9862 NP_109597 W288C not found in SNVbox database
394 NP_001070868 K489M not found in SNVbox database
810 NP_001070868 P273A not found in SNVbox database
2024 NP_001070868 Y672C not found in SNVbox database
2101 NP_001070868 G194R not found in SNVbox database
3453 NP_001070868 E21D not found in SNVbox database
3797 NP_001070868 D479E not found in SNVbox database
Reference base specified for sequencing variant TCGA-CC-A7IL-01A-11D-A33Q-10 chr19:58864478 C>A does not match reference base at that coordinate in hg19.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr10:52603786 T>A maps to NM_138932.2 R65R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A3KG-01A-11D-A20W-10 chr12:9241794 C>A did not map to a codon.
Sequencing variant TCGA-DD-A3A9-01A-11D-A25V-10 chr12:9258834 C>T maps to NM_000014.4 G367G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CK-01A-11D-A20W-10 chr12:9221387 T>C maps to NM_000014.4 P1438P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5262-01A-01D-A12Z-10 chr12:9027103 C>T maps to NM_144670.3 V1435V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr12:8990975 C>T maps to NM_144670.3 T300T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IL-01A-11D-A33Q-10 chr12:8988263 T>C did not map to a codon.
Sequencing variant TCGA-DD-A113-01A-11D-A12Z-10 chr12:9020502 G>A maps to NM_144670.3 E1261E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-4073-01B-02D-A12Z-10 chr3:151545692 T>G maps to NM_001086.2 Y311*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NR-01A-11D-A30V-10 chr3:151545467 A>G maps to NM_001086.2 S236S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A6M6-01A-11D-A32G-10 chr4:170991791 T>C maps to ENST00000509167 K226K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr16:70292099 G>A maps to ENST00000418685 C679C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LG-A6GG-01A-11D-A30V-10 chr16:70299542 A>G maps to ENST00000418685 Y423Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-4073-01B-02D-A12Z-10 chr4:57204729 C>A maps to NM_181806.2 G1045G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A5SI-01A-31D-A27I-10 chr4:57215516 G>T maps to NM_181806.2 Y800*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7ME-01A-11D-A33K-10 chr4:57219582 T>C maps to NM_181806.2 P521P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5264-01A-01D-A12Z-10 chr7:121756963 G>C maps to NM_005763.3 P245P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39Y-01A-11D-A20W-10 chr17:79094084 C>G maps to NM_001080395.2 L1217L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr9:107620922 T>A maps to NM_005502.3 S200S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39V-01A-11D-A20W-10 chr17:67210856 G>A maps to NM_080282.3 R332*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr2:215833479 A>G maps to NM_173076.2 D1914D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr2:215797447 G>T maps to NM_173076.2 A2566A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr2:215807646 A>G did not map to a codon.
Sequencing variant TCGA-BC-4073-01B-02D-A12Z-10 chr7:48318704 T>A maps to NM_152701.3 I2638I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MC-01A-11D-A22F-10 chr7:48319232 A>G maps to NM_152701.3 K2814K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr7:48634409 G>A did not map to a codon.
Sequencing variant TCGA-DD-A115-01A-11D-A12Z-10 chr7:48311638 A>G maps to NM_152701.3 K792K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EG-01A-11D-A20W-10 chr7:48313396 A>G maps to NM_152701.3 L1378L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EJ-01A-11D-A152-10 chr7:48318517 T>A maps to NM_152701.3 L2576*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NK-01A-11D-A28X-10 chr7:48287834 G>T did not map to a codon.
Sequencing variant TCGA-FV-A496-01A-11D-A25V-10 chr7:48559879 C>T maps to NM_152701.3 R4681*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A7M8-01A-11D-A33Q-10 chr7:48273679 A>T maps to NM_152701.3 K277*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A7M9-01A-23D-A34Z-10 chr7:48431662 G>T maps to NM_152701.3 E3934*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr7:48412075 T>C maps to NM_152701.3 F3705F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr7:48559634 A>T did not map to a codon.
Sequencing variant TCGA-BC-A10Z-01A-11D-A12Z-10 chr9:139904509 G>A maps to ENST00000355090 F2170F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39Z-01A-11D-A20W-10 chr9:139913716 A>G maps to ENST00000355090 Y519Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr16:2339467 C>T maps to NM_001089.2 E889E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A6M4-01A-11D-A32G-10 chr16:2338102 G>T maps to NM_001089.2 S976S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr16:2348542 T>C did not map to a codon.
Sequencing variant TCGA-DD-A39Z-01A-11D-A20W-10 chr1:94502754 C>A maps to NM_000350.2 T1253T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A7PZ-01A-11D-A33Q-10 chr1:94548998 T>A did not map to a codon.
Sequencing variant TCGA-G3-A5SJ-01A-11D-A27I-10 chr1:94577091 C>T maps to NM_000350.2 P68P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A6M4-01A-11D-A32G-10 chr1:94510166 A>C did not map to a codon.
Sequencing variant TCGA-ED-A7PZ-01A-11D-A33Q-10 chr17:67283766 A>T maps to ENST00000392677 A676A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A7M9-01A-23D-A34Z-10 chr17:67287402 C>T maps to ENST00000392677 K520K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr17:67111076 T>C maps to NM_080284.2 G536G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5263-01A-01D-A12Z-10 chr19:1051262 A>T maps to NM_019112.3 K932*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr19:1042060 A>T did not map to a codon.
Sequencing variant TCGA-BC-A3KF-01A-11D-A20W-10 chr17:66879990 A>G maps to NM_007168.2 T1176T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr17:66873814 T>C maps to NM_007168.2 L1308L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11A-01A-11D-A12Z-10 chr17:66873751 C>T maps to NM_007168.2 A1329A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10T-01A-11D-A12Z-10 chr7:87179343 C>T maps to NM_000927.3 R459R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-O8-A75V-01A-11D-A32G-10 chr7:87168616 G>T maps to NM_000927.3 L788L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A4XI-01A-11D-A25V-10 chr2:169791713 G>A maps to NM_003742.2 L1012L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A66Y-01A-11D-A30V-10 chr7:20785062 T>A did not map to a codon.
Sequencing variant TCGA-MI-A75E-01A-11D-A32G-10 chr7:20685482 C>A maps to NM_001163941.1 A261A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MA-01A-11D-A33Q-10 chr7:20738173 G>A did not map to a codon.
Sequencing variant TCGA-DD-A1EL-01A-11D-A152-10 chr2:220079776 C>A maps to NM_005689.2 T394T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39X-01A-11D-A20W-10 chr23:74295253 A>G did not map to a codon.
Sequencing variant TCGA-EP-A26S-01A-11D-A16V-10 chr23:74288849 C>A did not map to a codon.
Sequencing variant TCGA-KR-A7K2-01A-12D-A33Q-10 chr16:16139803 C>T maps to ENST00000399408 Y384Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A0-01A-11D-A20W-10 chr6:43413440 C>A maps to NM_033450.2 I1017I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7II-01A-11D-A33K-10 chr16:48119515 G>T maps to NM_033226.2 L1272L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25V-01A-11D-A16V-10 chr16:48149505 G>A maps to NM_033226.2 L603L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr13:95858956 G>T maps to NM_005845.3 I330I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5263-01A-01D-A12Z-10 chr3:183667833 T>A maps to NM_005688.2 A1008A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10R-01A-11D-A12Z-10 chr23:153001603 G>C did not map to a codon.
Sequencing variant TCGA-G3-A25T-01A-11D-A16V-10 chr23:152991038 C>T did not map to a codon.
Sequencing variant TCGA-DD-A73G-01A-22D-A32G-10 chr6:30557648 C>T maps to NM_001025091.1 L711L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11D-01A-11D-A12Z-10 chr2:44073331 G>T maps to NM_022437.2 L68L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A26S-01A-11D-A16V-10 chr2:44099244 G>T maps to NM_022437.2 T365T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75I-01A-11D-A32G-10 chr14:51368575 T>A maps to ENST00000337334 R270R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BW-A5NP-01A-11D-A27I-10 chr15:89738536 C>T maps to NM_152924.4 P387P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr15:89694905 A>G did not map to a codon.
Sequencing variant TCGA-CC-A3M9-01A-11D-A20W-10 chr18:19263895 C>T maps to NM_138340.4 A180A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A1-01A-11D-A20W-10 chr3:100569516 T>C maps to ENST00000471714 P478P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr9:133761036 G>T maps to NM_007313.2 S1139S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr4:8029483 A>T did not map to a codon.
Sequencing variant TCGA-LG-A6GG-01A-11D-A30V-10 chr4:8031434 G>A maps to NM_001130083.1 S372S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5261-01A-01D-A12Z-10 chr17:973213 A>T maps to NM_021962.2 S337S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NO-01A-11D-A28X-10 chr11:34189527 T>G maps to NM_145804.2 P525P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CK-01A-11D-A20W-10 chr17:35631110 A>G maps to NM_198834.1 Y327Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A6M6-01A-11D-A32G-10 chr17:35545225 C>T maps to NM_198834.1 R1589R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A112-01A-11D-A12Z-10 chr12:109617829 C>T maps to NM_001093.3 Q586*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A23B-01A-11D-A16V-10 chr12:109679058 A>G maps to NM_001093.3 K1665K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A7S9-01A-11D-A33Q-10 chr12:109637210 C>A maps to NM_001093.3 R878R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A7SB-01A-21D-A34Z-10 chr11:134131729 T>C maps to NM_014384.2 D346D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MA-01A-11D-A20W-10 chr1:76216191 T>C maps to ENST00000370834 Y335Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A2QQ-01A-11D-A22F-10 chr10:124812581 A>G maps to NM_001609.3 A378A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A123-01A-11D-A12Z-10 chr17:7126516 G>A maps to ENST00000356839 E427E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25S-01A-11D-A16V-10 chr17:7124265 T>C maps to ENST00000356839 N168N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3M9-01A-11D-A20W-10 chr15:89417181 C>A maps to NM_013227.3 V2481V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73B-01A-12D-A32G-10 chr15:89400396 G>A maps to NM_013227.3 R1527R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25S-01A-11D-A16V-10 chr15:89386655 G>A maps to NM_013227.3 L276L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KR-A7K8-01A-11D-A33K-10 chr15:89395100 C>A maps to NM_013227.3 I701I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MA-01A-11D-A33Q-10 chr15:89401572 G>A maps to NM_013227.3 S1919S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr17:7249577 T>C maps to NM_014716.3 I290I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A6M6-01A-11D-A32G-10 chr17:7254301 G>A maps to NM_014716.3 A702A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr3:195112842 T>A maps to NM_012287.5 A29A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5259-01A-31D-A20W-10 chr6:160184054 G>T maps to NM_005891.2 E54*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A7M6-01A-11D-A33Q-10 chr6:160197284 C>T maps to NM_005891.2 V246V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A9-01A-11D-A25V-10 chr10:27486369 T>A maps to ENST00000375888 K532*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NI-01A-11D-A27I-10 chr11:44073228 T>A maps to NM_001031854.2 S244S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KC-01A-11D-A20W-10 chr11:44072128 G>T maps to NM_001031854.2 E198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A9-01A-11D-A25V-10 chr17:61573827 C>T maps to NM_000789.3 L1152L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MD-01A-12D-A34Z-10 chr23:23731289 T>C did not map to a codon.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr2:111556609 T>A maps to NM_001142807.1 V160V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7II-01A-11D-A33K-10 chr2:111556209 T>C maps to NM_001142807.1 C123C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A1HT-01A-11D-A12Z-10 chr2:277012 C>T maps to NM_004300.3 T109T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr3:141011191 T>C maps to NM_001037172.1 S196S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MC-01A-11D-A22F-10 chr3:132061393 A>C did not map to a codon.
Sequencing variant TCGA-BC-A112-01A-11D-A12Z-10 chr19:51298213 C>T maps to NM_033068.2 I386I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BW-A5NO-01A-11D-A27I-10 chr23:70824087 G>A did not map to a codon.
Sequencing variant TCGA-T1-A6J8-01A-11D-A32G-10 chr5:131298317 C>T maps to NM_001009185.1 Q589Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NI-01A-11D-A27I-10 chr16:20494378 G>A did not map to a codon.
Sequencing variant TCGA-RC-A6M6-01A-11D-A32G-10 chr16:20476837 G>A did not map to a codon.
Sequencing variant TCGA-DD-A116-01A-11D-A12Z-10 chr15:35084615 G>A maps to NM_005159.4 V203V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11D-01A-11D-A12Z-10 chr1:18152299 G>C maps to NM_030812.2 L129L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CK-01A-11D-A20W-10 chr19:8807892 G>A maps to NM_178525.3 L387L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10Z-01A-11D-A12Z-10 chr1:236881237 C>A maps to NM_001103.2 G69G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11C-01A-11D-A12Z-10 chr1:236906332 T>C maps to NM_001103.2 T415T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A5SM-01A-12D-A28X-10 chr11:66330588 G>A maps to NM_001104.1 K877K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A7PZ-01A-11D-A33Q-10 chr19:39207844 G>A maps to NM_004924.3 P344P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A3JL-01A-11D-A20W-10 chr10:104247918 A>C maps to NM_005736.3 T101T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IL-01A-11D-A33Q-10 chr2:98275015 A>C maps to NM_005735.3 P177P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A118-01A-11D-A12Z-10 chr7:152549221 C>G maps to NM_020445.4 L321L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A5W4-01A-11D-A28X-10 chr3:53911740 A>C maps to NM_022899.4 L148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25W-01A-11D-A16V-10 chr3:53905466 C>T maps to NM_022899.4 G453G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10U-01A-11D-A12Z-10 chr23:127185962 C>T did not map to a codon.
Sequencing variant TCGA-BC-4073-01B-02D-A12Z-10 chr12:52374780 G>T maps to NM_020328.3 V203V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NI-01A-11D-A27I-10 chr2:148657132 C>T maps to NM_001616.3 Q124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A7M5-01A-11D-A33Q-10 chr2:148653867 A>T did not map to a codon.
Sequencing variant TCGA-RC-A6M6-01A-11D-A32G-10 chr2:148674982 A>G maps to NM_001616.3 A268A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A217-01A-11D-A152-10 chr12:52307457 C>T maps to NM_001077401.1 V143V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25S-01A-11D-A16V-10 chr12:52309853 C>T maps to NM_001077401.1 Y361Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A116-01A-11D-A12Z-10 chr4:123301310 G>A maps to NM_139243.3 A29A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr4:123336765 T>A maps to NM_139243.3 T494T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A7SK-01A-11D-A34Z-10 chr16:84230531 C>T maps to NM_139174.3 G650G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A0-01A-11D-A20W-10 chr17:42854588 G>C maps to NM_002390.4 G579G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A6M4-01A-11D-A32G-10 chr17:42854924 C>T maps to NM_002390.4 I619I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A7M9-01A-23D-A34Z-10 chr8:39505934 G>A maps to NM_014237.2 E373E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr14:70989893 A>G maps to NM_003814.4 S577S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39Z-01A-11D-A20W-10 chr2:207414829 T>C maps to NM_003812.2 G293G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr2:207346033 T>C did not map to a codon.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr2:207424749 T>A maps to NM_003812.2 I359I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr2:207436494 G>T maps to NM_003812.2 G537G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IF-01A-11D-A33K-10 chr4:175898868 G>A maps to NM_014269.4 Q731Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73A-01A-12D-A32G-10 chr4:175897951 C>T maps to NM_014269.4 L426L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr4:175897602 A>T maps to NM_014269.4 P309P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25S-01A-11D-A16V-10 chr8:39022553 C>T maps to NM_145004.5 F224F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr8:24346836 C>T maps to ENST00000380789 G419G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BD-A2L6-01A-11D-A20W-10 chr21:28211904 C>A did not map to a codon.
Sequencing variant TCGA-DD-A4NN-01A-11D-A28X-10 chr21:28210545 T>C maps to NM_006988.3 E752E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75I-01A-11D-A32G-10 chr21:28210527 C>T maps to NM_006988.3 Q758Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A459-01A-11D-A25V-10 chr5:33648937 G>A maps to NM_030955.2 Q490*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A7M5-01A-11D-A33Q-10 chr5:33576425 T>C maps to NM_030955.2 R1235R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NJ-01A-11D-A27I-10 chr15:100594227 G>A maps to NM_139057.2 N723N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7II-01A-11D-A33K-10 chr16:77355099 C>T did not map to a codon.
Sequencing variant TCGA-G3-A25S-01A-11D-A16V-10 chr16:77389916 G>T maps to NM_199355.2 I460I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25Z-01A-11D-A16V-10 chr16:77328999 T>C maps to NM_199355.2 T942T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr5:128863438 A>T did not map to a codon.
Sequencing variant TCGA-ED-A66Y-01A-11D-A30V-10 chr5:128887586 A>C maps to NM_133638.3 P447P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MA-01A-11D-A33Q-10 chr5:178562942 G>A maps to NM_014244.4 D684D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr5:178566985 C>G maps to NM_014244.4 R560R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5264-01A-01D-A12Z-10 chr12:43833852 C>A maps to ENST00000389420 G770G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IF-01A-11D-A33K-10 chr12:43860552 T>C maps to ENST00000389420 K423K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73G-01A-22D-A32G-10 chr12:43837681 A>G maps to ENST00000389420 Y734Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A7PZ-01A-11D-A33Q-10 chr12:43826448 A>G maps to ENST00000389420 H962H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr12:43847741 G>A maps to ENST00000389420 I576I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MF-01A-11D-A33K-10 chr12:43846136 A>T maps to ENST00000389420 V673V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A7-01A-11D-A22F-10 chr4:73176809 A>G maps to NM_014243.1 C670C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K7-A6G5-01A-11D-A30V-10 chr21:28296455 C>T maps to NM_007038.3 Q903Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr21:28306844 T>A maps to NM_007038.3 G543G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr5:64510630 A>G maps to NM_197941.2 T855T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5261-01A-01D-A12Z-10 chr15:79069905 G>A maps to ENST00000258883 D449D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr15:79080628 G>A maps to ENST00000258883 D422D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25U-01A-11D-A16V-10 chr15:79058505 G>A maps to ENST00000258883 T1249T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EK-01A-11D-A20W-10 chr3:64579955 C>T maps to NM_182920.1 W1445*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A26S-01A-11D-A16V-10 chr3:64582655 G>C maps to NM_182920.1 T1343T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BW-A5NO-01A-11D-A27I-10 chr9:18777037 C>G maps to NM_001040272.4 L937L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MB-01A-11D-A20W-10 chr9:18636001 T>C maps to NM_001040272.4 G221G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A217-01A-11D-A152-10 chr9:136402627 G>A maps to ENST00000393061 G173G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A3JL-01A-11D-A20W-10 chr15:84611386 T>C maps to NM_207517.2 C719C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr15:84694001 T>C maps to NM_207517.2 S1490S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1E9-01A-21D-A152-10 chr1:150531571 T>C maps to ENST00000369039 P921P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73G-01A-22D-A32G-10 chr1:150529205 G>A maps to ENST00000369039 R585R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr1:150526447 C>A maps to ENST00000369039 R327R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IK-01A-12D-A33Q-10 chr1:154569744 T>C did not map to a codon.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr1:154573590 T>C maps to ENST00000292205 L552L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A23B-01A-11D-A16V-10 chr16:75646505 G>A maps to NM_012091.3 I226I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr7:45717818 C>T maps to NM_021116.2 L619L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EG-01A-11D-A20W-10 chr1:167874252 G>C maps to NM_018417.4 V42V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr1:167849365 T>C maps to NM_018417.4 R401R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A113-01A-11D-A12Z-10 chr5:7773142 G>A maps to NM_020546.2 V771V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr5:7817091 G>C maps to NM_020546.2 V999V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr14:24792118 A>T maps to NM_139247.3 L778*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25W-01A-11D-A16V-10 chr3:123018992 G>T maps to NM_183357.2 A958A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73F-01A-11D-A32G-10 chr16:50339756 C>T maps to NM_001114.3 R583R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IK-01A-12D-A33Q-10 chr8:131797637 A>T maps to NM_001115.2 P1048P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A113-01A-11D-A12Z-10 chr8:131793000 G>A maps to NM_001115.2 Q1131*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NJ-01A-11D-A27I-10 chr8:131949434 G>A maps to NM_001115.2 C455C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A3RK-01A-11D-A22F-10 chr8:131848680 C>A maps to NM_001115.2 T839T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr8:131795973 G>T maps to NM_001115.2 I1077I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A5UC-01A-11D-A28X-10 chr16:4033249 G>A maps to NM_001116.3 S834S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr16:4164948 G>T maps to NM_001116.3 T165T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr7:31125005 A>G maps to ENST00000409489 K206K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RG-A7D4-01A-12D-A33Q-10 chr4:100232813 C>T did not map to a codon.
Sequencing variant TCGA-RC-A6M5-01A-11D-A32G-10 chr4:100052693 C>G maps to ENST00000505590 V287V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A496-01A-11D-A25V-10 chr2:3502748 C>T maps to NM_018269.3 L175L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A3R2-01A-11D-A22F-10 chr1:202914286 C>A maps to NM_015999.3 L147L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NN-01A-11D-A28X-10 chr20:49508565 A>C maps to NM_181442.1 P895P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A5SM-01A-12D-A28X-10 chr22:24837234 C>T maps to NM_000675.4 N339N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10W-01A-11D-A12Z-10 chr1:112042757 A>T maps to NM_000677.3 G257G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A112-01A-11D-A12Z-10 chr1:112042805 C>T maps to NM_000677.3 L241L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BW-A5NO-01A-11D-A27I-10 chr3:119306691 C>A maps to NM_001125.2 L347L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73E-01A-12D-A32G-10 chr3:119306619 G>A maps to NM_001125.2 V323V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A112-01A-11D-A12Z-10 chr5:159398904 G>A maps to NM_000679.3 L323L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GJ-A6C0-01A-12D-A30V-10 chr20:4228866 G>T maps to NM_000678.3 C246*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr20:4228554 C>A maps to NM_000678.3 L350L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MF-01A-11D-A33K-10 chr4:3768932 G>A maps to NM_000683.3 P200P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr11:67047307 A>T did not map to a codon.
Sequencing variant TCGA-ED-A7PY-01A-11D-A33Q-10 chr22:40742603 C>A maps to NM_000026.2 R14R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CH-01A-11D-A22F-10 chr14:105196357 T>C maps to NM_199165.1 S43S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10Q-01A-11D-A12Z-10 chr7:44147092 A>G maps to NM_001129.3 A217A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K7-A6G5-01A-11D-A30V-10 chr15:89169542 C>T maps to NM_022767.3 R35*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A7M5-01A-11D-A33Q-10 chr5:148682069 T>C maps to NM_152406.2 P139P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A112-01A-11D-A12Z-10 chr10:116060311 C>A maps to NM_001001936.1 P560P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A5UE-01A-11D-A28X-10 chr10:116061115 A>C maps to NM_001001936.1 A513A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KR-A7K0-01A-12D-A33Q-10 chr4:88048837 C>T maps to NM_001166693.1 Q983*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10Y-01A-11D-A12Z-10 chr23:147744244 T>A did not map to a codon.
Sequencing variant TCGA-BD-A2L6-01A-11D-A20W-10 chr23:148037576 A>G did not map to a codon.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr23:147743515 A>G did not map to a codon.
Sequencing variant TCGA-MI-A75I-01A-11D-A32G-10 chr23:148072844 G>C did not map to a codon.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr23:147967465 A>T did not map to a codon.
Sequencing variant TCGA-UB-A7MD-01A-12D-A34Z-10 chr23:148037266 A>T did not map to a codon.
Sequencing variant TCGA-DD-A3A9-01A-11D-A25V-10 chr2:100194856 C>T maps to NM_001025108.1 T975T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25T-01A-11D-A16V-10 chr18:12329713 T>C maps to NM_006796.2 R748R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K7-A6G5-01A-11D-A30V-10 chr18:12356734 T>G maps to NM_006796.2 G374G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10W-01A-11D-A12Z-10 chr17:76198607 G>A maps to NM_001145526.1 K61K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MC-01A-11D-A22F-10 chr17:76183501 G>A maps to NM_001145526.1 K17K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NN-01A-11D-A28X-10 chr12:58125708 G>A maps to NM_001122772.1 L612L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K7-A5RG-01A-11D-A28X-10 chr12:58121177 C>G maps to NM_001122772.1 T1015T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7II-01A-11D-A33K-10 chr15:87097614 G>A maps to NM_152336.2 K901K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A113-01A-11D-A12Z-10 chr15:86810274 A>G maps to NM_152336.2 S556S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr15:86702251 A>C maps to NM_152336.2 A115A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr15:87097674 C>A maps to NM_152336.2 S921S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BD-A2L6-01A-11D-A20W-10 chr11:47712148 C>T maps to ENST00000357610 G370G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BW-A5NP-01A-11D-A27I-10 chr11:47727468 C>T maps to ENST00000357610 W78*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IF-01A-11D-A33K-10 chr6:32149150 C>T maps to ENST00000375070 R396R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IL-01A-11D-A33Q-10 chr1:100356774 G>T did not map to a codon.
Sequencing variant TCGA-QA-A7B7-01A-11D-A32G-10 chr1:100350157 T>C maps to ENST00000311030 V861V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A5KG-01A-11D-A27I-10 chr1:15909712 T>G maps to NM_024758.3 A150A. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-EP-A2KB-01A-11D-A183-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-NI-A4U2-01A-11D-A28X-10 chr6:32138302 G>A maps to NM_032741.4 L137L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25S-01A-11D-A16V-10 chr21:45397992 C>G maps to NM_001037553.1 Y278*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25T-01A-11D-A16V-10 chr8:41469487 A>G maps to NM_178819.3 T226T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73E-01A-12D-A32G-10 chr1:230846422 A>G maps to NM_000029.3 N58N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr9:88292375 A>C maps to ENST00000395847 S137S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75I-01A-11D-A32G-10 chr5:177649436 G>A maps to NM_153373.2 N282N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A7PZ-01A-11D-A33Q-10 chr1:247013751 T>A maps to ENST00000428671 P1890P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QA-A7B7-01A-11D-A32G-10 chr1:247031036 G>T maps to ENST00000428671 I1093I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NF-01A-11D-A27I-10 chr1:110560139 T>A maps to NM_006621.4 A329A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EG-01A-11D-A20W-10 chr1:27876867 G>T maps to NM_001029882.2 R587R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LG-A6GG-01A-11D-A30V-10 chr6:135715920 A>C maps to NM_017651.4 T1034T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25U-01A-11D-A16V-10 chr11:62290410 C>A maps to NM_001620.1 V3826V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39X-01A-11D-A20W-10 chr14:105407780 T>C maps to NM_138420.2 E4669E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A5SM-01A-12D-A28X-10 chr14:105420944 C>T maps to NM_138420.2 S281S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A7M6-01A-11D-A33Q-10 chr5:427998 G>A maps to NM_020731.3 P284P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A7XO-01A-11D-A34Z-10 chr14:77931883 T>G maps to NM_012111.2 A188A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39V-01A-11D-A20W-10 chr6:31583457 C>T maps to NM_001623.3 D33D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HP-A5N0-01A-11D-A28X-10 chr23:129264034 G>A did not map to a codon.
Sequencing variant TCGA-DD-A3A0-01A-11D-A20W-10 chr22:21328151 G>T maps to NM_144704.2 V117V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A114-01A-11D-A12Z-10 chr6:106978190 G>T did not map to a codon.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr6:106999725 G>T did not map to a codon.
Sequencing variant TCGA-FV-A4ZQ-01A-11D-A25V-10 chr6:106968958 G>T maps to NM_001624.2 P884P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A7PZ-01A-11D-A33Q-10 chr1:159043067 A>G maps to NM_004833.1 Y74Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr1:159038417 T>A maps to NM_004833.1 A112A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11A-01A-11D-A12Z-10 chr1:4772502 C>G maps to NM_018836.3 A191A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EI-01A-11D-A12Z-10 chr14:96875278 G>A did not map to a codon.
Sequencing variant TCGA-G3-A7M5-01A-11D-A33Q-10 chr14:96875252 G>A maps to NM_152327.2 W158*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EA-01A-11D-A12Z-10 chr13:42877119 C>A maps to NM_016248.2 S1413*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-O8-A75V-01A-11D-A32G-10 chr13:42876850 A>T maps to NM_016248.2 P1323P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A118-01A-11D-A12Z-10 chr6:151670984 A>T maps to NM_005100.3 K487*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A115-01A-11D-A12Z-10 chr15:86236557 A>G maps to NM_006738.4 K1784K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A7PX-01A-51D-A34Z-10 chr15:86124169 A>T maps to NM_006738.4 G957G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A7PX-01A-51D-A34Z-10 chr15:86124170 C>T maps to NM_006738.4 Q958*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr15:86273744 A>G maps to NM_006738.4 E2367E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr15:86286976 C>A maps to NM_006738.4 T2775T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A66X-01A-11D-A30V-10 chr12:4724997 C>T maps to NM_006422.2 S823S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-4073-01B-02D-A12Z-10 chr23:49955716 A>T did not map to a codon.
Sequencing variant TCGA-CC-A3MA-01A-11D-A20W-10 chr23:49958533 T>C did not map to a codon.
Sequencing variant TCGA-CC-A7IK-01A-12D-A33Q-10 chr23:49958227 A>G did not map to a codon.
Sequencing variant TCGA-DD-A39Y-01A-11D-A20W-10 chr23:49963344 T>C did not map to a codon.
Sequencing variant TCGA-G3-A7M9-01A-23D-A34Z-10 chr23:49957906 G>T did not map to a codon.
Sequencing variant TCGA-BC-A10R-01A-11D-A12Z-10 chr14:33165313 A>T maps to NM_004274.4 K1000*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5258-01A-01D-A12Z-10 chr14:33014860 A>G maps to NM_004274.4 T334T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr7:91706166 A>G did not map to a codon.
Sequencing variant TCGA-MI-A75I-01A-11D-A32G-10 chr7:91669985 A>C did not map to a codon.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr7:91724334 A>T did not map to a codon.
Sequencing variant TCGA-G3-A25T-01A-11D-A16V-10 chr9:117113245 G>A maps to NM_030767.4 P1038P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr9:117118382 T>A maps to NM_030767.4 A960A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25T-01A-11D-A16V-10 chr1:109363222 A>G maps to NM_152763.3 C731C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A217-01A-11D-A152-10 chr10:5009198 T>C maps to NM_001353.5 V111V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73G-01A-22D-A32G-10 chr10:5139643 C>A maps to NM_003739.4 R91R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NI-01A-11D-A27I-10 chr10:4875658 G>T did not map to a codon.
Sequencing variant TCGA-CC-A7IJ-01A-11D-A33Q-10 chr1:19612756 G>A maps to NM_012067.2 D108D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A459-01A-11D-A25V-10 chr1:19596174 T>A did not map to a codon.
Sequencing variant TCGA-UB-A7MA-01A-11D-A33Q-10 chr19:40746008 G>T maps to NM_001626.3 V194V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25T-01A-11D-A16V-10 chr23:55040037 A>G did not map to a codon.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr4:74274384 T>C maps to NM_000477.5 C115C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr4:74275125 T>C maps to NM_000477.5 L179L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr4:74275204 G>A did not map to a codon.
Sequencing variant TCGA-G3-A3CJ-01A-11D-A20W-10 chr4:74282070 G>A did not map to a codon.
Sequencing variant TCGA-DD-A39Z-01A-11D-A20W-10 chr15:58306386 T>C maps to NM_003888.2 Q70Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25U-01A-11D-A16V-10 chr15:58247427 C>A maps to NM_003888.2 T508T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr15:101438326 C>T maps to NM_000693.2 L274L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A5SM-01A-12D-A28X-10 chr12:112220987 C>T maps to NM_000690.2 A82A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A6UC-01A-21D-A33K-10 chr5:125896799 T>C maps to NM_001182.3 E296E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NV-01A-11D-A30V-10 chr16:30080631 C>T maps to ENST00000395248 G236G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7II-01A-11D-A33K-10 chr16:5121882 G>A maps to NM_019109.4 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CK-01A-11D-A20W-10 chr12:38714456 T>C maps to NM_001013620.3 F288F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A5SJ-01A-11D-A27I-10 chr22:50303560 C>T maps to NM_024105.3 P215P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr23:110980010 G>T did not map to a codon.
Sequencing variant TCGA-G3-A25V-01A-11D-A16V-10 chr23:110951315 T>C did not map to a codon.
Sequencing variant TCGA-CC-5258-01A-01D-A12Z-10 chr3:129811028 C>A maps to NM_001136152.1 R73R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr9:101980977 C>T maps to NM_033087.3 E163E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A69H-01A-11D-A30V-10 chr3:183963595 T>C maps to NM_005787.5 T67T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A7SB-01A-21D-A34Z-10 chr13:37524128 G>A maps to NM_013338.4 R309*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A9-01A-11D-A25V-10 chr11:111740960 C>T maps to ENST00000428306 W320*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25S-01A-11D-A16V-10 chr2:29445232 G>A maps to NM_004304.3 F1164F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A7M5-01A-11D-A33Q-10 chr17:18088099 C>T maps to ENST00000261650 V181V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A114-01A-11D-A12Z-10 chr2:73677971 C>T maps to NM_015120.4 Q1439*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A7-01A-11D-A22F-10 chr2:73679797 T>A maps to NM_015120.4 Y2047*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10W-01A-11D-A12Z-10 chr17:6905063 C>T maps to NM_000697.2 H365H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A3I0-01A-11D-A22F-10 chr17:7980385 C>T maps to NM_001139.2 L399L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A3R2-01A-11D-A22F-10 chr17:7983974 C>A did not map to a codon.
Sequencing variant TCGA-CC-5262-01A-01D-A12Z-10 chr4:113352529 A>G maps to NM_025144.3 K609K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A2QR-01A-11D-A20W-10 chr18:56247583 C>A maps to NM_052947.3 E142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NO-01A-11D-A28X-10 chr15:85400701 A>C maps to NM_020778.4 T1113T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A459-01A-11D-A25V-10 chr15:85401061 G>T maps to NM_020778.4 L1233L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr1:21902358 G>T maps to NM_000478.4 A377A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A5UC-01A-11D-A28X-10 chr2:233272462 C>A maps to NM_031313.2 R154R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr2:202593825 C>T maps to NM_020919.3 K887K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A115-01A-11D-A12Z-10 chr2:202633599 T>G maps to NM_020919.3 S3S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr3:46722797 C>T maps to NM_147129.3 R458R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-O8-A75V-01A-11D-A32G-10 chr3:46727833 T>C maps to NM_147129.3 T210T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RG-A7D4-01A-12D-A33Q-10 chr2:202436740 T>C maps to NM_001168221.1 L252L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IJ-01A-11D-A33Q-10 chr2:202211383 C>A maps to NM_139163.2 V83V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr2:203834659 A>G maps to NM_024744.14 V324V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A23B-01A-11D-A16V-10 chr11:46419098 T>C maps to ENST00000458649 P1266P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25S-01A-11D-A16V-10 chr11:46430117 T>C maps to ENST00000458649 T1116T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IK-01A-12D-A33Q-10 chr16:56435756 T>A did not map to a codon.
Sequencing variant TCGA-CC-A7IL-01A-11D-A33Q-10 chr16:56396834 G>A maps to NM_001144.4 Q640*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CK-01A-11D-A20W-10 chr16:56443341 A>G maps to NM_001144.4 F169F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A3R3-01A-11D-A22F-10 chr23:109444277 C>T did not map to a codon.
Sequencing variant TCGA-BC-A69H-01A-11D-A30V-10 chr2:128628830 C>T maps to NM_031445.2 T170T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A495-01A-11D-A25V-10 chr23:112022292 C>G did not map to a codon.
Sequencing variant TCGA-DD-A73C-01A-12D-A33K-10 chr11:94533438 C>T maps to NM_130847.2 V361V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A7M9-01A-23D-A34Z-10 chr3:134076548 A>C maps to ENST00000514516 *838G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25S-01A-11D-A16V-10 chr1:115217492 C>T maps to NM_000036.2 K593K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11D-01A-11D-A12Z-10 chr1:110171047 C>T maps to ENST00000393689 S500S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75C-01A-11D-A32G-10 chr11:10527412 C>T maps to NM_000480.2 I771I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25V-01A-11D-A16V-10 chr3:49458963 A>G maps to NM_000481.3 S100S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NQ-01A-21D-A28X-10 chr7:2740123 G>A maps to NM_133463.1 G13G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75H-01A-11D-A32G-10 chr17:66246520 G>T maps to NM_016627.4 E65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A7SB-01A-21D-A34Z-10 chr14:77275408 T>C maps to NM_015305.3 P214P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EF-01A-11D-A12Z-10 chr8:108297061 G>T maps to NM_001146.3 P351P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1ED-01A-11D-A152-10 chr8:6420323 A>G maps to NM_001147.2 T44T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NJ-01A-11D-A27I-10 chr20:861811 A>C did not map to a codon.
Sequencing variant TCGA-DD-A4NG-01A-11D-A27I-10 chr1:178822881 A>G maps to NM_004673.3 H288H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A5SL-01A-11D-A27I-10 chr1:63063266 T>A maps to NM_014495.2 I10I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11D-01A-11D-A12Z-10 chr8:41559137 T>C maps to ENST00000415018 L797L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EB-01A-11D-A12Z-10 chr4:114278314 A>T maps to NM_001148.4 S2847S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RG-A7D4-01A-12D-A33Q-10 chr4:114275908 A>G maps to NM_001148.4 T2045T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr10:61829457 A>C maps to NM_020987.2 S3727S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr10:61956317 T>G maps to NM_020987.2 L585L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7II-01A-11D-A33K-10 chr17:54559742 G>A maps to NM_153228.2 Q709Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NQ-01A-21D-A28X-10 chr17:54535231 T>C maps to NM_153228.2 C486C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10Q-01A-11D-A12Z-10 chr17:4082166 G>A maps to NM_016376.3 S862S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A3RK-01A-11D-A22F-10 chr17:4098291 G>A maps to NM_016376.3 D451D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1E9-01A-21D-A152-10 chr5:139876826 C>T maps to ENST00000253810 Q990*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A3I1-01A-11D-A22F-10 chr5:139889379 T>C maps to ENST00000253810 C1308C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A3I1-01A-11D-A22F-10 chr5:139917172 A>T maps to ENST00000253810 S2426S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MB-01A-11D-A20W-10 chr7:92028082 T>C maps to NM_019004.1 S1030S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NV-01A-11D-A30V-10 chr7:92027848 A>G maps to NM_019004.1 S952S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KR-A7K0-01A-12D-A33Q-10 chr12:133319811 T>G maps to NM_015114.1 V427V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25S-01A-11D-A16V-10 chr2:241492432 C>T maps to ENST00000401804 L126L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A9-01A-11D-A25V-10 chr5:72857021 T>C maps to NM_023039.4 K127K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25S-01A-11D-A16V-10 chr13:111536108 C>T maps to NM_017664.2 T241T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MD-01A-12D-A34Z-10 chr13:111532382 G>C maps to NM_017664.2 S288S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MC-01A-11D-A22F-10 chr16:89352531 C>T maps to NM_013275.4 T269T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EA-01A-11D-A12Z-10 chr16:89349769 T>C maps to NM_013275.4 K1060K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A3KF-01A-11D-A20W-10 chr18:9255793 A>G maps to NM_015208.3 K843K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EI-01A-11D-A12Z-10 chr18:9258430 C>A maps to NM_015208.3 A1722A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GJ-A6C0-01A-12D-A30V-10 chr17:27940597 T>C maps to NM_152345.4 *627Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A26S-01A-11D-A16V-10 chr4:73990632 C>T maps to NM_032217.3 Q1163Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr4:74005965 T>C maps to NM_032217.3 P789P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr10:27306631 T>C maps to NM_014915.2 L1435L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CK-01A-11D-A20W-10 chr10:27337836 A>C maps to NM_014915.2 T569T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K7-A5RG-01A-11D-A28X-10 chr10:27356182 T>C maps to NM_014915.2 K370K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IG-01A-11D-A33K-10 chr10:37455582 G>T maps to ENST00000374660 A649A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A9-01A-11D-A25V-10 chr10:37507996 C>T maps to ENST00000374660 A1182A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A3I0-01A-11D-A22F-10 chr10:37506692 T>C maps to ENST00000374660 L1115L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A4ZP-01A-12D-A25V-10 chr10:37442510 G>A maps to ENST00000374660 E517E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75E-01A-11D-A32G-10 chr18:14763925 A>C maps to NM_001145029.1 A354A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr5:93989110 A>T maps to NM_032290.3 I339I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RG-A7D4-01A-12D-A33Q-10 chr5:94022287 A>G maps to NM_032290.3 S662S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11C-01A-11D-A12Z-10 chr1:145474730 T>A maps to NM_001039888.2 L468*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr2:197954756 C>A did not map to a codon.
Sequencing variant TCGA-G3-A25T-01A-11D-A16V-10 chr1:173596299 T>C did not map to a codon.
Sequencing variant TCGA-BC-A10Z-01A-11D-A12Z-10 chr8:101540170 G>A maps to NM_198401.2 V124V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11C-01A-11D-A12Z-10 chr12:56648359 A>G did not map to a codon.
Sequencing variant TCGA-G3-A6UC-01A-21D-A33K-10 chr5:55472049 A>G maps to NM_024669.2 L81L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25S-01A-11D-A16V-10 chr9:101552845 C>T maps to ENST00000375018 G134G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A0-01A-11D-A20W-10 chr7:36445865 T>G maps to NM_018685.2 L188L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EF-01A-11D-A12Z-10 chr12:5936959 G>A maps to ENST00000356134 A286A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MA-01A-11D-A20W-10 chr12:101333216 A>G maps to ENST00000392977 E95E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EF-01A-11D-A12Z-10 chr12:101365127 C>T maps to ENST00000392977 A167A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NG-01A-11D-A27I-10 chr19:17443814 G>A maps to NM_020959.2 R170R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A7S9-01A-11D-A33Q-10 chr19:17442016 G>T maps to NM_020959.2 I237I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A1HT-01A-11D-A12Z-10 chr11:418529 C>T maps to NM_001012302.2 S730S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EF-01A-11D-A12Z-10 chr15:69076892 G>A maps to NM_006305.3 C123C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75G-01A-11D-A32G-10 chr12:48866815 C>T maps to NM_012404.2 C123C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75C-01A-11D-A32G-10 chr15:90335705 C>T maps to NM_001150.2 W779*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A69H-01A-11D-A30V-10 chr2:69379335 C>T maps to NM_032208.2 I329I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr2:69304559 T>C maps to NM_032208.2 S194S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr4:80899211 T>A maps to NM_001145794.1 R432R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75C-01A-11D-A32G-10 chr9:75782425 A>T maps to NM_000700.1 T272T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BD-A3EP-01A-11D-A22F-10 chr8:124705520 C>T maps to NM_001003954.1 W227*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr4:122607463 G>T maps to NM_001154.3 R25R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MF-01A-11D-A33K-10 chr1:150960817 G>A did not map to a codon.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr4:113174412 G>A did not map to a codon.
Sequencing variant TCGA-DD-A3A7-01A-11D-A22F-10 chr22:29724845 G>A maps to NM_001127.3 H938H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39Z-01A-11D-A20W-10 chr16:71779498 T>C maps to ENST00000423132 R606R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39Z-01A-11D-A20W-10 chr16:71798317 C>A maps to ENST00000423132 G308*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-O8-A75V-01A-11D-A32G-10 chr19:16319966 C>A maps to NM_001130524.1 V175V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1E9-01A-21D-A152-10 chr19:50302170 C>T maps to NM_014203.2 I309I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A6M3-01A-11D-A32G-10 chr19:50306438 G>A maps to NM_014203.2 Q771Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A3KF-01A-11D-A20W-10 chr11:992670 A>T maps to ENST00000332231 K481*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MA-01A-11D-A20W-10 chr11:993285 T>C maps to ENST00000332231 A486A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IK-01A-12D-A33Q-10 chr17:33921085 G>T maps to NM_001030006.1 G13*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr17:33925249 A>G maps to NM_001030006.1 G13G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A112-01A-11D-A12Z-10 chr5:77412059 T>C did not map to a codon.
Sequencing variant TCGA-G3-A7M6-01A-11D-A33Q-10 chr5:77298848 T>C maps to NM_003664.3 S1054S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A3KG-01A-11D-A20W-10 chr15:83331626 C>A maps to NM_004644.3 R865R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25Z-01A-11D-A16V-10 chr15:83331890 G>T maps to NM_004644.3 T845T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T1-A6J8-01A-11D-A32G-10 chr15:83330628 C>T maps to NM_004644.3 G969G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr19:2138616 C>T did not map to a codon.
Sequencing variant TCGA-G3-A25S-01A-11D-A16V-10 chr8:42012432 T>C maps to NM_006803.3 P76P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PD-A5DF-01A-11D-A27I-10 chr15:51223096 C>T maps to NM_007347.3 H266H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EB-01A-11D-A12Z-10 chr9:72064663 C>A maps to NM_001163.3 E673*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NK-01A-11D-A28X-10 chr9:72131730 C>T maps to NM_001163.3 Q132Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A3I1-01A-11D-A22F-10 chr15:29398964 C>T maps to NM_005503.3 S620S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BD-A2L6-01A-11D-A20W-10 chr11:6422249 G>C maps to ENST00000389906 Y547*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A8-01A-11D-A22F-10 chr5:112111379 C>G maps to NM_001127510.2 Y159*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NP-01A-11D-A28X-10 chr5:112111323 A>G did not map to a codon.
Sequencing variant TCGA-KR-A7K7-01A-11D-A33K-10 chr5:112174285 C>T maps to NM_001127510.2 Q999*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NN-01A-11D-A28X-10 chr19:1456315 G>A maps to NM_005883.2 A243A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NJ-01A-11D-A27I-10 chr18:10468487 C>T maps to ENST00000423585 L78L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A12J-01A-11D-A12Z-10 chr18:10471886 C>T maps to ENST00000423585 A252A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75H-01A-11D-A32G-10 chr18:10488025 C>A maps to ENST00000423585 I563I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A5SI-01A-31D-A27I-10 chr3:49719194 C>T maps to ENST00000438011 S493S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MF-01A-11D-A33K-10 chr3:49720484 C>T maps to ENST00000438011 L672L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr23:55033577 A>T did not map to a codon.
Sequencing variant TCGA-DD-A73E-01A-12D-A32G-10 chr15:63571456 C>T maps to NM_031301.3 L71L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10Q-01A-11D-A12Z-10 chr11:43364047 A>G maps to NM_001142930.1 G521G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr19:36370025 C>A maps to NM_001024807.1 I588I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A5SL-01A-11D-A27I-10 chr19:36363454 C>T maps to NM_001024807.1 H307H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IG-01A-11D-A33K-10 chr2:21246407 C>A maps to NM_000384.2 E865*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A113-01A-11D-A12Z-10 chr2:21228861 A>C maps to NM_000384.2 T3626T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A66Y-01A-11D-A30V-10 chr2:21249794 A>G maps to NM_000384.2 A703A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25W-01A-11D-A16V-10 chr2:21235441 G>T maps to NM_000384.2 S1433*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KR-A7K2-01A-12D-A33Q-10 chr2:21229488 G>T maps to NM_000384.2 T3417T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr22:39421149 A>C maps to NM_152426.3 R96R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MF-01A-11D-A33K-10 chr22:39421640 T>C maps to NM_152426.3 Y190Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11A-01A-11D-A12Z-10 chr11:116701501 C>T maps to ENST00000360377 A41A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr3:195306236 C>A maps to ENST00000421243 P60P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A4ZQ-01A-11D-A25V-10 chr17:64210646 A>G maps to NM_000042.2 N302N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NS-01A-11D-A30V-10 chr22:36587461 G>A maps to ENST00000332987 A235A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25V-01A-11D-A16V-10 chr6:31625486 T>C maps to NM_019101.2 T176T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A6M4-01A-11D-A32G-10 chr23:84301521 A>G did not map to a codon.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr12:105605023 T>A maps to NM_018171.3 R119R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IK-01A-12D-A33Q-10 chr1:154296108 G>C maps to NM_080429.2 L178L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A1-01A-11D-A20W-10 chr9:33442306 T>C maps to NM_004925.3 A234A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A12J-01A-11D-A12Z-10 chr9:33386143 G>A maps to NM_001170.1 V152V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39Z-01A-11D-A20W-10 chr15:35166046 A>G maps to NM_014691.2 P1193P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10Z-01A-11D-A12Z-10 chr23:66766452 G>A did not map to a codon.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr23:66766305 A>G did not map to a codon.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr23:66937426 A>C did not map to a codon.
Sequencing variant TCGA-CC-5263-01A-01D-A12Z-10 chr23:47428284 G>T did not map to a codon.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr23:47430810 T>A did not map to a codon.
Sequencing variant TCGA-G3-A25T-01A-11D-A16V-10 chr11:72404495 G>T maps to NM_001040118.2 T1276T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25U-01A-11D-A16V-10 chr11:72407663 G>T maps to NM_001040118.2 R1068R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A123-01A-11D-A12Z-10 chr5:141036085 C>A maps to NM_022481.5 L1258L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MB-01A-11D-A20W-10 chr5:141059771 G>A maps to NM_022481.5 P94P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A116-01A-11D-A12Z-10 chr5:141033642 C>A maps to NM_022481.5 L1503L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39W-01A-11D-A20W-10 chr5:141051869 T>A did not map to a codon.
Sequencing variant TCGA-ED-A7XP-01A-11D-A34Z-10 chr11:118452208 G>A maps to ENST00000359415 R125R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A7SK-01A-11D-A34Z-10 chr4:75312479 T>A maps to NM_001657.2 I97I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A7SK-01A-11D-A34Z-10 chr4:75482234 T>A maps to NM_001657.2 I97I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1ED-01A-11D-A152-10 chr3:57563093 A>G maps to NM_001660.3 D93D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MA-01A-11D-A20W-10 chr11:6501573 A>G maps to NM_012402.2 P26P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr4:148802994 G>T maps to NM_024605.3 G316*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39X-01A-11D-A20W-10 chr4:148778701 A>G did not map to a codon.
Sequencing variant TCGA-G3-A7M7-01A-12D-A34Z-10 chr10:32150409 C>G maps to NM_018287.5 G287G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A7M9-01A-23D-A34Z-10 chr2:144314010 C>A maps to NM_018460.3 G320G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MA-01A-11D-A20W-10 chr16:24958828 A>G maps to NM_001006634.1 P405P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EH-01A-11D-A12Z-10 chr6:129927036 G>A maps to NM_033515.2 N450N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr6:129937449 T>C did not map to a codon.
Sequencing variant TCGA-NI-A4U2-01A-11D-A28X-10 chr11:110477434 G>A maps to NM_020809.2 R272*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A9-01A-11D-A25V-10 chr4:86852133 A>T maps to NM_031305.2 S17S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4ND-01A-11D-A25V-10 chr2:69049533 C>T maps to NM_001007231.2 D421D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr2:69043418 A>G did not map to a codon.
Sequencing variant TCGA-G3-A7M5-01A-11D-A33Q-10 chr2:69034417 G>A maps to NM_001007231.2 Q160Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3M9-01A-11D-A20W-10 chr5:142435641 A>T maps to NM_015071.4 K475*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11A-01A-11D-A12Z-10 chr18:6887165 C>T maps to ENST00000400091 H488H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11C-01A-11D-A12Z-10 chr3:119087230 C>G maps to NM_020754.2 G72G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A66Y-01A-11D-A30V-10 chr3:119134791 C>A maps to NM_020754.2 S1339*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A2QR-01A-11D-A20W-10 chr11:128932246 T>C maps to NM_001142685.1 G283G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25Y-01A-11D-A16V-10 chr11:129034322 C>A did not map to a codon.
Sequencing variant TCGA-DD-A113-01A-11D-A12Z-10 chr19:36278139 G>A maps to ENST00000007510 P891P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MA-01A-11D-A33Q-10 chr19:36278733 C>T maps to ENST00000007510 I1089I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MA-01A-11D-A20W-10 chr23:130220616 T>C did not map to a codon.
Sequencing variant TCGA-FV-A3R2-01A-11D-A22F-10 chr23:130219932 G>T did not map to a codon.
Sequencing variant TCGA-DD-A118-01A-11D-A12Z-10 chr23:153185068 G>T did not map to a codon.
Sequencing variant TCGA-ED-A4XI-01A-11D-A25V-10 chr14:32563378 T>A maps to NM_001030055.1 Y1168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A118-01A-11D-A12Z-10 chr23:11206889 C>T did not map to a codon.
Sequencing variant TCGA-DD-A4ND-01A-11D-A25V-10 chr23:11162338 G>A did not map to a codon.
Sequencing variant TCGA-G3-A25W-01A-11D-A16V-10 chr1:17981128 A>G did not map to a codon.
Sequencing variant TCGA-RC-A6M3-01A-11D-A32G-10 chr1:156917231 C>T maps to NM_198236.1 V784V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25S-01A-11D-A16V-10 chr11:120329985 A>G maps to NM_015313.2 L828L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A5KG-01A-11D-A27I-10 chr17:8215881 C>T maps to NM_173728.3 L175L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr11:73066690 A>G maps to NM_014786.3 L1189L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A69H-01A-11D-A30V-10 chr19:7535138 C>G maps to NM_001130955.1 L1159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A118-01A-11D-A12Z-10 chr19:7516108 C>T maps to NM_001130955.1 T416T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-O8-A75V-01A-11D-A32G-10 chr19:7528839 G>A maps to NM_001130955.1 K736K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EB-01A-11D-A12Z-10 chr23:135767929 G>C did not map to a codon.
Sequencing variant TCGA-DD-A1EL-01A-11D-A152-10 chr23:135757210 C>G did not map to a codon.
Sequencing variant TCGA-FV-A4ZP-01A-12D-A25V-10 chr23:135863019 C>T did not map to a codon.
Sequencing variant TCGA-DD-A3A7-01A-11D-A22F-10 chr13:111927940 C>A maps to NM_001113511.1 I466I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EB-01A-11D-A12Z-10 chr23:62926263 G>T did not map to a codon.
Sequencing variant TCGA-BC-A10W-01A-11D-A12Z-10 chr1:27056353 G>A maps to NM_006015.4 Q450Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5262-01A-01D-A12Z-10 chr1:27099007 C>T maps to NM_006015.4 Q1142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EH-01A-11D-A12Z-10 chr1:27105549 C>T maps to NM_006015.4 R1721*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39W-01A-11D-A20W-10 chr1:27099007 C>T maps to NM_006015.4 Q1142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A23B-01A-11D-A16V-10 chr1:27101341 G>T maps to NM_006015.4 E1542*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LG-A6GG-01A-11D-A30V-10 chr1:27102065 A>T did not map to a codon.
Sequencing variant TCGA-CC-5264-01A-01D-A12Z-10 chr6:157502281 C>G maps to ENST00000367148 V1145V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A3KF-01A-11D-A20W-10 chr12:46231165 T>C maps to NM_152641.2 C362C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A5SL-01A-11D-A27I-10 chr12:46245722 C>T maps to NM_152641.2 R1273*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7ME-01A-11D-A33K-10 chr19:968402 A>T did not map to a codon.
Sequencing variant TCGA-CC-A7II-01A-11D-A33K-10 chr15:74836780 C>T maps to ENST00000395077 V168V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A6M6-01A-11D-A32G-10 chr15:74836588 T>C maps to ENST00000395077 D104D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NV-01A-11D-A30V-10 chr10:63850752 A>T maps to NM_032199.2 R511*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A9-01A-11D-A25V-10 chr23:100240895 C>A did not map to a codon.
Sequencing variant TCGA-GJ-A6C0-01A-12D-A30V-10 chr3:160395170 C>T maps to NM_025047.2 Q13*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A495-01A-11D-A25V-10 chr2:152670805 T>C maps to NM_012097.3 T44T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr16:18810099 C>T maps to NM_015161.1 L31L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73C-01A-12D-A33K-10 chr4:57384921 C>A maps to ENST00000360096 S96*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A217-01A-11D-A152-10 chr10:23297250 C>A maps to NM_173081.3 R626R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11C-01A-11D-A12Z-10 chr10:23326200 T>C maps to NM_173081.3 A804A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LG-A6GG-01A-11D-A30V-10 chr10:23244757 C>T maps to NM_173081.3 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EK-01A-11D-A20W-10 chr23:100808328 C>A did not map to a codon.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr23:100808408 A>G did not map to a codon.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr23:100880233 A>T did not map to a codon.
Sequencing variant TCGA-BC-A10T-01A-11D-A12Z-10 chr23:100871411 G>T did not map to a codon.
Sequencing variant TCGA-CC-A7IK-01A-12D-A33Q-10 chr23:100871177 C>A did not map to a codon.
Sequencing variant TCGA-UB-A7ME-01A-11D-A33K-10 chr1:150788839 T>A maps to NM_001668.3 S615S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T1-A6J8-01A-11D-A32G-10 chr15:80873587 A>T maps to NM_014862.3 P587P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10R-01A-11D-A12Z-10 chr11:13398210 C>T maps to ENST00000403290 D450D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A495-01A-11D-A25V-10 chr23:69501564 C>T did not map to a codon.
Sequencing variant TCGA-HP-A5N0-01A-11D-A28X-10 chr11:74980003 C>T did not map to a codon.
Sequencing variant TCGA-DD-A118-01A-11D-A12Z-10 chr23:2835843 C>T did not map to a codon.
Sequencing variant TCGA-CC-A7IL-01A-11D-A33Q-10 chr23:3019188 A>G did not map to a codon.
Sequencing variant TCGA-DD-A11A-01A-11D-A12Z-10 chr5:149677215 C>T maps to NM_001012301.2 W424*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75H-01A-11D-A32G-10 chr5:149677631 A>G maps to NM_001012301.2 G285G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr11:3681382 C>T maps to NM_004314.2 Q212*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A69H-01A-11D-A30V-10 chr4:77025762 A>G maps to NM_001130016.1 P328P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7ME-01A-11D-A33K-10 chr11:3661592 A>T maps to NM_001079536.1 A22A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A0-01A-11D-A20W-10 chr22:19959473 G>T maps to NM_001670.2 R906R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A216-01A-11D-A152-10 chr23:25033825 C>G did not map to a codon.
Sequencing variant TCGA-CC-A5UD-01A-11D-A28X-10 chr23:25033711 T>A did not map to a codon.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr8:17933072 T>A maps to NM_004315.4 S50S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5258-01A-01D-A12Z-10 chr8:131164980 C>T did not map to a codon.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr8:131130887 A>G maps to NM_018482.2 Y547Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39Y-01A-11D-A20W-10 chr2:9515030 T>C maps to NM_003887.2 D568D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A216-01A-11D-A152-10 chr2:239353033 T>C maps to NM_001040445.1 P182P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25V-01A-11D-A16V-10 chr23:63445127 T>C did not map to a codon.
Sequencing variant TCGA-BW-A5NP-01A-11D-A27I-10 chr10:5683745 G>A maps to NM_024701.3 F232F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MA-01A-11D-A20W-10 chr10:5691032 G>A maps to NM_024701.3 V139V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5258-01A-01D-A12Z-10 chr7:123270024 T>C maps to NM_080928.3 C482C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr17:42255626 C>T maps to NM_080863.4 L411L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5258-01A-01D-A12Z-10 chr14:94405768 G>A maps to ENST00000434324 G434G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A23B-01A-11D-A16V-10 chr14:94405780 C>T maps to ENST00000434324 L430L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A7M7-01A-12D-A34Z-10 chr7:95157218 C>T maps to NM_016116.2 Y194Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A9-01A-11D-A25V-10 chr4:177190076 T>C maps to NM_080874.3 V61V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IK-01A-12D-A33Q-10 chr10:73892878 T>C maps to NM_001198800.1 K269K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A5UD-01A-11D-A28X-10 chr1:155449285 T>A maps to ENST00000368346 A1125A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr1:155451022 T>C maps to ENST00000368346 P546P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10W-01A-11D-A12Z-10 chr20:32856829 C>A maps to NM_001672.2 R86R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A8-01A-11D-A22F-10 chr23:1752179 G>A did not map to a codon.
Sequencing variant TCGA-G3-A7M7-01A-12D-A34Z-10 chr19:12856229 G>T maps to NM_004317.2 E117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A5UD-01A-11D-A28X-10 chr7:97484709 T>A maps to NM_183356.3 G364G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A4XI-01A-11D-A25V-10 chr2:190531502 G>T maps to NM_019048.2 L215L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A7M5-01A-11D-A33Q-10 chr19:51015947 G>A maps to NM_001114598.1 I134I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K7-A5RG-01A-11D-A28X-10 chr1:176853523 G>T maps to ENST00000281881 L1067L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr9:119858431 T>A did not map to a codon.
Sequencing variant TCGA-DD-A1EF-01A-11D-A12Z-10 chr20:31016043 A>G maps to ENST00000375687 E122E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39Z-01A-11D-A20W-10 chr20:31024705 T>C maps to ENST00000375687 G1397G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25T-01A-11D-A16V-10 chr20:31019175 C>T maps to ENST00000375687 S257S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A5UD-01A-11D-A28X-10 chr18:31320037 A>T maps to NM_030632.1 T890T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr7:117003769 A>G maps to NM_130768.2 H436H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A3R3-01A-11D-A22F-10 chr8:124382253 T>C maps to NM_014109.3 E246E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A5SJ-01A-11D-A27I-10 chr8:124408567 C>T maps to NM_014109.3 L10L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A3RK-01A-11D-A22F-10 chr2:23980354 A>G maps to NM_017552.1 C1337C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25S-01A-11D-A16V-10 chr19:3905456 C>T maps to NM_033064.4 N54N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A7PZ-01A-11D-A33Q-10 chr1:161832996 A>T maps to NM_007348.2 S538S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IK-01A-12D-A33Q-10 chr6:32085718 T>A maps to NM_004381.4 P447P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A82E-01A-11D-A34Z-10 chr12:53928284 C>G did not map to a codon.
Sequencing variant TCGA-BC-A10U-01A-11D-A12Z-10 chr16:10574814 A>G maps to NM_024997.2 A543A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A2QR-01A-11D-A20W-10 chr16:10527418 G>A maps to NM_024997.2 E291E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr11:72538272 G>T maps to NM_033388.1 V469V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr11:64681336 C>T maps to ENST00000421419 P182P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A23B-01A-11D-A16V-10 chr11:64664265 G>T maps to ENST00000421419 P1744P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39Z-01A-11D-A20W-10 chr14:96798728 C>A maps to NM_018036.5 E461*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75G-01A-11D-A32G-10 chr14:96781502 G>A maps to NM_018036.5 S1210S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75I-01A-11D-A32G-10 chr2:242590730 G>A maps to ENST00000337606 R171R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39X-01A-11D-A20W-10 chr19:10659670 T>C maps to NM_032885.4 G309G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A113-01A-11D-A12Z-10 chr14:51087445 T>A did not map to a codon.
Sequencing variant TCGA-BC-A10W-01A-11D-A12Z-10 chr11:108127031 G>T maps to NM_000051.3 E739*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr11:108175445 T>C maps to NM_000051.3 H1847H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A6M4-01A-11D-A32G-10 chr16:81076058 T>C maps to NM_015251.2 T212T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39X-01A-11D-A20W-10 chr12:7050121 T>C maps to NM_001940.3 T1098T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A2QQ-01A-11D-A22F-10 chr12:7047885 C>T maps to NM_001940.3 V920V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25V-01A-11D-A16V-10 chr12:7047717 A>G maps to NM_001940.3 E864E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5264-01A-01D-A12Z-10 chr15:25953216 C>T maps to NM_024490.3 L827L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HP-A5N0-01A-11D-A28X-10 chr5:160113231 G>A maps to NM_025153.2 P108P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A7SK-01A-11D-A34Z-10 chr5:159992726 T>C maps to NM_025153.2 T1373T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K7-A5RF-01A-11D-A28X-10 chr23:138878507 T>A did not map to a codon.
Sequencing variant TCGA-BC-A10Y-01A-11D-A12Z-10 chr19:19756557 C>T maps to NM_020410.2 L1134L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A23B-01A-11D-A16V-10 chr19:19756682 T>C maps to NM_020410.2 K1120K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A5UE-01A-11D-A28X-10 chr1:17331928 C>A maps to NM_022089.2 R76R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EA-01A-11D-A12Z-10 chr3:194126803 G>A maps to NM_024524.3 A1175A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IJ-01A-11D-A33Q-10 chr3:193025124 G>A maps to NM_198505.2 N853N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5262-01A-01D-A12Z-10 chr1:160104351 G>T maps to NM_000702.3 E636*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IK-01A-12D-A33Q-10 chr1:160098467 C>A maps to NM_000702.3 R348R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr19:42471492 C>A did not map to a codon.
Sequencing variant TCGA-DD-A3A9-01A-11D-A25V-10 chr1:160141548 T>C did not map to a codon.
Sequencing variant TCGA-FV-A496-01A-11D-A25V-10 chr1:160121862 T>G maps to NM_144699.3 A11A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5262-01A-01D-A12Z-10 chr23:119505027 G>T did not map to a codon.
Sequencing variant TCGA-G3-A25Z-01A-11D-A16V-10 chr23:119509403 T>C did not map to a codon.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr16:28914130 C>A maps to NM_173201.3 T881T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr12:110729904 C>A maps to NM_170665.3 A100A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LG-A6GG-01A-11D-A30V-10 chr12:89998054 G>A maps to ENST00000428670 S837S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A7SK-01A-11D-A34Z-10 chr12:89992430 T>C maps to NM_001001323.1 V1147V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr3:10370617 T>A maps to NM_001001331.2 S1204S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3M9-01A-11D-A20W-10 chr23:152835146 C>T did not map to a codon.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr3:130714896 G>T maps to NM_001001486.1 E690*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10Y-01A-11D-A12Z-10 chr16:84486811 A>T maps to ENST00000416219 K634*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5260-01A-01D-A12Z-10 chr16:84482137 G>T did not map to a codon.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr16:84459338 A>T did not map to a codon.
Sequencing variant TCGA-G3-A25S-01A-11D-A16V-10 chr19:36050919 G>A maps to NM_000704.2 I281I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1ED-01A-11D-A152-10 chr12:57038964 G>A maps to NM_001686.3 A100A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25U-01A-11D-A16V-10 chr12:54063080 G>A maps to NM_005176.5 V111V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A113-01A-11D-A12Z-10 chr23:153657460 T>A did not map to a codon.
Sequencing variant TCGA-G3-A25V-01A-11D-A16V-10 chr12:124221769 T>C maps to NM_012463.3 C330C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MF-01A-11D-A33K-10 chr16:67472439 A>T maps to NM_004691.4 P349P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr7:128505617 G>T maps to ENST00000492758 E144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr6:31513187 G>T maps to NM_130463.2 A118A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25V-01A-11D-A16V-10 chr8:54742069 C>A maps to NM_015941.2 L80L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5259-01A-31D-A20W-10 chr23:77244074 T>C did not map to a codon.
Sequencing variant TCGA-DD-A11D-01A-11D-A12Z-10 chr23:77243770 T>A did not map to a codon.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr23:77258576 T>C did not map to a codon.
Sequencing variant TCGA-DD-A1EK-01A-11D-A20W-10 chr13:52548362 G>A maps to NM_000053.2 A331A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75H-01A-11D-A32G-10 chr4:42583636 C>A did not map to a codon.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr4:42446618 T>C maps to NM_006095.2 G997G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NI-01A-11D-A27I-10 chr13:26586734 C>A maps to NM_016529.4 G1148G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25V-01A-11D-A16V-10 chr13:26411377 C>T maps to NM_016529.4 P944P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr13:26349094 G>T maps to NM_016529.4 E893*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25W-01A-11D-A16V-10 chr19:1807172 G>A maps to NM_138813.2 D203D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A7PZ-01A-11D-A33Q-10 chr20:50305603 T>A maps to NM_006045.1 S266S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A6M4-01A-11D-A32G-10 chr1:47110922 T>C maps to NM_022745.3 L198L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EF-01A-11D-A12Z-10 chr3:142215985 C>T maps to NM_001184.3 Q1869Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A7M7-01A-12D-A34Z-10 chr3:142275250 A>C maps to NM_001184.3 S684S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75G-01A-11D-A32G-10 chr3:142217616 C>A did not map to a codon.
Sequencing variant TCGA-BC-A217-01A-11D-A152-10 chr3:48506378 G>A maps to NM_130384.1 K735K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A113-01A-11D-A12Z-10 chr10:117607491 T>A maps to NM_207303.2 P1336P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HP-A5MZ-01A-21D-A27I-10 chr10:117486765 T>C maps to NM_207303.2 L1268L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A3KF-01A-11D-A20W-10 chr23:76856033 C>T did not map to a codon.
Sequencing variant TCGA-DD-A1ED-01A-11D-A152-10 chr23:76972656 T>C did not map to a codon.
Sequencing variant TCGA-DD-A4NK-01A-11D-A28X-10 chr23:76938216 G>A did not map to a codon.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr23:76938244 T>A did not map to a codon.
Sequencing variant TCGA-DD-A39Z-01A-11D-A20W-10 chr12:111963043 T>C maps to NM_002973.3 A376A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NK-01A-11D-A28X-10 chr16:28846464 T>A maps to NM_148414.1 P840P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A4XI-01A-11D-A25V-10 chr16:28846410 A>G maps to NM_148414.1 P822P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EB-01A-11D-A12Z-10 chr23:13337138 G>T did not map to a codon.
Sequencing variant TCGA-DD-A3A2-01A-11D-A20W-10 chr3:63982026 G>A maps to NM_001177387.1 S843S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A459-01A-11D-A25V-10 chr20:54961583 T>A maps to NM_198437.1 T16T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T1-A6J8-01A-11D-A32G-10 chr7:69583170 A>T maps to NM_015570.2 G192G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EL-01A-11D-A152-10 chr12:63544148 C>T maps to NM_000706.3 P156P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BW-A5NP-01A-11D-A27I-10 chr16:347720 C>T did not map to a codon.
Sequencing variant TCGA-FV-A23B-01A-11D-A16V-10 chr16:339438 C>T did not map to a codon.
Sequencing variant TCGA-FV-A3R2-01A-11D-A22F-10 chr16:360069 C>A did not map to a codon.
Sequencing variant TCGA-FV-A4ZQ-01A-11D-A25V-10 chr16:396950 C>A maps to NM_003502.3 V25V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A114-01A-11D-A12Z-10 chr17:63532594 G>A maps to NM_004655.3 L662L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CK-01A-11D-A20W-10 chr17:63534325 G>A maps to NM_004655.3 R399*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr17:79170792 C>G maps to ENST00000269392 V573V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EL-01A-11D-A152-10 chr17:79172745 G>A maps to ENST00000269392 P406P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A4ZQ-01A-11D-A25V-10 chr15:45007634 C>T maps to NM_004048.2 Q28*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr3:160803873 A>G maps to NM_033168.2 H223H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A123-01A-11D-A12Z-10 chr6:71603894 G>A maps to NM_080742.2 N224N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr19:17919062 A>T maps to NM_014256.3 T149T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A459-01A-11D-A25V-10 chr12:122691676 T>A maps to NM_030765.2 A293A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A7PZ-01A-11D-A33Q-10 chr2:232263635 A>T maps to NM_145236.2 *402C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5263-01A-01D-A12Z-10 chr12:668556 G>A maps to NM_173593.3 W953*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr12:660160 T>C maps to NM_173593.3 D357D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A217-01A-11D-A152-10 chr21:42622761 T>A maps to NM_012105.3 P356P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A5SM-01A-12D-A28X-10 chr21:42598203 C>A maps to NM_012105.3 L108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr8:38067824 A>G maps to NM_004874.2 E396E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A115-01A-11D-A12Z-10 chr17:79409034 G>A maps to ENST00000436173 V220V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A9-01A-11D-A25V-10 chr17:79424535 G>T maps to ENST00000436173 V1653V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IG-01A-11D-A33K-10 chr8:143623347 C>T maps to NM_001702.2 G1251G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A7-01A-11D-A22F-10 chr1:32206013 G>A maps to NM_001703.2 D641D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39V-01A-11D-A20W-10 chr6:69703823 A>G maps to NM_001704.2 A633A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr6:69949084 C>T maps to NM_001704.2 L927L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BW-A5NQ-01A-11D-A27I-10 chr16:1384727 C>A maps to NM_003933.4 I22I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A118-01A-11D-A12Z-10 chr3:52440294 G>A maps to NM_004656.2 Q253*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A9-01A-11D-A25V-10 chr3:52441333 T>A did not map to a codon.
Sequencing variant TCGA-G3-A25T-01A-11D-A16V-10 chr3:52439873 G>A maps to NM_004656.2 Q280*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NO-01A-11D-A28X-10 chr14:35255189 A>G maps to NM_013448.2 L542L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A66X-01A-11D-A30V-10 chr7:72891606 G>A maps to NM_032408.3 F728F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39Y-01A-11D-A20W-10 chr12:56997485 T>C did not map to a codon.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr2:160242971 A>C maps to NM_013450.2 L1121L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7ME-01A-11D-A33K-10 chr4:123664495 T>C maps to NM_152618.2 D483D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10X-01A-11D-A12Z-10 chr7:33192379 A>G maps to NM_198428.2 G60G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A7-01A-11D-A22F-10 chr7:33192463 G>A did not map to a codon.
Sequencing variant TCGA-G3-A5SM-01A-12D-A28X-10 chr3:107491986 C>T maps to NM_001142568.1 C473C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A7SK-01A-11D-A34Z-10 chr1:156616629 G>A maps to NM_021948.3 A43A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr1:156622304 A>T maps to NM_021948.3 P521P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A459-01A-11D-A25V-10 chr17:59155890 G>A did not map to a codon.
Sequencing variant TCGA-DD-A114-01A-11D-A12Z-10 chr12:50236855 C>A maps to NM_181708.2 T5T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10Z-01A-11D-A12Z-10 chr14:99640712 G>C maps to NM_138576.2 G820G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7ME-01A-11D-A33K-10 chr14:99641807 G>C maps to NM_138576.2 Y455*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MA-01A-11D-A20W-10 chr18:60795977 T>C maps to NM_000633.2 E200E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CH-01A-11D-A22F-10 chr18:60795936 C>T maps to NM_000633.2 W214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NN-01A-11D-A28X-10 chr20:30309742 T>A maps to NM_138578.1 A93A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73B-01A-12D-A32G-10 chr3:187447679 G>A maps to NM_001706.4 S171S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KC-01A-11D-A20W-10 chr3:187447391 T>C maps to NM_001706.4 E267E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NI-A4U2-01A-11D-A28X-10 chr11:112064702 G>T maps to NM_031938.4 E207*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5259-01A-31D-A20W-10 chr23:39922122 T>A did not map to a codon.
Sequencing variant TCGA-ED-A7PZ-01A-11D-A33Q-10 chr23:39932114 T>A did not map to a codon.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr23:39913171 G>T did not map to a codon.
Sequencing variant TCGA-FV-A23B-01A-11D-A16V-10 chr23:39922118 G>T did not map to a codon.
Sequencing variant TCGA-BC-A216-01A-11D-A152-10 chr23:129159155 C>T did not map to a codon.
Sequencing variant TCGA-BW-A5NP-01A-11D-A27I-10 chr23:129147852 A>G did not map to a codon.
Sequencing variant TCGA-BW-A5NP-01A-11D-A27I-10 chr23:129162762 A>T did not map to a codon.
Sequencing variant TCGA-NI-A4U2-01A-11D-A28X-10 chr23:129149865 C>G did not map to a codon.
Sequencing variant TCGA-DD-A116-01A-11D-A12Z-10 chr3:197238765 T>G maps to NM_203315.2 *344C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3M9-01A-11D-A20W-10 chr11:27681096 T>C did not map to a codon.
Sequencing variant TCGA-DD-A118-01A-11D-A12Z-10 chr1:49242455 C>T maps to NM_024603.2 L16L. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-DD-A4NP-01A-11D-A28X-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-DD-A4NP-01A-11D-A28X-10 chr7:93628604 A>G maps to NM_005868.4 G7G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39V-01A-11D-A20W-10 chr3:133185753 C>A maps to NM_003571.2 S325*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A118-01A-11D-A12Z-10 chr23:102005368 C>A did not map to a codon.
Sequencing variant TCGA-DD-A39X-01A-11D-A20W-10 chr23:102004755 T>C did not map to a codon.
Sequencing variant TCGA-FV-A495-01A-11D-A25V-10 chr23:102004067 G>A did not map to a codon.
Sequencing variant TCGA-HP-A5N0-01A-11D-A28X-10 chr20:61637463 G>A maps to NM_080606.3 D205D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NK-01A-11D-A28X-10 chr3:5025202 C>T maps to NM_003670.2 L355L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr10:60553241 A>G did not map to a codon.
Sequencing variant TCGA-DD-A3A5-01A-11D-A22F-10 chr12:32369237 G>T maps to NM_001714.2 E91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25U-01A-11D-A16V-10 chr12:32520625 C>A maps to NM_001714.2 S929S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73G-01A-22D-A32G-10 chr2:127806197 C>T maps to NM_139343.1 W562*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MC-01A-11D-A22F-10 chr2:32640006 G>T maps to NM_016252.3 E550*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11C-01A-11D-A12Z-10 chr2:32773059 A>G maps to NM_016252.3 E4318E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EG-01A-11D-A20W-10 chr2:32733176 T>C maps to NM_016252.3 A3277A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NV-01A-11D-A30V-10 chr15:91347542 C>A maps to NM_000057.2 V1235V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr15:91304195 A>G maps to NM_000057.2 K531K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25S-01A-11D-A16V-10 chr10:102045884 T>C maps to NM_173809.2 K47K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A495-01A-11D-A25V-10 chr8:22052003 G>A maps to NM_006129.4 S448S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10Q-01A-11D-A12Z-10 chr23:50653811 T>G did not map to a codon.
Sequencing variant TCGA-DD-A4NH-01A-11D-A27I-10 chr23:50658923 T>A did not map to a codon.
Sequencing variant TCGA-DD-A1EG-01A-11D-A20W-10 chr7:33976995 C>A maps to NM_133468.3 C105*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A3R2-01A-11D-A22F-10 chr7:34118586 G>T maps to NM_133468.3 S399S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A9-01A-11D-A25V-10 chr2:203332239 A>G did not map to a codon.
Sequencing variant TCGA-ED-A7PZ-01A-11D-A33Q-10 chr2:203379608 A>T did not map to a codon.
Sequencing variant TCGA-MI-A75E-01A-11D-A32G-10 chr2:203421180 G>A maps to NM_001204.6 K931K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NO-01A-11D-A28X-10 chr23:15560133 T>A did not map to a codon.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr23:15534283 C>T did not map to a codon.
Sequencing variant TCGA-CC-A1HT-01A-11D-A12Z-10 chr15:83926505 A>G maps to NM_001717.3 D891D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11A-01A-11D-A12Z-10 chr15:83933192 A>G maps to NM_001717.3 H270H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr9:16437126 G>T maps to NM_017637.5 P355P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IJ-01A-11D-A33Q-10 chr1:151015462 C>A maps to NM_138278.3 T155T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr1:151018275 A>G maps to NM_138278.3 L285L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr3:112993375 A>T maps to ENST00000273395 P463P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IK-01A-12D-A33Q-10 chr3:113004362 C>T maps to ENST00000273395 A1037A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr3:112987287 C>T maps to ENST00000273395 S173S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25Y-01A-11D-A16V-10 chr3:112998755 G>T maps to ENST00000273395 S703S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A5W4-01A-11D-A28X-10 chr7:134346579 T>C maps to NM_001724.4 H107H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NF-01A-11D-A27I-10 chr20:36937388 G>T maps to NM_001725.2 V105V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10T-01A-11D-A12Z-10 chr17:65889634 T>G maps to ENST00000321892 A861A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A7M7-01A-12D-A34Z-10 chr17:41245777 A>G maps to ENST00000471181 S590S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10U-01A-11D-A12Z-10 chr23:154299925 G>A did not map to a codon.
Sequencing variant TCGA-G3-A25W-01A-11D-A16V-10 chr23:154348354 A>G did not map to a codon.
Sequencing variant TCGA-BC-A112-01A-11D-A12Z-10 chr6:32948466 C>A maps to ENST00000395289 S828*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NN-01A-11D-A28X-10 chr19:15349579 C>A maps to NM_058243.2 E1332*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EH-01A-11D-A12Z-10 chr16:50357575 A>C maps to NM_001173984.2 Y455*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CH-01A-11D-A22F-10 chr16:50357552 A>T maps to NM_001173984.2 L463*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A26S-01A-11D-A16V-10 chr5:137504196 A>G maps to NM_006696.3 L275L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A5SM-01A-12D-A28X-10 chr5:137501702 G>A maps to NM_139199.1 I364I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr1:92428481 T>C maps to ENST00000347608 D69D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr1:92442751 T>C maps to ENST00000347608 S269S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A66X-01A-11D-A30V-10 chr17:59821817 G>A maps to NM_032043.2 D744D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr17:59793425 T>A did not map to a codon.
Sequencing variant TCGA-O8-A75V-01A-11D-A32G-10 chr11:66109565 C>A did not map to a codon.
Sequencing variant TCGA-DD-A3A9-01A-11D-A25V-10 chr3:9776288 G>A maps to NM_001003694.1 E155E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MA-01A-11D-A20W-10 chr19:55816893 C>T maps to NM_032430.1 L610L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MB-01A-11D-A20W-10 chr21:40590494 A>G maps to NM_018963.3 G1158G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A5UD-01A-11D-A28X-10 chr23:79989644 T>A did not map to a codon.
Sequencing variant TCGA-G3-A5SK-01A-11D-A27I-10 chr23:79984392 G>A did not map to a codon.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr23:79979303 T>C did not map to a codon.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr23:79999578 T>C did not map to a codon.
Sequencing variant TCGA-CC-A7IF-01A-11D-A33K-10 chr19:579632 G>A maps to NM_001728.2 L183L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A5SL-01A-11D-A27I-10 chr15:83698991 G>T maps to NM_025238.3 Y317*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr15:83718867 T>C maps to NM_025238.3 T207T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr12:108008835 A>C did not map to a codon.
Sequencing variant TCGA-DD-A113-01A-11D-A12Z-10 chr14:105716438 C>T maps to NM_033271.2 G296G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A459-01A-11D-A25V-10 chr14:93714871 G>A maps to NM_001002860.2 R691*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A3R2-01A-11D-A22F-10 chr14:93720037 G>T maps to NM_001002860.2 I569I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25W-01A-11D-A16V-10 chr6:38256181 G>A maps to NM_052893.1 V440V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KR-A7K0-01A-12D-A33Q-10 chr4:75675928 G>T maps to NM_001729.2 V94V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr5:72798772 C>A maps to NM_001037637.1 I116I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25U-01A-11D-A16V-10 chr23:100611052 A>G did not map to a codon.
Sequencing variant TCGA-G3-A7M6-01A-11D-A33Q-10 chr23:100608969 G>C did not map to a codon.
Sequencing variant TCGA-CC-A7IK-01A-12D-A33Q-10 chr3:112185076 C>A maps to NM_181780.3 E250*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5263-01A-01D-A12Z-10 chr6:26390935 G>A did not map to a codon.
Sequencing variant TCGA-MI-A75I-01A-11D-A32G-10 chr6:26409956 A>G maps to NM_007048.5 T304T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr6:105572511 T>A maps to NM_007073.4 R186R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MB-01A-11D-A20W-10 chr17:56388535 C>A maps to NM_004758.2 L1040L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KR-A7K7-01A-11D-A33K-10 chr17:56400052 G>A maps to NM_004758.2 L427L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EF-01A-11D-A12Z-10 chr7:16720996 G>T maps to NM_014038.2 E103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A216-01A-11D-A152-10 chr10:127426554 A>G maps to ENST00000356792 L609L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MB-01A-11D-A20W-10 chr10:127431771 A>G maps to ENST00000356792 R839R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25U-01A-11D-A16V-10 chr10:102750243 T>C maps to NM_021830.4 H512H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5262-01A-01D-A12Z-10 chr10:50533356 C>A maps to NM_001135196.1 R923R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr10:50530955 C>T maps to NM_001135196.1 V122V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A7XP-01A-11D-A34Z-10 chr11:93494679 G>A did not map to a codon.
Sequencing variant TCGA-DD-A4NG-01A-11D-A27I-10 chr11:122774638 A>G maps to NM_024806.2 Q117Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr11:108264017 A>G maps to NM_152587.3 A216A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EL-01A-11D-A152-10 chr11:108253792 T>C maps to NM_152587.3 E299E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NH-01A-11D-A27I-10 chr11:86048469 A>G maps to NM_016401.3 P106P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25U-01A-11D-A16V-10 chr12:64661043 C>T maps to NM_001170633.1 L596L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3M9-01A-11D-A20W-10 chr14:77311221 G>A maps to NM_194287.2 G235G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25V-01A-11D-A16V-10 chr14:50459530 T>C maps to NM_001012706.1 R89R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KR-A7K0-01A-12D-A33Q-10 chr14:50550626 T>C maps to NM_001014830.1 T239T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10Q-01A-11D-A12Z-10 chr14:58605152 A>T maps to ENST00000438670 S326S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr15:75499849 A>T maps to NM_015492.4 P487P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A2QR-01A-11D-A20W-10 chr15:40628994 T>C maps to NM_207380.2 K298K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MA-01A-11D-A20W-10 chr15:34646647 G>A maps to ENST00000438749 V349V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A2QR-01A-11D-A20W-10 chr16:81095082 G>A maps to NM_152337.2 L291L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MC-01A-11D-A33Q-10 chr16:89724815 A>T maps to NM_153025.1 A65A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr16:58148803 G>T maps to NM_013242.2 I162I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr17:42750731 A>C did not map to a codon.
Sequencing variant TCGA-CC-A5UD-01A-11D-A28X-10 chr17:56621178 A>T maps to NM_001038704.1 V123V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IG-01A-11D-A33K-10 chr18:43796311 A>T maps to NM_145055.3 K156*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A7M6-01A-11D-A33Q-10 chr18:21110005 A>G maps to NM_013326.3 E503E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr18:21104399 A>G maps to NM_013326.3 S338S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A116-01A-11D-A12Z-10 chr19:4658076 T>A maps to NM_019107.3 A154A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr19:758322 T>C maps to NM_173481.2 T459T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A5-01A-11D-A22F-10 chr19:758169 C>T maps to NM_173481.2 A408A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73E-01A-12D-A32G-10 chr1:22987599 C>T maps to NM_000491.3 T161T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A116-01A-11D-A12Z-10 chr5:159776747 T>C maps to NM_031908.4 P140P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NI-01A-11D-A27I-10 chr5:159797620 C>A maps to NM_031908.4 P8P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A7SK-01A-11D-A34Z-10 chr5:159797620 C>A maps to NM_031908.4 P8P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5258-01A-01D-A12Z-10 chr11:47611681 G>A maps to NM_031909.2 G227G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A9-01A-11D-A25V-10 chr12:7242775 C>G maps to ENST00000290575 P114P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A116-01A-11D-A12Z-10 chr12:7177504 G>A maps to NM_001734.3 V539V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr1:244681970 T>G maps to NM_001130957.1 V169V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IG-01A-11D-A33K-10 chr1:162344017 G>T maps to NM_182581.3 I202I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr1:11009709 G>A maps to NM_001170754.1 L421L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1ED-01A-11D-A152-10 chr1:231360123 T>C maps to ENST00000421623 S262S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr1:75039092 A>G maps to NM_001002912.4 Y767Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A114-01A-11D-A12Z-10 chr1:75037156 C>A maps to NM_001002912.4 E1413*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A3-01A-11D-A22F-10 chr1:184446675 T>A maps to NM_030806.3 T11T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A5W4-01A-11D-A28X-10 chr1:23698087 A>G did not map to a codon.
Sequencing variant TCGA-CC-5262-01A-01D-A12Z-10 chr1:23697597 T>A did not map to a codon.
Sequencing variant TCGA-G3-A25V-01A-11D-A16V-10 chr1:23696027 T>C maps to ENST00000507744 L80L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A7PZ-01A-11D-A33Q-10 chr1:228290667 C>A maps to NM_024319.2 A59A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A9-01A-11D-A25V-10 chr1:25570118 C>A maps to NM_020317.3 S226S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A7PZ-01A-11D-A33Q-10 chr1:25571744 G>A maps to NM_020317.3 L190L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A110-01A-11D-A12Z-10 chr1:223568583 C>T maps to NM_152610.2 L589L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A7M6-01A-11D-A33Q-10 chr1:223568586 T>C maps to NM_152610.2 P590P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73E-01A-12D-A32G-10 chr1:60520923 G>A maps to NM_152377.2 N98N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A4-01A-11D-A22F-10 chr1:34667860 G>T did not map to a codon.
Sequencing variant TCGA-DD-A3A9-01A-11D-A25V-10 chr1:34667799 C>T maps to NM_001134734.1 L462L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr1:34662931 G>T maps to NM_001134734.1 E143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EL-01A-11D-A152-10 chr20:42826207 C>A maps to NM_016470.6 L121L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A7PZ-01A-11D-A33Q-10 chr20:31043959 C>T maps to NM_080616.3 L116L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr20:2796252 T>A maps to NM_080739.2 G110G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr20:3274838 A>G maps to NM_001009984.1 P728P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A9-01A-11D-A25V-10 chr20:35238001 A>T did not map to a codon.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr20:20144824 T>A maps to ENST00000389655 A386A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A0-01A-11D-A20W-10 chr22:32789990 T>C did not map to a codon.
Sequencing variant TCGA-BW-A5NO-01A-11D-A27I-10 chr22:19839037 T>C maps to NM_024627.5 V249V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NV-01A-11D-A30V-10 chr21:43309316 G>T maps to NM_015500.1 L669L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11A-01A-11D-A12Z-10 chr11:118984631 C>T maps to NM_014807.3 P520P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7II-01A-11D-A33K-10 chr2:27804121 C>A maps to NM_032266.3 P1561P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr2:27803185 A>G maps to NM_032266.3 R1249R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr2:27803791 T>C maps to NM_032266.3 P1451P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BD-A3EP-01A-11D-A22F-10 chr2:24261848 C>T maps to NM_025203.2 V172V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A4-01A-11D-A22F-10 chr2:24262241 A>G maps to NM_025203.2 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A0-01A-11D-A20W-10 chr2:200824538 T>C maps to NM_024520.2 A195A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5259-01A-31D-A20W-10 chr2:219225313 G>T maps to NM_198559.1 E132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MF-01A-11D-A33K-10 chr2:219225306 C>T maps to NM_198559.1 L129L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EL-01A-11D-A152-10 chr2:29294436 G>A maps to NM_001029883.1 T897T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-O8-A75V-01A-11D-A32G-10 chr2:29294546 C>A maps to NM_001029883.1 E861*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A6M6-01A-11D-A32G-10 chr2:29297115 T>C maps to NM_001029883.1 T4T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39Z-01A-11D-A20W-10 chr2:191064867 G>A maps to NM_032321.2 G94G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EG-01A-11D-A20W-10 chr19:6718128 G>A maps to NM_000064.2 G160G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73D-01A-12D-A32G-10 chr19:6697549 G>A maps to NM_000064.2 L867L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IK-01A-12D-A33Q-10 chr3:112736435 T>A maps to NM_015412.3 A40A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EG-01A-11D-A20W-10 chr3:126270922 G>A maps to NM_152533.1 P44P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RG-A7D4-01A-12D-A33Q-10 chr3:128292488 G>A maps to NM_007354.2 R28R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25S-01A-11D-A16V-10 chr3:118870135 A>G maps to NM_152539.2 V536V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A9-01A-11D-A25V-10 chr3:157296100 C>T maps to NM_001099777.2 F112F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr3:143708571 G>A maps to NM_173552.3 R394R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10U-01A-11D-A12Z-10 chr3:138669224 C>T maps to NM_001040061.2 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73G-01A-22D-A32G-10 chr1:207288821 A>G maps to NM_000715.3 L130L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K7-A6G5-01A-11D-A30V-10 chr4:100463065 G>C did not map to a codon.
Sequencing variant TCGA-ED-A459-01A-11D-A25V-10 chr4:113461975 C>A did not map to a codon.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr4:76489570 T>G maps to NM_178497.2 Y105*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73E-01A-12D-A32G-10 chr4:146648099 A>G maps to NM_001080531.1 S115S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25W-01A-11D-A16V-10 chr4:146650319 G>T did not map to a codon.
Sequencing variant TCGA-DD-A39X-01A-11D-A20W-10 chr9:123738975 A>G did not map to a codon.
Sequencing variant TCGA-DD-A73G-01A-22D-A32G-10 chr9:123768306 T>A maps to NM_001735.2 K818*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr5:31534521 T>C maps to NM_018356.2 F75F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A113-01A-11D-A12Z-10 chr5:43446539 A>C maps to NM_022483.4 L144L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25W-01A-11D-A16V-10 chr5:37227753 T>C maps to NM_023073.3 L429L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11B-01A-11D-A16Z-10 chr5:41201722 G>A maps to NM_001115131.1 P79P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr5:41186294 T>C maps to NM_001115131.1 A201A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr5:41143007 T>A maps to NM_001115131.1 T908T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A110-01A-11D-A12Z-10 chr6:34574640 A>C maps to NM_024294.2 L184L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A4XI-01A-11D-A25V-10 chr6:31079841 C>T maps to NM_014070.2 W98*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MC-01A-11D-A22F-10 chr6:121642786 T>C maps to ENST00000275159 E103E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IL-01A-11D-A33Q-10 chr6:121434234 G>A maps to ENST00000275159 Q1089*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A495-01A-11D-A25V-10 chr6:121625733 A>G maps to ENST00000275159 N269N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39Z-01A-11D-A20W-10 chr6:43970787 G>T maps to NM_153246.4 R218R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr6:31627615 C>A maps to NM_021184.3 E37*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr6:127902352 T>C maps to NM_001010905.1 F200F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NF-01A-11D-A27I-10 chr6:24714569 A>G maps to NM_030939.4 S135S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73C-01A-12D-A33K-10 chr7:40535936 C>A maps to NM_001193311.1 V354V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A5UE-01A-11D-A28X-10 chr7:42949410 C>T maps to NM_001099858.1 G421G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A5SL-01A-11D-A27I-10 chr7:6631387 C>T maps to NM_024067.2 Q102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A9-01A-11D-A25V-10 chr7:112579748 C>T maps to NM_152556.2 P19P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5261-01A-01D-A12Z-10 chr8:49985397 C>T maps to NM_001007176.3 S3S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10Z-01A-11D-A12Z-10 chr8:144124679 G>A did not map to a codon.
Sequencing variant TCGA-ED-A7XP-01A-11D-A34Z-10 chr9:72459517 C>T maps to NM_001010940.1 R80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr9:88842777 A>T maps to NM_001010907.1 P78P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A7M9-01A-23D-A34Z-10 chr9:100667206 C>A maps to NM_016481.3 V378V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A26S-01A-11D-A16V-10 chr9:89763701 G>T maps to NM_001001709.2 G19G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A2QR-01A-11D-A20W-10 chr9:140147364 G>A maps to ENST00000388931 S248S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11C-01A-11D-A12Z-10 chr9:34385757 G>T maps to NM_032596.3 R53R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A3RK-01A-11D-A22F-10 chr9:86571247 G>A maps to NM_032307.3 N56N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr9:27556626 T>C maps to NM_018325.2 R341R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A3R3-01A-11D-A22F-10 chr9:114462239 A>G maps to NM_173521.3 D995D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BD-A2L6-01A-11D-A20W-10 chr9:74586498 C>T maps to NM_182505.3 C96C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr9:136270406 T>C maps to NM_153710.3 S635S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IK-01A-12D-A33Q-10 chr8:86250478 A>T did not map to a codon.
Sequencing variant TCGA-DD-A3A4-01A-11D-A22F-10 chr8:86360369 T>C maps to NM_005181.3 A257A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A216-01A-11D-A152-10 chr17:58235785 C>T maps to NM_000717.3 P241P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A459-01A-11D-A25V-10 chr1:9027784 C>A maps to ENST00000413627 Y217*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75G-01A-11D-A32G-10 chr8:61135273 G>T maps to NM_004056.4 I224I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BW-A5NO-01A-11D-A27I-10 chr9:35674207 T>C maps to NM_001216.2 P84P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EA-01A-11D-A12Z-10 chr2:231624745 A>G maps to NM_001130850.1 K10K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr22:24455826 G>A did not map to a codon.
Sequencing variant TCGA-BC-A10T-01A-11D-A12Z-10 chr11:67223229 C>T maps to NM_145200.3 Y112Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr1:65142575 A>G did not map to a codon.
Sequencing variant TCGA-FV-A23B-01A-11D-A16V-10 chr19:13363876 C>A maps to NM_023035.2 R1602R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A23B-01A-11D-A16V-10 chr19:13410089 A>T maps to NM_023035.2 L790*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25U-01A-11D-A16V-10 chr19:13476248 C>A maps to NM_023035.2 A222A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A116-01A-11D-A12Z-10 chr9:140901280 C>G maps to ENST00000277549 V680V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EL-01A-11D-A152-10 chr9:140953172 G>C maps to ENST00000277549 V1488V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QA-A7B7-01A-11D-A32G-10 chr9:140865850 C>T maps to ENST00000277549 R451R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A5W4-01A-11D-A28X-10 chr12:2229595 G>T maps to NM_199460.2 L159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A118-01A-11D-A12Z-10 chr12:2788716 G>A maps to NM_199460.2 A1781A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75E-01A-11D-A32G-10 chr12:2794934 G>A maps to NM_199460.2 L1952L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr3:53700543 G>A maps to NM_001128840.1 W366*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EJ-01A-11D-A152-10 chr3:53707150 C>T maps to NM_001128840.1 S406S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A9-01A-11D-A25V-10 chr1:181706681 C>T maps to ENST00000357570 Y1148Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NG-01A-11D-A27I-10 chr1:181767516 G>A maps to ENST00000357570 P2163P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A7M5-01A-11D-A33Q-10 chr1:181689966 T>A maps to ENST00000357570 P644P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A8-01A-11D-A22F-10 chr23:49062153 G>T did not map to a codon.
Sequencing variant TCGA-DD-A3A2-01A-11D-A20W-10 chr16:1251934 G>A maps to NM_021098.2 V495V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr22:39994206 T>C maps to NM_021096.3 L96L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A5UD-01A-11D-A28X-10 chr1:201060849 G>A maps to NM_000069.2 L204L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A5SK-01A-11D-A27I-10 chr1:201058469 G>A maps to NM_000069.2 I272I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A7PZ-01A-11D-A33Q-10 chr3:50418546 G>A maps to ENST00000435965 I221I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A7M5-01A-11D-A33Q-10 chr3:54880436 T>A maps to NM_018398.2 Y523*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PD-A5DF-01A-11D-A27I-10 chr3:54905637 C>A maps to NM_018398.2 R567R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BD-A3EP-01A-11D-A22F-10 chr17:37341066 G>T maps to NM_000723.3 I233I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CJ-01A-11D-A20W-10 chr10:18439888 T>C maps to NM_201596.2 N66N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73E-01A-12D-A32G-10 chr2:152729008 T>C did not map to a codon.
Sequencing variant TCGA-FV-A495-01A-11D-A25V-10 chr22:36960730 G>A maps to NM_006078.3 R213R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A2QQ-01A-11D-A22F-10 chr19:54445426 G>A maps to NM_031896.4 A236A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr19:54444785 A>C maps to NM_031896.4 R163R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LG-A6GG-01A-11D-A30V-10 chr19:54485673 G>T maps to NM_031895.5 P283P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IJ-01A-11D-A33Q-10 chr2:27456322 T>G maps to NM_004341.3 A1045A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KC-01A-11D-A20W-10 chr2:27460319 C>T maps to NM_004341.3 A1490A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5258-01A-01D-A12Z-10 chr11:115085442 C>G maps to NM_014333.3 L293L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73C-01A-12D-A33K-10 chr11:115111038 G>A maps to NM_014333.3 L76L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EJ-01A-11D-A152-10 chr3:86114752 A>G did not map to a codon.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr3:85961526 A>T maps to NM_153184.3 V171V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A3KF-01A-11D-A20W-10 chr3:62385128 C>T maps to ENST00000383709 Q1343Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A459-01A-11D-A25V-10 chr3:62518734 T>A did not map to a codon.
Sequencing variant TCGA-CC-A5UE-01A-11D-A28X-10 chr7:122303419 T>C maps to NM_001167940.1 K219K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A5UD-01A-11D-A28X-10 chr12:54118966 T>A maps to NM_020898.2 V20V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73B-01A-12D-A32G-10 chr12:54118935 C>A maps to NM_020898.2 E31*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HP-A5N0-01A-11D-A28X-10 chr7:93055778 G>A maps to NM_001164737.1 I472I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25V-01A-11D-A16V-10 chr10:105218130 G>T maps to NM_001001412.3 L126L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A5-01A-11D-A22F-10 chr1:1847134 T>C maps to NM_138705.2 C13C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5263-01A-01D-A12Z-10 chr7:71571274 G>T maps to NM_031468.3 I83I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10Z-01A-11D-A12Z-10 chr19:13054679 G>T maps to NM_004343.3 E403*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5261-01A-01D-A12Z-10 chr10:135140402 G>A maps to NM_015722.3 C113C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73G-01A-22D-A32G-10 chr10:135140486 G>T maps to NM_015722.3 T85T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A5UE-01A-11D-A28X-10 chr10:12858285 G>A maps to NM_153498.2 P264P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr5:149602598 C>T maps to NM_015981.3 W473*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75H-01A-11D-A32G-10 chr7:44281926 C>A maps to NM_001220.4 E237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73F-01A-11D-A32G-10 chr1:20811830 G>T maps to NM_018584.5 P14P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75I-01A-11D-A32G-10 chr17:3779537 G>T maps to ENST00000381771 S363S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr12:121701740 A>G maps to NM_006549.3 R209R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NQ-01A-21D-A28X-10 chr1:7700464 C>T maps to NM_015215.2 P172P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73F-01A-11D-A32G-10 chr1:7723458 C>T maps to NM_015215.2 R284R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A496-01A-11D-A25V-10 chr1:7724691 G>T maps to NM_015215.2 S695S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr12:67699019 G>T maps to NM_018448.3 V524V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr12:67703829 A>T maps to NM_018448.3 R1059*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr3:12858224 T>A maps to NM_001162499.1 L598L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25U-01A-11D-A16V-10 chr6:17463258 G>A maps to NM_006366.2 Q85Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A23B-01A-11D-A16V-10 chr6:44150675 A>G did not map to a codon.
Sequencing variant TCGA-BC-A3KG-01A-11D-A20W-10 chr19:39226820 C>G maps to NM_144691.3 P504P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QA-A7B7-01A-11D-A32G-10 chr2:31010122 G>T maps to ENST00000295055 T23T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr2:30966295 T>A maps to ENST00000295055 S466S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A5SM-01A-12D-A28X-10 chr11:76834774 G>A maps to ENST00000360841 Q634Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39W-01A-11D-A20W-10 chr19:36637096 G>C did not map to a codon.
Sequencing variant TCGA-G3-A25U-01A-11D-A16V-10 chr16:55601228 A>G maps to NM_032330.1 E187E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr7:2983943 T>A maps to NM_032415.4 K196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IF-01A-11D-A33K-10 chr19:48734193 C>T maps to NM_001184900.1 E204E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr12:25267702 G>A maps to NM_018272.3 Q500*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A459-01A-11D-A25V-10 chr15:40917525 G>T maps to NM_170589.3 P1714P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EB-01A-11D-A12Z-10 chr23:41428984 T>C did not map to a codon.
Sequencing variant TCGA-G3-A25T-01A-11D-A16V-10 chr11:104897622 A>G maps to NM_033292.2 I354I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A7XP-01A-11D-A34Z-10 chr11:104819258 C>A did not map to a codon.
Sequencing variant TCGA-CC-A7IJ-01A-11D-A33Q-10 chr11:104872820 C>A maps to NM_001136112.1 V230V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11C-01A-11D-A12Z-10 chr10:115457350 G>A maps to NM_033338.4 P66P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A7-01A-11D-A22F-10 chr6:90562906 T>C maps to NM_012115.3 D26D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A9-01A-11D-A25V-10 chr6:90581016 C>T maps to NM_012115.3 D1934D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10R-01A-11D-A12Z-10 chr1:15821774 A>G maps to NM_001229.3 T347T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr14:92126217 A>G maps to NM_024764.2 F465F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A26S-01A-11D-A16V-10 chr19:38827957 G>T maps to NM_021185.4 V28V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A23B-01A-11D-A16V-10 chr16:88958804 G>A maps to NM_005187.5 S156S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11A-01A-11D-A12Z-10 chr4:169923356 C>G did not map to a codon.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr21:44488624 C>A maps to ENST00000398168 E104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr22:39530448 C>T maps to NM_175709.3 A185A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10Z-01A-11D-A12Z-10 chr19:14038068 G>A maps to NM_017721.4 E769E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73C-01A-12D-A33K-10 chr4:15516352 T>A maps to NM_001080522.2 G247G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MB-01A-11D-A20W-10 chr10:70515290 A>G maps to NM_018237.2 Q541Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NI-A4U2-01A-11D-A28X-10 chr18:57136702 A>T did not map to a codon.
Sequencing variant TCGA-T1-A6J8-01A-11D-A32G-10 chr18:57363934 G>A maps to NM_133459.3 I46I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr18:57122129 T>A maps to NM_133459.3 K203*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A459-01A-11D-A25V-10 chr2:219897275 G>A maps to NM_194302.2 F187F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A2QR-01A-11D-A20W-10 chr2:219892383 G>A maps to NM_194302.2 F733F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NV-01A-11D-A30V-10 chr4:185606651 G>T maps to NM_152683.2 G396*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25T-01A-11D-A16V-10 chr23:48919844 T>C did not map to a codon.
Sequencing variant TCGA-BC-A3KF-01A-11D-A20W-10 chr13:44433972 T>C maps to NM_144974.3 A130A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75E-01A-11D-A32G-10 chr13:44433942 C>T maps to NM_144974.3 G140G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EB-01A-11D-A12Z-10 chr7:31691633 G>T maps to NM_194300.2 R931R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A5SL-01A-11D-A27I-10 chr7:31683404 C>A maps to NM_194300.2 I807I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5262-01A-01D-A12Z-10 chr3:42787465 C>A maps to NM_144719.3 S258S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25Y-01A-11D-A16V-10 chr3:42754744 G>A maps to NM_144719.3 R594R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QA-A7B7-01A-11D-A32G-10 chr19:13873869 G>A maps to NM_030818.2 S393S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39X-01A-11D-A20W-10 chr7:92952971 T>A maps to NM_017667.2 V635V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A3R3-01A-11D-A22F-10 chr7:92935294 A>G maps to NM_017667.2 E536E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr16:57760017 C>A maps to NM_032269.5 P599P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr7:128434788 G>T maps to NM_022742.3 E105*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25T-01A-11D-A16V-10 chr7:128454945 T>C maps to NM_022742.3 T1006T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QA-A7B7-01A-11D-A32G-10 chr7:128449529 A>G maps to NM_022742.3 T544T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CK-01A-11D-A20W-10 chr17:79639184 G>A maps to NM_199287.2 Q220Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KR-A7K8-01A-11D-A33K-10 chr17:79638801 C>T maps to NM_199287.2 R176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A5SJ-01A-11D-A27I-10 chr2:109405346 C>A maps to NM_144978.1 S64*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr2:223168827 A>T maps to NM_153038.1 P69P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A9-01A-11D-A25V-10 chr2:74707913 C>T maps to ENST00000393965 K495K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CJ-01A-11D-A20W-10 chr17:18498057 T>C did not map to a codon.
Sequencing variant TCGA-G3-A7M7-01A-12D-A34Z-10 chr2:197595662 A>C maps to NM_001080539.1 S1021S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A114-01A-11D-A12Z-10 chr19:49920646 C>A maps to NM_144688.4 I523I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A9-01A-11D-A25V-10 chr23:49103271 C>T did not map to a codon.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr23:49105131 G>T did not map to a codon.
Sequencing variant TCGA-DD-A3A9-01A-11D-A25V-10 chr11:27384585 C>A maps to NM_030771.1 S52S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BW-A5NP-01A-11D-A27I-10 chr3:180361988 G>A maps to NM_181426.1 S528S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A6UC-01A-21D-A33K-10 chr3:180359905 A>T maps to NM_181426.1 L583L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10T-01A-11D-A12Z-10 chr12:94706793 C>T did not map to a codon.
Sequencing variant TCGA-ED-A7PZ-01A-11D-A33Q-10 chr12:102419816 C>G did not map to a codon.
Sequencing variant TCGA-EP-A12J-01A-11D-A12Z-10 chr17:80115730 G>A maps to ENST00000445854 Q712*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MB-01A-11D-A20W-10 chr10:61612352 T>C maps to ENST00000395341 E137E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25V-01A-11D-A16V-10 chr12:119916934 T>C maps to NM_178499.3 A126A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr19:46498358 C>A maps to NM_001080402.1 L7L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NF-01A-11D-A27I-10 chr12:111342551 C>T maps to NM_152591.1 P501P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QA-A7B7-01A-11D-A32G-10 chr12:111336786 C>T maps to NM_152591.1 Y400Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25W-01A-11D-A16V-10 chr12:49298805 G>T maps to NM_033124.4 R70R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75I-01A-11D-A32G-10 chr12:49298897 T>C did not map to a codon.
Sequencing variant TCGA-FV-A2QQ-01A-11D-A22F-10 chr3:49200369 C>A maps to NM_022903.3 L424L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CJ-01A-11D-A20W-10 chr11:32739624 T>C maps to NM_001008391.2 Q68Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A6UC-01A-21D-A33K-10 chr2:132290492 G>A maps to NM_138770.1 E311E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A5W4-01A-11D-A28X-10 chr2:130898810 G>T maps to NM_207310.1 P201P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A6UC-01A-21D-A33K-10 chr2:130897612 C>T maps to NM_207310.1 E311E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A123-01A-11D-A12Z-10 chr19:46914888 C>T maps to NM_032040.3 A393A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr3:112357720 A>T maps to ENST00000447230 P355P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7II-01A-11D-A33K-10 chr11:86108767 A>G maps to NM_001156474.1 K247K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NV-01A-11D-A30V-10 chr11:118869171 T>G maps to NM_198489.1 A51A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39W-01A-11D-A20W-10 chr2:55589548 T>C maps to ENST00000436346 Q174Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25S-01A-11D-A16V-10 chr11:64111851 A>G maps to NM_032251.5 K613K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10Y-01A-11D-A12Z-10 chr14:91770247 C>T maps to NM_001080414.2 T1144T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MB-01A-11D-A20W-10 chr14:91770229 G>A maps to NM_001080414.2 N1150N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NJ-01A-11D-A27I-10 chr14:91780182 C>T maps to NM_001080414.2 E659E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr14:91739337 G>T maps to NM_001080414.2 P1906P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5262-01A-01D-A12Z-10 chr2:118716045 T>G maps to NM_019044.4 L300L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr19:4249222 A>G did not map to a codon.
Sequencing variant TCGA-CC-A7II-01A-11D-A33K-10 chr19:41822392 C>T maps to NM_052848.1 L51L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73E-01A-12D-A32G-10 chr4:26491838 G>A maps to NM_000730.2 P17P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr11:6292238 A>G did not map to a codon.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr17:34398400 A>T maps to NM_002988.2 *90C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr17:32583295 A>G maps to NM_002982.3 S44S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CK-01A-11D-A20W-10 chr4:122740570 G>A maps to NM_001237.3 L320L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr14:20784550 T>C maps to NM_182849.1 S44S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A9-01A-11D-A25V-10 chr23:50037909 G>C did not map to a codon.
Sequencing variant TCGA-G3-A7M5-01A-11D-A33Q-10 chr23:50053767 A>T did not map to a codon.
Sequencing variant TCGA-PD-A5DF-01A-11D-A27I-10 chr23:50090666 A>G did not map to a codon.
Sequencing variant TCGA-RC-A7SK-01A-11D-A34Z-10 chr23:50037975 T>A did not map to a codon.
Sequencing variant TCGA-CC-A7IF-01A-11D-A33K-10 chr16:2499458 G>T maps to NM_001761.2 G465G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr16:2499280 A>T did not map to a codon.
Sequencing variant TCGA-G3-A3CK-01A-11D-A20W-10 chr5:162866369 A>C maps to NM_199246.1 L36L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MA-01A-11D-A20W-10 chr10:97816896 T>C maps to NM_001134375.1 A211A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10T-01A-11D-A12Z-10 chr5:159682608 C>T maps to NM_024565.5 R278R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EF-01A-11D-A12Z-10 chr1:1322748 C>T maps to NM_030937.4 E475E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr15:55664084 C>T maps to ENST00000442196 K204K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A2-01A-11D-A20W-10 chr17:40831633 G>A maps to NM_016602.2 R342R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A7M7-01A-12D-A34Z-10 chr6:167550437 C>T maps to NM_004367.5 T240T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A459-01A-11D-A25V-10 chr17:38711881 A>G maps to NM_001838.3 Y83Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A7SK-01A-11D-A34Z-10 chr4:139965790 A>T did not map to a codon.
Sequencing variant TCGA-DD-A73E-01A-12D-A32G-10 chr12:69986799 A>G maps to NM_006431.2 A265A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr21:30437363 A>C maps to NM_006585.2 G229G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73C-01A-12D-A33K-10 chr21:30439332 T>C maps to NM_006585.2 V147V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr22:17072000 C>A maps to NM_014406.4 V480V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25S-01A-11D-A16V-10 chr1:117560027 G>A maps to NM_004258.3 E515E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IK-01A-12D-A33Q-10 chr6:74407155 C>T maps to NM_133493.3 I36I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A459-01A-11D-A25V-10 chr6:109690221 T>A did not map to a codon.
Sequencing variant TCGA-DD-A1EI-01A-11D-A12Z-10 chr19:43866282 A>G maps to NM_020406.2 Q375Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39W-01A-11D-A20W-10 chr1:158299816 G>T maps to NM_001764.2 V144V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5260-01A-01D-A12Z-10 chr1:158325698 C>T maps to NM_030893.3 Y236Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75I-01A-11D-A32G-10 chr1:158325806 C>A maps to NM_030893.3 T272T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A3JL-01A-11D-A20W-10 chr1:117311335 C>A maps to NM_001767.3 P329P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NJ-01A-11D-A27I-10 chr3:112066564 T>A maps to NM_001004196.2 S219S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A2QR-01A-11D-A20W-10 chr19:35832036 C>G maps to NM_001771.3 V501V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11C-01A-11D-A12Z-10 chr12:6559456 C>T maps to NM_001242.4 T129T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CI-01A-11D-A20W-10 chr6:47576857 G>A did not map to a codon.
Sequencing variant TCGA-EP-A3JL-01A-11D-A20W-10 chr17:72539018 C>A maps to NM_006678.3 E170*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A3JL-01A-11D-A20W-10 chr17:72539019 G>T maps to NM_006678.3 P169P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A6M4-01A-11D-A32G-10 chr17:72519755 G>A maps to NM_174892.2 T172T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr17:41924619 G>A maps to NM_145273.3 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A459-01A-11D-A25V-10 chr4:15841651 T>G maps to NM_001775.2 T221T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EL-01A-11D-A152-10 chr19:45911585 T>C maps to ENST00000423698 G122G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73B-01A-12D-A32G-10 chr12:6926464 G>C maps to NM_000616.4 S375S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25S-01A-11D-A16V-10 chr12:6923450 T>C maps to NM_000616.4 L120L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A7PZ-01A-11D-A33Q-10 chr11:35236396 A>T did not map to a codon.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr1:160648871 C>T maps to NM_001778.2 V234V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73B-01A-12D-A32G-10 chr11:60882525 A>G did not map to a codon.
Sequencing variant TCGA-CC-5259-01A-31D-A20W-10 chr1:157804416 G>A maps to NM_005894.2 G166G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr1:157803105 A>C maps to NM_005894.2 V305V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A459-01A-11D-A25V-10 chr11:60777230 C>G maps to NM_006725.3 S323S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr11:60785417 A>G maps to NM_006725.3 S590S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IF-01A-11D-A33K-10 chr17:7483021 G>C maps to NM_001251.2 G9G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A2QQ-01A-11D-A22F-10 chr11:2417937 G>T maps to NM_004356.3 V214V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K7-A6G5-01A-11D-A30V-10 chr20:23066707 G>T maps to NM_012072.3 S41*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A7PZ-01A-11D-A33Q-10 chr3:111342599 G>T did not map to a codon.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr19:14512304 A>G maps to NM_078481.2 E335E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MC-01A-11D-A22F-10 chr23:2644347 G>A did not map to a codon.
Sequencing variant TCGA-DD-A3A9-01A-11D-A25V-10 chr1:20940333 G>A did not map to a codon.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr9:99286008 T>C did not map to a codon.
Sequencing variant TCGA-BC-A3KF-01A-11D-A20W-10 chr5:137537069 T>C maps to NM_004661.3 K161K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A66Y-01A-11D-A30V-10 chr19:10506762 C>T maps to NM_007065.3 V73V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25T-01A-11D-A16V-10 chr6:110551183 A>G maps to NM_015891.2 G530G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75G-01A-11D-A32G-10 chr6:110540595 A>T maps to NM_015891.2 K374*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr6:110522885 A>G maps to NM_015891.2 T134T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A6M4-01A-11D-A32G-10 chr1:227216679 G>T maps to ENST00000366766 T1370T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73E-01A-12D-A32G-10 chr11:64603630 G>A maps to NM_017525.2 A542A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr22:19502320 C>T maps to NM_001178010.1 L455L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NK-01A-11D-A28X-10 chr22:19481905 G>T did not map to a codon.
Sequencing variant TCGA-FV-A23B-01A-11D-A16V-10 chr22:19486622 G>T did not map to a codon.
Sequencing variant TCGA-UB-A7MA-01A-11D-A33Q-10 chr1:193094334 C>A maps to NM_024529.4 V75V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr2:174230177 A>C did not map to a codon.
Sequencing variant TCGA-CC-A7IK-01A-12D-A33Q-10 chr3:45187698 T>A maps to NM_022842.3 A27A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5260-01A-01D-A12Z-10 chr16:68856128 G>A did not map to a codon.
Sequencing variant TCGA-DD-A3A8-01A-11D-A22F-10 chr16:68845608 A>G maps to NM_004360.3 T285T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A7S9-01A-11D-A33Q-10 chr16:68849485 G>A maps to NM_004360.3 E463E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73A-01A-12D-A32G-10 chr16:64984769 G>A maps to NM_001797.2 N598N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LG-A6GG-01A-11D-A30V-10 chr16:65016063 G>A maps to NM_001797.2 P380P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MA-01A-11D-A20W-10 chr16:66946025 T>C maps to NM_004062.2 A522A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr5:19544065 A>G maps to NM_004934.3 D434D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A2QQ-01A-11D-A22F-10 chr5:19473466 A>C maps to NM_004934.3 A747A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A7PZ-01A-11D-A33Q-10 chr18:59158022 T>C maps to NM_031891.2 Y79Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr18:59166655 G>T maps to NM_031891.2 E162*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A7XO-01A-11D-A34Z-10 chr10:73330626 C>A maps to ENST00000398860 I240I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A23B-01A-11D-A16V-10 chr10:73491945 G>A maps to ENST00000398860 E1311E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr10:73269836 A>T did not map to a codon.
Sequencing variant TCGA-FV-A2QQ-01A-11D-A22F-10 chr20:60348087 G>T maps to NM_001794.2 L142L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A5SM-01A-12D-A28X-10 chr20:60499389 A>G did not map to a codon.
Sequencing variant TCGA-CC-A3MA-01A-11D-A20W-10 chr5:31305283 T>C maps to NM_004932.2 L335L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A113-01A-11D-A12Z-10 chr5:31297483 A>G maps to NM_004932.2 G204G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73E-01A-12D-A32G-10 chr5:31323298 C>T maps to NM_004932.2 L753L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IF-01A-11D-A33K-10 chr18:63511190 T>A maps to NM_004361.2 P375P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BW-A5NO-01A-11D-A27I-10 chr5:26902657 C>A maps to NM_016279.3 E394*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MB-01A-11D-A20W-10 chr5:26906840 C>A maps to NM_016279.3 V210V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NO-01A-11D-A28X-10 chr5:26881250 T>G maps to NM_016279.3 R788R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr10:85970914 T>A maps to NM_033100.2 A493A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A12J-01A-11D-A12Z-10 chr10:85960358 C>T maps to NM_033100.2 D147D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A3I1-01A-11D-A22F-10 chr10:85971459 T>A maps to NM_033100.2 T514T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39V-01A-11D-A20W-10 chr5:176011756 C>T maps to NM_001171976.1 H825H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A66Y-01A-11D-A30V-10 chr7:105662821 T>C maps to NM_152750.4 V668V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IK-01A-12D-A33Q-10 chr3:49832412 A>T maps to NM_001007540.2 P384P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25T-01A-11D-A16V-10 chr17:37619235 C>G maps to NM_016507.2 P304P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A12J-01A-11D-A12Z-10 chr7:40085552 T>C maps to NM_003718.4 G824G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75H-01A-11D-A32G-10 chr7:40027407 A>C maps to NM_003718.4 A474A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IG-01A-11D-A33K-10 chr12:56365393 C>G maps to NM_001798.3 P294P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NF-01A-11D-A27I-10 chr17:30814787 G>A maps to NM_003885.2 L50L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5258-01A-01D-A12Z-10 chr9:123202152 C>T maps to NM_018249.4 L1082L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A23B-01A-11D-A16V-10 chr9:123199605 G>A maps to NM_018249.4 L1308L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A495-01A-11D-A25V-10 chr9:123298711 T>C maps to NM_018249.4 S200S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25Y-01A-11D-A16V-10 chr9:123308035 C>A maps to NM_018249.4 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11A-01A-11D-A12Z-10 chr23:18622798 G>A did not map to a codon.
Sequencing variant TCGA-DD-A11C-01A-11D-A12Z-10 chr23:18664146 A>G did not map to a codon.
Sequencing variant TCGA-EP-A12J-01A-11D-A12Z-10 chr5:115146945 T>C maps to NM_001801.2 T105T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr11:125891233 A>G maps to ENST00000392693 S86S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A2QQ-01A-11D-A22F-10 chr17:15510885 A>T did not map to a codon.
Sequencing variant TCGA-G3-A7M9-01A-23D-A34Z-10 chr17:15522793 G>A maps to ENST00000261644 A11A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NR-01A-11D-A30V-10 chr4:85540552 T>C maps to NM_001263.3 F149F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr4:85562070 A>G maps to NM_001263.3 E320E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr19:43013272 T>C maps to NM_001712.4 V523V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A118-01A-11D-A12Z-10 chr19:45206799 C>A maps to ENST00000396750 G138G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr19:42265919 C>G maps to NM_002483.4 Y249*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IJ-01A-11D-A33Q-10 chr19:43098935 C>T maps to NM_001816.3 W15*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39X-01A-11D-A20W-10 chr2:37455987 T>C maps to NM_005760.2 K116K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EI-01A-11D-A12Z-10 chr22:18028981 A>G maps to ENST00000400579 A1314A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A23B-01A-11D-A16V-10 chr22:17626007 C>A did not map to a codon.
Sequencing variant TCGA-RC-A6M6-01A-11D-A32G-10 chr1:15788105 G>T maps to ENST00000375924 G60G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11D-01A-11D-A12Z-10 chr11:47504290 C>A maps to NM_001172639.1 G241*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KR-A7K7-01A-11D-A33K-10 chr11:47510521 A>T maps to NM_001172639.1 A42A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NO-01A-11D-A28X-10 chr15:72582279 C>T maps to NM_052840.4 A201A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A7-01A-11D-A22F-10 chr22:46807620 C>T maps to NM_014246.1 P1549P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GJ-A6C0-01A-12D-A30V-10 chr22:46782347 G>A maps to NM_014246.1 N2230N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A5W4-01A-11D-A28X-10 chr1:109814046 G>A maps to NM_001408.2 L2572L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7II-01A-11D-A33K-10 chr1:109810615 G>T maps to NM_001408.2 L2084L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39X-01A-11D-A20W-10 chr1:109793708 C>T maps to NM_001408.2 P336P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39Y-01A-11D-A20W-10 chr1:109813220 A>G maps to NM_001408.2 T2494T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A7PZ-01A-11D-A33Q-10 chr1:109801477 G>A maps to NM_001408.2 S1245S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CK-01A-11D-A20W-10 chr1:109795271 C>T maps to NM_001408.2 G857G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IJ-01A-11D-A33Q-10 chr3:48697292 C>T maps to NM_001407.2 V925V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IK-01A-12D-A33Q-10 chr3:48689875 G>T maps to NM_001407.2 C1915*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75E-01A-11D-A32G-10 chr3:48696461 G>A maps to NM_001407.2 V1202V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BW-A5NO-01A-11D-A27I-10 chr4:104065712 C>T maps to NM_001813.2 Q1640Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73A-01A-12D-A32G-10 chr13:25466999 T>C maps to NM_018451.3 L999L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25Y-01A-11D-A16V-10 chr13:25466800 C>A maps to NM_018451.3 E1066*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A7XO-01A-11D-A34Z-10 chr2:25016356 C>T maps to ENST00000473706 L5L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A5SI-01A-31D-A27I-10 chr4:56835288 C>T maps to NM_025009.3 Q369*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-4073-01B-02D-A12Z-10 chr15:49048387 A>G maps to NM_001194998.1 C1019C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39Z-01A-11D-A20W-10 chr15:49090247 A>G maps to NM_001194998.1 L30L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3M9-01A-11D-A20W-10 chr1:243291603 T>A did not map to a codon.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr18:13113582 A>T did not map to a codon.
Sequencing variant TCGA-G3-A25S-01A-11D-A16V-10 chr18:13049024 C>T maps to NM_032142.3 T745T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A9-01A-11D-A25V-10 chr20:34090340 A>C maps to NM_007186.3 R1382R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EC-01A-21D-A12Z-10 chr12:88508194 A>C did not map to a codon.
Sequencing variant TCGA-G3-A3CH-01A-11D-A22F-10 chr12:88478473 A>C maps to NM_025114.3 S1531S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr1:180013221 A>G maps to NM_014810.4 E1512E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25Y-01A-11D-A16V-10 chr1:179989458 C>T maps to NM_014810.4 S850S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr10:95275259 G>T maps to NM_018131.4 T209T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A9-01A-11D-A25V-10 chr3:138256156 C>A maps to NM_024491.2 T166T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NI-01A-11D-A27I-10 chr18:12699182 C>T maps to NM_024899.2 R105R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A459-01A-11D-A25V-10 chr3:101451369 G>A maps to ENST00000327230 L200L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75E-01A-11D-A32G-10 chr2:182412567 T>C maps to NM_001030311.2 A406A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr2:182413407 T>A maps to NM_001030311.2 K384*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IL-01A-11D-A33Q-10 chr16:66976620 G>A maps to NM_003869.5 P515P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KR-A7K0-01A-12D-A33Q-10 chr16:66976599 G>A maps to NM_003869.5 W508*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EF-01A-11D-A12Z-10 chr16:67006589 G>A maps to NM_024922.5 E487E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25Y-01A-11D-A16V-10 chr16:66998382 A>G maps to NM_024922.5 G228G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A0-01A-11D-A20W-10 chr16:57005937 C>T maps to NM_000078.2 D231D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A7M6-01A-11D-A33Q-10 chr6:31915209 C>T maps to ENST00000437789 H692H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr1:196715033 C>A maps to NM_000186.3 S1133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A6-01A-11D-A22F-10 chr1:196800930 G>A maps to NM_002113.2 P265P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25U-01A-11D-A16V-10 chr1:196965239 C>A maps to ENST00000367414 V317V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A7M9-01A-23D-A34Z-10 chr4:110682849 T>A did not map to a codon.
Sequencing variant TCGA-CC-5264-01A-01D-A12Z-10 chr7:117292986 T>G did not map to a codon.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr7:117232659 T>C maps to NM_000492.3 S813S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A6M4-01A-11D-A32G-10 chr7:117306999 C>T maps to NM_000492.3 I1427I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A26S-01A-11D-A16V-10 chr19:49558232 G>A maps to ENST00000377280 G19G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A7M9-01A-23D-A34Z-10 chr1:151502576 C>T maps to NM_020770.2 L767L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A113-01A-11D-A12Z-10 chr15:41247962 G>A maps to NM_024111.3 A262A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EF-01A-11D-A12Z-10 chr19:4408945 C>T maps to NM_005483.2 A50A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IK-01A-12D-A33Q-10 chr10:50873040 A>G maps to NM_020549.4 P732P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NI-01A-11D-A27I-10 chr10:50863254 C>T maps to NM_020549.4 A583A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75C-01A-11D-A32G-10 chr1:146747920 G>A maps to NM_004284.3 Q513Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IK-01A-12D-A33Q-10 chr1:6206300 C>T maps to NM_015557.2 W591*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25T-01A-11D-A16V-10 chr20:40052165 C>T maps to NM_032221.3 R1507R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A5UD-01A-11D-A28X-10 chr8:61765634 C>T maps to NM_017780.2 L2117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LG-A6GG-01A-11D-A30V-10 chr8:61769251 A>G maps to NM_017780.2 S2471S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CK-01A-11D-A20W-10 chr16:53358773 A>C maps to ENST00000219084 S2887S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75G-01A-11D-A32G-10 chr16:53296957 G>A maps to ENST00000219084 W1423*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A459-01A-11D-A25V-10 chr3:53857408 G>A maps to NM_018397.4 A209A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A5UD-01A-11D-A28X-10 chr11:125514070 A>T maps to NM_001274.4 K337*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IK-01A-12D-A33Q-10 chr19:16634006 G>A maps to NM_006387.5 F612F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QA-A7B7-01A-11D-A32G-10 chr14:93397787 C>G maps to NM_001275.3 T183T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A7M5-01A-11D-A33Q-10 chr20:5904187 G>A maps to NM_001819.2 E466E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11D-01A-11D-A12Z-10 chr1:111861753 C>T maps to NM_201653.2 L310L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A495-01A-11D-A25V-10 chr23:72783226 C>A did not map to a codon.
Sequencing variant TCGA-BC-A10Z-01A-11D-A12Z-10 chr3:430966 C>G maps to NM_006614.2 G760G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A114-01A-11D-A12Z-10 chr23:85218968 C>G did not map to a codon.
Sequencing variant TCGA-DD-A4NI-01A-11D-A27I-10 chr23:85302519 G>A did not map to a codon.
Sequencing variant TCGA-RC-A6M4-01A-11D-A32G-10 chr1:241799047 T>G maps to NM_001821.3 T7T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73B-01A-12D-A32G-10 chr17:78968446 G>T maps to NM_024591.4 E44*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A6M3-01A-11D-A32G-10 chr17:78972940 G>A maps to NM_024591.4 V198V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GJ-A6C0-01A-12D-A30V-10 chr8:23104432 G>A maps to NM_152272.3 R75R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11D-01A-11D-A12Z-10 chr7:29519791 G>A maps to NM_001039936.1 Q22Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11A-01A-11D-A12Z-10 chr23:109919505 A>G did not map to a codon.
Sequencing variant TCGA-CC-A7IJ-01A-11D-A33Q-10 chr7:136701544 G>T did not map to a codon.
Sequencing variant TCGA-FV-A2QR-01A-11D-A20W-10 chr7:136701055 G>T did not map to a codon.
Sequencing variant TCGA-CC-A3MB-01A-11D-A20W-10 chr1:240072217 G>A maps to NM_000740.2 A489A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73D-01A-12D-A32G-10 chr11:46407537 C>G maps to NM_000741.2 L190L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A9-01A-11D-A25V-10 chr15:34356471 A>G maps to NM_012125.3 K518K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10W-01A-11D-A12Z-10 chr8:27320513 A>G maps to NM_000742.3 S482S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75E-01A-11D-A32G-10 chr8:27321443 G>A maps to NM_000742.3 H172H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A7SK-01A-11D-A34Z-10 chr8:27324789 G>T maps to NM_000742.3 V135V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75C-01A-11D-A32G-10 chr15:78894344 T>A maps to NM_000743.4 P213P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73F-01A-11D-A32G-10 chr20:61981052 G>A maps to NM_000744.5 G570G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A9-01A-11D-A25V-10 chr1:154543703 C>T maps to NM_000748.2 A135A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A123-01A-11D-A12Z-10 chr15:78927918 G>C maps to NM_000750.3 R22R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39Z-01A-11D-A20W-10 chr2:233400021 G>T maps to NM_000751.1 *518Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A5SM-01A-12D-A28X-10 chr2:233390975 T>C maps to NM_000751.1 C17C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A23B-01A-11D-A16V-10 chr2:101014571 G>A maps to NM_004854.3 L75L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73B-01A-12D-A32G-10 chr12:105151022 C>A maps to NM_018413.5 Y167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GJ-A6C0-01A-12D-A30V-10 chr3:126260673 G>A maps to NM_152889.1 P93P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5258-01A-01D-A12Z-10 chr10:125769677 C>T maps to NM_015892.3 W558*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25V-01A-11D-A16V-10 chr3:142841014 C>T maps to NM_004267.3 Q453*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A1-01A-11D-A20W-10 chr10:73767841 C>T maps to NM_004273.4 S351S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr23:46433645 G>T did not map to a codon.
Sequencing variant TCGA-UB-A7MD-01A-12D-A34Z-10 chr18:24496570 G>A maps to NM_031422.4 V328V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr15:101718546 A>G maps to NM_014918.4 H485H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A6M3-01A-11D-A32G-10 chr10:101989280 C>A maps to NM_001278.3 R3R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73B-01A-12D-A32G-10 chr14:65398945 T>C maps to NM_145165.2 *114Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A4XI-01A-11D-A25V-10 chr19:42798804 A>G maps to NM_015125.3 P1459P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NJ-01A-11D-A27I-10 chr3:9911994 A>G maps to ENST00000430427 T83T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A459-01A-11D-A25V-10 chr19:19656086 G>A maps to NM_153221.2 V911V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NI-A4U2-01A-11D-A28X-10 chr19:19654086 A>G maps to NM_153221.2 R336R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr19:19651055 A>T maps to NM_153221.2 G69G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25V-01A-11D-A16V-10 chr2:175244953 G>A maps to NM_004882.3 I114I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A23B-01A-11D-A16V-10 chr16:69167466 A>G maps to NM_032830.2 R35R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr10:60047331 T>C maps to NM_018464.3 C83C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NQ-01A-21D-A28X-10 chr10:60037076 A>T maps to NM_018464.3 K78*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr12:120271924 A>T maps to ENST00000392521 A208A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr12:120214541 T>C maps to ENST00000392521 R590R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A2QR-01A-11D-A20W-10 chr12:120172997 C>T maps to ENST00000392521 T1041T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr2:113518342 T>A did not map to a codon.
Sequencing variant TCGA-BC-A3KG-01A-11D-A20W-10 chr11:46829628 G>A maps to ENST00000415402 P310P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IL-01A-11D-A33Q-10 chr19:45810803 G>T maps to NM_001824.3 G294G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25W-01A-11D-A16V-10 chr1:154947278 C>T maps to NM_001826.2 R20*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr2:122205081 A>G maps to NM_015282.2 A581A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A112-01A-11D-A12Z-10 chr3:33626377 C>G maps to ENST00000359576 L702L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr3:33759301 G>T maps to ENST00000359576 R65R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75I-01A-11D-A32G-10 chr1:87029374 C>G maps to ENST00000263723 L160L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NI-A4U2-01A-11D-A28X-10 chr23:49854826 G>T did not map to a codon.
Sequencing variant TCGA-DD-A1EB-01A-11D-A12Z-10 chr3:190030688 G>T maps to NM_021101.4 V120V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A9-01A-11D-A25V-10 chr7:90042145 A>G maps to NM_001185072.2 T52T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IJ-01A-11D-A33Q-10 chr21:31538833 A>C maps to NM_012131.2 A34A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr8:8560186 G>T maps to NM_194284.2 L93L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A3KF-01A-11D-A20W-10 chr14:38725215 C>A maps to NM_175060.1 A4A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A4ZP-01A-12D-A25V-10 chr16:11114146 C>T maps to ENST00000409790 A467A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KR-A7K8-01A-11D-A33K-10 chr12:10228255 T>C did not map to a codon.
Sequencing variant TCGA-HP-A5N0-01A-11D-A28X-10 chr12:10147805 C>A maps to NM_016509.3 G160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NV-01A-11D-A30V-10 chr3:45077343 G>A maps to NM_003278.2 A179A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A7-01A-11D-A22F-10 chr2:71043462 G>A maps to NM_173535.2 G350G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A3I0-01A-11D-A22F-10 chr2:71043684 A>G maps to NM_173535.2 N276N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MF-01A-11D-A33K-10 chr12:8612253 T>C maps to NM_001007033.1 H61H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A3R3-01A-11D-A22F-10 chr4:141313502 T>C maps to NM_004362.2 K507K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr12:122773082 T>C maps to ENST00000302528 E1200E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr1:155234092 T>A maps to ENST00000424156 R210*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T1-A6J8-01A-11D-A32G-10 chr15:74919877 A>G did not map to a codon.
Sequencing variant TCGA-BC-A217-01A-11D-A152-10 chr5:178040783 A>T maps to NM_020666.2 A201A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11C-01A-11D-A12Z-10 chr13:77569323 A>G maps to NM_006493.2 P149P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NO-01A-11D-A28X-10 chr13:77566253 G>C maps to NM_006493.2 T56T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11D-01A-11D-A12Z-10 chr6:35762976 G>A maps to NM_001832.2 S95S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MC-01A-11D-A22F-10 chr15:65443161 T>C maps to NM_006660.3 *634*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A5SM-01A-12D-A28X-10 chr3:140123516 G>A maps to NM_022131.2 E182E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5263-01A-01D-A12Z-10 chr17:57759021 T>C maps to NM_004859.3 H1088H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BW-A5NO-01A-11D-A27I-10 chr22:19207464 T>A maps to NM_007098.3 R950*. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-DD-A39Y-01A-11D-A20W-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr6:123319263 T>C maps to NM_001010852.2 Y114Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A23B-01A-11D-A16V-10 chr6:123319162 C>T maps to NM_001010852.2 Q81*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39Z-01A-11D-A20W-10 chr12:22215330 A>G maps to NM_018686.3 K359K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A112-01A-11D-A12Z-10 chr16:81736274 G>A did not map to a codon.
Sequencing variant TCGA-CC-A7IK-01A-12D-A33Q-10 chr16:81691393 C>A maps to NM_198390.2 T218T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25W-01A-11D-A16V-10 chr16:66613723 C>A maps to NM_144673.2 R72R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73A-01A-12D-A32G-10 chr5:79026633 C>T maps to NM_153610.3 D682D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr8:88218280 A>C maps to NM_173538.2 P164P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A6M4-01A-11D-A32G-10 chr8:88249210 T>C maps to NM_173538.2 Y214Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr8:88365946 T>G maps to NM_173538.2 P412P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr3:128890512 T>A maps to NM_001127192.1 R30*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5259-01A-31D-A20W-10 chr23:150912894 G>T did not map to a codon.
Sequencing variant TCGA-ED-A66Y-01A-11D-A30V-10 chr23:150912331 C>T did not map to a codon.
Sequencing variant TCGA-G3-A6UC-01A-21D-A33K-10 chr2:98996754 C>A maps to NM_001298.2 S111S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KR-A7K0-01A-12D-A33Q-10 chr11:6265536 C>T maps to NM_001037329.2 P542P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LG-A6GG-01A-11D-A30V-10 chr11:6261356 C>T maps to NM_001037329.2 R111R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr16:57935437 G>A maps to NM_001297.4 L962L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BW-A5NP-01A-11D-A27I-10 chr11:66050238 C>T maps to NM_182553.1 C62C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25S-01A-11D-A16V-10 chr11:66050757 T>G maps to NM_182553.1 Y117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-4073-01B-02D-A12Z-10 chr23:21624910 A>G did not map to a codon.
Sequencing variant TCGA-BC-A10Z-01A-11D-A12Z-10 chr23:21627707 G>T did not map to a codon.
Sequencing variant TCGA-DD-A113-01A-11D-A12Z-10 chr23:21550126 T>C did not map to a codon.
Sequencing variant TCGA-DD-A1EA-01A-11D-A12Z-10 chr23:21545014 G>A did not map to a codon.
Sequencing variant TCGA-DD-A1ED-01A-11D-A152-10 chr23:21458841 A>G did not map to a codon.
Sequencing variant TCGA-DD-A73C-01A-12D-A33K-10 chr23:21515934 C>A did not map to a codon.
Sequencing variant TCGA-EP-A26S-01A-11D-A16V-10 chr10:101120688 C>A maps to NM_020348.2 I605I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5262-01A-01D-A12Z-10 chr10:104679475 A>G maps to NM_017649.3 K413K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NK-01A-11D-A28X-10 chr3:32757736 A>G maps to NM_015442.1 K198K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5258-01A-01D-A12Z-10 chr19:54646891 C>T maps to NM_014516.3 G21G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A5UD-01A-11D-A28X-10 chr7:135095304 T>A maps to NM_001190850.1 K261*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K7-A5RF-01A-11D-A28X-10 chr5:179956353 A>G maps to NM_015455.3 G26G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A115-01A-11D-A12Z-10 chr12:56708751 T>C did not map to a codon.
Sequencing variant TCGA-DD-A73D-01A-12D-A32G-10 chr6:88854114 C>T maps to NM_016083.4 A293A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr1:246784774 C>T maps to NM_152609.2 L142L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75H-01A-11D-A32G-10 chr9:34552229 G>T maps to NM_147164.1 P349P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A112-01A-11D-A12Z-10 chr9:17457519 A>G did not map to a codon.
Sequencing variant TCGA-BC-A216-01A-11D-A152-10 chr12:41410482 G>A did not map to a codon.
Sequencing variant TCGA-DD-A39Z-01A-11D-A20W-10 chr12:41318437 C>G maps to NM_001843.2 P160P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A5KG-01A-11D-A27I-10 chr1:205041629 C>A maps to NM_005076.3 G917G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NJ-01A-11D-A27I-10 chr11:99827703 C>T maps to NM_014361.2 V280V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73E-01A-12D-A32G-10 chr11:99690404 G>T maps to NM_014361.2 L62L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A6UC-01A-21D-A33K-10 chr3:1189705 G>A maps to NM_014461.2 W5*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A7S9-01A-11D-A33Q-10 chr7:146825913 G>T maps to NM_014141.5 E357*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11A-01A-11D-A12Z-10 chr9:39140552 G>T maps to NM_033655.3 G613G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3M9-01A-11D-A20W-10 chr2:125555775 A>T maps to NM_130773.2 T1031T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A7SK-01A-11D-A34Z-10 chr2:125192134 A>T maps to NM_130773.2 K202*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A2QR-01A-11D-A20W-10 chr17:7842847 T>C maps to NM_001037144.4 A315A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr17:40715080 G>C maps to NM_001042532.2 L176L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr7:51096494 T>C maps to ENST00000395542 K848K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1E9-01A-21D-A152-10 chr7:51095516 C>T maps to ENST00000395542 K1174K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr7:51095618 T>G maps to ENST00000395542 T1140T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A9-01A-11D-A25V-10 chr2:165548774 G>A maps to ENST00000392717 L1162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73A-01A-12D-A32G-10 chr17:71199898 C>T maps to NM_018714.2 A783A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A1HT-01A-11D-A12Z-10 chr1:230819334 G>C maps to NM_007357.2 A394A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr13:40293425 C>T maps to ENST00000255468 L479L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A5W4-01A-11D-A28X-10 chr1:103480064 A>T did not map to a codon.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr1:103453233 T>A maps to NM_080629.2 A831A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11C-01A-11D-A12Z-10 chr1:103461592 G>A maps to NM_080629.2 P761P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr1:103461544 C>T maps to NM_080629.2 K777K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr1:103484376 A>T maps to NM_080629.2 P461P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EL-01A-11D-A152-10 chr6:33144990 C>A maps to NM_080680.2 G661G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A1-01A-11D-A20W-10 chr6:33141807 G>T maps to NM_080680.2 R837R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A23B-01A-11D-A16V-10 chr6:33146491 A>G maps to NM_080680.2 D561D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr6:33143843 A>G maps to NM_080680.2 G739G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5262-01A-01D-A12Z-10 chr6:75853092 T>A maps to ENST00000322507 R1568*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A7PZ-01A-11D-A33Q-10 chr6:75887628 T>A maps to ENST00000322507 L729L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75C-01A-11D-A32G-10 chr10:71688712 G>T maps to ENST00000356340 G470G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7ME-01A-11D-A33K-10 chr10:71692350 A>T maps to ENST00000356340 P562P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EA-01A-11D-A12Z-10 chr9:101749574 G>A did not map to a codon.
Sequencing variant TCGA-UB-A7MA-01A-11D-A33Q-10 chr9:101748303 C>A maps to NM_001855.3 P186P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-4073-01B-02D-A12Z-10 chr1:32151293 T>G maps to NM_001856.3 P654P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A7PZ-01A-11D-A33Q-10 chr1:32157243 C>A did not map to a codon.
Sequencing variant TCGA-G3-A25W-01A-11D-A16V-10 chr1:32120417 T>C maps to NM_001856.3 R1444R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MA-01A-11D-A33Q-10 chr1:32133202 G>A maps to NM_001856.3 T1110T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr1:32124124 T>G maps to NM_001856.3 P1328P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr10:105794487 A>T maps to NM_000494.3 P1219P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11D-01A-11D-A12Z-10 chr21:46917552 A>G maps to ENST00000359759 E1302E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EL-01A-11D-A152-10 chr21:46888234 C>A maps to ENST00000359759 P477P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A6M4-01A-11D-A32G-10 chr21:46911136 A>T did not map to a codon.
Sequencing variant TCGA-BC-A10U-01A-11D-A12Z-10 chr6:70852681 C>T maps to NM_001858.4 S532S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr7:94040244 T>C maps to NM_000089.3 A414A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A6UC-01A-21D-A33K-10 chr7:94027069 G>A maps to NM_000089.3 E27E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A7M5-01A-11D-A33Q-10 chr7:94029551 A>T maps to NM_000089.3 T59T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr20:61947980 T>C maps to ENST00000326996 S874S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PD-A5DF-01A-11D-A27I-10 chr20:61937234 G>T maps to ENST00000326996 E114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A1HT-01A-11D-A12Z-10 chr6:56035644 A>G maps to NM_030820.3 G276G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr6:55940291 T>C maps to NM_030820.3 G632G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5263-01A-01D-A12Z-10 chr8:139736901 C>A maps to NM_152888.1 G735*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A6M6-01A-11D-A32G-10 chr8:139620229 G>T maps to NM_152888.1 G1327G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7II-01A-11D-A33K-10 chr5:177669081 G>T maps to ENST00000390654 G514G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T1-A6J8-01A-11D-A32G-10 chr5:177673418 C>A maps to ENST00000390654 S444S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr1:86340971 T>C maps to NM_152890.5 E1024E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A2QR-01A-11D-A20W-10 chr9:117015213 T>A did not map to a codon.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr7:7530241 T>A maps to NM_001037763.2 P354P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73A-01A-12D-A32G-10 chr2:189856232 C>T maps to NM_000090.3 G291G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A7PZ-01A-11D-A33Q-10 chr2:189861937 C>A maps to NM_000090.3 G603G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr2:189864284 T>A maps to NM_000090.3 P737P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EF-01A-11D-A12Z-10 chr13:111077154 A>G maps to NM_001846.2 G85G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr13:111144453 A>G maps to NM_001846.2 G1164G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr2:227886776 G>A maps to ENST00000396625 G1401G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11D-01A-11D-A12Z-10 chr2:227892672 A>T maps to ENST00000396625 P1342P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr2:227875173 G>T maps to ENST00000396625 G1459G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A113-01A-11D-A12Z-10 chr23:107834826 C>T did not map to a codon.
Sequencing variant TCGA-DD-A1EB-01A-11D-A12Z-10 chr23:107807133 C>A did not map to a codon.
Sequencing variant TCGA-DD-A3A8-01A-11D-A22F-10 chr23:107910380 A>G did not map to a codon.
Sequencing variant TCGA-EP-A2KC-01A-11D-A20W-10 chr23:107834315 T>C did not map to a codon.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr23:107821342 T>A did not map to a codon.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr23:107464586 A>G did not map to a codon.
Sequencing variant TCGA-DD-A4NQ-01A-21D-A28X-10 chr23:107681208 A>T did not map to a codon.
Sequencing variant TCGA-DD-A73F-01A-11D-A32G-10 chr23:107402852 G>T did not map to a codon.
Sequencing variant TCGA-KR-A7K7-01A-11D-A33K-10 chr23:107422544 A>C did not map to a codon.
Sequencing variant TCGA-RC-A6M4-01A-11D-A32G-10 chr23:107423749 A>T did not map to a codon.
Sequencing variant TCGA-CC-A3MC-01A-11D-A22F-10 chr9:137630605 T>C maps to NM_000093.3 P482P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RG-A7D4-01A-12D-A33Q-10 chr9:137713940 A>T did not map to a codon.
Sequencing variant TCGA-BW-A5NQ-01A-11D-A27I-10 chr2:238255171 C>A maps to NM_004369.3 G2356*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5261-01A-01D-A12Z-10 chr2:238249680 G>A maps to NM_004369.3 S2626S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EG-01A-11D-A20W-10 chr2:238285640 G>A maps to NM_004369.3 V948V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EL-01A-11D-A152-10 chr2:238280489 C>T maps to NM_004369.3 S1390S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A495-01A-11D-A25V-10 chr2:238245048 A>G maps to NM_004369.3 T2898T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EA-01A-11D-A12Z-10 chr3:130113754 C>T maps to ENST00000312481 D1005D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A66X-01A-11D-A30V-10 chr3:130107780 G>A maps to ENST00000312481 A740A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr3:130092492 G>A maps to ENST00000312481 L4L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A3KG-01A-11D-A20W-10 chr3:130282158 C>T maps to NM_001102608.1 S104S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NH-01A-11D-A27I-10 chr3:48610138 T>A maps to NM_000094.3 K2289*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr3:48625361 T>C maps to NM_000094.3 E907E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr3:48609830 T>C maps to NM_000094.3 G2320G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CJ-01A-11D-A20W-10 chr3:48608293 C>T maps to NM_000094.3 R2424R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5261-01A-01D-A12Z-10 chr3:99514181 C>T maps to ENST00000429802 L480L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11A-01A-11D-A12Z-10 chr1:36565804 C>T maps to NM_005202.2 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LG-A6GG-01A-11D-A30V-10 chr6:70981792 T>A did not map to a codon.
Sequencing variant TCGA-MI-A75I-01A-11D-A32G-10 chr6:71004220 C>A maps to NM_001851.4 T115T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr1:40777785 T>A did not map to a codon.
Sequencing variant TCGA-MI-A75G-01A-11D-A32G-10 chr18:334784 G>A maps to NM_130386.2 P591P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A114-01A-11D-A12Z-10 chr13:76111798 C>A did not map to a codon.
Sequencing variant TCGA-DD-A3A1-01A-11D-A20W-10 chr19:18899994 G>A maps to NM_000095.2 L168L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10U-01A-11D-A12Z-10 chr7:99686934 C>T maps to NM_006833.4 C33C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A113-01A-11D-A12Z-10 chr2:237998515 A>G maps to NM_006710.4 E70E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K7-A6G5-01A-11D-A30V-10 chr14:74428465 G>T maps to NM_182476.1 E413*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EB-01A-11D-A12Z-10 chr4:47746440 A>C maps to NM_006587.2 P259P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25U-01A-11D-A16V-10 chr15:68937509 T>C maps to NM_006091.3 R9R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10Y-01A-11D-A12Z-10 chr16:84623755 G>A maps to NM_021149.2 R91R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MC-01A-11D-A22F-10 chr17:13980194 A>G maps to NM_001303.3 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A12J-01A-11D-A12Z-10 chr20:30227826 C>T maps to NM_032609.2 N58N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A4XI-01A-11D-A25V-10 chr12:120878336 A>G maps to NM_004373.2 E109E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr12:120875943 T>C maps to NM_004373.2 G5G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A3I0-01A-11D-A22F-10 chr8:68658310 G>T maps to NM_020361.4 C18*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BW-A5NO-01A-11D-A27I-10 chr19:17068703 A>G maps to ENST00000443236 T802T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A2-01A-11D-A20W-10 chr19:17115179 G>A maps to ENST00000443236 S249S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A118-01A-11D-A12Z-10 chr17:28772897 G>T maps to NM_001304.4 A911A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A2QR-01A-11D-A20W-10 chr17:28770948 T>C maps to NM_001304.4 L835L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73D-01A-12D-A32G-10 chr4:15067829 C>T maps to NM_001177382.1 G977G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A112-01A-11D-A12Z-10 chr10:93999726 G>A maps to NM_014912.4 I127I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25Z-01A-11D-A16V-10 chr5:173382914 G>T maps to NM_030627.2 V655V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MC-01A-11D-A22F-10 chr10:101825000 G>A maps to NM_001308.2 R235*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NS-01A-11D-A30V-10 chr10:101823464 G>T maps to NM_001308.2 S259S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NQ-01A-21D-A28X-10 chr20:34220600 C>A maps to NM_003915.5 R54R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73G-01A-22D-A32G-10 chr8:87549816 C>A maps to NM_003909.3 Y162*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A217-01A-11D-A152-10 chr6:36712087 G>T maps to NM_020939.1 P482P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25T-01A-11D-A16V-10 chr3:9756639 G>A did not map to a codon.
Sequencing variant TCGA-BD-A3EP-01A-11D-A22F-10 chr8:145634527 G>T maps to NM_013291.2 Y5*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1ED-01A-11D-A152-10 chr14:92621559 T>C maps to NM_017437.1 G445G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LG-A6GG-01A-11D-A30V-10 chr14:92609349 A>G maps to NM_017437.1 V284V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NG-01A-11D-A27I-10 chr1:1257365 T>G did not map to a codon.
Sequencing variant TCGA-G3-A25Z-01A-11D-A16V-10 chr11:68525192 A>G maps to NM_001876.3 S747S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75H-01A-11D-A32G-10 chr7:29160617 A>G maps to NM_031311.3 C20C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr7:29103851 T>A did not map to a codon.
Sequencing variant TCGA-G3-A7M6-01A-11D-A33Q-10 chr23:88008953 G>A did not map to a codon.
Sequencing variant TCGA-G3-A25T-01A-11D-A16V-10 chr10:125601902 G>A maps to NM_198148.2 F205F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5261-01A-01D-A12Z-10 chr4:8605902 C>T maps to NM_001014447.2 Q233*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A8-01A-11D-A22F-10 chr4:8621091 C>T maps to NM_001014447.2 A569A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BD-A2L6-01A-11D-A20W-10 chr1:207739188 A>G maps to NM_000651.4 Q1291Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MB-01A-11D-A20W-10 chr1:207679428 G>A did not map to a codon.
Sequencing variant TCGA-ED-A459-01A-11D-A25V-10 chr1:207679330 T>A maps to NM_000651.4 Y68*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr1:207741307 A>G maps to NM_000651.4 G1364G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BW-A5NO-01A-11D-A27I-10 chr1:207870920 G>A maps to NM_175710.1 Q312Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr1:207890959 C>T maps to NM_175710.1 I522I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr1:207646132 A>T maps to NM_001006658.2 P529P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25S-01A-11D-A16V-10 chr1:207641905 C>T maps to NM_001006658.2 I160I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MA-01A-11D-A33Q-10 chr1:207651317 T>A maps to NM_001006658.2 T997T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25V-01A-11D-A16V-10 chr7:65617295 G>A maps to NM_014478.4 K133K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A7S9-01A-11D-A33Q-10 chr19:4171378 G>A did not map to a codon.
Sequencing variant TCGA-ED-A5KG-01A-11D-A27I-10 chr16:3817805 C>T maps to NM_004380.2 V1055V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr16:3778390 G>T maps to NM_004380.2 A2219A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T1-A6J8-01A-11D-A32G-10 chr5:76249896 C>G maps to NM_001882.3 T73T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A5UE-01A-11D-A28X-10 chr17:43861913 G>T maps to NM_001145146.1 G2*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IK-01A-12D-A33Q-10 chr17:43910819 C>A maps to NM_001145146.1 I311I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75H-01A-11D-A32G-10 chr17:43911987 A>T did not map to a codon.
Sequencing variant TCGA-CC-5259-01A-31D-A20W-10 chr2:36691796 T>C maps to NM_016441.2 N330N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr2:36771540 C>A maps to NM_016441.2 T882T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11C-01A-11D-A12Z-10 chr6:43274202 A>G maps to ENST00000449267 C127C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A7SK-01A-11D-A34Z-10 chr6:49668497 C>G did not map to a codon.
Sequencing variant TCGA-DD-A4NF-01A-11D-A27I-10 chr6:49698948 A>G maps to NM_001190986.1 N202N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3M9-01A-11D-A20W-10 chr8:75932131 A>G maps to NM_031461.5 T385T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A23B-01A-11D-A16V-10 chr19:18707745 T>A maps to NM_004750.4 K271*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75G-01A-11D-A32G-10 chr23:1327775 G>C did not map to a codon.
Sequencing variant TCGA-G3-A7M5-01A-11D-A33Q-10 chr20:20033132 T>A maps to NM_016652.4 R113*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LG-A6GG-01A-11D-A30V-10 chr1:152382363 T>A maps to NM_016190.2 T398T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73F-01A-11D-A32G-10 chr7:86986878 T>C maps to NM_001143935.1 L58L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10R-01A-11D-A12Z-10 chr1:153924494 T>C maps to NM_181715.2 P332P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A7SK-01A-11D-A34Z-10 chr1:153920973 G>A maps to NM_181715.2 H607H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A3JL-01A-11D-A20W-10 chr15:91150627 T>C maps to NM_022769.3 A165A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HP-A5N0-01A-11D-A28X-10 chr12:107395608 T>C maps to NM_004075.3 E176E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73G-01A-22D-A32G-10 chr22:27026302 G>A did not map to a codon.
Sequencing variant TCGA-MI-A75G-01A-11D-A32G-10 chr2:208986519 G>T maps to NM_006891.3 Y134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73C-01A-12D-A33K-10 chr21:35003836 T>C maps to ENST00000416217 Q31Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4ND-01A-11D-A25V-10 chr12:53553481 A>G maps to NM_015989.4 N438N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr20:47675053 A>G maps to NM_001316.2 T18T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A1HT-01A-11D-A12Z-10 chr8:3081363 G>T maps to NM_033225.5 G1457G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3M9-01A-11D-A20W-10 chr8:2799991 A>C did not map to a codon.
Sequencing variant TCGA-CC-A3M9-01A-11D-A20W-10 chr8:3443700 T>C maps to NM_033225.5 T393T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39V-01A-11D-A20W-10 chr8:2954518 T>C maps to NM_033225.5 G2330G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39W-01A-11D-A20W-10 chr8:3267014 C>T maps to NM_033225.5 E558E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A4-01A-11D-A22F-10 chr8:2876119 C>T maps to NM_033225.5 T2636T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr8:2967693 A>G maps to NM_033225.5 D2198D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr8:3216814 G>T maps to NM_033225.5 R1055R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MC-01A-11D-A33Q-10 chr8:3216737 G>A maps to NM_033225.5 A1080A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3M9-01A-11D-A20W-10 chr1:34498285 T>G maps to ENST00000373381 P102P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A5UD-01A-11D-A28X-10 chr1:34038175 G>A maps to ENST00000373381 G2524G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11C-01A-11D-A12Z-10 chr1:34037318 A>G maps to ENST00000373381 T2550T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr1:34128579 T>A maps to ENST00000373381 K1349*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BD-A2L6-01A-11D-A20W-10 chr8:113668401 A>G maps to NM_198123.1 G995G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IF-01A-11D-A33K-10 chr8:113418768 G>T maps to NM_198123.1 S1931S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr8:113326784 A>T maps to NM_198123.1 Y2474*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IJ-01A-11D-A33Q-10 chr8:113326811 A>G maps to NM_198123.1 S2465S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NR-01A-11D-A30V-10 chr8:114031311 A>G maps to NM_198123.1 F338F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NV-01A-11D-A30V-10 chr8:113519058 C>A did not map to a codon.
Sequencing variant TCGA-DD-A73E-01A-12D-A32G-10 chr8:113585850 T>A maps to NM_198123.1 L1307L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QA-A7B7-01A-11D-A32G-10 chr8:113569136 T>G maps to NM_198123.1 G1363G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A6M4-01A-11D-A32G-10 chr8:113529404 A>T maps to NM_198123.1 T1538T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr8:113237149 A>T maps to NM_198123.1 P3658P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr8:113702109 T>A maps to NM_198123.1 I714I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BD-A3EP-01A-11D-A22F-10 chr4:71115097 T>C maps to NM_005212.2 T157T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A6M6-01A-11D-A32G-10 chr13:37679219 C>G maps to NM_145203.5 L58L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HP-A5N0-01A-11D-A28X-10 chr3:47618645 T>C maps to ENST00000383738 G290G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10Z-01A-11D-A12Z-10 chr8:68105730 T>G maps to ENST00000389042 G1151G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr8:67976716 A>T maps to ENST00000389042 R28R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IK-01A-12D-A33Q-10 chr8:68107737 C>T maps to ENST00000389042 F1227F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr3:39185785 G>T maps to NM_033027.3 R208R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K7-A5RF-01A-11D-A28X-10 chr3:39184866 C>G maps to NM_033027.3 V483V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A2QR-01A-11D-A20W-10 chr12:51457624 C>A maps to NM_030809.1 T512T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr12:77253333 A>G maps to NM_001321.1 Y166Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A2-01A-11D-A20W-10 chr11:19204230 C>A maps to NM_003476.3 E191*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7ME-01A-11D-A33K-10 chr20:23856825 T>A maps to NM_001900.4 *143L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IL-01A-11D-A33Q-10 chr20:23584365 T>A maps to NM_001008693.2 R87R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr20:23586296 T>G maps to NM_001008693.2 R69R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IG-01A-11D-A33K-10 chr20:23546706 T>C maps to NM_080610.2 V86V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A118-01A-11D-A12Z-10 chr23:100078294 G>T did not map to a codon.
Sequencing variant TCGA-KR-A7K2-01A-12D-A33Q-10 chr23:100086582 A>G did not map to a codon.
Sequencing variant TCGA-CC-A7IF-01A-11D-A33K-10 chr10:53458520 T>A maps to NM_015235.2 P263P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KR-A7K8-01A-11D-A33K-10 chr23:134947977 G>C did not map to a codon.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr23:153880819 G>T did not map to a codon.
Sequencing variant TCGA-BC-A112-01A-11D-A12Z-10 chr4:1206150 G>A maps to NM_001328.2 I400I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7II-01A-11D-A33K-10 chr10:126715002 G>A maps to NM_022802.2 P442P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A495-01A-11D-A25V-10 chr20:56073608 C>T maps to NM_080618.2 K663K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IK-01A-12D-A33Q-10 chr18:77455995 A>T maps to NM_004715.3 K140*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K7-A5RF-01A-11D-A28X-10 chr3:37988644 A>C maps to NM_001008392.1 P59P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K7-A6G5-01A-11D-A30V-10 chr15:44816345 T>C maps to NM_016396.2 L459L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39Z-01A-11D-A20W-10 chr1:70881688 A>G maps to NM_001902.5 K73K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A9-01A-11D-A25V-10 chr5:138266251 G>T maps to ENST00000355078 E701*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10Y-01A-11D-A12Z-10 chr2:80085160 C>T maps to ENST00000402739 S107S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A115-01A-11D-A12Z-10 chr2:80101326 A>G maps to ENST00000402739 R237R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NK-01A-11D-A28X-10 chr2:80801439 G>T did not map to a codon.
Sequencing variant TCGA-BC-A10U-01A-11D-A12Z-10 chr3:41266134 T>C maps to NM_001904.3 P44P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr3:41275033 T>C maps to NM_001904.3 G400G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A66Y-01A-11D-A30V-10 chr20:36431329 G>T maps to NM_030877.3 E365*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A7XO-01A-11D-A34Z-10 chr20:36470821 G>A did not map to a codon.
Sequencing variant TCGA-DD-A11C-01A-11D-A12Z-10 chr11:57569522 C>T maps to NM_001085458.1 H425H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A496-01A-11D-A25V-10 chr11:57577635 G>T maps to NM_001085458.1 G831*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A217-01A-11D-A152-10 chr5:10992756 C>A maps to NM_001332.2 S1039S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39Y-01A-11D-A20W-10 chr5:11159821 G>A maps to NM_001332.2 I675I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NG-01A-11D-A27I-10 chr5:11117630 A>T maps to NM_001332.2 C736*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A2-01A-11D-A20W-10 chr1:206325311 A>C maps to ENST00000361052 A184A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NI-A4U2-01A-11D-A28X-10 chr1:150778407 C>A maps to NM_000396.3 E110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A3R2-01A-11D-A22F-10 chr9:90342997 G>A maps to NM_145918.2 L61L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25U-01A-11D-A16V-10 chr1:150722587 T>C maps to NM_004079.4 E229E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A5UE-01A-11D-A28X-10 chr7:117351761 T>A maps to NM_033427.2 S1607S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NR-01A-11D-A30V-10 chr7:117398013 C>T maps to NM_033427.2 P1061P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A12J-01A-11D-A12Z-10 chr16:88776354 C>T maps to ENST00000378384 F51F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A112-01A-11D-A12Z-10 chr10:17169923 C>G did not map to a codon.
Sequencing variant TCGA-CC-A5UD-01A-11D-A28X-10 chr10:16877185 T>A maps to NM_001081.3 R3397*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1ED-01A-11D-A152-10 chr10:17024536 A>G maps to NM_001081.3 R1547R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EF-01A-11D-A12Z-10 chr10:17130261 A>G maps to NM_001081.3 C616C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MD-01A-12D-A34Z-10 chr10:16882373 C>T maps to NM_001081.3 S3329S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr7:148451109 A>G maps to NM_003592.2 Q61Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A7XP-01A-11D-A34Z-10 chr2:225376242 T>C maps to NM_003590.3 V237V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MA-01A-11D-A33Q-10 chr2:225367699 T>C maps to NM_003590.3 Q489Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A2-01A-11D-A20W-10 chr13:113898776 G>T maps to NM_001008895.1 E428*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A217-01A-11D-A152-10 chr23:119669736 A>C did not map to a codon.
Sequencing variant TCGA-UB-A7MA-01A-11D-A33Q-10 chr6:43005506 G>A maps to NM_001168370.1 T1756T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HP-A5MZ-01A-21D-A27I-10 chr6:43166473 C>A maps to ENST00000354495 P977P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr6:43155008 T>A maps to ENST00000354495 P471P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A5SI-01A-31D-A27I-10 chr2:180815589 G>A maps to NM_020943.2 A627A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A2-01A-11D-A20W-10 chr17:36977154 T>A maps to NM_017748.3 K64*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A5SK-01A-11D-A27I-10 chr17:36958365 C>T maps to NM_017748.3 E419E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39X-01A-11D-A20W-10 chr5:64079685 T>C maps to NM_005869.2 R92R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11A-01A-11D-A12Z-10 chr10:102003452 A>G did not map to a codon.
Sequencing variant TCGA-DD-A39V-01A-11D-A20W-10 chr11:107309855 A>G maps to NM_152434.2 G208G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73E-01A-12D-A32G-10 chr11:107299751 A>G maps to NM_152434.2 C402C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A5SK-01A-11D-A27I-10 chr4:49046852 A>G maps to NM_025087.2 R618R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr19:42937970 A>G maps to NM_198477.1 S39S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-O8-A75V-01A-11D-A32G-10 chr4:74964376 T>C maps to NM_002089.3 K83K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75I-01A-11D-A32G-10 chr23:70836902 A>T did not map to a codon.
Sequencing variant TCGA-DD-A4NS-01A-11D-A30V-10 chr2:136872510 G>A maps to NM_001008540.1 L333L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A2QR-01A-11D-A20W-10 chr11:118764606 G>A maps to NM_001716.3 G118G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10Q-01A-11D-A12Z-10 chr2:237489914 C>T maps to NM_020311.2 H269H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A23B-01A-11D-A16V-10 chr23:30578386 C>A did not map to a codon.
Sequencing variant TCGA-DD-A1ED-01A-11D-A152-10 chr23:35966466 T>C did not map to a codon.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr23:35989739 T>G did not map to a codon.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr23:35971755 A>G did not map to a codon.
Sequencing variant TCGA-DD-A73E-01A-12D-A32G-10 chr23:45060067 C>A did not map to a codon.
Sequencing variant TCGA-DD-A73F-01A-11D-A32G-10 chr23:45011085 C>T did not map to a codon.
Sequencing variant TCGA-DD-A39Z-01A-11D-A20W-10 chr23:40489972 A>G did not map to a codon.
Sequencing variant TCGA-DD-A73F-01A-11D-A32G-10 chr23:40498274 T>G did not map to a codon.
Sequencing variant TCGA-DD-A1ED-01A-11D-A152-10 chr23:105876228 A>G did not map to a codon.
Sequencing variant TCGA-ED-A5KG-01A-11D-A27I-10 chr23:23934444 G>A did not map to a codon.
Sequencing variant TCGA-FV-A495-01A-11D-A25V-10 chr23:23953336 C>A did not map to a codon.
Sequencing variant TCGA-G3-A25S-01A-11D-A16V-10 chr23:23953504 A>G did not map to a codon.
Sequencing variant TCGA-RG-A7D4-01A-12D-A33Q-10 chr17:4058037 G>A maps to NM_144611.3 A154A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25V-01A-11D-A16V-10 chr1:202935659 A>G maps to NM_016243.2 P78P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25W-01A-11D-A16V-10 chr15:22956490 C>A maps to NM_014608.2 S576S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A114-01A-11D-A12Z-10 chr5:156768086 G>T maps to ENST00000442283 R890R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A7-01A-11D-A22F-10 chr5:156727772 C>G maps to ENST00000442283 A146A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A7M5-01A-11D-A33Q-10 chr5:156816274 C>T maps to ENST00000442283 L1121L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A123-01A-11D-A12Z-10 chr23:83128876 G>T did not map to a codon.
Sequencing variant TCGA-CC-A5UD-01A-11D-A28X-10 chr23:83126556 G>A did not map to a codon.
Sequencing variant TCGA-CC-A7IK-01A-12D-A33Q-10 chr23:83128469 G>T did not map to a codon.
Sequencing variant TCGA-DD-A11A-01A-11D-A12Z-10 chr23:83129261 G>A did not map to a codon.
Sequencing variant TCGA-DD-A3A9-01A-11D-A25V-10 chr23:83129238 A>G did not map to a codon.
Sequencing variant TCGA-FV-A496-01A-11D-A25V-10 chr23:83128348 T>A did not map to a codon.
Sequencing variant TCGA-DD-A1EF-01A-11D-A12Z-10 chr9:105767036 T>C maps to NM_001340.3 L81L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr9:105767560 T>C maps to NM_001340.3 D216D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A1HT-01A-11D-A12Z-10 chr8:143993482 T>C maps to NM_000498.3 T475T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A9-01A-11D-A25V-10 chr8:143994783 G>A maps to NM_000498.3 A346A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr15:75013935 T>C maps to NM_000499.3 G316G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1ED-01A-11D-A152-10 chr15:75047230 T>C maps to NM_000761.3 F451F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GJ-A6C0-01A-12D-A30V-10 chr2:38301744 G>A maps to NM_000104.3 Q263*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10Z-01A-11D-A12Z-10 chr2:72371120 G>A maps to NM_019885.2 R142R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A7SF-01A-11D-A34Z-10 chr19:41594949 C>T maps to NM_000766.3 S99S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A2-01A-11D-A20W-10 chr19:41354234 G>C maps to NM_000762.5 V181V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A113-01A-11D-A12Z-10 chr10:96493058 G>T maps to NM_000772.2 T385T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39X-01A-11D-A20W-10 chr10:96447909 G>A maps to NM_000772.2 W120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A7M7-01A-12D-A34Z-10 chr10:96796968 A>G maps to NM_000770.3 D463D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73D-01A-12D-A32G-10 chr19:41622415 G>A maps to NM_000774.3 V76V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NK-01A-11D-A28X-10 chr6:46620283 C>T maps to NM_016593.3 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A12J-01A-11D-A12Z-10 chr6:46607277 C>T maps to NM_016593.3 L147L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39Y-01A-11D-A20W-10 chr7:99364062 G>A maps to NM_017460.3 R268*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A6M6-01A-11D-A32G-10 chr7:99447234 C>T maps to NM_022820.3 L196L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IF-01A-11D-A33K-10 chr7:99270217 G>T maps to NM_000777.3 V101V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10T-01A-11D-A12Z-10 chr1:47603267 C>A maps to NM_001010969.2 L37L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr1:47264910 G>A maps to NM_001099772.1 W53*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NI-01A-11D-A27I-10 chr19:16000328 C>T maps to NM_001082.3 R274R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IK-01A-12D-A33Q-10 chr19:15636152 G>A maps to NM_173483.3 L2L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A12J-01A-11D-A12Z-10 chr19:15760905 C>T maps to NM_000896.2 T277T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-O8-A75V-01A-11D-A32G-10 chr8:65537038 C>A maps to NM_004820.3 L60L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A9-01A-11D-A25V-10 chr23:77528232 T>C did not map to a codon.
Sequencing variant TCGA-DD-A39X-01A-11D-A20W-10 chr14:59793327 A>G maps to NM_014992.1 T425T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A3KF-01A-11D-A20W-10 chr1:57480889 T>C maps to ENST00000371231 Q403Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25W-01A-11D-A16V-10 chr5:39376176 G>T maps to NM_001343.2 S723S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73G-01A-22D-A32G-10 chr13:72049303 G>A maps to ENST00000359684 G738G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr23:85906100 A>T did not map to a codon.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr23:86069719 A>G did not map to a codon.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr23:85404069 G>T did not map to a codon.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr23:85769361 G>T did not map to a codon.
Sequencing variant TCGA-DD-A1EK-01A-11D-A20W-10 chr14:59112757 G>T maps to NM_016651.5 E473*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KC-01A-11D-A20W-10 chr3:49569128 C>T maps to NM_004393.4 T395T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A8-01A-11D-A22F-10 chr11:61496464 C>A maps to NM_006133.2 L278L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A3R2-01A-11D-A22F-10 chr11:61502407 C>A maps to NM_006133.2 I354I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A6M6-01A-11D-A32G-10 chr7:6474590 C>T maps to NM_139179.3 G160G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A115-01A-11D-A12Z-10 chr9:90272969 G>A maps to NM_004938.2 A617A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EJ-01A-11D-A152-10 chr9:90318035 G>A maps to NM_004938.2 L988L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A5SM-01A-12D-A28X-10 chr2:159651943 T>A did not map to a codon.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr1:159176131 C>G maps to NM_001122951.2 P303P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A7M5-01A-11D-A33Q-10 chr1:159175432 C>T maps to NM_001122951.2 T70T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1E9-01A-21D-A152-10 chr1:173825829 G>A maps to NM_018122.4 L567L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EA-01A-11D-A12Z-10 chr3:16639044 A>G maps to NM_001190811.1 Y102Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A6M4-01A-11D-A32G-10 chr9:121929739 G>A maps to NM_014618.2 G636G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NF-01A-11D-A27I-10 chr23:125685360 G>A did not map to a codon.
Sequencing variant TCGA-DD-A4NV-01A-11D-A30V-10 chr23:125685426 C>T did not map to a codon.
Sequencing variant TCGA-BC-A3KG-01A-11D-A20W-10 chr23:125299292 G>T did not map to a codon.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr23:125298936 C>A did not map to a codon.
Sequencing variant TCGA-K7-A5RF-01A-11D-A28X-10 chr23:125298988 G>A did not map to a codon.
Sequencing variant TCGA-QA-A7B7-01A-11D-A32G-10 chr14:69520834 C>T maps to NM_003861.2 V856V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EB-01A-11D-A12Z-10 chr23:27998515 G>A did not map to a codon.
Sequencing variant TCGA-G3-A7M5-01A-11D-A33Q-10 chr23:27999288 T>A did not map to a codon.
Sequencing variant TCGA-FV-A3I0-01A-11D-A22F-10 chr23:27765468 C>T did not map to a codon.
Sequencing variant TCGA-MI-A75G-01A-11D-A32G-10 chr17:43101863 T>C maps to NM_001128631.1 T211T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MA-01A-11D-A20W-10 chr6:117861868 A>G maps to ENST00000338728 Q380Q. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-MI-A75G-01A-11D-A32G-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-DD-A73D-01A-12D-A32G-10 chr11:6661101 A>G maps to NM_003737.2 T581T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr11:6644032 T>A maps to NM_003737.2 L2958L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5259-01A-31D-A20W-10 chr4:155243494 A>T maps to NM_017639.3 V933V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A1HT-01A-11D-A12Z-10 chr4:155226012 C>A maps to NM_017639.3 G1350*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MB-01A-11D-A20W-10 chr4:155278417 T>C maps to NM_017639.3 E251E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IF-01A-11D-A33K-10 chr4:155412381 C>T maps to NM_001142552.1 R42R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr4:155226267 T>C maps to NM_017639.3 Q1337Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A2-01A-11D-A20W-10 chr4:155157678 C>A maps to NM_017639.3 E2254*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A6M4-01A-11D-A32G-10 chr4:155256018 C>G did not map to a codon.
Sequencing variant TCGA-DD-A3A8-01A-11D-A22F-10 chr4:71889377 A>G maps to ENST00000504952 Q168Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25T-01A-11D-A16V-10 chr4:71888085 A>G maps to ENST00000504952 E70E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10Y-01A-11D-A12Z-10 chr13:36385024 G>T maps to NM_004734.4 Y545*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NI-01A-11D-A27I-10 chr4:151168790 C>A maps to NM_001040261.4 I622I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3M9-01A-11D-A20W-10 chr1:114454509 A>G maps to NM_022836.3 S432S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EI-01A-11D-A12Z-10 chr10:14976378 C>T maps to NM_001033855.1 Q226Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr12:91546949 A>T maps to NM_133503.2 L223L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A1-01A-11D-A20W-10 chr3:53326494 T>A maps to ENST00000480258 A329A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A6UC-01A-21D-A33K-10 chr11:126201384 G>A maps to NM_014026.3 T154T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A116-01A-11D-A12Z-10 chr1:155003098 C>A maps to NM_144622.2 R276R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25S-01A-11D-A16V-10 chr9:34614116 G>A maps to NM_024348.2 L164L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39X-01A-11D-A20W-10 chr16:23654295 T>C maps to NM_032486.3 S23S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39Y-01A-11D-A20W-10 chr3:182665123 T>C did not map to a codon.
Sequencing variant TCGA-DD-A11C-01A-11D-A12Z-10 chr4:52779747 T>C maps to ENST00000451288 *337Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39Y-01A-11D-A20W-10 chr23:110574141 G>T did not map to a codon.
Sequencing variant TCGA-G3-A25T-01A-11D-A16V-10 chr23:110644537 A>G did not map to a codon.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr11:61091479 T>A maps to NM_001923.3 K298*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10R-01A-11D-A12Z-10 chr11:47260381 A>G maps to NM_000107.2 E422E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25V-01A-11D-A16V-10 chr11:47256455 C>A maps to NM_000107.2 S284*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25W-01A-11D-A16V-10 chr7:50607705 G>T maps to NM_000790.3 P74P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5262-01A-01D-A12Z-10 chr14:53522390 T>C maps to NM_001160148.1 K744K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A123-01A-11D-A12Z-10 chr14:53540462 A>G maps to NM_001160148.1 D464D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr14:53521252 T>C maps to NM_001160148.1 S780S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MR-A520-01A-11D-A25V-10 chr1:20980768 G>A maps to NM_005216.4 F264F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A7M6-01A-11D-A33Q-10 chr6:30861166 C>A maps to NM_013994.2 L438L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr20:3180749 T>G did not map to a codon.
Sequencing variant TCGA-RC-A6M4-01A-11D-A32G-10 chr2:15736868 A>T maps to NM_004939.1 T48T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GJ-A6C0-01A-12D-A30V-10 chr16:70363838 G>A maps to NM_007242.4 L297L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75I-01A-11D-A32G-10 chr24:15024658 G>T did not map to a codon.
Sequencing variant TCGA-G3-A25U-01A-11D-A16V-10 chr5:176939386 C>A maps to NM_016222.2 R519R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A1-01A-11D-A20W-10 chr5:134121197 T>A maps to ENST00000452510 T462T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A459-01A-11D-A25V-10 chr5:134117756 A>T maps to ENST00000452510 L342L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A3RK-01A-11D-A22F-10 chr5:134152220 T>A maps to ENST00000452510 A846A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr10:70666603 A>G maps to NM_024045.1 E75E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr23:23019626 A>G did not map to a codon.
Sequencing variant TCGA-DD-A3A8-01A-11D-A22F-10 chr7:44609639 A>T maps to NM_019082.2 P366P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A217-01A-11D-A152-10 chr4:169382957 C>T maps to NM_001012967.1 W166*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A495-01A-11D-A25V-10 chr8:91031396 T>C maps to NM_001359.1 P138P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A4ZP-01A-12D-A25V-10 chr1:161091966 C>G maps to ENST00000368005 L339L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75I-01A-11D-A32G-10 chr19:42713935 T>A maps to NM_133328.2 R169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25U-01A-11D-A16V-10 chr6:35289120 G>T maps to NM_022047.3 G610G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr16:90023995 C>A maps to NM_207514.1 P161P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr16:90021592 G>A maps to NM_207514.1 L108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BD-A3EP-01A-11D-A22F-10 chr6:49936571 T>A maps to NM_001037729.1 K23*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A5SI-01A-31D-A27I-10 chr6:18249917 C>T maps to NM_003472.3 E242E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BW-A5NO-01A-11D-A27I-10 chr7:140301983 C>A maps to NM_015689.3 E72*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr7:140285438 A>G maps to NM_015689.3 L399L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A2QQ-01A-11D-A22F-10 chr1:111738546 T>A maps to NM_024901.3 S212S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr8:142185461 A>T maps to NM_014957.2 L733L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr8:142188200 C>A maps to NM_014957.2 V834V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A9-01A-11D-A25V-10 chr15:65959790 G>C maps to ENST00000443035 S1746*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75G-01A-11D-A32G-10 chr15:66031082 T>C maps to ENST00000443035 V254V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EL-01A-11D-A152-10 chr1:153913915 C>G maps to NM_014856.2 A352A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5262-01A-01D-A12Z-10 chr9:19325934 A>G did not map to a codon.
Sequencing variant TCGA-CC-5259-01A-31D-A20W-10 chr11:9192220 G>A maps to NM_015213.2 F670F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr12:31605206 T>C maps to NM_144973.3 K432K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K7-A5RF-01A-11D-A28X-10 chr12:31552685 C>A maps to NM_144973.3 L990L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NR-01A-11D-A30V-10 chr1:68954708 G>A maps to NM_001114120.1 G160G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KR-A7K0-01A-12D-A33Q-10 chr5:59940644 G>T maps to NM_018369.2 V212V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IF-01A-11D-A33K-10 chr12:100660785 A>T maps to ENST00000422147 L23L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10T-01A-11D-A12Z-10 chr22:32188762 C>T maps to NM_001136029.1 R243*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A3KF-01A-11D-A20W-10 chr8:124037285 A>G maps to NM_024295.4 A90A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5262-01A-01D-A12Z-10 chr8:124054283 A>G maps to NM_024295.4 L27L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NK-01A-11D-A28X-10 chr7:24758743 C>T maps to NM_001127453.1 Q166Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A113-01A-11D-A12Z-10 chr8:145540246 G>A maps to NM_012079.4 L479L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EA-01A-11D-A12Z-10 chr11:75508293 T>G maps to NM_032564.3 A242A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NQ-01A-21D-A28X-10 chr11:75509439 G>T maps to NM_032564.3 G326G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A6UC-01A-21D-A33K-10 chr22:19124883 T>C maps to NM_022719.2 E329E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A7M7-01A-12D-A34Z-10 chr22:20307213 G>A maps to NM_033257.3 L73L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10T-01A-11D-A12Z-10 chr12:56332337 C>T maps to NM_201554.1 D131D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1ED-01A-11D-A152-10 chr12:56345832 T>C maps to NM_201554.1 A534A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75I-01A-11D-A32G-10 chr7:14741335 G>A maps to NM_004080.2 D162D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KR-A7K8-01A-11D-A33K-10 chr2:234299113 C>A maps to NM_152879.2 V111V. Only missense variants will be evaluated by CHASM.
Reference base specified for sequencing variant TCGA-DD-A3A3-01A-11D-A22F-10 chr3:186006617 C>A does not match reference base at that coordinate in hg19.
Sequencing variant TCGA-RC-A6M3-01A-11D-A32G-10 chr3:185997720 G>A maps to NM_001346.2 D237D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39Z-01A-11D-A20W-10 chr13:42764599 C>T maps to NM_178009.2 S658S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MA-01A-11D-A20W-10 chr7:137374711 A>G maps to NM_004717.2 A146A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr7:137170143 A>T maps to NM_004717.2 S801S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr23:50125537 A>G did not map to a codon.
Sequencing variant TCGA-DD-A3A9-01A-11D-A25V-10 chr23:50147102 C>T did not map to a codon.
Sequencing variant TCGA-DD-A39V-01A-11D-A20W-10 chr4:967111 C>A maps to NM_001347.2 P53P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A3RK-01A-11D-A22F-10 chr2:74185302 A>G maps to NM_080916.1 P246P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39V-01A-11D-A20W-10 chr1:55340776 G>A maps to NM_014762.3 R201*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73E-01A-12D-A32G-10 chr11:71146468 C>T maps to NM_001360.2 E460E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr14:24507077 C>T maps to NM_001082488.1 G85G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr14:60619872 A>G maps to NM_016029.2 G139G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A26S-01A-11D-A16V-10 chr17:9683304 A>G maps to ENST00000330255 C106C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A7PZ-01A-11D-A33Q-10 chr10:12126674 G>T maps to NM_018706.5 R149R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RG-A7D4-01A-12D-A33Q-10 chr4:24531240 T>A maps to NM_001358.2 T751T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39W-01A-11D-A20W-10 chr6:30624170 G>A maps to NM_003587.4 T809T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NL-01A-11D-A28X-10 chr6:30624803 A>G maps to NM_003587.4 D691D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25V-01A-11D-A16V-10 chr6:30633482 G>T maps to NM_003587.4 R232R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A1-01A-11D-A20W-10 chr19:47876047 C>A maps to NM_014681.5 A610A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NF-01A-11D-A27I-10 chr19:47861353 C>T maps to NM_014681.5 L417L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A3R3-01A-11D-A22F-10 chr20:37621022 C>T maps to NM_021931.3 H179H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A3KF-01A-11D-A20W-10 chr12:125451368 T>A maps to NM_032656.3 S520S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A3R3-01A-11D-A22F-10 chr12:125455934 C>G maps to NM_032656.3 V368V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25U-01A-11D-A16V-10 chr16:72142232 C>A maps to NM_014003.3 S1024S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A5-01A-11D-A22F-10 chr2:39088479 G>A maps to NM_198963.1 R358*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IK-01A-12D-A33Q-10 chr17:41582012 G>A maps to NM_004941.1 A516A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-O8-A75V-01A-11D-A32G-10 chr17:41590857 G>T maps to NM_004941.1 T877T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr1:182836132 A>T maps to NM_001357.4 G504G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LG-A6GG-01A-11D-A30V-10 chr23:95940061 A>C did not map to a codon.
Sequencing variant TCGA-DD-A11A-01A-11D-A12Z-10 chr13:60498942 A>C maps to NM_001042517.1 L712L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr14:95560493 C>A did not map to a codon.
Sequencing variant TCGA-ED-A4XI-01A-11D-A25V-10 chr20:61511820 A>G maps to NM_033081.2 S1829S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A4ZQ-01A-11D-A25V-10 chr20:61512903 C>A maps to NM_033081.2 A1468A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A6UC-01A-21D-A33K-10 chr20:61525547 T>A did not map to a codon.
Sequencing variant TCGA-RC-A7SF-01A-11D-A34Z-10 chr1:54359900 A>G maps to NM_000792.5 P6P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A5UE-01A-11D-A28X-10 chr21:47952071 G>T maps to ENST00000318711 V410V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A9-01A-11D-A25V-10 chr21:47931357 G>A maps to ENST00000318711 K312K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr1:68512863 G>A maps to NM_004675.2 R39R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39V-01A-11D-A20W-10 chr15:66604084 T>A maps to NM_001143688.1 P194P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A7PZ-01A-11D-A33Q-10 chr2:232894735 A>G maps to NM_152383.4 R104R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr2:232889006 A>T maps to NM_152383.4 P77P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr1:231829653 A>T maps to NM_001164537.1 T50T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MF-01A-11D-A33K-10 chr1:231931027 G>T maps to NM_001164537.1 E591*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A5UC-01A-11D-A28X-10 chr1:223176571 C>A maps to NM_032890.2 T611T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25U-01A-11D-A16V-10 chr15:40659779 G>T maps to NM_033510.1 T489T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr23:153996704 A>G did not map to a codon.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr11:11988501 T>C maps to ENST00000450094 R224R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5261-01A-01D-A12Z-10 chr3:38150948 T>A maps to NM_007335.2 P1052P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr3:38080907 C>T maps to NM_007335.2 R64R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A9-01A-11D-A25V-10 chr11:84634118 A>T did not map to a codon.
Sequencing variant TCGA-BC-A10Z-01A-11D-A12Z-10 chr23:69669638 A>G did not map to a codon.
Sequencing variant TCGA-CC-A7IJ-01A-11D-A33Q-10 chr10:79569436 G>A maps to NM_004747.3 I1505I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7II-01A-11D-A33K-10 chr8:1514021 G>T maps to ENST00000357934 L410L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CJ-01A-11D-A20W-10 chr8:1497491 C>T maps to ENST00000357934 P233P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39Z-01A-11D-A20W-10 chr1:35334623 G>A maps to NM_001080418.1 G689G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A118-01A-11D-A12Z-10 chr14:55618446 G>T maps to NM_014750.4 I778I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A23B-01A-11D-A16V-10 chr6:170592755 C>T maps to NM_005618.3 E537E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GJ-A6C0-01A-12D-A30V-10 chr14:75359657 C>T maps to NM_001933.4 P188P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A7PZ-01A-11D-A33Q-10 chr17:48050404 C>A maps to NM_001934.2 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10Q-01A-11D-A12Z-10 chr1:44684029 C>T maps to NM_019100.4 L147L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HP-A5MZ-01A-21D-A27I-10 chr10:124335945 G>A maps to ENST00000368915 V105V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10Q-01A-11D-A12Z-10 chr23:32486706 C>A did not map to a codon.
Sequencing variant TCGA-BC-A10R-01A-11D-A12Z-10 chr23:31496393 G>A did not map to a codon.
Sequencing variant TCGA-CC-A7II-01A-11D-A33K-10 chr23:32834719 T>A did not map to a codon.
Sequencing variant TCGA-CC-A7IK-01A-12D-A33Q-10 chr23:32481604 T>A did not map to a codon.
Sequencing variant TCGA-DD-A115-01A-11D-A12Z-10 chr23:31525445 T>C did not map to a codon.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr23:32366625 T>C did not map to a codon.
Sequencing variant TCGA-DD-A1EB-01A-11D-A12Z-10 chr23:31200853 C>A did not map to a codon.
Sequencing variant TCGA-DD-A4NN-01A-11D-A28X-10 chr23:31747755 G>A did not map to a codon.
Sequencing variant TCGA-ED-A5KG-01A-11D-A27I-10 chr23:31525468 G>T did not map to a codon.
Sequencing variant TCGA-ED-A7PZ-01A-11D-A33Q-10 chr23:32429920 G>T did not map to a codon.
Sequencing variant TCGA-ED-A7XP-01A-11D-A34Z-10 chr23:31496266 C>A did not map to a codon.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr23:32490307 G>T did not map to a codon.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr23:32715996 A>T did not map to a codon.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr23:32328323 A>G did not map to a codon.
Sequencing variant TCGA-FV-A23B-01A-11D-A16V-10 chr23:31462649 G>T did not map to a codon.
Sequencing variant TCGA-FV-A2QR-01A-11D-A20W-10 chr23:31497177 T>C did not map to a codon.
Sequencing variant TCGA-FV-A495-01A-11D-A25V-10 chr23:31165435 G>A did not map to a codon.
Sequencing variant TCGA-KR-A7K2-01A-12D-A33Q-10 chr23:32486814 A>G did not map to a codon.
Sequencing variant TCGA-DD-A4NA-01A-11D-A25V-10 chr5:78322294 G>A maps to NM_013391.2 A714A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MA-01A-11D-A33Q-10 chr5:78320119 G>A maps to NM_013391.2 L742L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73B-01A-12D-A32G-10 chr19:35992754 G>A maps to NM_001035516.3 G17G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CJ-01A-11D-A20W-10 chr19:36000833 C>T maps to NM_033317.4 G339G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75H-01A-11D-A32G-10 chr4:88584444 T>C maps to NM_004407.3 D505D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A9-01A-11D-A25V-10 chr9:990927 C>T maps to NM_021240.2 Q448*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A5SK-01A-11D-A27I-10 chr9:22447694 G>T maps to NM_022160.2 E211*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MA-01A-11D-A33Q-10 chr1:50886866 C>G maps to NM_032110.1 A114A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IK-01A-12D-A33Q-10 chr1:53932265 A>T did not map to a codon.
Sequencing variant TCGA-DD-A3A0-01A-11D-A20W-10 chr5:118569089 A>G maps to NM_005509.4 Q2777Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A3-01A-11D-A22F-10 chr5:118484602 A>G maps to NM_005509.4 P1027P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5259-01A-31D-A20W-10 chr15:51828801 T>A maps to NM_001174116.1 A625A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A7-01A-11D-A22F-10 chr15:51839581 C>T maps to NM_001174116.1 W197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EI-01A-11D-A12Z-10 chr3:52393976 C>T maps to ENST00000273600 Q1485*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HP-A5N0-01A-11D-A28X-10 chr3:52393978 G>A maps to ENST00000273600 Q1485Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39Z-01A-11D-A20W-10 chr12:124305127 A>G maps to NM_207437.3 G1216G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A26S-01A-11D-A16V-10 chr12:124377823 C>T maps to NM_207437.3 L2896L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A23B-01A-11D-A16V-10 chr12:124415999 G>T maps to NM_207437.3 L4181L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25S-01A-11D-A16V-10 chr12:124257448 C>T maps to NM_207437.3 F94F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25V-01A-11D-A16V-10 chr12:124341691 T>C maps to NM_207437.3 D2058D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-O8-A75V-01A-11D-A32G-10 chr12:124419243 C>T maps to NM_207437.3 P4400P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A4-01A-11D-A22F-10 chr7:21657265 C>T maps to NM_003777.3 R1380R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25V-01A-11D-A16V-10 chr7:21940748 C>T maps to NM_003777.3 Y4483Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A7M5-01A-11D-A33Q-10 chr7:21757497 A>T maps to NM_003777.3 T2370T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr7:21630533 A>T did not map to a codon.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr7:21646302 T>C maps to NM_003777.3 Y1268Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5262-01A-01D-A12Z-10 chr3:57438656 A>G maps to NM_178504.4 N1210N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5262-01A-01D-A12Z-10 chr3:57443513 C>T maps to NM_178504.4 K1067K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IK-01A-12D-A33Q-10 chr3:57394213 C>A maps to NM_178504.4 L2004L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A3I1-01A-11D-A22F-10 chr3:57454648 T>C maps to NM_178504.4 E721E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A7M6-01A-11D-A33Q-10 chr3:57356457 C>T maps to NM_178504.4 T2611T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A1-01A-11D-A20W-10 chr17:76472712 C>A maps to ENST00000389840 E2685*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A5-01A-11D-A22F-10 chr17:76462859 C>A maps to ENST00000389840 R2925R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NQ-01A-21D-A28X-10 chr17:76482176 G>T maps to ENST00000389840 I2366I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A23B-01A-11D-A16V-10 chr17:76528758 G>T maps to ENST00000389840 V973V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A2QQ-01A-11D-A22F-10 chr17:76565545 G>A maps to ENST00000389840 L370L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A112-01A-11D-A12Z-10 chr17:7701532 C>T maps to NM_020877.2 I2763I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr17:7644138 G>A maps to NM_020877.2 R506R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A2QR-01A-11D-A20W-10 chr17:7721765 T>C maps to NM_020877.2 A3508A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5259-01A-31D-A20W-10 chr16:21061287 T>A maps to NM_017539.1 P1430P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K7-A5RG-01A-11D-A28X-10 chr16:20981195 T>C maps to NM_017539.1 P2792P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A5UD-01A-11D-A28X-10 chr5:13830158 A>T maps to NM_001369.2 P2075P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73C-01A-12D-A33K-10 chr5:13830841 C>T maps to NM_001369.2 G1975G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73G-01A-22D-A32G-10 chr5:13866358 C>T maps to NM_001369.2 Q1362Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A3JL-01A-11D-A20W-10 chr5:13794080 A>G maps to NM_001369.2 D2658D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A495-01A-11D-A25V-10 chr5:13820596 A>G maps to NM_001369.2 A2233A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KR-A7K8-01A-11D-A33K-10 chr5:13776634 G>A maps to NM_001369.2 R3096*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A112-01A-11D-A12Z-10 chr2:84774639 C>T maps to NM_001370.1 R364*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MB-01A-11D-A20W-10 chr2:84924793 A>G maps to NM_001370.1 L2540L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EK-01A-11D-A20W-10 chr2:84931192 C>T maps to NM_001370.1 V2744V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39Y-01A-11D-A20W-10 chr2:84954803 C>T maps to NM_001370.1 T3328T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A2-01A-11D-A20W-10 chr2:84777069 T>C maps to NM_001370.1 N458N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A12J-01A-11D-A12Z-10 chr2:85043136 G>A maps to NM_001370.1 K4101K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr2:84955002 C>A maps to NM_001370.1 R3395R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LG-A6GG-01A-11D-A30V-10 chr2:84832703 A>T maps to NM_001370.1 T1054T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr2:84954899 A>G maps to NM_001370.1 R3360R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MA-01A-11D-A20W-10 chr2:196750894 T>C maps to NM_018897.2 R1836R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A5UC-01A-11D-A28X-10 chr2:196759698 C>A did not map to a codon.
Sequencing variant TCGA-DD-A113-01A-11D-A12Z-10 chr2:196674471 C>T maps to NM_018897.2 R3295R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A7-01A-11D-A22F-10 chr2:196682481 T>C maps to NM_018897.2 Q3121Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NH-01A-11D-A27I-10 chr2:196740507 G>T maps to NM_018897.2 P2059P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75C-01A-11D-A32G-10 chr2:196866479 A>T maps to NM_018897.2 A364A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A1HT-01A-11D-A12Z-10 chr6:38781905 G>T did not map to a codon.
Sequencing variant TCGA-CC-A5UC-01A-11D-A28X-10 chr6:38891939 T>C did not map to a codon.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr6:38994403 T>A maps to ENST00000327475 V4587V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EL-01A-11D-A152-10 chr6:38747835 A>T maps to ENST00000327475 K700*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A3-01A-11D-A22F-10 chr6:38747841 G>T did not map to a codon.
Sequencing variant TCGA-G3-A25U-01A-11D-A16V-10 chr6:38690903 C>A maps to ENST00000327475 R95R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CJ-01A-11D-A20W-10 chr6:38690854 G>A maps to ENST00000327475 P78P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75E-01A-11D-A32G-10 chr6:38775435 T>A maps to ENST00000327475 L1055L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MD-01A-12D-A34Z-10 chr6:38795994 A>G maps to ENST00000327475 E1361E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5258-01A-01D-A12Z-10 chr17:11738187 G>A maps to NM_001372.3 A3160A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EL-01A-11D-A152-10 chr17:11535902 G>T did not map to a codon.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr17:11661006 C>T maps to NM_001372.3 T2331T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A5SJ-01A-11D-A27I-10 chr17:11573030 C>G maps to NM_001372.3 P1091P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HP-A5N0-01A-11D-A28X-10 chr17:11593044 G>A maps to NM_001372.3 L1302L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A5SM-01A-12D-A28X-10 chr9:34514528 C>T maps to NM_012144.2 D569D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11C-01A-11D-A12Z-10 chr9:33037025 G>A maps to NM_001539.2 K296K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A496-01A-11D-A25V-10 chr19:14629101 G>A maps to NM_006145.1 I20I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IJ-01A-11D-A33Q-10 chr7:157155964 G>T did not map to a codon.
Sequencing variant TCGA-MI-A75E-01A-11D-A32G-10 chr7:157208728 G>A maps to NM_058246.3 K306K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr7:157160146 G>T maps to NM_058246.3 G106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11A-01A-11D-A12Z-10 chr3:128181898 G>A maps to NM_153330.2 L64L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A5-01A-11D-A22F-10 chr10:22207779 C>T maps to NM_022365.3 W219*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr5:138760774 T>C maps to NM_152686.3 T196T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A1-01A-11D-A20W-10 chr7:102957428 C>T maps to NM_014377.1 E425E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LG-A6GG-01A-11D-A30V-10 chr7:102953435 C>T maps to NM_014377.1 A583A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MB-01A-11D-A20W-10 chr9:114411854 A>G maps to NM_001015882.2 K204K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73G-01A-22D-A32G-10 chr13:96409902 A>G maps to NM_006260.4 K133K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A7M6-01A-11D-A33Q-10 chr8:66992664 G>T maps to NM_033105.4 L129L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A3KG-01A-11D-A20W-10 chr2:27500669 G>A maps to NM_173650.1 R54R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr1:65867510 C>A maps to ENST00000371069 T725T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr1:65852602 A>G maps to ENST00000371069 L368L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr1:28536548 C>T maps to NM_014280.2 L111L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr23:153633397 C>T did not map to a codon.
Sequencing variant TCGA-DD-A4NH-01A-11D-A27I-10 chr23:153633193 T>C did not map to a codon.
Sequencing variant TCGA-DD-A118-01A-11D-A12Z-10 chr19:12987091 A>C maps to NM_001375.2 S265S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A113-01A-11D-A12Z-10 chr11:6566485 T>A maps to NM_144666.2 P1439P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A9-01A-11D-A25V-10 chr11:6579425 T>C maps to NM_144666.2 P2967P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NG-01A-11D-A27I-10 chr11:6567457 T>C maps to NM_144666.2 Y1763Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr12:32854461 A>G maps to ENST00000381000 Q72Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73G-01A-22D-A32G-10 chr1:172356430 C>T maps to ENST00000359070 I749I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IL-01A-11D-A33Q-10 chr2:25467522 T>C did not map to a codon.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr1:94342287 T>C maps to NM_014597.4 E401E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A113-01A-11D-A12Z-10 chr16:30018187 G>T maps to NM_003586.2 R266R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A3-01A-11D-A22F-10 chr16:30018526 C>T maps to NM_003586.2 K207K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr16:30020839 G>T maps to NM_003586.2 R101R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NO-01A-11D-A28X-10 chr2:225653872 C>A maps to NM_014689.2 G1776*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25W-01A-11D-A16V-10 chr2:225634957 G>T maps to NM_014689.2 L2138L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A113-01A-11D-A12Z-10 chr23:117752663 T>G did not map to a codon.
Sequencing variant TCGA-DD-A118-01A-11D-A12Z-10 chr23:117788709 C>T did not map to a codon.
Sequencing variant TCGA-DD-A3A9-01A-11D-A25V-10 chr23:117752605 A>G did not map to a codon.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr23:117722104 A>G did not map to a codon.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr23:117722146 T>G did not map to a codon.
Sequencing variant TCGA-KR-A7K0-01A-12D-A33Q-10 chr5:169186740 G>T maps to NM_004946.2 L803L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr5:169122910 G>T maps to NM_004946.2 T316T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EL-01A-11D-A152-10 chr3:51398051 C>T maps to NM_004947.4 T1665T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25T-01A-11D-A16V-10 chr3:51395250 C>A maps to NM_004947.4 L1582L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NI-01A-11D-A27I-10 chr7:111517083 A>G did not map to a codon.
Sequencing variant TCGA-G3-A5SM-01A-12D-A28X-10 chr7:111387427 A>G maps to ENST00000428084 I1496I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LG-A6GG-01A-11D-A30V-10 chr7:111575683 C>G did not map to a codon.
Sequencing variant TCGA-G3-A25U-01A-11D-A16V-10 chr8:25174643 G>A maps to NM_024940.6 L480L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EL-01A-11D-A152-10 chr19:11363498 G>T maps to ENST00000319867 R90R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25Y-01A-11D-A16V-10 chr19:11339689 G>A maps to ENST00000319867 L914L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MA-01A-11D-A33Q-10 chr19:11363511 C>A maps to ENST00000319867 L85L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr1:62995053 T>G maps to ENST00000371140 S1225S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MA-01A-11D-A33Q-10 chr1:63001216 C>T maps to ENST00000371140 L1186L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A1-01A-11D-A20W-10 chr13:99515317 C>T maps to ENST00000428223 R1178R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr13:99519791 T>C did not map to a codon.
Sequencing variant TCGA-UB-A7MD-01A-12D-A34Z-10 chr13:99533810 C>T did not map to a codon.
Sequencing variant TCGA-DD-A73E-01A-12D-A32G-10 chr2:74783057 C>T maps to NM_001381.3 A164A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HP-A5N0-01A-11D-A28X-10 chr5:176936801 C>T did not map to a codon.
Sequencing variant TCGA-G3-A25V-01A-11D-A16V-10 chr4:3491479 G>A maps to ENST00000389653 K243K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IK-01A-12D-A33Q-10 chr6:83862022 A>G maps to NM_015018.2 A2022A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4ND-01A-11D-A25V-10 chr21:37618217 C>T maps to NM_005128.2 L1314L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A6M4-01A-11D-A32G-10 chr21:37618610 C>T maps to NM_005128.2 L1445L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10Z-01A-11D-A12Z-10 chr19:2217052 G>A maps to ENST00000221482 G836G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr6:30919180 T>A maps to NM_080870.3 P980P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NR-01A-11D-A30V-10 chr19:38713009 G>A maps to NM_001135155.1 C122C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11C-01A-11D-A12Z-10 chr14:73181158 T>C maps to NM_012074.3 E192E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A112-01A-11D-A12Z-10 chr9:130699763 G>A maps to ENST00000373110 V14V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr2:116593731 G>T did not map to a codon.
Sequencing variant TCGA-CC-A7IG-01A-11D-A33K-10 chr11:66259029 C>A maps to NM_005700.3 G288G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr11:66249886 C>T maps to NM_005700.3 P72P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25W-01A-11D-A16V-10 chr11:66262717 C>A maps to NM_005700.3 I477I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr11:66258739 T>C maps to NM_005700.3 S228S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A1HT-01A-11D-A12Z-10 chr7:154263940 C>T maps to NM_130797.2 A189A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75H-01A-11D-A32G-10 chr7:154593129 A>T maps to NM_130797.2 G455G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QA-A7B7-01A-11D-A32G-10 chr19:4695539 G>T maps to ENST00000357909 P480P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10W-01A-11D-A12Z-10 chr3:109028178 T>C did not map to a codon.
Sequencing variant TCGA-BW-A5NP-01A-11D-A27I-10 chr3:109026918 G>T maps to NM_138815.3 S206S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr19:54139944 T>A maps to NM_001012728.1 G93G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NJ-01A-11D-A27I-10 chr7:35013142 T>C maps to NM_015283.1 L226L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75I-01A-11D-A32G-10 chr7:34981497 T>C did not map to a codon.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr7:35053221 G>A maps to NM_015283.1 P96P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A4ZQ-01A-11D-A25V-10 chr10:134012416 C>A maps to NM_006426.2 Y251*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25Z-01A-11D-A16V-10 chr10:134018355 T>C maps to NM_006426.2 D547D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25U-01A-11D-A16V-10 chr2:27162929 C>A maps to NM_020134.3 R327R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NQ-01A-21D-A28X-10 chr2:74745707 T>A maps to NM_133637.2 P673P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr11:65688798 A>T did not map to a codon.
Sequencing variant TCGA-BC-A10U-01A-11D-A12Z-10 chr23:100513347 C>G did not map to a codon.
Sequencing variant TCGA-BC-A217-01A-11D-A152-10 chr18:28650706 A>T maps to ENST00000438199 P758P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4ND-01A-11D-A25V-10 chr18:28650774 T>A maps to ENST00000438199 K736*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A0-01A-11D-A20W-10 chr18:28604327 T>C maps to NM_001941.3 E254E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10Z-01A-11D-A12Z-10 chr21:41505790 G>T maps to NM_001389.3 T1184T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BW-A5NP-01A-11D-A27I-10 chr21:41427742 C>A maps to NM_001389.3 T1648T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7II-01A-11D-A33K-10 chr21:42064796 G>A maps to NM_001389.3 S149S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EK-01A-11D-A20W-10 chr21:41719858 G>T maps to NM_001389.3 A316A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39Z-01A-11D-A20W-10 chr21:41455833 C>G did not map to a codon.
Sequencing variant TCGA-DD-A39Z-01A-11D-A20W-10 chr21:41455834 C>A maps to NM_001389.3 G1411*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A23B-01A-11D-A16V-10 chr11:117389232 T>C maps to NM_020693.2 T546T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A5SM-01A-12D-A28X-10 chr11:117342744 C>T maps to NM_020693.2 W991*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr18:65178260 T>C maps to NM_032160.2 E1205E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr18:65180192 A>G maps to NM_032160.2 F561F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NI-01A-11D-A27I-10 chr18:29115250 T>C maps to NM_001943.3 D433D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EF-01A-11D-A12Z-10 chr18:28956906 T>C maps to NM_001134453.1 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25S-01A-11D-A16V-10 chr18:28991245 G>A maps to NM_001134453.1 S749S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11A-01A-11D-A12Z-10 chr20:35383169 C>T maps to NM_001145315.1 Q319Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BW-A5NP-01A-11D-A27I-10 chr6:7580847 C>T maps to NM_004415.2 T1475T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MA-01A-11D-A20W-10 chr6:7580097 C>G maps to NM_004415.2 S1225S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A2QQ-01A-11D-A22F-10 chr6:7585456 G>A maps to NM_004415.2 Q2654Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75I-01A-11D-A32G-10 chr6:7571704 A>T maps to NM_004415.2 S597S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A3KG-01A-11D-A20W-10 chr6:56497658 T>C maps to ENST00000361203 A1055A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MB-01A-11D-A20W-10 chr6:56418421 A>G maps to ENST00000361203 C4845C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr6:56328484 G>A maps to ENST00000361203 R7375*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73G-01A-22D-A32G-10 chr6:56341126 G>A maps to ENST00000361203 A7017A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr6:56350121 G>T maps to ENST00000361203 I6854I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EB-01A-11D-A12Z-10 chr1:205180510 G>A maps to NM_015375.2 F51F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A0-01A-11D-A20W-10 chr1:212238256 A>G did not map to a codon.
Sequencing variant TCGA-BC-A217-01A-11D-A152-10 chr18:32438290 A>G maps to NM_001390.4 E498E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr15:49935631 C>T maps to NM_001144955.1 L258L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr7:76112437 A>T maps to NM_020892.2 P294P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EG-01A-11D-A20W-10 chr15:45386374 G>A maps to NM_014080.4 H1540H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39Y-01A-11D-A20W-10 chr17:80020817 A>G maps to NM_022156.3 P143P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MB-01A-11D-A20W-10 chr7:107216858 A>G maps to NM_181581.1 E176E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10R-01A-11D-A12Z-10 chr1:221912366 G>A maps to NM_007207.3 T240T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BW-A5NQ-01A-11D-A27I-10 chr1:221879680 G>A maps to NM_007207.3 T313T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A7M5-01A-11D-A33Q-10 chr1:161723026 T>G maps to NM_007240.1 A279A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5261-01A-01D-A12Z-10 chr23:44703614 G>A did not map to a codon.
Sequencing variant TCGA-DD-A11B-01A-11D-A16Z-10 chr1:167095693 C>T maps to NM_001080426.1 S442S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EF-01A-11D-A12Z-10 chr1:167095360 G>A maps to NM_001080426.1 K331K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A3I0-01A-11D-A22F-10 chr1:167096332 G>C maps to NM_001080426.1 G655G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25U-01A-11D-A16V-10 chr1:167096470 C>A maps to NM_001080426.1 S701S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LG-A6GG-01A-11D-A30V-10 chr1:167096125 G>C maps to NM_001080426.1 L586L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A8-01A-11D-A22F-10 chr10:112262620 T>C maps to NM_004419.3 Y174Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A118-01A-11D-A12Z-10 chr12:89743031 C>A maps to NM_001946.2 *382L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10Q-01A-11D-A12Z-10 chr23:152914787 G>A did not map to a codon.
Sequencing variant TCGA-UB-A7MD-01A-12D-A34Z-10 chr17:7137467 G>A maps to NM_004422.2 I38I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IJ-01A-11D-A33Q-10 chr14:102508726 G>A maps to NM_001376.4 V4094V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A115-01A-11D-A12Z-10 chr14:102466375 G>A maps to NM_001376.4 G1285G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A7M9-01A-23D-A34Z-10 chr14:102446825 T>G maps to NM_001376.4 T300T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BD-A3EP-01A-11D-A22F-10 chr11:103027463 A>G maps to NM_001080463.1 E1364E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NV-01A-11D-A30V-10 chr11:103229041 T>C maps to NM_001080463.1 S4044S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr11:103152946 T>C maps to NM_001080463.1 L3608L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr11:103058311 A>G maps to NM_001080463.1 Q2379Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75G-01A-11D-A32G-10 chr11:102984321 A>G maps to NM_001080463.1 E84E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A3KF-01A-11D-A20W-10 chr2:44032354 A>G maps to NM_001193464.1 E322E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A3-01A-11D-A22F-10 chr17:56166588 C>T maps to NM_080677.2 F73F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25U-01A-11D-A16V-10 chr23:37701139 C>A did not map to a codon.
Sequencing variant TCGA-CC-A7IL-01A-11D-A33Q-10 chr21:38865316 A>T did not map to a codon.
Sequencing variant TCGA-EP-A3JL-01A-11D-A20W-10 chr21:38865435 G>T maps to NM_001396.3 G357*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A7SK-01A-11D-A34Z-10 chr2:71827926 G>A maps to NM_001130987.1 P1284P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr2:71780940 C>T maps to NM_001130987.1 C663C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BW-A5NO-01A-11D-A27I-10 chr2:207527924 A>G maps to NM_001093730.1 N445N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A82E-01A-11D-A34Z-10 chr2:207528077 T>C maps to NM_001093730.1 Q394Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A9-01A-11D-A25V-10 chr15:55783380 T>A maps to NM_130810.2 T115T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr13:96237035 C>A maps to NM_198968.2 V826V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A6M4-01A-11D-A32G-10 chr3:137787108 T>G maps to NM_173543.2 P572P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A5UC-01A-11D-A28X-10 chr3:108363328 G>A maps to NM_014648.3 W487*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QA-A7B7-01A-11D-A32G-10 chr3:108407749 C>T maps to NM_014648.3 C1165C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A6M4-01A-11D-A32G-10 chr3:108405432 T>A did not map to a codon.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr3:108396341 A>T did not map to a codon.
Sequencing variant TCGA-DD-A1EK-01A-11D-A20W-10 chr2:11593706 C>G did not map to a codon.
Sequencing variant TCGA-BC-A216-01A-11D-A152-10 chr11:19251119 T>A maps to NM_024680.2 K592*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr16:2282754 A>C did not map to a codon.
Sequencing variant TCGA-LG-A6GG-01A-11D-A30V-10 chr3:15475935 T>G maps to NM_033083.6 P139P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A496-01A-11D-A25V-10 chr5:158139189 G>A maps to NM_024007.3 N507N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10Z-01A-11D-A12Z-10 chr8:25715970 G>A maps to NM_022659.2 S464S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IF-01A-11D-A33K-10 chr1:43637962 A>G maps to NM_001159936.1 L44L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HP-A5N0-01A-11D-A28X-10 chr1:43630463 T>C maps to NM_001159936.1 K295K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A7M9-01A-23D-A34Z-10 chr10:74912125 T>G maps to NM_001135752.1 P279P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10W-01A-11D-A12Z-10 chr2:233344955 C>A maps to NM_004826.2 L745L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25Y-01A-11D-A16V-10 chr19:39322022 A>G maps to NM_001398.2 S62S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11D-01A-11D-A12Z-10 chr23:69249365 A>T did not map to a codon.
Sequencing variant TCGA-G3-A7M5-01A-11D-A33Q-10 chr15:74925258 G>A maps to NM_025083.3 V407V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HP-A5N0-01A-11D-A28X-10 chr1:184702093 G>T maps to NM_025191.3 I163I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A12J-01A-11D-A12Z-10 chr4:148457096 G>A maps to NM_001957.3 A272A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A7SK-01A-11D-A34Z-10 chr4:148463733 C>T maps to NM_001957.3 N416N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NN-01A-11D-A28X-10 chr13:78474005 T>C maps to ENST00000377211 K484K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A6M6-01A-11D-A32G-10 chr13:78477335 C>G maps to ENST00000377211 L342L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A69H-01A-11D-A30V-10 chr12:93205204 T>C maps to NM_003566.3 L683L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75C-01A-11D-A32G-10 chr12:93205144 A>G maps to NM_003566.3 H703H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A26S-01A-11D-A16V-10 chr20:62122017 C>A maps to NM_001958.2 A281A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LG-A6GG-01A-11D-A30V-10 chr1:245250659 T>A maps to ENST00000421886 *299K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A496-01A-11D-A25V-10 chr17:60493467 C>T maps to NM_001144933.1 D417D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25S-01A-11D-A16V-10 chr12:3782652 T>C maps to NM_001144958.1 E210E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A1-01A-11D-A20W-10 chr22:43936087 G>A maps to NM_022785.3 D1266D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QA-A7B7-01A-11D-A32G-10 chr1:63998375 C>T maps to NM_032437.2 A145A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A8-01A-11D-A22F-10 chr8:16956031 A>G maps to NM_181723.2 T318T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25V-01A-11D-A16V-10 chr3:19962060 T>C did not map to a codon.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr3:19921297 T>C did not map to a codon.
Sequencing variant TCGA-FV-A2QQ-01A-11D-A22F-10 chr6:52334231 G>A maps to NM_018100.3 L413L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A118-01A-11D-A12Z-10 chr23:44091922 C>T did not map to a codon.
Sequencing variant TCGA-DD-A39Z-01A-11D-A20W-10 chr23:44109536 A>G did not map to a codon.
Sequencing variant TCGA-FV-A23B-01A-11D-A16V-10 chr23:44109451 A>G did not map to a codon.
Sequencing variant TCGA-RC-A6M4-01A-11D-A32G-10 chr23:44109643 G>T did not map to a codon.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr17:42937414 T>C did not map to a codon.
Sequencing variant TCGA-MI-A75G-01A-11D-A32G-10 chr4:110915961 C>T maps to NM_001963.4 P977P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A7SB-01A-21D-A34Z-10 chr4:110862302 T>C did not map to a codon.
Sequencing variant TCGA-RC-A7SF-01A-11D-A34Z-10 chr4:110925745 G>T maps to NM_001963.4 E1087*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5259-01A-31D-A20W-10 chr23:13645317 G>C did not map to a codon.
Sequencing variant TCGA-CC-A7II-01A-11D-A33K-10 chr5:38438474 C>T maps to ENST00000354891 A794A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A113-01A-11D-A12Z-10 chr5:38406943 T>A maps to ENST00000354891 P281P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39Z-01A-11D-A20W-10 chr5:38337732 T>C did not map to a codon.
Sequencing variant TCGA-FV-A2QQ-01A-11D-A22F-10 chr5:38451431 A>G maps to ENST00000354891 R861R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RG-A7D4-01A-12D-A33Q-10 chr5:38409152 C>T maps to ENST00000354891 H432H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr7:55224337 G>T maps to NM_005228.3 P373P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25W-01A-11D-A16V-10 chr10:64575690 G>A maps to NM_001136178.1 A33A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MB-01A-11D-A20W-10 chr8:22548279 G>A maps to NM_004430.2 D290D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MB-01A-11D-A20W-10 chr15:42245960 C>A did not map to a codon.
Sequencing variant TCGA-DD-A1EK-01A-11D-A20W-10 chr3:184910060 G>A maps to NM_001966.3 L709L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EF-01A-11D-A12Z-10 chr9:140707933 C>T maps to NM_024757.4 N1044N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73C-01A-12D-A33K-10 chr6:31860512 T>A did not map to a codon.
Sequencing variant TCGA-G3-A3CK-01A-11D-A20W-10 chr12:104698074 C>T maps to NM_001008394.1 D121D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr3:150285798 G>A maps to NM_032025.3 K220K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A115-01A-11D-A12Z-10 chr15:40268640 C>T maps to NM_001013703.2 C615C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-4073-01B-02D-A12Z-10 chr2:27590023 C>T maps to NM_172195.3 E330E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IJ-01A-11D-A33Q-10 chr2:27590909 C>A maps to NM_172195.3 L249L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A4-01A-11D-A22F-10 chr3:183855594 T>A did not map to a codon.
Sequencing variant TCGA-BC-A10Y-01A-11D-A12Z-10 chr23:24084189 T>C did not map to a codon.
Sequencing variant TCGA-MI-A75I-01A-11D-A32G-10 chr10:120801557 G>A maps to NM_003750.2 P1158P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IL-01A-11D-A33Q-10 chr8:117658833 C>T maps to ENST00000411422 Q293Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25T-01A-11D-A16V-10 chr11:32610276 T>C maps to NM_006360.3 L105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K7-A6G5-01A-11D-A30V-10 chr4:99850251 G>A maps to NM_001130679.1 V4V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10R-01A-11D-A12Z-10 chr3:184039488 G>T maps to NM_001194947.1 E380*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A116-01A-11D-A12Z-10 chr3:184049264 G>A maps to NM_001194947.1 V1429V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25W-01A-11D-A16V-10 chr11:10828410 T>C maps to ENST00000429377 G94G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MA-01A-11D-A20W-10 chr14:103803077 T>C maps to NM_183004.3 R73R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MF-01A-11D-A33K-10 chr17:7212997 C>G maps to NM_001143760.1 S45*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MF-01A-11D-A33K-10 chr19:855637 C>T maps to NM_001972.2 N147N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A123-01A-11D-A12Z-10 chr19:11569051 G>A maps to NM_001420.3 A179A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A23B-01A-11D-A16V-10 chr19:11577474 G>A maps to NM_001420.3 F59F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A3-01A-11D-A22F-10 chr23:129200819 G>T did not map to a codon.
Sequencing variant TCGA-G3-A25U-01A-11D-A16V-10 chr11:34527176 T>C maps to NM_198381.1 T50T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5261-01A-01D-A12Z-10 chr23:47496429 C>T did not map to a codon.
Sequencing variant TCGA-CC-A5UD-01A-11D-A28X-10 chr5:95242486 C>G did not map to a codon.
Sequencing variant TCGA-DD-A39W-01A-11D-A20W-10 chr5:95224586 C>T maps to NM_012081.5 E637E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CK-01A-11D-A20W-10 chr5:95236729 T>A maps to NM_012081.5 K266*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr11:107526787 A>G maps to NM_018712.3 T276T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr4:141448649 T>C did not map to a codon.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr4:111119422 G>A maps to NM_024090.2 I23I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EG-01A-11D-A20W-10 chr5:60050626 G>A maps to NM_024930.2 Q224*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IK-01A-12D-A33Q-10 chr1:79411968 G>T maps to NM_022159.3 T105T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IL-01A-11D-A33Q-10 chr1:79472324 C>A maps to NM_022159.3 P5P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr1:79404923 G>T maps to NM_022159.3 C115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25V-01A-11D-A16V-10 chr1:79356901 C>T did not map to a codon.
Sequencing variant TCGA-BC-A3KF-01A-11D-A20W-10 chr4:101396222 T>C maps to NM_016242.3 T77T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A113-01A-11D-A12Z-10 chr4:101401080 A>T maps to NM_016242.3 T60T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr23:153607909 G>T did not map to a codon.
Sequencing variant TCGA-UB-A7MD-01A-12D-A34Z-10 chr16:1826217 C>T maps to NM_001010865.1 L438L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MC-01A-11D-A22F-10 chr18:2891528 C>T maps to NM_032048.2 C468C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A26S-01A-11D-A16V-10 chr19:46112991 A>G maps to NM_001193268.1 L828L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NI-01A-11D-A27I-10 chr11:62376465 T>C maps to ENST00000278845 R300R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73D-01A-12D-A32G-10 chr11:62373663 C>T maps to ENST00000278845 Q510Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NA-01A-11D-A25V-10 chr2:42488345 C>T maps to NM_019063.3 R142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25W-01A-11D-A16V-10 chr14:89124555 G>T maps to ENST00000380664 S1284S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A6M6-01A-11D-A32G-10 chr12:13366480 C>A maps to NM_001423.2 C49*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NJ-01A-11D-A27I-10 chr19:14877173 G>T maps to NM_013447.2 S169S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73E-01A-12D-A32G-10 chr19:14740910 G>T maps to NM_032571.3 T584T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr19:14765978 T>A did not map to a codon.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr19:14749128 A>T maps to NM_032571.3 G424G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A5SJ-01A-11D-A27I-10 chr2:73160941 G>A maps to NM_004097.2 R244R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KR-A7K0-01A-12D-A33Q-10 chr11:94823276 T>G maps to NM_015036.2 A62A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BD-A2L6-01A-11D-A20W-10 chr9:130587247 A>T maps to NM_001114753.1 T274T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr17:77073754 T>C maps to NM_001042573.1 Y75Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10W-01A-11D-A12Z-10 chr1:8930510 C>T maps to NM_001428.2 K80K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr12:7026811 G>C maps to NM_001975.2 R126R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-O8-A75V-01A-11D-A32G-10 chr23:129813672 T>C did not map to a codon.
Sequencing variant TCGA-RC-A7SF-01A-11D-A34Z-10 chr23:129813523 T>C did not map to a codon.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr8:120594813 A>G maps to NM_006209.3 N576N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr6:132006561 A>T maps to NM_005021.3 I393I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A6M4-01A-11D-A32G-10 chr4:185074756 C>T maps to NM_153343.3 W124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10R-01A-11D-A12Z-10 chr17:77711820 G>A maps to NM_178543.3 V451V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K7-A5RF-01A-11D-A28X-10 chr22:40216998 T>C maps to NM_152512.3 A277A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A9-01A-11D-A25V-10 chr10:97626019 T>C maps to NM_001098175.1 P478P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A7PY-01A-11D-A33Q-10 chr10:97626109 G>A maps to NM_001098175.1 K508K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11B-01A-11D-A16Z-10 chr3:40442396 C>T maps to NM_001248.2 L61L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A23B-01A-11D-A16V-10 chr22:41545853 T>C maps to NM_001429.3 P823P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GJ-A6C0-01A-12D-A30V-10 chr22:41574845 T>C maps to NM_001429.3 A2377A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7II-01A-11D-A33K-10 chr12:132445445 G>T maps to ENST00000333577 L94L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PD-A5DF-01A-11D-A27I-10 chr12:132512743 G>T maps to ENST00000333577 A1800A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A3R3-01A-11D-A22F-10 chr20:34761812 C>A maps to NM_012156.2 G38G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NI-A4U2-01A-11D-A28X-10 chr20:34773212 C>T maps to NM_012156.2 T247T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A66Y-01A-11D-A30V-10 chr18:5419717 C>A maps to NM_012307.2 E500*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr18:5416314 T>C maps to NM_012307.2 T523T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NE-01A-11D-A27I-10 chr5:111643178 C>G maps to NM_022140.3 T36T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75C-01A-11D-A32G-10 chr5:111598278 C>T did not map to a codon.
Sequencing variant TCGA-FV-A4ZQ-01A-11D-A25V-10 chr9:112004034 G>A maps to NM_018424.2 D488D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A123-01A-11D-A12Z-10 chr10:32576203 T>C did not map to a codon.
Sequencing variant TCGA-RC-A7SK-01A-11D-A34Z-10 chr1:38185616 A>G maps to NM_001099439.1 F842F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11B-01A-11D-A16Z-10 chr1:16464911 T>C maps to NM_004431.3 G279G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K7-A6G5-01A-11D-A30V-10 chr1:16464615 C>T maps to NM_004431.3 W348*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25Z-01A-11D-A16V-10 chr3:89391166 C>A maps to NM_005233.5 A411A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10Z-01A-11D-A12Z-10 chr2:222347237 G>T maps to NM_004438.3 V384V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IK-01A-12D-A33Q-10 chr2:222301133 T>A maps to NM_004438.3 A777A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A7S9-01A-11D-A33Q-10 chr2:222428733 C>T maps to NM_004438.3 G180G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A1HT-01A-11D-A12Z-10 chr4:66361223 G>A maps to NM_004439.5 I316I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KR-A7K0-01A-12D-A33Q-10 chr4:66467890 G>T maps to NM_004439.5 I126I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10T-01A-11D-A12Z-10 chr3:96706229 A>T maps to NM_001080448.2 V169V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A5W4-01A-11D-A28X-10 chr3:97194244 C>T maps to NM_001080448.2 A648A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75I-01A-11D-A32G-10 chr3:97185270 A>C maps to ENST00000514100 P5P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A1HT-01A-11D-A12Z-10 chr6:94124468 A>T maps to NM_004440.3 S38S. Only missense variants will be evaluated by CHASM.
Reference base specified for sequencing variant TCGA-FV-A4ZQ-01A-11D-A25V-10 chr6:93982123 G>T does not match reference base at that coordinate in hg19.
Sequencing variant TCGA-MI-A75G-01A-11D-A32G-10 chr6:93969102 G>A maps to NM_004440.3 S631S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IK-01A-12D-A33Q-10 chr1:22895780 G>A did not map to a codon.
Sequencing variant TCGA-K7-A5RG-01A-11D-A28X-10 chr1:22902825 C>T maps to NM_020526.3 D92D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A459-01A-11D-A25V-10 chr1:23222043 T>A maps to ENST00000400191 A557A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IG-01A-11D-A33K-10 chr3:184295207 C>A maps to NM_004443.3 R478R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NL-01A-11D-A28X-10 chr7:100402888 A>T maps to NM_004444.4 S911S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr7:142563374 C>T maps to NM_004445.3 A364A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73G-01A-22D-A32G-10 chr7:142562073 C>T maps to NM_004445.3 S172S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KR-A7K0-01A-12D-A33Q-10 chr8:27382881 G>T maps to ENST00000458037 A354A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr1:92495734 C>A maps to NM_173567.4 S33S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K7-A5RF-01A-11D-A28X-10 chr6:145948713 G>A maps to NM_005670.3 C278C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A3KG-01A-11D-A20W-10 chr19:11491861 G>T maps to NM_000121.3 T203T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BD-A3EP-01A-11D-A22F-10 chr8:144940353 G>A maps to NM_031308.1 R2356R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A116-01A-11D-A12Z-10 chr8:144945357 G>T maps to NM_031308.1 V688V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CK-01A-11D-A20W-10 chr1:220146577 A>G did not map to a codon.
Sequencing variant TCGA-NI-A4U2-01A-11D-A28X-10 chr1:220193424 T>C maps to NM_004446.2 P418P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BW-A5NO-01A-11D-A27I-10 chr12:15813578 T>C maps to NM_004447.5 K302K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MB-01A-11D-A20W-10 chr12:15774277 T>C maps to NM_004447.5 E814E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NG-01A-11D-A27I-10 chr19:55598912 A>T maps to NM_133180.2 S701S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A5UC-01A-11D-A28X-10 chr12:56478883 A>T maps to NM_001982.2 K114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10X-01A-11D-A12Z-10 chr2:212251836 T>C maps to NM_005235.2 E1074E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LG-A6GG-01A-11D-A30V-10 chr12:1192436 A>C maps to NM_178040.2 V259V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BW-A5NO-01A-11D-A27I-10 chr3:56183106 G>A maps to ENST00000460849 I401I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73A-01A-12D-A32G-10 chr3:56468630 G>T maps to ENST00000460849 V135V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A6M6-01A-11D-A32G-10 chr2:128038081 C>A maps to NM_000122.1 E490*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A3KF-01A-11D-A20W-10 chr16:14024745 A>G maps to NM_005236.2 S324S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr16:14020497 A>T maps to NM_005236.2 K157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A5UD-01A-11D-A28X-10 chr23:71425151 G>T did not map to a codon.
Sequencing variant TCGA-QA-A7B7-01A-11D-A32G-10 chr23:71426313 A>G did not map to a codon.
Sequencing variant TCGA-DD-A1EB-01A-11D-A12Z-10 chr5:60200655 A>G maps to NM_000082.3 H148H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EK-01A-11D-A20W-10 chr19:42753846 A>C maps to NM_006494.2 G139G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A2QQ-01A-11D-A22F-10 chr5:172359508 G>A maps to NM_001031711.2 R204R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr16:23707248 G>A maps to NM_033266.3 L574L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11C-01A-11D-A12Z-10 chr14:53149117 C>A maps to NM_014584.1 L81L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10U-01A-11D-A12Z-10 chr1:236416757 A>G maps to NM_019891.3 C90C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25Y-01A-11D-A16V-10 chr12:112460308 G>T maps to NM_006817.3 G213G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A112-01A-11D-A12Z-10 chr18:19112483 G>A maps to NM_052911.2 F775F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7II-01A-11D-A33K-10 chr6:152129175 C>A maps to NM_001122741.1 Y43*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A7M7-01A-12D-A34Z-10 chr6:152415518 G>A did not map to a codon.
Sequencing variant TCGA-CC-A7II-01A-11D-A33K-10 chr14:64727460 G>T maps to NM_001437.2 R220R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NO-01A-11D-A28X-10 chr8:95680360 C>T maps to NM_017697.3 D372D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K7-A5RG-01A-11D-A28X-10 chr8:95676927 C>T maps to NM_017697.3 S216S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75C-01A-11D-A32G-10 chr14:76905704 G>A maps to NM_004452.3 S3S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr5:137843999 G>A maps to NM_004730.2 D436D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A23B-01A-11D-A16V-10 chr19:36135134 A>G did not map to a codon.
Sequencing variant TCGA-FV-A3I0-01A-11D-A22F-10 chr1:157069138 G>A maps to NM_001004341.2 A30A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KR-A7K0-01A-12D-A33Q-10 chr4:5798958 G>T maps to NM_153717.2 L699L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5262-01A-01D-A12Z-10 chr4:5578156 G>A maps to NM_147127.4 L1028L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KC-01A-11D-A20W-10 chr17:29632210 T>C maps to NM_006495.3 P139P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10Y-01A-11D-A12Z-10 chr17:74003348 C>T maps to NM_001988.2 E1979E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A23B-01A-11D-A16V-10 chr17:74015069 G>T maps to NM_001988.2 A403A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr2:176948255 G>A maps to NM_001080458.1 G83G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A115-01A-11D-A12Z-10 chr22:29694813 G>A maps to NM_013986.3 R508R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A12J-01A-11D-A12Z-10 chr9:140201463 C>A maps to NM_017820.3 E857*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EF-01A-11D-A12Z-10 chr1:242035388 G>A maps to NM_006027.4 K441K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-4073-01B-02D-A12Z-10 chr4:56759927 G>A maps to NM_018261.3 R645R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A4ZQ-01A-11D-A25V-10 chr14:57713484 G>A maps to ENST00000340918 Q72*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HP-A5MZ-01A-21D-A27I-10 chr14:57698354 T>C maps to ENST00000340918 K341K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IL-01A-11D-A33Q-10 chr9:37783970 T>C maps to NM_016042.2 P138P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr11:108398907 A>G maps to NM_015065.2 C149C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A6UC-01A-21D-A33K-10 chr11:108381598 C>T maps to NM_015065.2 Q1545Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A2QR-01A-11D-A20W-10 chr8:28575570 G>T maps to NM_001440.2 V665V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IK-01A-12D-A33Q-10 chr8:72229892 A>T maps to NM_000503.4 G150G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11A-01A-11D-A12Z-10 chr8:72233981 G>T maps to NM_000503.4 G135G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A216-01A-11D-A152-10 chr20:45702936 T>C maps to ENST00000360649 S213S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A69H-01A-11D-A30V-10 chr6:65612319 A>G maps to ENST00000370616 C905C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MA-01A-11D-A20W-10 chr6:64498004 A>G maps to ENST00000370616 G2572G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IJ-01A-11D-A33Q-10 chr6:65622635 T>A maps to ENST00000370616 R794R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A8-01A-11D-A22F-10 chr6:65767614 G>A maps to ENST00000370616 Q677*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73F-01A-11D-A32G-10 chr6:65301373 A>G maps to ENST00000370616 S1462S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25W-01A-11D-A16V-10 chr6:65300536 A>G maps to ENST00000370616 D1741D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CH-01A-11D-A22F-10 chr6:65612307 G>A maps to ENST00000370616 V909V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7ME-01A-11D-A33K-10 chr6:65707539 G>A maps to ENST00000370616 Q732*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A112-01A-11D-A12Z-10 chr17:40871172 T>C maps to ENST00000264646 A242A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39X-01A-11D-A20W-10 chr6:159190396 C>T maps to NM_001111077.1 R435R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NE-01A-11D-A27I-10 chr6:159206579 G>T maps to NM_001111077.1 L76L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MA-01A-11D-A20W-10 chr13:113803257 C>T maps to NM_000504.3 G298G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A112-01A-11D-A12Z-10 chr6:6145911 G>A maps to NM_000129.3 D713D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IG-01A-11D-A33K-10 chr6:6248625 G>T maps to NM_000129.3 C239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A6M6-01A-11D-A32G-10 chr19:17001134 G>T maps to NM_003950.2 V287V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr1:169512353 T>C did not map to a codon.
Sequencing variant TCGA-BC-A112-01A-11D-A12Z-10 chr23:154158683 C>G did not map to a codon.
Sequencing variant TCGA-DD-A1ED-01A-11D-A152-10 chr23:154124422 A>G did not map to a codon.
Sequencing variant TCGA-DD-A4NV-01A-11D-A30V-10 chr23:154158629 T>C did not map to a codon.
Sequencing variant TCGA-ED-A459-01A-11D-A25V-10 chr23:154158500 T>A did not map to a codon.
Sequencing variant TCGA-DD-A73D-01A-12D-A32G-10 chr1:46867760 A>G did not map to a codon.
Sequencing variant TCGA-CC-5259-01A-31D-A20W-10 chr8:82371528 C>A maps to NM_001080526.1 P39P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75C-01A-11D-A32G-10 chr11:70049615 C>T maps to NM_003824.3 S17S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10Z-01A-11D-A12Z-10 chr15:80465404 G>A maps to NM_000137.1 G252G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr2:97757305 T>A maps to NM_199336.1 T46T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BD-A2L6-01A-11D-A20W-10 chr12:50291318 C>T maps to NM_012306.2 V121V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BD-A3EP-01A-11D-A22F-10 chr12:50281166 A>T did not map to a codon.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr12:50294961 T>A maps to NM_012306.2 P54P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr1:109171191 A>T maps to NM_001010883.2 S276S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11B-01A-11D-A16Z-10 chr23:55172690 T>C did not map to a codon.
Sequencing variant TCGA-MI-A75G-01A-11D-A32G-10 chr23:55187568 C>T did not map to a codon.
Sequencing variant TCGA-CC-A5UE-01A-11D-A28X-10 chr5:14601218 G>T maps to NM_019018.2 G70G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A112-01A-11D-A12Z-10 chr10:14563196 C>A maps to NM_031453.2 E305*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr10:14563993 T>A maps to NM_031453.2 P226P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IK-01A-12D-A33Q-10 chr5:153413429 T>C maps to ENST00000442256 S115S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr6:170657248 T>A maps to NM_032448.1 P676P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MA-01A-11D-A20W-10 chr23:54162987 T>C did not map to a codon.
Sequencing variant TCGA-G3-A25S-01A-11D-A16V-10 chr23:54160308 G>T did not map to a codon.
Sequencing variant TCGA-HP-A5N0-01A-11D-A28X-10 chr23:133927918 G>A did not map to a codon.
Sequencing variant TCGA-G3-A25U-01A-11D-A16V-10 chr13:51855052 C>T maps to NM_145019.2 P470P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25Y-01A-11D-A16V-10 chr2:225244373 G>A maps to NM_001122779.1 T428T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75C-01A-11D-A32G-10 chr2:225266001 T>A maps to NM_001122779.1 R162*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KR-A7K2-01A-12D-A33Q-10 chr23:134166685 C>A did not map to a codon.
Sequencing variant TCGA-FV-A3I1-01A-11D-A22F-10 chr23:134156304 G>A did not map to a codon.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr9:130279259 G>T maps to NM_022833.2 A283A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NL-01A-11D-A28X-10 chr19:17664296 A>G maps to ENST00000335393 A673A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10R-01A-11D-A12Z-10 chr23:92965113 A>G did not map to a codon.
Sequencing variant TCGA-DD-A3A9-01A-11D-A25V-10 chr23:92964818 A>G did not map to a codon.
Sequencing variant TCGA-G3-A3CK-01A-11D-A20W-10 chr23:92964585 A>G did not map to a codon.
Sequencing variant TCGA-CC-5262-01A-01D-A12Z-10 chr17:40737143 T>C maps to NM_178126.3 Q242Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A7SF-01A-11D-A34Z-10 chr6:71243557 G>T did not map to a codon.
Sequencing variant TCGA-FV-A2QQ-01A-11D-A22F-10 chr4:89772241 T>C maps to NM_014883.2 L312L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MB-01A-11D-A20W-10 chr4:187077240 T>C maps to ENST00000356371 C448C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A4XI-01A-11D-A25V-10 chr4:187073130 A>G maps to ENST00000356371 K297K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EI-01A-11D-A12Z-10 chr1:55075293 C>A maps to NM_176782.2 E469*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr23:68725239 C>A did not map to a codon.
Sequencing variant TCGA-DD-A115-01A-11D-A12Z-10 chr6:117083205 T>C maps to NM_001085480.2 K108K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A6M4-01A-11D-A32G-10 chr1:179783083 T>C maps to NM_173509.2 C88C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25V-01A-11D-A16V-10 chr15:98995195 A>G maps to NM_182562.2 P76P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IJ-01A-11D-A33Q-10 chr10:15290659 C>A maps to NM_001010924.1 A244A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25W-01A-11D-A16V-10 chr10:15255746 G>A maps to NM_001010924.1 L614L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr2:187627315 A>G maps to NM_177454.3 G749G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A113-01A-11D-A12Z-10 chr15:93198580 G>T maps to NM_207446.2 T103T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25S-01A-11D-A16V-10 chr2:29259441 C>A maps to NM_199280.2 S818S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75C-01A-11D-A32G-10 chr2:29222108 G>T maps to NM_199280.2 G68*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr14:45535807 C>T maps to ENST00000361462 T1529T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25S-01A-11D-A16V-10 chr14:45432958 G>A maps to ENST00000361462 A445A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A6-01A-11D-A22F-10 chr6:119327609 A>G did not map to a codon.
Sequencing variant TCGA-BC-A10U-01A-11D-A12Z-10 chr10:15858831 A>G did not map to a codon.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr10:15883431 T>C maps to NM_024948.2 E134E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A3KF-01A-11D-A20W-10 chr7:30821783 A>G maps to NM_032222.2 E125E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A2-01A-11D-A20W-10 chr16:57206204 C>T maps to NM_024946.2 K102K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IK-01A-12D-A33Q-10 chr10:128973669 C>G maps to NM_001039762.2 G330G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5264-01A-01D-A12Z-10 chr4:159048702 A>T maps to NM_001128424.1 S472S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11C-01A-11D-A12Z-10 chr1:179013020 C>T maps to NM_014864.3 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A7M5-01A-11D-A33Q-10 chr10:46272807 A>T maps to ENST00000399588 K744*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A9-01A-11D-A25V-10 chr9:97082513 A>G maps to NM_017561.1 C448C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25T-01A-11D-A16V-10 chr23:153735767 A>G did not map to a codon.
Sequencing variant TCGA-CC-A3MA-01A-11D-A20W-10 chr21:42720629 T>C maps to ENST00000398652 P238P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A1-01A-11D-A20W-10 chr23:79699172 C>T did not map to a codon.
Sequencing variant TCGA-DD-A4NF-01A-11D-A27I-10 chr23:79698051 G>A did not map to a codon.
Sequencing variant TCGA-DD-A73C-01A-12D-A33K-10 chr23:79698132 A>T did not map to a codon.
Sequencing variant TCGA-DD-A73F-01A-11D-A32G-10 chr23:79698374 C>T did not map to a codon.
Sequencing variant TCGA-NI-A4U2-01A-11D-A28X-10 chr23:79698450 G>A did not map to a codon.
Sequencing variant TCGA-BC-A10W-01A-11D-A12Z-10 chr23:34148611 A>G did not map to a codon.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr23:34149062 A>T did not map to a codon.
Sequencing variant TCGA-DD-A3A9-01A-11D-A25V-10 chr23:34150302 C>T did not map to a codon.
Sequencing variant TCGA-FV-A3I1-01A-11D-A22F-10 chr23:34149523 G>C did not map to a codon.
Sequencing variant TCGA-G3-A25T-01A-11D-A16V-10 chr23:34149593 C>A did not map to a codon.
Sequencing variant TCGA-HP-A5N0-01A-11D-A28X-10 chr23:34149906 C>A did not map to a codon.
Sequencing variant TCGA-RC-A6M6-01A-11D-A32G-10 chr23:34149527 G>C did not map to a codon.
Sequencing variant TCGA-UB-A7MA-01A-11D-A33Q-10 chr23:34149695 G>A did not map to a codon.
Sequencing variant TCGA-BW-A5NO-01A-11D-A27I-10 chr23:34961244 G>A did not map to a codon.
Sequencing variant TCGA-DD-A113-01A-11D-A12Z-10 chr23:34962849 C>T did not map to a codon.
Sequencing variant TCGA-DD-A73B-01A-12D-A32G-10 chr23:34962715 A>T did not map to a codon.
Sequencing variant TCGA-DD-A3A1-01A-11D-A20W-10 chr23:37026589 G>A did not map to a codon.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr23:37027899 C>T did not map to a codon.
Sequencing variant TCGA-DD-A113-01A-11D-A12Z-10 chr5:137681159 A>G maps to NM_001135647.1 R261R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EK-01A-11D-A20W-10 chr23:152857987 G>T did not map to a codon.
Sequencing variant TCGA-DD-A4NI-01A-11D-A27I-10 chr23:152858106 C>A did not map to a codon.
Sequencing variant TCGA-CC-A3MB-01A-11D-A20W-10 chr1:177247855 A>T maps to NM_021165.2 L390L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A5SL-01A-11D-A27I-10 chr1:177245346 G>A maps to NM_021165.2 L263L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr1:177226312 A>G maps to NM_021165.2 G154G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr1:190067336 T>A maps to NM_199051.1 L704L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K7-A5RF-01A-11D-A28X-10 chr1:190068068 G>A maps to NM_199051.1 C460C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IF-01A-11D-A33K-10 chr9:139612123 C>A maps to NM_152421.3 Y53*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10W-01A-11D-A12Z-10 chr14:67671394 G>A maps to NM_173526.3 W167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr19:50971075 A>G maps to ENST00000391816 L184L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25S-01A-11D-A16V-10 chr19:50979110 G>T maps to ENST00000391816 I113I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A7PZ-01A-11D-A33Q-10 chr1:78325805 C>T maps to NM_198549.2 R424*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NF-01A-11D-A27I-10 chr11:95522612 G>T maps to NM_144664.4 T10T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr6:54805799 T>C maps to NM_001010872.1 P677P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75H-01A-11D-A32G-10 chr17:18874755 T>C maps to NM_001039999.2 L796L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A1-01A-11D-A20W-10 chr6:17601072 C>T maps to NM_016255.2 Q145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr23:8767069 T>A did not map to a codon.
Sequencing variant TCGA-DD-A115-01A-11D-A12Z-10 chr16:89813299 T>C did not map to a codon.
Sequencing variant TCGA-DD-A3A1-01A-11D-A20W-10 chr16:89849429 C>T maps to NM_000135.2 R517R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73A-01A-12D-A32G-10 chr23:14876076 C>T did not map to a codon.
Sequencing variant TCGA-CC-A3MC-01A-11D-A22F-10 chr3:10128832 C>T maps to NM_033084.3 Y1117Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39Y-01A-11D-A20W-10 chr3:10108948 T>C maps to NM_033084.3 T814T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-O8-A75V-01A-11D-A32G-10 chr3:10076195 G>C maps to NM_033084.3 L83L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A1-01A-11D-A20W-10 chr11:22646564 A>G maps to NM_022725.3 T264T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A3KF-01A-11D-A20W-10 chr14:45623915 A>G maps to NM_020937.2 K400K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MA-01A-11D-A20W-10 chr10:127697828 C>T maps to ENST00000368692 D348D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A8-01A-11D-A22F-10 chr2:163029732 T>C did not map to a codon.
Sequencing variant TCGA-CC-A3MA-01A-11D-A20W-10 chr13:99038052 A>T maps to NM_005766.2 G248G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1ED-01A-11D-A152-10 chr13:99063058 T>C maps to NM_005766.2 D558D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25T-01A-11D-A16V-10 chr13:98896770 A>G maps to NM_001001715.2 K66K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IK-01A-12D-A33Q-10 chr2:242380933 C>A maps to NM_014808.2 A458A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A115-01A-11D-A12Z-10 chr2:242343250 C>T maps to NM_014808.2 C64C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A5SL-01A-11D-A27I-10 chr2:242430490 A>G maps to NM_014808.2 K840K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A4XI-01A-11D-A25V-10 chr6:5369075 G>A maps to NM_006567.3 E91E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EC-01A-21D-A12Z-10 chr2:223505622 T>A maps to NM_005687.3 V99V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MD-01A-12D-A34Z-10 chr1:172633480 C>T maps to NM_000639.1 P134P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5263-01A-01D-A12Z-10 chr17:80039103 G>A maps to NM_004104.4 R2177R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A5UD-01A-11D-A28X-10 chr17:80049389 C>T maps to NM_004104.4 V400V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A113-01A-11D-A12Z-10 chr17:80047247 C>A maps to NM_004104.4 E660*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NV-01A-11D-A30V-10 chr17:80039091 T>C maps to NM_004104.4 Q2181Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73B-01A-12D-A32G-10 chr17:80045028 C>T maps to NM_004104.4 E1108E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A5SL-01A-11D-A27I-10 chr17:80040958 C>T maps to NM_004104.4 K1866K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75I-01A-11D-A32G-10 chr17:80040838 C>T maps to NM_004104.4 Q1906Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr7:150774996 A>G maps to NM_006712.3 V336V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10W-01A-11D-A12Z-10 chr4:187541013 C>T maps to ENST00000260147 L2245L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73C-01A-12D-A33K-10 chr4:187557323 G>T maps to ENST00000260147 I1346I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-O8-A75V-01A-11D-A32G-10 chr4:187539093 A>G maps to ENST00000260147 N2885N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr4:187538293 C>T maps to ENST00000260147 V2983V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr4:187539225 T>A maps to ENST00000260147 S2841S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BW-A5NQ-01A-11D-A27I-10 chr5:150885500 G>A maps to NM_001447.2 G4225G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A118-01A-11D-A12Z-10 chr5:150932948 C>G did not map to a codon.
Sequencing variant TCGA-DD-A1EF-01A-11D-A12Z-10 chr5:150922776 G>A maps to NM_001447.2 N2637N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A9-01A-11D-A25V-10 chr5:150945318 G>A maps to NM_001447.2 D1058D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NV-01A-11D-A30V-10 chr5:150947397 A>T maps to NM_001447.2 A365A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A495-01A-11D-A25V-10 chr5:150948273 G>T maps to NM_001447.2 I73I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75G-01A-11D-A32G-10 chr5:150925185 G>T maps to NM_001447.2 P1834P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BD-A3EP-01A-11D-A22F-10 chr11:92616494 C>A maps to ENST00000298047 A4291A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A115-01A-11D-A12Z-10 chr11:92534437 G>C maps to ENST00000298047 G2753G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1E9-01A-21D-A152-10 chr11:92534029 C>T maps to ENST00000298047 H2617H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A23B-01A-11D-A16V-10 chr11:92087170 T>A maps to ENST00000298047 G631G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A4ZP-01A-12D-A25V-10 chr11:92531021 A>T maps to ENST00000298047 K1615*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A5SK-01A-11D-A27I-10 chr11:92538484 T>C maps to ENST00000298047 D3021D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A6UC-01A-21D-A33K-10 chr11:92531035 C>T maps to ENST00000298047 V1619V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75E-01A-11D-A32G-10 chr11:92495074 G>T maps to ENST00000298047 V1241V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NK-01A-11D-A28X-10 chr4:126400894 G>A did not map to a codon.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr4:126328165 A>T maps to NM_024582.4 L1813L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BD-A3EP-01A-11D-A22F-10 chr23:150884641 A>G did not map to a codon.
Sequencing variant TCGA-FV-A23B-01A-11D-A16V-10 chr23:150889962 C>A did not map to a codon.
Sequencing variant TCGA-KR-A7K2-01A-12D-A33Q-10 chr17:73914084 G>A maps to ENST00000389570 R757R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73G-01A-22D-A32G-10 chr1:16096973 C>G maps to NM_017556.2 Y204*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr22:45943007 C>T maps to ENST00000348697 A455A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A5UD-01A-11D-A28X-10 chr3:13670760 T>C maps to NM_001165035.1 F937F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IL-01A-11D-A33Q-10 chr15:48888573 A>G maps to NM_000138.4 P148P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A9-01A-11D-A25V-10 chr15:48719787 G>A maps to NM_000138.4 R2394*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75I-01A-11D-A32G-10 chr15:48764820 G>A maps to NM_000138.4 L1421L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1ED-01A-11D-A152-10 chr5:127712454 A>G maps to NM_001999.3 F647F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EH-01A-11D-A12Z-10 chr5:127681088 A>T maps to NM_001999.3 A1059A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A495-01A-11D-A25V-10 chr5:127686698 T>C did not map to a codon.
Sequencing variant TCGA-MI-A75G-01A-11D-A32G-10 chr5:127685695 A>G maps to NM_001999.3 D938D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75G-01A-11D-A32G-10 chr5:127704956 T>C maps to NM_001999.3 A722A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr5:127609595 T>G maps to NM_001999.3 P2592P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr5:127653901 A>G maps to NM_001999.3 G1552G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MF-01A-11D-A33K-10 chr5:127680140 G>T maps to NM_001999.3 I1093I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25U-01A-11D-A16V-10 chr19:8154495 G>T maps to NM_032447.3 T2103T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75H-01A-11D-A32G-10 chr19:8167617 A>G maps to NM_032447.3 T1693T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A6M3-01A-11D-A32G-10 chr19:8161855 G>A maps to NM_032447.3 C1774C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr16:30680872 G>C maps to ENST00000356166 P950P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5262-01A-01D-A12Z-10 chr16:30939816 G>A maps to NM_001099784.2 K239K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NJ-01A-11D-A27I-10 chr17:37421706 C>A did not map to a codon.
Sequencing variant TCGA-NI-A4U2-01A-11D-A28X-10 chr13:77589640 A>T maps to NM_012158.2 T182T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LG-A6GG-01A-11D-A30V-10 chr6:99374695 C>A maps to NM_012160.3 E57*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5260-01A-01D-A12Z-10 chr9:37518349 C>T maps to NM_012166.2 V762V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IK-01A-12D-A33Q-10 chr9:37541573 T>C maps to NM_012166.2 P64P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KR-A7K8-01A-11D-A33K-10 chr10:5945116 A>T maps to NM_032807.3 R97*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7ME-01A-11D-A33K-10 chr10:5945115 G>C maps to NM_032807.3 P96P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr19:39517610 T>A maps to NM_178820.3 R203*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A5UE-01A-11D-A28X-10 chr16:87364935 G>A maps to NM_024735.3 A526A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25W-01A-11D-A16V-10 chr14:55819115 C>A maps to NM_152231.1 R670R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IJ-01A-11D-A33Q-10 chr8:101153046 G>A maps to NM_001029860.3 Q479*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KR-A7K7-01A-11D-A33K-10 chr8:101153179 T>C maps to NM_001029860.3 L434L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr3:196304622 A>T maps to NM_001105573.1 L206L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10R-01A-11D-A12Z-10 chr6:52957295 C>T maps to NM_012347.4 Y251Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A9-01A-11D-A25V-10 chr9:123526905 C>T maps to NM_012164.3 T432T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EL-01A-11D-A152-10 chr10:103371083 A>G maps to ENST00000331272 S401S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5259-01A-31D-A20W-10 chr4:153273837 A>T maps to NM_018315.4 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A4-01A-11D-A22F-10 chr12:117465264 G>A maps to NM_153348.2 T536T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A115-01A-11D-A12Z-10 chr19:55386822 T>C did not map to a codon.
Sequencing variant TCGA-G3-A25S-01A-11D-A16V-10 chr14:75200776 A>G did not map to a codon.
Sequencing variant TCGA-G3-A3CK-01A-11D-A20W-10 chr14:75190044 A>C maps to NM_015962.4 L121L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A216-01A-11D-A152-10 chr19:40360957 G>T maps to NM_003890.2 R5150R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73D-01A-12D-A32G-10 chr19:40408467 C>T maps to NM_003890.2 K1457K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr1:161479766 C>T maps to NM_001136219.1 I174I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10U-01A-11D-A12Z-10 chr1:157739785 G>A maps to NM_030764.3 G155G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25Y-01A-11D-A16V-10 chr1:157667131 C>T maps to NM_052939.3 Q214Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A9-01A-11D-A25V-10 chr1:157494213 G>A maps to NM_031281.2 V698V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr1:157497527 G>A maps to NM_031281.2 P613P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr1:159779342 A>G maps to NM_001004310.2 S252S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RG-A7D4-01A-12D-A33Q-10 chr1:159778187 A>C maps to NM_001004310.2 P91P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr1:161682965 T>A maps to NM_001184866.1 P315P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1E9-01A-21D-A152-10 chr1:155289685 A>G maps to NM_001135821.1 Q342Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A9-01A-11D-A25V-10 chr19:4793794 G>A maps to NM_018708.2 A643A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr19:4792960 C>A maps to NM_018708.2 T365T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BW-A5NP-01A-11D-A27I-10 chr11:61563318 C>T maps to NM_004111.4 S162S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A26S-01A-11D-A16V-10 chr2:97359396 G>A maps to NM_001113382.1 V1176V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr2:97315364 T>C maps to NM_001113382.1 T115T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EG-01A-11D-A20W-10 chr8:125103756 C>T maps to NM_001039112.2 H1495H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A3R2-01A-11D-A22F-10 chr8:125072473 C>G maps to NM_001039112.2 T976T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T1-A6J8-01A-11D-A32G-10 chr7:19184880 G>T maps to NM_152898.2 P35P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr7:19184844 T>A maps to NM_152898.2 R47R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NI-A4U2-01A-11D-A28X-10 chr6:36979513 C>T maps to NM_173558.3 R137R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A112-01A-11D-A12Z-10 chr12:32760994 G>A maps to NM_139241.2 L366L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BW-A5NP-01A-11D-A27I-10 chr3:14964027 G>A maps to NM_152536.3 R1260R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr3:14860936 C>A maps to NM_152536.3 S120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A5SM-01A-12D-A28X-10 chr3:14862980 G>T maps to NM_152536.3 T801T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EG-01A-11D-A20W-10 chr23:137717736 C>T did not map to a codon.
Sequencing variant TCGA-UB-A7ME-01A-11D-A33K-10 chr5:170876190 C>T maps to NM_003862.2 V97V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NN-01A-11D-A28X-10 chr8:16850700 G>A maps to NM_019851.2 D172D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr19:49261302 A>T maps to NM_019113.2 P152P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A23B-01A-11D-A16V-10 chr6:167438329 A>G maps to NM_007045.2 L289L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A66Y-01A-11D-A30V-10 chr10:123276884 C>T maps to ENST00000357555 A363A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A69H-01A-11D-A30V-10 chr4:1807576 C>T maps to NM_000142.4 C582C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39V-01A-11D-A20W-10 chr4:1808892 G>A maps to NM_000142.4 Q775Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr7:76829023 T>C maps to NM_006682.2 E29E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NQ-01A-21D-A28X-10 chr1:27941375 C>A maps to NM_005248.2 V360V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A69H-01A-11D-A30V-10 chr4:153896513 G>T maps to NM_033393.2 E691*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75E-01A-11D-A32G-10 chr2:105977826 A>G maps to ENST00000344213 C361C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MC-01A-11D-A22F-10 chr6:97053844 A>G maps to NM_020482.4 R134R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A7SK-01A-11D-A34Z-10 chr16:67267988 G>T maps to NM_013241.2 L539L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5259-01A-31D-A20W-10 chr18:34182637 G>A maps to NM_025135.2 G240G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A1-01A-11D-A20W-10 chr18:34182679 A>G maps to NM_025135.2 K254K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25U-01A-11D-A16V-10 chr18:34289289 G>A maps to NM_025135.2 S648S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A3R2-01A-11D-A22F-10 chr6:110059525 A>G did not map to a codon.
Sequencing variant TCGA-BC-A10W-01A-11D-A12Z-10 chr2:164466793 C>A maps to NM_018086.2 T516T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MR-A520-01A-11D-A25V-10 chr2:164467789 T>C maps to NM_018086.2 E184E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BW-A5NO-01A-11D-A27I-10 chr6:76024439 C>A maps to NM_015687.2 E370*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5263-01A-01D-A12Z-10 chr6:76024217 T>A maps to NM_015687.2 K444*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IL-01A-11D-A33Q-10 chr6:76024769 G>A maps to NM_015687.2 Q260*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73F-01A-11D-A32G-10 chr6:76124502 A>T maps to NM_015687.2 S62S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A3I0-01A-11D-A22F-10 chr3:99643071 A>G did not map to a codon.
Sequencing variant TCGA-FV-A2QQ-01A-11D-A22F-10 chr17:39975630 C>T maps to NM_021939.3 D299D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A5SK-01A-11D-A27I-10 chr17:39975543 A>G maps to NM_021939.3 L270L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-4073-01B-02D-A12Z-10 chr9:115948580 C>T maps to ENST00000446284 Q507Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LG-A6GG-01A-11D-A30V-10 chr12:2904410 G>A did not map to a codon.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr6:35604881 A>C maps to NM_001145775.1 V53V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A7SK-01A-11D-A34Z-10 chr2:179343058 T>C maps to ENST00000350591 L56L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BW-A5NO-01A-11D-A27I-10 chr1:152283188 A>G maps to NM_002016.1 S1391S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A5UD-01A-11D-A28X-10 chr1:152279630 T>G maps to NM_002016.1 S2577S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A9-01A-11D-A25V-10 chr1:152286776 G>A maps to NM_002016.1 D195D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A5SK-01A-11D-A27I-10 chr1:152279759 G>A maps to NM_002016.1 H2534H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A6UC-01A-21D-A33K-10 chr1:152282594 G>T maps to NM_002016.1 R1589R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-O8-A75V-01A-11D-A32G-10 chr1:152287878 A>T maps to NM_002016.1 Y18*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QA-A7B7-01A-11D-A32G-10 chr1:152280080 G>T maps to NM_002016.1 A2427A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RG-A7D4-01A-12D-A33Q-10 chr1:152279555 G>T maps to NM_002016.1 G2602G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7ME-01A-11D-A33K-10 chr1:152276111 C>T maps to NM_002016.1 A3750A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7ME-01A-11D-A33K-10 chr1:152278841 T>A maps to NM_002016.1 T2840T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IK-01A-12D-A33Q-10 chr1:152326655 G>T maps to NM_001014342.2 S1202S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75C-01A-11D-A32G-10 chr1:152323835 C>A maps to NM_001014342.2 G2142G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10R-01A-11D-A12Z-10 chr23:153595781 G>A did not map to a codon.
Sequencing variant TCGA-DD-A3A9-01A-11D-A25V-10 chr23:153580980 G>T did not map to a codon.
Sequencing variant TCGA-FV-A495-01A-11D-A25V-10 chr23:153586829 A>T did not map to a codon.
Sequencing variant TCGA-G3-A25U-01A-11D-A16V-10 chr23:153592414 A>G did not map to a codon.
Sequencing variant TCGA-G3-A3CK-01A-11D-A20W-10 chr3:58141693 C>G maps to NM_001164317.1 Y2291*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75E-01A-11D-A32G-10 chr3:58089690 C>T maps to NM_001164317.1 L497L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10R-01A-11D-A12Z-10 chr7:128489493 G>A maps to NM_001458.4 G1687G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73E-01A-12D-A32G-10 chr7:128486942 G>C maps to NM_001458.4 G1424G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr7:128488062 A>T maps to NM_001458.4 P1507P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr7:128494856 T>A maps to NM_001458.4 A2342A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IK-01A-12D-A33Q-10 chr11:63883946 C>A maps to NM_013280.4 R70R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NI-01A-11D-A27I-10 chr14:86089798 C>G maps to NM_013231.4 Y647*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A7XP-01A-11D-A34Z-10 chr14:86089753 G>A maps to NM_013231.4 G632G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A6UC-01A-21D-A33K-10 chr14:86089138 C>A maps to NM_013231.4 L427L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A1HT-01A-11D-A12Z-10 chr20:14307369 C>T maps to NM_198391.2 R261R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A123-01A-11D-A12Z-10 chr13:28942732 T>C maps to NM_001160030.1 S728S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A1HT-01A-11D-A12Z-10 chr13:28883064 C>G did not map to a codon.
Sequencing variant TCGA-ED-A7PZ-01A-11D-A33Q-10 chr13:29001940 G>A maps to NM_002019.4 S408S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr13:28601379 T>C did not map to a codon.
Sequencing variant TCGA-BC-A5W4-01A-11D-A28X-10 chr5:180048542 C>T maps to NM_182925.4 Q673Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A116-01A-11D-A12Z-10 chr5:180047635 G>C maps to NM_182925.4 L793L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A2QR-01A-11D-A20W-10 chr5:180036904 C>A maps to NM_182925.4 V1269V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr5:180037026 T>A did not map to a codon.
Sequencing variant TCGA-G3-A6UC-01A-21D-A33K-10 chr15:33359764 A>G maps to NM_001103184.2 S107S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A6UC-01A-21D-A33K-10 chr15:33359983 A>T maps to NM_001103184.2 S34S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A2QQ-01A-11D-A22F-10 chr2:153471432 T>C maps to NM_052905.3 D377D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25U-01A-11D-A16V-10 chr2:153475550 G>A maps to NM_052905.3 L502L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CH-01A-11D-A22F-10 chr23:147018118 T>C did not map to a codon.
Sequencing variant TCGA-DD-A11A-01A-11D-A12Z-10 chr23:147084805 A>C did not map to a codon.
Sequencing variant TCGA-ED-A459-01A-11D-A25V-10 chr2:216261911 T>C maps to NM_212482.1 A1184A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25S-01A-11D-A16V-10 chr2:216238043 C>G did not map to a codon.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr17:80674714 C>T maps to NM_024619.3 G28G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A1HT-01A-11D-A12Z-10 chr6:159655416 C>T maps to NM_032532.2 S1291S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A5SM-01A-12D-A28X-10 chr6:159655440 C>A maps to NM_032532.2 R1299R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A7SB-01A-21D-A34Z-10 chr6:159655129 C>T maps to NM_032532.2 L1196L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5258-01A-01D-A12Z-10 chr13:49710510 A>G maps to NM_001079673.1 R178R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A12J-01A-11D-A12Z-10 chr3:172098772 T>C maps to NM_022763.3 L1065L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NQ-01A-21D-A28X-10 chr8:42911626 C>T maps to NM_002027.2 A46A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A2QR-01A-11D-A20W-10 chr8:42939882 T>C maps to NM_002027.2 Y292Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A496-01A-11D-A25V-10 chr11:71847150 C>T maps to ENST00000442948 D51D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A23B-01A-11D-A16V-10 chr2:28626981 G>T maps to NM_005253.3 R37R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr16:86544399 C>A maps to NM_001451.2 Y75*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A113-01A-11D-A12Z-10 chr14:29237216 C>A maps to NM_005249.3 R244R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A7-01A-11D-A22F-10 chr5:169535371 C>A maps to NM_012188.4 P298P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RG-A7D4-01A-12D-A33Q-10 chr5:169535272 G>A maps to NM_012188.4 E265E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3M9-01A-11D-A20W-10 chr16:86612388 G>C maps to NM_005250.2 L20L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr13:41239791 G>A maps to NM_002015.3 I186I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EB-01A-11D-A12Z-10 chr23:70316753 C>G did not map to a codon.
Sequencing variant TCGA-DD-A3A9-01A-11D-A25V-10 chr23:70320819 G>A did not map to a codon.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr11:118842682 C>A maps to NM_181721.2 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr23:55650628 C>A did not map to a codon.
Sequencing variant TCGA-ED-A82E-01A-11D-A34Z-10 chr19:52249926 G>T maps to NM_002029.3 I107I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr19:52249743 A>T maps to NM_002029.3 P168P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BD-A2L6-01A-11D-A20W-10 chr10:95441347 C>A maps to NM_145246.4 E226*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KC-01A-11D-A20W-10 chr10:95436449 T>C did not map to a codon.
Sequencing variant TCGA-CC-A1HT-01A-11D-A12Z-10 chr4:79328917 C>T maps to NM_025074.6 Q1411*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73F-01A-11D-A32G-10 chr4:79229241 T>C maps to NM_025074.6 G519G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr4:79455680 C>A maps to NM_025074.6 L3668L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A4ZQ-01A-11D-A25V-10 chr4:79166409 C>T maps to NM_025074.6 A80A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75H-01A-11D-A32G-10 chr4:79391154 G>A maps to NM_025074.6 P2427P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RG-A7D4-01A-12D-A33Q-10 chr4:79158772 T>C did not map to a codon.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr4:79229363 G>T did not map to a codon.
Sequencing variant TCGA-DD-A39Y-01A-11D-A20W-10 chr9:14863880 A>G maps to ENST00000380880 L85L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25V-01A-11D-A16V-10 chr9:14851596 A>G maps to ENST00000380880 S282S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BW-A5NO-01A-11D-A27I-10 chr13:39266352 C>A maps to NM_207361.4 T1624T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IJ-01A-11D-A33Q-10 chr13:39422757 T>C maps to NM_207361.4 L2110L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A1-01A-11D-A20W-10 chr13:39343835 T>C maps to NM_207361.4 D1844D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A3JL-01A-11D-A20W-10 chr13:39261906 C>A maps to NM_207361.4 G142G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25S-01A-11D-A16V-10 chr13:39265054 G>T maps to NM_207361.4 E1192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A7M5-01A-11D-A33Q-10 chr13:39454461 A>T maps to NM_207361.4 T3016T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KR-A7K7-01A-11D-A33K-10 chr13:39264295 G>T maps to NM_207361.4 E939*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LG-A6GG-01A-11D-A30V-10 chr13:39262722 A>C maps to NM_207361.4 V414V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr13:39262740 A>T maps to NM_207361.4 A420A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KR-A7K0-01A-12D-A33Q-10 chr6:168464372 G>A maps to NM_024919.3 Q238*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NI-A4U2-01A-11D-A28X-10 chr9:85863363 G>A maps to NM_174938.4 A421A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A6M4-01A-11D-A32G-10 chr3:69221074 G>A maps to NM_015123.1 N1014N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A123-01A-11D-A12Z-10 chr23:131212314 G>A did not map to a codon.
Sequencing variant TCGA-DD-A3A9-01A-11D-A25V-10 chr23:131212019 G>A did not map to a codon.
Sequencing variant TCGA-KR-A7K2-01A-12D-A33Q-10 chr10:49447718 C>A maps to NM_001018071.3 T239T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EB-01A-11D-A12Z-10 chr23:12712562 T>C did not map to a codon.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr6:41739272 T>A did not map to a codon.
Sequencing variant TCGA-CC-A3MA-01A-11D-A20W-10 chr4:48545871 A>G maps to NM_015030.1 V1848V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A5UD-01A-11D-A28X-10 chr4:48529664 T>C maps to NM_015030.1 V2382V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A9-01A-11D-A25V-10 chr4:48607808 T>A maps to NM_015030.1 I261I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A5UD-01A-11D-A28X-10 chr14:44975743 T>C maps to NM_032135.3 E149E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A496-01A-11D-A25V-10 chr14:44975317 G>T maps to NM_032135.3 V291V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25W-01A-11D-A16V-10 chr7:5645020 C>T maps to ENST00000340250 G472G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LG-A6GG-01A-11D-A30V-10 chr15:83437678 A>G maps to NM_001007122.2 T502T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7II-01A-11D-A33K-10 chr11:30255241 A>T maps to NM_001018080.1 P95P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr2:49190264 A>G maps to NM_000145.3 S565S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NQ-01A-21D-A28X-10 chr2:186673298 C>T maps to NM_173651.2 V6511V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A6M4-01A-11D-A32G-10 chr2:186670101 G>T maps to NM_173651.2 E5446*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A7M6-01A-11D-A33Q-10 chr4:162431552 C>A maps to NM_020116.3 E446*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr23:31089829 T>A did not map to a codon.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr17:61902422 A>G maps to NM_017647.3 T232T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A112-01A-11D-A12Z-10 chr1:78429796 G>A maps to ENST00000436586 R352*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr15:91423152 C>T maps to NM_002569.2 Q439*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75G-01A-11D-A32G-10 chr19:49253496 C>A maps to NM_000148.3 E348*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A115-01A-11D-A12Z-10 chr19:5844840 G>A maps to NM_001097641.1 L4L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A6M4-01A-11D-A32G-10 chr19:5866695 T>A maps to NM_002034.2 A347A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KR-A7K0-01A-12D-A33Q-10 chr14:66082779 G>A maps to NM_178155.1 Q96Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IJ-01A-11D-A33Q-10 chr19:35614351 C>T maps to NM_021910.2 A111A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr5:39130698 T>C maps to ENST00000263405 G620G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73C-01A-12D-A33K-10 chr5:39137760 C>A maps to ENST00000263405 E495*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KR-A7K8-01A-11D-A33K-10 chr3:46008640 C>A maps to NM_024513.2 E729*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NQ-01A-21D-A28X-10 chr6:112035596 A>G maps to NM_153047.1 D99D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr6:112021439 T>C maps to NM_002037.3 V243V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr8:28385434 G>C maps to NM_017412.3 G386G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LG-A6GG-01A-11D-A30V-10 chr7:72849305 C>T maps to NM_003508.2 F323F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A7M8-01A-11D-A33Q-10 chr19:3532453 C>T maps to NM_001136198.1 Q350*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NI-A4U2-01A-11D-A28X-10 chr19:3522995 G>A maps to NM_001136198.1 Q3Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BD-A2L6-01A-11D-A20W-10 chr4:76579226 A>C maps to NM_203505.2 P255P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4ND-01A-11D-A25V-10 chr2:169757873 A>C maps to NM_021176.2 I11I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10W-01A-11D-A12Z-10 chr4:144378869 T>C maps to NM_207123.2 G541G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5258-01A-01D-A12Z-10 chr4:144336700 C>A maps to NM_207123.2 Y48*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1E9-01A-21D-A152-10 chr4:144354860 A>G maps to NM_207123.2 E195E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NI-A4U2-01A-11D-A28X-10 chr23:153940658 G>A did not map to a codon.
Sequencing variant TCGA-G3-A25T-01A-11D-A16V-10 chr6:29576389 A>G maps to NM_001470.2 P660P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr6:29595352 C>T maps to NM_001470.2 Q189Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HP-A5MZ-01A-21D-A27I-10 chr9:101340351 G>A maps to NM_005458.7 C108C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39W-01A-11D-A20W-10 chr21:27141413 G>A maps to NM_002040.3 A412A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr15:50578222 T>A maps to NM_002041.4 P359P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr5:161300200 C>A maps to NM_001127648.1 R112R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A113-01A-11D-A12Z-10 chr23:151393309 T>C did not map to a codon.
Sequencing variant TCGA-DD-A11D-01A-11D-A12Z-10 chr23:151424437 T>A did not map to a codon.
Sequencing variant TCGA-G3-A7M5-01A-11D-A33Q-10 chr23:151336876 G>C did not map to a codon.
Sequencing variant TCGA-CC-5264-01A-01D-A12Z-10 chr4:46930407 G>T maps to NM_000809.2 S500*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IK-01A-12D-A33Q-10 chr4:46967018 G>A maps to NM_000809.2 Q368*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A9-01A-11D-A25V-10 chr4:46967001 A>T maps to NM_000809.2 P373P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25U-01A-11D-A16V-10 chr5:160972295 G>A maps to NM_021911.2 P58P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr5:160753449 A>G maps to NM_021911.2 Y372Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A9-01A-11D-A25V-10 chr15:26793134 T>C maps to NM_021912.4 R409R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10Z-01A-11D-A12Z-10 chr4:46060338 C>A maps to NM_173536.3 G271*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr4:46067445 G>A maps to NM_173536.3 H159H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr4:46066494 G>T maps to NM_173536.3 P196P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr4:46099286 C>A maps to NM_173536.3 G62*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10W-01A-11D-A12Z-10 chr5:161580268 G>A maps to NM_198903.2 R481R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CJ-01A-11D-A20W-10 chr5:161569293 G>A maps to NM_198903.2 K338K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr15:27777743 A>T did not map to a codon.
Sequencing variant TCGA-BD-A3EP-01A-11D-A22F-10 chr23:151815445 A>C did not map to a codon.
Sequencing variant TCGA-CC-A1HT-01A-11D-A12Z-10 chr23:151821043 C>A did not map to a codon.
Sequencing variant TCGA-DD-A118-01A-11D-A12Z-10 chr23:151806784 C>T did not map to a codon.
Sequencing variant TCGA-G3-A5SK-01A-11D-A27I-10 chr23:151818956 T>C did not map to a codon.
Sequencing variant TCGA-K7-A6G5-01A-11D-A30V-10 chr23:151821123 G>C did not map to a codon.
Sequencing variant TCGA-DD-A3A9-01A-11D-A25V-10 chr3:97753824 G>A maps to NM_001105580.1 L3L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75I-01A-11D-A32G-10 chr3:97736567 T>A did not map to a codon.
Sequencing variant TCGA-DD-A11D-01A-11D-A12Z-10 chr2:171715378 T>A maps to NM_000817.2 P529P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NG-01A-11D-A27I-10 chr10:26505806 C>T maps to NM_001134366.1 P23P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10Z-01A-11D-A12Z-10 chr3:30827848 C>A maps to NM_207359.2 E434*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NG-01A-11D-A27I-10 chr3:30819693 C>A maps to NM_207359.2 E457*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A3JL-01A-11D-A20W-10 chr3:30827898 C>T did not map to a codon.
Sequencing variant TCGA-G3-A25V-01A-11D-A16V-10 chr23:49173764 A>G did not map to a codon.
Sequencing variant TCGA-G3-A25V-01A-11D-A16V-10 chr4:887730 G>T maps to NM_005255.2 R270R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LG-A6GG-01A-11D-A30V-10 chr4:887683 G>T maps to NM_005255.2 Y285*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NF-01A-11D-A27I-10 chr11:68458397 C>G maps to NM_015973.3 L105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MD-01A-12D-A34Z-10 chr11:68455539 G>A maps to NM_015973.3 E65E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10U-01A-11D-A12Z-10 chr11:65810798 C>A maps to NM_033036.2 E159*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11C-01A-11D-A12Z-10 chr11:65810616 G>A maps to NM_033036.2 D219D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10Q-01A-11D-A12Z-10 chr15:49531473 C>T maps to NM_002044.2 I138I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr2:155295138 C>A maps to NM_052917.2 T477T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10Q-01A-11D-A12Z-10 chr1:230410234 G>A maps to NM_004481.3 L495L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NI-01A-11D-A27I-10 chr12:51758077 C>T maps to NM_007210.3 V292V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A123-01A-11D-A12Z-10 chr12:4848461 G>T maps to NM_017417.1 E215*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EG-01A-11D-A20W-10 chr18:74962809 G>A maps to NM_001480.3 V102V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A5SK-01A-11D-A27I-10 chr18:74980683 G>T maps to NM_001480.3 A292A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EL-01A-11D-A152-10 chr9:34649405 G>T did not map to a codon.
Sequencing variant TCGA-K7-A6G5-01A-11D-A30V-10 chr16:81390416 C>T maps to NM_022041.3 L221L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EB-01A-11D-A12Z-10 chr11:62407127 A>G maps to NM_198335.2 F38F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NI-01A-11D-A27I-10 chr15:42646623 A>G maps to NM_212465.2 L7L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr9:128124886 A>G maps to NM_015635.2 A1442A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr22:29706427 G>T did not map to a codon.
Sequencing variant TCGA-G3-A25V-01A-11D-A16V-10 chr17:34079488 G>T maps to NM_139285.2 I127I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr12:101018226 A>C maps to NM_174942.1 P548P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A6M6-01A-11D-A32G-10 chr17:9846499 C>A maps to NM_201433.1 L223L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A7M9-01A-23D-A34Z-10 chr8:11615851 C>T maps to NM_002052.3 V399V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A9-01A-11D-A25V-10 chr1:153785890 A>G maps to NM_020699.2 F418F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4ND-01A-11D-A25V-10 chr7:56049253 C>T maps to NM_001483.1 Q123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CK-01A-11D-A20W-10 chr9:136029632 G>A maps to NM_021996.4 I125I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CK-01A-11D-A20W-10 chr1:89480300 G>T maps to NM_018284.2 A119A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A0-01A-11D-A20W-10 chr1:89847412 C>T maps to NM_198460.2 L344L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr1:89843996 A>G maps to NM_198460.2 E150E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75E-01A-11D-A32G-10 chr1:89607247 A>T maps to NM_207398.2 A483A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A5UE-01A-11D-A28X-10 chr2:27741788 G>T maps to NM_001486.3 A519A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CJ-01A-11D-A20W-10 chr1:94354635 C>T maps to NM_002061.2 L245L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A7M9-01A-23D-A34Z-10 chr1:94354617 C>T maps to NM_002061.2 S251S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5261-01A-01D-A12Z-10 chr6:10529560 A>G maps to NM_145649.4 A139A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10X-01A-11D-A12Z-10 chr1:118441790 T>C maps to NM_017686.3 K228K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73F-01A-11D-A32G-10 chr10:48428811 G>A maps to NM_004962.2 D358D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A496-01A-11D-A25V-10 chr10:48413955 C>T maps to NM_016204.1 T304T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr10:48416369 A>G maps to NM_016204.1 I108I. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-BC-A10Y-01A-11D-A12Z-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CC-A7II-01A-11D-A33K-10 chr20:34025504 C>G maps to NM_000557.2 G68G. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-G3-A25S-01A-11D-A16V-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-EP-A26S-01A-11D-A16V-10 chr5:37815755 G>A maps to NM_001190468.1 I228I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A26S-01A-11D-A16V-10 chr23:69644839 C>T did not map to a codon.
Sequencing variant TCGA-HP-A5MZ-01A-21D-A27I-10 chr11:75150966 G>A maps to NM_030792.6 L505L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr5:154311782 A>G maps to NM_015465.3 I179I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7II-01A-11D-A33K-10 chr5:154287211 T>C maps to NM_015465.3 S778S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr5:154317546 T>C maps to NM_015465.3 P49P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NA-01A-11D-A25V-10 chr23:14027049 G>A did not map to a codon.
Sequencing variant TCGA-G3-A7M6-01A-11D-A33Q-10 chr23:14027289 T>A did not map to a codon.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr2:17959313 A>T maps to NM_001130009.1 I416I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A5SL-01A-11D-A27I-10 chr17:42988812 C>T maps to NM_002055.3 L306L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr3:158364695 C>A maps to ENST00000264263 R178R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-4073-01B-02D-A12Z-10 chr6:13470847 T>C did not map to a codon.
Sequencing variant TCGA-G3-A25Y-01A-11D-A16V-10 chr2:69581699 C>T maps to ENST00000357308 R202R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11C-01A-11D-A12Z-10 chr8:21560352 C>T maps to NM_001495.4 L394L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EK-01A-11D-A20W-10 chr6:55198737 A>G maps to NM_207410.2 K104K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A7M7-01A-12D-A34Z-10 chr17:73236488 G>C maps to NM_138619.2 L399L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A4-01A-11D-A22F-10 chr19:38877739 G>A maps to NM_152657.3 S54S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73G-01A-22D-A32G-10 chr22:25024303 G>C maps to NM_005265.2 L504L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MA-01A-11D-A33Q-10 chr22:24628912 G>C maps to NM_001099781.1 P158P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A118-01A-11D-A12Z-10 chr17:61995227 C>T maps to NM_000515.3 V116V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A3KF-01A-11D-A20W-10 chr17:40342898 G>A maps to NM_032484.4 R369*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A115-01A-11D-A12Z-10 chr5:42713545 G>A maps to NM_000163.2 W267*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A9-01A-11D-A25V-10 chr2:233710579 G>A maps to ENST00000373566 T1170T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5258-01A-01D-A12Z-10 chr7:150390063 G>T maps to NM_015660.2 V230V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75G-01A-11D-A32G-10 chr7:150327196 C>A maps to ENST00000438845 E12*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr12:110421239 T>C maps to NM_057169.3 A187A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr12:110390998 G>A maps to NM_057169.3 H380H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25W-01A-11D-A16V-10 chr12:110390904 G>T maps to NM_057169.3 R412R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr1:35259855 C>A maps to NM_002060.2 V14V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MB-01A-11D-A20W-10 chr1:147230515 T>C maps to NM_005266.5 G277G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10R-01A-11D-A12Z-10 chr1:147380862 C>T maps to NM_005267.4 Q261*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73F-01A-11D-A32G-10 chr1:147380858 C>T maps to NM_005267.4 S259S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BW-A5NO-01A-11D-A27I-10 chr1:39340261 A>G maps to NM_030772.4 N503N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A5-01A-11D-A22F-10 chr23:70444423 C>T did not map to a codon.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr1:35223305 T>A maps to NM_005268.2 G125G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr13:20797361 G>T maps to NM_001110221.2 T86T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HP-A5MZ-01A-21D-A27I-10 chr15:35044888 G>A maps to NM_020660.1 V252V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr3:141884550 T>C maps to NM_001039547.2 P501P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BD-A3EP-01A-11D-A22F-10 chr23:100658873 G>T did not map to a codon.
Sequencing variant TCGA-BC-A10Z-01A-11D-A12Z-10 chr3:33099713 C>T maps to NM_000404.2 L200L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5264-01A-01D-A12Z-10 chr3:33106972 C>T maps to NM_000404.2 G178G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75H-01A-11D-A32G-10 chr2:220102299 G>T maps to NM_024506.3 Y541*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr11:134177094 T>C maps to NM_001080407.2 D318D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75C-01A-11D-A32G-10 chr15:69560736 T>C maps to NM_015554.1 D336D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39V-01A-11D-A20W-10 chr9:6592199 T>C maps to NM_000170.2 T475T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4ND-01A-11D-A25V-10 chr9:6558588 C>A maps to NM_000170.2 G674G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7ME-01A-11D-A33K-10 chr9:131296077 A>T maps to NM_001003722.1 A498A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr2:121743963 G>T maps to NM_005270.4 G689G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A0-01A-11D-A20W-10 chr7:42012093 G>T maps to NM_000168.5 R649R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A495-01A-11D-A25V-10 chr7:42262747 G>A maps to NM_000168.5 A35A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75E-01A-11D-A32G-10 chr7:42005487 G>A maps to NM_000168.5 H1061H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11A-01A-11D-A12Z-10 chr12:75875765 T>A maps to NM_006851.2 S109S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11D-01A-11D-A12Z-10 chr6:38650626 C>T maps to NM_006708.2 E111E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73G-01A-22D-A32G-10 chr23:48631827 G>A did not map to a codon.
Sequencing variant TCGA-DD-A73E-01A-12D-A32G-10 chr23:14550360 G>C did not map to a codon.
Sequencing variant TCGA-BC-A69H-01A-11D-A30V-10 chr23:102978842 A>C did not map to a codon.
Sequencing variant TCGA-DD-A73D-01A-12D-A32G-10 chr23:102974159 C>T did not map to a codon.
Sequencing variant TCGA-DD-A73E-01A-12D-A32G-10 chr4:158043480 G>C did not map to a codon.
Sequencing variant TCGA-MI-A75I-01A-11D-A32G-10 chr12:56868405 A>G maps to NM_013267.2 S382S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GJ-A6C0-01A-12D-A30V-10 chr12:129360596 G>A maps to ENST00000442111 R69R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NQ-01A-21D-A28X-10 chr12:104388180 G>C maps to NM_031302.3 A233A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NI-01A-11D-A27I-10 chr19:48182829 C>T maps to NM_015711.3 Q135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KC-01A-11D-A20W-10 chr19:48204843 G>A maps to NM_015711.3 E1285E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr19:48197946 G>T maps to NM_015711.3 L953L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3M9-01A-11D-A20W-10 chr19:48257973 A>G maps to NM_015710.4 T293T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr23:120181980 G>A did not map to a codon.
Sequencing variant TCGA-G3-A25Y-01A-11D-A16V-10 chr23:120182438 G>A did not map to a codon.
Sequencing variant TCGA-RG-A7D4-01A-12D-A33Q-10 chr23:120182070 C>G did not map to a codon.
Sequencing variant TCGA-CC-A5UD-01A-11D-A28X-10 chr1:182353641 A>G maps to NM_002065.5 R340R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NE-01A-11D-A27I-10 chr11:58491954 C>T maps to NM_201648.2 L5L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NF-01A-11D-A27I-10 chr11:58607043 A>G maps to NM_145016.3 Y14Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A2QR-01A-11D-A20W-10 chr1:29040627 T>C maps to NM_006582.2 D355D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EJ-01A-11D-A152-10 chr19:19744902 T>C maps to NM_016573.2 A727A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IL-01A-11D-A33Q-10 chr3:49759577 G>A maps to NM_013334.2 D257D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr3:155629066 A>G maps to NM_003875.2 K295K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IG-01A-11D-A33K-10 chr20:57428697 G>T maps to NM_080425.2 G126G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EI-01A-11D-A12Z-10 chr3:50231027 G>A maps to NM_000172.3 W127*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11D-01A-11D-A12Z-10 chr1:1721848 G>A maps to NM_002074.2 D228D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IJ-01A-11D-A33Q-10 chr9:36223376 C>T maps to NM_001128227.2 L499L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A5-01A-11D-A22F-10 chr1:68171259 C>G did not map to a codon.
Sequencing variant TCGA-DD-A3A3-01A-11D-A22F-10 chr1:84971731 G>A maps to NM_005274.2 Q15*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11C-01A-11D-A12Z-10 chr17:47284178 G>A maps to NM_001198754.1 L50L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73A-01A-12D-A32G-10 chr17:47284154 A>G maps to NM_001198754.1 N58N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NK-01A-11D-A28X-10 chr23:54566596 C>A did not map to a codon.
Sequencing variant TCGA-CC-A7II-01A-11D-A33K-10 chr6:42928678 C>T maps to NM_018960.4 C58C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A9-01A-11D-A25V-10 chr1:231411878 A>G did not map to a codon.
Sequencing variant TCGA-KR-A7K2-01A-12D-A33Q-10 chr14:53245073 A>G maps to NM_198066.3 Y170Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A1-01A-11D-A20W-10 chr9:131022365 G>A maps to NM_004486.4 L594L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75H-01A-11D-A32G-10 chr15:34673743 C>T maps to NM_181077.3 Q560Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75H-01A-11D-A32G-10 chr15:34819964 C>T maps to NM_001023567.4 Q560Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NG-01A-11D-A27I-10 chr3:121416716 G>A maps to ENST00000393667 Q885*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KR-A7K0-01A-12D-A33Q-10 chr1:155736386 G>A maps to ENST00000368331 D959D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NE-01A-11D-A27I-10 chr1:170508681 C>A maps to NM_152281.2 C156*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A3R2-01A-11D-A22F-10 chr17:45015969 T>G maps to NM_054022.2 T161T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25W-01A-11D-A16V-10 chr16:20328666 G>A maps to NM_001007240.1 H431H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A5SK-01A-11D-A27I-10 chr3:128781112 T>C maps to NM_000174.3 D177D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MA-01A-11D-A20W-10 chr10:113940242 A>G maps to NM_020918.4 T71T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A4ZQ-01A-11D-A25V-10 chr10:113935463 C>A maps to NM_020918.4 G103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr1:217783742 C>A did not map to a codon.
Sequencing variant TCGA-O8-A75V-01A-11D-A32G-10 chr17:42552195 C>A did not map to a codon.
Sequencing variant TCGA-DD-A73C-01A-12D-A33K-10 chr23:132887922 T>G did not map to a codon.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr23:132458432 C>A did not map to a codon.
Sequencing variant TCGA-UB-A7MF-01A-11D-A33K-10 chr13:94680116 T>C maps to NM_005708.3 A282A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A7-01A-11D-A22F-10 chr14:67346715 A>T maps to NM_020806.4 G118G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A7XP-01A-11D-A34Z-10 chr14:67389469 G>T maps to NM_020806.4 E182*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BD-A2L6-01A-11D-A20W-10 chr19:34887541 C>A maps to NM_000175.3 R417R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73B-01A-12D-A32G-10 chr19:34890536 G>T did not map to a codon.
Sequencing variant TCGA-CC-5262-01A-01D-A12Z-10 chr4:176556172 G>A maps to NM_005277.3 A240A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39Z-01A-11D-A20W-10 chr23:13803852 A>G did not map to a codon.
Sequencing variant TCGA-DD-A3A9-01A-11D-A25V-10 chr23:13801603 C>T did not map to a codon.
Sequencing variant TCGA-DD-A1EC-01A-21D-A12Z-10 chr1:27210696 C>A maps to NM_018066.3 E272*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73F-01A-11D-A32G-10 chr23:136113471 G>T did not map to a codon.
Sequencing variant TCGA-DD-A73G-01A-22D-A32G-10 chr23:136112566 C>T did not map to a codon.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr23:135488039 A>T did not map to a codon.
Sequencing variant TCGA-DD-A1EB-01A-11D-A12Z-10 chr23:135487871 T>C did not map to a codon.
Sequencing variant TCGA-DD-A1EF-01A-11D-A12Z-10 chr23:135453611 A>G did not map to a codon.
Sequencing variant TCGA-ED-A7XO-01A-11D-A34Z-10 chr23:135441569 T>C did not map to a codon.
Sequencing variant TCGA-K7-A5RG-01A-11D-A28X-10 chr23:135431900 T>A did not map to a codon.
Sequencing variant TCGA-DD-A1EC-01A-21D-A12Z-10 chr16:57601899 C>T maps to ENST00000349457 A318A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A9-01A-11D-A25V-10 chr6:46823750 A>G maps to NM_015234.4 S1307S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A3KF-01A-11D-A20W-10 chr23:129518584 A>G did not map to a codon.
Sequencing variant TCGA-CC-A7IF-01A-11D-A33K-10 chr23:129518889 T>A did not map to a codon.
Sequencing variant TCGA-BC-A216-01A-11D-A152-10 chr13:27332980 C>T maps to NM_005288.3 A328A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A7PZ-01A-11D-A33Q-10 chr10:134942774 C>T maps to ENST00000368577 V1021V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr10:134910584 C>T maps to ENST00000368577 V578V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A5UE-01A-11D-A28X-10 chr8:37693182 C>A maps to NM_032777.9 R649R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5260-01A-01D-A12Z-10 chr4:22389480 C>T maps to NM_145290.2 V1271V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IJ-01A-11D-A33Q-10 chr4:22425951 A>G maps to NM_145290.2 I489I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A1-01A-11D-A20W-10 chr4:22425933 C>T maps to NM_145290.2 L495L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A23B-01A-11D-A16V-10 chr11:64055318 G>T maps to NM_001170726.1 V236V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10Z-01A-11D-A12Z-10 chr7:37780402 T>C maps to NM_181791.1 S136S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr23:9711665 T>C did not map to a codon.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr2:131487677 C>T maps to NM_207364.2 Y318Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5262-01A-01D-A12Z-10 chr3:154055823 C>T maps to NM_001038705.1 E620E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A5UE-01A-11D-A28X-10 chr3:154146873 G>A maps to NM_001038705.1 R177R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LG-A6GG-01A-11D-A30V-10 chr3:119886208 G>C maps to NM_153002.2 A705A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr3:119886436 A>T maps to NM_153002.2 P629P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A3I1-01A-11D-A22F-10 chr1:9188903 G>A maps to NM_024980.4 A61A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A69H-01A-11D-A30V-10 chr10:25464384 C>A maps to NM_020752.2 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A5UD-01A-11D-A28X-10 chr10:25701320 T>G maps to NM_020752.2 L418L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75G-01A-11D-A32G-10 chr10:25464990 C>T maps to NM_020752.2 A214A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4ND-01A-11D-A25V-10 chr3:150916345 C>A maps to NM_013308.3 S276S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A495-01A-11D-A25V-10 chr23:53106557 G>A did not map to a codon.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr23:53106452 T>C did not map to a codon.
Sequencing variant TCGA-FV-A495-01A-11D-A25V-10 chr23:78426849 C>G did not map to a codon.
Sequencing variant TCGA-MI-A75C-01A-11D-A32G-10 chr23:78427072 A>G did not map to a codon.
Sequencing variant TCGA-FV-A496-01A-11D-A25V-10 chr17:36485932 G>A maps to ENST00000398597 S1174S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NI-01A-11D-A27I-10 chr12:12815346 T>C maps to NM_006143.2 P12P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr7:107114660 T>A maps to NM_005295.2 I52I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CK-01A-11D-A20W-10 chr1:200843248 T>G maps to NM_005298.2 *362E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HP-A5N0-01A-11D-A28X-10 chr6:167571100 G>A maps to NM_005299.2 F73F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25Z-01A-11D-A16V-10 chr23:41555140 A>G did not map to a codon.
Sequencing variant TCGA-HP-A5N0-01A-11D-A28X-10 chr23:41555816 A>T did not map to a codon.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr2:105858392 C>A maps to NM_007227.3 S26S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LG-A6GG-01A-11D-A30V-10 chr23:150349505 C>A did not map to a codon.
Sequencing variant TCGA-UB-A7MA-01A-11D-A33Q-10 chr23:150348391 G>T did not map to a codon.
Sequencing variant TCGA-MI-A75I-01A-11D-A32G-10 chr3:51990738 C>A maps to NM_080865.3 P357P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A123-01A-11D-A12Z-10 chr23:19017391 C>A did not map to a codon.
Sequencing variant TCGA-DD-A1EC-01A-21D-A12Z-10 chr14:91700518 G>T maps to ENST00000238699 T302T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BD-A2L6-01A-11D-A20W-10 chr2:54081698 C>T maps to NM_006794.2 L65L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5260-01A-01D-A12Z-10 chr23:41586731 T>A did not map to a codon.
Sequencing variant TCGA-FV-A495-01A-11D-A25V-10 chr23:41586978 T>A did not map to a codon.
Sequencing variant TCGA-CC-A7IJ-01A-11D-A33Q-10 chr12:54757482 G>C maps to NM_020370.2 L51L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A115-01A-11D-A12Z-10 chr12:54757476 G>A maps to NM_020370.2 T53T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr12:54757017 T>C maps to NM_020370.2 K206K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A3I1-01A-11D-A22F-10 chr3:151017870 C>A maps to NM_023915.3 T6T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr1:147408745 A>T maps to NM_016334.3 L16L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BW-A5NP-01A-11D-A27I-10 chr5:90000210 G>A maps to NM_032119.3 S2764S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5263-01A-01D-A12Z-10 chr5:89910834 C>A maps to NM_032119.3 S69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A5UD-01A-11D-A28X-10 chr5:89971057 A>T did not map to a codon.
Sequencing variant TCGA-DD-A39Y-01A-11D-A20W-10 chr5:89968412 A>G maps to NM_032119.3 G1601G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A7PZ-01A-11D-A33Q-10 chr5:90070013 G>A maps to NM_032119.3 Q4099Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr5:89971069 G>A maps to NM_032119.3 Q1707Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MA-01A-11D-A33Q-10 chr5:89990342 C>T maps to NM_032119.3 S2590S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr5:90077395 G>T did not map to a codon.
Sequencing variant TCGA-CC-A3MA-01A-11D-A20W-10 chr23:101909697 G>T did not map to a codon.
Sequencing variant TCGA-CC-A3MA-01A-11D-A20W-10 chr23:101912552 T>C did not map to a codon.
Sequencing variant TCGA-DD-A118-01A-11D-A12Z-10 chr23:101911926 C>T did not map to a codon.
Sequencing variant TCGA-G3-A25T-01A-11D-A16V-10 chr23:101911001 G>T did not map to a codon.
Sequencing variant TCGA-G3-A3CJ-01A-11D-A20W-10 chr23:101971960 G>A did not map to a codon.
Sequencing variant TCGA-G3-A7M5-01A-11D-A33Q-10 chr23:101970490 A>G did not map to a codon.
Sequencing variant TCGA-CC-A7IJ-01A-11D-A33Q-10 chr16:19883201 C>T maps to NM_016235.1 E322E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr6:117114123 T>A maps to NM_148963.2 P654P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25W-01A-11D-A16V-10 chr5:176025337 A>G maps to NM_052899.2 L500L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75G-01A-11D-A32G-10 chr5:176025587 C>T maps to NM_052899.2 V416V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5258-01A-01D-A12Z-10 chr10:47000007 G>T maps to NM_014696.3 P376P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NH-01A-11D-A27I-10 chr10:46999761 C>T maps to NM_014696.3 A294A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A5SJ-01A-11D-A27I-10 chr4:90171126 A>G maps to NM_198281.2 N45N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25W-01A-11D-A16V-10 chr17:80011841 G>A maps to NM_212492.1 L115L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5258-01A-01D-A12Z-10 chr17:7216696 A>G did not map to a codon.
Sequencing variant TCGA-BC-A10Y-01A-11D-A12Z-10 chr9:139234259 G>A maps to NM_001145638.1 Q357Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39X-01A-11D-A20W-10 chr9:139244073 G>A maps to NM_001145638.1 W438*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr9:139250845 C>T maps to NM_001145638.1 I555I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5259-01A-31D-A20W-10 chr6:28478621 G>A maps to NM_182701.1 N49N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A9-01A-11D-A25V-10 chr6:28473512 T>A maps to NM_182701.1 G142G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73C-01A-12D-A33K-10 chr19:35501095 C>G maps to NM_020895.3 T142T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A5UC-01A-11D-A28X-10 chr11:123483490 C>A maps to ENST00000456860 R512R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11A-01A-11D-A12Z-10 chr5:125759318 T>C maps to NM_023927.2 D7D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NI-01A-11D-A27I-10 chr22:47073041 A>T did not map to a codon.
Sequencing variant TCGA-ED-A66Y-01A-11D-A30V-10 chr22:47033857 G>C did not map to a codon.
Sequencing variant TCGA-FV-A4ZP-01A-12D-A25V-10 chr2:11752721 G>A maps to NM_014668.3 G1036G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11A-01A-11D-A12Z-10 chr2:10132261 G>A maps to NM_198182.2 Q483Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A114-01A-11D-A12Z-10 chr8:102611375 G>A maps to NM_024915.3 A365A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CK-01A-11D-A20W-10 chr5:153065883 C>T maps to NM_001114183.1 R377*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr4:158262574 T>C maps to NM_000826.3 Y668Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A118-01A-11D-A12Z-10 chr23:122538726 A>G did not map to a codon.
Sequencing variant TCGA-DD-A11D-01A-11D-A12Z-10 chr23:122616685 G>A did not map to a codon.
Sequencing variant TCGA-DD-A4NS-01A-11D-A30V-10 chr23:122536847 C>A did not map to a codon.
Sequencing variant TCGA-QA-A7B7-01A-11D-A32G-10 chr23:122538599 G>T did not map to a codon.
Sequencing variant TCGA-QA-A7B7-01A-11D-A32G-10 chr23:122538600 G>T did not map to a codon.
Sequencing variant TCGA-UB-A7MA-01A-11D-A33Q-10 chr23:122598766 G>A did not map to a codon.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr11:105781252 G>T maps to NM_000829.3 V417V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A7M5-01A-11D-A33Q-10 chr11:105769113 A>T maps to NM_000829.3 L282L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr11:105795168 A>G maps to NM_000829.3 R507R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr11:105795273 T>A maps to NM_000829.3 P542P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MF-01A-11D-A33K-10 chr11:105795189 T>A maps to NM_000829.3 S514S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A7M6-01A-11D-A33Q-10 chr10:87362150 G>T maps to NM_017551.2 S970*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10W-01A-11D-A12Z-10 chr4:94006347 T>G maps to NM_001510.2 P149P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A5-01A-11D-A22F-10 chr4:94436381 T>C maps to NM_001510.2 L671L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr21:30971253 G>T maps to ENST00000327783 R368R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr1:37315909 A>G did not map to a codon.
Sequencing variant TCGA-G3-A7M6-01A-11D-A33Q-10 chr1:37270815 G>T maps to NM_000831.3 I779I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EB-01A-11D-A12Z-10 chr11:120827653 T>C maps to NM_014619.2 S622S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr19:42510880 A>G maps to NM_002088.3 P651P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A5UD-01A-11D-A28X-10 chr16:10032378 T>A maps to NM_000833.3 G148G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IL-01A-11D-A33Q-10 chr16:9934502 C>A did not map to a codon.
Sequencing variant TCGA-DD-A3A9-01A-11D-A25V-10 chr16:9862845 G>A maps to NM_000833.3 G819G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73C-01A-12D-A33K-10 chr16:9862752 C>T maps to NM_000833.3 T850T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr16:9857311 G>T maps to NM_000833.3 S1363S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr16:9943749 G>T maps to NM_000833.3 S397S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A23B-01A-11D-A16V-10 chr16:9943614 G>A maps to NM_000833.3 I442I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CK-01A-11D-A20W-10 chr16:10273989 T>C maps to NM_000833.3 A93A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39X-01A-11D-A20W-10 chr17:72848171 A>G maps to NM_000835.3 P326P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39Z-01A-11D-A20W-10 chr19:48908505 G>A maps to NM_000836.2 V327V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NV-01A-11D-A30V-10 chr19:48945413 C>T maps to NM_000836.2 I816I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A6M4-01A-11D-A32G-10 chr19:48925127 T>A maps to NM_000836.2 Y726*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QA-A7B7-01A-11D-A32G-10 chr12:66838426 G>A maps to ENST00000359742 Q542*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr23:48853704 T>C did not map to a codon.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr23:48855661 G>A did not map to a codon.
Sequencing variant TCGA-G3-A5SJ-01A-11D-A27I-10 chr23:48834813 G>A did not map to a codon.
Sequencing variant TCGA-KR-A7K2-01A-12D-A33Q-10 chr3:141497428 C>A maps to NM_139209.2 T101T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7ME-01A-11D-A33K-10 chr3:141535711 G>T maps to NM_139209.2 G494G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr19:47425268 C>T maps to NM_004491.4 Q1113*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10W-01A-11D-A12Z-10 chr6:146720307 A>T maps to NM_000838.3 S711S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EI-01A-11D-A12Z-10 chr6:146480535 A>G maps to NM_000838.3 E251E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A9-01A-11D-A25V-10 chr6:146755590 C>T maps to NM_000838.3 L1082L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5259-01A-31D-A20W-10 chr7:86416220 C>T maps to NM_000840.2 R371R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A7SK-01A-11D-A34Z-10 chr7:86493596 G>T did not map to a codon.
Sequencing variant TCGA-CC-A3M9-01A-11D-A20W-10 chr6:34029742 T>A maps to NM_000841.1 K267*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NS-01A-11D-A30V-10 chr6:34003576 A>G maps to NM_000841.1 Y770Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr6:34004200 A>G maps to NM_000841.1 Y562Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11C-01A-11D-A12Z-10 chr11:88583096 C>T maps to NM_001143831.2 A296A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NE-01A-11D-A27I-10 chr5:178408749 C>A maps to NM_000843.3 E848*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A9-01A-11D-A25V-10 chr3:7620821 C>T maps to NM_181874.2 A743A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10R-01A-11D-A12Z-10 chr17:42428481 C>T maps to NM_002087.2 S262S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A23B-01A-11D-A16V-10 chr23:16142450 G>T did not map to a codon.
Sequencing variant TCGA-G3-A25S-01A-11D-A16V-10 chr4:42895630 C>T maps to NM_001080476.2 G116G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EI-01A-11D-A12Z-10 chr17:38068751 T>C did not map to a codon.
Sequencing variant TCGA-G3-A3CJ-01A-11D-A20W-10 chr19:42736819 T>G maps to NM_019884.2 R371R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11A-01A-11D-A12Z-10 chr3:119634999 G>A maps to NM_002093.3 R167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KR-A7K2-01A-12D-A33Q-10 chr9:124065339 C>G maps to NM_000177.4 Y167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-4073-01B-02D-A12Z-10 chr6:52858984 C>A maps to NM_001512.3 V19V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10Q-01A-11D-A12Z-10 chr4:106766664 T>C maps to NM_001031720.2 V611V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MA-01A-11D-A20W-10 chr4:106650633 T>C maps to NM_001031720.2 P406P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A6M3-01A-11D-A32G-10 chr10:106025864 C>T maps to NM_004832.2 T163T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11D-01A-11D-A12Z-10 chr2:144903284 C>A maps to NM_001164629.2 V67V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A6UC-01A-21D-A33K-10 chr1:89325565 T>C maps to NM_001514.5 K178K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BW-A5NP-01A-11D-A27I-10 chr19:6381583 C>T maps to NM_002096.2 Q293Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5261-01A-01D-A12Z-10 chr7:73932487 C>G maps to NM_016328.2 A147A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr7:74211993 A>T maps to NM_173537.2 T619T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A26S-01A-11D-A16V-10 chr13:28009316 A>G maps to NM_002097.2 K307K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A9-01A-11D-A25V-10 chr16:27506736 G>A maps to NM_001520.3 Y809Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NI-A4U2-01A-11D-A28X-10 chr16:27549249 T>A did not map to a codon.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr16:27509072 T>C maps to NM_001520.3 P745P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr2:27550058 C>A maps to NM_001521.2 L834L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr22:46719147 G>T maps to NM_016426.6 T498T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr22:46704833 G>T maps to NM_016426.6 A252A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IL-01A-11D-A33Q-10 chr11:106810593 C>A maps to ENST00000282249 V266V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A7PZ-01A-11D-A33Q-10 chr11:106810254 C>T maps to ENST00000282249 L379L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25S-01A-11D-A16V-10 chr4:156715006 G>T did not map to a codon.
Sequencing variant TCGA-MI-A75I-01A-11D-A32G-10 chr4:156724874 G>T maps to ENST00000502959 E527*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-4073-01B-02D-A12Z-10 chr12:14774138 G>T maps to NM_004963.3 I871I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A8-01A-11D-A22F-10 chr23:108684674 A>G did not map to a codon.
Sequencing variant TCGA-BC-A112-01A-11D-A12Z-10 chr4:44692731 A>T did not map to a codon.
Sequencing variant TCGA-BC-A110-01A-11D-A12Z-10 chr7:65440042 G>A maps to NM_000181.3 Q310*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A4-01A-11D-A22F-10 chr7:65435331 T>C maps to NM_000181.3 K471K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr7:65435343 G>T maps to NM_000181.3 I467I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr23:2774544 A>G did not map to a codon.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr20:23345334 G>T maps to NM_022482.3 R105R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HP-A5N0-01A-11D-A28X-10 chr19:549778 C>G maps to NM_005317.2 G254G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr12:48723754 G>C maps to NM_181788.1 P227P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A6M4-01A-11D-A32G-10 chr3:129266303 C>A maps to NM_153833.1 P53P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EA-01A-11D-A12Z-10 chr1:9305493 G>A maps to NM_004285.3 W167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K7-A5RG-01A-11D-A28X-10 chr3:15613197 T>A maps to NM_012260.2 K358*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T1-A6J8-01A-11D-A32G-10 chr19:35775693 G>A maps to NM_021175.2 T31T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MA-01A-11D-A33Q-10 chr20:7915179 C>A maps to NM_017545.2 T80T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A5UD-01A-11D-A28X-10 chr1:156594456 T>A maps to NM_021817.2 P207P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25T-01A-11D-A16V-10 chr1:156593365 A>G maps to NM_021817.2 P28P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75H-01A-11D-A32G-10 chr19:19369443 C>T maps to NM_023002.2 G235G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1E9-01A-21D-A152-10 chr8:122641076 C>T maps to NM_005328.2 S168S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LG-A6GG-01A-11D-A30V-10 chr8:122626465 A>T maps to NM_005328.2 V514V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11C-01A-11D-A12Z-10 chr19:36106171 G>A maps to NM_015302.1 Q123Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10W-01A-11D-A12Z-10 chr9:19070269 A>G maps to NM_017645.3 N441N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39V-01A-11D-A20W-10 chr5:156479624 G>A maps to NM_001173393.1 T140T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A3-01A-11D-A22F-10 chr11:5269687 C>T maps to ENST00000440157 L120L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75G-01A-11D-A32G-10 chr7:106820463 A>G maps to NM_012257.3 P42P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-4073-01B-02D-A12Z-10 chr23:11139891 G>C did not map to a codon.
Sequencing variant TCGA-DD-A4NA-01A-11D-A25V-10 chr23:11139830 G>A did not map to a codon.
Sequencing variant TCGA-CC-A3MC-01A-11D-A22F-10 chr23:153224781 C>A did not map to a codon.
Sequencing variant TCGA-DD-A1EF-01A-11D-A12Z-10 chr23:153222831 C>T did not map to a codon.
Sequencing variant TCGA-DD-A39X-01A-11D-A20W-10 chr23:153220033 C>T did not map to a codon.
Sequencing variant TCGA-G3-A5SM-01A-12D-A28X-10 chr15:73617653 G>A maps to NM_005477.2 S574S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A6M4-01A-11D-A32G-10 chr15:73615217 G>A maps to NM_005477.2 P1072P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr1:32087136 C>T maps to NM_001525.2 L228L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr6:55142233 A>G maps to NM_001526.3 S273S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11B-01A-11D-A16Z-10 chr22:50688344 C>A maps to NM_032019.5 V146V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A6UC-01A-21D-A33K-10 chr22:50688855 C>A maps to NM_032019.5 P97P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NP-01A-11D-A28X-10 chr5:141007749 G>C maps to NM_003883.3 Y232*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73E-01A-12D-A32G-10 chr5:141008782 C>T maps to NM_003883.3 T189T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A6M6-01A-11D-A32G-10 chr2:240056267 G>A maps to NM_006037.3 S350S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T1-A6J8-01A-11D-A32G-10 chr2:240158360 C>G did not map to a codon.
Sequencing variant TCGA-DD-A3A8-01A-11D-A22F-10 chr23:71788677 G>C did not map to a codon.
Sequencing variant TCGA-CC-5262-01A-01D-A12Z-10 chr7:18833075 G>A did not map to a codon.
Sequencing variant TCGA-ED-A4XI-01A-11D-A25V-10 chr7:18688119 G>A maps to NM_178425.2 L427L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr7:18687566 C>T maps to NM_178425.2 L399L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr2:242186198 G>T maps to NM_005336.3 R640R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A5KG-01A-11D-A27I-10 chr16:50106572 G>T maps to NM_182922.2 V190V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73C-01A-12D-A33K-10 chr14:73964941 G>T maps to ENST00000334988 I774I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr14:31819852 A>G maps to ENST00000389961 L822L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5258-01A-01D-A12Z-10 chr17:58156055 C>T did not map to a codon.
Sequencing variant TCGA-DD-A11D-01A-11D-A12Z-10 chr6:138734130 C>T maps to NM_014320.2 G178G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr14:31641122 G>A maps to NM_015382.2 Q426*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A5UE-01A-11D-A28X-10 chr1:45469576 C>T maps to NM_024602.5 T793T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25S-01A-11D-A16V-10 chr7:43506064 A>G maps to NM_015052.3 S937S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BW-A5NQ-01A-11D-A27I-10 chr2:197080656 T>A maps to NM_020760.1 S1513S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A23B-01A-11D-A16V-10 chr3:124724108 C>A maps to NM_020733.1 T1099T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A9-01A-11D-A25V-10 chr12:66704295 A>T maps to NM_033647.2 K530*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr9:100698474 C>A maps to NM_018437.3 E51*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5264-01A-01D-A12Z-10 chr23:65393435 C>G did not map to a codon.
Sequencing variant TCGA-MI-A75H-01A-11D-A32G-10 chr23:65408257 T>C did not map to a codon.
Sequencing variant TCGA-BC-A112-01A-11D-A12Z-10 chr11:93822053 C>A maps to NM_001098672.1 A738A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25W-01A-11D-A16V-10 chr11:93778946 A>G maps to NM_001098672.1 K93K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr15:63916006 G>T maps to ENST00000261887 R4510R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr15:63915039 G>T maps to ENST00000261887 T4554T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QA-A7B7-01A-11D-A32G-10 chr15:63978598 A>G maps to ENST00000261887 L2062L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T1-A6J8-01A-11D-A32G-10 chr15:63988456 T>A maps to ENST00000261887 R1663*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MA-01A-11D-A20W-10 chr15:28427624 T>C maps to NM_004667.4 S2953S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A5UE-01A-11D-A28X-10 chr15:28518062 C>A maps to NM_004667.4 L296L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr15:28493785 A>G maps to NM_004667.4 A1049A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11A-01A-11D-A12Z-10 chr15:28457605 T>A maps to NM_004667.4 K2304*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CK-01A-11D-A20W-10 chr15:28482109 G>A maps to NM_004667.4 A1334A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A4ZQ-01A-11D-A25V-10 chr4:89318062 A>G maps to NM_017912.3 P316P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LG-A6GG-01A-11D-A30V-10 chr4:89329770 T>C did not map to a codon.
Sequencing variant TCGA-G3-A25W-01A-11D-A16V-10 chr3:57233896 G>T maps to NM_003865.2 S17*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A2QR-01A-11D-A20W-10 chr6:126080599 C>T maps to NM_012259.2 H222H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr6:26091581 A>G maps to NM_000410.3 Q127Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25W-01A-11D-A16V-10 chr1:145414810 C>T maps to NM_213653.3 P10P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A4XI-01A-11D-A25V-10 chr1:91784928 T>C maps to NM_001017975.3 L867L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr4:3443799 G>C maps to ENST00000511533 L24L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A7SK-01A-11D-A34Z-10 chr17:79663472 A>T maps to NM_004712.4 K494*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75G-01A-11D-A32G-10 chr10:94450054 G>T maps to NM_002729.4 P104P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BW-A5NP-01A-11D-A27I-10 chr3:108076863 C>T maps to NM_007072.2 R287*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A7SK-01A-11D-A34Z-10 chr1:100542806 A>G maps to NM_033055.2 A326A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A5SL-01A-11D-A27I-10 chr9:97216241 G>A maps to NM_032558.2 T306T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A7SB-01A-21D-A34Z-10 chr2:191110919 T>A maps to NM_014362.3 K257*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BD-A2L6-01A-11D-A20W-10 chr19:46812016 G>A maps to NM_152795.2 K182K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-O8-A75V-01A-11D-A32G-10 chr19:46815883 T>C maps to NM_152795.2 S333S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A9-01A-11D-A25V-10 chr12:123338689 C>T maps to NM_003959.1 L226L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A3KF-01A-11D-A20W-10 chr1:114500749 T>C maps to ENST00000426820 D677D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr1:114499247 G>T did not map to a codon.
Sequencing variant TCGA-DD-A116-01A-11D-A12Z-10 chr22:19376068 A>G maps to NM_003325.3 C315C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr6:26156942 A>T maps to NM_005321.2 K109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr6:26156945 A>T maps to NM_005321.2 K110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NB-01A-12D-A25V-10 chr6:27100891 G>A maps to NM_021064.4 K14K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BW-A5NO-01A-11D-A27I-10 chr6:26158525 C>G maps to NM_138720.1 Y43*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11A-01A-11D-A12Z-10 chr6:26158594 C>T maps to NM_138720.1 F66F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LG-A6GG-01A-11D-A30V-10 chr6:26184112 C>G maps to NM_003523.2 R30R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr6:27100193 C>A maps to NM_021058.3 V112V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QA-A7B7-01A-11D-A32G-10 chr6:26032225 C>A maps to NM_003537.3 L21L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KR-A7K8-01A-11D-A33K-10 chr6:26045685 T>A maps to NM_003531.2 A16A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CJ-01A-11D-A20W-10 chr1:149858904 A>G maps to NM_003517.2 K127K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73B-01A-12D-A32G-10 chr6:12120241 C>T maps to NM_002114.2 Q72*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CH-01A-11D-A22F-10 chr6:12121665 G>A maps to NM_002114.2 L546L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-O8-A75V-01A-11D-A32G-10 chr6:12122421 A>T maps to NM_002114.2 P798P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A5UD-01A-11D-A28X-10 chr6:143092422 C>A maps to NM_006734.3 L1151L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5259-01A-31D-A20W-10 chr1:42048713 C>G maps to NM_024503.3 R585R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MA-01A-11D-A33Q-10 chr1:42041240 C>T maps to NM_024503.3 P1727P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25U-01A-11D-A16V-10 chr10:71148961 C>T maps to ENST00000439900 L684L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10Q-01A-11D-A12Z-10 chr2:75104367 G>A maps to NM_000189.4 E317E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5262-01A-01D-A12Z-10 chr2:75107696 G>T did not map to a codon.
Sequencing variant TCGA-FV-A23B-01A-11D-A16V-10 chr5:176317834 C>T maps to NM_002115.2 T174T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A7M6-01A-11D-A33Q-10 chr10:71025433 C>T maps to NM_025130.3 C822C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr19:37854184 A>T maps to NM_181786.2 P496P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr6:32905063 A>G maps to NM_002118.4 N169N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-O8-A75V-01A-11D-A32G-10 chr21:38128886 C>A maps to NM_000411.5 G655G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4ND-01A-11D-A25V-10 chr11:118955776 G>A did not map to a codon.
Sequencing variant TCGA-CC-A5UC-01A-11D-A28X-10 chr1:185992214 T>C maps to NM_031935.2 A1893A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A9-01A-11D-A25V-10 chr1:186077692 T>A maps to NM_031935.2 P3651P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A7PY-01A-11D-A33Q-10 chr1:185897697 T>G maps to NM_031935.2 L484*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A7XP-01A-11D-A34Z-10 chr1:185976271 G>A maps to NM_031935.2 L1496L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25W-01A-11D-A16V-10 chr1:186088389 G>T maps to NM_031935.2 A3972A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KR-A7K0-01A-12D-A33Q-10 chr1:185985309 C>A maps to NM_031935.2 Y1710*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr1:185902888 A>T maps to NM_031935.2 G587G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr1:186092185 A>G maps to NM_031935.2 T4111T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A110-01A-11D-A12Z-10 chr23:150155723 A>T did not map to a codon.
Sequencing variant TCGA-O8-A75V-01A-11D-A32G-10 chr6:55378943 G>A maps to NM_019036.2 S178S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr5:74638582 A>G maps to NM_000859.2 P51P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr21:40720226 T>A maps to NM_004965.6 A39A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39X-01A-11D-A20W-10 chr23:80371832 T>C did not map to a codon.
Sequencing variant TCGA-RC-A6M4-01A-11D-A32G-10 chr23:80370662 C>A did not map to a codon.
Sequencing variant TCGA-ED-A459-01A-11D-A25V-10 chr22:35789563 A>T maps to NM_002133.2 T280T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A5SM-01A-12D-A28X-10 chr10:124908049 G>A maps to NM_005519.1 E52E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A123-01A-11D-A12Z-10 chr10:124896949 C>T maps to NM_001105574.1 G259G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A2-01A-11D-A20W-10 chr12:121426819 C>T maps to NM_000545.5 R171*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73C-01A-12D-A33K-10 chr12:121416898 T>A did not map to a codon.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr17:36091618 G>A maps to NM_000458.2 Q338*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A5UE-01A-11D-A28X-10 chr14:21679443 C>A maps to NM_031314.2 E287*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10W-01A-11D-A12Z-10 chr1:12908010 C>T maps to NM_001013631.1 A44A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3M9-01A-11D-A20W-10 chr1:12907410 T>C maps to NM_001013631.1 A244A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A459-01A-11D-A25V-10 chr23:100667969 G>T did not map to a codon.
Sequencing variant TCGA-MI-A75G-01A-11D-A32G-10 chr23:100668005 G>T did not map to a codon.
Sequencing variant TCGA-G3-A25T-01A-11D-A16V-10 chr19:39329656 T>C did not map to a codon.
Sequencing variant TCGA-BC-A69H-01A-11D-A30V-10 chr19:41785001 G>A maps to NM_007040.3 V269V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr5:78692727 T>C did not map to a codon.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr14:23745569 A>G maps to NM_020834.2 S289S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IG-01A-11D-A33K-10 chr1:60324101 A>G maps to NM_015888.4 R415R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A496-01A-11D-A25V-10 chr1:150680867 G>A maps to NM_032132.4 N137N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IK-01A-12D-A33Q-10 chr7:27224508 C>A maps to NM_005523.5 A85A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A459-01A-11D-A25V-10 chr7:27187128 A>T maps to NM_024014.2 Y80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A3I0-01A-11D-A22F-10 chr17:46628058 A>G maps to NM_002146.4 P311P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A7M8-01A-11D-A33Q-10 chr17:46688034 C>A maps to NM_004502.3 P82P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A112-01A-11D-A12Z-10 chr12:54382989 G>A maps to NM_017409.3 L263L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75I-01A-11D-A32G-10 chr12:54403334 T>C maps to NM_022658.3 Y89Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39V-01A-11D-A20W-10 chr12:54394043 A>G maps to NM_006897.1 L24L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A5SK-01A-11D-A27I-10 chr2:176964642 G>C maps to NM_021193.3 A38A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A6M6-01A-11D-A32G-10 chr1:45793224 C>T maps to NM_032756.2 R135R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EL-01A-11D-A152-10 chr19:35556779 C>T maps to NM_182983.2 S353S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11D-01A-11D-A12Z-10 chr16:72110625 C>T maps to ENST00000228226 N268N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39W-01A-11D-A20W-10 chr3:148868467 G>A did not map to a codon.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr22:26860233 G>C maps to NM_022081.4 P454P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A3I0-01A-11D-A22F-10 chr11:18333520 T>C maps to NM_181507.1 G53G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10T-01A-11D-A12Z-10 chr10:103825803 C>T maps to NM_024747.4 F191F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A2QR-01A-11D-A20W-10 chr10:100904082 C>T maps to NM_021828.4 L174L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A6M4-01A-11D-A32G-10 chr10:100995493 T>A maps to NM_021828.4 L22L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IF-01A-11D-A33K-10 chr11:6453021 T>C maps to NM_000613.2 V326V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A0-01A-11D-A20W-10 chr3:186390577 A>G maps to NM_000412.2 R187R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BW-A5NQ-01A-11D-A27I-10 chr5:175110733 G>A maps to NM_001131055.1 K166K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A217-01A-11D-A152-10 chr18:22057508 C>A maps to NM_021624.3 R386R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr1:152191382 G>A maps to NM_001009931.1 R908*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A7SB-01A-21D-A34Z-10 chr4:11401188 T>C maps to NM_005114.2 R147R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A3I1-01A-11D-A22F-10 chr13:97484794 C>T maps to NM_153456.2 S253S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr17:40706434 C>T maps to NM_000413.2 I184I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11D-01A-11D-A12Z-10 chr4:88293883 C>A maps to NM_016245.3 S178S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MB-01A-11D-A20W-10 chr9:99006631 T>C maps to NM_000197.1 K217K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A4XI-01A-11D-A25V-10 chr1:162760595 A>G maps to NM_016371.2 R2R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr16:30997765 T>C maps to NM_025193.3 A115A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A6M3-01A-11D-A32G-10 chr16:84163812 C>T maps to NM_031463.4 L148L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25W-01A-11D-A16V-10 chr6:122737442 T>C did not map to a codon.
Sequencing variant TCGA-CC-A7II-01A-11D-A33K-10 chr6:44218825 A>G maps to NM_007355.2 L333L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3M9-01A-11D-A20W-10 chr10:118458223 C>A maps to NM_025015.2 T156T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A496-01A-11D-A25V-10 chr20:3728928 G>A maps to NM_052970.4 S247S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HP-A5N0-01A-11D-A28X-10 chr10:14890637 C>T maps to NM_016299.2 I84I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A217-01A-11D-A152-10 chr6:31777907 T>C maps to NM_005527.3 Q614Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr6:31779394 C>A maps to NM_005527.3 E119*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A23B-01A-11D-A16V-10 chr6:31778552 A>G maps to NM_005527.3 A399A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CK-01A-11D-A20W-10 chr14:65008466 C>T maps to NM_021979.3 I300I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A7-01A-11D-A22F-10 chr11:122931846 G>A maps to NM_006597.3 N62N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A66Y-01A-11D-A30V-10 chr13:31715295 A>C maps to NM_006644.2 L606*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10Q-01A-11D-A12Z-10 chr23:135593728 A>C did not map to a codon.
Sequencing variant TCGA-CC-5261-01A-01D-A12Z-10 chr23:135593319 C>G did not map to a codon.
Sequencing variant TCGA-DD-A1EB-01A-11D-A12Z-10 chr23:135582922 T>G did not map to a codon.
Sequencing variant TCGA-DD-A3A5-01A-11D-A22F-10 chr5:63256469 C>T maps to NM_000524.2 L359L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K7-A5RG-01A-11D-A28X-10 chr5:63256700 C>T maps to NM_000524.2 R282R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25S-01A-11D-A16V-10 chr6:78172409 G>A maps to NM_000863.1 S237S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A9-01A-11D-A25V-10 chr3:88040702 C>T maps to NM_000866.3 L268L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11D-01A-11D-A12Z-10 chr13:47409331 G>A maps to NM_000621.3 S352S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A113-01A-11D-A12Z-10 chr23:113965761 C>G did not map to a codon.
Sequencing variant TCGA-FV-A23B-01A-11D-A16V-10 chr23:114141873 G>T did not map to a codon.
Sequencing variant TCGA-G3-A5SM-01A-12D-A28X-10 chr23:114141439 C>T did not map to a codon.
Sequencing variant TCGA-G3-A7M6-01A-11D-A33Q-10 chr23:114141283 C>G did not map to a codon.
Sequencing variant TCGA-ED-A7XO-01A-11D-A34Z-10 chr3:183772620 C>A maps to NM_130770.2 Y60*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25T-01A-11D-A16V-10 chr5:147889386 G>T maps to NM_001040173.2 S236S. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-CC-5262-01A-01D-A12Z-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CC-5262-01A-01D-A12Z-10 chr7:154862968 C>T maps to NM_024012.2 C120C. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-CC-A7IF-01A-11D-A33K-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr10:92503354 A>T maps to NM_019859.3 L463*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IL-01A-11D-A33Q-10 chr2:74757926 A>G maps to NM_013247.4 A230A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A7PX-01A-51D-A34Z-10 chr4:8304196 G>A maps to NM_053044.3 K353K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25W-01A-11D-A16V-10 chr4:8293155 G>T maps to NM_053044.3 V256V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A5SM-01A-12D-A28X-10 chr4:8295869 C>T maps to NM_053044.3 A331A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A6UC-01A-21D-A33K-10 chr4:3241783 T>A maps to NM_002111.6 *3143R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HP-A5N0-01A-11D-A28X-10 chr4:3237425 G>T maps to NM_002111.6 L2902L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr4:3189595 A>T maps to NM_002111.6 P1736P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A123-01A-11D-A12Z-10 chr23:53588742 T>C did not map to a codon.
Sequencing variant TCGA-DD-A3A9-01A-11D-A25V-10 chr23:53563160 G>C did not map to a codon.
Sequencing variant TCGA-DD-A4NQ-01A-21D-A28X-10 chr23:53655711 C>T did not map to a codon.
Sequencing variant TCGA-DD-A73F-01A-11D-A32G-10 chr23:53577954 G>T did not map to a codon.
Sequencing variant TCGA-ED-A459-01A-11D-A25V-10 chr23:53672380 T>A did not map to a codon.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr23:53579841 G>T did not map to a codon.
Sequencing variant TCGA-DD-A3A2-01A-11D-A20W-10 chr3:50332787 G>A maps to NM_003549.2 P82P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A116-01A-11D-A12Z-10 chr7:123517142 T>A maps to NM_012269.2 P460P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5258-01A-01D-A12Z-10 chr16:70884512 C>G maps to NM_032821.2 V4162V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A115-01A-11D-A12Z-10 chr16:70891689 G>T maps to NM_032821.2 V4070V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EG-01A-11D-A20W-10 chr11:118926261 C>T maps to NM_001130991.1 P69P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A5SM-01A-12D-A28X-10 chr11:118924949 T>C did not map to a codon.
Sequencing variant TCGA-MI-A75G-01A-11D-A32G-10 chr11:118922611 T>A maps to NM_001130991.1 A419A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MB-01A-11D-A20W-10 chr9:95051644 C>T maps to ENST00000375660 L21L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A3KF-01A-11D-A20W-10 chr1:220276068 A>G maps to NM_018060.3 Q300Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NI-A4U2-01A-11D-A28X-10 chr4:88732683 C>T maps to NM_004967.3 S192S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11C-01A-11D-A12Z-10 chr19:10404830 G>A maps to NM_003259.3 V609V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr1:6292059 C>A maps to NM_012405.3 E192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MA-01A-11D-A20W-10 chr10:94274761 T>C maps to NM_004969.3 E233E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A7SF-01A-11D-A34Z-10 chr10:94267912 A>G maps to NM_004969.3 F370F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EB-01A-11D-A12Z-10 chr15:78454583 T>C maps to NM_005530.2 D162D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A217-01A-11D-A152-10 chr23:153055244 G>A did not map to a codon.
Sequencing variant TCGA-RC-A6M4-01A-11D-A32G-10 chr10:1094802 C>T did not map to a codon.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr8:39785505 T>A maps to NM_002164.4 A338A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5259-01A-31D-A20W-10 chr8:39873102 C>A maps to NM_194294.2 I415I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A216-01A-11D-A152-10 chr23:148577999 A>G did not map to a codon.
Sequencing variant TCGA-DD-A3A2-01A-11D-A20W-10 chr23:148582536 C>T did not map to a codon.
Sequencing variant TCGA-DD-A1EK-01A-11D-A20W-10 chr4:994397 A>T did not map to a codon.
Sequencing variant TCGA-ED-A7XP-01A-11D-A34Z-10 chr19:18284656 C>T maps to NM_006332.3 T2T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A5UD-01A-11D-A28X-10 chr2:163124063 T>C maps to NM_022168.2 V941V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr10:91144105 C>T maps to NM_001010987.2 L346L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EL-01A-11D-A152-10 chr10:91099875 A>G maps to NM_001549.4 Q488Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RG-A7D4-01A-12D-A33Q-10 chr9:21206859 G>A maps to NM_002171.1 V79V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr9:21217241 A>G maps to NM_002173.2 S21S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75G-01A-11D-A32G-10 chr9:21409381 A>G maps to NM_002170.3 K69K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NN-01A-11D-A28X-10 chr21:34721746 T>C maps to NM_000629.2 H347H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73C-01A-12D-A33K-10 chr9:21481102 C>T maps to NM_176891.4 K197K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5259-01A-31D-A20W-10 chr6:137519199 T>A maps to NM_000416.2 R480*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A9-01A-11D-A25V-10 chr7:112102234 G>A did not map to a codon.
Sequencing variant TCGA-RC-A6M3-01A-11D-A32G-10 chr16:1630795 C>T maps to NM_014714.3 T496T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BD-A3EP-01A-11D-A22F-10 chr2:27679433 T>C maps to NM_015662.1 R1105R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A110-01A-11D-A12Z-10 chr3:107937443 T>C maps to ENST00000457963 V175V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11C-01A-11D-A12Z-10 chr3:159976323 A>G maps to ENST00000483754 L946L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75I-01A-11D-A32G-10 chr13:21175873 A>G maps to NM_175605.3 T290T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr15:65621486 C>A did not map to a codon.
Sequencing variant TCGA-DD-A3A1-01A-11D-A20W-10 chr15:99467824 G>A maps to NM_000875.3 P898P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A9-01A-11D-A25V-10 chr15:99451928 C>T maps to NM_000875.3 Y421Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A216-01A-11D-A152-10 chr17:47117453 G>A did not map to a codon.
Sequencing variant TCGA-K7-A5RG-01A-11D-A28X-10 chr17:47119723 T>C maps to NM_006546.3 D354D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7II-01A-11D-A33K-10 chr7:23509623 T>A maps to NM_006547.2 K36*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NI-01A-11D-A27I-10 chr7:23353254 A>G maps to NM_006547.2 Y471Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5263-01A-01D-A12Z-10 chr6:160454026 G>T maps to NM_000876.2 G367*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A8-01A-11D-A22F-10 chr6:160491063 C>T maps to NM_000876.2 R1473*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MD-01A-12D-A34Z-10 chr6:160454116 A>C maps to NM_000876.2 R397R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A7SB-01A-21D-A34Z-10 chr17:38610217 G>A maps to NM_001552.2 L182L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T1-A6J8-01A-11D-A32G-10 chr19:46543654 G>A maps to NM_001002923.1 C30C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A7XO-01A-11D-A34Z-10 chr1:201196307 A>T maps to NM_001164586.1 A3695A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K7-A5RG-01A-11D-A28X-10 chr1:201184847 G>T maps to NM_001164586.1 G3059G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QA-A7B7-01A-11D-A32G-10 chr11:68701271 A>T maps to NM_002180.2 P476P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr19:51828606 C>A maps to NM_001101372.1 A133A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr23:130408625 T>A did not map to a codon.
Sequencing variant TCGA-NI-A4U2-01A-11D-A28X-10 chr23:130408572 C>T did not map to a codon.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr23:130419758 G>T did not map to a codon.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr3:151160800 T>C maps to NM_178822.4 P1978P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A0-01A-11D-A20W-10 chr3:151176326 G>T maps to NM_178822.4 P57P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25S-01A-11D-A16V-10 chr3:151155691 A>G maps to NM_178822.4 S2219S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25S-01A-11D-A16V-10 chr3:118621408 A>G maps to NM_152538.2 P417P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75I-01A-11D-A32G-10 chr3:118647488 G>A maps to NM_152538.2 T96T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7II-01A-11D-A33K-10 chr11:18743086 G>A maps to NM_173588.3 L125L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr11:18743195 G>A maps to NM_173588.3 A88A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-4073-01B-02D-A12Z-10 chr1:117158699 A>T did not map to a codon.
Sequencing variant TCGA-G3-A3CK-01A-11D-A20W-10 chr21:41160115 G>A did not map to a codon.
Sequencing variant TCGA-G3-A7M5-01A-11D-A33Q-10 chr21:41151110 A>T maps to NM_001080444.1 L271L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr11:133807313 G>A maps to NM_014987.1 S212S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A4XI-01A-11D-A25V-10 chr11:133799609 C>T maps to NM_014987.1 W529*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25T-01A-11D-A16V-10 chr11:133801030 T>C did not map to a codon.
Sequencing variant TCGA-O8-A75V-01A-11D-A32G-10 chr11:133790931 G>A maps to NM_014987.1 N896N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A5SK-01A-11D-A27I-10 chr12:99028192 T>A did not map to a codon.
Sequencing variant TCGA-G3-A25T-01A-11D-A16V-10 chr9:111665217 T>C maps to NM_003640.3 S585S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25T-01A-11D-A16V-10 chr1:206647813 G>T maps to NM_014002.3 T76T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25Z-01A-11D-A16V-10 chr1:206649566 C>T maps to NM_014002.3 R134R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr23:153770549 T>C did not map to a codon.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr7:50467946 C>T maps to NM_006060.3 C394C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EG-01A-11D-A20W-10 chr7:50467991 C>T maps to NM_006060.3 S409S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A4ZQ-01A-11D-A25V-10 chr2:213914449 G>A maps to ENST00000342002 L193L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A496-01A-11D-A25V-10 chr17:37922297 G>A maps to NM_012481.3 Y425Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25S-01A-11D-A16V-10 chr12:56428967 C>T maps to NM_022465.3 I537I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A459-01A-11D-A25V-10 chr11:117869878 G>T maps to NM_001558.3 S420S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75E-01A-11D-A32G-10 chr11:117869719 C>T maps to NM_001558.3 S367S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25S-01A-11D-A16V-10 chr5:158750287 C>T maps to NM_002187.2 V46V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A6M6-01A-11D-A32G-10 chr5:158753701 C>T did not map to a codon.
Sequencing variant TCGA-CC-A7IK-01A-12D-A33Q-10 chr19:18186613 C>A maps to NM_005535.1 L215L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11C-01A-11D-A12Z-10 chr19:18188363 G>A maps to NM_005535.1 Q171*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IF-01A-11D-A33K-10 chr1:67833703 T>C maps to NM_001559.2 I485I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A118-01A-11D-A12Z-10 chr23:117895249 T>A did not map to a codon.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr23:117910393 A>G did not map to a codon.
Sequencing variant TCGA-CC-A7IK-01A-12D-A33Q-10 chr23:114244203 A>G did not map to a codon.
Sequencing variant TCGA-ED-A7PZ-01A-11D-A33Q-10 chr23:114249117 A>T did not map to a codon.
Sequencing variant TCGA-BC-A112-01A-11D-A12Z-10 chr16:88705411 G>A maps to NM_013278.3 L10L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EL-01A-11D-A152-10 chr22:17585698 A>G maps to NM_014339.5 P310P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A3-01A-11D-A22F-10 chr22:17577965 G>A maps to NM_014339.5 T51T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A7M5-01A-11D-A33Q-10 chr3:57148801 A>T maps to NM_017563.3 A76A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A1-01A-11D-A20W-10 chr11:112020883 G>C maps to NM_001562.2 S46*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A5UD-01A-11D-A28X-10 chr11:71712349 A>G maps to NM_001145057.1 R113R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K7-A6G5-01A-11D-A30V-10 chr11:71711532 C>T maps to NM_001145057.1 P55P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NA-01A-11D-A25V-10 chr2:103013027 C>T maps to NM_003855.2 S436S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr2:113593195 T>C did not map to a codon.
Sequencing variant TCGA-BD-A3EP-01A-11D-A22F-10 chr2:113831956 G>T maps to NM_032556.4 L28L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11D-01A-11D-A12Z-10 chr23:29973330 A>T did not map to a codon.
Sequencing variant TCGA-K7-A5RG-01A-11D-A28X-10 chr23:29973746 C>T did not map to a codon.
Sequencing variant TCGA-BC-A217-01A-11D-A152-10 chr23:105011222 T>C did not map to a codon.
Sequencing variant TCGA-CC-A3MA-01A-11D-A20W-10 chr23:104478543 T>C did not map to a codon.
Sequencing variant TCGA-DD-A4NF-01A-11D-A27I-10 chr23:105011410 C>A did not map to a codon.
Sequencing variant TCGA-K7-A5RG-01A-11D-A28X-10 chr23:104999215 A>G did not map to a codon.
Sequencing variant TCGA-RC-A6M4-01A-11D-A32G-10 chr23:105011033 A>T did not map to a codon.
Sequencing variant TCGA-DD-A3A9-01A-11D-A25V-10 chr2:102968227 A>G maps to NM_016232.4 V506V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NI-01A-11D-A27I-10 chr2:102836403 A>G maps to NM_003854.2 K306K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11D-01A-11D-A12Z-10 chr6:137323492 C>G did not map to a codon.
Sequencing variant TCGA-DD-A3A8-01A-11D-A22F-10 chr3:136708319 T>C maps to NM_144717.3 D148D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A5-01A-11D-A22F-10 chr16:27460190 C>T maps to NM_181079.4 L424L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25Y-01A-11D-A16V-10 chr16:27460453 G>T maps to NM_181079.4 T511T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73G-01A-22D-A32G-10 chr14:23842467 C>T maps to NM_022789.3 T47T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A6M3-01A-11D-A32G-10 chr19:14150477 G>A did not map to a codon.
Sequencing variant TCGA-DD-A73G-01A-22D-A32G-10 chr9:6241765 C>T maps to NM_033439.3 A24A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10Z-01A-11D-A12Z-10 chr19:50393088 C>T maps to NM_172374.1 T536T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75G-01A-11D-A32G-10 chr16:27374562 G>T maps to NM_000418.2 G630G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr16:27374492 C>G maps to NM_000418.2 S607*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10T-01A-11D-A12Z-10 chr5:55247871 T>C maps to NM_002184.3 K528K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A118-01A-11D-A12Z-10 chr5:55272093 G>A maps to NM_002184.3 Q5*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A113-01A-11D-A12Z-10 chr5:135231423 G>A maps to NM_000590.1 L28L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A69H-01A-11D-A30V-10 chr23:155233209 G>T did not map to a codon.
Sequencing variant TCGA-CC-A1HT-01A-11D-A12Z-10 chr23:155239666 C>A did not map to a codon.
Sequencing variant TCGA-MI-A75H-01A-11D-A32G-10 chr23:155233486 C>T did not map to a codon.
Sequencing variant TCGA-K7-A5RG-01A-11D-A28X-10 chr3:121712593 T>A maps to ENST00000344209 P334P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BW-A5NO-01A-11D-A27I-10 chr19:10791741 C>T maps to NM_017620.2 G335G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73E-01A-12D-A32G-10 chr19:15233712 C>A maps to NM_006844.3 S198S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EA-01A-11D-A12Z-10 chr8:82591404 T>C maps to NM_001144878.1 T145T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10R-01A-11D-A12Z-10 chr3:100972617 T>A maps to NM_016247.2 G387G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IK-01A-12D-A33Q-10 chr3:100948246 C>A maps to NM_016247.2 E1204*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr1:62582320 C>A maps to NM_176877.2 A1591A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A3KF-01A-11D-A20W-10 chr11:61906199 A>G maps to NM_001040694.1 E377E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A3KF-01A-11D-A20W-10 chr7:120607622 T>C maps to NM_019071.2 D159D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1ED-01A-11D-A152-10 chr2:220439446 A>G maps to NM_002191.3 R100R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A7PZ-01A-11D-A33Q-10 chr2:220439763 C>A maps to NM_002191.3 S206*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73B-01A-12D-A32G-10 chr7:41729921 C>A maps to NM_002192.2 E203*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A496-01A-11D-A25V-10 chr12:57849889 C>T maps to NM_031479.3 A104A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5258-01A-01D-A12Z-10 chr4:143043285 T>C maps to NM_003866.2 G710G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25S-01A-11D-A16V-10 chr4:143043366 G>T maps to NM_003866.2 A683A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr4:143007365 T>C maps to NM_003866.2 L806L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10Z-01A-11D-A12Z-10 chr2:234112783 G>A maps to ENST00000359570 L996L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-4073-01B-02D-A12Z-10 chr11:71948270 C>T maps to NM_001567.3 Q995*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MC-01A-11D-A22F-10 chr11:71944786 A>G maps to NM_001567.3 K737K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IK-01A-12D-A33Q-10 chr11:71948759 C>T maps to NM_001567.3 L1158L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr11:15247244 G>T maps to NM_001031853.3 A394A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr11:15262002 T>C maps to NM_001031853.3 R515R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MC-01A-11D-A22F-10 chr7:155093274 G>C did not map to a codon.
Sequencing variant TCGA-ED-A7XP-01A-11D-A34Z-10 chr7:155094007 C>T maps to ENST00000344756 A195A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11A-01A-11D-A12Z-10 chr1:67266849 C>A maps to NM_005478.3 E19*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11C-01A-11D-A12Z-10 chr19:7126663 T>C did not map to a codon.
Sequencing variant TCGA-CC-A3M9-01A-11D-A20W-10 chr7:1529319 T>A did not map to a codon.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr7:1513872 C>A maps to ENST00000389470 P2134P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11D-01A-11D-A12Z-10 chr7:1539151 C>A maps to ENST00000389470 L395L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11C-01A-11D-A12Z-10 chr8:19682424 G>A maps to NM_018142.2 L316L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QA-A7B7-01A-11D-A32G-10 chr11:62415199 A>T maps to NM_030628.1 V784V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr13:52025247 T>A maps to NM_012141.2 G84G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A116-01A-11D-A12Z-10 chr1:212184717 T>C maps to NM_015434.3 Q185Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CK-01A-11D-A20W-10 chr8:95892460 A>C maps to NM_017864.2 *996S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A3R2-01A-11D-A22F-10 chr6:33690706 G>A maps to NM_054111.4 G341G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr6:154480992 A>G maps to NM_001130700.1 P429P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NF-01A-11D-A27I-10 chr1:44424561 G>A did not map to a codon.
Sequencing variant TCGA-DD-A3A8-01A-11D-A22F-10 chr14:24654742 G>A maps to ENST00000458132 C400C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A7M9-01A-23D-A34Z-10 chr12:30816573 A>C maps to NM_006390.3 L481L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BW-A5NP-01A-11D-A27I-10 chr1:201827624 A>C maps to NM_018085.4 A424A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75I-01A-11D-A32G-10 chr1:201817699 T>C maps to NM_018085.4 H164H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IJ-01A-11D-A33Q-10 chr3:121514403 G>A maps to NM_001023570.2 Q296*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr3:121527777 C>A maps to NM_001023570.2 E158*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10W-01A-11D-A12Z-10 chr1:32673298 G>A maps to NM_001160042.1 R419R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A69H-01A-11D-A30V-10 chr7:2625880 G>A maps to NM_152558.3 K288K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A7-01A-11D-A22F-10 chr3:51937030 A>G maps to NM_152397.2 H26H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MA-01A-11D-A20W-10 chr15:67553701 A>G maps to NM_001031715.2 T48T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A118-01A-11D-A12Z-10 chr15:91020962 T>C maps to NM_003870.3 S1057S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A118-01A-11D-A12Z-10 chr23:53279674 C>T did not map to a codon.
Sequencing variant TCGA-G3-A5SM-01A-12D-A28X-10 chr23:53277364 C>T did not map to a codon.
Sequencing variant TCGA-UB-A7MC-01A-11D-A33Q-10 chr23:53277342 C>T did not map to a codon.
Sequencing variant TCGA-DD-A39Y-01A-11D-A20W-10 chr12:271221 C>A maps to NM_001170738.1 G858G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A9-01A-11D-A25V-10 chr12:266235 G>A maps to NM_001170738.1 E733E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A7M5-01A-11D-A33Q-10 chr7:123097529 T>A maps to NM_178827.4 R700*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A7-01A-11D-A22F-10 chr23:153278075 T>C did not map to a codon.
Sequencing variant TCGA-DD-A3A9-01A-11D-A25V-10 chr23:153284219 C>T did not map to a codon.
Sequencing variant TCGA-G3-A5SK-01A-11D-A27I-10 chr12:66611015 G>T did not map to a codon.
Sequencing variant TCGA-DD-A1EH-01A-11D-A12Z-10 chr4:185320191 C>A maps to NM_002199.3 E191*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A7PY-01A-11D-A33Q-10 chr4:185339322 T>A maps to NM_002199.3 K137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IJ-01A-11D-A33Q-10 chr1:234743410 G>A maps to NM_182972.2 T412T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5262-01A-01D-A12Z-10 chr6:393365 A>T maps to NM_002460.3 K72*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IF-01A-11D-A33K-10 chr6:393202 G>A maps to NM_002460.3 V17V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr1:209974641 G>A maps to NM_006147.2 P39P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr19:44222898 G>A maps to NM_019612.3 S63S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EL-01A-11D-A152-10 chr19:44099394 C>T maps to NM_001007561.2 V32V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25Y-01A-11D-A16V-10 chr19:44097314 C>T maps to NM_001007561.2 L245L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NV-01A-11D-A30V-10 chr13:110436225 G>A maps to NM_003749.2 G725G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11D-01A-11D-A12Z-10 chr23:107977030 G>T did not map to a codon.
Sequencing variant TCGA-DD-A1EA-01A-11D-A12Z-10 chr23:107976585 G>A did not map to a codon.
Sequencing variant TCGA-DD-A4NJ-01A-11D-A27I-10 chr23:107979137 C>T did not map to a codon.
Sequencing variant TCGA-G3-A5SM-01A-12D-A28X-10 chr23:107977916 G>A did not map to a codon.
Sequencing variant TCGA-G3-A6UC-01A-21D-A33K-10 chr23:107977379 T>C did not map to a codon.
Sequencing variant TCGA-ED-A7XP-01A-11D-A34Z-10 chr5:3599649 C>A maps to NM_024337.3 R196R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr5:1878690 C>A maps to NM_016358.2 E318*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MC-01A-11D-A33Q-10 chr15:89182608 C>T maps to NM_002201.4 S4S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25S-01A-11D-A16V-10 chr5:50685753 C>T maps to NM_002202.2 P251P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10Z-01A-11D-A12Z-10 chr15:76632728 C>G maps to NM_145805.1 T208T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A66X-01A-11D-A30V-10 chr20:13279760 C>T maps to NM_080826.1 D350D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A9-01A-11D-A25V-10 chr14:77948665 G>A maps to NM_199296.2 Y324Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25Z-01A-11D-A16V-10 chr19:18545773 G>T maps to NM_016368.4 T542T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr16:312090 G>T did not map to a codon.
Sequencing variant TCGA-G3-A5SM-01A-12D-A28X-10 chr16:314813 C>A maps to NM_032039.2 V484V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QA-A7B7-01A-11D-A32G-10 chr16:312456 C>T maps to NM_032039.2 L292L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A216-01A-11D-A152-10 chr1:145532145 C>T maps to NM_003637.3 R264*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A6M4-01A-11D-A32G-10 chr1:145532112 A>T did not map to a codon.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr15:68609679 C>A maps to ENST00000423218 E880*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr15:68624265 C>T maps to ENST00000423218 E567E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EL-01A-11D-A152-10 chr5:52353864 A>G maps to NM_002203.3 Q369Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A2QR-01A-11D-A20W-10 chr5:52356812 A>T maps to NM_002203.3 I465I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CK-01A-11D-A20W-10 chr5:52347344 T>C maps to NM_002203.3 Y245Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr5:52369004 G>A maps to NM_002203.3 L829L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A5UE-01A-11D-A28X-10 chr17:48149395 G>T maps to NM_002204.2 E336*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IL-01A-11D-A33Q-10 chr2:182323027 C>T maps to NM_000885.4 C101C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A2QQ-01A-11D-A22F-10 chr2:182358112 C>T maps to NM_000885.4 G405G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A459-01A-11D-A25V-10 chr2:173344404 A>T maps to ENST00000264106 T514T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10T-01A-11D-A12Z-10 chr12:56087101 C>T did not map to a codon.
Sequencing variant TCGA-G3-A25T-01A-11D-A16V-10 chr12:56086981 G>T maps to ENST00000347027 G929G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A5SM-01A-12D-A28X-10 chr12:56092543 C>G maps to ENST00000347027 L360L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A5SJ-01A-11D-A27I-10 chr10:15559198 G>T maps to NM_003638.1 T1050T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A6M6-01A-11D-A32G-10 chr10:15688878 T>G maps to NM_003638.1 A391A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr3:37774279 A>C maps to NM_002207.2 S715S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A496-01A-11D-A25V-10 chr16:31419145 G>A maps to ENST00000444228 A322A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GJ-A6C0-01A-12D-A30V-10 chr16:31414895 C>T maps to ENST00000444228 Q228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr16:30500451 C>T maps to NM_002209.2 S352S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10W-01A-11D-A12Z-10 chr16:31284709 C>T maps to NM_001145808.1 N243N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A217-01A-11D-A152-10 chr16:31372493 T>C maps to NM_000887.3 D324D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A9-01A-11D-A25V-10 chr16:31390891 C>T maps to NM_000887.3 H931H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A8-01A-11D-A22F-10 chr2:9552532 T>C maps to NM_004763.3 G51G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr21:46330222 G>T maps to NM_000211.3 P41P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EH-01A-11D-A12Z-10 chr17:45387554 G>C maps to NM_000212.2 T784T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NE-01A-11D-A27I-10 chr17:45361989 A>G maps to NM_000212.2 A181A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A3I1-01A-11D-A22F-10 chr1:63974242 T>C did not map to a codon.
Sequencing variant TCGA-DD-A3A0-01A-11D-A20W-10 chr3:124578236 G>A maps to NM_002213.3 V71V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75H-01A-11D-A32G-10 chr2:161029223 C>A maps to NM_000888.3 R259R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr12:53586192 G>A maps to NM_000889.1 T692T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A1HT-01A-11D-A12Z-10 chr7:20445702 T>A maps to NM_002214.2 L644L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A2QR-01A-11D-A20W-10 chr7:20438492 C>A maps to NM_002214.2 S386*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11A-01A-11D-A12Z-10 chr13:102366887 T>G maps to NM_004791.1 G460G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CK-01A-11D-A20W-10 chr3:52823732 G>C maps to NM_002215.2 T728T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MA-01A-11D-A20W-10 chr3:52842645 A>G maps to NM_002217.3 E874E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25V-01A-11D-A16V-10 chr3:52828854 T>C maps to NM_002217.3 A12A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A5UD-01A-11D-A28X-10 chr3:52861119 A>G maps to ENST00000485816 A115A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A495-01A-11D-A25V-10 chr3:52863214 C>T maps to ENST00000485816 V57V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr3:52860031 T>A did not map to a codon.
Sequencing variant TCGA-ED-A459-01A-11D-A25V-10 chr10:7627888 G>T maps to ENST00000256861 Y361*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A2-01A-11D-A20W-10 chr5:156675954 T>C maps to NM_005546.3 L577L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A6UC-01A-21D-A33K-10 chr23:78618460 G>C did not map to a codon.
Sequencing variant TCGA-RC-A7SF-01A-11D-A34Z-10 chr23:78618535 G>A did not map to a codon.
Sequencing variant TCGA-G3-A3CK-01A-11D-A20W-10 chr13:48832329 T>C maps to NM_021999.4 V174V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5263-01A-01D-A12Z-10 chr14:93483122 C>T maps to NM_014216.4 E48E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A5SM-01A-12D-A28X-10 chr14:93542959 G>A maps to NM_014216.4 R34*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73G-01A-22D-A32G-10 chr1:226829807 C>T maps to NM_002221.3 E755E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A7M9-01A-23D-A34Z-10 chr1:226923398 T>G maps to NM_002221.3 G587G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr1:226835067 T>A maps to NM_002221.3 A682A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IJ-01A-11D-A33Q-10 chr12:26752254 C>T maps to NM_002223.2 R1275R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11C-01A-11D-A12Z-10 chr12:26647250 T>C maps to NM_002223.2 S1735S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A7SK-01A-11D-A34Z-10 chr12:26647154 A>G maps to NM_002223.2 N1767N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A1HT-01A-11D-A12Z-10 chr21:35208754 G>A maps to NM_003024.2 V1160V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A5SL-01A-11D-A27I-10 chr21:35169913 T>C did not map to a codon.
Sequencing variant TCGA-RC-A7S9-01A-11D-A33Q-10 chr21:35258603 G>A maps to NM_003024.2 P1619P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A5UD-01A-11D-A28X-10 chr2:24438935 A>G maps to NM_006277.2 D1324D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NA-01A-11D-A25V-10 chr1:152883643 G>C maps to NM_005547.2 V457V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MA-01A-11D-A33Q-10 chr1:152884006 G>T maps to NM_005547.2 V578V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3M9-01A-11D-A20W-10 chr2:128247423 G>A maps to NM_017969.2 R715*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LG-A6GG-01A-11D-A30V-10 chr2:128249665 T>A did not map to a codon.
Sequencing variant TCGA-BC-A10Z-01A-11D-A12Z-10 chr19:49248990 A>G maps to NM_182575.2 P42P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73E-01A-12D-A32G-10 chr20:10654130 G>T maps to NM_000214.2 L16L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K7-A5RG-01A-11D-A28X-10 chr20:10644620 A>G maps to NM_000214.2 N143N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A4ZQ-01A-11D-A25V-10 chr19:17947998 C>T maps to NM_000215.3 L575L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NL-01A-11D-A28X-10 chr4:6083467 T>C maps to NM_001099433.1 R323R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IK-01A-12D-A33Q-10 chr5:147030070 G>A maps to NM_014790.3 L223L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr6:15497297 C>T maps to NM_004973.2 I614I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-4073-01B-02D-A12Z-10 chr7:139819019 C>A did not map to a codon.
Sequencing variant TCGA-CC-A3M9-01A-11D-A20W-10 chr7:139791730 C>T maps to NM_030647.1 A868A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-4073-01B-02D-A12Z-10 chr14:59965465 T>G maps to ENST00000356057 Y174*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10Y-01A-11D-A12Z-10 chr10:64952866 G>A maps to NM_032776.1 C1969C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A118-01A-11D-A12Z-10 chr10:64967084 G>A maps to NM_032776.1 C1448C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EF-01A-11D-A12Z-10 chr10:64950773 G>A maps to NM_032776.1 S2057S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EF-01A-11D-A12Z-10 chr10:64966478 G>C maps to NM_032776.1 Y1650*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A2QR-01A-11D-A20W-10 chr1:227922401 G>A maps to NM_023007.2 G172G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A217-01A-11D-A152-10 chr15:42126944 C>T maps to NM_005090.3 C24C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75C-01A-11D-A32G-10 chr15:42126966 C>T maps to NM_005090.3 L32L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr15:42134020 A>T maps to NM_005090.3 S396S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NF-01A-11D-A27I-10 chr20:42788301 G>C maps to NM_020433.4 R375R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IJ-01A-11D-A33Q-10 chr16:87723912 C>A maps to NM_020655.2 G649G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10Z-01A-11D-A12Z-10 chr14:24040534 G>A maps to NM_032452.2 Q469*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A7SB-01A-21D-A34Z-10 chr6:24358007 T>A maps to NM_181337.3 A47A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IK-01A-12D-A33Q-10 chr23:8503724 A>T did not map to a codon.
Sequencing variant TCGA-ED-A7PZ-01A-11D-A33Q-10 chr3:124437875 G>A maps to NM_001024660.3 L2840L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr1:62739083 C>A maps to NM_181712.4 V564V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11C-01A-11D-A12Z-10 chr17:40270417 G>A maps to NM_021078.2 F359F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LG-A6GG-01A-11D-A30V-10 chr3:20156481 T>G did not map to a codon.
Sequencing variant TCGA-PD-A5DF-01A-11D-A27I-10 chr3:20113880 C>G maps to NM_003884.4 P120P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EL-01A-11D-A152-10 chr18:44625670 C>A maps to ENST00000356157 P406P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A23B-01A-11D-A16V-10 chr10:102824162 C>A maps to NM_030929.4 P219P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A7SK-01A-11D-A34Z-10 chr3:127702968 T>C maps to NM_207335.2 L574L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25W-01A-11D-A16V-10 chr1:111060013 G>T maps to NM_005549.2 R466R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A5-01A-11D-A22F-10 chr1:111147254 G>T maps to NM_004974.2 T50T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A5SJ-01A-11D-A27I-10 chr12:5153807 C>T maps to NM_002234.2 F165F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A3KF-01A-11D-A20W-10 chr8:73849086 G>A maps to NM_004770.2 L499L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39Y-01A-11D-A20W-10 chr11:17757950 G>A maps to NM_001112741.1 A134A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr11:17801168 A>T maps to NM_001112741.1 P557P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A217-01A-11D-A152-10 chr1:110775554 G>A maps to NM_001039574.2 S614S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BD-A3EP-01A-11D-A22F-10 chr23:48823419 T>C did not map to a codon.
Sequencing variant TCGA-MI-A75E-01A-11D-A32G-10 chr18:77659125 C>T maps to NM_012283.1 S237S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QA-A7B7-01A-11D-A32G-10 chr18:77623987 C>A maps to NM_012283.1 Y107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NI-01A-11D-A27I-10 chr16:84270992 C>A maps to NM_172347.2 T33T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A7M5-01A-11D-A33Q-10 chr16:84270674 G>A maps to NM_172347.2 C139C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A112-01A-11D-A12Z-10 chr7:150671892 C>A maps to NM_000238.2 G71G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A3R2-01A-11D-A22F-10 chr7:150644108 A>T maps to NM_000238.2 T1062T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A6M4-01A-11D-A32G-10 chr12:49943272 C>T maps to NM_012284.1 R506R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A26S-01A-11D-A16V-10 chr3:19554730 C>T maps to NM_144633.2 P783P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr3:19575098 T>C maps to NM_144633.2 Y944Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr3:19492663 A>T maps to NM_144633.2 P531P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EA-01A-11D-A12Z-10 chr11:17409284 C>T maps to NM_000525.3 S118S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A7M5-01A-11D-A33Q-10 chr17:68128986 T>A maps to NM_018658.1 I253I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5261-01A-01D-A12Z-10 chr17:68172289 T>C maps to NM_000891.2 N370N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A9-01A-11D-A25V-10 chr17:68171824 C>T maps to NM_000891.2 G215G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KC-01A-11D-A20W-10 chr2:47748597 G>C maps to NM_022055.1 L247L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A9-01A-11D-A25V-10 chr14:90651206 C>T maps to NM_022054.2 L363L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NJ-01A-11D-A27I-10 chr14:90651289 G>T maps to NM_022054.2 G390G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73B-01A-12D-A32G-10 chr10:118969677 C>G maps to NM_181840.1 S341S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75I-01A-11D-A32G-10 chr1:215259975 C>G maps to NM_001017425.2 S104S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LG-A6GG-01A-11D-A30V-10 chr2:26915802 G>T maps to NM_002246.2 L20L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KC-01A-11D-A20W-10 chr6:39159106 G>T maps to NM_003740.3 P353P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MB-01A-11D-A20W-10 chr10:78669795 T>C maps to NM_001161352.1 E1025E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NJ-01A-11D-A27I-10 chr10:78761221 T>A maps to NM_001161352.1 R737*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25U-01A-11D-A16V-10 chr10:79010978 A>G maps to NM_001161352.1 L192L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A5W4-01A-11D-A28X-10 chr19:18099243 C>T maps to ENST00000222249 L377L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A3I0-01A-11D-A22F-10 chr19:18092828 G>A maps to ENST00000222249 T287T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BW-A5NQ-01A-11D-A27I-10 chr5:113798832 C>T maps to NM_021614.2 D363D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1E9-01A-21D-A152-10 chr11:2869139 C>T maps to NM_000218.2 G646G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr8:133153568 C>T maps to NM_004519.2 L424L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A5SI-01A-31D-A27I-10 chr8:133141973 C>G maps to NM_004519.2 V718V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QA-A7B7-01A-11D-A32G-10 chr6:73331991 G>T maps to NM_001160133.1 A25A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25S-01A-11D-A16V-10 chr9:138661868 C>A maps to ENST00000298480 L529L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EA-01A-11D-A12Z-10 chr1:196309630 T>C maps to NM_198503.2 R541R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39X-01A-11D-A20W-10 chr1:196295980 A>G maps to NM_198503.2 Y714Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NV-01A-11D-A30V-10 chr8:36666268 A>C maps to NM_001031836.2 I230I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A66Y-01A-11D-A30V-10 chr8:36788611 G>T maps to NM_001031836.2 R960R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25U-01A-11D-A16V-10 chr8:36776401 C>A maps to NM_001031836.2 I861I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KR-A7K7-01A-11D-A33K-10 chr8:110980790 G>A maps to NM_014379.2 Y343Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A113-01A-11D-A12Z-10 chr9:2718690 C>T maps to NM_133497.2 L318L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-4073-01B-02D-A12Z-10 chr5:143586732 C>T maps to NM_020768.3 P152P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39X-01A-11D-A20W-10 chr22:37453517 C>T maps to ENST00000403888 G164G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A26S-01A-11D-A16V-10 chr16:2732725 G>A maps to NM_018992.3 R59R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10U-01A-11D-A12Z-10 chr4:44449750 T>A maps to NM_198353.2 K264*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EB-01A-11D-A12Z-10 chr4:44176878 G>A maps to NM_198353.2 I450I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NL-01A-11D-A28X-10 chr4:44176929 C>T maps to NM_198353.2 K433K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5264-01A-01D-A12Z-10 chr19:48886579 T>C maps to NM_006801.2 L203L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10U-01A-11D-A12Z-10 chr6:18215296 C>A maps to ENST00000388870 T724T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25W-01A-11D-A16V-10 chr11:66975110 C>A maps to NM_012308.2 L146L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A4ZQ-01A-11D-A25V-10 chr2:86709143 G>A maps to NM_001146688.1 T868T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25Y-01A-11D-A16V-10 chr9:6793122 T>C maps to NM_015061.3 G45G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr9:7046859 A>T did not map to a codon.
Sequencing variant TCGA-DD-A39V-01A-11D-A20W-10 chr1:202704643 C>T maps to ENST00000367264 L1148L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25W-01A-11D-A16V-10 chr1:202710670 C>T maps to ENST00000367264 V959V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A5SK-01A-11D-A27I-10 chr23:53228046 A>T did not map to a codon.
Sequencing variant TCGA-G3-A5SM-01A-12D-A28X-10 chr23:53246990 C>A did not map to a codon.
Sequencing variant TCGA-G3-A25V-01A-11D-A16V-10 chr24:21897300 C>T did not map to a codon.
Sequencing variant TCGA-K7-A5RF-01A-11D-A28X-10 chr24:21901514 T>C did not map to a codon.
Sequencing variant TCGA-MI-A75I-01A-11D-A32G-10 chr23:44870265 T>G did not map to a codon.
Sequencing variant TCGA-BW-A5NO-01A-11D-A27I-10 chr17:7751675 C>T maps to NM_001080424.1 I690I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A3I0-01A-11D-A22F-10 chr17:7755290 C>T maps to NM_001080424.1 F1396F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-4073-01B-02D-A12Z-10 chr4:55955861 G>A maps to NM_002253.2 S1100S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3M9-01A-11D-A20W-10 chr4:55946221 G>T maps to NM_002253.2 Y1319*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75I-01A-11D-A32G-10 chr4:55963910 G>C maps to NM_002253.2 A844A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr4:55984966 C>T maps to NM_002253.2 R54R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr18:61034243 C>T maps to NM_002035.2 V36V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25Y-01A-11D-A16V-10 chr18:61018192 T>G maps to NM_002035.2 G179G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A113-01A-11D-A12Z-10 chr7:142639988 G>A maps to NM_000420.2 D638D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr12:91445248 T>G maps to NM_007035.3 A311A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10Y-01A-11D-A12Z-10 chr19:6420135 T>C maps to NM_003685.2 E165E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr9:2807905 T>C did not map to a codon.
Sequencing variant TCGA-CC-5258-01A-01D-A12Z-10 chr17:26967657 G>A maps to NM_014680.2 F270F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A7S9-01A-11D-A33Q-10 chr17:26970214 G>C maps to NM_014680.2 S121S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A5SL-01A-11D-A27I-10 chr5:141313822 T>C maps to NM_014773.3 L306L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-4073-01B-02D-A12Z-10 chr8:48508455 C>G maps to NM_001080394.1 S394*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NN-01A-11D-A28X-10 chr8:48309165 A>T maps to NM_001080394.1 S252S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A23B-01A-11D-A16V-10 chr8:48625237 G>A maps to NM_001080394.1 L664L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73D-01A-12D-A32G-10 chr8:126044595 T>A maps to ENST00000377985 P1079P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K7-A6G5-01A-11D-A30V-10 chr4:6863164 C>T maps to NM_014743.2 S352S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A118-01A-11D-A12Z-10 chr14:75136703 A>G maps to NM_001039479.1 A578A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr1:35928255 A>G maps to NM_024874.4 S420S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11B-01A-11D-A16Z-10 chr19:34791641 C>T maps to NM_014686.3 N88N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39X-01A-11D-A20W-10 chr19:34818734 C>T maps to NM_014686.3 F302F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A3R2-01A-11D-A22F-10 chr19:34810942 C>T maps to NM_014686.3 G209G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QA-A7B7-01A-11D-A32G-10 chr19:34839932 C>T maps to NM_014686.3 H900H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MB-01A-11D-A20W-10 chr14:35593209 A>G maps to NM_014672.2 G253G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr14:35596744 T>C maps to NM_014672.2 Y365Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NI-A4U2-01A-11D-A28X-10 chr6:127768212 C>T maps to NM_014702.4 E417E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A7M5-01A-11D-A33Q-10 chr16:85114998 G>A did not map to a codon.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr14:58924598 A>G maps to ENST00000354386 Q548Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75C-01A-11D-A32G-10 chr1:155891366 A>C maps to NM_014949.2 Y355*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EL-01A-11D-A152-10 chr5:5466616 T>C did not map to a codon.
Sequencing variant TCGA-DD-A4NK-01A-11D-A28X-10 chr5:5463007 T>A maps to NM_015325.1 Y1187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr5:5489286 A>G maps to NM_015325.1 A2215A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73A-01A-12D-A32G-10 chr6:84910597 A>T maps to NM_014895.2 S248S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-4073-01B-02D-A12Z-10 chr12:105509005 A>T maps to NM_015275.1 G122G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MC-01A-11D-A22F-10 chr12:105519875 C>G maps to NM_015275.1 S294*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A26S-01A-11D-A16V-10 chr12:105557964 G>A maps to NM_015275.1 E1078E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25T-01A-11D-A16V-10 chr4:123238012 C>T maps to NM_015312.3 L3556L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A6M4-01A-11D-A32G-10 chr4:123268770 G>A maps to NM_015312.3 Q4322Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr4:123113384 A>T maps to NM_015312.3 G301G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K7-A5RG-01A-11D-A28X-10 chr5:175774611 A>T maps to NM_020444.3 T303T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LG-A6GG-01A-11D-A30V-10 chr5:175774921 A>C did not map to a codon.
Sequencing variant TCGA-DD-A4NS-01A-11D-A30V-10 chr23:118250522 A>G did not map to a codon.
Sequencing variant TCGA-ED-A4XI-01A-11D-A25V-10 chr23:118230574 G>A did not map to a codon.
Sequencing variant TCGA-ED-A7PZ-01A-11D-A33Q-10 chr23:118223433 A>T did not map to a codon.
Sequencing variant TCGA-FV-A2QR-01A-11D-A20W-10 chr23:118221123 T>C did not map to a codon.
Sequencing variant TCGA-G3-A25T-01A-11D-A16V-10 chr23:118230609 C>A did not map to a codon.
Sequencing variant TCGA-G3-A7M8-01A-11D-A33Q-10 chr23:118281507 T>C did not map to a codon.
Sequencing variant TCGA-ED-A7XO-01A-11D-A34Z-10 chr4:57180855 G>A maps to NM_020722.1 A396A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A4ZP-01A-12D-A25V-10 chr4:57181428 G>A maps to NM_020722.1 S587S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7ME-01A-11D-A33K-10 chr4:57179475 C>A maps to NM_020722.1 A156A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39Z-01A-11D-A20W-10 chr10:24834952 A>T maps to NM_019590.3 T1844T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K7-A6G5-01A-11D-A30V-10 chr10:24508648 A>G maps to NM_019590.3 S55S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5264-01A-01D-A12Z-10 chr6:138550955 T>C maps to NM_020340.4 D129D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11C-01A-11D-A12Z-10 chr6:138612923 G>A maps to NM_020340.4 S1034S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A9-01A-11D-A25V-10 chr6:138531045 G>A did not map to a codon.
Sequencing variant TCGA-DD-A3A9-01A-11D-A25V-10 chr6:138655565 C>T maps to NM_020340.4 D1861D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A4XI-01A-11D-A25V-10 chr6:138629874 G>C did not map to a codon.
Sequencing variant TCGA-RG-A7D4-01A-12D-A33Q-10 chr6:138619873 C>T maps to NM_020340.4 F1260F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr7:86571333 A>G maps to NM_001142749.2 S247S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr8:95531220 T>C maps to NM_015496.3 E835E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr7:138554405 G>A maps to NM_001164665.1 D1551D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K7-A5RG-01A-11D-A28X-10 chr7:138564335 A>G maps to NM_001164665.1 D1431D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A7XP-01A-11D-A34Z-10 chr6:56918370 A>C maps to NM_020931.2 I358I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr6:56917491 T>C maps to NM_020931.2 F65F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7II-01A-11D-A33K-10 chr22:44681336 C>A maps to NM_001099294.1 P190P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A23B-01A-11D-A16V-10 chr20:36874513 G>A maps to NM_001029864.1 L6L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25U-01A-11D-A16V-10 chr1:233489582 C>A maps to NM_032435.2 T339T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr9:115421703 C>A maps to NM_133465.2 T502T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A5SK-01A-11D-A27I-10 chr3:113373817 T>C maps to NM_001009899.2 L2237L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BW-A5NQ-01A-11D-A27I-10 chr23:73960549 C>A did not map to a codon.
Sequencing variant TCGA-DD-A4NR-01A-11D-A30V-10 chr23:73960185 A>G did not map to a codon.
Sequencing variant TCGA-G3-A5SK-01A-11D-A27I-10 chr23:73962087 T>A did not map to a codon.
Sequencing variant TCGA-BW-A5NQ-01A-11D-A27I-10 chr9:5922602 A>G maps to NM_001017969.2 G1131G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5263-01A-01D-A12Z-10 chr9:5922995 C>T maps to NM_001017969.2 Q1000Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7II-01A-11D-A33K-10 chr9:5923024 A>G maps to NM_001017969.2 L991L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11C-01A-11D-A12Z-10 chr9:5920262 G>T maps to NM_001017969.2 L1911L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39X-01A-11D-A20W-10 chr9:5920643 A>G maps to NM_001017969.2 T1784T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39Y-01A-11D-A20W-10 chr9:5921057 T>C maps to NM_001017969.2 S1646S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RG-A7D4-01A-12D-A33Q-10 chr10:94376540 G>A maps to NM_004523.3 L360L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MB-01A-11D-A20W-10 chr6:17834224 T>C maps to NM_022113.4 E411E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A7M5-01A-11D-A33Q-10 chr6:17794910 T>A maps to NM_022113.4 I989I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A495-01A-11D-A25V-10 chr8:28950345 C>G maps to NM_015254.3 V1458V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CK-01A-11D-A20W-10 chr8:28974374 T>C maps to NM_015254.3 R1270R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CK-01A-11D-A20W-10 chr8:28974383 T>C maps to NM_015254.3 L1267L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25T-01A-11D-A16V-10 chr1:200544759 G>T maps to NM_014875.2 P1175P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73B-01A-12D-A32G-10 chr20:16387060 A>G maps to NM_024704.4 F551F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr20:16492141 T>C maps to NM_024704.4 R159R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25T-01A-11D-A16V-10 chr20:16360075 T>C maps to NM_024704.4 E857E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr20:16485048 T>A maps to NM_024704.4 R382*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr1:21013988 T>C maps to NM_020816.2 L610L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NF-01A-11D-A27I-10 chr11:28116255 G>A maps to NM_031217.3 H139H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A6M4-01A-11D-A32G-10 chr17:43010039 C>A did not map to a codon.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr1:10363424 A>T maps to NM_183416.3 K728*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A7PY-01A-11D-A33Q-10 chr10:91498041 G>A maps to ENST00000416354 A1178A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A6M4-01A-11D-A32G-10 chr10:91520383 T>C maps to ENST00000416354 N1624N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr10:91469184 A>G maps to ENST00000416354 S106S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A114-01A-11D-A12Z-10 chr12:39726714 C>G maps to ENST00000395670 T894T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr12:39727051 T>A maps to ENST00000395670 R817*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NH-01A-11D-A27I-10 chr1:200959772 C>A maps to NM_017596.2 R922R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25V-01A-11D-A16V-10 chr1:200959271 C>T maps to NM_017596.2 E1008E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A7M9-01A-23D-A34Z-10 chr1:200945971 G>A maps to NM_017596.2 L1446L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3M9-01A-11D-A20W-10 chr16:29811025 C>T maps to NM_007317.1 V356V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5263-01A-01D-A12Z-10 chr1:245847618 G>A maps to NM_018012.3 A781A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IK-01A-12D-A33Q-10 chr1:245850811 C>A maps to NM_018012.3 V1509V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A66X-01A-11D-A30V-10 chr1:245530500 G>A maps to NM_018012.3 A277A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75G-01A-11D-A32G-10 chr1:245849629 T>C maps to NM_018012.3 S1115S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr1:245850541 A>T maps to NM_018012.3 T1419T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr9:86495241 T>A maps to NM_017576.1 A871A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A3KF-01A-11D-A20W-10 chr5:61669512 G>A did not map to a codon.
Sequencing variant TCGA-FV-A2QR-01A-11D-A20W-10 chr5:61659120 A>G maps to NM_001098511.1 K412K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr17:51901221 C>T maps to NM_032559.4 N276N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A3-01A-11D-A22F-10 chr17:51901389 G>T maps to NM_032559.4 V332V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr23:69572475 A>G did not map to a codon.
Sequencing variant TCGA-MI-A75I-01A-11D-A32G-10 chr23:69595073 A>G did not map to a codon.
Sequencing variant TCGA-CC-A7IL-01A-11D-A33Q-10 chr12:57971811 C>A maps to NM_004984.2 L794L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A7SF-01A-11D-A34Z-10 chr12:57957421 T>C maps to NM_004984.2 N79N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr6:39387772 A>T maps to NM_145027.4 S587S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LG-A6GG-01A-11D-A30V-10 chr6:39311592 T>A did not map to a codon.
Sequencing variant TCGA-DD-A3A4-01A-11D-A22F-10 chr6:33372735 A>G maps to NM_002263.3 E288E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25W-01A-11D-A16V-10 chr6:33371611 T>C maps to NM_002263.3 R154R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A5W4-01A-11D-A28X-10 chr19:55378065 G>A maps to ENST00000355608 Q416Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BD-A3EP-01A-11D-A22F-10 chr1:158061245 C>T maps to ENST00000368173 T473T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1ED-01A-11D-A152-10 chr19:36350513 T>C maps to NM_199180.2 A218A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5264-01A-01D-A12Z-10 chr1:204159886 C>A maps to ENST00000306118 E48*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5264-01A-01D-A12Z-10 chr4:55599300 T>A maps to NM_000222.2 C809*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr4:55564701 C>A maps to NM_000222.2 S197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73D-01A-12D-A32G-10 chr4:55604593 G>T did not map to a codon.
Sequencing variant TCGA-ED-A459-01A-11D-A25V-10 chr12:88900156 T>A did not map to a codon.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr13:33635813 C>T maps to NM_004795.3 L866L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BW-A5NO-01A-11D-A27I-10 chr4:39439383 T>C maps to NM_175737.3 T458T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CK-01A-11D-A20W-10 chr4:39409342 A>T maps to NM_175737.3 G258G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A7SK-01A-11D-A34Z-10 chr4:39448205 G>T maps to NM_175737.3 L620L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A4ZQ-01A-11D-A25V-10 chr14:104153536 A>G maps to ENST00000334553 P590P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr11:66029591 A>T did not map to a codon.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr11:66031563 G>T maps to NM_022822.2 L330L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3M9-01A-11D-A20W-10 chr19:45853936 G>A maps to NM_177417.2 E437E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25W-01A-11D-A16V-10 chr6:43033407 T>C maps to NM_201523.1 P198P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A118-01A-11D-A12Z-10 chr2:10188153 C>T maps to NM_003597.4 S230S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A9-01A-11D-A25V-10 chr13:74387347 G>T maps to NM_007249.4 T249T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr13:74420057 C>A maps to NM_007249.4 S192S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MA-01A-11D-A20W-10 chr3:126071498 G>A maps to NM_014079.3 G89G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr1:44595053 C>T maps to NM_173484.3 N37N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-4073-01B-02D-A12Z-10 chr10:3824156 C>A maps to NM_001300.5 E118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10R-01A-11D-A12Z-10 chr23:56291628 G>A did not map to a codon.
Sequencing variant TCGA-G3-A5SJ-01A-11D-A27I-10 chr13:70549803 G>A maps to NM_020866.2 Q210*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr13:70535470 A>G maps to NM_020866.2 A262A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MB-01A-11D-A20W-10 chr17:40010297 G>A maps to NM_018143.1 Y607Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A6M3-01A-11D-A32G-10 chr23:117053616 C>T did not map to a codon.
Sequencing variant TCGA-G3-A7M5-01A-11D-A33Q-10 chr23:24006692 C>A did not map to a codon.
Sequencing variant TCGA-HP-A5N0-01A-11D-A28X-10 chr23:24006090 A>C did not map to a codon.
Sequencing variant TCGA-G3-A25V-01A-11D-A16V-10 chr3:47376271 T>C maps to NM_025010.4 A287A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A66Y-01A-11D-A30V-10 chr4:166238987 A>G maps to NM_001161521.1 A544A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A7M5-01A-11D-A33Q-10 chr3:183381338 A>T maps to NM_017644.3 V338V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MA-01A-11D-A20W-10 chr5:136963984 C>A did not map to a codon.
Sequencing variant TCGA-DD-A1EL-01A-11D-A152-10 chr6:53517091 G>T maps to NM_001003760.4 A403A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25Y-01A-11D-A16V-10 chr23:21675561 C>T did not map to a codon.
Sequencing variant TCGA-CC-5259-01A-31D-A20W-10 chr23:86873048 C>A did not map to a codon.
Sequencing variant TCGA-MI-A75H-01A-11D-A32G-10 chr23:86877344 G>T did not map to a codon.
Sequencing variant TCGA-CC-A7II-01A-11D-A33K-10 chr3:183210426 G>T maps to NM_130446.2 I473I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A4ZQ-01A-11D-A25V-10 chr3:183209981 C>G maps to NM_130446.2 P533P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr4:88098000 A>G maps to NM_020803.3 G372G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11A-01A-11D-A12Z-10 chr9:21334287 G>A maps to NM_018847.2 L191L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A216-01A-11D-A152-10 chr19:51535231 G>A maps to NM_019598.2 R119R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10Z-01A-11D-A12Z-10 chr19:51465086 A>T maps to NM_001012964.1 R165R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10Z-01A-11D-A12Z-10 chr19:51503357 C>T maps to NM_144505.1 Q174Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A3JL-01A-11D-A20W-10 chr19:51503825 T>A maps to NM_144505.1 A73A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1E9-01A-21D-A152-10 chr19:51507093 G>A maps to NM_012315.1 L157L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A9-01A-11D-A25V-10 chr19:51506440 T>G maps to NM_012315.1 R227R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A2QQ-01A-11D-A22F-10 chr12:10587103 C>T maps to NM_002260.3 P104P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A7SK-01A-11D-A34Z-10 chr12:10584706 A>G maps to NM_002260.3 H194H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A5UD-01A-11D-A28X-10 chr12:10561526 T>A maps to NM_013431.2 T90T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A9-01A-11D-A25V-10 chr10:135038186 G>A maps to ENST00000368572 Q1683Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr10:135013093 C>G maps to ENST00000368572 S966*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39Z-01A-11D-A20W-10 chr12:123022961 T>C maps to NM_014708.4 H109H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr13:50285128 T>C maps to NM_002267.3 S267S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr6:117047734 A>T maps to NM_002269.2 A401A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EI-01A-11D-A12Z-10 chr2:88327722 A>G maps to NM_016618.1 F120F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IG-01A-11D-A33K-10 chr22:29490381 G>C maps to NM_032045.4 G78G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MB-01A-11D-A20W-10 chr19:10671690 G>C maps to NM_023008.3 S223S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MB-01A-11D-A20W-10 chr7:91851227 T>C maps to NM_194456.1 E517E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr12:53069529 T>C did not map to a codon.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr12:53069399 A>C maps to NM_006121.3 S504S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A7SK-01A-11D-A34Z-10 chr17:39017948 G>C maps to NM_000223.3 V483V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39X-01A-11D-A20W-10 chr12:53039092 G>A maps to NM_000423.2 R544*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A5SM-01A-12D-A28X-10 chr12:53041618 A>G maps to NM_000423.2 T381T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A5SJ-01A-11D-A27I-10 chr17:39084784 C>G maps to NM_015515.3 L237L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr17:38855853 T>C maps to NM_019016.2 S401S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NI-01A-11D-A27I-10 chr12:53189358 G>A maps to ENST00000309505 G156G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr12:53189819 T>A maps to ENST00000309505 R3*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10Z-01A-11D-A12Z-10 chr17:39534379 G>T maps to NM_021013.3 C414*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A7PZ-01A-11D-A33Q-10 chr17:39637037 C>G maps to NM_002280.4 L104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HP-A5MZ-01A-21D-A27I-10 chr17:39643886 G>A maps to NM_003771.4 Q268*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NK-01A-11D-A28X-10 chr17:39116561 G>A maps to NM_213656.3 Y396Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A5SJ-01A-11D-A27I-10 chr17:39118509 G>T maps to NM_213656.3 T300T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10W-01A-11D-A12Z-10 chr12:53202116 G>T maps to NM_002272.2 I436I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A459-01A-11D-A25V-10 chr17:39135186 C>T maps to NM_182497.3 E355E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A7PZ-01A-11D-A33Q-10 chr17:39140201 G>T maps to NM_182497.3 R108R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr17:39137241 C>T maps to NM_182497.3 Q283Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A114-01A-11D-A12Z-10 chr12:52910559 C>A maps to NM_000424.3 E434*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10Z-01A-11D-A12Z-10 chr12:52841355 G>A maps to NM_005555.3 L476L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A7SF-01A-11D-A34Z-10 chr12:52845421 G>T maps to NM_005555.3 P147P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr12:53010080 A>G maps to NM_175068.2 N177N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A116-01A-11D-A12Z-10 chr12:52826870 C>A maps to ENST00000252245 E276*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25U-01A-11D-A16V-10 chr12:53169278 G>T maps to NM_015848.4 S236S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr12:53086272 C>T maps to NM_175078.2 L453L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5263-01A-01D-A12Z-10 chr12:53237936 G>A maps to NM_173352.2 I329I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K7-A6G5-01A-11D-A30V-10 chr12:53242689 G>A maps to NM_173352.2 Q9*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NO-01A-11D-A28X-10 chr12:53216819 A>G maps to NM_175834.2 L449L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr12:52682241 T>C did not map to a codon.
Sequencing variant TCGA-CC-5261-01A-01D-A12Z-10 chr12:52708546 G>A maps to NM_002282.3 S450S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HP-A5N0-01A-11D-A28X-10 chr12:52760928 C>T maps to NM_002283.3 V87V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BD-A3EP-01A-11D-A22F-10 chr12:52699515 G>T maps to NM_002284.3 E324*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1E9-01A-21D-A152-10 chr12:52699950 C>A maps to NM_002284.3 A378A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A6M6-01A-11D-A32G-10 chr17:39723991 C>A maps to NM_000226.3 G469*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr17:39728013 A>G maps to NM_000226.3 S77S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73F-01A-11D-A32G-10 chr21:31744147 T>C maps to NM_181621.3 R128R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A5SM-01A-12D-A28X-10 chr21:31852612 G>A maps to NM_181607.1 Y8Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-O8-A75V-01A-11D-A32G-10 chr21:31852476 C>A maps to NM_181607.1 G54*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EL-01A-11D-A152-10 chr17:39150289 G>T maps to NM_033185.2 C20*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A116-01A-11D-A12Z-10 chr17:39324103 A>G maps to NM_033187.1 S107S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A69H-01A-11D-A30V-10 chr17:39254309 C>T maps to NM_031960.2 V9V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr11:1605912 A>G maps to NM_001005922.1 S189S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11C-01A-11D-A12Z-10 chr11:1606218 C>A maps to NM_001005922.1 G87G. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-K7-A5RF-01A-11D-A28X-10. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-MI-A75I-01A-11D-A32G-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-DD-A3A9-01A-11D-A25V-10 chr11:1629510 G>A maps to NM_001012708.2 C35C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7II-01A-11D-A33K-10 chr11:71249151 C>T maps to ENST00000422553 C38C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A5SM-01A-12D-A28X-10 chr21:32185532 G>C maps to NM_175857.3 L2L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NS-01A-11D-A30V-10 chr12:118198838 G>A maps to ENST00000339824 R321R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A3R2-01A-11D-A22F-10 chr12:118298109 T>A maps to ENST00000339824 K103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KR-A7K7-01A-11D-A33K-10 chr12:118199276 C>T maps to ENST00000339824 T175T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A6M4-01A-11D-A32G-10 chr14:56122804 A>G maps to NM_001079521.1 L949L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5262-01A-01D-A12Z-10 chr3:134339675 G>A maps to NM_178554.4 D169D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5264-01A-01D-A12Z-10 chr3:134369795 G>A maps to NM_178554.4 L3L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CH-01A-11D-A22F-10 chr3:134366277 G>A maps to NM_178554.4 H66H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5258-01A-01D-A12Z-10 chr2:143718191 G>A did not map to a codon.
Sequencing variant TCGA-DD-A39Y-01A-11D-A20W-10 chr23:153128286 A>G did not map to a codon.
Sequencing variant TCGA-DD-A4NF-01A-11D-A27I-10 chr23:153129930 T>C did not map to a codon.
Sequencing variant TCGA-DD-A4NK-01A-11D-A28X-10 chr23:153135688 C>A did not map to a codon.
Sequencing variant TCGA-DD-A4NV-01A-11D-A30V-10 chr23:153133460 A>G did not map to a codon.
Sequencing variant TCGA-FV-A3I1-01A-11D-A22F-10 chr23:153136307 C>A did not map to a codon.
Sequencing variant TCGA-G3-A3CK-01A-11D-A20W-10 chr8:71581339 G>A maps to NM_016027.2 Q6*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A3I1-01A-11D-A22F-10 chr1:201351822 C>T maps to NM_005558.3 L477L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A69H-01A-11D-A30V-10 chr18:7002348 A>G maps to NM_005559.2 D1432D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BW-A5NQ-01A-11D-A27I-10 chr18:6958644 A>G maps to NM_005559.2 L2599L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A7PZ-01A-11D-A33Q-10 chr6:129591827 C>T maps to NM_000426.3 G794G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CJ-01A-11D-A20W-10 chr6:129636957 G>T maps to NM_000426.3 E1263*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr6:129498935 G>T maps to NM_000426.3 P464P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr6:129618939 T>A maps to NM_000426.3 P989P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr6:129636778 A>T maps to NM_000426.3 P1238P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A112-01A-11D-A12Z-10 chr18:21331051 G>T maps to ENST00000416669 R285R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EL-01A-11D-A152-10 chr6:112457354 T>C maps to NM_001105206.1 K1128K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25S-01A-11D-A16V-10 chr20:60886537 A>G maps to NM_005560.3 N3287N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75C-01A-11D-A32G-10 chr7:107580786 G>A maps to NM_002291.2 P1136P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75E-01A-11D-A32G-10 chr7:107616133 G>A maps to NM_002291.2 R397*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10W-01A-11D-A12Z-10 chr3:49169090 G>A maps to NM_002292.3 Y175Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A7S9-01A-11D-A33Q-10 chr3:49162917 C>A did not map to a codon.
Sequencing variant TCGA-CC-5264-01A-01D-A12Z-10 chr1:209789917 G>A maps to NM_000228.2 Q1094*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A112-01A-11D-A12Z-10 chr7:107763584 A>G maps to NM_007356.2 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr7:107720066 A>G maps to NM_007356.2 I622I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25T-01A-11D-A16V-10 chr7:107696360 T>C maps to NM_007356.2 R1157R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A113-01A-11D-A12Z-10 chr1:183085928 A>G maps to NM_002293.3 E485E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A1-01A-11D-A20W-10 chr1:183095397 G>T did not map to a codon.
Sequencing variant TCGA-K7-A6G5-01A-11D-A30V-10 chr1:183101588 G>A maps to NM_002293.3 T1207T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25T-01A-11D-A16V-10 chr9:133963172 C>A maps to ENST00000355048 I1494I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MD-01A-12D-A34Z-10 chr9:133914251 C>T maps to ENST00000355048 P326P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr13:113973925 C>T maps to NM_005561.3 S235S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr2:211341072 G>C maps to NM_001136575.1 S16S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A7PZ-01A-11D-A33Q-10 chr12:50869367 A>T maps to ENST00000429001 S638S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A7XP-01A-11D-A34Z-10 chr12:50869601 A>G maps to ENST00000429001 R716R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr23:64744927 T>C did not map to a codon.
Sequencing variant TCGA-G3-A25U-01A-11D-A16V-10 chr23:64744885 G>T did not map to a codon.
Sequencing variant TCGA-CC-5263-01A-01D-A12Z-10 chr16:29001266 C>A maps to NM_014387.3 S241S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A6M4-01A-11D-A32G-10 chr6:150005470 T>A maps to NM_004690.2 R252*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KR-A7K0-01A-12D-A33Q-10 chr2:30480369 A>G maps to NM_030915.3 E67E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39Z-01A-11D-A20W-10 chr20:36974924 G>A maps to NM_004139.2 G2G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A495-01A-11D-A25V-10 chr20:36983751 G>A maps to NM_004139.2 L177L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CK-01A-11D-A20W-10 chr1:225611702 T>C maps to NM_194442.1 V25V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A12J-01A-11D-A12Z-10 chr21:40800131 T>C maps to NM_152505.3 K96K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr1:152636871 T>C maps to NM_178430.2 S97S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A123-01A-11D-A12Z-10 chr9:130912581 G>A maps to ENST00000373013 P68P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25W-01A-11D-A16V-10 chr9:139641976 C>A maps to NM_198946.2 R43R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11D-01A-11D-A12Z-10 chr9:139651620 C>A did not map to a codon.
Sequencing variant TCGA-DD-A3A2-01A-11D-A20W-10 chr9:139878136 G>T maps to NM_207510.3 L33L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BW-A5NQ-01A-11D-A27I-10 chr5:169689859 C>T maps to NM_005565.3 S268S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5263-01A-01D-A12Z-10 chr5:169697819 G>A maps to NM_005565.3 D142D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LG-A6GG-01A-11D-A30V-10 chr2:136567009 C>T maps to NM_002299.2 L969L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A6UC-01A-21D-A33K-10 chr15:66850162 G>C maps to NM_207338.2 P273P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39Z-01A-11D-A20W-10 chr10:88478581 C>T maps to NM_001171610.1 D657D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73E-01A-12D-A32G-10 chr16:75147447 C>A maps to NM_153486.3 T380T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RG-A7D4-01A-12D-A33Q-10 chr22:44893692 T>A did not map to a codon.
Sequencing variant TCGA-DD-A4NF-01A-11D-A27I-10 chr4:109084857 C>T did not map to a codon.
Sequencing variant TCGA-LG-A6GG-01A-11D-A30V-10 chr1:154966208 C>A maps to NM_018655.2 T42T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NI-01A-11D-A27I-10 chr19:54967842 C>A maps to ENST00000431846 R492R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A7M9-01A-23D-A34Z-10 chr19:54966689 G>A maps to ENST00000431846 A323A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A9-01A-11D-A25V-10 chr1:66102181 A>G maps to NM_002303.5 K994K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr1:66067255 T>C maps to NM_002303.5 T392T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr3:189838133 C>T maps to NM_018192.3 G129G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr3:189691794 T>A did not map to a codon.
Sequencing variant TCGA-MI-A75G-01A-11D-A32G-10 chr17:25972915 C>T maps to NM_009587.2 S202S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MB-01A-11D-A20W-10 chr19:35622721 C>T maps to NM_139284.2 L143L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A3R2-01A-11D-A22F-10 chr11:27389535 C>A maps to NM_018490.2 E912*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A5UD-01A-11D-A28X-10 chr12:71960644 A>T maps to NM_003667.2 S341S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr12:71955572 C>T maps to NM_003667.2 S266S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A3R2-01A-11D-A22F-10 chr1:202249944 C>A maps to NM_001017403.1 T227T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A9-01A-11D-A25V-10 chr2:48915237 C>T maps to NM_000233.3 K566K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A4ZP-01A-12D-A25V-10 chr2:48925800 C>T maps to NM_000233.3 L273L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr2:48925835 T>A maps to NM_000233.3 R262*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73C-01A-12D-A33K-10 chr5:77805628 A>G maps to NM_005779.2 C136C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KR-A7K8-01A-11D-A33K-10 chr7:103969490 G>T maps to NM_199000.2 L88L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr9:126794983 T>C maps to NM_004789.3 *407Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr9:139089344 T>G maps to NM_014564.3 P345P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr1:75602349 C>T maps to NM_001001933.1 R27R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75I-01A-11D-A32G-10 chr1:75608865 A>G maps to NM_001001933.1 R151R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A3R3-01A-11D-A22F-10 chr5:38482265 C>A maps to NM_002310.5 E909*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39W-01A-11D-A20W-10 chr17:33310395 C>T maps to NM_013975.3 P124P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr19:54803145 T>C maps to ENST00000251375 S177S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr19:54803146 G>C maps to ENST00000251375 S177*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A217-01A-11D-A152-10 chr19:54823335 C>A maps to NM_021250.2 G69G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A116-01A-11D-A12Z-10 chr19:55148211 G>A maps to ENST00000427581 V663V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A7SK-01A-11D-A34Z-10 chr19:55143683 C>A maps to ENST00000427581 V255V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr19:54721081 A>G maps to NM_001081450.1 D593D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5262-01A-01D-A12Z-10 chr19:55175419 A>T maps to ENST00000391733 A93A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr11:27523453 T>C maps to NM_018362.3 A17A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-O8-A75V-01A-11D-A32G-10 chr19:2290104 C>G maps to NM_001101391.1 G557G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr21:15516948 T>C maps to NM_198996.2 P451P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25Y-01A-11D-A16V-10 chr21:15579151 A>G maps to NM_198996.2 V31V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10W-01A-11D-A12Z-10 chr1:145497478 G>A maps to NM_153713.1 L228L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A1HT-01A-11D-A12Z-10 chr17:73569580 C>G maps to NM_001031803.1 P915P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EJ-01A-11D-A152-10 chr18:56998711 C>A maps to NM_005570.3 T478T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A459-01A-11D-A25V-10 chr15:75115898 G>T did not map to a codon.
Sequencing variant TCGA-DD-A4NQ-01A-21D-A28X-10 chr2:97405771 C>T maps to NM_001142292.1 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A459-01A-11D-A25V-10 chr7:156556490 T>A did not map to a codon.
Sequencing variant TCGA-CC-A3MB-01A-11D-A20W-10 chr1:156108484 C>T maps to NM_170707.2 G635G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A7SK-01A-11D-A34Z-10 chr1:156100405 A>G did not map to a codon.
Sequencing variant TCGA-BC-A10U-01A-11D-A12Z-10 chr5:126145937 G>T maps to NM_005573.3 E237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A5UD-01A-11D-A28X-10 chr7:123302236 T>A maps to NM_207163.1 I199I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3M9-01A-11D-A20W-10 chr7:97822980 T>C maps to NM_014916.3 P1068P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CJ-01A-11D-A20W-10 chr7:97821053 G>A maps to NM_014916.3 W426*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr9:129455876 A>T maps to NM_001174147.1 A272A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73F-01A-11D-A32G-10 chr5:96350726 C>T maps to NM_005575.2 A768A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A3R2-01A-11D-A22F-10 chr4:54373547 C>G maps to NM_001126328.1 G237G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5258-01A-01D-A12Z-10 chr13:28143355 A>C maps to NM_153371.3 T155T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A217-01A-11D-A152-10 chr2:43903341 G>A maps to NM_001101330.1 H40H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KR-A7K8-01A-11D-A33K-10 chr12:12514203 C>T maps to NM_058169.3 S41S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5264-01A-01D-A12Z-10 chr19:5699210 G>A maps to NM_004793.2 F504F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr8:12586493 A>G maps to NM_152271.3 V642V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EC-01A-21D-A12Z-10 chr2:100906809 G>A maps to NM_198461.3 D610D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A5UC-01A-11D-A28X-10 chr23:118145796 A>G did not map to a codon.
Sequencing variant TCGA-G3-A25U-01A-11D-A16V-10 chr23:118148214 G>A did not map to a codon.
Sequencing variant TCGA-G3-A25W-01A-11D-A16V-10 chr23:118148309 C>A did not map to a codon.
Sequencing variant TCGA-BW-A5NQ-01A-11D-A27I-10 chr8:23217773 G>A maps to NM_002318.2 P120P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10W-01A-11D-A12Z-10 chr2:74763251 T>C maps to NM_032603.2 E373E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr2:74761506 A>G maps to NM_032603.2 N625N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75G-01A-11D-A32G-10 chr10:100011439 T>A maps to NM_032211.6 A657A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10U-01A-11D-A12Z-10 chr6:161006133 A>C maps to NM_005577.2 S1411S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HP-A5MZ-01A-21D-A27I-10 chr6:160966523 G>A maps to NM_005577.2 C1782C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr1:85331281 A>C maps to NM_012152.2 S174S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A116-01A-11D-A12Z-10 chr23:78011333 A>T did not map to a codon.
Sequencing variant TCGA-G3-A3CH-01A-11D-A22F-10 chr23:78010877 T>C did not map to a codon.
Sequencing variant TCGA-BC-A217-01A-11D-A152-10 chr4:62936604 T>C maps to ENST00000506720 A1574A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A7PZ-01A-11D-A33Q-10 chr4:62862047 T>C maps to ENST00000506720 F1092F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr4:62758608 A>T maps to ENST00000506720 R572R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EB-01A-11D-A12Z-10 chr18:2923819 T>C maps to NM_014646.2 K709K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4ND-01A-11D-A25V-10 chr18:2939525 T>C maps to NM_014646.2 S258S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr20:39986060 C>A maps to NM_022896.1 I671I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr20:39978720 C>G maps to NM_022896.1 S262S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A26S-01A-11D-A16V-10 chr17:56329583 C>T maps to NM_006151.2 C274C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A7SB-01A-21D-A34Z-10 chr17:56332170 G>A did not map to a codon.
Sequencing variant TCGA-FV-A3R3-01A-11D-A22F-10 chr9:104071697 C>A maps to NM_017753.2 P197P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A3I1-01A-11D-A22F-10 chr1:99771770 T>C maps to NM_014839.4 N499N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25T-01A-11D-A16V-10 chr4:151408924 A>G maps to NM_006726.3 P2181P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EB-01A-11D-A12Z-10 chr3:197592313 T>C maps to ENST00000425562 A579A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A5UE-01A-11D-A28X-10 chr7:100174772 A>G maps to NM_002319.3 L434L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MR-A520-01A-11D-A25V-10 chr19:39804839 C>T maps to NM_020862.1 A379A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1E9-01A-21D-A152-10 chr6:40400288 G>A maps to NM_020737.1 I188I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KR-A7K0-01A-12D-A33Q-10 chr6:40360308 G>A maps to NM_020737.1 G581G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr14:42356397 C>A maps to NM_152447.3 T190T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IJ-01A-11D-A33Q-10 chr14:42356466 C>T maps to NM_152447.3 D213D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75I-01A-11D-A32G-10 chr14:42356422 C>A maps to NM_152447.3 R199R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EL-01A-11D-A152-10 chr19:4538449 C>A maps to NM_052972.2 G182G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A459-01A-11D-A25V-10 chr7:133881818 A>T maps to NM_144648.1 R503*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr7:133876487 T>C maps to NM_144648.1 D472D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KC-01A-11D-A20W-10 chr7:133812143 C>T maps to NM_144648.1 L8L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NO-01A-11D-A28X-10 chr3:66465345 T>C maps to NM_015541.2 Q215Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EL-01A-11D-A152-10 chr1:113658967 G>T maps to NM_014813.1 E864*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr4:110791335 A>G maps to NM_198506.2 Q432Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25W-01A-11D-A16V-10 chr12:25232337 T>A maps to ENST00000354454 Y82*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IL-01A-11D-A33Q-10 chr8:105511590 C>A maps to NM_013437.4 S143S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A1-01A-11D-A20W-10 chr8:105503083 G>A maps to NM_013437.4 A799A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MA-01A-11D-A20W-10 chr2:141092034 T>C maps to NM_018557.2 L4070L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IK-01A-12D-A33Q-10 chr2:141459797 C>A maps to NM_018557.2 G2072*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr2:141777525 A>G maps to NM_018557.2 S645S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A5SJ-01A-11D-A27I-10 chr2:141122262 C>A maps to NM_018557.2 G3700*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NA-01A-11D-A25V-10 chr2:170029678 G>A maps to NM_004525.2 Y3690Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NI-A4U2-01A-11D-A28X-10 chr2:170055350 C>T maps to NM_004525.2 L2841L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr2:170097672 A>G maps to NM_004525.2 C1290C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QA-A7B7-01A-11D-A32G-10 chr19:33696162 C>T maps to NM_002333.3 Q163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73C-01A-12D-A33K-10 chr11:46880820 C>A maps to ENST00000256991 E1856*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr11:46896442 G>T maps to ENST00000256991 V1424V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5258-01A-01D-A12Z-10 chr12:12291265 T>C maps to NM_002336.2 Q1200Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A496-01A-11D-A25V-10 chr1:53727879 C>T did not map to a codon.
Sequencing variant TCGA-CC-5264-01A-01D-A12Z-10 chr2:44201377 G>A maps to NM_133259.3 Q356*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IJ-01A-11D-A33Q-10 chr2:44176799 T>G did not map to a codon.
Sequencing variant TCGA-G3-A7M8-01A-11D-A33Q-10 chr2:44209518 A>G maps to NM_133259.3 I68I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A6M6-01A-11D-A32G-10 chr2:44162018 T>A did not map to a codon.
Sequencing variant TCGA-G3-A3CH-01A-11D-A22F-10 chr5:192438 C>T maps to NM_001080478.1 D262D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A4XI-01A-11D-A25V-10 chr3:194081706 G>A maps to NM_001135057.2 Y28Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25Z-01A-11D-A16V-10 chr6:25492250 C>A maps to NM_017640.5 R407R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IG-01A-11D-A33K-10 chr10:50121828 G>A maps to NM_001006939.3 R124R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BD-A2L6-01A-11D-A20W-10 chr9:26995538 C>A maps to NM_022901.2 E365*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73G-01A-22D-A32G-10 chr15:99828119 C>T maps to NM_144598.2 R117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75H-01A-11D-A32G-10 chr3:169565965 A>T maps to NM_024727.2 S423S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A118-01A-11D-A12Z-10 chr11:76371940 G>T maps to NM_001128922.1 A232A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr16:67375857 A>C did not map to a codon.
Sequencing variant TCGA-K7-A6G5-01A-11D-A30V-10 chr17:30351739 G>T maps to ENST00000327564 G591*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75I-01A-11D-A32G-10 chr17:30348371 G>T maps to ENST00000327564 P96P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr1:70616863 T>G maps to NM_017768.4 P488P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7ME-01A-11D-A33K-10 chr1:46746116 G>A maps to ENST00000254454 A602A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EF-01A-11D-A12Z-10 chr12:122676080 C>A maps to NM_001098519.1 G352G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A7M8-01A-11D-A33Q-10 chr15:71329547 C>T maps to NM_017691.3 S578S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr19:51022207 G>A maps to NM_001080457.1 S254S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A114-01A-11D-A12Z-10 chr11:40137652 G>T maps to NM_020929.1 R64R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11C-01A-11D-A12Z-10 chr11:40137650 C>T maps to NM_020929.1 R64R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A2QQ-01A-11D-A22F-10 chr1:165533061 T>A did not map to a codon.
Sequencing variant TCGA-HP-A5MZ-01A-21D-A27I-10 chr3:120067724 G>T maps to NM_001099678.1 L122L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25Y-01A-11D-A16V-10 chr8:133673829 A>G maps to ENST00000250173 C18C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MD-01A-12D-A34Z-10 chr8:133634903 C>T maps to ENST00000250173 R289R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr1:70460298 A>G maps to NM_020794.2 L291L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25W-01A-11D-A16V-10 chr1:70501868 C>T maps to NM_020794.2 T649T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K7-A6G5-01A-11D-A30V-10 chr19:7960520 G>A maps to NM_025061.3 T11T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1ED-01A-11D-A152-10 chr8:86022369 C>T maps to NM_033402.4 L111L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75I-01A-11D-A32G-10 chr8:86048193 A>G maps to NM_033402.4 Q775Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10Z-01A-11D-A12Z-10 chr12:85546124 C>A maps to NM_001079910.1 S1466*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75H-01A-11D-A32G-10 chr12:85450883 G>A maps to NM_001079910.1 V771V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NI-A4U2-01A-11D-A28X-10 chr12:85518184 A>T maps to NM_001079910.1 R1299*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NI-A4U2-01A-11D-A28X-10 chr12:85554389 G>C did not map to a codon.
Sequencing variant TCGA-ED-A5KG-01A-11D-A27I-10 chr1:74507288 A>T maps to NM_001105659.1 V442V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr15:101595196 C>A maps to NM_024652.3 A1367A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A9-01A-11D-A25V-10 chr15:101592135 T>A maps to NM_024652.3 P1220P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KR-A7K8-01A-11D-A33K-10 chr15:101569224 G>A maps to NM_024652.3 R917R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr12:40760829 G>A maps to NM_198578.3 L2471L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A7-01A-11D-A22F-10 chr12:40687369 A>T maps to NM_198578.3 K905*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4ND-01A-11D-A25V-10 chr12:40707955 T>G maps to NM_198578.3 V1573V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr3:3887041 T>C maps to NM_020873.5 D239D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11C-01A-11D-A12Z-10 chr7:110763772 A>G maps to NM_018334.4 E315E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A0-01A-11D-A20W-10 chr7:110764582 A>G maps to NM_018334.4 P585P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A459-01A-11D-A25V-10 chr7:110763112 T>A maps to NM_018334.4 T95T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr7:110764147 T>C maps to NM_018334.4 V440V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr2:80529618 C>A maps to NM_178839.4 V442V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-4073-01B-02D-A12Z-10 chr2:77745673 A>G maps to NM_001134745.1 L441L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75E-01A-11D-A32G-10 chr3:194371615 T>C maps to NM_018385.2 V471V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A496-01A-11D-A25V-10 chr19:34687543 A>G maps to NM_001114093.1 S97S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr19:35758315 G>A maps to NM_205834.2 R531R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NI-01A-11D-A27I-10 chr2:33246000 T>C maps to ENST00000354476 N197N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EG-01A-11D-A20W-10 chr14:75018977 C>T maps to NM_000428.2 E437E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A2QQ-01A-11D-A22F-10 chr14:74989511 G>T maps to NM_000428.2 P880P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr14:75078476 C>T maps to NM_000428.2 G57G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr19:41133126 C>T maps to ENST00000308370 D1477D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NF-01A-11D-A27I-10 chr19:41133673 C>T maps to ENST00000308370 T1543T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39Z-01A-11D-A20W-10 chr15:41799393 G>C maps to NM_002344.5 A480A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BD-A3EP-01A-11D-A22F-10 chr6:144184606 A>G maps to NM_032860.3 R457R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25S-01A-11D-A16V-10 chr23:114541214 A>G did not map to a codon.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr1:160784285 T>G maps to ENST00000263285 L269L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73E-01A-12D-A32G-10 chr2:99861784 A>G maps to NM_175735.3 H107H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr2:99870711 G>T maps to NM_175735.3 S4S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A6M4-01A-11D-A32G-10 chr19:13211832 G>A maps to NM_005583.4 S51S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3M9-01A-11D-A20W-10 chr19:43969675 T>A maps to NM_014400.2 A16A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K7-A5RF-01A-11D-A28X-10 chr19:43968546 G>A maps to NM_014400.2 N47N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EF-01A-11D-A12Z-10 chr1:235904820 C>T maps to NM_000081.2 S2753S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NQ-01A-21D-A28X-10 chr1:235973622 G>T maps to NM_000081.2 T165T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73B-01A-12D-A32G-10 chr1:235915326 A>G maps to NM_000081.2 N2535N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A5SJ-01A-11D-A27I-10 chr1:235964398 T>A did not map to a codon.
Sequencing variant TCGA-DD-A3A7-01A-11D-A22F-10 chr10:29581508 C>T maps to NM_032517.4 D113D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25U-01A-11D-A16V-10 chr1:9992005 A>G maps to NM_032368.3 L153L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A5UD-01A-11D-A28X-10 chr8:20112614 G>A maps to NM_021020.2 R26R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr8:20110757 C>T maps to NM_021020.2 K228K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EL-01A-11D-A152-10 chr1:39788628 T>C maps to ENST00000361689 T1400T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NK-01A-11D-A28X-10 chr1:39920642 T>A maps to ENST00000361689 A4924A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A6M4-01A-11D-A32G-10 chr1:39929342 A>C maps to ENST00000361689 G5187G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr20:15967783 A>G maps to ENST00000310348 E378E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25Y-01A-11D-A16V-10 chr7:2041756 C>T did not map to a codon.
Sequencing variant TCGA-LG-A6GG-01A-11D-A30V-10 chr7:2252878 C>T maps to NM_003550.2 E318E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25S-01A-11D-A16V-10 chr11:47308083 A>G maps to NM_003682.3 K884K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EB-01A-11D-A12Z-10 chr1:166974344 G>A maps to NM_032858.1 L227L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A496-01A-11D-A25V-10 chr19:35800858 G>C maps to NM_002361.3 P438P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73G-01A-22D-A32G-10 chr23:148798395 T>A did not map to a codon.
Sequencing variant TCGA-MI-A75G-01A-11D-A32G-10 chr23:148798281 C>T did not map to a codon.
Sequencing variant TCGA-BW-A5NO-01A-11D-A27I-10 chr23:151900289 G>T did not map to a codon.
Sequencing variant TCGA-ED-A4XI-01A-11D-A25V-10 chr23:151093076 A>T did not map to a codon.
Sequencing variant TCGA-G3-A6UC-01A-21D-A33K-10 chr23:151870007 G>T did not map to a codon.
Sequencing variant TCGA-RC-A6M4-01A-11D-A32G-10 chr23:149013279 T>A did not map to a codon.
Sequencing variant TCGA-CC-A3MA-01A-11D-A20W-10 chr23:27839846 A>G did not map to a codon.
Sequencing variant TCGA-DD-A39Y-01A-11D-A20W-10 chr23:35820407 A>G did not map to a codon.
Sequencing variant TCGA-CC-5259-01A-31D-A20W-10 chr23:26157855 A>T did not map to a codon.
Sequencing variant TCGA-DD-A1EL-01A-11D-A152-10 chr23:26157601 T>A did not map to a codon.
Sequencing variant TCGA-G3-A25S-01A-11D-A16V-10 chr23:30254252 C>A did not map to a codon.
Sequencing variant TCGA-MI-A75I-01A-11D-A32G-10 chr23:30260450 C>A did not map to a codon.
Sequencing variant TCGA-DD-A3A9-01A-11D-A25V-10 chr23:26212301 C>A did not map to a codon.
Sequencing variant TCGA-CC-A7IK-01A-12D-A33Q-10 chr23:140996542 T>C did not map to a codon.
Sequencing variant TCGA-DD-A11D-01A-11D-A12Z-10 chr23:140993821 T>C did not map to a codon.
Sequencing variant TCGA-DD-A1EI-01A-11D-A12Z-10 chr23:140993325 G>C did not map to a codon.
Sequencing variant TCGA-ED-A7PZ-01A-11D-A33Q-10 chr23:140994575 C>A did not map to a codon.
Sequencing variant TCGA-CC-A3M9-01A-11D-A20W-10 chr23:141291369 G>A did not map to a codon.
Sequencing variant TCGA-LG-A6GG-01A-11D-A30V-10 chr23:141291160 A>T did not map to a codon.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr23:141291575 A>T did not map to a codon.
Sequencing variant TCGA-CC-5259-01A-31D-A20W-10 chr23:140983103 T>C did not map to a codon.
Sequencing variant TCGA-CC-A1HT-01A-11D-A12Z-10 chr23:140985120 A>G did not map to a codon.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr23:140969386 C>T did not map to a codon.
Sequencing variant TCGA-RC-A7SB-01A-21D-A34Z-10 chr23:140953291 C>T did not map to a codon.
Sequencing variant TCGA-G3-A5SM-01A-12D-A28X-10 chr23:51638376 T>C did not map to a codon.
Sequencing variant TCGA-G3-A7M6-01A-11D-A33Q-10 chr23:51639741 G>A did not map to a codon.
Sequencing variant TCGA-DD-A4NN-01A-11D-A28X-10 chr23:75649899 G>A did not map to a codon.
Sequencing variant TCGA-GJ-A6C0-01A-12D-A30V-10 chr23:75648382 G>A did not map to a codon.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr23:75004448 A>G did not map to a codon.
Sequencing variant TCGA-DD-A114-01A-11D-A12Z-10 chr23:75004286 C>T did not map to a codon.
Sequencing variant TCGA-FV-A496-01A-11D-A25V-10 chr23:75003420 C>T did not map to a codon.
Sequencing variant TCGA-G3-A5SL-01A-11D-A27I-10 chr23:75003637 G>A did not map to a codon.
Sequencing variant TCGA-MI-A75G-01A-11D-A32G-10 chr15:23890417 G>A maps to NM_019066.4 P824P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EL-01A-11D-A152-10 chr1:114137183 T>C did not map to a codon.
Sequencing variant TCGA-DD-A11D-01A-11D-A12Z-10 chr12:10766086 G>A maps to NM_018048.3 H15H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5259-01A-31D-A20W-10 chr6:10818122 C>A maps to NM_005906.3 E80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73E-01A-12D-A32G-10 chr6:10784805 C>A did not map to a codon.
Sequencing variant TCGA-DD-A39W-01A-11D-A20W-10 chr2:95713852 G>A maps to NM_002371.2 E81E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A217-01A-11D-A152-10 chr18:56401613 G>A did not map to a codon.
Sequencing variant TCGA-CC-A7IG-01A-11D-A33K-10 chr9:72723139 T>C maps to NM_153267.4 Y54Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr4:140651773 G>T maps to ENST00000509479 S709S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A0-01A-11D-A20W-10 chr4:140811104 C>T maps to ENST00000509479 Q495Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A9-01A-11D-A25V-10 chr23:149638230 T>C did not map to a codon.
Sequencing variant TCGA-DD-A4NK-01A-11D-A28X-10 chr23:149671632 G>C did not map to a codon.
Sequencing variant TCGA-QA-A7B7-01A-11D-A32G-10 chr1:118065533 A>G maps to NM_006699.3 L627L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10Y-01A-11D-A12Z-10 chr9:140001760 C>T maps to NM_016219.3 P542P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A3KG-01A-11D-A20W-10 chr5:109091086 A>G maps to NM_002372.2 E255E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-4073-01B-02D-A12Z-10 chr19:12776598 C>G maps to NM_000528.3 P60P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K7-A6G5-01A-11D-A30V-10 chr19:12757460 T>C maps to NM_000528.3 S1003S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A4ZQ-01A-11D-A25V-10 chr4:103590161 A>G maps to NM_005908.3 D425D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KR-A7K0-01A-12D-A33Q-10 chr12:12483616 C>A maps to NM_018050.2 E214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A7PZ-01A-11D-A33Q-10 chr23:43603115 A>T did not map to a codon.
Sequencing variant TCGA-G3-A25S-01A-11D-A16V-10 chr23:43571196 A>G did not map to a codon.
Sequencing variant TCGA-DD-A1EB-01A-11D-A12Z-10 chr23:43652776 G>T did not map to a codon.
Sequencing variant TCGA-FV-A3I1-01A-11D-A22F-10 chr23:43655029 T>A did not map to a codon.
Sequencing variant TCGA-ED-A459-01A-11D-A25V-10 chr15:43819172 T>A maps to ENST00000382031 T2072T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25U-01A-11D-A16V-10 chr15:43816464 T>C maps to ENST00000382031 L1170L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A5UD-01A-11D-A28X-10 chr5:71494848 T>C maps to NM_005909.3 Y1889Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11D-01A-11D-A12Z-10 chr5:71491563 T>A maps to NM_005909.3 A794A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73A-01A-12D-A32G-10 chr5:71493189 C>T maps to NM_005909.3 Y1336Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr19:17837555 C>T maps to NM_018174.4 R455*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr2:210557751 T>A maps to NM_002374.3 P286P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A3-01A-11D-A22F-10 chr2:210517998 C>A maps to NM_002374.3 G35G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KR-A7K0-01A-12D-A33Q-10 chr2:210594613 C>T maps to NM_002374.3 F1732F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10Q-01A-11D-A12Z-10 chr15:66777395 A>C maps to NM_002755.3 V254V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A7M9-01A-23D-A34Z-10 chr15:66729187 G>A maps to NM_002755.3 A132A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A115-01A-11D-A12Z-10 chr17:67521064 C>T maps to NM_002758.3 L229L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11D-01A-11D-A12Z-10 chr19:40704414 G>A maps to NM_002446.3 P272P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NB-01A-12D-A25V-10 chr19:40698303 G>A maps to NM_002446.3 V122V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr12:53878894 G>A maps to NM_001193511.1 L362L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73A-01A-12D-A32G-10 chr12:53875040 T>A maps to NM_001193511.1 S868S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10Y-01A-11D-A12Z-10 chr23:19410151 G>A did not map to a codon.
Sequencing variant TCGA-CC-A1HT-01A-11D-A12Z-10 chr23:19418727 T>C did not map to a codon.
Sequencing variant TCGA-CC-5261-01A-01D-A12Z-10 chr2:128075797 C>A maps to NM_006609.3 E381*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IG-01A-11D-A33K-10 chr17:61768463 G>A maps to NM_203351.1 E436E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7II-01A-11D-A33K-10 chr6:161507444 G>T maps to NM_005922.2 E803*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A3I1-01A-11D-A22F-10 chr6:161470523 T>G maps to NM_005922.2 L407*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr6:161523728 A>T did not map to a codon.
Sequencing variant TCGA-DD-A11A-01A-11D-A12Z-10 chr6:136913603 A>G maps to NM_005923.3 D1009D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39Z-01A-11D-A20W-10 chr6:136932526 T>C did not map to a codon.
Sequencing variant TCGA-DD-A3A0-01A-11D-A20W-10 chr6:136935402 T>C maps to NM_005923.3 E724E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr6:136882715 G>T maps to NM_005923.3 T1314T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A5UD-01A-11D-A28X-10 chr1:27684709 C>T maps to NM_004672.3 P959P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A5SL-01A-11D-A27I-10 chr10:30747089 C>A maps to NM_005204.2 L317L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39V-01A-11D-A20W-10 chr2:39535116 T>C maps to NM_003618.2 S362S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IF-01A-11D-A33K-10 chr6:136704839 T>A maps to NM_001198609.1 S224S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11C-01A-11D-A12Z-10 chr6:136682316 T>C maps to NM_001198609.1 R539R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EF-01A-11D-A12Z-10 chr6:136742908 C>T maps to NM_001198609.1 K54K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10W-01A-11D-A12Z-10 chr23:20074813 T>C did not map to a codon.
Sequencing variant TCGA-CC-A3M9-01A-11D-A20W-10 chr23:135314088 C>G did not map to a codon.
Sequencing variant TCGA-DD-A4ND-01A-11D-A25V-10 chr23:135309505 T>C did not map to a codon.
Sequencing variant TCGA-FV-A3R2-01A-11D-A22F-10 chr23:135318410 T>C did not map to a codon.
Sequencing variant TCGA-G3-A25T-01A-11D-A16V-10 chr6:36100411 G>A maps to NM_002754.3 L88L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10T-01A-11D-A12Z-10 chr15:52357195 A>G maps to NM_002748.3 *722*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NS-01A-11D-A30V-10 chr15:52342239 T>G maps to NM_002748.3 L202L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T1-A6J8-01A-11D-A32G-10 chr15:52357166 A>T maps to NM_002748.3 T712T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IF-01A-11D-A33K-10 chr17:19285376 G>T maps to NM_139034.2 P587P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73D-01A-12D-A32G-10 chr3:50677795 G>A did not map to a codon.
Sequencing variant TCGA-CC-A7II-01A-11D-A33K-10 chr2:27248562 C>T maps to NM_012326.2 G194G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr17:44049222 A>G did not map to a codon.
Sequencing variant TCGA-DD-A73C-01A-12D-A33K-10 chr2:217124226 C>T maps to NM_020814.2 S347S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NI-01A-11D-A27I-10 chr5:10403535 T>A maps to NM_005885.2 T405T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A4XI-01A-11D-A25V-10 chr1:220826559 G>A maps to NM_018650.3 Q618Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A7SK-01A-11D-A34Z-10 chr12:57910050 A>C maps to NM_004990.2 A829A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IK-01A-12D-A33Q-10 chr5:68715679 G>A maps to NM_001038603.2 R156R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39Z-01A-11D-A20W-10 chr3:186938874 G>A maps to NM_001879.5 A619A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11B-01A-11D-A16Z-10 chr19:12975698 G>T maps to NM_014975.2 T481T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NF-01A-11D-A27I-10 chr19:12969449 G>A maps to NM_014975.2 V421V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10Z-01A-11D-A12Z-10 chr1:46500282 A>G maps to NM_015112.2 T1314T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A114-01A-11D-A12Z-10 chr1:46485311 G>A maps to NM_015112.2 Q411Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25V-01A-11D-A16V-10 chr1:46472010 A>G maps to NM_015112.2 V282V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75I-01A-11D-A32G-10 chr2:85770058 T>C maps to NM_005911.4 S329S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A6M6-01A-11D-A32G-10 chr19:3783883 G>A maps to NM_002378.3 R171R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A3I1-01A-11D-A22F-10 chr8:99045369 T>C maps to ENST00000254898 S894S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25T-01A-11D-A16V-10 chr8:98973648 T>C maps to ENST00000254898 C283C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KR-A7K7-01A-11D-A33K-10 chr20:3845078 G>T maps to NM_020746.3 E268*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-4073-01B-02D-A12Z-10 chr18:47800055 C>A maps to ENST00000424334 E493*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A0-01A-11D-A20W-10 chr18:47801525 T>C maps to ENST00000424334 P345P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A5UC-01A-11D-A28X-10 chr2:149226009 T>C maps to ENST00000404807 N166N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75H-01A-11D-A32G-10 chr2:149227545 T>C maps to ENST00000404807 S678S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr10:54528160 A>C maps to NM_000242.2 S161S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MA-01A-11D-A33Q-10 chr16:84118637 C>T maps to NM_003791.2 G412G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A7PZ-01A-11D-A33Q-10 chr23:21887621 C>T did not map to a codon.
Sequencing variant TCGA-LG-A6GG-01A-11D-A30V-10 chr18:58039129 G>A maps to NM_005912.2 I151I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr18:13826627 C>T maps to NM_005913.2 S288S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EB-01A-11D-A12Z-10 chr3:182756876 G>C maps to NM_020166.3 V438V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A9-01A-11D-A25V-10 chr3:182788805 T>A maps to NM_020166.3 K248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-4073-01B-02D-A12Z-10 chr5:70936897 T>A maps to NM_022132.4 V356V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr23:138701842 A>T did not map to a codon.
Sequencing variant TCGA-FV-A2QQ-01A-11D-A22F-10 chr23:138670588 A>G did not map to a codon.
Sequencing variant TCGA-HP-A5N0-01A-11D-A28X-10 chr23:138728987 C>A did not map to a codon.
Sequencing variant TCGA-ED-A459-01A-11D-A25V-10 chr13:113730401 G>A maps to NM_001112732.1 A534A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RG-A7D4-01A-12D-A33Q-10 chr22:41075733 G>T maps to NM_005297.3 S95S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73C-01A-12D-A33K-10 chr10:13234348 C>G maps to NM_182751.2 A538A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr6:52129385 T>A maps to ENST00000419835 *854C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A0-01A-11D-A20W-10 chr21:47685324 T>C maps to NM_003906.3 A1048A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr6:119136766 T>C maps to ENST00000316316 P884P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75H-01A-11D-A32G-10 chr1:85403449 T>G maps to NM_153259.2 P441P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A116-01A-11D-A12Z-10 chr8:6296582 G>A maps to NM_024596.3 E182E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr5:94245050 T>C maps to NM_024717.4 E519E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CH-01A-11D-A22F-10 chr6:30673413 G>A maps to NM_014641.2 P1182P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A113-01A-11D-A12Z-10 chr7:114655973 T>C maps to NM_199072.4 I351I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NK-01A-11D-A28X-10 chr2:63832430 C>T maps to NM_005917.3 G231G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A118-01A-11D-A12Z-10 chr6:90371907 T>C maps to NM_014611.1 S4821S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A459-01A-11D-A25V-10 chr6:90380709 A>G maps to NM_014611.1 S4628S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A459-01A-11D-A25V-10 chr6:90381951 C>A maps to NM_014611.1 S4587S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr6:90438700 T>C maps to NM_014611.1 L1766L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr6:90371807 C>A maps to NM_014611.1 E4855*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MD-01A-12D-A34Z-10 chr6:90452951 C>G maps to NM_014611.1 L1455L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A114-01A-11D-A12Z-10 chr3:168819858 G>A maps to NM_004991.3 R920R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A5SM-01A-12D-A28X-10 chr3:168810744 C>A did not map to a codon.
Sequencing variant TCGA-MI-A75H-01A-11D-A32G-10 chr3:168838895 C>A maps to NM_004991.3 S360S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A7M5-01A-11D-A33Q-10 chr23:153295882 T>A did not map to a codon.
Sequencing variant TCGA-DD-A3A1-01A-11D-A20W-10 chr5:6374435 C>T did not map to a codon.
Sequencing variant TCGA-EP-A26S-01A-11D-A16V-10 chr23:70349265 T>C did not map to a codon.
Sequencing variant TCGA-G3-A25Z-01A-11D-A16V-10 chr23:70338631 G>C did not map to a codon.
Sequencing variant TCGA-DD-A1EF-01A-11D-A12Z-10 chr3:150873990 C>T maps to NM_053002.4 A200A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CJ-01A-11D-A20W-10 chr3:151107816 C>A maps to NM_053002.4 I1799I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T1-A6J8-01A-11D-A32G-10 chr17:60088410 G>A maps to NM_005121.2 D489D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr12:116446846 T>C maps to NM_015335.4 S457S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5262-01A-01D-A12Z-10 chr23:40572165 C>T did not map to a codon.
Sequencing variant TCGA-ED-A7PY-01A-11D-A33Q-10 chr23:40511062 G>T did not map to a codon.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr23:40522222 G>A did not map to a codon.
Sequencing variant TCGA-RC-A6M3-01A-11D-A32G-10 chr23:40562815 T>C did not map to a codon.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr12:27181240 A>G maps to NM_004264.3 E94E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25Z-01A-11D-A16V-10 chr6:131917144 C>A maps to ENST00000403834 P985P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-4073-01B-02D-A12Z-10 chr17:38185194 T>C maps to NM_014815.3 S431S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NH-01A-11D-A27I-10 chr9:134738509 G>A maps to NM_004269.2 T247T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IK-01A-12D-A33Q-10 chr15:100214725 A>G maps to ENST00000338042 T173T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25U-01A-11D-A16V-10 chr15:100230446 G>A maps to ENST00000338042 G224G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EB-01A-11D-A12Z-10 chr5:88025143 G>T maps to NM_002397.4 S285S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IL-01A-11D-A33Q-10 chr5:126774131 A>C maps to NM_032446.2 P702P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr15:66222096 A>T maps to NM_032445.2 T511T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3M9-01A-11D-A20W-10 chr1:3425654 C>T maps to ENST00000452816 T579T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EL-01A-11D-A152-10 chr1:3428669 C>A maps to ENST00000452816 G367G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BW-A5NP-01A-11D-A27I-10 chr19:42839239 G>A maps to ENST00000251268 L204L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr19:42874932 A>G maps to ENST00000251268 K2362K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A8-01A-11D-A22F-10 chr19:42866313 C>T maps to ENST00000251268 C1931C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NG-01A-11D-A27I-10 chr19:42837806 G>T maps to ENST00000251268 E80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25T-01A-11D-A16V-10 chr19:42839305 T>C maps to ENST00000251268 S226S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr6:46801091 A>T maps to NM_005588.2 R476*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25V-01A-11D-A16V-10 chr2:112702623 C>T maps to NM_006343.2 Y190Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A123-01A-11D-A12Z-10 chr4:99955477 A>G maps to NM_015143.2 R88R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39X-01A-11D-A20W-10 chr4:99960537 T>C maps to NM_015143.2 S118S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr12:95905677 A>C maps to NM_006838.3 P324P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A3RK-01A-11D-A22F-10 chr10:126454117 T>C maps to NM_212554.2 K153K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1ED-01A-11D-A152-10 chr11:62434057 T>C maps to NM_001043229.1 T86T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr1:171759655 A>T maps to NM_015935.4 A458A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5262-01A-01D-A12Z-10 chr7:128119311 T>G maps to NM_018396.2 P101P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CK-01A-11D-A20W-10 chr12:51323794 T>C maps to NM_014033.3 F199F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NA-01A-11D-A25V-10 chr1:156051765 T>C maps to NM_001093725.1 G8G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BD-A2L6-01A-11D-A20W-10 chr18:48723393 C>A maps to NM_016626.4 G99G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NQ-01A-21D-A28X-10 chr1:17301518 C>G did not map to a codon.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr17:19289685 G>C maps to NM_001198695.1 P83P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7ME-01A-11D-A33K-10 chr12:8807069 A>T maps to NM_003480.2 A60A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A112-01A-11D-A12Z-10 chr2:228220419 C>T maps to NM_020194.4 T280T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10T-01A-11D-A12Z-10 chr15:89450542 A>C maps to NM_005928.2 S90S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NV-01A-11D-A30V-10 chr3:196744153 C>T maps to NM_005929.5 T240T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A216-01A-11D-A152-10 chr3:179103487 C>T maps to NM_033540.2 G598G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T1-A6J8-01A-11D-A32G-10 chr3:179093111 G>T maps to NM_033540.2 L360L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IF-01A-11D-A33K-10 chr3:158525237 A>C maps to NM_022736.2 G191G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A2QR-01A-11D-A20W-10 chr3:158527009 T>C maps to NM_022736.2 A210A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10T-01A-11D-A12Z-10 chr2:24240355 G>A maps to ENST00000338315 L193L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11B-01A-11D-A16Z-10 chr8:145735130 C>T maps to NM_138431.1 Q139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3M9-01A-11D-A20W-10 chr1:205568281 T>C maps to NM_181644.4 Y464Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A5UD-01A-11D-A28X-10 chr2:191301291 G>A maps to NM_017694.3 L179L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A3KF-01A-11D-A20W-10 chr15:42003111 T>C maps to ENST00000219905 S883S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BW-A5NP-01A-11D-A27I-10 chr15:42054411 G>A maps to ENST00000219905 K2581K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A5UC-01A-11D-A28X-10 chr15:42059141 C>A maps to ENST00000219905 L3003L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EB-01A-11D-A12Z-10 chr15:42059126 G>A maps to ENST00000219905 K2998K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NK-01A-11D-A28X-10 chr15:41988801 A>T maps to ENST00000219905 K532*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73F-01A-11D-A32G-10 chr15:42028492 G>A maps to ENST00000219905 W1344*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A7M6-01A-11D-A33Q-10 chr15:41961694 G>A maps to ENST00000219905 L201L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A69H-01A-11D-A30V-10 chr7:141755414 C>T maps to ENST00000475668 T1124T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A5UD-01A-11D-A28X-10 chr7:141765269 T>A did not map to a codon.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr7:141755834 C>T maps to ENST00000475668 Y1173Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A2-01A-11D-A20W-10 chr7:141726933 G>T maps to ENST00000475668 A334A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NI-01A-11D-A27I-10 chr7:141764226 T>C maps to ENST00000475668 C1463C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A5SJ-01A-11D-A27I-10 chr7:141763306 T>C maps to ENST00000475668 N1422N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A5UD-01A-11D-A28X-10 chr5:180218675 C>T maps to NM_001114617.1 A432A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KR-A7K7-01A-11D-A33K-10 chr14:50089029 G>A maps to NM_002408.3 W348*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NB-01A-12D-A25V-10 chr5:179226058 G>A maps to NM_054013.3 S419S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A6UC-01A-21D-A33K-10 chr2:135095831 G>A maps to NM_002410.3 A216A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr17:74921069 C>A maps to NM_198955.1 R361R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3M9-01A-11D-A20W-10 chr3:127413988 C>T maps to NM_007283.5 L215L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MA-01A-11D-A33Q-10 chr19:41281479 C>T maps to NM_006533.2 I11I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A9-01A-11D-A25V-10 chr1:222822188 C>T maps to NM_198551.2 Q1210*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A7PZ-01A-11D-A33Q-10 chr1:1561030 A>T maps to NM_080875.2 K439*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EG-01A-11D-A20W-10 chr6:31380099 A>C did not map to a codon.
Sequencing variant TCGA-CC-A7IK-01A-12D-A33Q-10 chr6:109766713 T>A maps to NM_022765.3 K898*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EI-01A-11D-A12Z-10 chr6:109768570 G>A maps to NM_022765.3 Q687*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A7M5-01A-11D-A33Q-10 chr11:12265544 C>T maps to NM_014632.2 L890L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10R-01A-11D-A12Z-10 chr22:18358242 G>A maps to NM_001136004.1 P825P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BD-A3EP-01A-11D-A22F-10 chr22:18299503 G>C maps to NM_015241.2 L1799L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MC-01A-11D-A22F-10 chr22:18374288 G>C maps to NM_015241.2 A552A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A9-01A-11D-A25V-10 chr22:18347689 C>T maps to NM_015241.2 V860V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr22:38321665 A>T did not map to a codon.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr22:38318311 C>A maps to NM_033386.2 P301P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr23:10437802 C>T did not map to a codon.
Sequencing variant TCGA-EP-A2KC-01A-11D-A20W-10 chr23:38664208 A>G did not map to a codon.
Sequencing variant TCGA-BC-A10T-01A-11D-A12Z-10 chr23:107169327 A>G did not map to a codon.
Sequencing variant TCGA-FV-A3R3-01A-11D-A22F-10 chr23:107084300 C>T did not map to a codon.
Sequencing variant TCGA-ED-A4XI-01A-11D-A25V-10 chr1:67436524 T>C maps to NM_001077700.2 P269P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73F-01A-11D-A32G-10 chr17:4789859 G>A maps to NM_153827.4 R296R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr7:7612423 A>G maps to NM_019005.3 K106K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3M9-01A-11D-A20W-10 chr13:24384000 A>G maps to NM_005932.3 D572D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IK-01A-12D-A33Q-10 chr13:24410480 C>T maps to NM_005932.3 R517R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A4-01A-11D-A22F-10 chr13:24330757 C>T did not map to a codon.
Sequencing variant TCGA-DD-A11B-01A-11D-A16Z-10 chr17:5392626 C>T maps to NM_024039.1 Q149*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IK-01A-12D-A33Q-10 chr3:70008477 A>G maps to ENST00000448226 R362R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A4-01A-11D-A22F-10 chr3:70014269 C>A maps to ENST00000448226 I484I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A2QR-01A-11D-A20W-10 chr3:69813024 C>T maps to NM_006722.2 F11F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5260-01A-01D-A12Z-10 chr10:129901091 T>A maps to NM_002417.4 G3004G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1E9-01A-21D-A152-10 chr10:129901193 G>A maps to NM_002417.4 P2970P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A7M5-01A-11D-A33Q-10 chr16:14304133 A>G maps to NM_014048.3 R63R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr16:14340580 A>T maps to NM_014048.3 T488T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BW-A5NQ-01A-11D-A27I-10 chr15:23812393 G>T maps to NM_005664.3 E489*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A5SM-01A-12D-A28X-10 chr15:23811327 G>A maps to NM_005664.3 S133S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr4:185646184 A>G maps to NM_024629.3 A82A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25T-01A-11D-A16V-10 chr12:6861204 A>G maps to NM_005439.2 I22I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EA-01A-11D-A12Z-10 chr3:37048517 T>C maps to NM_000249.3 P139P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr14:75516321 A>G maps to NM_001040108.1 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KR-A7K2-01A-12D-A33Q-10 chr16:74708936 A>C maps to NM_152649.2 G434G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10Q-01A-11D-A12Z-10 chr11:118373506 G>A maps to NM_001197104.1 V2300V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A5UD-01A-11D-A28X-10 chr11:118347663 C>T maps to NM_001197104.1 R1101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A5UE-01A-11D-A28X-10 chr11:118376453 C>T maps to NM_001197104.1 R3283*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25T-01A-11D-A16V-10 chr11:118343415 C>T maps to NM_001197104.1 P514P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A5SJ-01A-11D-A27I-10 chr11:118342445 C>G maps to NM_001197104.1 S191*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A114-01A-11D-A12Z-10 chr12:49443881 C>A maps to NM_003482.3 V1163V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A7-01A-11D-A22F-10 chr12:49416061 C>A did not map to a codon.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr12:49421090 T>C maps to NM_003482.3 P4886P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10T-01A-11D-A12Z-10 chr7:151833917 C>A maps to ENST00000355193 *4969L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10U-01A-11D-A12Z-10 chr7:151884487 C>A maps to ENST00000355193 E1623*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10Y-01A-11D-A12Z-10 chr7:151873591 A>C maps to ENST00000355193 V2982V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A5SM-01A-12D-A28X-10 chr7:151860410 C>T maps to ENST00000355193 Q3417Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73E-01A-12D-A32G-10 chr19:36221664 C>A maps to NM_014727.1 C1778*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A7PZ-01A-11D-A33Q-10 chr19:36214898 C>T maps to NM_014727.1 R1109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr19:36229092 G>T did not map to a codon.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr19:36222959 T>C maps to NM_014727.1 A1863A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25U-01A-11D-A16V-10 chr19:36216119 G>C did not map to a codon.
Alternatively spliced codon TCGA-G3-A3CJ-01A-11D-A20W-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr19:36221016 G>C maps to NM_014727.1 L1689L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MB-01A-11D-A20W-10 chr7:104746371 C>T maps to NM_182931.2 Q840*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr19:6222581 A>G maps to NM_005934.3 R220R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75H-01A-11D-A32G-10 chr19:6226989 T>A maps to NM_005934.3 K182*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IK-01A-12D-A33Q-10 chr6:168352221 A>T maps to ENST00000400822 P1388P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NK-01A-11D-A28X-10 chr17:36876673 G>A maps to NM_005937.3 R735R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CJ-01A-11D-A20W-10 chr17:36861959 C>T maps to NM_005937.3 C25C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25S-01A-11D-A16V-10 chr13:49796479 C>A maps to NM_001507.1 T402T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5263-01A-01D-A12Z-10 chr2:238449166 G>A maps to NM_024101.5 A427A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A5SM-01A-12D-A28X-10 chr16:2257267 G>T maps to NM_022372.4 L165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MF-01A-11D-A33K-10 chr16:2257034 G>C did not map to a codon.
Sequencing variant TCGA-T1-A6J8-01A-11D-A32G-10 chr7:73009990 C>A maps to NM_032951.2 T762T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3M9-01A-11D-A20W-10 chr4:146575234 A>G maps to NM_172250.2 Q303Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A6M6-01A-11D-A32G-10 chr1:45966040 G>T maps to NM_015506.2 E13*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A1HT-01A-11D-A12Z-10 chr3:154890001 G>T did not map to a codon.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr3:154889934 C>A maps to NM_007289.2 G670G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QA-A7B7-01A-11D-A32G-10 chr1:2524343 G>A maps to NM_033467.3 H643H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1E9-01A-21D-A152-10 chr23:135049604 T>G did not map to a codon.
Sequencing variant TCGA-DD-A1E9-01A-21D-A152-10 chr23:135049611 T>C did not map to a codon.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr23:135053249 T>A did not map to a codon.
Sequencing variant TCGA-DD-A3A9-01A-11D-A25V-10 chr11:102662134 C>T maps to NM_002421.3 K375K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr11:102642847 T>A did not map to a codon.
Sequencing variant TCGA-ED-A459-01A-11D-A25V-10 chr11:102737121 G>A maps to ENST00000326227 S323S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr11:102742327 T>G maps to ENST00000326227 S207S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr14:23310815 A>G maps to NM_004995.2 Q75Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A4XI-01A-11D-A25V-10 chr8:89180167 C>A maps to NM_005941.4 E147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75I-01A-11D-A32G-10 chr8:89053952 T>A maps to NM_005941.4 G520G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A3RK-01A-11D-A22F-10 chr16:55517933 T>A maps to NM_004530.4 I129I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A5UE-01A-11D-A28X-10 chr10:127455371 G>A maps to NM_147191.1 G523G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr20:33839776 C>A maps to NM_006690.3 R155R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73A-01A-12D-A32G-10 chr4:90856219 T>C maps to NM_007351.2 I463I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10W-01A-11D-A12Z-10 chr22:28193393 C>T maps to NM_002430.2 S1046S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IF-01A-11D-A33K-10 chr22:28196150 G>A maps to NM_002430.2 C127C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11B-01A-11D-A16Z-10 chr22:28194926 C>T maps to NM_002430.2 Q535Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73E-01A-12D-A32G-10 chr14:61275079 C>T maps to NM_002431.3 T118T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A5-01A-11D-A22F-10 chr1:158812125 T>C maps to NM_002432.1 C61C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A5SL-01A-11D-A27I-10 chr1:158813150 C>T maps to NM_002432.1 P116P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A6M6-01A-11D-A32G-10 chr1:158817561 T>C maps to NM_002432.1 N344N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A7PZ-01A-11D-A33Q-10 chr7:156802351 A>T did not map to a codon.
Sequencing variant TCGA-DD-A11A-01A-11D-A12Z-10 chr5:52405550 C>T maps to NM_176806.2 P3P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1ED-01A-11D-A152-10 chr5:52402916 C>A maps to NM_004531.3 E30*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A3KF-01A-11D-A20W-10 chr2:223559204 T>C maps to NM_058165.2 T201T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BD-A2L6-01A-11D-A20W-10 chr16:77228316 G>T maps to NM_014940.2 R187R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A4ZP-01A-12D-A25V-10 chr12:62926221 G>T maps to ENST00000393630 E469*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39Z-01A-11D-A20W-10 chr21:37747485 T>C maps to ENST00000290384 A905A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25Y-01A-11D-A16V-10 chr21:37741556 C>A maps to ENST00000290384 R632R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KR-A7K2-01A-12D-A33Q-10 chr21:37736427 C>A maps to ENST00000290384 S498*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A9-01A-11D-A25V-10 chr23:106185318 C>A did not map to a codon.
Sequencing variant TCGA-CC-5264-01A-01D-A12Z-10 chr23:102931736 C>A did not map to a codon.
Sequencing variant TCGA-DD-A11B-01A-11D-A16Z-10 chr12:122097219 G>A maps to NM_173855.4 A60A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A9-01A-11D-A25V-10 chr23:14910892 A>G did not map to a codon.
Sequencing variant TCGA-UB-A7MF-01A-11D-A33K-10 chr23:14915352 A>G did not map to a codon.
Sequencing variant TCGA-MI-A75H-01A-11D-A32G-10 chr1:113231595 T>C maps to NM_020963.3 Y59Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr22:50580529 C>T maps to NM_018995.2 D697D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HP-A5MZ-01A-21D-A27I-10 chr9:13126732 A>G maps to ENST00000319217 D1501D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr2:71376543 A>G maps to NM_005791.2 L619L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr13:20237232 C>T maps to ENST00000414242 V662V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25U-01A-11D-A16V-10 chr12:123647655 T>C maps to NM_022782.2 P826P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A6M3-01A-11D-A32G-10 chr1:43805038 T>C maps to NM_005373.2 D163D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr17:56357775 C>A maps to ENST00000340482 E67*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A1HT-01A-11D-A12Z-10 chr23:154013424 C>T did not map to a codon.
Sequencing variant TCGA-DD-A4NH-01A-11D-A27I-10 chr23:154010039 C>T did not map to a codon.
Sequencing variant TCGA-FV-A3R2-01A-11D-A22F-10 chr23:154007593 T>C did not map to a codon.
Sequencing variant TCGA-DD-A1EL-01A-11D-A152-10 chr2:202557681 C>T maps to NM_033066.2 V50V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CK-01A-11D-A20W-10 chr2:202549802 C>T maps to NM_033066.2 G186G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A3-01A-11D-A22F-10 chr7:24690138 A>G maps to ENST00000409253 V195V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NQ-01A-21D-A28X-10 chr7:24705232 C>T maps to ENST00000409253 S312S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10T-01A-11D-A12Z-10 chr10:28420524 T>C maps to NM_173496.3 V137V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NV-01A-11D-A30V-10 chr10:28378705 T>C maps to NM_173496.3 E339E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5263-01A-01D-A12Z-10 chr18:11889441 T>A maps to ENST00000344987 P146P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A6M5-01A-11D-A32G-10 chr10:18122742 C>T maps to NM_002438.2 N251N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10W-01A-11D-A12Z-10 chr17:60765747 A>T maps to NM_006039.3 T1015T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5262-01A-01D-A12Z-10 chr17:60744894 G>T did not map to a codon.
Sequencing variant TCGA-DD-A115-01A-11D-A12Z-10 chr17:60743464 C>T maps to NM_006039.3 T177T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39V-01A-11D-A20W-10 chr17:60767530 C>A maps to NM_006039.3 R1253R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73E-01A-12D-A32G-10 chr17:60767108 G>A maps to NM_006039.3 L1187L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A2QQ-01A-11D-A22F-10 chr17:60766319 G>T maps to NM_006039.3 T1111T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25T-01A-11D-A16V-10 chr17:60759722 C>A maps to NM_006039.3 I977I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr17:60744224 G>T maps to NM_006039.3 E323*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A3I0-01A-11D-A22F-10 chr4:6642726 C>T maps to NM_033296.1 H46H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BW-A5NQ-01A-11D-A27I-10 chr11:18955437 C>A maps to NM_147199.3 A298A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GJ-A6C0-01A-12D-A30V-10 chr11:18159633 G>T maps to NM_054031.3 L295L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A3R2-01A-11D-A22F-10 chr4:78806453 A>G maps to NM_020236.3 P149P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10T-01A-11D-A12Z-10 chr11:66206165 G>T maps to NM_016050.3 I20I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A26S-01A-11D-A16V-10 chr11:68664054 C>G maps to NM_181514.1 V108V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MA-01A-11D-A33Q-10 chr11:68658836 G>T maps to NM_181514.1 R194R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A7SB-01A-21D-A34Z-10 chr17:36478417 G>C maps to NM_032351.3 L287L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39Z-01A-11D-A20W-10 chr11:73536777 G>A maps to NM_016055.5 R46R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A5-01A-11D-A22F-10 chr2:74699317 G>C maps to NM_053050.3 A89A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39Z-01A-11D-A20W-10 chr6:42185569 C>A maps to NM_018141.3 A6A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A115-01A-11D-A12Z-10 chr19:39421983 G>A did not map to a codon.
Sequencing variant TCGA-DD-A1EI-01A-11D-A12Z-10 chr10:75010747 A>G maps to NM_016065.3 G92G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25W-01A-11D-A16V-10 chr3:15094001 G>T maps to NM_022497.3 P156P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A7PZ-01A-11D-A33Q-10 chr7:140710337 T>C maps to NM_053035.2 K32K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10Z-01A-11D-A12Z-10 chr11:10651166 C>A maps to NM_001098579.1 L155L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39W-01A-11D-A20W-10 chr11:10602111 G>A maps to NM_001098579.1 T786T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MB-01A-11D-A20W-10 chr11:60184402 G>A maps to NM_032597.3 W654*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73G-01A-22D-A32G-10 chr11:59837693 C>T maps to NM_006138.4 P211P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr11:60073589 G>A maps to NM_148975.1 V188V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BD-A3EP-01A-11D-A22F-10 chr11:59947378 A>G maps to NM_152852.1 A69A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A113-01A-11D-A12Z-10 chr11:59947426 G>T maps to NM_152852.1 I53I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EG-01A-11D-A20W-10 chr2:47639550 A>T did not map to a codon.
Sequencing variant TCGA-T1-A6J8-01A-11D-A32G-10 chr1:76262909 T>G maps to NM_002440.2 A80A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73A-01A-12D-A32G-10 chr23:11783625 C>A did not map to a codon.
Sequencing variant TCGA-BW-A5NO-01A-11D-A27I-10 chr10:51562360 C>T maps to NM_002443.2 D102D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A118-01A-11D-A12Z-10 chr23:64957170 C>T did not map to a codon.
Sequencing variant TCGA-DD-A39W-01A-11D-A20W-10 chr23:64955216 G>A did not map to a codon.
Sequencing variant TCGA-ED-A7PZ-01A-11D-A33Q-10 chr8:16035437 A>T maps to ENST00000445506 S38S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A23B-01A-11D-A16V-10 chr3:49722241 T>A maps to NM_020998.3 L566L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11A-01A-11D-A12Z-10 chr3:49936588 T>C maps to NM_002447.2 V446V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A7M6-01A-11D-A33Q-10 chr3:49933286 G>A maps to NM_002447.2 I941I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A7-01A-11D-A22F-10 chr5:174151961 G>A maps to NM_002449.4 E100E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A3I0-01A-11D-A22F-10 chr16:56692644 C>T maps to ENST00000394501 C30C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39Y-01A-11D-A20W-10 chr1:38288326 T>C maps to NM_005955.2 T411T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A1-01A-11D-A20W-10 chr1:38281194 G>A maps to NM_005955.2 I625I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A3KG-01A-11D-A20W-10 chr1:93545088 G>T did not map to a codon.
Sequencing variant TCGA-G3-A25W-01A-11D-A16V-10 chr10:135211953 T>C maps to NM_138384.2 L100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A6UC-01A-21D-A33K-10 chr14:64914954 A>G maps to NM_005956.3 K733K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11B-01A-11D-A16Z-10 chr23:149814212 C>T did not map to a codon.
Sequencing variant TCGA-MI-A75G-01A-11D-A32G-10 chr23:149818233 G>A did not map to a codon.
Sequencing variant TCGA-DD-A3A8-01A-11D-A22F-10 chr23:149905791 G>T did not map to a codon.
Sequencing variant TCGA-EP-A26S-01A-11D-A16V-10 chr23:149905904 A>G did not map to a codon.
Sequencing variant TCGA-NI-A4U2-01A-11D-A28X-10 chr23:149895738 G>T did not map to a codon.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr23:149867739 A>G did not map to a codon.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr1:149902440 T>C did not map to a codon.
Sequencing variant TCGA-ED-A459-01A-11D-A25V-10 chr1:149904190 T>A maps to NM_001145862.1 S339S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A113-01A-11D-A12Z-10 chr3:9703949 G>A did not map to a codon.
Sequencing variant TCGA-DD-A114-01A-11D-A12Z-10 chr17:56582858 C>A maps to NM_004687.4 V359V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CK-01A-11D-A20W-10 chr17:56584191 T>G maps to NM_004687.4 A301A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73A-01A-12D-A32G-10 chr13:25826055 A>T maps to NM_004685.3 P471P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75G-01A-11D-A32G-10 chr8:17228585 G>T maps to NM_004686.4 C90*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A3I1-01A-11D-A22F-10 chr23:63548662 G>T did not map to a codon.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr23:63490846 C>G did not map to a codon.
Sequencing variant TCGA-BC-A216-01A-11D-A152-10 chr4:187455190 C>T maps to NM_005958.3 R235R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A112-01A-11D-A12Z-10 chr1:11303172 A>G maps to NM_004958.3 H470H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KC-01A-11D-A20W-10 chr1:11316987 A>T did not map to a codon.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr8:125580778 T>C did not map to a codon.
Sequencing variant TCGA-BC-A3KG-01A-11D-A20W-10 chr4:100532579 C>T maps to ENST00000511045 Y680Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75I-01A-11D-A32G-10 chr4:100532576 G>A maps to ENST00000511045 Q679Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr8:17541869 T>C maps to NM_001001924.2 A935A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr13:30066784 T>C maps to NM_001033602.2 L1180L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A3KF-01A-11D-A20W-10 chr1:155180141 T>C maps to NM_002455.3 Y178Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10U-01A-11D-A12Z-10 chr19:9057201 C>A maps to NM_024690.2 E10082*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5259-01A-31D-A20W-10 chr19:9065779 A>T maps to NM_024690.2 T7222T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5263-01A-01D-A12Z-10 chr19:9045798 G>C maps to NM_024690.2 T11944T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3M9-01A-11D-A20W-10 chr19:9011460 A>G maps to NM_024690.2 D12924D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IK-01A-12D-A33Q-10 chr19:9065587 A>T maps to NM_024690.2 S7286S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A113-01A-11D-A12Z-10 chr19:9074277 G>A maps to NM_024690.2 Q4390*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A118-01A-11D-A12Z-10 chr19:9087245 G>T maps to NM_024690.2 I1523I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A8-01A-11D-A22F-10 chr19:9057571 G>T maps to NM_024690.2 T9958T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A4XI-01A-11D-A25V-10 chr19:9059728 G>C maps to NM_024690.2 S9239S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A4ZP-01A-12D-A25V-10 chr19:9060556 G>A maps to NM_024690.2 S8963S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25W-01A-11D-A16V-10 chr19:9048402 A>G maps to NM_024690.2 S11076S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25Z-01A-11D-A16V-10 chr19:9028260 G>A maps to NM_024690.2 G12177G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A7M5-01A-11D-A33Q-10 chr19:9062326 T>A maps to NM_024690.2 S8373S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A7M5-01A-11D-A33Q-10 chr19:9082589 A>T maps to NM_024690.2 A3075A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LG-A6GG-01A-11D-A30V-10 chr19:9074548 A>T maps to NM_024690.2 I4299I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75H-01A-11D-A32G-10 chr19:9072821 G>T maps to NM_024690.2 S4875*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-O8-A75V-01A-11D-A32G-10 chr19:9088913 C>T maps to NM_024690.2 W967*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr19:9067174 A>T maps to NM_024690.2 T6757T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr19:9069193 G>A maps to NM_024690.2 A6084A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EF-01A-11D-A12Z-10 chr7:100678399 G>T maps to NM_001040105.1 E1235*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39W-01A-11D-A20W-10 chr7:100686942 G>A maps to NM_001040105.1 T4082T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A6M6-01A-11D-A32G-10 chr7:100682889 T>C maps to NM_001040105.1 S2731S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EJ-01A-11D-A152-10 chr11:1077627 G>A maps to ENST00000441003 L126L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NI-A4U2-01A-11D-A28X-10 chr11:1095257 G>A maps to ENST00000441003 K2026K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr6:30955853 A>C maps to NM_001010909.2 P528P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr6:30955028 A>T maps to NM_001010909.2 T359T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IK-01A-12D-A33Q-10 chr3:195515684 G>T maps to NM_018406.5 I922I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A9-01A-11D-A25V-10 chr3:195507287 T>C maps to NM_018406.5 V3721V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NA-01A-11D-A25V-10 chr3:195512354 C>T maps to NM_018406.5 P2032P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr3:195517319 G>C maps to NM_018406.5 T377T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A2QQ-01A-11D-A22F-10 chr3:195513176 G>T maps to NM_018406.5 A1758A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A3R3-01A-11D-A22F-10 chr3:195513065 G>T maps to NM_018406.5 V1795V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A7M5-01A-11D-A33Q-10 chr3:195511178 T>A maps to NM_018406.5 S2424S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39Z-01A-11D-A20W-10 chr11:1256341 C>T maps to ENST00000447027 C889C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A1-01A-11D-A20W-10 chr11:1276337 G>A maps to ENST00000447027 K5247K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75G-01A-11D-A32G-10 chr11:1248992 C>A maps to ENST00000447027 A252A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr11:1261068 T>C maps to ENST00000447027 N1211N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr11:1031238 G>C maps to NM_005961.2 Y168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A12J-01A-11D-A12Z-10 chr11:1016212 A>G maps to NM_005961.2 P2196P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A113-01A-11D-A12Z-10 chr4:71346649 T>A maps to NM_152291.2 Y63*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K7-A5RG-01A-11D-A28X-10 chr4:71346646 C>T maps to NM_152291.2 S62S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10W-01A-11D-A12Z-10 chr9:113563238 G>T maps to ENST00000189978 E867*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr1:45800075 A>G maps to NM_001128425.1 P48P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr16:88724395 G>T maps to NM_002461.1 T61T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T1-A6J8-01A-11D-A32G-10 chr16:29848050 G>C maps to NM_017458.3 L227L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A5UD-01A-11D-A28X-10 chr4:2252294 C>A maps to NM_006454.2 R202R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BD-A3EP-01A-11D-A22F-10 chr23:3241430 A>T did not map to a codon.
Sequencing variant TCGA-CC-A7IK-01A-12D-A33Q-10 chr23:3240279 C>A did not map to a codon.
Sequencing variant TCGA-DD-A1EB-01A-11D-A12Z-10 chr23:3240504 T>A did not map to a codon.
Sequencing variant TCGA-FV-A3I1-01A-11D-A22F-10 chr23:3227925 G>A did not map to a codon.
Sequencing variant TCGA-G3-A5SM-01A-12D-A28X-10 chr23:3248324 T>G did not map to a codon.
Sequencing variant TCGA-HP-A5N0-01A-11D-A28X-10 chr23:3238422 G>C did not map to a codon.
Sequencing variant TCGA-K7-A6G5-01A-11D-A30V-10 chr23:3248696 G>A did not map to a codon.
Sequencing variant TCGA-RG-A7D4-01A-12D-A33Q-10 chr23:3239232 G>T did not map to a codon.
Sequencing variant TCGA-DD-A4NI-01A-11D-A27I-10 chr17:4446342 G>A maps to NM_001105538.1 T919T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73C-01A-12D-A33K-10 chr17:4442760 A>C maps to NM_001105538.1 L1312L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A6UC-01A-21D-A33K-10 chr20:42338683 C>T maps to NM_002466.2 Y529Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NV-01A-11D-A30V-10 chr19:50958839 T>C maps to NM_004533.3 P759P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MA-01A-11D-A33Q-10 chr19:50957537 G>A maps to NM_004533.3 P642P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5264-01A-01D-A12Z-10 chr13:77641990 A>G maps to NM_015057.4 S4060S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75E-01A-11D-A32G-10 chr13:77750663 C>A maps to NM_015057.4 E1814*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BD-A3EP-01A-11D-A22F-10 chr17:48603555 C>T maps to NM_032133.4 S742S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MA-01A-11D-A33Q-10 chr17:48586028 C>T maps to NM_032133.4 G41G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr6:153043210 T>A maps to NM_025107.2 P177P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A113-01A-11D-A12Z-10 chr15:48470359 C>T maps to NM_016132.3 P25P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A7SB-01A-21D-A34Z-10 chr12:81101779 G>A maps to NM_002469.2 R94R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A216-01A-11D-A152-10 chr17:10404039 T>C maps to NM_005963.3 L1256L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EF-01A-11D-A12Z-10 chr17:10404576 C>T maps to NM_005963.3 L1196L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A23B-01A-11D-A16V-10 chr17:10404675 G>T maps to NM_005963.3 A1163A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A6UC-01A-21D-A33K-10 chr17:10399269 G>C maps to NM_005963.3 T1722T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr17:10416940 A>T did not map to a codon.
Sequencing variant TCGA-CC-A5UE-01A-11D-A28X-10 chr17:8390876 C>T maps to ENST00000360416 R1640R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EG-01A-11D-A20W-10 chr17:8455400 A>G maps to ENST00000360416 F294F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25W-01A-11D-A16V-10 chr17:8381679 T>C maps to ENST00000360416 R1894R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A113-01A-11D-A12Z-10 chr16:15931794 C>T maps to NM_001040114.1 L105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A6M5-01A-11D-A32G-10 chr16:15815346 G>T maps to NM_001040114.1 R1511R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A7SK-01A-11D-A34Z-10 chr16:15931899 C>A maps to NM_001040114.1 T70T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr17:10212853 G>C maps to NM_003802.2 V1650V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A3JL-01A-11D-A20W-10 chr3:108220703 T>C did not map to a codon.
Sequencing variant TCGA-FV-A4ZQ-01A-11D-A25V-10 chr3:108204061 G>T maps to NM_014981.1 I350I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KR-A7K2-01A-12D-A33Q-10 chr3:108117573 C>T maps to NM_014981.1 R1701R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10Q-01A-11D-A12Z-10 chr17:10432776 C>A maps to NM_017534.5 E1047*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3M9-01A-11D-A20W-10 chr17:10432946 C>T maps to NM_017534.5 Q1017Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73E-01A-12D-A32G-10 chr17:10549293 C>T maps to NM_002470.2 E318E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NE-01A-11D-A27I-10 chr17:10352332 C>A maps to NM_017533.2 E1405*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr14:23865973 T>G maps to NM_002471.3 R741R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EB-01A-11D-A12Z-10 chr14:23897840 G>A maps to NM_000257.2 N482N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EL-01A-11D-A152-10 chr14:23894543 G>T maps to NM_000257.2 A790A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A7SK-01A-11D-A34Z-10 chr14:23901920 C>T maps to NM_000257.2 R143R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr14:23892878 C>A maps to NM_000257.2 L992L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NE-01A-11D-A27I-10 chr17:10304672 G>A maps to NM_002472.2 T1009T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MF-01A-11D-A33K-10 chr17:10307685 G>T maps to NM_002472.2 L883L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MB-01A-11D-A20W-10 chr22:36696311 T>C did not map to a codon.
Sequencing variant TCGA-FV-A3R3-01A-11D-A22F-10 chr22:36737553 G>A maps to NM_002473.4 F117F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A7M9-01A-23D-A34Z-10 chr22:36689428 C>T maps to NM_002473.4 E1347E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KR-A7K8-01A-11D-A33K-10 chr22:36700183 G>T maps to NM_002473.4 L749L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr22:36684452 C>A maps to NM_002473.4 E1593*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A112-01A-11D-A12Z-10 chr17:45299201 G>C maps to NM_002476.2 R156R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A23B-01A-11D-A16V-10 chr12:56553888 C>A maps to NM_079423.3 G102G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IG-01A-11D-A33K-10 chr6:16145304 T>A maps to NM_013262.3 V335V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A217-01A-11D-A152-10 chr3:123411615 G>A maps to NM_053025.3 G1177G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr20:30419869 C>A maps to NM_033118.3 A547A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A112-01A-11D-A12Z-10 chr5:16701662 G>A maps to NM_012334.2 F947F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A5UD-01A-11D-A28X-10 chr5:16704766 T>A maps to NM_012334.2 K733*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A26S-01A-11D-A16V-10 chr5:16701446 T>C maps to NM_012334.2 R1019R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25Z-01A-11D-A16V-10 chr5:16783574 A>G maps to NM_012334.2 G157G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr5:16711258 G>T maps to NM_012334.2 V675V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MC-01A-11D-A33Q-10 chr13:109707404 G>A maps to NM_015011.1 K998K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25T-01A-11D-A16V-10 chr17:27421739 G>A maps to NM_078471.3 D1546D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EB-01A-11D-A12Z-10 chr22:26423607 T>C maps to ENST00000407587 D2558D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr22:26176137 A>C maps to ENST00000407587 T730T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A23B-01A-11D-A16V-10 chr12:57441108 T>C maps to NM_005379.2 L136L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A9-01A-11D-A25V-10 chr2:192228451 A>T did not map to a codon.
Sequencing variant TCGA-G3-A25U-01A-11D-A16V-10 chr17:31075958 A>G maps to NM_015194.1 D511D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A216-01A-11D-A152-10 chr15:59450528 A>C maps to NM_004998.2 T945T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25S-01A-11D-A16V-10 chr15:59470654 G>T maps to NM_004998.2 V662V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A123-01A-11D-A12Z-10 chr7:45005390 C>T maps to NM_033054.2 W742*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4ND-01A-11D-A25V-10 chr12:109879425 C>T maps to NM_001101421.3 Q833*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A217-01A-11D-A152-10 chr10:26462897 T>C maps to NM_017433.4 A1235A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IJ-01A-11D-A33Q-10 chr10:26455034 C>G maps to NM_017433.4 R1013R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A2QQ-01A-11D-A22F-10 chr10:26436360 C>A maps to NM_017433.4 V836V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5263-01A-01D-A12Z-10 chr2:171242773 T>C maps to NM_138995.3 L456L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A114-01A-11D-A12Z-10 chr2:171260815 G>T maps to NM_138995.3 P779P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A113-01A-11D-A12Z-10 chr18:47500943 C>T maps to NM_001080467.2 G366G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39Y-01A-11D-A20W-10 chr15:52571841 A>G maps to NM_018728.3 S56S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr6:76576646 A>T did not map to a codon.
Sequencing variant TCGA-DD-A1EH-01A-11D-A12Z-10 chr11:76917165 G>A maps to NM_000260.3 P1887P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LG-A6GG-01A-11D-A30V-10 chr11:76858872 G>A maps to NM_000260.3 T54T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr11:76903161 A>T maps to NM_000260.3 K1331*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A114-01A-11D-A12Z-10 chr2:128335797 G>T maps to ENST00000389524 E314*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39Y-01A-11D-A20W-10 chr15:72193621 G>A maps to ENST00000424560 L1020L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A7-01A-11D-A22F-10 chr15:72338582 T>G maps to ENST00000424560 R108R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25U-01A-11D-A16V-10 chr19:17317096 C>T maps to NM_004145.3 A1766A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr1:171605646 G>C maps to NM_000261.1 Y311*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10R-01A-11D-A12Z-10 chr17:12666486 C>T maps to NM_001146312.1 P829P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A459-01A-11D-A25V-10 chr10:95116493 T>A maps to NM_013451.3 R1078*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A495-01A-11D-A25V-10 chr10:95161195 G>A maps to NM_013451.3 R366*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A4XI-01A-11D-A25V-10 chr18:3155036 C>T maps to NM_003803.3 K517K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr18:3187545 C>A maps to NM_003803.3 T287T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KR-A7K0-01A-12D-A33Q-10 chr18:3067313 C>T maps to NM_003803.3 E1668E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RG-A7D4-01A-12D-A33Q-10 chr18:3134721 C>A maps to NM_003803.3 G770G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NN-01A-11D-A28X-10 chr8:2054128 T>C maps to NM_003970.2 C944C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A5SI-01A-31D-A27I-10 chr8:1998978 G>A maps to NM_003970.2 A33A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr4:120079174 A>G did not map to a codon.
Sequencing variant TCGA-DD-A3A1-01A-11D-A20W-10 chr19:46393961 G>A maps to NM_001012643.2 L373L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NG-01A-11D-A27I-10 chr20:62839415 G>A maps to NM_004535.2 E289E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NG-01A-11D-A27I-10 chr20:62839433 G>A maps to NM_004535.2 E295E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr2:1983302 C>A maps to ENST00000399161 E27*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A115-01A-11D-A12Z-10 chr2:1946919 G>A maps to ENST00000399161 D113D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A8-01A-11D-A22F-10 chr2:1926592 C>T maps to ENST00000399161 E316E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73E-01A-12D-A32G-10 chr2:1915790 C>A did not map to a codon.
Sequencing variant TCGA-ED-A7PZ-01A-11D-A33Q-10 chr2:1926445 C>T maps to ENST00000399161 E365E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A3I0-01A-11D-A22F-10 chr16:48595689 A>T maps to NM_153029.3 S288S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10Z-01A-11D-A12Z-10 chr13:33017686 T>C maps to NM_033111.3 K329K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A3RK-01A-11D-A22F-10 chr13:33110777 T>C maps to ENST00000505213 K129K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EB-01A-11D-A12Z-10 chr4:140272692 A>G maps to NM_057175.3 L314L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A7SK-01A-11D-A34Z-10 chr4:140299907 A>G did not map to a codon.
Sequencing variant TCGA-CC-A3MB-01A-11D-A20W-10 chr13:41891034 T>C maps to NM_024561.4 I36I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A5SJ-01A-11D-A27I-10 chr13:41905449 T>C maps to NM_024561.4 S284S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KR-A7K0-01A-12D-A33Q-10 chr12:112481515 G>C maps to NM_024953.3 S721S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr7:117828429 A>T maps to NM_016200.4 L57L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EB-01A-11D-A12Z-10 chr3:175293975 G>T did not map to a codon.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr17:59667967 T>A maps to NM_199290.3 R192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr9:138905768 C>T maps to NM_144653.3 L366L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A459-01A-11D-A25V-10 chr1:1687957 G>A maps to ENST00000344463 F306F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MA-01A-11D-A20W-10 chr4:164058389 T>C maps to NM_138386.2 S297S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5262-01A-01D-A12Z-10 chr17:40696105 G>A maps to NM_000263.3 Q694Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73B-01A-12D-A32G-10 chr17:42083958 C>T maps to NM_153006.2 S326S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25T-01A-11D-A16V-10 chr13:101881827 G>A maps to NM_052867.2 A514A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75H-01A-11D-A32G-10 chr13:101735198 T>G maps to NM_052867.2 A1242A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75E-01A-11D-A32G-10 chr23:72433657 A>G did not map to a codon.
Sequencing variant TCGA-MI-A75H-01A-11D-A32G-10 chr23:72434297 A>G did not map to a codon.
Sequencing variant TCGA-CC-5258-01A-01D-A12Z-10 chr23:92927475 T>A did not map to a codon.
Sequencing variant TCGA-BC-A10U-01A-11D-A12Z-10 chr7:102743977 C>T maps to ENST00000455523 K433K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KC-01A-11D-A20W-10 chr7:102760529 G>A maps to ENST00000455523 L218L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10Z-01A-11D-A12Z-10 chr15:60758887 C>A maps to NM_024611.4 E145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A118-01A-11D-A12Z-10 chr1:46083193 G>A maps to NM_002482.3 P739P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5258-01A-01D-A12Z-10 chr11:34137374 G>A maps to NM_024662.2 V167V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25Z-01A-11D-A16V-10 chr19:55997776 C>T maps to NM_020378.3 A25A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EJ-01A-11D-A152-10 chr11:19955619 C>G maps to ENST00000396087 S633S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25S-01A-11D-A16V-10 chr11:20127076 A>G maps to ENST00000396087 R2274R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MF-01A-11D-A33K-10 chr11:20057522 C>A maps to ENST00000396087 S952S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IK-01A-12D-A33Q-10 chr12:78362414 C>A maps to NM_014903.4 R202R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NG-01A-11D-A27I-10 chr2:15378652 G>C maps to NM_015909.2 S1961*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A7SK-01A-11D-A34Z-10 chr2:15523422 C>T maps to NM_015909.2 E1092E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr2:15679481 T>A did not map to a codon.
Sequencing variant TCGA-BW-A5NQ-01A-11D-A27I-10 chr13:35692391 C>T maps to ENST00000400445 Q704*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A5UD-01A-11D-A28X-10 chr13:35923306 T>A maps to ENST00000400445 L1989*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr13:35729981 T>A maps to ENST00000400445 I839I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EB-01A-11D-A12Z-10 chr13:35672499 G>T maps to ENST00000400445 L546L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A66Y-01A-11D-A30V-10 chr13:35806706 C>T maps to ENST00000400445 F1909F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr13:35731382 T>C maps to ENST00000400445 D940D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MF-01A-11D-A33K-10 chr13:36202216 G>T did not map to a codon.
Sequencing variant TCGA-FV-A496-01A-11D-A25V-10 chr2:204067443 A>T maps to NM_001114132.1 G2453G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A217-01A-11D-A152-10 chr3:47030820 C>G maps to NM_015175.1 L141L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr3:47042831 G>T maps to NM_015175.1 L1516L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr8:90995075 T>C maps to NM_002485.4 P15P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A12J-01A-11D-A12Z-10 chr1:148004748 C>T maps to ENST00000310701 L860L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25W-01A-11D-A16V-10 chr17:41347051 T>G maps to NM_005899.3 P582P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BD-A3EP-01A-11D-A22F-10 chr11:113085205 T>A maps to ENST00000316851 S343S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A113-01A-11D-A12Z-10 chr21:22664427 G>A maps to NM_004540.2 R162R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr19:19359572 C>A maps to NM_004386.2 Y1234*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EH-01A-11D-A12Z-10 chr11:134029861 G>A maps to NM_015261.2 V1264V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75G-01A-11D-A32G-10 chr22:50961496 C>A maps to NM_001185011.1 R528R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr9:100410501 C>A maps to NM_002486.4 P298P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25S-01A-11D-A16V-10 chr1:36026741 A>G maps to NM_001014839.1 K330K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IL-01A-11D-A33Q-10 chr3:172351795 T>C maps to NM_001146276.1 P272P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LG-A6GG-01A-11D-A30V-10 chr2:183866686 A>G maps to NM_205842.1 H205H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A5UD-01A-11D-A28X-10 chr12:50190490 A>G maps to NM_001037806.3 G384G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A8-01A-11D-A22F-10 chr12:50186243 C>A maps to NM_001037806.3 L1259L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A459-01A-11D-A25V-10 chr3:48716128 T>A maps to NM_016453.2 P611P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A459-01A-11D-A25V-10 chr2:232326344 T>A maps to NM_005381.2 A173A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NQ-01A-21D-A28X-10 chr19:3206307 C>T maps to NM_020170.3 Q462*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A112-01A-11D-A12Z-10 chr2:24991259 A>T maps to NM_003743.4 *1442Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A7M7-01A-12D-A34Z-10 chr2:24962369 A>C maps to NM_003743.4 R1091R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IK-01A-12D-A33Q-10 chr8:71036124 G>A maps to NM_006540.2 P1429P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39Z-01A-11D-A20W-10 chr20:46275953 A>G maps to NM_181659.2 G1130G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr10:51585412 A>G maps to NM_001145260.1 K520K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10W-01A-11D-A12Z-10 chr20:33337354 C>T maps to NM_014071.2 T881T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr20:33324499 T>A maps to NM_014071.2 R1986*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10Z-01A-11D-A12Z-10 chr17:15973500 G>T maps to ENST00000395857 P1513P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A5UD-01A-11D-A28X-10 chr6:41309646 T>C maps to NM_004828.3 S170S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EB-01A-11D-A12Z-10 chr6:41309740 G>T maps to ENST00000373086 P178P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A5SJ-01A-11D-A27I-10 chr15:23931944 G>T maps to NM_002487.2 L140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A7M7-01A-12D-A34Z-10 chr14:21486185 C>T maps to NM_201537.1 L303L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A3KG-01A-11D-A20W-10 chr10:75566199 A>G maps to NM_003635.3 A427A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A1HT-01A-11D-A12Z-10 chr4:119154260 T>C maps to NM_004784.2 N638N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A23B-01A-11D-A16V-10 chr4:118975958 A>G maps to NM_004784.2 T298T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr4:119174752 T>A maps to NM_004784.2 S833S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A8-01A-11D-A22F-10 chr4:115792013 C>T maps to NM_022569.1 W543*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr4:115858494 G>A maps to NM_022569.1 G462G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A496-01A-11D-A25V-10 chr19:19626947 A>C maps to ENST00000252576 L50L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr6:97339047 T>A maps to NM_014165.3 K154*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A7XP-01A-11D-A34Z-10 chr1:39494584 C>T maps to NM_004552.2 F63F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A8-01A-11D-A22F-10 chr11:67799629 G>A maps to NM_002496.3 L4L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A4XI-01A-11D-A25V-10 chr18:9119503 A>G maps to NM_021074.4 E72E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K7-A5RF-01A-11D-A28X-10 chr21:44324090 A>G maps to NM_021075.3 Q323Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5259-01A-31D-A20W-10 chr2:152502667 T>C maps to NM_001164507.1 K2504K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11A-01A-11D-A12Z-10 chr2:152552145 G>C maps to NM_001164507.1 P540P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39Z-01A-11D-A20W-10 chr2:152534625 G>A maps to NM_001164507.1 L1111L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HP-A5N0-01A-11D-A28X-10 chr2:152528993 G>T maps to NM_001164507.1 A1396A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A7SB-01A-21D-A34Z-10 chr2:152499356 T>C maps to NM_001164507.1 K2729K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A7SB-01A-21D-A34Z-10 chr2:152525646 T>G did not map to a codon.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr2:152466568 A>G maps to NM_001164507.1 D4028D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr10:21178772 C>A did not map to a codon.
Sequencing variant TCGA-BC-A10Z-01A-11D-A12Z-10 chr8:91946572 G>C maps to NM_022351.4 G245G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MA-01A-11D-A20W-10 chr15:56207943 T>C maps to ENST00000508342 R362R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr18:56002762 A>G maps to NM_001144967.1 E373E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MF-01A-11D-A33K-10 chr18:56033298 A>G maps to NM_001144967.1 R634R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MC-01A-11D-A22F-10 chr15:75641491 C>T maps to NM_024608.2 S82S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A5UD-01A-11D-A28X-10 chr4:178256895 T>C maps to NM_018248.2 Y111Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73A-01A-12D-A32G-10 chr1:211840445 A>T maps to ENST00000366998 G371G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A0-01A-11D-A20W-10 chr13:52707931 T>C maps to NM_002498.2 K443K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75G-01A-11D-A32G-10 chr13:52718080 T>C maps to NM_002498.2 K282K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A3KG-01A-11D-A20W-10 chr9:127101925 G>T maps to NM_001166171.1 L267L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr1:198233310 A>G maps to NM_133494.2 E106E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BW-A5NQ-01A-11D-A27I-10 chr11:20699517 C>A maps to NM_006157.3 I32I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1E9-01A-21D-A152-10 chr12:45270409 T>C maps to NM_001145107.1 R33R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr15:73541515 G>A maps to NM_002499.3 L574L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr1:156641501 T>A maps to NM_006617.1 L826L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A3R2-01A-11D-A22F-10 chr18:70417751 G>A maps to NM_153181.2 I361I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39V-01A-11D-A20W-10 chr11:74716843 T>C maps to NM_006656.5 P231P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7II-01A-11D-A33K-10 chr10:105350083 C>A maps to NM_004210.4 C560*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EJ-01A-11D-A152-10 chr12:55420792 T>C maps to NM_021191.2 S190S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EB-01A-11D-A12Z-10 chr5:134871329 G>A maps to NM_006161.2 S17S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A2QR-01A-11D-A20W-10 chr17:29576137 G>C did not map to a codon.
Sequencing variant TCGA-G3-A3CK-01A-11D-A20W-10 chr17:29496953 T>C maps to NM_001042492.2 H175H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A1HT-01A-11D-A12Z-10 chr22:30069413 G>T maps to NM_181832.2 E427*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A3RK-01A-11D-A22F-10 chr14:24843035 C>A maps to NM_001136022.1 V628V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr14:24843544 C>A maps to NM_001136022.1 A645A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5264-01A-01D-A12Z-10 chr12:54687078 G>T maps to NM_001136023.1 P67P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NO-01A-11D-A28X-10 chr2:178098809 C>A maps to NM_006164.3 E79*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A6M5-01A-11D-A32G-10 chr7:26224601 T>C maps to NM_004289.6 N428N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EH-01A-11D-A12Z-10 chr1:61920982 C>T maps to NM_001145512.1 Y552Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25T-01A-11D-A16V-10 chr4:103533726 T>C maps to NM_003998.3 S852S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KR-A7K2-01A-12D-A33Q-10 chr4:103518689 A>G maps to NM_003998.3 L503L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10W-01A-11D-A12Z-10 chr19:39397948 G>A maps to NM_002503.3 P236P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A113-01A-11D-A12Z-10 chr19:39395720 C>A maps to NM_002503.3 A82A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr11:129752347 T>C maps to NM_006165.3 E385E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A118-01A-11D-A12Z-10 chr20:34286441 C>T maps to NM_021100.4 L56L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A4ZQ-01A-11D-A25V-10 chr2:69642380 T>A maps to NM_001002755.1 T140T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A113-01A-11D-A12Z-10 chr9:33351694 G>A maps to NM_002504.4 Q854Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39Y-01A-11D-A20W-10 chr9:33295417 G>A maps to NM_002504.4 T342T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A7M9-01A-23D-A34Z-10 chr4:47850328 T>A maps to NM_152995.4 R863*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NI-01A-11D-A27I-10 chr6:41048593 G>A maps to NM_002505.4 Q40Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25S-01A-11D-A16V-10 chr1:41215258 A>G maps to ENST00000308733 E64E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A112-01A-11D-A12Z-10 chr1:115829017 G>A maps to NM_002506.2 F133F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr1:115829386 T>A maps to NM_002506.2 T10T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A5-01A-11D-A22F-10 chr3:25805745 A>T maps to NM_018297.3 I101I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11C-01A-11D-A12Z-10 chr23:17744746 T>C did not map to a codon.
Sequencing variant TCGA-DD-A73C-01A-12D-A33K-10 chr23:17746801 C>T did not map to a codon.
Sequencing variant TCGA-RC-A6M4-01A-11D-A32G-10 chr23:17745540 T>C did not map to a codon.
Sequencing variant TCGA-RG-A7D4-01A-12D-A33Q-10 chr1:236193032 G>A maps to NM_002508.2 Q519*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A115-01A-11D-A12Z-10 chr20:25485595 G>A maps to NM_025176.4 S212S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10Y-01A-11D-A12Z-10 chr5:36976271 G>A maps to NM_133433.3 S421S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39W-01A-11D-A20W-10 chr5:37007557 A>C maps to NM_133433.3 T1407T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73A-01A-12D-A32G-10 chr5:37008168 T>C maps to NM_133433.3 C1433C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A5KG-01A-11D-A27I-10 chr5:37016247 C>T maps to NM_133433.3 L1584L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IK-01A-12D-A33Q-10 chr9:107533136 T>A maps to NM_018376.2 Y146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25U-01A-11D-A16V-10 chr3:52513790 A>G maps to NM_007184.3 T443T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A4XI-01A-11D-A25V-10 chr6:124979396 A>T maps to NM_001040214.1 P113P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IJ-01A-11D-A33Q-10 chr6:28227196 T>C maps to NM_001007531.1 S16S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A2QQ-01A-11D-A22F-10 chr19:51875421 A>G maps to NM_005601.3 F99F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39X-01A-11D-A20W-10 chr3:23942421 C>A maps to NM_020345.3 L71L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr8:41503970 G>A maps to ENST00000425142 V265V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A112-01A-11D-A12Z-10 chr3:173998708 C>T maps to NM_014932.2 A696A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A66Y-01A-11D-A30V-10 chr23:70387138 A>C did not map to a codon.
Sequencing variant TCGA-G3-A25U-01A-11D-A16V-10 chr23:70389118 G>A did not map to a codon.
Sequencing variant TCGA-RC-A7SB-01A-21D-A34Z-10 chr23:70389591 A>G did not map to a codon.
Sequencing variant TCGA-BC-A3KG-01A-11D-A20W-10 chr23:6069291 C>A did not map to a codon.
Sequencing variant TCGA-CC-5260-01A-01D-A12Z-10 chr23:5821678 T>C did not map to a codon.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr23:6069057 G>T did not map to a codon.
Sequencing variant TCGA-DD-A118-01A-11D-A12Z-10 chr23:5811322 A>G did not map to a codon.
Sequencing variant TCGA-DD-A1EJ-01A-11D-A152-10 chr23:5811265 G>A did not map to a codon.
Sequencing variant TCGA-DD-A4NJ-01A-11D-A27I-10 chr23:5821237 G>T did not map to a codon.
Sequencing variant TCGA-DD-A73A-01A-12D-A32G-10 chr23:5810975 G>A did not map to a codon.
Sequencing variant TCGA-ED-A459-01A-11D-A25V-10 chr23:6069269 A>T did not map to a codon.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr23:5810964 T>A did not map to a codon.
Sequencing variant TCGA-MI-A75I-01A-11D-A32G-10 chr24:16941899 A>G did not map to a codon.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr17:26499543 T>A maps to NM_016231.4 L350*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MC-01A-11D-A22F-10 chr2:32463204 G>A maps to NM_021209.4 I839I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr16:57067551 A>G maps to NM_032206.3 K838K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A2-01A-11D-A20W-10 chr11:7981808 G>A maps to NM_176821.3 N450N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A5W4-01A-11D-A28X-10 chr19:56321585 G>A maps to NM_145007.3 Y130Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CK-01A-11D-A20W-10 chr19:56320454 A>C maps to NM_145007.3 L507L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A12J-01A-11D-A12Z-10 chr19:54313460 G>A maps to ENST00000391773 H484H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25S-01A-11D-A16V-10 chr19:56423970 T>C maps to NM_176810.2 E404E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BW-A5NQ-01A-11D-A27I-10 chr11:7064360 C>G maps to NM_176822.3 V368V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RG-A7D4-01A-12D-A33Q-10 chr11:7063784 A>G maps to NM_176822.3 P176P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IL-01A-11D-A33Q-10 chr19:56372856 C>A maps to NM_134444.4 T654T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73F-01A-11D-A32G-10 chr19:56369796 C>T maps to NM_134444.4 I346I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr19:56565057 C>A maps to NM_153447.4 I1061I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A7SB-01A-21D-A34Z-10 chr19:56539101 G>A maps to NM_153447.4 L501L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HP-A5N0-01A-11D-A28X-10 chr19:56241198 G>A maps to NM_176820.2 L664L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-O8-A75V-01A-11D-A32G-10 chr11:119054108 C>A maps to NM_024618.2 V963V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A3KG-01A-11D-A20W-10 chr6:142400003 C>T maps to NM_002511.2 T153T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5261-01A-01D-A12Z-10 chr6:142396835 G>C maps to NM_002511.2 T374T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A7M7-01A-12D-A34Z-10 chr3:160960386 C>T maps to ENST00000472947 C321C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr17:49237414 C>T maps to ENST00000393198 Y92Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75G-01A-11D-A32G-10 chr3:139297766 C>T maps to ENST00000296202 V80V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A5SM-01A-12D-A28X-10 chr16:4519431 C>T maps to NM_020677.3 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A8-01A-11D-A22F-10 chr2:232392879 C>T maps to NM_006056.4 R284R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75H-01A-11D-A32G-10 chr12:132636049 G>A maps to NM_024078.1 V365V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr9:33469274 C>G maps to NM_022917.4 P264P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A459-01A-11D-A25V-10 chr9:33466414 T>A maps to NM_022917.4 P700P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MD-01A-12D-A34Z-10 chr6:13620547 C>G maps to NM_016167.3 T203T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5263-01A-01D-A12Z-10 chr7:156743258 A>T maps to NM_138400.1 A276A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25S-01A-11D-A16V-10 chr23:70514266 T>C did not map to a codon.
Sequencing variant TCGA-DD-A73A-01A-12D-A32G-10 chr12:117698356 C>G maps to ENST00000338101 A760A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A12J-01A-11D-A12Z-10 chr12:117768409 G>A maps to ENST00000338101 P155P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A3I1-01A-11D-A22F-10 chr12:117723944 C>T maps to ENST00000338101 S418S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LG-A6GG-01A-11D-A30V-10 chr12:117655926 G>A maps to ENST00000338101 R1439*. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-CC-A3M9-01A-11D-A20W-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-DD-A3A9-01A-11D-A25V-10 chr7:150698350 C>T maps to NM_000603.4 A422A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10W-01A-11D-A12Z-10 chr1:120539926 G>A maps to NM_024408.2 C148C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25Y-01A-11D-A16V-10 chr1:120512320 A>G maps to NM_024408.2 N307N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A5SJ-01A-11D-A27I-10 chr1:145281399 G>T maps to ENST00000454606 L122L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PD-A5DF-01A-11D-A27I-10 chr1:145281613 C>T maps to ENST00000454606 L194L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr19:15281191 A>G maps to NM_000435.2 S1688S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A3-01A-11D-A22F-10 chr19:15303035 G>A maps to NM_000435.2 P138P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr19:15290990 T>G maps to NM_000435.2 P1073P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr19:15299986 T>A did not map to a codon.
Sequencing variant TCGA-DD-A3A9-01A-11D-A25V-10 chr6:32188290 T>A maps to NM_004557.3 T350T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A6UC-01A-21D-A33K-10 chr6:32166273 C>A maps to NM_004557.3 A1560A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KR-A7K2-01A-12D-A33Q-10 chr6:32163285 T>C maps to NM_004557.3 S1980S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25Z-01A-11D-A16V-10 chr14:26917335 A>T maps to ENST00000449198 T468T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75G-01A-11D-A32G-10 chr14:26949266 T>G maps to ENST00000449198 R138R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr19:46444122 C>T maps to NM_002516.2 Q159Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A113-01A-11D-A12Z-10 chr23:100105358 G>A did not map to a codon.
Sequencing variant TCGA-ED-A66Y-01A-11D-A30V-10 chr23:100104410 T>C did not map to a codon.
Sequencing variant TCGA-RC-A6M4-01A-11D-A32G-10 chr23:100104831 G>C did not map to a codon.
Sequencing variant TCGA-CC-A7IK-01A-12D-A33Q-10 chr6:155776019 G>A maps to NM_015718.2 C60C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A66Y-01A-11D-A30V-10 chr6:155750072 C>A maps to NM_015718.2 E334*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A6M4-01A-11D-A32G-10 chr6:155774562 G>A maps to NM_015718.2 V105V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A26S-01A-11D-A16V-10 chr11:89069053 C>G maps to NM_016931.3 R525R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5261-01A-01D-A12Z-10 chr15:69348933 G>A maps to NM_024505.3 K732K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A115-01A-11D-A12Z-10 chr2:101580592 T>C maps to NM_002518.3 V224V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr14:34269081 G>C maps to NM_001164749.1 P523P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr14:34270266 C>G maps to NM_001164749.1 Y918*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25U-01A-11D-A16V-10 chr11:66191181 C>A maps to NM_178864.3 I314I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-O8-A75V-01A-11D-A32G-10 chr17:79860623 A>G maps to NM_148896.3 *126W. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10Z-01A-11D-A12Z-10 chr7:44579860 C>T maps to NM_013389.2 L45L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A2QR-01A-11D-A20W-10 chr7:44555504 C>T maps to NM_013389.2 K1258K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25S-01A-11D-A16V-10 chr7:44555742 G>T maps to NM_013389.2 I1218I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A7SK-01A-11D-A34Z-10 chr7:44578552 A>G maps to NM_013389.2 S481S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A5UE-01A-11D-A28X-10 chr20:57288475 G>A maps to NM_024663.3 K334K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IL-01A-11D-A33Q-10 chr10:72015501 C>A maps to ENST00000277942 L168L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr2:110926055 T>C maps to NM_000272.3 E199E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25U-01A-11D-A16V-10 chr2:110959032 A>G maps to NM_000272.3 A36A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5258-01A-01D-A12Z-10 chr3:132407636 T>C maps to ENST00000393156 V994V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25W-01A-11D-A16V-10 chr3:132418878 A>G maps to ENST00000393156 S590S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A123-01A-11D-A12Z-10 chr19:36339601 C>T maps to NM_004646.3 R369R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EL-01A-11D-A152-10 chr19:36340536 T>A maps to NM_004646.3 S209S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NI-01A-11D-A27I-10 chr1:182794947 C>G maps to NM_030769.1 V257V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr2:232790143 C>T maps to NM_024409.1 L124L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25W-01A-11D-A16V-10 chr1:153660155 T>C maps to NM_000906.3 P713P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A6M6-01A-11D-A32G-10 chr1:153653013 C>T maps to NM_000906.3 T253T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr1:153661566 C>T maps to NM_000906.3 I852I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MF-01A-11D-A33K-10 chr1:153654208 C>T maps to NM_000906.3 D355D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IK-01A-12D-A33Q-10 chr10:129350902 A>T maps to NM_001030013.1 *90C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LG-A6GG-01A-11D-A30V-10 chr7:34917717 T>A maps to NM_207173.1 A352A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A7-01A-11D-A22F-10 chr7:25267919 C>T did not map to a codon.
Sequencing variant TCGA-DD-A3A0-01A-11D-A20W-10 chr19:50881824 G>A maps to NM_007121.4 Q173Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NK-01A-11D-A28X-10 chr19:50881835 C>A maps to NM_007121.4 S177*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A7M5-01A-11D-A33Q-10 chr3:119530548 C>G maps to NM_022002.2 T204T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A9-01A-11D-A25V-10 chr12:95422247 T>C maps to NM_003297.2 L482L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A7SK-01A-11D-A34Z-10 chr12:95451646 T>C maps to NM_003297.2 Q184Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73E-01A-12D-A32G-10 chr5:142680053 T>A maps to NM_001024094.1 I582I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25U-01A-11D-A16V-10 chr4:149181130 T>C maps to ENST00000511528 E632E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A9-01A-11D-A25V-10 chr9:127284983 T>C maps to NM_033334.2 *481W. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25Z-01A-11D-A16V-10 chr10:115385894 G>T maps to ENST00000369358 R727R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10Y-01A-11D-A12Z-10 chr7:107866733 G>A maps to ENST00000379032 R213R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5264-01A-01D-A12Z-10 chr7:107836239 A>G maps to ENST00000379032 C476C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr7:107820769 C>T maps to ENST00000379032 P916P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A12J-01A-11D-A12Z-10 chr7:107824933 G>A maps to ENST00000379032 R720R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NI-A4U2-01A-11D-A28X-10 chr8:32621589 C>T maps to NM_013956.3 Y536Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr5:139232520 G>T maps to NM_013982.2 R470R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KC-01A-11D-A20W-10 chr10:84498383 T>C maps to ENST00000404547 T335T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A115-01A-11D-A12Z-10 chr23:105152836 C>A did not map to a codon.
Sequencing variant TCGA-DD-A3A9-01A-11D-A25V-10 chr23:105179195 A>G did not map to a codon.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr23:105153327 T>G did not map to a codon.
Sequencing variant TCGA-RG-A7D4-01A-12D-A33Q-10 chr2:206581087 C>A maps to NM_201266.1 I141I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A5UE-01A-11D-A28X-10 chr2:50463973 G>T maps to ENST00000404971 R1207R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr2:50149220 G>T maps to ENST00000404971 S1502*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NI-01A-11D-A27I-10 chr2:50464016 C>A maps to ENST00000404971 L1192L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A7PY-01A-11D-A33Q-10 chr2:51255366 G>T maps to ENST00000404971 C15*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr2:50463974 C>A maps to ENST00000404971 V1206V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73C-01A-12D-A33K-10 chr11:64434902 C>T maps to NM_015080.3 G539G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A26S-01A-11D-A16V-10 chr11:64434896 T>C maps to NM_015080.3 G541G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A5-01A-11D-A22F-10 chr14:80328057 C>A maps to NM_004796.4 I979I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A26S-01A-11D-A16V-10 chr5:176562163 G>A maps to NM_022455.4 V20V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr5:176722360 T>C maps to NM_022455.4 S2664S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A5SK-01A-11D-A27I-10 chr5:176721087 C>A maps to NM_022455.4 S2240*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5259-01A-31D-A20W-10 chr23:152018892 A>G did not map to a codon.
Sequencing variant TCGA-MI-A75E-01A-11D-A32G-10 chr8:59536324 A>G maps to NM_001144772.1 Y164Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr8:59498515 A>G maps to NM_001144772.1 N861N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A7M8-01A-11D-A33Q-10 chr5:6602578 A>G maps to NM_017755.5 D664D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A6UC-01A-21D-A33K-10 chr3:93802962 A>G maps to NM_022072.3 T45T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr4:40800849 A>G maps to NM_024677.4 P443P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73C-01A-12D-A33K-10 chr2:18765783 C>T maps to ENST00000455492 W317*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A1HT-01A-11D-A12Z-10 chr12:5603520 G>A maps to NM_001102654.1 K60K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T1-A6J8-01A-11D-A32G-10 chr12:5604081 C>T maps to NM_001102654.1 L247L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25W-01A-11D-A16V-10 chr12:96181033 G>A maps to NM_021229.3 L90L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10U-01A-11D-A12Z-10 chr1:107937922 C>T maps to NM_001113226.1 P345P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A7PZ-01A-11D-A33Q-10 chr9:135116363 C>A maps to NM_032536.2 R430R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11D-01A-11D-A12Z-10 chr9:87570245 G>T maps to NM_006180.3 T662T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A123-01A-11D-A12Z-10 chr15:88472661 G>T maps to NM_001012338.1 A631A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NK-01A-11D-A28X-10 chr15:88423566 G>A maps to NM_001012338.1 F756F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A23B-01A-11D-A16V-10 chr15:88727469 G>T maps to NM_001012338.1 T103T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A459-01A-11D-A25V-10 chr12:86276026 T>A maps to NM_006183.3 T129T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25V-01A-11D-A16V-10 chr20:61340804 G>T maps to NM_002531.2 T82T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A23B-01A-11D-A16V-10 chr2:11798784 T>C maps to NM_012344.3 S351S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A6UC-01A-21D-A33K-10 chr1:205273291 C>T maps to ENST00000441520 T435T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A4XI-01A-11D-A25V-10 chr14:32031296 C>T maps to NM_025152.2 T44T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RG-A7D4-01A-12D-A33Q-10 chr14:32030677 T>C maps to NM_025152.2 G11G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A7-01A-11D-A22F-10 chr23:51075988 C>A did not map to a codon.
Sequencing variant TCGA-EP-A3RK-01A-11D-A22F-10 chr23:51238813 A>C did not map to a codon.
Sequencing variant TCGA-DD-A4NV-01A-11D-A30V-10 chr5:102886633 G>A maps to NM_031438.2 F439F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr1:145589343 T>C maps to NM_001012758.2 G28G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr10:12219891 C>A maps to ENST00000378937 A76A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25T-01A-11D-A16V-10 chr10:12221082 A>G maps to ENST00000378937 D73D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A4XI-01A-11D-A25V-10 chr4:123814210 T>C maps to NM_007083.3 E241E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A7-01A-11D-A22F-10 chr1:229636532 A>G maps to NM_018230.2 S161S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BW-A5NO-01A-11D-A27I-10 chr9:131764255 G>A did not map to a codon.
Sequencing variant TCGA-G3-A25V-01A-11D-A16V-10 chr7:135330243 T>G maps to NM_015135.2 L1904L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A7M9-01A-23D-A34Z-10 chr7:135300724 A>G maps to NM_015135.2 L1124L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BW-A5NP-01A-11D-A27I-10 chr1:154127336 G>A maps to NM_207308.2 Q62*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5263-01A-01D-A12Z-10 chr1:154033435 A>G maps to NM_207308.2 Y910Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A7M9-01A-23D-A34Z-10 chr1:154067566 C>G maps to NM_207308.2 G677G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BW-A5NP-01A-11D-A27I-10 chr4:77065332 T>C maps to ENST00000458189 G88G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A3R2-01A-11D-A22F-10 chr19:50411918 C>A maps to NM_012346.4 V382V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EA-01A-11D-A12Z-10 chr17:5319993 A>G maps to NM_002532.3 L102L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr11:3716711 T>C maps to NM_016320.4 R1378R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A5SL-01A-11D-A27I-10 chr11:3797195 A>T maps to NM_016320.4 S137S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NI-A4U2-01A-11D-A28X-10 chr11:3707424 C>G did not map to a codon.
Sequencing variant TCGA-CC-A7IF-01A-11D-A33K-10 chr19:16890276 G>C did not map to a codon.
Sequencing variant TCGA-EP-A26S-01A-11D-A16V-10 chr19:16874715 T>C maps to ENST00000438489 L737L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A3I1-01A-11D-A22F-10 chr23:101615540 G>A did not map to a codon.
Sequencing variant TCGA-BC-A216-01A-11D-A152-10 chr23:102335093 C>A did not map to a codon.
Sequencing variant TCGA-CC-A7II-01A-11D-A33K-10 chr23:102334692 G>A did not map to a codon.
Sequencing variant TCGA-DD-A3A7-01A-11D-A22F-10 chr23:102332619 G>C did not map to a codon.
Sequencing variant TCGA-DD-A73E-01A-12D-A32G-10 chr23:102337748 G>T did not map to a codon.
Sequencing variant TCGA-ED-A4XI-01A-11D-A25V-10 chr23:102334163 C>T did not map to a codon.
Sequencing variant TCGA-DD-A4NI-01A-11D-A27I-10 chr23:101095773 G>C did not map to a codon.
Sequencing variant TCGA-BC-A112-01A-11D-A12Z-10 chr7:8791056 T>A maps to NM_152745.2 T158T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NF-01A-11D-A27I-10 chr12:57618995 T>C maps to NM_007224.3 H131H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A118-01A-11D-A12Z-10 chr12:113344970 G>T maps to NM_001032409.1 E43*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10T-01A-11D-A12Z-10 chr1:228462083 C>T maps to NM_001098623.1 D1874D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A110-01A-11D-A12Z-10 chr1:228495848 G>T maps to NM_001098623.1 A4168A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7II-01A-11D-A33K-10 chr1:228503596 C>A maps to NM_001098623.1 G4354G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11A-01A-11D-A12Z-10 chr1:228511095 C>T maps to NM_001098623.1 C5147C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NF-01A-11D-A27I-10 chr1:228451985 G>T maps to NM_001098623.1 V1585V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NF-01A-11D-A27I-10 chr1:228466999 G>T maps to NM_001098623.1 T2417T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NK-01A-11D-A28X-10 chr1:228526697 T>C maps to NM_001098623.1 N5743N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73E-01A-12D-A32G-10 chr1:228467594 C>T maps to NM_001098623.1 C2490C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A5SJ-01A-11D-A27I-10 chr1:228538635 G>A maps to NM_001098623.1 P6137P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KR-A7K0-01A-12D-A33Q-10 chr1:228560354 C>T maps to NM_001098623.1 A7292A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A6M4-01A-11D-A32G-10 chr1:228528926 C>A maps to NM_001098623.1 V5943V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NI-01A-11D-A27I-10 chr2:220432566 C>A maps to NM_015311.2 P469P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A4ZP-01A-12D-A25V-10 chr15:28230304 C>T maps to NM_000275.2 W423*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MA-01A-11D-A20W-10 chr23:128695174 A>G did not map to a codon.
Sequencing variant TCGA-G3-A25Z-01A-11D-A16V-10 chr23:128722191 C>T did not map to a codon.
Sequencing variant TCGA-ED-A5KG-01A-11D-A27I-10 chr8:103572782 C>A maps to NM_024410.3 R142R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A7-01A-11D-A22F-10 chr1:86814444 T>G maps to ENST00000370567 T641T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10T-01A-11D-A12Z-10 chr15:76019646 A>G maps to NM_175881.3 G197G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A3R2-01A-11D-A22F-10 chr17:8243609 C>T maps to NM_153007.4 Q81*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A3-01A-11D-A22F-10 chr23:13779283 A>G did not map to a codon.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr10:50948861 A>G maps to NM_018245.2 H678H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39X-01A-11D-A20W-10 chr6:72003033 A>G maps to NM_024576.3 R91R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A4ZQ-01A-11D-A25V-10 chr9:95155380 A>G maps to NM_033014.2 D138D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr1:102270333 A>G maps to ENST00000338858 N299N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1E9-01A-21D-A152-10 chr13:53617268 G>A maps to NM_006418.3 K200K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A7PY-01A-11D-A33Q-10 chr18:55103727 C>T maps to NM_004852.2 P260P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr3:193374928 G>T maps to NM_130837.2 E747*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A9-01A-11D-A25V-10 chr11:132306091 T>C maps to NM_002545.3 K275K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5263-01A-01D-A12Z-10 chr23:67283855 T>A did not map to a codon.
Sequencing variant TCGA-ED-A7PZ-01A-11D-A33Q-10 chr23:67293090 A>T did not map to a codon.
Sequencing variant TCGA-BD-A3EP-01A-11D-A22F-10 chr8:145112136 C>T maps to ENST00000360660 L503L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr20:62729929 C>T maps to NM_000913.3 A297A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10W-01A-11D-A12Z-10 chr6:154412234 C>A maps to NM_001145279.1 V357V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EF-01A-11D-A12Z-10 chr1:203468894 G>T maps to NM_014359.3 L216L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A9-01A-11D-A25V-10 chr11:6867578 T>C maps to ENST00000379831 I226I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A66X-01A-11D-A30V-10 chr11:7949332 G>A maps to NM_001004461.1 R293*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr6:29408613 C>A maps to NM_013941.2 S274S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr11:123901211 A>T maps to ENST00000375021 K295*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CJ-01A-11D-A20W-10 chr11:123894414 G>C maps to NM_001001953.1 G232G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IL-01A-11D-A33Q-10 chr19:15918703 G>A maps to NM_013940.2 T48T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A7XO-01A-11D-A34Z-10 chr19:15905583 T>C maps to NM_001004466.1 C242C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KR-A7K7-01A-11D-A33K-10 chr1:159410509 G>A maps to NM_012351.2 *321*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QA-A7B7-01A-11D-A32G-10 chr1:158435494 C>A maps to NM_001004473.1 T48T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A217-01A-11D-A152-10 chr12:56030749 C>A maps to NM_206899.1 G25G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A66Y-01A-11D-A30V-10 chr1:158449816 T>A maps to NM_001004472.1 V50V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5263-01A-01D-A12Z-10 chr11:59481144 G>T maps to NM_001005324.1 P58P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HP-A5N0-01A-11D-A28X-10 chr1:158576233 G>T maps to NM_001004478.1 G2G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr14:20666490 A>T maps to NM_001005503.1 K333*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39W-01A-11D-A20W-10 chr6:29342650 C>T maps to ENST00000396806 V138V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T1-A6J8-01A-11D-A32G-10 chr10:45799381 G>T maps to NM_001004297.2 A163A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EF-01A-11D-A12Z-10 chr9:107379993 T>C maps to NM_001001956.1 V164V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5264-01A-01D-A12Z-10 chr9:107457697 T>A maps to NM_001004484.1 A332A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NV-01A-11D-A30V-10 chr9:107457350 C>T maps to NM_001004484.1 L217L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A23B-01A-11D-A16V-10 chr23:130678191 A>G did not map to a codon.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr1:247978551 G>T maps to NM_001001966.1 G160G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IF-01A-11D-A33K-10 chr1:248844792 C>A maps to NM_001004734.1 V271V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr17:3119513 C>A maps to NM_014565.2 Y200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A5UE-01A-11D-A28X-10 chr9:125391805 G>A maps to NM_001004450.1 S3S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A12J-01A-11D-A12Z-10 chr17:3300969 C>G maps to NM_003553.2 L245L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CI-01A-11D-A20W-10 chr17:3336388 A>T maps to NM_003554.1 T249T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NK-01A-11D-A28X-10 chr16:3254986 G>A maps to NM_012360.1 V247V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr9:125437542 C>T maps to NM_001005234.1 I45I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39X-01A-11D-A20W-10 chr9:125512278 C>T maps to ENST00000373684 Y87Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73G-01A-22D-A32G-10 chr9:125315780 T>C maps to NM_001004457.1 Y111Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-4073-01B-02D-A12Z-10 chr11:57970714 G>A maps to NM_001004459.1 A313A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr7:144015435 C>T maps to NM_001005287.1 T73T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr7:143792916 C>A maps to NM_001004135.1 T239T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NQ-01A-21D-A28X-10 chr7:143807040 T>A maps to NM_001005480.2 Y122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr11:6806882 C>T maps to NM_001004489.2 T205T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EB-01A-11D-A12Z-10 chr11:6790152 G>A maps to NM_001004490.1 F12F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CJ-01A-11D-A20W-10 chr11:74799966 G>A maps to NM_001005285.1 Y264Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A1HT-01A-11D-A12Z-10 chr1:247614390 A>G maps to NM_001004492.1 N298N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IK-01A-12D-A33Q-10 chr6:27879560 A>G maps to NM_033057.2 C179C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10R-01A-11D-A12Z-10 chr1:248684958 C>T maps to NM_001013355.1 T4T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr1:248685870 T>C maps to NM_001013355.1 S308S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A7SK-01A-11D-A34Z-10 chr6:29430100 C>A maps to NM_030883.3 L185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A115-01A-11D-A12Z-10 chr6:29556101 C>A maps to NM_007160.3 P127P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr6:29141975 A>G maps to NM_030905.2 L188L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A12J-01A-11D-A12Z-10 chr1:248263610 G>T maps to NM_175911.2 E312*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75C-01A-11D-A32G-10 chr1:248263222 C>T maps to NM_175911.2 A182A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11D-01A-11D-A12Z-10 chr1:248224573 A>T maps to NM_001004687.1 T197T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11A-01A-11D-A12Z-10 chr1:248112613 C>A maps to NM_001001963.1 S152*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11D-01A-11D-A12Z-10 chr1:248112749 A>T maps to NM_001001963.1 T197T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A5SJ-01A-11D-A27I-10 chr1:248367190 G>T maps to NM_001004689.1 V274V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A1-01A-11D-A20W-10 chr1:248308862 C>A maps to NM_001004690.1 P138P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10R-01A-11D-A12Z-10 chr1:248756793 G>T maps to NM_001004693.1 I92I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IL-01A-11D-A33Q-10 chr1:248458205 G>A maps to NM_001004692.1 L225L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75E-01A-11D-A32G-10 chr1:248458181 C>T maps to NM_001004692.1 K233K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10U-01A-11D-A12Z-10 chr1:248813315 G>T maps to NM_001001824.1 Y290*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A9-01A-11D-A25V-10 chr1:248737674 A>C maps to NM_001001821.1 Y128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NF-01A-11D-A27I-10 chr1:248737386 G>C maps to NM_001001821.1 T224T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10U-01A-11D-A12Z-10 chr1:248525892 A>G maps to NM_001004696.1 L337L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10R-01A-11D-A12Z-10 chr1:248551625 C>T maps to NM_001005471.1 A239A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NK-01A-11D-A28X-10 chr1:248551235 G>T maps to NM_001005471.1 G109G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K7-A5RF-01A-11D-A28X-10 chr5:180582508 C>T maps to NM_206880.1 A189A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5264-01A-01D-A12Z-10 chr6:29012334 A>T maps to NM_030903.3 I206I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NS-01A-11D-A30V-10 chr1:247655365 G>T maps to NM_001004698.2 G313*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A8-01A-11D-A22F-10 chr5:180166443 G>A maps to NM_001001657.1 V205V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A114-01A-11D-A12Z-10 chr19:8842139 C>A maps to NM_001004699.1 L250L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A114-01A-11D-A12Z-10 chr11:55135485 T>C maps to NM_001005275.1 L43L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr11:55110909 A>G maps to NM_001005274.1 K78K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A9-01A-11D-A25V-10 chr11:51412083 G>A maps to NM_001005272.3 F104F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RG-A7D4-01A-12D-A33Q-10 chr11:51411560 G>A maps to NM_001005272.3 L279L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr11:48239230 A>G maps to NM_001005470.1 A290A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A5SM-01A-12D-A28X-10 chr11:55371774 C>A maps to NM_001004700.1 V25V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A3KG-01A-11D-A20W-10 chr11:50003746 A>T maps to NM_001005270.2 A97A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A7PY-01A-11D-A33Q-10 chr11:55322153 G>C maps to NM_001001920.1 A124A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25Z-01A-11D-A16V-10 chr11:48347262 G>A maps to NM_001004702.1 G257G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr11:55433037 C>T maps to NM_001004704.1 I132I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A5UD-01A-11D-A28X-10 chr11:59283044 C>A maps to NM_001004711.1 V220V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IK-01A-12D-A33Q-10 chr15:102346470 A>G maps to NM_001005326.1 R183R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr14:20483232 C>A maps to NM_001004712.1 L40L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr14:20444393 T>C maps to NM_001005486.1 V239V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr14:20586545 A>C maps to NM_001004715.1 I327I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25V-01A-11D-A16V-10 chr14:20528667 C>T maps to NM_001004717.1 H155H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5263-01A-01D-A12Z-10 chr14:20249421 G>A maps to NM_001005500.1 *314*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MC-01A-11D-A33Q-10 chr14:20249254 C>A maps to NM_001005500.1 Y258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IJ-01A-11D-A33Q-10 chr11:55405982 C>A maps to NM_001004124.1 T50T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A7M5-01A-11D-A33Q-10 chr11:48285787 A>T maps to NM_001004726.1 K126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A5KG-01A-11D-A27I-10 chr11:4967859 C>A maps to NM_001005329.1 L157L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BW-A5NO-01A-11D-A27I-10 chr11:4944786 A>G maps to NM_001005237.1 S261S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr11:5020778 A>G maps to NM_001004755.1 L189L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NF-01A-11D-A27I-10 chr11:5021108 G>A maps to NM_001004755.1 K299K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39V-01A-11D-A20W-10 chr11:4869814 A>G maps to NM_001004758.1 F208F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NS-01A-11D-A30V-10 chr11:4869688 G>T maps to NM_001004758.1 A250A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A3I0-01A-11D-A22F-10 chr11:4904014 T>C maps to NM_001004759.1 L323L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10R-01A-11D-A12Z-10 chr11:5878725 C>A maps to NM_001005168.1 L69L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10U-01A-11D-A12Z-10 chr11:5566528 G>T maps to NM_001005289.1 A75A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A118-01A-11D-A12Z-10 chr11:4567047 T>C maps to NM_001004137.1 L210L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A69H-01A-11D-A30V-10 chr11:5776242 C>G maps to NM_001005175.2 L91L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A114-01A-11D-A12Z-10 chr11:4825511 C>A maps to ENST00000380382 P112P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MF-01A-11D-A33K-10 chr11:4825733 G>A maps to ENST00000380382 T38T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A7M5-01A-11D-A33Q-10 chr11:55798175 T>A maps to NM_001001921.1 P94P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IK-01A-12D-A33Q-10 chr11:58126347 A>G maps to NM_001005489.1 S65S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A112-01A-11D-A12Z-10 chr11:55541186 A>T maps to NM_001001967.1 R92*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A112-01A-11D-A12Z-10 chr11:55606430 C>A maps to NM_001005496.1 L68L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3M9-01A-11D-A20W-10 chr11:55587761 T>C maps to ENST00000395203 Y221Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NV-01A-11D-A30V-10 chr11:55587563 A>T maps to ENST00000395203 G155G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75C-01A-11D-A32G-10 chr11:55587641 C>T maps to ENST00000395203 F181F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A12J-01A-11D-A12Z-10 chr11:55761411 C>T maps to NM_003697.1 S230S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LG-A6GG-01A-11D-A30V-10 chr3:97851771 G>T maps to NM_001005338.1 V77V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A3I1-01A-11D-A22F-10 chr3:97868345 C>A maps to NM_001005514.1 I39I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NG-01A-11D-A27I-10 chr3:98109589 G>C maps to NM_001005516.1 L27L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A8-01A-11D-A22F-10 chr11:55595155 G>T maps to NM_001004739.1 V154V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A7M5-01A-11D-A33Q-10 chr11:56344759 A>T maps to NM_001004741.1 T146T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NE-01A-11D-A27I-10 chr11:56237769 A>G maps to NM_001004742.1 D68D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NK-01A-11D-A28X-10 chr11:56258000 A>T maps to NM_001005282.1 P282P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11D-01A-11D-A12Z-10 chr11:7846817 G>T maps to NM_153445.1 R234R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A5UD-01A-11D-A28X-10 chr11:56185420 A>T maps to NM_001004744.1 A96A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A114-01A-11D-A12Z-10 chr11:55999980 A>C maps to NM_001004746.1 S227S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A6M6-01A-11D-A32G-10 chr11:56000067 A>G maps to NM_001004746.1 H198H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A7SK-01A-11D-A34Z-10 chr6:29323798 A>T maps to NM_030876.5 P58P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K7-A5RG-01A-11D-A28X-10 chr12:55945799 G>T maps to NM_001005494.1 E264*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K7-A5RG-01A-11D-A28X-10 chr12:55886940 A>G maps to NM_001005519.1 P265P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CH-01A-11D-A22F-10 chr1:247875184 C>T maps to NM_001005286.1 T291T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A7-01A-11D-A22F-10 chr1:158669565 G>A maps to NM_001005279.1 L293L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A6M6-01A-11D-A32G-10 chr1:158669509 T>A maps to NM_001005279.1 I311I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr1:158669602 T>C maps to NM_001005279.1 A280A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25T-01A-11D-A16V-10 chr1:158724982 C>A maps to NM_001005184.1 L126L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EF-01A-11D-A12Z-10 chr11:123676274 C>T maps to NM_001005325.1 Q261Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GJ-A6C0-01A-12D-A30V-10 chr11:123676931 G>T maps to NM_001005325.1 T42T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NO-01A-11D-A28X-10 chr1:158747386 C>A maps to NM_001005278.1 V13V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BW-A5NQ-01A-11D-A27I-10 chr1:158516971 C>T maps to NM_001005189.1 K308K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A114-01A-11D-A12Z-10 chr19:9324916 C>T maps to NM_001005191.2 L199L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr19:9226011 A>T maps to ENST00000293614 L143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73D-01A-12D-A32G-10 chr11:124440803 A>C maps to NM_001005194.1 T280T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr11:124440851 G>T maps to NM_001005194.1 T296T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A5KG-01A-11D-A27I-10 chr11:124294074 C>T maps to NM_001005196.1 E231E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25S-01A-11D-A16V-10 chr11:124310342 G>T maps to NM_012378.1 T213T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr11:124310402 A>T maps to NM_012378.1 Y193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IF-01A-11D-A33K-10 chr11:124095696 A>C maps to NM_001007249.1 T100T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr11:124095465 T>A maps to NM_001007249.1 T23T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A113-01A-11D-A12Z-10 chr11:56113636 T>C maps to NM_001002907.1 Y41Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr11:56114423 A>T maps to NM_001002907.1 K304*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5258-01A-01D-A12Z-10 chr11:55927259 G>T maps to NM_001004058.2 Y178*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A5UD-01A-11D-A28X-10 chr11:55926910 C>A maps to NM_001004058.2 E295*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr11:55926968 A>C maps to NM_001004058.2 S275S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LG-A6GG-01A-11D-A30V-10 chr12:48919695 A>G maps to NM_001005203.2 V94V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr12:48919701 C>G maps to NM_001005203.2 G96G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A5W4-01A-11D-A28X-10 chr11:56468747 T>C maps to NM_001013358.1 D295D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5259-01A-31D-A20W-10 chr11:56468093 C>A maps to NM_001013358.1 T77T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr11:56468657 T>G maps to NM_001013358.1 Y265*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NI-A4U2-01A-11D-A28X-10 chr12:55524127 T>C maps to NM_001005243.1 S192S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25S-01A-11D-A16V-10 chr3:31705615 G>A maps to NM_017784.4 R735R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75G-01A-11D-A32G-10 chr20:60835073 G>A maps to NM_144498.1 E25E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7ME-01A-11D-A33K-10 chr7:24881963 A>T maps to NM_015550.2 T445T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3M9-01A-11D-A20W-10 chr17:45885989 G>A maps to NM_145798.2 A778A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A6M4-01A-11D-A32G-10 chr17:45890655 T>C maps to NM_145798.2 R571R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A12J-01A-11D-A12Z-10 chr19:54602892 C>A did not map to a codon.
Sequencing variant TCGA-K7-A5RG-01A-11D-A28X-10 chr19:54600386 A>T maps to NM_130771.3 P49P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25Y-01A-11D-A16V-10 chr2:190618640 C>A did not map to a codon.
Sequencing variant TCGA-RC-A7SK-01A-11D-A34Z-10 chr16:83994226 C>T maps to NM_013370.3 A169A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5264-01A-01D-A12Z-10 chr2:26725218 G>T maps to NM_194248.2 S220*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NG-01A-11D-A27I-10 chr4:4199474 C>A maps to NM_177998.1 G362G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A6M4-01A-11D-A32G-10 chr4:4228501 A>T maps to NM_177998.1 P30P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr4:4199318 A>T maps to NM_177998.1 C414*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A112-01A-11D-A12Z-10 chr5:76932768 C>G maps to NM_032109.2 R108R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NV-01A-11D-A30V-10 chr5:76932918 C>A maps to NM_032109.2 L58L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NQ-01A-21D-A28X-10 chr11:63755855 C>A maps to ENST00000422031 R73R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A4ZP-01A-12D-A25V-10 chr23:48814824 A>G did not map to a codon.
Sequencing variant TCGA-G3-A25V-01A-11D-A16V-10 chr23:69282481 C>A did not map to a codon.
Sequencing variant TCGA-DD-A4NV-01A-11D-A30V-10 chr1:149915758 G>A maps to NM_020205.2 F843F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NI-A4U2-01A-11D-A28X-10 chr2:63283429 A>T maps to NM_014562.3 S348S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11B-01A-11D-A16Z-10 chr12:29597094 A>G maps to NM_183378.2 S1000S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NR-01A-11D-A30V-10 chr12:29598310 G>T maps to NM_183378.2 Y927*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25U-01A-11D-A16V-10 chr12:29628066 C>A maps to NM_183378.2 T509T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75I-01A-11D-A32G-10 chr12:29628110 C>A maps to NM_183378.2 G495*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr12:29580581 G>T did not map to a codon.
Sequencing variant TCGA-DD-A1EG-01A-11D-A20W-10 chr1:111957946 T>C maps to ENST00000369728 L456L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr14:23237246 A>T maps to NM_005015.3 V162V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MB-01A-11D-A20W-10 chr5:41794834 A>G maps to NM_000436.3 T372T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A6M4-01A-11D-A32G-10 chr5:41739503 C>G maps to NM_000436.3 G503G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5259-01A-31D-A20W-10 chr8:107719000 G>T maps to NM_001198533.1 E418*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr8:107691474 A>G maps to NM_001198533.1 G86G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A7-01A-11D-A22F-10 chr3:25833479 T>A maps to NM_017897.2 G323G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A6M3-01A-11D-A32G-10 chr3:25833158 G>T maps to NM_017897.2 V216V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A6UC-01A-21D-A33K-10 chr12:133197657 G>A maps to NM_170683.2 K282K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A6M4-01A-11D-A32G-10 chr22:21369504 A>T maps to NM_005446.3 P14P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr22:21380893 C>A maps to NM_005446.3 S438S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A69H-01A-11D-A30V-10 chr3:152553753 A>G maps to NM_002563.2 V61V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr23:78216942 C>A did not map to a codon.
Sequencing variant TCGA-DD-A4ND-01A-11D-A25V-10 chr23:69478611 T>C did not map to a codon.
Sequencing variant TCGA-K7-A5RF-01A-11D-A28X-10 chr23:69479047 C>A did not map to a codon.
Sequencing variant TCGA-NI-A4U2-01A-11D-A28X-10 chr23:1585346 C>A did not map to a codon.
Sequencing variant TCGA-G3-A25V-01A-11D-A16V-10 chr5:131531149 A>G maps to NM_001142599.1 G465G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A69H-01A-11D-A30V-10 chr23:90690698 T>A did not map to a codon.
Sequencing variant TCGA-G3-A6UC-01A-21D-A33K-10 chr23:90690654 C>T did not map to a codon.
Sequencing variant TCGA-UB-A7ME-01A-11D-A33K-10 chr23:90691011 G>T did not map to a codon.
Sequencing variant TCGA-DD-A115-01A-11D-A12Z-10 chr11:65988181 G>A maps to NM_018026.2 L373L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A1-01A-11D-A20W-10 chr22:43284654 A>C maps to NM_001184970.1 V201V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25S-01A-11D-A16V-10 chr1:17563889 G>A maps to NM_013358.2 S465S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K7-A6G5-01A-11D-A30V-10 chr1:17565193 C>T maps to NM_013358.2 A514A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5258-01A-01D-A12Z-10 chr23:55117890 G>A did not map to a codon.
Sequencing variant TCGA-RC-A7SB-01A-21D-A34Z-10 chr12:103237548 T>C maps to NM_000277.1 L358L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25T-01A-11D-A16V-10 chr4:57302495 T>C did not map to a codon.
Sequencing variant TCGA-DD-A11C-01A-11D-A12Z-10 chr3:196547329 G>A maps to NM_002577.4 V414V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MB-01A-11D-A20W-10 chr23:110439077 A>T did not map to a codon.
Sequencing variant TCGA-DD-A113-01A-11D-A12Z-10 chr23:110439119 T>C did not map to a codon.
Sequencing variant TCGA-G3-A7M9-01A-23D-A34Z-10 chr23:110416298 A>G did not map to a codon.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr23:110391046 T>C did not map to a codon.
Sequencing variant TCGA-RC-A6M4-01A-11D-A32G-10 chr19:39664256 G>T maps to NM_005884.3 G235G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73A-01A-12D-A32G-10 chr15:40564636 C>T maps to NM_020168.4 A357A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr20:9624844 T>A maps to NM_177990.2 A44A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A7-01A-11D-A22F-10 chr16:23646315 T>C maps to NM_024675.3 K517K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A3RK-01A-11D-A22F-10 chr1:100154969 C>G maps to NM_017734.4 S385*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A3R3-01A-11D-A22F-10 chr12:56720645 T>C maps to NM_001127460.2 S339S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7II-01A-11D-A33K-10 chr13:28794510 G>A maps to NM_175854.7 A332A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A6UC-01A-21D-A33K-10 chr20:3893206 G>A maps to NM_153638.2 V446V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5259-01A-31D-A20W-10 chr16:50259195 A>G maps to NM_001040284.2 V585V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KR-A7K2-01A-12D-A33Q-10 chr2:61014135 T>C maps to NM_022894.3 N407N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HP-A5N0-01A-11D-A28X-10 chr9:118950192 C>G maps to NM_002581.3 S392S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5261-01A-01D-A12Z-10 chr1:176671814 G>A maps to NM_020318.2 S1103S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CH-01A-11D-A22F-10 chr1:176564725 C>T maps to NM_020318.2 P662P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A7M8-01A-11D-A33Q-10 chr1:176709305 C>T maps to NM_020318.2 D1375D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A112-01A-11D-A12Z-10 chr10:34400171 C>T maps to NM_019619.3 V1332V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K7-A5RF-01A-11D-A28X-10 chr10:34671813 G>A maps to NM_019619.3 P351P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr2:206036932 A>T did not map to a codon.
Sequencing variant TCGA-ED-A7XP-01A-11D-A34Z-10 chr1:226590005 C>T maps to NM_001618.3 R65R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NI-01A-11D-A27I-10 chr3:122418684 A>T maps to NM_017554.2 T428T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A2QR-01A-11D-A20W-10 chr3:122419293 T>C maps to NM_017554.2 T631T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A6-01A-11D-A22F-10 chr15:65563338 G>A maps to NM_017851.4 A82A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A2QQ-01A-11D-A22F-10 chr14:20822995 A>C maps to NM_005484.3 A277A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A66Y-01A-11D-A30V-10 chr3:122271264 C>T maps to NM_031458.2 Q404Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11D-01A-11D-A12Z-10 chr23:150840759 A>T did not map to a codon.
Sequencing variant TCGA-G3-A25W-01A-11D-A16V-10 chr23:150839638 G>T did not map to a codon.
Sequencing variant TCGA-UB-A7MD-01A-12D-A34Z-10 chr23:150842572 C>G did not map to a codon.
Sequencing variant TCGA-DD-A39Z-01A-11D-A20W-10 chr11:59423449 T>C maps to NM_152716.2 A264A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A459-01A-11D-A25V-10 chr11:59420492 T>A did not map to a codon.
Sequencing variant TCGA-G3-A7M9-01A-23D-A34Z-10 chr10:102584501 G>A maps to NM_003987.3 V362V. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-G3-A25T-01A-11D-A16V-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-FV-A495-01A-11D-A25V-10 chr7:127255086 T>C maps to NM_006193.2 P61P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25T-01A-11D-A16V-10 chr2:113993091 G>A maps to NM_003466.3 S322S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr7:154738502 T>C maps to NM_007349.3 T981T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EA-01A-11D-A12Z-10 chr3:52662938 G>A maps to ENST00000296302 R472*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10W-01A-11D-A12Z-10 chr11:66618557 A>G maps to NM_022172.2 L726L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A23B-01A-11D-A16V-10 chr11:66618381 G>A maps to NM_022172.2 L746L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CK-01A-11D-A20W-10 chr11:66618657 C>G maps to NM_022172.2 A692A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MF-01A-11D-A33K-10 chr11:66639214 G>A maps to NM_022172.2 R88R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5258-01A-01D-A12Z-10 chr5:134246023 G>C did not map to a codon.
Sequencing variant TCGA-DD-A1EG-01A-11D-A20W-10 chr21:47320945 C>A maps to NM_020528.2 C86*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A5SI-01A-31D-A27I-10 chr21:47330913 C>A maps to NM_020528.2 C190*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25U-01A-11D-A16V-10 chr3:51993961 C>T maps to NM_033010.2 V155V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MC-01A-11D-A33Q-10 chr13:100925471 C>A maps to NM_000282.3 R313R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NV-01A-11D-A30V-10 chr5:141244053 C>G maps to NM_032420.2 L614L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75G-01A-11D-A32G-10 chr5:141248169 T>C maps to NM_032420.2 L289L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr4:134084264 C>A maps to NM_032961.1 G977G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr23:91131827 A>T did not map to a codon.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr23:91873263 T>A did not map to a codon.
Sequencing variant TCGA-DD-A114-01A-11D-A12Z-10 chr23:91090987 C>T did not map to a codon.
Sequencing variant TCGA-DD-A3A9-01A-11D-A25V-10 chr23:91133860 G>C did not map to a codon.
Sequencing variant TCGA-G3-A7M5-01A-11D-A33Q-10 chr23:91132751 C>A did not map to a codon.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr23:91873833 C>T did not map to a codon.
Sequencing variant TCGA-BC-A10Y-01A-11D-A12Z-10 chr24:4925277 C>T did not map to a codon.
Sequencing variant TCGA-CC-A3M9-01A-11D-A20W-10 chr24:4966400 G>C did not map to a codon.
Sequencing variant TCGA-DD-A11B-01A-11D-A16Z-10 chr24:4925134 A>T did not map to a codon.
Sequencing variant TCGA-DD-A1EI-01A-11D-A12Z-10 chr24:4968284 C>A did not map to a codon.
Sequencing variant TCGA-EP-A3JL-01A-11D-A20W-10 chr24:4968506 A>G did not map to a codon.
Sequencing variant TCGA-G3-A5SI-01A-31D-A27I-10 chr24:5605944 A>T did not map to a codon.
Sequencing variant TCGA-MI-A75G-01A-11D-A32G-10 chr24:4967402 A>G did not map to a codon.
Sequencing variant TCGA-RC-A6M3-01A-11D-A32G-10 chr24:4967708 A>T did not map to a codon.
Sequencing variant TCGA-RC-A7SK-01A-11D-A34Z-10 chr24:4968004 A>G did not map to a codon.
Sequencing variant TCGA-ED-A82E-01A-11D-A34Z-10 chr5:141336990 C>A maps to NM_016580.2 L142L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25Y-01A-11D-A16V-10 chr5:141335556 G>A maps to NM_016580.2 T620T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A112-01A-11D-A12Z-10 chr10:56128942 C>T maps to NM_001142763.1 V142V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5259-01A-31D-A20W-10 chr10:55996687 C>A maps to NM_001142763.1 E299*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3M9-01A-11D-A20W-10 chr10:55568667 A>T maps to NM_001142769.1 A1719A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IF-01A-11D-A33K-10 chr10:55582875 G>T maps to NM_001142763.1 S1544*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NK-01A-11D-A28X-10 chr10:55591091 A>G maps to NM_001142763.1 V1400V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K7-A5RF-01A-11D-A28X-10 chr10:55719517 G>A maps to NM_001142763.1 I1037I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K7-A5RG-01A-11D-A28X-10 chr10:55581782 A>G maps to NM_001142763.1 S1908S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T1-A6J8-01A-11D-A32G-10 chr10:55583048 T>C maps to NM_001142763.1 Q1486Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NF-01A-11D-A27I-10 chr13:58298753 G>T maps to NM_001040429.2 E936*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A7PY-01A-11D-A33Q-10 chr13:58299286 G>A maps to NM_001040429.2 E1113E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A7SB-01A-21D-A34Z-10 chr13:58299073 G>C maps to NM_001040429.2 A1042A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10R-01A-11D-A12Z-10 chr23:99658622 T>A did not map to a codon.
Sequencing variant TCGA-CC-A3M9-01A-11D-A20W-10 chr23:99551539 G>T did not map to a codon.
Sequencing variant TCGA-DD-A1E9-01A-21D-A152-10 chr23:99662111 G>A did not map to a codon.
Sequencing variant TCGA-DD-A1ED-01A-11D-A152-10 chr23:99657570 T>C did not map to a codon.
Sequencing variant TCGA-CC-5260-01A-01D-A12Z-10 chr13:61987586 C>T maps to NM_022843.3 S215S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IL-01A-11D-A33Q-10 chr4:30724306 G>T maps to NM_001173523.1 G421G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11D-01A-11D-A12Z-10 chr4:30723823 G>T maps to NM_001173523.1 L260L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A8-01A-11D-A22F-10 chr4:30921950 G>A maps to NM_001173523.1 T1117T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A26S-01A-11D-A16V-10 chr4:30726037 T>A maps to NM_001173523.1 S998S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A5SM-01A-12D-A28X-10 chr4:30726250 C>T maps to NM_032456.1 P1069P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A118-01A-11D-A12Z-10 chr13:53422355 A>G maps to NM_002590.2 S72S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5259-01A-31D-A20W-10 chr13:67801362 C>A maps to NM_203487.2 E404*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A4XI-01A-11D-A25V-10 chr13:67801109 A>T maps to NM_203487.2 L488*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11D-01A-11D-A12Z-10 chr5:140167845 G>A maps to NM_018900.2 P657P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MD-01A-12D-A34Z-10 chr5:140167890 C>T maps to NM_018900.2 S672S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10R-01A-11D-A12Z-10 chr5:140237873 T>C maps to NM_018901.2 S747S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A3I1-01A-11D-A22F-10 chr5:140235698 C>T maps to NM_018901.2 A22A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A7S9-01A-11D-A33Q-10 chr5:140237150 C>T maps to NM_018901.2 Y506Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IJ-01A-11D-A33Q-10 chr5:140250481 G>A maps to NM_018902.3 A598A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A114-01A-11D-A12Z-10 chr5:140250370 G>A maps to NM_018902.3 A561A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr5:140250199 G>A maps to NM_018902.3 S504S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A1-01A-11D-A20W-10 chr5:140249053 G>A maps to NM_018902.3 E122E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EC-01A-21D-A12Z-10 chr5:140255563 C>G maps to NM_018903.2 T169T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr5:140257187 C>T maps to NM_018903.2 L711L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EF-01A-11D-A12Z-10 chr5:140175841 C>T maps to NM_018905.2 G431G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IG-01A-11D-A33K-10 chr5:140180919 C>A maps to NM_018906.2 G46G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A12J-01A-11D-A12Z-10 chr5:140182752 C>G maps to NM_018906.2 P657P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A7-01A-11D-A22F-10 chr5:140187338 A>G maps to NM_018907.2 V189V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A4XI-01A-11D-A25V-10 chr5:140187737 C>A maps to NM_018907.2 G322G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-4073-01B-02D-A12Z-10 chr5:140208266 G>A maps to NM_018909.2 K197K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A1HT-01A-11D-A12Z-10 chr5:140210048 A>G maps to NM_018909.2 L791L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11D-01A-11D-A12Z-10 chr5:140209427 A>T maps to NM_018909.2 S584S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39V-01A-11D-A20W-10 chr5:140209064 C>T maps to NM_018909.2 F463F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A118-01A-11D-A12Z-10 chr5:140216085 G>T maps to NM_018910.2 A706A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KC-01A-11D-A20W-10 chr5:140215320 C>T maps to NM_018910.2 N451N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IG-01A-11D-A33K-10 chr5:140222939 G>A maps to NM_018911.2 A678A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EK-01A-11D-A20W-10 chr5:140222267 G>A maps to NM_018911.2 A454A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr5:140308411 A>G maps to NM_018898.3 P645P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NJ-01A-11D-A27I-10 chr5:140348024 A>G maps to NM_018899.5 P558P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IF-01A-11D-A33K-10 chr5:140433010 T>A maps to NM_013340.2 A652A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A5SL-01A-11D-A27I-10 chr5:140572646 C>T maps to NM_018930.3 P174P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A7M9-01A-23D-A34Z-10 chr5:140573687 C>A maps to NM_018930.3 Y521*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr5:140572208 T>C maps to NM_018930.3 S28S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EB-01A-11D-A12Z-10 chr5:140580795 C>T maps to NM_018931.2 N483N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr5:140579923 G>T maps to NM_018931.2 E193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NI-A4U2-01A-11D-A28X-10 chr5:140579643 C>T maps to NM_018931.2 I99I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A7PZ-01A-11D-A33Q-10 chr5:140595368 G>A maps to NM_018933.2 S558S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25T-01A-11D-A16V-10 chr5:140627377 C>T maps to NM_018935.2 T744T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr5:140563036 T>A maps to NM_020957.1 V301V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HP-A5MZ-01A-21D-A27I-10 chr5:140503230 C>T maps to NM_018938.2 L551L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A4XI-01A-11D-A25V-10 chr5:140516629 G>A maps to NM_015669.2 P538P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A7M6-01A-11D-A33Q-10 chr5:140530761 G>A maps to NM_018939.2 E308E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A217-01A-11D-A152-10 chr5:140554545 G>A maps to NM_018940.2 R710R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A5SM-01A-12D-A28X-10 chr5:140558832 A>G maps to NM_019120.2 T406T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25U-01A-11D-A16V-10 chr5:140810433 G>T maps to NM_003735.2 P36P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EF-01A-11D-A12Z-10 chr5:140723656 C>T maps to NM_018916.3 L19L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39W-01A-11D-A20W-10 chr5:140744160 C>T maps to NM_018918.2 G88G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A4ZP-01A-12D-A25V-10 chr5:140745936 C>A maps to NM_018918.2 T680T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5262-01A-01D-A12Z-10 chr5:140755533 G>A maps to NM_018919.2 T628T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A1HT-01A-11D-A12Z-10 chr5:140753694 G>T maps to NM_018919.2 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4ND-01A-11D-A25V-10 chr5:140755725 C>T maps to NM_018919.2 Y692Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73E-01A-12D-A32G-10 chr5:140773531 T>C maps to NM_032088.1 C384C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LG-A6GG-01A-11D-A30V-10 chr5:140740664 A>C maps to NM_018923.2 A321A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr5:140751343 A>T maps to NM_018924.2 V461V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3M9-01A-11D-A20W-10 chr5:140798232 G>A maps to NM_018927.2 Q269Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10W-01A-11D-A12Z-10 chr5:140856090 T>C maps to NM_002588.2 P136P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A112-01A-11D-A12Z-10 chr5:140855946 G>C maps to NM_002588.2 V88V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A7SB-01A-21D-A34Z-10 chr5:140856285 C>A maps to NM_002588.2 A201A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NH-01A-11D-A27I-10 chr5:140869877 C>T maps to NM_018929.2 N357N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MD-01A-12D-A34Z-10 chr2:120385298 G>A maps to NM_001029996.3 S243S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A3KF-01A-11D-A20W-10 chr11:82872484 G>A maps to NM_015885.3 V103V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A7M7-01A-12D-A34Z-10 chr11:82879584 G>A maps to NM_015885.3 L736L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr17:36891667 G>T maps to NM_007144.2 T281T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73A-01A-12D-A32G-10 chr14:24567762 C>T maps to NM_004563.2 D180D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75G-01A-11D-A32G-10 chr14:24572376 C>T maps to NM_004563.2 L461L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BD-A3EP-01A-11D-A22F-10 chr7:82389960 A>G maps to NM_033026.5 S5094S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MA-01A-11D-A20W-10 chr7:82580360 A>G maps to NM_033026.5 V3181V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr7:82580708 T>A maps to NM_033026.5 T3065T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11A-01A-11D-A12Z-10 chr7:82583265 A>G maps to NM_033026.5 L2335L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1E9-01A-21D-A152-10 chr7:82595461 G>A maps to NM_033026.5 L1214L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EK-01A-11D-A20W-10 chr7:82580516 T>G maps to NM_033026.5 S3129S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A5SM-01A-12D-A28X-10 chr7:82791800 C>A maps to NM_033026.5 A36A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A7M5-01A-11D-A33Q-10 chr7:82582708 T>A maps to NM_033026.5 P2520P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr7:82764679 A>T maps to NM_033026.5 L729*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A2QR-01A-11D-A20W-10 chr8:52746161 T>C maps to NM_052937.2 G166G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EB-01A-11D-A12Z-10 chr20:5096122 T>C maps to NM_002592.2 T226T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A6M6-01A-11D-A32G-10 chr21:47856894 A>T maps to NM_006031.5 T3000T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75E-01A-11D-A32G-10 chr14:71444964 G>A maps to NM_014982.2 E637E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7II-01A-11D-A33K-10 chr11:65394884 G>A maps to NM_032223.2 A1178A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A7SF-01A-11D-A34Z-10 chr1:161254247 A>C maps to NM_001102566.1 R62R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr20:17410142 A>T maps to NM_002594.2 G228G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25Z-01A-11D-A16V-10 chr20:17208108 C>T maps to NM_002594.2 H53H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25W-01A-11D-A16V-10 chr19:1484036 C>T maps to NM_017573.3 A386A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr23:24597451 A>G did not map to a codon.
Sequencing variant TCGA-DD-A1EL-01A-11D-A152-10 chr17:79864759 C>A maps to NM_001184917.1 R202R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A9-01A-11D-A25V-10 chr1:186413278 G>T maps to ENST00000340129 I215I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11C-01A-11D-A12Z-10 chr10:105162877 C>T maps to NM_014976.1 L80L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3M9-01A-11D-A20W-10 chr9:5549464 C>A maps to NM_025239.3 T164T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IL-01A-11D-A33Q-10 chr19:34895343 C>G maps to NM_032346.1 A3A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BD-A3EP-01A-11D-A22F-10 chr10:112641039 T>C maps to NM_014456.4 A31A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A5SM-01A-12D-A28X-10 chr4:56458268 A>C did not map to a codon.
Sequencing variant TCGA-G3-A25U-01A-11D-A16V-10 chr11:773564 A>G maps to NM_182612.2 S104S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MB-01A-11D-A20W-10 chr6:165863851 T>C did not map to a codon.
Sequencing variant TCGA-RC-A7SK-01A-11D-A34Z-10 chr6:165801927 C>A maps to NM_001130690.1 L557L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MA-01A-11D-A33Q-10 chr6:165827144 C>T maps to NM_001130690.1 T374T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IK-01A-12D-A33Q-10 chr2:178769915 T>A did not map to a codon.
Sequencing variant TCGA-DD-A1ED-01A-11D-A152-10 chr12:54970384 G>A maps to NM_000924.3 V469V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K7-A6G5-01A-11D-A30V-10 chr12:20766492 C>A maps to NM_000921.3 A376A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CK-01A-11D-A20W-10 chr19:10531542 C>A maps to NM_001111307.1 R35R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A3R3-01A-11D-A22F-10 chr5:58511684 C>A maps to NM_001104631.1 E189*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5259-01A-31D-A20W-10 chr1:144923731 T>A maps to NM_014644.4 A242A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A5UD-01A-11D-A28X-10 chr1:144854657 T>A did not map to a codon.
Sequencing variant TCGA-DD-A1EA-01A-11D-A12Z-10 chr1:144915561 C>T maps to NM_014644.4 Q621Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73D-01A-12D-A32G-10 chr1:144868026 G>T maps to NM_014644.4 Y1804*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CK-01A-11D-A20W-10 chr1:144921894 A>G maps to NM_014644.4 F378F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr17:79618687 T>C maps to ENST00000331056 E108E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MB-01A-11D-A20W-10 chr8:66636574 T>C maps to ENST00000401827 K359K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A118-01A-11D-A12Z-10 chr15:85660889 T>A maps to NM_002605.2 G518G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MD-01A-12D-A34Z-10 chr15:85664188 G>A maps to NM_002605.2 L632L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MA-01A-11D-A33Q-10 chr5:76633095 G>C maps to NM_003719.3 L251L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QA-A7B7-01A-11D-A32G-10 chr21:44117596 C>T maps to NM_001001570.1 H97H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10Y-01A-11D-A12Z-10 chr7:550577 C>T maps to NM_002607.5 R107R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25Y-01A-11D-A16V-10 chr22:39621840 G>A maps to NM_002608.2 Q205*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EB-01A-11D-A12Z-10 chr11:103870888 G>A maps to NM_025208.4 Y73Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A9-01A-11D-A25V-10 chr23:19371269 C>T did not map to a codon.
Sequencing variant TCGA-MI-A75G-01A-11D-A32G-10 chr23:19367483 A>G did not map to a codon.
Sequencing variant TCGA-DD-A11D-01A-11D-A12Z-10 chr11:35016490 C>T maps to NM_003477.2 D426D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr16:333348 T>A maps to NM_006849.2 P60P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NF-01A-11D-A27I-10 chr7:148703055 C>T maps to NM_004911.4 K407K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BD-A3EP-01A-11D-A22F-10 chr3:122849446 C>A maps to NM_006810.3 V298V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr2:173423556 C>T maps to ENST00000392571 S106S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A116-01A-11D-A12Z-10 chr23:24549825 A>C did not map to a codon.
Sequencing variant TCGA-G3-A7M6-01A-11D-A33Q-10 chr23:24513000 G>C did not map to a codon.
Sequencing variant TCGA-EP-A3JL-01A-11D-A20W-10 chr7:95222150 G>A maps to NM_002612.3 V150V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A26S-01A-11D-A16V-10 chr16:66918396 A>G maps to NM_020786.2 E70E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NI-01A-11D-A27I-10 chr16:70170121 G>A maps to NM_017990.3 R341R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BW-A5NQ-01A-11D-A27I-10 chr4:39876001 T>A maps to NM_001100399.1 A728A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr4:39850469 C>T did not map to a codon.
Sequencing variant TCGA-KR-A7K2-01A-12D-A33Q-10 chr4:39905760 T>C maps to NM_001100399.1 K428K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A459-01A-11D-A25V-10 chr10:27024490 C>T maps to NM_014317.3 L337L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EB-01A-11D-A12Z-10 chr6:107475921 G>C maps to NM_020381.3 Y367*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5263-01A-01D-A12Z-10 chr16:15126796 A>T maps to NM_015027.2 K551*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11D-01A-11D-A12Z-10 chr16:15103554 G>A maps to NM_015027.2 E222E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr16:15127207 C>A maps to NM_015027.2 L588L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25Y-01A-11D-A16V-10 chr20:1963616 T>C maps to NM_024411.4 K38K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39Y-01A-11D-A20W-10 chr10:102777928 G>A maps to NM_001195263.1 D483D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75I-01A-11D-A32G-10 chr10:102783277 G>A maps to NM_001195263.1 L153L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5258-01A-01D-A12Z-10 chr10:119078451 T>C maps to NM_173791.3 A343A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A5W4-01A-11D-A28X-10 chr3:73433850 G>A maps to NM_015009.1 N622N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A217-01A-11D-A152-10 chr12:41967430 G>T maps to NM_001164595.1 L950L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A6UC-01A-21D-A33K-10 chr12:41949557 T>A maps to NM_001164595.1 L454*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CK-01A-11D-A20W-10 chr17:62407076 C>T did not map to a codon.
Sequencing variant TCGA-DD-A11D-01A-11D-A12Z-10 chr2:216930059 C>G maps to NM_018441.5 T133T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CK-01A-11D-A20W-10 chr2:216923625 T>A maps to NM_018441.5 P166P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr1:32101090 T>A maps to NM_012392.3 G19G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BD-A3EP-01A-11D-A22F-10 chr19:57334961 G>A maps to NM_006210.2 F160F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A2QQ-01A-11D-A22F-10 chr19:57326458 C>T maps to NM_006210.2 V1117V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MD-01A-12D-A34Z-10 chr19:57325651 C>T maps to NM_006210.2 R1386R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10Y-01A-11D-A12Z-10 chr14:56746413 A>G maps to NM_021255.2 Q76Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73E-01A-12D-A32G-10 chr8:57353831 T>C maps to NM_001135690.1 *268*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5258-01A-01D-A12Z-10 chr2:239167285 C>T did not map to a codon.
Sequencing variant TCGA-BW-A5NQ-01A-11D-A27I-10 chr1:7887613 A>G maps to ENST00000377532 P875P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EL-01A-11D-A152-10 chr1:7887220 A>G maps to ENST00000377532 K744K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr22:30975864 G>T maps to NM_014303.2 P409P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A7SK-01A-11D-A34Z-10 chr7:92122386 A>G maps to NM_000466.2 D1029D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LG-A6GG-01A-11D-A30V-10 chr8:77895733 A>T maps to NM_001172087.1 L227L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LG-A6GG-01A-11D-A30V-10 chr8:77895736 A>T maps to NM_001172087.1 P226P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr12:7344168 T>C maps to NM_001131023.1 P122P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25U-01A-11D-A16V-10 chr12:7343826 G>T maps to NM_001131023.1 V78V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A5SL-01A-11D-A27I-10 chr3:179592186 T>C maps to NM_016559.1 P218P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr6:42933449 G>A maps to NM_000287.3 R814*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NJ-01A-11D-A27I-10 chr23:54978365 T>G did not map to a codon.
Sequencing variant TCGA-FV-A495-01A-11D-A25V-10 chr23:54989779 C>T did not map to a codon.
Sequencing variant TCGA-LG-A6GG-01A-11D-A30V-10 chr23:54982654 A>C did not map to a codon.
Sequencing variant TCGA-DD-A1EF-01A-11D-A12Z-10 chr10:6258733 T>C maps to NM_004566.3 N144N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A459-01A-11D-A25V-10 chr10:3161000 G>A maps to NM_002627.3 E490E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr6:28268677 A>G maps to NM_032507.3 R349R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A113-01A-11D-A12Z-10 chr1:249211814 G>A maps to NM_170725.2 L344L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25V-01A-11D-A16V-10 chr1:249211484 C>T maps to NM_170725.2 N234N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A7M7-01A-12D-A34Z-10 chr1:249211311 C>T maps to NM_170725.2 Q177*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BW-A5NP-01A-11D-A27I-10 chr1:230468773 G>A maps to ENST00000321327 C393C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K7-A5RF-01A-11D-A28X-10 chr1:10468142 C>T maps to NM_002631.2 T155T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K7-A5RF-01A-11D-A28X-10 chr5:114572219 C>A did not map to a codon.
Sequencing variant TCGA-G3-A25V-01A-11D-A16V-10 chr19:17627037 C>A maps to NM_012088.2 P115P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-4073-01B-02D-A12Z-10 chr1:153279732 G>A maps to NM_052891.1 T22T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NN-01A-11D-A28X-10 chr1:153277441 G>T maps to NM_052891.1 A119A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MB-01A-11D-A20W-10 chr6:83889642 T>C maps to ENST00000416472 G305G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CK-01A-11D-A20W-10 chr6:83896733 T>C maps to ENST00000416472 Q178Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A216-01A-11D-A152-10 chr15:99512658 T>C maps to NM_001102612.2 A122A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A7SK-01A-11D-A34Z-10 chr15:99512763 C>A maps to NM_001102612.2 V87V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BW-A5NP-01A-11D-A27I-10 chr11:100996841 A>C maps to NM_000926.4 L562*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11D-01A-11D-A12Z-10 chr11:100998682 C>T maps to NM_000926.4 A373A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LG-A6GG-01A-11D-A30V-10 chr11:100999048 T>C maps to NM_000926.4 G251G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QA-A7B7-01A-11D-A32G-10 chr11:100998997 G>C maps to NM_000926.4 V268V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr6:13160508 T>C maps to NM_030948.1 Y163Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr20:58180074 C>G maps to NM_080672.3 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1ED-01A-11D-A152-10 chr20:58342289 C>A maps to NM_080672.3 L197L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NJ-01A-11D-A27I-10 chr20:58416547 G>A maps to NM_080672.3 R515R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73F-01A-11D-A32G-10 chr5:125944166 C>A maps to NM_032177.3 L274L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11B-01A-11D-A16Z-10 chr12:7078679 G>A maps to NM_001144831.1 S91S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11C-01A-11D-A12Z-10 chr1:33799861 G>A maps to ENST00000419414 T530T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr1:33836102 A>T maps to ENST00000419414 A165A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A6M3-01A-11D-A32G-10 chr3:169867032 C>G did not map to a codon.
Sequencing variant TCGA-DD-A4NF-01A-11D-A27I-10 chr23:22117126 G>A did not map to a codon.
Sequencing variant TCGA-G3-A25U-01A-11D-A16V-10 chr23:22196425 C>A did not map to a codon.
Sequencing variant TCGA-G3-A7M5-01A-11D-A33Q-10 chr23:22056645 A>C did not map to a codon.
Sequencing variant TCGA-ED-A7PZ-01A-11D-A33Q-10 chr6:170112535 T>A maps to NM_018288.3 S301S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A5SL-01A-11D-A27I-10 chr6:170112621 C>A maps to NM_018288.3 E273*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75E-01A-11D-A32G-10 chr6:170116082 G>A maps to NM_018288.3 Q171*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75H-01A-11D-A32G-10 chr6:170114881 G>T maps to NM_018288.3 V250V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39Y-01A-11D-A20W-10 chr13:50098317 A>G maps to NM_001040443.1 P245P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5262-01A-01D-A12Z-10 chr23:46844300 A>G did not map to a codon.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr9:123636995 T>C maps to NM_015651.1 P8P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NJ-01A-11D-A27I-10 chr9:96435948 C>T maps to NM_005392.3 L811L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11A-01A-11D-A12Z-10 chr11:45975167 T>C maps to ENST00000257821 K335K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EI-01A-11D-A12Z-10 chr22:45289354 G>A maps to NM_138415.3 S314S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5259-01A-31D-A20W-10 chr22:41863490 A>G maps to NM_032758.3 D68D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr23:133547941 A>G did not map to a codon.
Sequencing variant TCGA-G3-A5SJ-01A-11D-A27I-10 chr23:133527958 A>G did not map to a codon.
Sequencing variant TCGA-DD-A1EL-01A-11D-A152-10 chr23:54022183 T>C did not map to a codon.
Sequencing variant TCGA-DD-A3A4-01A-11D-A22F-10 chr23:54044137 A>C did not map to a codon.
Sequencing variant TCGA-DD-A4NF-01A-11D-A27I-10 chr23:54022131 C>T did not map to a codon.
Sequencing variant TCGA-HP-A5N0-01A-11D-A28X-10 chr23:54011483 G>A did not map to a codon.
Sequencing variant TCGA-DD-A3A8-01A-11D-A22F-10 chr1:120266058 G>C maps to NM_006623.3 L117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EB-01A-11D-A12Z-10 chr6:79688428 C>A did not map to a codon.
Sequencing variant TCGA-DD-A39Z-01A-11D-A20W-10 chr6:79692704 T>C maps to NM_017934.5 K889K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LG-A6GG-01A-11D-A30V-10 chr6:79688416 C>G maps to NM_017934.5 V927V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11D-01A-11D-A12Z-10 chr23:71855111 T>C did not map to a codon.
Sequencing variant TCGA-DD-A39Y-01A-11D-A20W-10 chr23:71873286 T>C did not map to a codon.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr23:71915636 C>T did not map to a codon.
Sequencing variant TCGA-BC-A10Q-01A-11D-A12Z-10 chr23:18919621 A>T did not map to a codon.
Sequencing variant TCGA-BC-A10R-01A-11D-A12Z-10 chr23:18972508 A>C did not map to a codon.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr16:47727354 A>T maps to NM_000293.2 R944R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K7-A5RG-01A-11D-A28X-10 chr16:30760207 A>T maps to NM_000294.2 K23*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr16:30764550 A>T did not map to a codon.
Sequencing variant TCGA-G3-A3CJ-01A-11D-A20W-10 chr11:118526375 C>T maps to NM_015157.2 Y1312Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr3:111604196 C>T maps to NM_001134438.1 L425L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A3KF-01A-11D-A20W-10 chr18:60563016 A>G maps to NM_194449.2 L739L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr2:170557708 A>T maps to NM_001008489.3 P76P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73G-01A-22D-A32G-10 chr11:606502 C>T maps to ENST00000264555 L506L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A26S-01A-11D-A16V-10 chr11:609442 A>G maps to ENST00000264555 E1329E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A5SJ-01A-11D-A27I-10 chr11:587379 C>A maps to ENST00000264555 L112L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A7SF-01A-11D-A34Z-10 chr11:592653 C>G maps to ENST00000264555 L200L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A3R2-01A-11D-A22F-10 chr1:114255974 G>A maps to NM_006608.2 Q237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A12J-01A-11D-A12Z-10 chr7:77569479 C>A maps to ENST00000427986 S534*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr7:77567112 A>T maps to ENST00000427986 A475A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A6M4-01A-11D-A32G-10 chr20:43804640 T>G maps to NM_002638.3 P73P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11A-01A-11D-A12Z-10 chr22:21174844 A>G maps to NM_058004.2 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A4ZP-01A-12D-A25V-10 chr22:21153476 G>A maps to NM_058004.2 P578P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CK-01A-11D-A20W-10 chr1:151280252 C>A maps to NM_002651.2 E339*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A7PZ-01A-11D-A33Q-10 chr18:44408007 T>G maps to NM_004671.2 I474I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A112-01A-11D-A12Z-10 chr19:4037689 C>T maps to NM_015897.2 G450G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5264-01A-01D-A12Z-10 chr13:73369661 T>C maps to NM_006346.2 P173P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5260-01A-01D-A12Z-10 chr11:85712083 A>G maps to ENST00000393343 A337A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11B-01A-11D-A16Z-10 chr1:172413126 C>A did not map to a codon.
Sequencing variant TCGA-BC-A10Y-01A-11D-A12Z-10 chr2:46839476 T>A maps to NM_002643.3 A109A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A110-01A-11D-A12Z-10 chr9:35093207 T>C did not map to a codon.
Sequencing variant TCGA-DD-A3A8-01A-11D-A22F-10 chr1:207103701 G>A maps to NM_002644.3 T752T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NI-01A-11D-A27I-10 chr11:17141376 C>T maps to NM_002645.2 W934*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73G-01A-22D-A32G-10 chr11:17191174 A>G maps to NM_002645.2 A38A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73F-01A-11D-A32G-10 chr1:204393999 G>A maps to NM_002646.3 R1629*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75G-01A-11D-A32G-10 chr1:204429746 G>C maps to NM_002646.3 R451R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1ED-01A-11D-A152-10 chr3:178943816 T>C maps to NM_006218.2 G828G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A7XP-01A-11D-A34Z-10 chr7:106545718 A>T maps to NM_002649.2 K1066*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K7-A5RG-01A-11D-A28X-10 chr19:18279668 G>T maps to NM_005027.2 E648*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10W-01A-11D-A12Z-10 chr3:130435260 A>G maps to NM_014602.2 L770L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MA-01A-11D-A20W-10 chr3:130449232 A>G maps to NM_014602.2 L502L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A23B-01A-11D-A16V-10 chr17:8790505 G>T maps to NM_001142633.1 T604T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5261-01A-01D-A12Z-10 chr2:209190042 C>T maps to NM_015040.3 G836G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25T-01A-11D-A16V-10 chr2:209203239 G>T maps to NM_015040.3 A1540A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A5SJ-01A-11D-A27I-10 chr2:209190270 C>T maps to NM_015040.3 P912P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RG-A7D4-01A-12D-A33Q-10 chr2:209218740 A>G maps to NM_015040.3 L1988L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A5UD-01A-11D-A28X-10 chr7:99987595 C>G maps to NM_013439.2 V180V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A5W4-01A-11D-A28X-10 chr23:71401593 C>A did not map to a codon.
Sequencing variant TCGA-FV-A3I1-01A-11D-A22F-10 chr23:71417257 C>A did not map to a codon.
Sequencing variant TCGA-RC-A6M4-01A-11D-A32G-10 chr10:22829004 T>A did not map to a codon.
Sequencing variant TCGA-K7-A5RG-01A-11D-A28X-10 chr17:36955560 G>A maps to NM_003559.4 S39S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr12:57989717 T>C maps to NM_024779.4 G139G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A496-01A-11D-A25V-10 chr12:57985225 C>T maps to NM_024779.4 L52L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5259-01A-31D-A20W-10 chr9:71491628 A>T maps to NM_003558.2 P79P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NR-01A-11D-A30V-10 chr11:67261259 G>T maps to NM_004910.2 G1019G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-O8-A75V-01A-11D-A32G-10 chr11:67266191 C>T maps to NM_004910.2 V453V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10Z-01A-11D-A12Z-10 chr12:123497235 G>A maps to NM_020845.2 T113T. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-T1-A6J8-01A-11D-A32G-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-BC-A216-01A-11D-A152-10 chr12:130834406 C>T maps to NM_004764.4 N313N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A118-01A-11D-A12Z-10 chr12:130830385 A>G maps to NM_004764.4 T93T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5259-01A-31D-A20W-10 chr8:22146164 T>C maps to NM_001135721.1 N324N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A496-01A-11D-A25V-10 chr8:22136991 T>G maps to NM_001135721.1 A31A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IG-01A-11D-A33K-10 chr11:94316705 C>A maps to NM_152431.2 C202*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr11:94354058 A>T maps to NM_152431.2 P820P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CI-01A-11D-A20W-10 chr16:2162835 T>C maps to NM_001009944.2 A1038A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A3KF-01A-11D-A20W-10 chr7:47873951 T>C maps to NM_138295.3 A2053A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A5UC-01A-11D-A28X-10 chr7:47886598 A>C maps to NM_138295.3 A1677A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr7:47947752 G>T maps to NM_138295.3 A441A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LG-A6GG-01A-11D-A30V-10 chr7:47886592 T>A maps to NM_138295.3 A1679A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr7:47970704 T>A maps to NM_138295.3 R245*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A9-01A-11D-A25V-10 chr6:51917940 G>A maps to NM_138694.3 L691L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr6:51491879 A>T maps to NM_138694.3 T3900T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NF-01A-11D-A27I-10 chr8:110393731 A>G maps to ENST00000426474 T99T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A495-01A-11D-A25V-10 chr8:110539188 G>T maps to ENST00000426474 G4222*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25Y-01A-11D-A16V-10 chr8:110495216 G>A maps to ENST00000426474 G3153G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73E-01A-12D-A32G-10 chr6:123039082 A>G maps to ENST00000368446 K57K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5264-01A-01D-A12Z-10 chr9:131476849 G>A maps to NM_013355.3 L497L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MB-01A-11D-A20W-10 chr9:131469011 T>C maps to NM_013355.3 A144A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10Q-01A-11D-A12Z-10 chr21:44450021 G>A maps to NM_004571.3 T374T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr21:44430255 A>G maps to NM_004571.3 V91V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10T-01A-11D-A12Z-10 chr11:125237752 C>T maps to NM_022062.2 T33T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A4ZP-01A-12D-A25V-10 chr1:201291110 G>A maps to NM_000299.3 V472V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr12:33031342 C>T maps to NM_004572.3 E157E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CJ-01A-11D-A20W-10 chr11:397013 G>A maps to NM_007183.2 G171G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BD-A3EP-01A-11D-A22F-10 chr2:159481872 C>T maps to NM_003628.3 Q363*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K7-A5RG-01A-11D-A28X-10 chr11:63365557 T>C maps to NM_001128203.1 G31G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A217-01A-11D-A152-10 chr22:31533848 T>A maps to NM_015715.3 K305*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A5SL-01A-11D-A27I-10 chr1:186948507 A>G maps to NM_024420.2 P674P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25V-01A-11D-A16V-10 chr15:42364566 T>C maps to NM_178034.3 G447G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr15:42364509 A>G maps to NM_178034.3 N466N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MC-01A-11D-A33Q-10 chr15:42378518 A>G maps to NM_178034.3 Y93Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RG-A7D4-01A-12D-A33Q-10 chr15:42298316 G>A maps to NM_001080490.1 N103N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MD-01A-12D-A34Z-10 chr15:42280319 C>A maps to NM_001080490.1 L557L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A2QQ-01A-11D-A22F-10 chr15:42436337 T>A maps to ENST00000397272 T662T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25S-01A-11D-A16V-10 chr22:38508272 C>T maps to NM_003560.2 E772E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75I-01A-11D-A32G-10 chr6:46682255 A>T maps to NM_001168357.1 P137P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A3KF-01A-11D-A20W-10 chr2:160879269 A>G maps to NM_007366.4 H400H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A7-01A-11D-A22F-10 chr2:160833797 T>G maps to NM_007366.4 R800R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25T-01A-11D-A16V-10 chr2:160804062 T>C maps to NM_007366.4 R1239R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A7SK-01A-11D-A34Z-10 chr2:160808015 A>T maps to NM_007366.4 T1125T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A3KF-01A-11D-A20W-10 chr9:26905634 A>G maps to NM_001031689.2 S754S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EB-01A-11D-A12Z-10 chr9:26923263 C>A maps to NM_001031689.2 L317L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr23:133700149 G>A did not map to a codon.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr23:133700329 C>A did not map to a codon.
Sequencing variant TCGA-BW-A5NP-01A-11D-A27I-10 chr10:75673402 C>T maps to NM_002658.3 N189N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A3I0-01A-11D-A22F-10 chr2:28825785 C>T maps to NM_153021.4 A924A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A7M5-01A-11D-A33Q-10 chr2:28752184 C>A maps to NM_153021.4 V109V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A2QQ-01A-11D-A22F-10 chr15:40585895 G>A maps to NM_004573.2 R697R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A7SB-01A-21D-A34Z-10 chr15:40584570 C>T maps to NM_004573.2 E800E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A9-01A-11D-A25V-10 chr11:64029999 G>A maps to NM_000932.2 V720V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A459-01A-11D-A25V-10 chr11:64023033 A>T maps to NM_000932.2 A181A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr20:9352960 T>A maps to NM_001172646.1 I199I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EA-01A-11D-A12Z-10 chr20:9319626 A>C maps to NM_001172646.1 T104T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K7-A6G5-01A-11D-A30V-10 chr20:9449314 G>T maps to NM_001172646.1 E1116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr20:9449298 G>A maps to NM_001172646.1 K1110K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7II-01A-11D-A33K-10 chr17:43196347 C>A maps to NM_133373.3 R249R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A9-01A-11D-A25V-10 chr10:95791759 G>A maps to ENST00000371380 K319K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A112-01A-11D-A12Z-10 chr20:39794968 C>T maps to NM_002660.2 R645R. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-UB-A7MB-01A-11D-A33Q-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-FV-A23B-01A-11D-A16V-10 chr2:198950751 G>A maps to NM_006226.3 E837E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr3:111394181 C>A maps to ENST00000312791 V30V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EB-01A-11D-A12Z-10 chr5:41381971 C>T maps to NM_001005473.2 V256V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr17:4712847 T>C did not map to a codon.
Sequencing variant TCGA-RC-A7SB-01A-21D-A34Z-10 chr19:40872765 C>T maps to NM_012268.2 G63G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25S-01A-11D-A16V-10 chr1:242451666 A>T maps to NM_152666.2 C164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LG-A6GG-01A-11D-A30V-10 chr1:242264075 A>G maps to NM_152666.2 F416F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IK-01A-12D-A33Q-10 chr8:145001889 G>A maps to NM_201380.2 A1285A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr8:144996710 G>T maps to NM_201380.2 L2599L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25W-01A-11D-A16V-10 chr2:68607904 A>G maps to NM_002664.2 A83A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75C-01A-11D-A32G-10 chr12:19436366 A>G maps to ENST00000429027 T489T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BW-A5NQ-01A-11D-A27I-10 chr1:204197268 C>A maps to ENST00000367191 R1011R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A7M8-01A-11D-A33Q-10 chr1:204214796 C>A maps to ENST00000367191 E680*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75I-01A-11D-A32G-10 chr1:204210870 G>A maps to ENST00000367191 I768I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CJ-01A-11D-A20W-10 chr2:131884341 A>G maps to ENST00000409158 E92E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr6:151152097 A>G maps to NM_001029884.1 T617T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A6M4-01A-11D-A32G-10 chr16:67320229 T>C maps to NM_001129729.1 D832D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr16:67322136 G>A maps to NM_001129729.1 S1096S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7II-01A-11D-A33K-10 chr5:143612 C>A maps to NM_052909.3 I246I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NB-01A-12D-A25V-10 chr5:161902 C>T maps to NM_052909.3 S475S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10U-01A-11D-A12Z-10 chr12:93148008 C>G maps to NM_001004330.2 Y153*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1E9-01A-21D-A152-10 chr14:68038987 G>A maps to NM_020715.2 L574L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25U-01A-11D-A16V-10 chr2:43919651 G>T did not map to a codon.
Sequencing variant TCGA-CC-A5UC-01A-11D-A28X-10 chr1:16060356 C>T maps to ENST00000420314 S1099S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A217-01A-11D-A152-10 chr1:150131672 C>G maps to ENST00000443480 L426L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A9-01A-11D-A25V-10 chr6:161137784 C>T maps to NM_000301.3 I259I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A5SK-01A-11D-A27I-10 chr6:161139736 A>G maps to NM_000301.3 E321E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr6:161160114 A>G maps to NM_000301.3 S631S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A23B-01A-11D-A16V-10 chr9:19126217 A>G maps to NM_001122.2 Y40Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5261-01A-01D-A12Z-10 chr19:4517617 G>A maps to NM_001080400.1 A33A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IK-01A-12D-A33Q-10 chr19:4511837 T>A maps to NM_001080400.1 K698*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A4XI-01A-11D-A25V-10 chr20:21213369 A>T did not map to a codon.
Sequencing variant TCGA-FV-A3I1-01A-11D-A22F-10 chr20:21142903 T>A maps to NM_018474.4 S266S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A0-01A-11D-A20W-10 chr5:57753127 C>T maps to NM_006622.2 R296R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CK-01A-11D-A20W-10 chr5:57752799 T>C maps to NM_006622.2 K376K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr5:57750785 T>A maps to NM_006622.2 L606L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A23B-01A-11D-A16V-10 chr1:12027090 T>C maps to ENST00000376369 C613C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A116-01A-11D-A12Z-10 chr23:103041517 A>G did not map to a codon.
Sequencing variant TCGA-NI-A4U2-01A-11D-A28X-10 chr23:103042815 G>T did not map to a codon.
Sequencing variant TCGA-BC-A10R-01A-11D-A12Z-10 chr3:142388292 C>T maps to NM_001172312.1 S44S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10W-01A-11D-A12Z-10 chr3:126739123 G>T maps to NM_032242.3 R1325R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11D-01A-11D-A12Z-10 chr3:126708419 G>A maps to NM_032242.3 L328L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A12J-01A-11D-A12Z-10 chr3:126733601 C>A maps to NM_032242.3 A935A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25S-01A-11D-A16V-10 chr3:126737195 G>T maps to NM_032242.3 L1240L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A7M5-01A-11D-A33Q-10 chr1:208252775 T>A maps to NM_025179.3 A805A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75I-01A-11D-A32G-10 chr23:153698840 C>A did not map to a codon.
Sequencing variant TCGA-CC-A3MC-01A-11D-A22F-10 chr7:131925876 C>A maps to NM_020911.1 E518*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr7:131908375 T>C maps to NM_020911.1 P669P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A5KG-01A-11D-A27I-10 chr7:132193185 G>A maps to NM_020911.1 D89D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A5SJ-01A-11D-A27I-10 chr7:131910918 C>T did not map to a codon.
Sequencing variant TCGA-G3-A6UC-01A-21D-A33K-10 chr7:131829963 G>T maps to NM_020911.1 I1713I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IK-01A-12D-A33Q-10 chr3:48455149 T>A maps to NM_001130082.1 A1488A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr3:48465276 T>C maps to NM_001130082.1 V248V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr22:50720690 C>T maps to NM_012401.2 R1013R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10U-01A-11D-A12Z-10 chr23:153039046 A>G did not map to a codon.
Sequencing variant TCGA-DD-A4NJ-01A-11D-A27I-10 chr23:153034489 G>A did not map to a codon.
Sequencing variant TCGA-EP-A26S-01A-11D-A16V-10 chr23:153039371 T>A did not map to a codon.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr23:153032891 G>T did not map to a codon.
Sequencing variant TCGA-G3-A5SM-01A-12D-A28X-10 chr23:153035891 C>A did not map to a codon.
Sequencing variant TCGA-G3-A5SM-01A-12D-A28X-10 chr23:153042727 G>A did not map to a codon.
Sequencing variant TCGA-DD-A11A-01A-11D-A12Z-10 chr3:129303387 G>A maps to NM_015103.2 I623I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1E9-01A-21D-A152-10 chr3:129286592 C>A maps to NM_015103.2 T1307T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10U-01A-11D-A12Z-10 chr20:56227216 C>A maps to NM_020182.3 P252P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10Z-01A-11D-A12Z-10 chr20:56227369 C>T maps to NM_020182.3 R201R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A5UD-01A-11D-A28X-10 chr20:56227156 T>A maps to NM_020182.3 A272A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr20:56228120 C>A maps to NM_020182.3 E96*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3M9-01A-11D-A20W-10 chr8:82357105 G>C maps to NM_002677.3 S64S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A4XI-01A-11D-A25V-10 chr9:139313080 C>G maps to NM_015160.1 P355P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A0-01A-11D-A20W-10 chr6:160241521 G>A maps to NM_173516.1 A512A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10W-01A-11D-A12Z-10 chr10:118310665 C>T maps to NM_000936.2 S127S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7ME-01A-11D-A33K-10 chr10:118202640 A>T maps to NM_001011709.2 I93I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11A-01A-11D-A12Z-10 chr23:152226797 C>T did not map to a codon.
Sequencing variant TCGA-EP-A12J-01A-11D-A12Z-10 chr23:152225434 A>G did not map to a codon.
Sequencing variant TCGA-ED-A459-01A-11D-A25V-10 chr23:152159794 A>T did not map to a codon.
Sequencing variant TCGA-GJ-A6C0-01A-12D-A30V-10 chr19:46973077 A>T maps to NM_018215.3 P405P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr6:36238347 C>T maps to ENST00000457797 L38L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A5UC-01A-11D-A28X-10 chr22:44328954 C>T maps to NM_025225.2 P228P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A7SB-01A-21D-A34Z-10 chr23:7889812 C>A did not map to a codon.
Sequencing variant TCGA-DD-A4NS-01A-11D-A30V-10 chr19:7615935 G>A maps to NM_001166111.1 T718T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IJ-01A-11D-A33Q-10 chr7:108113027 A>G maps to NM_015723.2 S722S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A26S-01A-11D-A16V-10 chr7:108131856 A>T maps to NM_015723.2 P560P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39Z-01A-11D-A20W-10 chr2:55906856 A>G maps to NM_033109.3 T213T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr2:55910943 T>A maps to NM_033109.3 P143P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MC-01A-11D-A33Q-10 chr5:74998429 C>T maps to NM_001099271.1 K171K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73G-01A-22D-A32G-10 chr23:84562233 C>A did not map to a codon.
Sequencing variant TCGA-RC-A6M6-01A-11D-A32G-10 chr23:84561302 A>G did not map to a codon.
Sequencing variant TCGA-CC-5261-01A-01D-A12Z-10 chr23:24741359 G>A did not map to a codon.
Sequencing variant TCGA-DD-A3A2-01A-11D-A20W-10 chr23:24744102 G>T did not map to a codon.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr19:50921164 C>T maps to ENST00000391817 L1121L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10Y-01A-11D-A12Z-10 chr14:50140882 A>G maps to NM_002692.3 D125D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr6:43555152 A>T maps to NM_006502.2 A139A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A2-01A-11D-A20W-10 chr5:74872758 G>C did not map to a codon.
Sequencing variant TCGA-G3-A25W-01A-11D-A16V-10 chr5:74892707 T>C maps to NM_016218.2 S730S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr3:121208147 C>T maps to ENST00000393672 Q1346Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr3:121263592 T>G maps to ENST00000393672 G241G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NV-01A-11D-A30V-10 chr4:57889911 C>T maps to NM_000938.1 Q951*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A7PZ-01A-11D-A33Q-10 chr4:57873095 A>T maps to NM_000938.1 L444L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11D-01A-11D-A12Z-10 chr11:62532652 G>T did not map to a codon.
Sequencing variant TCGA-CC-A7II-01A-11D-A33K-10 chr8:22105779 G>T maps to NM_001722.2 E159*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MD-01A-12D-A34Z-10 chr20:18464199 T>C maps to NM_006466.2 *317Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-4073-01B-02D-A12Z-10 chr19:621783 C>A maps to NM_005035.3 T638T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A113-01A-11D-A12Z-10 chr7:53104218 C>T maps to NM_182595.3 L285L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25Z-01A-11D-A16V-10 chr13:29242665 A>G maps to NM_015932.5 L73L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EB-01A-11D-A12Z-10 chr14:77751295 T>A maps to NM_013382.5 K525*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr14:77746806 C>A did not map to a codon.
Sequencing variant TCGA-CC-5262-01A-01D-A12Z-10 chr7:94947701 T>G maps to NM_000446.5 T26T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr8:99170219 G>T maps to NM_015029.2 A932A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A69H-01A-11D-A30V-10 chr23:48375572 C>T did not map to a codon.
Sequencing variant TCGA-BC-A112-01A-11D-A12Z-10 chr7:124464093 T>C maps to NM_015450.2 S609S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10U-01A-11D-A12Z-10 chr18:14542728 A>G maps to ENST00000444806 D139D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75H-01A-11D-A32G-10 chr18:14511959 G>A maps to ENST00000444806 L522L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A7S9-01A-11D-A33Q-10 chr18:14537871 A>G maps to ENST00000444806 A246A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73G-01A-22D-A32G-10 chr2:131976217 C>A maps to NM_001083538.1 G81G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A7M5-01A-11D-A33Q-10 chr14:19553602 A>T maps to NM_001005356.2 K63*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A7M5-01A-11D-A33Q-10 chr14:20020033 T>A maps to ENST00000439503 K63*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A69H-01A-11D-A30V-10 chr1:167384896 T>C maps to NM_002697.3 S717S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr23:82764126 C>A did not map to a codon.
Sequencing variant TCGA-DD-A4NV-01A-11D-A30V-10 chr23:82763683 C>T did not map to a codon.
Sequencing variant TCGA-RC-A6M4-01A-11D-A32G-10 chr23:82764108 G>T did not map to a codon.
Sequencing variant TCGA-DD-A73A-01A-12D-A32G-10 chr4:147561764 G>A maps to NM_004575.2 K345K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73F-01A-11D-A32G-10 chr8:128428641 G>A maps to NM_001159542.1 K177K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CJ-01A-11D-A20W-10 chr10:71969337 C>A maps to NM_021129.3 A205A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CI-01A-11D-A20W-10 chr1:56989986 G>A maps to NM_003713.4 Y179Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr23:18797262 G>T did not map to a codon.
Sequencing variant TCGA-G3-A25U-01A-11D-A16V-10 chr4:76809469 A>G maps to NM_006239.2 A143A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39V-01A-11D-A20W-10 chr1:203037704 C>T maps to ENST00000367238 F1070F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr12:27832960 T>A maps to NM_003622.3 L621*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11A-01A-11D-A12Z-10 chr6:36823792 T>C maps to NM_016059.4 A99A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A7M7-01A-12D-A34Z-10 chr22:22049305 G>A maps to NM_148175.2 Q471Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A2QR-01A-11D-A20W-10 chr6:149867087 G>A maps to NM_139126.2 T18T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25Z-01A-11D-A16V-10 chr16:4943554 G>T maps to NM_002705.4 T493T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IL-01A-11D-A33Q-10 chr22:22277761 C>T maps to NM_014634.3 L356L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5258-01A-01D-A12Z-10 chr12:63087750 A>G maps to NM_020700.1 L368L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A3RK-01A-11D-A22F-10 chr12:63195712 G>A maps to NM_020700.1 R213R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A23B-01A-11D-A16V-10 chr12:63083508 G>A maps to NM_020700.1 Y405Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A116-01A-11D-A12Z-10 chr12:111162540 C>T maps to NM_002710.2 W149*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MB-01A-11D-A20W-10 chr12:80191130 T>C maps to NM_001143885.1 G712G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A4XI-01A-11D-A25V-10 chr12:80199548 C>T did not map to a codon.
Sequencing variant TCGA-CC-5263-01A-01D-A12Z-10 chr19:55606962 T>C maps to NM_017607.2 E412E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25S-01A-11D-A16V-10 chr14:104204198 T>C did not map to a codon.
Sequencing variant TCGA-KR-A7K8-01A-11D-A33K-10 chr15:41120818 A>C maps to NM_001130143.1 A7A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11C-01A-11D-A12Z-10 chr12:54975805 T>C maps to NM_006741.3 P119P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A6UC-01A-21D-A33K-10 chr7:113558466 A>T maps to NM_002711.3 V195V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr7:113519016 G>T maps to NM_002711.3 C710*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr7:113520087 T>A maps to NM_002711.3 A353A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5259-01A-31D-A20W-10 chr23:49126932 C>T did not map to a codon.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr23:49143176 A>G did not map to a codon.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr7:94540282 T>C maps to NM_001166160.1 S286S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25U-01A-11D-A16V-10 chr8:30643818 G>A maps to NM_001009552.1 Q288*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11A-01A-11D-A12Z-10 chr11:111624196 T>C maps to NM_181699.2 L378L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KR-A7K0-01A-12D-A33Q-10 chr11:111636081 T>C maps to NM_181699.2 L47L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A3R2-01A-11D-A22F-10 chr5:146077623 C>T maps to ENST00000394414 K150K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IJ-01A-11D-A33Q-10 chr3:135721146 T>C maps to NM_002718.4 D269D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A0-01A-11D-A20W-10 chr3:135721002 T>C maps to NM_002718.4 D221D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EG-01A-11D-A20W-10 chr14:102349776 G>A maps to NM_002719.3 E169E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11C-01A-11D-A12Z-10 chr6:42975773 C>T maps to NM_006245.2 I276I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IK-01A-12D-A33Q-10 chr14:63860612 T>C maps to ENST00000422769 A324A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A26S-01A-11D-A16V-10 chr14:63858559 C>T maps to ENST00000422769 W376*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MB-01A-11D-A20W-10 chr8:22333118 A>G maps to ENST00000397775 R118R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr18:9557374 T>C maps to NM_001042388.1 K678K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A5-01A-11D-A22F-10 chr14:94697003 G>A maps to NM_058237.1 V125V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr14:94716579 A>G maps to NM_058237.1 E561E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A3RK-01A-11D-A22F-10 chr19:46890687 G>A maps to NM_006247.2 R371R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A2QQ-01A-11D-A22F-10 chr19:46857047 C>T maps to NM_006247.2 I55I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IK-01A-12D-A33Q-10 chr9:127920662 T>A did not map to a codon.
Sequencing variant TCGA-HP-A5N0-01A-11D-A28X-10 chr10:103909722 C>T maps to NM_015062.3 S1644S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KR-A7K0-01A-12D-A33Q-10 chr1:40539786 A>G maps to ENST00000372783 H318H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CH-01A-11D-A22F-10 chr6:32130606 G>A maps to NM_138717.1 G269G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25T-01A-11D-A16V-10 chr18:77710728 G>A maps to NM_025078.4 L66L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A5SL-01A-11D-A27I-10 chr2:11300639 G>C maps to NM_152391.3 L64L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A7PZ-01A-11D-A33Q-10 chr23:48931535 G>T did not map to a codon.
Sequencing variant TCGA-UB-A7MD-01A-12D-A34Z-10 chr22:22892515 G>A maps to NM_206954.1 L195L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr1:12921327 G>C maps to NM_023014.1 L373L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EF-01A-11D-A12Z-10 chr1:12943155 T>C maps to NM_001009611.2 L20L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr12:11546399 T>A maps to NM_006248.3 P204P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A0-01A-11D-A20W-10 chr6:106553018 C>T maps to NM_001198.3 P328P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LG-A6GG-01A-11D-A30V-10 chr6:106553642 A>T maps to NM_001198.3 A536A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RG-A7D4-01A-12D-A33Q-10 chr6:106552730 C>T maps to NM_001198.3 S232S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NE-01A-11D-A27I-10 chr6:100062538 T>C maps to ENST00000359773 P686P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NI-A4U2-01A-11D-A28X-10 chr8:70981669 C>T maps to NM_024504.2 P142P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A7-01A-11D-A22F-10 chr21:43241420 A>C did not map to a codon.
Sequencing variant TCGA-EP-A26S-01A-11D-A16V-10 chr21:43291639 C>T maps to NM_022115.3 A168A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A5SL-01A-11D-A27I-10 chr21:43221870 G>A maps to NM_022115.3 T1351T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75G-01A-11D-A32G-10 chr21:43248678 C>A maps to NM_022115.3 T825T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25W-01A-11D-A16V-10 chr1:3350305 G>A maps to NM_022114.3 L1254L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IK-01A-12D-A33Q-10 chr1:14108237 A>T maps to NM_012231.4 T1316T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A3-01A-11D-A22F-10 chr1:14108627 G>A maps to NM_012231.4 L1446L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A7-01A-11D-A22F-10 chr4:121737606 C>A did not map to a codon.
Sequencing variant TCGA-G3-A6UC-01A-21D-A33K-10 chr4:81123281 C>A maps to NM_001099403.1 G222G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K7-A6G5-01A-11D-A30V-10 chr5:23526528 A>G maps to NM_020227.2 P444P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11D-01A-11D-A12Z-10 chr1:45977036 G>A maps to NM_181697.1 V188V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LG-A6GG-01A-11D-A30V-10 chr23:23693212 C>G did not map to a codon.
Sequencing variant TCGA-DD-A4NJ-01A-11D-A27I-10 chr5:176732981 C>G maps to NM_013237.2 V143V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A2-01A-11D-A20W-10 chr5:145176019 T>G maps to NM_182960.2 R165R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IK-01A-12D-A33Q-10 chr20:47296239 G>A maps to NM_020820.3 Y496Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A116-01A-11D-A12Z-10 chr8:68939467 G>T maps to NM_024870.2 L151L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11D-01A-11D-A12Z-10 chr8:69104676 G>A maps to NM_024870.2 G1507G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A7XO-01A-11D-A34Z-10 chr8:68864763 G>T maps to NM_024870.2 L45L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5262-01A-01D-A12Z-10 chr10:72358775 G>T maps to NM_005041.4 S234*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HP-A5N0-01A-11D-A28X-10 chr10:72357967 A>G maps to NM_005041.4 S503S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A7S9-01A-11D-A33Q-10 chr10:72358909 C>T maps to NM_005041.4 L189L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A3JL-01A-11D-A20W-10 chr1:186277379 T>A maps to NM_005807.3 A843A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A3JL-01A-11D-A20W-10 chr1:186277382 A>C maps to NM_005807.3 P844P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A459-01A-11D-A25V-10 chr12:11036771 T>A maps to NM_006250.2 S15S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11A-01A-11D-A12Z-10 chr3:64084857 G>T maps to NM_198859.3 R802R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10R-01A-11D-A12Z-10 chr23:49032069 G>A did not map to a codon.
Sequencing variant TCGA-ED-A7PX-01A-51D-A34Z-10 chr14:94245605 G>A maps to NM_178013.3 R49*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BW-A5NO-01A-11D-A27I-10 chr1:57173334 C>A maps to NM_006252.3 T536T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5260-01A-01D-A12Z-10 chr1:57161706 G>A maps to NM_006252.3 T221T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NS-01A-11D-A30V-10 chr19:14208611 C>T maps to NM_002730.3 P170P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A3KG-01A-11D-A20W-10 chr7:151372541 T>C maps to NM_016203.3 P216P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75G-01A-11D-A32G-10 chr7:151254298 T>C maps to NM_016203.3 T566T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73B-01A-12D-A32G-10 chr2:219688556 G>A maps to NM_017431.2 G466G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11A-01A-11D-A12Z-10 chr11:6340704 C>T maps to NM_145040.2 L158L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A6M6-01A-11D-A32G-10 chr2:45879476 G>T maps to NM_005400.2 E80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25W-01A-11D-A16V-10 chr19:54403528 T>C maps to NM_002739.3 L442L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr19:54401218 C>A maps to NM_002739.3 R316R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr14:61920070 G>T maps to NM_006255.3 S320S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A114-01A-11D-A12Z-10 chr10:6470192 G>T maps to NM_006257.2 P699P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A7SF-01A-11D-A34Z-10 chr10:6521124 G>T maps to NM_006257.2 V394V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7II-01A-11D-A33K-10 chr14:30100158 G>A maps to NM_002742.2 A487A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A216-01A-11D-A152-10 chr8:48856411 C>A did not map to a codon.
Sequencing variant TCGA-CC-5259-01A-31D-A20W-10 chr8:48815177 T>A maps to NM_006904.6 K1074*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CK-01A-11D-A20W-10 chr8:48856411 C>A did not map to a codon.
Sequencing variant TCGA-GJ-A6C0-01A-12D-A30V-10 chr8:48732068 A>G maps to NM_006904.6 N3112N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75I-01A-11D-A32G-10 chr8:48715983 T>G maps to NM_006904.6 R3268R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RG-A7D4-01A-12D-A33Q-10 chr8:48794655 C>T maps to NM_006904.6 V1592V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10Z-01A-11D-A12Z-10 chr10:54048600 C>T maps to NM_001098512.1 L594L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A7SF-01A-11D-A34Z-10 chr11:76063482 C>T maps to NM_004705.2 Q237Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T1-A6J8-01A-11D-A32G-10 chr23:3533925 G>T did not map to a codon.
Sequencing variant TCGA-CC-A3MC-01A-11D-A22F-10 chr19:50187271 C>A maps to NM_001536.3 C167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10W-01A-11D-A12Z-10 chr4:148563936 C>T did not map to a codon.
Sequencing variant TCGA-DD-A3A0-01A-11D-A20W-10 chr4:148559832 T>C maps to NM_138364.2 E796E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A1-01A-11D-A20W-10 chr11:20409580 G>T maps to NM_005788.3 V15V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MC-01A-11D-A33Q-10 chr20:4680288 C>T maps to NM_001080123.1 F141F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-4073-01B-02D-A12Z-10 chr17:27038627 G>T maps to ENST00000415329 T17T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IG-01A-11D-A33K-10 chr19:36297612 C>A maps to NM_021232.1 G342G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25U-01A-11D-A16V-10 chr2:68882572 C>A maps to NM_138964.2 T349T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A3KF-01A-11D-A20W-10 chr4:71275488 C>T maps to NM_021225.4 T148T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EF-01A-11D-A12Z-10 chr4:16035129 A>G maps to NM_006017.2 I102I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr4:16025969 A>T maps to NM_006017.2 Y214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5262-01A-01D-A12Z-10 chr2:95952936 C>T maps to NM_144707.2 A717A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25V-01A-11D-A16V-10 chr2:95942073 C>T maps to NM_144707.2 G199G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MA-01A-11D-A20W-10 chr3:93611836 A>G maps to NM_000313.3 N365N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr1:214170675 G>T maps to NM_002763.3 S266S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A110-01A-11D-A12Z-10 chr19:54631458 A>G maps to NM_015629.3 E319E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A23B-01A-11D-A16V-10 chr1:109242491 T>C maps to NM_018061.2 S497S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73F-01A-11D-A32G-10 chr9:116045491 G>T did not map to a codon.
Sequencing variant TCGA-EP-A2KC-01A-11D-A20W-10 chr9:116049015 C>T maps to NM_004697.3 F281F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KR-A7K0-01A-12D-A33Q-10 chr6:4032470 A>G maps to NM_003913.4 K240K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IK-01A-12D-A33Q-10 chr20:62612636 G>T maps to NM_012469.3 A13A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A0-01A-11D-A20W-10 chr20:62614444 T>C maps to NM_012469.3 D39D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KR-A7K2-01A-12D-A33Q-10 chr20:62659866 G>A maps to NM_012469.3 L792L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-4073-01B-02D-A12Z-10 chr23:12838903 A>G did not map to a codon.
Sequencing variant TCGA-G3-A25W-01A-11D-A16V-10 chr23:12838908 G>C did not map to a codon.
Sequencing variant TCGA-BC-A10R-01A-11D-A12Z-10 chr19:50124860 G>A maps to NM_020719.1 S1901S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75G-01A-11D-A32G-10 chr19:50119468 C>T maps to NM_020719.1 S1830S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25S-01A-11D-A16V-10 chr5:120022232 C>T maps to NM_016644.1 G225G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr5:120022244 T>C maps to NM_016644.1 P229P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EL-01A-11D-A152-10 chr19:42814119 T>C maps to NM_199285.2 P128P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75E-01A-11D-A32G-10 chr22:45255713 G>C maps to ENST00000352766 A537A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A7XP-01A-11D-A34Z-10 chr23:37285114 C>A did not map to a codon.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr23:37312752 T>C did not map to a codon.
Sequencing variant TCGA-DD-A4NV-01A-11D-A30V-10 chr23:150869169 C>A did not map to a codon.
Sequencing variant TCGA-CC-A1HT-01A-11D-A12Z-10 chr3:9991577 A>G maps to NM_207351.3 D74D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MR-A520-01A-11D-A25V-10 chr7:142460285 C>T maps to ENST00000486171 D167D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A495-01A-11D-A25V-10 chr6:27220729 T>C did not map to a codon.
Sequencing variant TCGA-CC-A3M9-01A-11D-A20W-10 chr6:84233540 C>A maps to NM_153362.2 T127T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GJ-A6C0-01A-12D-A30V-10 chr6:84233978 G>A maps to NM_153362.2 L273L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11A-01A-11D-A12Z-10 chr3:46755768 G>A maps to NM_013270.4 D231D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr16:58320071 T>G maps to NM_001080492.1 I97I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A7PZ-01A-11D-A33Q-10 chr15:55931837 A>T did not map to a codon.
Sequencing variant TCGA-CC-A7IF-01A-11D-A33K-10 chr9:79322770 C>T maps to NM_015225.2 E1473E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr9:79318668 C>T maps to NM_015225.2 T2620T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A1-01A-11D-A20W-10 chr9:79322806 C>T maps to NM_015225.2 K1461K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr19:40903670 T>A maps to NM_181882.2 R196R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KR-A7K2-01A-12D-A33Q-10 chr8:143763523 C>T maps to ENST00000301258 L116L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A5UD-01A-11D-A28X-10 chr5:139189339 A>T maps to NM_032289.2 A105A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A115-01A-11D-A12Z-10 chr5:139193050 G>T maps to NM_032289.2 E177*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11C-01A-11D-A12Z-10 chr5:139189231 T>C maps to NM_032289.2 H69H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A9-01A-11D-A25V-10 chr5:139219613 G>A maps to NM_032289.2 E657E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A7S9-01A-11D-A33Q-10 chr8:18730004 G>A maps to ENST00000440756 L123L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A2QQ-01A-11D-A22F-10 chr2:113940278 C>T maps to NM_012455.2 D82D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KC-01A-11D-A20W-10 chr19:43382064 G>A maps to NM_006905.2 L144L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IK-01A-12D-A33Q-10 chr19:43576074 T>C maps to NM_031246.3 S247S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A6UC-01A-21D-A33K-10 chr19:43234065 G>T maps to NM_021016.3 P284P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A4ZQ-01A-11D-A25V-10 chr19:43699213 A>G maps to NM_002780.3 P307P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39Z-01A-11D-A20W-10 chr19:43430130 G>T maps to NM_002783.2 S346*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A4ZP-01A-12D-A25V-10 chr19:43259368 C>T maps to NM_182707.2 E253E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A4-01A-11D-A22F-10 chr9:15506557 C>A did not map to a codon.
Sequencing variant TCGA-DD-A3A8-01A-11D-A22F-10 chr9:127115963 T>C maps to NM_002799.2 K249K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5261-01A-01D-A12Z-10 chr7:102988208 G>A maps to NM_002803.2 K17K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A3KF-01A-11D-A20W-10 chr19:40486010 G>A maps to NM_006503.2 L292L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73D-01A-12D-A32G-10 chr2:231931710 C>T maps to NM_002807.3 G132G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A23B-01A-11D-A16V-10 chr17:30806342 C>T maps to NM_002815.2 N329N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CJ-01A-11D-A20W-10 chr17:65346350 T>C maps to NM_002816.3 E133E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A7SK-01A-11D-A34Z-10 chr1:151237943 G>T maps to ENST00000368881 V171V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11C-01A-11D-A12Z-10 chr9:123595661 C>A maps to NM_005047.2 R82R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39Z-01A-11D-A20W-10 chr9:123589184 T>C maps to NM_005047.2 R224R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25Y-01A-11D-A16V-10 chr14:24615415 C>A did not map to a codon.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr2:54101523 T>C maps to NM_014614.2 K1684K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A2QR-01A-11D-A20W-10 chr20:1145054 T>C maps to NM_006814.3 P233P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A3KF-01A-11D-A20W-10 chr18:12718586 T>C maps to NM_020232.4 V120V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A3JL-01A-11D-A20W-10 chr1:109823807 C>A maps to ENST00000409138 S195S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25Z-01A-11D-A16V-10 chr1:109824627 C>A maps to ENST00000409138 R44R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr1:109824546 T>G maps to ENST00000409138 P71P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A5UC-01A-11D-A28X-10 chr1:97250799 A>G maps to ENST00000370197 T298T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10Y-01A-11D-A12Z-10 chr9:98268743 C>A maps to NM_000264.3 A113A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MB-01A-11D-A20W-10 chr23:23411905 A>T did not map to a codon.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr23:23397833 C>T did not map to a codon.
Sequencing variant TCGA-CC-A7IL-01A-11D-A33Q-10 chr23:23410845 G>A did not map to a codon.
Sequencing variant TCGA-ED-A7XO-01A-11D-A34Z-10 chr23:23398174 C>A did not map to a codon.
Sequencing variant TCGA-HP-A5N0-01A-11D-A28X-10 chr23:23411940 C>T did not map to a codon.
Sequencing variant TCGA-MI-A75C-01A-11D-A32G-10 chr1:11591709 C>T maps to NM_020780.1 H1106H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr1:11589856 T>C maps to NM_020780.1 R981R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A5UD-01A-11D-A28X-10 chr10:89712016 G>T did not map to a codon.
Sequencing variant TCGA-DD-A3A0-01A-11D-A20W-10 chr10:89717724 T>A maps to NM_000314.4 C250*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A7M8-01A-11D-A33Q-10 chr14:52735239 G>A maps to NM_000953.2 P236P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7II-01A-11D-A33K-10 chr9:139873557 C>A maps to ENST00000224167 G76G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr1:71418660 T>G maps to NM_198718.1 R396R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5258-01A-01D-A12Z-10 chr20:48140753 A>G maps to NM_000961.3 S232S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A9-01A-11D-A25V-10 chr9:114348378 T>A maps to NM_001146108.1 T92T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr1:186645248 T>C maps to NM_000963.2 K346K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr2:209345824 A>T maps to NM_005048.2 R338*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A5W4-01A-11D-A28X-10 chr8:27255269 A>T maps to NM_004103.3 K57*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A112-01A-11D-A12Z-10 chr20:62162198 G>T maps to NM_005975.2 S305*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IL-01A-11D-A33Q-10 chr7:136936110 C>T maps to NM_002825.5 W106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NP-01A-11D-A28X-10 chr7:136938300 G>T maps to NM_002825.5 R67R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A69H-01A-11D-A30V-10 chr19:50361894 C>A maps to NM_017432.3 I342I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A0-01A-11D-A20W-10 chr4:87556465 A>G maps to NM_080685.2 E19E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CK-01A-11D-A20W-10 chr2:131117001 G>T maps to NM_014369.3 T104T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A112-01A-11D-A12Z-10 chr14:88938676 G>A maps to NM_007039.3 Q928*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A12J-01A-11D-A12Z-10 chr1:114380290 A>G maps to NM_015967.5 Y577Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IL-01A-11D-A33Q-10 chr3:47449185 G>T did not map to a codon.
Sequencing variant TCGA-CC-A7IG-01A-11D-A33K-10 chr11:18754796 G>T maps to NM_032781.3 I401I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr11:18754886 G>A maps to NM_032781.3 A371A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NI-01A-11D-A27I-10 chr15:75782643 T>A did not map to a codon.
Sequencing variant TCGA-BC-A69H-01A-11D-A30V-10 chr20:2988017 G>A maps to NM_002836.3 P286P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IK-01A-12D-A33Q-10 chr20:2987987 A>T did not map to a codon.
Sequencing variant TCGA-G3-A5SL-01A-11D-A27I-10 chr20:3002001 G>A maps to NM_002836.3 G363G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BW-A5NQ-01A-11D-A27I-10 chr12:70986131 T>C maps to NM_001109754.1 R570R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr12:70989898 T>C maps to NM_001109754.1 K396K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NI-01A-11D-A27I-10 chr12:70988331 C>T maps to NM_001109754.1 G477G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73F-01A-11D-A32G-10 chr12:71003576 G>A maps to NM_002837.3 A6A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75C-01A-11D-A32G-10 chr12:70953300 C>T maps to NM_001109754.1 E1512E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr9:8486104 C>T maps to NM_002839.3 G904G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25Z-01A-11D-A16V-10 chr10:129871632 C>A maps to NM_006504.4 T499T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr10:129869163 G>T maps to NM_006504.4 P462P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5262-01A-01D-A12Z-10 chr1:44069657 C>T maps to NM_002840.3 N945N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr1:44083443 C>A maps to NM_002840.3 I1411I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A2-01A-11D-A20W-10 chr3:62240817 T>C maps to NM_002841.3 P829P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A496-01A-11D-A25V-10 chr11:48185170 G>T did not map to a codon.
Sequencing variant TCGA-CC-A3MB-01A-11D-A20W-10 chr6:128388888 T>C maps to ENST00000368210 R644R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5258-01A-01D-A12Z-10 chr18:8088801 C>T maps to NM_001105244.1 T603T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NB-01A-12D-A25V-10 chr18:7888161 C>T maps to NM_001105244.1 L85L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NO-01A-11D-A28X-10 chr18:8247841 G>T did not map to a codon.
Sequencing variant TCGA-FV-A4ZP-01A-12D-A25V-10 chr18:8143666 C>G maps to NM_001105244.1 V730V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10U-01A-11D-A12Z-10 chr12:71139794 G>A maps to NM_002849.2 H270H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A4ZQ-01A-11D-A25V-10 chr20:41101119 G>A maps to ENST00000373198 Y412Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K7-A5RG-01A-11D-A28X-10 chr20:40980733 G>T maps to ENST00000373198 T584T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10W-01A-11D-A12Z-10 chr1:29641991 C>T maps to NM_005704.4 S1122S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75H-01A-11D-A32G-10 chr1:29609328 G>C maps to NM_005704.4 A670A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IK-01A-12D-A33Q-10 chr7:121653533 T>A maps to NM_002851.2 S1478S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A5SK-01A-11D-A27I-10 chr7:121653215 G>C maps to NM_002851.2 G1372G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39V-01A-11D-A20W-10 chr4:37962091 G>T maps to NM_006607.2 E13*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A5SM-01A-12D-A28X-10 chr16:1535963 G>A maps to NM_001013658.1 C466C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A5UD-01A-11D-A28X-10 chr8:144899154 G>A maps to NM_078480.1 S435S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A5SM-01A-12D-A28X-10 chr8:144899576 T>A maps to NM_078480.1 P356P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73G-01A-22D-A32G-10 chr2:20454711 G>A maps to ENST00000361078 L930L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NR-01A-11D-A30V-10 chr7:105121548 A>G maps to NM_019042.3 Y375Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39Z-01A-11D-A20W-10 chr12:44148625 G>A maps to NM_031292.3 A141A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A26S-01A-11D-A16V-10 chr7:99818612 C>A maps to NM_024070.3 C240*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LG-A6GG-01A-11D-A30V-10 chr11:119508958 T>A did not map to a codon.
Sequencing variant TCGA-DD-A114-01A-11D-A12Z-10 chr19:45391366 G>T maps to NM_001042724.1 E450*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NN-01A-11D-A28X-10 chr1:161044014 G>A maps to NM_030916.2 T383T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr1:161044158 G>T maps to NM_030916.2 P335P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5262-01A-01D-A12Z-10 chr2:1664716 G>T maps to NM_012293.1 R591R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A7M7-01A-12D-A34Z-10 chr2:1638056 A>G maps to NM_012293.1 P1453P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr8:52320841 G>C maps to NM_144651.4 P1114P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CK-01A-11D-A20W-10 chr8:52323846 A>G maps to NM_144651.4 R675R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KR-A7K0-01A-12D-A33Q-10 chr3:58383368 T>G maps to NM_017771.3 L341*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-4073-01B-02D-A12Z-10 chr20:32298386 C>A maps to NM_007238.4 G117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A5-01A-11D-A22F-10 chr16:31212987 C>T maps to NM_013258.4 W169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25T-01A-11D-A16V-10 chr11:64522269 A>T maps to NM_005609.2 Y298*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A1-01A-11D-A20W-10 chr1:158908886 T>A maps to NM_152501.3 S143S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1E9-01A-21D-A152-10 chr12:9344849 G>T maps to NM_002864.2 I495I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A4ZQ-01A-11D-A25V-10 chr2:37580078 G>T did not map to a codon.
Sequencing variant TCGA-DD-A4NI-01A-11D-A27I-10 chr4:122301703 C>G maps to NM_198179.2 P33P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25T-01A-11D-A16V-10 chr6:107113738 T>C maps to NM_018292.4 C483C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A216-01A-11D-A152-10 chr11:32987852 A>G maps to NM_001076786.1 E1530E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr11:32956866 T>C maps to NM_001076786.1 L1226L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25V-01A-11D-A16V-10 chr11:32956304 A>G maps to NM_001076786.1 P1038P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73A-01A-12D-A32G-10 chr12:57660556 A>T maps to ENST00000438036 S748S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A7SB-01A-21D-A34Z-10 chr12:57663678 A>G maps to ENST00000438036 L533L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T1-A6J8-01A-11D-A32G-10 chr11:66039303 A>C maps to NM_030981.2 S17S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10Q-01A-11D-A12Z-10 chr5:176728923 A>G did not map to a codon.
Sequencing variant TCGA-CC-A3MC-01A-11D-A22F-10 chr1:156035801 G>A maps to NM_020387.2 E48E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A23B-01A-11D-A16V-10 chr1:156035735 C>A maps to NM_020387.2 T26T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75G-01A-11D-A32G-10 chr1:156039507 C>G maps to NM_020387.2 T160T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A4ZQ-01A-11D-A25V-10 chr15:55527009 T>A maps to NM_183235.1 T41T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A2QR-01A-11D-A20W-10 chr4:13462449 T>C maps to NM_004249.3 G88G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11B-01A-11D-A16Z-10 chr8:61496801 G>T maps to NM_002865.1 S74S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A113-01A-11D-A12Z-10 chr6:146865245 G>A maps to NM_006834.3 W80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A66Y-01A-11D-A30V-10 chr23:129306276 G>T did not map to a codon.
Sequencing variant TCGA-UB-A7ME-01A-11D-A33K-10 chr2:135878430 C>T maps to NM_001172435.1 R231*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25U-01A-11D-A16V-10 chr1:220364459 G>A maps to ENST00000358951 S479S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A123-01A-11D-A12Z-10 chr23:102755565 T>A did not map to a codon.
Sequencing variant TCGA-HP-A5MZ-01A-21D-A27I-10 chr1:229434758 G>T maps to NM_004578.2 E161*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A118-01A-11D-A12Z-10 chr23:13727289 G>A did not map to a codon.
Sequencing variant TCGA-BC-A69H-01A-11D-A30V-10 chr23:103080317 C>T did not map to a codon.
Sequencing variant TCGA-DD-A11D-01A-11D-A12Z-10 chr17:5235400 A>G maps to NM_004703.4 K107K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73B-01A-12D-A32G-10 chr9:127996063 T>C maps to NM_005833.3 A308A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A112-01A-11D-A12Z-10 chr14:24738188 C>T maps to NM_182836.1 Q242Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25V-01A-11D-A16V-10 chr14:24737765 G>T maps to NM_182836.1 V320V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10U-01A-11D-A12Z-10 chr1:202858124 C>G maps to NM_002871.3 G34G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A1-01A-11D-A20W-10 chr22:37622733 C>T maps to NM_002872.3 K186K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A4ZQ-01A-11D-A25V-10 chr2:17696822 C>A maps to NM_001099218.2 E954*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CJ-01A-11D-A20W-10 chr8:95390863 T>C did not map to a codon.
Sequencing variant TCGA-O8-A75V-01A-11D-A32G-10 chr3:51690040 G>A maps to NM_015106.2 Q1027Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr7:4843188 T>G maps to NM_018059.4 P829P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A9-01A-11D-A25V-10 chr11:36596384 A>T maps to NM_000448.2 K511*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KR-A7K0-01A-12D-A33Q-10 chr11:36597508 G>A maps to NM_000448.2 L885L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr11:36596842 A>C maps to NM_000448.2 A663A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A9-01A-11D-A25V-10 chr11:36614458 G>T maps to NM_000536.3 C420*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr11:36614914 A>G maps to NM_000536.3 N268N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39Y-01A-11D-A20W-10 chr17:17700881 C>A maps to ENST00000395776 L1540L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MF-01A-11D-A33K-10 chr17:17696771 C>T maps to ENST00000395776 S170S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5259-01A-31D-A20W-10 chr23:17819078 C>T did not map to a codon.
Sequencing variant TCGA-DD-A3A9-01A-11D-A25V-10 chr23:17818830 A>G did not map to a codon.
Sequencing variant TCGA-ED-A7XO-01A-11D-A34Z-10 chr23:17819378 G>A did not map to a codon.
Sequencing variant TCGA-CC-5263-01A-01D-A12Z-10 chr18:9535917 A>T maps to NM_006788.3 K651*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr18:9535700 T>C maps to NM_006788.3 H578H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-4073-01B-02D-A12Z-10 chr20:20571890 C>T maps to NM_020343.3 Q757Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A5UD-01A-11D-A28X-10 chr20:20585825 T>A maps to NM_020343.3 R677R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4ND-01A-11D-A25V-10 chr20:20621444 C>A maps to NM_020343.3 L150L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7ME-01A-11D-A33K-10 chr20:37117218 T>G maps to NM_020336.2 P48P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25Z-01A-11D-A16V-10 chr1:178866878 C>A maps to NM_152663.3 T504T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BW-A5NO-01A-11D-A27I-10 chr8:85785540 C>G maps to NM_001100391.1 T211T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A4ZP-01A-12D-A25V-10 chr8:85799989 T>C maps to NM_001100391.1 D292D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3M9-01A-11D-A20W-10 chr2:109380630 A>G maps to NM_006267.4 K1212K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73B-01A-12D-A32G-10 chr2:109380984 T>C maps to NM_006267.4 D1330D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25V-01A-11D-A16V-10 chr2:109347858 G>T maps to NM_006267.4 G112*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MC-01A-11D-A22F-10 chr19:5931459 T>C maps to NM_007322.2 A216A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr9:6012661 T>A maps to NM_012416.2 S982S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11B-01A-11D-A16Z-10 chr1:21940576 A>G maps to NM_001145658.1 H163H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39Y-01A-11D-A20W-10 chr4:99313178 T>C maps to NM_001100426.1 N196N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BW-A5NQ-01A-11D-A27I-10 chr23:131348420 G>C did not map to a codon.
Sequencing variant TCGA-CC-A7IF-01A-11D-A33K-10 chr4:160243509 G>T maps to NM_014247.2 E128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39Z-01A-11D-A20W-10 chr2:173852990 T>C maps to NM_007023.3 I406I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A23B-01A-11D-A16V-10 chr11:47463161 C>A did not map to a codon.
Sequencing variant TCGA-KR-A7K7-01A-11D-A33K-10 chr6:88227930 A>G maps to NM_020320.3 C489C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A3KF-01A-11D-A20W-10 chr5:86682656 A>G maps to NM_002890.1 E954E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A123-01A-11D-A12Z-10 chr5:86637133 A>T maps to NM_002890.1 K349*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39X-01A-11D-A20W-10 chr5:86659273 T>C maps to NM_002890.1 D521D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr3:141290357 T>C maps to ENST00000452898 F377F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IK-01A-12D-A33Q-10 chr13:114766317 G>T maps to ENST00000389544 T618T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr13:114780787 C>T maps to ENST00000389544 V441V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75G-01A-11D-A32G-10 chr1:178427345 A>G maps to ENST00000263528 E962E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75C-01A-11D-A32G-10 chr19:15569402 G>T maps to NM_022904.1 A242A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NI-01A-11D-A27I-10 chr15:79350801 C>T maps to NM_002891.4 E135E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr15:79254551 A>G maps to NM_002891.4 S1252S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25U-01A-11D-A16V-10 chr2:33752433 C>A maps to NM_170672.2 A346A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IF-01A-11D-A33K-10 chr19:38907808 C>A did not map to a codon.
Sequencing variant TCGA-DD-A4NK-01A-11D-A28X-10 chr19:38912648 G>A maps to ENST00000405332 C56C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A3KG-01A-11D-A20W-10 chr11:13031941 G>T maps to ENST00000340901 V381V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A1HT-01A-11D-A12Z-10 chr10:45479553 C>T maps to NM_032023.3 D122D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NA-01A-11D-A25V-10 chr10:45486411 A>G maps to NM_032023.3 K234K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MF-01A-11D-A33K-10 chr10:45478108 T>A maps to NM_032023.3 P93P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EC-01A-21D-A12Z-10 chr1:206730942 G>T maps to NM_182665.2 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-4073-01B-02D-A12Z-10 chr4:74451009 T>G maps to NM_201431.1 R184R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NG-01A-11D-A27I-10 chr12:26217449 C>A maps to NM_001164747.1 T41T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr12:86198973 G>A maps to NM_005447.3 R272*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A7-01A-11D-A22F-10 chr1:65280432 C>T maps to ENST00000294428 S613S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A113-01A-11D-A12Z-10 chr13:48881511 G>A maps to NM_000321.2 W78*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NJ-01A-11D-A27I-10 chr13:48951169 G>A maps to NM_000321.2 Q444Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A66Y-01A-11D-A30V-10 chr13:48951052 G>A did not map to a codon.
Sequencing variant TCGA-G3-A25Y-01A-11D-A16V-10 chr13:48953727 A>G did not map to a codon.
Sequencing variant TCGA-RC-A7S9-01A-11D-A33Q-10 chr13:48953787 T>C did not map to a codon.
Sequencing variant TCGA-CC-5259-01A-31D-A20W-10 chr8:53540729 T>G did not map to a codon.
Sequencing variant TCGA-EP-A3RK-01A-11D-A22F-10 chr8:53536344 T>C maps to NM_014781.4 V1594V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5261-01A-01D-A12Z-10 chr18:20562243 G>A maps to ENST00000360790 P164P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EB-01A-11D-A12Z-10 chr2:28065966 A>G maps to NM_022128.1 L161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr20:35632145 T>A maps to NM_002895.2 R999*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73G-01A-22D-A32G-10 chr20:35663858 G>A maps to NM_002895.2 T652T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10W-01A-11D-A12Z-10 chr16:53504484 A>G maps to NM_005611.3 P812P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NH-01A-11D-A27I-10 chr16:53524209 T>C maps to NM_005611.3 *1140R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr16:53498135 A>G did not map to a codon.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr20:34242509 C>T maps to NM_001198838.1 P245P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NI-01A-11D-A27I-10 chr8:94747567 T>C maps to NM_203390.2 P357P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A9-01A-11D-A25V-10 chr12:114296691 C>T maps to NM_016196.3 G856G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25Z-01A-11D-A16V-10 chr5:150072841 T>C maps to NM_018047.2 K313K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EH-01A-11D-A12Z-10 chr5:145641134 G>A maps to NM_018989.1 R652R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A7PZ-01A-11D-A33Q-10 chr7:127978349 T>G maps to NM_018077.2 L165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IK-01A-12D-A33Q-10 chr23:48433626 A>T did not map to a codon.
Sequencing variant TCGA-DD-A3A7-01A-11D-A22F-10 chr20:34312494 T>C maps to NM_184234.1 S228S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A5SJ-01A-11D-A27I-10 chr20:34319989 G>A maps to NM_184234.1 R57*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A69H-01A-11D-A30V-10 chr19:36120132 G>T maps to NM_024321.3 P26P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EI-01A-11D-A12Z-10 chr4:155719371 A>G maps to NM_144979.3 A187A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A113-01A-11D-A12Z-10 chr4:40440061 G>A maps to NM_001098634.1 Y283Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11C-01A-11D-A12Z-10 chr3:50095359 G>A maps to NM_005777.2 R631R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr2:161133885 A>G maps to NM_016836.3 P357P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-4073-01B-02D-A12Z-10 chr3:29781251 C>G maps to NM_001003793.2 L147L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A5SL-01A-11D-A27I-10 chr3:30032667 A>G maps to NM_001003793.2 E425E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A9-01A-11D-A25V-10 chr23:135957308 A>G did not map to a codon.
Sequencing variant TCGA-BC-A69H-01A-11D-A30V-10 chr10:48389746 C>T maps to NM_002900.2 Q377Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EF-01A-11D-A12Z-10 chr10:48388578 G>A maps to NM_002900.2 L767L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KR-A7K7-01A-11D-A33K-10 chr10:48389260 C>T maps to NM_002900.2 L539L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NV-01A-11D-A30V-10 chr1:10068316 A>C maps to ENST00000377192 G160G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MB-01A-11D-A20W-10 chr9:125613388 T>C maps to NM_001100588.1 K1117K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IK-01A-12D-A33Q-10 chr6:46424644 T>C maps to ENST00000405162 G23G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A66X-01A-11D-A30V-10 chr1:17752172 G>A maps to NM_018715.2 Y129Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr11:63680388 G>A maps to NM_173587.3 L308L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A7SK-01A-11D-A34Z-10 chr1:211451496 C>G maps to NM_001136223.1 Y185*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5261-01A-01D-A12Z-10 chr1:167666538 G>A maps to NM_052862.3 E226E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IK-01A-12D-A33Q-10 chr1:167659344 T>A maps to NM_052862.3 I86I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr17:9804354 C>T maps to NM_002903.2 P148P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A113-01A-11D-A12Z-10 chr8:74209534 C>T maps to NM_172037.3 V132V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr19:10131463 G>A maps to NM_015725.2 L174L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A7PZ-01A-11D-A33Q-10 chr17:34257109 C>A maps to NM_145654.3 R82R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A118-01A-11D-A12Z-10 chr14:24646589 G>T did not map to a codon.
Sequencing variant TCGA-MI-A75I-01A-11D-A32G-10 chr9:36122843 A>G maps to NM_021111.2 A906A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A8-01A-11D-A22F-10 chr12:21644630 A>G maps to NM_032941.2 D12D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73C-01A-12D-A33K-10 chr12:21630877 C>T maps to NM_032941.2 K242K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RG-A7D4-01A-12D-A33Q-10 chr11:65422088 G>T maps to NM_021975.3 S472S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5259-01A-31D-A20W-10 chr7:103292163 G>T maps to ENST00000428762 I612I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5261-01A-01D-A12Z-10 chr7:103130237 G>A maps to ENST00000428762 H3238H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MA-01A-11D-A20W-10 chr7:103162471 A>G maps to ENST00000428762 S2555S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73B-01A-12D-A32G-10 chr7:103202065 A>G maps to ENST00000428762 P1814P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HP-A5N0-01A-11D-A28X-10 chr7:103179711 A>G maps to ENST00000428762 D2331D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25U-01A-11D-A16V-10 chr11:73106526 G>T maps to NM_152222.1 L428L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A7-01A-11D-A22F-10 chr23:17156983 C>T did not map to a codon.
Sequencing variant TCGA-G3-A25S-01A-11D-A16V-10 chr23:17095519 C>T did not map to a codon.
Sequencing variant TCGA-BC-A69H-01A-11D-A30V-10 chr10:43600448 G>A maps to NM_020975.4 T225T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11C-01A-11D-A12Z-10 chr10:43613902 A>G maps to NM_020975.4 K789K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A496-01A-11D-A25V-10 chr10:43615626 G>A maps to NM_020975.4 E902E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A2QR-01A-11D-A20W-10 chr2:100029413 C>T did not map to a codon.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr6:111686476 T>C maps to NM_002912.3 T2248T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25W-01A-11D-A16V-10 chr6:111709274 C>A maps to NM_002912.3 V292V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LG-A6GG-01A-11D-A30V-10 chr6:111688371 T>A maps to NM_002912.3 R2207*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LG-A6GG-01A-11D-A30V-10 chr6:111693803 C>T maps to NM_002912.3 K1918K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39Z-01A-11D-A20W-10 chr19:1827476 T>C maps to NM_020695.3 P437P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A3KF-01A-11D-A20W-10 chr4:39352985 T>C maps to ENST00000381897 K38K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A0-01A-11D-A20W-10 chr3:186507956 T>A maps to NM_181573.2 K324*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CJ-01A-11D-A20W-10 chr12:118464812 A>G maps to NM_007370.4 T261T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr22:32586881 C>T maps to NM_001098527.2 E338E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75E-01A-11D-A32G-10 chr22:32754309 C>T maps to NM_001098535.1 V84V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A123-01A-11D-A12Z-10 chr19:14092956 G>A maps to NM_002918.4 T199T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25S-01A-11D-A16V-10 chr9:3346709 G>A maps to NM_134428.1 Q58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A3R2-01A-11D-A22F-10 chr1:151316340 T>C maps to NM_000449.3 E191E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A113-01A-11D-A12Z-10 chr23:109695250 T>C did not map to a codon.
Sequencing variant TCGA-EP-A2KC-01A-11D-A20W-10 chr23:109695029 T>A did not map to a codon.
Sequencing variant TCGA-FV-A3R2-01A-11D-A22F-10 chr23:109695877 C>T did not map to a codon.
Sequencing variant TCGA-MI-A75I-01A-11D-A32G-10 chr23:109695555 A>G did not map to a codon.
Sequencing variant TCGA-RC-A6M4-01A-11D-A32G-10 chr23:109693861 A>G did not map to a codon.
Sequencing variant TCGA-DD-A3A4-01A-11D-A22F-10 chr1:183885769 G>T maps to NM_015149.3 E682*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10W-01A-11D-A12Z-10 chr6:33261660 G>C maps to NM_004761.3 L473L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11D-01A-11D-A12Z-10 chr5:98129452 T>A maps to NM_001012761.2 L478*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A6-01A-11D-A22F-10 chr23:46951498 C>A did not map to a codon.
Sequencing variant TCGA-MI-A75G-01A-11D-A32G-10 chr23:46949221 G>T did not map to a codon.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr9:35752014 A>G maps to ENST00000456972 A315A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NQ-01A-21D-A28X-10 chr2:107041398 G>A maps to ENST00000304514 Y1008Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr2:108487606 A>G maps to NM_182588.2 E1049E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A3I0-01A-11D-A22F-10 chr2:108487291 T>C maps to NM_182588.2 D944D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A5SM-01A-12D-A28X-10 chr2:108488191 G>C maps to NM_182588.2 G1244G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A5SM-01A-12D-A28X-10 chr2:108488197 A>C maps to NM_182588.2 T1246T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A5-01A-11D-A22F-10 chr2:113147587 A>C maps to NM_005054.2 T978T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A26S-01A-11D-A16V-10 chr5:176798893 C>A maps to ENST00000398128 R508R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NK-01A-11D-A28X-10 chr8:54792095 G>A maps to NM_170587.2 R148R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A7PZ-01A-11D-A33Q-10 chr8:54792131 C>T maps to NM_170587.2 D160D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11C-01A-11D-A12Z-10 chr8:101118125 C>A maps to NM_015668.3 A8A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A495-01A-11D-A25V-10 chr8:100994296 A>G maps to NM_015668.3 I1076I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QA-A7B7-01A-11D-A32G-10 chr8:100999805 A>G maps to NM_015668.3 I1020I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A112-01A-11D-A12Z-10 chr1:163039294 T>A maps to NM_001102445.2 G104G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A7M5-01A-11D-A33Q-10 chr1:163043348 T>A maps to NM_001102445.2 S202S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MB-01A-11D-A20W-10 chr14:72945004 A>G maps to NM_004296.4 R274R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A1-01A-11D-A20W-10 chr1:240978078 T>C did not map to a codon.
Sequencing variant TCGA-DD-A11C-01A-11D-A12Z-10 chr16:111694 C>T did not map to a codon.
Sequencing variant TCGA-CC-A5UD-01A-11D-A28X-10 chr17:30616019 A>T maps to NM_138328.2 T168T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25S-01A-11D-A16V-10 chr15:90023511 G>T maps to NM_016321.1 S217*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A0-01A-11D-A20W-10 chr3:129251108 C>T maps to NM_000539.3 G182G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75I-01A-11D-A32G-10 chr3:49400012 G>A maps to NM_001664.2 P108P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BW-A5NO-01A-11D-A27I-10 chr5:95067574 C>T maps to NM_014899.3 I5I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IF-01A-11D-A33K-10 chr23:119243260 C>G did not map to a codon.
Sequencing variant TCGA-BC-A10Z-01A-11D-A12Z-10 chr8:144460479 C>T maps to ENST00000422773 Y141Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NH-01A-11D-A27I-10 chr23:53457368 G>A did not map to a codon.
Sequencing variant TCGA-DD-A3A9-01A-11D-A25V-10 chr22:45810270 A>G maps to NM_015653.3 R61R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5260-01A-01D-A12Z-10 chr11:214284 C>T maps to NM_021932.4 Q517*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5258-01A-01D-A12Z-10 chr12:130927133 G>T maps to NM_015347.4 R238R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5259-01A-31D-A20W-10 chr22:20458547 G>C maps to NM_015672.1 L918L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A6M4-01A-11D-A32G-10 chr6:73102429 T>A maps to NM_014989.4 A1512A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5260-01A-01D-A12Z-10 chr8:104897855 A>G maps to NM_001100117.2 P343P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A495-01A-11D-A25V-10 chr8:104930678 C>A maps to NM_001100117.2 R683R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CK-01A-11D-A20W-10 chr8:104898095 T>G maps to NM_001100117.2 S423S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10W-01A-11D-A12Z-10 chr14:93118695 G>A maps to NM_024832.3 Q434Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A7M9-01A-23D-A34Z-10 chr7:105189008 T>A maps to NM_021930.4 L283*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr14:24806549 A>T maps to NM_006871.3 S339S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A6M6-01A-11D-A32G-10 chr14:24807238 G>T maps to NM_006871.3 T224T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr18:40554044 A>T maps to NM_002930.2 A76A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A7PZ-01A-11D-A33Q-10 chr15:89754010 G>T maps to NM_000326.4 I238I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A3KF-01A-11D-A20W-10 chr23:73814205 T>A did not map to a codon.
Sequencing variant TCGA-CC-A123-01A-11D-A12Z-10 chr23:73811890 A>T did not map to a codon.
Sequencing variant TCGA-CC-A7IK-01A-12D-A33Q-10 chr23:73812675 T>C did not map to a codon.
Sequencing variant TCGA-DD-A73D-01A-12D-A32G-10 chr23:73812011 T>A did not map to a codon.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr23:73812564 T>A did not map to a codon.
Sequencing variant TCGA-DD-A3A1-01A-11D-A20W-10 chr16:67683060 C>T maps to NM_001013838.1 F558F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A7PZ-01A-11D-A33Q-10 chr14:21270098 T>A maps to NM_198235.2 S43S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A6M3-01A-11D-A32G-10 chr14:21269972 G>A maps to NM_198235.2 V85V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25T-01A-11D-A16V-10 chr14:20979190 T>C maps to ENST00000430083 T215T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4ND-01A-11D-A25V-10 chr23:119005301 T>A did not map to a codon.
Sequencing variant TCGA-DD-A39Y-01A-11D-A20W-10 chr11:71671840 T>C maps to NM_018320.4 A49A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr11:71705853 A>G maps to NM_018320.4 E239E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EK-01A-11D-A20W-10 chr3:49739577 G>A did not map to a codon.
Sequencing variant TCGA-G3-A25S-01A-11D-A16V-10 chr3:49753578 G>C maps to NM_022064.2 L1128L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr23:105970374 G>T did not map to a codon.
Sequencing variant TCGA-ED-A7PX-01A-51D-A34Z-10 chr5:141358343 A>G maps to NM_183399.1 Q261Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10Z-01A-11D-A12Z-10 chr5:158603764 C>A maps to NM_144726.2 E194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A9-01A-11D-A25V-10 chr6:127607829 C>T maps to ENST00000368314 S24S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr6:127608495 T>C maps to ENST00000368314 S246S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IJ-01A-11D-A33Q-10 chr4:141888998 A>G maps to NM_020724.1 I171I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr17:74151645 T>C maps to NM_052916.2 G565G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr3:196199328 T>C maps to NM_152617.3 S359S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11A-01A-11D-A12Z-10 chr13:25435485 C>T maps to ENST00000381927 P1334P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EK-01A-11D-A20W-10 chr13:25439063 A>G maps to ENST00000381927 G1392G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5263-01A-01D-A12Z-10 chr6:13977394 T>C maps to NM_001165033.1 S15S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr11:117109395 A>T maps to NM_207343.2 R63*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11B-01A-11D-A16Z-10 chr7:5681007 C>A did not map to a codon.
Multiple mappings detected for codon TCGA-EP-A2KC-01A-11D-A20W-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-EP-A2KC-01A-11D-A20W-10 chr1:45111113 A>T maps to ENST00000453887 K468*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A8-01A-11D-A22F-10 chr11:119206380 A>G maps to NM_032015.3 V183V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A113-01A-11D-A12Z-10 chr13:26788011 A>G maps to NM_005977.3 C669C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LG-A6GG-01A-11D-A30V-10 chr13:26789148 T>A maps to NM_005977.3 T290T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A5UD-01A-11D-A28X-10 chr3:78717372 T>A maps to NM_002941.3 T570T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A3I1-01A-11D-A22F-10 chr3:78685013 A>G maps to NM_002941.3 S1094S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr3:77629213 A>T maps to ENST00000332191 A815A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EH-01A-11D-A12Z-10 chr11:124763621 C>A maps to NM_019055.5 L503L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A3R2-01A-11D-A22F-10 chr11:124766855 G>T maps to NM_019055.5 V124V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LG-A6GG-01A-11D-A30V-10 chr2:11337475 T>A did not map to a codon.
Sequencing variant TCGA-RC-A7SF-01A-11D-A34Z-10 chr1:64643502 G>T maps to NM_005012.2 L593L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr9:94486207 G>T maps to NM_004560.2 V856V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr9:94488969 T>A maps to NM_004560.2 A413A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NJ-01A-11D-A27I-10 chr6:117709157 A>C maps to NM_002944.2 L600*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A23B-01A-11D-A16V-10 chr6:117718162 G>A maps to NM_002944.2 L232L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HP-A5N0-01A-11D-A28X-10 chr6:117638329 A>G maps to NM_002944.2 Y2037Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LG-A6GG-01A-11D-A30V-10 chr6:117686250 T>A maps to NM_002944.2 T1030T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MB-01A-11D-A20W-10 chr8:55542177 T>C maps to NM_006269.1 A1912A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A459-01A-11D-A25V-10 chr8:55541214 G>A maps to NM_006269.1 W1591*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75C-01A-11D-A32G-10 chr8:55533948 C>T maps to NM_006269.1 P141P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A6M3-01A-11D-A32G-10 chr8:55539234 T>C maps to NM_006269.1 P931P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A2-01A-11D-A20W-10 chr8:10469480 C>T maps to NM_178857.5 S709S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A5SM-01A-12D-A28X-10 chr8:10468547 C>T maps to NM_178857.5 Q1020Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75G-01A-11D-A32G-10 chr8:10470653 G>A maps to NM_178857.5 D318D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A0-01A-11D-A20W-10 chr15:41826957 A>G maps to NM_015540.2 A239A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A9-01A-11D-A25V-10 chr1:92789744 G>A maps to NM_024813.2 W423*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr23:38145014 C>A did not map to a codon.
Sequencing variant TCGA-G3-A25W-01A-11D-A16V-10 chr23:38144822 A>C did not map to a codon.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr2:89036183 C>T maps to NM_144563.2 V243V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr1:24022367 A>G maps to NM_000975.3 K159K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A7M8-01A-11D-A33Q-10 chr3:23960000 C>T maps to NM_002948.2 Y81Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NE-01A-11D-A27I-10 chr1:6257753 G>T maps to NM_000983.3 C25*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CK-01A-11D-A20W-10 chr9:127622524 G>A maps to NM_007209.3 S53S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr15:66795503 T>A did not map to a codon.
Sequencing variant TCGA-RC-A7SB-01A-21D-A34Z-10 chr12:120636497 G>A maps to NM_053275.3 S170S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A3KF-01A-11D-A20W-10 chr3:58302306 A>G maps to NM_007042.3 R76R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-4073-01B-02D-A12Z-10 chr10:92660342 T>C maps to ENST00000458617 A260A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KC-01A-11D-A20W-10 chr16:2013232 G>A maps to NM_002952.3 L98L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7ME-01A-11D-A33K-10 chr11:75115171 G>A maps to NM_001005.3 V153V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EL-01A-11D-A152-10 chr24:2722743 A>G did not map to a codon.
Sequencing variant TCGA-CC-5262-01A-01D-A12Z-10 chr24:22941542 C>T did not map to a codon.
Sequencing variant TCGA-DD-A1EB-01A-11D-A12Z-10 chr1:26898356 C>T maps to NM_001006665.1 G599G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A3KG-01A-11D-A20W-10 chr23:20194412 C>A did not map to a codon.
Sequencing variant TCGA-DD-A1EH-01A-11D-A12Z-10 chr23:20252925 G>A did not map to a codon.
Sequencing variant TCGA-DD-A39W-01A-11D-A20W-10 chr23:20227475 T>A did not map to a codon.
Sequencing variant TCGA-ED-A66Y-01A-11D-A30V-10 chr23:20181159 T>A did not map to a codon.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr23:20181108 C>T did not map to a codon.
Sequencing variant TCGA-FV-A23B-01A-11D-A16V-10 chr23:20206010 G>A did not map to a codon.
Sequencing variant TCGA-BW-A5NO-01A-11D-A27I-10 chr23:83359654 T>C did not map to a codon.
Sequencing variant TCGA-CC-5259-01A-31D-A20W-10 chr23:83389789 C>T did not map to a codon.
Sequencing variant TCGA-CC-A3MB-01A-11D-A20W-10 chr23:83389803 T>C did not map to a codon.
Sequencing variant TCGA-CC-A7IK-01A-12D-A33Q-10 chr23:83352787 C>T did not map to a codon.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr23:83390123 A>C did not map to a codon.
Sequencing variant TCGA-DD-A73E-01A-12D-A32G-10 chr1:213415975 C>T maps to NM_012424.3 A962A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A9-01A-11D-A25V-10 chr20:17616197 C>A maps to ENST00000377813 E817*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KR-A7K2-01A-12D-A33Q-10 chr6:7231436 C>A maps to NM_001003699.3 L1035L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A2QQ-01A-11D-A22F-10 chr8:103237177 G>T maps to NM_015713.4 I130I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr10:99148092 C>A maps to NM_015179.3 L311L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NV-01A-11D-A30V-10 chr1:218475634 G>A did not map to a codon.
Sequencing variant TCGA-BC-A10Y-01A-11D-A12Z-10 chr21:45092190 A>G maps to NM_015056.2 E72E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73A-01A-12D-A32G-10 chr3:51969470 C>T maps to NM_004704.3 V286V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CK-01A-11D-A20W-10 chr8:67341482 G>A maps to NM_015169.3 L39L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25Y-01A-11D-A16V-10 chr2:7033835 T>C did not map to a codon.
Sequencing variant TCGA-MR-A520-01A-11D-A25V-10 chr1:15988084 C>G maps to NM_006511.1 A574A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25U-01A-11D-A16V-10 chr11:77412596 G>T maps to NM_016578.3 T559T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25W-01A-11D-A16V-10 chr11:77378438 T>C maps to NM_016578.3 E1283E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NQ-01A-21D-A28X-10 chr21:43896038 G>A maps to NM_080860.2 D282D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A26S-01A-11D-A16V-10 chr7:5967915 T>C maps to NM_173565.3 E781E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KR-A7K2-01A-12D-A33Q-10 chr7:6797424 G>A maps to NM_173565.3 E39E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A1-01A-11D-A20W-10 chr19:46305377 C>A maps to NM_030785.3 E600*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NK-01A-11D-A28X-10 chr1:38082336 C>T maps to NM_001038633.2 E35E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A26S-01A-11D-A16V-10 chr8:109094800 T>C maps to NM_178565.4 Q22Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A8-01A-11D-A22F-10 chr3:157920989 G>A maps to NM_016625.2 E150E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A7PZ-01A-11D-A33Q-10 chr19:12936624 T>A maps to NM_031429.1 G227G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NE-01A-11D-A27I-10 chr20:62324186 C>T maps to ENST00000482936 D894D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25U-01A-11D-A16V-10 chr20:62311204 C>T maps to ENST00000482936 Y347Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10W-01A-11D-A12Z-10 chr10:63999450 C>A maps to NM_145307.2 V148V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EH-01A-11D-A12Z-10 chr14:101348749 G>A maps to NM_001134888.2 N792N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EB-01A-11D-A12Z-10 chr14:60074127 G>T maps to NM_021136.2 T616T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EB-01A-11D-A12Z-10 chr14:60097162 C>A did not map to a codon.
Sequencing variant TCGA-G3-A25W-01A-11D-A16V-10 chr18:67871370 A>G maps to NM_173630.3 P116P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7ME-01A-11D-A33K-10 chr4:71656986 A>T maps to NM_014961.3 A461A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EL-01A-11D-A152-10 chr17:41143399 T>A maps to NM_173079.2 P503P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NR-01A-11D-A30V-10 chr8:92998418 T>C maps to NM_175634.2 K404K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MF-01A-11D-A33K-10 chr8:93023241 G>T maps to NM_175634.2 I182I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KR-A7K8-01A-11D-A33K-10 chr1:25229110 G>A maps to NM_001031680.2 R264R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IG-01A-11D-A33K-10 chr1:155292169 G>A maps to NM_001105203.1 R202R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A3-01A-11D-A22F-10 chr1:155296519 C>T maps to NM_001105203.1 L671L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KR-A7K0-01A-12D-A33Q-10 chr1:155292685 C>A maps to NM_001105203.1 L374L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A23B-01A-11D-A16V-10 chr9:35555120 C>T maps to NM_001135999.1 P693P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KR-A7K2-01A-12D-A33Q-10 chr3:127831761 C>T maps to NM_003707.2 E110E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5263-01A-01D-A12Z-10 chr5:33937816 C>A maps to NM_016568.3 V324V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A5SK-01A-11D-A27I-10 chr5:33938059 G>A maps to NM_016568.3 W405*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr6:33162735 A>G maps to ENST00000374685 P484P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A69H-01A-11D-A30V-10 chr1:165398165 T>A maps to NM_006917.4 P29P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NF-01A-11D-A27I-10 chr1:165386377 C>A maps to NM_006917.4 T174T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A114-01A-11D-A12Z-10 chr19:38974063 G>A maps to NM_000540.2 V1614V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NQ-01A-21D-A28X-10 chr19:39071080 C>T maps to NM_000540.2 R4861R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NI-A4U2-01A-11D-A28X-10 chr19:38964294 A>G maps to NM_000540.2 K1348K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr19:39076639 G>T maps to NM_000540.2 E4956*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A112-01A-11D-A12Z-10 chr1:237433795 G>C did not map to a codon.
Sequencing variant TCGA-DD-A3A8-01A-11D-A22F-10 chr1:237586487 A>T maps to NM_001035.2 L315L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NL-01A-11D-A28X-10 chr1:237947911 C>T maps to NM_001035.2 S4300S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A459-01A-11D-A25V-10 chr1:237868575 G>A maps to NM_001035.2 L3171L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A5KG-01A-11D-A27I-10 chr1:237947092 G>A maps to NM_001035.2 T4027T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A12J-01A-11D-A12Z-10 chr1:237774078 G>T maps to NM_001035.2 S1567S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr1:237947884 C>T maps to NM_001035.2 F4291F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A7M5-01A-11D-A33Q-10 chr1:237804196 T>G maps to NM_001035.2 L2372L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KR-A7K2-01A-12D-A33Q-10 chr1:237670086 A>G maps to NM_001035.2 K897K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10R-01A-11D-A12Z-10 chr15:34105062 G>C did not map to a codon.
Sequencing variant TCGA-BC-A3KF-01A-11D-A20W-10 chr15:33993259 A>G maps to NM_001036.3 L2154L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MC-01A-11D-A22F-10 chr15:33936689 C>A maps to NM_001036.3 V1245V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IG-01A-11D-A33K-10 chr15:33954428 C>T maps to NM_001036.3 S1566S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr15:34105179 C>T maps to NM_001036.3 V3458V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr9:91617110 C>T maps to NM_005226.2 L332L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A7XO-01A-11D-A34Z-10 chr9:91616132 G>A maps to NM_005226.2 P6P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr19:10624586 C>T maps to NM_001166215.1 S367S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr19:10625480 A>G maps to NM_001166215.1 A69A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1ED-01A-11D-A152-10 chr3:45744959 A>G maps to NM_014016.3 E21E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr13:23906629 A>G maps to NM_014363.4 A3795A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1E9-01A-21D-A152-10 chr13:23915815 A>G maps to NM_014363.4 T733T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NF-01A-11D-A27I-10 chr13:23907795 G>A maps to NM_014363.4 L3407L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr13:23908201 A>G maps to NM_014363.4 V3271V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A7M5-01A-11D-A33Q-10 chr13:23910454 T>G maps to NM_014363.4 T2520T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75E-01A-11D-A32G-10 chr13:23911711 G>T maps to NM_014363.4 S2101S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75G-01A-11D-A32G-10 chr13:23905054 A>G maps to NM_014363.4 L4320L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-4073-01B-02D-A12Z-10 chr19:5653398 C>T maps to ENST00000433404 D498D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr19:5654110 A>G maps to ENST00000433404 K522K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HP-A5N0-01A-11D-A28X-10 chr19:5621380 A>G maps to NM_014649.2 P71P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5259-01A-31D-A20W-10 chr23:134989875 C>A did not map to a codon.
Sequencing variant TCGA-CC-A5UD-01A-11D-A28X-10 chr23:134994076 A>T did not map to a codon.
Sequencing variant TCGA-CC-A7IK-01A-12D-A33Q-10 chr23:134986662 A>T did not map to a codon.
Sequencing variant TCGA-CC-A7IL-01A-11D-A33Q-10 chr23:134988644 C>G did not map to a codon.
Sequencing variant TCGA-ED-A459-01A-11D-A25V-10 chr23:134983799 C>G did not map to a codon.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr23:134993959 A>C did not map to a codon.
Sequencing variant TCGA-DD-A4NR-01A-11D-A30V-10 chr16:51173573 A>C maps to ENST00000251020 S853S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr16:51175283 G>T maps to ENST00000251020 S283S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HP-A5N0-01A-11D-A28X-10 chr14:21992349 T>A maps to NM_005407.1 G504G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A26S-01A-11D-A16V-10 chr18:76754126 C>T maps to NM_171999.2 C712C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75G-01A-11D-A32G-10 chr19:14199509 C>T maps to ENST00000269724 P374P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73C-01A-12D-A33K-10 chr1:878690 C>G maps to ENST00000443100 T541T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39X-01A-11D-A20W-10 chr19:39868420 C>G maps to NM_018028.2 A467A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NP-01A-11D-A28X-10 chr19:39866422 C>T maps to NM_018028.2 H267H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr7:92732404 C>T maps to NM_017654.3 L1002L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A3-01A-11D-A22F-10 chr7:92733943 G>A maps to NM_017654.3 P489P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr10:71917591 T>G maps to NM_020150.4 A92A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75C-01A-11D-A32G-10 chr5:133945275 T>A maps to NM_016103.3 S111S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A3KF-01A-11D-A20W-10 chr9:136578160 T>C maps to NM_007101.3 A412A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25U-01A-11D-A16V-10 chr9:136561447 G>A maps to NM_007101.3 A568A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73E-01A-12D-A32G-10 chr17:26723268 C>T maps to ENST00000379061 T711T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NP-01A-11D-A28X-10 chr12:108929238 T>C maps to NM_014706.3 R484R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A9-01A-11D-A25V-10 chr6:148841001 G>A maps to NM_015278.3 K394K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr6:148864813 A>T did not map to a codon.
Sequencing variant TCGA-DD-A1EL-01A-11D-A152-10 chr23:128926327 C>A did not map to a codon.
Sequencing variant TCGA-DD-A11C-01A-11D-A12Z-10 chr3:18436226 A>T maps to ENST00000332610 P313P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25U-01A-11D-A16V-10 chr3:18456692 T>C maps to ENST00000332610 Q185Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A5SL-01A-11D-A27I-10 chr22:50886720 A>T maps to ENST00000337034 A1778A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75H-01A-11D-A32G-10 chr11:9868631 T>C did not map to a codon.
Sequencing variant TCGA-DD-A4NP-01A-11D-A28X-10 chr12:123815841 C>T maps to NM_001167856.1 T330T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr12:123798233 T>C maps to NM_001167856.1 K1051K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A118-01A-11D-A12Z-10 chr19:1109389 C>T maps to NM_014963.2 A1083A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A4XI-01A-11D-A25V-10 chr19:50156750 A>G maps to NM_021228.2 E1035E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A2QR-01A-11D-A20W-10 chr15:75310252 C>T maps to ENST00000361900 F112F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A112-01A-11D-A12Z-10 chr3:47476583 C>A maps to NM_012235.2 E56*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A7M6-01A-11D-A33Q-10 chr15:77057676 C>A did not map to a codon.
Sequencing variant TCGA-CC-A5UE-01A-11D-A28X-10 chr8:27779610 C>A maps to NM_173833.5 A131A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr4:83602014 T>C maps to NM_001037582.2 S138S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A66Y-01A-11D-A30V-10 chr11:62038371 G>A maps to NM_002411.2 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25U-01A-11D-A16V-10 chr11:62040427 G>C did not map to a codon.
Sequencing variant TCGA-DD-A73F-01A-11D-A32G-10 chr7:12610489 G>A maps to NM_001112706.2 K26K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75G-01A-11D-A32G-10 chr2:239006993 T>C maps to NM_016510.4 *446Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EB-01A-11D-A12Z-10 chr23:17768331 G>T did not map to a codon.
Sequencing variant TCGA-G3-A25V-01A-11D-A16V-10 chr23:17769992 C>T did not map to a codon.
Sequencing variant TCGA-BC-A10R-01A-11D-A12Z-10 chr23:18283817 G>C did not map to a codon.
Sequencing variant TCGA-BC-A10U-01A-11D-A12Z-10 chr3:38835300 A>G maps to NM_006514.2 Y67Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NP-01A-11D-A28X-10 chr3:38791582 G>T maps to NM_006514.2 I616I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73G-01A-22D-A32G-10 chr3:38739070 G>T maps to NM_006514.2 P1880P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BD-A3EP-01A-11D-A22F-10 chr3:38921488 T>C maps to ENST00000302328 G1115G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3M9-01A-11D-A20W-10 chr3:38991631 T>A maps to ENST00000302328 I74I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr3:38926833 A>G maps to ENST00000302328 F1003F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IJ-01A-11D-A33Q-10 chr3:38938563 A>T maps to ENST00000302328 R725R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73E-01A-12D-A32G-10 chr3:38921512 T>C maps to ENST00000302328 L1107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A3KG-01A-11D-A20W-10 chr2:166854613 C>T maps to NM_001165963.1 G1470G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A123-01A-11D-A12Z-10 chr2:166897746 T>C maps to NM_001165963.1 G803G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A0-01A-11D-A20W-10 chr2:166866300 T>C maps to NM_001165963.1 G1310G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73E-01A-12D-A32G-10 chr2:166898865 T>C maps to NM_001165963.1 L704L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K7-A6G5-01A-11D-A30V-10 chr19:35524521 C>T maps to NM_199037.3 T109T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr11:118037685 C>T maps to NM_004588.4 E188E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25V-01A-11D-A16V-10 chr11:123516372 G>T maps to NM_018400.3 S47S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A7M5-01A-11D-A33Q-10 chr11:123524464 A>T maps to NM_018400.3 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr17:62022890 G>T maps to NM_000334.4 A1183A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-4073-01B-02D-A12Z-10 chr3:38645328 A>G maps to NM_001099404.1 H588H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3M9-01A-11D-A20W-10 chr3:38645541 C>T maps to NM_001099404.1 R517R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NI-A4U2-01A-11D-A28X-10 chr3:38620986 C>T did not map to a codon.
Sequencing variant TCGA-BC-A3KF-01A-11D-A20W-10 chr2:167297977 G>A maps to NM_002976.2 D695D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KR-A7K0-01A-12D-A33Q-10 chr2:167298064 G>T maps to NM_002976.2 L666L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr2:167298133 T>C maps to NM_002976.2 A643A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5264-01A-01D-A12Z-10 chr12:52056825 C>T maps to NM_014191.2 G75G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A4ZP-01A-12D-A25V-10 chr12:52115517 C>T maps to NM_014191.2 R608R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A23B-01A-11D-A16V-10 chr16:23366663 T>C maps to ENST00000307331 S255S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr1:1222885 A>T did not map to a codon.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr16:23223398 T>C maps to NM_001039.3 C407C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7II-01A-11D-A33K-10 chr8:144891810 G>A maps to NM_182706.3 P536P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39Z-01A-11D-A20W-10 chr8:144890959 C>T maps to NM_182706.3 W645*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-O8-A75V-01A-11D-A32G-10 chr8:144885834 C>T maps to NM_182706.3 E1132E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A7PY-01A-11D-A33Q-10 chr20:644967 G>A maps to NM_033129.3 L91L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75G-01A-11D-A32G-10 chr22:43608518 C>T maps to NM_173050.2 E711E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25V-01A-11D-A16V-10 chr6:35201067 G>A maps to ENST00000394681 K234K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CK-01A-11D-A20W-10 chr1:169847816 C>A maps to NM_181093.2 G103G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MB-01A-11D-A20W-10 chr4:76882409 T>C maps to NM_018115.2 E411E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A5SK-01A-11D-A27I-10 chr8:97621748 G>A maps to NM_002998.3 K193K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr1:243433404 A>C did not map to a codon.
Sequencing variant TCGA-CC-A5UD-01A-11D-A28X-10 chr7:4201421 A>T maps to NM_152744.3 P1578P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NE-01A-11D-A27I-10 chr7:4014120 C>T maps to NM_152744.3 S646S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10U-01A-11D-A12Z-10 chr17:71382608 C>T maps to NM_001144952.1 S1491S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5258-01A-01D-A12Z-10 chr17:71503641 G>A maps to NM_001144952.1 S53S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BW-A5NQ-01A-11D-A27I-10 chr2:192701014 C>T maps to NM_004657.5 E304E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A459-01A-11D-A25V-10 chr12:57324232 G>A maps to NM_148897.2 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7ME-01A-11D-A33K-10 chr17:75186882 A>T did not map to a codon.
Sequencing variant TCGA-DD-A3A9-01A-11D-A25V-10 chr22:30899671 C>T maps to NM_174977.3 W41*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A9-01A-11D-A25V-10 chr9:139361446 A>G maps to NM_014866.1 Y1297Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A3I0-01A-11D-A22F-10 chr9:139370174 C>A maps to NM_014866.1 V631V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75C-01A-11D-A32G-10 chr9:139371482 C>A maps to NM_014866.1 V195V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A5UE-01A-11D-A28X-10 chr1:177934192 C>T maps to NM_033127.2 E174E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75H-01A-11D-A32G-10 chr1:145109583 G>A maps to NM_004892.4 T82T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25Y-01A-11D-A16V-10 chr14:39555105 A>G maps to NM_006364.2 L230L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A9-01A-11D-A25V-10 chr4:110442310 C>T maps to NM_006323.2 L762L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A7XP-01A-11D-A34Z-10 chr4:110384262 C>T maps to NM_006323.2 Q114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr4:110453793 G>T did not map to a codon.
Sequencing variant TCGA-G3-A5SL-01A-11D-A27I-10 chr4:110442574 G>A did not map to a codon.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr10:75525660 A>T maps to NM_198597.1 V490V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr4:119666158 T>C maps to ENST00000379735 E589E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A8-01A-11D-A22F-10 chr14:81964802 C>T maps to NM_005065.4 Q309Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75E-01A-11D-A32G-10 chr20:13830845 C>A maps to NM_025229.1 L646L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr4:25849270 G>T maps to NM_015187.3 P126P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EK-01A-11D-A20W-10 chr1:169696928 A>G maps to NM_000450.2 L473L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NI-01A-11D-A27I-10 chr7:83643575 A>G maps to NM_006080.2 D253D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LG-A6GG-01A-11D-A30V-10 chr7:83675691 A>C maps to NM_006080.2 L205L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5263-01A-01D-A12Z-10 chr7:80432005 G>T maps to NM_006379.2 G297G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr7:80457898 A>G did not map to a codon.
Sequencing variant TCGA-BC-A10R-01A-11D-A12Z-10 chr7:84666318 C>G maps to NM_152754.2 V359V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11A-01A-11D-A12Z-10 chr7:84666203 C>T did not map to a codon.
Sequencing variant TCGA-BC-A3KG-01A-11D-A20W-10 chr7:83029464 T>G maps to NM_012431.2 I415I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A116-01A-11D-A12Z-10 chr7:83037732 C>T maps to NM_012431.2 G207G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73B-01A-12D-A32G-10 chr7:83035264 T>C maps to NM_012431.2 E308E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25W-01A-11D-A16V-10 chr7:83026016 T>C maps to NM_012431.2 T465T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10R-01A-11D-A12Z-10 chr3:50220185 G>T maps to NM_004186.3 A291A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25U-01A-11D-A16V-10 chr3:50211495 A>G maps to NM_004186.3 A95A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr3:52471560 C>A maps to NM_020163.1 G620G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25S-01A-11D-A16V-10 chr2:74901761 G>C maps to NM_004263.3 G320G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr2:74907006 G>T maps to NM_004263.3 G662*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A5UE-01A-11D-A28X-10 chr5:9066572 C>T maps to NM_003966.2 R753R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr5:9122916 A>G maps to NM_003966.2 G544G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MA-01A-11D-A33Q-10 chr3:122632772 C>T maps to NM_001031702.2 Q688Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A9-01A-11D-A25V-10 chr5:115811299 C>G did not map to a codon.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr5:115823893 T>C did not map to a codon.
Sequencing variant TCGA-G3-A7M5-01A-11D-A33Q-10 chr15:48058328 T>A maps to NM_153618.1 Y532*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75E-01A-11D-A32G-10 chr15:48058316 T>G maps to NM_153618.1 S528S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr15:48058821 A>G maps to NM_153618.1 G552G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73F-01A-11D-A32G-10 chr15:74703982 G>A maps to NM_003612.3 G497G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25T-01A-11D-A16V-10 chr20:43837122 A>G maps to NM_003007.3 Q395Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr20:43851484 T>C maps to NM_003008.2 N404N. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-BC-A112-01A-11D-A12Z-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-QA-A7B7-01A-11D-A32G-10 chr1:87379755 C>A maps to NM_004261.3 V13V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MB-01A-11D-A20W-10 chr1:26139197 T>A maps to NM_020451.2 T434T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EL-01A-11D-A152-10 chr5:42804756 C>A did not map to a codon.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr4:25160666 T>G maps to NM_016955.3 A59A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A5UD-01A-11D-A28X-10 chr2:242283229 A>T maps to ENST00000391972 R289*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr22:42377811 C>A maps to NM_145733.2 T58T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MA-01A-11D-A20W-10 chr17:56603140 T>C maps to NM_004574.3 G151G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25Z-01A-11D-A16V-10 chr17:56599412 G>T maps to NM_004574.3 R238R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CK-01A-11D-A20W-10 chr23:118827050 T>C did not map to a codon.
Sequencing variant TCGA-UB-A7MC-01A-11D-A33Q-10 chr1:67895953 G>T maps to NM_001018067.1 G10G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A216-01A-11D-A152-10 chr1:31907018 C>A maps to NM_178865.4 L447L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr14:94845815 G>A maps to NM_001127707.1 P350P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr14:94750484 T>C maps to NM_001100607.1 Q384Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MR-A520-01A-11D-A25V-10 chr14:94912672 C>A maps to NM_001080451.1 L304L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A7PZ-01A-11D-A33Q-10 chr14:95088800 A>T maps to ENST00000393080 T372T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7ME-01A-11D-A33K-10 chr18:61323100 G>A maps to NM_006919.2 R321R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NI-01A-11D-A27I-10 chr1:173880935 C>T did not map to a codon.
Sequencing variant TCGA-CC-A7IG-01A-11D-A33K-10 chr17:1657771 T>C maps to NM_000934.3 L474L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10Z-01A-11D-A12Z-10 chr19:40929015 C>A maps to NM_013376.3 G146G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr2:64863855 G>A maps to NM_014755.2 N50N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NS-01A-11D-A30V-10 chr2:179997117 T>C maps to NM_178123.4 Q295Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A6UC-01A-21D-A33K-10 chr3:47164904 A>G maps to NM_014159.6 S407S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A7SK-01A-11D-A34Z-10 chr3:47098370 T>C maps to NM_014159.6 T2301T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr14:99865384 T>C maps to NM_032233.2 K472K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr14:99927678 T>C did not map to a codon.
Sequencing variant TCGA-RC-A7SB-01A-21D-A34Z-10 chr3:9517711 G>A maps to ENST00000407969 V1441V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BW-A5NO-01A-11D-A27I-10 chr1:150900276 G>A maps to NM_001145415.1 V29V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MB-01A-11D-A20W-10 chr1:150933422 C>G maps to NM_001145415.1 S962*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A9-01A-11D-A25V-10 chr1:150915463 T>C maps to NM_001145415.1 D270D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A66Y-01A-11D-A30V-10 chr17:27309007 G>T maps to NM_178860.4 I35I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EB-01A-11D-A12Z-10 chr22:26706635 G>A maps to NM_021115.4 R505R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr16:29891257 A>G maps to NM_201575.2 P500P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IK-01A-12D-A33Q-10 chr1:149898427 G>A maps to NM_005850.3 S182S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NV-01A-11D-A30V-10 chr22:32007129 C>T maps to NM_001007467.1 G752G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A23B-01A-11D-A16V-10 chr22:32009156 G>T maps to NM_001007467.1 A840A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MB-01A-11D-A20W-10 chr3:52962210 A>C maps to NM_016329.3 P348P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10R-01A-11D-A12Z-10 chr10:7285627 G>A maps to NM_001018039.1 L338L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A3JL-01A-11D-A20W-10 chr10:7327858 G>T maps to NM_001018039.1 S165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75G-01A-11D-A32G-10 chr1:168204372 A>T maps to NM_199344.2 K91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr6:30899267 T>C maps to NM_205854.2 T78T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr10:81371580 C>A maps to NM_001093770.2 A15A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LG-A6GG-01A-11D-A30V-10 chr10:81317057 A>C maps to NM_001098668.2 G218G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A459-01A-11D-A25V-10 chr10:120914638 T>A maps to NM_213649.1 K223*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr4:52890299 A>C maps to NM_000232.4 S260S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EJ-01A-11D-A152-10 chr7:94232700 T>A maps to NM_001099401.1 P242P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr13:23898514 T>A maps to NM_000231.2 L237L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A6M3-01A-11D-A32G-10 chr8:14181673 G>A maps to NM_139167.2 R92*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr1:67148047 C>T maps to ENST00000237247 T441T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73A-01A-12D-A32G-10 chr6:134494620 G>A maps to NM_001143676.1 I199I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10Q-01A-11D-A12Z-10 chr10:52103373 A>G maps to ENST00000361543 P173P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A5-01A-11D-A22F-10 chr22:25275470 C>A maps to NM_001039948.2 I546I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25U-01A-11D-A16V-10 chr17:2276332 T>C maps to NM_014853.2 L625L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr22:40803250 G>T maps to NM_015705.4 T429T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A4ZQ-01A-11D-A25V-10 chr1:156785886 C>T did not map to a codon.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr9:130536279 C>G maps to NM_170600.2 V168V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A26S-01A-11D-A16V-10 chr23:80457735 T>C did not map to a codon.
Sequencing variant TCGA-CC-A7IK-01A-12D-A33Q-10 chr2:235951204 G>T maps to NM_014521.2 E598*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr1:249106272 C>G maps to NM_030645.1 L336L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A113-01A-11D-A12Z-10 chr9:17787405 C>A maps to NM_003026.2 A120A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11A-01A-11D-A12Z-10 chr9:17795713 G>A maps to NM_003026.2 V344V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11C-01A-11D-A12Z-10 chr9:17786385 A>G maps to NM_003026.2 R65R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K7-A5RG-01A-11D-A28X-10 chr9:17789514 T>A maps to NM_003026.2 A197A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr9:17793436 T>A maps to NM_003026.2 T267T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5262-01A-01D-A12Z-10 chr1:87189993 A>G did not map to a codon.
Sequencing variant TCGA-KR-A7K7-01A-11D-A33K-10 chr23:19560150 C>T did not map to a codon.
Sequencing variant TCGA-K7-A5RF-01A-11D-A28X-10 chr10:105362907 G>T maps to ENST00000369774 S689S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5261-01A-01D-A12Z-10 chr5:145393599 C>T maps to NM_152550.3 D345D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5264-01A-01D-A12Z-10 chr5:148411194 C>A maps to NM_024577.3 G353*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K7-A5RF-01A-11D-A28X-10 chr5:148407629 G>T maps to NM_024577.3 I555I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7ME-01A-11D-A33K-10 chr2:234272 C>T did not map to a codon.
Sequencing variant TCGA-NI-A4U2-01A-11D-A28X-10 chr19:51171700 G>A maps to ENST00000391814 S1180S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QA-A7B7-01A-11D-A32G-10 chr19:51169903 G>T maps to ENST00000391814 G1779G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A6M4-01A-11D-A32G-10 chr19:51169669 T>C maps to ENST00000391814 P1857P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr19:51189491 A>G did not map to a codon.
Sequencing variant TCGA-DD-A113-01A-11D-A12Z-10 chr11:70333709 C>T maps to ENST00000338508 P890P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75H-01A-11D-A32G-10 chr22:51113570 T>C maps to NM_001080420.1 Y53Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75E-01A-11D-A32G-10 chr19:430741 T>C maps to NM_012435.2 P372P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3M9-01A-11D-A20W-10 chr15:49135765 C>T maps to NM_203349.3 G441G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr16:46633833 G>T maps to NM_024745.4 G418G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25W-01A-11D-A16V-10 chr19:4280288 C>A maps to NM_020209.3 R77R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A123-01A-11D-A12Z-10 chr15:45465912 A>G maps to ENST00000437903 V275V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A6M6-01A-11D-A32G-10 chr4:42400219 C>T maps to NM_001080505.1 D49D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr4:42403329 C>A maps to NM_001080505.1 P193P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A110-01A-11D-A12Z-10 chr19:41089576 G>A maps to NM_138392.3 A373A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A7PZ-01A-11D-A33Q-10 chr17:18250859 T>A maps to NM_004169.3 K157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EL-01A-11D-A152-10 chr12:57626599 T>C maps to NM_005412.5 T277T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NE-01A-11D-A27I-10 chr3:157820589 C>G maps to NM_003030.4 R168R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr6:146276323 T>A maps to ENST00000367503 P45P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A116-01A-11D-A12Z-10 chr23:9863963 G>T did not map to a codon.
Sequencing variant TCGA-HP-A5N0-01A-11D-A28X-10 chr23:9841726 G>A did not map to a codon.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr4:77675937 C>T maps to NM_020859.3 A1434A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr4:77660861 T>C maps to NM_020859.3 A512A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A6M3-01A-11D-A32G-10 chr4:77660339 A>C maps to NM_020859.3 S338S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A69H-01A-11D-A30V-10 chr23:50350825 G>T did not map to a codon.
Sequencing variant TCGA-CC-A3MB-01A-11D-A20W-10 chr23:50351122 T>C did not map to a codon.
Sequencing variant TCGA-DD-A3A9-01A-11D-A25V-10 chr23:50345796 A>G did not map to a codon.
Sequencing variant TCGA-DD-A4NF-01A-11D-A27I-10 chr23:50376661 G>A did not map to a codon.
Sequencing variant TCGA-GJ-A6C0-01A-12D-A30V-10 chr23:50378092 C>T did not map to a codon.
Sequencing variant TCGA-DD-A39Y-01A-11D-A20W-10 chr3:164758753 T>C maps to NM_001041.3 E711E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A4XI-01A-11D-A25V-10 chr11:124517356 A>G maps to NM_170601.3 N290N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NK-01A-11D-A28X-10 chr16:48396329 G>A maps to NM_001006610.1 Q35*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A112-01A-11D-A12Z-10 chr11:117053473 C>T maps to NM_001040455.1 F218F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A3KG-01A-11D-A20W-10 chr20:3672110 G>A maps to NM_023068.3 H1489H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IK-01A-12D-A33Q-10 chr20:3674259 C>A maps to NM_023068.3 P1114P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A113-01A-11D-A12Z-10 chr20:3673731 G>A maps to NM_023068.3 G1185G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A26S-01A-11D-A16V-10 chr20:3682280 A>G maps to NM_023068.3 P412P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr19:50453265 A>T maps to NM_052884.2 L686L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IG-01A-11D-A33K-10 chr18:43418740 G>T maps to NM_213602.2 A185A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr18:43417042 A>G maps to NM_213602.2 T34T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A3KF-01A-11D-A20W-10 chr19:52130940 T>C maps to ENST00000222107 R352R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EL-01A-11D-A152-10 chr19:51645631 G>A maps to NM_014385.2 L2L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73D-01A-12D-A32G-10 chr19:51960895 C>A maps to NM_014442.2 G184G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A66X-01A-11D-A30V-10 chr19:51961350 T>C maps to NM_014442.2 Q97Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IK-01A-12D-A33Q-10 chr19:51630383 T>A maps to NM_014441.2 P282P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A69H-01A-11D-A30V-10 chr21:44841638 C>T maps to NM_173354.3 A126A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IJ-01A-11D-A33Q-10 chr21:44845965 C>T maps to NM_173354.3 R31R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr11:116746721 A>G maps to ENST00000445177 L360L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EB-01A-11D-A12Z-10 chr5:138287485 T>C maps to ENST00000509534 A292A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39X-01A-11D-A20W-10 chr21:38095409 C>A maps to NM_005069.3 G174G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CK-01A-11D-A20W-10 chr21:38117327 C>T maps to NM_005069.3 C489C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25Z-01A-11D-A16V-10 chr15:75694203 A>G maps to NM_001145357.1 S505S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IK-01A-12D-A33Q-10 chr19:16973708 A>C maps to NM_015260.1 T427T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10R-01A-11D-A12Z-10 chr14:72139333 G>T maps to NM_015556.1 P1033P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MB-01A-11D-A20W-10 chr14:72205029 A>G maps to NM_015556.1 E1753E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EF-01A-11D-A12Z-10 chr14:72054831 A>T maps to NM_015556.1 A81A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A4ZQ-01A-11D-A25V-10 chr14:72190402 C>T maps to NM_015556.1 F1437F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr1:232577102 A>T maps to NM_020808.3 G1192G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5260-01A-01D-A12Z-10 chr19:38610465 C>T maps to NM_015073.1 L938L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MC-01A-11D-A22F-10 chr19:38633245 A>G maps to NM_015073.1 V1143V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A6UC-01A-21D-A33K-10 chr20:1551499 G>C maps to NM_006065.3 A345A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EB-01A-11D-A12Z-10 chr12:120741414 C>T maps to NM_012240.2 I17I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr6:13588599 G>A maps to NM_012241.3 K51K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A496-01A-11D-A25V-10 chr14:61186833 G>C maps to NM_017420.4 S398*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KC-01A-11D-A20W-10 chr7:26779583 C>T did not map to a codon.
Sequencing variant TCGA-DD-A11B-01A-11D-A16Z-10 chr6:31929370 T>C maps to NM_006929.4 S279S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EA-01A-11D-A12Z-10 chr5:54635849 A>G maps to NM_015360.4 A176A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A26S-01A-11D-A16V-10 chr5:54637585 T>C maps to NM_015360.4 Y256Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CK-01A-11D-A20W-10 chr5:54619961 T>A maps to NM_015360.4 L92*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A5SI-01A-31D-A27I-10 chr5:54624615 A>C maps to NM_015360.4 S164S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A3R2-01A-11D-A22F-10 chr5:133494205 A>C maps to NM_170679.2 P132P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39Y-01A-11D-A20W-10 chr4:48384603 A>G maps to NM_020846.1 A294A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr1:160582367 A>G maps to NM_003037.2 P289P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EI-01A-11D-A12Z-10 chr1:160461020 A>G maps to NM_001184714.1 T180T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75E-01A-11D-A32G-10 chr1:159802825 A>G maps to NM_020125.2 P176P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-4073-01B-02D-A12Z-10 chr13:103701771 C>T maps to NM_000452.2 T262T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1ED-01A-11D-A152-10 chr13:103698605 A>G maps to NM_000452.2 Y308Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NO-01A-11D-A28X-10 chr13:103705044 A>T maps to NM_000452.2 V170V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A7M6-01A-11D-A33Q-10 chr23:153715954 G>T did not map to a codon.
Sequencing variant TCGA-DD-A115-01A-11D-A12Z-10 chr8:82606129 G>A maps to NM_001010893.2 L360L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73G-01A-22D-A32G-10 chr2:219254738 C>T maps to NM_000578.3 T314T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EL-01A-11D-A152-10 chr15:48593510 G>T did not map to a codon.
Sequencing variant TCGA-DD-A4NI-01A-11D-A27I-10 chr15:48533794 A>G maps to NM_000338.2 V433V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25Z-01A-11D-A16V-10 chr15:48595051 T>C maps to NM_000338.2 N1090N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K7-A5RG-01A-11D-A28X-10 chr16:56920368 C>A maps to NM_000339.2 I673I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73D-01A-12D-A32G-10 chr20:44664101 C>A maps to NM_001134771.1 T92T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr20:44676617 A>G did not map to a codon.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr20:44684871 A>G maps to NM_001134771.1 E980E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11B-01A-11D-A16Z-10 chr5:1079606 G>A maps to NM_006598.2 I434I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EF-01A-11D-A12Z-10 chr7:100452000 G>T did not map to a codon.
Sequencing variant TCGA-CC-A3M9-01A-11D-A20W-10 chr7:135377153 A>G maps to NM_012450.2 T379T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr18:43310401 C>A maps to NM_001146037.1 T95T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A4ZP-01A-12D-A25V-10 chr18:43310323 C>A maps to NM_001146037.1 P69P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EF-01A-11D-A12Z-10 chr13:99371493 G>A maps to NM_005073.3 L213L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A3I0-01A-11D-A22F-10 chr1:113471852 A>G maps to NM_003051.3 A26A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MC-01A-11D-A22F-10 chr6:111540207 C>T maps to NM_018593.4 F426F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr1:110918149 T>C maps to NM_004696.1 T422T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr17:73100203 G>C maps to ENST00000450736 A471A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IG-01A-11D-A33K-10 chr6:25811665 A>G maps to NM_005074.3 L380L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IJ-01A-11D-A33Q-10 chr6:25799087 G>C maps to NM_005074.3 G443G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NV-01A-11D-A30V-10 chr6:25917286 T>C maps to NM_005835.2 L226L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LG-A6GG-01A-11D-A30V-10 chr6:25850685 C>T did not map to a codon.
Sequencing variant TCGA-DD-A1EL-01A-11D-A152-10 chr6:25762252 C>T maps to NM_005495.2 N21N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MA-01A-11D-A20W-10 chr11:22381051 A>G maps to NM_020346.2 R184R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IF-01A-11D-A33K-10 chr11:22380970 T>G maps to NM_020346.2 A157A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A3I0-01A-11D-A22F-10 chr11:22399123 G>T maps to NM_020346.2 G529G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EF-01A-11D-A12Z-10 chr2:228567036 C>T did not map to a codon.
Sequencing variant TCGA-G3-A25Z-01A-11D-A16V-10 chr2:228563989 C>A maps to NM_025243.3 T147T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A6UC-01A-21D-A33K-10 chr9:4544612 T>C maps to NM_004170.5 T46T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KC-01A-11D-A20W-10 chr19:47280544 G>A maps to NM_005628.2 L392L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr19:15083652 G>A maps to NM_005071.1 Q24*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LG-A6GG-01A-11D-A30V-10 chr19:15063776 C>A maps to NM_005071.1 E488*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10U-01A-11D-A12Z-10 chr1:53555551 G>C maps to NM_006671.4 L427L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NJ-01A-11D-A27I-10 chr2:113416961 A>G maps to NM_005415.3 K410K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A8-01A-11D-A22F-10 chr6:160543146 G>A maps to NM_003057.2 Q60Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A3I1-01A-11D-A22F-10 chr11:63059094 A>T maps to NM_001039752.3 I162I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr11:64323630 C>T maps to NM_018484.2 L54L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A459-01A-11D-A25V-10 chr11:64366297 C>A maps to NM_144585.2 R325R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CI-01A-11D-A20W-10 chr11:64367213 C>T maps to NM_144585.2 F379F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr11:64359431 T>A did not map to a codon.
Sequencing variant TCGA-CC-5264-01A-01D-A12Z-10 chr3:38347843 C>T maps to NM_004803.3 H109H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T1-A6J8-01A-11D-A32G-10 chr3:38347894 C>T maps to NM_004803.3 G126G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-4073-01B-02D-A12Z-10 chr6:110763663 C>T maps to NM_033125.2 L322L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-4073-01B-02D-A12Z-10 chr14:23816359 G>A maps to NM_020372.2 A426A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr11:62886695 T>A maps to NM_001136506.1 A206A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25U-01A-11D-A16V-10 chr11:62848564 G>T maps to NM_001136506.1 S475S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr5:131647951 A>G maps to NM_003059.2 S164S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25S-01A-11D-A16V-10 chr11:62751009 C>A maps to NM_004790.3 L209L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NI-01A-11D-A27I-10 chr11:62768190 C>A did not map to a codon.
Sequencing variant TCGA-DD-A4NI-01A-11D-A27I-10 chr9:19528052 C>T maps to NM_020344.2 A521A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T1-A6J8-01A-11D-A32G-10 chr9:19576991 G>T maps to NM_020344.2 L386L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MA-01A-11D-A20W-10 chr20:19698203 C>T maps to NM_020689.3 S584S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A7M6-01A-11D-A33Q-10 chr20:19560718 G>C did not map to a codon.
Sequencing variant TCGA-CC-5259-01A-31D-A20W-10 chr2:172700889 G>A maps to NM_003705.3 Q152*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NI-A4U2-01A-11D-A28X-10 chr7:95838257 T>C maps to NM_001160210.1 T120T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73E-01A-12D-A32G-10 chr10:70243245 A>T maps to NM_152707.2 S314S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LG-A6GG-01A-11D-A30V-10 chr1:108686248 T>C maps to NM_013386.3 E338E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A112-01A-11D-A12Z-10 chr12:98991698 T>C maps to NM_213611.2 V115V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39X-01A-11D-A20W-10 chr13:45978524 C>T maps to NM_001010875.2 V110V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A5SI-01A-31D-A27I-10 chr8:23429091 C>T maps to NM_016612.2 L247L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NI-A4U2-01A-11D-A28X-10 chr23:118603837 T>G did not map to a codon.
Sequencing variant TCGA-BW-A5NP-01A-11D-A27I-10 chr7:107423493 G>A maps to NM_000111.2 F388F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr3:48669736 T>A maps to NM_022911.2 R176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A459-01A-11D-A25V-10 chr8:92352643 T>A maps to NM_134266.1 P297P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr19:59022229 G>A maps to NM_012254.2 L252L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EB-01A-11D-A12Z-10 chr5:128368890 C>A maps to NM_001017372.1 Y592*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IG-01A-11D-A33K-10 chr6:44198615 C>T maps to ENST00000313248 L331L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73F-01A-11D-A32G-10 chr6:44197694 G>T maps to ENST00000313248 V201V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MC-01A-11D-A33Q-10 chr11:66135013 A>G maps to NM_001532.2 F218F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A8-01A-11D-A22F-10 chr1:43394605 C>A maps to NM_006516.2 L357L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IG-01A-11D-A33K-10 chr22:24224832 G>T maps to NM_030807.3 S298S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EL-01A-11D-A152-10 chr12:40158660 C>A did not map to a codon.
Sequencing variant TCGA-DD-A114-01A-11D-A12Z-10 chr12:7981449 C>A maps to NM_153449.2 E199*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr17:7189181 C>T maps to NM_001042.2 N427N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EK-01A-11D-A20W-10 chr20:62373480 A>G did not map to a codon.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr20:62373569 C>T maps to NM_020062.3 L223L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75G-01A-11D-A32G-10 chr1:9117612 C>A maps to NM_003039.2 E63*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A23B-01A-11D-A16V-10 chr1:211751519 G>C maps to NM_021194.2 G145G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BW-A5NO-01A-11D-A27I-10 chr8:118175765 G>T maps to NM_173851.2 E276*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25U-01A-11D-A16V-10 chr5:176821188 C>A maps to NM_003052.4 I389I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr5:176814992 A>T did not map to a codon.
Sequencing variant TCGA-DD-A11C-01A-11D-A12Z-10 chr23:48763796 A>G did not map to a codon.
Sequencing variant TCGA-G3-A25Z-01A-11D-A16V-10 chr5:139947620 C>A maps to NM_080670.2 V289V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IG-01A-11D-A33K-10 chr3:112300031 C>T maps to NM_017945.2 S356S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QA-A7B7-01A-11D-A32G-10 chr17:47784393 C>T maps to ENST00000415270 E84E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A26S-01A-11D-A16V-10 chr6:44223036 G>A maps to NM_178148.2 Y235Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr6:137245641 T>A maps to NM_001008783.1 G353G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NB-01A-12D-A25V-10 chr1:234041460 C>T maps to NM_173508.2 I80I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EG-01A-11D-A20W-10 chr5:150666920 G>T maps to NM_001145017.1 P239P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr11:92899081 A>G did not map to a codon.
Sequencing variant TCGA-DD-A113-01A-11D-A12Z-10 chr21:43962521 C>T maps to NM_018964.3 N165N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EL-01A-11D-A152-10 chr21:43954848 C>T maps to NM_018964.3 D60D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr17:79234065 C>T maps to NM_001037984.1 L420L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BD-A3EP-01A-11D-A22F-10 chr12:46756926 T>C maps to NM_018976.4 E352E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr12:46760940 T>C maps to NM_018976.4 L133L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A5SL-01A-11D-A27I-10 chr3:50251706 C>T maps to NM_006841.4 V25V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A5UD-01A-11D-A28X-10 chr10:18282138 G>A maps to NM_001145195.1 V484V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KR-A7K2-01A-12D-A33Q-10 chr10:18289659 T>C maps to NM_001145195.1 D555D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr10:18250688 A>C maps to NM_001145195.1 L147L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25Y-01A-11D-A16V-10 chr3:125786987 G>C maps to NM_001008485.1 P25P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5259-01A-31D-A20W-10 chr1:75683602 T>G maps to NM_152697.4 A524A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A7M5-01A-11D-A33Q-10 chr1:75716964 A>T maps to NM_152697.4 L92*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A5W4-01A-11D-A28X-10 chr1:8384367 A>T maps to ENST00000377479 G27G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A116-01A-11D-A12Z-10 chr8:142231706 G>A maps to NM_001080431.1 G82G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EG-01A-11D-A20W-10 chr8:142231724 G>A maps to NM_001080431.1 C76C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MB-01A-11D-A20W-10 chr9:115652238 G>A maps to NM_033051.3 P241P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PD-A5DF-01A-11D-A27I-10 chr17:19452980 A>T maps to ENST00000395585 P163P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A5SL-01A-11D-A27I-10 chr2:220503555 C>A maps to NM_201574.2 V1023V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A217-01A-11D-A152-10 chr4:72412080 T>C maps to NM_001098484.2 Y819Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A23B-01A-11D-A16V-10 chr4:72423586 C>A maps to NM_001098484.2 I974I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75G-01A-11D-A32G-10 chr12:51864174 G>T did not map to a codon.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr12:51865211 A>G maps to NM_001039960.1 L600L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr22:32495286 C>A maps to NM_000343.3 P466P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5261-01A-01D-A12Z-10 chr16:24888676 G>A maps to NM_052944.2 T192T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A3R3-01A-11D-A22F-10 chr16:24902217 A>G maps to NM_052944.2 G231G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HP-A5MZ-01A-21D-A27I-10 chr19:18001722 G>A maps to NM_000453.2 P560P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr12:101551062 A>T maps to NM_145913.3 R609R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1ED-01A-11D-A152-10 chr3:11072873 T>C maps to NM_003042.3 Y445Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A7M9-01A-23D-A34Z-10 chr12:85277688 G>T maps to NM_182767.4 A235A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NV-01A-11D-A30V-10 chr5:1245973 C>G maps to NM_182632.2 P556P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A5SM-01A-12D-A28X-10 chr5:1244794 C>T maps to NM_182632.2 V523V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A66X-01A-11D-A30V-10 chr5:1219157 C>T maps to NM_001003841.2 G438G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NA-01A-11D-A25V-10 chr16:55725912 T>C maps to NM_001043.3 N289N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75I-01A-11D-A32G-10 chr16:55725900 C>T maps to NM_001043.3 P285P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11D-01A-11D-A12Z-10 chr3:45807035 G>A maps to NM_020208.3 A432A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IG-01A-11D-A33K-10 chr5:1406398 A>T maps to NM_001044.4 V501V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NH-01A-11D-A27I-10 chr5:1409892 G>A maps to NM_001044.4 L447L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A496-01A-11D-A25V-10 chr1:44468279 C>T maps to NM_201649.2 L327L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25W-01A-11D-A16V-10 chr1:44466892 A>G maps to NM_201649.2 Y499Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MA-01A-11D-A20W-10 chr8:87242257 A>G maps to NM_138817.2 F83F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NF-01A-11D-A27I-10 chr8:87229801 A>T maps to NM_138817.2 L359*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A7XO-01A-11D-A34Z-10 chr19:33349419 A>T maps to NM_014270.4 A301A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A5SJ-01A-11D-A27I-10 chr19:33324220 T>A maps to NM_014270.4 V411V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10T-01A-11D-A12Z-10 chr2:40656835 T>G maps to NM_021097.2 T195T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A118-01A-11D-A12Z-10 chr2:40656070 T>A maps to NM_021097.2 T450T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A216-01A-11D-A152-10 chr14:70633753 C>T maps to NM_183002.1 K462K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A5SJ-01A-11D-A27I-10 chr14:70634239 G>A maps to NM_183002.1 N300N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-O8-A75V-01A-11D-A32G-10 chr14:70634965 G>A maps to NM_183002.1 V58V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K7-A5RG-01A-11D-A28X-10 chr5:481702 G>A maps to NM_004174.2 I498I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A9-01A-11D-A25V-10 chr2:103124607 C>A maps to NM_001011552.3 I423I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10R-01A-11D-A12Z-10 chr16:67282982 G>A maps to NM_004594.2 Q22Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11D-01A-11D-A12Z-10 chr23:135080329 T>A did not map to a codon.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr23:135067789 G>A did not map to a codon.
Sequencing variant TCGA-FV-A495-01A-11D-A25V-10 chr23:135067805 G>A did not map to a codon.
Sequencing variant TCGA-MR-A520-01A-11D-A25V-10 chr23:135122262 G>C did not map to a codon.
Sequencing variant TCGA-NI-A4U2-01A-11D-A28X-10 chr23:135106597 A>G did not map to a codon.
Sequencing variant TCGA-BC-4073-01B-02D-A12Z-10 chr23:46541902 G>A did not map to a codon.
Sequencing variant TCGA-GJ-A6C0-01A-12D-A30V-10 chr20:48497558 C>T maps to ENST00000417961 I435I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K7-A5RG-01A-11D-A28X-10 chr3:143292966 C>T maps to NM_173653.3 W321*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A112-01A-11D-A12Z-10 chr12:21329793 A>G maps to NM_006446.4 L148L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MA-01A-11D-A20W-10 chr12:21068947 T>C maps to NM_019844.2 L626L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A3I0-01A-11D-A22F-10 chr3:133654649 G>A maps to NM_005630.2 C594C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5260-01A-01D-A12Z-10 chr11:74904563 G>A maps to NM_007256.4 P459P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73A-01A-12D-A32G-10 chr15:92459623 G>T maps to NM_013272.3 V194V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75G-01A-11D-A32G-10 chr20:61287811 C>G maps to NM_016354.3 P2P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A7XO-01A-11D-A34Z-10 chr5:101592901 T>C maps to NM_180991.4 G462G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A113-01A-11D-A12Z-10 chr17:33680371 A>G maps to NM_152270.3 P635P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73A-01A-12D-A32G-10 chr17:33679757 C>A maps to NM_152270.3 G775*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A217-01A-11D-A152-10 chr17:33749276 G>T maps to NM_018042.3 L257L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A6UC-01A-21D-A33K-10 chr17:33769275 C>A maps to NM_144682.5 E410*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A9-01A-11D-A25V-10 chr10:98764565 C>T maps to NM_003061.2 E1198E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NV-01A-11D-A30V-10 chr10:98945407 C>T maps to NM_003061.2 G8G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A8-01A-11D-A22F-10 chr4:20535248 A>G maps to ENST00000273739 A585A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25T-01A-11D-A16V-10 chr4:20611767 T>C maps to ENST00000273739 F1288F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A7M5-01A-11D-A33Q-10 chr4:20487847 A>T maps to ENST00000273739 R189*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10Y-01A-11D-A12Z-10 chr5:168119628 G>A maps to NM_003062.2 P1053P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5263-01A-01D-A12Z-10 chr5:168127669 A>G maps to NM_003062.2 T953T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CI-01A-11D-A20W-10 chr5:168189662 G>A maps to NM_003062.2 S497S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HP-A5N0-01A-11D-A28X-10 chr5:168233530 C>A maps to NM_003062.2 T285T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RG-A7D4-01A-12D-A33Q-10 chr5:168123357 G>A maps to NM_003062.2 N1007N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EA-01A-11D-A12Z-10 chr13:84454265 G>A maps to NM_052910.1 I459I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EJ-01A-11D-A152-10 chr13:84454186 G>A maps to NM_052910.1 L486L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73F-01A-11D-A32G-10 chr13:84454718 A>T maps to NM_052910.1 G308G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MA-01A-11D-A20W-10 chr23:144905986 G>A did not map to a codon.
Sequencing variant TCGA-DD-A1EI-01A-11D-A12Z-10 chr23:144904542 C>A did not map to a codon.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr23:144906049 C>A did not map to a codon.
Sequencing variant TCGA-FV-A495-01A-11D-A25V-10 chr23:144903984 C>A did not map to a codon.
Sequencing variant TCGA-G3-A5SK-01A-11D-A27I-10 chr23:144905413 T>A did not map to a codon.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr23:144904335 A>T did not map to a codon.
Sequencing variant TCGA-G3-A25T-01A-11D-A16V-10 chr3:164908426 T>C maps to NM_014926.2 K64K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A6M6-01A-11D-A32G-10 chr3:164908255 G>A maps to NM_014926.2 F121F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A3KG-01A-11D-A20W-10 chr23:142717431 A>G did not map to a codon.
Sequencing variant TCGA-DD-A3A1-01A-11D-A20W-10 chr23:142717684 T>C did not map to a codon.
Sequencing variant TCGA-DD-A4NV-01A-11D-A30V-10 chr23:142717870 G>T did not map to a codon.
Sequencing variant TCGA-MI-A75H-01A-11D-A32G-10 chr3:57898306 T>A maps to ENST00000428312 L616L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73F-01A-11D-A32G-10 chr15:59192011 A>G maps to NM_024755.2 A238A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25T-01A-11D-A16V-10 chr13:37453766 T>C maps to NM_001127217.2 R20R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A115-01A-11D-A12Z-10 chr1:40839818 G>A maps to NM_022733.2 V9V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A5-01A-11D-A22F-10 chr23:128641994 T>A did not map to a codon.
Sequencing variant TCGA-CC-A5UE-01A-11D-A28X-10 chr19:11096862 A>T did not map to a codon.
Sequencing variant TCGA-CC-5260-01A-01D-A12Z-10 chr23:53409454 T>A did not map to a codon.
Sequencing variant TCGA-DD-A1EL-01A-11D-A152-10 chr9:106894407 T>G did not map to a codon.
Sequencing variant TCGA-BC-A3KF-01A-11D-A20W-10 chr10:112338436 T>C maps to NM_005445.3 N134N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7II-01A-11D-A33K-10 chr3:160134113 G>T maps to NM_005496.3 E450*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NF-01A-11D-A27I-10 chr9:72879294 G>T maps to NM_015110.3 S87S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A3I0-01A-11D-A22F-10 chr2:17877587 G>A maps to ENST00000381272 R860*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EF-01A-11D-A12Z-10 chr18:2795978 A>T maps to NM_015295.2 K1918*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr18:2694532 T>C maps to NM_015295.2 D294D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr18:2726475 T>C maps to NM_015295.2 P909P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A9-01A-11D-A25V-10 chr17:18167687 G>A maps to NM_148886.1 L336L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KC-01A-11D-A20W-10 chr17:18166171 C>T maps to NM_148886.1 A57A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NQ-01A-21D-A28X-10 chr16:18853629 A>G maps to ENST00000389467 H2122H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr16:18846413 C>T maps to ENST00000389467 L2710L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-O8-A75V-01A-11D-A32G-10 chr16:18852977 G>T maps to ENST00000389467 S2202*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A116-01A-11D-A12Z-10 chr1:156220787 C>A did not map to a codon.
Sequencing variant TCGA-G3-A25T-01A-11D-A16V-10 chr17:2203158 C>A maps to NM_017575.4 V296V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A5SI-01A-31D-A27I-10 chr17:2203671 A>G maps to NM_017575.4 A125A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A112-01A-11D-A12Z-10 chr10:112053907 T>C maps to NM_005871.3 *239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11C-01A-11D-A12Z-10 chr10:112063291 T>C maps to NM_005871.3 Q18Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39Z-01A-11D-A20W-10 chr10:112063339 T>C maps to NM_005871.3 S2S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr20:4168038 C>T maps to ENST00000443211 F581F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A1-01A-11D-A20W-10 chr11:6412064 G>A maps to NM_000543.4 R79R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr2:130939135 T>A maps to NM_017951.4 P13P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr23:21761891 T>C did not map to a codon.
Sequencing variant TCGA-DD-A3A8-01A-11D-A22F-10 chr2:88396263 G>C maps to NM_198274.3 L283L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25S-01A-11D-A16V-10 chr2:88410003 C>T maps to NM_198274.3 S482S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5262-01A-01D-A12Z-10 chr1:214501024 G>T maps to NM_020197.2 L221L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73G-01A-22D-A32G-10 chr1:246021832 G>A maps to NM_001167740.1 A347A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BD-A3EP-01A-11D-A22F-10 chr22:21235342 A>G maps to NM_004782.3 K147K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr6:84311119 T>A maps to NM_014841.2 A398A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A7XO-01A-11D-A34Z-10 chr6:84270662 C>A maps to NM_014841.2 G816*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr6:84300972 A>G maps to NM_014841.2 S657S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr9:15447090 A>T did not map to a codon.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr5:121739501 A>G maps to ENST00000379533 S71S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25Y-01A-11D-A16V-10 chr5:121767680 C>T maps to ENST00000379533 C447C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr5:121780394 T>C maps to ENST00000379533 S567S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NH-01A-11D-A27I-10 chr2:242004718 C>T maps to NM_001080437.1 L906L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A7M8-01A-11D-A33Q-10 chr2:241979570 C>T maps to NM_001080437.1 C375C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr17:47022063 G>T maps to NM_007241.2 I11I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A3KF-01A-11D-A20W-10 chr3:43388905 G>A maps to NM_017719.4 A385A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5261-01A-01D-A12Z-10 chr2:96952175 C>T maps to NM_014014.3 P1292P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1E9-01A-21D-A152-10 chr20:2443294 G>C maps to ENST00000339610 P224P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NI-01A-11D-A27I-10 chr15:25221502 G>T maps to NM_022805.2 L69L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A2QQ-01A-11D-A22F-10 chr20:32000380 C>T maps to NM_003098.2 Q303Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3M9-01A-11D-A20W-10 chr8:121644854 C>T maps to NM_021021.3 T275T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NG-01A-11D-A27I-10 chr8:121824004 C>A maps to NM_021021.3 E27*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75H-01A-11D-A32G-10 chr8:51617236 G>A maps to NM_018967.2 V372V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IG-01A-11D-A33K-10 chr2:1241789 G>A did not map to a codon.
Sequencing variant TCGA-ED-A7PZ-01A-11D-A33Q-10 chr2:1094064 C>T maps to NM_018968.3 V98V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A7SF-01A-11D-A34Z-10 chr2:1204796 G>T maps to NM_018968.3 S200S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A7SK-01A-11D-A34Z-10 chr14:78198863 G>A maps to NM_012245.2 A285A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5258-01A-01D-A12Z-10 chr7:26412161 T>A maps to ENST00000446848 C218*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10T-01A-11D-A12Z-10 chr23:70281774 G>C did not map to a codon.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr23:70282706 G>A did not map to a codon.
Sequencing variant TCGA-BC-A5W4-01A-11D-A28X-10 chr7:17890005 T>C maps to ENST00000417048 V391V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A113-01A-11D-A12Z-10 chr7:17833731 C>T maps to ENST00000417048 K985K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A7PY-01A-11D-A33Q-10 chr6:86223593 G>A maps to NM_153816.3 N859N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A112-01A-11D-A12Z-10 chr5:53815182 G>A maps to NM_052870.2 V467V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10Q-01A-11D-A12Z-10 chr11:130785771 A>G maps to NM_014758.2 N21N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EL-01A-11D-A152-10 chr1:99203827 G>C maps to NM_015976.4 V387V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5261-01A-01D-A12Z-10 chr7:2317902 G>A maps to NM_013321.2 I44I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A6M3-01A-11D-A32G-10 chr6:107956285 G>A maps to NM_018013.3 P746P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7II-01A-11D-A33K-10 chr18:67992705 C>T maps to NM_004232.3 Q268*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A6UC-01A-21D-A33K-10 chr17:36508354 C>T maps to NM_014598.2 V76V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A110-01A-11D-A12Z-10 chr21:34925205 T>A maps to NM_138927.1 P1223P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EB-01A-11D-A12Z-10 chr4:186533093 C>T maps to ENST00000355634 W1075*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A3-01A-11D-A22F-10 chr10:108339224 C>A maps to NM_001013031.1 L1091L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A7M9-01A-23D-A34Z-10 chr10:108459040 G>A maps to NM_001013031.1 F448F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BW-A5NQ-01A-11D-A27I-10 chr4:7726888 C>T maps to NM_020777.2 Q874*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IG-01A-11D-A33K-10 chr4:7705957 G>T maps to NM_020777.2 S605S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A23B-01A-11D-A16V-10 chr4:7730137 C>A maps to NM_020777.2 T977T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-O8-A75V-01A-11D-A32G-10 chr4:7725464 C>T maps to NM_020777.2 D822D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PD-A5DF-01A-11D-A27I-10 chr4:7714543 G>A maps to NM_020777.2 E651E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A217-01A-11D-A152-10 chr11:121474905 A>G maps to NM_003105.5 T1508T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11C-01A-11D-A12Z-10 chr11:121383717 T>C maps to NM_003105.5 L316L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EF-01A-11D-A12Z-10 chr11:121421353 A>G maps to NM_003105.5 G747G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A7PY-01A-11D-A33Q-10 chr11:121476236 A>G maps to NM_003105.5 A1635A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr11:121478829 T>C maps to NM_003105.5 S1728S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NK-01A-11D-A28X-10 chr22:38369603 C>T maps to NM_006941.3 R433R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A7SF-01A-11D-A34Z-10 chr22:38379512 G>T maps to NM_006941.3 R93R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73G-01A-22D-A32G-10 chr2:5834086 G>T maps to NM_003108.3 E412*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A112-01A-11D-A12Z-10 chr3:137483874 C>G maps to NM_004189.2 P83P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K7-A6G5-01A-11D-A30V-10 chr3:181431519 T>G did not map to a codon.
Sequencing variant TCGA-RC-A6M3-01A-11D-A32G-10 chr13:95363706 G>A maps to NM_007084.2 T199T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr23:139587140 G>T did not map to a codon.
Sequencing variant TCGA-MI-A75C-01A-11D-A32G-10 chr5:157053725 T>C maps to NM_178424.1 T628T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11B-01A-11D-A16Z-10 chr11:15994639 T>A maps to NM_001145819.1 P747P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A5SJ-01A-11D-A27I-10 chr17:70119054 C>T maps to NM_000346.3 A209A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A7PX-01A-51D-A34Z-10 chr2:231067439 T>G maps to NM_080424.2 T301T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A6UC-01A-21D-A33K-10 chr2:231090582 G>A maps to NM_007237.4 G8G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr2:174820456 T>C maps to NM_003111.4 P261P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73F-01A-11D-A32G-10 chr7:21521736 T>C maps to NM_003112.3 H701H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25T-01A-11D-A16V-10 chr2:171573769 G>A maps to NM_001003845.2 T351T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A5UD-01A-11D-A28X-10 chr12:53723036 A>T maps to NM_001173467.1 A63A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr6:88757709 G>A maps to NM_030960.2 G29G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BW-A5NO-01A-11D-A27I-10 chr2:214727352 G>T did not map to a codon.
Sequencing variant TCGA-RC-A6M4-01A-11D-A32G-10 chr1:118623784 A>G maps to NM_206996.2 D716D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A82E-01A-11D-A34Z-10 chr17:26906775 C>T maps to NM_006461.3 Q959Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KC-01A-11D-A20W-10 chr17:26912925 C>A maps to NM_006461.3 E566*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A4XI-01A-11D-A25V-10 chr17:49048125 C>A maps to ENST00000376407 T1265T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K7-A6G5-01A-11D-A30V-10 chr23:140335727 G>T did not map to a codon.
Sequencing variant TCGA-K7-A6G5-01A-11D-A30V-10 chr23:140785699 G>T did not map to a codon.
Sequencing variant TCGA-DD-A4NE-01A-11D-A27I-10 chr2:32341262 T>C maps to NM_014946.3 L360L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NF-01A-11D-A27I-10 chr13:24864809 T>C maps to ENST00000424834 Y993Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A3RK-01A-11D-A22F-10 chr13:24798143 C>T maps to ENST00000424834 D396D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A2QQ-01A-11D-A22F-10 chr4:52948585 T>C maps to NM_145263.2 A463A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EB-01A-11D-A12Z-10 chr11:133714430 G>T maps to NM_174927.1 G80G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EG-01A-11D-A20W-10 chr11:133711935 A>G maps to NM_174927.1 *168R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A1HT-01A-11D-A12Z-10 chr20:48523373 C>A maps to NM_006038.3 T115T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A217-01A-11D-A152-10 chr17:48629416 G>A maps to NM_022827.2 A611A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25T-01A-11D-A16V-10 chr17:48625119 T>C maps to NM_022827.2 S39S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25Y-01A-11D-A16V-10 chr17:48629416 G>A maps to NM_022827.2 A611A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A112-01A-11D-A12Z-10 chr16:89764068 C>G maps to NM_152339.3 L316L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25T-01A-11D-A16V-10 chr16:89764257 G>A maps to NM_152339.3 P253P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A3-01A-11D-A22F-10 chr4:123900510 C>T maps to NM_145207.2 A613A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr4:123859403 A>T maps to NM_145207.2 S486S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr15:45713245 T>C maps to NM_024063.2 A700A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr14:88892682 T>C maps to NM_018418.4 S160S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10U-01A-11D-A12Z-10 chr8:145101781 C>T maps to NM_198572.2 L567L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10W-01A-11D-A12Z-10 chr6:44328191 T>C maps to NM_145026.3 A99A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A459-01A-11D-A25V-10 chr11:64939932 C>T maps to NM_001008778.1 L125L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25S-01A-11D-A16V-10 chr5:35618117 C>T maps to NM_024867.3 Q7*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BD-A2L6-01A-11D-A20W-10 chr2:220354313 G>A maps to NM_005876.4 A2858A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NO-01A-11D-A28X-10 chr2:220342148 G>T maps to NM_005876.4 E1571*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A4ZQ-01A-11D-A25V-10 chr2:220348818 C>T maps to NM_005876.4 Q2212*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75I-01A-11D-A32G-10 chr2:220336991 T>C maps to NM_005876.4 A1293A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A7SK-01A-11D-A34Z-10 chr2:220333677 C>T maps to NM_005876.4 L1133L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10W-01A-11D-A12Z-10 chr1:16260811 C>T maps to NM_015001.2 L2693L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr1:16261623 C>A maps to NM_015001.2 P2963P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr15:44876207 A>G maps to NM_025137.3 C1890C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EF-01A-11D-A12Z-10 chr2:228884726 A>T maps to NM_001142644.1 I281I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NF-01A-11D-A27I-10 chr2:228881310 G>T maps to NM_001142644.1 S1420*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KR-A7K2-01A-12D-A33Q-10 chr2:228882605 G>A maps to NM_001142644.1 S988S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A114-01A-11D-A12Z-10 chr23:62570623 G>A did not map to a codon.
Sequencing variant TCGA-DD-A3A9-01A-11D-A25V-10 chr23:62570077 A>G did not map to a codon.
Sequencing variant TCGA-KR-A7K0-01A-12D-A33Q-10 chr16:28995278 G>A did not map to a codon.
Sequencing variant TCGA-BC-A10U-01A-11D-A12Z-10 chr5:136314375 A>G maps to NM_004598.3 D429D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K7-A5RG-01A-11D-A28X-10 chr4:168155167 T>A maps to NM_016950.2 K53*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr2:234978569 A>G did not map to a codon.
Sequencing variant TCGA-K7-A6G5-01A-11D-A30V-10 chr1:153004985 G>A maps to NM_003125.2 E55E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IK-01A-12D-A33Q-10 chr1:152944447 C>T maps to NM_173080.1 Q28*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39Y-01A-11D-A20W-10 chr4:124322781 G>A maps to NM_199327.1 S12S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5258-01A-01D-A12Z-10 chr13:80911450 G>C maps to NM_005842.2 S130S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75H-01A-11D-A32G-10 chr23:155003828 T>C did not map to a codon.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr3:140785584 G>T maps to NM_080862.1 V213V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25U-01A-11D-A16V-10 chr1:158619677 C>A maps to NM_003126.2 L1179L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A6M4-01A-11D-A32G-10 chr1:158589012 T>G maps to NM_003126.2 R2177R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MA-01A-11D-A33Q-10 chr1:158637738 C>T maps to NM_003126.2 E649E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A0-01A-11D-A20W-10 chr9:131374458 G>C maps to NM_001130438.2 L1659L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NR-01A-11D-A30V-10 chr14:65241979 G>A maps to ENST00000389723 L1573L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr14:65267542 A>G maps to ENST00000389723 Y273Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr2:54882215 A>G maps to NM_003128.2 S1944S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A5-01A-11D-A22F-10 chr2:54859818 T>C maps to NM_003128.2 A1227A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A82E-01A-11D-A34Z-10 chr2:54857136 C>T maps to NM_003128.2 I926I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25V-01A-11D-A16V-10 chr2:54885137 A>G maps to NM_003128.2 A2066A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IJ-01A-11D-A33Q-10 chr11:66472169 G>A maps to NM_006946.2 S859S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr11:66468659 G>T maps to NM_006946.2 T970T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25T-01A-11D-A16V-10 chr11:66482854 T>C maps to NM_006946.2 T107T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr19:41071394 G>A maps to NM_020971.2 R1994R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EC-01A-21D-A12Z-10 chr19:41056208 C>A maps to NM_020971.2 V1550V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EA-01A-11D-A12Z-10 chr15:42154363 T>C maps to ENST00000320955 E2504E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EL-01A-11D-A152-10 chr15:42152869 A>G maps to ENST00000320955 A2634A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A3I1-01A-11D-A22F-10 chr15:42158098 C>T maps to ENST00000320955 E2275E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A5SK-01A-11D-A27I-10 chr15:42159171 G>A maps to ENST00000320955 T2155T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MD-01A-12D-A34Z-10 chr15:42178393 G>A maps to ENST00000320955 T353T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A3JL-01A-11D-A20W-10 chr2:45616466 G>A maps to NM_018079.4 D990D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10U-01A-11D-A12Z-10 chr16:30724537 A>T maps to NM_006662.2 K714*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A123-01A-11D-A12Z-10 chr16:30721367 T>C maps to NM_006662.2 S351S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25Y-01A-11D-A16V-10 chr16:30750594 A>G maps to NM_006662.2 G3078G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-O8-A75V-01A-11D-A32G-10 chr17:36719590 A>C maps to NM_025248.2 A236A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EA-01A-11D-A12Z-10 chr7:76029846 G>T maps to NM_080744.1 G77G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7ME-01A-11D-A33K-10 chr7:76023204 G>C maps to NM_080744.1 P321P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-4073-01B-02D-A12Z-10 chr17:17719658 G>A maps to NM_001005291.2 A722A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11B-01A-11D-A16Z-10 chr17:17719327 G>A maps to NM_001005291.2 S773S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EF-01A-11D-A12Z-10 chr5:121358097 C>G maps to NM_152546.2 S367S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr5:121309962 C>A maps to NM_152546.2 R37R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11A-01A-11D-A12Z-10 chr12:64505682 C>T maps to NM_020762.2 I687I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5264-01A-01D-A12Z-10 chr1:11119331 G>A maps to NM_003132.2 Q80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75I-01A-11D-A32G-10 chr14:35492188 G>C maps to NM_003136.3 S410S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BW-A5NO-01A-11D-A27I-10 chr4:57344755 A>G did not map to a codon.
Sequencing variant TCGA-CC-A1HT-01A-11D-A12Z-10 chr7:104787042 C>T maps to ENST00000336613 P259P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A3-01A-11D-A22F-10 chr23:38020248 G>A did not map to a codon.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr23:38013811 G>T did not map to a codon.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr23:99901348 T>C did not map to a codon.
Sequencing variant TCGA-BC-A3KF-01A-11D-A20W-10 chr22:26887636 G>A maps to NM_001013694.2 *340*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MA-01A-11D-A20W-10 chr1:24997899 A>G maps to NM_005839.3 G808G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EK-01A-11D-A20W-10 chr16:2814971 T>C maps to NM_016333.3 D1481D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39Y-01A-11D-A20W-10 chr16:2812845 T>C maps to NM_016333.3 L773L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A7PZ-01A-11D-A33Q-10 chr7:75896668 G>A maps to ENST00000388802 W308*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr12:119588875 C>A maps to NM_194286.2 V377V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EF-01A-11D-A12Z-10 chr7:100485881 T>C maps to NM_015908.5 G811G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73B-01A-12D-A32G-10 chr7:100478942 G>T maps to NM_015908.5 E54*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CK-01A-11D-A20W-10 chr5:80762866 T>A maps to ENST00000380182 S196S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10T-01A-11D-A12Z-10 chr11:67075196 C>T maps to NM_017857.3 A260A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1ED-01A-11D-A152-10 chr7:149500387 C>T maps to NM_198455.2 S2639S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NS-01A-11D-A30V-10 chr7:149520824 C>T maps to NM_198455.2 Q4472*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PD-A5DF-01A-11D-A27I-10 chr7:149523814 C>G maps to NM_198455.2 T4881T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EB-01A-11D-A12Z-10 chr1:155988137 T>C maps to ENST00000368312 L78L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A2QR-01A-11D-A20W-10 chr3:187388042 G>A maps to NM_001048.3 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75H-01A-11D-A32G-10 chr23:48125756 C>A did not map to a codon.
Sequencing variant TCGA-UB-A7MF-01A-11D-A33K-10 chr23:48054254 T>A did not map to a codon.
Sequencing variant TCGA-BC-A10R-01A-11D-A12Z-10 chr23:52677344 T>C did not map to a codon.
Sequencing variant TCGA-BC-A10Z-01A-11D-A12Z-10 chr11:130058533 C>T maps to NM_021978.3 A117A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A26S-01A-11D-A16V-10 chr8:53085084 G>T maps to NM_014682.2 S112S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EL-01A-11D-A152-10 chr16:70432283 C>T maps to NM_006927.3 L50L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IK-01A-12D-A33Q-10 chr1:44395832 A>G maps to NM_174963.2 K425K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11A-01A-11D-A12Z-10 chr1:44363937 C>A maps to NM_174963.2 T212T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KR-A7K8-01A-11D-A33K-10 chr2:86075255 C>T maps to NM_003896.3 A130A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10W-01A-11D-A12Z-10 chr2:107459743 G>A maps to NM_001142351.1 T230T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IF-01A-11D-A33K-10 chr2:107423270 G>A maps to NM_001142351.1 L485L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A7XP-01A-11D-A34Z-10 chr2:107460244 G>T maps to NM_001142351.1 G63G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25U-01A-11D-A16V-10 chr17:74562308 G>T maps to NM_006456.2 S334S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A123-01A-11D-A12Z-10 chr1:77333365 G>A maps to NM_030965.1 K2K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A4-01A-11D-A22F-10 chr15:92988126 C>T maps to NM_006011.3 Y270Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NI-A4U2-01A-11D-A28X-10 chr18:55024674 G>A maps to NM_015879.2 P278P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MC-01A-11D-A22F-10 chr3:52558207 C>T maps to NM_015136.2 D2545D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A6M4-01A-11D-A32G-10 chr3:52558210 C>T maps to NM_015136.2 T2546T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7II-01A-11D-A33K-10 chr12:104077059 C>A maps to NM_017564.9 T961T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NK-01A-11D-A28X-10 chr12:104136327 T>A maps to NM_017564.9 C2009*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A459-01A-11D-A25V-10 chr12:104067721 A>T maps to NM_017564.9 I803I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A23B-01A-11D-A16V-10 chr12:104118856 C>T maps to NM_017564.9 R1596R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75G-01A-11D-A32G-10 chr12:104136186 C>T maps to NM_017564.9 C1962C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RG-A7D4-01A-12D-A33Q-10 chr12:104157268 G>C did not map to a codon.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr12:104107484 C>A maps to NM_017564.9 T1492T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr3:36534677 T>C maps to NM_003149.1 N241N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A6M6-01A-11D-A32G-10 chr12:57640643 G>A maps to NM_145064.1 R182R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A5SM-01A-12D-A28X-10 chr23:123195633 G>A did not map to a codon.
Sequencing variant TCGA-BC-A10R-01A-11D-A12Z-10 chr7:99800187 C>A maps to NM_012447.2 S892*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A7-01A-11D-A22F-10 chr13:33681022 G>C maps to NM_178007.2 L1024L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10Z-01A-11D-A12Z-10 chr17:37814041 C>T maps to NM_006804.3 F104F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K7-A5RG-01A-11D-A28X-10 chr18:51851175 T>G maps to NM_139171.1 I183I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K7-A5RF-01A-11D-A28X-10 chr2:96861115 C>T maps to NM_020151.3 R154R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MA-01A-11D-A20W-10 chr23:67937130 T>C did not map to a codon.
Sequencing variant TCGA-MI-A75E-01A-11D-A32G-10 chr12:56742762 A>G maps to NM_005419.3 Y507Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A7PZ-01A-11D-A33Q-10 chr12:57498538 C>G maps to NM_003153.4 G353G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EK-01A-11D-A20W-10 chr8:74600946 T>C maps to NM_001164380.1 E72E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5262-01A-01D-A12Z-10 chr8:23712003 C>T maps to NM_003155.2 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A5SI-01A-31D-A27I-10 chr8:23709889 C>A maps to NM_003155.2 V42V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr5:172744893 C>A maps to NM_003714.2 E289*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A116-01A-11D-A12Z-10 chr7:89854614 G>A maps to NM_152999.3 V73V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A2QQ-01A-11D-A22F-10 chr7:89854506 A>G maps to NM_152999.3 G37G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NE-01A-11D-A27I-10 chr2:120005535 A>T maps to NM_182915.2 T268T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A7M9-01A-23D-A34Z-10 chr2:120005514 C>A maps to NM_182915.2 P261P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MD-01A-12D-A34Z-10 chr7:87910334 A>G maps to NM_024636.2 Y348Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr1:47717101 T>C maps to NM_001048166.1 A1191A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr11:63970926 G>T maps to ENST00000358794 A511A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr5:171509350 C>T maps to NM_005990.3 Q656Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11B-01A-11D-A16Z-10 chr19:1221319 G>A maps to NM_000455.4 P281P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MA-01A-11D-A20W-10 chr2:197021353 T>C maps to NM_004226.3 R48R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A3-01A-11D-A22F-10 chr8:99719382 G>A maps to ENST00000354930 Q198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KR-A7K0-01A-12D-A33Q-10 chr5:146752850 T>C maps to NM_001112724.1 I299I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3M9-01A-11D-A20W-10 chr11:8496344 T>C maps to NM_030906.2 P36P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75H-01A-11D-A32G-10 chr11:8457663 A>G maps to NM_030906.2 L324L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IK-01A-12D-A33Q-10 chr2:169020388 A>T maps to NM_013233.2 G144G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75H-01A-11D-A32G-10 chr1:36809504 G>A maps to ENST00000373130 A325A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75I-01A-11D-A32G-10 chr1:26227523 C>A maps to NM_203399.1 E145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75C-01A-11D-A32G-10 chr8:27099965 G>A maps to NM_030795.2 F19F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EJ-01A-11D-A152-10 chr2:48809394 G>A maps to NM_172311.2 V541V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CK-01A-11D-A20W-10 chr2:48818837 A>T maps to NM_172311.2 S659S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A26S-01A-11D-A16V-10 chr14:81737181 A>C maps to NM_033104.2 L815L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A5SM-01A-12D-A28X-10 chr10:70644910 C>T maps to NM_001130161.2 P453P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25V-01A-11D-A16V-10 chr12:16053884 A>G maps to ENST00000025399 E323E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A3KF-01A-11D-A20W-10 chr11:125474113 A>T maps to NM_152713.3 R160R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A7-01A-11D-A22F-10 chr20:57251325 C>T maps to NM_001001433.1 L319L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr20:57246217 A>G maps to NM_001001433.1 T219T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A3I0-01A-11D-A22F-10 chr16:31045530 C>T maps to ENST00000394998 L37L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr1:180953834 T>C maps to NM_005819.4 A223A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr6:132796760 A>G maps to NM_003569.2 P42P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A2QQ-01A-11D-A22F-10 chr9:130428512 C>A maps to NM_003165.3 L244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5263-01A-01D-A12Z-10 chr1:109340798 G>T maps to NM_007269.2 R463R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75E-01A-11D-A32G-10 chr1:109340860 T>C did not map to a codon.
Sequencing variant TCGA-ED-A459-01A-11D-A25V-10 chr17:53077022 A>T maps to NM_178509.5 I106I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A0-01A-11D-A20W-10 chr6:147631273 A>G maps to NM_001127715.1 R324R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39X-01A-11D-A20W-10 chr3:120941903 A>G maps to NM_014980.2 R337R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr3:120871321 A>G did not map to a codon.
Sequencing variant TCGA-G3-A25T-01A-11D-A16V-10 chr14:25281917 A>G maps to NM_014178.6 C210C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25V-01A-11D-A16V-10 chr12:10775258 C>A maps to NM_018423.2 L315L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EB-01A-11D-A12Z-10 chr13:53254290 G>T did not map to a codon.
Sequencing variant TCGA-DD-A1ED-01A-11D-A152-10 chr13:53237229 G>C did not map to a codon.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr13:53227238 G>A did not map to a codon.
Sequencing variant TCGA-MI-A75H-01A-11D-A32G-10 chr8:70551047 C>T maps to NM_001128206.1 Q836*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IK-01A-12D-A33Q-10 chr4:70620913 G>A maps to NM_014465.3 L8L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A5UD-01A-11D-A28X-10 chr2:108999918 A>T maps to NM_006588.2 K190*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr3:4458809 A>G did not map to a codon.
Sequencing variant TCGA-CC-A7IK-01A-12D-A33Q-10 chr17:27017149 C>T maps to NM_003170.3 S1131S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr17:27025000 A>G maps to NM_003170.3 E1467E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EC-01A-21D-A12Z-10 chr10:70951451 A>G maps to NM_003171.3 T261T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr10:70968758 A>T maps to NM_003171.3 R777*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A5UC-01A-11D-A28X-10 chr9:114911629 T>A maps to NM_022486.3 T89T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EF-01A-11D-A12Z-10 chr9:114820917 A>T maps to NM_022486.3 S633S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A2QR-01A-11D-A20W-10 chr22:24582053 G>A maps to NM_019601.3 E470E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A0-01A-11D-A20W-10 chr1:223402545 G>T maps to NM_017982.3 I303I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr23:48558574 A>T did not map to a codon.
Sequencing variant TCGA-FV-A23B-01A-11D-A16V-10 chr11:67942643 C>T maps to NM_017635.3 R128R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr15:91769903 G>A maps to NM_014848.4 E137E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1ED-01A-11D-A152-10 chr5:75587050 C>T maps to NM_014979.1 N381N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BW-A5NQ-01A-11D-A27I-10 chr9:113312195 C>T maps to ENST00000374463 E240E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A5UC-01A-11D-A28X-10 chr9:113137702 C>T maps to ENST00000374463 V3518V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A7PZ-01A-11D-A33Q-10 chr11:9750887 A>T did not map to a codon.
Sequencing variant TCGA-G3-A5SJ-01A-11D-A27I-10 chr23:16761851 C>A did not map to a codon.
Sequencing variant TCGA-DD-A113-01A-11D-A12Z-10 chr20:58467322 G>A maps to NM_014258.2 Q696*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A9-01A-11D-A25V-10 chr20:58489027 A>G did not map to a codon.
Sequencing variant TCGA-DD-A115-01A-11D-A12Z-10 chr6:10894135 G>T maps to NM_001040274.2 G39*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr1:85647969 T>C maps to NM_032184.1 R785R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr9:93650164 A>G maps to NM_003177.5 P572P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A118-01A-11D-A12Z-10 chr19:46319168 G>A maps to NM_004819.2 D1209D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr22:32914295 A>G maps to NM_003490.3 P448P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10T-01A-11D-A12Z-10 chr6:152676099 T>C maps to NM_182961.2 V3540V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10Z-01A-11D-A12Z-10 chr6:152765605 A>T maps to NM_182961.2 A1259A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MA-01A-11D-A20W-10 chr6:152763359 T>C maps to NM_182961.2 S1286S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr6:152765647 G>T maps to NM_182961.2 L1245L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IK-01A-12D-A33Q-10 chr6:152652649 G>A maps to NM_182961.2 I4390I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A4XI-01A-11D-A25V-10 chr6:152638094 A>G maps to NM_182961.2 N5533N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A3R3-01A-11D-A22F-10 chr6:152644791 C>T maps to NM_182961.2 E5246E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25W-01A-11D-A16V-10 chr6:152683373 G>T maps to NM_182961.2 A3410A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr6:152555814 T>C maps to NM_182961.2 L6839L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr6:152831365 C>T maps to NM_182961.2 K181K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10W-01A-11D-A12Z-10 chr14:64596546 G>A maps to NM_182914.2 V4689V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A123-01A-11D-A12Z-10 chr14:64520041 C>T maps to NM_182914.2 L3137L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MB-01A-11D-A20W-10 chr14:64519804 T>C maps to NM_182914.2 I3058I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39V-01A-11D-A20W-10 chr14:64497757 C>T maps to NM_182914.2 Q2302*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A0-01A-11D-A20W-10 chr14:64494279 A>T maps to NM_182914.2 L2161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NI-01A-11D-A27I-10 chr14:64457169 A>G maps to NM_182914.2 A785A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A7PZ-01A-11D-A33Q-10 chr14:64522759 C>G maps to NM_182914.2 P3281P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NS-01A-11D-A30V-10 chr22:39746104 C>A maps to NM_004711.4 V30V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5259-01A-31D-A20W-10 chr10:75414001 G>A maps to NM_001114133.1 R48*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr10:75407618 A>T maps to NM_001114133.1 P597P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4ND-01A-11D-A25V-10 chr23:49049851 C>A did not map to a codon.
Sequencing variant TCGA-CC-A7II-01A-11D-A33K-10 chr12:79689883 C>T maps to NM_005639.2 P170P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5262-01A-01D-A12Z-10 chr12:33592364 C>T maps to NM_198992.3 W31*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EG-01A-11D-A20W-10 chr11:66811278 G>A maps to NM_001177880.1 P264P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10R-01A-11D-A12Z-10 chr1:202572234 G>A maps to NM_177402.4 D119D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr1:202571583 A>T maps to NM_177402.4 P185P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A116-01A-11D-A12Z-10 chr18:40850323 G>A maps to NM_020783.3 H420H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39Z-01A-11D-A20W-10 chr18:40853606 C>A maps to NM_020783.3 G263*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KR-A7K0-01A-12D-A33Q-10 chr11:61323665 G>A maps to NM_004200.2 R15R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11B-01A-11D-A16Z-10 chr11:1856574 C>A maps to NM_138567.3 L62L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73C-01A-12D-A33K-10 chr11:7335069 T>C maps to NM_175733.3 S314S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A7M6-01A-11D-A33Q-10 chr11:7273525 C>T maps to NM_175733.3 L37L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A6M4-01A-11D-A32G-10 chr11:7437385 A>G maps to NM_175733.3 G386G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A116-01A-11D-A12Z-10 chr11:85436896 A>G maps to ENST00000359152 N725N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr11:85436398 G>T maps to ENST00000359152 P891P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MB-01A-11D-A20W-10 chr23:37913594 T>C did not map to a codon.
Sequencing variant TCGA-CC-5258-01A-01D-A12Z-10 chr11:64900940 T>C maps to NM_172230.2 A44A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr6:166578330 T>A maps to NM_003181.2 K209*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73C-01A-12D-A33K-10 chr6:132938435 A>G maps to NM_001033080.1 F303F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NI-01A-11D-A27I-10 chr6:132859670 G>C maps to NM_175057.3 V81V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A7M5-01A-11D-A33Q-10 chr23:30870986 G>A did not map to a codon.
Sequencing variant TCGA-CC-5262-01A-01D-A12Z-10 chr10:123843040 G>T maps to NM_206862.2 P342P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EB-01A-11D-A12Z-10 chr10:123846535 G>T maps to NM_206862.2 R1507R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr10:123848020 T>C maps to NM_206862.2 L1830L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25S-01A-11D-A16V-10 chr10:71175878 G>A maps to NM_001057.2 V67V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11C-01A-11D-A12Z-10 chr4:104640337 A>G maps to NM_001059.2 P165P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A4ZP-01A-12D-A25V-10 chr4:104511151 C>G did not map to a codon.
Sequencing variant TCGA-ED-A66X-01A-11D-A30V-10 chr17:35804824 T>C maps to NM_001166105.1 L187L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A7M9-01A-23D-A34Z-10 chr4:7056060 C>T maps to NM_152293.2 A181A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BD-A2L6-01A-11D-A20W-10 chr23:70604839 A>G did not map to a codon.
Sequencing variant TCGA-BD-A3EP-01A-11D-A22F-10 chr23:70607150 A>G did not map to a codon.
Sequencing variant TCGA-CC-5259-01A-31D-A20W-10 chr23:70617218 G>A did not map to a codon.
Sequencing variant TCGA-CC-A5UE-01A-11D-A28X-10 chr23:70674055 T>C did not map to a codon.
Sequencing variant TCGA-DD-A115-01A-11D-A12Z-10 chr23:70680628 A>G did not map to a codon.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr23:70601682 A>G did not map to a codon.
Sequencing variant TCGA-G3-A25U-01A-11D-A16V-10 chr23:70597451 G>T did not map to a codon.
Sequencing variant TCGA-G3-A3CK-01A-11D-A20W-10 chr16:84216852 C>T maps to NM_005679.2 A135A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BW-A5NO-01A-11D-A27I-10 chr10:8006084 G>T maps to NM_031923.2 T204T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EL-01A-11D-A152-10 chr20:60578220 C>A maps to NM_003185.3 S827S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BW-A5NQ-01A-11D-A27I-10 chr18:23854649 C>T maps to ENST00000418698 V207V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A2-01A-11D-A20W-10 chr10:105142993 G>C did not map to a codon.
Sequencing variant TCGA-DD-A1EA-01A-11D-A12Z-10 chr23:100547905 T>A did not map to a codon.
Sequencing variant TCGA-ED-A459-01A-11D-A25V-10 chr6:42036239 A>T maps to NM_138572.2 T225T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A5W4-01A-11D-A28X-10 chr23:77392437 C>A did not map to a codon.
Sequencing variant TCGA-DD-A11C-01A-11D-A12Z-10 chr1:47685718 G>A maps to ENST00000371883 L225L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr2:160087090 C>A maps to NM_033394.2 P1718P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11C-01A-11D-A12Z-10 chr2:160053177 C>T maps to NM_033394.2 H1013H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MC-01A-11D-A22F-10 chr17:61476232 C>T maps to ENST00000389520 R1023*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A5-01A-11D-A22F-10 chr12:118639246 G>T maps to NM_016281.3 R281R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr6:32820939 C>A maps to NM_000593.5 G218G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CK-01A-11D-A20W-10 chr6:32821434 G>A maps to NM_000593.5 D53D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A496-01A-11D-A25V-10 chr1:234536929 T>A maps to NM_005646.3 L1356L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73E-01A-12D-A32G-10 chr5:33448801 G>A maps to ENST00000455217 W98*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11B-01A-11D-A16Z-10 chr1:150470187 A>G maps to NM_025150.3 T401T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IG-01A-11D-A33K-10 chr1:6635434 C>T maps to NM_138697.3 R415*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr1:6639184 C>T maps to NM_138697.3 A689A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A2QQ-01A-11D-A22F-10 chr5:9629276 T>A maps to NM_019599.2 K290*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-O8-A75V-01A-11D-A32G-10 chr5:9630120 G>A maps to NM_019599.2 I8I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MC-01A-11D-A22F-10 chr7:141673255 A>G maps to NM_176817.4 L78L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A7-01A-11D-A22F-10 chr7:141672568 A>T maps to NM_176817.4 A307A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-4073-01B-02D-A12Z-10 chr7:142919944 C>T maps to NM_176882.1 F258F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BD-A2L6-01A-11D-A20W-10 chr7:143175216 C>T maps to NM_176883.2 F84F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr12:11244576 A>G maps to ENST00000422992 A84A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A2QR-01A-11D-A20W-10 chr12:10954419 G>A maps to NM_023919.2 S250S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-4073-01B-02D-A12Z-10 chr16:71606498 A>G maps to NM_000353.2 P167P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr7:27833955 T>C maps to ENST00000409980 N475N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A69H-01A-11D-A30V-10 chr16:30370139 T>A did not map to a codon.
Sequencing variant TCGA-G3-A25U-01A-11D-A16V-10 chr16:30380802 G>T maps to NM_015527.3 T234T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A3-01A-11D-A22F-10 chr9:131566319 G>T maps to NM_018201.3 S280S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr3:100002652 C>T maps to ENST00000394144 P158P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IF-01A-11D-A33K-10 chr23:48418241 G>T did not map to a codon.
Sequencing variant TCGA-DD-A115-01A-11D-A12Z-10 chr17:15642099 C>T maps to NM_178571.4 H151H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BW-A5NQ-01A-11D-A27I-10 chr2:101648733 C>G maps to NM_001102426.1 V629V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5259-01A-31D-A20W-10 chr2:101670762 G>A maps to NM_001102426.1 A131A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11C-01A-11D-A12Z-10 chr4:141622703 G>T maps to NM_015130.2 I65I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr5:179298473 G>A maps to NM_198868.2 Y824Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A2QQ-01A-11D-A22F-10 chr5:179306632 T>A maps to NM_198868.2 K471*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25V-01A-11D-A16V-10 chr3:186272530 T>C maps to NM_001134415.1 T352T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EA-01A-11D-A12Z-10 chr4:107092413 T>C maps to NM_001163436.1 E691E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A7SF-01A-11D-A34Z-10 chr23:9677337 C>G did not map to a codon.
Sequencing variant TCGA-CC-A7IL-01A-11D-A33Q-10 chr24:6939609 A>C did not map to a codon.
Sequencing variant TCGA-BC-A3KF-01A-11D-A20W-10 chr6:170871003 G>A maps to NM_003194.4 Q60Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A3KF-01A-11D-A20W-10 chr6:134305775 C>T maps to NM_004865.2 Q150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A5UD-01A-11D-A28X-10 chr2:162279936 C>A maps to NM_006593.2 R416R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A7SB-01A-21D-A34Z-10 chr2:162273412 C>T maps to NM_006593.2 S164S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5261-01A-01D-A12Z-10 chr22:19751755 G>A maps to NM_080647.1 P197P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr11:67406937 T>C maps to NM_005995.4 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75I-01A-11D-A32G-10 chr17:59485644 C>T maps to NM_005994.3 T639T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NI-01A-11D-A27I-10 chr7:35242185 C>A maps to NM_001077653.2 S400S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7II-01A-11D-A33K-10 chr17:45820044 G>A maps to NM_013351.1 V187V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A1-01A-11D-A20W-10 chr23:79282218 T>C did not map to a codon.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr23:79282235 C>A did not map to a codon.
Sequencing variant TCGA-MI-A75I-01A-11D-A32G-10 chr23:79283540 T>G did not map to a codon.
Sequencing variant TCGA-DD-A1EJ-01A-11D-A152-10 chr12:115112602 G>A maps to NM_016569.3 A379A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A6M3-01A-11D-A32G-10 chr17:59560351 T>A maps to ENST00000393853 P372P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IG-01A-11D-A33K-10 chr12:114823366 C>A maps to NM_000192.3 T223T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A5UE-01A-11D-A28X-10 chr7:139655332 T>A maps to NM_001166253.1 P252P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A118-01A-11D-A12Z-10 chr23:102842039 A>T did not map to a codon.
Sequencing variant TCGA-G3-A3CJ-01A-11D-A20W-10 chr23:101395773 T>C did not map to a codon.
Sequencing variant TCGA-G3-A3CJ-01A-11D-A20W-10 chr23:101395777 C>T did not map to a codon.
Sequencing variant TCGA-G3-A5SJ-01A-11D-A27I-10 chr23:102508743 T>C did not map to a codon.
Sequencing variant TCGA-BC-A3KG-01A-11D-A20W-10 chr23:13681571 T>A did not map to a codon.
Sequencing variant TCGA-G3-A3CJ-01A-11D-A20W-10 chr18:44560925 A>T maps to NM_016427.2 L237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MD-01A-12D-A34Z-10 chr18:44560132 A>T maps to NM_016427.2 A501A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MF-01A-11D-A33K-10 chr10:133058600 C>T maps to NM_174937.3 P259P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10W-01A-11D-A12Z-10 chr6:31129626 G>T maps to NM_007109.2 T214T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10W-01A-11D-A12Z-10 chr6:134212867 G>A maps to NM_003206.3 V156V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5259-01A-31D-A20W-10 chr18:53018189 G>A maps to ENST00000398339 T240T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A5UE-01A-11D-A28X-10 chr1:152080283 T>G maps to NM_007113.2 L1803L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EK-01A-11D-A20W-10 chr1:152083975 C>A maps to NM_007113.2 E573*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr1:152084201 G>T maps to NM_007113.2 R497R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr11:67818044 C>A maps to NM_006019.3 I776I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CH-01A-11D-A22F-10 chr11:67811700 C>T maps to NM_006019.3 L304L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KC-01A-11D-A20W-10 chr11:59620708 C>A maps to NM_001062.3 E403*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A118-01A-11D-A12Z-10 chr5:149769582 T>C maps to ENST00000451292 T1097T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5259-01A-31D-A20W-10 chr21:33954533 G>A maps to ENST00000431216 H285H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39Y-01A-11D-A20W-10 chr11:33083145 C>T maps to NM_001145541.1 H282H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A4ZQ-01A-11D-A25V-10 chr1:67242055 C>T maps to NM_152665.2 L102L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr12:111066599 A>G maps to NM_001082538.2 P167P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A3KF-01A-11D-A20W-10 chr12:124158355 A>T maps to NM_024809.3 S154S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A2-01A-11D-A20W-10 chr12:124184292 T>C maps to NM_024809.3 T516T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5258-01A-01D-A12Z-10 chr1:179623393 T>G maps to ENST00000444136 L740*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11A-01A-11D-A12Z-10 chr1:179631315 T>A maps to ENST00000444136 P800P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A9-01A-11D-A25V-10 chr1:179659882 T>C maps to ENST00000444136 A971A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73E-01A-12D-A32G-10 chr1:179604968 G>C maps to ENST00000444136 R489R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A459-01A-11D-A25V-10 chr1:179562718 G>A maps to ENST00000444136 R119R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A2QR-01A-11D-A20W-10 chr1:179564921 C>G maps to ENST00000444136 S267*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A7M5-01A-11D-A33Q-10 chr1:179600020 A>T maps to ENST00000444136 L364L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A8-01A-11D-A22F-10 chr9:100235829 C>T maps to NM_014290.2 L667L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25S-01A-11D-A16V-10 chr9:100232862 T>C maps to NM_014290.2 F551F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr14:104470584 A>G maps to NM_153046.2 G498G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr1:151751632 T>C maps to NM_001083965.1 L169L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73G-01A-22D-A32G-10 chr14:102904369 C>T maps to NM_014844.3 S802S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BD-A3EP-01A-11D-A22F-10 chr11:121058615 C>T maps to NM_005422.2 T2025T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A3JL-01A-11D-A20W-10 chr11:120989399 C>T maps to NM_005422.2 I392I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A9-01A-11D-A25V-10 chr9:27173268 A>G maps to NM_000459.3 G270G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A7M9-01A-23D-A34Z-10 chr9:27206620 C>A maps to NM_000459.3 A802A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75C-01A-11D-A32G-10 chr17:6718549 G>T maps to NM_053285.1 I187I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11C-01A-11D-A12Z-10 chr12:53453407 A>G maps to NM_170754.2 P661P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A5SM-01A-12D-A28X-10 chr12:53448149 C>G maps to NM_170754.2 P149P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MA-01A-11D-A20W-10 chr14:20859790 T>C maps to NM_007110.4 A688A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr14:20871534 C>A did not map to a codon.
Sequencing variant TCGA-MI-A75H-01A-11D-A32G-10 chr8:73944309 A>G maps to NM_017489.2 Q327Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr5:1254533 G>A maps to NM_198253.2 L1082L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25Z-01A-11D-A16V-10 chr10:70333687 C>A maps to NM_030625.2 A531A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A23B-01A-11D-A16V-10 chr2:74317137 T>C maps to ENST00000409262 P908P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr19:43920079 C>T maps to NM_031451.4 T21T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr23:69772027 A>T did not map to a codon.
Sequencing variant TCGA-FV-A2QQ-01A-11D-A22F-10 chr23:69942514 G>A did not map to a codon.
Sequencing variant TCGA-CC-A7IK-01A-12D-A33Q-10 chr17:56663387 A>T maps to ENST00000240361 P954P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BD-A3EP-01A-11D-A22F-10 chr8:30701384 G>A maps to NM_031271.3 R1717*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KR-A7K0-01A-12D-A33Q-10 chr8:30694574 C>A maps to NM_031271.3 G2692G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A115-01A-11D-A12Z-10 chr2:71215837 G>A maps to NM_144582.2 V161V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73D-01A-12D-A32G-10 chr15:56683605 C>T maps to NM_198524.1 D187D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K7-A6G5-01A-11D-A30V-10 chr1:36060159 C>T maps to NM_178548.3 A404A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A8-01A-11D-A22F-10 chr16:4308229 G>A maps to NM_003223.2 G281G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr12:51492561 A>G maps to NM_005653.4 D472D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25U-01A-11D-A16V-10 chr2:121995247 A>G maps to NM_014553.2 L318L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25U-01A-11D-A16V-10 chr3:141678611 C>A maps to NM_001178139.1 G319*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A66Y-01A-11D-A30V-10 chr23:48888981 C>T did not map to a codon.
Sequencing variant TCGA-G3-A7M6-01A-11D-A33Q-10 chr23:48895553 C>T did not map to a codon.
Sequencing variant TCGA-RC-A6M6-01A-11D-A32G-10 chr6:41658399 C>T did not map to a codon.
Sequencing variant TCGA-DD-A1EB-01A-11D-A12Z-10 chr7:115624438 C>A maps to NM_012252.2 V19V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K7-A6G5-01A-11D-A30V-10 chr3:100467365 T>G maps to NM_001007565.2 G398G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11D-01A-11D-A12Z-10 chr7:93516720 T>C maps to NM_006528.2 P161P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EF-01A-11D-A12Z-10 chr8:133961018 A>G did not map to a codon.
Sequencing variant TCGA-CC-5258-01A-01D-A12Z-10 chr19:41850670 C>A maps to NM_000660.4 R205R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NG-01A-11D-A27I-10 chr1:218609330 A>G maps to NM_001135599.2 T286T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A113-01A-11D-A12Z-10 chr1:92187584 A>G maps to NM_003243.4 N334N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A3I0-01A-11D-A22F-10 chr2:105885896 G>A maps to NM_004257.4 T746T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LG-A6GG-01A-11D-A30V-10 chr2:105890084 T>A maps to NM_004257.4 P576P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A116-01A-11D-A12Z-10 chr23:89177753 G>A did not map to a codon.
Sequencing variant TCGA-DD-A1EB-01A-11D-A12Z-10 chr23:89177575 G>T did not map to a codon.
Sequencing variant TCGA-RC-A6M4-01A-11D-A32G-10 chr20:2384054 C>G maps to NM_198994.2 V334V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A6M4-01A-11D-A32G-10 chr15:43574766 T>A maps to NM_052955.2 P352P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KR-A7K0-01A-12D-A33Q-10 chr8:56698308 T>C maps to NM_024831.6 G66G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr11:2190969 C>T maps to NM_199292.2 E105E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10T-01A-11D-A12Z-10 chr2:43819170 C>A maps to ENST00000330266 E31*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A5W4-01A-11D-A28X-10 chr2:43779385 G>A maps to ENST00000330266 R924*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A4ZQ-01A-11D-A25V-10 chr16:67877083 G>T maps to NM_020457.2 S209S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CK-01A-11D-A20W-10 chr12:72070665 C>T maps to NM_031435.3 C155C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NE-01A-11D-A27I-10 chr1:6688627 C>T maps to NM_001195753.1 P48P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A3RK-01A-11D-A22F-10 chr1:6692556 T>C did not map to a codon.
Sequencing variant TCGA-G3-A25V-01A-11D-A16V-10 chr15:39880778 T>C maps to NM_003246.2 C508C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LG-A6GG-01A-11D-A30V-10 chr6:169639733 T>C maps to NM_003247.2 P363P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QA-A7B7-01A-11D-A32G-10 chr6:169639700 G>T maps to NM_003247.2 C374*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NA-01A-11D-A25V-10 chr1:155175005 G>A maps to NM_007112.3 R130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73E-01A-12D-A32G-10 chr1:155172875 C>A did not map to a codon.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr19:362298 G>A maps to NM_016585.3 G347G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr6:128150864 T>G maps to NM_001164685.1 A155A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr19:2810299 A>T did not map to a codon.
Sequencing variant TCGA-DD-A4NJ-01A-11D-A27I-10 chr19:2794766 A>C maps to NM_003249.3 R79R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39Y-01A-11D-A20W-10 chr17:38230770 T>C maps to NM_003250.5 C10C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A118-01A-11D-A12Z-10 chr1:36757041 C>T maps to NM_005119.3 Q605*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A4XI-01A-11D-A25V-10 chr15:71548959 A>G maps to NM_024817.2 P307P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5264-01A-01D-A12Z-10 chr7:11416258 G>A maps to ENST00000423059 Y1609Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39W-01A-11D-A20W-10 chr7:11486896 T>C maps to ENST00000423059 G920G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NO-01A-11D-A28X-10 chr7:11445999 A>G maps to ENST00000423059 C1388C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A7SB-01A-21D-A34Z-10 chr16:20749099 T>C maps to ENST00000431224 T281T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr21:32639201 G>T maps to NM_003253.2 S29S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A5UD-01A-11D-A28X-10 chr6:155569179 C>T maps to ENST00000456144 P1233P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr4:153691589 A>G maps to NM_145720.2 Y189Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr8:144681731 G>A maps to NM_032862.4 L553L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A7PZ-01A-11D-A33Q-10 chr5:156381474 A>T maps to NM_138379.2 P117P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr12:56827888 T>C maps to NM_003920.3 G22G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A9-01A-11D-A25V-10 chr19:39980381 G>A maps to NM_001001563.1 E431E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A459-01A-11D-A25V-10 chr3:12198365 A>G maps to NM_003256.2 C102C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5259-01A-31D-A20W-10 chr6:54186161 C>T maps to NM_014464.3 Q163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11D-01A-11D-A12Z-10 chr6:54254593 T>C maps to NM_014464.3 A434A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25S-01A-11D-A16V-10 chr11:126162957 A>G maps to NM_148910.2 L218L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75I-01A-11D-A32G-10 chr15:30010588 C>A maps to NM_003257.3 E1253*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25S-01A-11D-A16V-10 chr9:71849422 A>G maps to NM_004817.3 K580K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A5SK-01A-11D-A27I-10 chr9:71840271 G>T maps to NM_004817.3 T335T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25U-01A-11D-A16V-10 chr3:53259912 C>A maps to ENST00000423516 V585V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73F-01A-11D-A32G-10 chr23:153556012 C>T did not map to a codon.
Sequencing variant TCGA-ED-A459-01A-11D-A25V-10 chr23:153558005 A>T did not map to a codon.
Sequencing variant TCGA-FV-A495-01A-11D-A25V-10 chr9:84208091 G>A maps to NM_005077.3 Q477*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KR-A7K0-01A-12D-A33Q-10 chr2:171853222 T>C maps to ENST00000360843 T709T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A9-01A-11D-A25V-10 chr4:166976352 T>C maps to ENST00000507499 N573N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A7SF-01A-11D-A34Z-10 chr4:166981306 G>A maps to ENST00000507499 V681V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MA-01A-11D-A33Q-10 chr4:166976397 A>G maps to ENST00000507499 A588A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NE-01A-11D-A27I-10 chr10:98144386 G>A maps to NM_012465.3 D717D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KR-A7K7-01A-11D-A33K-10 chr9:35703655 C>G maps to NM_006289.3 V2125V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K7-A6G5-01A-11D-A30V-10 chr15:63031554 A>G maps to NM_015059.2 P1232P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5264-01A-01D-A12Z-10 chr4:38799405 C>A maps to NM_003263.3 P349P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A5UE-01A-11D-A28X-10 chr4:38798658 G>A maps to NM_003263.3 T598T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CJ-01A-11D-A20W-10 chr4:38799867 C>G maps to NM_003263.3 V195V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NI-A4U2-01A-11D-A28X-10 chr4:38799345 C>T maps to NM_003263.3 G369G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr4:186997907 A>C maps to NM_003265.2 V45V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr9:120475740 A>T maps to NM_138554.3 S445S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73B-01A-12D-A32G-10 chr1:223284252 C>A maps to NM_003268.5 V707V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr1:223286220 G>T maps to NM_003268.5 L51L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5264-01A-01D-A12Z-10 chr23:12904608 A>G did not map to a codon.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr23:12905636 T>G did not map to a codon.
Sequencing variant TCGA-DD-A114-01A-11D-A12Z-10 chr23:12939182 T>C did not map to a codon.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr23:12938297 A>G did not map to a codon.
Sequencing variant TCGA-DD-A73G-01A-22D-A32G-10 chr23:12937741 G>A did not map to a codon.
Sequencing variant TCGA-G3-A25Y-01A-11D-A16V-10 chr23:12937427 C>G did not map to a codon.
Sequencing variant TCGA-G3-A7M6-01A-11D-A33Q-10 chr23:12937388 A>G did not map to a codon.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr23:12938412 C>A did not map to a codon.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr23:12939722 A>T did not map to a codon.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr10:102849343 G>T maps to NM_001085398.1 R107R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K7-A5RG-01A-11D-A28X-10 chr5:170738471 C>T maps to NM_021025.2 Q249*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10R-01A-11D-A12Z-10 chr8:38851170 A>G maps to NM_031940.3 G65G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10T-01A-11D-A12Z-10 chr3:149051079 G>A maps to NM_138786.3 F30F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25V-01A-11D-A16V-10 chr17:4686277 C>T maps to NM_003963.2 I175I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75I-01A-11D-A32G-10 chr15:83795554 C>T maps to NM_023003.3 Q253*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr20:30738605 G>T maps to NM_014742.3 V391V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5260-01A-01D-A12Z-10 chr9:75355073 T>A maps to NM_138691.2 L134L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr9:75404070 A>T maps to NM_138691.2 V354V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1ED-01A-11D-A152-10 chr9:75403362 A>G maps to NM_138691.2 A331A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A2-01A-11D-A20W-10 chr20:2582880 C>T maps to NM_080751.2 Y449Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7ME-01A-11D-A33K-10 chr19:54672011 G>A maps to NM_001145303.1 L234L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A6M6-01A-11D-A32G-10 chr17:76120808 C>T maps to NM_007267.6 P229P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BW-A5NP-01A-11D-A27I-10 chr1:205238235 G>A maps to NM_014858.3 Q302Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LG-A6GG-01A-11D-A30V-10 chr12:94972247 T>A maps to NM_020698.2 T351T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11A-01A-11D-A12Z-10 chr15:38229050 G>A maps to NM_152453.2 L48L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25U-01A-11D-A16V-10 chr7:44621074 C>T maps to NM_182547.2 R120R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EI-01A-11D-A12Z-10 chr12:48359719 C>T maps to NM_001143842.1 G117G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11D-01A-11D-A12Z-10 chr3:133099004 C>T maps to NM_001136469.1 T150T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39Z-01A-11D-A20W-10 chr11:85367379 A>G maps to NM_032273.3 K141K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10T-01A-11D-A12Z-10 chr2:96919803 G>A maps to NM_017849.3 L153L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A3KF-01A-11D-A20W-10 chr7:98460877 G>T maps to NM_001134450.1 T77T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A1-01A-11D-A20W-10 chr12:126138496 A>G maps to NM_052907.2 R826R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NV-01A-11D-A30V-10 chr12:125834659 G>T maps to NM_052907.2 E239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A0-01A-11D-A20W-10 chr11:87020677 T>C maps to NM_022918.3 L300L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A9-01A-11D-A25V-10 chr11:86782615 G>A maps to NM_022918.3 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr11:87029246 T>C maps to NM_022918.3 Y382Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HP-A5N0-01A-11D-A28X-10 chr19:42827877 G>C maps to ENST00000406159 T460T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A7M5-01A-11D-A33Q-10 chr4:38995619 T>A did not map to a codon.
Sequencing variant TCGA-CC-A7IK-01A-12D-A33Q-10 chr7:112412839 T>A maps to NM_022484.4 L514L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A5SM-01A-12D-A28X-10 chr7:150501447 A>G did not map to a codon.
Sequencing variant TCGA-FV-A496-01A-11D-A25V-10 chr6:159029440 C>T maps to NM_020823.1 F387F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73C-01A-12D-A33K-10 chr7:1589782 G>T maps to NM_001097620.1 I176I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3M9-01A-11D-A20W-10 chr23:148693146 C>A did not map to a codon.
Sequencing variant TCGA-DD-A113-01A-11D-A12Z-10 chr23:148690382 C>T did not map to a codon.
Sequencing variant TCGA-G3-A7M7-01A-12D-A34Z-10 chr23:153247690 G>A did not map to a codon.
Sequencing variant TCGA-RC-A6M3-01A-11D-A32G-10 chr9:74355006 A>G maps to NM_013390.2 S392S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25V-01A-11D-A16V-10 chr19:11453628 T>C maps to NM_198536.2 R144R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr22:25334134 T>A maps to ENST00000423535 P107P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A7M9-01A-23D-A34Z-10 chr2:27260449 G>A maps to NM_017727.4 Q344Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NH-01A-11D-A27I-10 chr11:124971200 T>A did not map to a codon.
Sequencing variant TCGA-G3-A25U-01A-11D-A16V-10 chr11:124972139 C>T did not map to a codon.
Sequencing variant TCGA-DD-A3A2-01A-11D-A20W-10 chr16:29979379 C>T maps to NM_194280.3 A130A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11C-01A-11D-A12Z-10 chr11:123753907 A>T maps to NM_001013743.1 R205R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A5SM-01A-12D-A28X-10 chr10:63212686 C>T maps to NM_178505.6 A51A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-O8-A75V-01A-11D-A32G-10 chr10:63195963 T>C maps to NM_178505.6 P78P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A1HT-01A-11D-A12Z-10 chr6:75974944 A>T did not map to a codon.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr6:75970579 T>C maps to NM_018247.3 P167P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75G-01A-11D-A32G-10 chr4:41951402 G>T did not map to a codon.
Sequencing variant TCGA-BC-A69H-01A-11D-A30V-10 chr9:108536209 G>A maps to NM_018112.1 W242*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73B-01A-12D-A32G-10 chr3:44906566 G>A maps to NM_144638.1 Q125Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A2QR-01A-11D-A20W-10 chr3:14180786 C>T maps to NM_024334.2 L330L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5263-01A-01D-A12Z-10 chr19:18731264 G>A maps to NM_012109.2 W316*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NO-01A-11D-A28X-10 chr15:43461807 G>T maps to NM_024956.3 V438V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KC-01A-11D-A20W-10 chr8:94800155 T>C maps to NM_153704.5 D499D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A5SL-01A-11D-A27I-10 chr8:94817075 A>G maps to NM_153704.5 E803E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HP-A5N0-01A-11D-A28X-10 chr8:133734356 G>T maps to ENST00000395406 T227T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A113-01A-11D-A12Z-10 chr1:156255313 A>T maps to NM_032323.2 P99P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NP-01A-11D-A28X-10 chr1:156255145 A>C maps to NM_032323.2 G43G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr15:42531865 A>G did not map to a codon.
Sequencing variant TCGA-MI-A75H-01A-11D-A32G-10 chr15:42519077 G>A maps to ENST00000389834 A443A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A3R2-01A-11D-A22F-10 chr17:7758490 C>T maps to NM_203411.1 A33A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10Z-01A-11D-A12Z-10 chr9:35841792 T>A did not map to a codon.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr17:7259190 T>C maps to NM_198154.1 Y87Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39W-01A-11D-A20W-10 chr17:7259753 C>T maps to NM_198154.1 I159I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NG-01A-11D-A27I-10 chr17:28656377 G>A maps to NM_206832.1 S84S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10U-01A-11D-A12Z-10 chr12:98938127 G>C did not map to a codon.
Sequencing variant TCGA-BC-A217-01A-11D-A152-10 chr3:33134373 C>G maps to NM_001039770.2 L438L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr4:68780362 A>G maps to NM_182606.3 D349D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr4:68789884 C>A did not map to a codon.
Sequencing variant TCGA-FV-A3R2-01A-11D-A22F-10 chr4:69095160 G>A maps to NM_182502.3 Q254*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BW-A5NP-01A-11D-A27I-10 chr4:68691557 G>A maps to NM_004262.2 V329V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5264-01A-01D-A12Z-10 chr4:68935723 A>G maps to NM_207407.2 P172P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10Z-01A-11D-A12Z-10 chr12:51237658 A>G maps to NM_182559.2 Q74Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A2QQ-01A-11D-A22F-10 chr11:117784523 T>C maps to ENST00000413475 S258S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr11:117789166 A>G maps to ENST00000413475 P135P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EG-01A-11D-A20W-10 chr21:19770596 T>C maps to NM_002772.2 T65T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr21:19732131 T>C maps to NM_002772.2 T274T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A112-01A-11D-A12Z-10 chr11:117979579 C>T maps to NM_019894.3 L184L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5259-01A-31D-A20W-10 chr3:111794165 A>G did not map to a codon.
Sequencing variant TCGA-G3-A25S-01A-11D-A16V-10 chr3:111764779 G>A maps to ENST00000443106 V214V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KR-A7K8-01A-11D-A33K-10 chr3:111785345 C>T maps to ENST00000443106 Q543*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73G-01A-22D-A32G-10 chr19:2399147 C>T maps to NM_182973.1 I123I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BW-A5NO-01A-11D-A27I-10 chr12:83290360 G>A maps to NM_152588.1 R473R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A123-01A-11D-A12Z-10 chr12:83250807 C>T maps to NM_152588.1 Q35*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MD-01A-12D-A34Z-10 chr17:42266395 C>T maps to NM_001076674.1 D14D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25Z-01A-11D-A16V-10 chr15:51397265 C>T maps to NM_207381.2 R36R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr17:16852253 A>G maps to NM_012452.2 H81H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5263-01A-01D-A12Z-10 chr13:24243205 C>A maps to NM_018647.2 V405V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IK-01A-12D-A33Q-10 chr13:43174892 A>G maps to NM_003701.3 L131L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-4073-01B-02D-A12Z-10 chr19:6670047 A>G maps to NM_003807.3 F11F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25T-01A-11D-A16V-10 chr17:7291785 A>G maps to NM_003985.3 S513S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A6M6-01A-11D-A32G-10 chr3:195610025 A>T did not map to a codon.
Sequencing variant TCGA-CC-5260-01A-01D-A12Z-10 chr8:9627613 A>T did not map to a codon.
Sequencing variant TCGA-DD-A11C-01A-11D-A12Z-10 chr8:9622230 A>G maps to NM_003747.2 Q1126Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25S-01A-11D-A16V-10 chr11:57080661 G>T maps to NM_033396.2 I500I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NQ-01A-21D-A28X-10 chr10:93558646 G>T did not map to a codon.
Sequencing variant TCGA-HP-A5N0-01A-11D-A28X-10 chr10:93558623 C>T maps to NM_025235.3 S59S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25U-01A-11D-A16V-10 chr23:99854570 C>A did not map to a codon.
Sequencing variant TCGA-CC-A3MB-01A-11D-A20W-10 chr1:175067579 T>G maps to NM_022093.1 S656S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NE-01A-11D-A27I-10 chr1:175105077 G>C did not map to a codon.
Sequencing variant TCGA-ED-A82E-01A-11D-A34Z-10 chr1:175048580 G>A maps to NM_022093.1 A174A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr19:55663249 G>A maps to ENST00000344887 I195I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A116-01A-11D-A12Z-10 chr5:72144244 G>T maps to NM_002270.3 E17*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3M9-01A-11D-A20W-10 chr19:12831731 T>C maps to NM_001136196.1 S20S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11C-01A-11D-A12Z-10 chr19:12817571 C>A maps to NM_001136196.1 L436L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A3KG-01A-11D-A20W-10 chr1:175360556 C>A maps to NM_003285.2 V458V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25T-01A-11D-A16V-10 chr1:175372510 G>A maps to NM_003285.2 D247D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A6UC-01A-21D-A33K-10 chr7:5352547 T>G maps to NM_001080495.2 S2658S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KR-A7K7-01A-11D-A33K-10 chr7:5416610 T>C maps to NM_001080495.2 P825P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr7:5353215 T>A maps to NM_001080495.2 K2436*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73A-01A-12D-A32G-10 chr16:24816120 C>A maps to NM_014494.2 A1311A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A7XO-01A-11D-A34Z-10 chr16:24831568 G>A maps to NM_014494.2 P1730P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A2QR-01A-11D-A20W-10 chr16:24801288 A>G maps to NM_014494.2 Q442Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25W-01A-11D-A16V-10 chr16:24802368 G>A maps to NM_014494.2 G802G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MC-01A-11D-A22F-10 chr22:40662451 C>T maps to ENST00000454349 Q754*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A1-01A-11D-A20W-10 chr22:40708593 G>T maps to ENST00000454349 G1521G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CJ-01A-11D-A20W-10 chr22:40657899 A>G maps to ENST00000454349 P74P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75G-01A-11D-A32G-10 chr17:76046693 G>A maps to NM_001142640.1 V517V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EH-01A-11D-A12Z-10 chr2:218696256 C>T maps to NM_022648.4 P973P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EL-01A-11D-A152-10 chr2:218745711 C>A maps to NM_022648.4 P321P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr7:47408178 T>A maps to NM_022748.11 P688P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75E-01A-11D-A32G-10 chr17:38638654 A>G maps to NM_032865.5 N505N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr6:32038105 G>T maps to ENST00000375244 L1692L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-O8-A75V-01A-11D-A32G-10 chr6:32064612 C>T maps to ENST00000375244 T339T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A7SK-01A-11D-A34Z-10 chr6:32012930 C>A maps to ENST00000375244 T3593T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EG-01A-11D-A20W-10 chr3:100093978 G>A maps to NM_014820.3 L370L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr17:38561111 A>G maps to ENST00000357601 D695D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr17:38556307 G>A maps to ENST00000357601 D1040D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A3KF-01A-11D-A20W-10 chr3:25670531 A>T maps to ENST00000264331 I598I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A8-01A-11D-A22F-10 chr3:25668096 G>A maps to ENST00000264331 L726L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11A-01A-11D-A12Z-10 chr17:18188781 G>A maps to NM_004618.3 Y550Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5260-01A-01D-A12Z-10 chr9:32544213 A>G maps to NM_005802.4 C103C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73C-01A-12D-A33K-10 chr9:32543941 G>C maps to NM_005802.4 S194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MF-01A-11D-A33K-10 chr9:32550783 C>T maps to NM_005802.4 P62P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25Z-01A-11D-A16V-10 chr9:130494465 G>A maps to NM_001085347.1 C271C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MR-A520-01A-11D-A25V-10 chr8:59852022 C>T maps to NM_014729.2 L83L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10R-01A-11D-A12Z-10 chr17:7578523 G>A maps to NM_001126112.1 Q136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BW-A5NQ-01A-11D-A27I-10 chr17:7578274 G>A maps to NM_001126112.1 Q192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5259-01A-31D-A20W-10 chr17:7579311 C>A maps to NM_001126112.1 T125T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5263-01A-01D-A12Z-10 chr17:7577106 A>T maps to NM_001126112.1 C277*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A1HT-01A-11D-A12Z-10 chr17:7578554 C>T did not map to a codon.
Sequencing variant TCGA-CC-A7IG-01A-11D-A33K-10 chr17:7578187 C>A maps to NM_001126112.1 E221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EI-01A-11D-A12Z-10 chr17:7578418 C>A maps to NM_001126112.1 E171*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A7-01A-11D-A22F-10 chr17:7578524 G>T maps to NM_001126112.1 C135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A3R2-01A-11D-A22F-10 chr17:7577021 G>A maps to NM_001126112.1 R306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A5SM-01A-12D-A28X-10 chr17:7574034 T>C did not map to a codon.
Sequencing variant TCGA-K7-A5RG-01A-11D-A28X-10 chr17:7576927 T>C did not map to a codon.
Sequencing variant TCGA-RC-A6M6-01A-11D-A32G-10 chr17:7577063 T>A maps to NM_001126112.1 K292*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T1-A6J8-01A-11D-A32G-10 chr17:7578289 C>T did not map to a codon.
Sequencing variant TCGA-UB-A7MD-01A-12D-A34Z-10 chr17:7579590 C>T did not map to a codon.
Sequencing variant TCGA-BC-A216-01A-11D-A152-10 chr1:224002031 G>A maps to NM_001031685.2 R67*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KC-01A-11D-A20W-10 chr11:44959104 C>A did not map to a codon.
Sequencing variant TCGA-ED-A7PZ-01A-11D-A33Q-10 chr8:95952314 G>T maps to NM_033285.3 S82S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NG-01A-11D-A27I-10 chr11:68854593 G>A maps to NM_139075.3 K700K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11A-01A-11D-A12Z-10 chr11:18050908 C>G did not map to a codon.
Sequencing variant TCGA-ED-A459-01A-11D-A25V-10 chr11:18057648 G>C maps to ENST00000341556 S53*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr12:72425318 T>C maps to ENST00000389376 I445I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KC-01A-11D-A20W-10 chr12:72388233 A>G maps to ENST00000389376 E325E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A7XP-01A-11D-A34Z-10 chr2:1440138 A>T maps to NM_000547.5 T155T. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-EP-A2KB-01A-11D-A183-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-MI-A75C-01A-11D-A32G-10 chr2:1459933 G>A maps to NM_000547.5 W233*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75G-01A-11D-A32G-10 chr2:1481039 G>T maps to NM_000547.5 P334P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A113-01A-11D-A12Z-10 chr11:6638384 C>T did not map to a codon.
Sequencing variant TCGA-DD-A3A7-01A-11D-A22F-10 chr16:67424966 C>T maps to NM_016140.2 K16K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MB-01A-11D-A20W-10 chr1:186340128 A>G maps to NM_003292.2 I101I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr3:127298923 T>C maps to NM_001136053.1 P22P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A7M5-01A-11D-A33Q-10 chr3:189028172 A>T did not map to a codon.
Sequencing variant TCGA-MI-A75G-01A-11D-A32G-10 chr1:3542441 A>G maps to NM_182752.3 K153K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A5UE-01A-11D-A28X-10 chr9:140093450 G>A maps to NM_001128228.2 S571S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr21:10908835 A>T maps to NM_199261.2 I503I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75G-01A-11D-A32G-10 chr11:36511423 C>T maps to NM_145803.1 E511E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11B-01A-11D-A16Z-10 chr2:202245371 A>T maps to NM_015049.2 L880*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EL-01A-11D-A152-10 chr2:202251195 G>A maps to NM_015049.2 L570L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-O8-A75V-01A-11D-A32G-10 chr2:202250956 T>C maps to NM_015049.2 A649A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A116-01A-11D-A12Z-10 chr4:118006516 G>A maps to NM_152402.2 P11P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MR-A520-01A-11D-A25V-10 chr4:118005751 A>T maps to NM_152402.2 I266I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25U-01A-11D-A16V-10 chr6:52373070 C>A maps to NM_012288.3 L172L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IG-01A-11D-A33K-10 chr21:45504035 C>T maps to NM_003274.4 L758L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr1:36605743 G>C maps to NM_014408.3 T22T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A7M9-01A-23D-A34Z-10 chr10:17202312 A>G maps to NM_004412.5 S150S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A7PZ-01A-11D-A33Q-10 chr6:41121499 G>A maps to NM_178174.2 P124P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A9-01A-11D-A25V-10 chr6:41196564 T>C maps to NM_198153.2 S59S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A3KF-01A-11D-A20W-10 chr6:42227242 G>T maps to NM_033502.2 P701P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A118-01A-11D-A12Z-10 chr23:152710778 C>T did not map to a codon.
Sequencing variant TCGA-FV-A4ZP-01A-12D-A25V-10 chr3:129695782 G>T maps to NM_007117.3 R151R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A9-01A-11D-A25V-10 chr12:72936135 A>G maps to NM_013381.2 Q551Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EI-01A-11D-A12Z-10 chr8:110131668 C>A maps to NM_003301.4 S394S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73F-01A-11D-A32G-10 chr7:28995703 C>T maps to NM_014817.3 G653G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KR-A7K7-01A-11D-A33K-10 chr7:28997602 C>T maps to NM_014817.3 P20P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A217-01A-11D-A152-10 chr13:50592278 T>C did not map to a codon.
Sequencing variant TCGA-G3-A25U-01A-11D-A16V-10 chr11:5718573 G>A did not map to a codon.
Sequencing variant TCGA-UB-A7MD-01A-12D-A34Z-10 chr6:30156976 C>A did not map to a codon.
Sequencing variant TCGA-CC-A7IK-01A-12D-A33Q-10 chr6:28876788 T>A maps to NM_006510.4 K283*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr11:6471834 A>G maps to NM_033278.2 A629A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A5UC-01A-11D-A28X-10 chr5:114462307 C>T maps to NM_018700.3 V693V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr6:25983701 A>T maps to NM_006355.2 A395A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A1HT-01A-11D-A12Z-10 chr3:140401303 C>A maps to NM_152616.4 S114S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25S-01A-11D-A16V-10 chr11:35684742 G>T maps to NM_017583.4 G28G. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-DD-A1EA-01A-11D-A12Z-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-RC-A7SF-01A-11D-A34Z-10 chr7:100732206 C>T maps to NM_030961.1 G538G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr3:160156797 A>G maps to ENST00000483754 N58N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A113-01A-11D-A12Z-10 chr11:5663671 T>C maps to NM_001003819.3 V624V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MA-01A-11D-A33Q-10 chr4:165962555 C>T maps to NM_152620.2 F444F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MA-01A-11D-A33Q-10 chr4:165962558 A>T maps to NM_152620.2 T445T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A66X-01A-11D-A30V-10 chr1:231349707 C>G maps to NM_001004342.3 L757L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A115-01A-11D-A12Z-10 chr3:32915308 G>A did not map to a codon.
Sequencing variant TCGA-BD-A2L6-01A-11D-A20W-10 chr4:189065203 T>A maps to NM_178556.3 L258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11D-01A-11D-A12Z-10 chr4:189026082 A>G maps to ENST00000326754 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10W-01A-11D-A12Z-10 chr5:14474100 A>G did not map to a codon.
Sequencing variant TCGA-BC-A10W-01A-11D-A12Z-10 chr5:14502745 T>C maps to NM_007118.2 S2797S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11C-01A-11D-A12Z-10 chr5:14502721 A>G maps to NM_007118.2 K2789K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A5SM-01A-12D-A28X-10 chr5:14374420 G>A maps to NM_007118.2 T1100T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A4ZP-01A-12D-A25V-10 chr14:92470461 C>T maps to NM_004239.3 Q1286Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EL-01A-11D-A152-10 chr2:230667053 G>A maps to ENST00000389044 A1013A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NI-01A-11D-A27I-10 chr2:230632437 T>A maps to ENST00000389044 T1985T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A66Y-01A-11D-A30V-10 chr2:230657706 T>A maps to ENST00000389044 R1348*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr5:901480 T>G maps to NM_004237.3 L157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73E-01A-12D-A32G-10 chr19:13220609 C>T maps to NM_001136035.2 E383E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-O8-A75V-01A-11D-A32G-10 chr14:103996383 T>A maps to ENST00000299201 G23G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5264-01A-01D-A12Z-10 chr2:29092900 A>G maps to NM_017910.3 C81C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EB-01A-11D-A12Z-10 chr22:46751485 G>A did not map to a codon.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr23:54955839 A>T did not map to a codon.
Sequencing variant TCGA-O8-A75V-01A-11D-A32G-10 chr12:49723687 C>T maps to NM_005480.3 L405L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr1:193045013 A>G maps to NM_004600.5 E215E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5258-01A-01D-A12Z-10 chr8:72948614 G>T maps to NM_007332.2 P821P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr8:72938309 T>A did not map to a codon.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr8:72983963 T>A maps to NM_007332.2 R84*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A3JL-01A-11D-A20W-10 chr13:38211432 T>C maps to NM_003306.1 L852L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A23B-01A-11D-A16V-10 chr13:38248409 G>A maps to NM_003306.1 S443S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NA-01A-11D-A25V-10 chr5:135692415 G>A maps to NM_020389.2 N220N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10R-01A-11D-A12Z-10 chr15:31295062 A>C maps to NM_002420.4 L1258L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A3KF-01A-11D-A20W-10 chr15:31355370 T>C maps to NM_002420.4 G283G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BW-A5NO-01A-11D-A27I-10 chr21:45811267 C>T maps to ENST00000397932 T518T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25U-01A-11D-A16V-10 chr21:45837839 G>A maps to ENST00000397932 T1059T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A5UC-01A-11D-A28X-10 chr9:73426149 C>A maps to ENST00000419692 P269P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IF-01A-11D-A33K-10 chr9:73442763 T>A maps to ENST00000419692 T265T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A66X-01A-11D-A30V-10 chr9:73477841 G>A maps to ENST00000419692 G89G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10Y-01A-11D-A12Z-10 chr9:77416899 C>T maps to NM_017662.4 A641A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75H-01A-11D-A32G-10 chr9:77442784 C>T maps to NM_017662.4 L250L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A6M4-01A-11D-A32G-10 chr9:77435309 G>T maps to NM_017662.4 I348I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73G-01A-22D-A32G-10 chr15:50884666 C>T maps to NM_017672.4 S1255S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NI-A4U2-01A-11D-A28X-10 chr2:234894477 C>T maps to NM_024080.4 L970L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A123-01A-11D-A12Z-10 chr8:116616800 T>A maps to NM_014112.2 L465L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A4ZQ-01A-11D-A25V-10 chr8:116427072 A>G maps to NM_014112.2 G1021G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A3-01A-11D-A22F-10 chr17:3493226 C>A maps to ENST00000399756 V306V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A3-01A-11D-A22F-10 chr17:3493238 G>A maps to ENST00000399756 N302N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25Y-01A-11D-A16V-10 chr17:16335313 C>A maps to NM_016113.4 P563P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10Q-01A-11D-A12Z-10 chr17:3417231 T>C maps to ENST00000381913 E785E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EA-01A-11D-A12Z-10 chr17:3427524 C>T maps to ENST00000381913 Q570Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73G-01A-22D-A32G-10 chr17:3417892 G>A maps to ENST00000381913 R758*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A115-01A-11D-A12Z-10 chr12:110234362 C>T maps to NM_021625.4 V433V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A115-01A-11D-A12Z-10 chr7:142612520 G>A maps to NM_019841.4 R414R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr7:142612493 C>A maps to NM_019841.4 G423G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr7:98609872 C>T maps to ENST00000359863 L3825L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25S-01A-11D-A16V-10 chr7:98562267 C>A maps to ENST00000359863 L2275L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A6M6-01A-11D-A32G-10 chr9:131072113 C>T maps to NM_015679.1 K237K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EK-01A-11D-A20W-10 chr9:135782756 C>A maps to NM_000368.4 E422*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A2QR-01A-11D-A20W-10 chr9:135798880 T>C did not map to a codon.
Sequencing variant TCGA-DD-A114-01A-11D-A12Z-10 chr16:2098718 C>T maps to NM_000548.3 Q35*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NH-01A-11D-A27I-10 chr16:2134405 C>T maps to NM_000548.3 Q1395*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25W-01A-11D-A16V-10 chr16:2112538 C>T maps to NM_000548.3 S433S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IG-01A-11D-A33K-10 chr3:150127751 C>T maps to NM_014779.2 S205S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25T-01A-11D-A16V-10 chr23:106959960 A>T did not map to a codon.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr11:18502149 C>T maps to NM_006292.2 Q372Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25Y-01A-11D-A16V-10 chr14:81609799 C>T maps to NM_000369.2 Y466Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr18:72998513 A>G maps to NM_005786.4 K339K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39X-01A-11D-A20W-10 chr19:31769300 C>G maps to NM_020856.2 L466L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A459-01A-11D-A25V-10 chr19:31768844 A>T maps to NM_020856.2 T618T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MC-01A-11D-A22F-10 chr5:110409216 C>T maps to NM_033035.4 C75C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MF-01A-11D-A33K-10 chr5:110409223 G>T maps to NM_033035.4 E78*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A23B-01A-11D-A16V-10 chr15:77339188 T>C maps to NM_005724.5 G250G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K7-A5RG-01A-11D-A28X-10 chr12:58141072 A>G maps to NM_005981.3 *211W. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr11:2337499 G>A maps to NM_139022.2 Q195Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A23B-01A-11D-A16V-10 chr23:38525509 G>C did not map to a codon.
Sequencing variant TCGA-DD-A4NK-01A-11D-A28X-10 chr2:3217958 G>A maps to ENST00000398659 I186I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MC-01A-11D-A22F-10 chr5:112769738 G>T maps to NM_032028.3 I266I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K7-A6G5-01A-11D-A30V-10 chr8:144695933 G>A maps to NM_003313.3 P239P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LG-A6GG-01A-11D-A30V-10 chr8:144698801 T>G maps to NM_003313.3 V27V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10X-01A-11D-A12Z-10 chr6:43223473 G>A maps to NM_032538.1 Q247Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MC-01A-11D-A22F-10 chr6:43250674 G>T maps to NM_032538.1 E733*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A5SM-01A-12D-A28X-10 chr6:43220562 G>A maps to NM_032538.1 E65E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A66X-01A-11D-A30V-10 chr15:43164897 G>A maps to ENST00000263802 H23H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5263-01A-01D-A12Z-10 chr3:39171741 G>T maps to ENST00000301819 E746*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A3KG-01A-11D-A20W-10 chr1:55248003 G>A maps to NM_001114108.1 I389I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EL-01A-11D-A152-10 chr15:99759188 C>A maps to NM_022905.4 V123V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NH-01A-11D-A27I-10 chr1:156551506 C>T maps to NM_001105669.2 G117G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NQ-01A-21D-A28X-10 chr1:156551494 C>T maps to NM_001105669.2 G113G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A1HT-01A-11D-A12Z-10 chr2:32859026 C>T maps to NM_017735.4 H117H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr2:32891804 A>T maps to NM_017735.4 P303P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39V-01A-11D-A20W-10 chr4:147824846 A>T maps to ENST00000513335 A171A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr4:147860986 T>A maps to ENST00000513335 K47*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IJ-01A-11D-A33Q-10 chr21:38461096 A>T did not map to a codon.
Sequencing variant TCGA-NI-A4U2-01A-11D-A28X-10 chr5:40716357 T>A maps to NM_012382.2 S226S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr18:21660555 C>T maps to NM_001135993.1 I156I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10W-01A-11D-A12Z-10 chr1:55194026 A>G maps to NM_004623.4 E201E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IJ-01A-11D-A33Q-10 chr9:135276846 C>T maps to NM_007344.2 A454A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A7SK-01A-11D-A34Z-10 chr9:135277158 A>T maps to NM_007344.2 P350P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1E9-01A-21D-A152-10 chr1:117644070 A>G maps to NM_003594.3 K1138K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A5SM-01A-12D-A28X-10 chr1:117644019 A>G maps to NM_003594.3 T1121T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr22:43459927 C>A did not map to a codon.
Sequencing variant TCGA-G3-A7M9-01A-23D-A34Z-10 chr22:43575636 G>A maps to NM_015140.3 A276A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39Z-01A-11D-A20W-10 chr6:167738684 C>T maps to NM_031949.4 S8S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A7PZ-01A-11D-A33Q-10 chr6:167754698 C>A maps to NM_031949.4 I437I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A3JL-01A-11D-A20W-10 chr2:219619006 T>C maps to NM_014640.4 S1165S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A5SM-01A-12D-A28X-10 chr14:76147886 G>T did not map to a codon.
Sequencing variant TCGA-CC-A7IG-01A-11D-A33K-10 chr20:30522614 C>T maps to NM_001008409.2 Q310*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BW-A5NO-01A-11D-A27I-10 chr2:179596522 G>A maps to NM_133378.4 S4449S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A5UE-01A-11D-A28X-10 chr2:179463971 G>A maps to NM_133378.4 L16282L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A5UE-01A-11D-A28X-10 chr2:179665289 G>T maps to NM_133378.4 R139R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr2:179431802 T>C maps to NM_133378.4 L23784L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IL-01A-11D-A33Q-10 chr2:179496877 C>T maps to NM_133378.4 V12013V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11A-01A-11D-A12Z-10 chr2:179659227 G>C maps to NM_133378.4 A432A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A7-01A-11D-A22F-10 chr2:179560595 A>G maps to NM_133378.4 Y9157Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73C-01A-12D-A33K-10 chr2:179435858 A>G maps to NM_133378.4 C22432C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73D-01A-12D-A32G-10 chr2:179560964 A>G maps to NM_133378.4 A9034A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73G-01A-22D-A32G-10 chr2:179410948 G>A maps to NM_133378.4 V29135V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A7PZ-01A-11D-A33Q-10 chr2:179407910 A>T maps to NM_133378.4 T29695T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A7PZ-01A-11D-A33Q-10 chr2:179611652 A>C maps to ENST00000375038 A5160A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A26S-01A-11D-A16V-10 chr2:179560595 A>G maps to NM_133378.4 Y9157Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr2:179413061 A>G maps to NM_133378.4 G28529G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr2:179393914 A>G maps to NM_133378.4 S32953S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr2:179396536 A>G maps to NM_133378.4 P32367P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25Z-01A-11D-A16V-10 chr2:179648461 T>C maps to NM_133378.4 P942P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K7-A5RG-01A-11D-A28X-10 chr2:179438597 C>T maps to NM_133378.4 L21519L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KR-A7K0-01A-12D-A33Q-10 chr2:179438087 A>G maps to NM_133378.4 Y21689Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NI-A4U2-01A-11D-A28X-10 chr2:179579149 C>T maps to NM_133378.4 W7540*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-O8-A75V-01A-11D-A32G-10 chr2:179593437 T>C maps to NM_133378.4 E5161E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr2:179398438 A>T maps to NM_133378.4 G31733G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr2:179477139 A>T maps to NM_133378.4 T14136T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr2:179584710 T>A maps to NM_133378.4 L6642L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PD-A5DF-01A-11D-A27I-10 chr8:63973813 T>C maps to NM_000370.3 Q278Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A3KG-01A-11D-A20W-10 chr18:29172905 T>A maps to ENST00000432547 A39A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr11:8111645 A>T maps to NM_003320.4 K96*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1ED-01A-11D-A152-10 chr12:49522076 G>A maps to NM_006082.2 S340S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr12:49666553 A>T maps to NM_032704.3 P298P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CK-01A-11D-A20W-10 chr10:5437355 G>A maps to NM_024803.2 Y110Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A123-01A-11D-A12Z-10 chr10:94783 C>A maps to NM_177987.2 L42L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A6M6-01A-11D-A32G-10 chr10:94663 A>T maps to NM_177987.2 G56G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25S-01A-11D-A16V-10 chr10:135099036 C>A maps to NM_006659.2 T606T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr16:28856081 G>T maps to NM_003321.4 T207T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39V-01A-11D-A20W-10 chr6:35471392 G>A maps to NM_003322.3 T422T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KR-A7K0-01A-12D-A33Q-10 chr6:35471362 G>A maps to NM_003322.3 N432N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A4ZP-01A-12D-A25V-10 chr18:9887133 A>T maps to NM_001098529.1 K220*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10W-01A-11D-A12Z-10 chr18:54293688 C>A did not map to a codon.
Sequencing variant TCGA-DD-A1ED-01A-11D-A152-10 chr16:72120694 T>C maps to NM_001142318.1 P97P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr19:10476356 G>A maps to NM_003331.4 L283L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EA-01A-11D-A12Z-10 chr18:671450 G>A maps to NM_001071.2 Q268Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A217-01A-11D-A152-10 chr15:41865514 G>A maps to NM_006293.3 E665E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5260-01A-01D-A12Z-10 chr7:66582481 G>A maps to NM_018264.2 P525P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MB-01A-11D-A20W-10 chr1:75199080 C>T maps to NM_138467.2 G51G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr1:75229760 A>G maps to NM_138467.2 L248L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A5SL-01A-11D-A27I-10 chr9:139973542 G>A maps to NM_207309.2 L262L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IG-01A-11D-A33K-10 chr23:47065467 A>G did not map to a codon.
Sequencing variant TCGA-DD-A3A9-01A-11D-A25V-10 chr23:47062207 A>G did not map to a codon.
Sequencing variant TCGA-FV-A23B-01A-11D-A16V-10 chr23:47065755 G>A did not map to a codon.
Sequencing variant TCGA-FV-A495-01A-11D-A25V-10 chr23:47072227 A>G did not map to a codon.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr23:47074243 G>A did not map to a codon.
Sequencing variant TCGA-BW-A5NO-01A-11D-A27I-10 chr4:68497489 C>A did not map to a codon.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr4:68534269 C>A maps to NM_018227.5 T264T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MD-01A-12D-A34Z-10 chr9:138837089 C>A maps to NM_016172.2 S220S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr9:33996316 T>C maps to NM_018449.2 T64T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr9:33953473 T>C did not map to a codon.
Sequencing variant TCGA-DD-A3A9-01A-11D-A25V-10 chr11:122659818 C>T maps to NM_032873.4 V261V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5259-01A-31D-A20W-10 chr4:103722608 A>C did not map to a codon.
Sequencing variant TCGA-DD-A1EF-01A-11D-A12Z-10 chr7:129520789 A>G maps to NM_003344.2 V25V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A4XI-01A-11D-A25V-10 chr4:39780008 A>G maps to NM_005339.4 K186K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr15:76183351 T>C maps to NM_173469.2 N342N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MD-01A-12D-A34Z-10 chr17:46988175 C>T maps to NM_023079.4 I108I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3M9-01A-11D-A20W-10 chr15:25616255 A>G maps to NM_000462.2 S358S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5261-01A-01D-A12Z-10 chr12:109972535 C>T maps to NM_183415.1 R1052R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A116-01A-11D-A12Z-10 chr12:109939173 A>G did not map to a codon.
Sequencing variant TCGA-G3-A25Z-01A-11D-A16V-10 chr7:157046655 A>G maps to NM_014671.2 E901E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A6UC-01A-21D-A33K-10 chr11:118245828 A>G maps to NM_004788.2 L452L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr1:110655546 G>T maps to NM_203412.1 E131*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MB-01A-11D-A20W-10 chr20:3102975 G>A maps to NM_014948.2 G103G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KR-A7K7-01A-11D-A33K-10 chr9:86297920 T>C maps to NM_013438.4 S131S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A5UC-01A-11D-A28X-10 chr23:56590708 C>G did not map to a codon.
Sequencing variant TCGA-DD-A4NG-01A-11D-A27I-10 chr11:5529135 C>A maps to NM_017481.2 G551G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A459-01A-11D-A25V-10 chr11:5537569 T>A maps to NM_145053.4 I34I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KR-A7K7-01A-11D-A33K-10 chr6:42610158 T>G maps to NM_015255.2 Y679*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr2:170897403 A>G maps to ENST00000442603 E1552E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10U-01A-11D-A12Z-10 chr1:19511590 A>G did not map to a codon.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr1:19433355 G>A maps to ENST00000375267 A4070A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A66Y-01A-11D-A30V-10 chr1:19478350 G>A maps to ENST00000375267 P2333P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A7XO-01A-11D-A34Z-10 chr1:19408021 C>A maps to ENST00000375267 L5018L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr1:19501461 G>T maps to ENST00000375267 R947R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K7-A5RF-01A-11D-A28X-10 chr1:19499467 C>T maps to ENST00000375267 E1137E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A3KF-01A-11D-A20W-10 chr8:103300479 C>T maps to NM_015902.4 E1576E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EF-01A-11D-A12Z-10 chr8:103293515 C>T did not map to a codon.
Sequencing variant TCGA-BC-A69H-01A-11D-A30V-10 chr11:62445984 C>A maps to NM_015853.3 E68*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A7S9-01A-11D-A33Q-10 chr2:136505939 G>T did not map to a codon.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr19:4448328 C>A maps to NM_025241.2 V175V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A3I0-01A-11D-A22F-10 chr3:196089288 C>T maps to NM_015562.1 E368E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3M9-01A-11D-A20W-10 chr13:76140946 G>A maps to NM_006002.3 L100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr1:192993076 C>A did not map to a codon.
Sequencing variant TCGA-DD-A113-01A-11D-A12Z-10 chr20:62577848 C>T maps to NM_017859.3 W87*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25W-01A-11D-A16V-10 chr3:48600436 G>A maps to NM_033199.3 R41*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MB-01A-11D-A20W-10 chr4:141484604 C>T maps to NM_021833.4 G131G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MF-01A-11D-A33K-10 chr4:141489131 C>T did not map to a codon.
Sequencing variant TCGA-FV-A496-01A-11D-A25V-10 chr22:19463068 G>C maps to ENST00000399525 S20S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr4:39510221 A>G maps to NM_003359.3 A290A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IF-01A-11D-A33K-10 chr13:96555131 A>G maps to NM_020121.3 D826D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EJ-01A-11D-A152-10 chr13:96599293 T>C maps to NM_020121.3 V558V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QA-A7B7-01A-11D-A32G-10 chr13:96579584 T>C maps to NM_020121.3 T661T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NB-01A-12D-A25V-10 chr2:234638002 G>T maps to NM_019093.2 L77L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A5SM-01A-12D-A28X-10 chr2:234526863 G>T maps to NM_019076.4 G171*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CK-01A-11D-A20W-10 chr2:234581245 T>A maps to NM_021027.2 R222R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RG-A7D4-01A-12D-A33Q-10 chr4:70504722 C>T maps to ENST00000514019 Q413Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39X-01A-11D-A20W-10 chr4:70160273 C>G maps to NM_053039.1 S446*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A6M4-01A-11D-A32G-10 chr4:70346459 C>G maps to NM_021139.2 V493V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MF-01A-11D-A33K-10 chr4:70359470 G>C maps to NM_021139.2 L270L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A110-01A-11D-A12Z-10 chr6:34802104 C>A maps to NM_017754.3 L150L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A2QQ-01A-11D-A22F-10 chr6:34827054 C>G maps to NM_017754.3 S974S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75H-01A-11D-A32G-10 chr12:100452949 C>T maps to NM_015054.1 W702*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr9:6493854 A>G maps to NM_152896.1 G509G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A459-01A-11D-A25V-10 chr12:132396632 A>G maps to NM_003565.2 P365P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1ED-01A-11D-A152-10 chr17:19705088 C>A did not map to a codon.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr3:41860959 A>G maps to NM_017886.2 V601V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A23B-01A-11D-A16V-10 chr19:17753722 G>A maps to ENST00000428389 H889H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10T-01A-11D-A12Z-10 chr15:54435881 G>A did not map to a codon.
Sequencing variant TCGA-DD-A39Z-01A-11D-A20W-10 chr15:54825123 T>A maps to ENST00000260323 V1852V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NL-01A-11D-A28X-10 chr15:54914612 A>G maps to ENST00000260323 V2065V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NI-A4U2-01A-11D-A28X-10 chr15:54590036 T>A maps to ENST00000260323 S1339S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EK-01A-11D-A20W-10 chr5:176305055 G>A maps to NM_133369.2 A599A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A2QQ-01A-11D-A22F-10 chr4:96141184 C>A maps to NM_003728.3 S417S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A5UD-01A-11D-A28X-10 chr8:35542097 A>T did not map to a codon.
Sequencing variant TCGA-DD-A1EL-01A-11D-A152-10 chr6:167708072 G>A maps to NM_018974.3 L52L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73G-01A-22D-A32G-10 chr12:109535498 G>A maps to NM_080911.2 K5K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EB-01A-11D-A12Z-10 chr16:1420137 G>A maps to ENST00000508903 S526S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A459-01A-11D-A25V-10 chr19:18967007 C>T maps to ENST00000418384 Q586*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NI-01A-11D-A27I-10 chr13:115052105 T>C did not map to a codon.
Sequencing variant TCGA-G3-A7M6-01A-11D-A33Q-10 chr23:118971719 C>G did not map to a codon.
Sequencing variant TCGA-BC-A10Y-01A-11D-A12Z-10 chr3:118909117 T>A maps to NM_006952.3 Y99*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EB-01A-11D-A12Z-10 chr7:48147818 C>T maps to NM_003364.2 A266A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IJ-01A-11D-A33Q-10 chr23:74494411 C>T did not map to a codon.
Sequencing variant TCGA-CC-A7II-01A-11D-A33K-10 chr1:46782225 G>T maps to NM_006004.2 V82V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CK-01A-11D-A20W-10 chr1:229779358 G>A maps to NM_014777.2 G1238G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10R-01A-11D-A12Z-10 chr9:131151970 C>T maps to NM_030914.2 D88D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73B-01A-12D-A32G-10 chr9:131152006 C>T maps to NM_030914.2 G100G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MB-01A-11D-A20W-10 chr3:126229601 C>T maps to NM_001165974.1 P54P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A7SF-01A-11D-A34Z-10 chr1:161011513 C>A maps to NM_007122.3 S133S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25Z-01A-11D-A16V-10 chr11:17530989 A>G maps to NM_153676.3 N642N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-4073-01B-02D-A12Z-10 chr1:216062250 T>A maps to ENST00000366943 G2580G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5259-01A-31D-A20W-10 chr1:216073534 C>T maps to ENST00000366943 S2492S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MB-01A-11D-A20W-10 chr1:216373461 A>G maps to ENST00000366943 S1106S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A118-01A-11D-A12Z-10 chr1:216073534 C>T maps to ENST00000366943 S2492S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A459-01A-11D-A25V-10 chr1:215972279 T>C maps to ENST00000366943 G3309G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A3I0-01A-11D-A22F-10 chr1:215932016 G>C maps to ENST00000366943 S3770*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A4ZQ-01A-11D-A25V-10 chr1:216062334 G>A maps to ENST00000366943 T2552T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25V-01A-11D-A16V-10 chr1:216538319 A>G maps to ENST00000366943 T253T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A5SK-01A-11D-A27I-10 chr1:215960063 T>C maps to ENST00000366943 S3445S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25Y-01A-11D-A16V-10 chr4:76703965 T>C maps to NM_003715.2 S219S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BW-A5NO-01A-11D-A27I-10 chr16:84801855 G>A maps to NM_005153.2 T630T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25W-01A-11D-A16V-10 chr13:27643522 T>C did not map to a codon.
Sequencing variant TCGA-G3-A25S-01A-11D-A16V-10 chr18:210404 T>C maps to NM_005151.3 C415C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MA-01A-11D-A20W-10 chr12:62790140 T>C maps to ENST00000280377 A879A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25S-01A-11D-A16V-10 chr12:62783236 A>G maps to ENST00000280377 G500G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73A-01A-12D-A32G-10 chr21:30411351 A>G maps to NM_006447.2 P246P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NI-A4U2-01A-11D-A28X-10 chr11:119228274 C>T maps to NM_004205.4 R509R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5261-01A-01D-A12Z-10 chr9:132636967 G>A maps to NM_001008563.3 K618K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A7M5-01A-11D-A33Q-10 chr9:132636871 A>T maps to NM_001008563.3 L586L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75I-01A-11D-A32G-10 chr1:161132172 C>T maps to NM_012475.4 L258L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr17:20919134 T>A maps to ENST00000455117 A324A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A3KF-01A-11D-A20W-10 chr21:17163835 C>T maps to ENST00000285681 S136S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75I-01A-11D-A32G-10 chr21:17250203 C>T maps to ENST00000285681 V995V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A5UE-01A-11D-A28X-10 chr23:132159789 C>A did not map to a codon.
Sequencing variant TCGA-DD-A73B-01A-12D-A32G-10 chr23:132161218 G>A did not map to a codon.
Sequencing variant TCGA-BD-A3EP-01A-11D-A22F-10 chr12:109519739 T>C maps to NM_032663.3 G261G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39Z-01A-11D-A20W-10 chr16:23093794 A>G maps to NM_020718.3 P638P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr16:23080458 G>T maps to NM_020718.3 I989I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A3KG-01A-11D-A20W-10 chr1:78183651 T>C maps to NM_015017.3 L637L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A66Y-01A-11D-A30V-10 chr2:61430399 T>G did not map to a codon.
Sequencing variant TCGA-G3-A7M5-01A-11D-A33Q-10 chr2:61520655 T>C maps to NM_014709.3 L1497L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A6M5-01A-11D-A32G-10 chr2:61607464 G>A maps to NM_014709.3 R285*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A116-01A-11D-A12Z-10 chr17:76802272 G>A maps to NM_025090.3 P727P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr17:76799930 C>A maps to NM_025090.3 T782T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1E9-01A-21D-A152-10 chr4:144107244 G>A maps to NM_032557.5 L214L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NA-01A-11D-A25V-10 chr4:144134994 T>C maps to NM_032557.5 P622P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr4:144133530 A>T maps to NM_032557.5 R520*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HP-A5MZ-01A-21D-A27I-10 chr3:49321559 G>A maps to NM_003363.3 P800P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A110-01A-11D-A12Z-10 chr2:234394445 G>A maps to NM_018218.2 P1136P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11C-01A-11D-A12Z-10 chr2:234394613 G>A maps to NM_018218.2 D1080D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75C-01A-11D-A32G-10 chr2:234442149 T>C maps to NM_018218.2 K493K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A7PZ-01A-11D-A33Q-10 chr7:6189833 G>A maps to ENST00000404835 P669P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A495-01A-11D-A25V-10 chr7:6194391 C>T maps to ENST00000404835 Y1069Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A5SJ-01A-11D-A27I-10 chr7:6183808 C>T maps to ENST00000404835 T324T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A7SF-01A-11D-A34Z-10 chr7:6185160 T>A maps to ENST00000404835 P335P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr7:6183733 A>T maps to ENST00000404835 P299P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr12:95922581 C>T did not map to a codon.
Sequencing variant TCGA-DD-A116-01A-11D-A12Z-10 chr11:11927067 T>C maps to ENST00000399455 Y321Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25S-01A-11D-A16V-10 chr1:22050538 T>C maps to NM_032236.5 E500E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A7-01A-11D-A22F-10 chr12:6973283 T>G maps to NM_001098536.1 P723P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LG-A6GG-01A-11D-A30V-10 chr4:120189489 G>A maps to NM_019050.2 K401K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A123-01A-11D-A12Z-10 chr10:75277369 T>C maps to NM_152586.3 P938P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4ND-01A-11D-A25V-10 chr17:5042894 G>A maps to NM_004505.2 W475*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A496-01A-11D-A25V-10 chr16:9000398 G>A maps to NM_003470.2 Q438*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3M9-01A-11D-A20W-10 chr23:41012218 C>T did not map to a codon.
Sequencing variant TCGA-CC-A3MA-01A-11D-A20W-10 chr23:41088998 A>G did not map to a codon.
Sequencing variant TCGA-MI-A75C-01A-11D-A32G-10 chr23:41002597 C>G did not map to a codon.
Sequencing variant TCGA-UB-A7ME-01A-11D-A33K-10 chr23:41069764 T>A did not map to a codon.
Sequencing variant TCGA-CC-A5UE-01A-11D-A28X-10 chr24:14951876 G>T did not map to a codon.
Sequencing variant TCGA-FV-A3R2-01A-11D-A22F-10 chr24:14968375 G>A did not map to a codon.
Sequencing variant TCGA-FV-A3R2-01A-11D-A22F-10 chr24:14968376 G>T did not map to a codon.
Sequencing variant TCGA-BC-A112-01A-11D-A12Z-10 chr12:101711354 C>T maps to NM_014503.2 A884A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A7M8-01A-11D-A33Q-10 chr12:101679569 T>C maps to NM_014503.2 N79N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A113-01A-11D-A12Z-10 chr6:144765509 G>T maps to NM_007124.2 E536*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73G-01A-22D-A32G-10 chr6:144875993 C>A maps to NM_007124.2 R2367R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25W-01A-11D-A16V-10 chr6:144783915 C>T maps to NM_007124.2 Q994*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EK-01A-11D-A20W-10 chr17:80332625 C>A maps to NM_018949.1 T142T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A4-01A-11D-A22F-10 chr23:47516682 A>G did not map to a codon.
Sequencing variant TCGA-RC-A6M6-01A-11D-A32G-10 chr16:70778458 C>A maps to NM_018052.3 V465V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A2-01A-11D-A20W-10 chr12:6575450 G>A maps to ENST00000396308 G22G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A1-01A-11D-A20W-10 chr17:8064967 G>A maps to ENST00000488857 S82S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11C-01A-11D-A12Z-10 chr1:160388868 C>T maps to NM_020335.2 R90R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A7M9-01A-23D-A34Z-10 chr18:9914270 G>T maps to NM_003574.5 G6G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KR-A7K0-01A-12D-A33Q-10 chr6:30893706 C>T maps to NM_001167734.1 Y1034Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr6:30892147 G>C maps to NM_001167734.1 V858V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr14:77237532 G>A maps to NM_014909.4 Q133Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CK-01A-11D-A20W-10 chr1:108322078 A>T maps to NM_006113.4 P119P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr23:154444800 C>G did not map to a codon.
Sequencing variant TCGA-DD-A1EH-01A-11D-A12Z-10 chr5:82833573 C>T maps to NM_004385.4 P1584P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A2QR-01A-11D-A20W-10 chr5:82835028 G>A maps to NM_004385.4 T2069T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A3R2-01A-11D-A22F-10 chr5:82836954 T>A maps to NM_004385.4 A2711A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25T-01A-11D-A16V-10 chr5:82817433 T>C maps to NM_004385.4 S1103S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A112-01A-11D-A12Z-10 chr23:7811708 G>C did not map to a codon.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr3:157031463 C>A maps to NM_001167912.1 G652G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73D-01A-12D-A32G-10 chr3:157098982 A>C maps to NM_001167912.1 L363L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A4ZP-01A-12D-A25V-10 chr17:56056621 C>T maps to NM_007146.2 Q343Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EB-01A-11D-A12Z-10 chr23:135618179 A>G did not map to a codon.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr3:38044029 G>T maps to NM_015873.3 L541L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A116-01A-11D-A12Z-10 chr10:17277862 A>T maps to NM_003380.3 P416P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-4073-01B-02D-A12Z-10 chr3:42577593 C>T maps to NM_004624.3 L399L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HP-A5N0-01A-11D-A28X-10 chr7:158851224 G>A maps to ENST00000402066 Y275Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A7SK-01A-11D-A34Z-10 chr19:53762413 T>A maps to NM_173856.2 Y262*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr3:51456167 A>G maps to ENST00000273612 C1133C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A217-01A-11D-A152-10 chr9:79824388 C>T maps to ENST00000376646 Q146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RG-A7D4-01A-12D-A33Q-10 chr9:79820238 A>G maps to ENST00000376646 K66K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A66X-01A-11D-A30V-10 chr8:100711795 G>T maps to NM_017890.3 L2055L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NV-01A-11D-A30V-10 chr15:62146684 T>G maps to NM_020821.2 R3745R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MB-01A-11D-A20W-10 chr1:12403093 A>G maps to NM_015378.2 G2957G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A459-01A-11D-A25V-10 chr1:12313849 T>A maps to NM_015378.2 T212T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr1:12516139 C>A maps to NM_015378.2 A4140A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A23B-01A-11D-A16V-10 chr1:12379554 T>C maps to NM_015378.2 G2472G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr1:12567011 A>G maps to NM_015378.2 L4300L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr17:40928288 C>A maps to NM_032353.2 S123S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A216-01A-11D-A152-10 chr11:134113162 G>A maps to NM_052875.3 E232E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MB-01A-11D-A20W-10 chr16:46708511 A>G maps to NM_018206.4 F325F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr11:60900810 T>C did not map to a codon.
Sequencing variant TCGA-O8-A75V-01A-11D-A32G-10 chr6:33218758 C>T maps to NM_022553.4 A677A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K7-A6G5-01A-11D-A30V-10 chr1:151158054 C>A maps to ENST00000354473 P104P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A6M4-01A-11D-A32G-10 chr1:151156880 T>A maps to ENST00000354473 R158R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A7PZ-01A-11D-A33Q-10 chr12:118533473 T>A maps to NM_019086.5 P75P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K7-A6G5-01A-11D-A30V-10 chr23:65253414 T>C did not map to a codon.
Sequencing variant TCGA-RC-A7S9-01A-11D-A33Q-10 chr23:65244889 A>G did not map to a codon.
Sequencing variant TCGA-RC-A7SK-01A-11D-A34Z-10 chr19:54554673 T>A maps to NM_198481.3 S128S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NK-01A-11D-A28X-10 chr14:74706314 G>A maps to NM_182894.2 V17V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3M9-01A-11D-A20W-10 chr6:142487369 T>C maps to NM_016485.3 L40L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A6M4-01A-11D-A32G-10 chr6:142468438 A>G maps to NM_016485.3 A5A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-4073-01B-02D-A12Z-10 chr1:117699310 A>G maps to NM_024626.2 V110V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A116-01A-11D-A12Z-10 chr17:26694413 G>C maps to NM_000638.3 G471G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5264-01A-01D-A12Z-10 chr16:22126724 G>A maps to NM_173615.3 L249L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IL-01A-11D-A33Q-10 chr16:22149724 A>G maps to NM_173615.3 V728V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A459-01A-11D-A25V-10 chr16:22126670 C>T maps to NM_173615.3 L231L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A5KG-01A-11D-A27I-10 chr16:22152957 A>T maps to NM_173615.3 S813S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A3KG-01A-11D-A20W-10 chr11:124013239 T>C maps to NM_014622.4 G705G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11C-01A-11D-A12Z-10 chr11:61036445 G>A maps to NM_152718.2 S610S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A459-01A-11D-A25V-10 chr11:61026644 T>A maps to NM_152718.2 S790S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7ME-01A-11D-A33K-10 chr11:61026464 G>C maps to NM_152718.2 T850T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25U-01A-11D-A16V-10 chr12:6161737 T>C maps to NM_000552.3 E719E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A7M6-01A-11D-A33Q-10 chr12:6125790 C>T maps to NM_000552.3 Q1734Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-4073-01B-02D-A12Z-10 chr10:88259808 A>G maps to ENST00000342368 R482R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4ND-01A-11D-A25V-10 chr23:48547189 G>T did not map to a codon.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr6:110426737 T>C maps to NM_003931.2 R195R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A5UD-01A-11D-A28X-10 chr7:123332583 C>T maps to NM_003941.2 P388P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10R-01A-11D-A12Z-10 chr12:14947912 T>C maps to NM_016312.2 S171S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5262-01A-01D-A12Z-10 chr12:14943651 T>C maps to NM_016312.2 V349V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CK-01A-11D-A20W-10 chr7:73105341 C>A maps to ENST00000423497 L153L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5262-01A-01D-A12Z-10 chr4:85707239 T>C maps to NM_014991.4 P1318P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IK-01A-12D-A33Q-10 chr4:85623578 T>G maps to NM_014991.4 A2841A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr4:85731415 A>G maps to NM_014991.4 L657L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A23B-01A-11D-A16V-10 chr4:85663039 T>C maps to NM_014991.4 G2036G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A5W4-01A-11D-A28X-10 chr4:10077079 G>A maps to NM_017491.3 S581S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BD-A3EP-01A-11D-A22F-10 chr4:10099481 A>G maps to NM_017491.3 S137S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T1-A6J8-01A-11D-A32G-10 chr4:177093602 A>G maps to NM_170710.4 V1099V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr4:177098696 A>G maps to NM_170710.4 L1247L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11C-01A-11D-A12Z-10 chr19:994279 G>A maps to NM_024100.3 L412L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39X-01A-11D-A20W-10 chr4:39191329 T>C maps to NM_025132.3 A73A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A1HT-01A-11D-A12Z-10 chr16:736890 A>G maps to ENST00000248142 S525S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39X-01A-11D-A20W-10 chr1:224588732 T>C maps to NM_025160.6 E446E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr9:116079109 A>G maps to NM_001012361.2 C341C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7II-01A-11D-A33K-10 chr2:128495605 A>C maps to NM_001006623.2 R249R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A4XI-01A-11D-A25V-10 chr2:128522412 A>G maps to NM_018383.4 I205I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr5:110430615 A>T did not map to a codon.
Sequencing variant TCGA-NI-A4U2-01A-11D-A28X-10 chr2:29129432 A>G maps to NM_015131.1 T157T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A112-01A-11D-A12Z-10 chr23:117528109 G>T did not map to a codon.
Sequencing variant TCGA-BC-A3KG-01A-11D-A20W-10 chr23:117566744 T>A did not map to a codon.
Sequencing variant TCGA-DD-A73C-01A-12D-A33K-10 chr23:48933030 G>A did not map to a codon.
Sequencing variant TCGA-G3-A25T-01A-11D-A16V-10 chr1:109553938 A>G maps to NM_001142550.1 S250S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IG-01A-11D-A33K-10 chr3:167277884 C>T maps to NM_178824.3 R206R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BD-A2L6-01A-11D-A20W-10 chr16:74943788 T>C maps to NM_030581.3 K472K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73C-01A-12D-A33K-10 chr16:74919608 C>T maps to NM_030581.3 E877E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A5UD-01A-11D-A28X-10 chr7:158672637 A>G maps to NM_018051.4 K279K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IJ-01A-11D-A33Q-10 chr7:158734668 G>C maps to NM_018051.4 P944P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73E-01A-12D-A32G-10 chr1:85561678 T>A maps to NM_145172.3 I413I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr1:241886641 C>A maps to NM_144625.4 T356T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CK-01A-11D-A20W-10 chr1:43638462 T>C maps to NM_001195831.1 G13G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7ME-01A-11D-A33K-10 chr1:43687774 G>A did not map to a codon.
Sequencing variant TCGA-DD-A11A-01A-11D-A12Z-10 chr18:54483319 T>C maps to NM_015285.2 P1083P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IG-01A-11D-A33K-10 chr15:44158352 G>T maps to NM_024908.3 L548L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr15:44158448 A>C maps to NM_024908.3 T580T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A8-01A-11D-A22F-10 chr1:67356849 C>T maps to NM_024763.4 L210L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25U-01A-11D-A16V-10 chr1:67292729 C>T did not map to a codon.
Sequencing variant TCGA-G3-A5SM-01A-12D-A28X-10 chr17:1630782 C>T maps to NM_001163809.1 Q844*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A5SK-01A-11D-A27I-10 chr7:151093227 C>G maps to ENST00000426624 R235R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A69H-01A-11D-A30V-10 chr7:134894444 C>T maps to NM_014149.3 R62R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr15:90272995 A>G maps to NM_020212.1 K402K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr1:27627863 A>G maps to ENST00000319394 K460K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39W-01A-11D-A20W-10 chr20:43743714 G>A maps to ENST00000307971 Q4*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1E9-01A-21D-A152-10 chr20:44181868 C>T maps to NM_130896.2 E164E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KR-A7K8-01A-11D-A33K-10 chr15:83481940 T>A maps to NM_001080435.1 V232V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A5UD-01A-11D-A28X-10 chr8:38133853 T>G maps to NM_023034.1 A1344A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NP-01A-11D-A28X-10 chr8:38133281 A>T maps to NM_023034.1 S1397S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39Y-01A-11D-A20W-10 chr17:38430225 T>C maps to NM_133264.4 S385S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A7M5-01A-11D-A33Q-10 chr7:29874393 G>T maps to NM_001080529.1 L18L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr7:29915477 A>C maps to NM_001080529.1 A41A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A3-01A-11D-A22F-10 chr8:134232983 G>A maps to NM_003882.2 P170P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A7XP-01A-11D-A34Z-10 chr6:112375574 C>A maps to NM_198239.1 L23L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NI-01A-11D-A27I-10 chr19:15538009 G>A maps to ENST00000389282 G1145G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10W-01A-11D-A12Z-10 chr12:1009714 A>C maps to NM_001184985.1 P2434P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr12:994232 T>C maps to NM_001184985.1 V1681V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A7M5-01A-11D-A33Q-10 chr9:96079848 G>A maps to ENST00000297954 A2225A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr9:96021604 T>A maps to ENST00000297954 P925P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K7-A6G5-01A-11D-A30V-10 chr7:116960720 G>A maps to NM_003391.2 A70A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A0-01A-11D-A20W-10 chr12:1741874 C>G maps to NM_032642.2 A44A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A3KF-01A-11D-A20W-10 chr3:13896148 A>G maps to NM_004625.3 G150G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KC-01A-11D-A20W-10 chr5:137426638 C>T maps to NM_058244.2 S311S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MB-01A-11D-A20W-10 chr17:44953862 G>T maps to NM_003396.1 E285*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A7M6-01A-11D-A33Q-10 chr8:31030548 G>A maps to NM_000553.4 W1410*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MA-01A-11D-A20W-10 chr17:25630656 T>A maps to NM_015626.8 Y158*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr12:118472834 C>G maps to ENST00000441406 G353G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11C-01A-11D-A12Z-10 chr19:34986660 A>G maps to ENST00000270288 A603A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73G-01A-22D-A32G-10 chr23:10085607 C>T did not map to a codon.
Sequencing variant TCGA-G3-A3CK-01A-11D-A20W-10 chr23:10094157 A>G did not map to a codon.
Sequencing variant TCGA-DD-A73A-01A-12D-A32G-10 chr16:69973253 A>G maps to NM_007014.3 G817G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25Z-01A-11D-A16V-10 chr16:69965733 C>T maps to NM_007014.3 R541R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10U-01A-11D-A12Z-10 chr19:7687526 G>A maps to NM_020196.2 A464A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A7M6-01A-11D-A33Q-10 chr1:168510342 A>G maps to NM_003175.3 R64R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A26S-01A-11D-A16V-10 chr2:168100449 T>C maps to NM_152381.5 L850L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75C-01A-11D-A32G-10 chr2:168102932 C>T maps to NM_152381.5 I1677I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75E-01A-11D-A32G-10 chr2:168107753 G>T maps to NM_152381.5 V3284V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75H-01A-11D-A32G-10 chr2:168115371 G>A maps to ENST00000420519 S805S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A6M6-01A-11D-A32G-10 chr2:168110642 C>A maps to ENST00000420519 C459*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A7SF-01A-11D-A34Z-10 chr2:168103400 A>G maps to NM_152381.5 K1833K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MD-01A-12D-A34Z-10 chr2:168106757 A>G maps to NM_152381.5 E2952E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A0-01A-11D-A20W-10 chr23:37553771 T>C did not map to a codon.
Sequencing variant TCGA-DD-A4NV-01A-11D-A30V-10 chr8:56015166 C>A maps to NM_052898.1 S40*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EC-01A-21D-A12Z-10 chr20:30585124 G>A maps to NM_001011718.1 W535*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MA-01A-11D-A33Q-10 chr20:30584707 C>T maps to NM_001011718.1 A396A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A7SF-01A-11D-A34Z-10 chr10:111642255 G>A maps to NM_020383.3 L325L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IG-01A-11D-A33K-10 chr23:128893169 A>T did not map to a codon.
Sequencing variant TCGA-G3-A25U-01A-11D-A16V-10 chr23:128896687 A>T did not map to a codon.
Sequencing variant TCGA-G3-A25Y-01A-11D-A16V-10 chr23:128893153 A>G did not map to a codon.
Sequencing variant TCGA-BC-A10W-01A-11D-A12Z-10 chr2:61706089 A>C maps to NM_003400.3 G1027G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr6:43515422 A>G maps to NM_020750.2 A694A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EB-01A-11D-A12Z-10 chr16:28112967 C>A maps to NM_015171.2 V1029V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MF-01A-11D-A33K-10 chr8:21827676 T>C maps to ENST00000434536 L94L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KR-A7K2-01A-12D-A33Q-10 chr1:180794055 T>C maps to NM_004736.3 L311L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7II-01A-11D-A33K-10 chr5:82406961 G>C maps to NM_022406.2 T85T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75E-01A-11D-A32G-10 chr5:82649042 C>T maps to NM_022406.2 D331D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1E9-01A-21D-A152-10 chr22:42042965 T>A maps to NM_001469.3 A280A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr3:142145679 T>A maps to NM_019001.3 S104S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr20:21369945 A>T maps to NM_012255.3 P941P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11D-01A-11D-A12Z-10 chr11:74617458 G>T maps to NM_182969.1 I268I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr3:38416702 C>T maps to NM_005108.3 H319H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A3KG-01A-11D-A20W-10 chr16:17211554 G>T maps to NM_022166.3 T835T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A82E-01A-11D-A34Z-10 chr16:17353088 G>A maps to NM_022166.3 A223A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr16:17353091 T>C maps to NM_022166.3 R222R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A7PZ-01A-11D-A33Q-10 chr1:43162927 C>T maps to NM_004559.3 F245F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75G-01A-11D-A32G-10 chr3:183480000 C>A maps to NM_018023.4 S627S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr12:69759664 G>T did not map to a codon.
Sequencing variant TCGA-G3-A25S-01A-11D-A16V-10 chr18:742993 T>C maps to NM_005433.3 R328R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A123-01A-11D-A12Z-10 chr19:11034658 G>A maps to NM_024029.3 I167I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MC-01A-11D-A22F-10 chr19:11034083 C>T did not map to a codon.
Sequencing variant TCGA-CC-A3MA-01A-11D-A20W-10 chr23:67731742 A>G did not map to a codon.
Sequencing variant TCGA-CC-5264-01A-01D-A12Z-10 chr4:44631479 A>G maps to NM_182592.2 N146N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NR-01A-11D-A30V-10 chr4:44626733 G>A maps to NM_182592.2 A188A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A6UC-01A-21D-A33K-10 chr14:75230509 G>T maps to NM_019589.2 P106P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25S-01A-11D-A16V-10 chr1:207224105 G>A maps to NM_018566.3 L90L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A3KF-01A-11D-A20W-10 chr5:112874843 A>G maps to NM_022828.3 K392K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NK-01A-11D-A28X-10 chr5:112926895 C>T maps to NM_022828.3 S1328S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39Y-01A-11D-A20W-10 chr1:29069726 A>G maps to NM_016258.2 P315P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A116-01A-11D-A12Z-10 chr8:64098979 G>A maps to ENST00000339066 G136G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5263-01A-01D-A12Z-10 chr7:75959523 C>G maps to NM_012479.3 S38S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A66X-01A-11D-A30V-10 chr14:100705844 G>T maps to NM_003403.3 P88P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A3KF-01A-11D-A20W-10 chr23:21875261 T>A did not map to a codon.
Sequencing variant TCGA-DD-A4NK-01A-11D-A28X-10 chr7:100344317 A>T maps to ENST00000349350 S308S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73B-01A-12D-A32G-10 chr7:100349485 C>A maps to ENST00000349350 V586V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A7M5-01A-11D-A33Q-10 chr7:100348275 C>T maps to ENST00000349350 D426D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MA-01A-11D-A33Q-10 chr7:100361667 G>T maps to ENST00000349350 V1372V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A82E-01A-11D-A34Z-10 chr3:166960378 G>A maps to ENST00000307529 S769S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A118-01A-11D-A12Z-10 chr23:2407375 G>A did not map to a codon.
Sequencing variant TCGA-MI-A75H-01A-11D-A32G-10 chr20:56179628 C>T maps to NM_030776.2 *430*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A3JL-01A-11D-A20W-10 chr8:81412171 A>G maps to NM_001105539.1 P472P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CK-01A-11D-A20W-10 chr11:114113006 C>T maps to NM_001018011.1 N524N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KR-A7K7-01A-11D-A33K-10 chr3:114070354 C>T maps to NM_001164342.1 T190T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7II-01A-11D-A33K-10 chr14:64954579 C>A maps to NM_006977.2 V123V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A26S-01A-11D-A16V-10 chr3:141162186 C>T maps to NM_001080412.2 S319S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A112-01A-11D-A12Z-10 chr12:57397204 C>T maps to NM_014830.2 T499T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25U-01A-11D-A16V-10 chr1:22839459 T>C maps to NM_014870.3 P835P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A112-01A-11D-A12Z-10 chr4:4303970 A>G maps to NM_145291.3 L136L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EK-01A-11D-A20W-10 chr1:154987975 G>A maps to ENST00000417934 E314E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MC-01A-11D-A33Q-10 chr1:33087488 C>A maps to NM_178547.2 E172*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NI-01A-11D-A27I-10 chr12:56515236 C>T maps to NM_032786.1 P297P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr23:64709114 T>C did not map to a codon.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr11:110035708 C>T maps to NM_033390.1 S633S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75E-01A-11D-A32G-10 chr6:149777856 C>A maps to NM_207360.2 E209*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1ED-01A-11D-A152-10 chr16:88666239 T>C maps to ENST00000452588 D348D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3M9-01A-11D-A20W-10 chr19:47569633 C>A maps to NM_015168.1 T1297T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5263-01A-01D-A12Z-10 chr22:41739419 C>T maps to ENST00000351589 G449G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73F-01A-11D-A32G-10 chr7:138761069 C>T maps to ENST00000464606 E675E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A3I1-01A-11D-A22F-10 chr7:138764381 C>A maps to ENST00000464606 V435V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr7:138749664 T>C maps to ENST00000464606 P773P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A459-01A-11D-A25V-10 chr1:52943443 T>A maps to NM_001009881.2 V653V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3M9-01A-11D-A20W-10 chr23:117960057 A>G did not map to a codon.
Sequencing variant TCGA-CC-A5UE-01A-11D-A28X-10 chr23:111698139 A>T did not map to a codon.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr23:111698805 A>G did not map to a codon.
Sequencing variant TCGA-FV-A495-01A-11D-A25V-10 chr18:60225964 T>G maps to NM_017742.4 L485*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K7-A6G5-01A-11D-A30V-10 chr18:60241962 T>G maps to NM_017742.4 P883P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A118-01A-11D-A12Z-10 chr4:25351158 G>T maps to NM_024936.2 E269*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A26S-01A-11D-A16V-10 chr23:77913189 G>T did not map to a codon.
Sequencing variant TCGA-G3-A7M9-01A-23D-A34Z-10 chr9:88967619 C>A maps to NM_024617.3 T165T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A3JL-01A-11D-A20W-10 chr9:37302183 G>A did not map to a codon.
Sequencing variant TCGA-RC-A6M4-01A-11D-A32G-10 chr12:42711633 A>G maps to NM_033114.3 D60D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A5SI-01A-31D-A27I-10 chr7:100004328 C>T maps to NM_017984.3 E386E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A123-01A-11D-A12Z-10 chr3:28566046 A>T maps to NM_001040432.1 A313A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MD-01A-12D-A34Z-10 chr2:207174746 G>A maps to NM_020923.1 W1832*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A5W4-01A-11D-A28X-10 chr9:131483967 C>T maps to ENST00000372667 L162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A118-01A-11D-A12Z-10 chr12:77203531 T>C maps to NM_015336.2 Y146Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39Y-01A-11D-A20W-10 chr8:17067944 T>C maps to NM_016353.4 P302P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EB-01A-11D-A12Z-10 chr3:44968181 C>T maps to NM_016598.2 *328*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25T-01A-11D-A16V-10 chr3:44986739 A>G maps to NM_016598.2 S117S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11D-01A-11D-A12Z-10 chr7:6624764 T>G maps to NM_018106.3 A205A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A118-01A-11D-A12Z-10 chr11:57466173 C>T maps to NM_015457.2 S422S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10W-01A-11D-A12Z-10 chr23:128946712 T>C did not map to a codon.
Sequencing variant TCGA-FV-A23B-01A-11D-A16V-10 chr10:31810467 T>C maps to NM_001174096.1 L736L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73F-01A-11D-A32G-10 chr9:131515867 C>T maps to NM_006336.2 E107E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39V-01A-11D-A20W-10 chr9:74970913 T>C maps to ENST00000437241 R251R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr8:135545137 A>G maps to NM_020863.3 P1018P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5260-01A-01D-A12Z-10 chr12:72057378 T>A maps to NM_144982.4 A4A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A0-01A-11D-A20W-10 chr16:72829896 G>C maps to NM_006885.3 P2228P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr16:72992019 C>T maps to NM_006885.3 K675K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NE-01A-11D-A27I-10 chr8:77618152 C>T maps to NM_024721.4 G610G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A2QR-01A-11D-A20W-10 chr8:77616370 G>A maps to NM_024721.4 Q16Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MB-01A-11D-A20W-10 chr16:75204018 A>G maps to NM_153688.2 S337S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25S-01A-11D-A16V-10 chr15:42720251 T>A maps to NM_022473.1 G1631G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A7M5-01A-11D-A33Q-10 chr15:42729474 T>C maps to NM_022473.1 L1544L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NV-01A-11D-A30V-10 chr19:36831782 C>T maps to NM_020917.2 K315K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25U-01A-11D-A16V-10 chr19:39899107 C>A maps to NM_003407.2 C250*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T1-A6J8-01A-11D-A32G-10 chr14:69256312 G>A maps to NM_004926.2 S318S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73G-01A-22D-A32G-10 chr2:43451847 G>A maps to NM_006887.4 F365F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A7-01A-11D-A22F-10 chr9:115805120 G>A maps to NM_003408.1 R593*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10Z-01A-11D-A12Z-10 chr4:188924569 T>A maps to NM_174900.3 A203A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LG-A6GG-01A-11D-A30V-10 chr4:188924649 C>A maps to NM_174900.3 S230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LG-A6GG-01A-11D-A30V-10 chr11:58347077 G>A maps to NM_053023.4 K108K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EF-01A-11D-A12Z-10 chr8:106331178 C>T maps to NM_012082.3 R4*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr19:3831766 G>C maps to NM_015174.1 S163S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A3I1-01A-11D-A22F-10 chr23:24229377 C>A did not map to a codon.
Sequencing variant TCGA-G3-A25U-01A-11D-A16V-10 chr14:73460000 A>G maps to NM_021260.2 P351P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A112-01A-11D-A12Z-10 chr5:79739076 C>G maps to NM_014733.3 S852*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73G-01A-22D-A32G-10 chr5:79734324 T>C maps to NM_014733.3 N607N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A112-01A-11D-A12Z-10 chr3:15126257 G>A maps to NM_022340.2 I194I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5264-01A-01D-A12Z-10 chr14:68238927 C>T did not map to a codon.
Sequencing variant TCGA-CC-A3MB-01A-11D-A20W-10 chr14:68248208 A>G maps to NM_015346.3 D1470D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IL-01A-11D-A33Q-10 chr14:68273375 T>C maps to NM_015346.3 L301L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A2QR-01A-11D-A20W-10 chr14:68220471 T>C maps to NM_015346.3 G2380G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IG-01A-11D-A33K-10 chr4:2273118 G>A maps to NM_020972.2 D817D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25S-01A-11D-A16V-10 chr4:2275873 A>G maps to NM_020972.2 A707A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr1:52761648 A>G maps to NM_004799.2 A1111A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A496-01A-11D-A25V-10 chr1:52761565 G>T did not map to a codon.
Sequencing variant TCGA-G3-A7M7-01A-12D-A34Z-10 chr16:2880750 G>T maps to NM_145252.2 E73*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QA-A7B7-01A-11D-A32G-10 chr16:2880716 C>T maps to NM_145252.2 G61G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A114-01A-11D-A12Z-10 chr20:62340060 G>T maps to NM_032527.4 L43L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A6UC-01A-21D-A33K-10 chr20:62340048 G>A maps to NM_032527.4 L39L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3M9-01A-11D-A20W-10 chr8:124266620 T>C maps to NM_007222.3 S522S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A116-01A-11D-A12Z-10 chr8:124267556 T>C maps to NM_007222.3 K210K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10Y-01A-11D-A12Z-10 chr8:123965264 C>A maps to NM_014943.3 S505S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A7-01A-11D-A22F-10 chr8:123963935 G>A maps to NM_014943.3 E62E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A7SF-01A-11D-A34Z-10 chr8:123965870 C>T maps to NM_014943.3 A707A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A495-01A-11D-A25V-10 chr3:147128636 C>T maps to NM_003412.3 F246F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr23:136649846 C>A did not map to a codon.
Sequencing variant TCGA-G3-A25Y-01A-11D-A16V-10 chr23:136649385 T>C did not map to a codon.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr19:57646377 C>A maps to NM_052882.1 G443*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A495-01A-11D-A25V-10 chr8:40532340 C>T maps to NM_024645.2 W153*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75H-01A-11D-A32G-10 chr1:40735690 G>T maps to NM_005857.3 V173V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A6M6-01A-11D-A32G-10 chr1:35563032 T>A maps to NM_024772.3 I95I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A26S-01A-11D-A16V-10 chr13:20567271 G>A maps to NM_001190965.1 G20G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5259-01A-31D-A20W-10 chr23:70467742 C>T did not map to a codon.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr23:70465849 A>G did not map to a codon.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr1:35846859 A>G maps to NM_005095.2 K394K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LG-A6GG-01A-11D-A30V-10 chr1:35884068 A>G maps to NM_005095.2 K1445K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A3JL-01A-11D-A20W-10 chr13:20411885 T>C maps to NM_001142684.1 T316T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A2QQ-01A-11D-A22F-10 chr1:42914267 G>T maps to NM_032257.4 Y98*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10Q-01A-11D-A12Z-10 chr20:45920578 T>C maps to ENST00000471951 E207E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr12:133727624 C>G maps to NM_015394.4 T15T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EF-01A-11D-A12Z-10 chr19:21910791 C>G did not map to a codon.
Sequencing variant TCGA-DD-A1EH-01A-11D-A12Z-10 chr7:64167563 T>C maps to NM_016220.3 H294H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A6M6-01A-11D-A32G-10 chr7:64166838 G>T maps to NM_016220.3 E53*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25S-01A-11D-A16V-10 chr5:43161947 T>C maps to ENST00000509156 T323T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr19:58945139 A>G maps to NM_003433.3 T557T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25V-01A-11D-A16V-10 chr20:18296814 T>C maps to ENST00000401790 C442C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3M9-01A-11D-A20W-10 chr19:19822649 A>G maps to NM_021030.2 C480C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5259-01A-31D-A20W-10 chr2:219508733 G>T maps to NM_001105537.1 A835A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr11:9499988 A>T maps to NM_003442.5 T142T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A114-01A-11D-A12Z-10 chr19:58216278 A>T maps to NM_001085384.1 A34A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-O8-A75V-01A-11D-A32G-10 chr8:146157909 G>T maps to NM_006958.2 S88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A26S-01A-11D-A16V-10 chr19:53572754 A>G maps to NM_001102603.1 N344N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A495-01A-11D-A25V-10 chr19:52090483 T>A maps to NM_007147.2 I300I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NI-01A-11D-A27I-10 chr19:44980915 T>A maps to NM_013256.3 V594V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IL-01A-11D-A33Q-10 chr6:27419759 T>C maps to NM_007149.2 Q526Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A8-01A-11D-A22F-10 chr23:152085855 C>T did not map to a codon.
Sequencing variant TCGA-EP-A2KC-01A-11D-A20W-10 chr23:152106688 C>T did not map to a codon.
Sequencing variant TCGA-FV-A23B-01A-11D-A16V-10 chr23:152101461 G>A did not map to a codon.
Sequencing variant TCGA-RC-A6M4-01A-11D-A32G-10 chr23:152110313 C>A did not map to a codon.
Sequencing variant TCGA-DD-A1EF-01A-11D-A12Z-10 chr9:104171114 G>A maps to NM_003452.2 R355R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A7SK-01A-11D-A34Z-10 chr11:3381364 C>T maps to NM_001130520.1 E291E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IL-01A-11D-A33Q-10 chr11:123600473 C>A maps to NM_003455.2 V154V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A114-01A-11D-A12Z-10 chr11:123600352 C>A maps to NM_003455.2 E195*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A216-01A-11D-A152-10 chr19:22171609 C>T maps to NM_007153.3 E35E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A5UC-01A-11D-A28X-10 chr19:22156011 G>T maps to NM_007153.3 P608P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr19:22156026 A>G maps to NM_007153.3 H603H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CJ-01A-11D-A20W-10 chr19:22155939 A>G maps to NM_007153.3 A632A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A459-01A-11D-A25V-10 chr19:58152705 T>G maps to NM_006385.3 P297P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A7SK-01A-11D-A34Z-10 chr19:58152693 T>C maps to NM_006385.3 S293S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4ND-01A-11D-A25V-10 chr20:52198138 G>C maps to NM_006526.2 T409T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5262-01A-01D-A12Z-10 chr19:44471486 A>C maps to NM_013359.2 L611L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr19:44470226 A>T maps to NM_013359.2 S191S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr19:44570977 A>T maps to NM_013361.4 K333*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr19:44610720 A>T maps to NM_013398.2 A136A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr19:44635249 C>A maps to NM_013362.2 S161S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A1HT-01A-11D-A12Z-10 chr19:44934679 A>G maps to NM_014518.2 D92D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5263-01A-01D-A12Z-10 chr19:44514562 C>G maps to NM_006300.3 S124S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A123-01A-11D-A12Z-10 chr19:44661605 C>G maps to NM_006630.2 T479T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A1-01A-11D-A20W-10 chr18:32920511 C>A maps to NM_006965.2 E35*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HP-A5N0-01A-11D-A28X-10 chr8:146107238 C>T maps to NM_021061.3 E448E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A23B-01A-11D-A16V-10 chr19:58453497 A>G maps to NM_005773.2 R226R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A7S9-01A-11D-A33Q-10 chr19:22271463 T>C maps to NM_033468.2 T304T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5259-01A-31D-A20W-10 chr19:37005747 T>A maps to NM_001166038.1 T131T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5263-01A-01D-A12Z-10 chr19:57723566 G>T maps to NM_003417.4 E368*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11D-01A-11D-A12Z-10 chr16:31926034 T>G maps to NM_003414.4 S155S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EC-01A-21D-A12Z-10 chr16:31925947 T>C maps to NM_003414.4 N126N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A7M9-01A-23D-A34Z-10 chr19:53303882 A>G maps to NM_006969.3 H405H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MD-01A-12D-A34Z-10 chr19:53304473 T>A maps to NM_006969.3 V208V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73G-01A-22D-A32G-10 chr22:22869867 A>G maps to NM_080740.3 D29D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11D-01A-11D-A12Z-10 chr22:22842865 A>G maps to NM_080764.2 S286S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A0-01A-11D-A20W-10 chr22:22842943 T>A maps to NM_080764.2 A260A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A4ZP-01A-12D-A25V-10 chr22:22843681 C>T maps to NM_080764.2 Q14Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A9-01A-11D-A25V-10 chr23:129349771 T>A did not map to a codon.
Sequencing variant TCGA-PD-A5DF-01A-11D-A27I-10 chr23:129349843 A>T did not map to a codon.
Sequencing variant TCGA-DD-A1EF-01A-11D-A12Z-10 chr19:44890915 T>C maps to NM_152354.3 S497S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr17:16470685 T>C maps to NM_020653.2 A120A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A8-01A-11D-A22F-10 chr6:87967390 G>A maps to NM_015021.1 G1348G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PD-A5DF-01A-11D-A27I-10 chr7:99662524 G>A maps to NM_017715.2 H94H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11B-01A-11D-A16Z-10 chr19:35174078 A>G maps to ENST00000221282 P51P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A82E-01A-11D-A34Z-10 chr6:28963998 T>G maps to NM_001010877.2 S260S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KR-A7K8-01A-11D-A33K-10 chr6:28963559 T>G maps to NM_001010877.2 R407R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5262-01A-01D-A12Z-10 chr6:43306776 T>A maps to NM_014345.2 L1653L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A4ZQ-01A-11D-A25V-10 chr6:43322733 C>A maps to NM_014345.2 G780*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73E-01A-12D-A32G-10 chr19:53384283 A>C maps to NM_207333.2 A365A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr19:58982591 G>T maps to NM_014347.2 E245*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10Z-01A-11D-A12Z-10 chr1:90486426 A>G maps to NM_182976.2 L417L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A459-01A-11D-A25V-10 chr1:90473062 A>T maps to NM_182976.2 G123G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr4:142145638 A>T did not map to a codon.
Sequencing variant TCGA-FV-A23B-01A-11D-A16V-10 chr19:14817511 T>A maps to NM_032433.2 A146A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr19:14828535 T>C maps to NM_032433.2 D297D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr20:45130945 T>A maps to NM_018102.3 T344T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A496-01A-11D-A25V-10 chr20:44588919 G>A maps to NM_022095.3 F649F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11D-01A-11D-A12Z-10 chr10:38343321 C>T maps to NM_006954.1 H90H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KR-A7K8-01A-11D-A33K-10 chr10:38343570 T>C maps to NM_006954.1 C173C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39Z-01A-11D-A20W-10 chr20:2465246 A>G maps to NM_024325.4 C120C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr19:53644358 A>G maps to NM_001172674.1 C575C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A7S9-01A-11D-A33Q-10 chr19:52468328 C>T maps to ENST00000391795 G533G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K7-A6G5-01A-11D-A30V-10 chr1:33760791 C>G maps to NM_152493.2 P344P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A1-01A-11D-A20W-10 chr8:28210088 C>T did not map to a codon.
Sequencing variant TCGA-G3-A3CK-01A-11D-A20W-10 chr18:32826112 C>T maps to NM_001135178.2 Q482*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-4073-01B-02D-A12Z-10 chr11:46726584 C>T maps to NM_024741.2 A445A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11D-01A-11D-A12Z-10 chr11:46726464 G>T maps to NM_024741.2 G405G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A459-01A-11D-A25V-10 chr23:47307357 T>C did not map to a codon.
Sequencing variant TCGA-FV-A3R2-01A-11D-A22F-10 chr14:74363142 G>A maps to NM_021188.1 P98P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MD-01A-12D-A34Z-10 chr19:53612424 C>T maps to NM_001164309.1 R291R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A23B-01A-11D-A16V-10 chr19:58004284 C>T maps to NM_001098491.1 L121L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MR-A520-01A-11D-A25V-10 chr16:49671019 C>T maps to NM_015069.2 L681L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr16:49764841 G>A maps to NM_015069.2 S39S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10Z-01A-11D-A12Z-10 chr19:21720691 A>T maps to NM_001001415.2 K613*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr19:21712458 G>T did not map to a codon.
Sequencing variant TCGA-EP-A26S-01A-11D-A16V-10 chr19:21990783 T>C maps to NM_003423.2 K685K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A7M6-01A-11D-A33Q-10 chr19:22000752 G>A maps to NM_003423.2 L56L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NS-01A-11D-A30V-10 chr19:21216303 G>T maps to NM_025189.3 E47*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr19:21239854 C>T maps to NM_025189.3 T247T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CK-01A-11D-A20W-10 chr19:52538391 A>T maps to NM_014650.2 S180S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10U-01A-11D-A12Z-10 chr1:23689652 T>C maps to NM_001077195.1 Q74Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A7SF-01A-11D-A34Z-10 chr10:31134174 C>T maps to NM_182755.2 Q734Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EA-01A-11D-A12Z-10 chr19:11888442 G>A maps to NM_152355.2 E7E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A9-01A-11D-A25V-10 chr19:11888523 G>A maps to NM_152355.2 Q34Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A118-01A-11D-A12Z-10 chr23:134494229 G>A did not map to a codon.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr6:56993603 A>T maps to NM_001031623.2 A130A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NN-01A-11D-A28X-10 chr19:37130124 T>A maps to NM_153257.2 I374I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5264-01A-01D-A12Z-10 chr9:109687218 T>G maps to NM_021224.4 S342S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A7XP-01A-11D-A34Z-10 chr9:109773121 G>A maps to NM_021224.4 K2444K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25T-01A-11D-A16V-10 chr9:109734382 T>C maps to NM_021224.4 P2175P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-O8-A75V-01A-11D-A32G-10 chr7:149462852 G>A maps to NM_207336.1 C246C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25W-01A-11D-A16V-10 chr19:50550099 T>C maps to NM_015428.1 N800N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A216-01A-11D-A152-10 chr19:12721446 C>T maps to NM_020714.2 E16E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3M9-01A-11D-A20W-10 chr1:247464446 C>A maps to NM_032752.1 E380*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr1:247492169 T>C did not map to a codon.
Sequencing variant TCGA-G3-A25T-01A-11D-A16V-10 chr10:77159616 C>T maps to NM_032772.4 T277T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10Z-01A-11D-A12Z-10 chr9:99522163 T>C maps to NM_014930.1 K316K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75E-01A-11D-A32G-10 chr9:99522337 T>C maps to NM_014930.1 K258K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr10:135123792 G>A did not map to a codon.
Sequencing variant TCGA-DD-A1EL-01A-11D-A152-10 chr20:62592676 C>A maps to NM_020713.1 L804L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr20:62594497 G>T maps to NM_020713.1 R640R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NS-01A-11D-A30V-10 chr8:146033059 C>T maps to NM_213605.2 R253R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EF-01A-11D-A12Z-10 chr18:14105689 C>T maps to NM_145287.3 Q283Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EL-01A-11D-A152-10 chr18:22775196 A>G maps to NM_015461.2 Y1195Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr18:22806399 T>C maps to NM_015461.2 E494E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NH-01A-11D-A27I-10 chr19:37045632 A>G maps to NM_001145649.1 S58S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25W-01A-11D-A16V-10 chr18:56646393 C>A maps to NM_018181.4 A1086A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A5UE-01A-11D-A28X-10 chr19:52941616 G>T maps to NM_001143939.1 E315*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A114-01A-11D-A12Z-10 chr19:30935047 C>T maps to NM_014717.1 R193R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11D-01A-11D-A12Z-10 chr19:30934909 G>C maps to NM_014717.1 L147L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25Y-01A-11D-A16V-10 chr19:31039498 G>T maps to NM_014717.1 S991S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7ME-01A-11D-A33K-10 chr19:31039816 C>T maps to NM_014717.1 T1097T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K7-A5RG-01A-11D-A28X-10 chr19:40520370 A>T maps to NM_178544.3 S398S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MB-01A-11D-A20W-10 chr19:58048845 A>G maps to ENST00000376233 K158K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A7PX-01A-51D-A34Z-10 chr19:58067686 G>C maps to NM_001039654.1 T13T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25T-01A-11D-A16V-10 chr19:2827727 C>T maps to NM_001102651.1 N80N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NI-A4U2-01A-11D-A28X-10 chr19:8932717 G>A maps to NM_144693.1 G27G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A115-01A-11D-A12Z-10 chr19:9580386 C>T did not map to a codon.
Sequencing variant TCGA-G3-A3CK-01A-11D-A20W-10 chr19:9578275 T>C maps to NM_152476.2 G449G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A8-01A-11D-A22F-10 chr19:12637748 T>C maps to NM_144976.3 G391G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5264-01A-01D-A12Z-10 chr19:36673861 C>A maps to ENST00000355114 E357*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5259-01A-31D-A20W-10 chr19:37210907 A>T maps to ENST00000423498 K427*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10T-01A-11D-A12Z-10 chr8:125987938 G>A maps to NM_152412.2 E19E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11A-01A-11D-A12Z-10 chr19:53014086 T>A maps to NM_001099694.1 P151P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25W-01A-11D-A16V-10 chr19:53015352 T>A maps to NM_001099694.1 G573G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A7M9-01A-23D-A34Z-10 chr19:56896170 C>T maps to NM_144690.1 G205G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr19:37644044 T>G maps to ENST00000356958 T252T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr19:37677106 C>T maps to NM_152279.3 G444G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73F-01A-11D-A32G-10 chr19:38189777 C>T maps to NM_032689.4 E418E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A9-01A-11D-A25V-10 chr5:123983010 A>G maps to NM_020747.2 S1022S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K7-A6G5-01A-11D-A30V-10 chr5:123979215 G>A maps to NM_020747.2 S1428S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr5:123983649 T>C maps to NM_020747.2 K809K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LG-A6GG-01A-11D-A30V-10 chr15:64967590 T>G maps to NM_015042.1 S846S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr19:52856963 C>T maps to NM_001161425.1 I31I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr19:53208495 A>G maps to NM_001161500.1 S604S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A3R2-01A-11D-A22F-10 chr9:116731401 C>T maps to ENST00000374126 D13D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25Y-01A-11D-A16V-10 chr3:40557546 C>A maps to NM_175888.2 T154T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A5UD-01A-11D-A28X-10 chr16:30793272 C>T maps to NM_001080417.1 Q792Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A3RK-01A-11D-A22F-10 chr16:30793869 T>C maps to NM_001080417.1 G593G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A2QR-01A-11D-A20W-10 chr16:30793662 G>A maps to NM_001080417.1 Y662Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K7-A5RF-01A-11D-A28X-10 chr16:30794702 T>A maps to NM_001080417.1 K316*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MA-01A-11D-A20W-10 chr23:47919902 T>C did not map to a codon.
Sequencing variant TCGA-DD-A4NR-01A-11D-A30V-10 chr23:47919573 T>A did not map to a codon.
Sequencing variant TCGA-DD-A3A8-01A-11D-A22F-10 chr2:71591323 A>G maps to NM_014497.3 P553P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A116-01A-11D-A12Z-10 chr1:91405647 C>T maps to NM_201269.1 E421E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr1:91403138 T>A maps to NM_201269.1 T1197T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr1:91405809 T>A maps to NM_201269.1 P367P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7II-01A-11D-A33K-10 chr23:22291220 G>T did not map to a codon.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr16:31088244 C>T maps to NM_014699.3 P200P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr1:182026596 G>T maps to NM_001009992.1 S183S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr7:99169919 G>T maps to NM_001083956.1 S98S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NI-01A-11D-A27I-10 chr9:40773312 C>A maps to NM_033160.5 G654G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A3RK-01A-11D-A22F-10 chr19:53669325 A>G maps to NM_024733.3 N139N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KC-01A-11D-A20W-10 chr19:56952617 G>A maps to ENST00000342634 P710P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A6M6-01A-11D-A32G-10 chr1:247201662 C>T maps to NM_033213.3 Q86Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr19:23836431 G>T maps to NM_138330.2 R435R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A7M7-01A-12D-A34Z-10 chr19:23844914 C>G did not map to a codon.
Sequencing variant TCGA-EP-A3RK-01A-11D-A22F-10 chr19:53747006 A>T maps to NM_182609.2 P53P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A7SB-01A-21D-A34Z-10 chr19:53740389 G>C maps to NM_182609.2 L530L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EF-01A-11D-A12Z-10 chr19:23927976 T>A maps to NM_138286.2 G125G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A2QR-01A-11D-A20W-10 chr19:23938329 C>A maps to NM_138286.2 V9V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr19:23926974 A>G maps to NM_138286.2 F459F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11C-01A-11D-A12Z-10 chr19:20117275 T>C maps to NM_033196.2 E345E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11B-01A-11D-A16Z-10 chr1:26694189 A>G maps to ENST00000436292 S71S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RG-A7D4-01A-12D-A33Q-10 chr1:26694243 A>G maps to ENST00000436292 H53H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A116-01A-11D-A12Z-10 chr1:151260006 C>T maps to NM_020832.1 L414L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A6UC-01A-21D-A33K-10 chr8:146067785 C>T maps to ENST00000446747 Q442*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10U-01A-11D-A12Z-10 chr19:12059505 A>T maps to NM_144566.1 K223*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr19:21477080 A>T maps to NM_021269.2 C229*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr19:57132816 A>T maps to NM_021216.4 A54A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A5SJ-01A-11D-A27I-10 chr23:84526389 T>C did not map to a codon.
Sequencing variant TCGA-ED-A4XI-01A-11D-A25V-10 chr7:57528610 T>A maps to NM_001159279.1 C148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A6UC-01A-21D-A33K-10 chr7:57529338 T>A maps to NM_001159279.1 L391*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75C-01A-11D-A32G-10 chr4:59394 C>T maps to NM_182524.2 Q26*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr4:436176 T>C maps to NM_133474.2 G693G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25W-01A-11D-A16V-10 chr23:134426309 T>G did not map to a codon.
Sequencing variant TCGA-BC-A5W4-01A-11D-A28X-10 chr6:35262246 C>T maps to NM_003427.3 T503T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr6:35260757 G>T maps to NM_003427.3 A422A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39Y-01A-11D-A20W-10 chr19:53959188 T>C maps to NM_001008401.3 R476R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39V-01A-11D-A20W-10 chr19:2934206 G>A maps to NM_021217.2 S306S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr19:2933801 A>G maps to NM_021217.2 C441C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MA-01A-11D-A20W-10 chr7:149129991 G>A maps to ENST00000440594 D458D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A7-01A-11D-A22F-10 chr7:148767723 G>T maps to NM_152411.3 R714R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr9:130206629 A>G maps to NM_007135.2 G217G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A3R3-01A-11D-A22F-10 chr19:38028240 C>T maps to NM_001013659.2 H227H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A123-01A-11D-A12Z-10 chr7:127013574 G>T maps to NM_176814.3 V605V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K7-A6G5-01A-11D-A30V-10 chr2:185800548 T>C maps to NM_194250.1 V142V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A118-01A-11D-A12Z-10 chr7:88964868 C>A maps to NM_181646.2 S858*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KC-01A-11D-A20W-10 chr7:88964536 C>T maps to NM_181646.2 H747H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25U-01A-11D-A16V-10 chr7:88963114 A>G maps to NM_181646.2 T273T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr7:88965400 A>T maps to NM_181646.2 T1035T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39Z-01A-11D-A20W-10 chr23:47775709 T>C did not map to a codon.
Sequencing variant TCGA-DD-A4NO-01A-11D-A28X-10 chr4:146695656 C>G did not map to a codon.
Sequencing variant TCGA-DD-A4NB-01A-12D-A25V-10 chr19:53117499 T>C maps to NM_018300.3 L106L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IG-01A-11D-A33K-10 chr17:33288614 G>T maps to NM_052857.3 P10P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5264-01A-01D-A12Z-10 chr20:57766857 A>C maps to NM_178457.1 R262R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25S-01A-11D-A16V-10 chr20:57767022 C>A maps to NM_178457.1 R317R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75C-01A-11D-A32G-10 chr20:57766653 C>T maps to NM_178457.1 Q194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MF-01A-11D-A33K-10 chr20:57768443 A>G maps to NM_178457.1 R790R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A5SM-01A-12D-A28X-10 chr19:57175243 C>T maps to NM_001005850.1 T463T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BW-A5NQ-01A-11D-A27I-10 chr14:102792470 C>T maps to NM_018335.3 A146A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr14:102805185 C>A maps to NM_018335.3 R565R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A5UD-01A-11D-A28X-10 chr19:52570323 T>A maps to NM_001136499.1 R271*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39Y-01A-11D-A20W-10 chr19:52569541 A>G maps to NM_001136499.1 H531H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr19:52569526 G>T maps to NM_001136499.1 T536T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11A-01A-11D-A12Z-10 chr19:53854647 G>A maps to NM_138374.1 A240A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75G-01A-11D-A32G-10 chr19:53848859 G>A maps to NM_138374.1 E39E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75H-01A-11D-A32G-10 chr19:53856523 A>T maps to NM_138374.1 K866*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A69H-01A-11D-A30V-10 chr19:21132331 G>T maps to NM_003429.4 G338*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MB-01A-11D-A20W-10 chr3:32030645 T>C maps to NM_001137674.1 T25T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A4-01A-11D-A22F-10 chr7:149557718 C>A maps to NM_001099220.1 C490*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A6M6-01A-11D-A32G-10 chr7:149558297 C>A maps to NM_001099220.1 I683I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr19:20229868 T>C maps to NM_007138.1 I502I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RG-A7D4-01A-12D-A33Q-10 chr19:23545411 T>C maps to NM_003430.2 R123R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr7:64864691 T>C maps to NM_152626.2 H555H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr19:20026108 T>C maps to NM_031218.3 D8D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IG-01A-11D-A33K-10 chr19:22941606 G>A maps to ENST00000397104 P277P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NI-01A-11D-A27I-10 chr19:22940609 C>A maps to ENST00000397104 G610*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25Y-01A-11D-A16V-10 chr17:34848720 C>T maps to NM_004773.2 T61T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr19:5455750 C>T maps to NM_181710.3 V83V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A112-01A-11D-A12Z-10 chr1:238053179 A>G maps to NM_021186.3 P129P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A459-01A-11D-A25V-10 chr7:50129225 T>A maps to NM_007009.2 P69P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A6M3-01A-11D-A32G-10 chr7:49977180 T>A maps to NM_007009.2 G333G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IL-01A-11D-A33Q-10 chr19:58597610 G>A maps to NM_001145542.1 D312D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr1:33955140 T>C maps to NM_145238.3 H235H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A26S-01A-11D-A16V-10 chr19:56735065 T>C maps to NM_024303.1 P174P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A7M9-01A-23D-A34Z-10 chr19:56704397 T>A maps to NM_001080456.2 S8S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A7M7-01A-12D-A34Z-10 chr2:187713758 G>C maps to NM_182521.2 L33L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A5SK-01A-11D-A27I-10 chr20:44506969 C>G maps to NM_080752.3 L591L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NE-01A-11D-A27I-10 chr19:13936367 C>T maps to NM_023072.2 D623D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EB-01A-11D-A12Z-10 chr6:116987856 C>A maps to NM_145062.2 E167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr6:116973311 T>A maps to NM_145062.2 T335T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EF-01A-11D-A12Z-10 chr10:58118597 C>T maps to NM_032997.2 Q197Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A3R3-01A-11D-A22F-10 chr23:57936065 G>A did not map to a codon.
Sequencing variant TCGA-MI-A75H-01A-11D-A32G-10 chr23:57936472 T>G did not map to a codon.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr17:3937450 A>G maps to NM_015113.3 L2148L. Only missense variants will be evaluated by CHASM.
