6841 NP_001070868 S653L not found in SNVbox database
7311 NP_109597 M136K not found in SNVbox database
345 NP_705833 Y31N not found in SNVbox database
530 NP_001070868 I562M not found in SNVbox database
839 NP_705833 S145R not found in SNVbox database
973 NP_001070868 D482G not found in SNVbox database
1077 NP_705833 S298N not found in SNVbox database
1094 NP_705833 K971N not found in SNVbox database
1130 NP_705833 V101I not found in SNVbox database
2888 NP_705833 S741P not found in SNVbox database
3824 NP_705833 H355Q not found in SNVbox database
3862 NP_705833 Y778H not found in SNVbox database
4965 NP_705833 C438R not found in SNVbox database
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-DD-A4NF-01A-11D-A27I-10 chr16:7568313 C>T maps to NM_145891.2 L85L. Only missense variants will be evaluated by CHASM.
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-DD-AAE7-01A-11D-A40R-10 chr12:9262918 T>C maps to NM_000014.4 V165V. 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-AACE-01A-11D-A40R-10 chr3:137849888 G>A maps to NM_016161.2 S70S. 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-A119-01A-11D-A12Z-10 chr3:151545788 T>C maps to NM_001086.2 D343D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39Y-01A-11D-A20W-10 chr3:151542579 A>G maps to NM_001086.2 G187G. 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-G3-AAUZ-01A-11D-A382-10 chr1:12785872 A>G maps to NM_001103170.1 G321G. 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-DD-A119-01A-11D-A12Z-10 chr2:69741752 C>T maps to NM_014911.3 Q542Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CG-01A-11D-A20W-10 chr2:69741743 T>C maps to NM_014911.3 Q545Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CG-01A-11D-A20W-10 chr2:69741752 C>T maps to NM_014911.3 Q542Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACP-01A-11D-A40R-10 chr16:70304224 C>A maps to ENST00000418685 L238L. 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-K7-AAU7-01A-11D-A382-10 chr16:70293020 C>T maps to ENST00000418685 V626V. 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-GJ-A9DB-01A-11D-A36X-10 chr6:44272420 C>T maps to NM_020745.2 Q571Q. 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-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-2Y-A9H1-01A-11D-A382-10 chr17:79093267 A>C maps to NM_001080395.2 A1332A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A8HV-01A-11D-A35Z-10 chr17:79096445 C>T maps to NM_001080395.2 A430A. 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-DD-AACI-01A-11D-A40R-10 chr17:79095854 T>A maps to NM_001080395.2 A627A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A0-01A-11D-A20W-10 chr9:107581924 A>G maps to NM_005502.3 A1061A. 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-G3-A3CG-01A-11D-A20W-10 chr17:67148260 T>C maps to NM_080282.3 K1440K. 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-DD-AACF-01A-11D-A40R-10 chr2:215854155 C>G maps to NM_173076.2 P1242P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAE3-01A-11D-A40R-10 chr2:215901701 C>G maps to NM_173076.2 L320L. 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-G3-AAV1-01A-11D-A382-10 chr2:215848387 G>A maps to NM_173076.2 L1455L. Only missense variants will be evaluated by CHASM.
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-A9FW-01A-11D-A36X-10 chr7:48428793 C>T maps to NM_152701.3 N3877N. Only missense variants will be evaluated by CHASM.
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-DD-AACU-01A-11D-A40R-10 chr7:48315127 C>T maps to NM_152701.3 I1955I. Only missense variants will be evaluated by CHASM.
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-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-G3-AAV4-01A-11D-A382-10 chr7:48315019 A>G maps to NM_152701.3 K1919K. 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-DD-AAEH-01A-11D-A40R-10 chr9:139906759 C>T maps to ENST00000355090 L1782L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr9:139910923 C>A did not map to a codon.
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-G3-AAV6-01A-21D-A36X-10 chr16:2342160 G>A maps to NM_001089.2 T831T. 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-DD-AACX-01A-11D-A40R-10 chr1:94466453 C>G maps to NM_000350.2 R2139R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAD5-01A-11D-A40R-10 chr1:94522309 G>A maps to NM_000350.2 A743A. 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-DD-A39X-01A-11D-A20W-10 chr17:67096940 A>G maps to NM_080284.2 P1003P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39Z-01A-11D-A20W-10 chr17:67119417 T>C maps to NM_080284.2 E466E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A0-01A-11D-A20W-10 chr17:67092458 G>A maps to NM_080284.2 V1110V. 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-DD-A1EE-01A-11D-A12Z-10 chr19:1051262 A>T maps to NM_019112.3 K932*. Only missense variants will be evaluated by CHASM.
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-DD-AAW1-01A-11D-A40P-10 chr17:66865907 C>T maps to NM_007168.2 L1508L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACE-01A-11D-A40R-10 chr17:66978769 C>T maps to NM_080283.3 L1551L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAD6-01A-11D-A40R-10 chr17:67013795 C>G did not map to a codon.
Sequencing variant TCGA-WQ-A9G7-01A-11D-A36X-10 chr17:67029867 G>A maps to NM_080283.3 P425P. 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-WQ-A9G7-01A-11D-A36X-10 chr1:229666150 C>A maps to NM_012089.2 G480G. 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-DD-A39Y-01A-11D-A20W-10 chr7:20698160 T>C maps to NM_001163941.1 A523A. 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-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-2Y-A9GY-01A-11D-A382-10 chr23:74295381 T>C did not map to a codon.
Sequencing variant TCGA-DD-A39X-01A-11D-A20W-10 chr23:74295253 A>G did not map to a codon.
Sequencing variant TCGA-DD-A39Y-01A-11D-A20W-10 chr7:150739103 A>G maps to ENST00000297504 E575E. Only missense variants will be evaluated by CHASM.
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-ED-A8O5-01A-11D-A35Z-10 chr6:43417801 A>C maps to NM_033450.2 G1456G. 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-DD-AAC8-01A-11D-A40R-10 chr16:48158121 A>T did not map to a codon.
Sequencing variant TCGA-G3-A3CG-01A-11D-A20W-10 chr16:48120708 C>T maps to NM_033226.2 E1219E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr17:48750985 G>T maps to NM_003786.3 E856*. 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-DD-AAE0-01A-11D-A40R-10 chr3:183667773 C>A maps to NM_005688.2 L1028L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAC9-01A-11D-A40R-10 chr11:17496562 G>A maps to ENST00000302539 Q54*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADF-01A-11D-A40R-10 chr11:17464327 C>T maps to ENST00000302539 E523E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A0-01A-11D-A20W-10 chr12:21960278 C>T did not map to a codon.
Sequencing variant TCGA-BC-A10R-01A-11D-A12Z-10 chr23:153001603 G>C did not map to a codon.
Sequencing variant TCGA-DD-A1EG-01A-11D-A20W-10 chr23:153009115 A>G did not map to a codon.
Sequencing variant TCGA-DD-AAE9-01A-11D-A40R-10 chr23:153005586 C>G did not map to a codon.
Sequencing variant TCGA-DD-AAE9-01A-11D-A40R-10 chr12:40012906 A>G maps to NM_005164.3 L171L. Only missense variants will be evaluated by CHASM.
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-ES-A2HS-01A-11D-A183-10 chr11:119029041 G>T maps to NM_001142505.1 T389T. 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-DD-AACM-01A-11D-A40R-10 chr3:111705758 A>G did not map to a codon.
Sequencing variant TCGA-DD-AACT-01A-11D-A40R-10 chr15:89659581 C>T maps to NM_152924.4 P8P. 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-AAED-01A-12D-A40R-10 chr18:19263880 C>T maps to NM_138340.4 L185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BD-A3EP-01A-11D-A22F-10 chr14:23072500 C>T maps to NM_022060.2 R107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADB-01A-11D-A40R-10 chr3:43743956 G>A maps to NM_016006.4 E128E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr2:204281667 A>G maps to ENST00000295851 E410E. 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-2Y-A9HB-01A-11D-A38X-10 chr9:133759734 G>C maps to NM_007313.2 L705L. 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-BC-A3KG-01A-11D-A20W-10 chr10:116201492 A>G maps to ENST00000277895 N730N. 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-ES-A2HS-01A-11D-A183-10 chr7:150553812 T>C maps to ENST00000416793 F85F. 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-WQ-A9G7-01A-11D-A36X-10 chr17:909328 G>A maps to NM_021962.2 T857T. 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-2Y-A9GU-01A-11D-A382-10 chr3:38178098 C>T maps to NM_001607.3 L83L. 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-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-CC-A8HT-01A-11D-A35Z-10 chr12:109616909 A>G maps to NM_001093.3 P485P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADB-01A-11D-A40R-10 chr12:109690863 C>T maps to NM_001093.3 G1982G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A2QR-01A-11D-A20W-10 chr12:109613959 A>G maps to NM_001093.3 A443A. 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-DD-AACQ-01A-11D-A40R-10 chr11:134127070 G>T maps to NM_014384.2 L100L. 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-DD-AACU-01A-11D-A40R-10 chr3:128621397 G>C maps to NM_014049.4 V295V. 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-G3-A3CG-01A-11D-A20W-10 chr1:76198377 C>T maps to ENST00000370834 A56A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WQ-A9G7-01A-11D-A36X-10 chr10:124812641 C>T maps to NM_001609.3 Y398Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39Y-01A-11D-A20W-10 chr17:7123921 G>A did not map to a codon.
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-EP-A2KB-01A-11D-A183-10 chr15:89398362 C>T maps to NM_013227.3 P849P. 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-EP-A2KA-01A-11D-A183-10 chr1:1231248 T>C maps to NM_030649.2 A524A. 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-ES-A2HT-01A-12D-A183-10 chr6:160197212 T>C maps to NM_005891.2 P222P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr6:160197290 A>G maps to NM_005891.2 P248P. 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-AAD8-01A-11D-A40R-10 chr17:43214133 G>A maps to NM_001135706.1 V95V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A5KG-01A-11D-A27I-10 chr17:32483119 C>T maps to NM_001094.4 K144K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NQ-01A-21D-A28X-10 chr12:50473751 C>T maps to NM_020039.2 G373G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr12:50474965 T>A did not map to a codon.
Sequencing variant TCGA-BC-4073-01B-02D-A12Z-10 chr2:220379822 C>A maps to NM_018674.4 S253*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZS-A9CF-01A-11D-A382-10 chr2:220396804 G>A maps to NM_018674.4 G397G. 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-2Y-A9H8-01A-11D-A38X-10 chr17:61568651 G>A maps to NM_000789.3 W941*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr17:61560880 A>G maps to NM_000789.3 G516G. 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-DD-AAW2-01A-11D-A40P-10 chr23:15609833 A>G did not map to a codon.
Sequencing variant TCGA-DD-A1EG-01A-11D-A20W-10 chr19:6307246 A>G maps to NM_133492.2 A181A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5C-A9VG-01A-11D-A36X-10 chr7:100490027 G>A maps to NM_000665.3 R494*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACT-01A-11D-A40R-10 chr7:100490379 G>A maps to NM_000665.3 G376G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WX-AA44-01A-11D-A38X-10 chr7:100488790 G>A maps to NM_000665.3 T574T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BD-A3EP-01A-11D-A22F-10 chr14:23548776 T>A maps to NM_014977.3 S647S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BD-A3EP-01A-11D-A22F-10 chr14:23549901 T>C maps to NM_014977.3 E272E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr14:23540643 C>A maps to NM_001164816.1 R36R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADB-01A-11D-A40R-10 chr17:40049359 C>A maps to ENST00000401700 V553V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-AA0U-01A-11D-A382-10 chr17:40030077 G>A maps to ENST00000401700 L920L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr9:32450102 C>G maps to NM_002197.2 A888A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39Y-01A-11D-A20W-10 chr9:32425906 T>G maps to NM_002197.2 T420T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADJ-01A-11D-A40R-10 chr9:32430519 A>T maps to NM_002197.2 I558I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MA-01A-11D-A20W-10 chr23:23726022 T>C did not map to a codon.
Sequencing variant TCGA-UB-A7MD-01A-12D-A34Z-10 chr23:23731289 T>C did not map to a codon.
Sequencing variant TCGA-DD-AAC9-01A-11D-A40R-10 chr4:8418224 G>A maps to NM_003501.2 G8G. Only missense variants will be evaluated by CHASM.
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-CC-A3MC-01A-11D-A22F-10 chr3:132061393 A>C did not map to a codon.
Sequencing variant TCGA-CC-A8HV-01A-11D-A35Z-10 chr3:132071586 A>C maps to NM_001134194.1 L296L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XR-A8TD-01A-12D-A38X-10 chr3:132061466 C>A maps to NM_001134194.1 V209V. Only missense variants will be evaluated by CHASM.
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-CC-A9FW-01A-11D-A36X-10 chr12:6756044 G>A maps to NM_032489.2 T59T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10U-01A-11D-A12Z-10 chr23:70824009 T>C did not map to a codon.
Sequencing variant TCGA-DD-AACP-01A-11D-A40R-10 chr23:70811973 A>G did not map to a codon.
Sequencing variant TCGA-G3-A3CG-01A-11D-A20W-10 chr23:70823975 A>G did not map to a codon.
Sequencing variant TCGA-DD-AACJ-01A-11D-A40R-10 chr11:125546341 A>G maps to NM_001612.5 Y195Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZS-A9CG-01A-11D-A36X-10 chr17:48539552 C>T maps to ENST00000427954 C197C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A2QR-01A-11D-A20W-10 chr16:89180758 A>G maps to NM_174917.2 S330S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAW0-01A-11D-A40R-10 chr10:114169430 A>T maps to NM_016234.3 L289L. Only missense variants will be evaluated by CHASM.
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-A39Y-01A-11D-A20W-10 chr16:20696512 A>G did not map to a codon.
Sequencing variant TCGA-DD-A4NI-01A-11D-A27I-10 chr16:20494378 G>A did not map to a codon.
Sequencing variant TCGA-G3-A3CG-01A-11D-A20W-10 chr20:25004119 C>T maps to NM_032501.2 L263L. Only missense variants will be evaluated by CHASM.
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-AADU-01A-11D-A40R-10 chr15:35084455 T>A maps to NM_005159.4 K215*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACC-01A-11D-A40R-10 chr3:179304421 T>G did not map to a codon.
Sequencing variant TCGA-DD-AADO-01A-11D-A40R-10 chr7:100246397 G>A maps to NM_016188.4 T172T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZS-A9CE-01A-11D-A36X-10 chr7:100247665 G>C maps to NM_016188.4 L154L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAW3-01A-11D-A40P-10 chr9:111617760 G>A maps to NM_006686.3 S150S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-AAV6-01A-21D-A36X-10 chr9:111617802 G>A maps to NM_006686.3 T136T. 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-LG-A9QD-01A-11D-A382-10 chr1:236900514 G>T did not map to a codon.
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-2Y-A9H3-01A-11D-A382-10 chr7:152457012 T>A did not map to a codon.
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-DD-AAE4-01A-11D-A40R-10 chr20:37378812 C>A maps to NM_024855.3 S179*. 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-DD-A1EE-01A-11D-A12Z-10 chr1:2938474 C>T maps to NM_080431.4 F75F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr2:158636912 T>C maps to NM_001111067.2 Q89Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A3KF-01A-11D-A20W-10 chr2:158390462 A>G maps to NM_145259.2 S483S. 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-DD-AADU-01A-11D-A40R-10 chr2:148674941 C>T maps to NM_001616.3 R255*. 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-DD-AADF-01A-11D-A40R-10 chr12:52309132 T>A maps to NM_001077401.1 A299A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39X-01A-11D-A20W-10 chr11:67412311 T>C maps to NM_080658.1 E221E. 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-DD-AAE2-01A-11D-A40R-10 chr4:123301298 A>T maps to NM_139243.3 P25P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAE2-01A-11D-A40R-10 chr4:123305083 A>G maps to NM_139243.3 Q164Q. 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-CC-A7IE-01A-21D-A382-10 chr16:84229450 G>A maps to NM_139174.3 P443P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACO-01A-11D-A40R-10 chr16:84228735 G>T maps to NM_139174.3 L295L. 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-4R-AA8I-01A-11D-A382-10 chr15:58936168 A>G maps to NM_001110.2 S248S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39Z-01A-11D-A20W-10 chr15:58919929 A>G maps to NM_001110.2 V443V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AA3A-01A-11D-A36X-10 chr15:58891887 A>C maps to NM_001110.2 A687A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACP-01A-11D-A40R-10 chr15:58936147 T>A maps to NM_001110.2 T255T. 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-2Y-A9H1-01A-11D-A382-10 chr10:127806604 A>G did not map to a codon.
Sequencing variant TCGA-5R-AA1C-01A-11D-A40R-10 chr10:127753570 C>A did not map to a codon.
Sequencing variant TCGA-DD-AACN-01A-11D-A40R-10 chr8:39467001 A>T did not map to a codon.
Sequencing variant TCGA-DD-AADO-01A-11D-A40R-10 chr8:39564350 A>C maps to NM_014237.2 R649R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADV-01A-11D-A38X-10 chr8:39564319 T>C maps to NM_014237.2 N638N. 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-AADM-01A-11D-A40R-10 chr7:87780309 T>A maps to NM_021723.3 I527I. 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-DD-AAC8-01A-11D-A40R-10 chr2:207436448 A>T did not map to a codon.
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-2Y-A9H9-01A-21D-A38X-10 chr8:24201030 G>T maps to NM_014265.4 E642*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9HA-01A-11D-A38X-10 chr8:24181393 C>A maps to NM_014265.4 I256I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9H3-01A-11D-A382-10 chr4:175897785 T>C maps to NM_014269.4 S370S. 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-CC-A9FW-01A-11D-A36X-10 chr1:120436832 C>A maps to NM_021794.2 R709R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACL-01A-11D-A40R-10 chr20:3652922 A>T maps to NM_025220.2 P485P. 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-DD-AACU-01A-11D-A40R-10 chr8:38913106 A>T maps to NM_003816.2 G469G. 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-A3CG-01A-11D-A20W-10 chr5:33684041 C>A maps to NM_030955.2 L251L. 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-CC-A7IE-01A-21D-A382-10 chr10:72518012 C>G maps to NM_139155.2 P1053P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A8HT-01A-11D-A35Z-10 chr5:5232630 T>C did not map to a codon.
Sequencing variant TCGA-DD-A1ED-01A-11D-A152-10 chr5:5303776 T>C maps to NM_139056.2 A1028A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAD2-01A-11D-A40R-10 chr5:5190169 T>A maps to NM_139056.2 T378T. 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-DD-AACD-01A-11D-A40R-10 chr15:100514720 G>A maps to NM_139057.2 C1058C. 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-CC-A7IH-01A-11D-A33K-10 chr5:128863438 A>T did not map to a codon.
Sequencing variant TCGA-DD-AACI-01A-11D-A40R-10 chr5:129019946 C>T maps to NM_133638.3 C927C. Only missense variants will be evaluated by CHASM.
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-WQ-A9G7-01A-11D-A36X-10 chr5:129039960 T>C maps to NM_133638.3 R1057R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACT-01A-11D-A40R-10 chr5:178541173 A>T maps to NM_014244.4 P1110P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A496-01A-11D-A25V-10 chr5:178552066 G>A maps to NM_014244.4 H955H. 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-2Y-A9H4-01A-11D-A382-10 chr12:43858525 G>T maps to ENST00000389420 Y459*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9H9-01A-21D-A38X-10 chr12:43846184 A>G maps to ENST00000389420 Y657Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5R-AA1D-01A-11D-A382-10 chr12:43748038 A>G maps to ENST00000389420 T1902T. 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-4R-AA8I-01A-11D-A382-10 chr4:73149371 C>T maps to NM_014243.1 L1033L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAC8-01A-11D-A40R-10 chr4:73181643 A>T maps to NM_014243.1 P510P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADF-01A-11D-A40R-10 chr21:28338521 G>T maps to NM_007038.3 P63P. 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-BC-A10W-01A-11D-A12Z-10 chr5:64558681 T>C maps to NM_197941.2 G576G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MA-01A-11D-A20W-10 chr5:64466486 C>T maps to NM_197941.2 Q1067Q. 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-DD-AAED-01A-12D-A40R-10 chr5:64521990 A>C maps to NM_197941.2 T663T. 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-DD-AACP-01A-11D-A40R-10 chr15:79090368 A>G maps to ENST00000258883 H181H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr3:64524965 A>G maps to NM_182920.1 T1842T. 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-DD-AACA-01A-11D-A40R-10 chr3:64582562 C>T maps to NM_182920.1 E1374E. 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-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-ES-A2HS-01A-11D-A183-10 chr9:18829937 A>G maps to NM_001040272.4 T1404T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr9:18681883 A>G maps to NM_001040272.4 G472G. 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-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-DD-AADM-01A-11D-A40R-10 chr7:959635 G>A maps to NM_006869.2 I119I. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-EP-A2KA-01A-11D-A183-10. Mapping will be selected arbitrarily.
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-EP-A2KA-01A-11D-A183-10 chr14:78374193 G>T maps to NM_020421.3 E264*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADF-01A-11D-A40R-10 chr7:140373720 C>T maps to NM_052853.3 I197I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39X-01A-11D-A20W-10 chr19:41220248 T>C maps to NM_024876.3 R52R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr19:41220242 C>T maps to NM_024876.3 L54L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CJ-01A-11D-A20W-10 chr8:145617319 A>G maps to NM_174922.3 K375K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr7:45743230 C>T maps to NM_021116.2 G868G. 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-ZS-A9CG-01A-11D-A36X-10 chr7:45750130 C>T maps to NM_021116.2 I979I. 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-4R-AA8I-01A-11D-A382-10 chr5:7706966 C>A maps to NM_020546.2 S407*. 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-DD-AACZ-01A-11D-A40R-10 chr2:25059803 G>C maps to NM_004036.3 P548P. 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-UB-AA0U-01A-11D-A382-10 chr3:123166783 C>T maps to NM_183357.2 L203L. 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-DD-AACI-01A-11D-A40R-10 chr8:131916176 A>G maps to NM_001115.2 T584T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACL-01A-11D-A40R-10 chr8:131896932 A>T maps to NM_001115.2 S662S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADV-01A-11D-A38X-10 chr8:131833592 G>A maps to NM_001115.2 Q917*. 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-K7-AAU7-01A-11D-A382-10 chr8:132052015 C>T maps to NM_001115.2 L188L. 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-G3-A3CG-01A-11D-A20W-10 chr4:2906528 G>T maps to NM_014189.2 L400L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WQ-A9G7-01A-11D-A36X-10 chr4:2910331 G>A did not map to a codon.
Sequencing variant TCGA-XR-A8TG-01A-11D-A35Z-10 chr4:2909498 C>A maps to NM_014189.2 S512S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10W-01A-11D-A12Z-10 chr2:70919546 C>T maps to NM_001185054.1 P231P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZP-A9CV-01A-11D-A382-10 chr2:70910803 G>A maps to NM_001185054.1 A348A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A0-01A-11D-A20W-10 chr10:111883899 T>C maps to NM_016824.3 S423S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADU-01A-11D-A40R-10 chr4:100201406 T>C maps to NM_000667.3 A286A. 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-DD-A39Y-01A-11D-A20W-10 chr4:100060246 A>G maps to ENST00000505590 C124C. Only missense variants will be evaluated by CHASM.
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.
Alternatively spliced codon TCGA-DD-AAD3-01A-11D-A40R-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-DD-AAD3-01A-11D-A40R-10 chr4:100002516 T>A maps to NM_000671.3 R115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAE0-01A-11D-A40R-10 chr2:3523231 G>A maps to NM_018269.3 D9D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADM-01A-11D-A40R-10 chr1:202920180 T>A maps to NM_015999.3 G6G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAE2-01A-11D-A40R-10 chr22:50921203 C>A maps to NM_024866.4 R107R. 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-2Y-A9GX-01A-11D-A382-10 chr18:77895929 C>T maps to NM_014913.3 P878P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADF-01A-11D-A40R-10 chr1:203134430 A>T maps to NM_001048230.1 I128I. 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-CC-A3MA-01A-11D-A20W-10 chr1:112033359 C>T maps to NM_020683.6 G125G. 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-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-DD-A119-01A-11D-A12Z-10 chr5:159399015 G>A maps to NM_000679.3 V360V. 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-G3-AAV0-01A-11D-A36X-10 chr10:112838914 C>T maps to NM_000681.3 F387F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACQ-01A-11D-A40R-10 chr8:37821736 T>A maps to NM_000025.2 *409L. 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-4R-AA8I-01A-11D-A382-10 chr22:26100173 C>T maps to NM_005160.3 G442G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACT-01A-11D-A40R-10 chr22:26083501 A>C did not map to a codon.
Sequencing variant TCGA-2Y-A9H8-01A-11D-A38X-10 chr7:44153376 G>A maps to NM_001129.3 G998G. 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-5R-AA1C-01A-11D-A40R-10 chr23:148037838 C>T did not map to a codon.
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-DD-A119-01A-11D-A12Z-10 chr23:148069085 A>G did not map to a codon.
Sequencing variant TCGA-DD-AAE0-01A-11D-A40R-10 chr23:147919195 C>T did not map to a codon.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr23:148037650 C>A did not map to a codon.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr23:148062275 T>C 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-BC-A10W-01A-11D-A12Z-10 chr2:100343585 T>C maps to NM_001025108.1 K373K. Only missense variants will be evaluated by CHASM.
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-ES-A2HT-01A-12D-A183-10 chr2:100209827 A>G maps to NM_001025108.1 S790S. 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-5C-A9VG-01A-11D-A36X-10 chr4:74357713 A>G maps to NM_001133.2 P323P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACX-01A-11D-A40R-10 chr4:74364861 C>T maps to NM_001133.2 Q441*. 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-CC-A3MB-01A-11D-A20W-10 chr4:74308084 T>C maps to NM_001134.1 Y185Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11C-01A-11D-A12Z-10 chr4:74319615 T>C did not map to a codon.
Sequencing variant TCGA-DD-AADY-01A-11D-A40R-10 chr2:64779984 C>G maps to ENST00000422803 A459A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAEH-01A-11D-A40R-10 chr2:64808324 T>G maps to ENST00000422803 A819A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr2:64779484 G>T maps to ENST00000422803 G293*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9HB-01A-11D-A38X-10 chr12:58120765 C>T maps to NM_001122772.1 L1109L. 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-G3-AAV7-01A-11D-A382-10 chr12:58131024 G>T maps to NM_001122772.1 G335G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-AAV7-01A-11D-A382-10 chr12:58131660 G>T maps to NM_001122772.1 L123L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAE7-01A-11D-A40R-10 chr10:51768607 G>C maps to NM_001077665.2 T241T. 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-DD-AADI-01A-11D-A40R-10 chr15:86791025 C>T maps to NM_152336.2 C171C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADO-01A-11D-A40R-10 chr15:87097620 A>G maps to NM_152336.2 A903A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-AAV0-01A-11D-A36X-10 chr15:86814916 C>T maps to NM_152336.2 G639G. 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-DD-AACK-01A-11D-A40R-10 chr1:50317107 G>C maps to NM_032785.3 P39P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr2:27279547 C>T maps to NM_021831.5 Q475*. 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-DD-AAD5-01A-11D-A40R-10 chr2:228401644 T>A maps to NM_001135187.1 A462A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAD5-01A-11D-A40R-10 chr2:228401647 T>A maps to NM_001135187.1 A463A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr7:100159951 C>T maps to NM_006076.4 D316D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EE-01A-11D-A12Z-10 chr5:76342269 C>T maps to NM_018046.4 G323G. 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-DD-AACC-01A-11D-A40R-10 chr1:100366398 T>G maps to ENST00000311030 P1191P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr1:100366212 G>T maps to ENST00000311030 A1129A. Only missense variants will be evaluated by CHASM.
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-4R-AA8I-01A-11D-A382-10 chr6:32138330 G>A maps to NM_032741.4 R127R. Only missense variants will be evaluated by CHASM.
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-4R-AA8I-01A-11D-A382-10 chr8:6590107 T>C maps to NM_018361.3 S144S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A1-01A-11D-A20W-10 chr15:78825562 G>T maps to NM_001013619.2 G225*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZS-A9CF-01A-11D-A382-10 chr2:178257522 G>T maps to NM_003659.3 A2A. 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-DD-AADJ-01A-11D-A40R-10 chr9:88272415 G>A maps to ENST00000395847 N281N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XR-A8TG-01A-11D-A35Z-10 chr9:88162137 T>C maps to ENST00000395847 A1189A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZP-A9CZ-01A-11D-A382-10 chr1:11808646 G>T maps to ENST00000376627 G159G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9H3-01A-11D-A382-10 chr1:247016530 C>T maps to ENST00000428671 E1513E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9H5-01A-11D-A382-10 chr1:247007206 G>A maps to ENST00000428671 Q2177*. 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-G3-AAV0-01A-11D-A36X-10 chr1:247027262 G>T maps to ENST00000428671 S1206*. 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-ZP-A9D0-01A-11D-A36X-10 chr1:247024558 A>C maps to ENST00000428671 P1296P. 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-DD-AAEI-01A-11D-A40R-10 chr1:27876697 C>T maps to NM_001029882.2 P643P. 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-2Y-A9GY-01A-11D-A382-10 chr11:62296755 T>C maps to NM_001620.1 K1711K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A8HT-01A-11D-A35Z-10 chr11:62288121 C>T maps to NM_001620.1 K4589K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAE3-01A-11D-A40R-10 chr11:62291790 T>A maps to NM_001620.1 T3366T. 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-WQ-A9G7-01A-11D-A36X-10 chr11:62289804 A>G maps to NM_001620.1 G4028G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XR-A8TG-01A-11D-A35Z-10 chr11:62292057 T>C maps to NM_001620.1 K3277K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr14:105414173 A>G maps to NM_138420.2 A2538A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr14:105414176 G>A maps to NM_138420.2 S2537S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5R-AA1C-01A-11D-A40R-10 chr14:105411350 C>T maps to NM_138420.2 K3479K. 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-WX-AA44-01A-11D-A38X-10 chr14:105406859 G>A maps to NM_138420.2 D4976D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XR-A8TE-01A-11D-A35Z-10 chr7:17362176 A>G maps to NM_001621.4 R102R. 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-DD-A39Y-01A-11D-A20W-10 chr14:77935520 C>A maps to NM_012111.2 R316R. 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-G3-A3CJ-01A-11D-A20W-10 chr14:77935520 C>A maps to NM_012111.2 R316R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr12:8759502 A>G maps to NM_020661.2 S38S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACF-01A-11D-A40R-10 chr9:133993146 G>T maps to NM_001185095.1 L95L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EG-01A-11D-A20W-10 chr23:129290532 T>C did not map to a codon.
Sequencing variant TCGA-DD-AACF-01A-11D-A40R-10 chr23:129270144 T>C did not map to a codon.
Sequencing variant TCGA-DD-AACT-01A-11D-A40R-10 chr23:129289156 T>C did not map to a codon.
Sequencing variant TCGA-DD-AAE9-01A-11D-A40R-10 chr23:129265688 T>C did not map to a codon.
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-EP-A2KB-01A-11D-A183-10 chr22:21329041 C>A maps to NM_144704.2 S219S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MA-01A-11D-A20W-10 chr6:106960806 A>G maps to NM_001624.2 R197R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADA-01A-11D-A40R-10 chr6:106967347 C>A maps to NM_001624.2 V347V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr6:106999725 G>T did not map to a codon.
Sequencing variant TCGA-FV-A2QR-01A-11D-A20W-10 chr6:106967047 T>C maps to NM_001624.2 P247P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CJ-01A-11D-A20W-10 chr6:106967098 T>C maps to NM_001624.2 V264V. 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-4R-AA8I-01A-11D-A382-10 chr7:6054889 A>C maps to NM_006303.3 P83P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1ED-01A-11D-A152-10 chr7:6063114 A>G maps to NM_006303.3 K252K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADI-01A-11D-A40R-10 chr17:6331739 G>A maps to NM_014336.3 C121C. 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-WX-AA44-01A-11D-A38X-10 chr1:33478934 G>T maps to NM_001625.3 A189A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9HA-01A-11D-A38X-10 chr14:96953299 G>A maps to NM_152327.2 L680L. 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-XR-A8TD-01A-12D-A38X-10 chr17:55182884 C>T maps to ENST00000427138 L62L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACI-01A-11D-A40R-10 chr17:19844214 G>A maps to NM_007202.2 L390L. 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-DD-A1EE-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-DD-AAEI-01A-11D-A40R-10 chr13:42876688 A>T maps to NM_016248.2 T1269T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr13:42891710 G>T maps to NM_016248.2 E1818*. 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-K7-AAU7-01A-11D-A382-10 chr6:151671010 C>T maps to NM_005100.3 G495G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39Y-01A-11D-A20W-10 chr15:86124121 T>C maps to NM_006738.4 A941A. 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-ES-A2HT-01A-12D-A183-10 chr15:86273921 A>G maps to NM_006738.4 K2426K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CG-01A-11D-A20W-10 chr15:86123971 C>T maps to NM_006738.4 D891D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-AAV0-01A-11D-A36X-10 chr15:86124903 C>G maps to NM_006738.4 S1202*. 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-5C-AAPD-01A-21D-A38X-10 chr12:4736120 G>T maps to NM_006422.2 A649A. 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-CC-A3MA-01A-11D-A20W-10 chr23:49958533 T>C 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-ES-A2HS-01A-11D-A183-10 chr23:49955743 T>C did not map to a codon.
Sequencing variant TCGA-2Y-A9GU-01A-11D-A382-10 chr14:33046346 G>T maps to NM_004274.4 E790*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr14:33293954 A>G maps to NM_004274.4 K2312K. 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-EP-A2KB-01A-11D-A183-10 chr7:91712763 C>A maps to NM_005751.4 S2814*. Only missense variants will be evaluated by CHASM.
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-ES-A2HT-01A-12D-A183-10 chr6:109837260 A>G maps to NM_001145128.2 Y1288Y. 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-WX-AA46-01A-11D-A38X-10 chr7:134136357 C>A maps to NM_001628.2 E72*. 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-G3-AAUZ-01A-11D-A382-10 chr10:5009210 T>G maps to NM_001353.5 L115L. 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-ZP-A9D2-01A-11D-A382-10 chr10:5136644 C>T maps to NM_003739.4 S3S. Only missense variants will be evaluated by CHASM.
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-DD-AAE7-01A-11D-A40R-10 chr1:243809236 T>A maps to NM_005465.3 G129G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YA-A8S7-01A-11D-A36X-10 chr16:53529085 C>T did not map to a codon.
Sequencing variant TCGA-DD-AACI-01A-11D-A40R-10 chr23:55052400 G>A 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-DD-A3A1-01A-11D-A20W-10 chr4:74277805 C>T maps to NM_000477.5 C269C. 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-LG-A9QD-01A-11D-A382-10 chr4:74282071 T>G did not map to a codon.
Sequencing variant TCGA-DD-AAC8-01A-11D-A40R-10 chr3:105266288 A>T maps to NM_001627.2 T432T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CG-01A-11D-A20W-10 chr3:105268981 T>C maps to NM_001627.2 S462S. Only missense variants will be evaluated by CHASM.
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-UB-AA0U-01A-11D-A382-10 chr9:38396812 C>T maps to NM_000692.3 T356T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACO-01A-11D-A40R-10 chr3:125856709 C>A maps to ENST00000273450 L400L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr11:67787181 A>G did not map to a codon.
Sequencing variant TCGA-CC-A9FW-01A-11D-A36X-10 chr6:24495385 C>T maps to NM_170740.1 L54L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr14:74534080 A>G did not map to a codon.
Sequencing variant TCGA-DD-AACD-01A-11D-A40R-10 chr5:125918579 T>C maps to NM_001182.3 L160L. 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-XR-A8TF-01A-11D-A35Z-10 chr6:135239909 T>C maps to NM_022568.3 A369A. 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-A8HT-01A-11D-A35Z-10 chr9:104187849 C>T maps to NM_000035.3 L228L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9GZ-01A-11D-A38X-10 chr17:26900923 G>A maps to NM_005165.2 S276S. 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-EP-A2KA-01A-11D-A183-10 chr23:110980010 G>T did not map to a codon.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr1:95448691 A>G maps to NM_144988.3 V197V. 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-A3A0-01A-11D-A20W-10 chr11:77812228 A>G maps to NM_024079.4 P454P. 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-UB-AA0U-01A-11D-A382-10 chr11:111706980 A>T maps to ENST00000428306 G728G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9GU-01A-11D-A382-10 chr2:29551300 A>G maps to NM_004304.3 C443C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CG-01A-11D-A20W-10 chr11:43940661 A>G maps to NM_139178.3 E248E. 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-2Y-A9GY-01A-11D-A382-10 chr2:73613064 G>A maps to NM_015120.4 E23E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A3KF-01A-11D-A20W-10 chr2:73799566 A>G maps to NM_015120.4 K3520K. 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-DD-AACE-01A-11D-A40R-10 chr2:73613064 G>A maps to NM_015120.4 E23E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADB-01A-11D-A40R-10 chr2:73680730 T>A maps to NM_015120.4 V2358V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XR-A8TD-01A-12D-A38X-10 chr2:73613064 G>A maps to NM_015120.4 E23E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZS-A9CG-01A-11D-A36X-10 chr2:73613064 G>A maps to NM_015120.4 E23E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAEG-01A-11D-A38X-10 chr17:7980037 G>A maps to NM_001139.2 Y433Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1ED-01A-11D-A152-10 chr17:8006757 T>C maps to ENST00000380149 P769P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EG-01A-11D-A20W-10 chr4:113333008 T>C maps to NM_025144.3 A101A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr4:113360846 A>G maps to NM_025144.3 L1119L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAD2-01A-11D-A40R-10 chr18:56204803 G>T maps to NM_052947.3 S872*. 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-CC-A8HV-01A-11D-A35Z-10 chr15:85399660 G>A maps to NM_020778.4 S766S. 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-DD-AAED-01A-12D-A40R-10 chr2:233243545 C>T maps to NM_001632.3 L12L. 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-DD-AAVX-01A-11D-A40R-10 chr3:46722031 C>A did not map to a codon.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr2:202400647 A>T maps to NM_001168217.1 A534A. 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-BC-A3KG-01A-11D-A20W-10 chr2:203848289 A>G maps to NM_024744.14 P707P. 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-DD-AAE4-01A-11D-A40R-10 chr12:85695156 T>C maps to NM_006982.2 F295F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr11:46456588 T>C did not map to a codon.
Sequencing variant TCGA-FV-A2QR-01A-11D-A20W-10 chr11:46431902 A>G maps to ENST00000458649 G1044G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WX-AA46-01A-11D-A38X-10 chr6:111196313 A>G maps to NM_001634.4 E2E. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-ES-A2HS-01A-11D-A183-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-DD-AADC-01A-11D-A40R-10 chr23:11316226 C>G did not map to a codon.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr23:11316393 A>G did not map to a codon.
Sequencing variant TCGA-G3-A3CJ-01A-11D-A20W-10 chr23:11316393 A>G did not map to a codon.
Sequencing variant TCGA-CC-A7IK-01A-12D-A33Q-10 chr16:56435756 T>A did not map to a codon.
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-2Y-A9GU-01A-11D-A382-10 chr12:53819693 G>A maps to NM_020547.2 L281L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A1-01A-11D-A20W-10 chr12:53823318 A>G maps to NM_020547.2 G350G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9H3-01A-11D-A382-10 chr11:118071325 T>C maps to NM_001098526.1 T258T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAD0-01A-11D-A40R-10 chr3:49755431 G>T maps to NM_198722.2 G489G. 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-DD-A39Y-01A-11D-A20W-10 chr14:103395266 T>C maps to NM_030943.3 P156P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr14:103396364 C>A maps to NM_030943.3 P316P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr23:112033909 G>T did not map to a codon.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr23:112021880 A>G did not map to a codon.
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-FV-A2QR-01A-11D-A20W-10 chr11:10500171 T>C maps to NM_000480.2 S116S. 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-AAV6-01A-21D-A36X-10 chr7:38429485 A>G maps to NM_001635.3 F633F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr4:71394474 G>A maps to NM_212557.2 Q110Q. 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-4R-AA8I-01A-11D-A382-10 chr17:79857926 A>T maps to NM_001002249.1 K81*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAE9-01A-11D-A40R-10 chr9:140075298 A>G maps to NM_013366.3 N517N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr9:140082405 A>G maps to NM_013366.3 P89P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr1:213178562 T>G maps to NM_144567.3 R316R. 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-4R-AA8I-01A-11D-A382-10 chr9:129854030 G>A maps to NM_012098.2 Y400Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADL-01A-11D-A40R-10 chr1:63070361 A>G maps to NM_014495.2 K419K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADL-01A-11D-A40R-10 chr1:63070370 A>G maps to NM_014495.2 A422A. 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-AACB-01A-11D-A40R-10 chr8:41542086 G>A maps to ENST00000415018 Y1504Y. 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-DD-A39Y-01A-11D-A20W-10 chr4:114276004 A>G maps to NM_001148.4 K2077K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAEH-01A-11D-A40R-10 chr4:114276433 G>A maps to NM_001148.4 E2220E. 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-2Y-A9H3-01A-11D-A382-10 chr10:61847907 G>T maps to NM_020987.2 L1179L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A3KF-01A-11D-A20W-10 chr10:61874002 A>G maps to NM_020987.2 V976V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EE-01A-11D-A12Z-10 chr10:61835055 C>T maps to NM_020987.2 T1861T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EG-01A-11D-A20W-10 chr10:61819138 A>G maps to NM_020987.2 A4215A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NI-A8LF-01A-11D-A35Z-10 chr10:61832736 C>T maps to NM_020987.2 V2634V. 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-ZP-A9D0-01A-11D-A36X-10 chr10:61832025 C>A maps to NM_020987.2 S2871S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39Y-01A-11D-A20W-10 chr2:190569758 T>C maps to NM_144708.3 P573P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr15:65219191 A>G maps to NM_182703.3 K188K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A0-01A-11D-A20W-10 chr17:54428174 T>C maps to NM_153228.2 C82C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAE6-01A-11D-A40R-10 chr17:54543823 A>T maps to NM_153228.2 S558S. 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-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-ZP-A9D4-01A-11D-A36X-10 chr5:139908467 G>A maps to ENST00000253810 V1979V. 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-EP-A2KB-01A-11D-A183-10 chr11:113266921 C>A maps to NM_178510.1 P272P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAE6-01A-11D-A40R-10 chr19:17393776 G>A maps to NM_152363.4 G142G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EG-01A-11D-A20W-10 chr12:133310971 A>G maps to NM_015114.1 S630S. 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-ZP-A9D4-01A-11D-A36X-10 chr2:241421601 C>G maps to ENST00000401804 G961G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACJ-01A-11D-A40R-10 chr7:16666728 T>A maps to NM_020319.2 G69G. 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-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-5C-A9VG-01A-11D-A36X-10 chr16:89347978 C>T maps to NM_013275.4 S1657S. 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-DD-AAE7-01A-11D-A40R-10 chr16:89349877 T>C maps to NM_013275.4 K1024K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr16:89346916 C>T maps to NM_013275.4 S2011S. 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-BC-A3KG-01A-11D-A20W-10 chr18:9256480 T>C maps to NM_015208.3 N1072N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A3KG-01A-11D-A20W-10 chr12:110468462 T>C maps to NM_033121.1 F416F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAW0-01A-11D-A40R-10 chr17:27939495 G>A maps to NM_152345.4 S445S. 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-DD-AAEG-01A-11D-A38X-10 chr4:73943152 T>A maps to NM_032217.3 R2502R. 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-G3-AAV4-01A-11D-A382-10 chr19:4202879 G>A maps to ENST00000262970 V231V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACL-01A-11D-A40R-10 chr10:27306541 T>A maps to NM_014915.2 I1465I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACL-01A-11D-A40R-10 chr10:27337851 T>A maps to NM_014915.2 I564I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr18:21214038 T>C maps to NM_173505.2 G135G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr18:21218860 G>T maps to NM_173505.2 V94V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr10:37447482 A>G maps to ENST00000374660 L567L. 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-DD-AACT-01A-11D-A40R-10 chr18:14842893 A>G did not map to a codon.
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-WX-AA47-01A-11D-A38X-10 chr1:145562471 C>T maps to NM_144698.3 S720S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr5:132150794 A>G maps to NM_175873.4 R494R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WX-AA44-01A-11D-A38X-10 chr5:132149933 A>T maps to NM_175873.4 A207A. 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-WQ-AB4B-01A-11D-A40P-10 chr2:197948232 C>T maps to NM_001195144.1 R439R. Only missense variants will be evaluated by CHASM.
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-A3A0-01A-11D-A20W-10 chr20:10032308 A>G did not map to a codon.
Sequencing variant TCGA-DD-AAC8-01A-11D-A40R-10 chr20:10033916 A>G maps to NM_198798.1 K676K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAE3-01A-11D-A40R-10 chr12:56641953 G>A maps to NM_173595.3 L611L. Only missense variants will be evaluated by CHASM.
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-CC-A3MA-01A-11D-A20W-10 chr23:118893081 T>C did not map to a codon.
Sequencing variant TCGA-DD-A39Z-01A-11D-A20W-10 chr6:90326288 A>G maps to ENST00000339746 T209T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADV-01A-11D-A38X-10 chr6:34935066 C>A maps to NM_015245.2 P83P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XR-A8TF-01A-11D-A35Z-10 chr9:101539737 T>A did not map to a codon.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr2:220097004 G>A maps to NM_001042410.1 W95*. 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-CC-A8HV-01A-11D-A35Z-10 chr11:69949237 G>T maps to NM_018043.5 E170*. 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-DD-AAEK-01A-11D-A40R-10 chr12:5853335 G>A maps to ENST00000356134 F443F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-AAV6-01A-21D-A36X-10 chr12:5860093 C>A maps to ENST00000356134 L363L. 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-A39X-01A-11D-A20W-10 chr12:45803138 G>A did not map to a codon.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr19:17434418 T>C maps to NM_020959.2 L1202L. 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-DD-AADE-01A-11D-A40R-10 chr15:90344727 G>C maps to NM_001150.2 T560T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr15:90346883 G>T maps to NM_001150.2 Y477*. 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-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-WQ-AB4B-01A-11D-A40P-10 chr2:69408988 C>T maps to NM_032208.2 G387G. 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-EP-A2KA-01A-11D-A183-10 chr4:169060640 T>C maps to NM_007193.3 C35C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A8O6-01A-11D-A35Z-10 chr10:81926705 C>G maps to NM_145869.1 G228G. 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-2Y-A9GZ-01A-11D-A38X-10 chr4:122602880 A>G maps to NM_001154.3 I113I. 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-ES-A2HS-01A-11D-A183-10 chr7:36763687 C>A maps to NM_001177506.1 S22S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAD2-01A-11D-A40R-10 chr2:201457897 A>G maps to NM_001159.3 T25T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NI-A8LF-01A-11D-A35Z-10 chr2:201462229 T>G 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-WX-AA46-01A-11D-A38X-10 chr22:29727787 C>G maps to NM_001127.3 L809L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EE-01A-11D-A12Z-10 chr16:71823202 G>A maps to ENST00000423132 G83G. 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-ES-A2HT-01A-12D-A183-10 chr14:24035856 T>A maps to NM_003917.2 T81T. 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-ZP-A9CV-01A-11D-A382-10 chr23:15864089 T>C did not map to a codon.
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-2Y-A9GW-01A-11D-A382-10 chr11:1000559 C>T maps to ENST00000332231 V696V. 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-ES-A2HT-01A-12D-A183-10 chr11:1009726 T>C maps to ENST00000332231 N885N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CG-01A-11D-A20W-10 chr11:1000574 T>C maps to ENST00000332231 P701P. 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-G3-AAV0-01A-11D-A36X-10 chr17:33968893 A>T did not map to a codon.
Sequencing variant TCGA-DD-A73E-01A-12D-A32G-10 chr3:183899819 G>T maps to ENST00000411763 L341L. 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-ES-A2HS-01A-11D-A183-10 chr15:83358198 A>G maps to NM_004644.3 D40D. 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-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-EP-A2KB-01A-11D-A183-10 chr7:99701747 G>T maps to ENST00000429084 E200*. 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-GJ-A3OU-01A-31D-A382-10 chr9:72071258 A>T maps to NM_001163.3 P564P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZS-A9CD-01A-11D-A36X-10 chr9:72131799 C>G maps to NM_001163.3 A109A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A8HV-01A-11D-A35Z-10 chr15:29406111 C>T maps to NM_005503.3 R691*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAW2-01A-11D-A40P-10 chr15:29346269 G>A maps to NM_005503.3 Q61Q. 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-EP-A2KA-01A-11D-A183-10 chr10:26825147 T>C did not map to a codon.
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-DD-AACI-01A-11D-A40R-10 chr5:112179021 A>T maps to NM_001127510.2 S2577S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A8O5-01A-11D-A35Z-10 chr5:112179351 A>T maps to NM_001127510.2 S2687S. Only missense variants will be evaluated by CHASM.
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-5C-AAPD-01A-21D-A38X-10 chr18:10471889 G>A maps to ENST00000423585 V253V. 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-DD-A1ED-01A-11D-A152-10 chr3:49712709 A>G maps to ENST00000438011 G80G. 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-AADF-01A-11D-A40R-10 chr23:55026951 G>A did not map to a codon.
Sequencing variant TCGA-2Y-A9GZ-01A-11D-A38X-10 chr15:63571386 G>A maps to NM_031301.3 L47L. Only missense variants will be evaluated by CHASM.
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-DD-AACJ-01A-11D-A40R-10 chr11:43340326 C>T maps to NM_001142930.1 D69D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9GV-01A-11D-A382-10 chr19:36363436 T>A maps to NM_001024807.1 P301P. 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-BC-A8YO-01A-11D-A36X-10 chr1:156562200 G>T maps to ENST00000446584 L130L. 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-DD-AACB-01A-11D-A40R-10 chr2:21256267 G>A maps to NM_000384.2 Q343*. 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-ES-A2HT-01A-12D-A183-10 chr2:21247879 G>T maps to NM_000384.2 A787A. 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-DD-AACM-01A-11D-A40R-10 chr22:39387542 C>G maps to ENST00000402182 A310A. 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-WQ-A9G7-01A-11D-A36X-10 chr22:39482297 C>T maps to NM_021822.3 H250H. 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-4R-AA8I-01A-11D-A382-10 chr12:56755671 A>C maps to NM_001638.2 A106A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5C-A9VG-01A-11D-A36X-10 chr17:64219852 C>T maps to NM_000042.2 E126E. 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-A119-01A-11D-A12Z-10 chr22:36537571 G>T maps to NM_145640.2 I295I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39Y-01A-11D-A20W-10 chr23:84306505 T>G did not map to a codon.
Sequencing variant TCGA-RC-A6M4-01A-11D-A32G-10 chr23:84301521 A>G did not map to a codon.
Sequencing variant TCGA-DD-AADI-01A-11D-A40R-10 chr3:57282310 C>T maps to NM_012096.2 D265D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A9FW-01A-11D-A36X-10 chr12:105591691 A>G maps to NM_018171.3 Y301Y. 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-G3-AAV0-01A-11D-A36X-10 chr9:33442435 C>T maps to NM_004925.3 E191E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr12:50368265 G>T did not map to a codon.
Sequencing variant TCGA-DD-AADR-01A-11D-A40R-10 chr15:58430832 G>A maps to NM_020980.3 A23A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAVP-01A-11D-A40R-10 chr5:115318982 G>T did not map to a codon.
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-DD-A39Z-01A-11D-A20W-10 chr15:35167041 T>C maps to NM_014691.2 R1087R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr15:35182512 A>G maps to NM_014691.2 L862L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WJ-A86L-01A-12D-A45V-10 chr15:35196557 T>C maps to NM_014691.2 K660K. 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-DD-A39X-01A-11D-A20W-10 chr23:66765175 A>T did not map to a codon.
Sequencing variant TCGA-DD-A39X-01A-11D-A20W-10 chr23:66765178 A>T did not map to a codon.
Sequencing variant TCGA-DD-A4NV-01A-11D-A30V-10 chr23:66766355 T>C did not map to a codon.
Sequencing variant TCGA-DD-AADY-01A-11D-A40R-10 chr23:66765172 A>T did not map to a codon.
Sequencing variant TCGA-DD-AAEI-01A-11D-A40R-10 chr23:66765175 A>T 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-QA-A7B7-01A-11D-A32G-10 chr23:66765175 A>T did not map to a codon.
Sequencing variant TCGA-QA-A7B7-01A-11D-A32G-10 chr23:66765178 A>T did not map to a codon.
Sequencing variant TCGA-RC-A7SH-01A-11D-A382-10 chr23:66931523 C>A 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-YA-A8S7-01A-11D-A36X-10 chr23:66765172 A>T did not map to a codon.
Sequencing variant TCGA-YA-A8S7-01A-11D-A36X-10 chr23:66765175 A>T did not map to a codon.
Sequencing variant TCGA-YA-A8S7-01A-11D-A36X-10 chr23:66765178 A>T did not map to a codon.
Sequencing variant TCGA-YA-A8S7-01A-11D-A36X-10 chr23:66765206 G>A did not map to a codon.
Sequencing variant TCGA-ZS-A9CD-01A-11D-A36X-10 chr23:66766367 C>T did not map to a codon.
Sequencing variant TCGA-ZS-A9CG-01A-11D-A36X-10 chr23:66766364 C>T 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-DD-A1EE-01A-11D-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-ES-A2HT-01A-12D-A183-10 chr23:47426697 A>G did not map to a codon.
Sequencing variant TCGA-DD-AACX-01A-11D-A40R-10 chr4:36230967 C>T maps to NM_015230.2 Q47Q. 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-DD-AAC9-01A-11D-A40R-10 chr5:141034963 G>A maps to NM_022481.5 R1372*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADP-01A-11D-A38X-10 chr5:141038046 C>T 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-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-DD-AACQ-01A-11D-A40R-10 chr20:61916215 A>T maps to ENST00000395285 T143T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAC8-01A-11D-A40R-10 chr8:68211584 A>C maps to NM_006421.3 L106L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5C-A9VG-01A-11D-A36X-10 chr20:47601302 C>T maps to NM_006420.2 Q666*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACJ-01A-11D-A40R-10 chr20:47605199 G>A did not map to a codon.
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-GJ-A9DB-01A-11D-A36X-10 chr4:148787951 G>A maps to NM_024605.3 Q229Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAVU-01A-11D-A40R-10 chr15:32925231 A>G maps to NM_014783.3 V386V. Only missense variants will be evaluated by CHASM.
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-4R-AA8I-01A-11D-A382-10 chr2:144313998 T>C maps to NM_018460.3 Y316Y. 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-DD-A39Y-01A-11D-A20W-10 chr10:99025638 A>G maps to NM_032900.4 S100S. Only missense variants will be evaluated by CHASM.
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-AACP-01A-11D-A40R-10 chr4:86916339 G>C maps to NM_001025616.2 L511L. 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-DD-AAEI-01A-11D-A40R-10 chr2:69014970 G>A did not map to a codon.
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-AAD8-01A-11D-A40R-10 chr5:142253058 A>T maps to NM_015071.4 I83I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZS-A9CD-01A-11D-A36X-10 chr17:43474145 G>A maps to ENST00000428638 A654A. 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-AAC9-01A-11D-A40R-10 chr1:161018500 C>T maps to NM_001025598.1 E770E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAW1-01A-11D-A40P-10 chr1:161021131 A>T maps to NM_001025598.1 P464P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MB-01A-11D-A20W-10 chr3:119133130 T>C maps to NM_020754.2 P785P. 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-2Y-A9GT-01A-11D-A382-10 chr11:128868355 T>C maps to NM_001142685.1 K337K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A3KF-01A-11D-A20W-10 chr11:128932192 T>C maps to NM_001142685.1 R301R. 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-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-CC-A3MB-01A-11D-A20W-10 chr23:130222733 C>T did not map to a codon.
Sequencing variant TCGA-DD-AADF-01A-11D-A40R-10 chr23:130215820 T>A 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-AADA-01A-11D-A40R-10 chr8:145759533 T>A maps to NM_025251.1 A889A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A118-01A-11D-A12Z-10 chr23:153185068 G>T did not map to a codon.
Sequencing variant TCGA-DD-AAVV-01A-11D-A40R-10 chr23:153173334 T>A did not map to a codon.
Sequencing variant TCGA-DD-AAVV-01A-11D-A40R-10 chr23:153173336 G>A did not map to a codon.
Sequencing variant TCGA-NI-A8LF-01A-11D-A35Z-10 chr23:153174960 G>A 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-A3A1-01A-11D-A20W-10 chr23:11682866 A>G did not map to a codon.
Sequencing variant TCGA-DD-AAC8-01A-11D-A40R-10 chr23:11204487 A>T did not map to a codon.
Sequencing variant TCGA-DD-AAD3-01A-11D-A40R-10 chr19:42409113 C>T maps to NM_199002.1 F740F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5C-A9VG-01A-11D-A36X-10 chr8:1905383 G>T maps to ENST00000398564 L1355L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9HB-01A-11D-A38X-10 chr1:18014159 C>G maps to NM_018125.3 T1034T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10W-01A-11D-A12Z-10 chr1:156909535 A>G maps to NM_198236.1 G1300G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EE-01A-11D-A12Z-10 chr1:156939121 C>A maps to NM_198236.1 G259G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACH-01A-11D-A40R-10 chr1:156908218 T>A maps to NM_198236.1 K1395*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr1:156908261 A>G maps to NM_198236.1 S1380S. Only missense variants will be evaluated by CHASM.
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-ZP-A9D2-01A-11D-A382-10 chr1:156918127 G>A maps to NM_198236.1 T696T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39X-01A-11D-A20W-10 chr11:120312471 T>C maps to NM_015313.2 A383A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZP-A9CV-01A-11D-A382-10 chr11:120280157 T>C maps to NM_015313.2 Y66Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9GV-01A-11D-A382-10 chr1:3390034 C>T maps to NM_014448.3 S418S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACL-01A-11D-A40R-10 chr11:73066956 A>T maps to NM_014786.3 K1208*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADJ-01A-11D-A40R-10 chr11:73021869 G>A maps to NM_014786.3 E729E. 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-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-ZP-A9CZ-01A-11D-A382-10 chr19:7528789 A>C maps to NM_001130955.1 R720R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10W-01A-11D-A12Z-10 chr5:148980771 A>G maps to NM_001001669.2 E96E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAE4-01A-11D-A40R-10 chr2:131785569 C>T maps to NM_015320.2 S160S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZP-A9D1-01A-11D-A382-10 chr2:131797620 C>T maps to NM_015320.2 D260D. 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-A3A0-01A-11D-A20W-10 chr13:111919987 T>C maps to NM_001113511.1 P369P. Only missense variants will be evaluated by CHASM.
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-AACK-01A-11D-A40R-10 chr13:111926287 A>T maps to NM_001113511.1 R422*. 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-DD-AACT-01A-11D-A40R-10 chr23:62926290 G>A did not map to a codon.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr23:62917039 G>T did not map to a codon.
Sequencing variant TCGA-2Y-A9HA-01A-11D-A38X-10 chr1:27023907 G>A maps to NM_006015.4 G338G. Only missense variants will be evaluated by CHASM.
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-CC-A9FS-01A-11D-A36X-10 chr1:27097795 A>T maps to NM_006015.4 K1129*. 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-DD-AAD5-01A-11D-A40R-10 chr1:27089689 G>C maps to NM_006015.4 G882G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAE7-01A-11D-A40R-10 chr1:27101212 C>T maps to NM_006015.4 Q1499*. 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-DD-AAE6-01A-11D-A40R-10 chr6:157222614 C>T maps to ENST00000367148 Q615*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr6:157502189 C>A maps to ENST00000367148 R1115R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3K-AAZ8-01A-12D-A38X-10 chr12:46231188 T>G maps to NM_152641.2 L370*. 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-CC-A7IE-01A-21D-A382-10 chr12:46254581 A>G did not map to a codon.
Sequencing variant TCGA-CC-A8HT-01A-11D-A35Z-10 chr12:46285640 T>A maps to NM_152641.2 C1667*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAC8-01A-11D-A40R-10 chr12:46205215 C>G maps to NM_152641.2 Y100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAVR-01A-11D-A40R-10 chr12:46231302 T>G maps to NM_152641.2 L381L. 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-G3-AAV4-01A-11D-A382-10 chr12:46243940 C>T maps to NM_152641.2 Q679*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-AA0U-01A-11D-A382-10 chr12:46246679 G>T did not map to a codon.
Sequencing variant TCGA-ZP-A9CV-01A-11D-A382-10 chr12:46230547 G>A maps to NM_152641.2 W266*. 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-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-WX-AA47-01A-11D-A38X-10 chr5:175798738 C>T maps to NM_173664.4 A192A. 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-CC-A9FW-01A-11D-A36X-10 chr3:93762020 A>T maps to NM_182896.2 K321*. 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-WQ-A9G7-01A-11D-A36X-10 chr3:97487016 C>T maps to NM_177976.1 C22C. 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-AADP-01A-11D-A38X-10 chr10:23235104 A>T maps to NM_173081.3 A27A. 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-AAEE-01A-11D-A40R-10 chr10:28276330 G>T maps to NM_018076.2 A122A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9GZ-01A-11D-A38X-10 chr3:138009427 C>A maps to ENST00000469044 I645I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A3KF-01A-11D-A20W-10 chr3:137960686 A>G maps to ENST00000469044 G300G. 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-DD-AAE8-01A-11D-A40R-10 chr23:100808334 G>C did not map to a codon.
Sequencing variant TCGA-DD-AAD6-01A-11D-A40R-10 chr23:100911128 G>T did not map to a codon.
Sequencing variant TCGA-DD-AADM-01A-11D-A40R-10 chr23:100911406 T>C did not map to a codon.
Sequencing variant TCGA-DD-AAE7-01A-11D-A40R-10 chr23:100912385 G>T did not map to a codon.
Sequencing variant TCGA-DD-AAE9-01A-11D-A40R-10 chr23:100911839 A>G did not map to a codon.
Sequencing variant TCGA-DD-AADV-01A-11D-A38X-10 chr23:100880298 C>T did not map to a codon.
Sequencing variant TCGA-DD-AAEI-01A-11D-A40R-10 chr23:100880946 T>G did not map to a codon.
Sequencing variant TCGA-DD-AAVY-01A-11D-A40R-10 chr23:100880444 T>A 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-ZP-A9CV-01A-11D-A382-10 chr23:100880945 A>G did not map to a codon.
Sequencing variant TCGA-2Y-A9GT-01A-11D-A382-10 chr23:100871589 C>A 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-DD-AAD0-01A-11D-A40R-10 chr23:100871396 C>T 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-EP-A2KA-01A-11D-A183-10 chr11:13408152 C>A maps to ENST00000403290 P577P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LG-A6GG-01A-11D-A30V-10 chr7:98955968 G>T maps to NM_006409.3 S240S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAE7-01A-11D-A40R-10 chr7:98985731 G>A maps to NM_005720.2 T80T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A2QR-01A-11D-A20W-10 chr12:110874443 T>C maps to NM_005719.2 G99G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZP-A9D0-01A-11D-A36X-10 chr1:183602267 T>C maps to ENST00000294742 L58L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAVZ-01A-11D-A40R-10 chr23:69498422 C>A did not map to a codon.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr23:69495999 C>T did not map to a codon.
Sequencing variant TCGA-FV-A495-01A-11D-A25V-10 chr23:69501564 C>T did not map to a codon.
Sequencing variant TCGA-ZP-A9D1-01A-11D-A382-10 chr23:69497339 A>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-A119-01A-11D-A12Z-10 chr15:98512599 T>C maps to NM_183376.2 Y291Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A8HT-01A-11D-A35Z-10 chr22:51065812 C>T maps to ENST00000395624 R82R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A9FS-01A-11D-A36X-10 chr22:51066153 G>A maps to ENST00000395624 A18A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A4XI-01A-11D-A25V-10 chr22:51064684 G>T maps to ENST00000395624 S292S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr22:51063860 A>G maps to ENST00000395624 P414P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73B-01A-12D-A32G-10 chr5:78280831 C>T maps to NM_000046.3 V80V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A118-01A-11D-A12Z-10 chr23:2835843 C>T did not map to a codon.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr23:2825610 A>G did not map to a codon.
Sequencing variant TCGA-DD-A39Z-01A-11D-A20W-10 chr23:2876321 T>C did not map to a codon.
Sequencing variant TCGA-G3-A3CJ-01A-11D-A20W-10 chr23:2861191 A>G 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-A39Y-01A-11D-A20W-10 chr23:2994594 T>C did not map to a codon.
Sequencing variant TCGA-BD-A3EP-01A-11D-A22F-10 chr17:66352819 A>G maps to NM_014960.3 R193R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9GZ-01A-11D-A38X-10 chr23:2947345 C>T did not map to a codon.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr23:2928165 T>C did not map to a codon.
Sequencing variant TCGA-DD-AADA-01A-11D-A40R-10 chr23:2951121 G>T 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-ED-A97K-01A-21D-A382-10 chr5:94922267 G>T maps to NM_198150.2 V234V. 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-A10W-01A-11D-A12Z-10 chr4:77018797 A>G maps to NM_001130016.1 G261G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MA-01A-11D-A20W-10 chr4:77003152 T>C maps to NM_001130016.1 T82T. 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-2Y-A9HA-01A-11D-A38X-10 chr23:25022794 C>A did not map to a codon.
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-G3-A3CG-01A-11D-A20W-10 chr8:17920691 A>G did not map to a codon.
Sequencing variant TCGA-RC-A6M4-01A-11D-A32G-10 chr11:122954394 A>T maps to NM_024769.2 S183S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WQ-A9G7-01A-11D-A36X-10 chr11:122968526 G>A maps to NM_024769.2 T54T. 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-4R-AA8I-01A-11D-A382-10 chr1:23763463 G>A maps to NM_017707.3 G472G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A2QR-01A-11D-A20W-10 chr1:23759639 A>G maps to NM_017707.3 C751C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-AAV4-01A-11D-A382-10 chr23:15306021 C>T did not map to a codon.
Sequencing variant TCGA-DD-A1EE-01A-11D-A12Z-10 chr23:63444956 C>A did not map to a codon.
Sequencing variant TCGA-DD-A1EE-01A-11D-A12Z-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-DD-AAVR-01A-11D-A40R-10 chr1:76397784 G>A maps to NM_080868.2 D64D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAVZ-01A-11D-A40R-10 chr14:94420804 G>A maps to ENST00000434324 A112A. 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-DD-A39Z-01A-11D-A20W-10 chr6:101095213 A>G maps to NM_006828.2 G1122G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K7-A5RG-01A-11D-A28X-10 chr11:8959173 T>A maps to NM_020646.1 R179*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CG-01A-11D-A20W-10 chr17:7077756 G>A maps to NM_001671.3 H126H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr1:155452063 G>A maps to ENST00000368346 S199S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BW-A5NQ-01A-11D-A27I-10 chr1:155385686 G>T maps to ENST00000368346 P1952P. 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-DD-A1ED-01A-11D-A152-10 chr1:155307889 A>G maps to ENST00000368346 P2936P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NN-01A-11D-A28X-10 chr1:155429585 G>T did not map to a codon.
Sequencing variant TCGA-DD-AAC8-01A-11D-A40R-10 chr1:155450302 T>A maps to ENST00000368346 T786T. 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-DD-AADE-01A-11D-A40R-10 chr7:65553860 C>G maps to NM_000048.3 L262L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9H0-01A-11D-A382-10 chr23:1742042 C>T did not map to a codon.
Sequencing variant TCGA-DD-AADM-01A-11D-A40R-10 chr23:1761897 C>G did not map to a codon.
Sequencing variant TCGA-BC-A3KF-01A-11D-A20W-10 chr23:1522163 A>C did not map to a codon.
Sequencing variant TCGA-DD-AAC8-01A-11D-A40R-10 chr23:1531640 G>A did not map to a codon.
Sequencing variant TCGA-XR-A8TF-01A-11D-A35Z-10 chr23:1571668 G>A did not map to a codon.
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-FV-A4ZQ-01A-11D-A25V-10 chr7:97482458 G>T maps to NM_183356.3 L463L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A3KG-01A-11D-A20W-10 chr2:190531151 T>C maps to NM_019048.2 Y98Y. 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-AAV2-01A-11D-A36X-10 chr16:29913161 C>T maps to NM_181718.3 A290A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACB-01A-11D-A40R-10 chr1:197065147 A>G maps to NM_018136.4 Y2989Y. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-CC-A3MB-01A-11D-A20W-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-2Y-A9H3-01A-11D-A382-10 chr1:176992546 G>A maps to ENST00000281881 P477P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADM-01A-11D-A40R-10 chr1:176913058 G>T maps to ENST00000281881 S790*. 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-WQ-A9G7-01A-11D-A36X-10 chr1:176926867 G>A maps to ENST00000281881 C619C. 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-2Y-A9H7-01A-11D-A38X-10 chr20:31021696 G>T maps to ENST00000375687 E566*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A9FW-01A-11D-A36X-10 chr20:31016224 G>A maps to ENST00000375687 Q157Q. Only missense variants will be evaluated by CHASM.
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-ZS-A9CF-01A-11D-A382-10 chr20:31024022 T>C maps to ENST00000375687 L1170L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CJ-01A-11D-A20W-10 chr2:26029193 A>G maps to NM_018263.4 P52P. 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-DD-A1ED-01A-11D-A152-10 chr18:31320167 T>C maps to NM_030632.1 L934L. 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-DD-AAC8-01A-11D-A40R-10 chr7:117060260 T>C maps to NM_130768.2 V132V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr10:89530706 A>T did not map to a codon.
Sequencing variant TCGA-DD-AACT-01A-11D-A40R-10 chr8:124383231 T>A did not map to a codon.
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-DD-A39Y-01A-11D-A20W-10 chr2:24033287 A>G maps to NM_017552.1 A784A. 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-DD-AADW-01A-11D-A38X-10 chr17:29159373 G>A maps to NM_024857.3 G3G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZS-A9CE-01A-11D-A36X-10 chr17:29187554 G>T maps to NM_024857.3 E1021*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-AAUZ-01A-11D-A382-10 chr19:50434172 A>C maps to NM_001193646.1 G22G. 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-CC-A3MA-01A-11D-A20W-10 chr12:53911112 T>C maps to NM_001130059.1 P431P. 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-5R-AAAM-01A-12D-A40R-10 chr2:234173606 T>C maps to ENST00000392018 C153C. 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-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-EP-A2KB-01A-11D-A183-10 chr14:96781571 C>A did not map to a codon.
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-DD-AAC8-01A-11D-A40R-10 chr3:112262915 T>A maps to NM_022488.3 T127T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADS-01A-11D-A40R-10 chr23:107381368 A>T did not map to a codon.
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-AAD5-01A-11D-A40R-10 chr14:51079993 T>C maps to ENST00000358385 V216V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CJ-01A-11D-A20W-10 chr14:51094798 A>G maps to ENST00000358385 K390K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAVW-01A-11D-A40R-10 chr2:38604336 C>T maps to NM_001135673.1 R22R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CG-01A-11D-A20W-10 chr11:63398634 C>T maps to NM_015459.3 L472L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADP-01A-11D-A38X-10 chr11:108205693 A>T did not map to a codon.
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-DD-AAD3-01A-11D-A40R-10 chr12:7045872 T>C maps to NM_001940.3 H481H. 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-2Y-A9H6-01A-11D-A38X-10 chr2:85981809 A>G maps to NM_032827.6 S166S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACI-01A-11D-A40R-10 chr15:25971122 A>G maps to NM_024490.3 V318V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9GZ-01A-11D-A38X-10 chr5:160059336 A>G maps to NM_025153.2 D473D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAC8-01A-11D-A40R-10 chr5:160071196 T>A maps to NM_025153.2 R272R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADE-01A-11D-A40R-10 chr5:160049549 G>A maps to NM_025153.2 R555*. 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-DD-AAED-01A-12D-A40R-10 chr3:182597382 C>T maps to NM_014616.1 C784C. 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-DD-AAC8-01A-11D-A40R-10 chr13:25283839 A>T maps to NM_001185085.1 G885G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr13:25276159 G>T maps to NM_001185085.1 E663*. Only missense variants will be evaluated by CHASM.
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-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-AADQ-01A-11D-A40R-10 chr1:17318783 G>T maps to NM_022089.2 V653V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CJ-01A-11D-A20W-10 chr1:17314702 G>T maps to NM_022089.2 S930*. 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-DD-A3A0-01A-11D-A20W-10 chr3:193029640 T>C maps to NM_198505.2 Q803Q. 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-CC-A8HU-01A-11D-A35Z-10 chr1:160100080 G>T maps to NM_000702.3 G551*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADB-01A-11D-A40R-10 chr1:160093073 A>G maps to NM_000702.3 T83T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5R-AAAM-01A-12D-A40R-10 chr1:160128806 C>A maps to NM_144699.3 R181R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EG-01A-11D-A20W-10 chr1:160136350 C>A maps to NM_144699.3 R361R. Only missense variants will be evaluated by CHASM.
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-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-DD-AADR-01A-11D-A40R-10 chr12:110778772 C>T maps to NM_170665.3 Q691*. 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-DD-AACI-01A-11D-A40R-10 chr12:90020266 T>A maps to ENST00000428670 K365*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAEB-01A-11D-A40R-10 chr12:90035971 G>C maps to ENST00000428670 G123G. 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-G3-A3CG-01A-11D-A20W-10 chr3:10443862 T>C maps to NM_001001331.2 E189E. 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-DD-AAC8-01A-11D-A40R-10 chr23:152845549 A>T did not map to a codon.
Sequencing variant TCGA-DD-AADN-01A-11D-A40R-10 chr23:152814215 C>T did not map to a codon.
Sequencing variant TCGA-DD-AADU-01A-11D-A40R-10 chr23:152801800 G>T did not map to a codon.
Sequencing variant TCGA-DD-AADY-01A-11D-A40R-10 chr23:152825343 A>T did not map to a codon.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr23:152821528 G>T did not map to a codon.
Sequencing variant TCGA-XR-A8TG-01A-11D-A35Z-10 chr23:152815621 A>C did not map to a codon.
Sequencing variant TCGA-BC-A3KG-01A-11D-A20W-10 chr3:130716554 A>G maps to NM_001001486.1 S783S. Only missense variants will be evaluated by CHASM.
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-A7IH-01A-11D-A33K-10 chr16:84459338 A>T did not map to a codon.
Sequencing variant TCGA-DD-AAD6-01A-11D-A40R-10 chr16:84402320 G>A did not map to a codon.
Sequencing variant TCGA-DD-A113-01A-11D-A12Z-10 chr23:153657460 T>A did not map to a codon.
Sequencing variant TCGA-DD-A39Y-01A-11D-A20W-10 chr23:153664090 T>C did not map to a codon.
Sequencing variant TCGA-DD-A3A0-01A-11D-A20W-10 chr17:40635053 A>G did not map to a codon.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr16:2564162 C>A maps to NM_001694.3 S20*. 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-DD-A3A0-01A-11D-A20W-10 chr3:113514006 T>C maps to NM_001690.3 C394C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAC8-01A-11D-A40R-10 chr8:20068077 A>T did not map to a codon.
Sequencing variant TCGA-FV-A2QR-01A-11D-A20W-10 chr8:20074765 A>G maps to NM_001693.3 S399S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAE7-01A-11D-A40R-10 chr8:104065038 A>G maps to NM_001695.4 E154E. 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-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-DD-A3A1-01A-11D-A20W-10 chr23:77284803 T>C did not map to a codon.
Sequencing variant TCGA-DD-AAC9-01A-11D-A40R-10 chr23:77245379 A>G did not map to a codon.
Sequencing variant TCGA-DD-AADG-01A-11D-A40R-10 chr23:77258570 A>T 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-2Y-A9H5-01A-11D-A382-10 chr18:55315839 C>T maps to NM_005603.4 S1212S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACH-01A-11D-A40R-10 chr18:55373802 G>C maps to NM_005603.4 V66V. 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-A39Y-01A-11D-A20W-10 chr15:35742949 T>C maps to NM_080650.3 E147E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr3:142272230 T>C maps to NM_001184.3 K881K. 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-DD-AAC8-01A-11D-A40R-10 chr3:142188238 T>A maps to NM_001184.3 I2164I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAEH-01A-11D-A40R-10 chr3:142278091 C>A did not map to a codon.
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-XR-A8TF-01A-11D-A35Z-10 chr20:3619492 C>T maps to NM_139321.2 Q1321*. 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-DD-AAC8-01A-11D-A40R-10 chr10:117059541 A>G did not map to a codon.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr10:117093837 C>T maps to NM_207303.2 C1028C. 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-XR-A8TG-01A-11D-A35Z-10 chr10:117154257 C>T maps to NM_207303.2 Q1089*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr23:76920178 T>C did not map to a codon.
Sequencing variant TCGA-BC-A3KF-01A-11D-A20W-10 chr23:76812949 T>C did not map to a codon.
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-DD-AAC8-01A-11D-A40R-10 chr23:76872152 C>G did not map to a codon.
Sequencing variant TCGA-DD-AAE3-01A-11D-A40R-10 chr23:76776918 C>T 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-ZP-A9D4-01A-11D-A36X-10 chr23:76938719 A>G 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-G3-A3CG-01A-11D-A20W-10 chr12:111926326 T>C maps to NM_002973.3 A891A. 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-AADM-01A-11D-A40R-10 chr7:105260693 G>A maps to NM_020725.1 F490F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr7:105260738 T>C maps to NM_020725.1 G475G. 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-ES-A2HS-01A-11D-A183-10 chr17:8110165 G>T maps to NM_004217.2 R147R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr7:70254961 C>T maps to NM_015570.2 D920D. 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-4R-AA8I-01A-11D-A382-10 chr7:32612908 C>T maps to NM_015060.1 H483H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EG-01A-11D-A20W-10 chr7:32535338 A>G maps to NM_015060.1 R6R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAVX-01A-11D-A40R-10 chr23:153171431 C>T did not map to a codon.
Sequencing variant TCGA-WX-AA44-01A-11D-A38X-10 chr23:153171244 C>T did not map to a codon.
Sequencing variant TCGA-DD-AACT-01A-11D-A40R-10 chr23:69269751 T>A did not map to a codon.
Sequencing variant TCGA-2Y-A9H7-01A-11D-A38X-10 chr16:396146 C>G did not map to a codon.
Sequencing variant TCGA-BW-A5NP-01A-11D-A27I-10 chr16:347720 C>T did not map to a codon.
Sequencing variant TCGA-CC-A9FS-01A-11D-A36X-10 chr16:347106 C>T maps to NM_003502.3 W635*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A9FU-01A-11D-A36X-10 chr16:360069 C>A did not map to a codon.
Sequencing variant TCGA-DD-AADS-01A-11D-A40R-10 chr16:347191 T>A maps to NM_003502.3 K607*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAE1-01A-11D-A40R-10 chr16:396739 G>A maps to NM_003502.3 Q96*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAE6-01A-11D-A40R-10 chr16:396163 C>A maps to NM_003502.3 E288*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAVS-01A-11D-A40R-10 chr16:354368 C>A maps to NM_003502.3 E397*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAVU-01A-11D-A40R-10 chr16:360037 G>A maps to NM_003502.3 Q351*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A8O5-01A-11D-A35Z-10 chr16:348174 C>T maps to NM_003502.3 W444*. Only missense variants will be evaluated by CHASM.
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-XR-A8TC-01A-11D-A35Z-10 chr16:347848 C>A maps to NM_003502.3 E553*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A8O5-01A-11D-A35Z-10 chr17:63534460 T>A maps to NM_004655.3 R354*. 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-AACQ-01A-11D-A40R-10 chr17:79167867 T>A maps to ENST00000269392 K730*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5C-A9VG-01A-11D-A36X-10 chr3:28382057 G>A maps to NM_022461.3 A17A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5R-AA1C-01A-11D-A40R-10 chr8:103855816 C>A maps to NM_148174.2 G22*. 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-DD-AACQ-01A-11D-A40R-10 chr11:134253921 G>T maps to NM_054025.2 P91P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr6:71603971 G>A maps to NM_080742.2 R199*. 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-DD-AADS-01A-11D-A40R-10 chr6:71603942 A>T maps to NM_080742.2 P208P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3K-AAZ8-01A-12D-A38X-10 chr11:62389401 C>T maps to NM_012200.2 K6K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADE-01A-11D-A40R-10 chr11:62388012 G>A maps to NM_012200.2 P71P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9GZ-01A-11D-A38X-10 chr12:122691553 C>T maps to NM_030765.2 P252P. 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.
Multiple mappings detected for codon TCGA-CC-5259-01A-31D-A20W-10. Mapping will be selected arbitrarily.
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-4R-AA8I-01A-11D-A382-10 chr16:67184216 A>G maps to NM_033309.2 L58L. 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-DD-A1EE-01A-11D-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-DD-AACL-01A-11D-A40R-10 chr11:379651 A>T maps to NM_178537.4 P813P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZP-A9D4-01A-11D-A36X-10 chr3:118948706 C>T maps to NM_212543.1 V80V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr18:29207085 T>C did not map to a codon.
Sequencing variant TCGA-DD-AACK-01A-11D-A40R-10 chr19:41860748 C>A maps to NM_030578.3 V128V. 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-5R-AA1C-01A-11D-A40R-10 chr21:30701997 C>A maps to NM_206866.1 S587*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADU-01A-11D-A40R-10 chr21:30698822 A>G maps to NM_206866.1 K226K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAVU-01A-11D-A40R-10 chr6:90661176 G>A maps to NM_001170794.1 T216T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADN-01A-11D-A40R-10 chr6:57037533 G>T maps to NM_004282.3 G13G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACK-01A-11D-A40R-10 chr8:38065142 T>C maps to NM_004874.2 S164S. 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-5R-AA1C-01A-11D-A40R-10 chr15:40751535 A>G maps to NM_014952.3 P291P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAD8-01A-11D-A40R-10 chr15:40757559 G>A maps to NM_014952.3 S693S. 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-WQ-A9G7-01A-11D-A36X-10 chr8:143563065 C>T maps to NM_001702.2 D708D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WQ-A9G7-01A-11D-A36X-10 chr8:143599548 C>T maps to NM_001702.2 G956G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZS-A9CG-01A-11D-A36X-10 chr8:143624959 A>G did not map to a codon.
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-5R-AA1C-01A-11D-A40R-10 chr6:70071151 T>C maps to NM_001704.2 N1329N. 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-EP-A2KB-01A-11D-A183-10 chr6:69684658 T>C maps to NM_001704.2 P510P. 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-A1EG-01A-11D-A20W-10 chr4:102946502 T>C maps to NM_017935.4 S477S. 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-DD-AADA-01A-11D-A40R-10 chr3:52437794 G>A maps to NM_004656.2 Q456*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADA-01A-11D-A40R-10 chr3:52441303 G>A maps to NM_004656.2 Q156*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADF-01A-11D-A40R-10 chr3:52439293 C>T maps to NM_004656.2 A316A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAVR-01A-11D-A40R-10 chr3:52436362 T>A maps to NM_004656.2 K711*. Only missense variants will be evaluated by CHASM.
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-ZS-A9CF-01A-11D-A382-10 chr2:215674278 C>A maps to NM_000465.2 R5R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAD3-01A-11D-A40R-10 chr1:91180224 A>T maps to NM_020063.1 A238A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACK-01A-11D-A40R-10 chr5:17275576 G>A maps to NM_006317.3 K84K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MB-01A-11D-A20W-10 chr6:31599887 T>C maps to NM_080686.2 P1146P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAE0-01A-11D-A40R-10 chr6:31600193 T>G maps to NM_080686.2 A1248A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr9:134353912 T>C maps to NM_013318.3 G1555G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A4ZP-01A-12D-A25V-10 chr9:134363452 C>T maps to NM_013318.3 A2065A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-AAV4-01A-11D-A382-10 chr9:134323168 C>G maps to NM_013318.3 A366A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A7SH-01A-11D-A382-10 chr9:134334700 G>A maps to NM_013318.3 P454P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACQ-01A-11D-A40R-10 chr1:171556149 A>G maps to ENST00000392078 V2586V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A8O5-01A-11D-A35Z-10 chr1:171511281 C>T maps to ENST00000392078 N1559N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A2QR-01A-11D-A20W-10 chr1:171510372 C>T maps to ENST00000392078 V1256V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IJ-01A-11D-A33Q-10 chr6:31608212 T>C maps to ENST00000404765 E1029E. 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-DD-AAE3-01A-11D-A40R-10 chr14:35331371 T>C maps to NM_013448.2 L90L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A2QR-01A-11D-A20W-10 chr14:35227927 T>C maps to NM_013448.2 K1456K. 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-A2HS-01A-11D-A183-10 chr12:56998904 C>T maps to NM_013449.3 R902R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAD0-01A-11D-A40R-10 chr2:160257108 C>A did not map to a codon.
Sequencing variant TCGA-DD-AAW3-01A-11D-A40P-10 chr2:160231233 C>A maps to NM_013450.2 E1346*. Only missense variants will be evaluated by CHASM.
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-ZS-A9CD-01A-11D-A36X-10 chr2:160181398 T>C maps to NM_013450.2 K2092K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADS-01A-11D-A40R-10 chr11:27114794 A>T maps to NM_003986.2 K139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr12:76740855 A>G maps to NM_024685.3 S303S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A8O6-01A-11D-A35Z-10 chr12:76741191 T>G maps to NM_024685.3 S191S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAE2-01A-11D-A40R-10 chr4:123663997 T>A maps to NM_152618.2 T317T. 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-DD-A3A1-01A-11D-A20W-10 chr16:56533695 T>C maps to NM_031885.3 A507A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAC8-01A-11D-A40R-10 chr2:170355993 A>T did not map to a codon.
Sequencing variant TCGA-DD-AACL-01A-11D-A40R-10 chr4:122789149 T>A maps to NM_176824.1 R30*. Only missense variants will be evaluated by CHASM.
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-ZS-A9CE-01A-11D-A36X-10 chr3:107492028 A>T maps to NM_001142568.1 I487I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr19:45322316 G>T maps to NM_005581.3 S447S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A3KF-01A-11D-A20W-10 chr1:156622301 A>G maps to NM_021948.3 S520S. 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-G3-AAV4-01A-11D-A382-10 chr23:152966417 C>T did not map to a codon.
Sequencing variant TCGA-DD-AAC8-01A-11D-A40R-10 chr20:52601944 T>A maps to NM_003657.2 K341*. 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-EP-A2KB-01A-11D-A183-10 chr17:59024695 G>T maps to ENST00000407086 G402*. Only missense variants will be evaluated by CHASM.
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-DD-AAEG-01A-11D-A38X-10 chr12:50236858 G>A maps to NM_181708.2 P4P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAVY-01A-11D-A40R-10 chr3:165548041 C>T maps to NM_000055.2 A260A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K7-AAU7-01A-11D-A382-10 chr14:99641662 C>A maps to NM_138576.2 E504*. 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-ZS-A9CG-01A-11D-A36X-10 chr14:99640841 C>T maps to NM_138576.2 P777P. 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-AAEG-01A-11D-A38X-10 chr19:50169298 G>A maps to NM_138639.1 R73R. 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-DD-AACC-01A-11D-A40R-10 chr3:187446199 C>T maps to NM_001706.4 T496T. 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-4R-AA8I-01A-11D-A382-10 chr11:118779168 G>A maps to NM_182557.2 G74G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACC-01A-11D-A40R-10 chr11:118771949 C>T maps to NM_182557.2 K834K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACI-01A-11D-A40R-10 chr6:136597257 C>A maps to NM_014739.2 E469*. 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-EP-A2KA-01A-11D-A183-10 chr23:39934378 G>T 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-4R-AA8I-01A-11D-A382-10 chr23:129185837 A>G 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-WQ-A9G7-01A-11D-A36X-10 chr23:129185868 T>C 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-4R-AA8I-01A-11D-A382-10 chr14:96730966 C>T maps to NM_000710.2 G316G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9H8-01A-11D-A38X-10 chr5:70782326 T>C maps to NM_018429.2 F362F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAD1-01A-11D-A40R-10 chr5:70806320 G>A maps to NM_018429.2 V1134V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAC8-01A-11D-A40R-10 chr23:18183180 A>T did not map to a codon.
Sequencing variant TCGA-DD-AACP-01A-11D-A40R-10 chr23:18189190 T>C did not map to a codon.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr4:42127599 C>T maps to NM_207406.3 E382E. Only missense variants will be evaluated by CHASM.
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.
Sequencing variant TCGA-DD-A1ED-01A-11D-A152-10 chr10:13541880 A>G maps to ENST00000396900 G115G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-AAV3-01A-11D-A36X-10 chr10:13523007 C>T maps to ENST00000396900 A318A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACF-01A-11D-A40R-10 chr19:12865363 A>G did not map to a codon.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr19:12866496 T>C maps to NM_017682.2 A261A. 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-ED-A8O5-01A-11D-A35Z-10 chr20:17489604 G>T maps to NM_001195.3 R222R. 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-EP-A2KA-01A-11D-A183-10 chr23:102004394 G>T 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-RC-A7SH-01A-11D-A382-10 chr12:26275004 A>T maps to NM_030762.2 A481A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A7SH-01A-11D-A382-10 chr10:60577442 G>C maps to NM_001080512.1 L885L. 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-DD-AAC8-01A-11D-A40R-10 chr12:32369350 A>T maps to NM_001714.2 A128A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39Z-01A-11D-A20W-10 chr9:95481865 T>C did not map to a codon.
Sequencing variant TCGA-DD-AAE1-01A-11D-A40R-10 chr9:95481420 C>T maps to NM_001003800.1 L502L. 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-EP-A2KB-01A-11D-A183-10 chr11:102206785 G>T maps to NM_182962.1 G472*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr2:32696134 C>T maps to NM_016252.3 L2179L. 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-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-AAC8-01A-11D-A40R-10 chr2:32661166 A>T maps to NM_016252.3 L1182L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACE-01A-11D-A40R-10 chr2:32774377 A>G did not map to a codon.
Sequencing variant TCGA-DD-AACJ-01A-11D-A40R-10 chr2:32724674 C>T maps to NM_016252.3 L2844L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EG-01A-11D-A20W-10 chr13:103486899 A>G maps to NM_017693.3 K373K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr15:91328232 T>C maps to NM_000057.2 A915A. 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-BC-A10U-01A-11D-A12Z-10 chr10:22618023 A>G maps to NM_005180.6 L206L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39X-01A-11D-A20W-10 chr10:22616562 T>C maps to NM_005180.6 V83V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CG-01A-11D-A20W-10 chr10:22618053 A>G maps to NM_005180.6 R216R. 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-WJ-A86L-01A-12D-A45V-10 chr23:50658935 G>T did not map to a codon.
Sequencing variant TCGA-DD-AAD3-01A-11D-A40R-10 chr6:7879307 T>C maps to NM_001718.4 D402D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr20:55758795 G>T maps to NM_001719.2 R314R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr1:39991421 C>A maps to NM_181809.3 I387I. Only missense variants will be evaluated by CHASM.
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-DD-AACZ-01A-11D-A40R-10 chr7:34118742 G>A maps to NM_133468.3 A451A. 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-DD-AADG-01A-11D-A40R-10 chr2:203383669 G>A maps to NM_001204.6 V249V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A7PZ-01A-11D-A33Q-10 chr2:203379608 A>T did not map to a codon.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr2:203420955 C>A maps to NM_001204.6 T856T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-AAV6-01A-21D-A36X-10 chr10:43312902 T>G maps to NM_014753.3 Y847*. 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-DD-AAD1-01A-11D-A40R-10 chr23:15560109 T>C did not map to a codon.
Sequencing variant TCGA-DD-AAEG-01A-11D-A38X-10 chr23:15555297 G>C 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-G3-AAUZ-01A-11D-A382-10 chr9:16738419 C>A maps to NM_017637.5 E23*. 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-DD-A39Y-01A-11D-A20W-10 chr1:151019161 A>G maps to NM_138278.3 *358W. 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-2Y-A9H3-01A-11D-A382-10 chr4:13603609 G>T maps to NM_148894.2 I1638I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3K-AAZ8-01A-12D-A38X-10 chr4:13578589 G>A maps to NM_148894.2 R2970R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IK-01A-12D-A33Q-10 chr4:13616093 T>C maps to NM_148894.2 L300L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EL-01A-11D-A152-10 chr4:13617011 C>A maps to NM_148894.2 T161T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A0-01A-11D-A20W-10 chr4:13582664 T>C maps to NM_148894.2 K2894K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75I-01A-11D-A32G-10 chr4:13610293 T>C did not map to a codon.
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-LG-A9QD-01A-11D-A382-10 chr20:36954701 C>A maps to NM_001725.2 I347I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZP-A9CY-01A-11D-A382-10 chr22:32827370 A>G maps to NM_174932.2 L394L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZS-A9CF-01A-11D-A382-10 chr20:31622066 G>A maps to NM_174897.2 V91V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9H6-01A-11D-A38X-10 chr17:65920660 A>G did not map to a codon.
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-DD-A39X-01A-11D-A20W-10 chr17:65971930 A>G maps to ENST00000321892 E2987E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr17:65960450 C>T maps to ENST00000321892 A2921A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr17:65850815 T>C maps to ENST00000321892 H458H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WQ-A9G7-01A-11D-A36X-10 chr17:65924472 A>G maps to ENST00000321892 K2044K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WX-AA46-01A-11D-A38X-10 chr17:65916144 G>T maps to ENST00000321892 E1941*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5C-A9VH-01A-11D-A36X-10 chr17:41246776 A>G maps to ENST00000471181 H257H. 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-DD-A39Z-01A-11D-A20W-10 chr13:32911476 A>G maps to NM_000059.3 G995G. 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-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-BC-A3KF-01A-11D-A20W-10 chr6:32946060 C>T maps to ENST00000395289 P579P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAC8-01A-11D-A40R-10 chr9:136905392 T>A did not map to a codon.
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-DD-AAE6-01A-11D-A40R-10 chr16:50354272 C>A maps to NM_001173984.2 E549*. 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-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-ZP-A9D4-01A-11D-A36X-10 chr5:892719 C>T did not map to a codon.
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-DD-A39Y-01A-11D-A20W-10 chr2:28210935 A>G maps to NM_004899.3 P94P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAE8-01A-11D-A40R-10 chr14:105766804 C>T maps to NM_001519.2 V54V. 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-G3-A3CG-01A-11D-A20W-10 chr17:59871068 T>C maps to NM_032043.2 E454E. 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-DD-AACI-01A-11D-A40R-10 chr23:135570515 T>A did not map to a codon.
Sequencing variant TCGA-2Y-A9GT-01A-11D-A382-10 chr19:55815038 C>T maps to NM_032430.1 P377P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAE7-01A-11D-A40R-10 chr19:55798666 T>A maps to NM_032430.1 L106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A2QR-01A-11D-A20W-10 chr19:55815938 A>G maps to NM_032430.1 S456S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A3KG-01A-11D-A20W-10 chr21:40571298 T>C maps to NM_018963.3 E1681E. 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-ES-A2HS-01A-11D-A183-10 chr21:40568901 C>T maps to NM_018963.3 R2031R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr23:79965041 C>T did not map to a codon.
Sequencing variant TCGA-5R-AAAM-01A-12D-A40R-10 chr23:79971673 T>C did not map to a codon.
Sequencing variant TCGA-CC-A5UD-01A-11D-A28X-10 chr23:79989644 T>A did not map to a codon.
Sequencing variant TCGA-DD-A3A1-01A-11D-A20W-10 chr23:79947358 T>C 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-DD-AAC8-01A-11D-A40R-10 chr19:579506 A>T maps to NM_001728.2 T141T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr19:582315 C>A maps to NM_001728.2 A360A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A8HT-01A-11D-A35Z-10 chr3:49691917 C>T maps to NM_003458.3 C1643C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-AAV0-01A-11D-A36X-10 chr3:49694956 C>A maps to NM_003458.3 A2656A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1ED-01A-11D-A152-10 chr10:93718880 T>C maps to NM_003972.2 G320G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-AAV5-01A-11D-A36X-10 chr10:93716305 G>A maps to NM_003972.2 E241E. 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-5C-A9VG-01A-11D-A36X-10 chr12:108013778 G>A maps to NM_001018072.1 L823L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A8O5-01A-11D-A35Z-10 chr12:108029087 C>T maps to NM_001018072.1 C886C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A116-01A-11D-A12Z-10 chr16:3651152 C>A maps to NM_032444.2 V330V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAEE-01A-11D-A40R-10 chr16:3633141 C>T maps to NM_032444.2 V1703V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAW2-01A-11D-A40P-10 chr16:3647562 C>A maps to NM_032444.2 T500T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3K-AAZ8-01A-12D-A38X-10 chr20:11899219 G>A maps to NM_014962.2 W99*. Only missense variants will be evaluated by CHASM.
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-A3CG-01A-11D-A20W-10 chr4:75673277 T>C maps to NM_001729.2 E170E. 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-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-ES-A2HT-01A-12D-A183-10 chr6:26413706 T>C maps to NM_007048.5 T443T. Only missense variants will be evaluated by CHASM.
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-DD-AAD1-01A-11D-A40R-10 chr6:26452497 G>A maps to NM_006994.4 P538P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BD-A3EP-01A-11D-A22F-10 chr5:180486678 C>T maps to NM_152547.4 H475H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A2QR-01A-11D-A20W-10 chr10:103190118 T>C maps to NM_033637.2 S22S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr2:111416239 C>T maps to NM_004336.3 T452T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39X-01A-11D-A20W-10 chr2:111408294 A>G maps to NM_004336.3 R677R. 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-DD-AAD8-01A-11D-A40R-10 chr17:56383219 G>T maps to NM_004758.2 S1744*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WQ-A9G7-01A-11D-A36X-10 chr17:56385232 G>A maps to NM_004758.2 R1601*. 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-DD-AADS-01A-11D-A40R-10 chr7:16720988 C>A maps to NM_014038.2 S100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9GZ-01A-11D-A38X-10 chr10:121616947 G>A maps to NM_024834.2 Q111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CG-01A-11D-A20W-10 chr10:121595142 G>C maps to NM_024834.2 S541*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr10:98743213 C>A maps to NM_015652.2 T689T. 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-4R-AA8I-01A-11D-A382-10 chr10:21804624 G>A maps to NM_207371.3 C709C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACZ-01A-11D-A40R-10 chr10:21805482 C>T maps to NM_207371.3 E423E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADW-01A-11D-A38X-10 chr10:21805719 A>G maps to NM_207371.3 H344H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAE4-01A-11D-A40R-10 chr10:21805719 A>G maps to NM_207371.3 H344H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr10:5789184 G>T maps to NM_017782.4 V1267V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A8HT-01A-11D-A35Z-10 chr10:5791216 A>C maps to NM_017782.4 R1945R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr10:100003863 A>G maps to ENST00000314594 E776E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAEK-01A-11D-A40R-10 chr10:99991444 G>A did not map to a codon.
Sequencing variant TCGA-DD-AAEB-01A-11D-A40R-10 chr10:104620106 C>A maps to NM_001136200.1 R54R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACE-01A-11D-A40R-10 chr10:11912119 G>A maps to NM_153256.3 L341L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr10:73511593 G>T maps to NM_022153.1 P243P. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-EP-A2KA-01A-11D-A183-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-5R-AA1C-01A-11D-A40R-10 chr10:50534396 G>A maps to NM_001135196.1 A1269A. 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-WX-AA46-01A-11D-A38X-10 chr10:50285294 C>T maps to NM_001031746.3 W201*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MC-01A-11D-A33Q-10 chr10:103766309 C>T maps to NM_024541.2 P345P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A0-01A-11D-A20W-10 chr10:105921775 A>G maps to ENST00000389588 A1120A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A9-01A-11D-A25V-10 chr10:105952056 A>G maps to ENST00000389588 Y483Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CJ-01A-11D-A20W-10 chr10:115529652 A>G maps to NM_182601.1 Q176Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9HA-01A-11D-A38X-10 chr10:120070723 T>C maps to NM_022063.2 A215A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACI-01A-11D-A40R-10 chr10:128150125 T>A maps to NM_001004298.2 V521V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr10:118116935 C>T maps to NM_198515.2 Q165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADM-01A-11D-A40R-10 chr10:118084529 T>C maps to NM_198515.2 L3L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADF-01A-11D-A40R-10 chr10:85933618 A>T maps to NM_207373.2 L4L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CK-01A-11D-A20W-10 chr11:64877951 A>G did not map to a codon.
Sequencing variant TCGA-2V-A95S-01A-11D-A36X-10 chr11:76175033 C>T maps to ENST00000393457 S248S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A3KF-01A-11D-A20W-10 chr11:76227255 T>C maps to ENST00000393457 A529A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr11:33628352 A>T maps to ENST00000389726 A1391A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr11:33573675 G>T maps to ENST00000389726 A957A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-AAUZ-01A-11D-A382-10 chr11:33628244 C>A maps to ENST00000389726 A1355A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-AAV0-01A-11D-A36X-10 chr11:33565295 T>A maps to ENST00000389726 I432I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr11:33564932 A>G maps to ENST00000389726 S311S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZP-A9CV-01A-11D-A382-10 chr11:33628361 C>T maps to ENST00000389726 N1394N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr11:30354501 A>G maps to NM_152316.1 K172K. 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-EP-A2KA-01A-11D-A183-10 chr11:16774368 T>C maps to NM_014267.5 S82S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAC8-01A-11D-A40R-10 chr11:124637131 T>A maps to ENST00000374979 A540A. Only missense variants will be evaluated by CHASM.
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-DD-AADM-01A-11D-A40R-10 chr11:122774671 T>C maps to NM_024806.2 Y128Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A8O5-01A-11D-A35Z-10 chr11:108264020 T>C maps to NM_152587.3 R215R. 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-BC-A3KG-01A-11D-A20W-10 chr11:66581346 T>C maps to ENST00000360962 Y351Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9H4-01A-11D-A382-10 chr12:27059305 C>T maps to NM_018164.2 Q670Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr12:91348402 A>G maps to NM_152638.2 H39H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39X-01A-11D-A20W-10 chr12:91348441 C>T maps to NM_152638.2 W26*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr12:32137296 A>G maps to NM_018169.3 K1136K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A114-01A-11D-A12Z-10 chr12:32137831 G>T maps to NM_018169.3 E1315*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K7-AAU7-01A-11D-A382-10 chr12:32138703 G>A maps to NM_018169.3 R1605R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr12:32137546 A>T maps to NM_018169.3 R1220*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CJ-01A-11D-A20W-10 chr12:21684113 T>C maps to NM_030572.2 S112S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A3KG-01A-11D-A20W-10 chr12:4599702 T>C maps to NM_020374.2 Q517Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr12:52470973 A>G maps to NM_021934.4 *219W. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9H2-01A-12D-A382-10 chr12:102569311 C>T maps to NM_017915.3 G291G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39X-01A-11D-A20W-10 chr12:112667540 T>C maps to NM_001109662.2 G1988G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A0-01A-11D-A20W-10 chr12:112703053 T>C maps to NM_001109662.2 R666R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CG-01A-11D-A20W-10 chr12:112613661 G>A maps to NM_001109662.2 V3652V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CJ-01A-11D-A20W-10 chr12:112685270 T>C maps to NM_001109662.2 S1272S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-AAV5-01A-11D-A36X-10 chr12:112617069 G>A maps to NM_001109662.2 Q3535*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LG-A9QC-01A-11D-A36X-10 chr12:112673431 G>A maps to NM_001109662.2 N1695N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WQ-A9G7-01A-11D-A36X-10 chr12:112613604 G>T maps to NM_001109662.2 A3671A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A1-01A-11D-A20W-10 chr12:64664452 A>G maps to NM_001170633.1 G542G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A9FU-01A-11D-A36X-10 chr12:7053298 G>T maps to NM_138425.2 S5S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9GU-01A-11D-A382-10 chr12:80707413 T>C did not map to a codon.
Sequencing variant TCGA-BC-A3KF-01A-11D-A20W-10 chr12:80714406 A>T maps to NM_173591.3 T1327T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A3KG-01A-11D-A20W-10 chr12:80722447 T>C maps to NM_173591.3 V1392V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EB-01A-11D-A12Z-10 chr12:80761992 A>G maps to NM_173591.3 V2164V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAC8-01A-11D-A40R-10 chr12:80655747 G>C did not map to a codon.
Sequencing variant TCGA-3K-AAZ8-01A-12D-A38X-10 chr12:25148919 T>A maps to NM_001101339.1 R76R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADD-01A-11D-A40R-10 chr13:39587546 A>G maps to NM_025138.3 P614P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAC8-01A-11D-A40R-10 chr13:43360936 T>A maps to NM_182508.2 I46I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-AAV1-01A-11D-A382-10 chr13:31495897 G>A maps to NM_032849.3 T234T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5260-01A-01D-A12Z-10 chr14:57075882 C>G maps to NM_017799.3 P232P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A2QR-01A-11D-A20W-10 chr14:57083975 A>G maps to NM_017799.3 R339R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A5-01A-11D-A22F-10 chr14:45700392 A>G maps to NM_018353.4 D515D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EE-01A-11D-A12Z-10 chr14:76668082 A>G maps to NM_017926.2 K446K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACZ-01A-11D-A40R-10 chr14:23567274 A>G maps to NM_017924.2 T136T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr14:31926575 A>C maps to NM_080664.2 P8P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A2QR-01A-11D-A20W-10 chr14:60585411 T>C did not map to a codon.
Sequencing variant TCGA-G3-A3CJ-01A-11D-A20W-10 chr14:60581570 A>G maps to ENST00000404681 G281G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XR-A8TC-01A-11D-A35Z-10 chr14:60590985 T>G maps to ENST00000404681 V699V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9GZ-01A-11D-A38X-10 chr14:81251870 C>A maps to NM_152446.3 E527*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MC-01A-11D-A22F-10 chr14:81251619 A>C maps to NM_152446.3 A610A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADJ-01A-11D-A40R-10 chr14:80993293 T>C maps to NM_152446.3 G997G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CK-01A-11D-A20W-10 chr14:77873884 A>G maps to NM_001113475.1 N151N. 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-CC-A7IH-01A-11D-A33K-10 chr14:77843997 T>A maps to NM_001010860.1 P79P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr14:99183502 G>T maps to NM_182560.2 G90G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CG-01A-11D-A20W-10 chr14:99182533 T>C maps to NM_182560.2 H2H. 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-NI-A8LF-01A-11D-A35Z-10 chr14:60928093 C>T maps to NM_174978.2 Q365Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9H1-01A-11D-A382-10 chr14:77493178 C>A maps to NM_024496.2 S319S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75G-01A-11D-A32G-10 chr14:77493781 C>T maps to NM_024496.2 Q118Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-4073-01B-02D-A12Z-10 chr14:74189520 C>T maps to NM_001043318.1 V868V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CG-01A-11D-A20W-10 chr14:74196574 A>C maps to NM_001043318.1 P621P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A113-01A-11D-A12Z-10 chr14:95918594 C>T maps to NM_152592.3 Q421Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADP-01A-11D-A38X-10 chr14:95932450 C>T maps to NM_152592.3 E148E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PD-A5DF-01A-11D-A27I-10 chr14:95909554 G>A maps to NM_152592.3 P616P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAEE-01A-11D-A40R-10 chr14:103570677 G>A maps to NM_001077594.1 E412E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5C-A9VG-01A-11D-A36X-10 chr14:23467695 C>T maps to NM_021944.2 R179R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39X-01A-11D-A20W-10 chr15:75197054 T>C did not map to a codon.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr15:24921715 G>A maps to NM_018958.2 L234L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-AA0V-01A-11D-A382-10 chr15:24923716 T>C maps to NM_018958.2 L901L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAW2-01A-11D-A40P-10 chr15:40675150 C>T maps to NM_033286.3 Q39*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A459-01A-11D-A25V-10 chr15:40675113 A>T maps to NM_033286.3 P26P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MC-01A-11D-A33Q-10 chr15:34376642 C>T maps to NM_020154.2 L207L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9GU-01A-11D-A382-10 chr15:75500059 C>T maps to NM_015492.4 G557G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAW1-01A-11D-A40P-10 chr15:75501100 G>A maps to NM_015492.4 Q904Q. 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-DD-AACE-01A-11D-A40R-10 chr15:90145126 A>G maps to NM_152259.3 S829S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr15:90142663 C>A maps to NM_152259.3 T670T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CJ-01A-11D-A20W-10 chr15:90138759 A>G maps to NM_152259.3 K606K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39Y-01A-11D-A20W-10 chr15:65871931 A>G maps to ENST00000420799 A493A. 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-DD-A119-01A-11D-A12Z-10 chr15:34640688 G>A maps to ENST00000438749 W197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WQ-A9G7-01A-11D-A36X-10 chr15:90784263 C>T maps to NM_001013657.2 Q42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WQ-A9G7-01A-11D-A36X-10 chr15:74043429 G>A maps to NM_001039614.1 D14D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADG-01A-11D-A40R-10 chr16:613775 C>A maps to ENST00000293874 S161*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAW0-01A-11D-A40R-10 chr16:1399609 C>T did not map to a codon.
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-ZS-A9CD-01A-11D-A36X-10 chr16:31519394 C>T maps to NM_022744.2 Q100Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39X-01A-11D-A20W-10 chr16:19619533 C>T maps to NM_020314.5 A362A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WX-AA46-01A-11D-A38X-10 chr16:89783144 G>T maps to NM_004913.2 A87A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9H1-01A-11D-A382-10 chr16:4794958 G>T maps to NM_139170.2 R330R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACN-01A-11D-A40R-10 chr16:49407993 T>A maps to NM_144602.2 A48A. 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-BC-A10Z-01A-11D-A12Z-10 chr17:72949119 C>T maps to NM_030630.2 W678*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAVX-01A-11D-A40R-10 chr17:17962264 C>T maps to NM_024052.4 Y230Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAW1-01A-11D-A40P-10 chr17:43332861 G>A maps to NM_152343.2 S229S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EG-01A-11D-A20W-10 chr17:45451901 A>G maps to NM_152347.4 G314G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WJ-A86L-01A-12D-A45V-10 chr17:34183787 G>A maps to NM_152781.2 Q392*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9H9-01A-21D-A38X-10 chr17:8140794 T>G maps to NM_025099.5 L230L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr17:8138159 A>G maps to NM_025099.5 A508A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr17:8131842 T>C maps to NM_025099.5 K1164K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr17:8133210 G>T maps to NM_025099.5 I1003I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XR-A8TG-01A-11D-A35Z-10 chr17:57289157 A>G maps to NM_018149.6 S582S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A8O5-01A-11D-A35Z-10 chr17:30665303 T>G maps to NM_022344.2 T138T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr17:30666838 C>A maps to NM_022344.2 E114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACQ-01A-11D-A40R-10 chr17:30179201 T>A maps to NM_018405.3 K171*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9GU-01A-11D-A382-10 chr17:71232523 C>T maps to NM_017941.4 T301T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A3KG-01A-11D-A20W-10 chr18:13643355 A>G did not map to a codon.
Sequencing variant TCGA-DD-A1EG-01A-11D-A20W-10 chr18:77796688 T>C maps to NM_024805.2 S60S. 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-A7M5-01A-11D-A33Q-10 chr18:52262215 G>A maps to NM_173629.1 W61*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39X-01A-11D-A20W-10 chr18:30517977 A>G maps to NM_001105528.1 G867G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAC8-01A-11D-A40R-10 chr18:30926214 T>A maps to NM_001105528.1 S206S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAVS-01A-11D-A40R-10 chr18:21001405 C>T maps to NM_032933.4 W41*. 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-4R-AA8I-01A-11D-A382-10 chr19:30503419 C>A maps to NM_003796.2 P469P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LG-A9QD-01A-11D-A382-10 chr19:30505900 T>G maps to NM_003796.2 V511V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACB-01A-11D-A40R-10 chr19:519038 G>A maps to NM_033513.2 P163P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr19:507709 T>C maps to NM_033513.2 A68A. 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-ZS-A9CD-01A-11D-A36X-10 chr19:757269 A>G maps to NM_173481.2 T108T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADF-01A-11D-A40R-10 chr19:1233485 A>G maps to ENST00000382477 Y326Y. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-CC-5259-01A-31D-A20W-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-BC-A3KG-01A-11D-A20W-10 chr19:2098974 A>G maps to NM_001039846.1 R185R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A3KG-01A-11D-A20W-10 chr19:50666319 G>A maps to NM_152358.2 F44F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAC8-01A-11D-A40R-10 chr19:50662760 A>T maps to NM_152358.2 Y128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAEB-01A-11D-A40R-10 chr19:16764844 C>T did not map to a codon.
Sequencing variant TCGA-CC-A3MA-01A-11D-A20W-10 chr19:36258937 G>A maps to NM_001039887.2 Q397Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MB-01A-11D-A20W-10 chr19:36258937 G>A maps to NM_001039887.2 Q397Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39X-01A-11D-A20W-10 chr19:36258937 G>A maps to NM_001039887.2 Q397Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A0-01A-11D-A20W-10 chr19:36252917 A>G did not map to a codon.
Sequencing variant TCGA-DD-A3A0-01A-11D-A20W-10 chr19:36258937 G>A maps to NM_001039887.2 Q397Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5C-A9VH-01A-11D-A36X-10 chr19:14006249 C>T maps to ENST00000454313 E47E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACL-01A-11D-A40R-10 chr19:7743419 C>A maps to NM_174918.2 G139G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A7PZ-01A-11D-A33Q-10 chr19:1014292 C>G maps to NM_001033026.1 G135G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A114-01A-11D-A12Z-10 chr19:44238559 G>T maps to NM_019108.2 T361T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr19:17384926 G>A maps to NM_014173.2 L159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACI-01A-11D-A40R-10 chr19:50984224 C>T maps to ENST00000376920 F223F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BD-A3EP-01A-11D-A22F-10 chr19:51770668 G>T maps to NM_173635.1 A151A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr19:51768724 A>T maps to NM_173635.1 G42G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr23:119760343 G>A did not map to a codon.
Sequencing variant TCGA-WQ-A9G7-01A-11D-A36X-10 chr23:119760166 C>G did not map to a codon.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr2:119915746 G>A maps to NM_182528.3 C33C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IE-01A-21D-A382-10 chr10:16562896 G>A maps to NM_001010908.1 P56P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr17:77043986 G>A maps to ENST00000392445 L231L. 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-DD-AADI-01A-11D-A40R-10 chr5:159776447 G>A maps to NM_031908.4 Y240Y. 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-A119-01A-11D-A12Z-10 chr4:15444245 T>C maps to NM_001135170.1 A238A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACU-01A-11D-A40R-10 chr12:7261739 T>A maps to NM_016546.2 R13*. 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-ZP-A9D1-01A-11D-A382-10 chr1:111494485 G>T maps to NM_018372.3 I340I. 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-DD-AAD0-01A-11D-A40R-10 chr1:169799443 C>A maps to NM_018186.2 T453T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GJ-A3OU-01A-31D-A382-10 chr1:169775143 G>C did not map to a codon.
Sequencing variant TCGA-2V-A95S-01A-11D-A36X-10 chr1:36786279 C>T maps to NM_001162530.1 L672L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr1:169388396 C>A maps to ENST00000367806 E357*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAD2-01A-11D-A40R-10 chr1:220870012 C>T maps to NM_024709.4 F123F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACI-01A-11D-A40R-10 chr1:179497526 T>C maps to NM_144696.4 H892H. 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-BW-A5NQ-01A-11D-A27I-10 chr1:170967420 T>C maps to NM_025063.2 S534S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAW1-01A-11D-A40P-10 chr1:170967476 C>A maps to NM_025063.2 S553*. 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-DD-AAD3-01A-11D-A40R-10 chr1:231376847 C>A maps to ENST00000421623 E14*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75E-01A-11D-A32G-10 chr1:182872215 G>A maps to ENST00000287709 T625T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACZ-01A-11D-A40R-10 chr1:19950008 G>T maps to ENST00000433528 G67*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CJ-01A-11D-A20W-10 chr1:169762227 T>G maps to NM_033418.1 I203I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACA-01A-11D-A40R-10 chr1:57206371 T>C maps to NM_001004303.4 L567L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CG-01A-11D-A20W-10 chr1:57207871 T>C maps to NM_001004303.4 E522E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A8HT-01A-11D-A35Z-10 chr1:75065586 C>T maps to NM_001002912.4 E506E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A8HT-01A-11D-A35Z-10 chr1:75065588 C>A maps to NM_001002912.4 E506*. 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-A119-01A-11D-A12Z-10 chr1:75037859 T>C maps to NM_001002912.4 G1178G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAC8-01A-11D-A40R-10 chr1:75038864 T>A maps to NM_001002912.4 A843A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9GT-01A-11D-A382-10 chr1:55118679 G>A maps to ENST00000454855 P27P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAEG-01A-11D-A38X-10 chr1:55118886 C>A maps to ENST00000454855 I96I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A459-01A-11D-A25V-10 chr1:55130861 A>G maps to ENST00000454855 S443S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A7SK-01A-11D-A34Z-10 chr1:55144943 A>T maps to ENST00000454855 G715G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr1:55119679 A>T maps to ENST00000454855 K361*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr1:55174687 G>A maps to ENST00000454855 G1252G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr1:112270029 G>A maps to NM_019099.4 R152*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10W-01A-11D-A12Z-10 chr1:230979275 C>A maps to NM_032800.2 E251*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A8HT-01A-11D-A35Z-10 chr1:230979534 G>T maps to NM_032800.2 A164A. 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-DD-AADR-01A-11D-A40R-10 chr1:162353115 A>G maps to NM_001135240.1 P197P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAD6-01A-11D-A40R-10 chr1:185113144 T>A maps to NM_030934.4 P224P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAVZ-01A-11D-A40R-10 chr1:185259913 C>T maps to NM_001105518.1 D894D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MB-01A-11D-A20W-10 chr1:186375350 T>C maps to NM_017847.5 D379D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39Z-01A-11D-A20W-10 chr1:186352260 A>G maps to NM_017847.5 E69E. 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-CC-A5UD-01A-11D-A28X-10 chr1:178490805 G>T did not map to a codon.
Sequencing variant TCGA-DD-A1EB-01A-11D-A12Z-10 chr1:178489806 G>C did not map to a codon.
Sequencing variant TCGA-ZP-A9D1-01A-11D-A382-10 chr1:178485748 G>T did not map to a codon.
Sequencing variant TCGA-RC-A7SH-01A-11D-A382-10 chr1:150255907 A>G maps to NM_144697.2 P77P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr1:222902171 T>C did not map to a codon.
Sequencing variant TCGA-2Y-A9GZ-01A-11D-A38X-10 chr1:109191342 G>A maps to ENST00000370031 L374L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5C-A9VH-01A-11D-A36X-10 chr1:109191370 G>A maps to ENST00000370031 F364F. 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-WQ-A9G7-01A-11D-A36X-10 chr1:25571730 G>A maps to NM_020317.3 N194N. 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-DD-A1EE-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-EP-A2KA-01A-11D-A183-10 chr1:156703276 C>T maps to NM_015997.3 Q201*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CG-01A-11D-A20W-10 chr1:43869390 T>G maps to ENST00000310739 A91A. 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-ES-A2HT-01A-12D-A183-10 chr1:60491089 A>G maps to NM_152377.2 G370G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LG-A9QD-01A-11D-A382-10 chr1:60521078 G>A maps to NM_152377.2 Q47*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACI-01A-11D-A40R-10 chr1:172577939 A>T maps to ENST00000367723 K1259*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAEH-01A-11D-A40R-10 chr1:172547510 C>T maps to ENST00000367723 L624L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAE9-01A-11D-A40R-10 chr1:156899103 G>C maps to NM_144702.2 T343T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39Y-01A-11D-A20W-10 chr1:34643425 T>C maps to NM_001134734.1 G12G. 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-ES-A2HS-01A-11D-A183-10 chr20:9496098 G>T did not map to a codon.
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-DD-A73G-01A-22D-A32G-10 chr20:35431375 C>T maps to NM_080627.2 Q1074Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr20:35406235 T>C did not map to a codon.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr20:35423003 T>A did not map to a codon.
Sequencing variant TCGA-XR-A8TG-01A-11D-A35Z-10 chr20:35414899 G>T maps to NM_080627.2 P1658P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr20:18407715 G>A maps to NM_001099407.1 Q317*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr20:18414337 A>G maps to NM_001099407.1 P273P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MA-01A-11D-A33Q-10 chr20:18393404 G>A maps to NM_001099407.1 F439F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAE1-01A-11D-A40R-10 chr20:32255992 C>T maps to NM_001024675.1 A230A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr20:2796265 G>T maps to NM_080739.2 E115*. 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-BC-A3KF-01A-11D-A20W-10 chr20:34611571 T>C maps to ENST00000373973 L440L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75E-01A-11D-A32G-10 chr20:34568391 T>C maps to ENST00000373973 P85P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADE-01A-11D-A40R-10 chr20:44515575 T>G maps to NM_080608.3 R88R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5259-01A-31D-A20W-10 chr20:58519114 T>A maps to NM_022106.2 A39A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr20:31671632 C>T maps to NM_182519.2 G210G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EL-01A-11D-A152-10 chr20:31672751 C>T maps to NM_182519.2 G244G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADI-01A-11D-A40R-10 chr20:3306870 A>G maps to NM_001009984.1 C387C. 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-AACQ-01A-11D-A40R-10 chr20:20071621 T>A did not map to a codon.
Sequencing variant TCGA-CC-A7IL-01A-11D-A33Q-10 chr20:34832688 G>T maps to NM_015511.3 R276R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10R-01A-11D-A12Z-10 chr20:55048452 T>A did not map to a codon.
Sequencing variant TCGA-CC-A7IG-01A-11D-A33K-10 chr20:31768350 G>T maps to NM_080574.2 L245L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACV-01A-11D-A40R-10 chr20:31814799 G>C did not map to a codon.
Sequencing variant TCGA-DD-A39Y-01A-11D-A20W-10 chr20:17950849 T>C maps to NM_052865.2 D116D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAEH-01A-11D-A40R-10 chr20:10602023 T>C maps to NM_001009608.1 P156P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WQ-A9G7-01A-11D-A36X-10 chr20:256673 C>T maps to NM_153269.1 E322E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr21:45755645 C>A maps to ENST00000397956 T46T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAE6-01A-11D-A40R-10 chr21:45949774 G>A maps to ENST00000443468 S234S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9HB-01A-11D-A38X-10 chr21:33641404 T>C maps to NM_018944.2 L215L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADO-01A-11D-A40R-10 chr21:47602715 G>A maps to NM_001142854.1 G5G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A8HT-01A-11D-A35Z-10 chr21:33984424 G>A maps to NM_021254.2 R43R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr22:32795592 A>G maps to NM_014306.4 P217P. 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-EP-A2KA-01A-11D-A183-10 chr22:32084214 T>C did not map to a codon.
Sequencing variant TCGA-DD-AADG-01A-11D-A40R-10 chr22:32546377 A>G maps to NM_001010859.1 L194L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A8O6-01A-11D-A35Z-10 chr22:32555160 G>C maps to NM_001010859.1 G14G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A5KG-01A-11D-A27I-10 chr22:45595760 G>A maps to NM_001009880.1 D336D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A3KF-01A-11D-A20W-10 chr11:73785298 T>C maps to ENST00000334126 K1650K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAD5-01A-11D-A40R-10 chr2:99767194 A>G maps to NM_144706.2 T92T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADE-01A-11D-A40R-10 chr2:99767089 T>C maps to NM_144706.2 D57D. 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-CC-A8HU-01A-11D-A35Z-10 chr2:27804118 C>T maps to NM_032266.3 N1560N. 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-G3-A3CJ-01A-11D-A20W-10 chr2:27800545 A>G maps to NM_032266.3 G369G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr2:220037322 G>A maps to NM_015680.4 F406F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAC8-01A-11D-A40R-10 chr2:27438565 A>T maps to NM_080592.3 I199I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr2:44933425 G>A maps to NM_024766.3 R146R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39Z-01A-11D-A20W-10 chr2:26644238 A>G maps to NM_145038.2 R109R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADV-01A-11D-A38X-10 chr2:26667691 C>T maps to NM_145038.2 H424H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr2:26624925 C>T maps to NM_145038.2 L23L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-AAV4-01A-11D-A382-10 chr2:70392229 G>A maps to NM_017880.1 T449T. 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-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-DD-AADY-01A-11D-A40R-10 chr2:88828587 C>T maps to NM_152670.2 Q47*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACF-01A-11D-A40R-10 chr2:27360537 C>A maps to NM_178553.3 G220G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADQ-01A-11D-A40R-10 chr2:27360804 G>T maps to NM_178553.3 S131S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IE-01A-21D-A382-10 chr2:241834940 T>C maps to NM_001085437.1 A158A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MC-01A-11D-A22F-10 chr2:99449387 G>A maps to NM_207362.2 D104D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A8HS-01A-11D-A35Z-10 chr2:232458828 G>A maps to NM_152614.2 Q389Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr2:219222347 G>A maps to NM_198559.1 V70V. 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-A4NO-01A-11D-A28X-10 chr2:55402926 T>C maps to NM_152385.2 *587W. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr2:55433451 A>G maps to NM_152385.2 S320S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADR-01A-11D-A40R-10 chr2:74842176 G>A maps to NM_138804.3 L114L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAVW-01A-11D-A40R-10 chr2:197672292 T>A maps to NM_213608.1 T76T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A3KG-01A-11D-A20W-10 chr2:85836674 T>C maps to NM_001013649.3 E87E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BW-A5NO-01A-11D-A27I-10 chr2:73456047 G>A maps to NM_032319.1 H107H. 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-AAD1-01A-11D-A40R-10 chr2:209045540 C>A did not map to a codon.
Sequencing variant TCGA-ED-A8O6-01A-11D-A35Z-10 chr2:242815104 G>A maps to NM_173821.2 T466T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A5SK-01A-11D-A27I-10 chr2:63631474 T>C maps to NM_015910.4 S381S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr2:191064798 T>C maps to NM_032321.2 C71C. 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-DD-AAD6-01A-11D-A40R-10 chr19:6677907 A>G maps to NM_000064.2 F1659F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAVW-01A-11D-A40R-10 chr19:6713206 C>T maps to NM_000064.2 L332L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr12:8212439 A>G maps to NM_004054.2 T114T. 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-AADG-01A-11D-A40R-10 chr3:112729967 T>C maps to NM_015412.3 K279K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr3:14724483 C>T maps to NM_032137.4 V88V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WX-AA44-01A-11D-A38X-10 chr3:14755615 C>T maps to NM_032137.4 A421A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAC8-01A-11D-A40R-10 chr3:194877311 T>A did not map to a codon.
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-ES-A2HS-01A-11D-A183-10 chr3:118870129 C>T maps to NM_152539.2 C534C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr3:8669445 T>C maps to NM_015931.1 G182G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr3:8661622 A>T maps to NM_015931.1 Y331*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A8HV-01A-11D-A35Z-10 chr3:196435516 A>T maps to NM_032898.3 T8T. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-GJ-A9DB-01A-11D-A36X-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr3:49841898 C>T maps to NM_203370.1 Q115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EE-01A-11D-A12Z-10 chr3:192516471 G>T maps to NM_178496.3 V393V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A3R2-01A-11D-A22F-10 chr3:192516789 C>T maps to NM_178496.3 W287*. 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-ES-A2HS-01A-11D-A183-10 chr3:47552680 A>G maps to NM_001031703.2 D30D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5R-AAAM-01A-12D-A40R-10 chr3:153220255 T>C maps to NM_001101337.1 D96D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39Y-01A-11D-A20W-10 chr1:207317163 T>C maps to NM_000715.3 A482A. 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-GJ-A6C0-01A-12D-A30V-10 chr4:57842962 C>T maps to NM_032313.2 R263R. 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-CC-A8HT-01A-11D-A35Z-10 chr4:113540195 C>T maps to NM_018392.4 Q334Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A459-01A-11D-A25V-10 chr4:113461975 C>A did not map to a codon.
Sequencing variant TCGA-BC-A217-01A-11D-A152-10 chr4:8469837 C>T maps to NM_152544.2 V564V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5262-01A-01D-A12Z-10 chr4:8469996 G>A maps to NM_152544.2 A617A. Only missense variants will be evaluated by CHASM.
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-A39X-01A-11D-A20W-10 chr4:184589186 A>G maps to NM_021942.4 A159A. 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-DD-A39X-01A-11D-A20W-10 chr9:123738975 A>G did not map to a codon.
Sequencing variant TCGA-DD-A39X-01A-11D-A20W-10 chr9:123776211 A>G maps to NM_001735.2 C732C. Only missense variants will be evaluated by CHASM.
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-DD-AACI-01A-11D-A40R-10 chr9:123789472 T>A maps to NM_001735.2 K280*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACV-01A-11D-A40R-10 chr9:123716024 T>C maps to NM_001735.2 K1628K. 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-A1EG-01A-11D-A20W-10 chr5:31541440 A>G maps to NM_018356.2 E308E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WX-AA44-01A-11D-A38X-10 chr5:31538642 A>G maps to NM_018356.2 P218P. 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-ES-A2HS-01A-11D-A183-10 chr5:43490730 A>G did not map to a codon.
Sequencing variant TCGA-FV-A2QR-01A-11D-A20W-10 chr5:56205564 C>T maps to NM_153706.3 N31N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39X-01A-11D-A20W-10 chr5:93807340 C>A maps to ENST00000513200 V517V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr5:154200872 G>A maps to NM_032385.3 G264G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A8YO-01A-11D-A36X-10 chr5:37170311 G>C maps to NM_023073.3 S2098*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EG-01A-11D-A20W-10 chr5:37115122 T>C maps to NM_023073.3 K3059K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EG-01A-11D-A20W-10 chr5:64931771 A>G maps to NM_001093755.1 G39G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr5:147281301 G>A maps to NM_206966.2 D35D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5R-AAAM-01A-12D-A40R-10 chr5:41912231 T>G maps to NM_175921.4 L183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11B-01A-11D-A12Z-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-DD-A1EE-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-DD-AAD2-01A-11D-A40R-10 chr6:165715429 C>A maps to NM_144980.3 P127P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5261-01A-01D-A12Z-10 chr6:30615169 C>T maps to NM_001161376.1 S54S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5259-01A-31D-A20W-10 chr6:48036325 C>G maps to NM_001013732.3 V22V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACJ-01A-11D-A40R-10 chr6:54095630 A>G maps to ENST00000502396 P946P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9HA-01A-11D-A38X-10 chr6:3751738 C>A maps to NM_183373.3 T9T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1ED-01A-11D-A152-10 chr6:97627436 T>C did not map to a codon.
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-DD-AAE8-01A-11D-A40R-10 chr6:121563445 A>G maps to ENST00000275159 H686H. 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-A3A5-01A-11D-A22F-10 chr6:127796692 G>A maps to NM_001012279.2 G826G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr6:127837003 T>C maps to NM_001012279.2 E252E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EG-01A-11D-A20W-10 chr6:130182309 A>G maps to NM_001010876.1 A8A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A0-01A-11D-A20W-10 chr6:107372313 A>G maps to NM_001142470.1 G204G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CG-01A-11D-A20W-10 chr6:151775691 A>G maps to NM_024573.1 A17A. 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-DD-AACP-01A-11D-A40R-10 chr6:31736937 G>A maps to NM_025258.2 R454*. 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-AAVV-01A-11D-A40R-10 chr6:170156444 A>G maps to NM_018341.1 E109E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr6:170154031 C>T maps to NM_018341.1 Q27*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAC9-01A-11D-A40R-10 chr6:35715162 G>T maps to NM_145028.3 V217V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-AAV3-01A-11D-A36X-10 chr6:151907028 C>A maps to ENST00000367290 V366V. 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-DD-AACH-01A-11D-A40R-10 chr7:31735230 A>T maps to NM_006658.4 I77I. 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-2Y-A9H5-01A-11D-A382-10 chr7:23338994 G>A maps to NM_138446.1 A8A. 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-DD-AADV-01A-11D-A38X-10 chr7:99755552 C>A maps to NM_018275.3 V140V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADB-01A-11D-A40R-10 chr7:43684912 A>G maps to NM_018224.2 P67P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EF-01A-11D-A12Z-10 chr7:100085892 C>T maps to ENST00000423930 G183G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAD8-01A-11D-A40R-10 chr7:100088251 A>G maps to ENST00000423930 A687A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75G-01A-11D-A32G-10 chr7:100085811 C>T maps to ENST00000423930 S156S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr7:100086258 A>T maps to ENST00000423930 S305S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HP-A5N0-01A-11D-A28X-10 chr7:139026138 C>T maps to NM_197964.3 A3A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YA-A8S7-01A-11D-A36X-10 chr7:120782176 A>G maps to NM_024913.4 T679T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A3KG-01A-11D-A20W-10 chr7:92163806 T>C maps to NM_032120.2 C180C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAD8-01A-11D-A40R-10 chr7:108524538 A>C maps to NM_001024607.1 P17P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9H2-01A-12D-A382-10 chr1:57378218 C>T maps to NM_000562.2 P508P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAD5-01A-11D-A40R-10 chr1:57320605 T>A maps to NM_000562.2 L11*. 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-2Y-A9H2-01A-12D-A382-10 chr8:146278705 C>T maps to ENST00000444534 R156*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAD5-01A-11D-A40R-10 chr8:69552725 C>T maps to NM_052958.2 N407N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADQ-01A-11D-A40R-10 chr8:96037271 G>T maps to NM_152416.2 P12P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACH-01A-11D-A40R-10 chr8:42401692 C>G maps to NM_001135675.1 T26T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A1-01A-11D-A20W-10 chr8:33358007 T>C maps to NM_001102401.1 R420R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WQ-A9G7-01A-11D-A36X-10 chr8:33357911 G>A maps to NM_001102401.1 S452S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A0-01A-11D-A20W-10 chr8:442413 C>T maps to NM_175075.3 P181P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9H6-01A-11D-A38X-10 chr8:67789681 T>C maps to NM_173518.4 Y128Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr8:144652225 C>A maps to NM_001100878.1 V351V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9HB-01A-11D-A38X-10 chr8:117950649 G>A maps to NM_001025357.2 L56L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A3KG-01A-11D-A20W-10 chr9:98691000 T>C maps to NM_001010895.2 L547L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BD-A3ER-01A-11D-A20W-10 chr9:35044762 G>T maps to NM_203299.2 E713*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A8HT-01A-11D-A35Z-10 chr9:35044801 C>T maps to NM_203299.2 L726L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADB-01A-11D-A40R-10 chr9:35045262 G>A maps to NM_203299.2 R879R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr9:72435840 C>T maps to NM_001010940.1 Q16*. Only missense variants will be evaluated by CHASM.
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-LG-A9QC-01A-11D-A36X-10 chr9:139927655 C>T maps to NM_207511.1 D47D. 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-EP-A2KA-01A-11D-A183-10 chr9:100667080 G>T maps to NM_016481.3 I420I. 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-A39Y-01A-11D-A20W-10 chr9:34385752 A>G maps to NM_032596.3 H54H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-AAV4-01A-11D-A382-10 chr9:34380992 G>T maps to NM_032596.3 G203G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZP-A9CV-01A-11D-A382-10 chr9:103212869 C>A maps to NM_001198805.1 C150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11D-01A-11D-A12Z-10 chr9:111899752 T>C maps to NM_014334.2 L339L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39Z-01A-11D-A20W-10 chr9:5361762 T>C maps to NM_018465.2 T69T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A5UD-01A-11D-A28X-10 chr9:111853342 T>A maps to NM_032012.3 R337*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAVR-01A-11D-A40R-10 chr9:111882013 C>A maps to NM_032012.3 V60V. 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-ES-A2HS-01A-11D-A183-10 chr9:114454020 A>G maps to NM_173521.3 S1348S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CG-01A-11D-A20W-10 chr9:114454236 T>C maps to NM_173521.3 K1276K. 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-BC-A10Y-01A-11D-A12Z-10 chr9:139732076 G>A maps to NM_001173988.1 G364G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A3KG-01A-11D-A20W-10 chr9:15777601 A>G maps to NM_173550.2 P892P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACT-01A-11D-A40R-10 chr9:15744564 A>T maps to NM_173550.2 K782*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr9:15784673 T>C maps to NM_173550.2 T1083T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A2QR-01A-11D-A20W-10 chr9:15695298 T>C maps to NM_173550.2 L428L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A7M6-01A-11D-A33Q-10 chr9:15777775 A>G maps to NM_173550.2 V950V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACC-01A-11D-A40R-10 chr9:136245945 C>T maps to NM_153710.3 L43L. 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-ED-A459-01A-11D-A25V-10 chr9:135739157 C>T maps to NM_152572.2 W76*. 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-AAW1-01A-11D-A40P-10 chr17:49825103 A>T maps to NM_001082534.1 S118S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAE1-01A-11D-A40R-10 chr19:49143043 C>T did not map to a codon.
Sequencing variant TCGA-LG-A9QD-01A-11D-A382-10 chr15:63632639 C>T maps to NM_001218.3 Q198Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WQ-A9G7-01A-11D-A36X-10 chr1:150234002 C>A maps to NM_012113.1 T74T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MB-01A-11D-A20W-10 chr23:15768151 G>A did not map to a codon.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr23:15768180 A>G did not map to a codon.
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-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-DD-AACX-01A-11D-A40R-10 chr22:24494015 A>G maps to NM_012295.3 S1326S. 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-G3-A3CJ-01A-11D-A20W-10 chr18:21723345 A>G maps to NM_138644.1 K56K. 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-5R-AA1C-01A-11D-A40R-10 chr19:13616902 T>G maps to NM_023035.2 R46R. 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-G3-AAV6-01A-21D-A36X-10 chr9:140773612 T>C did not map to a codon.
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-AAD0-01A-11D-A40R-10 chr12:2613672 C>T maps to ENST00000399634 F395F. 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-BC-A10W-01A-11D-A12Z-10 chr3:53839135 A>G maps to NM_001128840.1 R1904R. 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-ED-A97K-01A-21D-A382-10 chr3:53804515 G>A maps to NM_001128840.1 V1327V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IE-01A-21D-A382-10 chr1:181479648 C>A maps to ENST00000357570 A101A. 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-DD-AACI-01A-11D-A40R-10 chr1:181685266 T>A did not map to a codon.
Sequencing variant TCGA-ED-A8O5-01A-11D-A35Z-10 chr1:181765840 G>A maps to ENST00000357570 E2082E. 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-RC-A7SH-01A-11D-A382-10 chr1:181754898 G>A maps to ENST00000357570 E1910E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5R-AAAM-01A-12D-A40R-10 chr23:49065045 G>A did not map to a codon.
Sequencing variant TCGA-DD-AADJ-01A-11D-A40R-10 chr23:49072968 G>C did not map to a codon.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr23:49061724 T>C did not map to a codon.
Sequencing variant TCGA-WQ-A9G7-01A-11D-A36X-10 chr23:49082872 G>A did not map to a codon.
Sequencing variant TCGA-2Y-A9H5-01A-11D-A382-10 chr17:48703835 C>T maps to NM_018896.3 D2286D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9H6-01A-11D-A38X-10 chr17:48684343 C>T maps to NM_018896.3 D1502D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EE-01A-11D-A12Z-10 chr17:48695289 G>A maps to NM_018896.3 Q1742Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACZ-01A-11D-A40R-10 chr17:48655579 C>T maps to NM_018896.3 S652S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAD5-01A-11D-A40R-10 chr17:48653616 C>T maps to NM_018896.3 T618T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADB-01A-11D-A40R-10 chr17:48683347 G>A maps to NM_018896.3 W1462*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADI-01A-11D-A40R-10 chr17:48667881 C>T maps to NM_018896.3 S784S. Only missense variants will be evaluated by CHASM.
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-DD-AACI-01A-11D-A40R-10 chr16:1261287 T>A maps to NM_021098.2 G1448G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr16:1270003 G>A maps to NM_021098.2 L2024L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CJ-01A-11D-A20W-10 chr16:1252153 C>T maps to NM_021098.2 D568D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACH-01A-11D-A40R-10 chr22:40058778 A>T did not map to a codon.
Sequencing variant TCGA-DD-AACK-01A-11D-A40R-10 chr22:40069971 G>T maps to NM_021096.3 L1596L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAE7-01A-11D-A40R-10 chr22:40059827 G>A maps to NM_021096.3 Q1193Q. 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-ES-A2HT-01A-12D-A183-10 chr22:40068951 A>G did not map to a codon.
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-CC-A9FS-01A-11D-A36X-10 chr1:201012431 A>G maps to NM_000069.2 H1675H. 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-DD-A3A0-01A-11D-A20W-10 chr7:81662160 T>C maps to NM_000722.2 G365G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZP-A9CY-01A-11D-A382-10 chr7:81689805 G>T maps to NM_000722.2 R273R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BD-A3EP-01A-11D-A22F-10 chr3:50413238 C>T did not map to a codon.
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-LG-A6GG-01A-11D-A30V-10 chr12:1994035 G>T maps to NM_172364.4 A390A. 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-EP-A2KA-01A-11D-A183-10 chr12:49221408 C>T maps to NM_000725.2 P394P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39Z-01A-11D-A20W-10 chr2:152732941 T>C maps to NM_000726.3 G173G. 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-WQ-A9G7-01A-11D-A36X-10 chr22:36960547 G>A maps to NM_006078.3 S274S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9H6-01A-11D-A38X-10 chr17:65026621 C>T maps to NM_014405.3 S162S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZP-A9D1-01A-11D-A382-10 chr17:64961143 C>T maps to NM_014405.3 H39H. 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-G3-A3CI-01A-11D-A20W-10 chr19:54483250 C>T maps to NM_031895.5 F166F. 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-ZS-A9CF-01A-11D-A382-10 chr19:54485509 G>T maps to NM_031895.5 E229*. 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-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-A1EG-01A-11D-A20W-10 chr11:115099839 T>C maps to NM_014333.3 E238E. 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-AACM-01A-11D-A40R-10 chr11:115047194 T>A maps to NM_014333.3 *443L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A2QR-01A-11D-A20W-10 chr11:115049370 T>C maps to NM_014333.3 R401R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EE-01A-11D-A12Z-10 chr3:86114752 A>G did not map to a codon.
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-DD-AACP-01A-11D-A40R-10 chr3:62648032 G>A maps to ENST00000383709 R309*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACV-01A-11D-A40R-10 chr3:62467426 C>T maps to ENST00000383709 P1048P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADG-01A-11D-A40R-10 chr3:62459892 G>A maps to ENST00000383709 A1144A. 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-G3-AAV1-01A-11D-A382-10 chr3:62648032 G>T maps to ENST00000383709 R309R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A3KG-01A-11D-A20W-10 chr7:122255248 T>C maps to NM_001167940.1 E403E. Only missense variants will be evaluated by CHASM.
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-2Y-A9H9-01A-21D-A38X-10 chr6:7378873 G>A maps to NM_001170692.1 S221S. 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-DD-AACT-01A-11D-A40R-10 chr12:54105825 T>A maps to NM_020898.2 K660*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-AAV7-01A-11D-A382-10 chr12:54118960 C>A maps to NM_020898.2 R22R. 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-NI-A8LF-01A-11D-A35Z-10 chr7:93055706 G>A maps to NM_001164737.1 I496I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADV-01A-11D-A38X-10 chr10:105215374 T>A maps to NM_001001412.3 K229*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BD-A3EP-01A-11D-A22F-10 chr10:105209278 T>C maps to NM_015916.4 S140S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CG-01A-11D-A20W-10 chr19:47111478 T>C maps to NM_005184.2 F20F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A0-01A-11D-A20W-10 chr1:1847881 A>G maps to NM_138705.2 T27T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAE2-01A-11D-A40R-10 chr1:1848608 G>T maps to NM_138705.2 E175*. 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-BD-A3EP-01A-11D-A22F-10 chr19:13054663 T>C maps to NM_004343.3 D397D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAVQ-01A-11D-A40R-10 chr19:13054676 G>T maps to NM_004343.3 E402*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADF-01A-11D-A40R-10 chr7:128407567 A>T maps to ENST00000342367 R242R. 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.
Multiple mappings detected for codon TCGA-2Y-A9H7-01A-11D-A38X-10. Mapping will be selected arbitrarily.
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-G3-A3CJ-01A-11D-A20W-10 chr5:110820085 A>G maps to NM_001744.4 A448A. 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-2Y-A9H0-01A-11D-A382-10 chr9:138774766 T>C maps to ENST00000409386 G106G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9HB-01A-11D-A38X-10 chr9:138714940 C>T maps to ENST00000409386 T533T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr1:200817744 A>T maps to ENST00000236925 S627S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAC8-01A-11D-A40R-10 chr1:200818089 A>T maps to ENST00000236925 P742P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr1:200708966 T>C maps to ENST00000236925 A4A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr1:200817628 T>C maps to ENST00000236925 L589L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-AAV0-01A-11D-A36X-10 chr1:200819253 T>C maps to ENST00000236925 D1130D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9H0-01A-11D-A382-10 chr1:7725057 A>G maps to NM_015215.2 A817A. 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-DD-A1EG-01A-11D-A20W-10 chr12:67698890 T>C maps to NM_018448.3 I481I. 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-2Y-A9GY-01A-11D-A382-10 chr3:12845053 G>T maps to NM_001162499.1 E46*. 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-2Y-A9H8-01A-11D-A38X-10 chr17:76993227 C>T maps to NM_138793.3 A159A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39Z-01A-11D-A20W-10 chr5:179155614 A>G maps to ENST00000415618 S618S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A1-01A-11D-A20W-10 chr5:179133284 A>G maps to ENST00000415618 T101T. 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-5C-AAPD-01A-21D-A38X-10 chr6:44148396 G>T maps to NM_007058.3 E582*. Only missense variants will be evaluated by CHASM.
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-DD-AAC8-01A-11D-A40R-10 chr2:30966406 C>T maps to ENST00000295055 S429S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADK-01A-11D-A40R-10 chr2:30993222 T>C maps to ENST00000295055 Q160Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAEB-01A-11D-A40R-10 chr2:30993237 C>T maps to ENST00000295055 V155V. 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-DD-A1EG-01A-11D-A20W-10 chr11:76834766 C>T maps to ENST00000360841 L632L. 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-A39X-01A-11D-A20W-10 chr23:110490682 A>G did not map to a codon.
Sequencing variant TCGA-DD-AAW0-01A-11D-A40R-10 chr23:110495539 T>C did not map to a codon.
Sequencing variant TCGA-G3-A3CJ-01A-11D-A20W-10 chr23:110496326 A>G did not map to a codon.
Sequencing variant TCGA-G3-AAV0-01A-11D-A36X-10 chr23:110490681 G>T did not map to a codon.
Sequencing variant TCGA-WQ-A9G7-01A-11D-A36X-10 chr23:110491971 G>A did not map to a codon.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr1:230916292 C>T maps to NM_006615.2 H440H. 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-FV-A3I1-01A-11D-A22F-10 chr11:34112150 C>T maps to NM_005898.4 Q494*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr22:37888762 C>A maps to NM_014550.3 L841L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WQ-A9G7-01A-11D-A36X-10 chr22:37904629 A>G maps to NM_014550.3 H323H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr7:2956990 G>T maps to NM_032415.4 S879*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAEH-01A-11D-A40R-10 chr7:2978335 G>A maps to NM_032415.4 Q332*. 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-BC-A3KG-01A-11D-A20W-10 chr17:78163549 A>G did not map to a codon.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr5:40853233 G>A maps to NM_032587.3 L600L. 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-DD-AAEG-01A-11D-A38X-10 chr11:3039724 C>A maps to NM_001014437.2 L514L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr5:71015233 G>T maps to NM_004291.3 L38L. 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-G3-A3CJ-01A-11D-A20W-10 chr12:25308337 T>C maps to NM_018272.3 E69E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAEH-01A-11D-A40R-10 chr15:40943692 A>G maps to NM_170589.3 Q2105Q. 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-A3CJ-01A-11D-A20W-10 chr23:41495867 T>C did not map to a codon.
Sequencing variant TCGA-ZP-A9CY-01A-11D-A382-10 chr23:41379790 T>A did not map to a codon.
Sequencing variant TCGA-ZS-A9CE-01A-11D-A36X-10 chr23:41394031 A>G did not map to a codon.
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-CC-A8HV-01A-11D-A35Z-10 chr6:90572456 A>G maps to NM_012115.3 L343L. 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-2V-A95S-01A-11D-A36X-10 chr1:15820443 C>A maps to NM_001229.3 L367L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr1:160160792 A>G maps to NM_001231.4 Q84Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A3KG-01A-11D-A20W-10 chr3:121980427 T>C maps to NM_001178065.1 S182S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADS-01A-11D-A40R-10 chr3:121976017 G>T maps to NM_001178065.1 T92T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAE7-01A-11D-A40R-10 chr20:55027579 A>T maps to NM_020356.3 K450*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAE9-01A-11D-A40R-10 chr11:34478273 A>G maps to NM_001752.3 P322P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-AA0U-01A-11D-A382-10 chr11:65787819 G>A maps to NM_053054.3 L678L. 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-DD-AADF-01A-11D-A40R-10 chr19:38857881 C>G maps to NM_021185.4 R900R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BD-A3EP-01A-11D-A22F-10 chr10:74293539 A>G maps to NM_006077.3 G167G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZP-A9D1-01A-11D-A382-10 chr20:32207336 A>G maps to NM_005093.3 T154T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-AAV6-01A-21D-A36X-10 chr16:88968032 C>A maps to NM_005187.5 A61A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A3KG-01A-11D-A20W-10 chr3:105464837 T>C maps to NM_170662.3 T256T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAW3-01A-11D-A40P-10 chr3:105404273 T>C maps to NM_170662.3 K697K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACL-01A-11D-A40R-10 chr19:45303669 G>T maps to NM_012116.3 A465A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACA-01A-11D-A40R-10 chr18:70205485 G>C maps to NM_182511.3 L200L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAE1-01A-11D-A40R-10 chr18:70209068 G>A maps to NM_182511.3 S109S. 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 chr4:169931171 G>T maps to NM_032783.4 A23A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KR-A7K8-01A-11D-A33K-10 chr9:154794 T>C maps to NM_018491.3 R192R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IE-01A-21D-A382-10 chr7:26246055 C>T maps to NM_016587.2 V31V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr7:26248155 C>A maps to NM_016587.2 S104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5C-A9VH-01A-11D-A36X-10 chr17:77808905 C>A maps to NM_003655.2 E179*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr22:39262900 G>A maps to NM_014292.3 G184G. 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-A3A0-01A-11D-A20W-10 chr19:14023136 T>C maps to NM_017721.4 G66G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MB-01A-11D-A20W-10 chr4:15539667 A>G maps to NM_001080522.2 R637R. 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-ES-A2HT-01A-12D-A183-10 chr4:15572064 A>G maps to NM_001080522.2 R1180R. 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-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-DD-AACY-01A-11D-A40R-10 chr18:66678322 C>T maps to NM_024781.2 L472L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAE0-01A-11D-A40R-10 chr18:66504068 T>A maps to NM_024781.2 I23I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9HB-01A-11D-A38X-10 chr2:219886574 G>A maps to NM_194302.2 D1019D. 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-G3-AAV6-01A-21D-A36X-10 chr2:219888856 A>C maps to NM_194302.2 T825T. 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-DD-AACI-01A-11D-A40R-10 chr19:48806025 T>A maps to NM_144577.3 K352*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAE7-01A-11D-A40R-10 chr22:21988579 A>G maps to NM_152612.2 P114P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr2:27851423 G>A maps to ENST00000435516 P69P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WX-AA47-01A-11D-A38X-10 chr2:27849930 T>A maps to ENST00000435516 R410*. Only missense variants will be evaluated by CHASM.
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-DD-A3A1-01A-11D-A20W-10 chr5:68578777 A>G maps to NM_176816.3 A438A. 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-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-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-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-2Y-A9GX-01A-11D-A382-10 chr7:128450354 C>T maps to NM_022742.3 Q655*. 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-DD-A3A1-01A-11D-A20W-10 chr7:128445475 T>C maps to NM_022742.3 S282S. 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-DD-AACI-01A-11D-A40R-10 chr2:109408128 A>T did not map to a codon.
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-DD-AADO-01A-11D-A40R-10 chr3:123674899 T>C maps to NM_022757.4 E122E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CG-01A-11D-A20W-10 chr2:223169001 T>C maps to NM_153038.1 T127T. 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-RC-A7SH-01A-11D-A382-10 chr2:179736263 T>A maps to NM_173648.3 K699*. 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-DD-AAVX-01A-11D-A40R-10 chr2:74709805 C>T maps to ENST00000393965 G53G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WX-AA47-01A-11D-A38X-10 chr17:20768817 A>G maps to NM_001004306.1 Y192Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAW2-01A-11D-A40P-10 chr4:24839839 G>A maps to NM_001130726.2 R143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10W-01A-11D-A12Z-10 chr2:197521793 A>G maps to NM_001080539.1 E170E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACL-01A-11D-A40R-10 chr2:197540922 A>T maps to NM_001080539.1 A398A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WX-AA44-01A-11D-A38X-10 chr19:11532470 C>G maps to NM_145045.4 L488L. 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-AACQ-01A-11D-A40R-10 chr19:49901340 T>A maps to NM_144688.4 A190A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-AAV4-01A-11D-A382-10 chr19:49899025 G>A maps to NM_144688.4 G112G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZS-A9CD-01A-11D-A36X-10 chr4:77303824 A>G maps to NM_001042784.1 T284T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr1:46086572 A>G did not map to a codon.
Sequencing variant TCGA-DD-AACD-01A-11D-A40R-10 chr1:46087107 G>A maps to NM_001114938.2 S411S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADC-01A-11D-A40R-10 chr1:46088961 C>T maps to NM_001114938.2 A140A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BD-A3ER-01A-11D-A20W-10 chr1:93687489 C>T maps to NM_206886.2 I842I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr1:93677669 A>G maps to NM_206886.2 A567A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-AAV1-01A-11D-A382-10 chr1:93649645 A>G maps to NM_206886.2 E200E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr1:26586250 G>A maps to NM_022778.2 A433A. 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-2Y-A9GU-01A-11D-A382-10 chr1:43273172 T>G did not map to a codon.
Sequencing variant TCGA-2Y-A9GY-01A-11D-A382-10 chr1:44457669 G>A maps to NM_152499.1 R40R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr3:49293751 G>T maps to NM_178173.3 S274S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr3:126152004 A>G maps to ENST00000505024 K461K. 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-DD-AADQ-01A-11D-A40R-10 chr3:180377347 T>C maps to NM_181426.1 A210A. 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-DD-A3A0-01A-11D-A20W-10 chr12:94769730 A>G maps to NM_001042399.1 S288S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2V-A95S-01A-11D-A36X-10 chr17:63685337 T>A did not map to a codon.
Sequencing variant TCGA-DD-AAC8-01A-11D-A40R-10 chr17:64059101 T>A maps to NM_145036.3 L351L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IK-01A-12D-A33Q-10 chr3:113187198 T>C maps to NM_144718.3 S314S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAEG-01A-11D-A38X-10 chr3:113176013 C>T maps to NM_144718.3 K542K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A5SM-01A-12D-A28X-10 chr3:113212076 A>G maps to NM_144718.3 F156F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAVR-01A-11D-A40R-10 chr3:107096715 C>A maps to NM_032600.2 V94V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3M9-01A-11D-A20W-10 chr17:28511698 A>G maps to NM_032141.2 P228P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACQ-01A-11D-A40R-10 chr17:28507942 A>T maps to NM_032141.2 K176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EE-01A-11D-A12Z-10 chr17:80115730 G>A maps to ENST00000445854 Q712*. Only missense variants will be evaluated by CHASM.
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-WQ-AB4B-01A-11D-A40P-10 chr12:119978492 C>T maps to NM_178499.3 P542P. 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-MI-A75I-01A-11D-A32G-10 chr12:49298897 T>C did not map to a codon.
Sequencing variant TCGA-DD-AAE7-01A-11D-A40R-10 chr11:93104431 C>T maps to NM_181645.3 Q259*. Only missense variants will be evaluated by CHASM.
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-DD-AACT-01A-11D-A40R-10 chr2:130897153 G>T maps to NM_207310.1 R373R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAE6-01A-11D-A40R-10 chr2:130897516 G>A maps to NM_207310.1 D318D. 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-DD-A1EE-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-4R-AA8I-01A-11D-A382-10 chr3:112358125 G>A maps to ENST00000447230 I220I. 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-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-AACP-01A-11D-A40R-10 chr2:56419880 C>A maps to NM_001080433.1 G182G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZP-A9CV-01A-11D-A382-10 chr2:56611448 A>C maps to NM_001080433.1 R541R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A3KF-01A-11D-A20W-10 chr2:55562102 T>C maps to ENST00000436346 E618E. 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-EP-A2KB-01A-11D-A183-10 chr19:47764056 T>C maps to NM_015603.2 S141S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MB-01A-11D-A20W-10 chr11:82984886 T>C maps to NM_021825.3 R163R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr11:82985020 T>C maps to NM_021825.3 E147E. 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-FV-A2QR-01A-11D-A20W-10 chr5:169031186 A>G maps to NM_017785.4 P598P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr6:31113069 T>C maps to NM_001105564.1 L583L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACO-01A-11D-A40R-10 chr9:36170371 C>T maps to NM_005893.2 G291G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADR-01A-11D-A40R-10 chr9:36169648 C>A maps to NM_005893.2 S50S. 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-ZP-A9CY-01A-11D-A382-10 chr5:68471252 A>G maps to NM_031966.2 K324K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr23:50053331 A>G did not map to a codon.
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-DD-A119-01A-11D-A12Z-10 chr16:2503451 A>G maps to NM_001761.2 T543T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9GZ-01A-11D-A38X-10 chr5:162866372 T>C maps to NM_199246.1 I37I. Only missense variants will be evaluated by CHASM.
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-DD-AACX-01A-11D-A40R-10 chr3:156867721 T>C maps to NM_020307.2 V308V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADI-01A-11D-A40R-10 chr3:156876716 T>C maps to NM_020307.2 A142A. 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-DD-AACK-01A-11D-A40R-10 chr1:1334012 G>A maps to NM_030937.4 F109F. 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-DD-AADG-01A-11D-A40R-10 chr3:46414719 T>C maps to NM_001100168.1 F109F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XR-A8TF-01A-11D-A35Z-10 chr3:46415373 C>T maps to NM_001100168.1 F327F. 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-4R-AA8I-01A-11D-A382-10 chr3:39374346 C>A maps to NM_005201.3 A175A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACX-01A-11D-A40R-10 chr4:139966513 G>T maps to NM_012118.2 L394L. 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-DD-AAEH-01A-11D-A40R-10 chr1:156290761 A>G maps to NM_005998.4 S159S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5R-AAAM-01A-12D-A40R-10 chr17:33267595 T>G maps to NM_006584.3 I310I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9GY-01A-11D-A382-10 chr2:73479949 A>T maps to NM_006429.3 T531T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACI-01A-11D-A40R-10 chr2:73477550 C>A maps to NM_006429.3 V396V. 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-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-DD-A119-01A-11D-A12Z-10 chr1:117552526 A>G maps to NM_004258.3 R33R. 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-DD-A39X-01A-11D-A20W-10 chr6:74516713 T>C maps to NM_133493.3 S1036S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZP-A9CV-01A-11D-A382-10 chr12:7639353 C>T maps to NM_004244.4 E733E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EG-01A-11D-A20W-10 chr12:7521547 T>C maps to ENST00000416109 K1361K. 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-AACK-01A-11D-A40R-10 chr3:112693692 A>T maps to NM_138806.3 P4P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr19:35835729 A>G did not map to a codon.
Sequencing variant TCGA-XR-A8TG-01A-11D-A35Z-10 chr17:72613260 G>A maps to ENST00000426295 S169S. 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-ES-A2HS-01A-11D-A183-10 chr12:6926434 G>T maps to NM_000616.4 A365A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADJ-01A-11D-A40R-10 chr23:135741540 T>C did not map to a codon.
Sequencing variant TCGA-DD-AACG-01A-11D-A40R-10 chr11:35208382 A>T maps to NM_000610.3 P124P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACT-01A-11D-A40R-10 chr11:35219674 T>A maps to NM_000610.3 S268S. 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-4R-AA8I-01A-11D-A382-10 chr3:107798889 T>G maps to NM_001777.3 V116V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A3KF-01A-11D-A20W-10 chr1:160648862 A>G maps to NM_001778.2 I237I. Only missense variants will be evaluated by CHASM.
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-ES-A2HT-01A-12D-A183-10 chr11:60890418 G>A maps to NM_014207.3 V380V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACP-01A-11D-A40R-10 chr1:207498066 A>G maps to NM_001114752.1 K150K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CG-01A-11D-A20W-10 chr1:117087064 T>A maps to NM_001779.2 K78*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9GY-01A-11D-A382-10 chr1:157803135 G>A maps to NM_005894.2 F295F. Only missense variants will be evaluated by CHASM.
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-XR-A8TF-01A-11D-A35Z-10 chr1:157805703 T>G maps to NM_005894.2 T99T. 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-WJ-A86L-01A-12D-A45V-10 chr11:60785355 G>T maps to NM_006725.3 E570*. 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-DD-AADO-01A-11D-A40R-10 chr17:80274229 G>T maps to NM_006137.6 A151A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A0-01A-11D-A20W-10 chr5:149792275 G>A maps to NM_001025159.1 Q13*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9GW-01A-11D-A382-10 chr19:42383662 A>G maps to NM_001783.3 T146T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr17:62007734 A>G maps to NM_001039933.1 C44C. 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-WQ-A9G7-01A-11D-A36X-10 chr20:23065155 G>T maps to NM_012072.3 P558P. 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-DD-A119-01A-11D-A12Z-10 chr19:14516616 C>T maps to NM_078481.2 L563L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-AAV5-01A-11D-A36X-10 chr19:14517932 C>G maps to NM_078481.2 G756G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9GZ-01A-11D-A38X-10 chr23:150067007 G>T 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-BC-A3KG-01A-11D-A20W-10 chr10:12280453 A>G 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-DD-AAC8-01A-11D-A40R-10 chr5:54429258 A>T maps to NM_001170402.1 T226T. Only missense variants will be evaluated by CHASM.
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-DD-AACZ-01A-11D-A40R-10 chr5:137527197 T>C maps to NM_004661.3 G463G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BD-A3EP-01A-11D-A22F-10 chr17:45232067 A>G maps to NM_001114091.1 D309D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADR-01A-11D-A40R-10 chr17:45219594 C>A maps to NM_001114091.1 E466*. 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-DD-A39X-01A-11D-A20W-10 chr6:110540991 T>C maps to NM_015891.2 A420A. 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-2Y-A9H6-01A-11D-A38X-10 chr1:227223279 A>G maps to ENST00000366766 C1076C. 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-XR-A8TC-01A-11D-A35Z-10 chr1:227300123 C>T did not map to a codon.
Sequencing variant TCGA-CC-A3MA-01A-11D-A20W-10 chr14:103466023 A>G maps to NM_006035.3 G158G. 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-EP-A2KA-01A-11D-A183-10 chr11:64599914 C>T maps to NM_017525.2 L1024L. 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-LG-A9QD-01A-11D-A382-10 chr1:91985780 C>T maps to NM_001134420.1 A425A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WQ-A9G7-01A-11D-A36X-10 chr1:91985736 C>T maps to NM_001134420.1 R411*. 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-2Y-A9H1-01A-11D-A382-10 chr3:45132883 T>A maps to NM_022842.3 K592*. Only missense variants will be evaluated by CHASM.
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-DD-AACA-01A-11D-A40R-10 chr3:45152153 C>A maps to NM_022842.3 E279*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAE6-01A-11D-A40R-10 chr1:54618577 C>G maps to NM_201546.2 G6G. 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-A1EE-01A-11D-A12Z-10 chr16:68856128 G>A did not map to a codon.
Sequencing variant TCGA-DD-AADI-01A-11D-A40R-10 chr16:68849585 G>T maps to NM_004360.3 E497*. 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-2Y-A9H9-01A-21D-A38X-10 chr16:65026818 T>C maps to NM_001797.2 T214T. 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-DD-AACP-01A-11D-A40R-10 chr16:65005961 G>T maps to NM_001797.2 R466R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAE2-01A-11D-A40R-10 chr16:65025836 A>T maps to NM_001797.2 G215G. 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-G3-A3CG-01A-11D-A20W-10 chr16:83378492 T>C maps to ENST00000268613 N221N. 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-A39X-01A-11D-A20W-10 chr8:95161098 A>G maps to NM_001144663.1 Y600Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAC8-01A-11D-A40R-10 chr8:95174340 A>G maps to NM_001144663.1 D444D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADR-01A-11D-A40R-10 chr8:95182667 C>T maps to NM_001144663.1 P341P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAVP-01A-11D-A40R-10 chr8:95188825 G>T maps to NM_001144663.1 R123R. 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-G3-A3CG-01A-11D-A20W-10 chr5:19503116 A>G maps to NM_004934.3 T538T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAVS-01A-11D-A40R-10 chr18:64212132 G>A maps to NM_021153.2 Y261Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAD5-01A-11D-A40R-10 chr18:25589823 T>G maps to NM_001792.3 R187R. 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-G3-A3CJ-01A-11D-A20W-10 chr18:59221660 T>C maps to NM_031891.2 P713P. 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-2Y-A9GU-01A-11D-A382-10 chr20:44815545 T>A maps to NM_021248.1 R488R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADS-01A-11D-A40R-10 chr10:73560472 T>A maps to ENST00000398860 P2486P. 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-UB-A7MB-01A-11D-A33Q-10 chr10:73269836 A>T did not map to a codon.
Sequencing variant TCGA-DD-AADQ-01A-11D-A40R-10 chr20:58569359 T>C maps to NM_177980.2 N494N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WX-AA44-01A-11D-A38X-10 chr20:58564167 T>C maps to NM_177980.2 P411P. Only missense variants will be evaluated by CHASM.
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-ES-A2HS-01A-11D-A183-10 chr16:66426268 G>T maps to NM_001795.3 A400A. Only missense variants will be evaluated by CHASM.
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-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-DD-AACQ-01A-11D-A40R-10 chr16:61689605 C>T maps to NM_001796.2 L558L. 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-DD-AACV-01A-11D-A40R-10 chr5:26988367 G>A maps to NM_016279.3 Q25*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAVU-01A-11D-A40R-10 chr5:26885789 C>A maps to NM_016279.3 L605L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A8O5-01A-11D-A35Z-10 chr5:26902661 T>A maps to NM_016279.3 V392V. 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-ES-A2HT-01A-12D-A183-10 chr10:85968519 A>G maps to NM_033100.2 G401G. 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-LG-A9QD-01A-11D-A382-10 chr10:85970827 C>T maps to NM_033100.2 D464D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr5:175995733 T>C maps to NM_001171976.1 Y60Y. 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-DD-AADF-01A-11D-A40R-10 chr3:49831233 A>T did not map to a codon.
Sequencing variant TCGA-WQ-A9G7-01A-11D-A36X-10 chr3:49833196 G>A maps to NM_001007540.2 L237L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZP-A9D1-01A-11D-A382-10 chr11:621352 G>A maps to NM_021924.4 L204L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAW2-01A-11D-A40P-10 chr7:40133993 A>G maps to NM_003718.4 E1318E. 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-G3-A3CG-01A-11D-A20W-10 chr2:219825609 C>T maps to NM_003936.3 A356A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADG-01A-11D-A40R-10 chr9:123298693 G>A maps to NM_018249.4 H206H. 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-EP-A2KA-01A-11D-A183-10 chr7:92300835 C>T maps to NM_001145306.1 W184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACP-01A-11D-A40R-10 chr13:26911778 A>T maps to NM_001260.1 A68A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr4:76507087 T>C maps to ENST00000307465 S556S. 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-A3A0-01A-11D-A20W-10 chr23:18593548 A>G did not map to a codon.
Sequencing variant TCGA-DD-AACL-01A-11D-A40R-10 chr23:18606147 T>C did not map to a codon.
Sequencing variant TCGA-DD-AACV-01A-11D-A40R-10 chr23:18602432 G>A did not map to a codon.
Sequencing variant TCGA-UB-AA0V-01A-11D-A382-10 chr23:18627640 A>G did not map to a codon.
Sequencing variant TCGA-DD-AADQ-01A-11D-A40R-10 chr6:36652052 C>T maps to ENST00000448526 L93L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-AAV4-01A-11D-A382-10 chr11:2906107 C>T maps to NM_000076.2 P204P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XR-A8TG-01A-11D-A35Z-10 chr9:21971208 T>A did not map to a codon.
Sequencing variant TCGA-WQ-AB4B-01A-11D-A40P-10 chr4:184367701 G>T maps to NM_017632.2 E289*. Only missense variants will be evaluated by CHASM.
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-2Y-A9GT-01A-11D-A382-10 chr17:72999275 A>T did not map to a codon.
Sequencing variant TCGA-FV-A2QQ-01A-11D-A22F-10 chr17:15510885 A>T did not map to a codon.
Sequencing variant TCGA-WQ-A9G7-01A-11D-A36X-10 chr17:15492291 C>T maps to ENST00000261644 V782V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr17:15341249 G>T maps to ENST00000395926 S100*. 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-DD-AAW1-01A-11D-A40P-10 chr4:85564292 C>A maps to NM_001263.3 I383I. 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-4R-AA8I-01A-11D-A382-10 chr6:31084587 A>C maps to NM_001264.4 V268V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr6:31084098 G>A maps to NM_001264.4 F431F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAC8-01A-11D-A40R-10 chr13:28542903 G>A maps to NM_001265.3 Y80Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WX-AA44-01A-11D-A38X-10 chr23:72667260 C>A did not map to a codon.
Sequencing variant TCGA-DD-AACQ-01A-11D-A40R-10 chr6:4937881 C>G maps to ENST00000328908 V398V. 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-AADE-01A-11D-A40R-10 chr19:45026912 C>T maps to NM_001102597.1 L167L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EE-01A-11D-A12Z-10 chr19:42300659 G>A maps to NM_001815.2 G17G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5R-AA1C-01A-11D-A40R-10 chr19:42221464 G>A maps to NM_004363.2 Q350Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAC8-01A-11D-A40R-10 chr19:42223901 A>T maps to NM_004363.2 K516*. 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-2Y-A9GW-01A-11D-A382-10 chr19:42192076 G>T maps to NM_006890.3 A6A. 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-A119-01A-11D-A12Z-10 chr19:33793068 G>A maps to NM_004364.3 H84H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-T1-A6J8-01A-11D-A32G-10 chr19:33792918 C>T maps to NM_004364.3 A134A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A3KG-01A-11D-A20W-10 chr2:37455072 A>G maps to NM_005760.2 S421S. 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-AAVZ-01A-11D-A40R-10 chr1:15793936 C>T maps to ENST00000375924 H269H. Only missense variants will be evaluated by CHASM.
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-CC-A8HS-01A-11D-A35Z-10 chr1:151678724 C>T maps to NM_007185.4 Q367Q. 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-G3-AAV2-01A-11D-A36X-10 chr22:46792557 C>T maps to NM_014246.1 P1929P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WX-AA47-01A-11D-A38X-10 chr22:46930895 G>A maps to NM_014246.1 L724L. 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-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-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-DD-AACE-01A-11D-A40R-10 chr3:48698558 G>A maps to NM_001407.2 R503R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACF-01A-11D-A40R-10 chr3:48683635 G>A maps to NM_001407.2 H2450H. 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-DD-A39Y-01A-11D-A20W-10 chr2:27016083 T>C maps to NM_001809.3 T120T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73B-01A-12D-A32G-10 chr20:3765894 C>T maps to NM_001810.5 E412E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr16:90037949 G>A maps to NM_145039.3 G127G. 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-AACI-01A-11D-A40R-10 chr4:104066277 T>A maps to NM_001813.2 K1596*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EG-01A-11D-A20W-10 chr23:100357275 T>C did not map to a codon.
Sequencing variant TCGA-DD-A3A1-01A-11D-A20W-10 chr13:25478134 T>C maps to NM_018451.3 E918E. 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-DD-AAD5-01A-11D-A40R-10 chr22:42341232 T>C maps to NM_024053.3 T102T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACB-01A-11D-A40R-10 chr16:67862724 C>T maps to NM_025082.3 E434E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MB-01A-11D-A20W-10 chr9:123937426 A>G maps to NM_007018.4 A2293A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39Z-01A-11D-A20W-10 chr9:123857200 A>G maps to NM_007018.4 E128E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACG-01A-11D-A40R-10 chr5:122754207 A>C maps to NM_153223.3 G17G. 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-4R-AA8I-01A-11D-A382-10 chr15:49030736 G>A maps to NM_001194998.1 S1614S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MB-01A-11D-A20W-10 chr15:49060501 T>C maps to NM_001194998.1 K644K. 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-DD-AADV-01A-11D-A38X-10 chr15:49031450 A>G maps to NM_001194998.1 V1376V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr11:117214975 T>C maps to NM_014956.4 P59P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACX-01A-11D-A40R-10 chr1:243328221 T>A maps to NM_014812.2 R1014*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MB-01A-11D-A20W-10 chr18:13103588 T>C 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-DD-A1EE-01A-11D-A12Z-10 chr18:13056653 C>T maps to NM_032142.3 N1355N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr20:34090969 C>T maps to NM_007186.3 T1591T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MA-01A-11D-A20W-10 chr12:88523494 T>C maps to NM_025114.3 K276K. 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-FV-A2QR-01A-11D-A20W-10 chr12:88444169 T>C maps to NM_025114.3 T2390T. Only missense variants will be evaluated by CHASM.
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-ZP-A9D1-01A-11D-A382-10 chr12:88534998 A>T maps to NM_025114.3 L29*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MA-01A-11D-A20W-10 chr1:179972309 T>C maps to NM_014810.4 G340G. 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-DD-AACQ-01A-11D-A40R-10 chr9:80851281 A>T maps to NM_001098802.1 K6*. 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-DD-AAD8-01A-11D-A40R-10 chr9:14722568 G>C maps to NM_005454.2 L34L. 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 chr16:55862714 C>T maps to NM_001025195.1 W75*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZS-A9CF-01A-11D-A382-10 chr16:55853488 T>C maps to NM_001025195.1 R288R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9GV-01A-11D-A382-10 chr16:66971948 C>G maps to NM_003869.5 S93*. 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-CC-A7IK-01A-12D-A33Q-10 chr16:55897345 T>A maps to NM_001143685.1 K242*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADO-01A-11D-A40R-10 chr23:151997124 C>T did not map to a codon.
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-DD-A3A1-01A-11D-A20W-10 chr16:75338932 T>C maps to NM_006324.2 R266R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADE-01A-11D-A40R-10 chr23:47486302 G>C did not map to a codon.
Sequencing variant TCGA-WX-AA47-01A-11D-A38X-10 chr23:47483693 G>T 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-DD-AACL-01A-11D-A40R-10 chr1:151501989 A>G maps to NM_020770.2 Q687Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADG-01A-11D-A40R-10 chr10:90966683 G>T maps to NM_003956.3 L122L. 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-DD-AACE-01A-11D-A40R-10 chr19:4422570 G>A maps to NM_005483.2 E342E. 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-EP-A2KA-01A-11D-A183-10 chr10:50833614 C>A maps to NM_020549.4 P283P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACY-01A-11D-A40R-10 chr5:98262045 T>G maps to NM_001270.2 G15G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr5:98204196 A>T did not map to a codon.
Sequencing variant TCGA-XR-A8TG-01A-11D-A35Z-10 chr5:98192415 T>A maps to NM_001270.2 R1601*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1ED-01A-11D-A152-10 chr1:146731568 A>G maps to NM_004284.3 S191S. 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-DD-A3A0-01A-11D-A20W-10 chr15:93547896 T>C maps to NM_001271.3 G1443G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAC8-01A-11D-A40R-10 chr15:93552535 C>T maps to NM_001271.3 H1525H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EG-01A-11D-A20W-10 chr17:7806315 T>C maps to NM_001005271.2 N1203N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39Y-01A-11D-A20W-10 chr17:7802658 A>G did not map to a codon.
Sequencing variant TCGA-2Y-A9GY-01A-11D-A382-10 chr12:6682293 G>A maps to ENST00000309577 L1863L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9H6-01A-11D-A38X-10 chr12:6710862 C>A maps to ENST00000309577 E170*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr1:6202185 A>G did not map to a codon.
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-DD-AAC8-01A-11D-A40R-10 chr20:40127976 T>A maps to NM_032221.3 A291A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAE0-01A-11D-A40R-10 chr20:40050513 G>A maps to NM_032221.3 G1587G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-AAV0-01A-11D-A36X-10 chr20:40127985 T>C maps to NM_032221.3 E288E. 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-ES-A2HT-01A-12D-A183-10 chr8:61765122 T>C maps to NM_017780.2 P1987P. 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-DD-AAVU-01A-11D-A40R-10 chr14:21896308 C>T maps to NM_001170629.1 S440S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CJ-01A-11D-A20W-10 chr14:21865983 T>C maps to NM_001170629.1 E1683E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAD5-01A-11D-A40R-10 chr16:53307550 T>A maps to ENST00000219084 P1577P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAEA-01A-11D-A40R-10 chr16:53265377 A>G maps to ENST00000219084 V778V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr16:53358167 G>A maps to ENST00000219084 L2685L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CG-01A-11D-A20W-10 chr16:53338415 T>A maps to ENST00000219084 S2166S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CG-01A-11D-A20W-10 chr16:53338418 A>T maps to ENST00000219084 S2167S. 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-DD-A39X-01A-11D-A20W-10 chr20:5903683 T>C maps to NM_001819.2 S298S. 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-3K-AAZ8-01A-12D-A38X-10 chr1:111861227 T>A maps to NM_201653.2 I281I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IE-01A-21D-A382-10 chr1:111861236 C>T maps to NM_201653.2 P284P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr1:111857936 C>A maps to NM_201653.2 I120I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACJ-01A-11D-A40R-10 chr23:72783216 T>C did not map to a codon.
Sequencing variant TCGA-DD-AAD0-01A-11D-A40R-10 chr23:72783363 C>T did not map to a codon.
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-A1EE-01A-11D-A12Z-10 chr23:85218968 C>G did not map to a codon.
Sequencing variant TCGA-DD-A3A0-01A-11D-A20W-10 chr23:85282509 A>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-DD-AADO-01A-11D-A40R-10 chr23:85218701 C>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-BC-A3KF-01A-11D-A20W-10 chr2:175673732 T>C maps to NM_001822.4 E334E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A1-01A-11D-A20W-10 chr7:150935430 G>C maps to NM_019015.1 G661G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr3:184104452 C>T maps to NM_003741.2 P702P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-AA0V-01A-11D-A382-10 chr3:184103889 C>T maps to NM_003741.2 G625G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr11:62677348 G>A maps to NM_000738.2 Y408Y. Only missense variants will be evaluated by CHASM.
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-DD-A1ED-01A-11D-A152-10 chr11:3687609 G>A maps to NM_020402.2 S360S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr8:27320753 G>A maps to NM_000742.3 H402H. 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-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-A3A1-01A-11D-A20W-10 chr8:42611843 A>G maps to NM_004198.3 P166P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACV-01A-11D-A40R-10 chr15:32455505 C>T maps to NM_001190455.1 H349H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-AAV1-01A-11D-A382-10 chr15:32455517 G>A maps to NM_001190455.1 G353G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5C-A9VG-01A-11D-A36X-10 chr17:7359260 G>C did not map to a codon.
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-DD-AAE4-01A-11D-A40R-10 chr1:154548296 T>C maps to NM_000748.2 F466F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACQ-01A-11D-A40R-10 chr8:42587109 T>C maps to NM_000749.3 Y220Y. 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-DD-AAD1-01A-11D-A40R-10 chr2:233392133 T>A maps to NM_000751.1 T74T. 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-DD-AAC9-01A-11D-A40R-10 chr11:45672281 G>A maps to NM_003654.4 L64L. 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-DD-A39Z-01A-11D-A20W-10 chr15:40764275 T>C maps to NM_130468.3 P288P. 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-DD-A1EE-01A-11D-A12Z-10 chr10:125769677 C>T maps to NM_015892.3 W558*. 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-G3-AAV2-01A-11D-A36X-10 chr10:73767946 C>T maps to NM_004273.4 Y386Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3K-AAZ8-01A-12D-A38X-10 chr16:75563640 C>T maps to NM_024533.3 A214A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACF-01A-11D-A40R-10 chr23:46433906 G>A did not map to a codon.
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-WQ-A9G7-01A-11D-A36X-10 chr16:844173 T>C maps to ENST00000317063 S850S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr10:101982627 G>T maps to NM_001278.3 R104R. 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-DD-A1ED-01A-11D-A152-10 chr19:42793505 T>C maps to NM_015125.3 S436S. 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-FV-A2QR-01A-11D-A20W-10 chr19:42798457 T>C did not map to a codon.
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-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-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-2Y-A9H4-01A-11D-A382-10 chr3:50649060 C>T did not map to a codon.
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-2Y-A9H7-01A-11D-A38X-10 chr9:130943065 C>A maps to NM_012127.2 E206*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr9:130947924 A>G maps to NM_012127.2 P163P. 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-A3KF-01A-11D-A20W-10 chr11:46819405 A>G maps to ENST00000415402 A429A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A1-01A-11D-A20W-10 chr11:46818445 T>C maps to ENST00000415402 E461E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr11:46797921 T>C maps to ENST00000415402 R958R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAEE-01A-11D-A40R-10 chr14:103988749 G>A maps to NM_001823.3 N27N. 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-LG-A9QD-01A-11D-A382-10 chr2:122165164 G>A maps to NM_015282.2 L851L. 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-2Y-A9GT-01A-11D-A382-10 chr1:86954812 C>T maps to NM_001285.3 P439P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EG-01A-11D-A20W-10 chr1:86957055 T>C did not map to a codon.
Sequencing variant TCGA-DD-A39X-01A-11D-A20W-10 chr1:86904779 A>G maps to NM_006536.5 K398K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A3KF-01A-11D-A20W-10 chr1:87038339 C>T maps to ENST00000263723 G468G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39X-01A-11D-A20W-10 chr7:143043237 T>C maps to NM_000083.2 P726P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAEE-01A-11D-A40R-10 chr7:143018841 T>A maps to NM_000083.2 R199R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr4:170625276 C>T maps to NM_173872.2 V564V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACL-01A-11D-A40R-10 chr23:10166044 G>C did not map to a codon.
Sequencing variant TCGA-2Y-A9GT-01A-11D-A382-10 chr23:49840464 T>A did not map to a codon.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr23:49855055 A>G did not map to a codon.
Sequencing variant TCGA-NI-A4U2-01A-11D-A28X-10 chr23:49854826 G>T did not map to a codon.
Sequencing variant TCGA-DD-AAC8-01A-11D-A40R-10 chr1:16358336 A>T maps to NM_004070.3 T585T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10W-01A-11D-A12Z-10 chr1:16377073 C>T maps to NM_000085.3 A344A. Only missense variants will be evaluated by CHASM.
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-2Y-A9H1-01A-11D-A382-10 chr21:37833540 C>T maps to NM_001146077.1 L151L. 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-DD-AAE7-01A-11D-A40R-10 chr12:10131562 A>T did not map to a codon.
Sequencing variant TCGA-DD-AADE-01A-11D-A40R-10 chr12:10163363 T>C maps to NM_001129998.1 S2S. 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-DD-AADG-01A-11D-A40R-10 chr16:11217615 C>T maps to ENST00000409790 G762G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACK-01A-11D-A40R-10 chr12:10224015 C>T maps to NM_016511.2 K253K. 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-DD-AADM-01A-11D-A40R-10 chr19:7795686 C>G maps to NM_198492.3 A114A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAE9-01A-11D-A40R-10 chr12:8612283 A>G maps to NM_001007033.1 T71T. 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-DD-A1EE-01A-11D-A12Z-10 chr6:45922897 G>A maps to NM_001114086.1 F208F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A3KF-01A-11D-A20W-10 chr21:36081736 C>T maps to ENST00000360731 Y618Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A9FS-01A-11D-A36X-10 chr21:36042757 C>T maps to ENST00000360731 D357D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A2QR-01A-11D-A20W-10 chr12:122864936 T>C maps to ENST00000302528 T21T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAW1-01A-11D-A40P-10 chr7:73790426 A>T maps to NM_003388.4 K566*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACG-01A-11D-A40R-10 chr2:29366801 A>T maps to ENST00000379543 A292A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADF-01A-11D-A40R-10 chr2:29355070 T>A maps to ENST00000379543 T109T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACG-01A-11D-A40R-10 chr1:155238147 C>A maps to ENST00000368361 E164*. 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-DD-A1EG-01A-11D-A20W-10 chr15:74921280 A>G did not map to a codon.
Sequencing variant TCGA-DD-AACI-01A-11D-A40R-10 chr15:74914529 C>A maps to NM_001130028.1 R295R. 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-AAD8-01A-11D-A40R-10 chr14:95677209 G>C maps to NM_024734.3 G205G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADE-01A-11D-A40R-10 chr16:28495438 G>A maps to NM_000086.2 S226S. 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-4R-AA8I-01A-11D-A382-10 chr8:1719729 G>A maps to NM_018941.3 T170T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9H9-01A-21D-A38X-10 chr4:56308735 A>C maps to NM_004898.2 T656T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAE6-01A-11D-A40R-10 chr11:57427364 G>A maps to NM_006831.2 V139V. 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-EP-A2KA-01A-11D-A183-10 chr19:45489768 C>A maps to NM_001294.2 T243T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CG-01A-11D-A20W-10 chr19:45488527 A>G maps to NM_001294.2 T213T. 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-2Y-A9HA-01A-11D-A38X-10 chr3:140123534 C>A maps to NM_022131.2 C188*. 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-DD-A3A0-01A-11D-A20W-10 chr12:7295528 T>C maps to NM_014718.3 G535G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAW3-01A-11D-A40P-10 chr12:7288406 T>A maps to NM_014718.3 I200I. 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.
Sequencing variant TCGA-DD-A1EG-01A-11D-A20W-10 chr22:19189000 C>A maps to NM_007098.3 G1202*. Only missense variants will be evaluated by CHASM.
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-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-EP-A2KA-01A-11D-A183-10 chr16:81654515 T>C maps to NM_198390.2 H154H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr12:108685650 A>G maps to NM_001142344.1 T363T. 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-AAED-01A-12D-A40R-10 chr5:79031058 A>G maps to NM_153610.3 T2157T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr5:79034136 G>T maps to NM_153610.3 L3183L. 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-DD-AACI-01A-11D-A40R-10 chr8:88365868 A>G maps to NM_173538.2 R386R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADC-01A-11D-A40R-10 chr8:87951907 T>C maps to NM_173538.2 H119H. 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-5R-AAAM-01A-12D-A40R-10 chr3:128889413 C>T did not map to a codon.
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-4R-AA8I-01A-11D-A382-10 chr19:42893102 C>T maps to NM_032488.3 T29T. 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-ZP-A9CV-01A-11D-A382-10 chr23:150912120 G>T did not map to a codon.
Sequencing variant TCGA-ZP-A9CV-01A-11D-A382-10 chr23:150912139 A>G 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-DD-A39Y-01A-11D-A20W-10 chr11:6265176 A>G did not map to a codon.
Sequencing variant TCGA-DD-AACK-01A-11D-A40R-10 chr11:6261882 A>T maps to NM_001037329.2 K287*. 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-DD-AADQ-01A-11D-A40R-10 chr8:87755756 T>G maps to NM_019098.4 P33P. 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-2Y-A9H7-01A-11D-A38X-10 chr1:224559053 G>A maps to NM_014184.2 L107L. Only missense variants will be evaluated by CHASM.
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-A1EE-01A-11D-A12Z-10 chr23:21545014 G>A did not map to a codon.
Sequencing variant TCGA-DD-A1EG-01A-11D-A20W-10 chr6:154731498 T>C maps to NM_173515.2 R449R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr10:101136950 C>A maps to NM_020348.2 I772I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WQ-A9G7-01A-11D-A36X-10 chr10:101089164 G>A maps to NM_020348.2 A7A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39Y-01A-11D-A20W-10 chr16:58608979 A>G maps to NM_016284.3 A586A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACC-01A-11D-A40R-10 chr16:58572171 T>C did not map to a codon.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr16:58620482 T>C maps to NM_016284.3 E201E. 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-ED-A66X-01A-11D-A30V-10 chr19:54652190 C>A maps to NM_014516.3 G401G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5R-AA1C-01A-11D-A40R-10 chr7:135099082 A>T maps to NM_001190850.1 L186L. 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-DD-AADU-01A-11D-A40R-10 chr7:135080632 T>A maps to NM_001190850.1 I294I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9H3-01A-11D-A382-10 chr5:179980383 A>G did not map to a codon.
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-A3A1-01A-11D-A20W-10 chr4:78697512 A>G maps to ENST00000512485 P20P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAW0-01A-11D-A40R-10 chr4:78694247 A>G maps to ENST00000512485 T136T. 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-A1EE-01A-11D-A12Z-10 chr12:56708751 T>C did not map to a codon.
Sequencing variant TCGA-DD-AADD-01A-11D-A40R-10 chr7:99720106 G>A maps to NM_152755.1 E83E. Only missense variants will be evaluated by CHASM.
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-ES-A2HS-01A-11D-A183-10 chr1:246810802 T>C maps to NM_152609.2 L434L. 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-2Y-A9H9-01A-21D-A38X-10 chr9:17394650 A>G maps to NM_017738.2 Q733Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A216-01A-11D-A152-10 chr12:41410482 G>A did not map to a codon.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr12:41337845 A>G maps to NM_001843.2 G519G. Only missense variants will be evaluated by CHASM.
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-DD-AACL-01A-11D-A40R-10 chr12:41374783 T>A maps to NM_001843.2 R626R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADK-01A-11D-A40R-10 chr1:205027172 C>T maps to NM_005076.3 A65A. 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-CC-A3MB-01A-11D-A20W-10 chr3:3097903 A>G maps to NM_175607.1 *1027W. 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-2Y-A9H3-01A-11D-A382-10 chr3:1444078 A>G maps to NM_014461.2 P965P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MB-01A-11D-A20W-10 chr3:1337366 A>G maps to NM_014461.2 G179G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39Y-01A-11D-A20W-10 chr3:1367496 A>G did not map to a codon.
Sequencing variant TCGA-G3-A3CJ-01A-11D-A20W-10 chr3:1414127 A>G maps to NM_014461.2 K546K. 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-XR-A8TF-01A-11D-A35Z-10 chr3:1414519 A>T did not map to a codon.
Sequencing variant TCGA-DD-AAD8-01A-11D-A40R-10 chr17:40835881 C>A maps to NM_003632.2 S37S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAE3-01A-11D-A40R-10 chr7:146829530 C>A maps to NM_014141.5 L426L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAE3-01A-11D-A40R-10 chr7:147259227 A>G did not map to a codon.
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-XR-A8TE-01A-11D-A35Z-10 chr9:39078813 C>A maps to NM_033655.3 A1182A. 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-DD-AACI-01A-11D-A40R-10 chr2:125204372 C>G maps to NM_130773.2 T259T. 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-2Y-A9H0-01A-11D-A382-10 chr7:51096608 G>A maps to ENST00000395542 T810T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr7:51085258 A>G maps to ENST00000395542 L1341L. 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-DD-AACL-01A-11D-A40R-10 chr7:51095924 G>C maps to ENST00000395542 G1038G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr7:51111114 C>T maps to ENST00000395542 L539L. 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-AAC8-01A-11D-A40R-10 chr9:140166671 A>T maps to NM_015456.3 P495P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A7M9-01A-23D-A34Z-10 chr9:140158809 G>T did not map to a codon.
Sequencing variant TCGA-LG-A6GG-01A-11D-A30V-10 chr9:140160780 A>G did not map to a codon.
Sequencing variant TCGA-DD-AADD-01A-11D-A40R-10 chr14:31355228 T>G maps to NM_004086.2 T396T. 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-DD-AACT-01A-11D-A40R-10 chr17:71197660 C>G maps to NM_018714.2 T565T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A2QR-01A-11D-A20W-10 chr16:70553592 T>C maps to NM_015386.2 Q71Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9H3-01A-11D-A382-10 chr13:40256305 A>T did not map to a codon.
Sequencing variant TCGA-DD-A39Y-01A-11D-A20W-10 chr13:40297513 T>G maps to ENST00000255468 Y576*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NI-A8LF-01A-11D-A35Z-10 chr13:40256392 C>A maps to ENST00000255468 V293V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1ED-01A-11D-A152-10 chr16:69368966 A>G maps to NM_032382.4 R290R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAD6-01A-11D-A40R-10 chr16:69364960 T>C maps to NM_032382.4 L540L. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-BC-A8YO-01A-11D-A36X-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-2Y-A9GT-01A-11D-A382-10 chr1:103496800 C>A did not map to a codon.
Sequencing variant TCGA-2Y-A9GW-01A-11D-A382-10 chr1:103387109 T>A maps to NM_080629.2 P1236P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MB-01A-11D-A20W-10 chr1:103481280 A>G maps to NM_080629.2 P489P. Only missense variants will be evaluated by CHASM.
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-DD-A1EG-01A-11D-A20W-10 chr1:103453236 T>C maps to NM_080629.2 R830R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr1:103491373 T>C maps to NM_080629.2 K305K. 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-DD-AACI-01A-11D-A40R-10 chr6:33144071 G>A maps to NM_080680.2 D726D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADE-01A-11D-A40R-10 chr6:33154481 C>T maps to NM_080680.2 Q240Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADL-01A-11D-A40R-10 chr6:33157127 C>T maps to NM_080680.2 Q67Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAEH-01A-11D-A40R-10 chr6:33145003 T>C did not map to a codon.
Sequencing variant TCGA-2Y-A9H3-01A-11D-A382-10 chr6:75904565 T>A maps to ENST00000322507 I57I. 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-CC-A7IE-01A-21D-A382-10 chr6:75853039 A>G maps to ENST00000322507 F1585F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACD-01A-11D-A40R-10 chr6:75904604 T>C maps to ENST00000322507 S44S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACI-01A-11D-A40R-10 chr6:75875409 A>G maps to ENST00000322507 V932V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACL-01A-11D-A40R-10 chr6:75893245 C>A maps to ENST00000322507 E471*. 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-FV-A2QR-01A-11D-A20W-10 chr6:75806977 T>C maps to ENST00000322507 P2856P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A2QR-01A-11D-A20W-10 chr6:75864132 A>G maps to ENST00000322507 S1188S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CG-01A-11D-A20W-10 chr6:75893786 A>G maps to ENST00000322507 S357S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YA-A8S7-01A-11D-A36X-10 chr6:75904616 A>T maps to ENST00000322507 T40T. 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-AADG-01A-11D-A40R-10 chr8:121296006 T>A maps to NM_021110.1 V1319V. 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-DD-A1EE-01A-11D-A12Z-10 chr9:101749574 G>A did not map to a codon.
Sequencing variant TCGA-DD-A39Y-01A-11D-A20W-10 chr9:101765841 G>T maps to NM_001855.3 T391T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A0-01A-11D-A20W-10 chr9:101829177 T>C maps to NM_001855.3 A1222A. 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-DD-AACE-01A-11D-A40R-10 chr1:32131183 C>T maps to NM_001856.3 P1164P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACT-01A-11D-A40R-10 chr1:32163574 G>A maps to NM_001856.3 R197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAVR-01A-11D-A40R-10 chr1:32131189 G>A maps to NM_001856.3 G1162G. 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-WX-AA46-01A-11D-A38X-10 chr1:32157041 A>G maps to NM_001856.3 P458P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A2QR-01A-11D-A20W-10 chr10:105830328 T>C did not map to a codon.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr21:46910775 G>A maps to ENST00000359759 R1101R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A0-01A-11D-A20W-10 chr21:46899862 T>C maps to ENST00000359759 G847G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADR-01A-11D-A40R-10 chr21:46912478 G>A did not map to a codon.
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-EP-A2KA-01A-11D-A183-10 chr6:70897948 G>T maps to NM_001858.4 P1009P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39Z-01A-11D-A20W-10 chr17:48271981 T>C maps to NM_000088.3 G489G. 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-DD-A3A1-01A-11D-A20W-10 chr7:94056342 T>C maps to NM_000089.3 A1043A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACL-01A-11D-A40R-10 chr7:94053727 T>C maps to NM_000089.3 R882R. 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-DD-AA3A-01A-11D-A36X-10 chr20:61943319 G>A maps to ENST00000326996 A579A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACQ-01A-11D-A40R-10 chr20:61943818 T>A maps to ENST00000326996 S624S. 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-2Y-A9H3-01A-11D-A382-10 chr6:55924014 T>C maps to NM_030820.3 K878K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NE-01A-11D-A27I-10 chr8:139824125 G>A maps to NM_152888.1 P455P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACA-01A-11D-A40R-10 chr8:139856351 G>T maps to NM_152888.1 T236T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACI-01A-11D-A40R-10 chr8:139727942 T>C maps to NM_152888.1 K833K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACJ-01A-11D-A40R-10 chr8:139895406 G>T maps to NM_152888.1 G3G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADI-01A-11D-A40R-10 chr8:139696712 C>A did not map to a codon.
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-WQ-AB4B-01A-11D-A40P-10 chr8:139601630 G>A maps to NM_152888.1 G1582G. 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-DD-AADI-01A-11D-A40R-10 chr5:177695728 A>G did not map to a codon.
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-WQ-A9G7-01A-11D-A36X-10 chr5:177669108 G>C maps to ENST00000390654 G505G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADO-01A-11D-A40R-10 chr1:86289218 T>C maps to NM_152890.5 E1263E. 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-WX-AA47-01A-11D-A38X-10 chr1:86200502 T>A maps to NM_152890.5 K1643*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACZ-01A-11D-A40R-10 chr4:109765683 A>T maps to ENST00000333642 P540P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr9:117068855 C>A maps to NM_032888.2 T1665T. 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-BC-A8YO-01A-11D-A36X-10 chr7:7421216 T>A maps to NM_001037763.2 P721P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A0-01A-11D-A20W-10 chr7:7555462 A>G maps to NM_001037763.2 P288P. Only missense variants will be evaluated by CHASM.
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-5C-AAPD-01A-21D-A38X-10 chr12:48368645 C>T did not map to a codon.
Sequencing variant TCGA-DD-AADY-01A-11D-A40R-10 chr12:48373811 G>A maps to NM_001844.4 R887*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAEI-01A-11D-A40R-10 chr12:48378843 A>T maps to NM_001844.4 P589P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAVR-01A-11D-A40R-10 chr12:48376329 A>C maps to NM_001844.4 P752P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr12:48374363 C>T maps to NM_001844.4 Q866Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr12:48381090 G>A maps to NM_001844.4 N409N. 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-A39Y-01A-11D-A20W-10 chr13:110827093 T>C maps to NM_001845.4 G1067G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZS-A9CF-01A-11D-A382-10 chr13:110807651 C>T maps to NM_001845.4 W1578*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EE-01A-11D-A12Z-10 chr13:111117936 G>A maps to NM_001846.2 G654G. 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-WX-AA46-01A-11D-A38X-10 chr13:111125289 C>T maps to NM_001846.2 R740*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EG-01A-11D-A20W-10 chr2:228111435 G>C maps to NM_000091.4 L141L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A0-01A-11D-A20W-10 chr2:228174006 T>C maps to NM_000091.4 S1576S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACE-01A-11D-A40R-10 chr2:228141108 G>T maps to NM_000091.4 G646*. 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-AAC9-01A-11D-A40R-10 chr2:227919328 C>A maps to ENST00000396625 R947R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LG-A9QD-01A-11D-A382-10 chr2:227942712 C>T maps to ENST00000396625 G628G. 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-2Y-A9H9-01A-21D-A38X-10 chr23:107869538 G>T did not map to a codon.
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-AAC8-01A-11D-A40R-10 chr23:107823969 T>A did not map to a codon.
Sequencing variant TCGA-DD-AACA-01A-11D-A40R-10 chr23:107925028 T>C did not map to a codon.
Sequencing variant TCGA-DD-AACT-01A-11D-A40R-10 chr23:107867494 T>A did not map to a codon.
Sequencing variant TCGA-DD-AAD0-01A-11D-A40R-10 chr23:107821328 C>T did not map to a codon.
Sequencing variant TCGA-DD-AAD1-01A-11D-A40R-10 chr23:107824222 G>T did not map to a codon.
Sequencing variant TCGA-DD-AADI-01A-11D-A40R-10 chr23:107863657 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-BD-A3EP-01A-11D-A22F-10 chr23:107418369 T>C 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-CC-A8HT-01A-11D-A35Z-10 chr23:107464562 A>G did not map to a codon.
Sequencing variant TCGA-DD-A3A0-01A-11D-A20W-10 chr23:107448672 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-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-BD-A3EP-01A-11D-A22F-10 chr9:137593179 G>A 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-DD-A1EG-01A-11D-A20W-10 chr2:189951463 T>C maps to NM_000393.3 L226L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A2QR-01A-11D-A20W-10 chr2:189922081 T>C maps to NM_000393.3 R767R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADG-01A-11D-A40R-10 chr19:10092739 C>T did not map to a codon.
Sequencing variant TCGA-DD-AAEI-01A-11D-A40R-10 chr19:10087233 C>T maps to NM_015719.3 P1114P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZS-A9CG-01A-11D-A36X-10 chr19:10089906 T>A maps to NM_015719.3 T925T. Only missense variants will be evaluated by CHASM.
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-A3MA-01A-11D-A20W-10 chr2:238244874 A>G maps to NM_004369.3 A2956A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EE-01A-11D-A12Z-10 chr2:238249116 C>T maps to NM_004369.3 R2814R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A2QR-01A-11D-A20W-10 chr2:238244874 A>G maps to NM_004369.3 A2956A. 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-DD-AACC-01A-11D-A40R-10 chr3:130346160 A>C did not map to a codon.
Sequencing variant TCGA-ED-A8O5-01A-11D-A35Z-10 chr3:130290001 C>T maps to NM_001102608.1 V914V. 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-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-GJ-A9DB-01A-11D-A36X-10 chr1:36565002 G>C maps to NM_005202.2 P93P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A3KG-01A-11D-A20W-10 chr6:70991131 A>G maps to NM_001851.4 P279P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACL-01A-11D-A40R-10 chr6:70942394 A>T maps to NM_001851.4 P798P. 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-UB-A7MB-01A-11D-A33Q-10 chr1:40777785 T>A did not map to a codon.
Sequencing variant TCGA-2Y-A9HA-01A-11D-A38X-10 chr8:120103442 G>T maps to NM_006438.3 G92G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACV-01A-11D-A40R-10 chr2:3691386 C>T maps to ENST00000418971 D179D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADB-01A-11D-A40R-10 chr18:346625 C>T maps to NM_130386.2 L332L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADS-01A-11D-A40R-10 chr18:335066 G>A maps to NM_130386.2 G497G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAEE-01A-11D-A40R-10 chr18:347057 G>T maps to NM_130386.2 L188L. Only missense variants will be evaluated by CHASM.
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-ZP-A9D4-01A-11D-A36X-10 chr18:334823 G>T maps to NM_130386.2 G578G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACG-01A-11D-A40R-10 chr3:15507878 G>T maps to NM_005677.3 G261G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACT-01A-11D-A40R-10 chr10:22605411 C>T maps to NM_012071.2 S22S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A1-01A-11D-A20W-10 chr8:146076708 C>T maps to NM_001081003.1 G5G. 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-NI-A8LF-01A-11D-A35Z-10 chr19:18895753 C>T maps to NM_000095.2 W622*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADF-01A-11D-A40R-10 chr1:160303436 A>G maps to NM_001098398.1 D114D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EG-01A-11D-A20W-10 chr11:14487825 A>G did not map to a codon.
Sequencing variant TCGA-DD-AAW3-01A-11D-A40P-10 chr11:14512194 A>G maps to NM_001144061.1 P174P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACP-01A-11D-A40R-10 chr3:139096978 T>C maps to NM_004766.2 Q136Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr3:128984636 T>C did not map to a codon.
Sequencing variant TCGA-DD-AAVW-01A-11D-A40R-10 chr3:128986866 A>G maps to NM_016128.3 A544A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A3I1-01A-11D-A22F-10 chr3:128973579 C>A maps to NM_016128.3 I131I. 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-G3-A3CJ-01A-11D-A20W-10 chr14:74422602 T>C maps to NM_182476.1 A151A. 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-EP-A2KB-01A-11D-A183-10 chr16:30196583 G>T maps to NM_007074.3 P18P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WQ-A9G7-01A-11D-A36X-10 chr16:30198462 C>T maps to NM_007074.3 S185S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XR-A8TC-01A-11D-A35Z-10 chr11:67209970 G>C maps to NM_020441.2 V43V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5R-AA1C-01A-11D-A40R-10 chr15:69011782 T>C maps to NM_006091.3 Y401Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BD-A3ER-01A-11D-A20W-10 chr16:4414674 C>A maps to NM_024535.3 E354*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACI-01A-11D-A40R-10 chr16:4405165 T>A did not map to a codon.
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-DD-AAD6-01A-11D-A40R-10 chr10:101491745 G>A maps to NM_078470.4 L21L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-AAV0-01A-11D-A36X-10 chr10:101476152 T>C maps to NM_078470.4 R351R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2V-A95S-01A-11D-A36X-10 chr4:73931078 T>G maps to NM_173827.2 R162R. 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-WQ-A9G7-01A-11D-A36X-10 chr3:148925300 G>A maps to NM_000096.3 H295H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1ED-01A-11D-A152-10 chr16:19556462 T>C maps to NM_014711.4 D878D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A5SM-01A-12D-A28X-10 chr16:19551991 A>G maps to NM_014711.4 L644L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A8O5-01A-11D-A35Z-10 chr3:148596535 G>A did not map to a codon.
Sequencing variant TCGA-GJ-A3OU-01A-31D-A382-10 chr7:130007817 C>T maps to NM_080385.4 I370I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAE4-01A-11D-A40R-10 chr8:68536485 A>T maps to NM_020361.4 G39G. 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-3K-AAZ8-01A-12D-A38X-10 chr19:17004083 G>A maps to ENST00000443236 S1888S. 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-AA3A-01A-11D-A36X-10 chr19:17100488 G>T maps to ENST00000443236 C510*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADC-01A-11D-A40R-10 chr19:17017876 C>T maps to ENST00000443236 A1361A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACZ-01A-11D-A40R-10 chr17:28778775 T>C maps to NM_001304.4 D1039D. 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-BC-A3KF-01A-11D-A20W-10 chr15:83296064 A>G maps to ENST00000261723 A23A. 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-K7-A6G5-01A-11D-A30V-10 chr5:175306951 G>T maps to NM_001008220.1 A103A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr12:69326512 A>G maps to NM_001874.4 V35V. 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-EP-A2KA-01A-11D-A183-10 chr10:101824983 G>T maps to NM_001308.2 T240T. 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-2Y-A9H3-01A-11D-A382-10 chr6:36710254 G>A maps to NM_020939.1 P524P. 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-ES-A2HT-01A-12D-A183-10 chr16:89651219 C>T maps to NM_014427.4 Y257Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACX-01A-11D-A40R-10 chr16:12897628 G>T maps to NM_018340.2 S2*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9H3-01A-11D-A382-10 chr2:211442190 G>A maps to NM_001122633.1 W149*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39X-01A-11D-A20W-10 chr2:211476884 T>C maps to NM_001122633.1 A818A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAVY-01A-11D-A40R-10 chr2:211465357 T>C maps to NM_001122633.1 A549A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr2:211455600 C>T maps to NM_001122633.1 A312A. Only missense variants will be evaluated by CHASM.
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-AACT-01A-11D-A40R-10 chr8:145623167 C>T did not map to a codon.
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-DD-A3A1-01A-11D-A20W-10 chr14:92609577 T>C maps to NM_017437.1 T360T. 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-CC-A9FS-01A-11D-A36X-10 chr12:69652697 G>T maps to ENST00000266679 P378P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr11:68580045 T>A did not map to a codon.
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-DD-AADQ-01A-11D-A40R-10 chr23:88008449 C>T 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-DD-AACF-01A-11D-A40R-10 chr20:2775921 C>T did not map to a codon.
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-DD-AAD6-01A-11D-A40R-10 chr4:8594613 C>A maps to NM_001014447.2 A18A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAE3-01A-11D-A40R-10 chr4:8607786 C>T maps to NM_001014447.2 L261L. 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-ZP-A9D0-01A-11D-A36X-10 chr1:207748948 C>T maps to NM_000651.4 L1487L. 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-DD-AAVQ-01A-11D-A40R-10 chr16:1715077 A>G maps to NM_020825.3 P897P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GJ-A3OU-01A-31D-A382-10 chr16:1691137 A>C did not map to a codon.
Sequencing variant TCGA-WX-AA44-01A-11D-A38X-10 chr9:131866546 G>A maps to NM_000755.3 Y110Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAE2-01A-11D-A40R-10 chr1:197313447 C>T maps to NM_201253.2 S230S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr3:3221341 A>G maps to NM_016302.3 A10A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A3KF-01A-11D-A20W-10 chr7:137612917 G>A maps to NM_194071.2 T99T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACD-01A-11D-A40R-10 chr19:4171377 A>G did not map to a codon.
Sequencing variant TCGA-DD-AACI-01A-11D-A40R-10 chr19:4171377 A>G did not map to a codon.
Sequencing variant TCGA-DD-AACI-01A-11D-A40R-10 chr19:4171710 A>T maps to NM_032607.1 P377P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-AAV3-01A-11D-A36X-10 chr19:4171377 A>T did not map to a codon.
Sequencing variant TCGA-RC-A7S9-01A-11D-A33Q-10 chr19:4171378 G>A did not map to a codon.
Sequencing variant TCGA-DD-AAEE-01A-11D-A40R-10 chr7:28843946 G>T maps to NM_182898.2 P278P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr16:3799677 A>G maps to NM_004380.2 I1262I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACQ-01A-11D-A40R-10 chr16:3807811 T>A maps to NM_004380.2 K1203*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADM-01A-11D-A40R-10 chr16:3843531 C>T maps to NM_004380.2 Q357Q. 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-ES-A2HT-01A-12D-A183-10 chr16:3788624 A>G maps to NM_004380.2 R1443R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WQ-A9G7-01A-11D-A36X-10 chr16:3778435 C>T maps to NM_004380.2 Q2204Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAE2-01A-11D-A40R-10 chr11:85375724 G>A maps to NM_001039618.2 A65A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A9FW-01A-11D-A36X-10 chr22:50316311 C>T maps to NM_001135101.1 G264G. 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-DD-AAW2-01A-11D-A40P-10 chr2:36749316 A>T maps to NM_016441.2 A763A. 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-CC-A7IE-01A-21D-A382-10 chr6:49825046 C>A 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-DD-A3A0-01A-11D-A20W-10 chr8:75932281 T>C maps to NM_031461.5 C404C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACH-01A-11D-A40R-10 chr8:75932273 C>T maps to NM_031461.5 Q402*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADP-01A-11D-A38X-10 chr17:1359300 C>T maps to NM_016823.2 V37V. 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-DD-AACS-01A-11D-A40R-10 chr4:5853137 G>A maps to NM_001014809.1 S293S. Only missense variants will be evaluated by CHASM.
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-AACQ-01A-11D-A40R-10 chr1:17280851 G>T maps to NM_014675.3 R1107R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A0-01A-11D-A20W-10 chr7:86988624 A>G maps to NM_001143935.1 R101R. 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-ZS-A9CE-01A-11D-A36X-10 chr1:159683526 G>A maps to NM_000567.2 Q155*. 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-BD-A3EP-01A-11D-A22F-10 chr22:27026345 T>C maps to NM_001886.2 Y162Y. 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-DD-AADF-01A-11D-A40R-10 chr3:97605566 A>G maps to ENST00000182096 E467E. Only missense variants will be evaluated by CHASM.
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-AAE0-01A-11D-A40R-10 chr12:56676232 G>A maps to NM_004077.2 Q187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39Y-01A-11D-A20W-10 chr12:53553668 A>G did not map to a codon.
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-G3-A3CG-01A-11D-A20W-10 chr12:10853934 T>C maps to NM_003651.4 A357A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAE7-01A-11D-A40R-10 chr20:47695152 A>G maps to NM_001316.2 R492R. 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-XR-A8TF-01A-11D-A35Z-10 chr1:110466106 C>T maps to NM_000757.4 N288N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr5:149434852 T>C maps to NM_005211.3 K867K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZS-A9CF-01A-11D-A382-10 chr5:149435892 C>T maps to NM_005211.3 R777R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr23:1424528 G>A did not map to a codon.
Sequencing variant TCGA-DD-AAC8-01A-11D-A40R-10 chr22:37318308 C>T maps to ENST00000262825 S20S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9H0-01A-11D-A382-10 chr8:3165890 G>A maps to NM_033225.5 L1256L. 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-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-DD-AAD1-01A-11D-A40R-10 chr8:2800023 G>T maps to NM_033225.5 S3502*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADN-01A-11D-A40R-10 chr8:3087643 A>G maps to NM_033225.5 Y1421Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADN-01A-11D-A40R-10 chr8:3326339 C>A maps to NM_033225.5 T485T. 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-ES-A2HT-01A-12D-A183-10 chr8:2824170 T>C maps to NM_033225.5 E3007E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GJ-A3OU-01A-31D-A382-10 chr8:2823434 G>A maps to NM_033225.5 Q3048*. 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-XR-A8TF-01A-11D-A35Z-10 chr8:3046417 C>A maps to NM_033225.5 S1838S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9H5-01A-11D-A382-10 chr1:33999414 T>C maps to ENST00000373381 G3284G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9HA-01A-11D-A38X-10 chr1:34089021 C>T maps to ENST00000373381 L1850L. 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-AAW1-01A-11D-A40P-10 chr1:33985195 G>A maps to ENST00000373381 Y3566Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr1:34089067 T>C did not map to a codon.
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-ZP-A9CY-01A-11D-A382-10 chr1:34291373 G>T maps to ENST00000373381 V305V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZS-A9CD-01A-11D-A36X-10 chr1:34204786 C>T maps to ENST00000373381 L734L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9HA-01A-11D-A38X-10 chr8:113694806 C>A maps to NM_198123.1 G847G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A3KG-01A-11D-A20W-10 chr8:113364737 T>C maps to NM_198123.1 E2054E. 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-CC-A9FU-01A-11D-A36X-10 chr8:113697725 A>T maps to NM_198123.1 P797P. 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-DD-AAC8-01A-11D-A40R-10 chr8:113599329 T>A maps to NM_198123.1 R1284*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADI-01A-11D-A40R-10 chr8:113403005 C>A maps to NM_198123.1 G1941*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADN-01A-11D-A40R-10 chr8:113249530 G>A maps to NM_198123.1 Y3505Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr8:113331156 A>G maps to NM_198123.1 C2423C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-AAV2-01A-11D-A36X-10 chr8:113331117 C>A maps to NM_198123.1 T2436T. 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-CC-A8HT-01A-11D-A35Z-10 chr4:70810723 T>C did not map to a codon.
Sequencing variant TCGA-DD-AADV-01A-11D-A38X-10 chr4:70804904 C>A maps to NM_001890.1 S85S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EG-01A-11D-A20W-10 chr4:70824772 T>C maps to NM_001891.2 E31E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9H0-01A-11D-A382-10 chr13:37679129 T>C maps to NM_145203.5 L88L. 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-ES-A2HT-01A-12D-A183-10 chr16:58198046 A>G maps to NM_001896.2 P327P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADP-01A-11D-A38X-10 chr6:31635682 T>C maps to ENST00000375885 T56T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A9FS-01A-11D-A36X-10 chr15:75981257 C>A maps to NM_001897.4 G716G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACT-01A-11D-A40R-10 chr15:75968373 A>C maps to NM_001897.4 T2162T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADE-01A-11D-A40R-10 chr15:75980590 G>T maps to NM_001897.4 R939R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr3:47618663 A>G maps to ENST00000383738 D284D. 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-BC-A3KG-01A-11D-A20W-10 chr8:68007673 A>G maps to ENST00000389042 R254R. 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-DD-AADL-01A-11D-A40R-10 chr20:23433400 T>C maps to NM_130794.1 L16L. 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-4R-AA8I-01A-11D-A382-10 chr3:122060395 C>T maps to NM_005213.3 D93D. 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-DD-A39Y-01A-11D-A20W-10 chr23:100078881 T>C 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-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-BC-A3KF-01A-11D-A20W-10 chr2:219266305 T>C maps to NM_021198.1 A29A. 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-AACL-01A-11D-A40R-10 chr6:132270672 T>A maps to NM_001901.2 K261*. 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-AAVS-01A-11D-A40R-10 chr2:204736110 G>A maps to NM_005214.3 P156P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10W-01A-11D-A12Z-10 chr5:138260966 A>G maps to ENST00000355078 Q590Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACH-01A-11D-A40R-10 chr5:138269735 G>A maps to ENST00000355078 P916P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAE2-01A-11D-A40R-10 chr5:138223239 T>A maps to ENST00000355078 L402*. 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-A4NK-01A-11D-A28X-10 chr2:80801439 G>T did not map to a codon.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr2:80085186 C>A maps to ENST00000402739 S116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAEA-01A-11D-A40R-10 chr10:67726453 A>T maps to NM_013266.2 I772I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2V-A95S-01A-11D-A36X-10 chr9:111739249 T>A maps to NM_003798.2 K394*. Only missense variants will be evaluated by CHASM.
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-LG-A9QC-01A-11D-A36X-10 chr3:41266104 A>G maps to NM_001904.3 G34G. 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-WQ-A9G7-01A-11D-A36X-10 chr11:57583391 C>T maps to NM_001085458.1 D938D. 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-AACD-01A-11D-A40R-10 chr1:41449048 A>G maps to NM_001905.2 S29S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A8HT-01A-11D-A35Z-10 chr23:16707657 C>A did not map to a codon.
Sequencing variant TCGA-G3-AAV2-01A-11D-A36X-10 chr1:15772241 G>T maps to NM_007272.2 E264*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BD-A3EP-01A-11D-A22F-10 chr16:67964672 G>A maps to NM_001907.2 R92*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A3KG-01A-11D-A20W-10 chr20:44520237 C>T maps to NM_000308.2 L29L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XR-A8TF-01A-11D-A35Z-10 chr11:1785049 G>A maps to NM_001909.3 L14L. 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-BC-A3KF-01A-11D-A20W-10 chr14:25044538 A>G maps to NM_001911.2 G45G. 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-DD-AACQ-01A-11D-A40R-10 chr1:150722487 T>A maps to NM_004079.4 R263*. 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-A1EG-01A-11D-A20W-10 chr7:117398001 A>G maps to NM_033427.2 G1065G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACI-01A-11D-A40R-10 chr7:117361140 A>G maps to NM_033427.2 N1497N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAEA-01A-11D-A40R-10 chr7:117424329 A>G maps to NM_033427.2 Y749Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr16:88779223 G>A maps to ENST00000378384 P287P. 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-G3-AAV6-01A-21D-A36X-10 chr5:126993410 T>C maps to NM_001048252.2 D66D. 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-DD-AAD1-01A-11D-A40R-10 chr10:16982124 G>T maps to NM_001081.3 L1818L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAD6-01A-11D-A40R-10 chr10:17087152 C>A maps to NM_001081.3 T1175T. 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-2Y-A9GU-01A-11D-A382-10 chr23:119672025 A>G did not map to a codon.
Sequencing variant TCGA-BC-A217-01A-11D-A152-10 chr23:119669736 A>C did not map to a codon.
Sequencing variant TCGA-ZP-A9D1-01A-11D-A382-10 chr23:119677622 T>C did not map to a codon.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr6:43010876 G>T maps to NM_001168370.1 R1217R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACI-01A-11D-A40R-10 chr6:43160939 G>A maps to ENST00000354495 G794G. 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-WQ-A9G7-01A-11D-A36X-10 chr6:43172483 A>C did not map to a codon.
Sequencing variant TCGA-WQ-A9G7-01A-11D-A36X-10 chr6:43191999 C>A maps to ENST00000354495 S2458S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADY-01A-11D-A40R-10 chr12:111471986 C>T maps to NM_015267.3 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr12:111655741 G>A did not map to a codon.
Sequencing variant TCGA-DD-A3A1-01A-11D-A20W-10 chr10:124593455 T>C maps to NM_022034.4 G461G. 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-5C-A9VG-01A-11D-A36X-10 chr10:102013178 G>A maps to NM_018294.4 R208*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr11:107263570 T>C maps to NM_152434.2 R556R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACZ-01A-11D-A40R-10 chr4:48996765 A>G maps to NM_025087.2 G214G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CG-01A-11D-A20W-10 chr4:48990545 T>C maps to NM_025087.2 F32F. 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-WX-AA47-01A-11D-A38X-10 chr4:49005761 A>G maps to NM_025087.2 S271S. 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-DD-AACL-01A-11D-A40R-10 chr23:70836819 C>T did not map to a codon.
Sequencing variant TCGA-DD-AADL-01A-11D-A40R-10 chr23:70837371 T>C did not map to a codon.
Sequencing variant TCGA-DD-AAEH-01A-11D-A40R-10 chr23:70836724 G>T did not map to a codon.
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-DD-AACI-01A-11D-A40R-10 chr3:45988539 T>A maps to NM_006564.1 T189T. 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-G3-AAV6-01A-21D-A36X-10 chr23:144909206 A>G did not map to a codon.
Sequencing variant TCGA-MR-A520-01A-11D-A25V-10 chr23:144909485 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-DD-AAE7-01A-11D-A40R-10 chr23:35989800 T>A 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-XR-A8TD-01A-12D-A38X-10 chr23:35988969 C>T did not map to a codon.
Sequencing variant TCGA-ZS-A9CD-01A-11D-A36X-10 chr23:35969435 G>C did not map to a codon.
Sequencing variant TCGA-2Y-A9GT-01A-11D-A382-10 chr23:45016999 A>G 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-AACU-01A-11D-A40R-10 chr23:45051185 T>A did not map to a codon.
Sequencing variant TCGA-G3-A3CJ-01A-11D-A20W-10 chr23:45051112 C>T did not map to a codon.
Sequencing variant TCGA-3K-AAZ8-01A-12D-A38X-10 chr23:40506584 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-AAE1-01A-11D-A40R-10 chr23:148627335 C>T did not map to a codon.
Sequencing variant TCGA-MI-A75E-01A-11D-A32G-10 chr23:106486407 G>C did not map to a codon.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr23:134292207 T>C did not map to a codon.
Sequencing variant TCGA-DD-AAD6-01A-11D-A40R-10 chr23:134305028 C>A did not map to a codon.
Sequencing variant TCGA-DD-AADJ-01A-11D-A40R-10 chr23:118699266 C>A did not map to a codon.
Sequencing variant TCGA-ED-A8O5-01A-11D-A35Z-10 chr23:118675325 G>A 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-DD-AAC9-01A-11D-A40R-10 chr23:105879771 G>T did not map to a codon.
Sequencing variant TCGA-CC-A8HU-01A-11D-A35Z-10 chr23:23928462 C>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-BC-A10U-01A-11D-A12Z-10 chr23:36122658 T>C did not map to a codon.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr23:36156115 G>C did not map to a codon.
Sequencing variant TCGA-FV-A2QR-01A-11D-A20W-10 chr23:36156121 T>C did not map to a codon.
Sequencing variant TCGA-G3-A5SK-01A-11D-A27I-10 chr23:36103588 T>C did not map to a codon.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr3:50390718 T>C maps to NM_007022.3 S71S. Only missense variants will be evaluated by CHASM.
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-2Y-A9GZ-01A-11D-A38X-10 chr23:37668940 C>G did not map to a codon.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr23:37665716 G>T did not map to a codon.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr5:156816336 C>T maps to ENST00000442283 G1141G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A3KF-01A-11D-A20W-10 chr5:156721862 T>C maps to ENST00000442283 I93I. 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-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-A1EE-01A-11D-A12Z-10 chr23:83128876 G>T 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-DD-AACQ-01A-11D-A40R-10 chr23:83128058 T>C did not map to a codon.
Sequencing variant TCGA-DD-AAVR-01A-11D-A40R-10 chr23:83126540 A>T did not map to a codon.
Sequencing variant TCGA-ED-A8O6-01A-11D-A35Z-10 chr23:83128065 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-2Y-A9H9-01A-21D-A38X-10 chr9:105767524 A>T maps to NM_001340.3 T204T. Only missense variants will be evaluated by CHASM.
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-EP-A2KA-01A-11D-A183-10 chr9:105767095 A>G maps to NM_001340.3 K100K. 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-DD-A119-01A-11D-A12Z-10 chr16:50818356 G>A maps to ENST00000311559 L648L. 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-DD-AADO-01A-11D-A40R-10 chr10:104595083 C>T maps to NM_000102.3 W121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WQ-A9G7-01A-11D-A36X-10 chr10:104595101 A>G maps to NM_000102.3 A115A. 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-LG-A9QD-01A-11D-A382-10 chr2:204150446 G>A maps to ENST00000429815 E329E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BD-A3EP-01A-11D-A22F-10 chr2:72359541 C>T maps to NM_019885.2 L451L. 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-5C-A9VG-01A-11D-A36X-10 chr19:41512810 G>T maps to NM_000767.4 G162G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAW0-01A-11D-A40R-10 chr19:41518306 C>T maps to NM_000767.4 Q357*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-AAV6-01A-21D-A36X-10 chr19:41515200 C>T maps to NM_000767.4 I241I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9HA-01A-11D-A38X-10 chr10:96480253 A>G maps to NM_000772.2 R307R. 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-AADM-01A-11D-A40R-10 chr22:42525794 G>C maps to NM_000106.4 A99A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZS-A9CG-01A-11D-A36X-10 chr22:42525161 G>C maps to NM_000106.4 P126P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAE6-01A-11D-A40R-10 chr1:60377390 G>A maps to NM_000775.2 I191I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAC8-01A-11D-A40R-10 chr11:14902117 T>G maps to NM_024514.4 S188S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr11:14902276 A>G maps to NM_024514.4 D135D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IE-01A-21D-A382-10 chr7:1026831 C>T maps to NM_017781.2 A303A. 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-2Y-A9GX-01A-11D-A382-10 chr1:47606449 A>C did not map to a codon.
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-DD-AAD3-01A-11D-A40R-10 chr1:47611804 G>T maps to NM_001010969.2 L448L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACK-01A-11D-A40R-10 chr1:47278192 G>T maps to NM_001099772.1 G131G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADS-01A-11D-A40R-10 chr1:47279878 A>G did not map to a codon.
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-AACL-01A-11D-A40R-10 chr19:15794356 A>G maps to NM_023944.2 K234K. 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-YA-A8S7-01A-11D-A36X-10 chr8:59404950 C>T maps to NM_000780.3 Q392Q. 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-BC-A3KG-01A-11D-A20W-10 chr1:86048132 T>C maps to NM_001554.4 P223P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9GU-01A-11D-A382-10 chr23:77528344 C>A did not map to a codon.
Sequencing variant TCGA-DD-A3A9-01A-11D-A25V-10 chr23:77528232 T>C did not map to a codon.
Sequencing variant TCGA-DD-AAC8-01A-11D-A40R-10 chr17:76677125 T>A did not map to a codon.
Sequencing variant TCGA-2Y-A9GY-01A-11D-A382-10 chr2:158272221 A>G maps to NM_004288.4 H349H. Only missense variants will be evaluated by CHASM.
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-DD-A3A0-01A-11D-A20W-10 chr5:39377004 A>G maps to NM_001343.2 P628P. 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-4R-AA8I-01A-11D-A382-10 chr9:124534909 G>A maps to ENST00000408936 P701P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr9:124528985 C>T maps to ENST00000408936 T558T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A8HV-01A-11D-A35Z-10 chr13:72063269 C>T maps to ENST00000359684 P581P. 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-A9FW-01A-11D-A36X-10 chr23:85403710 C>A 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-WJ-A86L-01A-12D-A45V-10 chr23:86069739 G>T did not map to a codon.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr14:59113491 C>T maps to NM_016651.5 Y717Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr14:59112096 C>A maps to NM_016651.5 P252P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAC8-01A-11D-A40R-10 chr3:49570031 A>T maps to NM_004393.4 L696L. 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-AACT-01A-11D-A40R-10 chr13:106119491 T>C did not map to a codon.
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-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-AACG-01A-11D-A40R-10 chr1:173806172 C>T maps to NM_018122.4 G253G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9H0-01A-11D-A382-10 chr19:1429963 A>C did not map to a codon.
Sequencing variant TCGA-2Y-A9H3-01A-11D-A382-10 chr19:1434869 C>T maps to NM_018959.2 Q395*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr3:16639956 A>G did not map to a codon.
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-WX-AA46-01A-11D-A38X-10 chr9:136501519 C>T maps to NM_000787.3 S9S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr9:37860045 A>G maps to NM_024345.3 G389G. 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-DD-AACZ-01A-11D-A40R-10 chr23:125686534 G>A did not map to a codon.
Sequencing variant TCGA-2Y-A9H9-01A-21D-A38X-10 chr23:125299402 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-DD-AACI-01A-11D-A40R-10 chr23:125299818 G>A did not map to a codon.
Sequencing variant TCGA-YA-A8S7-01A-11D-A36X-10 chr8:104427709 T>C maps to NM_015420.6 N164N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAC8-01A-11D-A40R-10 chr2:172300030 A>T did not map to a codon.
Sequencing variant TCGA-DD-AADC-01A-11D-A40R-10 chr8:88885851 C>A maps to NM_152418.3 P116P. Only missense variants will be evaluated by CHASM.
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-2Y-A9GU-01A-11D-A382-10 chr1:168032857 G>C did not map to a codon.
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-4R-AA8I-01A-11D-A382-10 chr23:27765563 A>G did not map to a codon.
Sequencing variant TCGA-DD-A39V-01A-11D-A20W-10 chr23:27765410 G>A did not map to a codon.
Sequencing variant TCGA-DD-A4NA-01A-11D-A25V-10 chr23:27765398 A>G did not map to a codon.
Sequencing variant TCGA-DD-A4NN-01A-11D-A28X-10 chr23:27765413 G>A did not map to a codon.
Sequencing variant TCGA-DD-AADY-01A-11D-A40R-10 chr23:27766593 T>C 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-WJ-A86L-01A-12D-A45V-10 chr23:27765422 G>A did not map to a codon.
Sequencing variant TCGA-WQ-A9G7-01A-11D-A36X-10 chr23:27765398 A>G 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.
Sequencing variant TCGA-2Y-A9HA-01A-11D-A38X-10 chr18:50734121 T>A maps to NM_005215.3 L599*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39Y-01A-11D-A20W-10 chr18:50278697 A>G maps to NM_005215.3 G122G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADM-01A-11D-A40R-10 chr18:51057013 A>C maps to NM_005215.3 S1445S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAVU-01A-11D-A40R-10 chr18:50731598 G>C maps to NM_005215.3 G529G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr12:55042048 T>C maps to NM_053283.2 A13A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LG-A9QC-01A-11D-A36X-10 chr12:55038526 G>A maps to NM_053283.2 D101D. 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-AACQ-01A-11D-A40R-10 chr11:6651647 G>A maps to NM_003737.2 R1459R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAEA-01A-11D-A40R-10 chr11:6662052 C>A maps to NM_003737.2 V264V. 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-2Y-A9GU-01A-11D-A382-10 chr4:155219387 T>C maps to NM_017639.3 V1571V. 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-A7IE-01A-21D-A382-10 chr4:155252858 T>A maps to NM_017639.3 A747A. 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-DD-AADU-01A-11D-A40R-10 chr4:155411055 G>A maps to NM_001142552.1 G484G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAE4-01A-11D-A40R-10 chr4:155411568 G>A maps to NM_001142552.1 A313A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAE8-01A-11D-A40R-10 chr4:155157583 G>T maps to NM_017639.3 V2285V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAEA-01A-11D-A40R-10 chr4:155155900 C>A maps to NM_017639.3 L2846L. 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-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-AADO-01A-11D-A40R-10 chr13:36385015 A>G maps to NM_004734.4 C548C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WQ-A9G7-01A-11D-A36X-10 chr13:36700190 G>A maps to NM_004734.4 N28N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACI-01A-11D-A40R-10 chr3:36778743 G>A maps to NM_033403.1 H469H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACV-01A-11D-A40R-10 chr10:115612647 T>C maps to NM_014881.3 P98P. 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-AAD0-01A-11D-A40R-10 chr12:91552213 G>A maps to NM_133503.2 R133*. 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-ES-A2HS-01A-11D-A183-10 chr12:2062132 C>A maps to NM_152640.3 G325*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YA-A8S7-01A-11D-A36X-10 chr12:2062187 T>C maps to NM_152640.3 P306P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr5:112349075 A>G maps to NM_152624.4 G386G. 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-A3CJ-01A-11D-A20W-10 chr13:95121141 T>C maps to NM_001129889.1 R151R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-AA0U-01A-11D-A382-10 chr13:95112446 C>T maps to NM_001129889.1 G359G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr2:74593127 C>T maps to NM_004082.4 L926L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAD3-01A-11D-A40R-10 chr2:74596525 C>A maps to NM_004082.4 R495R. 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-2Y-A9H1-01A-11D-A382-10 chr3:182665420 C>A did not map to a codon.
Sequencing variant TCGA-BC-A10W-01A-11D-A12Z-10 chr3:182665119 T>C maps to NM_020640.2 E202E. 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-CC-A3MA-01A-11D-A20W-10 chr13:114112421 T>C maps to NM_001014283.1 G234G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K7-AAU7-01A-11D-A382-10 chr4:52757945 T>G maps to ENST00000451288 A189A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9GY-01A-11D-A382-10 chr23:110654105 G>T did not map to a codon.
Sequencing variant TCGA-DD-A39Y-01A-11D-A20W-10 chr23:110574141 G>T did not map to a codon.
Sequencing variant TCGA-DD-AACL-01A-11D-A40R-10 chr23:110644313 T>A did not map to a codon.
Sequencing variant TCGA-WJ-A86L-01A-12D-A45V-10 chr17:79993868 A>C maps to NM_016286.3 T234T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A5UE-01A-11D-A28X-10 chr11:61096942 G>A maps to NM_001923.3 R147R. Only missense variants will be evaluated by CHASM.
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-DD-AACI-01A-11D-A40R-10 chr7:50563116 T>A did not map to a codon.
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-DD-AACC-01A-11D-A40R-10 chr14:53540534 T>C maps to NM_001160148.1 E440E. 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-CC-A3MB-01A-11D-A20W-10 chr11:103908146 T>C maps to NM_001001711.2 R199R. 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-4R-AA8I-01A-11D-A382-10 chr6:30864467 C>T maps to NM_013994.2 S565S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr6:30862314 G>T maps to NM_013994.2 T460T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr1:162743269 T>C maps to NM_006182.2 C580C. 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-DD-A119-01A-11D-A12Z-10 chr2:15746377 A>G maps to NM_004939.1 S269S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAW3-01A-11D-A40P-10 chr2:15758309 G>T maps to NM_004939.1 G374G. Only missense variants will be evaluated by CHASM.
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-EP-A12J-01A-11D-A12Z-10 chr12:31255208 G>A maps to NM_030653.3 V745V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACZ-01A-11D-A40R-10 chr10:70719758 G>A maps to NM_004728.2 L95L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9GT-01A-11D-A382-10 chr14:94545833 C>T maps to NM_020414.3 E85E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1ED-01A-11D-A152-10 chr14:94528809 T>C maps to NM_020414.3 E292E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADI-01A-11D-A40R-10 chr23:134711159 C>A did not map to a codon.
Multiple mappings detected for codon TCGA-DD-AAC9-01A-11D-A40R-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr24:15026813 C>T did not map to a codon.
Sequencing variant TCGA-DD-AADV-01A-11D-A38X-10 chr24:15029319 G>C did not map to a codon.
Sequencing variant TCGA-MI-A75I-01A-11D-A32G-10 chr24:15024658 G>T did not map to a codon.
Sequencing variant TCGA-DD-AAD3-01A-11D-A40R-10 chr5:55081629 C>A maps to NM_024415.2 G265G. 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-DD-AAE6-01A-11D-A40R-10 chr5:134121266 C>T maps to ENST00000452510 I485I. 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-DD-AAW0-01A-11D-A40R-10 chr17:62496760 G>A maps to NM_004396.3 N449N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BD-A3ER-01A-11D-A20W-10 chr10:70706313 A>G maps to NM_024045.1 R714R. 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-DD-A1EG-01A-11D-A20W-10 chr23:23018953 A>G did not map to a codon.
Sequencing variant TCGA-DD-AADU-01A-11D-A40R-10 chr23:23018431 C>T did not map to a codon.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr23:23019626 A>G did not map to a codon.
Sequencing variant TCGA-XR-A8TF-01A-11D-A35Z-10 chr23:23019571 C>T did not map to a codon.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr12:113607595 G>T maps to NM_001111322.1 R465R. Only missense variants will be evaluated by CHASM.
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-DD-AACH-01A-11D-A40R-10 chr9:32457125 G>T maps to NM_014314.3 S924S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZP-A9D1-01A-11D-A382-10 chr11:118650349 A>T maps to NM_004397.4 S120S. 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-DD-AADE-01A-11D-A40R-10 chr4:169348265 A>G maps to NM_001012967.1 L629L. 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-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-EP-A2KA-01A-11D-A183-10 chr6:35288752 T>A did not map to a codon.
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-2Y-A9HA-01A-11D-A38X-10 chr6:49936538 C>A maps to NM_001037729.1 E34*. 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-DD-AAVU-01A-11D-A40R-10 chr20:30037859 T>C maps to NM_153324.2 Y29Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A8O5-01A-11D-A35Z-10 chr1:224380170 G>A maps to NM_003676.2 V321V. 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-ED-A8O5-01A-11D-A35Z-10 chr1:197509162 T>C maps to NM_001195215.1 V482V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A9FW-01A-11D-A36X-10 chr19:6475891 G>A maps to NM_024898.2 H245H. 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-DD-A1EG-01A-11D-A20W-10 chr7:140244509 A>G maps to NM_015689.3 S745S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAW1-01A-11D-A40P-10 chr7:140273640 T>A maps to NM_015689.3 P471P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A8O6-01A-11D-A35Z-10 chr1:115144130 T>A maps to ENST00000393274 K605*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAVZ-01A-11D-A40R-10 chr1:111730232 C>T maps to NM_024901.3 V470V. 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-WJ-A86L-01A-12D-A45V-10 chr8:142166009 G>T maps to NM_014957.2 T299T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9GY-01A-11D-A382-10 chr15:66021922 G>A maps to ENST00000443035 I420I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A1-01A-11D-A20W-10 chr15:65956953 T>C maps to ENST00000443035 G1822G. 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-FV-A2QR-01A-11D-A20W-10 chr1:153907314 C>T maps to NM_014856.2 Q898Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADP-01A-11D-A38X-10 chr9:19372062 A>G maps to NM_017925.4 A1638A. 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-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-DD-AAE3-01A-11D-A40R-10 chr22:32215182 A>G maps to NM_001136029.1 R614R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr8:120977516 A>G maps to NM_022783.2 E157E. 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-DD-AADB-01A-11D-A40R-10 chr1:10523575 T>C maps to NM_004401.2 Q181Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A2QR-01A-11D-A20W-10 chr1:3775364 C>T maps to ENST00000430539 N66N. 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-AAD0-01A-11D-A40R-10 chr7:24784272 C>T maps to NM_001127453.1 G104G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADE-01A-11D-A40R-10 chr7:24738644 T>A maps to NM_001127453.1 *497C. 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-CC-A7IE-01A-21D-A382-10 chr23:69420189 T>C did not map to a codon.
Sequencing variant TCGA-CC-A8HV-01A-11D-A35Z-10 chr23:69419696 C>A did not map to a codon.
Sequencing variant TCGA-DD-AAD0-01A-11D-A40R-10 chr23:69424177 C>A did not map to a codon.
Sequencing variant TCGA-G3-A3CJ-01A-11D-A20W-10 chr23:69424363 T>C did not map to a codon.
Sequencing variant TCGA-2Y-A9H5-01A-11D-A382-10 chr22:19126716 G>C maps to NM_022719.2 A259A. 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-DD-AACO-01A-11D-A40R-10 chr2:234360640 C>T maps to NM_152879.2 P733P. 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.
Sequencing variant TCGA-XR-A8TD-01A-12D-A38X-10 chr2:234355411 C>T maps to NM_152879.2 T463T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACI-01A-11D-A40R-10 chr17:54939188 T>A maps to NM_003647.2 L441*. 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-G3-AAV7-01A-11D-A382-10 chr7:137170152 T>A maps to NM_004717.2 S798S. 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-2Y-A9GZ-01A-11D-A38X-10 chr4:955622 C>T did not map to a codon.
Sequencing variant TCGA-DD-AACQ-01A-11D-A40R-10 chr11:46394021 A>T maps to NM_001105540.1 R512R. 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-EP-A2KA-01A-11D-A183-10 chr3:93779791 T>C maps to NM_001195643.1 *188*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACY-01A-11D-A40R-10 chr14:24517968 T>A maps to NM_001082488.1 I208I. 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-DD-AAW2-01A-11D-A40P-10 chr2:169952087 G>T maps to NM_001142271.1 V257V. 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-WQ-A9G7-01A-11D-A36X-10 chr4:24578248 G>A maps to NM_001358.2 R42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAW3-01A-11D-A40P-10 chr5:54581615 T>C maps to NM_019030.2 K380K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACQ-01A-11D-A40R-10 chr3:47889322 A>G maps to NM_138615.2 P721P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WQ-A9G7-01A-11D-A36X-10 chr10:127526921 A>C maps to NM_018180.2 L639*. 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-WJ-A86L-01A-12D-A45V-10 chr19:47865877 G>T maps to NM_014681.5 S507S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACI-01A-11D-A40R-10 chr20:37662953 A>G maps to NM_021931.3 Q687Q. 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 chr12:125435266 T>C maps to NM_032656.3 E984E. 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-GJ-A9DB-01A-11D-A36X-10 chr12:125470691 C>A maps to NM_032656.3 E76*. 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-4R-AA8I-01A-11D-A382-10 chr17:40263790 C>A maps to NM_024119.2 R40R. 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-DD-AAEG-01A-11D-A38X-10 chr1:182828231 C>T maps to NM_001357.4 Q374*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAD6-01A-11D-A40R-10 chr5:140958708 T>C maps to ENST00000398557 E293E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A1-01A-11D-A20W-10 chr23:96167499 G>A did not map to a codon.
Sequencing variant TCGA-FV-A4ZQ-01A-11D-A25V-10 chr23:96369846 G>T did not map to a codon.
Sequencing variant TCGA-LG-A6GG-01A-11D-A30V-10 chr23:95940061 A>C did not map to a codon.
Sequencing variant TCGA-CC-A3MA-01A-11D-A20W-10 chr13:60240728 G>A maps to NM_001042517.1 R1191*. Only missense variants will be evaluated by CHASM.
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-DD-AADF-01A-11D-A40R-10 chr13:60544096 T>A maps to NM_001042517.1 T685T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CG-01A-11D-A20W-10 chr13:60557951 T>C maps to NM_001042517.1 P477P. 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-DD-AACI-01A-11D-A40R-10 chr14:95577653 T>A maps to NM_177438.2 A752A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39Y-01A-11D-A20W-10 chr20:61513461 T>C maps to NM_033081.2 A1282A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAC8-01A-11D-A40R-10 chr20:61537424 T>A maps to NM_033081.2 K468*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAD1-01A-11D-A40R-10 chr20:61542448 C>A maps to NM_033081.2 R172R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAE7-01A-11D-A40R-10 chr20:61526439 A>G maps to NM_033081.2 S764S. Only missense variants will be evaluated by CHASM.
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-G3-A6UC-01A-21D-A33K-10 chr20:61525547 T>A did not map to a codon.
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-CC-A8HU-01A-11D-A35Z-10 chr21:47976000 G>T maps to ENST00000318711 V1166V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr21:47983805 C>A maps to ENST00000318711 T1376T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9GT-01A-11D-A382-10 chr10:468860 G>A maps to NM_014974.2 H169H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr1:68512695 G>A maps to NM_004675.2 G95G. 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-2Y-A9GW-01A-11D-A382-10 chr13:73346860 C>A maps to NM_014953.3 L452L. 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-2Y-A9H5-01A-11D-A382-10 chr2:232880380 G>A maps to NM_152383.4 Q70Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A0-01A-11D-A20W-10 chr2:233113946 A>G did not map to a codon.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr2:232880357 T>C maps to NM_152383.4 L63L. 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-NI-A8LF-01A-11D-A35Z-10 chr1:231829896 G>A maps to NM_001164537.1 R131R. 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-4R-AA8I-01A-11D-A382-10 chr15:40660889 C>T maps to NM_033510.1 C859C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACZ-01A-11D-A40R-10 chr15:40660664 C>A maps to NM_033510.1 G784G. 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-ZP-A9CY-01A-11D-A382-10 chr23:153991250 C>T 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-GJ-A9DB-01A-11D-A36X-10 chr11:11990019 G>A maps to ENST00000450094 D150D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39Z-01A-11D-A20W-10 chr19:49868004 C>T maps to NM_014419.3 F59F. 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-DD-AACD-01A-11D-A40R-10 chr3:38159098 T>C maps to NM_007335.2 S1494S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACT-01A-11D-A40R-10 chr3:38157965 C>T maps to NM_007335.2 T1293T. 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-WJ-A86L-01A-12D-A45V-10 chr3:38080871 T>A maps to NM_007335.2 S52S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAE7-01A-11D-A40R-10 chr3:197009693 C>T maps to NM_004087.2 V58V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9HA-01A-11D-A38X-10 chr11:84996277 G>A maps to NM_001142699.1 Q58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LG-A9QD-01A-11D-A382-10 chr23:69669568 A>C did not map to a codon.
Sequencing variant TCGA-YA-A8S7-01A-11D-A36X-10 chr23:69712084 C>G did not map to a codon.
Sequencing variant TCGA-DD-AAD2-01A-11D-A40R-10 chr17:7106631 G>A maps to NM_001365.3 I217I. Only missense variants will be evaluated by CHASM.
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-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-AAE6-01A-11D-A40R-10 chr20:35068156 G>A maps to ENST00000339266 R414R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr14:101201178 C>A maps to NM_003836.5 P366P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACL-01A-11D-A40R-10 chr19:39998580 A>T maps to NM_016941.3 L595L. 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-EP-A2KA-01A-11D-A183-10 chr10:124380738 G>T maps to ENST00000368915 S1817S. 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-2Y-A9H5-01A-11D-A382-10 chr23:32235036 A>T did not map to a codon.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr23:31496267 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-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-AACZ-01A-11D-A40R-10 chr23:32716094 C>A did not map to a codon.
Sequencing variant TCGA-DD-AAD2-01A-11D-A40R-10 chr23:32536159 C>A did not map to a codon.
Sequencing variant TCGA-DD-AADG-01A-11D-A40R-10 chr23:32827648 T>A did not map to a codon.
Sequencing variant TCGA-DD-AADN-01A-11D-A40R-10 chr23:32862918 C>A did not map to a codon.
Sequencing variant TCGA-DD-AAE7-01A-11D-A40R-10 chr23:31366710 T>G did not map to a codon.
Sequencing variant TCGA-DD-AAEG-01A-11D-A38X-10 chr23:32382768 A>T did not map to a codon.
Sequencing variant TCGA-DD-AAW3-01A-11D-A40P-10 chr23:32235164 A>T 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-ED-A8O5-01A-11D-A35Z-10 chr23:32663082 C>T 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-ES-A2HS-01A-11D-A183-10 chr23:32328323 A>G did not map to a codon.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr23:32509551 T>C 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-XR-A8TG-01A-11D-A35Z-10 chr23:32429886 T>C 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-WJ-A86L-01A-12D-A45V-10 chr19:36003634 G>A maps to NM_033317.4 Q162*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A8O5-01A-11D-A35Z-10 chr4:88583326 A>T maps to NM_004407.3 R133*. 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-CC-A9FU-01A-11D-A36X-10 chr1:50885039 G>T maps to NM_032110.1 S309*. 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-A39Z-01A-11D-A20W-10 chr5:118469313 A>G maps to NM_005509.4 K565K. Only missense variants will be evaluated by CHASM.
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-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-AAW1-01A-11D-A40P-10 chr15:51860704 T>A maps to NM_001174116.1 I88I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr15:51766615 G>T maps to NM_001174116.1 R2380R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACS-01A-11D-A40R-10 chr10:70192254 G>A maps to NM_001080449.1 V639V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9H8-01A-11D-A38X-10 chr3:52419369 G>A maps to ENST00000273600 E2844E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10W-01A-11D-A12Z-10 chr3:52429609 A>G maps to ENST00000273600 K3789K. 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-DD-AACI-01A-11D-A40R-10 chr12:124335526 G>A maps to NM_207437.3 S1947S. 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-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-AAV3-01A-11D-A36X-10 chr12:124360034 C>A maps to NM_207437.3 T2614T. 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-ZP-A9CV-01A-11D-A382-10 chr12:124358196 T>C maps to NM_207437.3 T2508T. 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-2Y-A9H6-01A-11D-A38X-10 chr3:57496651 G>A maps to NM_178504.4 Q112*. 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-DD-AAEI-01A-11D-A40R-10 chr3:57493369 C>T maps to NM_178504.4 Q299Q. 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-BC-A3KG-01A-11D-A20W-10 chr17:76421460 T>C maps to ENST00000389840 R4392R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IE-01A-21D-A382-10 chr17:76497895 C>T maps to ENST00000389840 R1739R. 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-ED-A8O5-01A-11D-A35Z-10 chr17:76497423 C>A maps to ENST00000389840 V1761V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr17:76456312 A>G maps to ENST00000389840 C3108C. 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-FV-A2QR-01A-11D-A20W-10 chr17:76464899 T>C maps to ENST00000389840 T2845T. 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-BC-A3KG-01A-11D-A20W-10 chr17:7636445 T>C maps to NM_020877.2 V147V. 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-DD-A39Y-01A-11D-A20W-10 chr17:7674121 T>C maps to NM_020877.2 S1411S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAVU-01A-11D-A40R-10 chr17:7720678 A>G maps to NM_020877.2 G3322G. 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-G3-AAV4-01A-11D-A382-10 chr17:7695574 G>A maps to NM_020877.2 T2353T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-AAV6-01A-21D-A36X-10 chr17:7682619 G>A maps to NM_020877.2 V1867V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9H3-01A-11D-A382-10 chr16:21139035 G>A maps to NM_017539.1 L394L. 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-DD-A39X-01A-11D-A20W-10 chr16:21011555 C>T maps to NM_017539.1 V2137V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACQ-01A-11D-A40R-10 chr16:21086767 A>T maps to NM_017539.1 T1028T. 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-4R-AA8I-01A-11D-A382-10 chr5:13911492 A>C did not map to a codon.
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-DD-AAC8-01A-11D-A40R-10 chr5:13928203 T>A maps to NM_001369.2 T92T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADL-01A-11D-A40R-10 chr5:13829747 G>A maps to NM_001369.2 A2105A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAE7-01A-11D-A40R-10 chr5:13718997 T>C maps to NM_001369.2 T4164T. 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-ES-A2HT-01A-12D-A183-10 chr5:13820547 C>A maps to NM_001369.2 E2250*. 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-A10W-01A-11D-A12Z-10 chr2:84949783 A>G maps to NM_001370.1 E3276E. 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-A3MA-01A-11D-A20W-10 chr2:84806670 T>C maps to NM_001370.1 P699P. 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-DD-AADL-01A-11D-A40R-10 chr2:84880998 G>A did not map to a codon.
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-DD-AADG-01A-11D-A40R-10 chr2:196765130 G>T maps to NM_018897.2 R1475R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADM-01A-11D-A40R-10 chr2:196636397 G>A maps to NM_018897.2 Q3807*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADO-01A-11D-A40R-10 chr2:196620955 A>G maps to NM_018897.2 N3829N. 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-YA-A8S7-01A-11D-A36X-10 chr2:196788419 G>A maps to NM_018897.2 L1242L. 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-DD-AADP-01A-11D-A38X-10 chr6:38897345 C>A maps to ENST00000327475 G3714G. 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-DD-AACA-01A-11D-A40R-10 chr17:11797764 C>A maps to NM_001372.3 T3786T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADI-01A-11D-A40R-10 chr17:11778276 A>T maps to NM_001372.3 P3418P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADL-01A-11D-A40R-10 chr17:11593002 C>T maps to NM_001372.3 D1288D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAVV-01A-11D-A40R-10 chr17:11783484 C>T maps to NM_001372.3 P3523P. Only missense variants will be evaluated by CHASM.
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-XR-A8TF-01A-11D-A35Z-10 chr17:11593506 G>A maps to NM_001372.3 R1456R. 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-CC-A3MA-01A-11D-A20W-10 chr15:78572630 T>C maps to NM_018602.3 P370P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADR-01A-11D-A40R-10 chr15:78568033 T>C maps to NM_018602.3 L310L. 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-4R-AA8I-01A-11D-A382-10 chr11:73675955 T>A maps to NM_153614.2 L123*. 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-DD-AAC8-01A-11D-A40R-10 chr7:157174946 T>C maps to NM_058246.3 P118P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACI-01A-11D-A40R-10 chr7:157160103 C>T maps to NM_058246.3 F91F. 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-2Y-A9H3-01A-11D-A382-10 chr1:6698363 C>T maps to NM_018198.3 A438A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr3:132169657 A>T maps to NM_015268.3 G168G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr3:132193830 G>T maps to NM_015268.3 E783*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YA-A8S7-01A-11D-A36X-10 chr3:132172974 A>G maps to NM_015268.3 Q302Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZP-A9CY-01A-11D-A382-10 chr3:132241674 C>T maps to NM_015268.3 R1893*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A1-01A-11D-A20W-10 chr12:56222421 T>C maps to NM_032364.5 G7G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr12:56221086 G>T maps to NM_032364.5 A452A. 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-DD-AAE3-01A-11D-A40R-10 chr12:49742903 C>G maps to NM_024902.2 A83A. 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-AACF-01A-11D-A40R-10 chr2:25190146 G>A maps to NM_016544.2 R35*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CG-01A-11D-A20W-10 chr21:34860753 A>C maps to NM_001040192.1 L316*. 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-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-DD-A39Z-01A-11D-A20W-10 chr17:40128752 A>G maps to NM_003315.3 *495Q. 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-DD-A4NH-01A-11D-A27I-10 chr23:153633193 T>C did not map to a codon.
Sequencing variant TCGA-DD-AAC8-01A-11D-A40R-10 chr23:153631373 C>T did not map to a codon.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr23:153631430 A>G 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-G3-AAV4-01A-11D-A382-10 chr2:230312119 G>A maps to NM_139072.3 A466A. 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-EP-A2KB-01A-11D-A183-10 chr11:6591489 C>A maps to NM_144666.2 Y4323*. 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-CC-A8HT-01A-11D-A35Z-10 chr1:172356292 C>A maps to ENST00000359070 S703S. 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-DD-A1ED-01A-11D-A152-10 chr10:101668877 A>G maps to ENST00000342239 S762S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LG-A9QC-01A-11D-A36X-10 chr19:10248603 T>G maps to NM_001130823.1 A1399A. 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-DD-AACZ-01A-11D-A40R-10 chr2:25505280 A>G maps to NM_175630.1 S159S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A8O5-01A-11D-A35Z-10 chr2:25466767 T>A maps to NM_175629.1 T645T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CJ-01A-11D-A20W-10 chr2:25467082 G>T maps to NM_175629.1 R598R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EG-01A-11D-A20W-10 chr2:220246819 T>C maps to NM_012100.2 T326T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr2:220251501 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-A1EE-01A-11D-A12Z-10 chr10:128840965 C>A maps to ENST00000398025 V675V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAW2-01A-11D-A40P-10 chr10:128835981 G>A did not map to a codon.
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-EP-A2KA-01A-11D-A183-10 chr2:225796363 C>A maps to NM_014689.2 E49*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr2:225652003 T>C maps to NM_014689.2 Q1843Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZS-A9CD-01A-11D-A36X-10 chr2:225750510 C>T maps to NM_014689.2 K208K. 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-DD-AADL-01A-11D-A40R-10 chr23:117676788 A>G did not map to a codon.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr23:117744274 T>C 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-2Y-A9GT-01A-11D-A382-10 chr5:169496160 T>A maps to NM_004946.2 Y1555*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5R-AA1C-01A-11D-A40R-10 chr5:169412918 C>T maps to NM_004946.2 Q996*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACU-01A-11D-A40R-10 chr5:169230173 C>T maps to NM_004946.2 L889L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAD8-01A-11D-A40R-10 chr5:169505976 A>G did not map to a codon.
Sequencing variant TCGA-DD-AAEI-01A-11D-A40R-10 chr5:169138989 C>T maps to NM_004946.2 R512*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-AAV4-01A-11D-A382-10 chr5:169494539 C>T maps to NM_004946.2 A1498A. Only missense variants will be evaluated by CHASM.
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-ZS-A9CF-01A-11D-A382-10 chr5:169101344 C>G maps to NM_004946.2 Y122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9H7-01A-11D-A38X-10 chr3:51297606 G>A maps to NM_004947.4 K735K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MB-01A-11D-A20W-10 chr3:51378809 A>G maps to NM_004947.4 K1303K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39Y-01A-11D-A20W-10 chr3:51198016 T>C maps to NM_004947.4 G307G. 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-LG-A6GG-01A-11D-A30V-10 chr7:111575683 C>G did not map to a codon.
Sequencing variant TCGA-DD-A39Y-01A-11D-A20W-10 chr8:25182969 A>T maps to NM_024940.6 K604*. 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-G3-AAV0-01A-11D-A36X-10 chr19:11339657 G>A maps to ENST00000319867 R924R. 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-WQ-A9G7-01A-11D-A36X-10 chr19:11322518 G>A maps to ENST00000319867 L1562L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9HB-01A-11D-A38X-10 chr1:63021550 T>C maps to ENST00000371140 S847S. 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-DD-AADL-01A-11D-A40R-10 chr1:62953083 C>A did not map to a codon.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr1:63099216 T>C maps to ENST00000371140 G356G. 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-XR-A8TC-01A-11D-A35Z-10 chr1:62958431 G>A maps to ENST00000371140 Y1768Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3K-AAZ8-01A-12D-A38X-10 chr9:376286 T>C maps to NM_203447.3 V729V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAC8-01A-11D-A40R-10 chr9:336699 T>A maps to NM_203447.3 V468V. 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-EP-A2KA-01A-11D-A183-10 chr13:99536144 A>G maps to ENST00000428223 G797G. 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-WQ-A9G7-01A-11D-A36X-10 chr8:21767271 C>T maps to NM_003974.2 S263S. 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-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-2Y-A9GS-01A-12D-A382-10 chr21:37617796 G>T maps to NM_005128.2 G1173G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr21:37600039 G>A maps to NM_005128.2 V510V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A8HT-01A-11D-A35Z-10 chr21:37603415 G>A maps to NM_005128.2 T778T. 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-DD-AAD5-01A-11D-A40R-10 chr21:37617604 C>T maps to NM_005128.2 H1109H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAEG-01A-11D-A38X-10 chr21:37581072 C>A maps to NM_005128.2 A184A. 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-BC-A10U-01A-11D-A12Z-10 chr6:30917878 G>A maps to NM_080870.3 R546R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EG-01A-11D-A20W-10 chr6:30918019 G>A maps to NM_080870.3 K593K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CG-01A-11D-A20W-10 chr6:30917314 A>G maps to NM_080870.3 P358P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-AAV1-01A-11D-A382-10 chr6:30918817 G>A maps to NM_080870.3 E859E. 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-AAEB-01A-11D-A40R-10 chr16:68023227 G>T maps to NM_022355.2 G356G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACO-01A-11D-A40R-10 chr19:38703031 C>T did not map to a codon.
Sequencing variant TCGA-CC-A8HV-01A-11D-A35Z-10 chr17:1945138 G>A maps to NM_001383.3 P440P. 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-DD-AACQ-01A-11D-A40R-10 chr2:116257156 T>C maps to NM_020868.3 L115L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAEH-01A-11D-A40R-10 chr2:116525976 C>T maps to NM_020868.3 I406I. Only missense variants will be evaluated by CHASM.
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-DD-A39Y-01A-11D-A20W-10 chr2:162875360 C>T did not map to a codon.
Sequencing variant TCGA-2Y-A9GZ-01A-11D-A38X-10 chr7:154561208 T>C maps to NM_130797.2 R322R. 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-G3-A3CG-01A-11D-A20W-10 chr9:140008790 A>G maps to NM_013379.2 T75T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A3KF-01A-11D-A20W-10 chr15:65739299 T>C maps to NM_197960.2 G873G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-AA0U-01A-11D-A382-10 chr15:65799616 T>C maps to NM_197960.2 L128L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZP-A9CY-01A-11D-A382-10 chr15:65746731 G>A maps to NM_197960.2 Q730*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EE-01A-11D-A12Z-10 chr19:4682766 G>A maps to ENST00000357909 N884N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr19:4700260 T>C maps to ENST00000357909 K426K. 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-DD-AAD8-01A-11D-A40R-10 chr3:109050837 G>A maps to NM_018189.3 P73P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39Y-01A-11D-A20W-10 chr6:74063603 A>G maps to NM_001025290.2 A88A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9H9-01A-21D-A38X-10 chr19:54140214 T>C maps to NM_001012728.1 C183C. 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-DD-AADA-01A-11D-A40R-10 chr12:63974526 G>A maps to NM_173812.4 L605L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr19:32968496 G>T maps to NM_001172774.1 T589T. 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-WQ-A9G7-01A-11D-A36X-10 chr10:134012410 G>A maps to NM_006426.2 P249P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1ED-01A-11D-A152-10 chr2:74751205 A>G maps to NM_133637.2 P220P. 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-DD-AADO-01A-11D-A40R-10 chr2:74752643 C>T maps to NM_133637.2 E71E. 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-2Y-A9GS-01A-12D-A382-10 chr5:174869970 G>C maps to NM_000794.3 V44V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CJ-01A-11D-A20W-10 chr22:31796694 T>C maps to NM_004147.3 T44T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10U-01A-11D-A12Z-10 chr23:100513347 C>G did not map to a codon.
Sequencing variant TCGA-DD-AACD-01A-11D-A40R-10 chr23:100507603 C>T did not map to a codon.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr23:100513517 A>G did not map to a codon.
Sequencing variant TCGA-UB-AA0V-01A-11D-A382-10 chr23:100496710 C>G did not map to a codon.
Sequencing variant TCGA-2V-A95S-01A-11D-A36X-10 chr18:28720138 A>T maps to NM_024421.2 I462I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADG-01A-11D-A40R-10 chr18:28719848 G>A maps to NM_024421.2 Q509*. Only missense variants will be evaluated by CHASM.
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-4R-AA8I-01A-11D-A382-10 chr18:28584132 T>A maps to NM_001941.3 I696I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EG-01A-11D-A20W-10 chr18:28611061 C>T maps to NM_001941.3 G77G. 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-AAC8-01A-11D-A40R-10 chr11:117314604 T>A maps to NM_020693.2 K1347*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACL-01A-11D-A40R-10 chr11:117299319 A>T maps to NM_020693.2 A2022A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACL-01A-11D-A40R-10 chr11:117375750 A>T maps to NM_020693.2 P750P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADB-01A-11D-A40R-10 chr11:117651412 G>T maps to NM_020693.2 P113P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAEB-01A-11D-A40R-10 chr11:117375714 G>A maps to NM_020693.2 I762I. 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-CC-A3MB-01A-11D-A20W-10 chr8:120850617 T>C maps to NM_024094.2 R318R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACL-01A-11D-A40R-10 chr6:116757980 A>T maps to NM_013352.2 R784*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr6:116757734 G>T maps to NM_013352.2 E702*. 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-BC-A3KG-01A-11D-A20W-10 chr18:29056123 T>C maps to NM_001944.2 C967C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AA3A-01A-11D-A36X-10 chr18:29039049 C>T maps to NM_001944.2 L143L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADG-01A-11D-A40R-10 chr18:29052250 C>T maps to NM_001944.2 A634A. 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-DD-AACI-01A-11D-A40R-10 chr18:28979345 A>T maps to NM_001134453.1 R373*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A2QR-01A-11D-A20W-10 chr18:28971040 C>T maps to NM_001134453.1 Q229*. 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-2Y-A9H5-01A-11D-A382-10 chr6:7585480 C>T maps to NM_004415.2 H2662H. 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-DD-A119-01A-11D-A12Z-10 chr6:7585892 C>T maps to NM_004415.2 L2800L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADN-01A-11D-A40R-10 chr6:7568672 G>T maps to NM_004415.2 E424*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADV-01A-11D-A38X-10 chr6:7583809 A>G maps to NM_004415.2 V2105V. 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-3K-AAZ8-01A-12D-A38X-10 chr4:88536435 C>T maps to NM_014208.3 S874S. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-BD-A3EP-01A-11D-A22F-10. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-DD-A1EH-01A-11D-A12Z-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-DD-AA3A-01A-11D-A36X-10 chr4:88536435 C>T maps to NM_014208.3 S874S. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-DD-AACD-01A-11D-A40R-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-DD-AACL-01A-11D-A40R-10 chr4:88536435 C>T maps to NM_014208.3 S874S. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-FV-A2QQ-01A-11D-A22F-10. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-RG-A7D4-01A-12D-A33Q-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-ZP-A9CY-01A-11D-A382-10 chr4:88536435 C>T maps to NM_014208.3 S874S. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-ZP-A9CY-01A-11D-A382-10. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-ZP-A9D0-01A-11D-A36X-10. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-ZS-A9CG-01A-11D-A36X-10. Mapping will be selected arbitrarily.
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-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-DD-AACI-01A-11D-A40R-10 chr6:56380271 T>G maps to ENST00000361203 L5973L. 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-EP-A2KA-01A-11D-A183-10 chr6:56376051 T>C maps to ENST00000361203 K6030K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr6:56358807 T>C maps to ENST00000361203 K6587K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr6:56436956 A>G maps to ENST00000361203 L4343L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A2QR-01A-11D-A20W-10 chr6:56443681 T>C maps to ENST00000361203 K4108K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XR-A8TF-01A-11D-A35Z-10 chr6:56505182 G>A maps to ENST00000361203 L539L. 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-A3A1-01A-11D-A20W-10 chr18:32428289 A>G maps to NM_001390.4 E432E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZP-A9D1-01A-11D-A382-10 chr2:25819005 C>T maps to NM_021907.3 G184G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3K-AAZ8-01A-12D-A38X-10 chr6:15663082 G>A maps to NM_032122.4 R6R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A3KG-01A-11D-A20W-10 chr15:49917369 T>C maps to NM_001144955.1 S2S. 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-UB-AA0V-01A-11D-A382-10 chr7:76132781 G>T maps to NM_020892.2 G477*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MA-01A-11D-A20W-10 chr12:58001167 C>T maps to NM_178502.2 A174A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACJ-01A-11D-A40R-10 chr3:122284853 G>A maps to NM_138287.3 P112P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9GU-01A-11D-A382-10 chr15:45443416 C>T maps to NM_175940.1 P995P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACT-01A-11D-A40R-10 chr15:45426493 G>A maps to NM_175940.1 L98L. 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-4R-AA8I-01A-11D-A382-10 chr15:45413419 C>T did not map to a codon.
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-K7-AAU7-01A-11D-A382-10 chr7:107217955 C>G maps to NM_181581.1 S302*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LG-A9QD-01A-11D-A382-10 chr5:172196040 A>G maps to NM_004417.3 T276T. 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-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-2Y-A9H1-01A-11D-A382-10 chr8:33449659 C>T maps to NM_024025.1 L169L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5C-AAPD-01A-21D-A38X-10 chr1:167095330 C>A maps to NM_001080426.1 A321A. 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-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-ES-A2HS-01A-11D-A183-10 chr12:89744395 G>T maps to NM_001946.2 S269S. 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-DD-AADQ-01A-11D-A40R-10 chr23:152915516 C>T did not map to a codon.
Sequencing variant TCGA-DD-AADE-01A-11D-A40R-10 chr17:7137428 C>A maps to NM_004422.2 A51A. Only missense variants will be evaluated by CHASM.
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-DD-A39Z-01A-11D-A20W-10 chr18:46906096 A>G maps to NM_017653.3 G75G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A1-01A-11D-A20W-10 chr18:46798652 A>G maps to NM_017653.3 I382I. 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-CC-A8HU-01A-11D-A35Z-10 chr14:102467510 C>T maps to NM_001376.4 S1405S. 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-DD-A39Y-01A-11D-A20W-10 chr14:102431078 A>G maps to NM_001376.4 E17E. 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-ZP-A9D1-01A-11D-A382-10 chr14:102446136 T>C maps to NM_001376.4 I200I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr16:66764023 G>T maps to NM_006141.2 P344P. 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-A1EG-01A-11D-A20W-10 chr11:103173918 T>C maps to NM_001080463.1 A3738A. 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-DD-AAD1-01A-11D-A40R-10 chr11:103191756 G>T did not map to a codon.
Sequencing variant TCGA-DD-AAVR-01A-11D-A40R-10 chr11:103026160 A>G maps to NM_001080463.1 L1225L. 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-CC-A7IL-01A-11D-A33Q-10 chr21:38865316 A>T did not map to a codon.
Sequencing variant TCGA-DD-AACK-01A-11D-A40R-10 chr21:38877654 C>T maps to NM_001396.3 R437*. Only missense variants will be evaluated by CHASM.
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-EP-A2KA-01A-11D-A183-10 chr1:206822048 T>C maps to NM_003582.2 C502C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9GY-01A-11D-A382-10 chr2:71740978 C>A maps to NM_001130987.1 Y229*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BD-A3ER-01A-11D-A20W-10 chr2:71871123 A>G maps to NM_001130987.1 K1519K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACZ-01A-11D-A40R-10 chr2:71795092 A>T maps to NM_001130987.1 K860*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr2:71892351 C>T maps to NM_001130987.1 C1745C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CG-01A-11D-A20W-10 chr2:71708029 A>T maps to NM_001130987.1 K37*. 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-BC-A8YO-01A-11D-A36X-10 chr2:207572183 A>G maps to NM_001093730.1 R46R. 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-DD-AAW1-01A-11D-A40P-10 chr15:55759145 T>A maps to NM_130810.2 R207*. 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-EP-A2KB-01A-11D-A183-10 chr13:96293970 G>A maps to NM_198968.2 Q59*. 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-DD-AADM-01A-11D-A40R-10 chr3:108380761 T>A maps to NM_014648.3 T746T. Only missense variants will be evaluated by CHASM.
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-A3KG-01A-11D-A20W-10 chr12:77421888 A>G maps to NM_203394.2 S638S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACI-01A-11D-A40R-10 chr12:77426864 T>A maps to NM_203394.2 A449A. 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-DD-AADQ-01A-11D-A40R-10 chr3:121573667 A>C maps to NM_018456.4 T112T. 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-DD-AADE-01A-11D-A40R-10 chr10:131671776 G>A maps to ENST00000355311 H240H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GJ-A9DB-01A-11D-A36X-10 chr10:131761726 G>T maps to ENST00000355311 S65S. 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-CC-A8HV-01A-11D-A35Z-10 chr1:43637223 A>C maps to NM_001159936.1 S138S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADO-01A-11D-A40R-10 chr1:43638005 C>T maps to NM_001159936.1 P29P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAE1-01A-11D-A40R-10 chr1:43637723 C>T maps to NM_001159936.1 E77E. 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-A3CJ-01A-11D-A20W-10 chr1:21564731 A>G maps to NM_001397.2 C428C. 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-DD-AACE-01A-11D-A40R-10 chr10:135180465 A>T maps to NM_004092.3 A182A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACM-01A-11D-A40R-10 chr6:139164327 C>T maps to NM_001195037.2 C185C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CJ-01A-11D-A20W-10 chr6:139159509 A>G maps to NM_001195037.2 S67S. 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-DD-AADS-01A-11D-A40R-10 chr23:69255444 G>T did not map to a codon.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr23:69247860 A>G did not map to a codon.
Sequencing variant TCGA-UB-AA0V-01A-11D-A382-10 chr23:65822602 G>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-CC-A3MA-01A-11D-A20W-10 chr16:67916723 T>C maps to NM_014329.3 S1195S. 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-2Y-A9GS-01A-12D-A382-10 chr5:83433152 A>C maps to NM_005711.3 V125V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5C-A9VG-01A-11D-A36X-10 chr5:83239360 G>A maps to NM_005711.3 D440D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5R-AAAM-01A-12D-A40R-10 chr20:57876549 T>C maps to NM_207034.1 C46C. 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-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-DD-AACZ-01A-11D-A40R-10 chr13:78472336 A>C maps to ENST00000377211 *533G. 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-DD-AACQ-01A-11D-A40R-10 chr12:93170693 T>A maps to NM_003566.3 R1347*. 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-2Y-A9HA-01A-11D-A38X-10 chr6:8090502 T>C maps to NM_004280.4 S100S. 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-2Y-A9H3-01A-11D-A382-10 chr17:60464700 G>A maps to NM_001144933.1 R77R. 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-BD-A3ER-01A-11D-A20W-10 chr17:28386623 G>A maps to NM_198529.3 W881*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A0-01A-11D-A20W-10 chr17:28407893 T>C maps to NM_198529.3 P1107P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACI-01A-11D-A40R-10 chr17:28296106 T>A maps to NM_198529.3 T163T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A8HT-01A-11D-A35Z-10 chr22:44168800 G>A maps to NM_022785.3 R108*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-AAV2-01A-11D-A36X-10 chr22:43976357 G>A maps to NM_022785.3 L1072L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WQ-A9G7-01A-11D-A36X-10 chr22:44168975 A>G maps to NM_022785.3 A49A. 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-A3A1-01A-11D-A20W-10 chr2:56149566 T>C maps to NM_001039349.1 K3K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A9FW-01A-11D-A36X-10 chr13:22084241 T>G did not map to a codon.
Sequencing variant TCGA-DD-AADL-01A-11D-A40R-10 chr13:22069446 C>T maps to NM_152726.2 K351K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39Z-01A-11D-A20W-10 chr3:19921260 C>T maps to NM_144715.3 L788L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr3:19921297 T>C did not map to a codon.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr6:52329889 C>A maps to NM_018100.3 R372R. Only missense variants will be evaluated by CHASM.
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-DD-AAD8-01A-11D-A40R-10 chr23:44101518 A>C 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-BC-A3KF-01A-11D-A20W-10 chr1:155057653 C>A maps to ENST00000505139 G67G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A3KF-01A-11D-A20W-10 chr1:155057656 C>G maps to ENST00000505139 P68P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A3KG-01A-11D-A20W-10 chr8:132991669 T>C did not map to a codon.
Sequencing variant TCGA-DD-AACA-01A-11D-A40R-10 chr8:132966068 C>T maps to NM_015137.3 R165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACL-01A-11D-A40R-10 chr14:23828141 C>T maps to NM_005864.2 P398P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A3KG-01A-11D-A20W-10 chr17:42960511 A>G maps to NM_004247.3 D147D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr17:42937414 T>C did not map to a codon.
Sequencing variant TCGA-WJ-A86L-01A-12D-A45V-10 chr17:42937332 C>T maps to NM_004247.3 L600L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACL-01A-11D-A40R-10 chr4:110882062 T>A maps to NM_001963.4 L369L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAD1-01A-11D-A40R-10 chr4:110865039 A>G maps to NM_001963.4 R184R. Only missense variants will be evaluated by CHASM.
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-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-DD-A3A1-01A-11D-A20W-10 chr23:13624531 T>C did not map to a codon.
Sequencing variant TCGA-2Y-A9H3-01A-11D-A382-10 chr5:38431348 T>C maps to ENST00000354891 L709L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A5UE-01A-11D-A28X-10 chr5:38412648 A>T maps to ENST00000354891 K465*. Only missense variants will be evaluated by CHASM.
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-DD-AAVV-01A-11D-A40R-10 chr5:38435261 C>T maps to ENST00000354891 C730C. Only missense variants will be evaluated by CHASM.
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-DD-AAC8-01A-11D-A40R-10 chr7:55273270 A>T maps to NM_005228.3 L1198L. 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-EP-A2KB-01A-11D-A183-10 chr7:55272979 C>A maps to NM_005228.3 P1101P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAD5-01A-11D-A40R-10 chr5:137801455 C>G maps to NM_001964.2 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EE-01A-11D-A12Z-10 chr10:64573580 G>A maps to NM_001136178.1 L273L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-AAV6-01A-21D-A36X-10 chr10:64573832 G>A maps to NM_001136178.1 L189L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A114-01A-11D-A12Z-10 chr2:73518959 G>A maps to NM_001965.3 R465R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XR-A8TF-01A-11D-A35Z-10 chr2:73519493 G>A maps to NM_001965.3 P287P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACT-01A-11D-A40R-10 chr11:65349552 C>T maps to NM_001099409.1 T470T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BD-A3EP-01A-11D-A22F-10 chr19:48244337 T>C maps to NM_014601.3 P427P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADO-01A-11D-A40R-10 chr19:48239729 G>A maps to NM_014601.3 A340A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAE9-01A-11D-A40R-10 chr19:48221837 G>A maps to NM_014601.3 S159S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XR-A8TG-01A-11D-A35Z-10 chr2:31472314 G>A maps to NM_014600.2 E161E. 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-A1EK-01A-11D-A20W-10 chr3:184910308 G>T maps to NM_001966.3 S626*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CG-01A-11D-A20W-10 chr3:184910634 T>C maps to NM_001966.3 G517G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CJ-01A-11D-A20W-10 chr9:140611474 A>G maps to NM_024757.4 K161K. 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-ES-A2HT-01A-12D-A183-10 chr6:31848832 A>G maps to ENST00000395728 D1135D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A0-01A-11D-A20W-10 chr11:125452298 G>A maps to ENST00000278903 K298K. Only missense variants will be evaluated by CHASM.
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-DD-AAE2-01A-11D-A40R-10 chr17:39847044 T>C maps to NM_005801.3 A103A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-AAV5-01A-11D-A36X-10 chr11:65767087 C>T maps to NM_032325.2 S85S. 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-AACI-01A-11D-A40R-10 chr7:6080783 T>A maps to NM_014413.3 P286P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XR-A8TE-01A-11D-A35Z-10 chr7:6064423 G>T maps to NM_014413.3 L591L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9GW-01A-11D-A382-10 chr2:88857340 G>A maps to NM_004836.5 L1088L. 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-EP-A2KA-01A-11D-A183-10 chr15:40301930 G>A maps to NM_001013703.2 V1231V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACQ-01A-11D-A40R-10 chr1:45340420 T>A maps to NM_020365.3 S377S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAE2-01A-11D-A40R-10 chr1:45345675 G>A maps to NM_020365.3 I263I. 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-DD-A3A4-01A-11D-A22F-10 chr3:183855594 T>A did not map to a codon.
Sequencing variant TCGA-5C-A9VG-01A-11D-A36X-10 chr8:141595330 G>A maps to NM_012154.3 S34S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr1:36298148 C>T maps to NM_017629.2 Q453*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1ED-01A-11D-A152-10 chr14:67841206 A>G maps to NM_004094.4 R88R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10Y-01A-11D-A12Z-10 chr23:24084189 T>C did not map to a codon.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr10:120801516 A>T maps to NM_003750.2 L1172*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CG-01A-11D-A20W-10 chr10:120832561 A>G maps to NM_003750.2 V127V. 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-ES-A2HT-01A-12D-A183-10 chr1:32696739 T>C maps to NM_003757.2 G307G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACO-01A-11D-A40R-10 chr15:44849748 G>T maps to NM_003758.2 E158*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-AA0V-01A-11D-A382-10 chr17:7477592 C>G maps to NM_001416.2 G13G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1ED-01A-11D-A152-10 chr12:53413701 A>G maps to ENST00000438209 A123A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A8HU-01A-11D-A35Z-10 chr4:99823067 A>C maps to NM_001130679.1 V28V. 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-DD-A39Y-01A-11D-A20W-10 chr2:233421123 A>G did not map to a codon.
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-BC-A10W-01A-11D-A12Z-10 chr3:184049875 T>A did not map to a codon.
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-EP-A2KA-01A-11D-A183-10 chr3:184049839 C>A maps to NM_001194947.1 L1535L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAE7-01A-11D-A40R-10 chr11:10823242 G>T maps to ENST00000429377 R533R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAE7-01A-11D-A40R-10 chr11:10826501 C>T maps to ENST00000429377 V176V. 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-DD-AAVZ-01A-11D-A40R-10 chr14:103806062 A>T maps to NM_183004.3 K332*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr17:12906872 A>G maps to NM_018127.6 D334D. 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-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-ES-A2HS-01A-11D-A183-10 chr1:50610678 A>G maps to NM_021952.3 T20T. 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-DD-AACZ-01A-11D-A40R-10 chr23:129205013 C>G did not map to a codon.
Sequencing variant TCGA-2Y-A9GU-01A-11D-A382-10 chr22:37769362 T>A maps to NM_052906.3 K738*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39Z-01A-11D-A20W-10 chr22:37771034 A>G maps to NM_052906.3 C180C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZP-A9D2-01A-11D-A382-10 chr12:96641038 G>T maps to NM_005230.2 E177*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WJ-A86L-01A-12D-A45V-10 chr1:205589081 C>A maps to NM_021795.2 S364S. Only missense variants will be evaluated by CHASM.
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-DD-AACL-01A-11D-A40R-10 chr5:95249475 T>A maps to NM_012081.5 V160V. 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-DD-AACM-01A-11D-A40R-10 chr4:141464673 T>C maps to NM_153702.3 L224L. 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-2Y-A9H7-01A-11D-A38X-10 chr2:85590251 G>A maps to NM_001135023.1 Q54Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9HA-01A-11D-A38X-10 chr2:85604560 G>A maps to NM_001135023.1 A234A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EB-01A-11D-A12Z-10 chr7:73474234 C>T maps to ENST00000358929 G513G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EH-01A-11D-A12Z-10 chr7:73474234 C>T maps to ENST00000358929 G513G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACZ-01A-11D-A40R-10 chr7:73442594 T>A maps to ENST00000358929 P26P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAVR-01A-11D-A40R-10 chr7:73452037 G>A maps to ENST00000358929 A55A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9H1-01A-11D-A382-10 chr1:43830910 G>A maps to NM_022821.2 F61F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39X-01A-11D-A20W-10 chr6:80635990 G>T maps to NM_022726.3 R70R. Only missense variants will be evaluated by CHASM.
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-DD-A119-01A-11D-A12Z-10 chr8:28016143 A>G maps to NM_018091.5 P417P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr8:27964301 T>A did not map to a codon.
Sequencing variant TCGA-XR-A8TF-01A-11D-A35Z-10 chr8:27957342 A>T did not map to a codon.
Sequencing variant TCGA-DD-AAC8-01A-11D-A40R-10 chr11:31669363 A>T maps to ENST00000395934 R335*. 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-ZP-A9CV-01A-11D-A382-10 chr1:79387444 A>G maps to NM_022159.3 C370C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAW0-01A-11D-A40R-10 chr5:49701579 G>A maps to NM_198449.2 Y193Y. Only missense variants will be evaluated by CHASM.
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-CC-A7IH-01A-11D-A33K-10 chr23:153607909 G>T did not map to a codon.
Sequencing variant TCGA-DD-AAW2-01A-11D-A40P-10 chr17:48457825 T>C maps to NM_001166131.1 V513V. Only missense variants will be evaluated by CHASM.
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-BC-A3KG-01A-11D-A20W-10 chr22:29611590 T>C maps to NM_133455.2 P97P. 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-DD-AAD1-01A-11D-A40R-10 chr18:2885111 T>A maps to NM_032048.2 P136P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZS-A9CE-01A-11D-A36X-10 chr18:2891711 G>A maps to NM_032048.2 G529G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACB-01A-11D-A40R-10 chr20:39992389 C>A maps to NM_052846.1 T134T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CJ-01A-11D-A20W-10 chr14:100375707 G>T maps to NM_001008707.1 A396A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr11:62370720 T>G did not map to a codon.
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-G3-A3CG-01A-11D-A20W-10 chr11:62370678 A>G maps to ENST00000278845 Y767Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A0-01A-11D-A20W-10 chr2:42544609 C>T maps to NM_019063.3 Y700Y. 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-DD-A39Y-01A-11D-A20W-10 chr14:89172627 T>C maps to ENST00000380664 K600K. 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-AADC-01A-11D-A40R-10 chr16:10631931 C>A did not map to a codon.
Sequencing variant TCGA-G3-A3CG-01A-11D-A20W-10 chr19:6921785 A>G maps to ENST00000381407 R563R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A8O5-01A-11D-A35Z-10 chr19:14863217 G>A maps to NM_013447.2 L571L. 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-G3-AAV5-01A-11D-A36X-10 chr7:155251299 G>A maps to NM_001427.3 R76R. 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-4R-AA8I-01A-11D-A382-10 chr17:77081341 C>T maps to NM_001042573.1 R540*. 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-G3-AAV3-01A-11D-A36X-10 chr17:4859416 C>A maps to NM_053013.3 S349*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XR-A8TF-01A-11D-A35Z-10 chr17:4857082 C>T maps to NM_053013.3 P129P. 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-WQ-A9G7-01A-11D-A36X-10 chr23:129759305 C>A 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-A3MA-01A-11D-A20W-10 chr6:132047294 A>G maps to NM_005021.3 K636K. 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-G3-A3CJ-01A-11D-A20W-10 chr6:132061521 T>A did not map to a codon.
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-DD-AAD8-01A-11D-A40R-10 chr1:150598959 C>A maps to NM_207042.1 E76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAW1-01A-11D-A40P-10 chr22:40283505 T>A maps to NM_152512.3 K83*. 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-A11B-01A-11D-A12Z-10 chr3:40442396 C>T maps to NM_001248.2 L61L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr3:40433586 G>A maps to NM_001248.2 V38V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39X-01A-11D-A20W-10 chr14:74443062 T>C maps to NM_001249.2 G202G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADS-01A-11D-A40R-10 chr10:101439110 C>G maps to NM_020354.3 S95S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACA-01A-11D-A40R-10 chr3:27763428 T>G maps to ENST00000449599 A119A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2V-A95S-01A-11D-A36X-10 chr22:41574170 G>A maps to NM_001429.3 Q2152Q. 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-DD-AAC8-01A-11D-A40R-10 chr12:132464276 A>T maps to ENST00000333577 G494G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADJ-01A-11D-A40R-10 chr12:132547104 G>A maps to ENST00000333577 Q2767Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADJ-01A-11D-A40R-10 chr12:132547107 G>A maps to ENST00000333577 Q2768Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr12:132549271 A>G maps to ENST00000333577 P2834P. 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-2Y-A9GY-01A-11D-A382-10 chr1:29314059 A>G maps to NM_001166005.1 E37E. 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-DD-AADK-01A-11D-A40R-10 chr18:5423478 G>A maps to NM_012307.2 Q413*. 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-EP-A2KA-01A-11D-A183-10 chr9:112013789 T>C maps to NM_019114.3 A427A. Only missense variants will be evaluated by CHASM.
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-2V-A95S-01A-11D-A36X-10 chr2:120922446 T>C maps to NM_020909.3 S641S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr10:32581986 G>A maps to NM_025209.2 R199*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A3KF-01A-11D-A20W-10 chr10:32576100 A>G maps to NM_025209.2 A359A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr2:47600663 C>T maps to ENST00000426238 Q75*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAE2-01A-11D-A40R-10 chr7:37989826 A>T maps to NM_017549.3 T288T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACH-01A-11D-A40R-10 chr1:38187383 C>T maps to NM_001099439.1 L698L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAD5-01A-11D-A40R-10 chr1:38227674 C>T maps to NM_001099439.1 Q84Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAD8-01A-11D-A40R-10 chr1:38197218 T>C maps to NM_001099439.1 T509T. Only missense variants will be evaluated by CHASM.
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-2Y-A9H3-01A-11D-A382-10 chr1:16464920 G>T maps to NM_004431.3 C276*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5C-A9VG-01A-11D-A36X-10 chr3:89528603 C>T maps to NM_005233.5 S968S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-AAV1-01A-11D-A382-10 chr3:89259350 C>T maps to NM_005233.5 N165N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WX-AA44-01A-11D-A38X-10 chr3:89390993 C>A maps to NM_005233.5 R354R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZS-A9CD-01A-11D-A36X-10 chr3:89480490 A>G maps to NM_005233.5 E776E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9H3-01A-11D-A382-10 chr2:222428898 G>T maps to NM_004438.3 Y125*. 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-DD-AAE6-01A-11D-A40R-10 chr2:222436896 C>T maps to NM_004438.3 R24R. 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-DD-AACT-01A-11D-A40R-10 chr3:96945198 T>G maps to NM_001080448.2 S402S. 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-5R-AAAM-01A-12D-A40R-10 chr6:93967864 G>A maps to NM_004440.3 Q688*. 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.
Sequencing variant TCGA-DD-AAVV-01A-11D-A40R-10 chr6:93956640 A>T maps to NM_004440.3 L865L. Only missense variants will be evaluated by CHASM.
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-XR-A8TD-01A-12D-A38X-10 chr6:93955016 C>A maps to NM_004440.3 E961*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9H9-01A-21D-A38X-10 chr1:22902960 A>T maps to NM_020526.3 T137T. 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-DD-A119-01A-11D-A12Z-10 chr1:22927918 T>C maps to NM_020526.3 A952A. 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-G3-AAUZ-01A-11D-A382-10 chr1:23232504 C>T maps to ENST00000400191 I597I. 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-AACE-01A-11D-A40R-10 chr7:100420007 A>T maps to NM_004444.4 P231P. 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-CC-A8HT-01A-11D-A35Z-10 chr7:142563350 G>C maps to NM_004445.3 R356R. 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-DD-AAC8-01A-11D-A40R-10 chr7:142562073 C>T maps to NM_004445.3 S172S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr1:226026999 G>T maps to NM_001136018.2 G225G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-AAV3-01A-11D-A36X-10 chr1:226027595 C>T maps to NM_001136018.2 L263L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A9FS-01A-11D-A36X-10 chr19:15343001 G>T maps to NM_001142886.1 T7T. 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-ZP-A9CZ-01A-11D-A382-10 chr17:19186881 C>G maps to NM_014964.4 T150T. 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-4R-AA8I-01A-11D-A382-10 chr8:144942557 T>A maps to NM_031308.1 K1622*. 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-DD-A39Y-01A-11D-A20W-10 chr8:144940596 G>A maps to NM_031308.1 P2275P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr8:144942462 G>T maps to NM_031308.1 T1653T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAE7-01A-11D-A40R-10 chr1:220156626 G>T maps to NM_004446.2 I1068I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr1:220170685 T>C did not map to a codon.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr1:220203777 T>C maps to NM_004446.2 P191P. 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-BC-A3KG-01A-11D-A20W-10 chr19:55594860 C>T maps to NM_133180.2 L444L. 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-G3-A3CG-01A-11D-A20W-10 chr19:55592799 C>A maps to NM_133180.2 A238A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9H6-01A-11D-A38X-10 chr11:720643 G>C maps to NM_022772.3 T125T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAW2-01A-11D-A40P-10 chr11:721562 A>T did not map to a codon.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr1:110300673 G>A maps to NM_139053.1 L243L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5R-AA1C-01A-11D-A40R-10 chr1:110293317 G>A maps to NM_139053.1 I579I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CJ-01A-11D-A20W-10 chr13:43543236 T>C maps to NM_001002264.1 R108R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BD-A3EP-01A-11D-A22F-10 chr5:96237301 C>T maps to NM_001130140.1 D555D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A2QR-01A-11D-A20W-10 chr5:96215716 T>C maps to NM_001130140.1 L110L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADM-01A-11D-A40R-10 chr17:37872629 C>T maps to NM_004448.2 N530N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAVR-01A-11D-A40R-10 chr17:37876051 G>A maps to NM_004448.2 L637L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr17:37872838 C>A maps to NM_004448.2 S573*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39Z-01A-11D-A20W-10 chr5:65321308 T>C maps to ENST00000506030 G273G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAVZ-01A-11D-A40R-10 chr5:65309394 T>C maps to ENST00000506030 S135S. 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-DD-AACD-01A-11D-A40R-10 chr12:56488187 C>A maps to NM_001982.2 G569G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LG-A9QD-01A-11D-A382-10 chr12:56474107 G>A maps to NM_001982.2 Q8Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A9FW-01A-11D-A36X-10 chr2:212537963 C>T maps to NM_005235.2 E547E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39X-01A-11D-A20W-10 chr2:212295714 T>C maps to NM_005235.2 R866R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACT-01A-11D-A40R-10 chr12:1137263 C>T maps to NM_178040.2 A65A. 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-EP-A2KA-01A-11D-A183-10 chr19:45920104 G>T maps to NM_202001.2 A192A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAD8-01A-11D-A40R-10 chr2:128044276 A>G did not map to a codon.
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-DD-A119-01A-11D-A12Z-10 chr10:50701216 C>T maps to NM_000124.2 W589*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-AAV6-01A-21D-A36X-10 chr10:50681068 T>C maps to NM_000124.2 T905T. 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-ES-A2HT-01A-12D-A183-10 chr23:71426581 T>C did not map to a codon.
Sequencing variant TCGA-FV-A2QR-01A-11D-A20W-10 chr23:71426724 T>C did not map to a codon.
Sequencing variant TCGA-2Y-A9GU-01A-11D-A382-10 chr5:60200667 A>C maps to NM_000082.3 V144V. Only missense variants will be evaluated by CHASM.
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-A2HT-01A-12D-A183-10 chr1:44818543 A>G maps to NM_024066.1 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A2QR-01A-11D-A20W-10 chr1:44778867 A>G maps to NM_024066.1 G213G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr10:101937925 G>T maps to NM_001100626.1 R90R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADE-01A-11D-A40R-10 chr2:158178163 T>C maps to NM_001009959.1 E171E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A3KG-01A-11D-A20W-10 chr9:5832862 C>T maps to NM_024896.2 G55G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADV-01A-11D-A38X-10 chr16:23713783 T>C maps to NM_033266.3 R384R. 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-A119-01A-11D-A12Z-10 chr12:112451274 T>C maps to NM_006817.3 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9H1-01A-11D-A382-10 chr9:102782995 G>T maps to NM_015051.1 I163I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A8O6-01A-11D-A35Z-10 chr1:8073830 G>A maps to NM_018948.3 S276S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1ED-01A-11D-A152-10 chr11:124624657 A>G maps to NM_138961.2 D203D. 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-4R-AA8I-01A-11D-A382-10 chr8:27646449 G>A maps to NM_001017420.2 Q406Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-AAV3-01A-11D-A36X-10 chr5:54281051 G>T maps to NM_007036.4 I98I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAC8-01A-11D-A40R-10 chr12:53684150 G>T maps to NM_012291.4 L1754L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9H3-01A-11D-A382-10 chr1:6488311 C>T maps to NM_031475.2 V107V. 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-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-EP-A2KB-01A-11D-A183-10 chr16:68265143 G>T maps to NM_024939.2 R550R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5C-A9VG-01A-11D-A36X-10 chr14:76957889 C>T maps to NM_004452.3 D296D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADP-01A-11D-A38X-10 chr14:76948998 T>C maps to NM_004452.3 P228P. 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-2Y-A9GT-01A-11D-A382-10 chr1:216680526 T>A did not map to a codon.
Sequencing variant TCGA-DD-AAC8-01A-11D-A40R-10 chr23:103499020 T>A did not map to a codon.
Sequencing variant TCGA-MI-A75I-01A-11D-A32G-10 chr23:103495143 C>G did not map to a codon.
Sequencing variant TCGA-WQ-A9G7-01A-11D-A36X-10 chr23:103498836 C>T did not map to a codon.
Sequencing variant TCGA-DD-AADQ-01A-11D-A40R-10 chr3:138183191 G>A maps to NM_031913.3 V307V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A1-01A-11D-A20W-10 chr2:67632363 A>G maps to NM_019002.3 T850T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39X-01A-11D-A20W-10 chr5:137844499 T>C maps to NM_004730.2 G363G. 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-4R-AA8I-01A-11D-A382-10 chr4:159620152 T>A maps to NM_004453.2 Y329*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YA-A8S7-01A-11D-A36X-10 chr4:159627389 G>A maps to NM_004453.2 W445*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACI-01A-11D-A40R-10 chr19:44012165 C>T maps to NM_014297.3 R214R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADB-01A-11D-A40R-10 chr19:44015586 A>T did not map to a codon.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr21:40191430 T>C maps to NM_005239.4 T272T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A1-01A-11D-A20W-10 chr1:157095520 T>C maps to NM_001145312.1 G217G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WQ-A9G7-01A-11D-A36X-10 chr3:185797805 A>G maps to NM_004454.2 F150F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAE7-01A-11D-A40R-10 chr6:36334436 T>A maps to NM_016135.2 P337P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BD-A3EP-01A-11D-A22F-10 chr4:5798817 C>T maps to NM_153717.2 R652R. 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-NI-A8LF-01A-11D-A35Z-10 chr4:5633651 G>A maps to NM_147127.4 H526H. 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-DD-AACI-01A-11D-A40R-10 chr1:93131550 T>G did not map to a codon.
Sequencing variant TCGA-WQ-A9G7-01A-11D-A36X-10 chr17:74005325 G>A maps to NM_001988.2 H1320H. 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-A2KB-01A-11D-A183-10 chr22:29692341 C>A maps to NM_013986.3 A431A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9GS-01A-12D-A382-10 chr15:41476593 A>G maps to NM_152596.2 F360F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr15:41482299 T>C maps to NM_152596.2 R239R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39X-01A-11D-A20W-10 chr15:41483690 T>C maps to NM_152596.2 Q213Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr14:69704316 C>A maps to NM_001193363.1 R440R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAD8-01A-11D-A40R-10 chr9:140247239 T>A did not map to a codon.
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-DD-AADA-01A-11D-A40R-10 chr1:242042425 G>A maps to NM_006027.4 L630L. 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-2Y-A9H3-01A-11D-A382-10 chr19:45721457 G>A maps to NM_138568.3 Y220Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39Y-01A-11D-A20W-10 chr7:133580479 A>G maps to NM_021807.3 A621A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACL-01A-11D-A40R-10 chr7:133749241 C>A maps to NM_021807.3 I962I. 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-DD-A3A0-01A-11D-A20W-10 chr10:94688163 A>G maps to NM_019053.4 Q319Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAD1-01A-11D-A40R-10 chr17:74085363 G>A maps to NM_001145297.2 Y364Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADR-01A-11D-A40R-10 chr1:231472536 C>A maps to NM_175876.3 E319*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACL-01A-11D-A40R-10 chr1:11142770 T>C maps to NM_001001998.1 Q418Q. 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-G3-AAV1-01A-11D-A382-10 chr11:108382003 A>C maps to NM_015065.2 S1410S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACI-01A-11D-A40R-10 chr8:118834755 T>A maps to NM_000127.2 L455L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADN-01A-11D-A40R-10 chr8:119122934 G>A maps to NM_000127.2 Y117Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAC8-01A-11D-A40R-10 chr11:44253900 A>T did not map to a codon.
Sequencing variant TCGA-G3-AAV4-01A-11D-A382-10 chr1:26349592 A>G maps to NM_004455.2 Q152Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr1:101339875 A>G maps to NM_001439.2 G205G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr8:28608211 T>C maps to NM_001440.2 P863P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACE-01A-11D-A40R-10 chr8:28573959 G>T maps to NM_001440.2 L128L. 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-DD-AACG-01A-11D-A40R-10 chr8:72182013 G>A maps to NM_000503.4 H337H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACQ-01A-11D-A40R-10 chr8:72129020 A>T maps to NM_000503.4 T422T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACI-01A-11D-A40R-10 chr6:133767788 A>T maps to ENST00000452339 L35L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr6:133767824 T>C maps to ENST00000452339 T47T. 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-A73F-01A-11D-A32G-10 chr6:65301373 A>G maps to ENST00000370616 S1462S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAVW-01A-11D-A40R-10 chr6:66042219 T>A maps to NM_001142801.1 I619I. 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-G3-A3CJ-01A-11D-A20W-10 chr6:66200485 C>A did not map to a codon.
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-ES-A2HT-01A-12D-A183-10 chr17:40870505 G>T maps to ENST00000264646 C302*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A9FW-01A-11D-A36X-10 chr7:148515059 T>A maps to NM_004456.3 T383T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1ED-01A-11D-A152-10 chr7:148507485 A>G maps to NM_004456.3 A656A. 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-EP-A2KA-01A-11D-A183-10 chr5:176833014 G>T maps to NM_000505.3 R55R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2V-A95S-01A-11D-A36X-10 chr6:6225009 A>T maps to NM_000129.3 T294T. 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-4R-AA8I-01A-11D-A382-10 chr1:197026473 A>G maps to NM_001994.2 H309H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADV-01A-11D-A38X-10 chr5:76129079 C>T maps to NM_005242.4 I216I. 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-DD-A119-01A-11D-A12Z-10 chr1:169510013 G>A maps to ENST00000367796 L1443L. 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-2Y-A9H9-01A-21D-A38X-10 chr23:154194336 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-CC-A3MA-01A-11D-A20W-10 chr23:154194404 C>T did not map to a codon.
Sequencing variant TCGA-DD-A3A0-01A-11D-A20W-10 chr23:154088731 A>G did not map to a codon.
Sequencing variant TCGA-DD-A3A0-01A-11D-A20W-10 chr23:154157275 C>T 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-2Y-A9H3-01A-11D-A382-10 chr8:82391105 T>C maps to NM_001442.2 R131R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr5:159626127 G>T maps to NM_001040442.1 T5T. Only missense variants will be evaluated by CHASM.
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-DD-AACU-01A-11D-A40R-10 chr2:96072724 G>A maps to NM_016044.2 S94S. 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-DD-AACI-01A-11D-A40R-10 chr17:74266432 C>T maps to NM_182565.3 A114A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr1:109171125 T>C maps to NM_001010883.2 C254C. 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-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-ES-A2HT-01A-12D-A183-10 chr3:58553081 A>G maps to ENST00000474531 G91G. 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-DD-AAVP-01A-11D-A40R-10 chr11:58919495 G>T maps to NM_198847.2 E119*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CG-01A-11D-A20W-10 chr11:58893057 G>A maps to NM_198947.3 V496V. 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-DD-A1EJ-01A-11D-A152-10 chr3:57646513 G>A maps to NM_152678.2 H224H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NI-A4U2-01A-11D-A28X-10 chr2:208478153 A>T maps to ENST00000272839 T109T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A6M6-01A-11D-A32G-10 chr12:58166536 T>A maps to NM_015433.2 S10S. 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-WQ-A9G7-01A-11D-A36X-10 chr6:170697397 C>A maps to NM_032448.1 A769A. 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-NI-A8LF-01A-11D-A35Z-10 chr23:54209039 C>T did not map to a codon.
Sequencing variant TCGA-XR-A8TD-01A-12D-A38X-10 chr23:54209301 G>C did not map to a codon.
Sequencing variant TCGA-XR-A8TD-01A-12D-A38X-10 chr23:54209317 A>G 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-DD-AACV-01A-11D-A40R-10 chr13:25744257 G>T maps to NM_152704.2 P500P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EE-01A-11D-A12Z-10 chr23:63410707 C>A did not map to a codon.
Sequencing variant TCGA-DD-A1EL-01A-11D-A152-10 chr23:63410707 C>A did not map to a codon.
Sequencing variant TCGA-DD-AADG-01A-11D-A40R-10 chr23:63412646 T>C did not map to a codon.
Sequencing variant TCGA-ED-A7XP-01A-11D-A34Z-10 chr23:63412193 A>G did not map to a codon.
Sequencing variant TCGA-G3-A25U-01A-11D-A16V-10 chr23:63410590 T>A did not map to a codon.
Sequencing variant TCGA-K7-A5RG-01A-11D-A28X-10 chr23:63412207 T>A did not map to a codon.
Sequencing variant TCGA-UB-A7MD-01A-12D-A34Z-10 chr23:63410477 C>T did not map to a codon.
Sequencing variant TCGA-DD-AACA-01A-11D-A40R-10 chr2:131522065 C>A maps to NM_001105195.1 G807G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADL-01A-11D-A40R-10 chr2:131520208 G>A maps to NM_001105195.1 G188G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9HA-01A-11D-A38X-10 chr2:225244882 C>A maps to NM_001122779.1 G259*. 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-EP-A2KB-01A-11D-A183-10 chr2:132249808 C>A maps to NM_001085365.1 A47A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-AAV6-01A-21D-A36X-10 chr2:130948159 G>A maps to ENST00000409255 G206G. Only missense variants will be evaluated by CHASM.
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-2Y-A9H0-01A-11D-A382-10 chr3:184062580 G>T maps to NM_144635.4 S308S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr1:1178922 G>A maps to NM_001014980.1 Q181*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADN-01A-11D-A40R-10 chr23:92964867 A>G did not map to a codon.
Sequencing variant TCGA-DD-AACK-01A-11D-A40R-10 chr6:71185405 T>A maps to NM_001162529.1 L113*. 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-DD-A39Y-01A-11D-A20W-10 chr4:89702435 A>G maps to NM_014883.2 T446T. Only missense variants will be evaluated by CHASM.
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-ES-A2HT-01A-12D-A183-10 chr5:79809579 T>C maps to NM_205548.1 D103D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZP-A9D1-01A-11D-A382-10 chr5:175530269 C>T maps to NM_001079529.2 N235N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACP-01A-11D-A40R-10 chr23:68748900 G>T did not map to a codon.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr23:68725239 C>A did not map to a codon.
Sequencing variant TCGA-BC-A3KG-01A-11D-A20W-10 chr11:6244469 T>C did not map to a codon.
Sequencing variant TCGA-DD-AADJ-01A-11D-A40R-10 chr9:136444247 G>A maps to NM_001080515.2 L133L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A6M4-01A-11D-A32G-10 chr8:79590889 A>G maps to NM_016010.2 P62P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RG-A7D4-01A-12D-A33Q-10 chr8:79598832 T>C maps to NM_016010.2 S114S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MB-01A-11D-A20W-10 chr5:74130326 A>G maps to NM_015566.1 C138C. 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-DD-AAD5-01A-11D-A40R-10 chr10:15256431 G>C maps to NM_001010924.1 P385P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACH-01A-11D-A40R-10 chr2:187559064 G>A maps to NM_177454.3 Q55Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WJ-A86L-01A-12D-A45V-10 chr2:187626927 G>A maps to NM_177454.3 W620*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACU-01A-11D-A40R-10 chr5:93294535 T>A maps to NM_032042.5 I171I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CJ-01A-11D-A20W-10 chr5:10236709 C>T maps to NM_199133.2 K108K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAE8-01A-11D-A40R-10 chr5:99871533 C>T maps to NM_198507.1 A100A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WQ-A9G7-01A-11D-A36X-10 chr10:102684350 C>T maps to NM_001136123.1 A531A. 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-DD-AACI-01A-11D-A40R-10 chr14:45473484 A>T maps to ENST00000361462 K854*. 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-WQ-AB4B-01A-11D-A40P-10 chr14:45496670 A>G maps to ENST00000361462 E1166E. 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-A2KA-01A-11D-A183-10 chr10:15821137 G>T maps to NM_024948.2 V397V. Only missense variants will be evaluated by CHASM.
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-AAE7-01A-11D-A40R-10 chr1:155220589 C>T maps to ENST00000368370 L330L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr4:92519976 C>T maps to NM_001145065.1 T824T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr4:91230221 T>C maps to NM_001145065.1 L263L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IF-01A-11D-A33K-10 chr10:86131216 G>T maps to ENST00000372088 E137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39Z-01A-11D-A20W-10 chr10:86131959 T>C maps to ENST00000372088 D384D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr10:86259680 G>A maps to NM_018999.2 G792G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CJ-01A-11D-A20W-10 chr4:2659603 A>G maps to ENST00000324666 E171E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10W-01A-11D-A12Z-10 chr5:176951435 T>C maps to ENST00000442143 K762K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAEG-01A-11D-A38X-10 chr5:176952089 C>T maps to ENST00000442143 L544L. 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-ZS-A9CD-01A-11D-A36X-10 chr10:128973668 G>A maps to NM_001039762.2 L331L. 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-2Y-A9GY-01A-11D-A382-10 chr23:103420442 C>G did not map to a codon.
Sequencing variant TCGA-DD-AACB-01A-11D-A40R-10 chr3:68466448 G>A maps to NM_213609.2 V46V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BD-A3EP-01A-11D-A22F-10 chr17:66538298 G>A maps to NM_017565.3 N312N. 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-AAV3-01A-11D-A36X-10 chr9:97084600 G>A maps to NM_017561.1 R242*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAC8-01A-11D-A40R-10 chr10:124672385 T>A maps to NM_001029888.1 S78S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A7SH-01A-11D-A382-10 chr6:116837130 G>T maps to NM_153711.2 V303V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5R-AA1D-01A-11D-A382-10 chr23:153735649 C>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-CC-A8HT-01A-11D-A35Z-10 chr7:121002989 C>A maps to NM_014888.2 E115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1ED-01A-11D-A152-10 chr7:129079891 T>C maps to ENST00000450266 F112F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A6-01A-11D-A22F-10 chr7:129110534 G>C maps to ENST00000450266 P700P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAW3-01A-11D-A40P-10 chr7:129102862 C>T maps to ENST00000450266 Y570Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MB-01A-11D-A20W-10 chr6:82461741 G>A maps to ENST00000369756 G120G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GJ-A9DB-01A-11D-A36X-10 chr6:82461741 G>A maps to ENST00000369756 G120G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LG-A9QD-01A-11D-A382-10 chr6:82459732 C>T maps to ENST00000369756 L417L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAE2-01A-11D-A40R-10 chr1:27333376 G>A maps to NM_052943.3 S112S. 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-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-2V-A95S-01A-11D-A36X-10 chr23:34148186 T>C did not map to a codon.
Sequencing variant TCGA-2Y-A9H9-01A-21D-A38X-10 chr23:34148401 T>A did not map to a codon.
Sequencing variant TCGA-DD-AADK-01A-11D-A40R-10 chr23:34148743 C>T did not map to a codon.
Sequencing variant TCGA-DD-AAE0-01A-11D-A40R-10 chr23:34149815 T>C did not map to a codon.
Sequencing variant TCGA-DD-AAEE-01A-11D-A40R-10 chr23:34149802 T>G 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-WQ-A9G7-01A-11D-A36X-10 chr23:34149343 C>T 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-ZS-A9CF-01A-11D-A382-10 chr23:34962124 C>T did not map to a codon.
Sequencing variant TCGA-DD-A39Y-01A-11D-A20W-10 chr23:37028803 T>C 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-DD-AAVZ-01A-11D-A40R-10 chr23:37027754 C>G 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-A119-01A-11D-A12Z-10 chr13:37586422 T>C maps to NM_001014286.2 Q668Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr13:37591495 T>C maps to NM_001014286.2 P626P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9GY-01A-11D-A382-10 chr23:24382425 G>C did not map to a codon.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr23:24383279 G>T did not map to a codon.
Sequencing variant TCGA-DD-A4NH-01A-11D-A27I-10 chr23:24382425 G>C did not map to a codon.
Sequencing variant TCGA-DD-AADI-01A-11D-A40R-10 chr23:24382419 G>C did not map to a codon.
Sequencing variant TCGA-DD-AAE6-01A-11D-A40R-10 chr23:24382494 G>C did not map to a codon.
Sequencing variant TCGA-DD-AAVQ-01A-11D-A40R-10 chr23:24383453 G>T did not map to a codon.
Sequencing variant TCGA-DD-AAVU-01A-11D-A40R-10 chr23:24381761 C>T did not map to a codon.
Sequencing variant TCGA-RC-A6M6-01A-11D-A32G-10 chr23:24383089 C>A did not map to a codon.
Sequencing variant TCGA-BD-A3EP-01A-11D-A22F-10 chr23:24329895 C>G did not map to a codon.
Sequencing variant TCGA-CC-A9FS-01A-11D-A36X-10 chr6:3850893 G>A maps to NM_012135.1 E283E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A3KG-01A-11D-A20W-10 chr11:114393610 T>C maps to ENST00000424269 K366K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr3:101520614 C>T maps to NM_145037.2 F210F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACI-01A-11D-A40R-10 chr17:644671 C>G maps to NM_024792.1 L212L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WQ-A9G7-01A-11D-A36X-10 chr18:29850319 G>A maps to ENST00000269209 N531N. Only missense variants will be evaluated by CHASM.
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-ZP-A9D1-01A-11D-A382-10 chr1:177199110 T>A maps to NM_021165.2 A33A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9H6-01A-11D-A38X-10 chr1:190067854 G>T maps to NM_199051.1 R532R. 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-DD-AAVP-01A-11D-A40R-10 chr1:190068053 G>T maps to NM_199051.1 T465T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CG-01A-11D-A20W-10 chr1:190067204 C>T maps to NM_199051.1 A748A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr17:6352637 T>C maps to NM_001195228.1 S199S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WQ-A9G7-01A-11D-A36X-10 chr6:24850822 A>G did not map to a codon.
Sequencing variant TCGA-G3-A3CG-01A-11D-A20W-10 chr20:49221179 A>G did not map to a codon.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr1:93309605 C>T maps to NM_001006605.3 V207V. 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-DD-AAE3-01A-11D-A40R-10 chr9:139617508 A>G maps to NM_152421.3 E193E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr18:72114419 T>C maps to NM_001044369.2 R99R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAE7-01A-11D-A40R-10 chr23:119410801 T>A did not map to a codon.
Sequencing variant TCGA-DD-AADQ-01A-11D-A40R-10 chr5:156590353 G>A maps to NM_130899.2 Q308*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACM-01A-11D-A40R-10 chr12:100041988 C>T maps to NM_153364.2 Q13*. 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-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-AACP-01A-11D-A40R-10 chr9:131832662 C>T maps to NM_032809.2 P571P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAE6-01A-11D-A40R-10 chr9:90536199 G>T maps to NM_001145124.1 E460*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAVV-01A-11D-A40R-10 chr9:90534167 A>C did not map to a codon.
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-2Y-A9H3-01A-11D-A382-10 chr5:94749834 C>T maps to NM_152548.2 L160L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr2:38178621 T>A maps to NM_144713.3 A88A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PD-A5DF-01A-11D-A27I-10 chr8:87520766 G>T maps to NM_016033.2 S28*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr17:18881094 A>G maps to NM_001039999.2 P628P. 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-4R-AA8I-01A-11D-A382-10 chr8:144809308 C>T maps to NM_198488.3 A774A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr8:144812416 A>G maps to NM_198488.3 P112P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACU-01A-11D-A40R-10 chr2:14774463 G>T maps to NM_145175.2 E121*. 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-DD-AACD-01A-11D-A40R-10 chr8:94730900 A>G did not map to a codon.
Sequencing variant TCGA-CC-A7IE-01A-21D-A382-10 chr2:33810622 C>A maps to ENST00000395190 E289*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9GW-01A-11D-A382-10 chr15:38773608 T>A maps to NM_173611.2 I282I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr19:38897602 C>A maps to NM_174905.3 T268T. 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-WQ-A9G7-01A-11D-A36X-10 chr23:8763402 C>T did not map to a codon.
Sequencing variant TCGA-DD-A39Y-01A-11D-A20W-10 chr16:89839739 T>C maps to NM_000135.2 G651G. Only missense variants will be evaluated by CHASM.
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-CC-A3MB-01A-11D-A20W-10 chr23:14868752 A>G did not map to a codon.
Sequencing variant TCGA-CC-A9FV-01A-11D-A36X-10 chr23:14862008 A>T did not map to a codon.
Sequencing variant TCGA-DD-A1EG-01A-11D-A20W-10 chr23:14863047 T>C did not map to a codon.
Sequencing variant TCGA-DD-A73A-01A-12D-A32G-10 chr23:14876076 C>T did not map to a codon.
Sequencing variant TCGA-CC-A9FS-01A-11D-A36X-10 chr9:97869518 C>T maps to NM_000136.2 L454L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9GZ-01A-11D-A38X-10 chr3:10083388 T>C maps to NM_033084.3 L260L. Only missense variants will be evaluated by CHASM.
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-DD-AAE7-01A-11D-A40R-10 chr3:10084811 T>C maps to NM_033084.3 L323L. 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-DD-AAW0-01A-11D-A40R-10 chr11:22646576 C>T maps to NM_022725.3 L260L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A3KF-01A-11D-A20W-10 chr9:35077011 A>G maps to NM_004629.1 L245L. 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-DD-AACT-01A-11D-A40R-10 chr14:45645055 A>G maps to NM_020937.2 K1033K. 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-DD-AAEA-01A-11D-A40R-10 chr2:163059607 G>T maps to NM_004460.2 Y365*. Only missense variants will be evaluated by CHASM.
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-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-2Y-A9GW-01A-11D-A382-10 chr19:13039210 G>T maps to NM_004461.2 L262L. 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-2Y-A9HB-01A-11D-A38X-10 chr17:80041426 A>G maps to NM_004104.4 I1769I. 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-DD-AADI-01A-11D-A40R-10 chr17:80042150 G>T maps to NM_004104.4 V1626V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAE2-01A-11D-A40R-10 chr17:80038616 G>A maps to NM_004104.4 S2259S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAVV-01A-11D-A40R-10 chr17:80038727 C>A maps to NM_004104.4 L2222L. 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-G3-A3CJ-01A-11D-A20W-10 chr5:7868133 A>G maps to NM_024091.3 A21A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADE-01A-11D-A40R-10 chr20:3128546 A>T maps to NM_021826.4 V390V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9H7-01A-11D-A38X-10 chr4:187630711 G>A maps to ENST00000260147 L90L. 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-BC-A3KG-01A-11D-A20W-10 chr4:187538164 A>G maps to ENST00000260147 C3026C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39Y-01A-11D-A20W-10 chr4:187517697 A>G maps to ENST00000260147 Y4335Y. 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-DD-AAD5-01A-11D-A40R-10 chr4:187541511 A>G maps to ENST00000260147 D2079D. 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-CC-A9FS-01A-11D-A36X-10 chr5:150886784 C>T maps to NM_001447.2 P4149P. 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-AADL-01A-11D-A40R-10 chr5:150923054 G>T maps to NM_001447.2 R2545R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr5:150905385 C>A maps to NM_001447.2 L3483L. 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-2Y-A9HB-01A-11D-A38X-10 chr11:92533684 A>T maps to ENST00000298047 V2502V. 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-CC-A7IE-01A-21D-A382-10 chr11:92495255 G>T maps to ENST00000298047 G1302*. 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-DD-AAVY-01A-11D-A40R-10 chr11:92533327 C>T maps to ENST00000298047 Y2383Y. 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-GJ-A9DB-01A-11D-A36X-10 chr11:92087689 T>C maps to ENST00000298047 Y804Y. 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-4R-AA8I-01A-11D-A382-10 chr4:126241912 A>C maps to NM_024582.4 A1449A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr4:126371392 T>C maps to NM_024582.4 T3074T. 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-ED-A97K-01A-21D-A382-10 chr4:126370126 C>T maps to NM_024582.4 Y2652Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr4:126328106 G>T maps to NM_024582.4 G1794*. 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-DD-AADI-01A-11D-A40R-10 chr23:150891212 G>A did not map to a codon.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr23:150889972 G>T did not map to a codon.
Sequencing variant TCGA-UB-AA0V-01A-11D-A382-10 chr23:150889929 G>T did not map to a codon.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr17:73910971 G>A maps to ENST00000389570 C876C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAE6-01A-11D-A40R-10 chr17:73910863 G>A maps to ENST00000389570 D912D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAEK-01A-11D-A40R-10 chr17:73922394 T>C maps to ENST00000389570 K222K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAEH-01A-11D-A40R-10 chr19:40331278 G>A maps to NM_001436.3 G53G. 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-WX-AA47-01A-11D-A38X-10 chr22:45937217 C>T maps to ENST00000348697 G344G. 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-ES-A2HT-01A-12D-A183-10 chr3:13678011 T>C maps to NM_001165035.1 G1094G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACL-01A-11D-A40R-10 chr14:92403333 T>A maps to ENST00000267620 I209I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9H0-01A-11D-A382-10 chr15:48779388 C>A maps to NM_000138.4 E1158*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9H5-01A-11D-A382-10 chr15:48736755 G>A maps to NM_000138.4 Q2007*. 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-A3A1-01A-11D-A20W-10 chr15:48738933 A>G maps to NM_000138.4 G1919G. 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-ES-A2HS-01A-11D-A183-10 chr15:48756204 A>T maps to NM_000138.4 C1652*. 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-2Y-A9GZ-01A-11D-A38X-10 chr5:127645696 G>A maps to NM_001999.3 V1726V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9H3-01A-11D-A382-10 chr5:127645692 C>A maps to NM_001999.3 G1728*. 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-DD-AACX-01A-11D-A40R-10 chr5:127744442 A>G maps to NM_001999.3 C334C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADI-01A-11D-A40R-10 chr5:127668622 T>C maps to NM_001999.3 G1401G. 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-G3-AAV4-01A-11D-A382-10 chr5:127595356 G>A maps to NM_001999.3 S2843S. Only missense variants will be evaluated by CHASM.
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-DD-AACF-01A-11D-A40R-10 chr19:8196465 G>A maps to NM_032447.3 P654P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-AAV0-01A-11D-A36X-10 chr19:8191481 G>A maps to NM_032447.3 T808T. 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-WQ-A9G7-01A-11D-A36X-10 chr19:8145941 G>A maps to NM_032447.3 G2466G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAW2-01A-11D-A40P-10 chr9:97367846 A>T maps to NM_001127628.1 A239A. 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-EP-A2KA-01A-11D-A183-10 chr19:9922013 G>T maps to NM_017703.1 S180*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADF-01A-11D-A40R-10 chr7:102603992 A>T maps to NM_145032.3 T237T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A1-01A-11D-A20W-10 chr12:1702305 A>G maps to NM_152441.2 S309S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr12:1702155 G>A maps to NM_152441.2 T359T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WQ-A9G7-01A-11D-A36X-10 chr16:744676 C>T maps to NM_153350.3 K416K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADF-01A-11D-A40R-10 chr5:107356641 A>T maps to NM_001163315.2 C602*. 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-2Y-A9H6-01A-11D-A38X-10 chr5:15936875 C>A maps to NM_012304.3 R353R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZP-A9CV-01A-11D-A382-10 chr5:15928341 C>T maps to NM_012304.3 I157I. 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-DD-AAEG-01A-11D-A38X-10 chr9:37541363 A>G maps to NM_012166.2 I134I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5R-AAAM-01A-12D-A40R-10 chr19:39435634 G>A maps to ENST00000448145 Q58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K7-AAU7-01A-11D-A382-10 chr10:5952980 C>T maps to NM_032807.3 C418C. 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-2Y-A9GW-01A-11D-A382-10 chr1:224345063 G>A maps to NM_015176.2 P241P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr14:39900874 A>G maps to NM_203301.3 T164T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr14:39900901 C>T maps to NM_203301.3 G155G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A0-01A-11D-A20W-10 chr2:230861590 T>C maps to NM_174899.4 D110D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CG-01A-11D-A20W-10 chr5:147788756 C>A maps to NM_205836.1 Y313*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CJ-01A-11D-A20W-10 chr3:121341493 A>G maps to NM_016298.3 R406R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9GW-01A-11D-A382-10 chr8:101146558 G>T maps to NM_001029860.3 R570R. 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-EP-A2KA-01A-11D-A183-10 chr8:101153749 T>A maps to NM_001029860.3 L244L. 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-DD-AAW0-01A-11D-A40R-10 chr1:11721247 G>A maps to ENST00000376768 R219R. 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-WQ-A9G7-01A-11D-A36X-10 chr6:153296637 G>A maps to NM_012177.3 Y74Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CJ-01A-11D-A20W-10 chr22:32887082 A>G maps to NM_012179.3 V294V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACT-01A-11D-A40R-10 chr4:175162347 T>A maps to NM_012180.2 K160*. 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-ES-A2HT-01A-12D-A183-10 chr10:103372235 T>C did not map to a codon.
Sequencing variant TCGA-G3-AAV6-01A-21D-A36X-10 chr9:139836597 G>C maps to NM_018998.2 A332A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WQ-A9G7-01A-11D-A36X-10 chr9:139835866 G>A maps to NM_018998.2 A431A. 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-ZS-A9CE-01A-11D-A36X-10 chr4:153245453 C>T maps to NM_033632.2 G579G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WQ-A9G7-01A-11D-A36X-10 chr1:161188699 C>T maps to NM_004106.1 Y76Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5C-A9VH-01A-11D-A36X-10 chr19:7763669 G>T maps to NM_002002.4 T31T. Only missense variants will be evaluated by CHASM.
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-5C-A9VG-01A-11D-A36X-10 chr19:40368474 G>A maps to NM_003890.2 F4291F. 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-DD-AAC9-01A-11D-A40R-10 chr19:40434028 G>T maps to NM_003890.2 V80V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr19:40433821 G>A maps to NM_003890.2 P149P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-AAV0-01A-11D-A36X-10 chr19:40366454 C>T maps to NM_003890.2 G4593G. 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-DD-AACF-01A-11D-A40R-10 chr19:17883503 A>G maps to NM_015122.2 L248L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A2-01A-11D-A20W-10 chr5:72347204 C>A maps to NM_138782.2 Y323*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZP-A9CV-01A-11D-A382-10 chr5:141027039 G>C maps to ENST00000354789 S252S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr1:27697418 A>G maps to NM_003665.2 S146S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5C-AAPD-01A-21D-A38X-10 chr1:157772290 C>T maps to NM_052938.4 Q161Q. 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-DD-AADN-01A-11D-A40R-10 chr1:157494288 C>T maps to NM_031281.2 G673G. 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-DD-AADS-01A-11D-A40R-10 chr1:159772231 T>A maps to NM_001004310.2 A6A. 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-AACT-01A-11D-A40R-10 chr1:161697119 A>T maps to NM_001002901.2 R317*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1ED-01A-11D-A152-10 chr19:4792762 A>G maps to NM_018708.2 E299E. 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-CC-A3MB-01A-11D-A20W-10 chr5:108380490 A>G maps to NM_005246.2 E608E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACZ-01A-11D-A40R-10 chr2:97368052 C>T maps to NM_001113382.1 R1760*. 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-A1ED-01A-11D-A152-10 chr8:125094660 A>G maps to NM_001039112.2 K1451K. 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-DD-AAC8-01A-11D-A40R-10 chr8:125103789 T>C maps to NM_001039112.2 F1506F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADE-01A-11D-A40R-10 chr8:125103742 G>T maps to NM_001039112.2 G1491*. 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-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-DD-AACA-01A-11D-A40R-10 chr3:62356921 C>A maps to NM_018008.3 E364*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9GU-01A-11D-A382-10 chr19:35940789 G>C maps to NM_005306.2 L58L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADW-01A-11D-A38X-10 chr4:155506804 T>C maps to NM_000508.3 G592G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CJ-01A-11D-A20W-10 chr4:155511791 T>C maps to NM_000508.3 T16T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9GT-01A-11D-A382-10 chr23:54496731 C>A did not map to a codon.
Sequencing variant TCGA-CC-A8HV-01A-11D-A35Z-10 chr23:54475584 G>A did not map to a codon.
Sequencing variant TCGA-G3-A3CG-01A-11D-A20W-10 chr6:36982464 A>G maps to NM_173558.3 A289A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9H5-01A-11D-A382-10 chr9:95797699 G>T maps to NM_033086.2 G669G. 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 chr12:95604471 A>G maps to NM_018351.3 S196S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr5:44388682 A>G maps to NM_004465.1 P34P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAVR-01A-11D-A40R-10 chr23:76711986 T>C 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-AACT-01A-11D-A40R-10 chr11:69518446 G>T maps to NM_005117.2 G66G. 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-DD-AAEI-01A-11D-A40R-10 chr15:49716641 G>T maps to NM_002009.3 E50*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A9FW-01A-11D-A36X-10 chr10:103535639 G>A maps to NM_033163.3 S6S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAEK-01A-11D-A40R-10 chr10:103530256 G>A maps to NM_033163.3 P188P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACT-01A-11D-A40R-10 chr8:38271456 G>A maps to NM_001174067.1 I788I. 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-G3-AAV4-01A-11D-A382-10 chr4:1017448 G>T maps to NM_021923.3 E125*. 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-FV-A2QR-01A-11D-A20W-10 chr4:153864457 T>C maps to NM_033393.2 T83T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACI-01A-11D-A40R-10 chr23:135291565 A>G did not map to a codon.
Sequencing variant TCGA-G3-A3CJ-01A-11D-A20W-10 chr23:135288587 C>T did not map to a codon.
Sequencing variant TCGA-BC-A10W-01A-11D-A12Z-10 chr1:38463118 T>C maps to NM_004468.3 G267G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADN-01A-11D-A40R-10 chr6:97052636 C>A maps to NM_020482.4 Y57*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A8HV-01A-11D-A35Z-10 chr16:67265129 G>A maps to NM_013241.2 D876D. 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-ZS-A9CD-01A-11D-A36X-10 chr16:67281172 C>A maps to NM_013241.2 G47G. 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-ZS-A9CE-01A-11D-A36X-10 chr18:34326997 G>T maps to NM_025135.2 E1203*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAE7-01A-11D-A40R-10 chr9:133799205 G>A maps to NM_001145106.1 Y258Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr11:65652449 G>T maps to NM_198897.1 R266R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39Y-01A-11D-A20W-10 chr6:110112749 A>G maps to NM_014845.5 A784A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAE0-01A-11D-A40R-10 chr6:110085142 G>A maps to NM_014845.5 W464*. 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-KR-A7K2-01A-12D-A33Q-10 chr6:110098137 A>G maps to NM_014845.5 Q588Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CJ-01A-11D-A20W-10 chr23:15365315 T>C 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-DD-A119-01A-11D-A12Z-10 chr2:164467711 A>G maps to NM_018086.2 H210H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5C-A9VH-01A-11D-A36X-10 chr6:76023249 C>T maps to NM_015687.2 G766G. 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-A1EE-01A-11D-A12Z-10 chr6:76024217 T>A maps to NM_015687.2 K444*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NR-01A-11D-A30V-10 chr6:76023701 G>A maps to NM_015687.2 R616*. 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-DD-A3A1-01A-11D-A20W-10 chr3:99567248 G>A maps to NM_001042459.1 R1091*. 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-DD-A1ED-01A-11D-A152-10 chr4:54265994 T>C maps to NM_030917.3 L268L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A1-01A-11D-A20W-10 chr4:54256721 T>C maps to NM_030917.3 P144P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAVY-01A-11D-A40R-10 chr4:54256023 A>G maps to NM_030917.3 R127R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACI-01A-11D-A40R-10 chr19:56109117 C>G maps to NM_032836.2 L38L. 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-ES-A2HS-01A-11D-A183-10 chr7:33028262 A>G maps to NM_007270.3 R346R. 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-DD-AAC8-01A-11D-A40R-10 chr1:152283806 T>A maps to NM_002016.1 V1185V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADU-01A-11D-A40R-10 chr1:152277557 T>A maps to NM_002016.1 A3268A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAW3-01A-11D-A40P-10 chr1:152283839 T>A maps to NM_002016.1 G1174G. 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-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 chr1:152278841 T>A maps to NM_002016.1 T2840T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9GU-01A-11D-A382-10 chr1:152324872 C>A maps to NM_001014342.2 G1797*. 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-DD-AADE-01A-11D-A40R-10 chr1:152326574 T>A maps to NM_001014342.2 G1229G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADI-01A-11D-A40R-10 chr1:152328830 A>G maps to NM_001014342.2 S477S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADS-01A-11D-A40R-10 chr1:152323286 T>A maps to NM_001014342.2 A2325A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAEG-01A-11D-A38X-10 chr1:152325269 C>A maps to NM_001014342.2 G1664G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-AAV7-01A-11D-A382-10 chr1:152324695 C>A maps to NM_001014342.2 G1856*. 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-XR-A8TG-01A-11D-A35Z-10 chr1:152328014 C>G maps to NM_001014342.2 G749G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10U-01A-11D-A12Z-10 chr14:21543016 C>G maps to NM_018071.3 G376G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BD-A3EP-01A-11D-A22F-10 chr14:21555548 G>A maps to NM_018071.3 S1438S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39Z-01A-11D-A20W-10 chr14:21544998 T>C maps to NM_018071.3 L662L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MA-01A-11D-A20W-10 chr23:71379911 T>C did not map to a codon.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr9:84607568 T>A maps to NM_001001670.2 I728I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr9:84608273 C>A maps to NM_001001670.2 S963S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr9:84608909 A>G maps to NM_001001670.2 K1175K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr23:153599341 C>T 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-2Y-A9H1-01A-11D-A382-10 chr3:58067390 G>A maps to NM_001164317.1 V225V. Only missense variants will be evaluated by CHASM.
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-5R-AA1C-01A-11D-A40R-10 chr7:128494869 C>T maps to NM_001458.4 L2347L. 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-DD-AACI-01A-11D-A40R-10 chr7:128486379 T>A maps to NM_001458.4 Y1330*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr7:128494725 C>A maps to NM_001458.4 A2329A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr7:128494662 G>A maps to NM_001458.4 P2308P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-AAV4-01A-11D-A382-10 chr7:128485211 C>T maps to NM_001458.4 G1231G. 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-UB-AA0U-01A-11D-A382-10 chr7:128478084 C>A maps to NM_001458.4 V338V. 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-CC-A8HT-01A-11D-A35Z-10 chr11:63883777 G>A maps to NM_013280.4 T13T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr14:86088964 C>A maps to NM_013231.4 L369L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A8HV-01A-11D-A35Z-10 chr14:86087998 C>A maps to NM_013231.4 V47V. 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-DD-AACB-01A-11D-A40R-10 chr14:86089390 G>A maps to NM_013231.4 E511E. 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 chr13:28883064 C>G did not map to a codon.
Sequencing variant TCGA-DD-A39X-01A-11D-A20W-10 chr13:28942735 C>T maps to NM_001160030.1 S727S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39X-01A-11D-A20W-10 chr13:28942738 T>C maps to NM_001160030.1 S726S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A9-01A-11D-A25V-10 chr13:28942738 T>C maps to NM_001160030.1 S726S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NV-01A-11D-A30V-10 chr13:28942738 T>C maps to NM_001160030.1 S726S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAE0-01A-11D-A40R-10 chr13:29012441 G>A maps to NM_002019.4 P143P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAVV-01A-11D-A40R-10 chr13:29041085 A>G maps to NM_002019.4 T114T. Only missense variants will be evaluated by CHASM.
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-DD-A3A1-01A-11D-A20W-10 chr13:28588597 T>C maps to NM_004119.2 A950A. 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-DD-AAD6-01A-11D-A40R-10 chr5:180040033 G>A maps to NM_182925.4 A1136A. 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-K7-A5RF-01A-11D-A28X-10 chr5:180048893 G>A maps to NM_182925.4 D556D. 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-2Y-A9HA-01A-11D-A38X-10 chr1:213068555 A>G did not map to a codon.
Sequencing variant TCGA-G3-A3CJ-01A-11D-A20W-10 chr1:213068595 G>T maps to NM_014053.2 T544T. Only missense variants will be evaluated by CHASM.
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-BC-A10W-01A-11D-A12Z-10 chr1:240370244 T>C maps to ENST00000406993 L854L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BD-A3EP-01A-11D-A22F-10 chr1:240370635 G>T maps to ENST00000406993 E985*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADP-01A-11D-A38X-10 chr1:240370097 G>A did not map to a codon.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr1:240371183 T>A maps to ENST00000406993 P1167P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZP-A9D1-01A-11D-A382-10 chr1:240601441 C>A maps to ENST00000406993 I1807I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAEA-01A-11D-A40R-10 chr17:43318780 C>A maps to NM_005892.3 P455P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WQ-A9G7-01A-11D-A36X-10 chr17:43322422 G>A maps to NM_005892.3 P892P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAED-01A-12D-A40R-10 chr2:153476053 A>G maps to NM_052905.3 P553P. 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-ES-A2HT-01A-12D-A183-10 chr12:50040684 G>T maps to NM_175736.4 I993I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5C-A9VH-01A-11D-A36X-10 chr1:171176858 T>C maps to NM_001460.2 L396L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CG-01A-11D-A20W-10 chr1:171072960 A>G maps to NM_006894.5 K56K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9GV-01A-11D-A382-10 chr23:147014108 G>A did not map to a codon.
Sequencing variant TCGA-DD-AAE3-01A-11D-A40R-10 chr23:147011691 A>T 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-DD-AAVZ-01A-11D-A40R-10 chr2:216241230 G>A maps to NM_212482.1 Y1959Y. Only missense variants will be evaluated by CHASM.
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-FV-A2QR-01A-11D-A20W-10 chr2:216239958 A>G maps to NM_212482.1 G2045G. Only missense variants will be evaluated by CHASM.
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-G3-AAV0-01A-11D-A36X-10 chr17:80684866 C>T maps to NM_024619.3 G250G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A3KF-01A-11D-A20W-10 chr11:47788669 G>C maps to NM_015308.2 T57T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACL-01A-11D-A40R-10 chr11:47744590 A>T maps to NM_015308.2 P914P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACX-01A-11D-A40R-10 chr11:47765676 C>T maps to NM_015308.2 V428V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAVV-01A-11D-A40R-10 chr6:159646689 T>C maps to NM_032532.2 R336R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr6:159618550 C>A maps to NM_032532.2 T66T. 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-XR-A8TF-01A-11D-A35Z-10 chr6:159642681 G>T maps to NM_032532.2 R240R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZS-A9CD-01A-11D-A36X-10 chr6:159653740 C>T maps to NM_032532.2 Q733*. 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-A2KB-01A-11D-A183-10 chr13:49781308 A>G maps to NM_001079673.1 Q1125Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACW-01A-11D-A40R-10 chr3:172052789 G>T maps to NM_022763.3 T566T. 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-4R-AA8I-01A-11D-A382-10 chr5:131007514 A>G maps to NM_133372.2 C874C. 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-DD-AADB-01A-11D-A40R-10 chr11:71906451 G>A maps to NM_016729.2 Q102Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAVU-01A-11D-A40R-10 chr11:94040365 T>C maps to NM_001080486.1 N121N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAEE-01A-11D-A40R-10 chr19:45974559 G>T did not map to a codon.
Sequencing variant TCGA-DD-AAD6-01A-11D-A40R-10 chr20:22562784 C>A maps to NM_021784.4 P365P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACA-01A-11D-A40R-10 chr6:1612041 G>C maps to NM_001453.2 G454G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACE-01A-11D-A40R-10 chr6:1612041 G>C maps to NM_001453.2 G454G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAW2-01A-11D-A40P-10 chr6:1612041 G>C maps to NM_001453.2 G454G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BD-A3EP-01A-11D-A22F-10 chr1:63789223 C>T maps to NM_012183.2 S165S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACK-01A-11D-A40R-10 chr1:63789823 G>A maps to NM_012183.2 A365A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GJ-A9DB-01A-11D-A36X-10 chr1:63788896 C>T maps to NM_012183.2 D56D. 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-AAW2-01A-11D-A40P-10 chr6:1391084 G>C maps to NM_001452.1 G301G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2V-A95S-01A-11D-A36X-10 chr14:29236982 G>A maps to NM_005249.3 G166G. 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-AACS-01A-11D-A40R-10 chr14:29237711 G>A maps to NM_005249.3 L409L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr14:29237530 C>A maps to NM_005249.3 S349*. 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-DD-A119-01A-11D-A12Z-10 chr12:8202063 T>C maps to NM_018416.2 G478G. 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-DD-AADK-01A-11D-A40R-10 chr2:48602536 A>C maps to NM_002158.3 L417L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3K-AAZ8-01A-12D-A38X-10 chr13:41134802 T>C maps to NM_002015.3 A275A. 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-A119-01A-11D-A12Z-10 chr23:70320732 T>C did not map to a codon.
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-DD-A39Z-01A-11D-A20W-10 chr3:71026862 C>T maps to NM_032682.4 A453A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADF-01A-11D-A40R-10 chr6:41566592 G>C maps to NM_001012426.1 L654L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADF-01A-11D-A40R-10 chr6:1313559 G>T maps to NM_033260.3 G207G. 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-FV-A2QR-01A-11D-A20W-10 chr23:55650772 A>G did not map to a codon.
Sequencing variant TCGA-WJ-A86L-01A-12D-A45V-10 chr23:55650547 C>T did not map to a codon.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr11:126147547 C>T maps to NM_017547.3 Y475Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9GW-01A-11D-A382-10 chr22:36900812 G>A maps to NM_001102371.1 S176S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZS-A9CF-01A-11D-A382-10 chr9:130565238 A>T maps to NM_004957.4 L12L. Only missense variants will be evaluated by CHASM.
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-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-CC-A8HT-01A-11D-A35Z-10 chr4:79387359 A>C did not map to a codon.
Sequencing variant TCGA-DD-AACE-01A-11D-A40R-10 chr4:79360142 T>C maps to NM_025074.6 D1818D. 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-G3-A3CJ-01A-11D-A20W-10 chr4:79458203 T>C maps to NM_025074.6 A3716A. 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-WJ-A86L-01A-12D-A45V-10 chr4:79350343 C>A maps to NM_025074.6 R1603R. Only missense variants will be evaluated by CHASM.
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-DD-A3A0-01A-11D-A20W-10 chr9:14737507 A>G maps to ENST00000380880 S2145S. 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-CC-A8HT-01A-11D-A35Z-10 chr13:39438521 G>T maps to NM_207361.4 E2588*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EE-01A-11D-A12Z-10 chr13:39265054 G>T maps to NM_207361.4 E1192*. 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-DD-AAD0-01A-11D-A40R-10 chr13:39435610 G>C maps to NM_207361.4 P2521P. 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-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-2Y-A9GZ-01A-11D-A38X-10 chr4:190878550 A>T did not map to a codon.
Sequencing variant TCGA-DD-AADA-01A-11D-A40R-10 chr6:116263780 T>C maps to NM_002031.2 T438T. 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-DD-A39Y-01A-11D-A20W-10 chr10:13838524 T>C maps to NM_018027.3 S90S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EG-01A-11D-A20W-10 chr3:69239068 A>G maps to NM_015123.1 S583S. 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-DD-AACX-01A-11D-A40R-10 chr14:52188701 G>T maps to ENST00000344768 E466*. 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-A1EE-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-DD-AACK-01A-11D-A40R-10 chr23:131212799 A>G did not map to a codon.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr9:37707439 C>T maps to NM_014907.2 P43P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr9:37737221 C>A maps to NM_014907.2 R511R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CG-01A-11D-A20W-10 chr9:37740138 T>C maps to NM_014907.2 P538P. Only missense variants will be evaluated by CHASM.
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-2Y-A9GU-01A-11D-A382-10 chr23:12736466 C>T did not map to a codon.
Sequencing variant TCGA-CC-A9FW-01A-11D-A36X-10 chr23:12736480 A>G did not map to a codon.
Sequencing variant TCGA-DD-A1EB-01A-11D-A12Z-10 chr23:12712562 T>C did not map to a codon.
Sequencing variant TCGA-DD-AACL-01A-11D-A40R-10 chr23:12735863 T>A did not map to a codon.
Sequencing variant TCGA-DD-AAEB-01A-11D-A40R-10 chr23:12735949 T>C did not map to a codon.
Sequencing variant TCGA-DD-AAVR-01A-11D-A40R-10 chr23:12701705 G>A did not map to a codon.
Sequencing variant TCGA-ZP-A9D1-01A-11D-A382-10 chr23:12516854 A>T did not map to a codon.
Sequencing variant TCGA-ZP-A9D4-01A-11D-A36X-10 chr23:12632899 G>A 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-YA-A8S7-01A-11D-A36X-10 chr13:32759190 C>T maps to NM_023037.2 L1075L. Only missense variants will be evaluated by CHASM.
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-DD-AACX-01A-11D-A40R-10 chr4:48636367 G>T maps to NM_015030.1 L20L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADG-01A-11D-A40R-10 chr4:48512965 C>T maps to NM_015030.1 E2727E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACL-01A-11D-A40R-10 chr2:183699693 T>A did not map to a codon.
Sequencing variant TCGA-WX-AA44-01A-11D-A38X-10 chr2:183703314 T>A maps to NM_001463.3 K207*. 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-DD-A1EE-01A-11D-A12Z-10 chr7:5643545 C>T maps to ENST00000340250 F394F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAC9-01A-11D-A40R-10 chr7:5633031 G>A maps to ENST00000340250 L161L. 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-DD-AADG-01A-11D-A40R-10 chr17:79495625 C>T maps to NM_001077182.2 Y23Y. 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-CC-A9FV-01A-11D-A36X-10 chr2:49295429 C>T did not map to a codon.
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-AAVV-01A-11D-A40R-10 chr15:40005704 G>C maps to NM_152597.4 R376R. 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-K7-AAU7-01A-11D-A382-10 chr5:52776662 G>C maps to NM_013409.1 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAD2-01A-11D-A40R-10 chr4:162577512 A>G maps to NM_020116.3 I287I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAD6-01A-11D-A40R-10 chr4:162307201 G>C maps to NM_020116.3 S747S. 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-WQ-A9G7-01A-11D-A36X-10 chr5:121187927 G>A maps to NM_177478.1 A90A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39Y-01A-11D-A20W-10 chr23:48341393 T>C 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-DD-AAE8-01A-11D-A40R-10 chr16:71317948 T>C maps to NM_018348.5 L625L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A97K-01A-21D-A382-10 chr6:37403497 C>T maps to NM_015050.2 S31S. 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-ES-A2HT-01A-12D-A183-10 chr1:78432757 T>C maps to ENST00000436586 K127K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZS-A9CE-01A-11D-A36X-10 chr1:78429309 C>A maps to ENST00000436586 E399*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A8HU-01A-11D-A35Z-10 chr1:24181041 C>A maps to NM_000147.4 V259V. 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-DD-AADL-01A-11D-A40R-10 chr15:91424927 C>T maps to NM_002569.2 V735V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr15:91423172 C>A maps to NM_002569.2 A445A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr15:91420415 C>A maps to NM_002569.2 R185R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WQ-A9G7-01A-11D-A36X-10 chr15:91424699 C>T maps to NM_002569.2 C659C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr16:31196407 C>T maps to NM_004960.3 G224G. 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-5R-AA1C-01A-11D-A40R-10 chr19:5832521 C>A maps to NM_001040701.1 T19T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A9FS-01A-11D-A36X-10 chr9:139925310 G>T maps to NM_004479.3 R294R. 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-ZS-A9CD-01A-11D-A36X-10 chr6:96651186 C>T maps to NM_006581.3 N52N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAD6-01A-11D-A40R-10 chr3:180666181 A>T maps to NM_005087.3 I106I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADL-01A-11D-A40R-10 chr19:35632087 C>T maps to NM_005031.3 I49I. 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-DD-AACC-01A-11D-A40R-10 chr5:39135011 G>T maps to ENST00000263405 I549I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZP-A9CV-01A-11D-A382-10 chr5:39141215 A>G maps to ENST00000263405 D449D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A8O6-01A-11D-A35Z-10 chr3:45977941 C>A maps to NM_024513.2 L1346L. 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-BD-A3EP-01A-11D-A22F-10 chr7:90894458 A>G maps to NM_003505.1 Q88Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MB-01A-11D-A20W-10 chr7:90894458 A>G maps to NM_003505.1 Q88Q. 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-DD-AAD5-01A-11D-A40R-10 chr2:208633106 C>T maps to NM_003468.3 L119L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-AAUZ-01A-11D-A382-10 chr10:35930024 G>A maps to NM_031866.2 C111C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr7:72849390 G>T maps to NM_003508.2 E352*. 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-DD-AAEE-01A-11D-A40R-10 chr19:3534790 A>G did not map to a codon.
Sequencing variant TCGA-DD-AAVV-01A-11D-A40R-10 chr19:3531920 G>A maps to NM_001136198.1 W279*. 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-AAE9-01A-11D-A40R-10 chr17:41063256 C>G maps to NM_000151.2 L296L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAEA-01A-11D-A40R-10 chr17:41059552 C>G maps to NM_000151.2 G118G. 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-FV-A2QR-01A-11D-A20W-10 chr23:153774306 G>A did not map to a codon.
Sequencing variant TCGA-UB-AA0U-01A-11D-A382-10 chr17:78092486 T>C maps to NM_001079804.1 S894S. 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-NI-A4U2-01A-11D-A28X-10 chr23:153940658 G>A did not map to a codon.
Sequencing variant TCGA-3K-AAZ8-01A-12D-A38X-10 chr22:17446134 T>G maps to NM_001037814.1 R438R. 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-ZP-A9CV-01A-11D-A382-10 chr15:50578219 T>C maps to NM_002041.4 K360K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9H1-01A-11D-A382-10 chr1:151070416 G>A maps to NM_144618.2 T187T. 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-A1EE-01A-11D-A12Z-10 chr4:46930407 G>T maps to NM_000809.2 S500*. 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-WQ-AB4B-01A-11D-A40P-10 chr15:27193199 C>A maps to NM_000810.3 V403V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YA-A8S7-01A-11D-A36X-10 chr15:27159961 T>G maps to NM_000810.3 S170S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAEA-01A-11D-A40R-10 chr5:161116700 G>T maps to NM_000811.2 E197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr5:161128526 G>A maps to NM_000811.2 L370L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A7SH-01A-11D-A382-10 chr5:161116133 C>T maps to NM_000811.2 L135L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BD-A3ER-01A-11D-A20W-10 chr5:160721289 A>T maps to NM_021911.2 L446*. 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-2Y-A9H1-01A-11D-A382-10 chr23:151123896 C>T did not map to a codon.
Sequencing variant TCGA-2Y-A9GS-01A-12D-A382-10 chr4:46043211 C>T maps to NM_173536.3 P397P. 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-DD-AAEI-01A-11D-A40R-10 chr5:161495109 T>C maps to NM_198903.2 P35P. 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-AA0V-01A-11D-A382-10 chr5:161580307 G>T maps to NM_198903.2 R494R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LG-A9QD-01A-11D-A382-10 chr15:27777999 C>A maps to NM_033223.4 V459V. 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-5C-A9VH-01A-11D-A36X-10 chr23:151818998 C>A 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-DD-A1EE-01A-11D-A12Z-10 chr23:151821043 C>A did not map to a codon.
Sequencing variant TCGA-DD-A39Y-01A-11D-A20W-10 chr23:151815554 T>C did not map to a codon.
Sequencing variant TCGA-DD-AADL-01A-11D-A40R-10 chr23:151818237 G>C 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-UB-AA0V-01A-11D-A382-10 chr23:151817746 G>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-DD-AAC8-01A-11D-A40R-10 chr10:26518687 T>C maps to NM_001134366.1 I274I. 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-DD-AADI-01A-11D-A40R-10 chr3:30842570 T>A maps to NM_207359.2 K354*. 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-EP-A2KA-01A-11D-A183-10 chr4:843757 C>T maps to NM_005255.2 V1252V. 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-DD-A39Y-01A-11D-A20W-10 chr14:88429766 A>G maps to NM_000153.2 T374T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr15:49611879 T>C maps to NM_002044.2 C349C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACX-01A-11D-A40R-10 chr5:153795395 C>T maps to NM_198321.3 T519T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZP-A9D0-01A-11D-A36X-10 chr5:153570578 G>A maps to NM_198321.3 A51A. 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-ZP-A9D4-01A-11D-A36X-10 chr2:155295174 A>G maps to NM_052917.2 G489G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACT-01A-11D-A40R-10 chr2:166615985 C>T maps to NM_004482.3 L311L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAVV-01A-11D-A40R-10 chr2:158115034 A>G maps to NM_014568.1 R147R. 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-DD-AADK-01A-11D-A40R-10 chr12:51773493 G>A maps to NM_007210.3 L24L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAE2-01A-11D-A40R-10 chr4:174223195 A>T did not map to a codon.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr12:132905783 C>T maps to NM_001122636.1 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LG-A9QD-01A-11D-A382-10 chr7:151704963 G>T maps to NM_145292.3 E321*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39X-01A-11D-A20W-10 chr4:173930372 A>G maps to NM_001034845.2 G472G. 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-4R-AA8I-01A-11D-A382-10 chr16:81411035 C>T maps to NM_022041.3 Y543Y. Only missense variants will be evaluated by CHASM.
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-ES-A2HT-01A-12D-A183-10 chr15:42621586 T>C maps to NM_198141.2 N528N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K7-AAU7-01A-11D-A382-10 chr9:128074845 A>G maps to NM_015635.2 L519L. 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-4R-AA8I-01A-11D-A382-10 chr22:29706651 C>T maps to NM_152236.1 R256*. 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-ED-A97K-01A-21D-A382-10 chr17:34072619 G>T maps to NM_139285.2 R632R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-AAV6-01A-21D-A36X-10 chr17:34072961 G>A maps to NM_139285.2 S518S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-AA0V-01A-11D-A382-10 chr17:34073119 C>A maps to NM_139285.2 E466*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr12:101016161 T>A did not map to a codon.
Sequencing variant TCGA-G3-A3CJ-01A-11D-A20W-10 chr12:101018208 A>G maps to NM_174942.1 G542G. 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-G3-AAV6-01A-21D-A36X-10 chr17:9850208 A>G did not map to a codon.
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-ES-A2HT-01A-12D-A183-10 chr23:48650744 T>C did not map to a codon.
Sequencing variant TCGA-DD-AACT-01A-11D-A40R-10 chr3:128205212 T>A did not map to a codon.
Sequencing variant TCGA-DD-AADN-01A-11D-A40R-10 chr3:128204629 G>A maps to NM_032638.4 L271L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MB-01A-11D-A20W-10 chr10:8115946 A>G maps to NM_001002295.1 G432G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACK-01A-11D-A40R-10 chr10:8097824 G>A maps to NM_001002295.1 R69R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAVP-01A-11D-A40R-10 chr10:8106025 C>T maps to NM_001002295.1 Y283Y. 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-3K-AAZ8-01A-12D-A38X-10 chr19:19612125 G>A maps to ENST00000404158 Q487Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADC-01A-11D-A40R-10 chr1:153788805 C>A maps to NM_020699.2 E387*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39X-01A-11D-A20W-10 chr15:45658282 A>G maps to ENST00000432007 P366P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-AA0U-01A-11D-A382-10 chr22:30683517 A>C maps to ENST00000434291 A261A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADI-01A-11D-A40R-10 chr1:155208418 C>T maps to NM_001005742.2 R159R. 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-5C-A9VG-01A-11D-A36X-10 chr3:81630425 G>A maps to ENST00000264326 L446L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BD-A3EP-01A-11D-A22F-10 chr10:104118302 T>C maps to NM_004193.2 S276S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACT-01A-11D-A40R-10 chr10:104018778 C>A maps to NM_004193.2 T28T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr9:136029418 G>T maps to NM_021996.4 R197R. 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-EP-A2KB-01A-11D-A183-10 chr1:89729495 C>A maps to NM_052942.3 G429*. 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-CC-A7IE-01A-21D-A382-10 chr4:72634107 A>G maps to ENST00000504199 F76F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACE-01A-11D-A40R-10 chr7:127225185 C>T maps to NM_024523.5 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A0-01A-11D-A20W-10 chr3:111842505 G>A maps to NM_001190259.1 P113P. 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-DD-AADG-01A-11D-A40R-10 chr12:120595712 G>T maps to NM_006836.1 I1009I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAD1-01A-11D-A40R-10 chr9:79117569 C>T maps to NM_001097636.1 D91D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A3KG-01A-11D-A20W-10 chr8:75276265 A>G maps to NM_018972.2 A247A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WQ-A9G7-01A-11D-A36X-10 chr8:75276244 C>T maps to NM_018972.2 C240C. 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-DD-AAVQ-01A-11D-A40R-10 chr10:48438407 G>A maps to NM_004962.2 S101S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A8O6-01A-11D-A35Z-10 chr19:18499390 G>A maps to NM_004864.2 G191G. 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.
Sequencing variant TCGA-ZS-A9CF-01A-11D-A382-10 chr10:48416486 G>A maps to NM_016204.1 S69S. Only missense variants will be evaluated by CHASM.
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-DD-AACZ-01A-11D-A40R-10 chr10:5842575 T>G maps to NM_001494.3 I46I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAE3-01A-11D-A40R-10 chr10:5808024 C>A maps to NM_001494.3 E428*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAE9-01A-11D-A40R-10 chr10:5836920 A>T maps to NM_001494.3 T105T. Only missense variants will be evaluated by CHASM.
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-ES-A2HT-01A-12D-A183-10 chr11:75152776 G>A maps to NM_030792.6 G413G. Only missense variants will be evaluated by CHASM.
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-5259-01A-31D-A20W-10 chr12:58008159 C>T maps to NM_001111270.1 L274L. 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-ES-A2HT-01A-12D-A183-10 chr16:2034923 T>C maps to NM_005262.2 C145C. 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-DD-AADG-01A-11D-A40R-10 chr6:13365292 C>G maps to NM_018988.2 V285V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAC8-01A-11D-A40R-10 chr2:69585595 C>T did not map to a codon.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr8:21562512 G>T maps to NM_001495.4 T343T. 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-2Y-A9H8-01A-11D-A38X-10 chr16:23486223 C>G did not map to a codon.
Sequencing variant TCGA-DD-AACQ-01A-11D-A40R-10 chr2:85780557 T>A maps to NM_000821.4 K318*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADI-01A-11D-A40R-10 chr19:38876401 T>C maps to NM_152657.3 P500P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADU-01A-11D-A40R-10 chr19:38876401 T>C maps to NM_152657.3 P500P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADY-01A-11D-A40R-10 chr19:38876398 A>G maps to NM_152657.3 A501A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADY-01A-11D-A40R-10 chr19:38876401 T>C maps to NM_152657.3 P500P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9GV-01A-11D-A382-10 chr17:34945742 C>T maps to NM_024835.3 R666*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACP-01A-11D-A40R-10 chr17:34916706 T>C maps to NM_024835.3 L175L. 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-AAE8-01A-11D-A40R-10 chr20:23965974 G>T maps to NM_178311.2 R186R. 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-4R-AA8I-01A-11D-A382-10 chr2:233612328 C>T maps to ENST00000373566 R16*. 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-DD-A3A1-01A-11D-A20W-10 chr7:150269811 A>G maps to ENST00000430830 E232E. 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-NI-A8LF-01A-11D-A35Z-10 chr7:150171328 G>A maps to NM_175571.2 P304P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACI-01A-11D-A40R-10 chr5:102432262 T>A maps to NM_017676.2 R426*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADR-01A-11D-A40R-10 chr19:14591236 C>A maps to NM_202470.1 E179*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACN-01A-11D-A40R-10 chr1:78601370 G>T maps to NM_017655.4 E298*. 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-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-4R-AA8I-01A-11D-A382-10 chr1:147230335 A>T maps to NM_005266.5 Y337*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr1:147380384 C>T maps to NM_005267.4 R101R. 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-DD-AAD5-01A-11D-A40R-10 chr1:147380357 C>A maps to NM_005267.4 Y92*. 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-G3-AAV0-01A-11D-A36X-10 chr1:35223440 C>G maps to NM_005268.2 P170P. 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-DD-AACZ-01A-11D-A40R-10 chr6:87994408 G>A maps to NM_198568.2 V74V. 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-DD-AACU-01A-11D-A40R-10 chr17:38519620 G>A maps to ENST00000337376 T149T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACP-01A-11D-A40R-10 chr9:86421240 T>C maps to NM_025211.3 E64E. 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-DD-AAVV-01A-11D-A40R-10 chr23:100662798 T>A did not map to a codon.
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-CC-A3MB-01A-11D-A20W-10 chr3:33110428 T>C maps to NM_000404.2 P93P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EE-01A-11D-A12Z-10 chr3:33106972 C>T maps to NM_000404.2 G178G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACQ-01A-11D-A40R-10 chr2:220104514 A>T maps to NM_024506.3 Y254*. 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-ES-A2HS-01A-11D-A183-10 chr11:134238602 G>T maps to NM_138342.3 G319*. 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-CC-A5UC-01A-11D-A28X-10 chr7:8125840 G>A maps to NM_138426.2 S439S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr15:69561465 T>C maps to NM_015554.1 H579H. 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-A8HS-01A-11D-A35Z-10 chr16:74640752 T>C maps to NM_012201.5 Q80Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr2:121746145 C>T maps to NM_005270.4 Q886*. 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-2Y-A9H3-01A-11D-A382-10 chr7:42011934 C>A did not map to a codon.
Sequencing variant TCGA-BC-A3KG-01A-11D-A20W-10 chr7:42005876 T>A maps to NM_000168.5 K932*. 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-WQ-A9G7-01A-11D-A36X-10 chr7:42017309 G>A maps to NM_000168.5 C553C. 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-BD-A3EP-01A-11D-A22F-10 chr12:75816821 A>G maps to NM_152436.1 K241K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr12:75816821 A>G maps to NM_152436.1 K241K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A0-01A-11D-A20W-10 chr16:4385329 T>C maps to NM_032575.2 C237C. 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-DD-AAE3-01A-11D-A40R-10 chr23:14550454 A>T did not map to a codon.
Sequencing variant TCGA-BC-A8YO-01A-11D-A36X-10 chr4:175636669 A>G maps to NM_006529.2 D181D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAE7-01A-11D-A40R-10 chr4:175580327 A>G maps to NM_006529.2 I316I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A69H-01A-11D-A30V-10 chr23:102978842 A>C did not map to a codon.
Sequencing variant TCGA-G3-A5SM-01A-12D-A28X-10 chr23:102973918 G>T 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-DD-AAVY-01A-11D-A40R-10 chr19:17691642 G>T maps to NM_024656.2 L510L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MF-01A-11D-A33K-10 chr19:17692113 G>A maps to NM_024656.2 W577*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EL-01A-11D-A152-10 chr1:183938535 G>T maps to NM_015101.2 P233P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EL-01A-11D-A152-10 chr1:183938538 G>T maps to NM_015101.2 V232V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr3:52730328 G>T maps to NM_018446.2 T151T. 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-4R-AA8I-01A-11D-A382-10 chr19:48202007 C>T maps to NM_015711.3 G1122G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAD0-01A-11D-A40R-10 chr19:48204912 C>T maps to NM_015711.3 L1308L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAVV-01A-11D-A40R-10 chr19:48185375 C>G maps to NM_015711.3 P750P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9GU-01A-11D-A382-10 chr23:120181748 G>A did not map to a codon.
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-WQ-A9G7-01A-11D-A36X-10 chr23:120181884 T>C did not map to a codon.
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-DD-AAD1-01A-11D-A40R-10 chr3:52324604 C>T maps to NM_145262.3 L83L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr1:29010171 A>G maps to NM_006582.2 V16V. 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-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-A1EG-01A-11D-A20W-10 chr3:49759217 G>A maps to NM_013334.2 G377G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IE-01A-21D-A382-10 chr3:155655378 G>A did not map to a codon.
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-ZS-A9CE-01A-11D-A36X-10 chr7:2771228 C>G maps to NM_007353.2 G244G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADU-01A-11D-A40R-10 chr17:63014399 G>A maps to NM_006572.4 L178L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9H4-01A-11D-A382-10 chr9:80144020 G>A maps to NM_004297.3 D91D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XR-A8TE-01A-11D-A35Z-10 chr9:80144155 A>G maps to NM_004297.3 S46S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZS-A9CF-01A-11D-A382-10 chr19:3155883 G>T maps to NM_002068.2 V226V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAVQ-01A-11D-A40R-10 chr7:79828587 C>T maps to NM_002069.5 G117G. 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-CC-A8HU-01A-11D-A35Z-10 chr20:57429285 C>T maps to NM_080425.2 P322P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAE6-01A-11D-A40R-10 chr20:57429420 C>T maps to NM_080425.2 A367A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACS-01A-11D-A40R-10 chr3:50232231 C>A maps to NM_000172.3 I299I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACL-01A-11D-A40R-10 chr7:80117907 T>A maps to NM_001102386.1 L82L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-AA0U-01A-11D-A382-10 chr22:23438484 C>T maps to NM_002073.2 D201D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr5:180668512 A>G maps to NM_006098.4 G136G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3K-AAZ8-01A-12D-A38X-10 chr3:179131379 A>C maps to NM_021629.3 T173T. 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-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-2Y-A9H1-01A-11D-A382-10 chr6:30520391 C>T maps to NM_005275.3 G317G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39Z-01A-11D-A20W-10 chr6:30523923 T>C maps to NM_005275.3 K19K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAE7-01A-11D-A40R-10 chr1:38061408 C>T maps to NM_013285.2 K5K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EG-01A-11D-A20W-10 chr3:52727058 A>G maps to NM_014366.4 R347R. 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-DD-AADV-01A-11D-A38X-10 chr5:141385880 T>C maps to NM_005471.4 R79R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADA-01A-11D-A40R-10 chr4:44713035 T>A maps to NM_138335.1 G176G. Only missense variants will be evaluated by CHASM.
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-G3-AAUZ-01A-11D-A382-10 chr12:102161839 G>T maps to NM_024312.4 C461*. 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-5R-AA1C-01A-11D-A40R-10 chr3:37396590 G>A did not map to a codon.
Sequencing variant TCGA-ZP-A9D4-01A-11D-A36X-10 chr3:37340442 T>C maps to NM_001172713.1 L334L. 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-DD-AACP-01A-11D-A40R-10 chr3:121410143 T>C maps to ENST00000393667 L2689L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CG-01A-11D-A20W-10 chr3:167728182 T>C maps to NM_014498.3 G655G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAD3-01A-11D-A40R-10 chr1:155823538 C>A maps to ENST00000368331 V11V. 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-AACT-01A-11D-A40R-10 chr6:117884419 A>G maps to NM_020399.3 Y462Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr6:117884506 T>C maps to NM_020399.3 G433G. 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-ES-A2HS-01A-11D-A183-10 chr16:58743422 A>G maps to NM_002080.2 T356T. 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-DD-A39Y-01A-11D-A20W-10 chr10:113935416 T>C maps to NM_020918.4 R118R. 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-A8HT-01A-11D-A35Z-10 chr2:96690204 G>A maps to NM_207328.2 L547L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACP-01A-11D-A40R-10 chr19:33579136 C>T maps to NM_018025.2 F57F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-O8-A75V-01A-11D-A32G-10 chr17:42552195 C>A did not map to a codon.
Sequencing variant TCGA-BC-A69H-01A-11D-A30V-10 chr1:46124753 C>A maps to NM_021639.4 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A1-01A-11D-A20W-10 chr1:46120862 T>C maps to NM_021639.4 G63G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-AAV5-01A-11D-A36X-10 chr7:99768965 C>T maps to NM_152742.1 R468R. Only missense variants will be evaluated by CHASM.
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-DD-A3A0-01A-11D-A20W-10 chr23:132438855 T>C did not map to a codon.
Sequencing variant TCGA-NI-A8LF-01A-11D-A35Z-10 chr23:132548887 G>C did not map to a codon.
Sequencing variant TCGA-BD-A3EP-01A-11D-A22F-10 chr13:92380784 G>T did not map to a codon.
Sequencing variant TCGA-DD-A3A0-01A-11D-A20W-10 chr13:92345687 A>G maps to NM_004466.4 S191S. Only missense variants will be evaluated by CHASM.
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-ZP-A9CZ-01A-11D-A382-10 chr14:67525477 T>A maps to NM_020806.4 L373L. 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-XR-A8TE-01A-11D-A35Z-10 chr4:176556160 G>A maps to NM_005277.3 D244D. 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-AACQ-01A-11D-A40R-10 chr23:13803758 T>A did not map to a codon.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr2:27852778 G>T maps to NM_007266.3 L69L. Only missense variants will be evaluated by CHASM.
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-BC-A10W-01A-11D-A12Z-10 chr2:207041287 A>G maps to NM_005279.3 C228C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A9FS-01A-11D-A36X-10 chr2:207041059 A>G maps to NM_005279.3 Y304Y. 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-AAC8-01A-11D-A40R-10 chr23:136113820 A>T did not map to a codon.
Sequencing variant TCGA-DD-AADC-01A-11D-A40R-10 chr23:136112558 C>T did not map to a codon.
Sequencing variant TCGA-DD-AAVY-01A-11D-A40R-10 chr23:136113549 A>G did not map to a codon.
Sequencing variant TCGA-DD-AADL-01A-11D-A40R-10 chr19:6730370 T>C maps to NM_001080452.1 E528E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9H3-01A-11D-A382-10 chr12:123187335 C>T maps to NM_177551.3 K165K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAVP-01A-11D-A40R-10 chr6:46976899 C>A maps to ENST00000283297 V758V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAD0-01A-11D-A40R-10 chr6:47647895 A>G maps to NM_153839.6 L119L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A2QR-01A-11D-A20W-10 chr6:47649350 A>G maps to NM_153839.6 E284E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9H1-01A-11D-A382-10 chr23:135427541 C>A 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-A119-01A-11D-A12Z-10 chr23:135430115 T>C 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-A1EE-01A-11D-A12Z-10 chr23:135453611 A>G 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-DD-A3A1-01A-11D-A20W-10 chr23:135438309 A>G did not map to a codon.
Sequencing variant TCGA-DD-AAC8-01A-11D-A40R-10 chr23:135431161 A>T did not map to a codon.
Sequencing variant TCGA-DD-AADQ-01A-11D-A40R-10 chr23:135443732 G>T did not map to a codon.
Sequencing variant TCGA-DD-AAED-01A-12D-A40R-10 chr23:135428110 C>A 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-G3-AAV6-01A-21D-A36X-10 chr23:135428653 T>C did not map to a codon.
Sequencing variant TCGA-WQ-A9G7-01A-11D-A36X-10 chr23:135431188 A>G did not map to a codon.
Sequencing variant TCGA-ZP-A9CY-01A-11D-A382-10 chr23:135429238 A>G did not map to a codon.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr6:47682483 A>G maps to NM_153838.3 G501G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAE3-01A-11D-A40R-10 chr6:47681895 C>T maps to NM_153838.3 A305A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAE8-01A-11D-A40R-10 chr6:47681899 T>C maps to NM_153838.3 L307L. 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-DD-AADN-01A-11D-A40R-10 chr6:46828583 C>A maps to NM_015234.4 L749L. 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-ES-A2HS-01A-11D-A183-10 chr23:129519157 G>T 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-DD-AAE4-01A-11D-A40R-10 chr10:134941949 G>A maps to ENST00000368577 G746G. 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-DD-AAED-01A-12D-A40R-10 chr8:37699536 C>T maps to NM_032777.9 T1227T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr4:22389384 A>G maps to NM_145290.2 G1303G. 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-G3-AAV5-01A-11D-A36X-10 chr4:22390452 C>T maps to NM_145290.2 E947E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACF-01A-11D-A40R-10 chr3:100387945 A>G maps to NM_032787.2 T711T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr14:105517771 A>G maps to NM_013345.2 A234A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MB-01A-11D-A20W-10 chr1:236305999 C>T maps to NM_003272.3 N26N. 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-CC-A3MB-01A-11D-A20W-10 chr17:72368627 A>G maps to ENST00000440684 R1389R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WX-AA44-01A-11D-A38X-10 chr17:72367913 C>T maps to ENST00000440684 T1151T. 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-DD-AAE4-01A-11D-A40R-10 chr23:9709455 A>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-4R-AA8I-01A-11D-A382-10 chr3:154146777 T>C maps to NM_001038705.1 S209S. 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-2Y-A9GT-01A-11D-A382-10 chr11:67220096 C>A maps to NM_206997.1 T33T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADL-01A-11D-A40R-10 chr3:119911829 G>A maps to NM_153002.2 R144*. 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-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-AAEB-01A-11D-A40R-10 chr12:6933885 C>T maps to NM_019858.1 S274S. 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-UB-A7MB-01A-11D-A33Q-10 chr8:145584306 G>A maps to NM_024531.3 L353L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A5UD-01A-11D-A28X-10 chr17:4936946 A>T maps to NM_017986.3 G279G. 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-2Y-A9GU-01A-11D-A382-10 chr23:78427213 G>A did not map to a codon.
Sequencing variant TCGA-DD-A3A0-01A-11D-A20W-10 chr23:78427230 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-DD-AADG-01A-11D-A40R-10 chr15:40093461 C>T maps to NM_007223.1 K473K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WQ-A9G7-01A-11D-A36X-10 chr15:40093623 C>T maps to NM_007223.1 A419A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAE3-01A-11D-A40R-10 chr13:99908039 A>G maps to NM_005292.3 Y29Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACD-01A-11D-A40R-10 chr13:99947895 G>A maps to NM_004951.4 I168I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAEA-01A-11D-A40R-10 chr13:99948231 A>T maps to NM_004951.4 I56I. 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-EP-A2KA-01A-11D-A183-10 chr8:142366955 G>T maps to NM_005293.2 P356P. 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-DD-AADM-01A-11D-A40R-10 chr7:107115515 A>G maps to NM_005295.2 L337L. 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-ZS-A9CG-01A-11D-A36X-10 chr1:200842405 C>T maps to NM_005298.2 L81L. 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-DD-AADQ-01A-11D-A40R-10 chr7:124404045 G>A maps to NM_005302.2 L329L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XR-A8TF-01A-11D-A35Z-10 chr7:124404435 T>A maps to NM_005302.2 K199*. Only missense variants will be evaluated by CHASM.
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-EP-A2KB-01A-11D-A183-10 chr23:150345210 G>T did not map to a codon.
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-DD-AAE9-01A-11D-A40R-10 chr2:231775506 A>T maps to NM_005683.3 A57A. Only missense variants will be evaluated by CHASM.
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-XR-A8TF-01A-11D-A35Z-10 chr6:97247592 T>A maps to NM_030784.2 A5A. 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-AAEA-01A-11D-A40R-10 chr23:19051753 A>G did not map to a codon.
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-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-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-2Y-A9H3-01A-11D-A382-10 chr5:90449148 C>T maps to NM_032119.3 Q6246*. 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-A1EE-01A-11D-A12Z-10 chr5:89910834 C>A maps to NM_032119.3 S69*. Only missense variants will be evaluated by CHASM.
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-DD-AACT-01A-11D-A40R-10 chr5:89943495 A>G maps to NM_032119.3 R1068R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAD5-01A-11D-A40R-10 chr5:90002211 G>A did not map to a codon.
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-A7MB-01A-11D-A33Q-10 chr5:90077395 G>T did not map to a codon.
Sequencing variant TCGA-ZS-A9CE-01A-11D-A36X-10 chr5:90074290 G>A maps to NM_032119.3 Q4238Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9H4-01A-11D-A382-10 chr23:101909784 C>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-A3A1-01A-11D-A20W-10 chr23:101910324 A>G did not map to a codon.
Sequencing variant TCGA-CC-A3MB-01A-11D-A20W-10 chr23:101970640 T>C did not map to a codon.
Sequencing variant TCGA-DD-A39Y-01A-11D-A20W-10 chr23:101970496 T>C 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-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-2Y-A9H9-01A-21D-A38X-10 chr6:117116995 T>C maps to NM_148963.2 Q517Q. 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-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-CC-A8HT-01A-11D-A35Z-10 chr10:46999959 G>T maps to NM_014696.3 L360L. 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-CC-5258-01A-01D-A12Z-10 chr17:7216696 A>G did not map to a codon.
Sequencing variant TCGA-DD-A1EE-01A-11D-A12Z-10 chr17:7216696 A>G did not map to a codon.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr9:139231494 C>T maps to NM_001145638.1 R182*. Only missense variants will be evaluated by CHASM.
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-BD-A3EP-01A-11D-A22F-10 chr9:139250947 C>T maps to NM_001145638.1 H589H. 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-DD-AAW3-01A-11D-A40P-10 chr9:139234262 C>T maps to NM_001145638.1 I358I. 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-DD-AAEE-01A-11D-A40R-10 chr6:32160268 C>A maps to NM_022107.1 E8*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CG-01A-11D-A20W-10 chr19:1104929 T>C did not map to a codon.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr5:54456943 T>C maps to NM_001008397.2 N109N. 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-AAD2-01A-11D-A40R-10 chr11:123474147 G>A maps to ENST00000456860 K219K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A6M3-01A-11D-A32G-10 chr11:123448101 G>T maps to ENST00000456860 T17T. 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-2Y-A9GZ-01A-11D-A38X-10 chr7:50680498 A>T maps to NM_005311.4 L378*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAVX-01A-11D-A40R-10 chr2:165381555 T>A maps to NM_004490.2 A212A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CG-01A-11D-A20W-10 chr2:165383604 T>C maps to NM_004490.2 L174L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr2:11778933 A>G maps to NM_014668.3 K1895K. 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-DD-AAC8-01A-11D-A40R-10 chr5:153085376 A>T maps to NM_001114183.1 K525*. 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-CC-A3MB-01A-11D-A20W-10 chr23:122551503 A>G did not map to a codon.
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-G3-AAV0-01A-11D-A36X-10 chr23:122551285 A>C did not map to a codon.
Sequencing variant TCGA-G3-AAV3-01A-11D-A36X-10 chr23:122387319 G>A 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-DD-AACL-01A-11D-A40R-10 chr11:105768992 A>T did not map to a codon.
Sequencing variant TCGA-DD-AAE4-01A-11D-A40R-10 chr11:105842661 T>A maps to NM_000829.3 V772V. 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-UB-AA0U-01A-11D-A382-10 chr11:105795409 C>T maps to NM_000829.3 Q588*. 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-AAEK-01A-11D-A40R-10 chr21:30968881 G>T maps to ENST00000327783 G405G. 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-2Y-A9GY-01A-11D-A382-10 chr6:102516349 C>T maps to NM_021956.4 N897N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9H2-01A-12D-A382-10 chr1:37356578 G>T maps to NM_000831.3 T78T. 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-DD-A1ED-01A-11D-A152-10 chr1:37291208 G>T maps to NM_000831.3 I583I. 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-DD-AADE-01A-11D-A40R-10 chr9:140056942 C>A maps to ENST00000371546 V634V. 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-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-DD-AACX-01A-11D-A40R-10 chr16:9943749 G>A maps to NM_000833.3 S397S. 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-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-AAW2-01A-11D-A40P-10 chr17:72838939 C>G maps to NM_000835.3 S1112S. 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-DD-AAD2-01A-11D-A40R-10 chr19:48918222 C>G maps to NM_000836.2 L505L. 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-WJ-A86L-01A-12D-A45V-10 chr9:104449359 C>T maps to NM_133445.2 W274*. 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-AADK-01A-11D-A40R-10 chr23:48840242 G>T 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-WQ-A9G7-01A-11D-A36X-10 chr23:48847396 T>C did not map to a codon.
Sequencing variant TCGA-YA-A8S7-01A-11D-A36X-10 chr13:114324084 C>A maps to NM_002929.2 A261A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZS-A9CE-01A-11D-A36X-10 chr13:114322306 G>A maps to NM_002929.2 G202G. Only missense variants will be evaluated by CHASM.
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-NI-A8LF-01A-11D-A35Z-10 chr19:47422763 G>T maps to NM_004491.4 E278*. 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-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-ES-A2HT-01A-12D-A183-10 chr6:146755355 C>T maps to NM_000838.3 F1003F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3K-AAZ8-01A-12D-A38X-10 chr3:51749598 G>T maps to NM_000839.3 E604*. 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-AACL-01A-11D-A40R-10 chr6:34003951 A>T maps to NM_000841.1 A645A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IE-01A-21D-A382-10 chr11:88386444 T>C maps to NM_001143831.2 P346P. 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-AADG-01A-11D-A40R-10 chr5:178418901 C>T maps to NM_000843.3 G229G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A1-01A-11D-A20W-10 chr3:7494417 C>T maps to NM_181874.2 Y433Y. 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-DD-AACC-01A-11D-A40R-10 chr3:7620314 C>T maps to NM_181874.2 T574T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADG-01A-11D-A40R-10 chr7:126173563 C>A maps to NM_001127323.1 V624V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A8O5-01A-11D-A35Z-10 chr7:126542719 G>C maps to NM_001127323.1 Y344*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADL-01A-11D-A40R-10 chr17:42427829 G>A maps to NM_002087.2 R161R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACQ-01A-11D-A40R-10 chr23:16170726 A>T did not map to a codon.
Sequencing variant TCGA-DD-AADI-01A-11D-A40R-10 chr4:42895606 C>A maps to NM_001080476.2 G108G. 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-4R-AA8I-01A-11D-A382-10 chr16:11981477 A>G maps to NM_002094.3 S302S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZP-A9D1-01A-11D-A382-10 chr16:11991859 A>G maps to NM_002094.3 L129L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WQ-A9G7-01A-11D-A36X-10 chr20:33519900 A>G maps to NM_000178.2 H290H. 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-DD-AAE7-01A-11D-A40R-10 chr6:52850271 G>T maps to NM_001512.3 G83G. 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-XR-A8TG-01A-11D-A35Z-10 chr1:110280322 T>C maps to NM_000849.4 Q141Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CJ-01A-11D-A20W-10 chr10:106022765 A>G maps to NM_004832.2 R132R. 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-DD-A39Z-01A-11D-A20W-10 chr2:48872209 T>C maps to NM_172311.2 G818G. 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-DD-A39X-01A-11D-A20W-10 chr11:18373438 A>G maps to NM_005316.3 Q355Q. 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-4R-AA8I-01A-11D-A382-10 chr2:197653947 C>T maps to NM_012086.2 Q291Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A8HV-01A-11D-A35Z-10 chr19:17452487 C>T maps to NM_133644.3 F517F. 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-EP-A2KB-01A-11D-A183-10 chr12:54858949 G>T maps to NM_144594.2 T6T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5C-AAPD-01A-21D-A38X-10 chr6:42146133 C>T maps to NM_000409.3 C106C. 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-CC-A8HU-01A-11D-A35Z-10 chr11:106810452 A>T maps to ENST00000282249 P313P. 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-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-2Y-A9H4-01A-11D-A382-10 chr12:14839105 G>A maps to NM_004963.3 T128T. 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-BC-A3KF-01A-11D-A20W-10 chr12:14829835 A>G maps to NM_004963.3 S300S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACZ-01A-11D-A40R-10 chr17:7909979 A>T maps to NM_000180.3 A442A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr23:108691375 G>A did not map to a codon.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr23:108628444 T>C did not map to a codon.
Sequencing variant TCGA-DD-A39X-01A-11D-A20W-10 chr23:108619160 T>C did not map to a codon.
Sequencing variant TCGA-DD-A39Y-01A-11D-A20W-10 chr23:108691368 T>C did not map to a codon.
Sequencing variant TCGA-DD-A3A1-01A-11D-A20W-10 chr23:108708491 A>G did not map to a codon.
Sequencing variant TCGA-DD-AAC8-01A-11D-A40R-10 chr23:108631784 A>T did not map to a codon.
Sequencing variant TCGA-DD-AAD0-01A-11D-A40R-10 chr23:108718937 C>T 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-DD-AADJ-01A-11D-A40R-10 chr2:189434771 A>G maps to NM_016315.2 T178T. Only missense variants will be evaluated by CHASM.
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-A1EE-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-DD-AAE2-01A-11D-A40R-10 chr3:148714620 C>T maps to NM_004130.3 F137F. 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-CC-A8HU-01A-11D-A35Z-10 chr11:45949842 C>T maps to NM_152312.3 R624*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A9FS-01A-11D-A36X-10 chr4:144801585 A>G maps to NM_198682.2 S38S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WQ-A9G7-01A-11D-A36X-10 chr12:21693400 G>T maps to NM_021957.3 I584I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr20:23345919 A>G maps to NM_022482.3 E300E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADY-01A-11D-A40R-10 chr20:23345919 A>G maps to NM_022482.3 E300E. Only missense variants will be evaluated by CHASM.
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-CC-A9FV-01A-11D-A36X-10 chr5:54404221 T>C maps to NM_006144.3 N209N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZP-A9D4-01A-11D-A36X-10 chr5:54320627 C>T maps to NM_002104.2 Q69*. 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-ZP-A9CV-01A-11D-A382-10 chr12:48723424 C>T maps to NM_181788.1 A117A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr7:44875218 T>C maps to ENST00000421098 K131K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADB-01A-11D-A40R-10 chr10:71855483 C>T maps to NM_018649.2 A221A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NI-A8LF-01A-11D-A35Z-10 chr17:73775165 A>C maps to NM_005324.3 A30A. 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-DD-A1EE-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-DD-AACY-01A-11D-A40R-10 chr2:43019664 G>A maps to NM_012205.2 R4R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A1-01A-11D-A20W-10 chr3:15613277 T>C did not map to a codon.
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-DD-A3A0-01A-11D-A20W-10 chr2:26426950 T>C maps to NM_000182.4 G400G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADO-01A-11D-A40R-10 chr2:26502109 G>A maps to NM_000183.2 L246L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr2:26502145 A>G maps to NM_000183.2 E258E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-AAV3-01A-11D-A36X-10 chr16:777614 G>T did not map to a codon.
Sequencing variant TCGA-DD-AAD5-01A-11D-A40R-10 chr12:96384224 T>C maps to NM_002108.2 L267L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr19:35775714 A>G maps to NM_021175.2 Q38Q. 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-BC-A3KG-01A-11D-A20W-10 chr20:7915281 T>C maps to NM_017545.2 R46R. 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-ZP-A9D1-01A-11D-A382-10 chr17:39890780 C>A maps to ENST00000310778 E36*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAD5-01A-11D-A40R-10 chr5:82940200 A>G maps to NM_001884.3 C252C. 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-DD-AAEK-01A-11D-A40R-10 chr19:19369377 G>A maps to NM_023002.2 N257N. 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-AADQ-01A-11D-A40R-10 chr19:52216885 G>A maps to NM_001523.2 L511L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A8HV-01A-11D-A35Z-10 chr8:122627071 A>G maps to NM_005328.2 G312G. 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-DD-AADR-01A-11D-A40R-10 chr18:43708090 A>G maps to NM_138443.3 *279W. 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-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-AAD3-01A-11D-A40R-10 chr16:227352 C>T maps to NM_000558.3 A124A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MA-01A-11D-A20W-10 chr5:139725514 T>C maps to NM_001945.2 A67A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAC8-01A-11D-A40R-10 chr5:139725616 T>A maps to NM_001945.2 L33L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAC9-01A-11D-A40R-10 chr5:139714266 G>A maps to NM_001945.2 S207S. 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-DD-A1ED-01A-11D-A152-10 chr7:106836395 A>G maps to NM_012257.3 G395G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAE2-01A-11D-A40R-10 chr7:106827062 T>G maps to NM_012257.3 V234V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAE2-01A-11D-A40R-10 chr7:106827074 T>C maps to NM_012257.3 A238A. 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-WQ-A9G7-01A-11D-A36X-10 chr7:106840667 C>T maps to NM_012257.3 Y483Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EG-01A-11D-A20W-10 chr6:135323882 A>G maps to NM_006620.3 F176F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9H5-01A-11D-A382-10 chr23:11132957 G>T did not map to a codon.
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 chr23:153225828 A>G did not map to a codon.
Sequencing variant TCGA-FV-A2QR-01A-11D-A20W-10 chr23:153230096 T>C did not map to a codon.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr12:104476617 T>C maps to NM_013320.2 D334D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A3KG-01A-11D-A20W-10 chr12:104461780 T>C maps to NM_013320.2 P123P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr12:104495756 A>G maps to NM_013320.2 A630A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9H9-01A-21D-A38X-10 chr5:45695976 G>A maps to NM_021072.2 G73G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAVP-01A-11D-A40R-10 chr1:155247572 G>T maps to NM_020897.1 V64V. Only missense variants will be evaluated by CHASM.
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-ZP-A9D4-01A-11D-A36X-10 chr15:73660428 G>A maps to NM_005477.2 A61A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACH-01A-11D-A40R-10 chr17:40336390 G>A maps to NM_001524.1 H59H. 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-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-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-WQ-A9G7-01A-11D-A36X-10 chr2:240056340 T>C did not map to a codon.
Sequencing variant TCGA-CC-A3MB-01A-11D-A20W-10 chr17:42168676 A>G maps to NM_001015053.1 L451L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9H5-01A-11D-A382-10 chr23:48678642 G>T did not map to a codon.
Sequencing variant TCGA-DD-A39Y-01A-11D-A20W-10 chr23:48663923 T>C did not map to a codon.
Sequencing variant TCGA-DD-AADM-01A-11D-A40R-10 chr23:48673108 G>T did not map to a codon.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr23:48661182 T>C did not map to a codon.
Sequencing variant TCGA-G3-A3CG-01A-11D-A20W-10 chr23:48661290 A>G did not map to a codon.
Sequencing variant TCGA-G3-A3CJ-01A-11D-A20W-10 chr23:48672875 A>G did not map to a codon.
Sequencing variant TCGA-G3-A3CJ-01A-11D-A20W-10 chr23:48675758 T>C did not map to a codon.
Sequencing variant TCGA-DD-AAE9-01A-11D-A40R-10 chr12:48179582 G>T maps to NM_015401.3 A886A. Only missense variants will be evaluated by CHASM.
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-DD-AADY-01A-11D-A40R-10 chr15:50535065 G>A maps to NM_002112.3 I460I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr6:22570436 C>T maps to NM_138574.2 G211G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39Z-01A-11D-A20W-10 chr15:83832755 A>G maps to NM_016073.2 H52H. 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-DD-A39Y-01A-11D-A20W-10 chr23:83577008 T>C did not map to a codon.
Sequencing variant TCGA-WQ-A9G7-01A-11D-A36X-10 chr23:83723917 G>A did not map to a codon.
Sequencing variant TCGA-ZS-A9CE-01A-11D-A36X-10 chr23:83723669 A>G did not map to a codon.
Sequencing variant TCGA-2Y-A9H0-01A-11D-A382-10 chr7:794223 A>G did not map to a codon.
Sequencing variant TCGA-DD-AAE7-01A-11D-A40R-10 chr16:50100276 G>T did not map to a codon.
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-EP-A2KA-01A-11D-A183-10 chr14:73969701 A>G maps to ENST00000334988 L621L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WQ-A9G7-01A-11D-A36X-10 chr14:73945439 G>A maps to ENST00000334988 P937P. 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-XR-A8TF-01A-11D-A35Z-10 chr14:31814461 T>C maps to ENST00000389961 L957L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39Y-01A-11D-A20W-10 chr2:37217793 T>C maps to NM_019024.1 P1898P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADE-01A-11D-A40R-10 chr2:37283647 G>A maps to NM_019024.1 V778V. 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-ZS-A9CG-01A-11D-A36X-10 chr5:41057462 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-ES-A2HS-01A-11D-A183-10 chr6:139487730 G>T maps to NM_016217.2 V194V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5R-AA1C-01A-11D-A40R-10 chr14:31597195 A>G maps to NM_015382.2 G1592G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MA-01A-11D-A20W-10 chr14:31583497 T>C maps to NM_015382.2 G1889G. 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-DD-A1EG-01A-11D-A20W-10 chr14:31575934 T>C maps to NM_015382.2 E2381E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A0-01A-11D-A20W-10 chr14:31576778 A>G maps to NM_015382.2 S2204S. 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-AAV4-01A-11D-A382-10 chr1:45469947 C>T maps to NM_024602.5 E748E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAW0-01A-11D-A40R-10 chr7:43447200 C>T maps to NM_015052.3 N224N. 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-DD-A39Z-01A-11D-A20W-10 chr2:197092979 T>C did not map to a codon.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr2:197172804 C>T maps to NM_020760.1 W813*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QA-A7B7-01A-11D-A32G-10 chr3:124732433 A>G maps to NM_020733.1 S663S. 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-EP-A2KA-01A-11D-A183-10 chr12:66731842 C>A maps to NM_033647.2 P1075P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADA-01A-11D-A40R-10 chr10:96350208 C>T maps to NM_018063.3 R510*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADN-01A-11D-A40R-10 chr10:96350288 G>A maps to NM_018063.3 Q536Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr4:84358186 G>A maps to NM_133636.2 G624G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZS-A9CE-01A-11D-A36X-10 chr17:65103748 C>A maps to NM_014877.3 E1593*. 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-ES-A2HS-01A-11D-A183-10 chr7:92825187 C>A maps to ENST00000453812 G433*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACA-01A-11D-A40R-10 chr23:65408258 C>T did not map to a codon.
Sequencing variant TCGA-WQ-A9G7-01A-11D-A36X-10 chr23:65483529 G>A did not map to a codon.
Sequencing variant TCGA-DD-AACU-01A-11D-A40R-10 chr11:93796812 G>A maps to NM_001098672.1 V185V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAVS-01A-11D-A40R-10 chr15:63916052 C>T maps to ENST00000261887 A4494A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAVV-01A-11D-A40R-10 chr15:63970129 A>G maps to ENST00000261887 T2328T. 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-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-DD-AAE0-01A-11D-A40R-10 chr15:28421671 G>A maps to NM_004667.4 P3196P. 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-ES-A2HT-01A-12D-A183-10 chr4:89397167 T>C maps to NM_016323.2 S523S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr4:89356959 T>C maps to NM_017912.3 P778P. 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-BD-A3EP-01A-11D-A22F-10 chr3:193854817 G>A maps to NM_005524.2 L91L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A1-01A-11D-A20W-10 chr15:72638892 G>C maps to ENST00000457859 Y446*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr15:72643537 C>T maps to ENST00000457859 W214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5R-AA1C-01A-11D-A40R-10 chr5:73981153 G>A maps to NM_000521.3 L23L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAEB-01A-11D-A40R-10 chr5:74009420 G>T maps to NM_000521.3 E288*. 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-DD-AAW0-01A-11D-A40R-10 chr1:40092691 G>A maps to NM_014571.3 A158A. 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-2Y-A9GY-01A-11D-A382-10 chr1:91841092 G>T maps to NM_001017975.3 P529P. 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-DD-AACL-01A-11D-A40R-10 chr7:81331974 A>T maps to NM_000601.4 P703P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EG-01A-11D-A20W-10 chr4:3443796 C>G maps to ENST00000511533 L23L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAE4-01A-11D-A40R-10 chr4:3446145 G>A maps to ENST00000511533 W236*. 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-WQ-A9G7-01A-11D-A36X-10 chr4:3444864 C>T maps to ENST00000511533 H129H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9H2-01A-12D-A382-10 chr8:43054561 C>T maps to ENST00000458501 H614H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MB-01A-11D-A20W-10 chr8:43047566 T>C maps to ENST00000458501 S485S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAC8-01A-11D-A40R-10 chr3:42735311 T>A did not map to a codon.
Sequencing variant TCGA-G3-A5SJ-01A-11D-A27I-10 chr4:145568033 C>T maps to NM_022475.1 C69C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZP-A9D4-01A-11D-A36X-10 chr4:145580920 T>C maps to NM_022475.1 L254L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5R-AA1D-01A-11D-A382-10 chr14:100135257 G>A maps to NM_032425.4 W607*. 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-CC-A8HT-01A-11D-A35Z-10 chr7:27570939 A>G maps to NM_152740.3 A241A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A1-01A-11D-A20W-10 chr7:27672028 A>G maps to NM_152740.3 A96A. 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-DD-AACB-01A-11D-A40R-10 chr9:35813495 G>T maps to NM_032593.2 V91V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CJ-01A-11D-A20W-10 chr6:126288055 A>G maps to NM_138571.4 K75K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr7:75184732 G>A maps to NM_005338.4 C650C. 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-DD-A3A0-01A-11D-A20W-10 chr1:114500896 T>C maps to ENST00000426820 C726C. 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-2Y-A9H1-01A-11D-A382-10 chr7:139316420 C>T maps to NM_022740.4 W385*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WQ-A9G7-01A-11D-A36X-10 chr11:33309021 T>C maps to NM_005734.3 T354T. Only missense variants will be evaluated by CHASM.
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-A1EE-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-A1EE-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-5R-AA1C-01A-11D-A40R-10 chr6:27114963 T>C maps to NM_080596.1 S19S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr6:25727450 G>T maps to NM_170610.2 P105P. 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-WQ-A9G7-01A-11D-A36X-10 chr6:26199791 T>C maps to NM_003522.3 P2P. 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-DD-AADB-01A-11D-A40R-10 chr6:27782902 A>T maps to NM_003521.2 K28*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADW-01A-11D-A38X-10 chr6:26021004 G>C maps to NM_003529.2 A96A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr6:26020866 C>A maps to NM_003529.2 R50R. 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-G3-AAV7-01A-11D-A382-10 chr6:26045842 C>T maps to NM_003531.2 Q69*. 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-5R-AAAM-01A-12D-A40R-10 chr6:27858204 A>C maps to NM_003535.2 P122P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACL-01A-11D-A40R-10 chr6:26104223 A>T maps to NM_003542.3 K17*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAVR-01A-11D-A40R-10 chr6:26104198 A>T maps to NM_003542.3 G8G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZP-A9D2-01A-11D-A382-10 chr6:26247103 A>G maps to NM_003547.2 T34T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAEA-01A-11D-A40R-10 chr6:26285637 G>A maps to NM_003543.3 I30I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CG-01A-11D-A20W-10 chr1:149859297 C>A maps to NM_175065.2 E57*. 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-5C-A9VH-01A-11D-A36X-10 chr6:12121245 T>C maps to NM_002114.2 Y406Y. 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-ES-A2HS-01A-11D-A183-10 chr6:12161736 G>T maps to NM_002114.2 E2185*. 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-CC-A8HT-01A-11D-A35Z-10 chr1:42047555 C>T maps to NM_024503.3 L971L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NV-01A-11D-A30V-10 chr1:42049186 G>T maps to NM_024503.3 R428R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-AAV0-01A-11D-A36X-10 chr1:41976244 T>A maps to NM_024503.3 P2366P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GJ-A9DB-01A-11D-A36X-10 chr1:42041240 C>T maps to NM_024503.3 P1727P. 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-DD-AACE-01A-11D-A40R-10 chr10:71158365 G>A maps to ENST00000439900 L832L. 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-A9FV-01A-11D-A36X-10 chr2:75109362 C>T maps to NM_000189.4 D612D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACE-01A-11D-A40R-10 chr2:75113491 C>T maps to NM_000189.4 D669D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACU-01A-11D-A40R-10 chr5:176314450 C>T did not map to a codon.
Sequencing variant TCGA-DD-AAE9-01A-11D-A40R-10 chr5:176318413 G>A maps to NM_002115.2 Y78Y. 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-DD-AACH-01A-11D-A40R-10 chr6:33053994 G>T did not map to a codon.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr6:29797327 C>T maps to ENST00000376828 D256D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9GV-01A-11D-A382-10 chr21:38126651 A>G maps to NM_000411.5 S692S. 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-ZP-A9D4-01A-11D-A36X-10 chr11:118963732 T>C did not map to a codon.
Sequencing variant TCGA-BC-A10W-01A-11D-A12Z-10 chr1:186064492 A>G maps to NM_031935.2 R3471R. Only missense variants will be evaluated by CHASM.
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-AAC8-01A-11D-A40R-10 chr1:186034406 G>T maps to NM_031935.2 G2517G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADA-01A-11D-A40R-10 chr1:186076062 A>T maps to NM_031935.2 G3606G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADF-01A-11D-A40R-10 chr1:186014949 G>A maps to NM_031935.2 L2145L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADG-01A-11D-A40R-10 chr1:186113434 A>C maps to NM_031935.2 A4685A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADM-01A-11D-A40R-10 chr1:186135943 T>C maps to NM_031935.2 I5148I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAEH-01A-11D-A40R-10 chr1:185704069 T>A maps to NM_031935.2 Y53*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAVZ-01A-11D-A40R-10 chr1:185892672 T>A maps to NM_031935.2 I391I. 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-ED-A8O6-01A-11D-A35Z-10 chr1:185988694 A>G maps to NM_031935.2 S1831S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-AAV7-01A-11D-A382-10 chr1:186088413 G>A maps to NM_031935.2 V3980V. 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-WQ-A9G7-01A-11D-A36X-10 chr1:186135391 C>A maps to NM_031935.2 C5132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WQ-AB4B-01A-11D-A40P-10 chr1:186047302 T>A maps to NM_031935.2 A2850A. 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-DD-A1EE-01A-11D-A12Z-10 chr23:150155723 A>T did not map to a codon.
Sequencing variant TCGA-DD-A3A0-01A-11D-A20W-10 chr23:150155772 A>G did not map to a codon.
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-WQ-A9G7-01A-11D-A36X-10 chr1:120298060 C>T maps to NM_005518.3 S392S. 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-DD-AAEH-01A-11D-A40R-10 chr19:1068486 C>T maps to NM_012292.2 G55G. Only missense variants will be evaluated by CHASM.
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-DD-AAD0-01A-11D-A40R-10 chr10:124895763 C>T maps to NM_001105574.1 A66A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADW-01A-11D-A38X-10 chr10:124895889 C>T maps to NM_001105574.1 H108H. 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-NI-A4U2-01A-11D-A28X-10 chr12:121434161 G>T maps to NM_000545.5 V351V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WJ-A86L-01A-12D-A45V-10 chr12:121437069 G>A did not map to a codon.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr17:36070597 G>T maps to NM_000458.2 A373A. Only missense variants will be evaluated by CHASM.
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-ZP-A9D2-01A-11D-A382-10 chr20:43052655 A>T did not map to a codon.
Sequencing variant TCGA-DD-AADO-01A-11D-A40R-10 chr7:26232907 A>G maps to NM_031243.2 F321F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr2:178083813 A>G maps to NM_194247.2 G337G. 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-DD-AAEG-01A-11D-A38X-10 chr14:21702343 G>A maps to NM_031314.2 S3S. 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-DD-A11A-01A-11D-A12Z-10 chr1:12907350 A>G maps to NM_001013631.1 D264D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr1:12907746 A>G maps to NM_001013631.1 P132P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADK-01A-11D-A40R-10 chr4:83294717 C>T maps to NM_031370.2 A38A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-AAV0-01A-11D-A36X-10 chr5:179046346 C>T maps to NM_005520.2 G153G. 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-DD-AACH-01A-11D-A40R-10 chr19:39329532 C>T did not map to a codon.
Sequencing variant TCGA-G3-AAV0-01A-11D-A36X-10 chr19:41787179 G>T maps to NM_007040.3 A333A. 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-G3-A3CG-01A-11D-A20W-10 chr8:42812265 T>C maps to NM_032410.3 A166A. 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-DD-AACL-01A-11D-A40R-10 chr7:27211676 A>G maps to NM_018951.3 N358N. 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-DD-AAD1-01A-11D-A40R-10 chr7:27187095 C>A maps to NM_024014.2 S91S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADL-01A-11D-A40R-10 chr7:27195945 G>C maps to NM_006896.3 G73G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A7SH-01A-11D-A382-10 chr7:27196119 C>A maps to NM_006896.3 T15T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CG-01A-11D-A20W-10 chr17:46805466 C>T maps to NM_006361.5 L163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WJ-A86L-01A-12D-A45V-10 chr17:46670489 G>A maps to NM_002147.3 I185I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9H2-01A-12D-A382-10 chr17:46675275 G>A maps to NM_018952.4 A79A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr17:46687953 G>A maps to NM_004502.3 G109G. 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-CC-5263-01A-01D-A12Z-10 chr17:46703430 G>A maps to NM_024017.4 S67S. 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-ES-A2HT-01A-12D-A183-10 chr12:54350170 T>C maps to NM_173860.1 L224L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAEE-01A-11D-A40R-10 chr12:54447993 G>T maps to NM_153633.2 S96S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A7SH-01A-11D-A382-10 chr12:54448086 C>T maps to NM_153633.2 S127S. 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-XR-A8TG-01A-11D-A35Z-10 chr2:176964606 C>T maps to NM_021193.3 F26F. 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-G3-A3CG-01A-11D-A20W-10 chr4:175443545 T>C maps to NM_000860.4 R19R. 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-EP-A2KB-01A-11D-A183-10 chr3:148880654 C>A maps to NM_032383.3 S824*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr3:148847620 G>T maps to NM_032383.3 A37A. Only missense variants will be evaluated by CHASM.
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-DD-AAE7-01A-11D-A40R-10 chr11:18333535 A>T maps to NM_181507.1 A48A. 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-K7-AAU7-01A-11D-A382-10 chr4:84216607 G>A maps to NM_006665.5 T507T. 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-WQ-A9G7-01A-11D-A36X-10 chr8:21976492 G>A maps to NM_005144.4 D1061D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A8O5-01A-11D-A35Z-10 chr11:63325962 T>G maps to NM_017878.1 A96A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACL-01A-11D-A40R-10 chr11:63235904 A>T maps to NM_054108.3 I136I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAW2-01A-11D-A40P-10 chr11:63257812 A>G maps to NM_054108.3 L57L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A112-01A-11D-A12Z-10 chr19:49657885 C>T maps to NM_002152.2 E203E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A3KF-01A-11D-A20W-10 chr19:49657915 T>C maps to NM_002152.2 E193E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EB-01A-11D-A12Z-10 chr19:49657885 C>T maps to NM_002152.2 E203E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EB-01A-11D-A12Z-10 chr19:49657915 T>C maps to NM_002152.2 E193E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EF-01A-11D-A12Z-10 chr19:49657915 T>C maps to NM_002152.2 E193E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39X-01A-11D-A20W-10 chr19:49657915 T>C maps to NM_002152.2 E193E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NA-01A-11D-A25V-10 chr19:49657915 T>C maps to NM_002152.2 E193E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NB-01A-12D-A25V-10 chr19:49657885 C>T maps to NM_002152.2 E203E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NB-01A-12D-A25V-10 chr19:49657915 T>C maps to NM_002152.2 E193E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A2QR-01A-11D-A20W-10 chr19:49657885 C>T maps to NM_002152.2 E203E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A2QR-01A-11D-A20W-10 chr19:49657915 T>C maps to NM_002152.2 E193E. 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-DD-AACQ-01A-11D-A40R-10 chr3:11300932 G>A maps to NM_001098211.1 S70S. 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-DD-A39Z-01A-11D-A20W-10 chr5:175111078 A>G maps to NM_001131055.1 S281S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9GZ-01A-11D-A38X-10 chr20:60791439 G>A maps to ENST00000317393 L320L. 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-DD-AAEG-01A-11D-A38X-10 chr1:152193173 G>A maps to NM_001009931.1 R311*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LG-A9QC-01A-11D-A36X-10 chr2:20838353 G>A maps to NM_022460.3 G155G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EE-01A-11D-A12Z-10 chr4:11400951 A>T maps to NM_005114.2 P226P. 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-CC-A3MA-01A-11D-A20W-10 chr16:22826065 T>C maps to NM_006043.1 G45G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr23:131763091 T>C did not map to a codon.
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-ES-A2HT-01A-12D-A183-10 chr9:99007624 A>G did not map to a codon.
Sequencing variant TCGA-WQ-A9G7-01A-11D-A36X-10 chr9:99006673 C>T maps to NM_000197.1 A203A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr5:118867100 T>A did not map to a codon.
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-DD-AAW3-01A-11D-A40P-10 chr8:145533249 T>A maps to NM_005526.2 L112L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZP-A9D0-01A-11D-A36X-10 chr6:122744788 A>G maps to NM_004506.3 L378L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADO-01A-11D-A40R-10 chr21:45076518 G>A maps to NM_007031.1 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WJ-A86L-01A-12D-A45V-10 chr14:102552709 A>T maps to NM_001017963.2 P124P. 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-CC-A5UD-01A-11D-A28X-10 chr20:3732437 G>A maps to NM_052970.4 L562L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EG-01A-11D-A20W-10 chr20:3723056 T>C did not map to a codon.
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-G3-A3CG-01A-11D-A20W-10 chr21:15748105 T>C maps to NM_006948.4 T205T. 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-DD-AAVY-01A-11D-A40R-10 chr14:65008433 G>A maps to NM_021979.3 S289S. 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-G3-A3CJ-01A-11D-A20W-10 chr5:132432854 T>C maps to NM_002154.3 G602G. 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-2Y-A9GU-01A-11D-A382-10 chr19:55777300 C>A maps to NM_012267.4 R282R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CG-01A-11D-A20W-10 chr19:55790904 T>G maps to NM_012267.4 S24S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-AA0U-01A-11D-A382-10 chr19:55790901 C>G maps to NM_012267.4 G25G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZS-A9CG-01A-11D-A36X-10 chr1:22178362 G>A maps to NM_005529.5 Y2309Y. 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-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-ED-A8O6-01A-11D-A35Z-10 chr6:87725375 C>A maps to NM_000865.2 C108*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A8HS-01A-11D-A35Z-10 chr3:88040771 A>G maps to NM_000866.3 A291A. 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-FV-A23B-01A-11D-A16V-10 chr23:114141873 G>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-K7-AAU7-01A-11D-A382-10 chr11:113775679 C>T maps to NM_006028.3 L9L. Only missense variants will be evaluated by CHASM.
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-ZP-A9D1-01A-11D-A382-10 chr3:183776323 C>A maps to NM_130770.2 A223A. 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-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-DD-A39Y-01A-11D-A20W-10 chr4:8307695 A>G did not map to a codon.
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-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-EP-A2KA-01A-11D-A183-10 chr8:38845472 C>T maps to NM_153692.3 H429H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACU-01A-11D-A40R-10 chr4:3131686 C>T maps to NM_002111.6 Q594*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAVR-01A-11D-A40R-10 chr4:3230457 T>C maps to NM_002111.6 S2655S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr4:3241605 G>T maps to NM_002111.6 L3083L. 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-DD-A1EG-01A-11D-A20W-10 chr21:33312480 T>C maps to NM_014586.1 L187L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A8O6-01A-11D-A35Z-10 chr21:33368208 C>T maps to NM_014586.1 T478T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MA-01A-11D-A20W-10 chr23:53565343 C>T 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-AAC8-01A-11D-A40R-10 chr23:53674398 T>C did not map to a codon.
Sequencing variant TCGA-DD-AAC8-01A-11D-A40R-10 chr23:53674401 T>C did not map to a codon.
Sequencing variant TCGA-DD-AAC8-01A-11D-A40R-10 chr23:53674403 T>C did not map to a codon.
Sequencing variant TCGA-DD-AACH-01A-11D-A40R-10 chr23:53617376 G>A did not map to a codon.
Sequencing variant TCGA-DD-AACK-01A-11D-A40R-10 chr23:53561498 T>A did not map to a codon.
Sequencing variant TCGA-DD-AACL-01A-11D-A40R-10 chr23:53619442 T>A did not map to a codon.
Sequencing variant TCGA-DD-AADF-01A-11D-A40R-10 chr23:53591648 A>G did not map to a codon.
Sequencing variant TCGA-DD-AADW-01A-11D-A38X-10 chr23:53603871 C>T did not map to a codon.
Sequencing variant TCGA-DD-AAE2-01A-11D-A40R-10 chr23:53672262 C>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-ED-A8O5-01A-11D-A35Z-10 chr23:53579726 A>T 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-G3-A3CG-01A-11D-A20W-10 chr23:53591669 T>C did not map to a codon.
Sequencing variant TCGA-G3-A3CJ-01A-11D-A20W-10 chr23:53630378 A>G did not map to a codon.
Sequencing variant TCGA-XR-A8TD-01A-12D-A38X-10 chr23:53579401 G>T did not map to a codon.
Sequencing variant TCGA-ZP-A9CY-01A-11D-A382-10 chr23:53574708 T>C 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-WQ-A9G7-01A-11D-A36X-10 chr7:123509037 C>T maps to NM_012269.2 C237C. 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-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-DD-AADP-01A-11D-A38X-10 chr1:220273890 G>T maps to NM_018060.3 V150V. 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-UB-AA0V-01A-11D-A382-10 chr2:203693672 T>C maps to NM_138468.4 Q20Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACK-01A-11D-A40R-10 chr19:10395558 C>T maps to NM_000201.2 P427P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9H3-01A-11D-A382-10 chr19:10403480 C>T maps to NM_003259.3 A385A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAC8-01A-11D-A40R-10 chr2:204820587 A>G maps to NM_012092.3 L96L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADQ-01A-11D-A40R-10 chr21:45655359 G>A maps to ENST00000400379 Y164Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACL-01A-11D-A40R-10 chr20:30193297 T>C maps to NM_002165.2 S36S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADM-01A-11D-A40R-10 chr1:23885467 T>G maps to NM_002167.3 R115R. 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-DD-AACL-01A-11D-A40R-10 chr10:94267963 T>A did not map to a codon.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr10:94291600 C>A maps to NM_004969.3 E189*. 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-DD-A1EE-01A-11D-A12Z-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-BC-A3KF-01A-11D-A20W-10 chr8:39776331 A>G did not map to a codon.
Sequencing variant TCGA-BC-A3KG-01A-11D-A20W-10 chr8:39785358 T>C maps to NM_002164.4 A289A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr8:39781034 T>C maps to NM_002164.4 T195T. Only missense variants will be evaluated by CHASM.
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-DD-A3A1-01A-11D-A20W-10 chr8:39836686 A>G maps to NM_194294.2 G112G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A2QR-01A-11D-A20W-10 chr8:39840205 A>G maps to NM_194294.2 E130E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A2-01A-11D-A20W-10 chr23:148582536 C>T did not map to a codon.
Sequencing variant TCGA-LG-A9QD-01A-11D-A382-10 chr23:148564323 A>G 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-2Y-A9H8-01A-11D-A38X-10 chr6:30712142 G>A maps to NM_003897.3 R51R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr9:131939317 G>T maps to NM_203434.2 R338R. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-DD-A1EG-01A-11D-A20W-10. Mapping will be selected arbitrarily.
Alternatively spliced codon TCGA-DD-A39Z-01A-11D-A20W-10. Mapping will be selected arbitrarily.
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-AAW2-01A-11D-A40P-10 chr2:163139080 C>A maps to NM_022168.2 L367L. 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-A119-01A-11D-A12Z-10 chr10:91066405 A>G maps to NM_001547.4 E231E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADR-01A-11D-A40R-10 chr11:320797 G>A maps to NM_021034.2 Q6*. 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-DD-AACI-01A-11D-A40R-10 chr9:21217202 A>G maps to NM_002173.2 N34N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAEI-01A-11D-A40R-10 chr9:21217148 G>A maps to NM_002173.2 C52C. 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-DD-AADW-01A-11D-A38X-10 chr9:21409228 A>T maps to NM_002170.3 S18S. 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-5R-AA1C-01A-11D-A40R-10 chr21:34635390 C>T maps to NM_207585.1 P378P. 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-BC-A3KG-01A-11D-A20W-10 chr12:68553389 T>C maps to NM_000619.2 K2K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACD-01A-11D-A40R-10 chr12:68551851 C>T maps to NM_000619.2 Q69Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A3KG-01A-11D-A20W-10 chr6:137528137 T>C maps to NM_000416.2 P54P. 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-A39X-01A-11D-A20W-10 chr21:34805150 A>G maps to ENST00000381995 P303P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39X-01A-11D-A20W-10 chr9:21141107 C>T maps to NM_002177.1 L154L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5C-A9VG-01A-11D-A36X-10 chr7:112102090 C>T maps to NM_001007245.2 I218I. 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-FV-A2QR-01A-11D-A20W-10 chr7:112095822 C>T maps to NM_001007245.2 Q34*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WQ-A9G7-01A-11D-A36X-10 chr3:50326694 C>A maps to ENST00000336089 R458R. Only missense variants will be evaluated by CHASM.
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-EP-A2KA-01A-11D-A183-10 chr2:27679375 A>G did not map to a codon.
Sequencing variant TCGA-2Y-A9H3-01A-11D-A382-10 chr3:107881359 G>A maps to ENST00000457963 A449A. 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-A1EE-01A-11D-A12Z-10 chr3:107937443 T>C maps to ENST00000457963 V175V. 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-DD-AAVZ-01A-11D-A40R-10 chr23:69353835 C>A did not map to a codon.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr15:65621486 C>A did not map to a codon.
Sequencing variant TCGA-DD-AAVU-01A-11D-A40R-10 chr15:65689262 C>T maps to NM_020962.1 A302A. Only missense variants will be evaluated by CHASM.
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-CC-A3MB-01A-11D-A20W-10 chr17:47103021 A>G maps to NM_006546.3 R93R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A1-01A-11D-A20W-10 chr3:185410533 T>C maps to NM_006548.4 E119E. 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-DD-AACO-01A-11D-A40R-10 chr7:23509594 C>T maps to NM_006547.2 P45P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADF-01A-11D-A40R-10 chr7:23391099 T>C maps to NM_006547.2 R169R. 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-A119-01A-11D-A12Z-10 chr6:160469466 A>G maps to NM_000876.2 E802E. 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-DD-AAVX-01A-11D-A40R-10 chr7:45931535 C>G maps to NM_000596.2 P175P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACJ-01A-11D-A40R-10 chr9:38411533 G>T maps to NM_001007563.1 R234R. 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-2V-A95S-01A-11D-A36X-10 chr1:201195084 G>T maps to NM_001164586.1 A3540A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BD-A3EP-01A-11D-A22F-10 chr1:201182024 A>G maps to NM_001164586.1 P2668P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A8HT-01A-11D-A35Z-10 chr1:201184916 G>A maps to NM_001164586.1 L3082L. 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-ES-A2HT-01A-12D-A183-10 chr22:23922197 C>T maps to NM_020070.2 R60R. 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-DD-AADG-01A-11D-A40R-10 chr23:130420011 A>G did not map to a codon.
Sequencing variant TCGA-DD-AADK-01A-11D-A40R-10 chr23:130417073 C>A did not map to a codon.
Sequencing variant TCGA-DD-AAVV-01A-11D-A40R-10 chr23:130420434 T>G did not map to a codon.
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-BC-A10W-01A-11D-A12Z-10 chr3:151154683 A>G maps to NM_178822.4 V2555V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IE-01A-21D-A382-10 chr3:151162740 G>A maps to NM_178822.4 P1676P. Only missense variants will be evaluated by CHASM.
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-DD-AACV-01A-11D-A40R-10 chr3:151171319 G>A maps to NM_178822.4 F189F. 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-DD-A39Y-01A-11D-A20W-10 chr21:41143129 C>A maps to NM_001080444.1 R236R. Only missense variants will be evaluated by CHASM.
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-CC-A8HU-01A-11D-A35Z-10 chr11:133794760 C>T maps to NM_014987.1 Q691Q. 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-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-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-DD-AAEA-01A-11D-A40R-10 chr1:206941983 G>A maps to NM_000572.2 N178N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XR-A8TF-01A-11D-A35Z-10 chr1:206945656 G>A maps to NM_000572.2 R42*. 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-ES-A2HT-01A-12D-A183-10 chr9:34659770 C>T maps to NM_001142784.1 L276L. Only missense variants will be evaluated by CHASM.
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-EP-A2KA-01A-11D-A183-10 chr19:18183012 C>A maps to NM_005535.1 S310S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LG-A9QC-01A-11D-A36X-10 chr19:18174686 G>A maps to NM_005535.1 I539I. 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-AACI-01A-11D-A40R-10 chr1:67855777 T>C maps to NM_001559.2 N671N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39Z-01A-11D-A20W-10 chr23:117874979 A>G did not map to a codon.
Sequencing variant TCGA-ZS-A9CE-01A-11D-A36X-10 chr23:117895238 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-DD-AAVQ-01A-11D-A40R-10 chr4:142653940 T>C maps to NM_000585.3 N143N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAVP-01A-11D-A40R-10 chr15:81598391 C>G maps to NM_172217.3 P1188P. Only missense variants will be evaluated by CHASM.
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-A1EE-01A-11D-A12Z-10 chr6:52101935 C>T maps to NM_052872.3 S95S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACL-01A-11D-A40R-10 chr6:52103727 C>T maps to NM_052872.3 S18S. 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-AAV6-01A-21D-A36X-10 chr22:17590238 C>T maps to NM_014339.5 G710G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A1-01A-11D-A20W-10 chr3:9972088 A>G maps to NM_153461.2 A499A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACQ-01A-11D-A40R-10 chr3:57135383 T>A maps to NM_017563.3 I329I. 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-CC-A9FS-01A-11D-A36X-10 chr3:9957184 G>A maps to NM_153483.2 P606P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr22:50439202 G>T maps to NM_001001694.2 R67R. 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-DD-A4NJ-01A-11D-A27I-10 chr2:113786632 A>T maps to NM_173178.1 C48*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAEG-01A-11D-A38X-10 chr2:102791044 A>G did not map to a codon.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr3:190338161 T>C maps to NM_002182.3 C212C. 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-DD-AAC8-01A-11D-A40R-10 chr23:105011035 A>T did not map to a codon.
Sequencing variant TCGA-DD-AADJ-01A-11D-A40R-10 chr23:104984618 A>T did not map to a codon.
Sequencing variant TCGA-FV-A2QR-01A-11D-A20W-10 chr23:104728323 T>C 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-AACX-01A-11D-A40R-10 chr6:137330582 G>T maps to NM_014432.2 S150S. Only missense variants will be evaluated by CHASM.
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-A119-01A-11D-A12Z-10 chr1:24463630 A>G maps to NM_021258.2 S115S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr12:56733287 G>T maps to NM_016584.2 G81*. 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-BC-A3KG-01A-11D-A20W-10 chr12:68619374 T>C maps to NM_018402.1 A54A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9GS-01A-12D-A382-10 chr16:28511193 C>T maps to NM_145659.3 E170E. 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-AACQ-01A-11D-A40R-10 chr1:24486038 T>A maps to NM_170743.2 R199*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LG-A9QD-01A-11D-A382-10 chr10:6061869 A>G maps to NM_000417.2 R206R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAE0-01A-11D-A40R-10 chr22:37524402 G>T maps to ENST00000406505 V468V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACL-01A-11D-A40R-10 chr23:70330768 T>A did not map to a codon.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr5:55164684 G>A maps to NM_139017.4 W74*. Only missense variants will be evaluated by CHASM.
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-WQ-A9G7-01A-11D-A36X-10 chr23:1484119 C>T did not map to a codon.
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-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-ES-A2HS-01A-11D-A183-10 chr1:154437807 A>G maps to NM_000565.2 P453P. 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-AAC8-01A-11D-A40R-10 chr5:35874563 T>A maps to NM_002185.2 P240P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K7-AAU7-01A-11D-A382-10 chr5:35867557 C>T maps to NM_002185.2 T124T. Only missense variants will be evaluated by CHASM.
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-DD-A1ED-01A-11D-A152-10 chr1:166891984 A>G maps to NM_199351.2 S352S. 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-AACB-01A-11D-A40R-10 chr2:131103252 C>T maps to NM_033416.1 H140H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr7:128034562 T>C maps to NM_000883.3 A547A. 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-DD-A39Z-01A-11D-A20W-10 chr3:100986352 A>G did not map to a codon.
Sequencing variant TCGA-5C-A9VG-01A-11D-A36X-10 chr10:105037735 G>T maps to NM_032727.3 V256V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A3KF-01A-11D-A20W-10 chr1:62593699 A>G maps to NM_176877.2 G1700G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACI-01A-11D-A40R-10 chr1:62263012 C>T maps to NM_176877.2 R439*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr1:62626600 C>A maps to NM_176877.2 A1800A. 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-ZP-A9CZ-01A-11D-A382-10 chr1:62299330 C>T maps to NM_176877.2 D662D. 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-ED-A82E-01A-11D-A34Z-10 chr11:61906403 G>T maps to NM_001040694.1 T406T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr14:105168019 C>T maps to ENST00000252520 R106R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAE7-01A-11D-A40R-10 chr14:105180663 C>A maps to ENST00000252520 P1055P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZP-A9CY-01A-11D-A382-10 chr13:111367801 G>T maps to NM_005537.3 V4V. 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-2Y-A9H0-01A-11D-A382-10 chr2:242662638 G>A maps to NM_032329.4 W211*. 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-DD-AACI-01A-11D-A40R-10 chr7:41730009 G>A maps to NM_002192.2 I173I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr7:41729529 G>T maps to NM_002192.2 I333I. 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-DD-A3A0-01A-11D-A20W-10 chr2:191233940 A>G maps to NM_002194.3 T193T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A3KF-01A-11D-A20W-10 chr4:143067029 T>C maps to NM_003866.2 E561E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADS-01A-11D-A40R-10 chr4:143324208 T>A did not map to a codon.
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-ES-A2HT-01A-12D-A183-10 chr9:139327477 G>A maps to NM_019892.3 T403T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A7SH-01A-11D-A382-10 chr10:121587246 T>C maps to NM_014937.2 L1118L. 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-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-2Y-A9HA-01A-11D-A38X-10 chr11:15134029 T>C maps to NM_001031853.3 P5P. 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-WJ-A86L-01A-12D-A45V-10 chr11:15243030 C>T maps to NM_001031853.3 G323G. 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-XR-A8TF-01A-11D-A35Z-10 chr19:17932270 A>T maps to NM_005543.2 P15P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A8O5-01A-11D-A35Z-10 chr9:5233726 A>G maps to NM_002195.1 S90S. 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-2Y-A9GW-01A-11D-A382-10 chr14:36005071 A>G maps to NM_032594.3 P538P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACK-01A-11D-A40R-10 chr14:36003922 A>T maps to NM_032594.3 A155A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAD8-01A-11D-A40R-10 chr19:7152759 C>T maps to NM_000208.2 L736L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADQ-01A-11D-A40R-10 chr1:156816467 G>C maps to NM_014215.2 P551P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr1:156813014 A>G maps to NM_014215.2 P969P. Only missense variants will be evaluated by CHASM.
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-A39Y-01A-11D-A20W-10 chr8:19675086 A>G maps to NM_018142.2 R13R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAEE-01A-11D-A40R-10 chr4:106604432 A>T maps to NM_020395.3 V282V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADE-01A-11D-A40R-10 chr17:59989027 A>G maps to NM_020748.2 L277L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAW0-01A-11D-A40R-10 chr17:59968915 G>T maps to NM_020748.2 V619V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAE9-01A-11D-A40R-10 chr1:153743173 C>T maps to ENST00000428986 A840A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAW2-01A-11D-A40P-10 chr1:153740304 T>A did not map to a codon.
Sequencing variant TCGA-G3-AAV0-01A-11D-A36X-10 chr11:77669832 T>A maps to NM_033547.3 A252A. 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-EP-A2KA-01A-11D-A183-10 chr13:51961530 C>A maps to NM_012141.2 S295S. 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-DD-A3A1-01A-11D-A20W-10 chr1:212141248 A>G maps to NM_015434.3 A695A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-AAV4-01A-11D-A382-10 chr1:212193462 C>T did not map to a codon.
Sequencing variant TCGA-DD-AAE7-01A-11D-A40R-10 chr8:95884162 T>G maps to NM_017864.2 V822V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAEB-01A-11D-A40R-10 chr8:95861724 A>T maps to NM_017864.2 S432S. 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-2Y-A9H4-01A-11D-A382-10 chr4:128625435 A>G maps to NM_015693.3 L519L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr6:33693355 C>T maps to NM_054111.4 T209T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAD8-01A-11D-A40R-10 chr6:33690511 G>A maps to NM_054111.4 I406I. 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-A1EG-01A-11D-A20W-10 chr10:59986873 A>G maps to NM_152230.4 G101G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACL-01A-11D-A40R-10 chr5:61833049 T>G maps to NM_001134779.1 G768G. Only missense variants will be evaluated by CHASM.
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-DD-AACH-01A-11D-A40R-10 chr14:24653202 C>G did not map to a codon.
Sequencing variant TCGA-DD-A39Y-01A-11D-A20W-10 chr13:98658547 A>G maps to NM_002271.4 R572R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CG-01A-11D-A20W-10 chr13:98645234 T>C maps to NM_002271.4 P271P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACZ-01A-11D-A40R-10 chr12:30837344 T>A maps to NM_006390.3 R71R. 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-A3MB-01A-11D-A20W-10 chr9:95411767 T>C maps to NM_022755.5 A127A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADF-01A-11D-A40R-10 chr2:237285769 T>A maps to ENST00000457693 K521*. 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-EP-A2KA-01A-11D-A183-10 chr7:2644522 G>A maps to NM_152558.3 V547V. 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-ES-A2HS-01A-11D-A183-10 chr15:67664645 C>A maps to NM_001031715.2 V317V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9H3-01A-11D-A382-10 chr15:90986672 G>A maps to NM_003870.3 T292T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5C-AAPD-01A-21D-A38X-10 chr1:156520098 G>A maps to NM_178229.4 R593R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACD-01A-11D-A40R-10 chr3:12963693 G>T maps to ENST00000429247 A593A. 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-DD-A39X-01A-11D-A20W-10 chr23:53310698 T>C did not map to a codon.
Sequencing variant TCGA-DD-A3A0-01A-11D-A20W-10 chr23:53264287 T>C did not map to a codon.
Sequencing variant TCGA-DD-AADF-01A-11D-A40R-10 chr23:53279806 G>T did not map to a codon.
Sequencing variant TCGA-DD-AADS-01A-11D-A40R-10 chr23:53272571 T>A did not map to a codon.
Sequencing variant TCGA-DD-AAED-01A-12D-A40R-10 chr23:53263731 G>A did not map to a codon.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr23:53277935 T>C 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-AADR-01A-11D-A40R-10 chr12:248118 C>A maps to NM_001170738.1 G530G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9GZ-01A-11D-A38X-10 chr23:153282004 G>T did not map to a codon.
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-DD-AACO-01A-11D-A40R-10 chr23:153277356 C>A did not map to a codon.
Sequencing variant TCGA-ZS-A9CF-01A-11D-A382-10 chr6:79577581 C>T maps to NM_001010844.1 Q97*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A3KG-01A-11D-A20W-10 chr3:10251315 T>C maps to NM_001570.3 P156P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A8HV-01A-11D-A35Z-10 chr12:66638954 C>G maps to NM_007199.2 P409P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A5SK-01A-11D-A27I-10 chr12:66611015 G>T did not map to a codon.
Sequencing variant TCGA-DD-AACC-01A-11D-A40R-10 chr15:78758780 G>A maps to NM_004136.2 Q193Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAE6-01A-11D-A40R-10 chr15:78778140 C>T maps to NM_004136.2 Y556Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr4:185340656 A>G maps to NM_002199.3 D51D. Only missense variants will be evaluated by CHASM.
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-DD-AAE4-01A-11D-A40R-10 chr19:46388495 C>A maps to NM_015649.1 L179L. 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-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-XR-A8TE-01A-11D-A35Z-10 chr7:128587365 C>T maps to NM_001098629.1 P188P. 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-5R-AAAM-01A-12D-A40R-10 chr19:44096252 G>A maps to NM_001007561.2 G599G. 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-AADM-01A-11D-A40R-10 chr13:110436753 C>A maps to NM_003749.2 L549L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9GV-01A-11D-A382-10 chr23:107977610 A>T did not map to a codon.
Sequencing variant TCGA-2Y-A9H4-01A-11D-A382-10 chr23:107978095 C>A did not map to a codon.
Sequencing variant TCGA-DD-AACI-01A-11D-A40R-10 chr23:107975900 G>T did not map to a codon.
Sequencing variant TCGA-ED-A459-01A-11D-A25V-10 chr23:107977706 T>A did not map to a codon.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr23:107979421 C>A did not map to a codon.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr23:107975815 G>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-ZP-A9CY-01A-11D-A382-10 chr23:107978081 C>T did not map to a codon.
Sequencing variant TCGA-2Y-A9HA-01A-11D-A38X-10 chr5:3601147 C>A maps to NM_024337.3 S479S. Only missense variants will be evaluated by CHASM.
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-DD-AACT-01A-11D-A40R-10 chr5:1879843 G>A maps to NM_016358.2 P170P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WX-AA44-01A-11D-A38X-10 chr5:1878256 G>A maps to NM_016358.2 G462G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZP-A9D4-01A-11D-A36X-10 chr16:55362675 G>A maps to NM_024335.2 E262E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADP-01A-11D-A38X-10 chr9:88889127 T>C maps to ENST00000452279 Q84Q. 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-BD-A3EP-01A-11D-A22F-10 chr5:50683548 T>C maps to NM_002202.2 S148S. 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-AAEA-01A-11D-A40R-10 chr20:33095535 T>C maps to ENST00000262650 Y883Y. 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-AACZ-01A-11D-A40R-10 chr5:52371062 A>G maps to NM_002203.3 E918E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr5:52376342 A>G maps to NM_002203.3 V977V. 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-G3-AAV0-01A-11D-A36X-10 chr5:52376394 C>T maps to NM_002203.3 Q995*. 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-ZP-A9CZ-01A-11D-A382-10 chr5:52370308 T>C did not map to a codon.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr17:42461044 T>C maps to NM_000419.3 P342P. 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-EP-A2KB-01A-11D-A183-10 chr17:48166577 C>A maps to NM_005501.2 P1050P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9H8-01A-11D-A38X-10 chr2:182358127 C>T maps to NM_000885.4 I410I. 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-DD-A39X-01A-11D-A20W-10 chr2:182358064 A>G maps to NM_000885.4 G389G. 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-DD-AACZ-01A-11D-A40R-10 chr12:54797996 G>A maps to NM_002205.2 L499L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAE7-01A-11D-A40R-10 chr12:54798980 G>T maps to NM_002205.2 P398P. 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-A5SM-01A-12D-A28X-10 chr12:56092543 C>G maps to ENST00000347027 L360L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr10:15590537 G>A maps to NM_003638.1 I932I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADO-01A-11D-A40R-10 chr10:15573078 C>T maps to NM_003638.1 Q984Q. 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-4R-AA8I-01A-11D-A382-10 chr3:37821427 A>G maps to NM_002207.2 A901A. 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-DD-AAD0-01A-11D-A40R-10 chr16:31422693 G>A maps to ENST00000444228 G537G. 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-DD-AAVY-01A-11D-A40R-10 chr17:3664406 A>G maps to NM_002208.4 G166G. 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-DD-AADQ-01A-11D-A40R-10 chr16:31336334 C>A maps to NM_001145808.1 I783I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAVY-01A-11D-A40R-10 chr16:31341475 C>G maps to NM_001145808.1 A1018A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CG-01A-11D-A20W-10 chr2:187531441 T>C maps to NM_002210.3 G726G. 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-G3-A3CJ-01A-11D-A20W-10 chr16:31382663 T>C maps to NM_000887.3 P617P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WX-AA44-01A-11D-A38X-10 chr23:70524434 C>A did not map to a codon.
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-ES-A2HS-01A-11D-A183-10 chr17:45363646 C>T maps to NM_000212.2 P212P. 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-CC-A3MB-01A-11D-A20W-10 chr17:73751905 T>C maps to NM_001005619.1 S1544S. Only missense variants will be evaluated by CHASM.
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-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-ZS-A9CD-01A-11D-A36X-10 chr13:102235650 T>C maps to NM_004791.1 C271C. 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-DD-AACM-01A-11D-A40R-10 chr3:52847498 T>G maps to ENST00000485816 R916R. 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-CC-5259-01A-31D-A20W-10 chr23:54780133 A>T did not map to a codon.
Sequencing variant TCGA-CC-A7IK-01A-12D-A33Q-10 chr23:54783988 G>C did not map to a codon.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr23:54786267 T>C did not map to a codon.
Sequencing variant TCGA-DD-A3A9-01A-11D-A25V-10 chr23:54823433 G>A did not map to a codon.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr23:54784887 T>C did not map to a codon.
Sequencing variant TCGA-FV-A3R3-01A-11D-A22F-10 chr23:54785171 G>A did not map to a codon.
Sequencing variant TCGA-RC-A6M4-01A-11D-A32G-10 chr23:54783458 G>A did not map to a codon.
Sequencing variant TCGA-RC-A7SH-01A-11D-A382-10 chr23:54784678 T>C did not map to a codon.
Sequencing variant TCGA-G3-A6UC-01A-21D-A33K-10 chr23:78618460 G>C did not map to a codon.
Sequencing variant TCGA-ZP-A9CV-01A-11D-A382-10 chr23:78616863 C>T 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-DD-AAC9-01A-11D-A40R-10 chr14:93408040 C>T maps to NM_014216.4 A370A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A8O6-01A-11D-A35Z-10 chr14:93407962 C>G maps to NM_014216.4 S396S. 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-DD-AACQ-01A-11D-A40R-10 chr3:4558208 G>T maps to ENST00000356617 G8*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr3:4730229 C>T maps to ENST00000356617 Q1248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr3:4735175 G>T maps to ENST00000356617 L1340L. 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-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-4R-AA8I-01A-11D-A382-10 chr10:106075737 C>T maps to NM_033397.2 P24P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr21:35140132 G>T did not map to a codon.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr21:35255855 T>C maps to NM_003024.2 P1519P. Only missense variants will be evaluated by CHASM.
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-DD-AADB-01A-11D-A40R-10 chr1:152883883 G>A maps to NM_005547.2 K537K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAVU-01A-11D-A40R-10 chr1:152883755 C>T maps to NM_005547.2 Q495*. 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-DD-AACQ-01A-11D-A40R-10 chr14:105609963 A>T maps to NM_002226.3 P1032P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACY-01A-11D-A40R-10 chr1:65311218 G>A maps to NM_002227.2 L698L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACI-01A-11D-A40R-10 chr9:5069059 A>G maps to NM_004972.3 T455T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAE7-01A-11D-A40R-10 chr9:5081812 T>G maps to NM_004972.3 P841P. 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-2Y-A9HB-01A-11D-A38X-10 chr4:6107373 C>T maps to NM_001099433.1 R150R. 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-DD-AAC8-01A-11D-A40R-10 chr21:27062286 T>C did not map to a codon.
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-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-DD-AACU-01A-11D-A40R-10 chr10:64968995 C>A did not map to a codon.
Sequencing variant TCGA-DD-AAD1-01A-11D-A40R-10 chr10:64974045 A>C maps to NM_032776.1 L627L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NI-A8LF-01A-11D-A35Z-10 chr10:64950794 G>C maps to NM_032776.1 G2050G. 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-DD-A3A7-01A-11D-A22F-10 chr16:27225072 G>C did not map to a codon.
Sequencing variant TCGA-DD-AACC-01A-11D-A40R-10 chr15:42127786 A>G maps to NM_005090.3 G158G. 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-2Y-A9HB-01A-11D-A38X-10 chr8:75157021 C>T maps to NM_020647.2 Q549Q. 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-ES-A2HS-01A-11D-A183-10 chr16:87723325 C>T maps to NM_020655.2 Q454*. 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-DD-A39Y-01A-11D-A20W-10 chr19:2254201 C>T maps to NM_144616.3 R82R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-AAV7-01A-11D-A382-10 chr14:23450782 A>C maps to NM_032876.4 Y231*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XR-A8TF-01A-11D-A35Z-10 chr14:23444238 G>A maps to NM_032876.4 G438G. 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-DD-AAC9-01A-11D-A40R-10 chr23:8503660 T>A did not map to a codon.
Sequencing variant TCGA-DD-AACA-01A-11D-A40R-10 chr23:8553365 C>T did not map to a codon.
Sequencing variant TCGA-ED-A8O5-01A-11D-A35Z-10 chr23:8667787 T>C did not map to a codon.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr23:8565288 G>T did not map to a codon.
Sequencing variant TCGA-WX-AA47-01A-11D-A38X-10 chr23:8504915 C>T did not map to a codon.
Sequencing variant TCGA-DD-AACT-01A-11D-A40R-10 chr3:124207121 A>G maps to NM_001024660.3 P1450P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAVV-01A-11D-A40R-10 chr3:124438223 A>G maps to NM_001024660.3 A2956A. Only missense variants will be evaluated by CHASM.
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-ZP-A9CV-01A-11D-A382-10 chr3:124201707 G>A maps to NM_001024660.3 K1413K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZS-A9CD-01A-11D-A36X-10 chr3:124160835 C>T maps to NM_001024660.3 Y1079Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADE-01A-11D-A40R-10 chr19:11286586 C>T maps to NM_015493.6 E621E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACI-01A-11D-A40R-10 chr19:8387767 A>C maps to NM_198471.2 G807G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAD2-01A-11D-A40R-10 chr19:8400164 T>C maps to NM_198471.2 Q182Q. 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-AACZ-01A-11D-A40R-10 chr1:62734067 T>A maps to NM_181712.4 K708*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr1:62739433 G>T maps to NM_181712.4 R448R. Only missense variants will be evaluated by CHASM.
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-G3-A3CG-01A-11D-A20W-10 chr18:44626698 C>T maps to ENST00000356157 I466I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAC8-01A-11D-A40R-10 chr3:127703118 T>A maps to NM_207335.2 *624K. 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-EP-A2KB-01A-11D-A183-10 chr15:65370196 C>A maps to NM_001101362.2 A348A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-AAV3-01A-11D-A36X-10 chr11:47594681 G>T maps to NM_018095.4 R469R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAE7-01A-11D-A40R-10 chr12:5020867 G>T maps to NM_000217.2 V108V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CG-01A-11D-A20W-10 chr1:111060285 A>T maps to NM_005549.2 L375*. 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-DD-AACA-01A-11D-A40R-10 chr1:111216297 C>T maps to NM_002232.3 S378S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WQ-A9G7-01A-11D-A36X-10 chr11:30034165 A>G maps to NM_002233.2 G20G. 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-DD-A3A0-01A-11D-A20W-10 chr3:155861083 T>C maps to NM_003471.3 P39P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9GW-01A-11D-A382-10 chr8:73848213 T>C maps to NM_004770.2 I208I. 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-AAVY-01A-11D-A40R-10 chr11:17758085 C>A maps to NM_001112741.1 L179L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9H3-01A-11D-A382-10 chr12:75601610 G>A maps to NM_139137.2 G51G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAED-01A-12D-A40R-10 chr12:75601376 C>A maps to NM_139137.2 V129V. 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-DD-AAC9-01A-11D-A40R-10 chr23:48823175 C>T did not map to a codon.
Sequencing variant TCGA-DD-AACT-01A-11D-A40R-10 chr23:48826084 C>T did not map to a codon.
Sequencing variant TCGA-BC-A3KG-01A-11D-A20W-10 chr7:119915321 C>T maps to NM_012281.2 S212S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9GX-01A-11D-A382-10 chr23:108868237 G>A did not map to a codon.
Sequencing variant TCGA-DD-AAD5-01A-11D-A40R-10 chr11:74168596 G>A maps to NM_005472.4 T4T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A8YO-01A-11D-A36X-10 chr2:11052593 C>T maps to NM_002236.4 S14S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EE-01A-11D-A12Z-10 chr2:11053358 C>T maps to NM_002236.4 S269S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr20:49626761 C>T maps to NM_002237.3 A38A. 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-2Y-A9H3-01A-11D-A382-10 chr2:42671523 G>C maps to NM_133329.5 T287T. 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-4R-AA8I-01A-11D-A382-10 chr7:150648806 C>T maps to NM_000238.2 A558A. 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-DD-AACP-01A-11D-A40R-10 chr7:150647094 G>A maps to NM_172056.1 A853A. 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-2Y-A9H0-01A-11D-A382-10 chr14:63473123 G>A maps to NM_139318.3 Y88Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3K-AAZ8-01A-12D-A38X-10 chr14:63246589 A>G maps to NM_139318.3 H625H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACL-01A-11D-A40R-10 chr17:61623091 T>A maps to NM_030779.2 P938P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADR-01A-11D-A40R-10 chr17:61620963 C>T maps to NM_030779.2 R726*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3K-AAZ8-01A-12D-A38X-10 chr3:19384191 T>C maps to NM_144633.2 L186L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACI-01A-11D-A40R-10 chr3:19575194 T>C maps to NM_144633.2 H976H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAEB-01A-11D-A40R-10 chr3:19554545 G>T maps to NM_144633.2 E722*. 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-G3-A3CG-01A-11D-A20W-10 chr10:103588903 A>G maps to NM_014591.4 G107G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EE-01A-11D-A12Z-10 chr17:21319097 G>T maps to NM_021012.4 L148L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A8HV-01A-11D-A35Z-10 chr21:39671701 G>A maps to NM_170736.1 K173K. 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-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-CC-A8HU-01A-11D-A35Z-10 chr6:39271871 G>T maps to NM_031460.3 G183G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAD3-01A-11D-A40R-10 chr6:39271748 G>A maps to NM_031460.3 F224F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADJ-01A-11D-A40R-10 chr6:39271860 G>T maps to NM_031460.3 S187*. 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-FV-A2QR-01A-11D-A20W-10 chr19:38817934 T>C maps to NM_004823.1 S278S. 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-DD-AACL-01A-11D-A40R-10 chr10:79397294 G>A maps to NM_001161352.1 L36L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9GW-01A-11D-A382-10 chr3:178960727 A>G maps to NM_171828.1 I266I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MA-01A-11D-A20W-10 chr19:18108963 C>T maps to ENST00000222249 Q478*. 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-XR-A8TF-01A-11D-A35Z-10 chr19:18092672 G>T maps to ENST00000222249 A235A. 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-A39Y-01A-11D-A20W-10 chr5:113698630 T>C maps to NM_021614.2 A53A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADG-01A-11D-A40R-10 chr5:113698856 G>T maps to NM_021614.2 E129*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-AAV1-01A-11D-A382-10 chr20:62045483 C>A maps to NM_172107.2 E530*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A3KG-01A-11D-A20W-10 chr8:133198355 T>C maps to NM_004519.2 G153G. 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-CC-A7IE-01A-21D-A382-10 chr8:99440320 C>T maps to NM_020697.2 F38F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IE-01A-21D-A382-10 chr9:138647015 G>T did not map to a codon.
Sequencing variant TCGA-DD-AACN-01A-11D-A40R-10 chr9:138662762 G>T maps to ENST00000298480 P610P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAE6-01A-11D-A40R-10 chr9:138660718 C>T maps to ENST00000298480 A482A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr9:138594133 G>T maps to ENST00000298480 P10P. 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-AACN-01A-11D-A40R-10 chr1:196394992 T>C maps to NM_198503.2 L370L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAW3-01A-11D-A40P-10 chr1:196398775 A>T maps to NM_198503.2 P250P. 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-DD-AACL-01A-11D-A40R-10 chr8:36768467 A>T maps to NM_001031836.2 G784G. 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-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-DD-AADA-01A-11D-A40R-10 chr9:2718410 G>A maps to NM_133497.2 A224A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WQ-A9G7-01A-11D-A36X-10 chr9:2718842 C>T maps to NM_133497.2 S368S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XR-A8TC-01A-11D-A35Z-10 chr9:2718362 C>T maps to NM_133497.2 D208D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAVP-01A-11D-A40R-10 chr19:34291424 G>T maps to ENST00000422820 A25A. 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-DD-A39Z-01A-11D-A20W-10 chr2:201369656 T>C maps to NM_152387.2 G62G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADJ-01A-11D-A40R-10 chr1:215768701 G>A maps to NM_016121.3 V274V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr13:45768399 G>T maps to NM_198404.2 P101P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAE3-01A-11D-A40R-10 chr3:58487085 T>G maps to NM_153331.3 T147T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr7:66098341 C>T maps to NM_153033.3 T75T. 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-DD-AADG-01A-11D-A40R-10 chr7:6505872 C>A maps to NM_006854.3 E145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10W-01A-11D-A12Z-10 chr1:23409727 A>G maps to NM_001009999.2 T834T. 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-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-DD-AAE3-01A-11D-A40R-10 chr5:137733998 A>G maps to NM_016604.3 K988K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-AAV0-01A-11D-A36X-10 chr5:137708412 A>G maps to NM_016604.3 K81K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9H1-01A-11D-A382-10 chr1:44170004 T>G maps to NM_014663.2 Y1053*. 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-A119-01A-11D-A12Z-10 chr23:53223018 C>T did not map to a codon.
Sequencing variant TCGA-DD-A3A1-01A-11D-A20W-10 chr23:53228323 T>C did not map to a codon.
Sequencing variant TCGA-DD-AAW2-01A-11D-A40P-10 chr23:53230775 T>C did not map to a codon.
Sequencing variant TCGA-FV-A2QR-01A-11D-A20W-10 chr23:53226131 T>C 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-CC-A9FW-01A-11D-A36X-10 chr24:21871365 T>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-G3-A3CJ-01A-11D-A20W-10 chr24:21870222 T>C 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-DD-A39Y-01A-11D-A20W-10 chr23:44941972 A>G 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-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-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-DD-AACQ-01A-11D-A40R-10 chr19:10610420 T>A maps to NM_203500.1 K97*. 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-DD-AACL-01A-11D-A40R-10 chr12:91449374 T>A maps to NM_007035.3 I228I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A8HV-01A-11D-A35Z-10 chr6:73933530 C>T maps to ENST00000370385 Q210Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADD-01A-11D-A40R-10 chr9:2812218 C>T did not map to a codon.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr9:2807905 T>C did not map to a codon.
Sequencing variant TCGA-DD-AACS-01A-11D-A40R-10 chr1:19571433 C>A maps to NM_015047.1 V62V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BD-A3EP-01A-11D-A22F-10 chr17:26961981 C>A maps to NM_014680.2 E875*. Only missense variants will be evaluated by CHASM.
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-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-DD-AACC-01A-11D-A40R-10 chr8:48647954 C>T maps to NM_001080394.1 C897C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr16:71957225 G>A maps to NM_014761.2 Q265Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4ND-01A-11D-A25V-10 chr16:85697086 G>A maps to NM_014615.2 Q837Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAD1-01A-11D-A40R-10 chr16:85699911 C>G maps to NM_014615.2 S1030*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A6M6-01A-11D-A32G-10 chr16:85696963 G>A maps to NM_014615.2 L796L. 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-EP-A2KA-01A-11D-A183-10 chr8:126093909 G>T maps to ENST00000377985 R176R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADQ-01A-11D-A40R-10 chr3:197409348 T>A maps to NM_014687.1 P706P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADQ-01A-11D-A40R-10 chr4:6865249 A>G maps to NM_014743.2 P1047P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr4:6882545 A>G maps to NM_014743.2 G1347G. 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-WQ-A9G7-01A-11D-A36X-10 chr4:6865897 A>G maps to NM_014743.2 G1263G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr6:42796556 G>A maps to NM_015349.1 T162T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADR-01A-11D-A40R-10 chr6:42796514 C>G maps to NM_015349.1 S148S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr6:42819933 A>G maps to NM_015349.1 P648P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BD-A3EP-01A-11D-A22F-10 chr14:105360105 C>T maps to ENST00000453495 F1433F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39Z-01A-11D-A20W-10 chr14:105350780 A>G maps to ENST00000453495 A556A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAVX-01A-11D-A40R-10 chr14:105359963 C>T maps to ENST00000453495 D1417D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr14:105349492 C>T maps to ENST00000453495 T234T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr14:75130469 G>A maps to NM_001039479.1 L809L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GJ-A9DB-01A-11D-A36X-10 chr14:75130766 C>T maps to NM_001039479.1 W735*. 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-A12Z-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-DD-A1EG-01A-11D-A20W-10 chr9:114213752 A>G maps to NM_001080398.1 P213P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr9:114172332 T>C maps to NM_001080398.1 K1024K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZP-A9CV-01A-11D-A382-10 chr9:114182325 T>C maps to NM_001080398.1 R688R. 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-DD-AACT-01A-11D-A40R-10 chr20:36642113 T>A maps to NM_014657.1 T35T. 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-4R-AA8I-01A-11D-A382-10 chr7:4825083 G>C did not map to a codon.
Sequencing variant TCGA-DD-A1EG-01A-11D-A20W-10 chr16:15705582 T>C maps to NM_014647.3 G1161G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr1:43895373 C>T maps to NM_015284.2 S490S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADF-01A-11D-A40R-10 chr1:43903331 G>A maps to NM_015284.2 L1220L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr1:43913357 G>T maps to NM_015284.2 S2244S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CG-01A-11D-A20W-10 chr1:43896221 A>G maps to NM_015284.2 E613E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr1:43908180 G>T maps to NM_015284.2 L1782L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr1:47149059 C>T maps to NM_014774.2 L408L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAE7-01A-11D-A40R-10 chr16:85112565 G>T maps to NM_014732.2 E287*. 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-BC-A10U-01A-11D-A12Z-10 chr12:22606892 C>G maps to ENST00000446597 G987G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IK-01A-12D-A33Q-10 chr12:22676442 T>A maps to ENST00000446597 I239I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A7SK-01A-11D-A34Z-10 chr12:22610087 T>A maps to ENST00000446597 T898T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr12:22606847 C>T maps to ENST00000446597 E1002E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAVR-01A-11D-A40R-10 chr16:27709793 G>A maps to NM_015202.2 K362K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BD-A3EP-01A-11D-A22F-10 chr1:3754079 G>A maps to NM_014704.3 R299*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75G-01A-11D-A32G-10 chr1:3740102 C>G maps to NM_014704.3 T796T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10Z-01A-11D-A12Z-10 chr13:42293770 C>A maps to NM_015058.1 G1024G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EG-01A-11D-A20W-10 chr13:42263624 A>G maps to NM_015058.1 P1332P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACB-01A-11D-A40R-10 chr13:42385466 A>G maps to NM_015058.1 L653L. Only missense variants will be evaluated by CHASM.
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-WQ-A9G7-01A-11D-A36X-10 chr9:138376418 G>A maps to NM_014811.3 P21P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A0-01A-11D-A20W-10 chr17:2604058 G>A maps to NM_015229.3 A324A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr17:2599485 A>G maps to NM_015229.3 A747A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-AAV3-01A-11D-A36X-10 chr17:2604932 G>A maps to NM_015229.3 L202L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LG-A9QC-01A-11D-A36X-10 chr1:39876449 C>T maps to NM_015038.1 S171S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9H9-01A-21D-A38X-10 chr18:8777844 A>G maps to ENST00000456698 R484R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr18:8718462 A>G maps to ENST00000456698 R365R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADB-01A-11D-A40R-10 chr18:8718622 C>T maps to ENST00000456698 R419*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A5KG-01A-11D-A27I-10 chr18:8824927 G>A maps to ENST00000456698 R1459R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A1HT-01A-11D-A12Z-10 chr14:55848811 G>A maps to NM_014924.3 R249*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WQ-A9G7-01A-11D-A36X-10 chr16:67214462 C>T maps to NM_001040715.1 P17P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9GU-01A-11D-A382-10 chr1:155887334 T>C maps to NM_014949.2 T465T. 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-2V-A95S-01A-11D-A36X-10 chr10:75561252 C>T maps to NM_015037.2 L1835L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADV-01A-11D-A38X-10 chr10:75558878 T>C maps to NM_015037.2 T1432T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9H1-01A-11D-A382-10 chr4:154525445 A>G maps to NM_001131007.1 S1094S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr5:5461627 A>G maps to NM_015325.1 K727K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAD0-01A-11D-A40R-10 chr5:5461381 C>T maps to NM_015325.1 P645P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADI-01A-11D-A40R-10 chr5:5463104 A>T maps to NM_015325.1 R1220*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAED-01A-12D-A40R-10 chr5:5462389 G>A maps to NM_015325.1 G981G. 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-XR-A8TD-01A-12D-A38X-10 chr5:5463127 A>G maps to NM_015325.1 E1227E. 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-G3-A3CJ-01A-11D-A20W-10 chr6:84930847 T>C maps to NM_014895.2 R33R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZS-A9CF-01A-11D-A382-10 chr6:84925112 C>T maps to NM_014895.2 E130E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr18:29437915 A>G maps to NM_014939.3 L925L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr18:29497604 G>T maps to NM_014939.3 Y126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A495-01A-11D-A25V-10 chr18:29419279 T>C maps to NM_014939.3 Q1326Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CG-01A-11D-A20W-10 chr18:29446818 A>G maps to NM_014939.3 C861C. 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-DD-A39Y-01A-11D-A20W-10 chr4:123145810 A>G maps to NM_015312.3 T924T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAC8-01A-11D-A40R-10 chr4:123246432 A>T maps to NM_015312.3 A3651A. 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-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-WJ-A86L-01A-12D-A45V-10 chr4:123179982 T>C maps to NM_015312.3 S2249S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr7:141362628 G>T maps to NM_001080392.1 R399R. 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-AAE3-01A-11D-A40R-10 chr15:81199077 C>A maps to NM_018689.1 R496R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IE-01A-21D-A382-10 chr23:118220841 C>T did not map to a codon.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr23:118284385 T>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-DD-AAC8-01A-11D-A40R-10 chr23:118230581 T>A did not map to a codon.
Sequencing variant TCGA-DD-AACU-01A-11D-A40R-10 chr23:118222962 T>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-A3CJ-01A-11D-A20W-10 chr23:118221021 T>C 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-DD-AACH-01A-11D-A40R-10 chr4:57173768 C>T maps to NM_020722.1 N63N. Only missense variants will be evaluated by CHASM.
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-ES-A2HS-01A-11D-A183-10 chr4:57181297 G>T maps to NM_020722.1 G544*. 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-WX-AA46-01A-11D-A38X-10 chr4:57180591 T>G maps to NM_020722.1 R308R. 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-DD-AAC8-01A-11D-A40R-10 chr10:24722116 T>C maps to NM_019590.3 D249D. 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-A119-01A-11D-A12Z-10 chr6:138629879 A>G maps to NM_020340.4 K1326K. Only missense variants will be evaluated by CHASM.
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-DD-AAE7-01A-11D-A40R-10 chr6:138584344 T>C maps to NM_020340.4 T575T. 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-FV-A2QR-01A-11D-A20W-10 chr3:128694727 T>C maps to NM_020741.2 T305T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A0-01A-11D-A20W-10 chr17:44109415 T>C maps to NM_015443.3 E1029E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11C-01A-11D-A12Z-10 chr10:72324190 T>C maps to NM_014431.2 Y778Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAW3-01A-11D-A40P-10 chr2:97274684 T>C maps to ENST00000421845 R500R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr1:109716106 T>C maps to NM_020775.3 N236N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K7-AAU7-01A-11D-A382-10 chr1:109734358 T>C maps to NM_020775.3 S519S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADS-01A-11D-A40R-10 chr7:86574265 A>T maps to NM_001142749.2 Y201*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAW0-01A-11D-A40R-10 chr7:86567440 C>G did not map to a codon.
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-DD-AADF-01A-11D-A40R-10 chr18:34752987 A>C maps to NM_020776.1 G489G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr15:52879346 C>T did not map to a codon.
Sequencing variant TCGA-CC-A9FS-01A-11D-A36X-10 chr11:101833466 T>C maps to NM_020802.2 H567H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADI-01A-11D-A40R-10 chr11:101863553 T>A maps to NM_020802.2 L1097*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAEK-01A-11D-A40R-10 chr11:101793444 C>T maps to NM_020802.2 R68*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CK-01A-11D-A20W-10 chr1:232941380 G>A maps to NM_019090.2 L204L. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-DD-A39X-01A-11D-A20W-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-DD-AA3A-01A-11D-A36X-10 chr3:113755520 C>T maps to NM_020817.1 R176R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5R-AA1C-01A-11D-A40R-10 chr14:94139741 C>T maps to ENST00000393153 L2289L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A1-01A-11D-A20W-10 chr14:94120352 T>C maps to ENST00000393153 A2149A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACV-01A-11D-A40R-10 chr14:94004492 C>T maps to ENST00000393153 T427T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5R-AA1C-01A-11D-A40R-10 chr8:95550551 G>A maps to NM_015496.3 Q68*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAC8-01A-11D-A40R-10 chr8:95539090 T>A maps to NM_015496.3 K461*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACV-01A-11D-A40R-10 chr8:95531277 A>G maps to NM_015496.3 F816F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACX-01A-11D-A40R-10 chr8:95508120 T>C did not map to a codon.
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-G3-A3CG-01A-11D-A20W-10 chr9:5772582 T>C maps to ENST00000414202 G1212G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr1:33238479 C>T maps to NM_020888.2 L1093L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr9:100074425 C>A maps to ENST00000375206 R281R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAC8-01A-11D-A40R-10 chr9:100116931 A>T maps to ENST00000375206 I1043I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XR-A8TF-01A-11D-A35Z-10 chr9:100105752 C>T maps to ENST00000375206 T985T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr4:1343356 A>G maps to NM_020894.2 A48A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9H1-01A-11D-A382-10 chr19:7670160 G>T maps to NM_001080429.2 A66A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADA-01A-11D-A40R-10 chr19:7676884 C>T maps to NM_001080429.2 P529P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5C-A9VG-01A-11D-A36X-10 chr7:138601673 G>A maps to NM_001164665.1 L900L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACI-01A-11D-A40R-10 chr7:138566237 C>T maps to NM_001164665.1 A1375A. 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-WJ-A86L-01A-12D-A45V-10 chr7:138552729 G>A maps to NM_001164665.1 I1640I. 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-2Y-A9GX-01A-11D-A382-10 chr10:118711418 C>T did not map to a codon.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr10:118713700 C>T maps to NM_001127211.1 T96T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A112-01A-11D-A12Z-10 chr18:43458390 T>C maps to NM_020964.2 V1964V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IE-01A-21D-A382-10 chr18:43532420 T>C maps to NM_020964.2 A399A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EJ-01A-11D-A152-10 chr18:43435549 G>C maps to NM_020964.2 P2515P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39X-01A-11D-A20W-10 chr18:43496027 A>G maps to NM_020964.2 A1176A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LG-A9QD-01A-11D-A382-10 chr18:43496495 C>T maps to NM_020964.2 Q1097Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZS-A9CF-01A-11D-A382-10 chr18:43505856 G>C maps to NM_020964.2 Y855*. 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-ES-A2HT-01A-12D-A183-10 chr19:18376582 T>C maps to NM_001145304.1 G589G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr2:176802231 A>G maps to NM_030650.1 C298C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADF-01A-11D-A40R-10 chr1:1895246 C>A maps to ENST00000434971 T545T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr20:36851951 A>G maps to NM_001029864.1 P752P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NB-01A-12D-A25V-10 chr9:20740267 C>T maps to NM_017794.3 H107H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr9:20907147 G>T did not map to a codon.
Sequencing variant TCGA-DD-AADE-01A-11D-A40R-10 chr1:233518138 C>T maps to NM_032435.2 V931V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IE-01A-21D-A382-10 chr2:61298746 A>T maps to NM_001129993.1 K53*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CG-01A-11D-A20W-10 chr2:61304084 A>G maps to NM_001129993.1 E154E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADC-01A-11D-A40R-10 chr9:115337109 T>G maps to NM_133465.2 A250A. 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-ZP-A9CY-01A-11D-A382-10 chr9:115337344 C>T maps to NM_133465.2 Q329*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WJ-A86L-01A-12D-A45V-10 chr1:11985676 G>T maps to ENST00000376576 I206I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MB-01A-11D-A20W-10 chr3:113379961 A>G maps to NM_001009899.2 T189T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A8HT-01A-11D-A35Z-10 chr3:113378344 T>C maps to NM_001009899.2 Q728Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NG-01A-11D-A27I-10 chr3:113376100 T>C maps to NM_001009899.2 Q1476Q. 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-2Y-A9H5-01A-11D-A382-10 chr23:73963442 A>C did not map to a codon.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr23:73963110 G>A did not map to a codon.
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-DD-AACP-01A-11D-A40R-10 chr23:73963967 G>A did not map to a codon.
Sequencing variant TCGA-DD-AACU-01A-11D-A40R-10 chr23:73962218 C>A did not map to a codon.
Sequencing variant TCGA-DD-AAEH-01A-11D-A40R-10 chr23:73963703 G>T did not map to a codon.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr23:73960459 C>A did not map to a codon.
Sequencing variant TCGA-G3-A3CJ-01A-11D-A20W-10 chr23:73960375 T>C 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-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-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-DD-AAEA-01A-11D-A40R-10 chr8:29035026 T>C maps to NM_015254.3 T263T. 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-DD-A1ED-01A-11D-A152-10 chr1:200572972 T>C maps to NM_014875.2 R619R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADM-01A-11D-A40R-10 chr1:200558356 C>T maps to NM_014875.2 L1034L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZP-A9D1-01A-11D-A382-10 chr1:200550339 A>G maps to NM_014875.2 Y1108Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A3KF-01A-11D-A20W-10 chr3:44816757 T>C maps to NM_020242.2 D25D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACF-01A-11D-A40R-10 chr3:44869716 A>G maps to NM_020242.2 V956V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EE-01A-11D-A12Z-10 chr20:16316591 T>C maps to NM_024704.4 T1230T. 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-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-DD-AADV-01A-11D-A38X-10 chr1:21036195 C>G maps to NM_020816.2 L202L. 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-RC-A6M4-01A-11D-A32G-10 chr17:43010039 C>A did not map to a codon.
Sequencing variant TCGA-DD-A39W-01A-11D-A20W-10 chr5:137519195 C>T maps to NM_005733.2 A355A. 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-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-BD-A3EP-01A-11D-A22F-10 chr1:200978070 G>A maps to NM_017596.2 A91A. 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-DD-AACO-01A-11D-A40R-10 chr1:200946497 C>A maps to NM_017596.2 S1376S. 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-BC-A3KG-01A-11D-A20W-10 chr16:29810069 T>G did not map to a codon.
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-GJ-A3OU-01A-31D-A382-10 chr14:104638071 C>T maps to NM_015656.1 L376L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9GY-01A-11D-A382-10 chr1:245847633 G>T maps to NM_018012.3 A786A. 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-DD-AACQ-01A-11D-A40R-10 chr1:245851009 T>A maps to NM_018012.3 A1575A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAVQ-01A-11D-A40R-10 chr1:245772751 G>A maps to NM_018012.3 S612S. 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-4R-AA8I-01A-11D-A382-10 chr9:86495340 A>G maps to NM_017576.1 A838A. 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-A39Z-01A-11D-A20W-10 chr17:51901303 C>T maps to NM_032559.4 Q304*. 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-4R-AA8I-01A-11D-A382-10 chr5:132069912 T>A maps to ENST00000403231 V88V. 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-DD-AAVV-01A-11D-A40R-10 chr5:154393730 G>A maps to NM_001099293.1 A104A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A3KG-01A-11D-A20W-10 chr10:32308887 C>T did not map to a codon.
Sequencing variant TCGA-DD-AACY-01A-11D-A40R-10 chr2:149868087 G>A maps to NM_004522.1 K924K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADN-01A-11D-A40R-10 chr6:39387780 T>C did not map to a codon.
Sequencing variant TCGA-G3-A3CG-01A-11D-A20W-10 chr6:39513358 C>T maps to NM_145027.4 K429K. 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-AACT-01A-11D-A40R-10 chr1:170001029 G>A maps to NM_014970.2 R280*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZP-A9D2-01A-11D-A382-10 chr1:170003615 A>T maps to NM_014970.2 L213L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAEK-01A-11D-A40R-10 chr8:145693162 G>A did not map to a codon.
Sequencing variant TCGA-DD-AADM-01A-11D-A40R-10 chr16:57805280 C>T maps to NM_005550.3 L198L. 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-AADO-01A-11D-A40R-10 chr1:158061203 G>T maps to ENST00000368173 V459V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MA-01A-11D-A20W-10 chr19:36351239 C>T maps to NM_199180.2 Q239*. 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-DD-AAE1-01A-11D-A40R-10 chr19:36351886 G>A maps to NM_199180.2 W335*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39X-01A-11D-A20W-10 chr11:126326263 G>A maps to NM_032531.3 N276N. 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-A3A1-01A-11D-A20W-10 chr4:55565811 T>C maps to NM_000222.2 P212P. 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-DD-AACN-01A-11D-A40R-10 chr4:55569978 T>C maps to NM_000222.2 V282V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAE4-01A-11D-A40R-10 chr4:55573354 A>T maps to NM_000222.2 A339A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A459-01A-11D-A25V-10 chr12:88900156 T>A did not map to a codon.
Sequencing variant TCGA-DD-AAD5-01A-11D-A40R-10 chr13:33629229 C>G maps to NM_004795.3 S459S. Only missense variants will be evaluated by CHASM.
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-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-DD-A3A0-01A-11D-A20W-10 chr14:104143835 A>G maps to ENST00000445352 E660E. 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-DD-AACL-01A-11D-A40R-10 chr6:43038458 A>T maps to NM_201523.1 A355A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACY-01A-11D-A40R-10 chr8:103663641 C>A maps to NM_005655.2 V306V. 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-DD-A1EG-01A-11D-A20W-10 chr13:73650023 A>G maps to NM_001730.3 *458W. 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-DD-AACI-01A-11D-A40R-10 chr23:56295810 T>A did not map to a codon.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr23:56291710 A>G did not map to a codon.
Sequencing variant TCGA-2Y-A9H1-01A-11D-A382-10 chr14:50192420 G>A maps to NM_172193.2 W167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A9FS-01A-11D-A36X-10 chr6:42988467 G>T maps to NM_057161.2 G382G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A1-01A-11D-A20W-10 chr16:87742991 C>T maps to NM_017566.3 G442G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr1:18808600 C>T maps to NM_152375.2 Q376*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9H0-01A-11D-A382-10 chr22:50987117 A>T maps to NM_138433.3 K175*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A3KG-01A-11D-A20W-10 chr1:161068354 C>T maps to NM_152366.4 A10A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EG-01A-11D-A20W-10 chr1:161068652 C>T maps to NM_152366.4 L110L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAW2-01A-11D-A40P-10 chr13:70314527 G>T maps to NM_020866.2 G600G. 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-2Y-A9H8-01A-11D-A38X-10 chr17:40021605 C>T maps to NM_018143.1 V6V. 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-ES-A2HT-01A-12D-A183-10 chr1:202887514 A>G maps to NM_021633.2 G117G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr23:117079480 C>T did not map to a codon.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr23:117053531 T>C did not map to a codon.
Sequencing variant TCGA-RC-A6M3-01A-11D-A32G-10 chr23:117053616 C>T did not map to a codon.
Sequencing variant TCGA-DD-AACL-01A-11D-A40R-10 chr18:30350113 C>T maps to NM_020805.1 V147V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A7M5-01A-11D-A33Q-10 chr23:24006692 C>A did not map to a codon.
Sequencing variant TCGA-DD-AAVQ-01A-11D-A40R-10 chr3:47371503 G>C maps to NM_025010.4 L155L. 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-DD-A39X-01A-11D-A20W-10 chr1:173720985 T>C maps to NM_014458.3 S227S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr22:20796518 G>A maps to NM_032775.3 S582S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MA-01A-11D-A20W-10 chr3:183381419 T>C maps to NM_017644.3 I365I. 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-AAE3-01A-11D-A40R-10 chr2:239049436 G>A maps to NM_198582.3 S14S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A8HU-01A-11D-A35Z-10 chr11:75139637 G>T maps to NM_001039548.2 I305I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADC-01A-11D-A40R-10 chr8:124664209 C>G maps to NM_001081675.2 P319P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAE7-01A-11D-A40R-10 chr8:124664884 C>T maps to NM_001081675.2 T94T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr23:86877224 G>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-DD-AAE0-01A-11D-A40R-10 chr23:86887267 C>T 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-G3-AAV6-01A-21D-A36X-10 chr3:183212025 C>A maps to NM_130446.2 S397S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr7:23180385 A>G did not map to a codon.
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-DD-AAVY-01A-11D-A40R-10 chr19:51563811 G>A maps to NM_015596.1 G39G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACF-01A-11D-A40R-10 chr19:51412003 G>T maps to NM_004917.3 S102S. 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-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-EP-A2KA-01A-11D-A183-10 chr19:51506517 T>C did not map to a codon.
Sequencing variant TCGA-GJ-A9DB-01A-11D-A36X-10 chr19:51507010 C>T maps to NM_012315.1 S184S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EG-01A-11D-A20W-10 chr4:187172370 A>T did not map to a codon.
Sequencing variant TCGA-DD-A115-01A-11D-A12Z-10 chr2:48718182 G>A maps to NM_001135629.2 L491L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XR-A8TE-01A-11D-A35Z-10 chr12:10603178 C>A did not map to a codon.
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-AACG-01A-11D-A40R-10 chr7:139168232 C>G maps to NM_198508.2 G52G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A5-01A-11D-A22F-10 chr12:10525807 T>A maps to NM_007360.3 K186*. 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-AADU-01A-11D-A40R-10 chr12:123106425 A>T did not map to a codon.
Sequencing variant TCGA-DD-A3A0-01A-11D-A20W-10 chr17:66038452 T>C maps to NM_002266.2 A185A. 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-AACU-01A-11D-A40R-10 chr1:152733602 A>T maps to NM_001025231.1 L513L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADW-01A-11D-A38X-10 chr1:152733002 C>T maps to NM_001025231.1 P313P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EG-01A-11D-A20W-10 chr7:149420822 A>T did not map to a codon.
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-2Y-A9GV-01A-11D-A382-10 chr12:53069228 G>A maps to NM_006121.3 S561S. 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-T1-A6J8-01A-11D-A32G-10 chr12:53069228 G>A maps to NM_006121.3 S561S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACK-01A-11D-A40R-10 chr17:38975888 A>T maps to NM_000421.3 L418*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACO-01A-11D-A40R-10 chr17:38975316 G>A maps to NM_000421.3 G490G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAW0-01A-11D-A40R-10 chr17:39018820 A>G maps to NM_000223.3 S461S. 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-WQ-A9G7-01A-11D-A36X-10 chr17:39019562 G>A maps to NM_000223.3 A376A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADS-01A-11D-A40R-10 chr17:39670927 T>A did not map to a codon.
Sequencing variant TCGA-DD-AADQ-01A-11D-A40R-10 chr17:39766281 C>T did not map to a codon.
Sequencing variant TCGA-DD-AACI-01A-11D-A40R-10 chr12:53343283 G>A maps to NM_000224.2 E109E. 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-EP-A2KB-01A-11D-A183-10 chr12:53040546 T>C maps to NM_000423.2 K482K. 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-DD-AAVY-01A-11D-A40R-10 chr17:39036073 A>G maps to NM_019010.2 H303H. 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-G3-A3CG-01A-11D-A20W-10 chr17:38926058 A>G maps to NM_181539.4 L306L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr17:38936686 A>T maps to NM_181537.3 L183L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZP-A9D1-01A-11D-A382-10 chr17:38936059 G>A maps to NM_181537.3 N246N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EG-01A-11D-A20W-10 chr17:38948684 A>G maps to NM_181535.3 P463P. 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-DD-AACZ-01A-11D-A40R-10 chr12:53189454 G>A maps to ENST00000309505 G124G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XR-A8TC-01A-11D-A35Z-10 chr17:39506782 C>A maps to NM_004138.2 R79R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A12J-01A-11D-A12Z-10 chr17:39525702 G>A maps to ENST00000394004 C101C. 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-DD-AAC8-01A-11D-A40R-10 chr17:39635248 T>A did not map to a codon.
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-ED-A8O5-01A-11D-A35Z-10 chr17:39644651 C>T did not map to a codon.
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-2Y-A9H8-01A-11D-A38X-10 chr17:39597053 A>G maps to NM_006771.3 I40I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XR-A8TG-01A-11D-A35Z-10 chr17:39594487 G>A maps to NM_006771.3 I366I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A1-01A-11D-A20W-10 chr17:39140492 A>G maps to NM_182497.3 S11S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADV-01A-11D-A38X-10 chr17:39140077 C>T did not map to a codon.
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-WJ-A86L-01A-12D-A45V-10 chr12:52884731 C>T maps to NM_005554.3 V274V. 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-EP-A2KA-01A-11D-A183-10 chr12:52826982 C>A maps to ENST00000252245 L238L. 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-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-WQ-A9G7-01A-11D-A36X-10 chr12:53227585 G>A maps to NM_175834.2 F153F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZS-A9CD-01A-11D-A36X-10 chr12:53225248 C>A maps to NM_175834.2 R213R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAVX-01A-11D-A40R-10 chr12:52681030 G>A maps to NM_002281.3 L368L. 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-4R-AA8I-01A-11D-A382-10 chr12:52799998 C>T maps to NM_033033.3 S21S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr12:52754780 G>A maps to NM_002283.3 S460S. 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-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-XR-A8TF-01A-11D-A35Z-10 chr17:39726457 T>A maps to NM_000226.3 T219T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr17:39183239 G>A maps to NM_031957.1 C56C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADF-01A-11D-A40R-10 chr21:46057579 G>T maps to NM_181688.1 P82P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A8HT-01A-11D-A35Z-10 chr21:46117301 C>A maps to NM_198699.1 C62*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZS-A9CF-01A-11D-A382-10 chr21:46047777 T>G maps to NM_198690.2 S230S. 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-DD-AAE2-01A-11D-A40R-10 chr21:31744027 T>A maps to NM_181621.3 S168S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EE-01A-11D-A12Z-10 chr21:31973498 C>A maps to NM_181620.1 C20*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr21:31709980 A>G maps to NM_001077711.1 P2P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EE-01A-11D-A12Z-10 chr17:39150289 G>T maps to NM_033185.2 C20*. 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-AACZ-01A-11D-A40R-10 chr17:39150196 A>T maps to NM_033185.2 C51*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr17:39279993 T>C maps to NM_031854.2 R127R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A8HU-01A-11D-A35Z-10 chr17:39316583 G>A maps to NM_032524.1 C120C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADN-01A-11D-A40R-10 chr17:39305698 T>C maps to NM_033188.3 R107R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr17:39261993 G>A maps to NM_001146041.1 R118R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WQ-A9G7-01A-11D-A36X-10 chr11:71293745 G>A maps to ENST00000376535 C46C. 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-DD-AACZ-01A-11D-A40R-10 chr11:1629045 G>A maps to ENST00000359229 C240C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NQ-01A-21D-A28X-10 chr11:1643104 G>C maps to ENST00000359229 S73S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-AA0U-01A-11D-A382-10 chr11:1651252 C>G maps to NM_001001480.2 G61G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25Z-01A-11D-A16V-10 chr11:71238414 C>A maps to ENST00000422553 G23G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACO-01A-11D-A40R-10 chr11:71249529 T>C maps to NM_021046.2 C143C. 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-AAC8-01A-11D-A40R-10 chr17:39388764 T>A maps to NM_031962.2 C4*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAD1-01A-11D-A40R-10 chr17:39388884 G>A maps to NM_031962.2 Q44Q. 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-DD-AAEA-01A-11D-A40R-10 chr3:119209505 T>C maps to NM_152305.2 Y302Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr1:52499376 T>C maps to NM_138417.2 E19E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A9FW-01A-11D-A36X-10 chr14:56079289 G>A did not map to a codon.
Sequencing variant TCGA-G3-AAV4-01A-11D-A382-10 chr14:56139681 A>G maps to NM_001079521.1 L1213L. 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-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-4R-AA8I-01A-11D-A382-10 chr23:153138118 G>A did not map to a codon.
Sequencing variant TCGA-BD-A3EP-01A-11D-A22F-10 chr23:153129903 T>C 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-DD-AACQ-01A-11D-A40R-10 chr23:153128940 C>A did not map to a codon.
Sequencing variant TCGA-DD-AACV-01A-11D-A40R-10 chr23:153135852 C>T did not map to a codon.
Sequencing variant TCGA-G3-A3CJ-01A-11D-A20W-10 chr23:153132509 T>C did not map to a codon.
Sequencing variant TCGA-GJ-A9DB-01A-11D-A36X-10 chr1:62672398 T>A maps to NM_019079.4 T33T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39X-01A-11D-A20W-10 chr20:42157386 T>C did not map to a codon.
Sequencing variant TCGA-DD-A73C-01A-12D-A33K-10 chr20:42159525 C>T maps to NM_032107.4 S405S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr6:130407319 T>C maps to NM_032438.2 L481L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A5KG-01A-11D-A27I-10 chr18:6243329 C>T maps to NM_173464.3 W141*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr18:6244509 C>T maps to NM_173464.3 S99S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACQ-01A-11D-A40R-10 chr15:63419549 A>T 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-2Y-A9HA-01A-11D-A38X-10 chr18:7026081 G>T maps to NM_005559.2 G766G. 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-DD-A39Z-01A-11D-A20W-10 chr18:7034665 T>C maps to NM_005559.2 T621T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACI-01A-11D-A40R-10 chr18:7013921 G>A maps to NM_005559.2 P1085P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACJ-01A-11D-A40R-10 chr18:7008501 C>A maps to NM_005559.2 V1369V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZP-A9D1-01A-11D-A382-10 chr18:6956652 T>G maps to NM_005559.2 P2692P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39Z-01A-11D-A20W-10 chr6:129621988 G>A maps to NM_000426.3 W1049*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACK-01A-11D-A40R-10 chr6:129813105 G>A maps to NM_000426.3 Q2653Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADP-01A-11D-A38X-10 chr6:129704302 C>T maps to NM_000426.3 Q1666*. 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-A39Y-01A-11D-A20W-10 chr18:21494697 A>G maps to ENST00000416669 G2508G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACL-01A-11D-A40R-10 chr18:21422659 A>T maps to ENST00000416669 S1185S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-AAV0-01A-11D-A36X-10 chr18:21343450 C>T maps to ENST00000416669 G382G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr6:112435866 T>C maps to NM_001105206.1 T1735T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr6:112466013 G>T maps to NM_001105206.1 T825T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACF-01A-11D-A40R-10 chr20:60898878 G>A maps to NM_005560.3 R1934R. 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-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-CC-A9FW-01A-11D-A36X-10 chr3:49161059 C>A maps to NM_002292.3 E1268*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr3:49162305 T>C maps to NM_002292.3 P979P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr3:49162735 T>C maps to NM_002292.3 T890T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-AAV0-01A-11D-A36X-10 chr3:49166161 G>A maps to NM_002292.3 L608L. 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-DD-A119-01A-11D-A12Z-10 chr1:209799288 G>A maps to NM_000228.2 T560T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EE-01A-11D-A12Z-10 chr1:209789917 G>A maps to NM_000228.2 Q1094*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9GS-01A-12D-A382-10 chr7:107696203 G>A maps to NM_007356.2 L1210L. 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-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-ES-A2HS-01A-11D-A183-10 chr1:183111867 C>T maps to NM_002293.3 D1591D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr1:183204832 G>A maps to NM_005562.2 P808P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAEH-01A-11D-A40R-10 chr1:183201973 A>G maps to NM_005562.2 E734E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADF-01A-11D-A40R-10 chr9:133936494 T>A maps to ENST00000355048 P744P. 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-DD-AAEG-01A-11D-A38X-10 chr7:55466206 G>T maps to NM_018697.3 R138R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XR-A8TF-01A-11D-A35Z-10 chr23:37431396 T>A did not map to a codon.
Sequencing variant TCGA-DD-AAE1-01A-11D-A40R-10 chr4:17586621 A>T maps to NM_015907.2 G189G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5C-A9VG-01A-11D-A36X-10 chr5:154172334 C>T maps to ENST00000377643 R240*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10W-01A-11D-A12Z-10 chr4:129127684 C>A maps to NM_018078.2 Y804*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACE-01A-11D-A40R-10 chr4:129028554 T>G maps to NM_032239.2 *359E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XR-A8TG-01A-11D-A35Z-10 chr4:129019440 C>T maps to NM_018078.2 Q257*. 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-EP-A2KA-01A-11D-A183-10 chr12:50822724 A>G maps to ENST00000429001 A64A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CG-01A-11D-A20W-10 chr12:50822862 T>C maps to ENST00000429001 Y110Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CJ-01A-11D-A20W-10 chr10:876908 T>C maps to NM_015155.1 E253E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAD8-01A-11D-A40R-10 chr15:71124686 T>A maps to NM_018357.2 R394*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MA-01A-11D-A20W-10 chr23:64754434 A>G did not map to a codon.
Sequencing variant TCGA-DD-A39Y-01A-11D-A20W-10 chr23:64754545 T>C did not map to a codon.
Sequencing variant TCGA-DD-AADD-01A-11D-A40R-10 chr23:64738078 T>G did not map to a codon.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr23:64744927 T>C did not map to a codon.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr19:8320762 C>T maps to NM_024552.2 H156H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NN-01A-11D-A28X-10 chr12:50529576 G>A maps to NM_147190.2 D270D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A3KF-01A-11D-A20W-10 chr2:169626075 A>G maps to ENST00000392687 E361E. Only missense variants will be evaluated by CHASM.
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-DD-AAD5-01A-11D-A40R-10 chr16:29001279 G>T maps to NM_014387.3 E246*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A5SI-01A-31D-A27I-10 chr6:149997736 C>T maps to NM_004690.2 L910L. 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-DD-AACI-01A-11D-A40R-10 chr1:203734780 A>T maps to NM_017773.3 R30*. 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-DD-AACQ-01A-11D-A40R-10 chr6:80196732 T>A maps to NM_181714.3 V694V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAVP-01A-11D-A40R-10 chr21:40778272 G>T maps to NM_152505.3 G516G. 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-XR-A8TG-01A-11D-A35Z-10 chr16:67976467 G>C maps to NM_000229.1 R182R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr1:152799971 G>A maps to NM_178348.2 Q8Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5262-01A-01D-A12Z-10 chr1:152777756 T>A maps to NM_178351.3 G66G. 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-ZP-A9D1-01A-11D-A382-10 chr1:152636634 C>A maps to NM_178430.2 P18P. 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-DD-A11D-01A-11D-A12Z-10 chr9:139651620 C>A did not map to a codon.
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-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-4R-AA8I-01A-11D-A382-10 chr10:103870858 A>G maps to NM_001113407.1 F72F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9H5-01A-11D-A382-10 chr11:18467771 C>T maps to NM_017448.3 I242I. 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-MR-A520-01A-11D-A25V-10 chr16:75146312 G>T maps to NM_153486.3 R489R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACP-01A-11D-A40R-10 chr23:140271003 A>G did not map to a codon.
Sequencing variant TCGA-CC-A8HT-01A-11D-A35Z-10 chr22:44893313 C>A maps to NM_032287.2 R41R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39Y-01A-11D-A20W-10 chr13:53277942 C>T maps to NM_007015.2 Q264Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NF-01A-11D-A27I-10 chr4:109084857 C>T did not map to a codon.
Sequencing variant TCGA-DD-AADQ-01A-11D-A40R-10 chr1:205388367 A>G maps to ENST00000367153 D65D. Only missense variants will be evaluated by CHASM.
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-3K-AAZ8-01A-12D-A38X-10 chr19:54964819 A>G maps to ENST00000431846 Q137Q. 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-WQ-A9G7-01A-11D-A36X-10 chr19:54965733 G>A maps to ENST00000431846 Q184Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WQ-AB4B-01A-11D-A40P-10 chr19:54967899 A>T maps to ENST00000431846 K511*. 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-UB-A7MB-01A-11D-A33Q-10 chr3:189691794 T>A did not map to a codon.
Sequencing variant TCGA-3K-AAZ8-01A-12D-A38X-10 chr12:6946250 G>A did not map to a codon.
Sequencing variant TCGA-BC-A3KG-01A-11D-A20W-10 chr8:29959444 C>T maps to NM_001128208.1 I16I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NB-01A-12D-A25V-10 chr7:2566468 G>T did not map to a codon.
Sequencing variant TCGA-ZP-A9CV-01A-11D-A382-10 chr7:2559887 C>T maps to NM_001040167.1 D131D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADF-01A-11D-A40R-10 chr11:63283716 A>T did not map to a codon.
Sequencing variant TCGA-DD-AADP-01A-11D-A38X-10 chr17:76968131 T>G maps to NM_005567.3 S428S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADB-01A-11D-A40R-10 chr19:39299452 C>T maps to NM_006149.3 K90K. Only missense variants will be evaluated by CHASM.
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-DD-A1EG-01A-11D-A20W-10 chr19:35617455 C>T maps to NM_139284.2 A339A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9H7-01A-11D-A38X-10 chr11:27389740 G>A maps to NM_018490.2 Y843Y. 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-UB-AA0U-01A-11D-A382-10 chr12:71977547 T>G maps to NM_003667.2 P586P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADB-01A-11D-A40R-10 chr1:202273759 T>A did not map to a codon.
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-2Y-A9H5-01A-11D-A382-10 chr13:39952661 G>C maps to NM_005780.2 G129G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADM-01A-11D-A40R-10 chr23:111914511 G>C did not map to a codon.
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-CC-A8HU-01A-11D-A35Z-10 chr7:103969250 C>T maps to NM_199000.2 A8A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACE-01A-11D-A40R-10 chr7:103969250 C>T maps to NM_199000.2 A8A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACL-01A-11D-A40R-10 chr7:103969250 C>T maps to NM_199000.2 A8A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACY-01A-11D-A40R-10 chr7:103969250 C>T maps to NM_199000.2 A8A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAVQ-01A-11D-A40R-10 chr7:103969250 C>T maps to NM_199000.2 A8A. 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-YA-A8S7-01A-11D-A36X-10 chr10:126150466 C>T maps to NM_022126.3 R12R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACI-01A-11D-A40R-10 chr17:35297688 C>T maps to NM_005568.3 C91C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZP-A9D1-01A-11D-A382-10 chr17:35300130 A>G maps to NM_005568.3 P308P. 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-DD-AAVX-01A-11D-A40R-10 chr1:75602885 T>A maps to NM_001001933.1 P69P. 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-DD-AACB-01A-11D-A40R-10 chr22:30640878 C>T maps to NM_002309.3 A21A. 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-EP-A2KB-01A-11D-A183-10 chr19:48630536 T>C maps to NM_000234.1 G667G. 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-DD-AAE2-01A-11D-A40R-10 chr19:55106838 C>A maps to NM_006863.1 P211P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACB-01A-11D-A40R-10 chr19:55086933 C>T maps to NM_001130917.1 H289H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZS-A9CD-01A-11D-A36X-10 chr19:55087300 C>A maps to NM_001130917.1 S327*. 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-BC-A8YO-01A-11D-A36X-10 chr19:54822849 G>A maps to NM_021250.2 S182S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAD2-01A-11D-A40R-10 chr19:54746591 G>A maps to ENST00000407860 P3P. 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-DD-AADO-01A-11D-A40R-10 chr19:55144167 C>T maps to ENST00000427581 S341S. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-5R-AA1C-01A-11D-A40R-10. Mapping will be selected arbitrarily.
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-DD-AAEA-01A-11D-A40R-10 chr19:54724953 C>A did not map to a codon.
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-4R-AA8I-01A-11D-A382-10 chr4:41621358 C>T maps to NM_014988.2 Y279Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAD6-01A-11D-A40R-10 chr7:73521438 C>G maps to NM_002314.2 V327V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAVV-01A-11D-A40R-10 chr4:83861044 T>C maps to NM_194282.2 K413K. 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-BC-A3KF-01A-11D-A20W-10 chr1:226420804 A>G maps to ENST00000366807 S655S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A3KG-01A-11D-A20W-10 chr9:27950198 A>G maps to NM_152570.1 S157S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A6M6-01A-11D-A32G-10 chr9:27949553 G>T maps to NM_152570.1 T372T. 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-A8HT-01A-11D-A35Z-10 chr19:42909570 C>T maps to NM_005357.2 G836G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NI-A8LF-01A-11D-A35Z-10 chr19:42914800 C>A maps to NM_005357.2 A359A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACU-01A-11D-A40R-10 chr10:90431670 T>C maps to NM_001198829.1 Y216Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZS-A9CD-01A-11D-A36X-10 chr10:90438429 A>T maps to NM_001198829.1 K407*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39Z-01A-11D-A20W-10 chr3:185226628 T>C maps to NM_139248.2 E435E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5C-A9VG-01A-11D-A36X-10 chr21:15535776 A>T maps to NM_198996.2 T344T. 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-4R-AA8I-01A-11D-A382-10 chr17:18138831 C>T maps to NM_004140.3 R445*. 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-AACL-01A-11D-A40R-10 chr17:73566300 C>T maps to NM_001031803.1 L613L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr17:73570324 T>C maps to NM_001031803.1 A979A. 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-DD-AACH-01A-11D-A40R-10 chr7:156555800 C>A did not map to a codon.
Sequencing variant TCGA-ED-A459-01A-11D-A25V-10 chr7:156556490 T>A did not map to a codon.
Sequencing variant TCGA-BD-A3EP-01A-11D-A22F-10 chr12:49500744 T>C maps to NM_018113.2 T52T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9H6-01A-11D-A38X-10 chr16:1020929 C>T maps to ENST00000262301 R17R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr1:156106160 G>T maps to NM_170707.2 G438G. Only missense variants will be evaluated by CHASM.
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-DD-AACI-01A-11D-A40R-10 chr5:126141267 A>G maps to NM_005573.3 E174E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9HA-01A-11D-A38X-10 chr7:123302962 T>A maps to NM_207163.1 P441P. 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-DD-AADF-01A-11D-A40R-10 chr7:123303031 A>G maps to NM_207163.1 K464K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WX-AA44-01A-11D-A38X-10 chr7:123302962 T>A maps to NM_207163.1 P441P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADS-01A-11D-A40R-10 chr7:97770824 A>T maps to NM_014916.3 P116P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A2QR-01A-11D-A20W-10 chr7:97821984 G>A maps to NM_014916.3 L736L. 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-DD-AACZ-01A-11D-A40R-10 chr19:49001082 G>A maps to NM_001080434.1 N1110N. 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-2Y-A9GS-01A-12D-A382-10 chr5:135188364 C>T maps to ENST00000420621 C92C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACQ-01A-11D-A40R-10 chr5:135188295 T>A maps to ENST00000420621 I69I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAE7-01A-11D-A40R-10 chr9:90746808 C>T maps to NM_001166137.1 A381A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A7M9-01A-23D-A34Z-10 chr9:90746826 A>G maps to NM_001166137.1 T375T. 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-UB-AA0V-01A-11D-A382-10 chr19:5719822 C>T maps to NM_004793.2 P107P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACJ-01A-11D-A40R-10 chr8:12589254 C>A maps to NM_152271.3 E560*. 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-CC-A7IE-01A-21D-A382-10 chr1:153233778 C>G maps to NM_000427.2 G118G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr15:74239485 C>T maps to NM_005576.2 H476H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZP-A9CY-01A-11D-A382-10 chr15:74235243 T>C maps to NM_005576.2 Y384Y. 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-DD-AAE6-01A-11D-A40R-10 chr2:74776518 C>T maps to NM_032603.2 K223K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAE7-01A-11D-A40R-10 chr2:74761506 A>G maps to NM_032603.2 N625N. 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-DD-AAVZ-01A-11D-A40R-10 chr10:100017526 G>A maps to NM_032211.6 C380C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9GU-01A-11D-A382-10 chr6:161016461 G>A maps to NM_005577.2 C1131C. 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-DD-A3A1-01A-11D-A20W-10 chr6:161016500 A>G maps to NM_005577.2 D1118D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr6:160978593 G>T maps to NM_005577.2 T1547T. 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-G3-AAV0-01A-11D-A36X-10 chr19:19737370 C>T maps to NM_004720.5 K241K. 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-G3-A3CH-01A-11D-A22F-10 chr23:78010877 T>C did not map to a codon.
Sequencing variant TCGA-DD-A39X-01A-11D-A20W-10 chr5:1467006 T>C did not map to a codon.
Sequencing variant TCGA-YA-A8S7-01A-11D-A36X-10 chr19:14274021 G>T maps to NM_001008701.2 T202T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr1:82409130 T>C maps to ENST00000370717 N292N. Only missense variants will be evaluated by CHASM.
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-AACP-01A-11D-A40R-10 chr2:11911613 G>A maps to ENST00000396099 T141T. 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-DD-AAEA-01A-11D-A40R-10 chr18:2926804 T>A did not map to a codon.
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-A2KA-01A-11D-A183-10 chr3:188327322 G>T maps to NM_005578.3 R268R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr9:104079723 A>G maps to NM_017753.2 V297V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr9:104079679 C>T maps to NM_017753.2 Q283*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACJ-01A-11D-A40R-10 chr19:813157 G>A maps to NM_024888.1 A551A. 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-CC-A8HV-01A-11D-A35Z-10 chr11:58318614 G>A maps to NM_004811.2 Q137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MB-01A-11D-A20W-10 chr4:151773417 A>G maps to NM_006726.3 F1148F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5R-AAAM-01A-12D-A40R-10 chr23:114357371 T>C did not map to a codon.
Sequencing variant TCGA-DD-AADF-01A-11D-A40R-10 chr23:114404862 T>A did not map to a codon.
Sequencing variant TCGA-XR-A8TF-01A-11D-A35Z-10 chr23:114414315 T>A did not map to a codon.
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-DD-AADV-01A-11D-A38X-10 chr19:39805142 G>A maps to NM_020862.1 P278P. 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-WX-AA44-01A-11D-A38X-10 chr19:39805159 C>A maps to NM_020862.1 E273*. 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-5C-A9VG-01A-11D-A36X-10 chr14:42356163 T>G maps to NM_152447.3 T112T. 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-ES-A2HT-01A-12D-A183-10 chr14:42356736 G>A maps to NM_152447.3 R303R. 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-2Y-A9H6-01A-11D-A38X-10 chr7:133821879 A>G maps to NM_144648.1 L134L. 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-4R-AA8I-01A-11D-A382-10 chr3:66449416 C>T maps to NM_015541.2 S403S. 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-AAE7-01A-11D-A40R-10 chr3:66431957 T>C maps to NM_015541.2 K905K. 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-CC-A3MB-01A-11D-A20W-10 chr12:59276666 T>C maps to NM_153377.3 P488P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2V-A95S-01A-11D-A36X-10 chr10:85982125 A>G maps to NM_001017924.2 D401D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9HA-01A-11D-A38X-10 chr4:110772896 T>A maps to NM_198506.2 A73A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr4:110791476 G>A maps to NM_198506.2 G479G. 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-DD-AACG-01A-11D-A40R-10 chr12:57594874 C>T maps to NM_002332.2 P3428P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACM-01A-11D-A40R-10 chr12:57586980 A>G maps to NM_002332.2 A2526A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr12:57539100 A>G maps to NM_002332.2 T223T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr12:57599188 C>A maps to NM_002332.2 R3797R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr6:150147436 A>G maps to NM_032832.5 G437G. 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-DD-AADC-01A-11D-A40R-10 chr8:105503524 A>G maps to NM_013437.4 S652S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9H5-01A-11D-A382-10 chr2:141457817 C>T did not map to a codon.
Sequencing variant TCGA-5R-AAAM-01A-12D-A40R-10 chr2:141473603 A>G maps to NM_018557.2 R1987R. 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-A7IE-01A-21D-A382-10 chr2:141083346 A>C maps to NM_018557.2 S4108S. 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-DD-A39Y-01A-11D-A20W-10 chr2:141812811 A>G maps to NM_018557.2 C475C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADN-01A-11D-A40R-10 chr2:141072504 T>A maps to NM_018557.2 L4268L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADQ-01A-11D-A40R-10 chr2:141739747 T>A maps to NM_018557.2 T956T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAEA-01A-11D-A40R-10 chr2:141812828 C>A did not map to a codon.
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-NI-A8LF-01A-11D-A35Z-10 chr2:142012193 G>A maps to NM_018557.2 C120C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WQ-A9G7-01A-11D-A36X-10 chr2:141709435 G>A maps to NM_018557.2 C987C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BD-A3ER-01A-11D-A20W-10 chr2:170076974 A>G maps to NM_004525.2 D1879D. 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-DD-AACI-01A-11D-A40R-10 chr2:170136922 G>T maps to NM_004525.2 A426A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACQ-01A-11D-A40R-10 chr2:170062840 T>A maps to NM_004525.2 S2463S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr2:170104008 A>G maps to NM_004525.2 T929T. 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-WQ-A9G7-01A-11D-A36X-10 chr2:170033018 G>A maps to NM_004525.2 C3491C. 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-A39Z-01A-11D-A20W-10 chr11:46890578 T>C maps to ENST00000256991 G1644G. 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-WQ-A9G7-01A-11D-A36X-10 chr11:68192641 C>T maps to NM_002335.2 R1103R. 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-DD-A3A0-01A-11D-A20W-10 chr12:12300339 A>G maps to NM_002336.2 A1119A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAE7-01A-11D-A40R-10 chr12:12332890 T>A maps to NM_002336.2 G466G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAEI-01A-11D-A40R-10 chr1:53716469 G>T maps to NM_004631.3 T856T. Only missense variants will be evaluated by CHASM.
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-EP-A2KB-01A-11D-A183-10 chr3:194080637 G>A maps to NM_001135057.2 Q385*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-AAV3-01A-11D-A36X-10 chr6:25420377 C>T maps to NM_017640.5 R59*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A1-01A-11D-A20W-10 chr14:24530140 T>C maps to NM_138360.3 F732F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr14:24523711 T>C maps to NM_138360.3 P118P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAC8-01A-11D-A40R-10 chr7:102574533 A>T maps to NM_001031692.2 T58T. 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-A119-01A-11D-A12Z-10 chr3:46569019 A>G maps to NM_024512.3 L275L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZP-A9CY-01A-11D-A382-10 chr10:72061217 G>A maps to NM_207119.1 I149I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39X-01A-11D-A20W-10 chr8:145748074 T>C maps to NM_001024678.3 G442G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A1-01A-11D-A20W-10 chr10:134151181 T>C maps to NM_030626.2 S108S. 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-FV-A2QR-01A-11D-A20W-10 chr15:99892587 C>T maps to NM_144598.2 R203*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr16:67241507 T>C maps to NM_001004055.1 *224W. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A8HT-01A-11D-A35Z-10 chr3:169574625 C>T maps to NM_024727.2 E174E. 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-ED-A8O5-01A-11D-A35Z-10 chr11:76376968 G>A maps to NM_001128922.1 A10A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZP-A9CV-01A-11D-A382-10 chr11:76372165 C>T maps to NM_001128922.1 A157A. 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-DD-AADU-01A-11D-A40R-10 chr17:62892811 A>G maps to NM_199340.2 D188D. 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-DD-A119-01A-11D-A12Z-10 chr3:26751505 T>C maps to NM_052953.2 L115L. 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-A39Z-01A-11D-A20W-10 chr1:3703706 T>C maps to NM_020710.2 G261G. 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-2Y-A9H5-01A-11D-A382-10 chr19:51021448 C>A maps to NM_001080457.1 R507R. 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-2Y-A9GY-01A-11D-A382-10 chr16:84203705 G>A maps to NM_178452.4 S424S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5C-A9VG-01A-11D-A36X-10 chr16:84188218 G>A maps to NM_178452.4 G130G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACQ-01A-11D-A40R-10 chr16:84203528 T>A maps to NM_178452.4 P365P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr11:552649 A>G maps to NM_198075.3 Q421Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WQ-A9G7-01A-11D-A36X-10 chr11:551774 C>A maps to NM_198075.3 G307G. Only missense variants will be evaluated by CHASM.
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-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-2Y-A9H5-01A-11D-A382-10 chr4:52861213 G>A maps to NM_001024611.1 Y658Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADI-01A-11D-A40R-10 chr4:52883569 A>G maps to NM_001024611.1 N70N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAD1-01A-11D-A40R-10 chr8:67929856 T>C maps to ENST00000421742 A42A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A5SM-01A-12D-A28X-10 chr8:67926749 A>G maps to ENST00000421742 N69N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5C-A9VG-01A-11D-A36X-10 chr1:70300493 C>T maps to NM_020794.2 L140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EG-01A-11D-A20W-10 chr1:70397187 A>G did not map to a codon.
Sequencing variant TCGA-DD-AACS-01A-11D-A40R-10 chr1:70504161 A>G maps to NM_020794.2 R847R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAW0-01A-11D-A40R-10 chr1:70502268 A>T maps to NM_020794.2 T712T. 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-ES-A2HT-01A-12D-A183-10 chr1:70505145 A>G maps to NM_020794.2 E1175E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39Z-01A-11D-A20W-10 chr1:90180438 A>G maps to NM_032270.4 E770E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39Y-01A-11D-A20W-10 chr1:90399469 A>G maps to NM_001134479.1 G281G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAEE-01A-11D-A40R-10 chr1:90400552 C>A maps to NM_001134479.1 L642L. 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-BC-A110-01A-11D-A12Z-10 chr8:86057621 A>T did not map to a codon.
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-DD-A1EE-01A-11D-A12Z-10 chr8:86057621 A>T did not map to a codon.
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-DD-AACI-01A-11D-A40R-10 chr3:37133030 T>C did not map to a codon.
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-DD-AACL-01A-11D-A40R-10 chr12:85466706 A>G maps to NM_001079910.1 E906E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAEB-01A-11D-A40R-10 chr12:85518022 C>T maps to NM_001079910.1 Q1245*. 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-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 chr12:40677798 C>T maps to NM_198578.3 S788S. 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-AAE0-01A-11D-A40R-10 chr1:204589033 G>A maps to NM_201630.1 C29C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39X-01A-11D-A20W-10 chr7:110764888 A>G maps to NM_018334.4 G687G. 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-DD-AADO-01A-11D-A40R-10 chr5:138209106 A>G maps to NM_015564.2 Y381Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACX-01A-11D-A40R-10 chr10:68686715 A>G maps to NM_178011.3 V14V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr2:77746552 A>G maps to NM_001134745.1 L148L. 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-CC-A3MA-01A-11D-A20W-10 chr20:60706421 T>C maps to NM_144703.2 A282A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACA-01A-11D-A40R-10 chr19:35758279 A>G maps to NM_205834.2 R519R. 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-AACG-01A-11D-A40R-10 chr6:31555455 C>T maps to NM_007161.3 L20L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AA3A-01A-11D-A36X-10 chr12:96394787 C>T maps to NM_000895.1 G605G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GJ-A9DB-01A-11D-A36X-10 chr14:24785801 G>A maps to NM_181657.3 T315T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9H1-01A-11D-A382-10 chr2:33359881 C>A maps to ENST00000354476 I352I. 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-G3-AAV0-01A-11D-A36X-10 chr2:33498741 G>A maps to ENST00000354476 V880V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A3KF-01A-11D-A20W-10 chr14:75070368 T>C maps to NM_000428.2 T178T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAVY-01A-11D-A40R-10 chr14:74988709 C>A maps to NM_000428.2 G898*. 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-DD-A3A1-01A-11D-A20W-10 chr11:65306670 G>T maps to NM_001130144.2 R1264R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39X-01A-11D-A20W-10 chr3:46501283 C>T maps to NM_002343.3 R23R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9H0-01A-11D-A382-10 chr15:41796630 C>G did not map to a codon.
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-G3-A3CJ-01A-11D-A20W-10 chr15:41805237 G>T maps to NM_002344.5 R42R. 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-DD-A4NE-01A-11D-A27I-10 chr12:91498001 G>A maps to NM_002345.3 T319T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A1-01A-11D-A20W-10 chr1:23420184 A>G maps to NM_001142546.1 T190T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACI-01A-11D-A40R-10 chr11:24936044 G>A maps to NM_001009909.2 L161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAEA-01A-11D-A40R-10 chr11:25004793 C>A maps to NM_001009909.2 P240P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1ED-01A-11D-A152-10 chr23:114540806 A>G did not map to a codon.
Sequencing variant TCGA-DD-AAEG-01A-11D-A38X-10 chr23:114536616 G>T did not map to a codon.
Sequencing variant TCGA-ZS-A9CE-01A-11D-A36X-10 chr23:114524333 G>A did not map to a codon.
Sequencing variant TCGA-DD-A3A0-01A-11D-A20W-10 chr3:158387375 A>G maps to NM_020169.3 A72A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9GS-01A-12D-A382-10 chr2:160708821 T>A maps to NM_001198759.1 K925*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A2QR-01A-11D-A20W-10 chr2:160676429 A>G maps to NM_001198759.1 N1320N. Only missense variants will be evaluated by CHASM.
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-EP-A2KA-01A-11D-A183-10 chr8:74941216 T>C maps to NM_015364.4 A137A. 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-EP-A2KA-01A-11D-A183-10 chr8:143846490 G>A maps to NM_023946.2 C74C. 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-NI-A8LF-01A-11D-A35Z-10 chr5:89815031 T>A maps to NM_198273.1 T175T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NH-01A-11D-A27I-10 chr1:235940365 G>A maps to NM_000081.2 A1819A. 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-DD-AADN-01A-11D-A40R-10 chr1:235897869 C>A maps to NM_000081.2 L2816L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAE3-01A-11D-A40R-10 chr1:235922870 T>C maps to NM_000081.2 Q2094Q. 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-DD-A1EG-01A-11D-A20W-10 chr3:45874601 A>G maps to NM_020347.2 D132D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAW2-01A-11D-A40P-10 chr3:45872440 T>C maps to NM_020347.2 A188A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAD6-01A-11D-A40R-10 chr22:21348000 G>A maps to NM_006767.3 W437*. 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-DD-AAD1-01A-11D-A40R-10 chr10:102766666 G>T maps to NM_032429.2 R584R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADO-01A-11D-A40R-10 chr13:36049723 A>T maps to NM_005584.4 A184A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NI-A8LF-01A-11D-A35Z-10 chr4:151505053 G>A maps to NM_006439.4 W291*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A9FS-01A-11D-A36X-10 chr7:20198210 C>T maps to NM_182762.3 Q591Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADD-01A-11D-A40R-10 chr7:20199560 T>G maps to NM_182762.3 S141S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1ED-01A-11D-A152-10 chr1:39934402 A>G maps to ENST00000361689 R5231R. 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-DD-AAD1-01A-11D-A40R-10 chr1:39750865 C>A maps to ENST00000361689 R420R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr1:39757652 C>T maps to ENST00000361689 H624H. 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-5C-AAPD-01A-21D-A38X-10 chr11:63767227 G>T maps to NM_014067.3 I224I. 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-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-EP-A2KA-01A-11D-A183-10 chr11:47307981 A>G did not map to a codon.
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-DD-AADG-01A-11D-A40R-10 chr23:152482571 C>A did not map to a codon.
Sequencing variant TCGA-ZS-A9CE-01A-11D-A36X-10 chr23:152482653 G>A did not map to a codon.
Sequencing variant TCGA-CC-A8HV-01A-11D-A35Z-10 chr23:148798033 C>G did not map to a codon.
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-2Y-A9H6-01A-11D-A38X-10 chr23:151283911 T>A 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-ZS-A9CF-01A-11D-A382-10 chr23:30269466 T>C 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-G3-AAV4-01A-11D-A382-10 chr23:27839800 C>T 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-RC-A7SH-01A-11D-A382-10 chr23:35820423 C>T 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-RC-A7SH-01A-11D-A382-10 chr23:26157399 G>A did not map to a codon.
Sequencing variant TCGA-DD-AAE2-01A-11D-A40R-10 chr23:30237135 G>C did not map to a codon.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr23:30236768 T>C did not map to a codon.
Sequencing variant TCGA-DD-AACL-01A-11D-A40R-10 chr23:30254844 T>A did not map to a codon.
Sequencing variant TCGA-DD-AACW-01A-11D-A40R-10 chr23:30261047 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-CC-A8HV-01A-11D-A35Z-10 chr23:26212736 C>G 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-2Y-A9H6-01A-11D-A38X-10 chr23:140995872 G>A 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-DD-AACG-01A-11D-A40R-10 chr23:140994995 G>T 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-2Y-A9H9-01A-21D-A38X-10 chr23:141290939 C>A did not map to a codon.
Sequencing variant TCGA-BC-A3KG-01A-11D-A20W-10 chr23:141291445 T>C 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-DD-A1EE-01A-11D-A12Z-10 chr23:140985120 A>G did not map to a codon.
Sequencing variant TCGA-DD-AACG-01A-11D-A40R-10 chr23:140984731 C>A did not map to a codon.
Sequencing variant TCGA-DD-AAW3-01A-11D-A40P-10 chr23:140926120 G>C 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-UB-AA0U-01A-11D-A382-10 chr23:140969561 G>T did not map to a codon.
Sequencing variant TCGA-CC-A8HU-01A-11D-A35Z-10 chr23:51638487 T>C 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-G3-AAV3-01A-11D-A36X-10 chr23:75649654 C>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-DD-A114-01A-11D-A12Z-10 chr23:75004286 C>T did not map to a codon.
Sequencing variant TCGA-DD-AACU-01A-11D-A40R-10 chr23:75004521 G>A 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-NI-A8LF-01A-11D-A35Z-10 chr3:184429510 C>T maps to NM_022149.4 S33S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACH-01A-11D-A40R-10 chr23:55478904 C>A did not map to a codon.
Sequencing variant TCGA-DD-AADU-01A-11D-A40R-10 chr15:23890780 C>T maps to NM_019066.4 A703A. Only missense variants will be evaluated by CHASM.
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-CC-A8HT-01A-11D-A35Z-10 chr3:65365035 C>T maps to NM_001033057.1 V965V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2V-A95S-01A-11D-A36X-10 chr7:77998507 T>C maps to NM_012301.3 K356K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAD3-01A-11D-A40R-10 chr7:77789510 G>T maps to NM_012301.3 T892T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADA-01A-11D-A40R-10 chr7:77797302 G>A maps to NM_012301.3 I842I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WX-AA44-01A-11D-A38X-10 chr7:77807383 T>G maps to NM_012301.3 R783R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AA3A-01A-11D-A36X-10 chr23:49020203 G>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-G3-A3CJ-01A-11D-A20W-10 chr8:33346291 T>C maps to NM_032509.3 A72A. Only missense variants will be evaluated by CHASM.
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-EP-A2KB-01A-11D-A183-10 chr9:72659501 C>T maps to NM_153267.4 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr5:179201139 G>A maps to NM_014757.4 P771P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10T-01A-11D-A12Z-10 chr11:95825205 C>T maps to NM_032427.1 Q663Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IF-01A-11D-A33K-10 chr11:95825256 T>C maps to NM_032427.1 Q646Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EB-01A-11D-A12Z-10 chr11:95825205 C>T maps to NM_032427.1 Q663Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CG-01A-11D-A20W-10 chr11:95825421 C>T maps to NM_032427.1 Q591Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-AAV4-01A-11D-A382-10 chr11:95712357 G>A maps to NM_032427.1 G1075G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QA-A7B7-01A-11D-A32G-10 chr11:95825256 T>C maps to NM_032427.1 Q646Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9H3-01A-11D-A382-10 chr4:140811089 C>T maps to ENST00000509479 Q500Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9H3-01A-11D-A382-10 chr4:140811101 C>T maps to ENST00000509479 Q496Q. 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-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-ES-A2HT-01A-12D-A183-10 chr1:26080013 C>T maps to NM_020379.2 L292L. 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-2V-A95S-01A-11D-A36X-10 chr4:6602389 G>A maps to NM_015274.1 P482P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAE3-01A-11D-A40R-10 chr4:6598949 C>T maps to NM_015274.1 L390L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MA-01A-11D-A20W-10 chr6:96052707 T>C maps to NM_024641.2 T220T. 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-DD-AAEA-01A-11D-A40R-10 chr23:43571156 A>G did not map to a codon.
Sequencing variant TCGA-ED-A7PZ-01A-11D-A33Q-10 chr23:43603115 A>T did not map to a codon.
Sequencing variant TCGA-BC-A8YO-01A-11D-A36X-10 chr23:43698228 T>A 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-DD-AACL-01A-11D-A40R-10 chr23:43656380 A>T did not map to a codon.
Sequencing variant TCGA-DD-AACM-01A-11D-A40R-10 chr23:43634422 T>A did not map to a codon.
Sequencing variant TCGA-DD-AAD3-01A-11D-A40R-10 chr23:43698251 C>A 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-ZS-A9CD-01A-11D-A36X-10 chr23:43698216 G>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-2Y-A9GX-01A-11D-A382-10 chr5:71492332 A>T maps to NM_005909.3 K1051*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9GX-01A-11D-A382-10 chr5:71495122 A>T maps to NM_005909.3 R1981*. 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-EP-A2KB-01A-11D-A183-10 chr5:71492349 T>C maps to NM_005909.3 G1056G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr5:71489754 T>C maps to NM_005909.3 P191P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5C-AAPD-01A-21D-A38X-10 chr19:17837233 G>T maps to NM_018174.4 R347R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADV-01A-11D-A38X-10 chr19:17837404 C>T maps to NM_018174.4 G404G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAED-01A-12D-A40R-10 chr19:17837677 C>T maps to NM_018174.4 G495G. 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-5C-A9VG-01A-11D-A36X-10 chr2:210560689 A>C maps to NM_002374.3 R1266R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10W-01A-11D-A12Z-10 chr2:210558810 T>C maps to NM_002374.3 T639T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10W-01A-11D-A12Z-10 chr2:210570347 A>G maps to NM_002374.3 R1543R. 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-DD-AADS-01A-11D-A40R-10 chr2:210560649 A>T maps to NM_002374.3 S1252S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CJ-01A-11D-A20W-10 chr2:210543359 A>G maps to NM_002374.3 E109E. 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-DD-AAE7-01A-11D-A40R-10 chr17:21203862 G>T maps to NM_145109.2 E58*. 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-CC-A8HT-01A-11D-A35Z-10 chr19:7975601 G>T maps to ENST00000425613 E239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A3KF-01A-11D-A20W-10 chr5:56178548 T>C maps to NM_005921.1 N1174N. 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-EP-A2KA-01A-11D-A183-10 chr11:65373550 C>T maps to NM_002419.3 L535L. 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-G3-A3CG-01A-11D-A20W-10 chr3:185146485 T>C maps to NM_004721.3 S39S. 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-DD-A1EE-01A-11D-A12Z-10 chr23:19379515 A>G did not map to a codon.
Sequencing variant TCGA-DD-AAC8-01A-11D-A40R-10 chr23:19418697 A>T did not map to a codon.
Sequencing variant TCGA-DD-AADA-01A-11D-A40R-10 chr23:19413260 T>A did not map to a codon.
Sequencing variant TCGA-DD-AAVY-01A-11D-A40R-10 chr23:19416358 G>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-DD-AAEA-01A-11D-A40R-10 chr2:128065256 G>C maps to NM_006609.3 V586V. 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-DD-AAD8-01A-11D-A40R-10 chr6:161470545 G>A maps to NM_005922.2 L414L. 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-A119-01A-11D-A12Z-10 chr6:136935338 C>A maps to NM_005923.3 E746*. Only missense variants will be evaluated by CHASM.
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-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-ZP-A9CV-01A-11D-A382-10 chr1:27686480 G>A maps to NM_004672.3 S729S. 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-2Y-A9H9-01A-21D-A38X-10 chr3:47910777 G>A maps to ENST00000426837 R2112*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9HA-01A-11D-A38X-10 chr3:47957486 C>A maps to ENST00000426837 L627L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A1-01A-11D-A20W-10 chr3:47960308 A>G maps to ENST00000426837 A201A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr19:39096217 G>A maps to NM_001042600.1 T451T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACT-01A-11D-A40R-10 chr11:64563809 C>A maps to NM_004579.2 R562R. 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-EP-A2KB-01A-11D-A183-10 chr2:39535143 G>A maps to NM_003618.2 P353P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAE8-01A-11D-A40R-10 chr2:102501673 G>A maps to NM_145686.2 L1118L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAVX-01A-11D-A40R-10 chr2:102477448 G>T did not map to a codon.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr2:102486260 T>C did not map to a codon.
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-G3-A3CJ-01A-11D-A20W-10 chr23:20031687 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-A39Y-01A-11D-A20W-10 chr23:135328495 A>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-XR-A8TG-01A-11D-A35Z-10 chr23:135318418 G>A did not map to a codon.
Sequencing variant TCGA-DD-AACK-01A-11D-A40R-10 chr22:50706331 G>A maps to NM_002751.5 L55L. 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-4R-AA8I-01A-11D-A382-10 chr17:19284127 T>C maps to NM_139034.2 G202G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr10:49628361 C>T maps to NM_139049.1 N205N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAW3-01A-11D-A40P-10 chr16:1816359 C>T maps to NM_015133.3 H922H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3K-AAZ8-01A-12D-A38X-10 chr5:179666987 C>T did not map to a codon.
Sequencing variant TCGA-DD-A73D-01A-12D-A32G-10 chr3:50677795 G>A did not map to a codon.
Sequencing variant TCGA-WQ-A9G7-01A-11D-A36X-10 chr12:112327907 C>T maps to NM_139078.1 C429C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr15:42107823 C>T maps to NM_001128608.1 D446D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADD-01A-11D-A40R-10 chr2:27245166 C>T maps to NM_012326.2 S27S. 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-2Y-A9GV-01A-11D-A382-10 chr17:60814028 A>T maps to NM_152598.2 P400P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3K-AAZ8-01A-12D-A38X-10 chr17:60821842 C>A maps to NM_152598.2 L143L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9GY-01A-11D-A382-10 chr5:16067613 G>T maps to NM_001102562.1 S392*. Only missense variants will be evaluated by CHASM.
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-EP-A2KB-01A-11D-A183-10 chr2:160605075 A>G maps to NM_022826.2 R425R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACK-01A-11D-A40R-10 chr2:119752066 G>T maps to NM_006770.3 E512*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACZ-01A-11D-A40R-10 chr2:119739021 G>T maps to NM_006770.3 G268G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39Y-01A-11D-A20W-10 chr1:220792018 C>T maps to NM_018650.3 P277P. 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-EP-A2KB-01A-11D-A183-10 chr11:63666538 C>T maps to NM_001039469.2 Q164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr19:45801086 T>C maps to NM_031417.3 G584G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-AAUZ-01A-11D-A382-10 chr19:45797638 A>G maps to NM_031417.3 R509R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZS-A9CD-01A-11D-A36X-10 chr19:45790826 C>T maps to NM_031417.3 R467*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACP-01A-11D-A40R-10 chr12:57910273 G>A maps to NM_004990.2 A871A. 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-AAC8-01A-11D-A40R-10 chr5:68715847 A>T maps to NM_001038603.2 T212T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADE-01A-11D-A40R-10 chr5:68715558 C>A maps to NM_001038603.2 S116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A2QR-01A-11D-A20W-10 chr6:29454971 T>C maps to NM_052967.1 S236S. 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-AAEG-01A-11D-A38X-10 chr3:186980346 G>C maps to NM_139125.3 A133A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9H1-01A-11D-A382-10 chr1:11102989 G>C maps to NM_006610.2 T277T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11B-01A-11D-A12Z-10 chr19:12975698 G>T maps to NM_014975.2 T481T. 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-DD-AAE7-01A-11D-A40R-10 chr1:46497889 A>T maps to NM_015112.2 P1076P. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-DD-AACZ-01A-11D-A40R-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-DD-A1EE-01A-11D-A12Z-10 chr10:27459954 T>G maps to NM_001172303.1 G689G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAVX-01A-11D-A40R-10 chr10:27454041 A>G maps to NM_001172303.1 R201R. 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-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-EP-A2KA-01A-11D-A183-10 chr16:29820870 G>T maps to NM_001042539.1 T430T. 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-DD-AAEA-01A-11D-A40R-10 chr3:152174104 A>G maps to NM_021038.3 T349T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADF-01A-11D-A40R-10 chr6:20131375 A>G maps to NM_001080480.1 D158D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAE1-01A-11D-A40R-10 chr18:74817195 G>A maps to NM_001025101.1 R8*. 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-DD-AAEA-01A-11D-A40R-10 chr20:54823964 A>G maps to ENST00000371389 Q59Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAE1-01A-11D-A40R-10 chr18:58039333 G>T maps to NM_005912.2 I83I. Only missense variants will be evaluated by CHASM.
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-BC-A3KG-01A-11D-A20W-10 chr11:119185941 A>G maps to NM_006500.2 P33P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr9:37888304 A>T maps to NM_033412.3 Y81*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A26S-01A-11D-A16V-10 chr18:29339766 G>A maps to NM_001034172.2 I286I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr23:103349275 C>T did not map to a codon.
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-DD-A1EG-01A-11D-A20W-10 chr5:70936849 T>C maps to NM_022132.4 D340D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LG-A9QD-01A-11D-A382-10 chr2:71351620 T>C maps to NM_032601.3 T31T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAD1-01A-11D-A40R-10 chr23:138686907 T>C did not map to a codon.
Sequencing variant TCGA-DD-AADS-01A-11D-A40R-10 chr23:138733893 T>C did not map to a codon.
Sequencing variant TCGA-G3-A3CG-01A-11D-A20W-10 chr23:138699700 T>C 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-UB-AA0U-01A-11D-A382-10 chr13:113741577 G>A maps to NM_001112732.1 L858L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A3KF-01A-11D-A20W-10 chr3:183028818 T>C did not map to a codon.
Sequencing variant TCGA-DD-A1EG-01A-11D-A20W-10 chr3:182946090 G>A maps to NM_015078.2 L703L. 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-BD-A3EP-01A-11D-A22F-10 chr6:100382374 C>A maps to NM_032503.2 T202T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EG-01A-11D-A20W-10 chr10:13239738 A>G maps to NM_182751.2 V698V. 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-DD-AACT-01A-11D-A40R-10 chr10:13243527 C>A maps to NM_182751.2 C783*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EA-01A-11D-A12Z-10 chr3:127323588 C>A maps to NM_004526.2 G125G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-AAV0-01A-11D-A36X-10 chr6:52132767 T>A did not map to a codon.
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-2Y-A9H9-01A-21D-A38X-10 chr21:47656823 G>C maps to NM_003906.3 P1901P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BD-A3EP-01A-11D-A22F-10 chr21:47676784 C>A maps to NM_003906.3 E1284*. 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-ZS-A9CG-01A-11D-A36X-10 chr8:48883069 G>A did not map to a codon.
Sequencing variant TCGA-BC-A8YO-01A-11D-A36X-10 chr22:35802595 C>T maps to NM_006739.3 A158A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADW-01A-11D-A38X-10 chr7:99693608 G>T maps to NM_005916.3 V461V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-AAV4-01A-11D-A382-10 chr7:99697717 T>C did not map to a codon.
Sequencing variant TCGA-GJ-A9DB-01A-11D-A36X-10 chr19:7593582 G>A maps to NM_020533.2 L326L. 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-AACI-01A-11D-A40R-10 chr1:85487860 G>A maps to NM_018298.9 T404T. 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-DD-AACL-01A-11D-A40R-10 chr8:6266839 A>T maps to NM_024596.3 T21T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr5:94275843 C>A maps to NM_024717.4 G373*. 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-A3CJ-01A-11D-A20W-10 chr5:94353089 T>C maps to NM_024717.4 L273L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EE-01A-11D-A12Z-10 chr15:94901713 C>T maps to NM_018349.3 L392L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39Z-01A-11D-A20W-10 chr15:94882651 A>G maps to NM_018349.3 L257L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WQ-A9G7-01A-11D-A36X-10 chr23:119739357 T>C did not map to a codon.
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-G3-AAV4-01A-11D-A382-10 chr6:30668319 G>A maps to NM_014641.2 F2064F. 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-AADD-01A-11D-A40R-10 chr6:37614142 C>T maps to ENST00000297153 Q688Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39X-01A-11D-A20W-10 chr14:47342699 A>G maps to NM_001113498.2 P896P. 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-AADF-01A-11D-A40R-10 chr2:207620147 T>A maps to NM_001039845.1 I165I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39X-01A-11D-A20W-10 chr12:68696472 T>C maps to NM_017440.4 P633P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CG-01A-11D-A20W-10 chr12:69207365 A>G maps to NM_002392.3 L44L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9H9-01A-21D-A38X-10 chr6:90377747 G>T maps to NM_014611.1 I4693I. 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-FV-A2QR-01A-11D-A20W-10 chr6:90411384 T>C maps to NM_014611.1 E2773E. 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-UB-AA0U-01A-11D-A382-10 chr6:90390401 C>T maps to NM_014611.1 L4057L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZP-A9D1-01A-11D-A382-10 chr6:90408664 T>C maps to NM_014611.1 P3029P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MA-01A-11D-A20W-10 chr6:84108171 A>G maps to NM_002395.4 S92S. 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-4R-AA8I-01A-11D-A382-10 chr23:153296805 G>A did not map to a codon.
Sequencing variant TCGA-G3-A7M5-01A-11D-A33Q-10 chr23:153295882 T>A did not map to a codon.
Sequencing variant TCGA-HP-A5N0-01A-11D-A28X-10 chr23:153296109 G>A did not map to a codon.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr17:37584011 A>G maps to NM_004774.3 S227S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A1-01A-11D-A20W-10 chr5:6374435 C>T did not map to a codon.
Sequencing variant TCGA-CC-A3MA-01A-11D-A20W-10 chr23:70357193 T>C did not map to a codon.
Sequencing variant TCGA-DD-A39Y-01A-11D-A20W-10 chr23:70344672 C>A did not map to a codon.
Sequencing variant TCGA-DD-AACA-01A-11D-A40R-10 chr23:70349273 T>A did not map to a codon.
Sequencing variant TCGA-DD-AAD5-01A-11D-A40R-10 chr23:70346906 G>T did not map to a codon.
Sequencing variant TCGA-DD-AADF-01A-11D-A40R-10 chr23:70354641 C>A did not map to a codon.
Sequencing variant TCGA-DD-AAE3-01A-11D-A40R-10 chr23:70352247 A>G did not map to a codon.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr23:70352237 G>T did not map to a codon.
Sequencing variant TCGA-BC-A10W-01A-11D-A12Z-10 chr3:150874117 G>A 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-DD-A1EG-01A-11D-A20W-10 chr3:150874053 A>G maps to NM_053002.4 P221P. 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-DD-A3A0-01A-11D-A20W-10 chr17:60028242 A>G maps to NM_005121.2 P2078P. 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-G3-A3CJ-01A-11D-A20W-10 chr12:116428867 A>G maps to NM_015335.4 A1297A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-AAV2-01A-11D-A36X-10 chr12:116443799 T>C did not map to a codon.
Sequencing variant TCGA-CC-5262-01A-01D-A12Z-10 chr23:40572165 C>T did not map to a codon.
Sequencing variant TCGA-DD-AADM-01A-11D-A40R-10 chr23:40526044 T>C did not map to a codon.
Sequencing variant TCGA-DD-AAVR-01A-11D-A40R-10 chr23:40526015 T>C 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-AACK-01A-11D-A40R-10 chr19:868160 T>A maps to NM_005481.2 T858T. Only missense variants will be evaluated by CHASM.
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-2Y-A9H4-01A-11D-A382-10 chr17:38186018 A>G maps to NM_014815.3 T416T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZP-A9CV-01A-11D-A382-10 chr17:38189359 T>C maps to NM_014815.3 T257T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A3KF-01A-11D-A20W-10 chr19:16687920 T>C maps to NM_004831.3 G240G. 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-2Y-A9GZ-01A-11D-A38X-10 chr8:118533156 G>T maps to NM_080651.2 G14G. 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-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-DD-AADA-01A-11D-A40R-10 chr16:3304620 G>A maps to NM_000243.2 A149A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A8O5-01A-11D-A35Z-10 chr16:3304269 C>T maps to NM_000243.2 K266K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr16:3306410 G>T maps to NM_000243.2 T59T. 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-G3-A3CJ-01A-11D-A20W-10 chr5:126792817 A>G did not map to a codon.
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-2Y-A9H1-01A-11D-A382-10 chr1:3407515 G>A maps to ENST00000452816 P1583P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5C-AAPD-01A-21D-A38X-10 chr1:3417557 G>C maps to ENST00000452816 P924P. 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-A1EG-01A-11D-A20W-10 chr19:42840480 C>T maps to ENST00000251268 H409H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39Z-01A-11D-A20W-10 chr19:42866591 A>G maps to ENST00000251268 G1967G. 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-ZS-A9CF-01A-11D-A382-10 chr19:42830442 C>T maps to ENST00000251268 A16A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAW0-01A-11D-A40R-10 chr9:123476252 C>T maps to ENST00000426959 P120P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5C-A9VG-01A-11D-A36X-10 chr15:37242601 C>T did not map to a codon.
Sequencing variant TCGA-2Y-A9HB-01A-11D-A38X-10 chr2:32157197 T>C maps to NM_015955.2 A50A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr17:41720882 C>A maps to NM_004527.3 A205A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAW0-01A-11D-A40R-10 chr7:15725802 G>A maps to NM_005924.4 H75H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAE7-01A-11D-A40R-10 chr6:46794121 T>C maps to NM_005588.2 T270T. 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-ES-A2HT-01A-12D-A183-10 chr18:29800205 T>C maps to NM_005925.2 *702R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A5UD-01A-11D-A28X-10 chr15:81295202 G>T maps to NM_022566.2 A197A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9GX-01A-11D-A382-10 chr15:90320133 A>G maps to NM_001039958.1 Q182Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr15:90320133 A>G maps to NM_001039958.1 Q182Q. 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-ES-A2HT-01A-12D-A183-10 chr12:95888768 A>G maps to NM_006838.3 K209K. 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-ED-A82E-01A-11D-A34Z-10 chr14:21464876 G>T maps to NM_001029991.1 G424G. 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-DD-AACQ-01A-11D-A40R-10 chr1:171761247 T>A maps to NM_015935.4 A522A. 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-2Y-A9H8-01A-11D-A38X-10 chr18:48703512 T>A maps to NM_016626.4 G396G. 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-WQ-A9G7-01A-11D-A36X-10 chr18:48723153 G>C maps to NM_016626.4 A179A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WX-AA44-01A-11D-A38X-10 chr18:48723153 G>C maps to NM_016626.4 A179A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAE3-01A-11D-A40R-10 chr19:1555359 G>T maps to NM_001174118.1 G657G. 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-DD-AACZ-01A-11D-A40R-10 chr1:17303682 C>A maps to NM_017459.2 L16L. Only missense variants will be evaluated by CHASM.
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-G3-A3CG-01A-11D-A20W-10 chr17:19288767 C>T did not map to a codon.
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-EP-A2KA-01A-11D-A183-10 chr15:89442943 G>T maps to NM_005928.2 Y323*. 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-5C-A9VH-01A-11D-A36X-10 chr11:119213688 G>T maps to NM_031433.2 P383P. 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-DD-AACO-01A-11D-A40R-10 chr3:158531836 C>T maps to NM_022736.2 L260L. 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-A12Z-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-5C-A9VG-01A-11D-A36X-10 chr15:41988635 C>T maps to ENST00000219905 V476V. 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-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-DD-AADM-01A-11D-A40R-10 chr15:42054034 A>G maps to ENST00000219905 V2548V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A8O5-01A-11D-A35Z-10 chr15:42034792 A>G maps to ENST00000219905 K1594K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr15:41989187 G>T maps to ENST00000219905 V660V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CJ-01A-11D-A20W-10 chr15:41988794 T>C maps to ENST00000219905 G529G. 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-G3-AAV0-01A-11D-A36X-10 chr15:41988767 C>T maps to ENST00000219905 F520F. 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-DD-AADB-01A-11D-A40R-10 chr7:141762460 C>T maps to ENST00000475668 Q1406*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADE-01A-11D-A40R-10 chr7:141764320 G>T maps to ENST00000475668 E1495*. 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-DD-AAEH-01A-11D-A40R-10 chr12:86373972 C>T maps to ENST00000393205 E206E. 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-4R-AA8I-01A-11D-A382-10 chr8:145752947 C>T maps to NM_001001795.1 A143A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BW-A5NP-01A-11D-A27I-10 chr7:22532993 G>A maps to ENST00000441815 Y329Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A8YO-01A-11D-A36X-10 chr3:127540604 G>T maps to NM_007283.5 L29L. 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-DD-AAE0-01A-11D-A40R-10 chr3:127414027 G>A maps to NM_007283.5 D202D. 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-AADB-01A-11D-A40R-10 chr14:39716659 A>G maps to NM_054024.3 L294L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAE4-01A-11D-A40R-10 chr14:39716434 T>A maps to NM_054024.3 A219A. 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-DD-AAC8-01A-11D-A40R-10 chr1:222801851 A>T maps to NM_198551.2 S430S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAE7-01A-11D-A40R-10 chr18:19437091 C>T maps to NM_020774.2 N889N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr18:19383905 T>C maps to NM_020774.2 A470A. 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-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-DD-A39Z-01A-11D-A20W-10 chr11:12183894 C>T maps to NM_014632.2 L65L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAD1-01A-11D-A40R-10 chr11:12237866 G>T did not map to a codon.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr11:12278378 G>A maps to NM_014632.2 T1001T. 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-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-DD-AAD5-01A-11D-A40R-10 chr22:18324652 C>T maps to NM_015241.2 E912E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADK-01A-11D-A40R-10 chr11:12315445 A>G maps to NM_032867.2 K156K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACA-01A-11D-A40R-10 chr22:38302533 G>T maps to NM_033386.2 L35L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACZ-01A-11D-A40R-10 chr22:38328561 C>G maps to NM_033386.2 V673V. Only missense variants will be evaluated by CHASM.
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-DD-AADA-01A-11D-A40R-10 chr23:10535299 A>T did not map to a codon.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr23:10450647 C>A did not map to a codon.
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-EP-A2KB-01A-11D-A183-10 chr23:107097838 C>T 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-AADV-01A-11D-A38X-10 chr5:56226566 T>C maps to ENST00000381226 L256L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr1:12082887 A>G did not map to a codon.
Sequencing variant TCGA-DD-AAC8-01A-11D-A40R-10 chr3:97686359 T>A maps to NM_153182.2 A26A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10T-01A-11D-A12Z-10 chr17:4796727 G>A did not map to a codon.
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-4R-AA8I-01A-11D-A382-10 chr13:24413823 G>A maps to NM_005932.3 Y434Y. 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-AACV-01A-11D-A40R-10 chr13:24411688 A>T did not map to a codon.
Sequencing variant TCGA-DD-A11B-01A-11D-A12Z-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-AADS-01A-11D-A40R-10 chr3:69788757 G>T maps to ENST00000448226 E4*. 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-DD-A3A1-01A-11D-A20W-10 chr10:129899524 C>T maps to NM_002417.4 K3234K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACY-01A-11D-A40R-10 chr20:10393868 A>C maps to NM_170784.1 L98L. 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-DD-A39X-01A-11D-A20W-10 chr7:131084061 A>G maps to NM_013255.4 E191E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADO-01A-11D-A40R-10 chr7:131113816 G>A maps to NM_013255.4 W291*. 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-A3CJ-01A-11D-A20W-10 chr15:23811294 T>C maps to NM_005664.3 S122S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr22:50515342 T>C did not map to a codon.
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-DD-A1EG-01A-11D-A20W-10 chr14:75515827 A>G maps to NM_001040108.1 A177A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39Z-01A-11D-A20W-10 chr14:75514921 T>C maps to NM_001040108.1 S479S. 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-ZP-A9D2-01A-11D-A382-10 chr14:75514825 A>G maps to NM_001040108.1 P511P. 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-DD-AADI-01A-11D-A40R-10 chr11:118347551 G>A maps to NM_001197104.1 V1063V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A2QR-01A-11D-A20W-10 chr11:118368715 A>G maps to NM_001197104.1 S1910S. 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-DD-AACF-01A-11D-A40R-10 chr12:49426792 G>A maps to NM_003482.3 Q3899*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAD6-01A-11D-A40R-10 chr12:49433089 G>A maps to NM_003482.3 L2761L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAVQ-01A-11D-A40R-10 chr12:49431177 G>A maps to NM_003482.3 R3321*. Only missense variants will be evaluated by CHASM.
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-5R-AAAM-01A-12D-A40R-10 chr19:36222960 C>T maps to NM_014727.1 R1864*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr19:36223464 A>G maps to NM_014727.1 E2005E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EG-01A-11D-A20W-10 chr19:36214630 C>A maps to ENST00000396924 R1024R. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-DD-A1EG-01A-11D-A20W-10. Mapping will be selected arbitrarily.
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-DD-AAD0-01A-11D-A40R-10 chr19:36219049 C>T maps to NM_014727.1 R1517*. 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-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-BC-A3KF-01A-11D-A20W-10 chr7:104717612 C>T maps to NM_182931.2 N324N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A3KG-01A-11D-A20W-10 chr7:104742346 A>G maps to NM_182931.2 E634E. 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-EP-A2KA-01A-11D-A183-10 chr10:21884282 C>T maps to NM_004641.3 L107L. 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-AAVY-01A-11D-A40R-10 chr6:168319444 G>T maps to ENST00000400822 E906*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A8O6-01A-11D-A35Z-10 chr6:168352525 G>T maps to ENST00000400822 E1490*. 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-WQ-A9G7-01A-11D-A36X-10 chr17:36876001 G>T did not map to a codon.
Sequencing variant TCGA-ED-A8O5-01A-11D-A35Z-10 chr6:33766965 G>T maps to NM_002418.2 S50S. 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-WQ-A9G7-01A-11D-A36X-10 chr12:122625583 G>A maps to NM_014938.3 A864A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MA-01A-11D-A20W-10 chr7:73011791 A>G maps to NM_032951.2 P441P. Only missense variants will be evaluated by CHASM.
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-A1HT-01A-11D-A12Z-10 chr3:154890001 G>T did not map to a codon.
Sequencing variant TCGA-DD-A3A0-01A-11D-A20W-10 chr3:154802866 A>G maps to NM_007289.2 S60S. Only missense variants will be evaluated by CHASM.
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-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-DD-AAEE-01A-11D-A40R-10 chr11:102650305 T>G maps to NM_002425.2 G92G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAW1-01A-11D-A40P-10 chr11:102650036 T>A maps to NM_002425.2 K135*. 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-BD-A3EP-01A-11D-A22F-10 chr22:24124434 C>T maps to NM_005940.3 D366D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr14:23315223 G>A maps to NM_004995.2 Q575Q. 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-DD-AAD2-01A-11D-A40R-10 chr12:56234592 C>T maps to NM_002429.4 R126R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr12:56234505 G>T maps to NM_002429.4 R155R. 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-DD-AACT-01A-11D-A40R-10 chr11:102495987 A>G maps to NM_004771.3 T21T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACU-01A-11D-A40R-10 chr11:102487622 A>T maps to NM_004771.3 P98P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAED-01A-12D-A40R-10 chr11:102477303 C>T maps to NM_004771.3 V305V. 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-AADQ-01A-11D-A40R-10 chr11:5013311 C>T maps to NM_021801.3 F238F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr11:5013444 A>G maps to NM_021801.3 G253G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9GU-01A-11D-A382-10 chr11:102713310 C>A did not map to a codon.
Sequencing variant TCGA-G3-A5SL-01A-11D-A27I-10 chr11:102711280 G>T maps to NM_002422.3 S223S. 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-DD-AACL-01A-11D-A40R-10 chr4:90857647 A>T maps to NM_007351.2 S939S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAE6-01A-11D-A40R-10 chr4:90856477 A>G maps to NM_007351.2 L549L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XR-A8TE-01A-11D-A35Z-10 chr4:90857797 G>A maps to NM_007351.2 S989S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAW2-01A-11D-A40P-10 chr10:99219815 A>G maps to ENST00000422291 H902H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A9FW-01A-11D-A36X-10 chr22:28195916 G>C maps to NM_002430.2 G205G. 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-UB-AA0U-01A-11D-A382-10 chr15:56736724 T>C maps to NM_018365.2 K201K. 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-A1EG-01A-11D-A20W-10 chr14:93650221 T>C maps to NM_022151.4 R122R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAW2-01A-11D-A40P-10 chr1:47075832 G>T maps to NM_145279.4 I206I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADE-01A-11D-A40R-10 chr18:33840137 G>A maps to NM_017947.2 Q803Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADS-01A-11D-A40R-10 chr18:33846709 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-ES-A2HS-01A-11D-A183-10 chr16:77225505 G>T maps to NM_014940.2 E42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5C-A9VG-01A-11D-A36X-10 chr12:62902145 A>G maps to ENST00000393630 R290R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A9FS-01A-11D-A36X-10 chr12:62946909 G>T maps to ENST00000393630 G1057*. 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-BC-A3KG-01A-11D-A20W-10 chr3:108705727 T>C maps to NM_014429.3 Q752Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAW3-01A-11D-A40P-10 chr3:108819340 G>A maps to NM_014429.3 D79D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A0-01A-11D-A20W-10 chr22:31334113 G>A maps to ENST00000397641 I384I. 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-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-A1EE-01A-11D-A12Z-10 chr23:102931736 C>A did not map to a codon.
Sequencing variant TCGA-DD-A11B-01A-11D-A12Z-10 chr12:122097219 G>A maps to NM_173855.4 A60A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A5SK-01A-11D-A27I-10 chr1:220935023 C>T maps to NM_017898.3 G157G. 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-DD-AACZ-01A-11D-A40R-10 chr23:14915269 A>T 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-DD-AADM-01A-11D-A40R-10 chr1:113237433 G>A maps to NM_020963.3 T512T. Only missense variants will be evaluated by CHASM.
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-CC-A3MB-01A-11D-A20W-10 chr6:132649227 T>C maps to NM_015529.2 G290G. 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-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-EP-A2KB-01A-11D-A183-10 chr15:75182886 G>T maps to NM_002435.1 A12A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr1:43812145 A>G maps to NM_005373.2 E337E. 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-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-DD-AAW1-01A-11D-A40P-10 chr23:154020560 C>T did not map to a codon.
Sequencing variant TCGA-NI-A8LF-01A-11D-A35Z-10 chr17:41975686 C>A maps to NM_005374.3 L31L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAD0-01A-11D-A40R-10 chr17:41898312 G>A maps to ENST00000398393 D291D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A2QR-01A-11D-A20W-10 chr17:41907093 A>G maps to ENST00000398393 P148P. 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-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-DD-AACK-01A-11D-A40R-10 chr10:28491162 C>A maps to NM_173496.3 L25L. 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-DD-AACI-01A-11D-A40R-10 chr17:17075127 C>T maps to NM_015134.2 R754*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5C-A9VG-01A-11D-A36X-10 chr19:18306855 A>C maps to NM_032683.2 R204R. 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-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-DD-AAE9-01A-11D-A40R-10 chr17:60742243 C>T maps to NM_006039.3 Q152*. 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-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-ES-A2HT-01A-12D-A183-10 chr11:94180592 C>T maps to NM_005591.3 R525R. 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-ED-A8O6-01A-11D-A35Z-10 chr11:68747516 G>A maps to NM_198923.2 T313T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAE8-01A-11D-A40R-10 chr11:68772955 G>A maps to NM_145015.4 Y274Y. 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-DD-AACL-01A-11D-A40R-10 chr11:18955671 G>T maps to NM_147199.3 L220L. 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-WQ-A9G7-01A-11D-A36X-10 chr11:18195144 C>T maps to NM_054032.3 S114S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACV-01A-11D-A40R-10 chr17:34958497 G>T maps to NM_024864.3 E87*. 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-DD-AAVY-01A-11D-A40R-10 chr6:44081734 G>A maps to NM_032111.2 R95*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAVY-01A-11D-A40R-10 chr8:55055239 G>A maps to NM_014175.3 T149T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A8O6-01A-11D-A35Z-10 chr8:55047917 C>T maps to NM_014175.3 A25A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IE-01A-21D-A382-10 chr11:68660462 T>C did not map to a codon.
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-CC-A3MB-01A-11D-A20W-10 chr22:19422403 T>C maps to NM_003776.2 L95L. 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-G3-A3CJ-01A-11D-A20W-10 chr14:23302669 A>G maps to NM_178336.2 K67K. 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-G3-AAV5-01A-11D-A36X-10 chr1:228295709 G>C maps to NM_181462.2 G34G. 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-ZS-A9CE-01A-11D-A36X-10 chr10:75010633 T>C maps to NM_016065.3 T130T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9H9-01A-21D-A38X-10 chr6:30587274 C>T maps to NM_014046.3 P28P. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-DD-A39Y-01A-11D-A20W-10. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-DD-AACX-01A-11D-A40R-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-DD-A39X-01A-11D-A20W-10 chr17:55918548 A>G maps to NM_016070.3 C96C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr8:80942311 G>T maps to NM_014018.2 R58R. 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-G3-A3CJ-01A-11D-A20W-10 chr21:35497666 T>C maps to NM_032476.3 R24R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr6:24418378 T>C maps to NM_020662.2 L302L. 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-A119-01A-11D-A12Z-10 chr11:60165353 T>A maps to NM_032597.3 I56I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACL-01A-11D-A40R-10 chr11:60170382 A>T did not map to a codon.
Sequencing variant TCGA-DD-AAVY-01A-11D-A40R-10 chr11:60184357 G>T maps to NM_032597.3 L639L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAEG-01A-11D-A38X-10 chr11:59857212 A>G maps to NM_000139.4 S35S. 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-BC-A3KF-01A-11D-A20W-10 chr11:59947439 T>C did not map to a codon.
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-ZP-A9D2-01A-11D-A382-10 chr11:59949191 T>C maps to NM_152852.1 S3S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACB-01A-11D-A40R-10 chr11:60107404 C>T maps to NM_139249.2 L141L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACG-01A-11D-A40R-10 chr11:60157017 T>C maps to NM_206939.1 Y165Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr11:60476244 C>A maps to NM_031457.1 A175A. 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-2Y-A9H8-01A-11D-A38X-10 chr1:76349303 A>C 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-2Y-A9H9-01A-21D-A38X-10 chr2:48018237 A>T maps to NM_000179.2 K145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr2:48027260 T>C maps to NM_000179.2 D713D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACV-01A-11D-A40R-10 chr17:55752441 T>C maps to NM_138962.2 S300S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A8HU-01A-11D-A35Z-10 chr23:11790750 G>A did not map to a codon.
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-BC-A3KG-01A-11D-A20W-10 chr12:65762780 A>G maps to NM_001031679.2 S89S. 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-DD-AACI-01A-11D-A40R-10 chr3:49928637 C>A maps to NM_002447.2 R1212R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADR-01A-11D-A40R-10 chr3:49932695 G>A maps to NM_002447.2 L1059L. 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-G3-AAV7-01A-11D-A382-10 chr4:4861841 G>A maps to NM_002448.3 K72K. 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-WX-AA46-01A-11D-A38X-10 chr16:56704899 G>A maps to NM_005951.2 *62*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAC8-01A-11D-A40R-10 chr16:56667699 T>A maps to NM_176870.2 C44*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XR-A8TF-01A-11D-A35Z-10 chr7:91503578 C>A maps to NM_006980.3 E177*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CG-01A-11D-A20W-10 chr12:107371778 A>G maps to NM_025198.3 G238G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10W-01A-11D-A12Z-10 chr1:38281032 A>G maps to NM_005955.2 S679S. 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-LG-A9QD-01A-11D-A382-10 chr8:66617099 T>G maps to NM_014637.3 L151L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9H6-01A-11D-A38X-10 chr2:74435848 G>T did not map to a codon.
Sequencing variant TCGA-DD-A3A1-01A-11D-A20W-10 chr4:75147265 A>G maps to NM_001144978.1 E310E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-AAUZ-01A-11D-A382-10 chr2:55470680 C>A maps to NM_002453.2 E479*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAC8-01A-11D-A40R-10 chr11:68517741 T>A maps to NM_004923.3 L129L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11B-01A-11D-A12Z-10 chr23:149814212 C>T did not map to a codon.
Sequencing variant TCGA-DD-AADD-01A-11D-A40R-10 chr23:149814283 A>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-A119-01A-11D-A12Z-10 chr23:149905885 A>G 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-UB-A7MB-01A-11D-A33Q-10 chr23:149867739 A>G did not map to a codon.
Sequencing variant TCGA-WQ-A9G7-01A-11D-A36X-10 chr23:149931128 G>A 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-GJ-A9DB-01A-11D-A36X-10 chr3:9739393 G>T did not map to a codon.
Sequencing variant TCGA-CC-A9FW-01A-11D-A36X-10 chr11:95595468 C>A maps to NM_016156.5 T108T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A5-01A-11D-A22F-10 chr22:30418641 G>C maps to NM_021090.3 A1127A. Only missense variants will be evaluated by CHASM.
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-DD-A3A0-01A-11D-A20W-10 chr8:17159698 A>G maps to NM_004686.4 T528T. 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-K7-AAU7-01A-11D-A382-10 chr4:187455202 T>C maps to NM_005958.3 P231P. 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-DD-A3A1-01A-11D-A20W-10 chr1:11301614 T>C maps to NM_004958.3 G512G. 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-4R-AA8I-01A-11D-A382-10 chr1:236959038 T>C did not map to a codon.
Sequencing variant TCGA-FV-A2QR-01A-11D-A20W-10 chr1:237038041 A>G maps to NM_000254.2 S830S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr8:125580778 T>C did not map to a codon.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr16:70708259 G>A maps to NM_138383.2 D334D. Only missense variants will be evaluated by CHASM.
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-2Y-A9GU-01A-11D-A382-10 chr8:17611233 G>A maps to NM_001001924.2 L695L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A3KG-01A-11D-A20W-10 chr8:17611714 A>G maps to NM_001001924.2 P534P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1ED-01A-11D-A152-10 chr8:17579295 A>G maps to NM_001001931.2 L39L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADM-01A-11D-A40R-10 chr8:17612098 G>A maps to NM_001001924.2 G406G. 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-2Y-A9GU-01A-11D-A382-10 chr13:29600031 C>T maps to NM_001033602.2 G409G. 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-DD-AAD2-01A-11D-A40R-10 chr13:29933427 C>T maps to NM_001033602.2 R989*. 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-DD-AADB-01A-11D-A40R-10 chr5:79285982 C>T maps to ENST00000512528 Q76Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADQ-01A-11D-A40R-10 chr3:124635176 A>G maps to NM_033049.3 F316F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2V-A95S-01A-11D-A36X-10 chr19:9063484 G>T maps to NM_024690.2 S7987S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9H8-01A-11D-A38X-10 chr19:9074290 C>A maps to NM_024690.2 V4385V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr19:9071611 A>G maps to NM_024690.2 S5278S. 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-A1ED-01A-11D-A152-10 chr19:9048765 A>G maps to NM_024690.2 S10955S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1ED-01A-11D-A152-10 chr19:9070573 A>G maps to NM_024690.2 P5624P. 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-DD-AAC8-01A-11D-A40R-10 chr19:9061255 A>T maps to NM_024690.2 S8730S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACF-01A-11D-A40R-10 chr19:9083168 A>T maps to NM_024690.2 T2882T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACT-01A-11D-A40R-10 chr19:9068491 A>T maps to NM_024690.2 T6318T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAD6-01A-11D-A40R-10 chr19:9091764 A>T maps to NM_024690.2 L17*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADD-01A-11D-A40R-10 chr19:9026241 A>T maps to NM_024690.2 R12248R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADO-01A-11D-A40R-10 chr19:9083708 T>G maps to NM_024690.2 V2702V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADV-01A-11D-A38X-10 chr19:9057496 G>A maps to NM_024690.2 T9983T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAW1-01A-11D-A40P-10 chr19:9075724 C>T maps to NM_024690.2 L3907L. 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-A3CJ-01A-11D-A20W-10 chr19:9024994 G>T maps to NM_024690.2 P12289P. 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-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-4R-AA8I-01A-11D-A382-10 chr7:100678584 C>T maps to NM_001040105.1 S1296S. 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-DD-A3A1-01A-11D-A20W-10 chr7:100680429 T>C maps to NM_001040105.1 A1911A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAC8-01A-11D-A40R-10 chr7:100677846 C>T maps to NM_001040105.1 S1050S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACI-01A-11D-A40R-10 chr7:100680018 T>C maps to NM_001040105.1 I1774I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr7:100675797 T>C maps to NM_001040105.1 T367T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CG-01A-11D-A20W-10 chr7:100684023 T>C maps to NM_001040105.1 G3109G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GJ-A6C0-01A-12D-A30V-10 chr7:100683042 C>T maps to NM_001040105.1 V2782V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GJ-A9DB-01A-11D-A36X-10 chr7:100679094 G>A maps to NM_001040105.1 P1466P. 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-2Y-A9H1-01A-11D-A382-10 chr11:1093304 C>G maps to ENST00000441003 T1708T. 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-DD-AADM-01A-11D-A40R-10 chr11:1081110 C>T maps to ENST00000441003 N469N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAEE-01A-11D-A40R-10 chr11:1084793 C>T maps to ENST00000441003 Y863Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAVU-01A-11D-A40R-10 chr11:1092674 C>A maps to ENST00000441003 T1498T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A66X-01A-11D-A30V-10 chr11:1083118 C>T maps to ENST00000441003 T673T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CG-01A-11D-A20W-10 chr11:1093298 G>A maps to ENST00000441003 T1706T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GJ-A6C0-01A-12D-A30V-10 chr11:1085940 G>T maps to ENST00000441003 T927T. 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-G3-AAV0-01A-11D-A36X-10 chr6:30955325 T>G maps to NM_001010909.2 T458T. 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-4R-AA8I-01A-11D-A382-10 chr3:195475921 C>T maps to NM_018406.5 T5295T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAE8-01A-11D-A40R-10 chr3:195474196 G>A maps to NM_018406.5 S5363S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-AAV5-01A-11D-A36X-10 chr3:195477873 G>A maps to NM_018406.5 L5253L. 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-AACH-01A-11D-A40R-10 chr11:1247914 C>T maps to ENST00000447027 G90G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADI-01A-11D-A40R-10 chr11:1258279 C>T maps to ENST00000447027 C1064C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADO-01A-11D-A40R-10 chr11:1271183 G>A maps to ENST00000447027 E4361E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-AAV1-01A-11D-A382-10 chr11:1279380 G>A maps to ENST00000447027 Q5504Q. 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-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-DD-AACH-01A-11D-A40R-10 chr11:1028286 C>G maps to NM_005961.2 A564A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACQ-01A-11D-A40R-10 chr11:1013918 G>T maps to NM_005961.2 G2374G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADB-01A-11D-A40R-10 chr11:1017613 G>A maps to NM_005961.2 T1729T. 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-DD-AACH-01A-11D-A40R-10 chr12:55248915 T>A maps to NM_058173.2 A25A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A3-01A-11D-A22F-10 chr14:57741432 T>C maps to ENST00000431972 D196D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A2QR-01A-11D-A20W-10 chr19:1362333 A>G maps to NM_032853.3 R400R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAEG-01A-11D-A38X-10 chr23:105450457 T>A did not map to a codon.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr23:105450465 A>G did not map to a codon.
Sequencing variant TCGA-BC-A5W4-01A-11D-A28X-10 chr3:52867654 G>T maps to ENST00000504329 T330T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADL-01A-11D-A40R-10 chr6:49416603 T>A maps to NM_000255.3 K457*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr1:45797950 G>T maps to NM_001128425.1 R274R. 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-DD-AAD2-01A-11D-A40R-10 chr16:88722114 T>A maps to NM_002461.1 T209T. 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-4R-AA8I-01A-11D-A382-10 chr16:29848107 G>A maps to NM_017458.3 G246G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAC8-01A-11D-A40R-10 chr16:29847022 A>T did not map to a codon.
Sequencing variant TCGA-DD-AACC-01A-11D-A40R-10 chr16:29848233 C>T maps to NM_017458.3 V288V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACF-01A-11D-A40R-10 chr16:29859234 G>T maps to NM_017458.3 G869G. 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-2Y-A9H3-01A-11D-A382-10 chr5:176734611 G>A maps to ENST00000423571 R225R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CG-01A-11D-A20W-10 chr10:112038991 A>G maps to NM_130439.3 G164G. 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-DD-A39Y-01A-11D-A20W-10 chr23:3241038 T>C did not map to a codon.
Sequencing variant TCGA-DD-AACQ-01A-11D-A40R-10 chr23:3241469 T>A did not map to a codon.
Sequencing variant TCGA-DD-AACY-01A-11D-A40R-10 chr23:3240424 C>T 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-UB-AA0V-01A-11D-A382-10 chr23:3235499 C>A did not map to a codon.
Sequencing variant TCGA-ZP-A9CZ-01A-11D-A382-10 chr23:3235460 G>C did not map to a codon.
Sequencing variant TCGA-WQ-A9G7-01A-11D-A36X-10 chr19:54377622 C>T maps to NM_001020818.1 S280S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CJ-01A-11D-A20W-10 chr6:135518298 T>C maps to NM_001130173.1 P468P. Only missense variants will be evaluated by CHASM.
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-EP-A2KA-01A-11D-A183-10 chr17:4458457 C>T maps to NM_001105538.1 T54T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GJ-A9DB-01A-11D-A36X-10 chr17:4451499 A>G maps to NM_001105538.1 N554N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5R-AAAM-01A-12D-A40R-10 chr8:67478975 A>G maps to NM_001080416.2 N631N. 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-ZS-A9CF-01A-11D-A382-10 chr12:102045034 C>T maps to NM_002465.2 L464L. 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-DD-AADS-01A-11D-A40R-10 chr11:47361215 T>A maps to ENST00000399249 K685*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAC8-01A-11D-A40R-10 chr13:77755970 C>A maps to NM_015057.4 L1602L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACT-01A-11D-A40R-10 chr13:77672194 T>A maps to NM_015057.4 R3032*. 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-4R-AA8I-01A-11D-A382-10 chr2:16082704 C>T maps to NM_005378.4 A173A. 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-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-DD-AAC8-01A-11D-A40R-10 chr17:10409338 A>T maps to NM_005963.3 T682T. 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-ES-A2HS-01A-11D-A183-10 chr17:8455421 A>G maps to ENST00000360416 D287D. 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-DD-AADJ-01A-11D-A40R-10 chr17:10210382 T>C did not map to a codon.
Sequencing variant TCGA-2Y-A9H2-01A-12D-A382-10 chr19:50713648 C>T maps to NM_001145809.1 P9P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A8HV-01A-11D-A35Z-10 chr19:50753872 C>T maps to NM_001145809.1 G586G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A5SI-01A-31D-A27I-10 chr19:50766673 C>T maps to NM_001145809.1 T897T. 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-2Y-A9H1-01A-11D-A382-10 chr17:10535930 C>T maps to NM_002470.2 V1606V. 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-AAE7-01A-11D-A40R-10 chr17:10543713 G>T maps to NM_002470.2 R788R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZS-A9CD-01A-11D-A36X-10 chr17:10543990 C>A maps to NM_002470.2 L726L. 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-DD-AAC8-01A-11D-A40R-10 chr17:10357188 A>T maps to NM_017533.2 L902*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACF-01A-11D-A40R-10 chr17:10350422 G>T maps to NM_017533.2 L1692L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACF-01A-11D-A40R-10 chr17:10363540 G>T maps to NM_017533.2 T415T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr14:23863387 G>A maps to NM_002471.3 F858F. 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-A1ED-01A-11D-A152-10 chr14:23862188 C>T maps to NM_002471.3 L1061L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAEE-01A-11D-A40R-10 chr14:23868177 C>T maps to NM_002471.3 K550K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr14:23865911 G>T maps to NM_002471.3 G761G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IE-01A-21D-A382-10 chr14:23884287 C>T maps to NM_000257.2 E1825E. 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-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-BC-A3KG-01A-11D-A20W-10 chr20:33586332 A>G maps to NM_020884.3 L1340L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAD6-01A-11D-A40R-10 chr20:33585320 G>T maps to NM_020884.3 E1251*. 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-ES-A2HT-01A-12D-A183-10 chr22:36684859 G>A maps to NM_002473.4 N1561N. 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-LG-A9QC-01A-11D-A36X-10 chr22:36702651 C>T maps to NM_002473.4 V615V. 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-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-DD-AAW1-01A-11D-A40P-10 chr6:16143346 A>T maps to NM_013262.3 I187I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr6:16144040 C>T maps to NM_013262.3 T258T. 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-DD-AAD6-01A-11D-A40R-10 chr3:123444794 C>A maps to NM_053025.3 L549L. 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-DD-AACL-01A-11D-A40R-10 chr16:46781874 C>T maps to NM_182493.2 G77G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADB-01A-11D-A40R-10 chr16:46761273 C>T maps to NM_182493.2 E596E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CJ-01A-11D-A20W-10 chr16:46781802 C>T maps to NM_182493.2 Q101Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADP-01A-11D-A38X-10 chr6:2685716 C>T maps to NM_001012418.3 K145K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr5:16818198 A>G maps to NM_012334.2 D66D. 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-CC-A9FW-01A-11D-A36X-10 chr5:16701800 C>T maps to NM_012334.2 Q901Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACQ-01A-11D-A40R-10 chr5:16779717 A>T maps to NM_012334.2 L289*. 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-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-CC-A8HT-01A-11D-A35Z-10 chr17:18036652 C>T maps to ENST00000205890 L1479L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr17:18024954 A>G maps to ENST00000205890 A947A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A9-01A-11D-A25V-10 chr13:109792699 G>A maps to NM_015011.1 K1358K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr13:109318306 C>A maps to NM_015011.1 P12P. 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-DD-AACD-01A-11D-A40R-10 chr17:27442454 C>T maps to NM_078471.3 P744P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADS-01A-11D-A40R-10 chr17:27448103 A>G maps to NM_078471.3 S499S. 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-G3-A3CG-01A-11D-A20W-10 chr17:27421006 A>G maps to NM_078471.3 C1604C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9H9-01A-21D-A38X-10 chr22:26243584 C>T maps to ENST00000407587 F1249F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr22:26306992 C>A maps to ENST00000407587 G1782G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5C-AAPD-01A-21D-A38X-10 chr22:26348382 A>G maps to ENST00000407587 R1990R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BD-A3EP-01A-11D-A22F-10 chr22:26164266 C>A maps to ENST00000407587 A130A. 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-DD-AAVV-01A-11D-A40R-10 chr22:26222448 G>C maps to ENST00000407587 V925V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CJ-01A-11D-A20W-10 chr22:26176035 A>G maps to ENST00000407587 R696R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAC8-01A-11D-A40R-10 chr17:34859821 G>T maps to NM_001163735.1 T648T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr17:34884034 T>C did not map to a codon.
Sequencing variant TCGA-DD-A1EE-01A-11D-A12Z-10 chr2:192160952 G>T did not map to a codon.
Sequencing variant TCGA-DD-AACP-01A-11D-A40R-10 chr17:1371775 G>C maps to NM_001080779.1 A875A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADQ-01A-11D-A40R-10 chr17:1378256 C>A maps to NM_001080779.1 A548A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EG-01A-11D-A20W-10 chr17:30980959 T>C maps to NM_015194.1 P832P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EG-01A-11D-A20W-10 chr17:31094665 A>G maps to NM_015194.1 A273A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A0-01A-11D-A20W-10 chr17:30965823 T>C maps to NM_015194.1 R875R. 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-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-AACE-01A-11D-A40R-10 chr7:45005788 C>A maps to NM_033054.2 L680L. 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-ES-A2HS-01A-11D-A183-10 chr10:26312956 A>G maps to NM_017433.4 P246P. 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-3K-AAZ8-01A-12D-A38X-10 chr2:171239699 G>A did not map to a codon.
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-ED-A8O5-01A-11D-A35Z-10 chr2:171323101 C>A maps to NM_138995.3 A965A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5R-AAAM-01A-12D-A40R-10 chr15:52635318 G>A maps to ENST00000358212 A1345A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A1-01A-11D-A20W-10 chr15:52697483 A>G maps to ENST00000358212 P351P. 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-A39X-01A-11D-A20W-10 chr15:52548895 G>A maps to NM_018728.3 N445N. 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-ED-A8O5-01A-11D-A35Z-10 chr15:52497231 G>A maps to NM_018728.3 S1550S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADO-01A-11D-A40R-10 chr6:76599976 G>A maps to ENST00000428345 R954R. 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-G3-A3CJ-01A-11D-A20W-10 chr2:128345985 A>G maps to ENST00000389524 R570R. 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-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-ZP-A9D1-01A-11D-A382-10 chr17:12608446 T>C maps to NM_001146312.1 L20L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5C-A9VG-01A-11D-A36X-10 chr10:95134585 T>A maps to NM_013451.3 T745T. 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-DD-AADL-01A-11D-A40R-10 chr1:203055031 C>A maps to NM_002479.4 E20*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39Y-01A-11D-A20W-10 chr18:3151803 A>G maps to NM_003803.3 G577G. 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-A3CJ-01A-11D-A20W-10 chr10:75394368 T>C maps to NM_021245.2 G125G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACL-01A-11D-A40R-10 chr4:120072180 T>A maps to NM_016599.3 S77S. 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-EP-A2KB-01A-11D-A183-10 chr5:150056367 T>C maps to NM_133371.3 R229R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A3KF-01A-11D-A20W-10 chr10:69918259 A>G maps to NM_032578.2 S445S. Only missense variants will be evaluated by CHASM.
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-AAE6-01A-11D-A40R-10 chr8:41798613 G>A maps to NM_006766.3 Q929*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WX-AA46-01A-11D-A38X-10 chr8:41812896 T>C maps to NM_006766.3 Q505Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BD-A3EP-01A-11D-A22F-10 chr10:76781898 A>G maps to NM_012330.2 E1094E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr10:76788661 A>G maps to NM_012330.2 E1360E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAD3-01A-11D-A40R-10 chr10:76789168 G>A maps to NM_012330.2 E1529E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr10:76788577 T>C maps to NM_012330.2 P1332P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LG-A9QD-01A-11D-A382-10 chr10:76789927 T>A maps to NM_012330.2 A1782A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr10:76788412 A>T maps to NM_012330.2 P1277P. 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-ZP-A9CZ-01A-11D-A382-10 chr20:62843407 C>T maps to NM_004535.2 A478A. 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-DD-AADU-01A-11D-A40R-10 chr2:1844608 T>A maps to ENST00000399161 S927S. Only missense variants will be evaluated by CHASM.
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-ES-A2HT-01A-12D-A183-10 chr2:1915832 C>A maps to ENST00000399161 T556T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADO-01A-11D-A40R-10 chr16:48576815 C>A maps to NM_153029.3 *897L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr16:48596337 G>T maps to NM_153029.3 I72I. 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-5C-A9VG-01A-11D-A36X-10 chr4:40122640 G>A maps to NM_018177.3 G970G. 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-DD-A119-01A-11D-A12Z-10 chr13:33012839 A>G maps to NM_033111.3 L728L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1ED-01A-11D-A152-10 chr13:33111158 A>G maps to NM_033111.3 S2S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2V-A95S-01A-11D-A36X-10 chr5:177548181 T>A maps to NM_015111.1 A312A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADO-01A-11D-A40R-10 chr5:177547300 G>T maps to NM_015111.1 T151T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADW-01A-11D-A38X-10 chr21:30257544 G>T maps to NM_013240.3 A41A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CG-01A-11D-A20W-10 chr21:30248784 T>C maps to NM_013240.3 K189K. 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-BC-A3KG-01A-11D-A20W-10 chr11:89892487 A>G maps to NM_005467.3 T324T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACL-01A-11D-A40R-10 chr11:89911261 T>A maps to NM_005467.3 L612*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAVW-01A-11D-A40R-10 chr12:57113525 C>T maps to NM_001113203.1 G596G. Only missense variants will be evaluated by CHASM.
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-DD-AAE0-01A-11D-A40R-10 chr17:59668028 G>A maps to NM_199290.3 V171V. 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-XR-A8TE-01A-11D-A35Z-10 chr1:1684345 G>C maps to ENST00000344463 G591G. 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-4R-AA8I-01A-11D-A382-10 chr9:130829074 G>A maps to NM_197956.3 D102D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACZ-01A-11D-A40R-10 chr5:70308628 T>A maps to NM_004536.2 L38L. 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-4R-AA8I-01A-11D-A382-10 chr19:13988406 C>T maps to NM_001098622.1 C115C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADF-01A-11D-A40R-10 chr19:13988409 C>A maps to NM_001098622.1 G116G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr20:25604492 A>T did not map to a codon.
Sequencing variant TCGA-DD-AAEH-01A-11D-A40R-10 chr20:25596728 G>C maps to NM_152667.2 T193T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XR-A8TC-01A-11D-A35Z-10 chr9:100823186 C>T maps to NM_018946.3 R86*. 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-CC-A9FW-01A-11D-A36X-10 chr23:92928251 C>A did not map to a codon.
Sequencing variant TCGA-DD-AACB-01A-11D-A40R-10 chr23:92927343 C>A did not map to a codon.
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-WQ-A9G7-01A-11D-A36X-10 chr8:144657635 C>T maps to ENST00000276844 T416T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MA-01A-11D-A20W-10 chr15:60741134 A>G maps to NM_024611.4 P677P. 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-DD-A3A0-01A-11D-A20W-10 chr11:34158557 T>C maps to NM_024662.2 Y732Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACA-01A-11D-A40R-10 chr17:72767892 A>C maps to NM_015654.3 P198P. 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-DD-A39X-01A-11D-A20W-10 chr11:20066857 C>T maps to ENST00000396087 L1205L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr11:20077343 T>C maps to ENST00000396087 L1581L. 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-4R-AA8I-01A-11D-A382-10 chr2:15607894 A>G maps to NM_015909.2 S637S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5C-AAPD-01A-21D-A38X-10 chr2:15651377 C>T maps to NM_015909.2 P281P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10W-01A-11D-A12Z-10 chr2:15534401 G>T maps to NM_015909.2 S1069*. 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-DD-AADP-01A-11D-A38X-10 chr2:15319164 G>A maps to NM_015909.2 R2263*. 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-2Y-A9H4-01A-11D-A382-10 chr13:36180582 C>T maps to ENST00000400445 Y2439Y. Only missense variants will be evaluated by CHASM.
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-A119-01A-11D-A12Z-10 chr13:36229064 T>C maps to ENST00000400445 C2682C. 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-ES-A2HT-01A-12D-A183-10 chr13:36046570 C>A maps to ENST00000400445 I2161I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A2QR-01A-11D-A20W-10 chr13:36046642 T>C maps to ENST00000400445 D2185D. 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-DD-AACF-01A-11D-A40R-10 chr2:204078360 T>C maps to NM_001114132.1 V2656V. Only missense variants will be evaluated by CHASM.
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-2Y-A9GT-01A-11D-A382-10 chr3:47046578 A>C maps to NM_015175.1 R2138R. 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-DD-AADS-01A-11D-A40R-10 chr3:47044766 C>T maps to NM_015175.1 L1896L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr3:47040567 G>T maps to NM_015175.1 R1168R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WX-AA44-01A-11D-A38X-10 chr3:47049822 A>G maps to NM_015175.1 A2590A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADO-01A-11D-A40R-10 chr8:90996752 C>A maps to NM_002485.4 G13*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CG-01A-11D-A20W-10 chr8:90960117 T>C maps to NM_002485.4 Q616Q. 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-DD-AACL-01A-11D-A40R-10 chr1:21799873 G>T maps to NM_032264.2 E246*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A2QR-01A-11D-A20W-10 chr8:102731719 T>C maps to NM_032041.2 E46E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9GX-01A-11D-A382-10 chr11:113075221 C>A maps to ENST00000316851 I113I. 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-CC-A3MB-01A-11D-A20W-10 chr11:134072726 T>C maps to NM_015261.2 E533E. 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-G3-A3CG-01A-11D-A20W-10 chr11:134072792 G>A maps to NM_015261.2 S511S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A1-01A-11D-A20W-10 chr4:17839330 T>C maps to NM_022346.3 A791A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADN-01A-11D-A40R-10 chr4:17829967 C>A maps to NM_022346.3 S574*. 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-DD-A3A0-01A-11D-A20W-10 chr9:100429053 T>C maps to NM_002486.4 V637V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAEA-01A-11D-A40R-10 chr9:100431135 T>C maps to NM_002486.4 D675D. 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-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-DD-AAVU-01A-11D-A40R-10 chr22:37272067 T>A maps to NM_013416.3 L334*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr2:106498260 G>A maps to NM_001004720.2 W235*. 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-ED-A97K-01A-21D-A382-10 chr2:133541515 G>A maps to NM_207363.2 S956S. 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-FV-A2QR-01A-11D-A20W-10 chr12:50189185 A>G maps to NM_001037806.3 P819P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr2:232325389 C>T maps to NM_005381.2 E267E. 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-AAV0-01A-11D-A36X-10 chr2:24929658 T>C maps to NM_003743.4 S440S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9H9-01A-21D-A38X-10 chr8:71037077 T>C maps to NM_006540.2 P1313P. 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-ED-A8O6-01A-11D-A35Z-10 chr8:71128947 G>A maps to NM_006540.2 P11P. 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-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-A3MB-01A-11D-A20W-10 chr17:15973761 A>G maps to ENST00000395857 P1426P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IE-01A-21D-A382-10 chr17:15976835 C>A maps to ENST00000395857 E1256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CG-01A-11D-A20W-10 chr17:15935795 G>C maps to ENST00000395857 G2393G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADN-01A-11D-A40R-10 chr19:55417691 C>T maps to NM_004829.5 Q24*. 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-AACL-01A-11D-A40R-10 chr6:41309623 A>T maps to NM_004828.3 R163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A3KG-01A-11D-A20W-10 chr18:2578923 A>G did not map to a codon.
Sequencing variant TCGA-DD-AAD0-01A-11D-A40R-10 chr15:23932088 C>A maps to NM_002487.2 P92P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr9:140109379 G>A maps to NM_001144026.1 L325L. 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-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-DD-A1EG-01A-11D-A20W-10 chr4:119035959 G>A did not map to a codon.
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-DD-AADB-01A-11D-A40R-10 chr4:115754811 G>T maps to NM_022569.1 V782V. 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-EP-A2KB-01A-11D-A183-10 chr15:41689119 A>G maps to NM_016013.2 P46P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A0-01A-11D-A20W-10 chr6:97338979 T>C maps to NM_014165.3 *176W. 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-DD-AAVR-01A-11D-A40R-10 chr3:120320136 G>A maps to NM_001168331.1 E120E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MB-01A-11D-A20W-10 chr2:207008849 G>A maps to ENST00000455934 A307A. 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-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-DD-A3A0-01A-11D-A20W-10 chr21:44323562 A>G maps to NM_021075.3 K147K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-AAV2-01A-11D-A36X-10 chr21:44324121 C>T maps to NM_021075.3 L334L. 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-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-A1EG-01A-11D-A20W-10 chr2:152424932 T>A did not map to a codon.
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-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-DD-AACI-01A-11D-A40R-10 chr10:21169806 A>T maps to ENST00000430741 A132A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr10:21104613 G>T maps to ENST00000430741 T727T. Only missense variants will be evaluated by CHASM.
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-DD-AAE9-01A-11D-A40R-10 chr8:91836942 A>T did not map to a codon.
Sequencing variant TCGA-2Y-A9GT-01A-11D-A382-10 chr1:16767318 C>T maps to NM_018090.4 I21I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A0-01A-11D-A20W-10 chr12:97328851 T>C maps to NM_001135175.1 S203S. 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-BC-A3KF-01A-11D-A20W-10 chr18:56008983 T>C maps to NM_001144967.1 P444P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACZ-01A-11D-A40R-10 chr18:56056333 C>T maps to NM_001144967.1 L855L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADI-01A-11D-A40R-10 chr18:56034977 G>A maps to NM_001144967.1 T688T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAEK-01A-11D-A40R-10 chr18:56001067 A>C maps to NM_001144967.1 R337R. 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-DD-AACW-01A-11D-A40R-10 chr22:29885875 G>A maps to NM_021076.3 K749K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADI-01A-11D-A40R-10 chr22:29885647 A>G maps to NM_021076.3 E673E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADI-01A-11D-A40R-10 chr22:29885650 A>C maps to NM_021076.3 A674A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAEG-01A-11D-A38X-10 chr22:29885650 A>C maps to NM_021076.3 A674A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAEH-01A-11D-A40R-10 chr22:29885647 A>G maps to NM_021076.3 E673E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAEH-01A-11D-A40R-10 chr22:29885650 A>C maps to NM_021076.3 A674A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADM-01A-11D-A40R-10 chr1:72748048 C>A maps to NM_173808.2 A43A. 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-G3-A3CG-01A-11D-A20W-10 chr15:75641527 A>G maps to NM_024608.2 P94P. 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-G3-A3CG-01A-11D-A20W-10 chr4:170502054 T>C did not map to a codon.
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-DD-AACL-01A-11D-A40R-10 chr3:52794924 A>G maps to NM_003157.4 N283N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9H5-01A-11D-A382-10 chr9:127074819 G>A maps to NM_001166171.1 S75S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9H9-01A-21D-A38X-10 chr9:127089632 C>T maps to NM_001166171.1 N211N. 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-4R-AA8I-01A-11D-A382-10 chr11:21135202 T>C maps to NM_006157.3 L457L. 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-CC-A3MB-01A-11D-A20W-10 chr11:20940816 T>C maps to NM_006157.3 D232D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EG-01A-11D-A20W-10 chr15:73470685 A>G maps to NM_002499.3 S403S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XR-A8TF-01A-11D-A35Z-10 chr15:73541946 T>G maps to NM_002499.3 S593S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACI-01A-11D-A40R-10 chr1:156640721 T>A maps to NM_006617.1 S1086S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WQ-A9G7-01A-11D-A36X-10 chr1:156640019 C>T maps to NM_006617.1 R1320R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZS-A9CG-01A-11D-A36X-10 chr1:156639239 C>T maps to NM_006617.1 Q1580Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACP-01A-11D-A40R-10 chr18:70526061 A>T maps to NM_153181.2 P155P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAEA-01A-11D-A40R-10 chr18:70532097 A>G maps to NM_153181.2 S54S. 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-AAEI-01A-11D-A40R-10 chr2:242758031 G>A maps to NM_001167599.1 P384P. 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-ES-A2HT-01A-12D-A183-10 chr12:55420694 C>T maps to NM_021191.2 L158L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39Z-01A-11D-A20W-10 chr17:29559882 T>C maps to NM_001042492.2 G1160G. 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-DD-A1EE-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-DD-A119-01A-11D-A12Z-10 chr1:204937943 A>G maps to ENST00000367172 A279A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACL-01A-11D-A40R-10 chr1:204923313 A>T did not map to a codon.
Sequencing variant TCGA-WJ-A86L-01A-12D-A45V-10 chr16:69727753 C>T maps to NM_138713.2 P1342P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A8HT-01A-11D-A35Z-10 chr18:77170793 G>T maps to NM_172387.1 P160P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADI-01A-11D-A40R-10 chr20:50158975 C>T maps to NM_012340.3 G21G. 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-DD-A119-01A-11D-A12Z-10 chr17:46136183 T>C maps to ENST00000362042 S519S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9H3-01A-11D-A382-10 chr7:26224236 C>T maps to NM_004289.6 Q307*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9HA-01A-11D-A38X-10 chr7:26224373 T>G maps to NM_004289.6 P352P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr19:3381966 C>T maps to ENST00000269778 I96I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr4:103498146 T>G maps to NM_003998.3 P174P. 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-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-FV-A2QR-01A-11D-A20W-10 chr8:145659588 G>A maps to NM_013432.4 A1053A. 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-AACF-01A-11D-A40R-10 chr11:129754015 A>G maps to NM_006165.3 S280S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADE-01A-11D-A40R-10 chr11:129745335 C>T maps to NM_006165.3 L615L. 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-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-A5SI-01A-31D-A27I-10 chr9:33295193 C>T maps to NM_002504.4 R268*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAVR-01A-11D-A40R-10 chr4:47850262 G>A maps to NM_152995.4 Q885*. 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-2Y-A9GY-01A-11D-A382-10 chr2:233759596 C>T maps to NM_019850.2 A286A. 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-AAEG-01A-11D-A38X-10 chr17:47590067 A>T did not map to a codon.
Sequencing variant TCGA-DD-AAVR-01A-11D-A40R-10 chr17:47590142 C>T maps to NM_002507.3 N352N. 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-A4NF-01A-11D-A27I-10 chr4:103912817 T>C maps to NM_139173.3 Q17Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr4:103822468 A>T maps to NM_139173.3 A451A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A7SH-01A-11D-A382-10 chr4:103987526 C>T maps to NM_178833.4 L76L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACZ-01A-11D-A40R-10 chr1:116380918 G>A maps to NM_005599.3 G25G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BD-A3EP-01A-11D-A22F-10 chr10:115644137 A>G maps to NM_198514.3 S346S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAEB-01A-11D-A40R-10 chr13:39613819 A>G maps to NM_001012754.2 Q119Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAED-01A-12D-A40R-10 chr22:42071124 G>A maps to ENST00000402458 L71L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5R-AAAM-01A-12D-A40R-10 chr23:17743755 A>G 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-DD-AACF-01A-11D-A40R-10 chr23:17746243 T>G did not map to a codon.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr23:17745287 C>A 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-DD-A39Z-01A-11D-A20W-10 chr23:71358562 T>C did not map to a codon.
Sequencing variant TCGA-DD-AADB-01A-11D-A40R-10 chr23:71358361 C>A did not map to a codon.
Sequencing variant TCGA-G3-A3CJ-01A-11D-A20W-10 chr23:71359403 T>C did not map to a codon.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr1:236228259 T>C maps to NM_002508.2 G40G. Only missense variants will be evaluated by CHASM.
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-AACE-01A-11D-A40R-10 chr14:52520492 T>C maps to NM_007361.3 P411P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADA-01A-11D-A40R-10 chr14:52485914 G>A maps to NM_007361.3 D964D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr20:25498458 A>G maps to NM_025176.4 G69G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAD5-01A-11D-A40R-10 chr15:23086387 C>A maps to NM_144599.4 A8A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WJ-A86L-01A-12D-A45V-10 chr15:23049158 G>A maps to NM_144599.4 N220N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9GX-01A-11D-A382-10 chr8:99208233 C>G did not map to a codon.
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-DD-AACL-01A-11D-A40R-10 chr5:37049312 G>A maps to NM_133433.3 E2288E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAD0-01A-11D-A40R-10 chr5:36971137 C>T maps to NM_133433.3 D257D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAD1-01A-11D-A40R-10 chr5:37048673 A>G maps to NM_133433.3 L2220L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADO-01A-11D-A40R-10 chr5:36986167 G>A maps to NM_133433.3 K962K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A2QR-01A-11D-A20W-10 chr5:37063995 A>G maps to NM_133433.3 G2655G. 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-BC-A3KG-01A-11D-A20W-10 chr1:161088599 T>C maps to NM_005600.2 P9P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACF-01A-11D-A40R-10 chr8:63161676 G>T maps to NM_173688.2 A15A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr8:63492102 A>G maps to NM_173688.2 S20S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9H8-01A-11D-A38X-10 chr23:119077492 T>C did not map to a codon.
Sequencing variant TCGA-CC-A3MA-01A-11D-A20W-10 chr23:119068492 T>C did not map to a codon.
Sequencing variant TCGA-G3-A3CG-01A-11D-A20W-10 chr23:119059317 G>T did not map to a codon.
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-ES-A2HS-01A-11D-A183-10 chr6:28227460 A>G maps to NM_001007531.1 E104E. 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-A1ED-01A-11D-A152-10 chr23:118724382 T>C did not map to a codon.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr23:118725225 T>C did not map to a codon.
Sequencing variant TCGA-2Y-A9H5-01A-11D-A382-10 chr10:101295219 C>A maps to NM_145285.2 A279A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EE-01A-11D-A12Z-10 chr17:33469090 A>G maps to NM_018096.3 D23D. 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-DD-AAD8-01A-11D-A40R-10 chr17:7318991 T>G maps to NM_020795.2 G400G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A8HT-01A-11D-A35Z-10 chr23:70375179 G>C 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-2Y-A9H2-01A-12D-A382-10 chr23:5821284 G>T did not map to a codon.
Sequencing variant TCGA-2Y-A9HB-01A-11D-A38X-10 chr23:5811118 C>A 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-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-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-DD-AADY-01A-11D-A40R-10 chr23:6069246 C>G 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-4R-AA8I-01A-11D-A382-10 chr24:16942178 G>A did not map to a codon.
Sequencing variant TCGA-DD-AAW3-01A-11D-A40P-10 chr24:16942169 G>T 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-FV-A2QR-01A-11D-A20W-10 chr16:3602249 T>C maps to ENST00000448023 G813G. 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-A3A0-01A-11D-A20W-10 chr16:57063747 A>G maps to NM_032206.3 L769L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A1-01A-11D-A20W-10 chr16:57060297 T>C maps to NM_032206.3 A481A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr16:57113153 T>C maps to NM_032206.3 A1729A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADP-01A-11D-A38X-10 chr17:5463295 C>T maps to NM_033004.3 T240T. 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-G3-AAV6-01A-21D-A36X-10 chr19:56320850 A>T maps to NM_145007.3 A375A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9H9-01A-21D-A38X-10 chr19:54314218 G>A maps to ENST00000391773 L232L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A8HT-01A-11D-A35Z-10 chr19:54313286 G>A maps to ENST00000391773 T542T. 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-EP-A2KA-01A-11D-A183-10 chr11:7091660 T>C maps to NM_176822.3 S1040S. 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-DD-AADF-01A-11D-A40R-10 chr19:55495066 T>A maps to NM_017852.3 T667T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr19:55497648 T>C maps to NM_017852.3 L778L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-AA0U-01A-11D-A382-10 chr1:247607348 G>A maps to NM_004895.4 T915T. 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-CC-A8HS-01A-11D-A35Z-10 chr19:56539530 C>T maps to NM_153447.4 D644D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACL-01A-11D-A40R-10 chr19:56520163 A>T maps to NM_153447.4 P151P. 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-5R-AA1D-01A-11D-A382-10 chr11:281191 G>T maps to NM_138329.1 P486P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-AA0U-01A-11D-A382-10 chr11:280375 G>A maps to NM_138329.1 K214K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39Y-01A-11D-A20W-10 chr19:55445100 T>C maps to ENST00000446217 E854E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADL-01A-11D-A40R-10 chr19:55451283 C>A maps to ENST00000446217 T329T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9GU-01A-11D-A382-10 chr19:56244025 G>A maps to NM_176820.2 R391*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr19:56244025 G>T maps to NM_176820.2 R391R. 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 chr15:85200577 A>G maps to NM_205858.1 G53G. 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-DD-A39X-01A-11D-A20W-10 chr3:160968076 A>G maps to ENST00000472947 E448E. 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-AADF-01A-11D-A40R-10 chr2:101096961 C>A maps to NM_001011717.1 S114*. 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-DD-AADE-01A-11D-A40R-10 chr2:232390062 T>C maps to NM_006056.4 S324S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACH-01A-11D-A40R-10 chr5:151784455 G>A maps to NM_020167.4 H73H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39Z-01A-11D-A20W-10 chr5:43628310 T>C maps to NM_182977.2 A262A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAEB-01A-11D-A40R-10 chr5:43650681 C>T maps to NM_182977.2 N570N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACL-01A-11D-A40R-10 chr10:96116931 T>A maps to NM_022451.9 P169P. 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-YA-A8S7-01A-11D-A36X-10 chr10:72195098 G>A maps to NM_018055.4 G278G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AA3A-01A-11D-A36X-10 chr22:38083916 G>T maps to NM_024313.2 R28R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MA-01A-11D-A33Q-10 chr16:67208999 G>A maps to NM_001185057.1 *220*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9H9-01A-21D-A38X-10 chr18:31599307 G>A maps to NM_003787.4 R344*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A8HT-01A-11D-A35Z-10 chr18:31709984 C>A did not map to a codon.
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-G3-AAV0-01A-11D-A36X-10 chr7:156743033 G>A maps to NM_138400.1 K201K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9GU-01A-11D-A382-10 chr23:70517736 A>C did not map to a codon.
Sequencing variant TCGA-2Y-A9GU-01A-11D-A382-10 chr23:70517752 C>T did not map to a codon.
Sequencing variant TCGA-DD-AAW2-01A-11D-A40P-10 chr20:2635440 G>A maps to NM_006392.2 L139L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BD-A3EP-01A-11D-A22F-10 chr12:117726018 C>A maps to ENST00000338101 T329T. Only missense variants will be evaluated by CHASM.
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.
Sequencing variant TCGA-CC-A7IE-01A-21D-A382-10 chr1:162336962 T>C maps to NM_014697.2 A409A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IE-01A-21D-A382-10 chr17:26096595 C>T maps to NM_000625.4 S608S. 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-DD-AAD6-01A-11D-A40R-10 chr19:50060188 G>A maps to NM_015953.3 P160P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAC8-01A-11D-A40R-10 chr2:169688004 A>T maps to NM_001171631.1 T122T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BW-A5NP-01A-11D-A27I-10 chr9:139395192 G>A maps to NM_017617.3 Y1915Y. 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-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-DD-A4ND-01A-11D-A25V-10 chr19:15291636 C>A maps to NM_000435.2 T999T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr19:15281633 G>T maps to NM_000435.2 S1580*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr19:15297799 C>A did not map to a codon.
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-CC-A3MA-01A-11D-A20W-10 chr6:32187546 A>G maps to NM_004557.3 S444S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A1-01A-11D-A20W-10 chr6:32188845 T>C maps to NM_004557.3 G236G. Only missense variants will be evaluated by CHASM.
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-DD-AACZ-01A-11D-A40R-10 chr6:32180405 T>A did not map to a codon.
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-DD-AAVP-01A-11D-A40R-10 chr17:79914894 T>A maps to NM_178493.5 K251*. 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-G3-AAV5-01A-11D-A36X-10 chr14:27064669 G>A maps to ENST00000449198 Q93*. 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-ES-A2HT-01A-12D-A183-10 chr19:46444041 G>A maps to NM_002516.2 P186P. 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-DD-A119-01A-11D-A12Z-10 chr6:155750088 T>C maps to NM_015718.2 P328P. 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-DD-A39Y-01A-11D-A20W-10 chr15:69331258 T>C maps to NM_024505.3 Y478Y. 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-DD-AAVS-01A-11D-A40R-10 chr14:34269936 G>A maps to NM_001164749.1 R808R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LG-A9QD-01A-11D-A382-10 chr11:108047093 T>A maps to NM_002519.2 T337T. 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-EP-A2KA-01A-11D-A183-10 chr18:21120465 G>T maps to NM_000271.4 I850I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9HB-01A-11D-A38X-10 chr7:44575495 G>A maps to NM_013389.2 V642V. 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-DD-AADA-01A-11D-A40R-10 chr7:44555417 G>A maps to NM_013389.2 V1287V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr7:44555531 A>G maps to NM_013389.2 P1249P. 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-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-DD-A119-01A-11D-A12Z-10 chr17:45679094 A>G maps to NM_006310.3 K574K. 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-DD-AADG-01A-11D-A40R-10 chr1:6029259 G>A maps to NM_015102.2 V113V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZP-A9D1-01A-11D-A382-10 chr1:5927957 T>G did not map to a codon.
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-AAC8-01A-11D-A40R-10 chr1:179530442 A>T maps to NM_014625.2 P144P. 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 chr5:170827198 A>G maps to NM_002520.6 K189K. 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-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-BD-A3ER-01A-11D-A20W-10 chr5:32724926 G>T did not map to a codon.
Sequencing variant TCGA-NI-A8LF-01A-11D-A35Z-10 chr5:32711929 C>T maps to ENST00000265074 G16G. 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-2Y-A9GZ-01A-11D-A38X-10 chr4:164246910 C>G did not map to a codon.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr4:164272693 T>C maps to NM_006174.2 I423I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9HA-01A-11D-A38X-10 chr23:30327146 C>T did not map to a codon.
Sequencing variant TCGA-2Y-A9HB-01A-11D-A38X-10 chr23:30327259 G>T did not map to a codon.
Sequencing variant TCGA-DD-AAD1-01A-11D-A40R-10 chr23:30327406 G>A did not map to a codon.
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-DD-AADE-01A-11D-A40R-10 chr19:50885831 G>C maps to NM_007121.4 L452L. 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-G3-AAUZ-01A-11D-A382-10 chr3:119530468 G>T maps to NM_022002.2 G178*. 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-4R-AA8I-01A-11D-A382-10 chr3:15057747 C>T maps to NM_003298.3 G140G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A8YO-01A-11D-A36X-10 chr6:108502143 C>A maps to ENST00000368983 I328I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A8O6-01A-11D-A35Z-10 chr6:108492695 C>T maps to ENST00000368983 G57G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr6:108497812 G>A maps to ENST00000368983 S159S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADB-01A-11D-A40R-10 chr5:142680244 T>A maps to NM_001024094.1 K519*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACK-01A-11D-A40R-10 chr4:149357528 T>A maps to ENST00000511528 R162*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADC-01A-11D-A40R-10 chr4:149115895 C>A did not map to a codon.
Sequencing variant TCGA-DD-AADU-01A-11D-A40R-10 chr12:52452484 G>A maps to ENST00000360284 L572L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACX-01A-11D-A40R-10 chr9:127253384 G>A maps to NM_004959.4 L371L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5R-AAAM-01A-12D-A40R-10 chr1:200008802 C>T maps to NM_205860.1 R28*. 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-BC-A3KG-01A-11D-A20W-10 chr10:115401183 T>C maps to ENST00000369358 E421E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADO-01A-11D-A40R-10 chr10:115372163 G>A maps to ENST00000369358 H1117H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACE-01A-11D-A40R-10 chr1:115256599 C>T did not map to a codon.
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-DD-A1EE-01A-11D-A12Z-10 chr1:52254982 A>G maps to NM_002525.2 C1195C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAE7-01A-11D-A40R-10 chr1:52281990 T>G maps to NM_002525.2 R546R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-AAV1-01A-11D-A382-10 chr8:32505643 G>A maps to NM_013959.3 S136S. 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-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-A39X-01A-11D-A20W-10 chr21:16339694 T>C maps to NM_003489.3 E273E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr21:16337048 T>C maps to NM_003489.3 K1155K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39Y-01A-11D-A20W-10 chr23:105153616 T>C 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-DD-AADI-01A-11D-A40R-10 chr23:105197131 G>A did not map to a codon.
Sequencing variant TCGA-DD-AAVX-01A-11D-A40R-10 chr6:30656497 C>A maps to NM_007243.1 R243R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5C-A9VG-01A-11D-A36X-10 chr16:67920014 C>A maps to NM_198443.1 A117A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAVS-01A-11D-A40R-10 chr10:33510746 T>C maps to NM_003873.5 V394V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACI-01A-11D-A40R-10 chr2:206641000 A>T maps to NM_018534.3 T824T. Only missense variants will be evaluated by CHASM.
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-DD-AAC8-01A-11D-A40R-10 chr20:333978 A>T maps to NM_024958.2 A105A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A8O6-01A-11D-A35Z-10 chr20:330325 C>T maps to NM_024958.2 R13R. 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-DD-AAD5-01A-11D-A40R-10 chr2:51255332 G>A maps to ENST00000404971 L27L. 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-ED-A97K-01A-21D-A382-10 chr2:51254751 G>A maps to ENST00000404971 G220G. 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-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-DD-AACK-01A-11D-A40R-10 chr14:79432392 T>G maps to NM_004796.4 R434R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACP-01A-11D-A40R-10 chr14:79746795 G>A maps to ENST00000440563 Q54Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZP-A9D0-01A-11D-A36X-10 chr14:80271456 A>G maps to NM_004796.4 P936P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9H1-01A-11D-A382-10 chr5:176721058 A>G maps to NM_022455.4 P2230P. 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-WQ-A9G7-01A-11D-A36X-10 chr17:44803928 G>A maps to NM_006178.2 A592A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A9FW-01A-11D-A36X-10 chr20:1447367 C>T maps to ENST00000476071 L34L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr8:59520363 G>T maps to NM_001144772.1 R272R. Only missense variants will be evaluated by CHASM.
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-DD-A4NF-01A-11D-A27I-10 chr3:93812982 G>T did not map to a codon.
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-DD-AADO-01A-11D-A40R-10 chr2:18765410 A>T maps to ENST00000455492 Y355*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A3KF-01A-11D-A20W-10 chr3:52558486 C>A maps to NM_001134231.1 *558L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAE7-01A-11D-A40R-10 chr6:86194983 G>T maps to NM_002526.2 G261G. 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-DD-AACI-01A-11D-A40R-10 chr11:132081913 A>T did not map to a codon.
Sequencing variant TCGA-G3-AAV2-01A-11D-A36X-10 chr16:2522556 C>T maps to NM_006181.1 C285C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr1:108023281 C>T maps to NM_001113226.1 C480C. 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-AACQ-01A-11D-A40R-10 chr1:156838009 G>A maps to NM_002529.3 G181G. 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-DD-A39X-01A-11D-A20W-10 chr9:87475991 A>G maps to NM_006180.3 R478R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACJ-01A-11D-A40R-10 chr9:87635233 T>A maps to NM_006180.3 I762I. 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-AACY-01A-11D-A40R-10 chr15:88670419 G>C maps to NM_001012338.1 T422T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAE3-01A-11D-A40R-10 chr15:88690617 G>T maps to NM_001012338.1 R138R. 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-2Y-A9H4-01A-11D-A382-10 chr2:11798628 C>T maps to NM_012344.3 G403G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XR-A8TF-01A-11D-A35Z-10 chr2:11809667 C>A maps to NM_012344.3 V196V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACB-01A-11D-A40R-10 chr1:205277741 C>A maps to ENST00000441520 R201R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A0-01A-11D-A20W-10 chr14:32142558 A>C did not map to a codon.
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-DD-AAE2-01A-11D-A40R-10 chr19:49407701 G>A maps to NM_006184.5 E78E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr11:17352476 T>A maps to ENST00000458064 L401*. 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-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-FV-A496-01A-11D-A25V-10 chr13:48611930 G>T maps to NM_018283.1 G17*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr10:12219830 G>T maps to ENST00000378937 R97R. 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-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-A3A1-01A-11D-A20W-10 chr14:73743384 C>T maps to NM_001005743.1 Q619Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADO-01A-11D-A40R-10 chr14:73750977 C>A maps to NM_001005743.1 E254*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CJ-01A-11D-A20W-10 chr14:73822378 T>C maps to NM_001005743.1 T27T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9HA-01A-11D-A38X-10 chr1:229631722 C>T maps to NM_018230.2 W297*. 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-G3-AAV4-01A-11D-A382-10 chr1:229641904 C>T maps to NM_018230.2 R61R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACQ-01A-11D-A40R-10 chr6:17616801 C>A maps to ENST00000430136 S1464S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WQ-A9G7-01A-11D-A36X-10 chr6:17629462 T>C maps to ENST00000430136 L1020L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5C-A9VG-01A-11D-A36X-10 chr5:37352899 C>A maps to NM_153485.1 L165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADG-01A-11D-A40R-10 chr5:37302982 T>C maps to NM_153485.1 L1115L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACT-01A-11D-A40R-10 chr11:47823483 T>C did not map to a codon.
Sequencing variant TCGA-BW-A5NO-01A-11D-A27I-10 chr9:131764255 G>A did not map to a codon.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr9:131750463 T>C maps to NM_015354.1 H844H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CJ-01A-11D-A20W-10 chr9:131745769 T>C maps to NM_015354.1 R634R. Only missense variants will be evaluated by CHASM.
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-EP-A2KA-01A-11D-A183-10 chr3:13429808 G>T maps to NM_024923.2 V226V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr3:13364884 G>A maps to NM_024923.2 P1564P. 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-DD-AA3A-01A-11D-A36X-10 chr1:154062057 G>A maps to NM_207308.2 R734*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9H1-01A-11D-A382-10 chr9:134073495 A>T maps to ENST00000451030 K1540*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39Y-01A-11D-A20W-10 chr9:134015960 T>C maps to ENST00000451030 A386A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACF-01A-11D-A40R-10 chr9:134073950 T>G maps to ENST00000451030 T1691T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACJ-01A-11D-A40R-10 chr2:184022186 T>A maps to NM_138285.3 S185S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39Z-01A-11D-A20W-10 chr12:102470581 A>G maps to NM_024057.2 L256L. 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-G3-A3CJ-01A-11D-A20W-10 chr23:106396416 T>C did not map to a codon.
Sequencing variant TCGA-G3-A3CJ-01A-11D-A20W-10 chr23:106410963 T>C did not map to a codon.
Sequencing variant TCGA-BC-A3KG-01A-11D-A20W-10 chr17:73205984 T>C maps to NM_024844.3 S65S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr17:5317450 G>T maps to NM_002532.3 T157T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1ED-01A-11D-A152-10 chr16:56852598 A>G maps to NM_014669.3 G171G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr16:56868678 G>T maps to NM_014669.3 G591*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAEK-01A-11D-A40R-10 chr11:3744591 G>T maps to NM_016320.4 A647A. 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-DD-AAD0-01A-11D-A40R-10 chr15:41657597 A>T did not map to a codon.
Sequencing variant TCGA-DD-AADR-01A-11D-A40R-10 chr1:224415336 G>A maps to NM_002533.2 L854L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr1:224475674 C>A maps to NM_002533.2 L532L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAE6-01A-11D-A40R-10 chr11:62563803 C>A maps to NM_006362.4 E434*. Only missense variants will be evaluated by CHASM.
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-A119-01A-11D-A12Z-10 chr23:102339710 A>G 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-AAC8-01A-11D-A40R-10 chr23:102338423 A>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-ZP-A9CZ-01A-11D-A382-10 chr23:101092558 A>T did not map to a codon.
Sequencing variant TCGA-DD-AACQ-01A-11D-A40R-10 chr17:722715 G>C maps to NM_022463.3 A261A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A496-01A-11D-A25V-10 chr17:704278 G>T maps to NM_022463.3 Y406*. Only missense variants will be evaluated by CHASM.
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-AADQ-01A-11D-A40R-10 chr2:139429157 C>T maps to NM_007226.2 L43L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr23:108779153 G>T did not map to a codon.
Sequencing variant TCGA-WQ-A9G7-01A-11D-A36X-10 chr14:24877346 T>C maps to NM_025081.2 A157A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9H4-01A-11D-A382-10 chr11:120082154 C>T maps to NM_178507.2 S56S. 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-ES-A2HS-01A-11D-A183-10 chr12:113354433 T>C maps to NM_001032409.1 L259L. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-DD-AADQ-01A-11D-A40R-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-2Y-A9GS-01A-12D-A382-10 chr1:228506636 C>A maps to NM_001098623.1 P4728P. 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-A8HT-01A-11D-A35Z-10 chr1:228503671 C>G maps to NM_001098623.1 P4379P. 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-A1EE-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-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-DD-AADB-01A-11D-A40R-10 chr1:228399588 T>G maps to NM_001098623.1 G35G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAVP-01A-11D-A40R-10 chr1:228496076 C>A maps to NM_001098623.1 T4244T. 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-A119-01A-11D-A12Z-10 chr2:220432975 T>C maps to NM_015311.2 E361E. 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-NI-A8LF-01A-11D-A35Z-10 chr4:48901943 T>C did not map to a codon.
Sequencing variant TCGA-2V-A95S-01A-11D-A36X-10 chr23:128694556 C>A did not map to a codon.
Sequencing variant TCGA-CC-A3MA-01A-11D-A20W-10 chr23:128695174 A>G did not map to a codon.
Sequencing variant TCGA-DD-A1EE-01A-11D-A12Z-10 chr23:128722191 C>T 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-WQ-A9G7-01A-11D-A36X-10 chr23:128701326 C>T did not map to a codon.
Sequencing variant TCGA-2Y-A9H1-01A-11D-A382-10 chr8:103572892 G>A maps to NM_024410.3 P178P. Only missense variants will be evaluated by CHASM.
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-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-2Y-A9H3-01A-11D-A382-10 chr23:123526163 T>A did not map to a codon.
Sequencing variant TCGA-2Y-A9H5-01A-11D-A382-10 chr23:123517914 T>G did not map to a codon.
Sequencing variant TCGA-5R-AAAM-01A-12D-A40R-10 chr23:123514878 T>C did not map to a codon.
Sequencing variant TCGA-DD-A1EF-01A-11D-A12Z-10 chr23:123517525 A>T did not map to a codon.
Sequencing variant TCGA-DD-A39Z-01A-11D-A20W-10 chr23:123654549 G>A did not map to a codon.
Sequencing variant TCGA-DD-A73G-01A-22D-A32G-10 chr23:123680737 C>T did not map to a codon.
Sequencing variant TCGA-DD-AACA-01A-11D-A40R-10 chr23:123514833 T>A did not map to a codon.
Sequencing variant TCGA-DD-AAD0-01A-11D-A40R-10 chr23:123870897 G>T did not map to a codon.
Sequencing variant TCGA-RC-A6M6-01A-11D-A32G-10 chr23:123540197 C>T did not map to a codon.
Sequencing variant TCGA-WQ-A9G7-01A-11D-A36X-10 chr23:123517730 G>A did not map to a codon.
Sequencing variant TCGA-CC-A3MA-01A-11D-A20W-10 chr5:167689610 C>G maps to NM_001122679.1 A2698A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A115-01A-11D-A12Z-10 chr5:166711892 C>T maps to NM_001122679.1 G17G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EG-01A-11D-A20W-10 chr5:167553852 C>T maps to NM_001122679.1 R768R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A7-01A-11D-A22F-10 chr5:167420041 C>G maps to NM_001122679.1 P347P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACM-01A-11D-A40R-10 chr4:183721164 C>T maps to NM_001080477.1 N2587N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAE3-01A-11D-A40R-10 chr4:183721240 C>T maps to NM_001080477.1 L2613L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr4:183651370 A>G maps to NM_001080477.1 R868R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr4:183549875 A>T maps to NM_001080477.1 A274A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XR-A8TG-01A-11D-A35Z-10 chr4:183721245 C>T maps to NM_001080477.1 D2614D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MB-01A-11D-A20W-10 chr11:78467980 A>G maps to NM_001098816.2 P875P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACS-01A-11D-A40R-10 chr11:78387280 G>A maps to NM_001098816.2 I1804I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADQ-01A-11D-A40R-10 chr11:78525436 G>T maps to NM_001098816.2 S562*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr11:78437178 C>A maps to NM_001098816.2 A1165A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CG-01A-11D-A20W-10 chr11:78482150 T>A maps to NM_001098816.2 R809*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75I-01A-11D-A32G-10 chr11:78369306 C>G maps to NM_001098816.2 A2702A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-AAV7-01A-11D-A382-10 chr23:13778503 C>G did not map to a codon.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr7:44687302 T>C maps to ENST00000444676 D154D. Only missense variants will be evaluated by CHASM.
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-AACG-01A-11D-A40R-10 chr20:61443980 G>T maps to NM_007346.2 G338G. 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-G3-A3CJ-01A-11D-A20W-10 chr23:70775861 A>G did not map to a codon.
Sequencing variant TCGA-BC-A10W-01A-11D-A12Z-10 chr2:174945975 A>G maps to ENST00000409546 S310S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAVU-01A-11D-A40R-10 chr19:9968429 G>A maps to NM_058164.2 L107L. 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-5C-A9VG-01A-11D-A36X-10 chr13:53603060 C>A maps to NM_006418.3 P30P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5C-A9VH-01A-11D-A36X-10 chr13:53608514 C>T maps to NM_006418.3 D79D. 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-2Y-A9H3-01A-11D-A382-10 chr9:127570168 C>T maps to NM_182487.2 D426D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACL-01A-11D-A40R-10 chr1:161968002 G>A maps to ENST00000451379 S363S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GJ-A9DB-01A-11D-A36X-10 chr21:34399754 C>A maps to NM_005806.2 S195S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-AAUZ-01A-11D-A382-10 chr15:53081883 T>G maps to NM_004498.1 G66G. 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-DD-AACI-01A-11D-A40R-10 chr6:74079022 G>A maps to NM_001080507.2 V92V. 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-CC-A9FS-01A-11D-A36X-10 chr3:193384161 A>G maps to NM_130837.2 Q952Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACL-01A-11D-A40R-10 chr3:193353248 A>T maps to NM_130837.2 K296*. 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-AAVV-01A-11D-A40R-10 chr8:145114665 G>A maps to ENST00000360660 Q67*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAW0-01A-11D-A40R-10 chr8:145113728 C>T maps to ENST00000360660 G178G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACL-01A-11D-A40R-10 chr10:88414683 A>C maps to NM_001030015.2 T48T. 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-DD-AACX-01A-11D-A40R-10 chr20:62729869 G>A maps to NM_000913.3 T277T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADE-01A-11D-A40R-10 chr6:154414484 T>A maps to NM_001008505.1 P415P. 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-2Y-A9H6-01A-11D-A38X-10 chr10:13154619 T>G maps to NM_021980.4 V179V. 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-DD-AAD8-01A-11D-A40R-10 chr12:55615503 T>A maps to NM_001005280.1 T232T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAE4-01A-11D-A40R-10 chr6:29408145 C>T maps to NM_013941.2 A118A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAEE-01A-11D-A40R-10 chr6:29408580 C>T maps to NM_013941.2 A263A. 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-LG-A9QD-01A-11D-A382-10 chr14:22102422 C>T maps to NM_001005466.1 L192L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADW-01A-11D-A38X-10 chr11:123886337 A>T maps to ENST00000375021 P19P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XR-A8TD-01A-12D-A38X-10 chr11:123886313 C>T maps to ENST00000375021 I11I. 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-CC-A8HT-01A-11D-A35Z-10 chr11:123893760 C>A maps to NM_001001953.1 G14G. 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-DD-AADI-01A-11D-A40R-10 chr19:15918066 G>A maps to NM_013940.2 L261L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A0-01A-11D-A20W-10 chr19:15838972 G>A maps to NM_013939.2 L40L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CJ-01A-11D-A20W-10 chr19:15838972 G>A maps to NM_013939.2 L40L. 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-DD-A1EG-01A-11D-A20W-10 chr12:56031280 A>G maps to NM_206899.1 T202T. 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-DD-AADL-01A-11D-A40R-10 chr1:158576491 G>T maps to NM_001004478.1 G88G. 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-2Y-A9H5-01A-11D-A382-10 chr6:29394995 C>A maps to NM_013937.2 R141R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BD-A3EP-01A-11D-A22F-10 chr14:20666183 C>G maps to NM_001005503.1 G230G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39X-01A-11D-A20W-10 chr14:20666183 C>G maps to NM_001005503.1 G230G. 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-AADG-01A-11D-A40R-10 chr14:20711204 C>G maps to NM_001004479.1 S85S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9HA-01A-11D-A38X-10 chr14:20692716 G>A maps to NM_001004480.1 G283G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MA-01A-11D-A20W-10 chr14:20692755 C>T maps to NM_001004480.1 Y296Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A8O5-01A-11D-A35Z-10 chr1:248004282 T>A maps to NM_001001959.1 R306*. 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-AAVV-01A-11D-A40R-10 chr9:107360935 C>A maps to NM_001004482.1 G253G. 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-2Y-A9GU-01A-11D-A382-10 chr23:130678587 C>G did not map to a codon.
Sequencing variant TCGA-LG-A9QD-01A-11D-A382-10 chr23:130678860 T>A did not map to a codon.
Sequencing variant TCGA-DD-AAW3-01A-11D-A40P-10 chr1:248512966 G>A maps to NM_001001918.1 V297V. 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-4R-AA8I-01A-11D-A382-10 chr17:3119840 G>A maps to NM_014565.2 S309S. 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-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-ZP-A9CY-01A-11D-A382-10 chr17:3336670 C>T maps to NM_003554.1 A155A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A3KF-01A-11D-A20W-10 chr16:3254974 T>C maps to NM_012360.1 S243S. 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-DD-AAVP-01A-11D-A40R-10 chr9:125239743 C>A maps to NM_001004451.1 A154A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACU-01A-11D-A40R-10 chr9:125273730 A>T maps to NM_054107.1 S217S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACX-01A-11D-A40R-10 chr9:125437749 C>A maps to NM_001005234.1 L114L. 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-DD-AACI-01A-11D-A40R-10 chr9:125316381 A>C maps to NM_001004457.1 R312R. 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-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-3K-AAZ8-01A-12D-A38X-10 chr11:6806963 G>A maps to NM_001004489.2 E232E. 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-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-DD-AADL-01A-11D-A40R-10 chr6:29054416 A>G maps to NM_001005226.2 S203S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A3KG-01A-11D-A20W-10 chr1:247695756 G>C maps to NM_198074.4 S19S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EG-01A-11D-A20W-10 chr1:247695756 G>C maps to NM_198074.4 S19S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CJ-01A-11D-A20W-10 chr1:247695756 G>C maps to NM_198074.4 S19S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAE6-01A-11D-A40R-10 chr1:247769165 T>G maps to NM_001001914.1 T93T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YA-A8S7-01A-11D-A36X-10 chr1:247768925 C>T maps to NM_001001914.1 I13I. 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-2V-A95S-01A-11D-A36X-10 chr6:29430082 C>T maps to NM_030883.3 V179V. 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-BC-A10U-01A-11D-A12Z-10 chr6:29556263 T>C maps to NM_007160.3 A181A. 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-DD-AAVW-01A-11D-A40R-10 chr6:29080266 G>T maps to NM_001005216.2 L200L. 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-ZS-A9CE-01A-11D-A36X-10 chr1:248224066 C>T maps to NM_001004687.1 I28I. 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-AAC8-01A-11D-A40R-10 chr1:248487042 T>C maps to NM_001004691.1 V276V. 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-DD-AAE6-01A-11D-A40R-10 chr1:248756757 G>A maps to NM_001004693.1 Y104Y. 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-DD-AAD1-01A-11D-A40R-10 chr1:248616772 T>A maps to NM_001004136.1 T225T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZS-A9CE-01A-11D-A36X-10 chr1:248616328 C>T maps to NM_001004136.1 I77I. 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-G3-A3CG-01A-11D-A20W-10 chr1:248436936 G>T maps to NM_001004695.1 L60L. 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-EP-A12J-01A-11D-A12Z-10 chr1:248525403 C>T maps to NM_001004696.1 L174L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CJ-01A-11D-A20W-10 chr1:248525053 C>T maps to NM_001004696.1 L58L. 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-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-BC-A3KG-01A-11D-A20W-10 chr6:29012811 A>C maps to NM_030903.3 L47L. 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-2Y-A9GU-01A-11D-A382-10 chr1:248059058 C>A maps to NM_001001957.2 T57T. 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 chr11:55135485 T>C maps to NM_001005275.1 L43L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACK-01A-11D-A40R-10 chr11:55135452 A>T maps to NM_001005275.1 K32*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A9FU-01A-11D-A36X-10 chr11:55111590 T>C maps to NM_001005274.1 S305S. 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-WQ-A9G7-01A-11D-A36X-10 chr11:49974681 T>C maps to NM_001001955.2 S236S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A1-01A-11D-A20W-10 chr11:55322069 A>G maps to NM_001001920.1 L96L. 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-DD-A1EE-01A-11D-A12Z-10 chr11:55339974 C>A maps to NM_001004701.2 I124I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9H9-01A-21D-A38X-10 chr11:48346804 A>T maps to NM_001004702.1 K105*. 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-DD-A1EE-01A-11D-A12Z-10 chr11:51516033 C>T maps to NM_001004703.1 P251P. 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-DD-A3A0-01A-11D-A20W-10 chr17:56247312 T>C maps to NM_001004707.3 G99G. 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-DD-AAE7-01A-11D-A40R-10 chr11:59282777 C>T maps to NM_001004711.1 H131H. 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-DD-AAVV-01A-11D-A40R-10 chr14:20403851 G>A maps to NM_001004063.2 V9V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr14:20502874 A>G maps to NM_001004714.1 L15L. 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-FV-A495-01A-11D-A25V-10 chr14:20586347 T>C maps to NM_001004715.1 P261P. 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-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-DD-AACF-01A-11D-A40R-10 chr14:20296044 G>A maps to NM_001004723.1 L146L. 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-DD-A39Y-01A-11D-A20W-10 chr14:20215939 C>T maps to NM_172194.1 V118V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XR-A8TG-01A-11D-A35Z-10 chr11:55418846 C>A maps to NM_001004059.2 I156I. 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-2Y-A9GZ-01A-11D-A38X-10 chr11:48266849 C>A maps to NM_001004727.1 Y65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADF-01A-11D-A40R-10 chr11:4976934 A>T maps to NM_001004748.1 I3I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADD-01A-11D-A40R-10 chr11:4967514 G>C maps to NM_001005329.1 L272L. 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-DD-AAC8-01A-11D-A40R-10 chr11:5373111 C>T maps to NM_001004750.1 R125R. 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-5C-A9VG-01A-11D-A36X-10 chr11:4936101 A>G maps to NM_001005238.1 S264S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADF-01A-11D-A40R-10 chr11:4936770 C>A maps to NM_001005238.1 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WQ-A9G7-01A-11D-A36X-10 chr11:5475290 T>C maps to NM_001004754.2 D191D. 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-CC-A8HV-01A-11D-A35Z-10 chr11:5221635 G>A maps to NM_001004760.2 R99*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A9FS-01A-11D-A36X-10 chr11:4389144 G>T maps to NM_001005161.3 A127A. 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-AACY-01A-11D-A40R-10 chr11:5799570 G>A maps to NM_001001922.2 L98L. 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-DD-AACT-01A-11D-A40R-10 chr11:5989216 T>G maps to NM_001146033.1 R170R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAE0-01A-11D-A40R-10 chr11:56409795 G>T maps to NM_001002925.1 I40I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADM-01A-11D-A40R-10 chr11:56431490 T>A maps to NM_001004730.1 A110A. 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-DD-A1ED-01A-11D-A152-10 chr11:58190476 T>C maps to NM_001005566.2 G86G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAW1-01A-11D-A40P-10 chr11:58274924 T>A maps to NM_001005218.1 I218I. 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-DD-AADU-01A-11D-A40R-10 chr11:55563594 T>A maps to NM_001004735.1 S188S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WX-AA44-01A-11D-A38X-10 chr11:55563747 C>T maps to NM_001004735.1 A239A. 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-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-DD-AAC8-01A-11D-A40R-10 chr11:55587485 T>A maps to ENST00000395203 I129I. 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-DD-AACI-01A-11D-A40R-10 chr3:97852434 A>T maps to NM_001005338.1 T298T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CG-01A-11D-A20W-10 chr3:97852335 G>A maps to NM_001005338.1 P265P. 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-3K-AAZ8-01A-12D-A38X-10 chr3:98001886 T>C maps to NM_001005482.1 A52A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAD1-01A-11D-A40R-10 chr11:55944929 G>A maps to NM_001005492.1 T279T. 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-3K-AAZ8-01A-12D-A38X-10 chr3:98072898 C>T maps to NM_001005517.1 L68L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADW-01A-11D-A38X-10 chr11:55579748 T>C maps to NM_001004738.1 D269D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-AAV0-01A-11D-A36X-10 chr11:55579060 T>A maps to NM_001004738.1 L40*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K7-AAU7-01A-11D-A382-10 chr11:55579073 C>A maps to NM_001004738.1 G44G. 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-DD-A119-01A-11D-A12Z-10 chr11:56380552 G>C maps to NM_001004740.1 V142V. 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-YA-A8S7-01A-11D-A36X-10 chr11:56344591 A>G maps to NM_001004741.1 V202V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39Y-01A-11D-A20W-10 chr11:56310223 G>T maps to NM_001005245.1 S170S. 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-AAVY-01A-11D-A40R-10 chr11:56237300 G>A maps to NM_001004742.1 R225*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZP-A9CV-01A-11D-A382-10 chr11:56237303 G>A maps to NM_001004742.1 L224L. 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-AACV-01A-11D-A40R-10 chr11:56230822 G>A maps to NM_001004743.1 Q19*. 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-DD-AADN-01A-11D-A40R-10 chr11:56185177 G>A maps to NM_001004744.1 F177F. 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-DD-AACL-01A-11D-A40R-10 chr11:56000214 T>A maps to NM_001004746.1 T149T. 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-G3-AAV5-01A-11D-A36X-10 chr11:55681632 A>G maps to NM_001001960.1 Y142Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr12:55945360 T>C maps to NM_001005494.1 S117S. 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-DD-AAC8-01A-11D-A40R-10 chr12:55886886 T>C maps to NM_001005519.1 H247H. 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-ED-A8O6-01A-11D-A35Z-10 chr12:55641388 G>T maps to NM_001005490.1 G106G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10W-01A-11D-A12Z-10 chr1:247875174 T>A maps to NM_001005286.1 K295*. 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-CC-A3MB-01A-11D-A20W-10 chr1:158669521 A>G maps to NM_001005279.1 G307G. 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-DD-AACJ-01A-11D-A40R-10 chr1:158669713 G>A maps to NM_001005279.1 V243V. 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-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-AACJ-01A-11D-A40R-10 chr1:158735539 C>T maps to NM_001005185.1 L311L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9H9-01A-21D-A38X-10 chr1:158746472 C>G maps to NM_001005278.1 *318S. 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-DD-AADG-01A-11D-A40R-10 chr11:57798663 G>C maps to NM_001005186.2 V80V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAC8-01A-11D-A40R-10 chr19:14991447 G>T maps to NM_030901.1 T240T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACX-01A-11D-A40R-10 chr19:14938489 A>C maps to NM_017506.1 A188A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A8O5-01A-11D-A35Z-10 chr19:14910798 G>A maps to NM_198944.1 C50C. 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-WQ-A9G7-01A-11D-A36X-10 chr19:9324679 G>A maps to NM_001005191.2 Y278Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A8O5-01A-11D-A35Z-10 chr19:9225701 A>T maps to ENST00000293614 S246S. 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-CC-A8HT-01A-11D-A35Z-10 chr19:9237266 A>G maps to NM_001001958.1 Y120Y. 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-GJ-A9DB-01A-11D-A36X-10 chr11:124440404 G>A maps to NM_001005194.1 L147L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3K-AAZ8-01A-12D-A38X-10 chr11:124294236 C>A maps to NM_001005196.1 L177L. 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-EP-A2KA-01A-11D-A183-10 chr11:124310837 C>T maps to NM_012378.1 L48L. 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-WJ-A86L-01A-12D-A45V-10 chr11:124310417 A>G maps to NM_012378.1 A188A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr11:124189724 A>G maps to NM_001002918.1 Y123Y. 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-CC-A9FS-01A-11D-A36X-10 chr11:124096062 G>A maps to NM_001007249.1 T222T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A9FS-01A-11D-A36X-10 chr11:56058115 G>T maps to NM_001005199.1 C141*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAVZ-01A-11D-A40R-10 chr11:56057635 A>G maps to NM_001005199.1 I301I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr11:55860941 T>G maps to NM_001003750.1 S53S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADQ-01A-11D-A40R-10 chr11:55905104 G>T maps to NM_001004064.1 V30V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WQ-A9G7-01A-11D-A36X-10 chr11:55905119 A>G maps to NM_001004064.1 I25I. 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-DD-AADO-01A-11D-A40R-10 chr11:56114329 T>C maps to NM_001002907.1 H272H. 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-DD-AAVP-01A-11D-A40R-10 chr11:56086231 C>T maps to NM_001005202.1 L150L. 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-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-DD-AADB-01A-11D-A40R-10 chr11:56468270 C>A maps to NM_001013358.1 S136S. 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-DD-AACM-01A-11D-A40R-10 chr11:56510312 T>C maps to NM_001005284.1 P325P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAEA-01A-11D-A40R-10 chr11:57886844 C>T maps to NM_001005211.1 E24E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAD3-01A-11D-A40R-10 chr12:55523605 A>G maps to NM_001005243.1 Q18Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADK-01A-11D-A40R-10 chr12:55524550 T>C maps to NM_001005243.1 I333I. 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-DD-AADO-01A-11D-A40R-10 chr11:57946996 C>T maps to NM_001005212.3 L27L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAE9-01A-11D-A40R-10 chr16:30964576 C>T maps to NM_152288.2 A100A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39Y-01A-11D-A20W-10 chr2:201778020 C>T maps to NM_006190.4 K548K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAD1-01A-11D-A40R-10 chr2:201798637 A>G maps to NM_006190.4 D256D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADO-01A-11D-A40R-10 chr7:103801579 T>C maps to NM_002553.3 L363L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr7:103808858 A>T maps to NM_181747.3 T313T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A8HV-01A-11D-A35Z-10 chr12:58087961 G>T maps to NM_006812.3 L6L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MB-01A-11D-A20W-10 chr11:59347664 A>G maps to NM_002556.2 S620S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACY-01A-11D-A40R-10 chr18:21758131 G>T maps to NM_080597.2 S646S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAVQ-01A-11D-A40R-10 chr18:21743142 T>C maps to NM_080597.2 *951*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-AAV3-01A-11D-A36X-10 chr18:21860861 T>A maps to NM_080597.2 R409*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A0-01A-11D-A20W-10 chr20:60861768 T>C did not map to a codon.
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-XR-A8TF-01A-11D-A35Z-10 chr20:60854387 C>T maps to NM_144498.1 L223L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9HB-01A-11D-A38X-10 chr7:24911673 C>T maps to NM_015550.2 V37V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1ED-01A-11D-A152-10 chr7:24849447 A>G maps to NM_015550.2 S765S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr7:24870475 G>T maps to NM_015550.2 R599R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A1-01A-11D-A20W-10 chr2:179197375 A>G maps to ENST00000392505 K127K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZS-A9CF-01A-11D-A382-10 chr2:179197656 T>C maps to ENST00000392505 Y182Y. 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-DD-A1EE-01A-11D-A12Z-10 chr12:76752566 T>A maps to NM_020841.4 K785*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EE-01A-11D-A12Z-10 chr19:54602892 C>A did not map to a codon.
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-ES-A2HS-01A-11D-A183-10 chr14:20920171 G>T maps to NM_017807.3 T124T. Only missense variants will be evaluated by CHASM.
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-2Y-A9H9-01A-21D-A38X-10 chr22:30659919 G>A maps to NM_020530.3 P237P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZP-A9D4-01A-11D-A36X-10 chr5:38921879 C>T maps to NM_003999.2 S583S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACY-01A-11D-A40R-10 chr2:19553488 T>G maps to NM_145260.2 A26A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr3:195944787 A>G maps to NM_152672.5 T38T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr16:21702949 C>T maps to ENST00000286149 S227S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10W-01A-11D-A12Z-10 chr2:26693458 A>G did not map to a codon.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr3:161221474 T>C maps to NM_001080440.1 H393H. 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-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-5R-AA1D-01A-11D-A382-10 chr11:63753946 C>T maps to ENST00000422031 Q44*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CJ-01A-11D-A20W-10 chr11:63764414 T>C did not map to a codon.
Sequencing variant TCGA-FV-A4ZP-01A-12D-A25V-10 chr23:48814824 A>G did not map to a codon.
Sequencing variant TCGA-5R-AA1D-01A-11D-A382-10 chr15:31776669 G>A maps to ENST00000382902 G543G. Only missense variants will be evaluated by CHASM.
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-ED-A8O6-01A-11D-A35Z-10 chr14:57270980 G>T maps to NM_021728.2 A66A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr14:57271043 T>C maps to NM_021728.2 K45K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACC-01A-11D-A40R-10 chr17:1945364 G>T maps to NM_080822.2 R8R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11B-01A-11D-A12Z-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-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-DD-A119-01A-11D-A12Z-10 chr11:65562181 C>T maps to NM_004561.2 H164H. 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-DD-AACT-01A-11D-A40R-10 chr8:107751705 A>T maps to NM_001198533.1 I686I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADG-01A-11D-A40R-10 chr8:107705035 T>G maps to NM_001198533.1 T202T. 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-WJ-A86L-01A-12D-A45V-10 chr3:8794827 G>A maps to NM_000916.3 H335H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A2QR-01A-11D-A20W-10 chr12:133196676 T>C maps to NM_170683.2 S183S. 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-4R-AA8I-01A-11D-A382-10 chr3:152554281 C>T maps to NM_002563.2 Y237Y. 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-AAED-01A-12D-A40R-10 chr23:78216620 G>T 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-DD-AAEH-01A-11D-A40R-10 chr11:73008129 T>C maps to NM_004154.3 Y189Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr23:1585321 A>G did not map to a codon.
Sequencing variant TCGA-DD-AA3A-01A-11D-A36X-10 chr10:74810843 G>T maps to NM_000917.3 Y289*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39Y-01A-11D-A20W-10 chr12:56503707 A>G maps to NM_006191.2 T206T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACI-01A-11D-A40R-10 chr8:101733712 C>G maps to NM_002568.3 P33P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACY-01A-11D-A40R-10 chr8:101721827 A>C maps to NM_002568.3 A368A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A66X-01A-11D-A30V-10 chr13:25671805 T>A maps to NM_030979.2 A490A. 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-DD-AAD2-01A-11D-A40R-10 chr23:90690667 A>G 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-A1E9-01A-21D-A152-10 chr14:23793426 C>T maps to NM_004643.3 T270T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr14:23794467 A>G maps to NM_004643.3 R298R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr16:88932214 C>T maps to NM_001080487.2 V130V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAD1-01A-11D-A40R-10 chr6:163735949 C>T maps to NM_152410.2 Y274Y. 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-DD-AADQ-01A-11D-A40R-10 chr11:47201828 C>A maps to NM_016223.4 E171*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr11:47199983 G>T maps to NM_016223.4 T364T. 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-ZP-A9D1-01A-11D-A382-10 chr1:17555181 G>T maps to NM_013358.2 E239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr1:17402248 C>T maps to NM_007365.2 V460V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WQ-AB4B-01A-11D-A40P-10 chr1:17410313 C>T maps to NM_007365.2 L319L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr11:117031925 A>G maps to NM_002572.3 R79R. 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-DD-AADS-01A-11D-A40R-10 chr4:57325637 A>T maps to NM_001079525.1 A411A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5C-A9VG-01A-11D-A36X-10 chr11:77060307 T>A maps to NM_001128620.1 A287A. Only missense variants will be evaluated by CHASM.
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-ED-A66Y-01A-11D-A30V-10 chr3:196509561 T>C maps to NM_002577.4 P15P. 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-DD-AADA-01A-11D-A40R-10 chr23:110459744 A>T 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-DD-AA3A-01A-11D-A36X-10 chr19:39663568 G>T maps to NM_005884.3 R72R. Only missense variants will be evaluated by CHASM.
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-DD-A39Y-01A-11D-A20W-10 chr20:9538332 A>G maps to NM_177990.2 A555A. 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-DD-AADF-01A-11D-A40R-10 chr4:169432855 T>A maps to NM_001166108.1 I67I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAE0-01A-11D-A40R-10 chr4:169602486 C>T maps to NM_001166108.1 A364A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACY-01A-11D-A40R-10 chr1:100152743 A>G maps to NM_017734.4 K171K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr1:100154876 C>A maps to NM_017734.4 S354*. 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-YA-A8S7-01A-11D-A36X-10 chr1:100152710 T>C maps to NM_017734.4 N160N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACI-01A-11D-A40R-10 chr5:102326045 T>C maps to NM_000919.3 A518A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAW1-01A-11D-A40P-10 chr5:102360940 G>T maps to NM_000919.3 V864V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADG-01A-11D-A40R-10 chr11:35454062 G>T maps to NM_015430.2 I685I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr12:56722128 C>A maps to NM_001127460.2 E156*. 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-DD-AACT-01A-11D-A40R-10 chr5:167986087 T>G maps to NM_024594.2 A337A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39Z-01A-11D-A20W-10 chr5:6743904 T>C maps to NM_006999.4 G149G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A9-01A-11D-A25V-10 chr14:73721643 G>A maps to ENST00000427855 P515P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr14:73719405 C>A maps to ENST00000427855 P339P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39Z-01A-11D-A20W-10 chr14:97022279 A>G maps to NM_032632.3 S587S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MA-01A-11D-A20W-10 chr7:4900925 T>C maps to NM_020144.4 A172A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9H2-01A-12D-A382-10 chr2:61014654 C>T maps to NM_022894.3 Y432Y. 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-5C-A9VH-01A-11D-A36X-10 chr1:176563999 T>C maps to NM_020318.2 R420R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A0-01A-11D-A20W-10 chr1:176708892 T>C maps to NM_020318.2 S1310S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACJ-01A-11D-A40R-10 chr1:176762738 C>T maps to NM_020318.2 P1688P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAD6-01A-11D-A40R-10 chr1:176563804 C>T maps to NM_020318.2 S355S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr1:176564278 C>T maps to NM_020318.2 Y513Y. 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-WQ-A9G7-01A-11D-A36X-10 chr3:142681758 G>A maps to NM_198504.2 H140H. 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-DD-AACQ-01A-11D-A40R-10 chr2:205912301 A>T did not map to a codon.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr2:205912376 A>G maps to ENST00000406610 S156S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACL-01A-11D-A40R-10 chr20:49366412 A>T maps to NM_032521.2 L169L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZS-A9CG-01A-11D-A36X-10 chr10:51028217 G>T maps to NM_003631.2 L923L. Only missense variants will be evaluated by CHASM.
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-G3-AAV5-01A-11D-A36X-10 chr8:145057701 G>A maps to NM_032789.3 L685L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr12:3931064 G>A maps to NM_020367.4 N174N. 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-EP-A2KA-01A-11D-A183-10 chr15:65578650 C>A maps to NM_017851.4 S38S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACP-01A-11D-A40R-10 chr14:20820472 T>C maps to NM_005484.3 D202D. 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-DD-A1ED-01A-11D-A152-10 chr3:122274537 A>G maps to NM_031458.2 H195H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAC8-01A-11D-A40R-10 chr22:44547367 C>A maps to NM_001003828.1 L293L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADB-01A-11D-A40R-10 chr22:44527388 G>C maps to NM_001003828.1 L166L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A0-01A-11D-A20W-10 chr22:44587942 T>C maps to NM_001137606.1 G173G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MA-01A-11D-A20W-10 chr23:150832683 A>G 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-2Y-A9GX-01A-11D-A382-10 chr2:242075393 A>G maps to ENST00000358649 L400L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr2:242063477 T>C maps to ENST00000358649 K930K. Only missense variants will be evaluated by CHASM.
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-EP-A2KB-01A-11D-A183-10 chr22:31724791 G>A maps to NM_014323.2 A542A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZS-A9CF-01A-11D-A382-10 chr10:102584453 C>A maps to NM_003987.3 P346P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1ED-01A-11D-A152-10 chr2:223086013 A>G maps to NM_181459.3 P295P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr2:223066864 G>T maps to NM_181459.3 P406P. 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-A2QR-01A-11D-A20W-10 chr7:127252031 T>C maps to NM_006193.2 V238V. Only missense variants will be evaluated by CHASM.
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-DD-A11A-01A-11D-A12Z-10 chr7:154760557 T>C maps to NM_007349.3 Q451Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11A-01A-11D-A12Z-10 chr7:154760560 C>T maps to NM_007349.3 Q450Q. 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-FV-A2QR-01A-11D-A20W-10 chr7:154759591 A>G maps to NM_007349.3 C609C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39Y-01A-11D-A20W-10 chr8:27668598 T>C maps to NM_018492.2 E216E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39Y-01A-11D-A20W-10 chr6:138539187 C>T maps to NM_021635.2 Q115Q. 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-DD-A1EE-01A-11D-A12Z-10 chr3:52662938 G>A maps to ENST00000296302 R472*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A5SI-01A-31D-A27I-10 chr3:52643630 G>T maps to ENST00000296302 V755V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADO-01A-11D-A40R-10 chr1:164776787 A>G maps to NM_002585.2 R237R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr11:66639567 G>T maps to NM_022172.2 T21T. 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-CC-5258-01A-01D-A12Z-10 chr5:134246023 G>C did not map to a codon.
Sequencing variant TCGA-CC-A7IE-01A-21D-A382-10 chr21:47350754 A>G maps to NM_020528.2 S284S. Only missense variants will be evaluated by CHASM.
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-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-2Y-A9H1-01A-11D-A382-10 chr23:91133724 T>C did not map to a codon.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr23:91873880 G>A did not map to a codon.
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-A3A9-01A-11D-A25V-10 chr23:91133860 G>C did not map to a codon.
Sequencing variant TCGA-DD-AACL-01A-11D-A40R-10 chr23:91132903 A>T did not map to a codon.
Sequencing variant TCGA-DD-AACP-01A-11D-A40R-10 chr23:91132816 G>T did not map to a codon.
Sequencing variant TCGA-DD-AAVV-01A-11D-A40R-10 chr23:91137936 G>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-4R-AA8I-01A-11D-A382-10 chr24:5369159 A>T did not map to a codon.
Sequencing variant TCGA-5C-A9VH-01A-11D-A36X-10 chr24:4967468 G>A 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-A1EI-01A-11D-A12Z-10 chr24:4968284 C>A did not map to a codon.
Sequencing variant TCGA-DD-AACK-01A-11D-A40R-10 chr24:4924911 T>A did not map to a codon.
Sequencing variant TCGA-DD-AADN-01A-11D-A40R-10 chr24:4967387 T>C 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-A7SK-01A-11D-A34Z-10 chr24:4968004 A>G did not map to a codon.
Sequencing variant TCGA-2V-A95S-01A-11D-A36X-10 chr5:141329102 G>A maps to NM_016580.2 G1008G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BD-A3EP-01A-11D-A22F-10 chr5:141335034 G>A maps to NM_016580.2 S794S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADS-01A-11D-A40R-10 chr5:141334584 G>A maps to NM_016580.2 A944A. Only missense variants will be evaluated by CHASM.
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-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-BC-A8YO-01A-11D-A36X-10 chr10:55849777 C>A maps to NM_001142763.1 G660*. 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-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-CC-A9FW-01A-11D-A36X-10 chr10:55955616 G>A maps to NM_001142763.1 A382A. 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-DD-A1EE-01A-11D-A12Z-10 chr13:58207558 C>T maps to NM_001040429.2 L293L. 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-ZP-A9CY-01A-11D-A382-10 chr4:138452549 T>A maps to NM_019035.3 I231I. Only missense variants will be evaluated by CHASM.
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-DD-AAEI-01A-11D-A40R-10 chr23:99596911 A>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-AACP-01A-11D-A40R-10 chr4:30921953 G>T maps to NM_001173523.1 P1118P. 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-2Y-A9GU-01A-11D-A382-10 chr13:53422136 G>A maps to NM_002590.2 S145S. 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-4R-AA8I-01A-11D-A382-10 chr5:140167659 C>T maps to NM_018900.2 R595R. 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-DD-AACA-01A-11D-A40R-10 chr5:140168106 G>C maps to NM_018900.2 A744A. 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-DD-AADB-01A-11D-A40R-10 chr5:140236127 A>G maps to NM_018901.2 A165A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADD-01A-11D-A40R-10 chr5:140235812 G>A maps to NM_018901.2 Q60Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADO-01A-11D-A40R-10 chr5:140237594 C>G maps to NM_018901.2 G654G. 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-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-5C-AAPD-01A-21D-A38X-10 chr5:140255591 G>T maps to NM_018903.2 E179*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADS-01A-11D-A40R-10 chr5:140255479 T>A maps to NM_018903.2 P141P. 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-2Y-A9GZ-01A-11D-A38X-10 chr5:140264042 C>A maps to NM_018904.2 G730G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACH-01A-11D-A40R-10 chr5:140262782 C>T maps to NM_018904.2 F310F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADS-01A-11D-A40R-10 chr5:140262776 A>T maps to NM_018904.2 L308L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAEB-01A-11D-A40R-10 chr5:140264084 G>T maps to NM_018904.2 A744A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACL-01A-11D-A40R-10 chr5:140175982 A>T maps to NM_018905.2 S478S. 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-DD-AAD2-01A-11D-A40R-10 chr5:140181354 C>T maps to NM_018906.2 S191S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAE7-01A-11D-A40R-10 chr5:140181279 G>A maps to NM_018906.2 S166S. 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-XR-A8TD-01A-12D-A38X-10 chr5:140182419 C>A maps to NM_018906.2 G546G. 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-ZP-A9CZ-01A-11D-A382-10 chr5:140188505 C>T maps to NM_018907.2 S578S. 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-AACL-01A-11D-A40R-10 chr5:140208515 T>A maps to NM_018909.2 S280S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WJ-A86L-01A-12D-A45V-10 chr5:140208116 G>A maps to NM_018909.2 L147L. 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-DD-AAE4-01A-11D-A40R-10 chr5:140222699 C>T maps to NM_018911.2 D598D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADL-01A-11D-A40R-10 chr5:140229699 G>A maps to NM_031857.1 A540A. 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-AACF-01A-11D-A40R-10 chr5:140308282 G>A maps to NM_018898.3 R602R. 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-DD-AADS-01A-11D-A40R-10 chr5:140348696 A>G maps to NM_018899.5 R782R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9HA-01A-11D-A38X-10 chr5:140432308 T>C maps to NM_013340.2 Y418Y. 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-DD-AADA-01A-11D-A40R-10 chr5:140432818 C>A maps to NM_013340.2 T588T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAE9-01A-11D-A40R-10 chr5:140432977 G>A maps to NM_013340.2 L641L. 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-DD-AACU-01A-11D-A40R-10 chr5:140594105 A>G maps to NM_018933.2 K137K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAEI-01A-11D-A40R-10 chr5:140595752 C>T maps to NM_018933.2 L686L. 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-DD-A39X-01A-11D-A20W-10 chr5:140626123 A>G maps to NM_018935.2 G326G. 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-2V-A95S-01A-11D-A36X-10 chr5:140480871 C>T maps to NM_018937.2 T213T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAC8-01A-11D-A40R-10 chr5:140481324 A>T maps to NM_018937.2 V364V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAE2-01A-11D-A40R-10 chr5:140482110 C>T maps to NM_018937.2 T626T. 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-BC-A10W-01A-11D-A12Z-10 chr5:140515855 T>C maps to NM_015669.2 A280A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACL-01A-11D-A40R-10 chr5:140515387 A>T maps to NM_015669.2 T124T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAVZ-01A-11D-A40R-10 chr5:140516626 C>T maps to NM_015669.2 S537S. 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-ZP-A9D2-01A-11D-A382-10 chr5:140515198 T>A maps to NM_015669.2 T61T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10W-01A-11D-A12Z-10 chr5:140530198 C>T maps to NM_018939.2 R121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A8HU-01A-11D-A35Z-10 chr5:140529885 C>T maps to NM_018939.2 F16F. 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-DD-AAVU-01A-11D-A40R-10 chr5:140554566 G>C maps to NM_018940.2 A717A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MA-01A-11D-A20W-10 chr5:140559336 C>T maps to NM_019120.2 T574T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAC8-01A-11D-A40R-10 chr5:140559336 C>T maps to NM_019120.2 T574T. 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-ZP-A9D0-01A-11D-A36X-10 chr5:140801282 G>A maps to NM_018914.2 V163V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XR-A8TF-01A-11D-A35Z-10 chr5:140810475 G>A maps to NM_003735.2 R50R. 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-AADJ-01A-11D-A40R-10 chr5:140735876 C>T maps to NM_018917.2 N370N. 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-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-EP-A2KA-01A-11D-A183-10 chr5:140762723 T>C maps to NM_018920.2 T86T. 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-DD-AACP-01A-11D-A40R-10 chr5:140783283 G>T maps to NM_018921.2 V255V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAEA-01A-11D-A40R-10 chr5:140784950 C>A maps to NM_032089.1 S811*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9GV-01A-11D-A382-10 chr5:140731302 G>A maps to NM_018922.2 L492L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A8O6-01A-11D-A35Z-10 chr5:140730928 C>T maps to NM_018922.2 R368*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CJ-01A-11D-A20W-10 chr5:140741738 G>C maps to NM_018923.2 R679R. 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-LG-A9QD-01A-11D-A382-10 chr5:140751547 G>A maps to NM_018924.2 E529E. 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-EP-A2KA-01A-11D-A183-10 chr5:140768681 G>T maps to NM_003736.2 E411*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr5:140769223 G>T maps to NM_003736.2 A591A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A8HV-01A-11D-A35Z-10 chr5:140778725 A>G maps to NM_018925.2 T344T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9GU-01A-11D-A382-10 chr5:140787867 C>A maps to NM_018926.2 I33I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZP-A9CY-01A-11D-A382-10 chr5:140787903 G>T maps to NM_018926.2 S45S. 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-DD-AADO-01A-11D-A40R-10 chr5:140797662 G>T maps to NM_018927.2 A79A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAW1-01A-11D-A40P-10 chr5:140799183 C>T maps to NM_018927.2 Y586Y. 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-AAC8-01A-11D-A40R-10 chr5:140865876 A>T maps to NM_018928.2 S379S. 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-DD-AADQ-01A-11D-A40R-10 chr5:140870855 C>T maps to NM_018929.2 H683H. 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-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-3K-AAZ8-01A-12D-A38X-10 chr10:105110553 C>T maps to NM_001011663.1 L90L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39X-01A-11D-A20W-10 chr20:44574500 C>T maps to NM_022104.3 S440S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAVR-01A-11D-A40R-10 chr20:44571776 G>T maps to NM_022104.3 E239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAE3-01A-11D-A40R-10 chr20:56138213 T>G maps to NM_002591.3 A247A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr20:56137171 C>T maps to NM_002591.3 S90S. 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-DD-AAW3-01A-11D-A40P-10 chr14:24572746 C>T maps to NM_004563.2 A499A. 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-2Y-A9GZ-01A-11D-A38X-10 chr7:82584099 T>A maps to NM_033026.5 K2057*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A3KG-01A-11D-A20W-10 chr7:82578935 T>C maps to NM_033026.5 V3656V. 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-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-DD-AACL-01A-11D-A40R-10 chr7:82595395 T>A maps to NM_033026.5 L1236L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADG-01A-11D-A40R-10 chr7:82538311 C>A maps to NM_033026.5 E4440*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr7:82390783 G>T maps to NM_033026.5 I5011I. 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-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-WQ-AB4B-01A-11D-A40P-10 chr7:82545901 G>A maps to NM_033026.5 Y3800Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACP-01A-11D-A40R-10 chr8:17823506 G>T did not map to a codon.
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-4R-AA8I-01A-11D-A382-10 chr21:47848329 C>T maps to NM_006031.5 L2506L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr21:47786942 A>G maps to NM_006031.5 K1018K. 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-DD-AAD5-01A-11D-A40R-10 chr14:71479826 A>G maps to NM_014982.2 Q968Q. 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-WJ-A86L-01A-12D-A45V-10 chr14:71524346 C>T maps to NM_014982.2 F1586F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BD-A3ER-01A-11D-A20W-10 chr1:233122170 C>A maps to NM_014801.3 T1969T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WQ-A9G7-01A-11D-A36X-10 chr11:65396884 T>C maps to NM_032223.2 P1333P. 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-DD-A39X-01A-11D-A20W-10 chr9:78790031 A>G maps to NM_001190482.1 T629T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-AAV4-01A-11D-A382-10 chr9:78722180 G>A maps to NM_001190482.1 L374L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr11:117100221 G>T maps to NM_004716.2 I113I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACP-01A-11D-A40R-10 chr1:55527162 C>G maps to NM_174936.3 S599S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAE9-01A-11D-A40R-10 chr1:55527046 G>T did not map to a codon.
Sequencing variant TCGA-MR-A8JO-01A-12D-A35Z-10 chr1:55521762 C>T maps to NM_174936.3 A299A. 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-ES-A2HT-01A-12D-A183-10 chr23:24605379 A>G did not map to a codon.
Sequencing variant TCGA-G3-A3CJ-01A-11D-A20W-10 chr23:24605385 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-4R-AA8I-01A-11D-A382-10 chr10:105182856 C>A maps to NM_014976.1 P870P. 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-G3-A3CJ-01A-11D-A20W-10 chr10:105160236 A>G maps to NM_014976.1 R62R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MB-01A-11D-A20W-10 chr6:170886664 A>G maps to NM_002598.3 D339D. 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-DD-AAC8-01A-11D-A40R-10 chr3:33840378 A>T maps to NM_001162429.1 A53A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZS-A9CD-01A-11D-A36X-10 chr3:33883511 G>A maps to NM_001162429.1 Q440Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9GY-01A-11D-A382-10 chr15:65421368 C>A did not map to a codon.
Sequencing variant TCGA-DD-AACM-01A-11D-A40R-10 chr2:101192855 A>G maps to NM_024065.4 T206T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADS-01A-11D-A40R-10 chr11:770991 C>A did not map to a codon.
Sequencing variant TCGA-CC-A3MB-01A-11D-A20W-10 chr6:165863851 T>C did not map to a codon.
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-2V-A95S-01A-11D-A36X-10 chr2:178936398 T>A maps to NM_016953.3 K256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9HA-01A-11D-A38X-10 chr2:178562091 T>G maps to NM_016953.3 S771S. 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-A39Y-01A-11D-A20W-10 chr2:183387040 T>C maps to NM_005019.3 G21G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A0-01A-11D-A20W-10 chr12:54968905 T>C maps to NM_000924.3 S363S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9H3-01A-11D-A382-10 chr7:31918661 C>T maps to NM_001191057.1 K124K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAEI-01A-11D-A40R-10 chr12:20806879 G>A did not map to a codon.
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-G3-A3CJ-01A-11D-A20W-10 chr1:66831429 T>C maps to NM_001037341.1 N455N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39Y-01A-11D-A20W-10 chr19:18322643 T>C maps to NM_000923.3 G572G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39X-01A-11D-A20W-10 chr5:58270499 A>G maps to NM_001104631.1 P807P. 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-5C-A9VG-01A-11D-A36X-10 chr1:144868125 G>A maps to NM_014644.4 N1771N. 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-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-DD-AAC8-01A-11D-A40R-10 chr1:144868113 G>T maps to NM_014644.4 A1775A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACQ-01A-11D-A40R-10 chr1:144930751 T>A maps to NM_001002811.1 L319L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADS-01A-11D-A40R-10 chr1:144892214 T>A maps to NM_001002812.1 *970L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A8O5-01A-11D-A35Z-10 chr1:144886224 C>T maps to NM_014644.4 Q1003Q. 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-G3-AAV2-01A-11D-A36X-10 chr1:144867972 A>T maps to NM_014644.4 S1822S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A3KG-01A-11D-A20W-10 chr4:120528277 A>G maps to NM_001083.3 P109P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr5:149324080 C>T maps to NM_000440.2 P52P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WQ-A9G7-01A-11D-A36X-10 chr5:149262996 G>A maps to NM_000440.2 I710I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACI-01A-11D-A40R-10 chr4:656886 A>T did not map to a codon.
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-2Y-A9H8-01A-11D-A38X-10 chr15:85652344 C>T maps to NM_002605.2 A366A. 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-DD-AAC8-01A-11D-A40R-10 chr21:44192596 A>T maps to NM_002606.2 R579*. 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-AACQ-01A-11D-A40R-10 chr4:55127496 A>T maps to NM_006206.4 T95T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACT-01A-11D-A40R-10 chr4:55143654 A>G maps to ENST00000507166 L389L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A3KG-01A-11D-A20W-10 chr5:149500489 T>C maps to NM_002609.3 R849R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADI-01A-11D-A40R-10 chr5:149515367 C>T maps to NM_002609.3 P38P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAE0-01A-11D-A40R-10 chr5:149504386 G>A maps to NM_002609.3 T605T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MB-01A-11D-A20W-10 chr23:19368149 A>G did not map to a codon.
Sequencing variant TCGA-DD-AAEE-01A-11D-A40R-10 chr23:19369496 C>T did not map to a codon.
Sequencing variant TCGA-ZP-A9D1-01A-11D-A382-10 chr23:19367461 T>G did not map to a codon.
Sequencing variant TCGA-BC-A10W-01A-11D-A12Z-10 chr4:96761828 T>C maps to NM_005390.4 A176A. Only missense variants will be evaluated by CHASM.
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-DD-AACA-01A-11D-A40R-10 chr16:336641 T>C maps to NM_006849.2 I443I. 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-DD-A119-01A-11D-A12Z-10 chr2:10925107 A>G maps to ENST00000381611 A454A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADV-01A-11D-A38X-10 chr1:26449067 A>G maps to NM_152835.3 *342W. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr1:26448824 A>G maps to NM_152835.3 T261T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACY-01A-11D-A40R-10 chr2:173429802 T>G did not map to a codon.
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-A119-01A-11D-A12Z-10 chr23:24521600 T>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-CC-A8HT-01A-11D-A35Z-10 chr4:95507589 G>A maps to NM_006457.3 K305K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACV-01A-11D-A40R-10 chr4:95539283 G>A maps to NM_006457.3 K350K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAVX-01A-11D-A40R-10 chr8:94935708 G>A maps to NM_001161778.1 E533E. 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-G3-A3CJ-01A-11D-A20W-10 chr13:33332688 T>C maps to ENST00000400481 C1069C. 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-DD-AACA-01A-11D-A40R-10 chr16:15069068 C>T maps to NM_015027.2 L5L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADV-01A-11D-A38X-10 chr16:15125628 A>T maps to NM_015027.2 V479V. 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-2Y-A9GS-01A-12D-A382-10 chr5:31983275 G>A maps to NM_178140.2 Q164Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr5:32088756 G>T maps to NM_178140.2 E1735*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A3KG-01A-11D-A20W-10 chr5:32089622 A>G maps to NM_178140.2 R2023R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADC-01A-11D-A40R-10 chr5:32087360 A>G maps to NM_178140.2 A1269A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9H9-01A-21D-A38X-10 chr11:119059806 C>T maps to ENST00000392817 L527L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADA-01A-11D-A40R-10 chr11:119058342 G>A maps to ENST00000392817 G263G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3K-AAZ8-01A-12D-A38X-10 chr23:153068844 C>T did not map to a codon.
Sequencing variant TCGA-DD-A1EG-01A-11D-A20W-10 chr23:153070035 A>G did not map to a codon.
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-2Y-A9H0-01A-11D-A382-10 chr10:119133942 G>A maps to NM_173791.3 Q266*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A9FU-01A-11D-A36X-10 chr1:47649701 C>A maps to NM_005764.3 E96*. 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-EP-A2KB-01A-11D-A183-10 chr3:73433256 A>G maps to NM_015009.1 P820P. 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-DD-A1ED-01A-11D-A152-10 chr12:41967380 G>T maps to NM_001164595.1 E934*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACG-01A-11D-A40R-10 chr12:41900358 T>C maps to NM_001164595.1 P315P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr12:41946514 C>A maps to NM_001164595.1 R421R. 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-ZP-A9CV-01A-11D-A382-10 chr12:41961650 G>T maps to NM_001164595.1 E512*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAEG-01A-11D-A38X-10 chr1:156878620 G>A maps to NM_001080471.1 T430T. Only missense variants will be evaluated by CHASM.
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-DD-AAD2-01A-11D-A40R-10 chr19:57325480 G>C maps to NM_006210.2 A1443A. 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-DD-A3A0-01A-11D-A20W-10 chr11:66243163 T>C maps to NM_145065.2 A312A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MA-01A-11D-A20W-10 chr17:4575333 T>G maps to ENST00000301396 P1128P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73A-01A-12D-A32G-10 chr17:4575507 C>T maps to ENST00000301396 E1070E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr17:4607241 C>T maps to ENST00000301396 P55P. 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-ZS-A9CD-01A-11D-A36X-10 chr19:33892755 C>A maps to NM_000285.3 E280*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9GY-01A-11D-A382-10 chr2:239161960 C>T maps to NM_022817.2 A901A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WQ-A9G7-01A-11D-A36X-10 chr1:7887310 C>T maps to ENST00000377532 N774N. 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-EP-A2KB-01A-11D-A183-10 chr4:152679944 T>C maps to NM_004564.2 A102A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9HA-01A-11D-A38X-10 chr7:92134133 C>G maps to NM_000466.2 L661L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A1-01A-11D-A20W-10 chr7:92123942 T>C maps to NM_000466.2 R928R. 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-DD-AADO-01A-11D-A40R-10 chr2:61258829 A>G maps to NM_002618.3 E123E. 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-WQ-A9G7-01A-11D-A36X-10 chr22:18561183 G>A maps to NM_017929.5 G14G. 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-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-XR-A8TG-01A-11D-A35Z-10 chr3:179689380 C>T did not map to a codon.
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-EP-A2KA-01A-11D-A183-10 chr6:137193355 T>C maps to NM_000288.3 S256S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-AA0V-01A-11D-A382-10 chr6:137191047 G>T maps to NM_000288.3 A218A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr4:74719171 C>T maps to NM_002620.2 F31F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9H3-01A-11D-A382-10 chr17:8168226 G>T maps to NM_012393.2 V688V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADR-01A-11D-A40R-10 chr12:53691668 C>T maps to NM_002624.3 H81H. 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-G3-AAV6-01A-21D-A36X-10 chr23:54978347 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-ES-A2HT-01A-12D-A183-10 chr10:6258144 A>G maps to NM_004566.3 G119G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A8YO-01A-11D-A36X-10 chr2:24342546 G>A maps to NM_199346.1 N87N. 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-DD-A119-01A-11D-A12Z-10 chr15:34395100 A>G maps to NM_152595.4 E123E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9HB-01A-11D-A38X-10 chr1:230492977 G>A maps to ENST00000321327 Q171*. 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-ES-A2HS-01A-11D-A183-10 chr1:230486727 A>G maps to ENST00000321327 C320C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAED-01A-12D-A40R-10 chr8:97797376 A>G maps to ENST00000325141 L84L. 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-DD-AAW1-01A-11D-A40P-10 chr14:75412965 C>T maps to NM_002632.4 K145K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9H3-01A-11D-A382-10 chr23:77359872 G>A did not map to a codon.
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-DD-AACQ-01A-11D-A40R-10 chr1:153276486 T>G did not map to a codon.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr4:37847312 G>T maps to NM_018290.3 P323P. 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-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-DD-AAD5-01A-11D-A40R-10 chr17:76411089 G>A maps to NM_024419.3 L511L. 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-DD-AACW-01A-11D-A40R-10 chr6:144095323 C>T maps to NM_001100164.1 R521*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADC-01A-11D-A40R-10 chr6:144086749 C>T maps to NM_001100164.1 P349P. 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-A1EG-01A-11D-A20W-10 chr1:28793166 T>C maps to NM_023923.3 A247A. 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-WQ-A9G7-01A-11D-A36X-10 chr12:9087823 C>T maps to ENST00000433083 S881S. 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-ES-A2HT-01A-12D-A183-10 chr1:33794699 T>C maps to ENST00000419414 T732T. 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-WX-AA44-01A-11D-A38X-10 chr3:169840462 T>G maps to NM_024947.3 R620R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NF-01A-11D-A27I-10 chr23:22117126 G>A did not map to a codon.
Sequencing variant TCGA-DD-AAC9-01A-11D-A40R-10 chr23:22263483 G>A did not map to a codon.
Sequencing variant TCGA-DD-AACI-01A-11D-A40R-10 chr23:22231053 T>C did not map to a codon.
Sequencing variant TCGA-G3-A3CG-01A-11D-A20W-10 chr23:22237188 A>G did not map to a codon.
Sequencing variant TCGA-G3-A3CG-01A-11D-A20W-10 chr23:22265969 T>C 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-2Y-A9GU-01A-11D-A382-10 chr5:133873702 C>A maps to ENST00000448712 S44*. 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-DD-AADF-01A-11D-A40R-10 chr23:46893037 C>T did not map to a codon.
Sequencing variant TCGA-G3-A3CJ-01A-11D-A20W-10 chr23:46884292 T>C did not map to a codon.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr4:129782995 A>G maps to NM_199320.2 K373K. Only missense variants will be evaluated by CHASM.
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-BC-A3KF-01A-11D-A20W-10 chr9:96438991 A>T maps to NM_005392.3 P983P. 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-4R-AA8I-01A-11D-A382-10 chr8:133848921 C>T maps to ENST00000395386 R684*. 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-A39Z-01A-11D-A20W-10 chr11:45991401 A>G maps to ENST00000257821 P222P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CG-01A-11D-A20W-10 chr11:45958087 A>G maps to ENST00000257821 P547P. 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-G3-A5SJ-01A-11D-A27I-10 chr23:133527958 A>G did not map to a codon.
Sequencing variant TCGA-CC-A8HU-01A-11D-A35Z-10 chr23:54013588 G>A did not map to a codon.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr23:54011485 A>G 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-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-DD-AADI-01A-11D-A40R-10 chr23:71813016 C>T did not map to a codon.
Sequencing variant TCGA-DD-AADM-01A-11D-A40R-10 chr23:71838612 C>G did not map to a codon.
Sequencing variant TCGA-DD-AADM-01A-11D-A40R-10 chr23:71838662 C>G 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-ES-A2HT-01A-12D-A183-10 chr23:71822974 G>A 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-DD-A1EG-01A-11D-A20W-10 chr23:18949831 T>C did not map to a codon.
Sequencing variant TCGA-BC-A3KG-01A-11D-A20W-10 chr16:47531307 A>G did not map to a codon.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr16:47698852 A>G maps to NM_000293.2 P798P. Only missense variants will be evaluated by CHASM.
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-DD-AAVS-01A-11D-A40R-10 chr12:76424918 C>T maps to NM_007350.3 Q201Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAC8-01A-11D-A40R-10 chr11:118502988 A>T maps to NM_015157.2 T785T. Only missense variants will be evaluated by CHASM.
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-ES-A2HS-01A-11D-A183-10 chr3:111658350 A>G maps to NM_001134438.1 K720K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CG-01A-11D-A20W-10 chr3:111671429 T>C maps to NM_001134438.1 S881S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr19:43998855 G>A maps to NM_198850.3 Q383*. 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-WJ-A86L-01A-12D-A45V-10 chr4:41748003 C>T maps to NM_003924.3 A255A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr11:609547 G>A maps to ENST00000264555 A1364A. 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-A2KA-01A-11D-A183-10 chr11:607102 C>A maps to ENST00000264555 S549S. 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-DD-A1EE-01A-11D-A12Z-10 chr7:77569479 C>A maps to ENST00000427986 S534*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A1-01A-11D-A20W-10 chr7:77551974 A>G maps to ENST00000427986 E333E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADM-01A-11D-A40R-10 chr7:77549625 A>G maps to ENST00000427986 K269K. 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-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-DD-AACT-01A-11D-A40R-10 chr18:44400938 T>C maps to NM_004671.2 P535P. 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-BC-A3KG-01A-11D-A20W-10 chr13:73366610 T>C maps to NM_006346.2 N93N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr13:73401962 T>C maps to NM_006346.2 H336H. 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-EP-A2KA-01A-11D-A183-10 chr11:85701368 A>G maps to ENST00000393343 S444S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAC8-01A-11D-A40R-10 chr22:38461006 A>C did not map to a codon.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr22:38465059 C>A maps to NM_012407.3 R124R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr15:65111378 C>T maps to ENST00000333425 L459L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A1-01A-11D-A20W-10 chr15:65108547 T>C maps to NM_025049.2 P625P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39Y-01A-11D-A20W-10 chr23:15349572 A>G 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-DD-AACP-01A-11D-A40R-10 chr18:59777110 T>C maps to NM_176787.4 V510V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADD-01A-11D-A40R-10 chr18:59757811 C>T did not map to a codon.
Sequencing variant TCGA-2Y-A9H1-01A-11D-A382-10 chr9:35092035 G>A maps to NM_032634.2 H616H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAD5-01A-11D-A40R-10 chr1:207106367 G>A maps to NM_002644.3 Q617*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5C-A9VH-01A-11D-A36X-10 chr17:34893441 A>G maps to NM_178517.3 T164T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAEI-01A-11D-A40R-10 chr4:89444728 C>T maps to NM_032906.3 K41K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACI-01A-11D-A40R-10 chr19:49954057 T>A maps to NM_017916.2 T46T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39Y-01A-11D-A20W-10 chr11:17113159 A>G maps to NM_002645.2 A1562A. 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-DD-AADM-01A-11D-A40R-10 chr3:138478167 T>G maps to NM_006219.1 I6I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADB-01A-11D-A40R-10 chr7:106509973 T>C maps to NM_002649.2 V656V. 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-DD-AACE-01A-11D-A40R-10 chr5:67576423 C>T maps to ENST00000396611 Q235*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACW-01A-11D-A40R-10 chr5:67590432 C>T maps to ENST00000396611 Q499*. 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-DD-A1EG-01A-11D-A20W-10 chr3:130454769 T>C maps to NM_014602.2 G270G. 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-DD-AACH-01A-11D-A40R-10 chr2:209195390 A>G maps to NM_015040.3 T1312T. 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-EP-A2KB-01A-11D-A183-10 chr7:99971977 C>A maps to NM_013439.2 R126R. 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-5C-A9VH-01A-11D-A36X-10 chr8:10690494 C>T did not map to a codon.
Sequencing variant TCGA-2V-A95S-01A-11D-A36X-10 chr7:77010639 T>C maps to NM_017439.3 Q186Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr10:22880590 G>T maps to NM_005028.4 A153A. Only missense variants will be evaluated by CHASM.
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-G3-AAV4-01A-11D-A382-10 chr9:130688227 G>A maps to NM_001135219.1 R227R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr23:15477840 C>T did not map to a codon.
Sequencing variant TCGA-BC-A3KG-01A-11D-A20W-10 chr17:65665661 A>G maps to NM_012417.2 G167G. 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-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-WQ-A9G7-01A-11D-A36X-10 chr12:123481369 G>T maps to NM_020845.2 S520S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A8HT-01A-11D-A35Z-10 chr17:6386916 G>A maps to NM_031220.3 F169F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr17:6386874 A>G maps to NM_031220.3 C183C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAC8-01A-11D-A40R-10 chr17:6373606 T>A maps to NM_031220.3 T582T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr10:3208565 C>T maps to ENST00000380989 Q91Q. Only missense variants will be evaluated by CHASM.
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-DD-AAW3-01A-11D-A40P-10 chr12:130832689 T>C maps to NM_004764.4 Y232Y. 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-DD-AAVV-01A-11D-A40R-10 chr22:25144936 G>T maps to NM_001008496.2 T462T. 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-EP-A2KB-01A-11D-A183-10 chr23:68381879 T>C did not map to a codon.
Sequencing variant TCGA-FV-A2QR-01A-11D-A20W-10 chr23:68382106 T>C did not map to a codon.
Sequencing variant TCGA-2V-A95S-01A-11D-A36X-10 chr16:2140498 G>A maps to NM_001009944.2 A4077A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9H7-01A-11D-A38X-10 chr16:2141434 G>A maps to NM_001009944.2 L3901L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A5SM-01A-12D-A28X-10 chr16:2157969 G>T maps to NM_001009944.2 R2327R. 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 chr7:47874577 G>T maps to NM_138295.3 T2038T. 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-AAEI-01A-11D-A40R-10 chr16:81208429 G>A maps to NM_052892.3 G891G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr16:81219116 C>T maps to NM_052892.3 W659*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACJ-01A-11D-A40R-10 chr10:102054309 G>A maps to NM_016112.2 F547F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A1-01A-11D-A20W-10 chr5:137257345 T>C maps to ENST00000230643 V450V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73F-01A-11D-A32G-10 chr22:46657637 G>T maps to NM_006071.1 R528R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CG-01A-11D-A20W-10 chr22:46654317 T>C maps to NM_006071.1 S1634S. 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-DD-AADD-01A-11D-A40R-10 chr6:51609282 A>G maps to NM_138694.3 Y3352Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZP-A9D1-01A-11D-A382-10 chr6:51917967 T>A maps to NM_138694.3 P682P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A3KG-01A-11D-A20W-10 chr8:110539226 T>C maps to ENST00000426474 V4234V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A8HT-01A-11D-A35Z-10 chr8:110408331 T>C maps to ENST00000426474 D296D. 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-DD-AAW1-01A-11D-A40P-10 chr8:110376803 A>T maps to ENST00000426474 T34T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr8:110457402 G>T maps to ENST00000426474 G1769*. 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-ZS-A9CE-01A-11D-A36X-10 chr8:110420350 A>G maps to ENST00000426474 K629K. 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-DD-AAC8-01A-11D-A40R-10 chr11:399155 A>G maps to NM_007183.2 T411T. 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-G3-AAV3-01A-11D-A36X-10 chr11:404566 T>A maps to NM_007183.2 *798K. 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-DD-A1EE-01A-11D-A12Z-10 chr22:31533848 T>A maps to NM_015715.3 K305*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MA-01A-11D-A20W-10 chr1:186919789 A>G maps to NM_024420.2 E422E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADA-01A-11D-A40R-10 chr1:186880395 C>T maps to NM_024420.2 R145*. 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-2Y-A9HA-01A-11D-A38X-10 chr19:48598745 A>C maps to NM_003706.2 P228P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr19:48609796 G>T maps to NM_001159322.1 T17T. 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-DD-AACH-01A-11D-A40R-10 chr15:42287600 G>A maps to NM_001080490.1 L373L. 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-DD-AACX-01A-11D-A40R-10 chr22:38524360 G>A maps to NM_003560.2 V421V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZP-A9CZ-01A-11D-A382-10 chr22:38525569 C>G did not map to a codon.
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-AACL-01A-11D-A40R-10 chr2:160873148 A>T maps to NM_007366.4 S509S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACQ-01A-11D-A40R-10 chr2:160884729 A>T maps to NM_007366.4 V366V. 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-UB-A7MB-01A-11D-A33Q-10 chr23:133700329 C>A did not map to a codon.
Sequencing variant TCGA-2Y-A9GS-01A-12D-A382-10 chr21:42551432 G>A maps to NM_182832.2 P41P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZP-A9CZ-01A-11D-A382-10 chr21:42551225 G>C maps to NM_182832.2 P110P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACK-01A-11D-A40R-10 chr4:84026084 T>C maps to NM_001130715.1 A69A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9H3-01A-11D-A382-10 chr2:28785967 T>G did not map to a codon.
Sequencing variant TCGA-DD-A1EG-01A-11D-A20W-10 chr2:28788182 T>C maps to NM_153021.4 L415L. 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-ZS-A9CE-01A-11D-A36X-10 chr2:28761187 T>C maps to NM_153021.4 N186N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39Y-01A-11D-A20W-10 chr12:14693775 T>C maps to NM_024829.5 R160R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9GT-01A-11D-A382-10 chr15:40588547 G>A maps to NM_004573.2 L549L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr15:40588495 C>T did not map to a codon.
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-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-AAEI-01A-11D-A40R-10 chr20:9424868 T>A maps to NM_001172646.1 S953S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr20:9438137 T>A did not map to a codon.
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-BC-A10W-01A-11D-A12Z-10 chr3:38049786 C>A maps to NM_001130964.1 V679V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAD5-01A-11D-A40R-10 chr3:38049271 G>A maps to NM_001130964.1 Q776*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAVU-01A-11D-A40R-10 chr17:43190625 C>T did not map to a codon.
Sequencing variant TCGA-CC-A7IE-01A-21D-A382-10 chr10:96084325 T>C did not map to a codon.
Sequencing variant TCGA-DD-A1ED-01A-11D-A152-10 chr10:96076425 T>C maps to ENST00000371380 G2085G. 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-ES-A2HS-01A-11D-A183-10 chr10:96076351 T>C maps to ENST00000371380 L2061L. 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.
Sequencing variant TCGA-DD-AACL-01A-11D-A40R-10 chr3:155198966 A>T maps to ENST00000340059 P1624P. 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-G3-AAV7-01A-11D-A382-10 chr2:198950088 T>C maps to NM_006226.3 S616S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr23:209879 G>A did not map to a codon.
Sequencing variant TCGA-BD-A3EP-01A-11D-A22F-10 chr23:215775 T>C did not map to a codon.
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-LG-A9QD-01A-11D-A382-10 chr3:111394160 G>A maps to ENST00000312791 G23G. 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-DD-AACG-01A-11D-A40R-10 chr5:41382469 A>T maps to NM_001005473.2 A90A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A3KG-01A-11D-A20W-10 chr12:18841041 A>G maps to ENST00000266505 T524T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39Y-01A-11D-A20W-10 chr12:18876314 T>C maps to ENST00000266505 E99E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A2QR-01A-11D-A20W-10 chr12:18841122 A>G maps to ENST00000266505 T497T. 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-ES-A2HS-01A-11D-A183-10 chr8:144990725 G>T maps to NM_201380.2 T4558T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZS-A9CE-01A-11D-A36X-10 chr2:68622842 G>A maps to NM_002664.2 E316E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A3KG-01A-11D-A20W-10 chr10:124172506 A>G maps to NM_021622.4 Q138Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39X-01A-11D-A20W-10 chr10:124189345 A>G maps to NM_021622.4 K369K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K7-AAU7-01A-11D-A382-10 chr8:38793564 G>C maps to NM_021623.1 S65S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9H2-01A-12D-A382-10 chr12:19467759 G>T maps to ENST00000429027 E684*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr12:19499935 A>G maps to ENST00000429027 E901E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr12:19489448 G>T maps to ENST00000429027 E817*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A2QR-01A-11D-A20W-10 chr12:19436348 T>C maps to ENST00000429027 P483P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-AAV7-01A-11D-A382-10 chr12:19501412 A>G maps to ENST00000429027 K988K. 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-CC-A9FU-01A-11D-A36X-10 chr1:204198157 G>A maps to ENST00000367191 G906G. 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-CC-A8HV-01A-11D-A35Z-10 chr11:16863173 G>A maps to ENST00000448080 A264A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr11:16838666 G>T maps to ENST00000448080 R516R. 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-CC-A3MA-01A-11D-A20W-10 chr6:151161731 A>G maps to NM_001029884.1 E1286E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A1-01A-11D-A20W-10 chr6:151152052 T>C maps to NM_001029884.1 G602G. 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-EP-A2KA-01A-11D-A183-10 chr19:39913583 C>T maps to NM_022835.2 P630P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAE3-01A-11D-A40R-10 chr14:65208352 A>G maps to ENST00000394691 E706E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CG-01A-11D-A20W-10 chr14:65208190 C>T maps to ENST00000394691 A652A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAC8-01A-11D-A40R-10 chr16:67319046 A>T maps to NM_001129729.1 G708G. 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-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-4R-AA8I-01A-11D-A382-10 chr1:6531574 G>A maps to NM_198681.2 P495P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39X-01A-11D-A20W-10 chr1:6529205 C>T maps to NM_198681.2 E792E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr12:6436813 C>A maps to NM_001144856.1 R689R. 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-G3-AAV4-01A-11D-A382-10 chr14:68028675 G>A maps to NM_020715.2 E143E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZS-A9CE-01A-11D-A36X-10 chr2:43927266 T>C maps to NM_172069.3 F390F. Only missense variants will be evaluated by CHASM.
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-DD-A119-01A-11D-A12Z-10 chr1:909217 C>T maps to ENST00000379409 L532L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A5SI-01A-31D-A27I-10 chr1:902176 G>T maps to ENST00000379409 P59P. 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-ZP-A9D4-01A-11D-A36X-10 chr1:150131450 G>A maps to ENST00000443480 E352E. 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-A3CG-01A-11D-A20W-10 chr6:161158037 A>C maps to NM_000301.3 R601R. 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-DD-A1EE-01A-11D-A12Z-10 chr9:19121142 G>A maps to NM_001122.2 G110G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CJ-01A-11D-A20W-10 chr19:4839251 T>C maps to NM_005817.4 G419G. 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-G3-A3CG-01A-11D-A20W-10 chr19:4510593 C>T maps to NM_001080400.1 G1112G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr19:4531822 C>T maps to NM_001013706.2 Q24Q. 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-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-DD-AAD3-01A-11D-A40R-10 chr5:57750577 T>C maps to NM_006622.2 T630T. 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-DD-A116-01A-11D-A12Z-10 chr23:103041517 A>G did not map to a codon.
Sequencing variant TCGA-DD-A1EE-01A-11D-A12Z-10 chr23:103041517 A>G did not map to a codon.
Sequencing variant TCGA-DD-A1EE-01A-11D-A12Z-10 chr23:103041635 G>A did not map to a codon.
Sequencing variant TCGA-DD-AAD1-01A-11D-A40R-10 chr4:155462029 A>G maps to NM_002669.2 T248T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-AAV1-01A-11D-A382-10 chr4:155460300 T>C maps to NM_002669.2 T369T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-AAV4-01A-11D-A382-10 chr4:155460254 A>G 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-DD-AADQ-01A-11D-A40R-10 chr23:114863610 C>T did not map to a codon.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr23:114883869 A>G did not map to a codon.
Sequencing variant TCGA-DD-AACO-01A-11D-A40R-10 chr3:146234855 G>T maps to NM_021105.2 I279I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADN-01A-11D-A40R-10 chr3:146234890 T>A maps to NM_021105.2 R268*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr3:146246439 A>G maps to NM_021105.2 P91P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAD6-01A-11D-A40R-10 chr3:145912236 G>A maps to NM_020353.2 F317F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EB-01A-11D-A12Z-10 chr20:31825879 G>T maps to NM_130852.2 L60L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADP-01A-11D-A38X-10 chr10:20290906 C>T maps to NM_032812.7 Q106*. 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-2Y-A9GU-01A-11D-A382-10 chr1:208272268 T>G maps to NM_025179.3 R551R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39X-01A-11D-A20W-10 chr1:208390745 G>A maps to NM_025179.3 R174R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACP-01A-11D-A40R-10 chr1:208202218 C>A maps to NM_025179.3 L1798L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACT-01A-11D-A40R-10 chr1:208212330 T>A did not map to a codon.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr1:208202172 A>G did not map to a codon.
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-5R-AAAM-01A-12D-A40R-10 chr23:153689564 C>T did not map to a codon.
Sequencing variant TCGA-DD-AADF-01A-11D-A40R-10 chr23:153690519 G>C did not map to a codon.
Sequencing variant TCGA-DD-AAVX-01A-11D-A40R-10 chr23:153691733 G>T did not map to a codon.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr23:153699868 A>G did not map to a codon.
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-DD-AAD1-01A-11D-A40R-10 chr7:132192558 A>T maps to NM_020911.1 I298I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAVP-01A-11D-A40R-10 chr7:132192828 A>C maps to NM_020911.1 S208S. Only missense variants will be evaluated by CHASM.
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-G3-AAV2-01A-11D-A36X-10 chr7:132192342 C>A maps to NM_020911.1 R370R. 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-EP-A2KA-01A-11D-A183-10 chr3:48465516 C>T maps to NM_001130082.1 V168V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADF-01A-11D-A40R-10 chr22:50722375 C>G maps to NM_012401.2 L769L. 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-CC-A3MA-01A-11D-A20W-10 chr23:153040830 A>G did not map to a codon.
Sequencing variant TCGA-DD-A1EE-01A-11D-A12Z-10 chr23:153035603 G>A 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-DD-AACL-01A-11D-A40R-10 chr23:153042748 G>T did not map to a codon.
Sequencing variant TCGA-DD-AADC-01A-11D-A40R-10 chr23:153033155 G>T 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-G3-A3CG-01A-11D-A20W-10 chr12:94697584 A>G maps to NM_005761.1 E1480E. Only missense variants will be evaluated by CHASM.
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-DD-AACF-01A-11D-A40R-10 chr3:129288752 C>T maps to NM_015103.2 G1266G. 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-DD-AAE0-01A-11D-A40R-10 chr16:72198722 T>C maps to NM_031293.2 R35R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr16:72184646 A>G maps to NM_031293.2 L166L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADI-01A-11D-A40R-10 chr15:74324991 C>G maps to NM_033238.2 S445*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr15:74327562 C>A maps to NM_033239.2 S587S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAE8-01A-11D-A40R-10 chr22:41973916 G>A maps to NM_002676.2 I187I. 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-EP-A2KB-01A-11D-A183-10 chr2:190656663 A>G maps to NM_000534.4 K43K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39Y-01A-11D-A20W-10 chr23:152937341 T>C did not map to a codon.
Sequencing variant TCGA-G3-A3CJ-01A-11D-A20W-10 chr6:160230044 A>G did not map to a codon.
Sequencing variant TCGA-DD-AACP-01A-11D-A40R-10 chr10:118306863 A>T maps to NM_000936.2 G35G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9H3-01A-11D-A382-10 chr10:118202686 G>C did not map to a codon.
Sequencing variant TCGA-DD-A3A0-01A-11D-A20W-10 chr10:118196247 A>G maps to NM_001011709.2 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAED-01A-12D-A40R-10 chr10:118225667 A>G maps to NM_001011709.2 T305T. 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-ZS-A9CE-01A-11D-A36X-10 chr14:74180324 C>T maps to NM_006029.4 L6L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A3KG-01A-11D-A20W-10 chr23:152226391 T>C did not map to a codon.
Sequencing variant TCGA-DD-A3A1-01A-11D-A20W-10 chr23:152226281 T>C 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-NI-A8LF-01A-11D-A35Z-10 chr23:152225495 G>C did not map to a codon.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr23:152158843 G>A did not map to a codon.
Multiple mappings detected for codon TCGA-2Y-A9GU-01A-11D-A382-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CC-A9FU-01A-11D-A36X-10 chr19:46997792 G>A maps to NM_020709.1 D310D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAVV-01A-11D-A40R-10 chr2:68385546 A>C maps to NM_020143.2 P81P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACK-01A-11D-A40R-10 chr6:36269663 A>T maps to ENST00000457797 K269*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr6:36270242 C>T maps to ENST00000457797 Q462*. 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-G3-A3CG-01A-11D-A20W-10 chr22:44283471 A>G maps to ENST00000216177 R254R. Only missense variants will be evaluated by CHASM.
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-G3-A3CG-01A-11D-A20W-10 chr12:89865460 A>G maps to NM_172240.2 A202A. 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-AACT-01A-11D-A40R-10 chr19:14047180 T>C maps to NM_024825.3 E113E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAC9-01A-11D-A40R-10 chr7:131241028 G>C maps to NM_001018111.2 P30P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACV-01A-11D-A40R-10 chr7:131241028 G>C maps to NM_001018111.2 P30P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACZ-01A-11D-A40R-10 chr7:131241034 C>G maps to NM_001018111.2 P28P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADO-01A-11D-A40R-10 chr7:131241028 G>C maps to NM_001018111.2 P30P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WJ-A86L-01A-12D-A45V-10 chr7:131241028 G>C maps to NM_001018111.2 P30P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WX-AA44-01A-11D-A38X-10 chr7:131241028 G>C maps to NM_001018111.2 P30P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XR-A8TE-01A-11D-A35Z-10 chr7:131241034 C>G maps to NM_001018111.2 P28P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XR-A8TF-01A-11D-A35Z-10 chr7:131241034 C>G maps to NM_001018111.2 P28P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZP-A9CZ-01A-11D-A382-10 chr7:131241028 G>C maps to NM_001018111.2 P30P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MA-01A-11D-A20W-10 chr3:127379377 A>G maps to NM_015720.2 E169E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-AAV0-01A-11D-A36X-10 chr3:127391217 G>T maps to NM_015720.2 L571L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NI-A8LF-01A-11D-A35Z-10 chr23:84600899 A>T 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-DD-AADY-01A-11D-A40R-10 chr20:30803115 G>A maps to NM_015352.1 Q97Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5261-01A-01D-A12Z-10 chr23:24741359 G>A did not map to a codon.
Sequencing variant TCGA-DD-A3A0-01A-11D-A20W-10 chr23:24741324 A>G did not map to a codon.
Sequencing variant TCGA-DD-A3A0-01A-11D-A20W-10 chr23:24844594 C>T 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-DD-AAC8-01A-11D-A40R-10 chr23:24757521 A>T did not map to a codon.
Sequencing variant TCGA-GJ-A3OU-01A-31D-A382-10 chr23:24861713 G>A did not map to a codon.
Sequencing variant TCGA-3K-AAZ8-01A-12D-A38X-10 chr8:42218855 C>A maps to NM_002690.1 P198P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAEA-01A-11D-A40R-10 chr8:42218870 A>G maps to NM_002690.1 E203E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAE9-01A-11D-A40R-10 chr19:50902182 T>C maps to ENST00000391817 D25D. Only missense variants will be evaluated by CHASM.
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-DD-A3A0-01A-11D-A20W-10 chr22:42991557 A>G maps to ENST00000415122 T309T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9H8-01A-11D-A38X-10 chr12:133254295 C>T maps to ENST00000455752 Q196Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr12:133218835 A>G maps to ENST00000455752 D1703D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EG-01A-11D-A20W-10 chr12:133249251 A>G maps to ENST00000455752 S552S. 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-2Y-A9H3-01A-11D-A382-10 chr15:89867411 G>A maps to NM_002693.2 Q666*. 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-DD-AACT-01A-11D-A40R-10 chr7:44119331 C>G maps to NM_013284.2 L160L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A3KF-01A-11D-A20W-10 chr3:121158913 T>C maps to ENST00000393672 G2574G. 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-DD-AAC8-01A-11D-A40R-10 chr3:121256055 C>G did not map to a codon.
Sequencing variant TCGA-DD-AACL-01A-11D-A40R-10 chr3:121208681 T>A maps to ENST00000393672 S1168S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAD6-01A-11D-A40R-10 chr3:121206680 A>G maps to ENST00000393672 N1835N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A2QR-01A-11D-A20W-10 chr3:121186372 A>G maps to ENST00000393672 P2456P. 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-A1EE-01A-11D-A12Z-10 chr2:86259501 C>A maps to NM_015425.3 E1389*. 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.
Alternatively spliced codon TCGA-DD-A39Y-01A-11D-A20W-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr12:106824061 T>C maps to NM_018082.5 S425S. Only missense variants will be evaluated by CHASM.
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-FV-A2QR-01A-11D-A20W-10 chr8:22106821 A>G maps to NM_001722.2 R307R. 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-DD-A1EE-01A-11D-A12Z-10 chr22:41928118 G>T maps to NM_138338.3 S113*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A5UD-01A-11D-A28X-10 chr7:53103630 G>A maps to NM_182595.3 P89P. 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-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-G3-A3CJ-01A-11D-A20W-10 chr7:95035442 A>G maps to NM_000305.2 P298P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A9FW-01A-11D-A36X-10 chr3:119378985 C>T maps to NM_022135.2 L95L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A1-01A-11D-A20W-10 chr13:38153043 T>C maps to NM_006475.2 T633T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XR-A8TF-01A-11D-A35Z-10 chr13:38159033 G>T maps to NM_006475.2 L309L. Only missense variants will be evaluated by CHASM.
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-DD-AAE9-01A-11D-A40R-10 chr8:43173613 C>T maps to NM_001005365.2 Q346*. 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-CC-A8HU-01A-11D-A35Z-10 chr22:16287879 C>A maps to NM_001136213.1 V2V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACV-01A-11D-A40R-10 chr14:20019995 G>A maps to ENST00000439503 S75S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADO-01A-11D-A40R-10 chr3:87313642 A>G maps to NM_001122757.1 L104L. 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-ED-A8O5-01A-11D-A35Z-10 chr1:167343487 G>A maps to NM_002697.3 T182T. Only missense variants will be evaluated by CHASM.
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-XR-A8TD-01A-12D-A38X-10 chr4:147560456 T>C maps to NM_004575.2 G55G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZS-A9CG-01A-11D-A36X-10 chr5:145719607 G>A maps to NM_002700.2 A206A. 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-DD-AACZ-01A-11D-A40R-10 chr7:39379607 T>A maps to NM_007252.3 P293P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39Y-01A-11D-A20W-10 chr10:71969412 A>G maps to NM_021129.3 P180P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CJ-01A-11D-A20W-10 chr10:71969412 A>G maps to NM_021129.3 P180P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A9FS-01A-11D-A36X-10 chr19:10218692 G>A maps to NM_001040664.2 E132E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZP-A9D2-01A-11D-A382-10 chr19:10221279 G>T maps to NM_001040664.2 E341*. 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-2Y-A9H1-01A-11D-A382-10 chr19:287715 G>A maps to NM_177543.1 D101D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WQ-A9G7-01A-11D-A36X-10 chr19:282793 C>T maps to NM_177543.1 S187S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IE-01A-21D-A382-10 chr22:46594480 C>T maps to NM_001001928.2 V67V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A8O5-01A-11D-A35Z-10 chr4:23803847 C>A maps to NM_013261.3 G714*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WQ-A9G7-01A-11D-A36X-10 chr5:149219651 C>T maps to NM_133263.3 H889H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAEB-01A-11D-A40R-10 chr4:57261619 A>G maps to NM_002703.3 D484D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WQ-A9G7-01A-11D-A36X-10 chr4:57269501 C>T maps to NM_002703.3 A156A. 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-DD-A1ED-01A-11D-A152-10 chr4:76797574 T>C maps to NM_006239.2 E395E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39X-01A-11D-A20W-10 chr4:76793206 C>T maps to NM_006239.2 K540K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9GZ-01A-11D-A38X-10 chr12:81719605 C>A maps to NM_003625.2 G864G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9H6-01A-11D-A38X-10 chr19:49651353 C>T maps to NM_003660.2 G950G. 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-AACU-01A-11D-A40R-10 chr11:7618804 A>G maps to NM_003621.2 T129T. 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-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-MR-A8JO-01A-12D-A35Z-10 chr17:58740433 G>T maps to NM_003620.3 E447*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5C-AAPD-01A-21D-A38X-10 chr17:56833447 G>A maps to NM_014906.3 E30E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5C-AAPD-01A-21D-A38X-10 chr17:56833450 G>C maps to NM_014906.3 P31P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr17:57058077 T>C maps to NM_014906.3 L652L. 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-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-AAEK-01A-11D-A40R-10 chr1:161140407 A>C did not map to a codon.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr1:161138328 C>A maps to NM_001122764.1 T193T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YA-A8S7-01A-11D-A36X-10 chr11:67166282 C>T maps to NM_001008709.1 V275V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9GZ-01A-11D-A38X-10 chr2:28975007 G>T maps to NM_002709.2 L6L. 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-DD-AACI-01A-11D-A40R-10 chr6:30570415 T>A maps to NM_002714.2 P670P. 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-DD-A39Z-01A-11D-A20W-10 chr12:80226242 T>C maps to NM_001143885.1 E172E. Only missense variants will be evaluated by CHASM.
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-2Y-A9H3-01A-11D-A382-10 chr19:45895302 G>A maps to NM_001142502.1 L550L. Only missense variants will be evaluated by CHASM.
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-WQ-A9G7-01A-11D-A36X-10 chr8:145724316 C>T maps to NM_032902.5 R117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WQ-A9G7-01A-11D-A36X-10 chr8:145727135 T>C maps to NM_032902.5 P479P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADU-01A-11D-A40R-10 chr17:37791908 C>T maps to ENST00000394271 R176R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XR-A8TF-01A-11D-A35Z-10 chr17:37791872 A>T maps to ENST00000394271 T164T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAD3-01A-11D-A40R-10 chr7:113518593 G>A maps to NM_002711.3 V851V. 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-2Y-A9HA-01A-11D-A38X-10 chr20:58514512 A>G maps to NM_006242.3 D158D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr23:49127167 G>A did not map to a codon.
Sequencing variant TCGA-5R-AAAM-01A-12D-A40R-10 chr23:49126706 G>T did not map to a codon.
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-ES-A2HS-01A-11D-A183-10 chr23:49143279 T>C did not map to a codon.
Sequencing variant TCGA-G3-A3CJ-01A-11D-A20W-10 chr23:49138447 G>A did not map to a codon.
Sequencing variant TCGA-DD-A3A0-01A-11D-A20W-10 chr2:242089945 G>A maps to NM_002712.1 S12S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EE-01A-11D-A12Z-10 chr8:30643818 G>A maps to NM_001009552.1 Q288*. 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-G3-AAV4-01A-11D-A382-10 chr8:26220350 T>C maps to NM_001177591.1 D273D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr3:135825068 C>T maps to NM_002718.4 N1078N. 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-A1EG-01A-11D-A20W-10 chr3:135745882 T>C maps to NM_002718.4 A735A. 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-G3-AAV0-01A-11D-A36X-10 chr3:135721278 T>C maps to NM_002718.4 N313N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADE-01A-11D-A40R-10 chr23:301662 C>A did not map to a codon.
Sequencing variant TCGA-ZS-A9CG-01A-11D-A36X-10 chr23:306922 T>C did not map to a codon.
Sequencing variant TCGA-DD-A1EG-01A-11D-A20W-10 chr14:35554855 C>T maps to NM_017917.2 E434E. 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-4R-AA8I-01A-11D-A382-10 chr6:42975947 C>T maps to NM_006245.2 Y289Y. 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-DD-AADC-01A-11D-A40R-10 chr14:63881863 T>C maps to ENST00000422769 V247V. 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-DD-A3A1-01A-11D-A20W-10 chr4:101953445 T>C maps to NM_000944.4 G439G. 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-AAE7-01A-11D-A40R-10 chr3:73113261 G>A maps to NM_174907.2 E201E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAW0-01A-11D-A40R-10 chr3:73046214 G>T maps to NM_174907.2 A9A. 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-DD-AADD-01A-11D-A40R-10 chr14:94711988 C>T maps to NM_058237.1 S470S. 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-2Y-A9H3-01A-11D-A382-10 chr19:46893575 C>T maps to NM_006247.2 N491N. 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-DD-A1EG-01A-11D-A20W-10 chr5:64878959 T>C maps to NM_015342.2 T482T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAEA-01A-11D-A40R-10 chr5:64868009 C>G maps to NM_015342.2 S289*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADJ-01A-11D-A40R-10 chr23:48759211 T>G did not map to a codon.
Sequencing variant TCGA-5R-AA1C-01A-11D-A40R-10 chr2:11317881 C>T maps to NM_152391.3 I179I. 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-DD-AAC8-01A-11D-A40R-10 chr19:8563755 G>A maps to NM_032152.4 A312A. Only missense variants will be evaluated by CHASM.
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-DD-AADG-01A-11D-A40R-10 chr1:13475240 C>T maps to NM_001099850.1 E296E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9GZ-01A-11D-A38X-10 chr1:12919904 G>T maps to NM_023014.1 T215T. 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-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-AACD-01A-11D-A40R-10 chr11:82536164 C>T did not map to a codon.
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-ZS-A9CG-01A-11D-A36X-10 chr6:106552763 C>T maps to NM_001198.3 V243V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr11:45241210 C>T maps to NM_020229.2 I249I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EE-01A-11D-A12Z-10 chr11:45246095 C>T maps to NM_020229.2 G391G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADB-01A-11D-A40R-10 chr11:45203391 G>T maps to NM_020229.2 T59T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A8YO-01A-11D-A36X-10 chr6:100061788 G>T maps to ENST00000359773 A436A. 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-LG-A9QD-01A-11D-A382-10 chr8:70981936 G>A maps to NM_024504.2 F53F. 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-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-G3-AAV4-01A-11D-A382-10 chr21:43221606 C>T maps to NM_022115.3 Q1439Q. 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-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-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-DD-AADG-01A-11D-A40R-10 chr5:23527458 G>A maps to NM_020227.2 G754G. 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-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-WQ-AB4B-01A-11D-A40P-10 chr20:47267527 C>T maps to NM_020820.3 L907L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WQ-AB4B-01A-11D-A40P-10 chr20:47267975 C>T maps to NM_020820.3 E871E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZP-A9D0-01A-11D-A36X-10 chr20:47262564 C>T maps to NM_020820.3 S1112S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BD-A3EP-01A-11D-A22F-10 chr8:68972974 T>C maps to NM_024870.2 L434L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MB-01A-11D-A20W-10 chr8:69002856 T>C maps to NM_024870.2 I719I. 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-AADK-01A-11D-A40R-10 chr8:69020462 T>A maps to NM_024870.2 V945V. 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-NI-A8LF-01A-11D-A35Z-10 chr8:68950407 T>C maps to NM_024870.2 T240T. 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-ZP-A9D1-01A-11D-A382-10 chr10:72357835 T>G maps to NM_005041.4 P547P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A3KF-01A-11D-A20W-10 chr1:186276410 G>A maps to NM_005807.3 K520K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACT-01A-11D-A40R-10 chr1:186266078 T>G maps to NM_005807.3 S24S. 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-GJ-A9DB-01A-11D-A36X-10 chr1:186277295 T>C maps to NM_005807.3 S815S. 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-4R-AA8I-01A-11D-A382-10 chr20:62198472 C>T maps to NM_001037335.2 T746T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A8-01A-11D-A22F-10 chr20:62190679 G>A maps to NM_001037335.2 L2623L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A97K-01A-21D-A382-10 chr12:42858347 C>T maps to NM_153026.2 R496R. 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-DD-AACH-01A-11D-A40R-10 chr3:64132536 G>T maps to NM_198859.3 S543S. 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-WQ-A9G7-01A-11D-A36X-10 chr23:49032589 C>T did not map to a codon.
Sequencing variant TCGA-DD-AAEH-01A-11D-A40R-10 chr12:57132216 C>T 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-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-ZP-A9D0-01A-11D-A36X-10 chr7:151329169 C>A maps to NM_016203.3 E247*. 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-AACI-01A-11D-A40R-10 chr17:66521089 A>C maps to NM_212472.1 G180G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr7:618964 G>T maps to NM_002735.2 P273P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAE8-01A-11D-A40R-10 chr7:106799921 T>C maps to NM_002736.2 L384L. 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-DD-AAC8-01A-11D-A40R-10 chr19:54401691 A>T did not map to a codon.
Sequencing variant TCGA-DD-AADG-01A-11D-A40R-10 chr19:54395039 G>T maps to NM_002739.3 T214T. 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-AAVQ-01A-11D-A40R-10 chr19:11558366 G>A maps to ENST00000436195 E321E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A3KG-01A-11D-A20W-10 chr1:2116023 G>A maps to NM_002744.4 L526L. 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-DD-AACY-01A-11D-A40R-10 chr19:47200428 G>A maps to ENST00000449438 T434T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAD6-01A-11D-A40R-10 chr19:47214209 G>T maps to ENST00000449438 C155*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAC8-01A-11D-A40R-10 chr8:48746958 T>A did not map to a codon.
Sequencing variant TCGA-DD-AACN-01A-11D-A40R-10 chr8:48846650 C>T did not map to a codon.
Sequencing variant TCGA-DD-AACP-01A-11D-A40R-10 chr8:48767934 C>T did not map to a codon.
Sequencing variant TCGA-DD-AADM-01A-11D-A40R-10 chr8:48774688 C>A did not map to a codon.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr8:48707063 T>A did not map to a codon.
Sequencing variant TCGA-G3-A3CK-01A-11D-A20W-10 chr8:48856411 C>A did not map to a codon.
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-2Y-A9GX-01A-11D-A382-10 chr4:82031669 G>A maps to NM_006259.1 N624N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-AAV3-01A-11D-A36X-10 chr4:82073195 G>A maps to NM_006259.1 Q335*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2V-A95S-01A-11D-A36X-10 chr2:179315143 A>G maps to NM_001139517.1 F9F. 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-2Y-A9GW-01A-11D-A382-10 chr23:3573253 G>A did not map to a codon.
Sequencing variant TCGA-BC-A3KF-01A-11D-A20W-10 chr23:3631157 A>G did not map to a codon.
Sequencing variant TCGA-DD-A1ED-01A-11D-A152-10 chr23:3573329 A>G did not map to a codon.
Sequencing variant TCGA-T1-A6J8-01A-11D-A32G-10 chr23:3533925 G>T did not map to a codon.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr2:238475760 A>G maps to NM_015893.1 R69R. Only missense variants will be evaluated by CHASM.
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-BC-A3KF-01A-11D-A20W-10 chr4:148559745 T>C maps to NM_138364.2 G825G. Only missense variants will be evaluated by CHASM.
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-ES-A2HS-01A-11D-A183-10 chr14:23393527 G>T maps to NM_006109.3 R384R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WJ-A86L-01A-12D-A45V-10 chr14:23398483 T>A maps to NM_006109.3 T29T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A8HT-01A-11D-A35Z-10 chr12:3701518 G>A did not map to a codon.
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-EP-A2KA-01A-11D-A183-10 chr2:128186177 C>A maps to ENST00000409048 R382R. 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-ZP-A9D1-01A-11D-A382-10 chr17:27030971 G>A maps to ENST00000415329 I233I. 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-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-ED-A8O5-01A-11D-A35Z-10 chr4:16077498 G>A maps to NM_006017.2 L11L. 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-DD-A119-01A-11D-A12Z-10 chr2:95940506 A>G maps to NM_144707.2 G58G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACI-01A-11D-A40R-10 chr2:95943752 G>T did not map to a codon.
Sequencing variant TCGA-ZS-A9CF-01A-11D-A382-10 chr2:95941841 C>A maps to NM_144707.2 A153A. 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-DD-AACT-01A-11D-A40R-10 chr14:75329265 A>T maps to ENST00000445876 A424A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr14:75330180 A>G maps to ENST00000445876 P119P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr11:60666656 G>T maps to NM_014502.4 A316A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZP-A9D1-01A-11D-A382-10 chr11:60670108 T>C maps to NM_014502.4 P136P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9H3-01A-11D-A382-10 chr1:52871470 A>T maps to NM_032864.3 K84*. 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-A1ED-01A-11D-A152-10 chr9:116053282 T>C maps to NM_004697.3 G454G. Only missense variants will be evaluated by CHASM.
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-DD-AAVX-01A-11D-A40R-10 chr2:153526801 C>A maps to ENST00000410080 E589*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADG-01A-11D-A40R-10 chr6:4032938 C>T maps to NM_003913.4 S396S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADQ-01A-11D-A40R-10 chr6:4060748 C>T maps to NM_003913.4 Q975*. 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-DD-AADJ-01A-11D-A40R-10 chr17:1582361 C>A maps to NM_006445.3 L516L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XR-A8TG-01A-11D-A35Z-10 chr17:1554096 C>T maps to NM_006445.3 *2336*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr12:49690225 T>C maps to ENST00000451891 D206D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADC-01A-11D-A40R-10 chr23:106890948 A>G did not map to a codon.
Sequencing variant TCGA-BC-4073-01B-02D-A12Z-10 chr23:12838903 A>G did not map to a codon.
Sequencing variant TCGA-BC-A3KF-01A-11D-A20W-10 chr17:57247211 A>G maps to NM_018304.3 T33T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39Z-01A-11D-A20W-10 chr17:57262913 A>G maps to NM_018304.3 E131E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-AAV7-01A-11D-A382-10 chr19:50119402 C>T maps to NM_020719.1 N1808N. 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-EP-A2KB-01A-11D-A183-10 chr19:5783321 C>A maps to NM_001134316.1 P312P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MA-01A-11D-A20W-10 chr22:45110468 A>G did not map to a codon.
Sequencing variant TCGA-G3-AAV7-01A-11D-A382-10 chr22:45132982 C>T maps to NM_001198721.1 P364P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAE7-01A-11D-A40R-10 chr11:36472811 G>A maps to NM_001160167.1 L213L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACL-01A-11D-A40R-10 chr23:37285108 A>G did not map to a codon.
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-2Y-A9H4-01A-11D-A382-10 chr11:32875006 A>G maps to NM_024081.4 P205P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A123-01A-11D-A12Z-10 chr3:9988525 C>A maps to NM_207351.3 S777S. Only missense variants will be evaluated by CHASM.
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-DD-AAW0-01A-11D-A40R-10 chr3:9988876 C>T maps to NM_207351.3 W660*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EG-01A-11D-A20W-10 chr6:27218542 A>G maps to NM_005865.3 G183G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACN-01A-11D-A40R-10 chr6:27223090 C>A maps to NM_005865.3 V514V. 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-G3-A3CG-01A-11D-A20W-10 chr6:27220675 T>C maps to NM_005865.3 S366S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAE9-01A-11D-A40R-10 chr16:2867808 C>A maps to NM_006799.2 C33*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAVP-01A-11D-A40R-10 chr11:86518741 G>C maps to NM_007173.4 G19G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5C-A9VG-01A-11D-A36X-10 chr16:2764243 C>T maps to NM_031948.3 V110V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr16:2834719 G>T maps to NM_152891.2 A256A. Only missense variants will be evaluated by CHASM.
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-EP-A2KB-01A-11D-A183-10 chr6:84234260 T>C maps to NM_153362.2 I367I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IE-01A-21D-A382-10 chr7:141537855 C>T maps to NM_001008270.2 Q78Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CG-01A-11D-A20W-10 chr4:152212523 A>G maps to NM_183375.2 R302R. 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-CC-A8HU-01A-11D-A35Z-10 chr19:687061 C>A maps to NM_214710.3 E170*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WX-AA44-01A-11D-A38X-10 chr10:25140373 T>C maps to NM_020200.5 P191P. 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-G3-AAV0-01A-11D-A36X-10 chr15:55972369 T>G maps to NM_173814.4 G285G. Only missense variants will be evaluated by CHASM.
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-DD-A119-01A-11D-A12Z-10 chr9:79461503 A>G maps to NM_015225.2 S145S. 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-DD-AACY-01A-11D-A40R-10 chr9:79322010 A>G maps to NM_015225.2 L1727L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADU-01A-11D-A40R-10 chr9:79321162 T>C maps to NM_015225.2 T2009T. 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-DD-A1EG-01A-11D-A20W-10 chr10:104163073 T>C maps to NM_002779.3 G986G. 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-DD-AACA-01A-11D-A40R-10 chr8:18662112 C>A did not map to a codon.
Sequencing variant TCGA-DD-AADN-01A-11D-A40R-10 chr8:18658786 A>C maps to ENST00000440756 A672A. 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-BC-A10W-01A-11D-A12Z-10 chr2:113958937 A>G maps to NM_012455.2 S1039S. 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-YA-A8S7-01A-11D-A36X-10 chr14:73637639 T>C maps to NM_000021.3 L75L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A7SH-01A-11D-A382-10 chr19:36236843 C>T maps to NM_172341.1 R5*. 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-2Y-A9GU-01A-11D-A382-10 chr19:43420364 C>T maps to NM_002782.3 Q113Q. 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-5R-AAAM-01A-12D-A40R-10 chr19:43766111 A>T maps to NM_002784.3 Y203*. 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-AADC-01A-11D-A40R-10 chr9:15469956 T>A maps to NM_001128217.1 K338*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr8:87076415 G>A maps to ENST00000276616 S210S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAE7-01A-11D-A40R-10 chr16:67969963 T>A maps to NM_002801.2 T95T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr14:23511751 G>T maps to NM_001099780.1 R106R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WQ-A9G7-01A-11D-A36X-10 chr17:36912244 T>C did not map to a codon.
Sequencing variant TCGA-ZS-A9CG-01A-11D-A36X-10 chr7:103008216 A>T maps to NM_002803.2 R369*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAE2-01A-11D-A40R-10 chr11:47441912 G>A maps to NM_002804.4 L343L. 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-AAD6-01A-11D-A40R-10 chr14:53185035 A>G maps to NM_002806.3 P241P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WX-AA46-01A-11D-A38X-10 chr14:53175061 G>T maps to NM_002806.3 E55*. 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-4R-AA8I-01A-11D-A382-10 chr17:30806364 C>T maps to NM_002815.2 R337*. 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-CC-A3MB-01A-11D-A20W-10 chr17:38140565 A>G maps to NM_002809.2 K80K. 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-DD-AACJ-01A-11D-A40R-10 chr3:64004652 A>C maps to ENST00000492933 L239L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10W-01A-11D-A12Z-10 chr2:54122146 T>C maps to NM_014614.2 T1303T. 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-XR-A8TG-01A-11D-A35Z-10 chr21:40549462 T>C maps to NM_003720.2 A230A. 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-DD-AADF-01A-11D-A40R-10 chr6:31106508 C>T maps to NM_014068.2 H40H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADI-01A-11D-A40R-10 chr13:20346622 T>G maps to NM_001042414.1 R145R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAVQ-01A-11D-A40R-10 chr7:56084930 A>G maps to NM_004577.3 F139F. 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-G3-A3CJ-01A-11D-A20W-10 chr9:72338480 T>C maps to NM_001099666.1 G236G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAVU-01A-11D-A40R-10 chr19:804890 G>A maps to NM_002819.4 Q223Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAW3-01A-11D-A40P-10 chr1:97250725 C>T maps to ENST00000370197 R274*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr7:99032619 G>A maps to NM_001198879.1 D131D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KC-01A-11D-A20W-10 chr7:99021403 A>G maps to NM_001198879.1 F687F. 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 chr23:23411679 T>C 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-DD-A1EG-01A-11D-A20W-10 chr23:23411606 A>G did not map to a codon.
Sequencing variant TCGA-DD-A3A0-01A-11D-A20W-10 chr23:23411676 T>C did not map to a codon.
Sequencing variant TCGA-DD-A3A1-01A-11D-A20W-10 chr23:23411616 T>C 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-DD-AACI-01A-11D-A40R-10 chr10:89720790 A>G maps to NM_000314.4 E314E. 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-4R-AA8I-01A-11D-A382-10 chr1:71437416 C>T did not map to a codon.
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-G3-A3CG-01A-11D-A20W-10 chr9:130887594 C>G maps to NM_025072.5 V135V. 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-DD-AAC8-01A-11D-A40R-10 chr1:186644522 A>T maps to NM_000963.2 A421A. 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-CC-A3MA-01A-11D-A20W-10 chr6:43097477 T>C maps to NM_002821.3 G127G. 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-EP-A2KA-01A-11D-A183-10 chr20:49197897 C>A maps to NM_002827.2 P395P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZP-A9CY-01A-11D-A382-10 chr12:112915713 C>A maps to ENST00000392596 A329A. 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-DD-AAC8-01A-11D-A40R-10 chr4:87638219 T>A maps to NM_080685.2 G445G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr4:87690932 G>T maps to NM_080685.2 E1506*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAE6-01A-11D-A40R-10 chr1:214585025 C>T did not map to a codon.
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-CC-A8HV-01A-11D-A35Z-10 chr1:114380833 T>C maps to NM_015967.5 K396K. 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-ED-A97K-01A-21D-A382-10 chr2:120712791 G>T maps to NM_002830.2 E625*. 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-G3-AAV0-01A-11D-A36X-10 chr1:202119443 T>G maps to ENST00000309017 L433L. 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-G3-AAV5-01A-11D-A36X-10 chr20:3005218 C>G maps to NM_002836.3 Y522*. 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-DD-AAC8-01A-11D-A40R-10 chr12:70983957 A>T maps to NM_001109754.1 L612L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACL-01A-11D-A40R-10 chr12:70989856 A>T maps to NM_001109754.1 S410S. 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-WQ-A9G7-01A-11D-A36X-10 chr12:70983908 G>A maps to NM_001109754.1 L629L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WQ-A9G7-01A-11D-A36X-10 chr12:70983920 G>A maps to NM_001109754.1 Q625*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5C-A9VG-01A-11D-A36X-10 chr9:8733789 C>T maps to NM_002839.3 T18T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACI-01A-11D-A40R-10 chr9:8404600 T>A maps to NM_002839.3 P1382P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACN-01A-11D-A40R-10 chr9:8341938 A>G maps to NM_002839.3 D1567D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACT-01A-11D-A40R-10 chr9:8527348 A>G maps to NM_002839.3 S182S. 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-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-A1EE-01A-11D-A12Z-10 chr19:55713469 C>T maps to NM_002842.3 G369G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACP-01A-11D-A40R-10 chr19:55715249 G>A maps to NM_002842.3 V262V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAD1-01A-11D-A40R-10 chr19:55715189 G>A maps to NM_002842.3 D282D. 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-DD-A39Y-01A-11D-A20W-10 chr6:128388714 A>G maps to ENST00000368210 A702A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAE2-01A-11D-A40R-10 chr6:128540088 A>G maps to ENST00000368210 N282N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZP-A9D1-01A-11D-A382-10 chr6:128388828 C>T maps to ENST00000368210 G664G. 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-AAE1-01A-11D-A40R-10 chr2:220172165 C>A maps to NM_002846.3 G94*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-AAV7-01A-11D-A382-10 chr7:157959680 G>C maps to NM_002847.3 A284A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr12:15704606 T>C did not map to a codon.
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-DD-AACT-01A-11D-A40R-10 chr19:5244416 G>A maps to NM_002850.3 G355G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9GU-01A-11D-A382-10 chr20:40979350 G>A maps to ENST00000373198 Y594Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9HA-01A-11D-A38X-10 chr20:41306595 C>A maps to ENST00000373198 E355*. 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-DD-AADB-01A-11D-A40R-10 chr7:121651009 C>A maps to NM_002851.2 S637*. 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-AAVY-01A-11D-A40R-10 chr17:40575008 G>T maps to NM_012232.5 S36*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr11:112097189 T>C maps to NM_000317.2 R8R. 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-5C-AAPD-01A-21D-A38X-10 chr2:20490527 C>T maps to ENST00000361078 Q392Q. 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-WQ-A9G7-01A-11D-A36X-10 chr8:30889770 G>A maps to NM_013357.2 I176I. 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-BC-A3KG-01A-11D-A20W-10 chr12:44132188 T>C maps to NM_031292.3 K456K. 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-G3-A3CJ-01A-11D-A20W-10 chr12:44139932 A>G maps to NM_031292.3 D393D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EE-01A-11D-A12Z-10 chr7:99818612 C>A maps to NM_024070.3 C240*. 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-ZP-A9D0-01A-11D-A36X-10 chr3:110837590 T>G maps to NM_015480.1 T197T. 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-2Y-A9HA-01A-11D-A38X-10 chr21:45545889 A>T did not map to a codon.
Sequencing variant TCGA-2Y-A9GT-01A-11D-A382-10 chr2:1648511 C>G maps to NM_012293.1 S1207S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr2:1670258 C>T did not map to a codon.
Sequencing variant TCGA-BC-A10W-01A-11D-A12Z-10 chr2:1652431 C>T maps to NM_012293.1 G1040G. 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-DD-AADY-01A-11D-A40R-10 chr2:1647158 C>T maps to NM_012293.1 V1311V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAW1-01A-11D-A40P-10 chr2:1652299 C>T maps to NM_012293.1 L1084L. 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-DD-AAD3-01A-11D-A40R-10 chr8:52287172 G>A maps to NM_144651.4 L1226L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CJ-01A-11D-A20W-10 chr8:52321456 A>G maps to NM_144651.4 A909A. 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-DD-AACY-01A-11D-A40R-10 chr3:58410539 T>G maps to NM_017771.3 P530P. 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-EP-A2KB-01A-11D-A183-10 chr17:79892335 T>C maps to ENST00000432920 E248E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9H2-01A-12D-A382-10 chr1:226109909 C>T maps to NM_013328.2 V104V. 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-CC-A8HT-01A-11D-A35Z-10 chr12:9356497 T>A maps to NM_002864.2 K45*. 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-DD-A11D-01A-11D-A12Z-10 chr20:3147348 A>G did not map to a codon.
Sequencing variant TCGA-2Y-A9GZ-01A-11D-A38X-10 chr6:163984602 C>T maps to ENST00000361752 V268V. 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-A119-01A-11D-A12Z-10 chr11:32955842 T>C maps to NM_001076786.1 G884G. 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-CC-A9FW-01A-11D-A36X-10 chr2:136389286 G>A did not map to a codon.
Sequencing variant TCGA-DD-AACG-01A-11D-A40R-10 chr2:136481726 C>G maps to ENST00000409606 V1056V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACH-01A-11D-A40R-10 chr2:136437816 T>A maps to ENST00000409606 S760S. 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-ZP-A9CZ-01A-11D-A382-10 chr12:57674221 C>T maps to ENST00000438036 Q439Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A9FW-01A-11D-A36X-10 chr12:72164379 A>T maps to NM_014999.2 A76A. Only missense variants will be evaluated by CHASM.
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-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-A12Z-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-DD-AACK-01A-11D-A40R-10 chr23:129318330 C>A did not map to a codon.
Sequencing variant TCGA-ED-A66Y-01A-11D-A30V-10 chr23:129306276 G>T did not map to a codon.
Sequencing variant TCGA-DD-AAD0-01A-11D-A40R-10 chr23:154490388 T>A did not map to a codon.
Sequencing variant TCGA-DD-AAVR-01A-11D-A40R-10 chr23:154493378 G>A did not map to a codon.
Sequencing variant TCGA-2Y-A9HA-01A-11D-A38X-10 chr5:57913468 G>A did not map to a codon.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr1:220387264 A>G maps to ENST00000358951 V79V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAC9-01A-11D-A40R-10 chr1:220340742 T>C did not map to a codon.
Sequencing variant TCGA-DD-AADO-01A-11D-A40R-10 chr1:220364507 T>C maps to ENST00000358951 Q463Q. 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-GJ-A3OU-01A-31D-A382-10 chr23:102192892 T>C 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-AAVR-01A-11D-A40R-10 chr17:40277842 C>T maps to NM_201434.1 Q203Q. 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-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-ZS-A9CF-01A-11D-A382-10 chr9:125719406 A>G maps to NM_012197.3 E23E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr1:174606550 T>C maps to NM_014857.3 H583H. 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-DD-AACF-01A-11D-A40R-10 chr14:24737795 G>A maps to NM_182836.1 N310N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr1:76253186 T>C maps to NM_004582.2 T3T. 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-DD-AADU-01A-11D-A40R-10 chr3:8988965 T>A maps to NM_020165.3 T68T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MB-01A-11D-A20W-10 chr8:117870612 A>G maps to NM_006265.2 S153S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MB-01A-11D-A20W-10 chr8:117870654 T>C maps to NM_006265.2 R139R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A8YO-01A-11D-A36X-10 chr9:110091935 G>T maps to NM_002874.3 *410L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CG-01A-11D-A20W-10 chr9:110064349 A>G maps to NM_002874.3 E61E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39Z-01A-11D-A20W-10 chr12:4665648 A>G maps to NM_001130862.1 K301K. 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-DD-A1EG-01A-11D-A20W-10 chr17:56798129 A>G maps to NM_058216.1 T287T. 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-DD-AACJ-01A-11D-A40R-10 chr3:51664803 G>T maps to NM_015106.2 E228*. Only missense variants will be evaluated by CHASM.
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-DD-AACF-01A-11D-A40R-10 chr7:4839834 G>T maps to NM_018059.4 P983P. 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-DD-AACL-01A-11D-A40R-10 chr11:36595109 A>T maps to NM_000448.2 K86*. 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-ES-A2HS-01A-11D-A183-10 chr5:34796131 G>T maps to NM_001145521.1 G86*. 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-4R-AA8I-01A-11D-A382-10 chr2:121036311 C>T maps to NM_002881.2 G24G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACV-01A-11D-A40R-10 chr14:36155746 C>A did not map to a codon.
Sequencing variant TCGA-DD-AAE2-01A-11D-A40R-10 chr14:36017744 C>A did not map to a codon.
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-AACL-01A-11D-A40R-10 chr20:20601244 A>T maps to NM_020343.3 A421A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADM-01A-11D-A40R-10 chr20:20505079 G>A maps to NM_020343.3 A1290A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CG-01A-11D-A20W-10 chr20:37202798 A>G maps to NM_020336.2 T1383T. 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-DD-AACG-01A-11D-A40R-10 chr9:135985071 T>C maps to NM_006266.2 R175R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACL-01A-11D-A40R-10 chr9:135977864 G>A maps to NM_006266.2 S669S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACX-01A-11D-A40R-10 chr9:135983385 G>A maps to NM_006266.2 L396L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5R-AA1D-01A-11D-A382-10 chr20:32664864 C>T maps to NM_016732.1 A230A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39V-01A-11D-A20W-10 chr20:32664867 C>T maps to NM_016732.1 G231G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAE1-01A-11D-A40R-10 chr20:32664876 C>T maps to NM_016732.1 G234G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADR-01A-11D-A40R-10 chr8:85774618 A>C maps to NM_001100391.1 R181R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAD8-01A-11D-A40R-10 chr5:170720951 G>A maps to NM_022897.3 R1003R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A0-01A-11D-A20W-10 chr2:109392276 A>G maps to NM_006267.4 E2794E. 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-DD-AADO-01A-11D-A40R-10 chr2:109384437 T>C maps to NM_006267.4 D2481D. 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-CC-5262-01A-01D-A12Z-10 chr9:6012697 G>T maps to NM_012416.2 T970T. 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-EP-A2KA-01A-11D-A183-10 chr17:2921395 G>A maps to NM_015085.4 V512V. 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-DD-A3A1-01A-11D-A20W-10 chr4:99342469 A>G maps to NM_001100426.1 E456E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XR-A8TF-01A-11D-A35Z-10 chr3:152880628 G>T maps to NM_002886.2 S49S. 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-4R-AA8I-01A-11D-A382-10 chr4:160264433 A>T maps to NM_014247.2 G883G. Only missense variants will be evaluated by CHASM.
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-AACQ-01A-11D-A40R-10 chr12:48143535 C>G maps to NM_001098531.2 V294V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAD2-01A-11D-A40R-10 chr12:48137436 T>A maps to NM_001098531.2 P567P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A6M6-01A-11D-A32G-10 chr12:48134733 C>A maps to NM_001098531.2 T671T. 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-DD-AAEK-01A-11D-A40R-10 chr2:173879263 C>T maps to NM_007023.3 V577V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAW2-01A-11D-A40P-10 chr7:22179654 C>T maps to ENST00000344041 S604S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9H4-01A-11D-A382-10 chr5:130769232 T>C maps to ENST00000514667 L1338L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAC9-01A-11D-A40R-10 chr5:130797636 C>T maps to ENST00000514667 L925L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADF-01A-11D-A40R-10 chr17:38348508 C>T maps to ENST00000456989 N549N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAD0-01A-11D-A40R-10 chr5:167919731 C>G maps to NM_002887.3 V83V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr5:167945065 T>C maps to NM_002887.3 T624T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39Y-01A-11D-A20W-10 chr6:88229962 T>C maps to NM_020320.3 G349G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr6:88229902 T>C maps to NM_020320.3 A369A. Only missense variants will be evaluated by CHASM.
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-DD-AAED-01A-12D-A40R-10 chr5:86659192 T>G maps to NM_002890.1 Y494*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-AA0U-01A-11D-A382-10 chr5:86629118 A>G maps to NM_002890.1 L288L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39X-01A-11D-A20W-10 chr3:141305545 C>T maps to ENST00000452898 R629*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADN-01A-11D-A40R-10 chr3:141289752 G>A did not map to a codon.
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-G3-AAV0-01A-11D-A36X-10 chr1:178408711 T>C did not map to a codon.
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-AAD2-01A-11D-A40R-10 chr10:43694570 G>A maps to ENST00000374459 I315I. 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-ES-A2HT-01A-12D-A183-10 chr15:79339197 C>A maps to NM_002891.4 V256V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-AAV7-01A-11D-A382-10 chr15:79296321 G>A maps to NM_002891.4 A773A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr5:80511699 A>G maps to NM_006909.1 K1120K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAE6-01A-11D-A40R-10 chr2:33764195 G>A maps to NM_170672.2 V399V. Only missense variants will be evaluated by CHASM.
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-DD-A3A0-01A-11D-A20W-10 chr20:4776513 T>C maps to NM_014737.2 R78R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-AAV5-01A-11D-A36X-10 chr12:65085253 C>T maps to NM_178169.2 Y154Y. 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-ED-A8O6-01A-11D-A35Z-10 chr10:45486498 C>T maps to NM_032023.3 G263G. 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-5C-A9VG-01A-11D-A36X-10 chr19:10431329 C>T did not map to a codon.
Sequencing variant TCGA-G3-A3CG-01A-11D-A20W-10 chr19:3771557 T>C maps to NM_032753.3 A61A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MA-01A-11D-A20W-10 chr13:49027247 G>A did not map to a codon.
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-WX-AA44-01A-11D-A38X-10 chr13:48923089 A>T 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-ZP-A9D4-01A-11D-A36X-10 chr8:53573154 C>T did not map to a codon.
Sequencing variant TCGA-BC-A3KF-01A-11D-A20W-10 chr23:16876929 T>C did not map to a codon.
Sequencing variant TCGA-DD-A3A1-01A-11D-A20W-10 chr23:16876871 A>G did not map to a codon.
Sequencing variant TCGA-DD-A3A1-01A-11D-A20W-10 chr18:20573439 A>G maps to ENST00000360790 P550P. 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-A39Z-01A-11D-A20W-10 chr16:53496561 T>C maps to NM_005611.3 L519L. 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-G3-A3CG-01A-11D-A20W-10 chr16:53513886 A>G maps to NM_005611.3 E955E. 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-2Y-A9GZ-01A-11D-A38X-10 chr23:47030584 T>G did not map to a codon.
Sequencing variant TCGA-DD-A39Y-01A-11D-A20W-10 chr23:47041606 A>G did not map to a codon.
Sequencing variant TCGA-DD-AACO-01A-11D-A40R-10 chr23:47030581 G>T did not map to a codon.
Sequencing variant TCGA-DD-AAVV-01A-11D-A40R-10 chr23:47030584 T>G did not map to a codon.
Sequencing variant TCGA-LG-A9QD-01A-11D-A382-10 chr23:47028881 G>C did not map to a codon.
Sequencing variant TCGA-XR-A8TC-01A-11D-A35Z-10 chr23:47030581 G>T 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-EP-A2KA-01A-11D-A183-10 chr11:66392657 C>A maps to NM_006328.3 A437A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr10:6143231 A>G did not map to a codon.
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-DD-A1ED-01A-11D-A152-10 chr14:73569995 A>C maps to NM_021239.2 R322R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr5:145634548 T>C maps to NM_018989.1 I496I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39Z-01A-11D-A20W-10 chr5:145613205 C>T maps to NM_018989.1 G348G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39Z-01A-11D-A20W-10 chr5:145613208 A>T maps to NM_018989.1 P349P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADE-01A-11D-A40R-10 chr5:145610480 G>A did not map to a codon.
Sequencing variant TCGA-GJ-A9DB-01A-11D-A36X-10 chr5:145664264 T>A maps to NM_018989.1 T1023T. 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-A1EG-01A-11D-A20W-10 chr23:48434039 A>G 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-DD-AAEG-01A-11D-A38X-10 chr20:34326924 C>T maps to NM_184234.1 L22L. 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-4R-AA8I-01A-11D-A382-10 chr11:66411227 C>T maps to NM_001198845.1 S215S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39X-01A-11D-A20W-10 chr23:106358784 T>C did not map to a codon.
Sequencing variant TCGA-DD-AACI-01A-11D-A40R-10 chr23:106312541 T>A did not map to a codon.
Sequencing variant TCGA-DD-AADU-01A-11D-A40R-10 chr23:106359255 G>A did not map to a codon.
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-G3-A3CJ-01A-11D-A20W-10 chr2:152107692 A>G maps to NM_198557.2 G267G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACK-01A-11D-A40R-10 chr2:238727031 A>G maps to NM_001080504.2 V491V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr4:40440442 G>A maps to NM_001098634.1 G156G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr3:50145540 T>A maps to NM_005778.2 Y360*. 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-A2HS-01A-11D-A183-10 chr22:36152190 A>G maps to NM_001082578.1 G370G. 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-DD-AADP-01A-11D-A38X-10 chr3:29804445 T>C maps to NM_001003793.2 N201N. 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-DD-A3A1-01A-11D-A20W-10 chr23:129546385 A>G did not map to a codon.
Sequencing variant TCGA-DD-AACG-01A-11D-A40R-10 chr23:129546794 G>T did not map to a codon.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr1:89449437 A>G maps to NM_019610.5 L24L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACU-01A-11D-A40R-10 chr11:7110725 C>T maps to NM_014469.4 G125G. Only missense variants will be evaluated by CHASM.
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-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-DD-A119-01A-11D-A12Z-10 chr9:125642093 T>C maps to NM_001100588.1 V384V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LG-A9QD-01A-11D-A382-10 chr1:24859571 G>A did not map to a codon.
Sequencing variant TCGA-DD-AADV-01A-11D-A38X-10 chr1:17743014 G>A maps to NM_018715.2 N329N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADB-01A-11D-A40R-10 chr15:91500106 G>A maps to NM_033544.2 W48*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1ED-01A-11D-A152-10 chr14:103173692 T>C maps to NM_015156.2 L165L. 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-ZP-A9CV-01A-11D-A382-10 chr11:63680389 G>A maps to NM_173587.3 S307S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9GU-01A-11D-A382-10 chr1:211462587 A>G maps to NM_001136223.1 Q263Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MB-01A-11D-A20W-10 chr1:211486824 T>C maps to NM_001136223.1 T459T. 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-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-G3-AAV4-01A-11D-A382-10 chr17:9808458 G>T maps to NM_002903.2 I13I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACS-01A-11D-A40R-10 chr1:211654727 G>A maps to NM_183059.2 N10N. 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-UB-A7MB-01A-11D-A33Q-10 chr2:18736711 T>C maps to NM_020905.3 T252T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr12:57351018 C>T maps to NM_003708.3 R76R. 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-ES-A2HT-01A-12D-A183-10 chr9:36063816 G>A maps to NM_021111.2 W99*. Only missense variants will be evaluated by CHASM.
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-CC-A7IE-01A-21D-A382-10 chr8:145737118 C>T maps to ENST00000428558 L1149L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAC8-01A-11D-A40R-10 chr8:145738778 C>T maps to ENST00000428558 Q762Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAVP-01A-11D-A40R-10 chr8:145738711 C>T maps to ENST00000428558 R784R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr11:65422121 A>G maps to NM_021975.3 A461A. 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-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-G3-AAV0-01A-11D-A36X-10 chr7:103185628 T>C maps to ENST00000428762 S2155S. 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-DD-AACI-01A-11D-A40R-10 chr20:30070205 G>T maps to NM_014012.4 R180R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACF-01A-11D-A40R-10 chr14:23355417 C>T maps to NM_173527.2 R235R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A25S-01A-11D-A16V-10 chr23:17095519 C>T did not map to a codon.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr12:15262427 C>T maps to NM_032918.2 G72G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LG-A9QC-01A-11D-A36X-10 chr12:15262378 G>T maps to NM_032918.2 R89R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MR-A8JO-01A-12D-A35Z-10 chr4:57797084 G>A maps to NM_005612.4 L687L. Only missense variants will be evaluated by CHASM.
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-ZP-A9D4-01A-11D-A36X-10 chr10:43609004 G>A maps to NM_020975.4 R587R. 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-ZS-A9CD-01A-11D-A36X-10 chr2:100058821 G>A maps to NM_016316.2 L154L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EG-01A-11D-A20W-10 chr6:111686476 T>C maps to NM_002912.3 T2248T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACA-01A-11D-A40R-10 chr6:111652971 T>C maps to NM_002912.3 K2647K. Only missense variants will be evaluated by CHASM.
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-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-LG-A9QC-01A-11D-A36X-10 chr6:111714107 T>C maps to NM_002912.3 L211L. 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-DD-A1EG-01A-11D-A20W-10 chr11:114316716 A>G maps to NM_015523.3 E146E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZP-A9D0-01A-11D-A36X-10 chr9:136272183 G>A maps to NM_020385.2 Q388*. 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-DD-AADS-01A-11D-A40R-10 chr9:79002392 T>A maps to ENST00000257452 L137L. 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-DD-A1EE-01A-11D-A12Z-10 chr3:16368287 C>T maps to NM_015150.1 K414K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr2:198480673 A>G maps to NM_144629.2 P360P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAD2-01A-11D-A40R-10 chr16:74678543 C>T maps to NM_018124.3 W294*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr16:74694848 G>A maps to NM_018124.3 Q167*. 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-DD-AACU-01A-11D-A40R-10 chr19:6013024 G>T maps to NM_000635.3 R291R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EE-01A-11D-A12Z-10 chr9:3346709 G>A maps to NM_134428.1 Q58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr12:107109248 G>A maps to ENST00000357881 L364L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-AAV7-01A-11D-A382-10 chr12:107103176 C>T maps to ENST00000357881 L310L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADO-01A-11D-A40R-10 chr1:151315081 C>T maps to NM_000449.3 G477G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A1-01A-11D-A20W-10 chr6:117198524 T>C maps to NM_173560.3 C29C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9GZ-01A-11D-A38X-10 chr15:56385626 G>A maps to NM_022841.5 C1433C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A9FU-01A-11D-A36X-10 chr3:101284815 A>G maps to NM_017819.2 R397R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-AAV0-01A-11D-A36X-10 chr3:101284683 A>G maps to NM_017819.2 L353L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADW-01A-11D-A38X-10 chr23:109697299 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-A119-01A-11D-A12Z-10 chr23:71349867 T>C 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-A3KG-01A-11D-A20W-10 chr19:11527334 C>T maps to NM_001161616.1 E126E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADR-01A-11D-A40R-10 chr15:93588469 C>A maps to NM_020211.2 E371*. 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-CC-A7IJ-01A-11D-A33Q-10 chr5:73069857 C>A maps to NM_001080479.2 V218V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr5:73163833 C>T maps to NM_001080479.2 T762T. Only missense variants will be evaluated by CHASM.
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-2Y-A9H4-01A-11D-A382-10 chr2:108488173 C>A maps to NM_182588.2 P1238P. 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-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-DD-AAC8-01A-11D-A40R-10 chr4:3424629 A>T did not map to a codon.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr4:3424104 G>T maps to NM_198229.2 S947S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAW0-01A-11D-A40R-10 chr6:153332801 A>C maps to NM_012419.4 T180T. 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-2Y-A9GS-01A-12D-A382-10 chr8:101076176 T>A maps to NM_015668.3 G273G. 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-DD-A3A0-01A-11D-A20W-10 chr9:116359109 C>T maps to NM_144488.4 G1158G. 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-ZS-A9CE-01A-11D-A36X-10 chr1:241094017 A>T maps to ENST00000407727 Y128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3K-AAZ8-01A-12D-A38X-10 chr5:63802552 G>A maps to NM_001029875.1 E34E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10W-01A-11D-A12Z-10 chr5:63802519 C>A maps to NM_001029875.1 I23I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11C-01A-11D-A12Z-10 chr16:111694 C>T did not map to a codon.
Sequencing variant TCGA-G3-AAV1-01A-11D-A382-10 chr1:39352190 T>C maps to ENST00000372985 L366L. Only missense variants will be evaluated by CHASM.
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-DD-A1EE-01A-11D-A12Z-10 chr15:90023511 G>T maps to NM_016321.1 S217*. 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-EP-A2KB-01A-11D-A183-10 chr3:129249880 G>A maps to NM_000539.3 W175*. 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-BD-A3EP-01A-11D-A22F-10 chr2:20647264 C>T maps to NM_004040.2 D13D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZS-A9CG-01A-11D-A36X-10 chr8:22865128 C>G maps to NM_001160036.1 V479V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9H9-01A-21D-A38X-10 chr12:122218861 G>A maps to NM_019034.2 I129I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZS-A9CG-01A-11D-A36X-10 chr16:723031 C>T maps to NM_138769.1 R544R. 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-5C-AAPD-01A-21D-A38X-10 chr23:53457917 T>C did not map to a codon.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr12:107209054 G>T maps to ENST00000392837 T238T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADW-01A-11D-A38X-10 chr17:12883407 T>C maps to NM_014859.4 S599S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10W-01A-11D-A12Z-10 chr5:38978734 A>T maps to ENST00000296782 Y257*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr5:38952347 G>T maps to ENST00000296782 S1026*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADM-01A-11D-A40R-10 chr2:152267845 T>G maps to NM_018151.4 V59V. 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-DD-AADK-01A-11D-A40R-10 chr1:42865093 G>A maps to NM_173642.3 K61K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADD-01A-11D-A40R-10 chr12:8866530 A>G maps to NM_020734.2 Q23Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAE3-01A-11D-A40R-10 chr6:73102483 C>A maps to NM_014989.4 G1530G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-AAV0-01A-11D-A36X-10 chr6:73017045 A>G maps to NM_014989.4 Q1312Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-AAV7-01A-11D-A382-10 chr6:73001643 C>A maps to NM_014989.4 R1249R. 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-DD-AAC9-01A-11D-A40R-10 chr8:104778483 A>G maps to NM_001100117.2 K139K. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-FV-A2QR-01A-11D-A20W-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-FV-A2QR-01A-11D-A20W-10 chr8:105257144 A>G maps to NM_001100117.2 K1112K. 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-DD-AAVR-01A-11D-A40R-10 chr20:19955802 C>T maps to ENST00000255006 S427S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11A-01A-11D-A12Z-10 chr7:105195557 C>T maps to NM_021930.4 R519*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1ED-01A-11D-A152-10 chr7:105205723 A>G maps to NM_021930.4 R629R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr6:7393523 A>G maps to NM_031480.2 G88G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MA-01A-11D-A20W-10 chr5:96514828 T>C maps to NM_018343.2 K45K. 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-EP-A2KA-01A-11D-A183-10 chr14:24808319 C>A maps to NM_006871.3 V124V. 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-CC-A7IE-01A-21D-A382-10 chr18:40554065 G>A maps to NM_002930.2 Y69Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAD1-01A-11D-A40R-10 chr18:40323616 G>A maps to NM_002930.2 A165A. 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-ES-A2HS-01A-11D-A183-10 chr1:40703877 G>C maps to NM_012421.3 R1168R. 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-G3-AAV2-01A-11D-A36X-10 chr19:14139179 C>A maps to NM_080864.2 S55*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9H2-01A-12D-A382-10 chr16:67688113 G>A maps to NM_001013838.1 E1061E. Only missense variants will be evaluated by CHASM.
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-G3-AAUZ-01A-11D-A382-10 chr6:151748615 C>T did not map to a codon.
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-EP-A2KA-01A-11D-A183-10 chr14:21270131 C>A maps to NM_198235.2 R32R. 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-5C-A9VG-01A-11D-A36X-10 chr14:21058714 C>T maps to NM_001024822.2 R56R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr6:167356556 C>T maps to ENST00000428859 R144R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9HA-01A-11D-A38X-10 chr2:86849811 C>T maps to NM_005667.3 K66K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CG-01A-11D-A20W-10 chr15:59377872 A>G maps to ENST00000434298 E822E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-AAV7-01A-11D-A382-10 chr17:19316309 C>A maps to NM_007148.4 G147G. 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-AADU-01A-11D-A40R-10 chr23:119005198 T>C 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-4R-AA8I-01A-11D-A382-10 chr3:49751387 G>A maps to NM_022064.2 R961R. 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-CC-A8HV-01A-11D-A35Z-10 chr23:105970235 G>A did not map to a codon.
Sequencing variant TCGA-DD-AAE0-01A-11D-A40R-10 chr23:105970507 G>A did not map to a codon.
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-DD-AACA-01A-11D-A40R-10 chr5:158586025 C>A maps to NM_144726.2 V576V. 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-DD-A119-01A-11D-A12Z-10 chr7:122342234 G>A maps to NM_198085.1 Y190Y. 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-2Y-A9GZ-01A-11D-A38X-10 chr17:74151750 G>A maps to NM_052916.2 D530D. 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-BC-A3KF-01A-11D-A20W-10 chr21:30329698 C>T maps to NM_015565.2 P995P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BD-A3EP-01A-11D-A22F-10 chr21:30339225 C>T maps to NM_015565.2 L575L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A113-01A-11D-A12Z-10 chr21:30354672 A>G maps to NM_015565.2 L244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAVS-01A-11D-A40R-10 chr17:4848076 G>A maps to NM_015528.1 Q273Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAEB-01A-11D-A40R-10 chr3:196199526 T>G maps to NM_152617.3 S293S. 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-A1EG-01A-11D-A20W-10 chr13:25363883 A>G maps to ENST00000381927 G303G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAE0-01A-11D-A40R-10 chr13:25433220 A>G maps to ENST00000381927 K1280K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAW3-01A-11D-A40P-10 chr13:25367347 T>C maps to ENST00000381927 D368D. 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-G3-AAV0-01A-11D-A36X-10 chr1:33430199 C>T maps to NM_153341.2 R29R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A8HS-01A-11D-A35Z-10 chr9:140115058 G>A maps to NM_031297.3 A202A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BD-A3ER-01A-11D-A20W-10 chr17:78321422 A>T maps to NM_020914.4 T3145T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39X-01A-11D-A20W-10 chr17:78280932 T>C maps to NM_020914.4 V860V. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-DD-A73E-01A-12D-A32G-10. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-DD-AACW-01A-11D-A40R-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-DD-AACW-01A-11D-A40R-10 chr17:78327345 G>A maps to NM_020914.4 E3535E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr17:78335537 G>A maps to NM_020914.4 L3784L. 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-A12Z-10 chr7:5681007 C>A did not map to a codon.
Sequencing variant TCGA-DD-A39Z-01A-11D-A20W-10 chr7:5781437 T>C maps to NM_207111.2 K70K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A1-01A-11D-A20W-10 chr13:79213207 T>C did not map to a codon.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr1:45115395 A>G maps to ENST00000453887 E504E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr1:45092000 A>G maps to ENST00000453887 E279E. Only missense variants will be evaluated by CHASM.
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.
Multiple mappings detected for codon TCGA-MR-A8JO-01A-12D-A35Z-10. Mapping will be selected arbitrarily.
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-CC-A3MB-01A-11D-A20W-10 chr14:24618769 C>T maps to NM_017999.4 Q263*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAE7-01A-11D-A40R-10 chr14:24617275 G>A maps to NM_017999.4 W95*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr14:24621042 C>A maps to NM_017999.4 R658R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr6:32148075 C>T maps to NM_006913.3 F172F. 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-BC-A3KG-01A-11D-A20W-10 chr12:117290507 A>G maps to NM_032814.3 A418A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACL-01A-11D-A40R-10 chr6:89600236 T>A maps to NM_003800.3 V291V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAD3-01A-11D-A40R-10 chr11:499112 G>A maps to NM_203389.1 F172F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9GU-01A-11D-A382-10 chr18:13746224 A>G maps to NM_003799.1 A382A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9H4-01A-11D-A382-10 chr18:13741654 T>A maps to NM_003799.1 Y313*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADO-01A-11D-A40R-10 chr17:695149 G>A maps to NM_018146.2 Q368Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9H9-01A-21D-A38X-10 chr1:104068796 G>T maps to NM_017619.3 P35P. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-ES-A2HT-01A-12D-A183-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-2Y-A9H5-01A-11D-A382-10 chr3:78706266 C>T maps to NM_002941.3 E865E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39Y-01A-11D-A20W-10 chr3:78719380 A>G maps to NM_002941.3 T471T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADA-01A-11D-A40R-10 chr3:78701074 G>A maps to NM_002941.3 A873A. 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-5C-A9VH-01A-11D-A36X-10 chr3:77147198 G>A maps to ENST00000332191 R32R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr3:77617563 C>A maps to ENST00000332191 T650T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAD2-01A-11D-A40R-10 chr11:124747875 G>A maps to NM_022370.3 T1010T. 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-2Y-A9H8-01A-11D-A38X-10 chr2:11341100 T>C maps to NM_004850.3 K964K. 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-WQ-A9G7-01A-11D-A36X-10 chr16:4851538 G>A maps to NM_024589.1 P55P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A2QR-01A-11D-A20W-10 chr5:10450065 T>C maps to NM_031916.3 C86C. Only missense variants will be evaluated by CHASM.
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-5R-AAAM-01A-12D-A40R-10 chr9:94493237 C>T maps to NM_004560.2 T379T. 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-DD-AACL-01A-11D-A40R-10 chr9:94495464 A>T maps to NM_004560.2 P292P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACP-01A-11D-A40R-10 chr9:94486329 G>A maps to NM_004560.2 Q816*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-AAV6-01A-21D-A36X-10 chr9:94487146 C>T maps to NM_004560.2 V543V. 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-ZS-A9CF-01A-11D-A382-10 chr15:60824051 T>A did not map to a codon.
Sequencing variant TCGA-2Y-A9GU-01A-11D-A382-10 chr9:77249680 A>T maps to ENST00000396204 S87S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A8HS-01A-11D-A35Z-10 chr6:117746712 G>T maps to NM_002944.2 S36*. 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-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-BC-A3KG-01A-11D-A20W-10 chr8:10480615 T>C maps to NM_178857.5 P32P. 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-EP-A2KB-01A-11D-A183-10 chr8:10469336 A>G maps to NM_178857.5 A757A. 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-AADD-01A-11D-A40R-10 chr23:46713107 G>T did not map to a codon.
Sequencing variant TCGA-DD-AADN-01A-11D-A40R-10 chr23:46713383 T>C did not map to a codon.
Sequencing variant TCGA-G3-A3CG-01A-11D-A20W-10 chr23:46713253 A>G did not map to a codon.
Sequencing variant TCGA-WQ-A9G7-01A-11D-A36X-10 chr23:46713332 T>C did not map to a codon.
Sequencing variant TCGA-DD-AACU-01A-11D-A40R-10 chr7:33134955 T>A maps to NM_203288.1 K186*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAEG-01A-11D-A38X-10 chr17:1780505 G>A maps to NM_002945.3 K196K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr15:41819623 G>T maps to NM_015540.2 I536I. 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-AADS-01A-11D-A40R-10 chr15:41812891 C>T maps to NM_015540.2 L1164L. 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-ES-A2HT-01A-12D-A183-10 chr1:92789691 A>G maps to NM_024813.2 E405E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr1:92789910 C>T maps to NM_024813.2 T478T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9H3-01A-11D-A382-10 chr1:68910484 T>C maps to NM_000329.2 P109P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A0-01A-11D-A20W-10 chr1:68896994 T>C maps to NM_000329.2 G436G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACL-01A-11D-A40R-10 chr23:38145016 T>A did not map to a codon.
Sequencing variant TCGA-DD-AACT-01A-11D-A40R-10 chr23:38182689 T>C did not map to a codon.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr23:38145014 C>A did not map to a codon.
Sequencing variant TCGA-DD-AAE7-01A-11D-A40R-10 chr16:53639513 G>C maps to NM_015272.2 T1238T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACS-01A-11D-A40R-10 chr12:113303257 G>A maps to NM_001143854.1 V90V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZS-A9CG-01A-11D-A36X-10 chr17:63675 T>A maps to NM_006987.3 A305A. Only missense variants will be evaluated by CHASM.
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-K7-AAU7-01A-11D-A382-10 chr16:89628069 C>T maps to NM_033251.1 Q111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr19:49994319 T>C maps to NM_012423.2 A122A. 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-CC-A8HS-01A-11D-A35Z-10 chr15:66795055 G>C maps to NM_000968.2 T105T. 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-DD-AACB-01A-11D-A40R-10 chr11:812568 G>T maps to NM_001004.3 G69G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACQ-01A-11D-A40R-10 chr3:128356920 T>A maps to NM_002950.3 P118P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9H6-01A-11D-A38X-10 chr20:35866807 C>A maps to NM_001135771.1 I597I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACB-01A-11D-A40R-10 chr20:35812640 G>T maps to NM_002951.3 T24T. 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-DD-AACZ-01A-11D-A40R-10 chr6:30314487 A>T did not map to a codon.
Sequencing variant TCGA-CC-A8HU-01A-11D-A35Z-10 chr19:39926514 C>A maps to NM_001020.4 L7L. 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-DD-AAC9-01A-11D-A40R-10 chr2:55460542 G>A maps to NM_001177413.1 Q31Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAEH-01A-11D-A40R-10 chr11:75115746 G>T maps to NM_001005.3 L190L. 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-CC-5262-01A-01D-A12Z-10 chr24:22941542 C>T did not map to a codon.
Sequencing variant TCGA-DD-AACB-01A-11D-A40R-10 chr1:26900659 C>A maps to NM_001006665.1 R735R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr6:166952272 C>A did not map to a codon.
Sequencing variant TCGA-2Y-A9GY-01A-11D-A382-10 chr23:20211661 A>C did not map to a codon.
Sequencing variant TCGA-2Y-A9HB-01A-11D-A38X-10 chr23:20206618 T>A did not map to a codon.
Sequencing variant TCGA-BC-A3KG-01A-11D-A20W-10 chr23:20194412 C>A did not map to a codon.
Sequencing variant TCGA-CC-A9FW-01A-11D-A36X-10 chr23:20179838 C>A did not map to a codon.
Sequencing variant TCGA-DD-A1EE-01A-11D-A12Z-10 chr23:20252925 G>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-DD-AACP-01A-11D-A40R-10 chr23:20187518 C>T did not map to a codon.
Sequencing variant TCGA-DD-AAEI-01A-11D-A40R-10 chr23:20185786 G>C 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-ED-A8O5-01A-11D-A35Z-10 chr23:20183140 T>C did not map to a codon.
Sequencing variant TCGA-ED-A8O5-01A-11D-A35Z-10 chr23:20213229 T>C 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-ZP-A9CV-01A-11D-A382-10 chr23:20187599 T>A did not map to a codon.
Sequencing variant TCGA-ZP-A9CV-01A-11D-A382-10 chr11:64137352 G>A maps to NM_003942.2 L595L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr14:91369166 A>G maps to NM_004755.2 S368S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAE6-01A-11D-A40R-10 chr14:91338566 C>A maps to NM_004755.2 E754*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9H2-01A-12D-A382-10 chr23:83359579 C>T 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-DD-AAE8-01A-11D-A40R-10 chr23:83419337 G>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-EP-A2KA-01A-11D-A183-10 chr1:213349822 G>T maps to NM_012424.3 G344G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr3:39453156 T>C maps to ENST00000443003 G177G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A8HT-01A-11D-A35Z-10 chr1:152127435 A>C maps to NM_001122965.1 T713T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAEG-01A-11D-A38X-10 chr17:78919548 G>C maps to NM_020761.2 P1036P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAVW-01A-11D-A40R-10 chr17:78796081 G>A maps to NM_020761.2 A324A. 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-ZP-A9CY-01A-11D-A382-10 chr20:17596111 T>C maps to ENST00000377813 L1338L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADC-01A-11D-A40R-10 chr6:7230407 G>T maps to NM_001003699.3 T692T. 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-DD-A39X-01A-11D-A20W-10 chr11:4127340 T>C maps to NM_001033.3 T58T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A0-01A-11D-A20W-10 chr11:4127277 T>C maps to NM_001033.3 A37A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACF-01A-11D-A40R-10 chr11:4148359 A>G maps to NM_001033.3 A522A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAE8-01A-11D-A40R-10 chr11:4159582 T>C maps to NM_001033.3 N783N. 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-EP-A2KA-01A-11D-A183-10 chr11:6622398 G>T maps to NM_015324.2 I299I. 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-CC-A9FS-01A-11D-A36X-10 chr17:48561892 C>T maps to NM_018346.1 Q400*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-AAV0-01A-11D-A36X-10 chr2:7017964 A>T maps to NM_080657.4 K12*. Only missense variants will be evaluated by CHASM.
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-2V-A95S-01A-11D-A36X-10 chr21:43912901 G>T maps to NM_080860.2 G80G. 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-ES-A2HS-01A-11D-A183-10 chr6:116943930 A>G maps to NM_001010892.2 L229L. 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-LG-A9QD-01A-11D-A382-10 chr8:108970400 G>A maps to NM_178565.4 Q175*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5C-A9VG-01A-11D-A36X-10 chr6:127440417 A>T maps to ENST00000368317 G27G. 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-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-AAV6-01A-21D-A36X-10 chr14:60193688 C>A maps to NM_021136.2 G571G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAD8-01A-11D-A40R-10 chr2:55253107 A>T maps to NM_020532.4 A709A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZP-A9CV-01A-11D-A382-10 chr2:55253875 A>G maps to NM_020532.4 G453G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr22:20229290 G>A maps to ENST00000425986 C540C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADF-01A-11D-A40R-10 chr18:67671401 G>T maps to NM_173630.3 L2222L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAEG-01A-11D-A38X-10 chr18:67715230 T>C maps to NM_173630.3 E1839E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WQ-A9G7-01A-11D-A36X-10 chr18:67753860 A>G maps to NM_173630.3 D1454D. 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-AACD-01A-11D-A40R-10 chr17:42389992 C>T maps to NM_001144825.1 I51I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACX-01A-11D-A40R-10 chr7:87369127 A>C maps to NM_138290.2 A177A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAD0-01A-11D-A40R-10 chr21:36193994 T>A did not map to a codon.
Sequencing variant TCGA-DD-AADO-01A-11D-A40R-10 chr8:93088271 A>T maps to NM_175634.2 S3S. 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-4R-AA8I-01A-11D-A382-10 chr6:45390465 A>G maps to ENST00000359524 Q133Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACE-01A-11D-A40R-10 chr6:45390468 G>A maps to ENST00000359524 Q134Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACT-01A-11D-A40R-10 chr6:45390465 A>G maps to ENST00000359524 Q133Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAVS-01A-11D-A40R-10 chr6:45390465 A>G maps to ENST00000359524 Q133Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WX-AA44-01A-11D-A38X-10 chr6:45390519 T>G maps to ENST00000359524 A151A. 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-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-DD-AAE3-01A-11D-A40R-10 chr9:35557956 T>C maps to NM_001135999.1 H1010H. 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-DD-AAE3-01A-11D-A40R-10 chr6:83905922 A>T maps to NM_033411.3 K271*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAE0-01A-11D-A40R-10 chr5:33937054 G>A maps to NM_016568.3 G70G. 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-WX-AA47-01A-11D-A38X-10 chr6:33162490 C>A maps to ENST00000374685 E528*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADJ-01A-11D-A40R-10 chr3:72427649 T>A maps to ENST00000477973 A279A. 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-DD-AACU-01A-11D-A40R-10 chr19:38995536 T>A maps to NM_000540.2 P2739P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACU-01A-11D-A40R-10 chr19:39009926 G>A maps to NM_000540.2 R3364R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADC-01A-11D-A40R-10 chr19:39034234 A>C maps to NM_000540.2 R3948R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADI-01A-11D-A40R-10 chr19:38993232 G>A maps to NM_000540.2 P2567P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr19:38948828 C>A maps to NM_000540.2 T688T. 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-2Y-A9H7-01A-11D-A38X-10 chr1:237947689 G>A maps to NM_001035.2 P4226P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1ED-01A-11D-A152-10 chr1:237789000 T>C maps to NM_001035.2 S2021S. Only missense variants will be evaluated by CHASM.
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-DD-AAC8-01A-11D-A40R-10 chr1:237823355 T>A maps to NM_001035.2 Y2760*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACI-01A-11D-A40R-10 chr1:237729921 C>T maps to NM_001035.2 A1090A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACI-01A-11D-A40R-10 chr1:237972235 A>T maps to NM_001035.2 V4778V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADN-01A-11D-A40R-10 chr1:237889574 G>A maps to NM_001035.2 K3564K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAW3-01A-11D-A40P-10 chr1:237804206 G>T maps to NM_001035.2 E2376*. 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-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-2Y-A9GY-01A-11D-A382-10 chr15:34130220 C>T maps to NM_001036.3 L4014L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5C-A9VG-01A-11D-A36X-10 chr15:33954905 G>T maps to NM_001036.3 V1725V. 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-BD-A3ER-01A-11D-A20W-10 chr15:33765651 C>T maps to NM_001036.3 T28T. 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-EP-A2KB-01A-11D-A183-10 chr15:33855060 C>A maps to NM_001036.3 S332S. 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-2Y-A9HA-01A-11D-A38X-10 chr1:153390689 C>T maps to NM_176823.3 L44L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACL-01A-11D-A40R-10 chr1:153391626 A>T maps to NM_176823.3 K50*. 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-DD-AACT-01A-11D-A40R-10 chr19:3179174 C>T maps to NM_003775.3 L129L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr19:10624904 C>A maps to NM_001166215.1 V261V. 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-2V-A95S-01A-11D-A36X-10 chr11:18266986 T>C maps to NM_030754.4 K102K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GJ-A3OU-01A-31D-A382-10 chr11:18266926 G>A maps to NM_030754.4 Y122Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr11:18253135 C>A maps to NM_006512.3 S102S. 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-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-4R-AA8I-01A-11D-A382-10 chr19:5661678 C>T maps to ENST00000433404 R671R. 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-DD-AADA-01A-11D-A40R-10 chr23:134988199 A>T did not map to a codon.
Sequencing variant TCGA-DD-AAVP-01A-11D-A40R-10 chr23:134990277 A>T 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-WQ-A9G7-01A-11D-A36X-10 chr23:134987455 G>A did not map to a codon.
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-2Y-A9HA-01A-11D-A38X-10 chr14:21992916 G>T maps to NM_005407.1 A315A. 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-DD-AACG-01A-11D-A40R-10 chr18:76755361 C>A maps to NM_171999.2 S1124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAW0-01A-11D-A40R-10 chr18:76753826 C>A maps to NM_171999.2 P612P. 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-XR-A8TD-01A-12D-A38X-10 chr18:76753073 G>A maps to NM_171999.2 P361P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZP-A9D1-01A-11D-A382-10 chr18:76757117 C>T maps to NM_171999.2 I1233I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr20:50408385 C>T maps to NM_020436.3 P212P. 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-AADL-01A-11D-A40R-10 chr8:119391801 G>A maps to NM_207506.2 Q154*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr17:48191302 G>A maps to NM_174920.2 D389D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACF-01A-11D-A40R-10 chr17:48194990 C>A maps to NM_174920.2 P93P. 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-AAE4-01A-11D-A40R-10 chr19:39867143 C>T maps to NM_018028.2 Y325Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADP-01A-11D-A38X-10 chr6:147830393 T>C maps to NM_001030060.2 S110S. 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-DD-AAC8-01A-11D-A40R-10 chr2:128747138 T>A maps to NM_001145928.1 S619S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-AAUZ-01A-11D-A382-10 chr13:21721330 G>A maps to NM_005870.4 K123K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-AAV0-01A-11D-A36X-10 chr19:55756526 C>T maps to ENST00000443936 Q255Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZP-A9D2-01A-11D-A382-10 chr19:55756721 G>A maps to ENST00000443936 Q217*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CJ-01A-11D-A20W-10 chr22:50876269 A>G did not map to a codon.
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-2Y-A9H6-01A-11D-A38X-10 chr9:136595228 A>C maps to NM_007101.3 T257T. 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-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-CC-A9FS-01A-11D-A36X-10 chr19:39412661 T>A maps to NM_001145901.1 P150P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAE4-01A-11D-A40R-10 chr19:39421214 T>C maps to NM_017827.3 A54A. 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-DD-A3A1-01A-11D-A20W-10 chr1:100571334 A>G maps to NM_194292.1 P511P. Only missense variants will be evaluated by CHASM.
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-DD-A39X-01A-11D-A20W-10 chr11:9871705 T>C maps to NM_030962.3 R890R. 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-2Y-A9H9-01A-21D-A38X-10 chr19:1116909 G>A maps to NM_014963.2 L574L. 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-RC-A7SF-01A-11D-A34Z-10 chr11:121177920 G>A maps to NM_001024956.2 L200L. 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-DD-A1EG-01A-11D-A20W-10 chr9:127904934 T>C maps to NM_173690.4 K25K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr9:127781125 T>C maps to NM_173690.4 G294G. 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-A3CJ-01A-11D-A20W-10 chr3:47459316 C>T did not map to a codon.
Sequencing variant TCGA-G3-A7M6-01A-11D-A33Q-10 chr15:77057676 C>A did not map to a codon.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr8:27509079 G>T maps to NM_016240.2 S54S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAW2-01A-11D-A40P-10 chr12:125299560 G>A maps to NM_005505.4 G128G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADF-01A-11D-A40R-10 chr1:246923256 A>T did not map to a codon.
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-DD-AAD8-01A-11D-A40R-10 chr13:78133956 G>A maps to NM_144777.2 R60R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CJ-01A-11D-A20W-10 chr13:78216917 T>C maps to NM_144777.2 C675C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A1-01A-11D-A20W-10 chr14:31139490 A>G maps to ENST00000311943 E303E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3K-AAZ8-01A-12D-A38X-10 chr2:224462659 A>G maps to NM_003469.4 N447N. 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-DD-A39Z-01A-11D-A20W-10 chr7:12620701 T>C maps to NM_001112706.2 S124S. Only missense variants will be evaluated by CHASM.
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-ES-A2HS-01A-11D-A183-10 chr7:12662451 A>G maps to NM_001112706.2 P231P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LG-A9QD-01A-11D-A382-10 chr7:12617695 G>A maps to NM_001112706.2 E69E. 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-DD-A39Y-01A-11D-A20W-10 chr23:17767570 A>G 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-ED-A8O5-01A-11D-A35Z-10 chr23:18276344 A>G 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-NI-A8LF-01A-11D-A35Z-10 chr3:38830493 C>T maps to NM_006514.2 L141L. 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-ZS-A9CF-01A-11D-A382-10 chr3:38962723 G>T maps to ENST00000302328 A245A. 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-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-EP-A2KB-01A-11D-A183-10 chr2:166900256 A>G maps to NM_001165963.1 G655G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZP-A9D0-01A-11D-A36X-10 chr2:166852579 A>G maps to NM_001165963.1 Y1508Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADO-01A-11D-A40R-10 chr2:166243455 T>C maps to NM_001040142.1 S1584S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADR-01A-11D-A40R-10 chr2:166172099 G>T maps to NM_001040142.1 L501L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WQ-A9G7-01A-11D-A36X-10 chr2:166032888 A>G maps to NM_006922.3 L6L. 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-DD-AADB-01A-11D-A40R-10 chr17:62045560 C>T maps to NM_000334.4 P286P. 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-G3-A3CJ-01A-11D-A20W-10 chr17:62026108 C>T maps to NM_000334.4 W1002*. 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-CC-A8HT-01A-11D-A35Z-10 chr3:38616807 G>A maps to NM_001099404.1 L1216L. Only missense variants will be evaluated by CHASM.
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-BC-A3KF-01A-11D-A20W-10 chr2:167142890 T>C maps to ENST00000303354 E520E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAE7-01A-11D-A40R-10 chr2:167136942 A>C maps to ENST00000303354 L757*. 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-DD-A39X-01A-11D-A20W-10 chr16:23223434 A>G maps to NM_001039.3 A419A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACP-01A-11D-A40R-10 chr16:23200751 G>A maps to NM_001039.3 K126K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAEI-01A-11D-A40R-10 chr16:23203677 A>C maps to NM_001039.3 S208S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39Z-01A-11D-A20W-10 chr22:50962275 A>G maps to NM_001169111.1 L189L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-AA0V-01A-11D-A382-10 chr4:174312526 A>T maps to NM_007281.2 T13T. 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-ES-A2HS-01A-11D-A183-10 chr8:144891810 G>C maps to NM_182706.3 P536P. 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-ZP-A9CZ-01A-11D-A382-10 chr8:144873557 C>T did not map to a codon.
Sequencing variant TCGA-DD-AAVU-01A-11D-A40R-10 chr17:45915689 C>T maps to NM_138355.3 R355R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACB-01A-11D-A40R-10 chr2:175292517 A>G maps to NM_024583.4 Q390Q. 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-ES-A2HS-01A-11D-A183-10 chr22:43610120 A>G maps to NM_173050.2 G676G. 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-DD-A3A1-01A-11D-A20W-10 chr11:9052314 A>G maps to ENST00000457346 C777C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr12:100708367 A>G maps to NM_017988.4 P357P. 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-UB-A7MB-01A-11D-A33Q-10 chr14:50318358 T>C maps to NM_004713.3 L51L. 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-EP-A2KA-01A-11D-A183-10 chr22:21998434 G>T maps to NM_022044.2 E213*. Only missense variants will be evaluated by CHASM.
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-AACL-01A-11D-A40R-10 chr7:3658709 A>T did not map to a codon.
Sequencing variant TCGA-DD-AADV-01A-11D-A38X-10 chr7:4153004 C>G maps to NM_152744.3 P1173P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACM-01A-11D-A40R-10 chr17:71361406 G>A maps to NM_001144952.1 S1765S. 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-ED-A8O6-01A-11D-A35Z-10 chr12:113874657 G>C maps to NM_138432.2 V258V. 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-ZS-A9CE-01A-11D-A36X-10 chr22:30803522 G>A maps to NM_012429.2 Q118Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39Z-01A-11D-A20W-10 chr22:30890135 C>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-2Y-A9GW-01A-11D-A382-10 chr16:5050722 G>A maps to NM_014692.1 G346G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MA-01A-11D-A20W-10 chr9:139358964 A>G maps to NM_014866.1 C1451C. 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-G3-A3CG-01A-11D-A20W-10 chr9:139368632 A>G maps to NM_014866.1 P1145P. 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-A3MB-01A-11D-A20W-10 chr1:177901666 T>C maps to NM_033127.2 G990G. 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-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-5C-A9VG-01A-11D-A36X-10 chr10:75528786 T>C maps to NM_198597.1 F767F. Only missense variants will be evaluated by CHASM.
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-DD-AACM-01A-11D-A40R-10 chr10:75519918 C>T maps to NM_198597.1 Q209*. 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-2Y-A9H5-01A-11D-A382-10 chr4:83800019 G>A maps to ENST00000505472 L89L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MA-01A-11D-A20W-10 chr10:102256017 A>G maps to NM_015490.3 A769A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACT-01A-11D-A40R-10 chr10:102250574 T>A maps to NM_015490.3 A846A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73A-01A-12D-A32G-10 chr6:108214764 A>T maps to NM_007214.4 L532*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADI-01A-11D-A40R-10 chr6:108214764 A>T maps to NM_007214.4 L532*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EG-01A-11D-A20W-10 chr14:81952088 T>C maps to NM_005065.4 R600R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EG-01A-11D-A20W-10 chr14:81961451 T>C maps to NM_005065.4 G386G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39Y-01A-11D-A20W-10 chr14:81970627 T>C maps to NM_005065.4 R177R. 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-2Y-A9H9-01A-21D-A38X-10 chr4:25767057 C>T did not map to a codon.
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-CC-A8HV-01A-11D-A35Z-10 chr1:169700979 C>T maps to NM_000450.2 E175E. 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-A39Z-01A-11D-A20W-10 chr1:151337177 T>C maps to ENST00000435071 E462E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9H4-01A-11D-A382-10 chr12:109017846 C>T maps to ENST00000228463 E79E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAD8-01A-11D-A40R-10 chr12:109017057 C>T maps to ENST00000228463 A342A. 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-DD-AAC9-01A-11D-A40R-10 chr7:83610773 T>A maps to NM_006080.2 S505S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACI-01A-11D-A40R-10 chr7:83610728 G>A maps to NM_006080.2 Y520Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADS-01A-11D-A40R-10 chr7:83610773 T>C maps to NM_006080.2 S505S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAEB-01A-11D-A40R-10 chr7:83610697 G>T maps to NM_006080.2 R531R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAEG-01A-11D-A38X-10 chr7:83643584 A>G maps to NM_006080.2 N250N. 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-2Y-A9H9-01A-21D-A38X-10 chr7:80378239 G>A maps to NM_006379.2 Q606*. 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-AAC8-01A-11D-A40R-10 chr7:84649626 A>T maps to NM_152754.2 T475T. Only missense variants will be evaluated by CHASM.
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-DD-AACZ-01A-11D-A40R-10 chr7:82997258 T>C maps to NM_012431.2 V657V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADO-01A-11D-A40R-10 chr7:83037793 A>T maps to NM_012431.2 L187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAE6-01A-11D-A40R-10 chr7:83095917 C>A did not map to a codon.
Sequencing variant TCGA-3K-AAZ8-01A-12D-A38X-10 chr3:50225205 T>C maps to NM_004186.3 D672D. 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-ZS-A9CE-01A-11D-A36X-10 chr3:50197096 C>A maps to NM_004186.3 T14T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACS-01A-11D-A40R-10 chr3:52472193 G>T maps to NM_020163.1 R511R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAD1-01A-11D-A40R-10 chr3:52471665 A>T maps to NM_020163.1 L585L. 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-DD-AAW3-01A-11D-A40P-10 chr15:90764626 C>T maps to NM_198925.2 S208S. 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-WQ-A9G7-01A-11D-A36X-10 chr2:74902503 G>A maps to NM_004263.3 L455L. 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-DD-A3A1-01A-11D-A20W-10 chr3:122642472 G>A maps to NM_001031702.2 P421P. 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-NI-A8LF-01A-11D-A35Z-10 chr1:151111133 G>T maps to NM_001178061.1 S143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACI-01A-11D-A40R-10 chr15:48062883 A>G maps to NM_153618.1 T708T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A8O5-01A-11D-A35Z-10 chr15:48056060 C>A maps to NM_153618.1 R254R. Only missense variants will be evaluated by CHASM.
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-ZS-A9CF-01A-11D-A382-10 chr15:74706912 G>T maps to NM_003612.3 T423T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADL-01A-11D-A40R-10 chr20:43850458 T>C maps to NM_003008.2 S62S. 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.
Multiple mappings detected for codon TCGA-BD-A3EP-01A-11D-A22F-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-DD-AACD-01A-11D-A40R-10 chr17:7466635 G>A maps to ENST00000321337 E81E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr17:7466513 C>A maps to ENST00000321337 R41R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9GW-01A-11D-A382-10 chr3:196613317 G>T maps to NM_152699.4 V422V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EE-01A-11D-A12Z-10 chr5:42804756 C>A did not map to a codon.
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-BC-A3KF-01A-11D-A20W-10 chr22:42392913 C>T maps to NM_145733.2 G340G. 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-WX-AA46-01A-11D-A38X-10 chr17:56604303 T>A maps to NM_004574.3 G32G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAVX-01A-11D-A40R-10 chr22:19707953 C>T maps to NM_002688.5 Y158Y. 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-G3-AAV7-01A-11D-A382-10 chr6:158535992 G>A maps to NM_032861.3 V504V. Only missense variants will be evaluated by CHASM.
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-EP-A2KA-01A-11D-A183-10 chr15:44089115 T>A maps to ENST00000319327 L289L. 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-DD-A39Z-01A-11D-A20W-10 chr14:94752492 A>G maps to NM_001100607.1 A365A. 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-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-BC-A3KG-01A-11D-A20W-10 chr14:94776278 T>C maps to NM_001756.3 T226T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZS-A9CF-01A-11D-A382-10 chr23:105279298 G>A did not map to a codon.
Sequencing variant TCGA-DD-AADM-01A-11D-A40R-10 chr18:61597342 C>T maps to NM_005024.1 N185N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A2QR-01A-11D-A20W-10 chr18:61587032 A>G maps to NM_005024.1 E128E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACV-01A-11D-A40R-10 chr18:61562580 G>A maps to NM_001143818.1 Q84Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr18:61569074 G>T maps to NM_001143818.1 E213*. 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-ZS-A9CE-01A-11D-A36X-10 chr18:61305146 T>A maps to NM_002974.2 K327*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9H3-01A-11D-A382-10 chr18:61460471 G>C maps to NM_001040147.1 V99V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACD-01A-11D-A40R-10 chr18:61449698 C>G maps to NM_001040147.1 S31S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZP-A9CY-01A-11D-A382-10 chr18:61654509 T>C maps to NM_198833.1 *375Q. 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-BC-A3KF-01A-11D-A20W-10 chr22:21138491 A>G maps to NM_000185.3 T374T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADS-01A-11D-A40R-10 chr13:51936117 T>C maps to NM_001101320.1 N420N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAVU-01A-11D-A40R-10 chr17:1678370 T>C maps to NM_002615.4 F221F. Only missense variants will be evaluated by CHASM.
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-DD-AACX-01A-11D-A40R-10 chr3:167542318 A>G maps to NM_005025.4 P375P. 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-G3-A3CJ-01A-11D-A20W-10 chr19:40929171 A>G maps to NM_013376.3 P94P. 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-AADO-01A-11D-A40R-10 chr1:210414922 A>G maps to NM_019605.3 E104E. 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-CC-A3MA-01A-11D-A20W-10 chr16:30978230 A>G maps to NM_014712.1 Q844Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GJ-A9DB-01A-11D-A36X-10 chr16:30982810 C>A maps to NM_014712.1 S1043S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EG-01A-11D-A20W-10 chr3:47164898 A>G maps to NM_014159.6 S409S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAD0-01A-11D-A40R-10 chr3:47161669 A>C did not map to a codon.
Sequencing variant TCGA-DD-AADD-01A-11D-A40R-10 chr3:47161865 C>T maps to NM_014159.6 E1420E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADK-01A-11D-A40R-10 chr3:47155364 C>T did not map to a codon.
Sequencing variant TCGA-DD-AAEB-01A-11D-A40R-10 chr3:47084190 C>A did not map to a codon.
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-4R-AA8I-01A-11D-A382-10 chr14:99929898 C>T maps to NM_032233.2 A40A. 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-DD-AAVR-01A-11D-A40R-10 chr9:135205037 T>G maps to ENST00000372169 P649P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A2QR-01A-11D-A20W-10 chr9:135202229 A>G maps to ENST00000372169 P1585P. 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-DD-AADD-01A-11D-A40R-10 chr22:30731655 G>C maps to NM_005877.4 L731L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACP-01A-11D-A40R-10 chr16:70588394 A>G maps to NM_012426.4 L483L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAVR-01A-11D-A40R-10 chr16:70605099 A>T maps to NM_012426.4 K1171*. 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-5R-AA1C-01A-11D-A40R-10 chr22:32009643 A>G maps to NM_001007467.1 K933K. 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-ES-A2HT-01A-12D-A183-10 chr22:31927043 A>G maps to NM_001007467.1 R89R. 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-DD-AAE9-01A-11D-A40R-10 chr10:7217970 A>G maps to NM_001018039.1 I655I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr10:7247789 T>C maps to NM_001018039.1 P477P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XR-A8TF-01A-11D-A35Z-10 chr10:7409743 C>A maps to NM_001018039.1 G101G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-AAV0-01A-11D-A36X-10 chr7:37955893 C>T maps to ENST00000223214 A104A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IK-01A-12D-A33Q-10 chr5:64023955 T>A maps to ENST00000513458 K86*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75C-01A-11D-A32G-10 chr6:89827582 G>A maps to ENST00000452027 P8P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr19:19129922 A>G maps to NM_001017392.3 A615A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A6M4-01A-11D-A32G-10 chr19:19136955 T>A maps to NM_001017392.3 G67G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr21:33068943 G>T maps to NM_020706.2 T299T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A9-01A-11D-A25V-10 chr19:45543520 C>T maps to NM_007056.2 V17V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YA-A8S7-01A-11D-A36X-10 chr19:45567464 G>A maps to NM_007056.2 P367P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A5UD-01A-11D-A28X-10 chr23:1718232 G>T did not map to a codon.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr23:1712974 T>C did not map to a codon.
Sequencing variant TCGA-DD-AADV-01A-11D-A38X-10 chr23:1720178 G>C did not map to a codon.
Sequencing variant TCGA-DD-AACL-01A-11D-A40R-10 chr6:99849419 T>A maps to NM_032870.2 R472*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A2QR-01A-11D-A20W-10 chr6:99862517 T>C maps to NM_032870.2 G6G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr17:74732954 C>T maps to NM_003016.4 P96P. 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-XR-A8TD-01A-12D-A38X-10 chr8:22021529 C>T maps to NM_003018.3 G190G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A9FU-01A-11D-A36X-10 chr10:120916265 T>A maps to NM_213649.1 V180V. 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-EP-A2KA-01A-11D-A183-10 chr2:73247366 C>T did not map to a codon.
Sequencing variant TCGA-ZP-A9D0-01A-11D-A36X-10 chr2:73250319 C>T maps to NM_144579.2 K91K. 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-DD-AADS-01A-11D-A40R-10 chr7:94259028 A>G did not map to a codon.
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-CC-A9FS-01A-11D-A36X-10 chr3:153943787 C>T maps to NM_015595.3 T693T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAEA-01A-11D-A40R-10 chr3:153909104 A>G maps to NM_015595.3 V556V. 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-2Y-A9GU-01A-11D-A382-10 chr6:134498799 C>G did not map to a codon.
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-DD-A1EA-01A-11D-A12Z-10 chr15:77425573 C>A maps to NM_024776.2 E1284*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EE-01A-11D-A12Z-10 chr15:77425573 C>A maps to NM_024776.2 E1284*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr4:108824504 G>T maps to NM_152621.5 T230T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CG-01A-11D-A20W-10 chr3:20219760 A>G did not map to a codon.
Sequencing variant TCGA-BC-A3KG-01A-11D-A20W-10 chr2:201400865 G>A did not map to a codon.
Sequencing variant TCGA-DD-AAEA-01A-11D-A40R-10 chr17:78184754 G>T maps to NM_000199.3 I335I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MR-A520-01A-11D-A25V-10 chr17:78188901 C>T maps to NM_000199.3 V95V. 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-EP-A2KA-01A-11D-A183-10 chr22:25280065 A>G maps to NM_001039948.2 S569S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACP-01A-11D-A40R-10 chr17:2276665 A>G maps to NM_014853.2 A653A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACH-01A-11D-A40R-10 chr22:40804804 G>T maps to NM_015705.4 E621*. 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-DD-AAVV-01A-11D-A40R-10 chr19:6755042 G>A maps to NM_005490.2 A260A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CJ-01A-11D-A20W-10 chr9:130536684 T>C maps to NM_170600.2 R33R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-AAV1-01A-11D-A382-10 chr8:19192208 T>A maps to NM_022071.3 S118S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CJ-01A-11D-A20W-10 chr23:80532636 C>T 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-G3-A3CJ-01A-11D-A20W-10 chr3:15311264 C>T maps to NM_004844.3 Q150Q. 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-CC-A7IE-01A-21D-A382-10 chr19:4366970 T>A maps to NM_003025.2 G22G. 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-EP-A2KA-01A-11D-A183-10 chr9:17791314 G>T maps to NM_003026.2 T237T. 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-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-DD-AAVR-01A-11D-A40R-10 chr5:171766053 G>A maps to NM_001017995.2 G685G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZP-A9CV-01A-11D-A382-10 chr5:145435594 G>A maps to NM_152550.3 W458*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr2:110015185 G>T maps to NM_001099289.1 A362A. 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-DD-A1EE-01A-11D-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-G3-AAV4-01A-11D-A382-10 chr19:51170471 G>T maps to ENST00000391814 S1590*. Only missense variants will be evaluated by CHASM.
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-AAE6-01A-11D-A40R-10 chr11:70333712 G>A maps to ENST00000338508 P889P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9GW-01A-11D-A382-10 chr22:51117296 G>A maps to NM_001080420.1 G183G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr22:51143418 G>T maps to NM_001080420.1 G658*. 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-DD-A39Y-01A-11D-A20W-10 chr17:7536254 T>C maps to NM_001040.3 R346R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr19:438993 G>A maps to NM_012435.2 G192G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr19:422412 C>A maps to NM_012435.2 A451A. 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-NI-A8LF-01A-11D-A35Z-10 chr15:49255155 G>A maps to NM_203349.3 F19F. 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-FV-A4ZP-01A-12D-A25V-10 chr16:46651614 C>T maps to NM_024745.4 L106L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr15:45490990 C>T maps to ENST00000437903 R151R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAD0-01A-11D-A40R-10 chr7:155595680 C>T maps to NM_000193.2 W434*. 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-5C-A9VH-01A-11D-A36X-10 chr3:48520584 C>T did not map to a codon.
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-A3A0-01A-11D-A20W-10 chr10:112769580 A>G maps to NM_007373.3 E511E. 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-4R-AA8I-01A-11D-A382-10 chr23:9866240 C>T did not map to a codon.
Sequencing variant TCGA-DD-A116-01A-11D-A12Z-10 chr23:9863963 G>T did not map to a codon.
Sequencing variant TCGA-DD-A3A0-01A-11D-A20W-10 chr23:9900714 T>C did not map to a codon.
Sequencing variant TCGA-DD-AACV-01A-11D-A40R-10 chr23:9864617 G>T did not map to a codon.
Sequencing variant TCGA-CC-A3MA-01A-11D-A20W-10 chr4:77663054 T>C maps to NM_020859.3 S1243S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAVQ-01A-11D-A40R-10 chr4:77662787 G>T maps to NM_020859.3 T1154T. 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-FV-A3R2-01A-11D-A22F-10 chr4:77661968 G>A maps to NM_020859.3 P881P. 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-CC-A7IE-01A-21D-A382-10 chr23:50341496 G>T did not map to a codon.
Sequencing variant TCGA-DD-A1EG-01A-11D-A20W-10 chr23:50351076 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-DD-AAC8-01A-11D-A40R-10 chr23:50377202 G>T 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-UB-AA0U-01A-11D-A382-10 chr23:50350751 T>C 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-DD-A3A0-01A-11D-A20W-10 chr3:164735839 G>A maps to NM_001041.3 S1146S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACY-01A-11D-A40R-10 chr3:164776810 C>T maps to NM_001041.3 R446R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAEE-01A-11D-A40R-10 chr3:164755791 C>T maps to NM_001041.3 R774R. 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-WQ-AB4B-01A-11D-A40P-10 chr3:150480231 C>T maps to NM_005067.5 L135L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr3:113300278 C>A maps to ENST00000393830 A245A. 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-EP-A2KB-01A-11D-A183-10 chr20:3670894 G>T maps to NM_023068.3 P1536P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XR-A8TD-01A-12D-A38X-10 chr20:3684556 G>A maps to NM_023068.3 A296A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACQ-01A-11D-A40R-10 chr19:50463580 A>T maps to NM_052884.2 C186*. 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-BC-A3KG-01A-11D-A20W-10 chr19:52002710 A>G maps to NM_053003.2 A356A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACM-01A-11D-A40R-10 chr19:52147071 C>T maps to NM_001098612.1 P324P. 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-4R-AA8I-01A-11D-A382-10 chr19:52034863 T>C maps to NM_001245.5 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADG-01A-11D-A40R-10 chr19:52031018 G>T maps to NM_001245.5 V390V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MB-01A-11D-A20W-10 chr19:51649118 A>G maps to NM_014385.2 T256T. 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-ES-A2HS-01A-11D-A183-10 chr19:51648214 A>G maps to NM_014385.2 T253T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9H1-01A-11D-A382-10 chr19:51958749 C>A maps to NM_014442.2 E325*. 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-DD-AAVX-01A-11D-A40R-10 chr19:51630326 A>G maps to NM_014441.2 P263P. 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-ES-A2HS-01A-11D-A183-10 chr21:44839237 G>A maps to NM_173354.3 Q414*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAEG-01A-11D-A38X-10 chr11:111574146 G>A maps to NM_015191.1 E316E. 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-CC-A7IH-01A-11D-A33K-10 chr1:115318965 C>G did not map to a codon.
Sequencing variant TCGA-DD-AAVP-01A-11D-A40R-10 chr1:115318965 C>G did not map to a codon.
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-5C-A9VG-01A-11D-A36X-10 chr19:16952598 G>C maps to NM_015260.1 G134G. 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-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-DD-A39Y-01A-11D-A20W-10 chr14:72152234 T>C maps to NM_015556.1 S1087S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A1-01A-11D-A20W-10 chr14:72176081 T>C maps to NM_015556.1 A1324A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr14:72090841 T>C maps to NM_015556.1 P569P. 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-4R-AA8I-01A-11D-A382-10 chr19:38573539 C>T maps to NM_015073.1 S445S. 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-ES-A2HT-01A-12D-A183-10 chr19:38633305 C>T maps to NM_015073.1 T1163T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACV-01A-11D-A40R-10 chr20:1551721 G>A maps to NM_006065.3 T271T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A3KG-01A-11D-A20W-10 chr20:1532595 G>C maps to ENST00000381621 P54P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WQ-A9G7-01A-11D-A36X-10 chr10:69648661 A>G maps to NM_012238.4 Q190Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A8HV-01A-11D-A35Z-10 chr11:219011 G>A maps to NM_012239.5 A333A. 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-DD-AACD-01A-11D-A40R-10 chr2:45233482 G>A maps to NM_016932.4 S234S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A8O6-01A-11D-A35Z-10 chr2:45171796 G>A maps to NM_005413.3 T299T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAC8-01A-11D-A40R-10 chr14:61186826 A>T maps to NM_017420.4 I400I. 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-WQ-A9G7-01A-11D-A36X-10 chr14:61190366 T>C maps to NM_017420.4 L142L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WX-AA47-01A-11D-A38X-10 chr19:46270085 G>A maps to NM_175875.4 A377A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADG-01A-11D-A40R-10 chr14:60976598 C>A maps to ENST00000381716 L220L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BD-A3EP-01A-11D-A22F-10 chr13:21750550 C>T maps to NM_145061.5 T22T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr13:21742125 C>A did not map to a codon.
Sequencing variant TCGA-DD-AADY-01A-11D-A40R-10 chr13:21742125 C>A did not map to a codon.
Sequencing variant TCGA-G3-A25Y-01A-11D-A16V-10 chr13:21742125 C>A did not map to a codon.
Sequencing variant TCGA-5C-A9VG-01A-11D-A36X-10 chr5:54649069 C>G maps to NM_015360.4 R502R. 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-DD-A39X-01A-11D-A20W-10 chr5:54603858 A>G maps to NM_015360.4 G6G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADI-01A-11D-A40R-10 chr5:54640444 A>G maps to NM_015360.4 E334E. 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-FV-A2QR-01A-11D-A20W-10 chr5:54635840 T>C maps to NM_015360.4 Y173Y. 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-2Y-A9H0-01A-11D-A382-10 chr13:78320727 A>G maps to ENST00000389459 K310K. 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-XR-A8TG-01A-11D-A35Z-10 chr4:48385694 C>A maps to NM_020846.1 S418S. 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-DD-AADM-01A-11D-A40R-10 chr14:70246026 A>T maps to NM_003049.3 S206S. 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-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-2Y-A9H5-01A-11D-A382-10 chr4:147431062 A>T did not map to a codon.
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-AAE6-01A-11D-A40R-10 chr2:219249061 C>T maps to NM_000578.3 Q83*. Only missense variants will be evaluated by CHASM.
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-CC-A7IE-01A-21D-A382-10 chr5:127520081 T>A maps to NM_001046.2 I1108I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACC-01A-11D-A40R-10 chr5:127483378 T>G maps to NM_001046.2 S613S. 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-DD-AAED-01A-12D-A40R-10 chr20:44669253 G>C maps to ENST00000372315 P285P. 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-CC-A8HT-01A-11D-A35Z-10 chr5:1073786 C>T maps to NM_006598.2 T734T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EE-01A-11D-A12Z-10 chr7:100452000 G>T did not map to a codon.
Sequencing variant TCGA-DD-A1EF-01A-11D-A12Z-10 chr7:100452000 G>T did not map to a codon.
Sequencing variant TCGA-DD-AAE6-01A-11D-A40R-10 chr7:100454562 G>A maps to NM_020246.2 L174L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAEK-01A-11D-A40R-10 chr7:122774579 G>A maps to NM_022444.3 R272R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr20:45239190 G>T maps to NM_022829.5 T145T. Only missense variants will be evaluated by CHASM.
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-DD-AACD-01A-11D-A40R-10 chr7:135370359 G>C maps to NM_012450.2 T505T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr17:6597476 G>T maps to NM_177550.3 T365T. 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-2Y-A9H3-01A-11D-A382-10 chr18:43248312 G>C did not map to a codon.
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-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-DD-AADI-01A-11D-A40R-10 chr2:230914606 G>A maps to NM_152527.4 G91G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73F-01A-11D-A32G-10 chr17:80195332 G>T maps to NM_001042423.1 V229V. 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-LG-A6GG-01A-11D-A30V-10 chr6:25850685 C>T did not map to a codon.
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-XR-A8TF-01A-11D-A35Z-10 chr11:22396317 T>A maps to NM_020346.2 A353A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A1-01A-11D-A20W-10 chr19:49937913 C>T maps to NM_020309.3 W194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A0-01A-11D-A20W-10 chr10:119026262 T>C maps to NM_003054.4 A337A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-AAV7-01A-11D-A382-10 chr1:169454947 G>T maps to NM_006996.2 L19L. Only missense variants will be evaluated by CHASM.
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-2Y-A9H5-01A-11D-A382-10 chr2:65248222 C>T maps to NM_003038.4 N514N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A2QR-01A-11D-A20W-10 chr19:47280495 A>G maps to NM_005628.2 L409L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9GU-01A-11D-A382-10 chr1:53571447 T>C did not map to a codon.
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-AAE3-01A-11D-A40R-10 chr1:53580428 C>A did not map to a codon.
Sequencing variant TCGA-DD-AAE3-01A-11D-A40R-10 chr8:42297136 T>C maps to NM_006749.3 V255V. 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-DD-AACQ-01A-11D-A40R-10 chr11:63057747 A>G maps to NM_001039752.3 L37L. 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-2Y-A9GV-01A-11D-A382-10 chr3:38347651 C>T maps to NM_004803.3 H45H. Only missense variants will be evaluated by CHASM.
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-DD-AAE4-01A-11D-A40R-10 chr3:38354540 G>A maps to NM_004803.3 E332E. 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-DD-AAD5-01A-11D-A40R-10 chr6:3273354 G>A maps to ENST00000436008 H673H. 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-DD-AACI-01A-11D-A40R-10 chr6:43269997 C>T maps to ENST00000372585 N374N. 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-2Y-A9GV-01A-11D-A382-10 chr20:4854659 T>A maps to NM_203327.1 K342*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A1-01A-11D-A20W-10 chr2:220028988 A>G maps to NM_001144890.1 A421A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACP-01A-11D-A40R-10 chr15:65943144 G>A maps to NM_004727.2 E886E. 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-2Y-A9H0-01A-11D-A382-10 chr15:48429128 A>C maps to NM_205850.2 I280I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAVX-01A-11D-A40R-10 chr15:48431226 C>T maps to NM_205850.2 S311S. Only missense variants will be evaluated by CHASM.
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-DD-AAVS-01A-11D-A40R-10 chr2:172641966 T>C maps to NM_003705.3 E618E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr7:95820552 C>A maps to NM_001160210.1 G208*. 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-EP-A2KA-01A-11D-A183-10 chr19:6456472 C>T maps to NM_024103.2 L147L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAE9-01A-11D-A40R-10 chr9:130866084 G>T maps to ENST00000373069 T250T. 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-BC-A3KG-01A-11D-A20W-10 chr13:45973082 A>G maps to NM_001010875.2 L249L. 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-DD-AAEB-01A-11D-A40R-10 chr4:128689944 C>T maps to NM_031291.2 V224V. 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-2Y-A9HA-01A-11D-A38X-10 chr3:39433405 G>T maps to NM_017875.2 G173G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAD1-01A-11D-A40R-10 chr23:118540511 T>C did not map to a codon.
Sequencing variant TCGA-DD-A39Z-01A-11D-A20W-10 chr23:118604918 A>G did not map to a codon.
Sequencing variant TCGA-NI-A4U2-01A-11D-A28X-10 chr23:118603837 T>G did not map to a codon.
Sequencing variant TCGA-DD-AACV-01A-11D-A40R-10 chr23:1506263 A>G did not map to a codon.
Sequencing variant TCGA-DD-AAW1-01A-11D-A40P-10 chr23:1508318 C>T did not map to a codon.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr4:984945 G>T maps to NM_213613.2 T182T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADG-01A-11D-A40R-10 chr12:58018904 G>A did not map to a codon.
Sequencing variant TCGA-2V-A95S-01A-11D-A36X-10 chr7:107431675 C>T maps to NM_000111.2 P129P. Only missense variants will be evaluated by CHASM.
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-DD-AAE3-01A-11D-A40R-10 chr8:92330491 G>T maps to NM_134266.1 E176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAEB-01A-11D-A40R-10 chr8:92346675 G>T did not map to a codon.
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-EP-A2KA-01A-11D-A183-10 chr6:35918963 C>A maps to NM_052961.3 R816R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WJ-A86L-01A-12D-A45V-10 chr1:205886473 C>A maps to NM_134325.2 G755G. 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-AADB-01A-11D-A40R-10 chr19:59010878 G>A maps to NM_012254.2 D549D. 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-BC-A3KF-01A-11D-A20W-10 chr15:85438312 C>T maps to NM_004213.3 L140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MA-01A-11D-A20W-10 chr15:85438312 C>T maps to NM_004213.3 L140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr15:85476373 A>G did not map to a codon.
Sequencing variant TCGA-DD-A1EG-01A-11D-A20W-10 chr15:85438312 C>T maps to NM_004213.3 L140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GJ-A9DB-01A-11D-A36X-10 chr9:86894923 C>T maps to NM_022127.2 G598G. 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-DD-AACX-01A-11D-A40R-10 chr11:66136931 G>A maps to NM_001532.2 P61P. 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-DD-AAW1-01A-11D-A40P-10 chr1:43393338 G>A maps to NM_006516.2 A405A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-AAUZ-01A-11D-A382-10 chr3:170732427 C>G maps to NM_000340.1 L67L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-AAV3-01A-11D-A36X-10 chr3:170732355 T>C maps to NM_000340.1 Q91Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YA-A8S7-01A-11D-A36X-10 chr3:170725002 G>A maps to NM_000340.1 T182T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EG-01A-11D-A20W-10 chr12:8085608 G>A maps to NM_006931.2 V81V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADS-01A-11D-A40R-10 chr12:8085599 G>A maps to NM_006931.2 F84F. 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-G3-A3CJ-01A-11D-A20W-10 chr20:62373697 A>G maps to NM_020062.3 A230A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAE7-01A-11D-A40R-10 chr1:9098488 C>T did not map to a codon.
Sequencing variant TCGA-DD-A3A0-01A-11D-A20W-10 chr2:32417461 A>G maps to NM_001193513.1 G154G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr1:101379225 A>T maps to NM_133496.4 G173G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9GW-01A-11D-A382-10 chr8:118159312 G>A maps to NM_173851.2 A64A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9GW-01A-11D-A382-10 chr5:176825094 G>A maps to NM_003052.4 W576*. 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-AACZ-01A-11D-A40R-10 chr4:25667798 T>A maps to NM_006424.2 P143P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAVX-01A-11D-A40R-10 chr4:25676184 C>G maps to NM_006424.2 G464G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr4:25678340 G>T maps to NM_006424.2 S681S. Only missense variants will be evaluated by CHASM.
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-WQ-A9G7-01A-11D-A36X-10 chr7:133979688 G>A maps to NM_032826.4 L298L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A1-01A-11D-A20W-10 chr1:67518480 A>G maps to NM_015139.2 P99P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9GY-01A-11D-A382-10 chr9:99113413 G>A maps to NM_007001.2 A153A. 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-BC-A3KG-01A-11D-A20W-10 chr19:16677348 G>A maps to NM_024881.4 S250S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAE2-01A-11D-A40R-10 chr19:16664489 C>A maps to NM_024881.4 *411Y. 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-DD-AACX-01A-11D-A40R-10 chr11:124949587 T>C maps to NM_198277.2 N153N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A2QR-01A-11D-A20W-10 chr12:46598343 A>G maps to NM_030674.3 L226L. 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-DD-AAE1-01A-11D-A40R-10 chr17:79257222 G>A maps to NM_001037984.1 L115L. 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-DD-AAD1-01A-11D-A40R-10 chr12:46764377 T>C maps to NM_018976.4 V77V. 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-DD-A119-01A-11D-A12Z-10 chr3:50251832 A>G did not map to a codon.
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-DD-A39Y-01A-11D-A20W-10 chr14:61497160 A>G did not map to a codon.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr14:61550408 C>A maps to NM_001172702.1 T515T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAEA-01A-11D-A40R-10 chr16:84075663 G>A maps to NM_001080442.1 L33L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACV-01A-11D-A40R-10 chr10:18242318 G>C maps to NM_001145195.1 G38G. 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-ES-A2HT-01A-12D-A183-10 chr19:2733300 C>G maps to NM_144564.4 S131S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAED-01A-12D-A40R-10 chr18:33703523 C>A maps to NM_012319.3 L358L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GJ-A9DB-01A-11D-A36X-10 chr4:103265761 C>A maps to NM_001135146.1 G20*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CJ-01A-11D-A20W-10 chr2:44513250 A>G maps to NM_000341.3 Q282Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACI-01A-11D-A40R-10 chr11:62648791 C>A maps to NM_001012661.1 A231A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr2:190426693 G>A maps to NM_014585.5 A542A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAVU-01A-11D-A40R-10 chr9:108126971 A>C maps to NM_080546.3 A408A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr19:10748542 C>T maps to NM_020428.3 Y569Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAVV-01A-11D-A40R-10 chr6:31839270 G>A maps to NM_025257.2 T199T. 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-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-DD-AADC-01A-11D-A40R-10 chr17:26731820 G>T maps to ENST00000440501 C298*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr9:115648747 A>T maps to NM_033051.3 I454I. 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-EP-A2KA-01A-11D-A183-10 chr17:19476160 T>C maps to ENST00000395585 D491D. 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-DD-AAEI-01A-11D-A40R-10 chr2:162738920 T>A maps to NM_001178015.1 I387I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr7:150761996 T>C maps to NM_003040.3 P174P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A7SH-01A-11D-A382-10 chr7:150767560 A>T maps to NM_003040.3 P489P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10W-01A-11D-A12Z-10 chr2:220506389 T>C maps to NM_201574.2 A1240A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NJ-01A-11D-A27I-10 chr2:220500540 C>T maps to NM_201574.2 Q734*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACQ-01A-11D-A40R-10 chr2:220501120 T>A maps to NM_201574.2 L790L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACU-01A-11D-A40R-10 chr2:220500392 A>T did not map to a codon.
Sequencing variant TCGA-DD-AADJ-01A-11D-A40R-10 chr2:220493161 A>T maps to NM_201574.2 P29P. 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-LG-A9QC-01A-11D-A36X-10 chr2:220500503 G>T maps to NM_201574.2 P721P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZP-A9D4-01A-11D-A36X-10 chr4:72205021 C>T maps to NM_003759.3 A19A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr12:51844747 A>G maps to NM_001039960.1 R73R. 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-DD-AADI-01A-11D-A40R-10 chr5:139743131 G>T maps to ENST00000507527 R381R. 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-CC-A9FW-01A-11D-A36X-10 chr11:26743146 G>A maps to NM_178498.3 R39*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr11:26700316 G>A maps to NM_178498.3 Y507Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACM-01A-11D-A40R-10 chr22:32620468 C>A maps to NM_014227.2 G484*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAC8-01A-11D-A40R-10 chr19:17988624 G>T maps to NM_000453.2 A264A. 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-2Y-A9H3-01A-11D-A382-10 chr12:101577958 T>C maps to NM_145913.3 P335P. 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-DD-AADR-01A-11D-A40R-10 chr12:301769 G>A maps to NM_003044.3 Y525Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAE7-01A-11D-A40R-10 chr12:330613 A>G maps to NM_016615.3 A538A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9GT-01A-11D-A382-10 chr23:115577962 A>G did not map to a codon.
Sequencing variant TCGA-DD-AADE-01A-11D-A40R-10 chr23:115590098 G>A did not map to a codon.
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-BC-A8YO-01A-11D-A36X-10 chr5:1219157 C>T maps to NM_001003841.2 G438G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAE6-01A-11D-A40R-10 chr5:1219040 C>G maps to NM_001003841.2 A399A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAVY-01A-11D-A40R-10 chr5:1221376 C>T maps to NM_001003841.2 F550F. 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-BC-A8YO-01A-11D-A36X-10 chr11:20660006 T>C maps to NM_004211.3 G624G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2V-A95S-01A-11D-A36X-10 chr3:14487225 T>C maps to NM_001134367.1 G77G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BD-A3EP-01A-11D-A22F-10 chr5:149578930 T>C did not map to a codon.
Sequencing variant TCGA-ZS-A9CF-01A-11D-A382-10 chr23:152959836 G>C did not map to a codon.
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-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-DD-A1ED-01A-11D-A152-10 chr3:170198198 C>T maps to NM_020949.2 K624K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr8:17422621 T>C maps to NM_001164771.1 P688P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39Y-01A-11D-A20W-10 chr23:70146022 A>G did not map to a codon.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr23:70149743 A>G did not map to a codon.
Sequencing variant TCGA-DD-AACQ-01A-11D-A40R-10 chr22:21384216 A>T maps to NM_004173.2 L469*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr16:87871522 T>C maps to NM_003486.5 E356E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A1-01A-11D-A20W-10 chr16:68344763 A>G maps to NM_032178.2 A22A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EG-01A-11D-A20W-10 chr19:33353025 T>C maps to NM_014270.4 G234G. 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-2Y-A9H8-01A-11D-A38X-10 chr19:47960452 C>T maps to NM_015063.2 T358T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAD8-01A-11D-A40R-10 chr19:47944675 T>A maps to NM_015063.2 I595I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A1-01A-11D-A20W-10 chr14:70512762 A>G maps to NM_183002.1 R895R. 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-UB-A7MB-01A-11D-A33Q-10 chr3:111888052 T>C maps to NM_183061.1 L1014L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10W-01A-11D-A12Z-10 chr1:173526508 G>A maps to NM_178527.3 L395L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADE-01A-11D-A40R-10 chr2:103300707 G>T maps to NM_003048.3 V446V. 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-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-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-DD-A3A1-01A-11D-A20W-10 chr12:21015741 A>G maps to NM_019844.2 G227G. 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-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-DD-AADS-01A-11D-A40R-10 chr15:92647604 T>A maps to NM_013272.3 L281*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9H9-01A-21D-A38X-10 chr5:101627073 C>A maps to NM_180991.4 E198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAEA-01A-11D-A40R-10 chr5:101627230 G>T maps to NM_180991.4 G145G. 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-5R-AAAM-01A-12D-A40R-10 chr8:70674090 T>A maps to NM_030958.2 G309G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACA-01A-11D-A40R-10 chr8:70744716 C>A maps to NM_030958.2 V64V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A3KG-01A-11D-A20W-10 chr5:101794139 T>C maps to NM_173488.3 R359R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A9FW-01A-11D-A36X-10 chr17:33679830 A>G maps to NM_152270.3 S750S. 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-DD-AAEE-01A-11D-A40R-10 chr17:33680409 C>A maps to NM_152270.3 E623*. 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-K7-AAU7-01A-11D-A382-10 chr17:33802436 T>C maps to ENST00000361112 G453G. 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-G3-A3CJ-01A-11D-A20W-10 chr17:33586257 T>C maps to NM_144975.3 Y183Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CG-01A-11D-A20W-10 chr10:98824596 T>C maps to NM_003061.2 E174E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A8YO-01A-11D-A36X-10 chr4:20535221 T>C maps to ENST00000273739 D576D. 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-DD-AAE0-01A-11D-A40R-10 chr4:20533634 T>C maps to ENST00000273739 L552L. 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-WX-AA44-01A-11D-A38X-10 chr4:20598094 T>C maps to ENST00000273739 D1139D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9GV-01A-11D-A382-10 chr5:168135070 A>G maps to NM_003062.2 N918N. 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-BD-A3EP-01A-11D-A22F-10 chr5:168093512 C>T maps to NM_003062.2 S1506S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39Y-01A-11D-A20W-10 chr5:168212943 T>C maps to NM_003062.2 G373G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAVP-01A-11D-A40R-10 chr5:168189635 G>A maps to NM_003062.2 P506P. 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-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-DD-AACU-01A-11D-A40R-10 chr23:144904521 A>G did not map to a codon.
Sequencing variant TCGA-DD-AADF-01A-11D-A40R-10 chr23:144906060 A>T did not map to a codon.
Sequencing variant TCGA-DD-AAED-01A-12D-A40R-10 chr23:144905308 T>A did not map to a codon.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr23:144905571 G>T 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-RC-A7SH-01A-11D-A382-10 chr23:144904693 G>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-ZP-A9D1-01A-11D-A382-10 chr23:144905171 G>T did not map to a codon.
Sequencing variant TCGA-ZP-A9D1-01A-11D-A382-10 chr23:144906449 T>A did not map to a codon.
Sequencing variant TCGA-CC-A7IE-01A-21D-A382-10 chr3:164907421 G>A maps to NM_014926.2 N399N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr3:164907027 G>T maps to NM_014926.2 R531R. 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-2Y-A9H5-01A-11D-A382-10 chr23:142718856 G>A did not map to a codon.
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-DD-AADG-01A-11D-A40R-10 chr23:142716501 T>A did not map to a codon.
Sequencing variant TCGA-DD-AADG-01A-11D-A40R-10 chr23:142716503 C>G did not map to a codon.
Sequencing variant TCGA-ED-A97K-01A-21D-A382-10 chr23:142718490 T>C did not map to a codon.
Sequencing variant TCGA-G3-A3CG-01A-11D-A20W-10 chr23:142716431 T>C did not map to a codon.
Sequencing variant TCGA-WQ-A9G7-01A-11D-A36X-10 chr23:142717164 G>A did not map to a codon.
Sequencing variant TCGA-WX-AA44-01A-11D-A38X-10 chr23:142717486 A>C did not map to a codon.
Sequencing variant TCGA-ZP-A9CV-01A-11D-A382-10 chr23:142718336 G>A did not map to a codon.
Sequencing variant TCGA-ZP-A9CV-01A-11D-A382-10 chr23:142718338 T>A did not map to a codon.
Sequencing variant TCGA-CC-A3MA-01A-11D-A20W-10 chr3:57846496 A>G maps to ENST00000428312 T253T. Only missense variants will be evaluated by CHASM.
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-AAE0-01A-11D-A40R-10 chr18:12427044 A>G maps to NM_006553.3 T99T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr20:43882354 A>G maps to NM_003064.2 C35C. 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-A3CJ-01A-11D-A20W-10 chr15:59204794 T>C maps to NM_024755.2 Q176Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WQ-A9G7-01A-11D-A36X-10 chr6:71546687 C>T maps to NM_001044305.1 S207S. 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-DD-AADD-01A-11D-A40R-10 chr23:128623008 T>C did not map to a codon.
Sequencing variant TCGA-DD-AAEE-01A-11D-A40R-10 chr23:128630826 C>T did not map to a codon.
Sequencing variant TCGA-DD-AAVP-01A-11D-A40R-10 chr23:128645790 T>C did not map to a codon.
Sequencing variant TCGA-BW-A5NP-01A-11D-A27I-10 chr9:2039814 G>A maps to NM_003070.3 Q235Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MA-01A-11D-A20W-10 chr9:2039814 G>A maps to NM_003070.3 Q235Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IJ-01A-11D-A33Q-10 chr9:2039814 G>A maps to NM_003070.3 Q235Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACT-01A-11D-A40R-10 chr9:2115819 A>T did not map to a codon.
Sequencing variant TCGA-DD-AADL-01A-11D-A40R-10 chr9:2123795 G>A maps to NM_003070.3 L1280L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CG-01A-11D-A20W-10 chr9:2039820 G>A maps to NM_003070.3 Q237Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A5UE-01A-11D-A28X-10 chr19:11096862 A>T did not map to a codon.
Sequencing variant TCGA-DD-A3A0-01A-11D-A20W-10 chr19:11099990 A>G did not map to a codon.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr4:144464785 T>A maps to NM_003601.2 G676G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CG-01A-11D-A20W-10 chr4:95197543 A>G maps to NM_001128429.1 K621K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACY-01A-11D-A40R-10 chr2:217341833 G>T maps to NM_014140.3 V810V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAE8-01A-11D-A40R-10 chr2:217293424 A>C maps to NM_014140.3 P418P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr2:217303198 G>T maps to NM_014140.3 P567P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAE7-01A-11D-A40R-10 chr12:56575847 G>T maps to NM_003075.3 I216I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZP-A9CV-01A-11D-A382-10 chr17:61911878 T>C maps to NM_001098426.1 G292G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-5260-01A-01D-A12Z-10 chr23:53409454 T>A did not map to a codon.
Sequencing variant TCGA-DD-AAD0-01A-11D-A40R-10 chr23:53442010 G>A did not map to a codon.
Sequencing variant TCGA-DD-AAEA-01A-11D-A40R-10 chr23:53421752 T>C did not map to a codon.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr23:53432728 T>C did not map to a codon.
Sequencing variant TCGA-G3-A3CJ-01A-11D-A20W-10 chr22:45767391 G>T maps to NM_148674.3 R758R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EE-01A-11D-A12Z-10 chr9:106894407 T>G 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-EP-A2KA-01A-11D-A183-10 chr9:106877082 A>G maps to NM_001042550.1 R548R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9H8-01A-11D-A38X-10 chr10:112349409 G>A maps to NM_005445.3 L451L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr10:112337616 C>T maps to NM_005445.3 R99*. Only missense variants will be evaluated by CHASM.
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-AADV-01A-11D-A38X-10 chr3:160148413 C>G maps to NM_005496.3 V941V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CG-01A-11D-A20W-10 chr3:160148404 A>G maps to NM_005496.3 Q938Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MB-01A-11D-A20W-10 chr9:72967129 T>C maps to NM_015110.3 S1063S. 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-DD-AADL-01A-11D-A40R-10 chr18:2763753 A>G maps to NM_015295.2 E1562E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADP-01A-11D-A38X-10 chr18:2697977 C>T maps to NM_015295.2 I427I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAEI-01A-11D-A40R-10 chr18:2772285 A>T maps to NM_015295.2 S1697S. 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-G3-AAV3-01A-11D-A36X-10 chr18:2747623 T>A maps to NM_015295.2 L1302L. 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-DD-AAEG-01A-11D-A38X-10 chr14:91927807 C>A maps to ENST00000417249 G770*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADE-01A-11D-A40R-10 chr2:55826139 C>T maps to NM_001122964.1 Q111Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XR-A8TF-01A-11D-A35Z-10 chr2:55825632 T>C maps to NM_001122964.1 P280P. 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-G3-AAV5-01A-11D-A36X-10 chr16:18861618 G>A maps to ENST00000389467 F1741F. 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-DD-A119-01A-11D-A12Z-10 chr17:2202372 A>G maps to NM_017575.4 P558P. Only missense variants will be evaluated by CHASM.
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-DD-AADD-01A-11D-A40R-10 chr1:183515341 G>A maps to ENST00000367537 W868*. 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-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-DD-A3A1-01A-11D-A20W-10 chr6:168944303 G>T did not map to a codon.
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-A1EG-01A-11D-A20W-10 chr11:6411959 G>T maps to NM_000543.4 A44A. 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-DD-AAW2-01A-11D-A40P-10 chr11:6411941 G>C maps to NM_000543.4 A38A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XR-A8TE-01A-11D-A35Z-10 chr11:6411971 T>G maps to NM_000543.4 A48A. 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-FV-A3I1-01A-11D-A22F-10 chr6:123110565 G>T maps to NM_006714.3 V25V. 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-ES-A2HS-01A-11D-A183-10 chr23:22010831 T>C did not map to a codon.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr22:31484695 T>C maps to ENST00000454496 A156A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MR-A8JO-01A-12D-A35Z-10 chr11:57310234 G>A maps to ENST00000457912 K58K. Only missense variants will be evaluated by CHASM.
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-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-G3-A3CG-01A-11D-A20W-10 chr2:73449932 A>G maps to NM_006062.2 E231E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WQ-A9G7-01A-11D-A36X-10 chr8:49832740 T>C maps to NM_003068.3 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A8HT-01A-11D-A35Z-10 chr16:88747781 C>A maps to NM_178310.3 L139L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NB-01A-12D-A25V-10 chr16:88747898 G>T maps to NM_178310.3 A100A. 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-2Y-A9GZ-01A-11D-A38X-10 chr6:84317434 A>T maps to NM_014841.2 S335S. 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-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-2Y-A9GW-01A-11D-A382-10 chr14:62248975 A>G maps to NM_003082.3 S279S. 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-DD-AADQ-01A-11D-A40R-10 chr5:121780325 C>A maps to ENST00000379533 A544A. Only missense variants will be evaluated by CHASM.
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-2Y-A9H7-01A-11D-A38X-10 chr5:176056619 C>T maps to NM_003085.3 K12K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39Y-01A-11D-A20W-10 chr2:241988109 A>G maps to NM_001080437.1 G477G. 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-ES-A2HS-01A-11D-A183-10 chr2:241979606 T>A did not map to a codon.
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-DD-AA3A-01A-11D-A36X-10 chr16:11770175 C>T maps to NM_003498.5 H87H. 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-DD-AAE7-01A-11D-A40R-10 chr1:31766195 C>A did not map to a codon.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr19:41268861 G>A maps to NM_004596.4 P161P. 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-DD-AADF-01A-11D-A40R-10 chr20:32026677 G>C maps to NM_003098.2 L155L. 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-DD-AACN-01A-11D-A40R-10 chr16:69318052 C>T maps to NM_006750.3 F417F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAD3-01A-11D-A40R-10 chr16:69333646 C>A maps to NM_006750.3 Y500*. 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-GJ-A3OU-01A-31D-A382-10 chr2:1271231 C>A maps to NM_018968.3 I391I. 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-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-G3-A3CJ-01A-11D-A20W-10 chr6:86259454 T>C maps to NM_153816.3 K259K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr2:27597621 T>C maps to NM_014748.2 A226A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-AAV0-01A-11D-A36X-10 chr2:27598431 G>A maps to NM_014748.2 V278V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAVU-01A-11D-A40R-10 chr5:53839037 C>T maps to NM_001102575.1 R551*. 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-CC-A3MA-01A-11D-A20W-10 chr11:130780179 T>C maps to NM_014758.2 L633L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACC-01A-11D-A40R-10 chr11:130785825 T>C maps to NM_014758.2 T3T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr20:44469555 G>T maps to NM_033421.2 P242P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAEB-01A-11D-A40R-10 chr4:186244737 A>G maps to NM_031953.2 K347K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACD-01A-11D-A40R-10 chr8:101612591 T>C maps to NM_152628.3 E253E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAD5-01A-11D-A40R-10 chr3:125195600 C>A did not map to a codon.
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-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-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-G3-A7M7-01A-12D-A34Z-10 chr13:36747868 G>A maps to ENST00000511166 S397S. 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-A1EE-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-A3A1-01A-11D-A20W-10 chr21:34923954 A>G maps to NM_138927.1 L806L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MA-01A-11D-A20W-10 chr4:186544674 G>A maps to ENST00000355634 S732S. 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-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-DD-A3A1-01A-11D-A20W-10 chr4:7730077 T>C maps to NM_020777.2 D957D. 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-DD-AADB-01A-11D-A40R-10 chr10:106937874 T>A maps to NM_014978.1 V651V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9HB-01A-11D-A38X-10 chr11:121393350 C>T maps to NM_003105.5 L487L. 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-AAEK-01A-11D-A40R-10 chr11:121360804 C>G maps to NM_003105.5 V248V. 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-2Y-A9GZ-01A-11D-A38X-10 chr2:5833473 C>T maps to NM_003108.3 G207G. 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-DD-AAE3-01A-11D-A40R-10 chr2:5832873 C>T maps to NM_003108.3 S7S. 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-2Y-A9GZ-01A-11D-A38X-10 chr13:95363826 A>G maps to NM_007084.2 A159A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73G-01A-22D-A32G-10 chr13:95363655 G>A maps to NM_007084.2 A216A. Only missense variants will be evaluated by CHASM.
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-DD-A3A1-01A-11D-A20W-10 chr23:139586971 T>C did not map to a codon.
Sequencing variant TCGA-DD-AADE-01A-11D-A40R-10 chr23:139586655 G>T did not map to a codon.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr23:139587140 G>T did not map to a codon.
Sequencing variant TCGA-WQ-A9G7-01A-11D-A36X-10 chr23:139586439 C>T did not map to a codon.
Sequencing variant TCGA-2Y-A9H1-01A-11D-A382-10 chr5:157078732 G>A maps to NM_178424.1 G118G. Only missense variants will be evaluated by CHASM.
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-EP-A2KA-01A-11D-A183-10 chr6:21595157 G>A maps to NM_003107.2 R131R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11B-01A-11D-A12Z-10 chr11:15994639 T>A maps to NM_001145819.1 P747P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADO-01A-11D-A40R-10 chr11:16077381 T>C maps to NM_001145819.1 P402P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr16:1033874 G>A maps to NM_014587.3 A190A. 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-DD-A3A1-01A-11D-A20W-10 chr12:53800444 A>G maps to NM_138473.2 E584E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACX-01A-11D-A40R-10 chr2:231368973 G>A maps to NM_001080391.1 K613K. 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-WQ-A9G7-01A-11D-A36X-10 chr2:231033881 A>G maps to NM_080424.2 G700G. 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-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-BC-A3KF-01A-11D-A20W-10 chr7:20824955 C>G maps to NM_182700.4 G160G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAVR-01A-11D-A40R-10 chr7:20825270 C>A maps to NM_182700.4 S55S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAW1-01A-11D-A40P-10 chr11:124551356 T>C did not map to a codon.
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-BD-A3EP-01A-11D-A22F-10 chr19:49110447 C>T maps to NM_133498.2 C71C. 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-G3-AAV1-01A-11D-A382-10 chr1:118584650 C>T maps to NM_206996.2 E943E. Only missense variants will be evaluated by CHASM.
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-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-DD-AADL-01A-11D-A40R-10 chr9:35811574 G>A maps to NM_001039592.1 G156G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr17:49072444 A>G maps to ENST00000376407 S734S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39X-01A-11D-A20W-10 chr17:49043632 T>C maps to ENST00000376407 *1323W. 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-BD-A3ER-01A-11D-A20W-10 chr7:123599551 C>G maps to NM_001174046.1 L353L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADR-01A-11D-A40R-10 chr23:140336532 C>A did not map to a codon.
Sequencing variant TCGA-G3-AAV4-01A-11D-A382-10 chr4:88411473 C>A maps to NM_004684.4 G494G. Only missense variants will be evaluated by CHASM.
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-4R-AA8I-01A-11D-A382-10 chr13:24858384 C>T maps to ENST00000424834 G796G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39Z-01A-11D-A20W-10 chr13:24874602 A>G maps to ENST00000424834 G1253G. 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-ES-A2HT-01A-12D-A183-10 chr13:24798392 A>G maps to ENST00000424834 K479K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr4:52917893 G>A maps to NM_145263.2 L8L. 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-EP-A2KA-01A-11D-A183-10 chr17:48628202 C>A maps to NM_022827.2 T436T. 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-DD-A119-01A-11D-A12Z-10 chr17:3365781 A>G maps to NM_001170695.1 G108G. 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-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-G3-AAV0-01A-11D-A36X-10 chr4:123868515 G>A maps to NM_145207.2 R529R. 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-DD-AAD8-01A-11D-A40R-10 chr15:45695490 C>T maps to NM_024063.2 R288R. 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-DD-AACD-01A-11D-A40R-10 chr14:88892811 C>G maps to NM_018418.4 P203P. 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-CC-A8HT-01A-11D-A35Z-10 chr15:97326944 C>A maps to NM_173499.3 A20A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADF-01A-11D-A40R-10 chr5:95018537 C>T maps to NM_031952.3 G7G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr8:145095688 C>T maps to NM_198572.2 S329S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr6:44336152 A>G maps to NM_145026.3 P204P. 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-BC-A3KF-01A-11D-A20W-10 chr5:35628605 G>T maps to NM_024867.3 G35*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A3KF-01A-11D-A20W-10 chr5:35792502 C>T maps to NM_024867.3 G1503G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACX-01A-11D-A40R-10 chr5:35807282 T>C maps to NM_024867.3 I1769I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9H8-01A-11D-A38X-10 chr2:220348088 C>A maps to NM_005876.4 A1968A. 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-DD-AACV-01A-11D-A40R-10 chr2:220326769 C>A maps to NM_005876.4 P869P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr2:220333747 C>A maps to NM_005876.4 R1157R. 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-2Y-A9H7-01A-11D-A38X-10 chr1:16263692 T>G maps to NM_015001.2 P3354P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A3KF-01A-11D-A20W-10 chr1:16174600 A>G maps to NM_015001.2 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MB-01A-11D-A20W-10 chr1:16254900 T>C maps to NM_015001.2 I722I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr1:16255353 A>G maps to NM_015001.2 E873E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACK-01A-11D-A40R-10 chr1:16255900 A>T maps to NM_015001.2 R1056*. 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-2Y-A9H4-01A-11D-A382-10 chr15:69238043 A>G maps to NM_145658.3 K57K. 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-WX-AA46-01A-11D-A38X-10 chr13:36905734 T>C did not map to a codon.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr15:65261627 A>G maps to NM_016630.3 P211P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WQ-A9G7-01A-11D-A36X-10 chr15:65268815 A>G maps to NM_016630.3 D101D. 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-EP-A2KB-01A-11D-A183-10 chr2:228881549 A>G maps to NM_001142644.1 S1340S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr2:228881963 G>T maps to NM_001142644.1 I1202I. 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-ES-A2HT-01A-12D-A183-10 chr20:44171498 G>T maps to ENST00000396669 C77*. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-DD-A39Z-01A-11D-A20W-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr18:12535543 T>C maps to NM_001128626.1 V220V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MB-01A-11D-A20W-10 chr16:29675096 C>T maps to NM_003123.3 D16D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BD-A3EP-01A-11D-A22F-10 chr16:28986618 C>T maps to NM_032038.2 R49R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KR-A7K0-01A-12D-A33Q-10 chr16:28995278 G>A did not map to a codon.
Sequencing variant TCGA-DD-A1EE-01A-11D-A12Z-10 chr17:4416594 C>T maps to NM_001124758.1 L142L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A5SM-01A-12D-A28X-10 chr17:4348360 G>T maps to NM_182538.4 V100V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10W-01A-11D-A12Z-10 chr1:32280898 T>C maps to NM_144569.4 T12T. Only missense variants will be evaluated by CHASM.
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-DD-AADA-01A-11D-A40R-10 chr5:136476318 G>A maps to NM_004598.3 T99T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADV-01A-11D-A38X-10 chr4:167658663 A>G maps to NM_016950.2 Y365Y. 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-4R-AA8I-01A-11D-A382-10 chr11:14264942 G>A did not map to a codon.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr17:47677853 C>T maps to NM_003563.3 G337G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr4:88903790 C>T maps to NM_001040058.1 L230L. 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-A9FW-01A-11D-A36X-10 chr1:153122522 T>A maps to NM_001014291.3 K22*. 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-4R-AA8I-01A-11D-A382-10 chr23:155004147 C>T did not map to a codon.
Sequencing variant TCGA-DD-AADM-01A-11D-A40R-10 chr23:155004066 T>C did not map to a codon.
Sequencing variant TCGA-DD-AAVZ-01A-11D-A40R-10 chr23:155004170 G>A did not map to a codon.
Sequencing variant TCGA-ZS-A9CD-01A-11D-A36X-10 chr23:155004357 T>G did not map to a codon.
Sequencing variant TCGA-DD-AACT-01A-11D-A40R-10 chr12:53460127 T>A maps to NM_032840.2 I388I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr12:53467189 C>T maps to NM_032840.2 L191L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr11:55653257 T>C maps to NM_032681.3 S118S. Only missense variants will be evaluated by CHASM.
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-CC-A7IE-01A-21D-A382-10 chr1:158650441 G>A maps to NM_003126.2 F203F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACI-01A-11D-A40R-10 chr1:158592933 C>A maps to NM_003126.2 E1987*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACP-01A-11D-A40R-10 chr1:158622439 G>A maps to NM_003126.2 Y1064Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAE6-01A-11D-A40R-10 chr1:158621154 A>T did not map to a codon.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr1:158641150 G>T maps to NM_003126.2 A527A. 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-EP-A2KA-01A-11D-A183-10 chr9:131337064 G>T maps to NM_001130438.2 E159*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr9:131344804 A>G maps to NM_001130438.2 A540A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-AA0U-01A-11D-A382-10 chr9:131353845 G>T maps to NM_001130438.2 E1033*. 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-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-ES-A2HT-01A-12D-A183-10 chr2:54871647 C>A maps to NM_003128.2 G1398G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AA3A-01A-11D-A36X-10 chr11:66472297 G>A maps to NM_006946.2 L817L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACT-01A-11D-A40R-10 chr11:66466554 T>A did not map to a codon.
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-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-AACT-01A-11D-A40R-10 chr19:41025769 A>T maps to NM_020971.2 L1122L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LG-A9QC-01A-11D-A36X-10 chr19:41078286 G>T did not map to a codon.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr15:42182403 C>A did not map to a codon.
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-BC-A3KG-01A-11D-A20W-10 chr20:36028551 A>G maps to ENST00000373558 K304K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr16:30727434 C>T maps to NM_006662.2 Q848*. 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-DD-AAD3-01A-11D-A40R-10 chr16:30720955 C>T maps to NM_006662.2 N252N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADL-01A-11D-A40R-10 chr16:30735748 T>C maps to NM_006662.2 V1668V. 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-A12Z-10 chr17:17719327 G>A maps to NM_001005291.2 S773S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZP-A9D1-01A-11D-A382-10 chr22:42280873 C>T maps to NM_004599.2 S689S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZS-A9CE-01A-11D-A36X-10 chr22:42266957 C>T maps to NM_004599.2 G262G. 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-DD-A39Y-01A-11D-A20W-10 chr12:64472775 C>T maps to NM_020762.2 C401C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAE9-01A-11D-A40R-10 chr3:9094836 G>C maps to NM_014850.2 S399S. 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-DD-A1EE-01A-11D-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-G3-AAV7-01A-11D-A382-10 chr7:104767482 A>G maps to ENST00000336613 Y624Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9H5-01A-11D-A382-10 chr23:153049750 C>G did not map to a codon.
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-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-A1ED-01A-11D-A152-10 chr1:24995724 T>C maps to NM_005839.3 P617P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2V-A95S-01A-11D-A36X-10 chr16:2819138 C>T maps to NM_016333.3 S2625S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr16:2818133 G>C maps to NM_016333.3 S2535S. 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-DD-A3A1-01A-11D-A20W-10 chr16:2813552 T>C maps to NM_016333.3 S1008S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACS-01A-11D-A40R-10 chr16:2819138 C>T maps to NM_016333.3 S2625S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAW0-01A-11D-A40R-10 chr16:2815587 C>T maps to NM_016333.3 R1687*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr16:2818025 T>C maps to NM_016333.3 P2499P. 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-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-BC-A10Z-01A-11D-A12Z-10 chr20:60747837 C>T maps to NM_198935.1 P339P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACL-01A-11D-A40R-10 chr12:109186286 C>T maps to NM_018984.3 Q556Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9GV-01A-11D-A382-10 chr7:149494389 C>A maps to NM_198455.2 L2288L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5R-AA1C-01A-11D-A40R-10 chr7:149518153 C>A maps to NM_198455.2 S4170*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A3KF-01A-11D-A20W-10 chr7:149489268 A>G maps to NM_198455.2 P1839P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A8HV-01A-11D-A35Z-10 chr7:149493598 G>A maps to NM_198455.2 E2226E. 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-AACK-01A-11D-A40R-10 chr7:149493828 T>A maps to NM_198455.2 T2276T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NI-A8LF-01A-11D-A35Z-10 chr7:149480010 C>G maps to NM_198455.2 S659S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NI-A8LF-01A-11D-A35Z-10 chr7:149480082 C>T maps to NM_198455.2 I683I. 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-DD-AACT-01A-11D-A40R-10 chr1:155989928 A>C maps to ENST00000368312 A29A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XR-A8TG-01A-11D-A35Z-10 chr1:155984781 A>C maps to ENST00000368312 T130T. 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-DD-A3A0-01A-11D-A20W-10 chr22:37602586 T>C maps to NM_001051.2 *419W. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACL-01A-11D-A40R-10 chr23:48123233 A>T did not map to a codon.
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-DD-AAD0-01A-11D-A40R-10 chr23:52682010 G>T did not map to a codon.
Sequencing variant TCGA-G3-AAV0-01A-11D-A36X-10 chr22:41252469 G>C maps to NM_003932.3 T25T. Only missense variants will be evaluated by CHASM.
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-DD-AADS-01A-11D-A40R-10 chr8:53055539 T>A maps to NM_014682.2 P706P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GJ-A9DB-01A-11D-A36X-10 chr8:53074115 C>T maps to NM_014682.2 V471V. 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-A3A1-01A-11D-A20W-10 chr11:126279254 A>G maps to ENST00000356132 A246A. 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-DD-AADI-01A-11D-A40R-10 chr2:107450507 C>T maps to NM_001142351.1 S346S. 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-ES-A2HT-01A-12D-A183-10 chr2:107459505 A>G maps to NM_001142351.1 L310L. 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-AAE7-01A-11D-A40R-10 chr1:77334300 A>G maps to NM_030965.1 Q45Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MI-A75G-01A-11D-A32G-10 chr1:77334300 A>G maps to NM_030965.1 Q45Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZP-A9D2-01A-11D-A382-10 chr1:77334300 A>G maps to NM_030965.1 Q45Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5C-AAPD-01A-21D-A38X-10 chr9:130649800 G>A maps to NM_013443.3 H258H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A0-01A-11D-A20W-10 chr7:116771957 A>G maps to ENST00000323984 R195R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACI-01A-11D-A40R-10 chr7:116862959 A>T maps to NM_021908.2 K562*. 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-4R-AA8I-01A-11D-A382-10 chr18:55024434 A>G maps to NM_015879.2 Q198Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr18:55027273 T>C maps to NM_015879.2 I303I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACJ-01A-11D-A40R-10 chr5:100231433 G>A maps to NM_005668.4 R57*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A8O5-01A-11D-A35Z-10 chr5:100222043 C>A maps to NM_175052.1 *169L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9GS-01A-12D-A382-10 chr10:17363215 C>G maps to NM_001004470.1 T286T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A9FS-01A-11D-A36X-10 chr10:17401545 C>T maps to NM_001004470.1 W115*. 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-AAC8-01A-11D-A40R-10 chr12:104071228 A>T did not map to a codon.
Sequencing variant TCGA-DD-AACX-01A-11D-A40R-10 chr12:104100583 T>C maps to NM_017564.9 C1337C. 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-DD-AACJ-01A-11D-A40R-10 chr12:57642929 C>T maps to NM_145064.1 E76E. 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-2Y-A9HB-01A-11D-A38X-10 chr23:123196844 G>C did not map to a codon.
Sequencing variant TCGA-DD-A1ED-01A-11D-A152-10 chr23:123200271 A>G did not map to a codon.
Sequencing variant TCGA-DD-A1EG-01A-11D-A20W-10 chr23:123217393 A>G did not map to a codon.
Sequencing variant TCGA-DD-AAE0-01A-11D-A40R-10 chr23:123205073 C>T did not map to a codon.
Sequencing variant TCGA-DD-AAVP-01A-11D-A40R-10 chr23:123182870 A>G did not map to a codon.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr23:123190044 C>A did not map to a codon.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr23:123190066 G>T did not map to a codon.
Sequencing variant TCGA-G3-A3CJ-01A-11D-A20W-10 chr23:123195125 A>G did not map to a codon.
Sequencing variant TCGA-G3-A5SM-01A-12D-A28X-10 chr23:123195633 G>A did not map to a codon.
Sequencing variant TCGA-WQ-A9G7-01A-11D-A36X-10 chr23:123191802 G>A did not map to a codon.
Sequencing variant TCGA-ZP-A9D0-01A-11D-A36X-10 chr23:123197039 T>C did not map to a codon.
Multiple mappings detected for codon TCGA-DD-A3A1-01A-11D-A20W-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-DD-AACQ-01A-11D-A40R-10 chr7:99798552 G>C maps to NM_012447.2 L674L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAW1-01A-11D-A40P-10 chr19:4325515 T>A maps to ENST00000314714 K286*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73F-01A-11D-A32G-10 chr8:38002820 A>G maps to NM_000349.2 G221G. 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-EP-A2KA-01A-11D-A183-10 chr13:33681004 T>C maps to NM_178007.2 E1030E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr13:33700280 T>C maps to NM_178007.2 G665G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MR-A8JO-01A-12D-A35Z-10 chr13:33704162 T>C maps to NM_178007.2 T209T. 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-G3-A3CG-01A-11D-A20W-10 chr18:51880862 A>C maps to NM_139171.1 V27V. 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-DD-A39X-01A-11D-A20W-10 chr23:67936250 A>G did not map to a codon.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr23:67938075 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-DD-A1EG-01A-11D-A20W-10 chr17:40456368 T>C maps to NM_003152.3 S393S. 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-A119-01A-11D-A12Z-10 chr20:47734535 T>C maps to NM_017453.2 G429G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADS-01A-11D-A40R-10 chr8:74464276 C>A maps to NM_001164380.1 L500L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAD3-01A-11D-A40R-10 chr4:77231062 G>T maps to NM_003943.3 G329G. 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-DD-AAC8-01A-11D-A40R-10 chr5:172744921 A>T maps to NM_003714.2 L279L. 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-DD-AAEB-01A-11D-A40R-10 chr1:47717254 C>T maps to NM_001048166.1 E1140E. 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 chr11:4112724 G>T maps to NM_003156.3 A585A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CJ-01A-11D-A20W-10 chr4:26997052 A>G maps to ENST00000382009 E237E. 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-2V-A95S-01A-11D-A36X-10 chr5:171471886 T>C maps to NM_005990.3 *969*. 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-ES-A2HS-01A-11D-A183-10 chr5:171520873 G>A maps to NM_005990.3 L366L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr19:1218438 T>G maps to NM_000455.4 L105*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11B-01A-11D-A12Z-10 chr19:1221319 G>A maps to NM_000455.4 P281P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACP-01A-11D-A40R-10 chr2:220480869 C>T maps to NM_052902.2 I1085I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-AAV3-01A-11D-A36X-10 chr2:220466723 C>T maps to NM_052902.2 P130P. 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-WX-AA44-01A-11D-A38X-10 chr2:197010769 A>C maps to NM_004226.3 G115G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACT-01A-11D-A40R-10 chr6:31940407 C>T maps to NM_032454.1 R147R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CJ-01A-11D-A20W-10 chr13:99109510 T>C maps to NM_003576.3 E402E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A0-01A-11D-A20W-10 chr8:99608283 T>C maps to ENST00000354930 R294R. 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-EP-A2KA-01A-11D-A183-10 chr4:5399970 G>T maps to NM_018401.1 G158*. 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-DD-AACK-01A-11D-A40R-10 chr2:219564007 A>T maps to NM_015690.3 P1247P. 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-DD-AACH-01A-11D-A40R-10 chr2:168986091 G>A maps to NM_013233.2 L350L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr1:36814367 C>A maps to ENST00000373130 V229V. 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-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-DD-AAD2-01A-11D-A40R-10 chr2:48809323 A>T maps to NM_172311.2 K518*. 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-DD-AADC-01A-11D-A40R-10 chr14:81743599 G>A maps to NM_033104.2 T685T. 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-CC-A3MB-01A-11D-A20W-10 chr10:70641819 A>G maps to NM_001130161.2 V139V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr10:70645468 T>C maps to NM_001130161.2 H639H. 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-DD-A4NI-01A-11D-A27I-10 chr2:202344879 C>T maps to NM_018571.5 D413D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A73D-01A-12D-A32G-10 chr2:202344885 C>T maps to NM_018571.5 Y415Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr2:37094973 A>T maps to NM_003162.2 Y510*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAEK-01A-11D-A40R-10 chr2:37129894 C>A did not map to a codon.
Sequencing variant TCGA-CC-A3MB-01A-11D-A20W-10 chr23:7177587 C>T did not map to a codon.
Sequencing variant TCGA-DD-A3A1-01A-11D-A20W-10 chr23:7268084 G>A did not map to a codon.
Sequencing variant TCGA-DD-AAW0-01A-11D-A40R-10 chr23:7252037 G>A did not map to a codon.
Sequencing variant TCGA-FV-A2QR-01A-11D-A20W-10 chr23:7177424 A>G did not map to a codon.
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-XR-A8TF-01A-11D-A35Z-10 chr11:125472791 C>T maps to NM_152713.3 L122L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr1:28128322 T>C maps to ENST00000373939 L141L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr1:28136790 C>A maps to ENST00000373939 S154*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr20:57242607 T>C maps to NM_001001433.1 G69G. 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-DD-AAW2-01A-11D-A40P-10 chr4:4426916 T>C maps to NM_016930.2 E245E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EG-01A-11D-A20W-10 chr16:31012909 A>G maps to NM_052874.3 D15D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WQ-A9G7-01A-11D-A36X-10 chr12:131283120 G>A maps to NM_194356.1 H245H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACI-01A-11D-A40R-10 chr11:62594818 T>C maps to NM_003164.3 T116T. 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-3K-AAZ8-01A-12D-A38X-10 chr17:9460749 C>T did not map to a codon.
Sequencing variant TCGA-DD-AAVQ-01A-11D-A40R-10 chr9:130423379 G>T did not map to a codon.
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-BC-A3KG-01A-11D-A20W-10 chr1:109342912 T>C maps to NM_007269.2 G507G. 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-DD-AAD5-01A-11D-A40R-10 chr1:109351497 A>G maps to NM_007269.2 *593W. 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-EP-A2KA-01A-11D-A183-10 chr17:53150292 C>A maps to NM_178509.5 A348A. 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-NI-A8LF-01A-11D-A35Z-10 chr6:147704134 G>A did not map to a codon.
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-DD-AACV-01A-11D-A40R-10 chr3:120998774 T>A maps to NM_014980.2 S694S. 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-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-A1EG-01A-11D-A20W-10 chr3:67660014 A>G maps to NM_003848.3 V30V. 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-DD-AA3A-01A-11D-A36X-10 chr8:70551052 A>G maps to NM_001128206.1 G837G. Only missense variants will be evaluated by CHASM.
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-ES-A2HT-01A-12D-A183-10 chr2:108910709 G>T maps to ENST00000437390 V59V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WQ-A9G7-01A-11D-A36X-10 chr2:108881279 G>T did not map to a codon.
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-DD-AADL-01A-11D-A40R-10 chr19:48389502 A>G maps to NM_003167.3 D4D. 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-G3-A3CJ-01A-11D-A20W-10 chr3:4403893 T>C maps to NM_182760.3 T353T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-AAV7-01A-11D-A382-10 chr17:73177178 T>C maps to NM_006937.3 K42K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BD-A3EP-01A-11D-A22F-10 chr7:882840 A>G did not map to a codon.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr7:881714 T>C maps to ENST00000456758 P191P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-AAV7-01A-11D-A382-10 chr7:878542 A>C maps to ENST00000456758 A120A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr22:39136283 G>T maps to ENST00000405018 A469A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9GY-01A-11D-A382-10 chr17:27014459 G>T maps to NM_003170.3 G993*. Only missense variants will be evaluated by CHASM.
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-AADQ-01A-11D-A40R-10 chr17:27028454 A>G did not map to a codon.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr17:27027430 G>T maps to NM_003170.3 A1569A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NI-A8LF-01A-11D-A35Z-10 chr17:27024666 T>G maps to NM_003170.3 A1413A. 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-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-DD-AAD1-01A-11D-A40R-10 chr9:114840896 C>T maps to NM_022486.3 P558P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9H3-01A-11D-A382-10 chr22:24583418 G>C did not map to a codon.
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-DD-A1ED-01A-11D-A152-10 chr23:48558561 T>C did not map to a codon.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr23:48558574 A>T did not map to a codon.
Sequencing variant TCGA-XR-A8TC-01A-11D-A35Z-10 chr23:48558696 G>C did not map to a codon.
Sequencing variant TCGA-CC-A8HS-01A-11D-A35Z-10 chr11:67957486 G>T maps to NM_017635.3 G19G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AA3A-01A-11D-A36X-10 chr11:67926441 A>G maps to NM_017635.3 H457H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAVS-01A-11D-A40R-10 chr1:149885086 G>A maps to NM_014849.3 P102P. 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-ES-A2HT-01A-12D-A183-10 chr15:91809825 A>G maps to NM_014848.4 K341K. 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-BC-A3KG-01A-11D-A20W-10 chr9:113171159 A>G maps to ENST00000374463 S2243S. 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-CC-A9FU-01A-11D-A36X-10 chr9:113170454 A>G maps to ENST00000374463 N2478N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EG-01A-11D-A20W-10 chr9:113191514 A>G maps to ENST00000374463 C1908C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAVV-01A-11D-A40R-10 chr10:29822161 C>T maps to NM_021738.2 K378K. 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-BC-A3KG-01A-11D-A20W-10 chr1:115537377 T>C maps to NM_003176.2 A921A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAE8-01A-11D-A40R-10 chr1:115400063 G>A did not map to a codon.
Sequencing variant TCGA-CC-A3MB-01A-11D-A20W-10 chr20:58442783 T>C maps to NM_014258.2 E1369E. Only missense variants will be evaluated by CHASM.
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-AACB-01A-11D-A40R-10 chr20:58489237 G>A maps to NM_014258.2 L235L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACT-01A-11D-A40R-10 chr20:58441391 C>A maps to NM_014258.2 E1426*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADQ-01A-11D-A40R-10 chr20:58496501 C>A maps to NM_014258.2 E11*. Only missense variants will be evaluated by CHASM.
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-DD-AAW0-01A-11D-A40R-10 chr6:10911071 G>T maps to NM_001040274.2 P296P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A8O5-01A-11D-A35Z-10 chr6:10924795 C>A maps to NM_001040274.2 V380V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A8HU-01A-11D-A35Z-10 chr19:15224668 C>T maps to NM_033025.4 D701D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACQ-01A-11D-A40R-10 chr19:15221085 T>A maps to NM_033025.4 L334L. 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-WQ-A9G7-01A-11D-A36X-10 chr19:46318889 T>A maps to NM_004819.2 G1251G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr23:47464462 C>T did not map to a codon.
Sequencing variant TCGA-DD-AADV-01A-11D-A38X-10 chr23:47479088 A>G did not map to a codon.
Sequencing variant TCGA-DD-AAEG-01A-11D-A38X-10 chr23:47434653 G>A did not map to a codon.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr23:47434131 G>A did not map to a codon.
Sequencing variant TCGA-G3-A3CJ-01A-11D-A20W-10 chr23:47466555 T>C did not map to a codon.
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-WQ-A9G7-01A-11D-A36X-10 chr6:86350163 C>T maps to NM_006372.4 Q89Q. 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-BD-A3ER-01A-11D-A20W-10 chr6:152668271 C>G maps to NM_182961.2 A4000A. 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-DD-A1EG-01A-11D-A20W-10 chr6:152472762 T>C maps to NM_182961.2 T8125T. 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-ED-A5KG-01A-11D-A27I-10 chr6:152536121 A>T maps to NM_182961.2 L7422*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr6:152457872 G>A maps to NM_182961.2 D8513D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A2QR-01A-11D-A20W-10 chr6:152647435 C>T maps to NM_182961.2 L5096L. 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-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-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-A119-01A-11D-A12Z-10 chr14:64630169 C>A maps to NM_182914.2 S5450S. 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-DD-AAC8-01A-11D-A40R-10 chr14:64408640 C>T maps to NM_182914.2 I92I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAC8-01A-11D-A40R-10 chr14:64408679 A>T maps to NM_182914.2 S105S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAD0-01A-11D-A40R-10 chr14:64653173 G>A maps to NM_182914.2 Q5863Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADY-01A-11D-A40R-10 chr14:64686098 G>T maps to NM_182914.2 E6611*. 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-ES-A2HS-01A-11D-A183-10 chr14:64630260 T>C maps to NM_182914.2 L5481L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-AAV7-01A-11D-A382-10 chr6:33405539 G>T maps to NM_006772.2 L286L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZP-A9D1-01A-11D-A382-10 chr6:33414443 C>A maps to NM_006772.2 S1225S. 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-BD-A3EP-01A-11D-A22F-10 chr21:34003926 A>T maps to NM_003895.3 L1406*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39Y-01A-11D-A20W-10 chr21:34053823 A>G maps to NM_003895.3 A484A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NB-01A-12D-A25V-10 chr21:34017977 T>C maps to NM_003895.3 P1162P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr21:34056409 G>A maps to NM_003895.3 R419*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9GX-01A-11D-A382-10 chr5:150029675 G>A maps to NM_001166209.1 L857L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A9FS-01A-11D-A36X-10 chr4:119952155 T>A maps to NM_133477.2 A742A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-AAUZ-01A-11D-A382-10 chr4:119947952 T>A maps to NM_133477.2 A143A. 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-DD-A1EG-01A-11D-A20W-10 chr10:75407600 A>G maps to NM_001114133.1 A603A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADC-01A-11D-A40R-10 chr10:75407831 G>T maps to NM_001114133.1 P526P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-AAV4-01A-11D-A382-10 chr17:35913871 A>T maps to NM_007247.4 S651S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WJ-A86L-01A-12D-A45V-10 chr17:35945537 C>T maps to NM_007247.4 Q124Q. 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-ES-A2HT-01A-12D-A183-10 chr10:46968620 C>T maps to NM_031912.3 P105P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9GY-01A-11D-A382-10 chr14:62551003 C>T maps to NM_031914.2 L509L. 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-AAVV-01A-11D-A40R-10 chr1:202568363 G>A maps to NM_177402.4 I345I. 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-BC-A3KG-01A-11D-A20W-10 chr19:55687411 T>C maps to NM_003180.2 R111R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACQ-01A-11D-A40R-10 chr1:114646328 C>T maps to ENST00000369545 L362L. 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-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-DD-A1EG-01A-11D-A20W-10 chr23:37981400 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-AACQ-01A-11D-A40R-10 chr6:132966653 T>A maps to NM_138327.1 L163L. 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-A39Z-01A-11D-A20W-10 chr22:39824029 A>G maps to NM_006116.2 A383A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IE-01A-21D-A382-10 chr6:149700568 C>A maps to NM_015093.4 L506L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADO-01A-11D-A40R-10 chr23:30871042 T>C did not map to a codon.
Sequencing variant TCGA-G3-A3CG-01A-11D-A20W-10 chr23:30864762 T>C did not map to a codon.
Sequencing variant TCGA-ZP-A9D0-01A-11D-A36X-10 chr23:30873585 T>A did not map to a codon.
Sequencing variant TCGA-DD-AACC-01A-11D-A40R-10 chr7:97363075 C>A maps to NM_003182.2 I55I. Only missense variants will be evaluated by CHASM.
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-A119-01A-11D-A12Z-10 chr10:123842980 A>G maps to NM_206862.2 E322E. 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 chr10:123845758 A>G maps to NM_206862.2 A1248A. 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-ZS-A9CG-01A-11D-A36X-10 chr10:123903125 G>C maps to NM_206862.2 S1913S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZS-A9CG-01A-11D-A36X-10 chr10:123969921 T>C maps to NM_206862.2 S1994S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9H2-01A-12D-A382-10 chr4:1746477 G>A maps to NM_006342.1 Q790Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr4:1725264 A>G maps to NM_006342.1 S39S. 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-AAC8-01A-11D-A40R-10 chr4:104511134 T>A maps to NM_001059.2 K368*. 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-DD-AAE7-01A-11D-A40R-10 chr17:35804826 G>A maps to NM_001166105.1 L187L. Only missense variants will be evaluated by CHASM.
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-DD-AAD0-01A-11D-A40R-10 chr4:7056325 G>T maps to NM_152293.2 E270*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CJ-01A-11D-A20W-10 chr3:9827070 A>G maps to NM_006354.2 P283P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9GT-01A-11D-A382-10 chr23:70643061 C>T did not map to a codon.
Sequencing variant TCGA-2Y-A9H3-01A-11D-A382-10 chr23:70617186 G>A did not map to a codon.
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-CC-A8HU-01A-11D-A35Z-10 chr23:70598215 T>A 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-DD-A1EE-01A-11D-A12Z-10 chr23:70680628 A>G did not map to a codon.
Sequencing variant TCGA-G3-AAV4-01A-11D-A382-10 chr23:70595089 C>T did not map to a codon.
Sequencing variant TCGA-G3-AAV5-01A-11D-A36X-10 chr6:34846456 T>C maps to NM_005643.2 L182L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CG-01A-11D-A20W-10 chr17:34171799 A>G maps to NM_139215.1 G499G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EG-01A-11D-A20W-10 chr2:10045014 A>T maps to NM_005680.2 K279*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A0-01A-11D-A20W-10 chr2:10045014 A>T maps to NM_005680.2 K279*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A1-01A-11D-A20W-10 chr2:10045014 A>T maps to NM_005680.2 K279*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CJ-01A-11D-A20W-10 chr2:10045014 A>T maps to NM_005680.2 K279*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr16:84212982 C>T maps to NM_005679.2 W725*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr16:84214783 C>T maps to NM_005679.2 P417P. 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-AACX-01A-11D-A40R-10 chr10:8051232 C>T maps to NM_031923.2 S836S. 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-A119-01A-11D-A12Z-10 chr18:23915176 A>G maps to ENST00000418698 L771L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr18:23847517 A>G maps to ENST00000418698 T176T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-AAV0-01A-11D-A36X-10 chr18:23937718 T>A maps to ENST00000418698 I799I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A2QR-01A-11D-A20W-10 chr10:105139429 A>G maps to NM_006951.3 G393G. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-BC-A3KG-01A-11D-A20W-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-G3-AAUZ-01A-11D-A382-10 chr7:99704952 A>G maps to ENST00000472509 A707A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EA-01A-11D-A12Z-10 chr23:100547905 T>A did not map to a codon.
Sequencing variant TCGA-DD-A3A0-01A-11D-A20W-10 chr23:100524208 T>C 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-ZP-A9D1-01A-11D-A382-10 chr5:68651606 T>C maps to NM_016283.4 L65L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9H8-01A-11D-A38X-10 chr23:77393576 A>C did not map to a codon.
Sequencing variant TCGA-BC-A5W4-01A-11D-A28X-10 chr23:77392437 C>A did not map to a codon.
Sequencing variant TCGA-DD-AAVS-01A-11D-A40R-10 chr23:77393270 T>C 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-BC-A3KG-01A-11D-A20W-10 chr2:159954260 A>G maps to NM_033394.2 K58K. 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-DD-AAEH-01A-11D-A40R-10 chr2:160050973 G>A maps to NM_033394.2 L983L. 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-2Y-A9H7-01A-11D-A38X-10 chr17:27778637 A>C maps to NM_020791.2 P24P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACQ-01A-11D-A40R-10 chr16:29990373 C>T maps to NM_016151.2 S144S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr16:30002498 G>T maps to NM_004783.2 L920L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9HA-01A-11D-A38X-10 chr12:118599688 C>A maps to NM_016281.3 T681T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A5W4-01A-11D-A28X-10 chr12:118588807 G>T maps to NM_016281.3 Y897*. 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-2V-A95S-01A-11D-A36X-10 chr6:33281113 G>T maps to NM_172208.2 R117R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr12:6562347 C>A maps to NM_018009.4 A60A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADB-01A-11D-A40R-10 chr1:234565277 G>A maps to NM_005646.3 L919L. 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-AAVU-01A-11D-A40R-10 chr12:53899545 C>G maps to NM_134323.1 G285G. 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-AACV-01A-11D-A40R-10 chr1:150471452 G>A maps to NM_025150.3 L494L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A8HV-01A-11D-A35Z-10 chr1:6631178 C>T maps to NM_138697.3 L134L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACW-01A-11D-A40R-10 chr1:6631121 G>A maps to NM_138697.3 T115T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr1:6630971 T>C maps to NM_138697.3 S65S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A2QR-01A-11D-A20W-10 chr1:6638905 G>A maps to NM_138697.3 V596V. 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-G3-A3CJ-01A-11D-A20W-10 chr1:1267319 T>G did not map to a codon.
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-G3-A3CJ-01A-11D-A20W-10 chr12:10978229 T>C maps to NM_023921.1 G213G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9GU-01A-11D-A382-10 chr7:141673138 G>C maps to NM_176817.4 Y117*. 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-CC-A9FS-01A-11D-A36X-10 chr7:141673087 G>A maps to NM_176817.4 S134S. 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-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-DD-AACB-01A-11D-A40R-10 chr12:11339507 C>T maps to NM_181429.1 L12L. 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-DD-A1E9-01A-21D-A152-10 chr12:11214719 T>C maps to NM_176887.2 L58L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1E9-01A-21D-A152-10 chr12:11214755 T>C maps to NM_176887.2 Q46Q. 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-WJ-A86L-01A-12D-A45V-10 chr4:38138874 G>A maps to NM_015173.2 T1142T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XR-A8TC-01A-11D-A35Z-10 chr22:30722678 C>A maps to ENST00000403477 S64S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CJ-01A-11D-A20W-10 chr16:30369600 A>G maps to NM_015527.3 T697T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACY-01A-11D-A40R-10 chr10:96269914 A>T maps to NM_015188.1 P556P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A2QR-01A-11D-A20W-10 chr10:96260079 T>C maps to NM_015188.1 T505T. 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-CC-A8HT-01A-11D-A35Z-10 chr17:77921557 C>T maps to NM_019020.2 A538A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAD0-01A-11D-A40R-10 chr17:77921566 G>A maps to NM_019020.2 D535D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr19:50391713 C>T maps to NM_024682.2 L594L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr4:26755499 G>T maps to NM_018317.2 L498L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAE6-01A-11D-A40R-10 chr4:26719628 A>G maps to NM_018317.2 S343S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9GW-01A-11D-A382-10 chr6:37281659 G>T maps to NM_017772.2 R386R. 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-AACX-01A-11D-A40R-10 chr23:48418425 T>C did not map to a codon.
Sequencing variant TCGA-CC-A9FW-01A-11D-A36X-10 chr17:15638738 T>A 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-EP-A2KA-01A-11D-A183-10 chr6:13316856 G>T maps to NM_016495.4 T155T. 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-AADO-01A-11D-A40R-10 chr2:101650197 T>C maps to NM_001102426.1 S527S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39Y-01A-11D-A20W-10 chr23:106116904 A>G did not map to a codon.
Sequencing variant TCGA-DD-AAD6-01A-11D-A40R-10 chr4:141555156 T>C maps to NM_015130.2 L897L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAE7-01A-11D-A40R-10 chr4:141543435 G>A maps to NM_015130.2 A1238A. 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-DD-A119-01A-11D-A12Z-10 chr17:80828169 C>A maps to NM_005993.4 V463V. 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-DD-A1EE-01A-11D-A12Z-10 chr12:64882344 A>G maps to NM_013254.3 R473R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADF-01A-11D-A40R-10 chr23:9677306 A>G did not map to a codon.
Sequencing variant TCGA-RC-A7SF-01A-11D-A34Z-10 chr23:9677337 C>G did not map to a codon.
Sequencing variant TCGA-RC-A7SH-01A-11D-A382-10 chr23:9677725 A>G did not map to a codon.
Sequencing variant TCGA-G3-AAV0-01A-11D-A36X-10 chr3:176750883 G>A maps to NM_024665.4 R431*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IL-01A-11D-A33Q-10 chr24:6939609 A>C did not map to a codon.
Sequencing variant TCGA-DD-A39Y-01A-11D-A20W-10 chr24:6938815 T>C did not map to a codon.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr16:2027158 T>C maps to NM_006453.2 G515G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WX-AA46-01A-11D-A38X-10 chr16:2025897 A>G maps to NM_006453.2 L359L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9GV-01A-11D-A382-10 chr6:170871003 G>A maps to NM_003194.4 Q60Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9H7-01A-11D-A38X-10 chr6:170871003 G>A maps to NM_003194.4 Q60Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39Z-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-DD-AACZ-01A-11D-A40R-10 chr6:170871003 G>A maps to NM_003194.4 Q60Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAE4-01A-11D-A40R-10 chr6:170871003 G>A maps to NM_003194.4 Q60Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAVW-01A-11D-A40R-10 chr6:170871003 G>A maps to NM_003194.4 Q60Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr6:170871003 G>A maps to NM_003194.4 Q60Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZS-A9CD-01A-11D-A36X-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-ES-A2HS-01A-11D-A183-10 chr6:134304018 G>A did not map to a codon.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr2:162275530 C>T maps to NM_006593.2 F366F. 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-DD-AADE-01A-11D-A40R-10 chr22:19748650 C>A maps to NM_080647.1 P86P. 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-AADD-01A-11D-A40R-10 chr7:35293156 C>G maps to NM_001077653.2 S25S. 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-A119-01A-11D-A12Z-10 chr17:45822239 C>T maps to NM_013351.1 D372D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9GZ-01A-11D-A38X-10 chr23:79282318 C>T did not map to a codon.
Sequencing variant TCGA-DD-A3A1-01A-11D-A20W-10 chr23:79282218 T>C did not map to a codon.
Sequencing variant TCGA-DD-AAEE-01A-11D-A40R-10 chr23:79277883 A>G 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-DD-A3A0-01A-11D-A20W-10 chr12:115112497 A>G maps to NM_016569.3 A414A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADO-01A-11D-A40R-10 chr17:59560477 T>C maps to ENST00000393853 P414P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZP-A9CY-01A-11D-A382-10 chr17:59557243 C>A maps to ENST00000393853 I235I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2V-A95S-01A-11D-A36X-10 chr12:114793369 A>C maps to NM_000192.3 V508V. 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-DD-AADG-01A-11D-A40R-10 chr16:30097547 A>C maps to NM_004608.3 *437G. 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-AADU-01A-11D-A40R-10 chr7:139719868 T>C maps to NM_001166253.1 N571N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr14:92258865 T>A maps to NM_001128596.1 K298*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACQ-01A-11D-A40R-10 chr20:62701906 C>T maps to NM_003195.4 H246H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr1:23710836 A>G did not map to a codon.
Sequencing variant TCGA-DD-A118-01A-11D-A12Z-10 chr23:102842039 A>T did not map to a codon.
Sequencing variant TCGA-DD-A1EG-01A-11D-A20W-10 chr23:101395772 G>T did not map to a codon.
Sequencing variant TCGA-DD-A1EG-01A-11D-A20W-10 chr23:101395777 C>T did not map to a codon.
Sequencing variant TCGA-DD-A39Y-01A-11D-A20W-10 chr23:101395772 G>T did not map to a codon.
Sequencing variant TCGA-DD-A39Y-01A-11D-A20W-10 chr23:101395777 C>T did not map to a codon.
Sequencing variant TCGA-DD-A39Y-01A-11D-A20W-10 chr23:101395785 A>G did not map to a codon.
Sequencing variant TCGA-DD-A3A0-01A-11D-A20W-10 chr23:101395773 T>C did not map to a codon.
Sequencing variant TCGA-DD-A3A0-01A-11D-A20W-10 chr23:101395777 C>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-DD-AAEI-01A-11D-A40R-10 chr23:13681524 T>C did not map to a codon.
Sequencing variant TCGA-CC-A8HU-01A-11D-A35Z-10 chr1:24080865 G>A maps to NM_003198.2 V595V. Only missense variants will be evaluated by CHASM.
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-G3-A3CJ-01A-11D-A20W-10 chr15:57484417 A>G maps to NM_207036.1 K151K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CK-01A-11D-A20W-10 chr20:590854 G>A maps to NM_004609.3 V9V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A3KF-01A-11D-A20W-10 chr22:42610351 T>C maps to NM_005650.1 Q320Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr22:42607069 C>A maps to NM_005650.1 S1414S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-AAV4-01A-11D-A382-10 chr22:42608025 C>A maps to NM_005650.1 E1096*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAVV-01A-11D-A40R-10 chr6:134210651 G>A maps to NM_003206.3 E39E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A0-01A-11D-A20W-10 chr16:89972661 G>A maps to NM_014972.2 E563E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A7SH-01A-11D-A382-10 chr16:89967153 C>T maps to NM_014972.2 Q445*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr18:52895533 G>A maps to ENST00000398339 S748S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADG-01A-11D-A40R-10 chr5:133481890 G>A did not map to a codon.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr2:85533588 T>C maps to NM_031283.2 S388S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr10:114901028 G>A maps to NM_030756.4 P190P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WX-AA46-01A-11D-A38X-10 chr20:61491545 T>C maps to NM_006602.2 Q254Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A5UE-01A-11D-A28X-10 chr1:152080268 T>C maps to NM_007113.2 E1808E. 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-DD-AACF-01A-11D-A40R-10 chr1:152086517 T>C maps to NM_007113.2 E13E. 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-WQ-AB4B-01A-11D-A40P-10 chr11:67815393 C>T maps to NM_006019.3 N503N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9GY-01A-11D-A382-10 chr11:59623354 G>T maps to NM_001062.3 C308*. 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-AACX-01A-11D-A40R-10 chr5:149753924 G>A maps to ENST00000451292 T353T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr6:167789460 T>C maps to NM_004610.3 R227R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr21:33951120 T>A maps to NM_144659.5 G127G. 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-G3-AAV3-01A-11D-A36X-10 chr12:111066707 T>C maps to NM_001082538.2 T203T. 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-EP-A2KB-01A-11D-A183-10 chr12:124189190 G>T maps to NM_024809.3 A575A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr10:97453398 A>G did not map to a codon.
Sequencing variant TCGA-WQ-A9G7-01A-11D-A36X-10 chr10:97453177 G>A maps to ENST00000371217 C122C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CG-01A-11D-A20W-10 chr12:104379507 T>C did not map to a codon.
Sequencing variant TCGA-XR-A8TG-01A-11D-A35Z-10 chr12:104379457 G>T maps to NM_003211.4 E348*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZS-A9CD-01A-11D-A36X-10 chr12:104378699 T>A did not map to a codon.
Sequencing variant TCGA-2Y-A9HB-01A-11D-A38X-10 chr14:90446919 G>T maps to NM_018319.3 R276R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr6:24653321 C>T maps to NM_016614.2 G232G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9GV-01A-11D-A382-10 chr10:115981224 A>G maps to NM_198795.1 K960K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADD-01A-11D-A40R-10 chr10:115966039 T>A maps to NM_198795.1 Y445*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACN-01A-11D-A40R-10 chr1:154516918 G>A maps to NM_001098475.1 E241E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAD2-01A-11D-A40R-10 chr1:154519927 G>T maps to NM_001098475.1 G332G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1ED-01A-11D-A152-10 chr13:61102825 T>C maps to NM_001146070.1 S489S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A8HU-01A-11D-A35Z-10 chr1:179564899 A>T maps to ENST00000444136 K260*. 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-A1EE-01A-11D-A12Z-10 chr1:179561758 A>G maps to ENST00000444136 E3E. 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-DD-AACO-01A-11D-A40R-10 chr1:179609570 A>G maps to ENST00000444136 R597R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAVX-01A-11D-A40R-10 chr1:179632574 A>G maps to ENST00000444136 P866P. 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-2Y-A9GY-01A-11D-A382-10 chr6:46657235 A>G maps to NM_001010870.2 P457P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9HA-01A-11D-A38X-10 chr6:46656122 G>T maps to NM_001010870.2 V86V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACL-01A-11D-A40R-10 chr6:46661685 A>T maps to NM_001010870.2 R1941*. 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-DD-AAC8-01A-11D-A40R-10 chr14:104433110 T>A maps to NM_153046.2 L236L. 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-FV-A2QR-01A-11D-A20W-10 chr6:35443340 A>G did not map to a codon.
Sequencing variant TCGA-DD-A39Y-01A-11D-A20W-10 chr12:3128310 T>C maps to NM_003213.3 A186A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACT-01A-11D-A40R-10 chr14:102898382 C>T maps to NM_014844.3 N445N. 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-DD-A39X-01A-11D-A20W-10 chr11:121060536 T>C maps to NM_005422.2 P2105P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAEE-01A-11D-A40R-10 chr11:121016727 C>A maps to NM_005422.2 G1336G. 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-AAEI-01A-11D-A40R-10 chr10:114046124 C>T maps to NM_058222.1 S153S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A0-01A-11D-A20W-10 chr9:27169565 C>T maps to NM_000459.3 Y189Y. 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-DD-AADB-01A-11D-A40R-10 chr9:27157868 C>T maps to NM_000459.3 S31S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr9:27212777 G>T maps to NM_000459.3 L920L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAC8-01A-11D-A40R-10 chr17:6718507 A>T maps to NM_053285.1 S201S. 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-ES-A2HS-01A-11D-A183-10 chr12:53456470 T>C maps to NM_170754.2 R1271R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr12:53455988 A>G maps to NM_170754.2 K1209K. 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-CC-A8HS-01A-11D-A35Z-10 chr14:20850190 C>T maps to NM_007110.4 L1435L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAE3-01A-11D-A40R-10 chr14:20876562 T>A maps to NM_007110.4 P12P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr14:20848599 G>T maps to NM_007110.4 P1599P. 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-DD-AADS-01A-11D-A40R-10 chr5:1266628 A>G maps to NM_198253.2 D868D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAEB-01A-11D-A40R-10 chr5:1294121 G>T maps to NM_198253.2 R293R. 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-DD-AACI-01A-11D-A40R-10 chr4:106157690 C>T maps to ENST00000513237 H885H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr2:74274103 T>C maps to ENST00000409262 L261L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr2:74328879 C>T maps to ENST00000409262 A1562A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADO-01A-11D-A40R-10 chr9:103092452 T>C did not map to a codon.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr9:103090231 T>C maps to NM_017746.3 K546K. 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-DD-A3A1-01A-11D-A20W-10 chr23:69964029 A>G did not map to a codon.
Sequencing variant TCGA-DD-AAC8-01A-11D-A40R-10 chr23:70072998 A>T did not map to a codon.
Sequencing variant TCGA-DD-AACL-01A-11D-A40R-10 chr23:69749739 A>C did not map to a codon.
Sequencing variant TCGA-DD-AACL-01A-11D-A40R-10 chr23:69964040 T>C 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-G3-A3CJ-01A-11D-A20W-10 chr23:70072998 A>G did not map to a codon.
Sequencing variant TCGA-ZP-A9CV-01A-11D-A382-10 chr23:69960591 A>G did not map to a codon.
Sequencing variant TCGA-5R-AAAM-01A-12D-A40R-10 chr23:104464277 A>C did not map to a codon.
Sequencing variant TCGA-ED-A4XI-01A-11D-A25V-10 chr23:104464382 G>T did not map to a codon.
Sequencing variant TCGA-WQ-A9G7-01A-11D-A36X-10 chr23:104464091 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-DD-AAE8-01A-11D-A40R-10 chr8:30695228 C>A maps to NM_031271.3 G2474G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAE9-01A-11D-A40R-10 chr8:30706086 A>G maps to NM_031271.3 C149C. 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-5C-AAPD-01A-21D-A38X-10 chr17:62265632 A>C maps to NM_018469.3 L780L. 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-2Y-A9GU-01A-11D-A382-10 chr15:56683536 T>A maps to NM_198524.1 I164I. 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-DD-AAEG-01A-11D-A38X-10 chr20:55206889 C>T maps to NM_003222.3 H188H. 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-4R-AA8I-01A-11D-A382-10 chr6:155578990 G>A maps to NM_016020.3 D340D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr12:51512403 C>A maps to NM_005653.4 G92*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAEE-01A-11D-A40R-10 chr12:51566148 C>T maps to NM_005653.4 V19V. 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-EP-A2KA-01A-11D-A183-10 chr2:121991664 A>T did not map to a codon.
Sequencing variant TCGA-WQ-A9G7-01A-11D-A36X-10 chr23:132352254 G>A did not map to a codon.
Sequencing variant TCGA-ED-A66Y-01A-11D-A30V-10 chr23:48888981 C>T did not map to a codon.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr23:48896667 A>G 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-DD-AAE3-01A-11D-A40R-10 chr22:26902860 G>A maps to NM_012143.2 I81I. 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-2Y-A9HB-01A-11D-A38X-10 chr8:133911107 C>T maps to NM_003235.4 Q1095*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A3KG-01A-11D-A20W-10 chr8:133941384 T>C maps to NM_003235.4 A1588A. 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-G3-AAV5-01A-11D-A36X-10 chr8:133899120 C>T maps to NM_003235.4 Q502*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADJ-01A-11D-A40R-10 chr13:95248351 G>A maps to NM_014305.2 P13P. Only missense variants will be evaluated by CHASM.
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-AACL-01A-11D-A40R-10 chr1:218609330 A>T maps to NM_001135599.2 T286T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9H2-01A-12D-A382-10 chr2:105892079 G>C maps to NM_004257.4 T534T. 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-DD-A1EE-01A-11D-A12Z-10 chr23:89177753 G>A did not map to a codon.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr15:43548801 C>T maps to NM_201631.3 K173K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-AAV6-01A-21D-A36X-10 chr20:2411161 G>C maps to NM_198994.2 L583L. Only missense variants will be evaluated by CHASM.
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-G3-A3CJ-01A-11D-A20W-10 chr8:56711513 A>G maps to NM_024831.6 E528E. 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-DD-AAD1-01A-11D-A40R-10 chr20:57568785 T>A maps to NM_198976.1 T525T. 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-EP-A2KB-01A-11D-A183-10 chr16:67876831 G>A maps to NM_020457.2 Q125Q. 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-DD-AACT-01A-11D-A40R-10 chr1:6685352 G>T did not map to a codon.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr1:6692464 G>T maps to NM_001195753.1 A116A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A3KG-01A-11D-A20W-10 chr22:21354222 A>G maps to NM_030573.2 T292T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-AAV7-01A-11D-A382-10 chr19:36530604 G>A maps to NM_152658.2 R98*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-AA0U-01A-11D-A382-10 chr4:83827763 A>T maps to NM_024672.4 L188L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A9FW-01A-11D-A36X-10 chr20:23029881 C>T maps to NM_000361.2 W87*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr15:39874934 C>T maps to NM_003246.2 G203G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr15:39881518 C>T maps to NM_003246.2 F630F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr15:39886307 C>A maps to NM_003246.2 T1092T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr6:169626379 T>C maps to NM_003247.2 E811E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAEA-01A-11D-A40R-10 chr6:169632797 G>A maps to NM_003247.2 P631P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAVP-01A-11D-A40R-10 chr6:169620433 T>G did not map to a codon.
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-EP-A2KA-01A-11D-A183-10 chr5:79351662 C>T maps to NM_003248.4 N116N. Only missense variants will be evaluated by CHASM.
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-DD-AAE0-01A-11D-A40R-10 chr6:128135073 G>A maps to NM_001164685.1 R238*. 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-DD-AACY-01A-11D-A40R-10 chr10:25312253 A>C maps to NM_024838.4 S34S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADR-01A-11D-A40R-10 chr10:25312661 A>T maps to NM_024838.4 T170T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A9FS-01A-11D-A36X-10 chr23:122761594 T>G did not map to a codon.
Sequencing variant TCGA-DD-AACI-01A-11D-A40R-10 chr23:122755373 T>A did not map to a codon.
Sequencing variant TCGA-DD-AACI-01A-11D-A40R-10 chr23:122755375 T>G did not map to a codon.
Sequencing variant TCGA-DD-AACY-01A-11D-A40R-10 chr23:122772801 T>G did not map to a codon.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr23:122760484 T>C did not map to a codon.
Sequencing variant TCGA-G3-AAV5-01A-11D-A36X-10 chr17:79848594 C>T maps to NM_005782.3 L120L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A9FS-01A-11D-A36X-10 chr22:29913066 C>G maps to NM_003678.4 L544L. 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-ES-A2HS-01A-11D-A183-10 chr13:52971399 T>A maps to NM_018676.3 K330*. 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-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-DD-AAVY-01A-11D-A40R-10 chr7:11416273 T>C maps to ENST00000423059 L1604L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GJ-A9DB-01A-11D-A36X-10 chr7:11416198 A>T maps to ENST00000423059 A1629A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr2:138373886 G>A did not map to a codon.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr2:138400204 T>A did not map to a codon.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr2:70441566 T>C maps to NM_022173.2 A316A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A8O6-01A-11D-A35Z-10 chr10:121338277 C>T maps to NM_001033925.1 W189*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZP-A9D4-01A-11D-A36X-10 chr10:121339461 A>C maps to NM_001033925.1 S161S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAEB-01A-11D-A40R-10 chr21:32638769 T>A maps to NM_003253.2 A173A. 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-G3-A3CJ-01A-11D-A20W-10 chr6:155565152 C>T maps to ENST00000456144 S1119S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A3KF-01A-11D-A20W-10 chr19:4817285 T>A maps to NM_182919.2 S368S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr1:43772514 C>A maps to NM_005424.2 S163S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WJ-A86L-01A-12D-A45V-10 chr1:43774663 C>T maps to NM_005424.2 I350I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9H6-01A-11D-A38X-10 chr4:113199371 T>A maps to NM_052864.2 R67R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr5:134785145 A>G maps to NM_001099221.1 *162Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A9FV-01A-11D-A36X-10 chr11:65124526 C>T maps to NM_145719.2 D416D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LG-A9QD-01A-11D-A382-10 chr11:65124367 A>G maps to NM_145719.2 E363E. 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-FV-A2QR-01A-11D-A20W-10 chr16:3348988 A>G maps to NM_033208.3 P542P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CG-01A-11D-A20W-10 chr3:114018525 C>A maps to ENST00000481065 I225I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr5:156353299 G>A maps to NM_138379.2 Q290*. 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-ES-A2HS-01A-11D-A183-10 chr5:156375499 A>G maps to NM_138379.2 V257V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr12:56814390 A>G maps to NM_003920.3 L1064L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-AAV0-01A-11D-A36X-10 chr12:56817447 C>T maps to NM_003920.3 E670E. 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-WX-AA44-01A-11D-A38X-10 chr12:56817447 C>T maps to NM_003920.3 E670E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9GX-01A-11D-A382-10 chr10:51592506 G>C maps to NM_006327.2 L209L. 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-DD-AADJ-01A-11D-A40R-10 chr23:47445001 G>T did not map to a codon.
Sequencing variant TCGA-WQ-A9G7-01A-11D-A36X-10 chr23:47444964 C>T did not map to a codon.
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-5R-AA1C-01A-11D-A40R-10 chr6:43473577 C>G maps to NM_001146016.1 G553G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A0-01A-11D-A20W-10 chr6:43473139 A>G maps to NM_001146016.1 E407E. 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-EP-A2KA-01A-11D-A183-10 chr9:71842714 T>C maps to NM_004817.3 S415S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr9:71845109 G>T maps to NM_004817.3 E545*. 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-DD-AAC8-01A-11D-A40R-10 chr3:53263100 T>A maps to ENST00000423516 S447S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr3:53289862 C>T maps to ENST00000423516 A32A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr3:53263136 G>A maps to ENST00000423516 S435S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9GS-01A-12D-A382-10 chr23:153556299 G>A 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-ES-A2HS-01A-11D-A183-10 chr23:153543545 T>C did not map to a codon.
Sequencing variant TCGA-2Y-A9H5-01A-11D-A382-10 chr9:84202720 C>A maps to NM_005077.3 G618*. Only missense variants will be evaluated by CHASM.
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-XR-A8TF-01A-11D-A35Z-10 chr9:84268952 T>A did not map to a codon.
Sequencing variant TCGA-DD-AADS-01A-11D-A40R-10 chr2:171863314 T>A maps to ENST00000360843 T552T. 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-2Y-A9H9-01A-21D-A38X-10 chr17:60685416 C>T maps to ENST00000326270 Q685*. 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-DD-A39Y-01A-11D-A20W-10 chr9:35717438 T>C did not map to a codon.
Sequencing variant TCGA-DD-AACA-01A-11D-A40R-10 chr15:62999359 C>T maps to NM_015059.2 Q694*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAVU-01A-11D-A40R-10 chr15:62990036 G>T maps to NM_015059.2 G481G. 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-ES-A2HS-01A-11D-A183-10 chr4:38776476 C>A maps to NM_030956.3 S245S. 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-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-DD-AADB-01A-11D-A40R-10 chr1:223284945 T>C maps to NM_003268.5 E476E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr1:223286027 G>A maps to NM_003268.5 Q116*. 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-DD-AAE7-01A-11D-A40R-10 chr4:38828946 G>T maps to NM_006068.3 L716L. 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-DD-A39X-01A-11D-A20W-10 chr23:12904277 A>G did not map to a codon.
Sequencing variant TCGA-DD-A39X-01A-11D-A20W-10 chr23:12905002 T>C did not map to a codon.
Sequencing variant TCGA-DD-AAC8-01A-11D-A40R-10 chr23:12906213 T>A 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-XR-A8TF-01A-11D-A35Z-10 chr23:12903872 A>T 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-A1EG-01A-11D-A20W-10 chr23:12938330 T>C 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-DD-AACV-01A-11D-A40R-10 chr23:12938751 T>C did not map to a codon.
Sequencing variant TCGA-DD-AADC-01A-11D-A40R-10 chr23:12940016 G>C did not map to a codon.
Sequencing variant TCGA-DD-AAED-01A-12D-A40R-10 chr23:12939762 A>G did not map to a codon.
Sequencing variant TCGA-DD-AAVQ-01A-11D-A40R-10 chr23:12939520 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-DD-AACH-01A-11D-A40R-10 chr10:102891822 C>G maps to NM_005521.3 P175P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A1-01A-11D-A20W-10 chr10:102849599 A>G maps to NM_001085398.1 S21S. 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-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-DD-AAD0-01A-11D-A40R-10 chr3:149205518 A>G maps to NM_004617.2 T126T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr17:4686301 T>C maps to NM_003963.2 G183G. 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-2Y-A9GT-01A-11D-A382-10 chr15:83781633 C>A maps to NM_023003.3 R60R. 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-FV-A3I0-01A-11D-A22F-10 chr8:105361091 G>T maps to NM_030788.2 G104G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr14:24662036 G>T maps to NM_006405.5 R262R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-AAV0-01A-11D-A36X-10 chr13:100206555 A>T did not map to a codon.
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-AAVY-01A-11D-A40R-10 chr9:75407156 T>C maps to NM_138691.2 N485N. 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-DD-AACX-01A-11D-A40R-10 chr20:2591138 C>T maps to NM_080751.2 Y496Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACB-01A-11D-A40R-10 chr15:81625500 A>T maps to ENST00000454937 P857P. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-DD-AADO-01A-11D-A40R-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr19:54664260 C>A maps to NM_001145303.1 V671V. 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.
Alternatively spliced codon TCGA-WQ-A9G7-01A-11D-A36X-10. Mapping will be selected arbitrarily.
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-5C-A9VG-01A-11D-A36X-10 chr16:19056298 C>T maps to NM_024847.3 C477C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MA-01A-11D-A20W-10 chr3:129546657 T>C maps to NM_001017395.3 G188G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1ED-01A-11D-A152-10 chr3:129370464 T>C maps to NM_001017395.3 V607V. 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-CC-A3MB-01A-11D-A20W-10 chr1:40713791 C>T maps to NM_001008740.3 L43L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACS-01A-11D-A40R-10 chr5:177021210 G>A maps to NM_017510.4 L161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39Y-01A-11D-A20W-10 chr9:103279041 A>G maps to NM_001198812.1 A257A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACI-01A-11D-A40R-10 chr2:192862988 T>A maps to NM_016192.2 A248A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GJ-A9DB-01A-11D-A36X-10 chr2:192820996 G>A maps to NM_016192.2 Q285*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr17:72815909 G>T maps to NM_017728.3 G220*. 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-AAW3-01A-11D-A40P-10 chr3:52877736 G>A maps to ENST00000504329 N206N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACP-01A-11D-A40R-10 chr12:108985574 G>A maps to NM_181724.2 D195D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr11:102272280 C>T maps to NM_052932.2 R197R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A3KF-01A-11D-A20W-10 chr11:85365265 T>C maps to NM_032273.3 T82T. 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-DD-AAE7-01A-11D-A40R-10 chr2:96930987 C>T maps to NM_017849.3 L44L. 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-GJ-A9DB-01A-11D-A36X-10 chr7:98445807 G>A maps to NM_001134450.1 V393V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr2:98382613 C>T maps to NM_015348.1 P1562P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EG-01A-11D-A20W-10 chr2:98460709 T>C maps to NM_015348.1 G166G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADF-01A-11D-A40R-10 chr11:60703649 T>A maps to NM_017870.3 A782A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACI-01A-11D-A40R-10 chr12:126139051 T>C maps to NM_052907.2 N1011N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACL-01A-11D-A40R-10 chr12:126138934 A>T maps to NM_052907.2 I972I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr12:126136984 A>G did not map to a codon.
Sequencing variant TCGA-K7-AAU7-01A-11D-A382-10 chr12:125834193 T>C maps to NM_052907.2 I83I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39Z-01A-11D-A20W-10 chr12:129694079 A>G maps to NM_133448.2 D476D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACH-01A-11D-A40R-10 chr12:129566301 A>G did not map to a codon.
Sequencing variant TCGA-DD-AACI-01A-11D-A40R-10 chr12:129558521 C>G maps to NM_133448.2 V1066V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr12:130184851 G>A maps to NM_133448.2 D157D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9GU-01A-11D-A382-10 chr11:87032350 A>T maps to NM_022918.3 P451P. 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-DD-AACE-01A-11D-A40R-10 chr4:159162712 A>C maps to NM_018342.4 A285A. 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-BC-A3KF-01A-11D-A20W-10 chr19:5737209 T>C maps to NM_152784.3 F151F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A9-01A-11D-A25V-10 chr19:5766133 C>G maps to NM_152784.3 G509G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACF-01A-11D-A40R-10 chr2:85828181 G>C maps to NM_001031738.2 P54P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr11:66062754 C>A maps to NM_153266.3 L346L. 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-EP-A2KB-01A-11D-A183-10 chr2:135308181 G>A maps to NM_030923.4 Y139Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WQ-A9G7-01A-11D-A36X-10 chr2:135470782 C>T maps to NM_030923.4 A103A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MB-01A-11D-A20W-10 chr23:109247198 A>G did not map to a codon.
Sequencing variant TCGA-2Y-A9H2-01A-12D-A382-10 chr7:112407740 G>T maps to NM_022484.4 S535S. Only missense variants will be evaluated by CHASM.
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-AAV1-01A-11D-A382-10 chr4:944243 A>T maps to NM_032326.2 T76T. 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-CC-A9FW-01A-11D-A36X-10 chr7:150488704 C>A maps to NM_014020.3 E243*. Only missense variants will be evaluated by CHASM.
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-DD-AAEA-01A-11D-A40R-10 chr4:148555392 A>G maps to NM_018241.2 L375L. 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-G3-A7M7-01A-12D-A34Z-10 chr23:153247690 G>A did not map to a codon.
Sequencing variant TCGA-2Y-A9H5-01A-11D-A382-10 chr9:74327049 G>C maps to NM_013390.2 S906S. Only missense variants will be evaluated by CHASM.
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-DD-AAD5-01A-11D-A40R-10 chr10:95660949 C>T maps to NM_001134658.1 V267V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr6:130762129 T>A maps to NM_052913.2 L188*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr2:27258127 A>G maps to NM_017727.4 E159E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LG-A9QC-01A-11D-A36X-10 chr2:27257067 G>A maps to NM_017727.4 V95V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2V-A95S-01A-11D-A36X-10 chr9:32784867 G>A maps to NM_212558.2 W229*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CJ-01A-11D-A20W-10 chr11:61165730 C>A did not map to a codon.
Sequencing variant TCGA-DD-A4NH-01A-11D-A27I-10 chr11:124971200 T>A 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-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-NI-A8LF-01A-11D-A35Z-10 chr14:61747676 C>T maps to NM_001017970.2 L63L. 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-AACL-01A-11D-A40R-10 chr3:119156669 T>A maps to NM_018266.1 K286*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAVX-01A-11D-A40R-10 chr1:32540607 G>T maps to NM_018056.2 G21*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZP-A9CZ-01A-11D-A382-10 chr1:32566141 C>T maps to NM_018056.2 D405D. 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-ED-A459-01A-11D-A25V-10 chr1:54272139 G>T maps to NM_018087.4 C314*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-AAV4-01A-11D-A382-10 chr1:54238114 G>A maps to NM_018087.4 P616P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-AAV3-01A-11D-A36X-10 chr12:64202487 G>A maps to NM_014254.1 K316K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAD3-01A-11D-A40R-10 chr1:33361531 G>T maps to NM_033504.2 R83R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-AA0U-01A-11D-A382-10 chr15:43473451 A>G maps to NM_024956.3 G520G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAC8-01A-11D-A40R-10 chr6:44116247 A>T did not map to a codon.
Sequencing variant TCGA-G3-AAV7-01A-11D-A382-10 chr14:77685212 G>T maps to NM_020431.2 V19V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5R-AA1C-01A-11D-A40R-10 chr8:94770708 A>G did not map to a codon.
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-DD-AADB-01A-11D-A40R-10 chr10:45429083 G>T did not map to a codon.
Sequencing variant TCGA-DD-AADQ-01A-11D-A40R-10 chr10:45406974 G>A maps to NM_001123376.1 V5V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr10:45429083 G>T did not map to a codon.
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-DD-A3A0-01A-11D-A20W-10 chr2:112839015 A>G maps to NM_032824.2 A253A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAD0-01A-11D-A40R-10 chr2:112839009 G>A maps to NM_032824.2 W251*. 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-DD-AADQ-01A-11D-A40R-10 chr16:422088 C>A maps to NM_021259.2 P738P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LG-A9QD-01A-11D-A382-10 chr16:422022 G>A maps to NM_021259.2 C760C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LG-A9QD-01A-11D-A382-10 chr16:422037 G>T maps to NM_021259.2 C755*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WQ-A9G7-01A-11D-A36X-10 chr17:48356248 G>A maps to NM_153229.2 P86P. Only missense variants will be evaluated by CHASM.
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-A39Z-01A-11D-A20W-10 chr17:7258601 T>C maps to NM_198154.1 L27L. 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-ED-A5KG-01A-11D-A27I-10 chr9:100325045 C>T maps to NM_003275.3 Q144*. 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-DD-AAE6-01A-11D-A40R-10 chr12:98921776 T>G maps to NM_003276.2 P131P. 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-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-DD-AADE-01A-11D-A40R-10 chr4:68938053 T>C maps to NM_207407.2 S167S. 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-DD-AAC8-01A-11D-A40R-10 chr11:117789472 T>G maps to ENST00000413475 A33A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr11:117780677 C>A maps to ENST00000413475 G317*. 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-DD-AADG-01A-11D-A40R-10 chr21:19726181 T>A did not map to a codon.
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-UB-A7MC-01A-11D-A33Q-10 chr21:19704473 A>G maps to NM_002772.2 P527P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADE-01A-11D-A40R-10 chr21:43805591 C>T maps to ENST00000380399 R250R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAE6-01A-11D-A40R-10 chr21:43802303 T>G maps to ENST00000380399 L358L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9GZ-01A-11D-A38X-10 chr11:117973864 C>T maps to NM_019894.3 H69H. 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-2V-A95S-01A-11D-A36X-10 chr22:37482383 C>T maps to ENST00000381792 K304K. 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-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-DD-AACI-01A-11D-A40R-10 chr12:83251360 T>A did not map to a codon.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr12:83526014 A>G maps to NM_152588.1 G786G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACI-01A-11D-A40R-10 chr12:88542127 A>T maps to NM_181783.3 I12I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACG-01A-11D-A40R-10 chr13:101289830 C>A maps to NM_032813.2 V320V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADI-01A-11D-A40R-10 chr7:150778971 G>T maps to NM_031434.3 G135G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAEK-01A-11D-A40R-10 chr7:150779557 C>T maps to NM_031434.3 T31T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr17:42266554 G>A maps to NM_001076674.1 L67L. 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-4R-AA8I-01A-11D-A382-10 chr18:66377256 C>G did not map to a codon.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr6:31544345 C>A maps to NM_000594.2 A74A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LG-A9QD-01A-11D-A382-10 chr6:138202371 G>T maps to NM_006290.2 R763R. 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-2Y-A9HB-01A-11D-A38X-10 chr8:22885266 C>T did not map to a codon.
Sequencing variant TCGA-ZP-A9D2-01A-11D-A382-10 chr8:22884791 G>A maps to NM_003842.4 R264*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAVU-01A-11D-A40R-10 chr18:60028928 G>A maps to NM_003839.2 L211L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A0-01A-11D-A20W-10 chr8:119945173 T>C maps to NM_002546.3 Q132Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADM-01A-11D-A40R-10 chr17:16842938 C>A maps to NM_012452.2 L268L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAVU-01A-11D-A40R-10 chr17:16843679 G>A maps to NM_012452.2 P197P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZP-A9D0-01A-11D-A36X-10 chr1:1140774 G>C maps to NM_004195.2 P95P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NI-A8LF-01A-11D-A35Z-10 chr13:24242839 C>T maps to NM_018647.2 G283G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9H0-01A-11D-A382-10 chr12:6438603 G>A maps to NM_001065.3 R414R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3K-AAZ8-01A-12D-A38X-10 chr6:47253740 G>A maps to NM_014452.3 I229I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr6:47202532 C>T maps to NM_014452.3 T537T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9GS-01A-12D-A382-10 chr1:6524729 A>G maps to ENST00000355862 C115C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-AAUZ-01A-11D-A382-10 chr1:1148456 C>G maps to NM_003327.3 R95R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WQ-A9G7-01A-11D-A36X-10 chr20:62328388 A>G maps to ENST00000482936 L1392L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAC8-01A-11D-A40R-10 chr1:12183819 G>A maps to NM_001243.3 T363T. 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-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-EP-A2KB-01A-11D-A183-10 chr8:9623749 T>C maps to NM_003747.2 G1185G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACB-01A-11D-A40R-10 chr11:57080661 G>A maps to NM_033396.2 I500I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr11:57069547 C>A maps to NM_033396.2 E1612*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A1-01A-11D-A20W-10 chr10:93609347 A>G maps to NM_025235.3 E897E. 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-2Y-A9H4-01A-11D-A382-10 chr23:99854660 C>T did not map to a codon.
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-DD-AADB-01A-11D-A40R-10 chr1:175048843 G>A did not map to a codon.
Sequencing variant TCGA-DD-AAW1-01A-11D-A40P-10 chr1:175053027 T>A maps to NM_022093.1 T397T. Only missense variants will be evaluated by CHASM.
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-LG-A9QD-01A-11D-A382-10 chr1:175046703 G>A maps to NM_022093.1 V50V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IE-01A-21D-A382-10 chr1:74737338 G>T maps to NM_001112808.2 G232*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IH-01A-11D-A33K-10 chr1:74833632 A>T maps to NM_001112808.2 K537*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAEA-01A-11D-A40R-10 chr1:74716452 G>A maps to NM_001112808.2 K212K. 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-DD-AAC8-01A-11D-A40R-10 chr19:12821576 T>A maps to NM_001136196.1 S376S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADF-01A-11D-A40R-10 chr7:128612494 T>A maps to ENST00000471166 T839T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAE6-01A-11D-A40R-10 chr1:175348808 C>T maps to NM_003285.2 W614*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CG-01A-11D-A20W-10 chr1:175348688 T>C maps to NM_003285.2 T654T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39X-01A-11D-A20W-10 chr7:5396832 G>T maps to NM_001080495.2 L1636L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAEB-01A-11D-A40R-10 chr7:5352634 T>G maps to NM_001080495.2 S2629S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAVP-01A-11D-A40R-10 chr7:5352832 G>A maps to NM_001080495.2 S2563S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr7:5391468 C>A maps to NM_001080495.2 S1817S. 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-2Y-A9HB-01A-11D-A38X-10 chr16:24826591 G>A maps to NM_014494.2 S1599S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39Z-01A-11D-A20W-10 chr16:24834277 T>C maps to NM_014494.2 A1819A. 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-DD-AACZ-01A-11D-A40R-10 chr16:24788428 A>G maps to NM_014494.2 P113P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAEI-01A-11D-A40R-10 chr16:24834980 C>T maps to NM_014494.2 H1914H. 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-DD-AACL-01A-11D-A40R-10 chr22:40708617 A>T maps to ENST00000454349 V1529V. 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-DD-A39Y-01A-11D-A20W-10 chr17:76075516 A>G maps to NM_001142640.1 A1081A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAVQ-01A-11D-A40R-10 chr17:76075531 C>T maps to NM_001142640.1 T1086T. 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-AADB-01A-11D-A40R-10 chr7:47476875 C>T maps to NM_022748.11 T62T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAE9-01A-11D-A40R-10 chr7:47440023 T>C maps to NM_022748.11 E295E. 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-WX-AA44-01A-11D-A38X-10 chr7:47343130 A>T maps to NM_022748.11 V958V. 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-DD-AADE-01A-11D-A40R-10 chr6:32038114 T>C maps to ENST00000375244 S1689S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAVX-01A-11D-A40R-10 chr6:32036841 A>G maps to ENST00000375244 L1887L. 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-XR-A8TG-01A-11D-A35Z-10 chr6:32046999 G>A maps to ENST00000375244 P1395P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr17:48941374 G>A maps to NM_005749.2 Q2*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACY-01A-11D-A40R-10 chr22:41833265 A>G maps to NM_016272.3 F28F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GJ-A9DB-01A-11D-A36X-10 chr11:1309925 G>A maps to ENST00000382211 D180D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACL-01A-11D-A40R-10 chr22:39078325 A>T did not map to a codon.
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-DD-AAEH-01A-11D-A40R-10 chr3:100105786 T>C maps to NM_014820.3 K120K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADS-01A-11D-A40R-10 chr20:39709834 A>G maps to NM_003286.2 T154T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9HB-01A-11D-A38X-10 chr8:144406771 C>A maps to NM_052963.1 A233A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9HB-01A-11D-A38X-10 chr17:38569013 C>T maps to ENST00000357601 L264L. 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-FV-A2QR-01A-11D-A20W-10 chr17:38552570 T>C maps to ENST00000357601 K1264K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WQ-A9G7-01A-11D-A36X-10 chr17:38564370 G>A maps to ENST00000357601 R486*. 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-ES-A2HT-01A-12D-A183-10 chr3:25671862 T>C maps to ENST00000264331 R501R. 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-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-DD-AADO-01A-11D-A40R-10 chr1:179815787 T>A maps to NM_145034.4 G277G. 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-DD-A3A1-01A-11D-A20W-10 chr20:42694557 C>G maps to ENST00000348077 S398S. 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-A1EE-01A-11D-A12Z-10 chr17:7577106 A>T maps to NM_001126112.1 C277*. 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-DD-AACG-01A-11D-A40R-10 chr17:7578274 G>A maps to NM_001126112.1 Q192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACV-01A-11D-A40R-10 chr17:7578499 G>A maps to NM_001126112.1 Q144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACZ-01A-11D-A40R-10 chr17:7577147 G>A maps to NM_001126112.1 L264L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAD8-01A-11D-A40R-10 chr17:7577609 T>A did not map to a codon.
Sequencing variant TCGA-DD-AADC-01A-11D-A40R-10 chr17:7578554 C>T did not map to a codon.
Sequencing variant TCGA-DD-AAED-01A-12D-A40R-10 chr17:7578554 C>T did not map to a codon.
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-G3-AAV4-01A-11D-A382-10 chr17:7578176 C>T maps to NM_001126112.1 E224E. Only missense variants will be evaluated by CHASM.
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-WJ-A86L-01A-12D-A45V-10 chr17:7578238 C>A maps to NM_001126112.1 E204*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WX-AA44-01A-11D-A38X-10 chr17:7576927 T>C did not map to a codon.
Sequencing variant TCGA-DD-A3A1-01A-11D-A20W-10 chr11:128807455 T>C maps to ENST00000263583 T86T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACQ-01A-11D-A40R-10 chr15:43724679 C>G maps to NM_001141980.1 V1129V. Only missense variants will be evaluated by CHASM.
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-WQ-A9G7-01A-11D-A36X-10 chr17:27899413 G>A maps to NM_138349.2 P256P. Only missense variants will be evaluated by CHASM.
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-AAW3-01A-11D-A40P-10 chr3:189584585 G>A maps to NM_003722.4 Q294Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5C-AAPD-01A-21D-A38X-10 chr1:3599744 G>A did not map to a codon.
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-A39Y-01A-11D-A20W-10 chr6:125541326 A>G maps to NM_003287.2 A41A. 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-DD-A1EG-01A-11D-A20W-10 chr9:35683239 T>G did not map to a codon.
Sequencing variant TCGA-DD-AAC8-01A-11D-A40R-10 chr1:154130186 T>C maps to NM_001043351.1 K225K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr19:16192749 C>T maps to NM_001145160.1 R90*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2V-A95S-01A-11D-A36X-10 chr2:1481105 C>T maps to NM_000547.5 L356L. 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-ZP-A9CY-01A-11D-A382-10 chr13:103268743 A>T did not map to a codon.
Sequencing variant TCGA-BC-A3KG-01A-11D-A20W-10 chr16:67425008 T>C maps to NM_016140.2 A2A. Only missense variants will be evaluated by CHASM.
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-DD-AACB-01A-11D-A40R-10 chr1:186304628 C>T maps to NM_003292.2 R1584R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZP-A9D1-01A-11D-A382-10 chr1:186329449 T>C maps to NM_003292.2 A382A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAC8-01A-11D-A40R-10 chr3:127295718 G>A maps to NM_001136053.1 T121T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-AAV0-01A-11D-A36X-10 chr1:3542010 G>A maps to NM_182752.3 V75V. Only missense variants will be evaluated by CHASM.
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-DD-AACA-01A-11D-A40R-10 chr19:48305637 T>C maps to NM_198479.2 P210P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACD-01A-11D-A40R-10 chr16:1306935 G>T maps to NM_012217.2 L131L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAE6-01A-11D-A40R-10 chr21:10933873 C>T maps to NM_199261.2 A335A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAE7-01A-11D-A40R-10 chr13:20056674 T>C maps to NM_199254.2 R44R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WQ-A9G7-01A-11D-A36X-10 chr13:20004676 A>G maps to NM_199254.2 C411C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39X-01A-11D-A20W-10 chr20:30366725 T>C maps to ENST00000340513 V331V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WX-AA46-01A-11D-A38X-10 chr3:185644396 A>T maps to NM_004593.2 S54S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WQ-A9G7-01A-11D-A36X-10 chr14:103371802 C>T maps to NM_145725.2 D463D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39Z-01A-11D-A20W-10 chr11:36520042 A>G maps to NM_145803.1 L148L. 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-UB-AA0V-01A-11D-A382-10 chr16:2221290 C>G maps to NM_032271.2 P125P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11B-01A-11D-A12Z-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-DD-AAW3-01A-11D-A40P-10 chr4:118005492 C>A maps to NM_152402.2 E353*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A3KG-01A-11D-A20W-10 chr6:52370843 T>C maps to NM_012288.3 E239E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAE0-01A-11D-A40R-10 chr16:3713464 C>T maps to NM_016292.2 V556V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BD-A3EP-01A-11D-A22F-10 chr21:45523363 G>A maps to NM_003274.4 L1244L. 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-G3-A3CJ-01A-11D-A20W-10 chr11:118889615 T>C maps to NM_016146.4 D37D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACH-01A-11D-A40R-10 chr14:39623437 G>A maps to NM_001079537.1 Q110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr8:141449295 T>C maps to NM_031466.5 R293R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADS-01A-11D-A40R-10 chr10:17191062 T>C maps to NM_004412.5 K384K. 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-BC-A3KG-01A-11D-A20W-10 chr6:123653051 C>T maps to NM_006073.2 E481E. 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-AACL-01A-11D-A40R-10 chr6:41162395 A>T maps to ENST00000373108 P243P. 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-DD-AAE3-01A-11D-A40R-10 chr6:41196729 T>C maps to NM_198153.2 A114A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr6:42200600 G>A maps to NM_033502.2 G1032G. 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-A3A0-01A-11D-A20W-10 chr6:42232471 C>T maps to NM_033502.2 G535G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACB-01A-11D-A40R-10 chr6:42196220 G>A maps to NM_033502.2 P1155P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A8HV-01A-11D-A35Z-10 chr23:152710778 C>G did not map to a codon.
Sequencing variant TCGA-DD-A118-01A-11D-A12Z-10 chr23:152710778 C>T did not map to a codon.
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-EP-A2KB-01A-11D-A183-10 chr20:376997 G>T maps to ENST00000422053 L274L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADO-01A-11D-A40R-10 chr6:30122219 G>T maps to NM_006778.3 L324L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr6:30121748 G>T maps to NM_006778.3 S481S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3K-AAZ8-01A-12D-A38X-10 chr1:228588703 G>A maps to NM_145214.2 L232L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAEK-01A-11D-A40R-10 chr17:15539430 C>T maps to ENST00000455584 E270E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BD-A3ER-01A-11D-A20W-10 chr4:154214186 G>A maps to NM_015271.3 T169T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr4:154216476 C>T maps to NM_015271.3 Q267*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADI-01A-11D-A40R-10 chr4:154191665 C>A maps to NM_015271.3 C70*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9H2-01A-12D-A382-10 chr5:64909989 G>A maps to NM_001656.3 R101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAC8-01A-11D-A40R-10 chr17:54981762 T>A maps to NM_005082.4 T260T. Only missense variants will be evaluated by CHASM.
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-DD-AAD0-01A-11D-A40R-10 chr5:114469809 G>A maps to NM_018700.3 S427S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9GZ-01A-11D-A38X-10 chr17:57181689 A>T maps to NM_015294.3 P29P. 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-DD-A119-01A-11D-A12Z-10 chr6:30297108 T>C maps to NM_021253.3 S5S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAEB-01A-11D-A40R-10 chr6:30303625 G>A maps to NM_021253.3 E218E. 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-DD-AADM-01A-11D-A40R-10 chr3:140401717 C>A maps to NM_152616.4 I252I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-AA0U-01A-11D-A382-10 chr3:140406639 G>A maps to NM_152616.4 K372K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr1:117661331 G>T maps to NM_025188.3 Y182*. 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-G3-A3CG-01A-11D-A20W-10 chr1:155148088 C>A maps to NM_025058.3 P97P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A12J-01A-11D-A12Z-10 chr5:180687427 C>T maps to NM_032765.2 E129E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAVX-01A-11D-A40R-10 chr7:100731595 C>T maps to NM_030961.1 L335L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADO-01A-11D-A40R-10 chr1:248039448 C>T maps to NM_015431.3 T373T. 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-G3-A3CG-01A-11D-A20W-10 chr4:165962540 T>C maps to NM_152620.2 T439T. 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-5C-A9VG-01A-11D-A36X-10 chr1:231299710 C>T maps to NM_001004342.3 H332H. 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-EP-A2KB-01A-11D-A183-10 chr15:45051021 G>T maps to NM_182985.3 T261T. 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-DD-A1EE-01A-11D-A12Z-10 chr3:32915308 G>A did not map to a codon.
Sequencing variant TCGA-2Y-A9GU-01A-11D-A382-10 chr16:31226232 C>T maps to NM_001008274.3 A58A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-AA0U-01A-11D-A382-10 chr16:31226433 C>T maps to NM_001008274.3 A125A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GJ-A9DB-01A-11D-A36X-10 chr4:189061020 G>A maps to NM_178556.3 K103K. 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-XR-A8TF-01A-11D-A35Z-10 chr22:38121211 C>T maps to NM_001039141.2 P883P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr19:6743584 C>T maps to ENST00000313244 N163N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADG-01A-11D-A40R-10 chr19:6743799 C>T maps to ENST00000313244 R199*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr2:230652244 A>G maps to ENST00000389044 V1630V. 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-A4NH-01A-11D-A27I-10 chr2:230632437 T>A maps to ENST00000389044 T1985T. 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-DD-AAC8-01A-11D-A40R-10 chr2:230638851 A>G maps to ENST00000389044 D1858D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACB-01A-11D-A40R-10 chr2:230656742 C>T maps to ENST00000389044 R1391R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACW-01A-11D-A40R-10 chr2:230655846 T>C maps to ENST00000389044 L1485L. 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-ES-A2HT-01A-12D-A183-10 chr2:230683118 T>C maps to ENST00000389044 T520T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAED-01A-12D-A40R-10 chr5:908113 G>A maps to NM_004237.3 L228L. 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-ZP-A9D4-01A-11D-A36X-10 chr5:912080 C>T maps to NM_004237.3 I330I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr15:64689806 A>G maps to NM_016213.4 A136A. 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-BC-A3KG-01A-11D-A20W-10 chr14:103999138 A>G maps to ENST00000299201 S184S. 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-A1EE-01A-11D-A12Z-10 chr2:29075272 C>T did not map to a codon.
Sequencing variant TCGA-DD-A3A0-01A-11D-A20W-10 chr2:29087913 A>G maps to NM_017910.3 S257S. 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-2Y-A9GZ-01A-11D-A38X-10 chr23:54955555 G>T did not map to a codon.
Sequencing variant TCGA-CC-A8HT-01A-11D-A35Z-10 chr23:54949457 C>T did not map to a codon.
Sequencing variant TCGA-DD-A39Y-01A-11D-A20W-10 chr23:54955826 A>G did not map to a codon.
Sequencing variant TCGA-DD-AACL-01A-11D-A40R-10 chr23:54956639 T>C did not map to a codon.
Sequencing variant TCGA-DD-AADK-01A-11D-A40R-10 chr23:54949796 C>A did not map to a codon.
Sequencing variant TCGA-DD-AAEH-01A-11D-A40R-10 chr23:54957050 T>C 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-ZS-A9CE-01A-11D-A36X-10 chr23:54955092 G>A did not map to a codon.
Sequencing variant TCGA-DD-AAVZ-01A-11D-A40R-10 chr12:49719612 G>A maps to NM_005480.3 L193L. Only missense variants will be evaluated by CHASM.
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-G3-A3CJ-01A-11D-A20W-10 chr8:72951123 A>G maps to NM_007332.2 D757D. Only missense variants will be evaluated by CHASM.
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-DD-AADR-01A-11D-A40R-10 chr4:122853581 C>T maps to NM_001130698.1 R277R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZP-A9CZ-01A-11D-A382-10 chr4:122833232 G>A maps to NM_001130698.1 R453*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39Y-01A-11D-A20W-10 chr13:38213436 C>T did not map to a codon.
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-WJ-A86L-01A-12D-A45V-10 chr13:38320589 C>T maps to NM_003306.1 V127V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A1-01A-11D-A20W-10 chr23:111090641 T>C did not map to a codon.
Sequencing variant TCGA-DD-AAE6-01A-11D-A40R-10 chr23:111195371 T>A did not map to a codon.
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-DD-AAE8-01A-11D-A40R-10 chr5:135551936 T>C maps to NM_020389.2 R790R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZS-A9CG-01A-11D-A36X-10 chr5:135692610 G>A maps to NM_020389.2 D155D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9GU-01A-11D-A382-10 chr15:31360289 G>A maps to NM_002420.4 I73I. 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-EP-A2KA-01A-11D-A183-10 chr15:31360166 G>A maps to NM_002420.4 P114P. 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-DD-A1ED-01A-11D-A152-10 chr11:2438954 A>G did not map to a codon.
Sequencing variant TCGA-ZP-A9D2-01A-11D-A382-10 chr11:2434046 G>A maps to ENST00000452833 P766P. 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-4R-AA8I-01A-11D-A382-10 chr15:50884114 T>C maps to NM_017672.4 A1439A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A1-01A-11D-A20W-10 chr15:50881854 T>C did not map to a codon.
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-DD-AACP-01A-11D-A40R-10 chr15:50884531 G>A maps to NM_017672.4 S1300S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAEK-01A-11D-A40R-10 chr2:234916712 G>T did not map to a codon.
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-2V-A95S-01A-11D-A36X-10 chr8:116427156 T>C maps to NM_014112.2 L993L. 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-DD-AACZ-01A-11D-A40R-10 chr8:116616719 A>G maps to NM_014112.2 S492S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACZ-01A-11D-A40R-10 chr8:116631491 A>T maps to NM_014112.2 L278*. 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-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-AACF-01A-11D-A40R-10 chr17:3417210 C>T maps to ENST00000381913 *792*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADM-01A-11D-A40R-10 chr7:142605696 C>A maps to NM_019841.4 E725*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAEB-01A-11D-A40R-10 chr7:142605859 C>T maps to NM_019841.4 G670G. 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-ES-A2HS-01A-11D-A183-10 chr7:142569465 C>T maps to NM_018646.2 Q724Q. 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-DD-AACY-01A-11D-A40R-10 chr7:98586441 G>T maps to ENST00000359863 L3152L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAE3-01A-11D-A40R-10 chr7:98513491 C>A maps to ENST00000359863 L782L. 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-CC-A9FS-01A-11D-A36X-10 chr16:2108809 G>A maps to NM_000548.3 W304*. Only missense variants will be evaluated by CHASM.
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-A1EE-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-AAV7-01A-11D-A382-10 chr16:2124224 C>T maps to NM_000548.3 Q794*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAC8-01A-11D-A40R-10 chr13:45148296 T>A maps to NM_183422.2 T638T. 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-DD-AAE7-01A-11D-A40R-10 chr3:150127757 T>G maps to NM_014779.2 T207T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAE2-01A-11D-A40R-10 chr19:54695355 C>T maps to NM_001077446.2 G47G. Only missense variants will be evaluated by CHASM.
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-ZP-A9CZ-01A-11D-A382-10 chr7:130356522 A>G maps to NM_052933.2 H212H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MR-A8JO-01A-12D-A35Z-10 chr7:130067811 T>C maps to NM_018718.1 K27K. 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-AAE4-01A-11D-A40R-10 chr18:73000059 C>T maps to NM_005786.4 L855L. 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-DD-AADG-01A-11D-A40R-10 chr19:31769255 A>G maps to NM_020856.2 T481T. 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-LG-A9QD-01A-11D-A382-10 chr19:31770239 G>A maps to NM_020856.2 S153S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-AAV5-01A-11D-A36X-10 chr19:50250009 G>A maps to NM_021733.1 R237*. 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-CC-A9FW-01A-11D-A36X-10 chr5:110409264 G>T maps to NM_033035.4 A91A. 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-3K-AAZ8-01A-12D-A38X-10 chr2:122522837 C>T maps to NM_004622.2 R194R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZS-A9CF-01A-11D-A382-10 chr1:231700449 T>C maps to NM_005999.2 V224V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr12:31132604 T>C maps to NM_001080509.2 D152D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1ED-01A-11D-A152-10 chr10:71255354 T>C maps to NM_012339.3 I121I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CJ-01A-11D-A20W-10 chr12:58140373 A>G maps to NM_005981.3 T105T. 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-2Y-A9GT-01A-11D-A382-10 chr11:850321 C>T maps to ENST00000409531 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAEA-01A-11D-A40R-10 chr11:862547 A>G did not map to a codon.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr4:99407999 G>T maps to NM_005723.3 L56L. 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-EP-A2KB-01A-11D-A183-10 chr6:41011696 C>T maps to NM_001159726.1 L112L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MB-01A-11D-A20W-10 chr23:53115033 T>C did not map to a codon.
Sequencing variant TCGA-DD-A1ED-01A-11D-A152-10 chr23:53114957 T>C did not map to a codon.
Sequencing variant TCGA-DD-A3A1-01A-11D-A20W-10 chr23:53115070 T>C did not map to a codon.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr23:53114010 C>T did not map to a codon.
Sequencing variant TCGA-XR-A8TF-01A-11D-A35Z-10 chr23:53112111 G>A did not map to a codon.
Sequencing variant TCGA-ZS-A9CE-01A-11D-A36X-10 chr23:53115088 T>A did not map to a codon.
Sequencing variant TCGA-DD-A3A1-01A-11D-A20W-10 chr6:116574325 C>T maps to ENST00000368611 L332L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1ED-01A-11D-A152-10 chr8:98288872 A>G maps to NM_033512.2 G400G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACL-01A-11D-A40R-10 chr2:54483165 A>G maps to NM_001003937.2 D41D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAC8-01A-11D-A40R-10 chr2:3358334 T>A maps to ENST00000398659 K38*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAE3-01A-11D-A40R-10 chr2:3193107 T>G maps to ENST00000398659 L414L. 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.
Multiple mappings detected for codon TCGA-ES-A2HS-01A-11D-A183-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-DD-AACA-01A-11D-A40R-10 chr22:37407301 A>G maps to NM_003312.4 D220D. 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-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-DD-A39X-01A-11D-A20W-10 chr6:43250733 A>G maps to NM_032538.1 E752E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAW2-01A-11D-A40P-10 chr6:43222807 C>T maps to NM_032538.1 R200*. 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-GJ-A9DB-01A-11D-A36X-10 chr6:43222833 C>T maps to NM_032538.1 V208V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZP-A9D1-01A-11D-A382-10 chr6:43226799 T>A maps to NM_032538.1 P347P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADY-01A-11D-A40R-10 chr1:231044766 C>T did not map to a codon.
Sequencing variant TCGA-DD-AAD1-01A-11D-A40R-10 chr3:180320102 C>T maps to NM_133462.3 L18L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WX-AA47-01A-11D-A38X-10 chr3:180328328 A>G maps to NM_133462.3 *771*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EG-01A-11D-A20W-10 chr9:130492951 T>C maps to NM_144965.1 A630A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACC-01A-11D-A40R-10 chr17:15903432 G>T maps to NM_017775.2 A183A. 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-DD-A1EE-01A-11D-A12Z-10 chr3:39171741 G>T maps to ENST00000301819 E746*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAD0-01A-11D-A40R-10 chr3:39159607 C>T maps to ENST00000301819 T255T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACQ-01A-11D-A40R-10 chr2:166781089 G>C maps to NM_024753.3 V495V. 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-AAD8-01A-11D-A40R-10 chr1:156555547 T>A maps to NM_001105669.2 A500A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAEE-01A-11D-A40R-10 chr7:138849980 G>T did not map to a codon.
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-CC-A3MB-01A-11D-A20W-10 chr4:147860978 A>G maps to ENST00000513335 P49P. 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-DD-AAD0-01A-11D-A40R-10 chr4:147724828 G>A maps to ENST00000513335 Y396Y. 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-DD-AADF-01A-11D-A40R-10 chr21:38567974 G>A did not map to a codon.
Sequencing variant TCGA-DD-AADF-01A-11D-A40R-10 chr21:38567996 G>T maps to NM_003316.3 E1747*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr2:74719855 C>A maps to NM_022492.4 C415*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EG-01A-11D-A20W-10 chr8:109468099 A>G did not map to a codon.
Sequencing variant TCGA-G3-A3CG-01A-11D-A20W-10 chr9:15177726 T>C maps to NM_152574.2 Q603Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A8HT-01A-11D-A35Z-10 chr18:21660786 G>A maps to NM_001135993.1 V233V. 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-4R-AA8I-01A-11D-A382-10 chr14:20757847 T>A maps to NM_138376.2 K421*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr14:91155975 C>T maps to NM_001010854.1 P286P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADS-01A-11D-A40R-10 chr14:91044611 T>A maps to NM_001010854.1 T716T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr14:91142947 G>T maps to NM_001010854.1 I357I. 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-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-DD-AADN-01A-11D-A40R-10 chr2:113277999 T>A maps to NM_153712.4 A339A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACW-01A-11D-A40R-10 chr22:43464504 C>T maps to NM_012263.4 K138K. 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-DD-AAD5-01A-11D-A40R-10 chr1:1119314 G>A maps to NM_001130045.1 P368P. Only missense variants will be evaluated by CHASM.
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-4R-AA8I-01A-11D-A382-10 chr6:167754935 G>A maps to NM_031949.4 T516T. 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-DD-AADN-01A-11D-A40R-10 chr3:9876554 T>C maps to NM_001025930.3 D772D. 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-DD-AADR-01A-11D-A40R-10 chr1:84386927 A>G did not map to a codon.
Sequencing variant TCGA-5R-AAAM-01A-12D-A40R-10 chr20:30510824 G>A maps to NM_001008409.2 Q211Q. Only missense variants will be evaluated by CHASM.
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-2V-A95S-01A-11D-A36X-10 chr2:179479397 G>A maps to NM_133378.4 T13713T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9GZ-01A-11D-A38X-10 chr2:179632560 T>C maps to NM_133378.4 G3132G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9H3-01A-11D-A382-10 chr2:179417551 C>T maps to NM_133378.4 V27457V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9H8-01A-11D-A38X-10 chr2:179567284 C>T maps to NM_133378.4 W8866*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3K-AAZ8-01A-12D-A38X-10 chr2:179424989 A>G maps to NM_133378.4 Y26055Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5R-AAAM-01A-12D-A40R-10 chr2:179436586 G>A maps to NM_133378.4 Q22190*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A3KG-01A-11D-A20W-10 chr2:179596302 T>C maps to NM_133378.4 P4486P. 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-A39Z-01A-11D-A20W-10 chr2:179640605 T>C maps to NM_133378.4 E1995E. 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-DD-AAC8-01A-11D-A40R-10 chr2:179575488 A>T maps to NM_133378.4 I8201I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAC8-01A-11D-A40R-10 chr2:179612799 A>T maps to ENST00000375038 L4778*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACZ-01A-11D-A40R-10 chr2:179438249 A>T maps to NM_133378.4 Y21635*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAD8-01A-11D-A40R-10 chr2:179407204 C>T maps to NM_133378.4 L29858L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADF-01A-11D-A40R-10 chr2:179560619 T>A maps to NM_133378.4 V9149V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADR-01A-11D-A40R-10 chr2:179474546 C>A maps to NM_133378.4 L14633L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAE7-01A-11D-A40R-10 chr2:179583265 A>G maps to NM_133378.4 V6945V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAW3-01A-11D-A40P-10 chr2:179427082 A>G maps to NM_133378.4 L25358L. 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-ED-A8O5-01A-11D-A35Z-10 chr2:179639714 A>T maps to NM_133378.4 A2241A. 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-EP-A2KB-01A-11D-A183-10 chr2:179476168 T>C maps to NM_133378.4 R14361R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr2:179647563 G>T maps to NM_133378.4 T1023T. 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-G3-AAV2-01A-11D-A36X-10 chr2:179413256 A>G maps to NM_133378.4 S28464S. 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-K7-AAU7-01A-11D-A382-10 chr2:179571275 G>A maps to NM_133378.4 N8531N. 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-ZS-A9CE-01A-11D-A36X-10 chr2:179422456 G>T maps to NM_133378.4 Y26640*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZS-A9CF-01A-11D-A382-10 chr2:179479289 A>T maps to NM_133378.4 T13749T. 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-DD-AAE2-01A-11D-A40R-10 chr20:43108746 A>T maps to NM_024331.3 T36T. 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-DD-AADM-01A-11D-A40R-10 chr19:54947006 G>A did not map to a codon.
Sequencing variant TCGA-DD-AAEK-01A-11D-A40R-10 chr7:2687141 C>A maps to NM_025250.2 R166R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZP-A9CY-01A-11D-A382-10 chr7:2689554 C>T maps to NM_025250.2 S268S. 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-DD-AAE9-01A-11D-A40R-10 chr2:130951584 G>T maps to NM_207312.2 S277*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A9FW-01A-11D-A36X-10 chr2:220115163 G>A maps to NM_006000.1 S419S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A66X-01A-11D-A30V-10 chr19:6495426 C>T maps to NM_006087.2 L361L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-AAV3-01A-11D-A36X-10 chr19:6496155 G>A maps to NM_006087.2 D118D. 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-2Y-A9GU-01A-11D-A382-10 chr10:135094883 G>A maps to NM_006659.2 I822I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAEI-01A-11D-A40R-10 chr10:135098647 G>A maps to NM_006659.2 L655L. 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-ZP-A9CV-01A-11D-A382-10 chr10:135101695 C>T maps to NM_006659.2 A553A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A0-01A-11D-A20W-10 chr13:113170853 T>C maps to NM_006322.4 R662R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr13:113174217 C>T maps to NM_006322.4 L621L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WQ-A9G7-01A-11D-A36X-10 chr13:113212589 G>A maps to NM_006322.4 S156S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr15:22873208 T>C maps to NM_052903.4 S1012S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9HA-01A-11D-A38X-10 chr22:50656995 G>A maps to NM_020461.3 S1625S. 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-5C-AAPD-01A-21D-A38X-10 chr1:151546816 G>T maps to NM_020127.2 V222V. 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-CC-A8HT-01A-11D-A35Z-10 chr11:62344400 C>A maps to NM_022830.2 V491V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADE-01A-11D-A40R-10 chr11:62343404 G>A maps to NM_022830.2 Q634*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9H0-01A-11D-A382-10 chr18:9399523 A>T maps to NM_020648.5 *224L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5C-A9VG-01A-11D-A36X-10 chr6:139609801 T>A maps to ENST00000358430 K79*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A3KG-01A-11D-A20W-10 chr6:139576757 T>C maps to ENST00000358430 A340A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr16:11785662 T>C maps to ENST00000356957 P488P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACC-01A-11D-A40R-10 chr17:6545139 A>G maps to NM_032731.3 V71V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAW2-01A-11D-A40P-10 chr18:9886754 A>C maps to NM_001098529.1 S93S. 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-DD-AAC8-01A-11D-A40R-10 chr7:37936558 A>T maps to NM_016616.4 A544A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LG-A9QC-01A-11D-A36X-10 chr7:37903053 T>C maps to NM_016616.4 C148C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A7SF-01A-11D-A34Z-10 chr7:37890295 A>T maps to NM_016616.4 K53*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACD-01A-11D-A40R-10 chr18:54291665 T>A maps to NM_004786.2 S74S. Only missense variants will be evaluated by CHASM.
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-WX-AA46-01A-11D-A38X-10 chr11:88924398 C>T maps to NM_000372.4 N283N. 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-2Y-A9H9-01A-21D-A38X-10 chr10:71905793 G>C maps to NM_173555.2 G183G. 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-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-DD-AACG-01A-11D-A40R-10 chr23:47065413 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-DD-AAVP-01A-11D-A40R-10 chr19:34925842 G>A maps to NM_005499.2 G143G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-AAV6-01A-21D-A36X-10 chr19:18684551 C>T maps to NM_003333.3 Q62*. Only missense variants will be evaluated by CHASM.
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-DD-AACW-01A-11D-A40R-10 chr9:138838154 C>A maps to NM_016172.2 A168A. 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-2Y-A9H6-01A-11D-A38X-10 chr9:33932568 C>T maps to NM_018449.2 T722T. 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-5C-A9VH-01A-11D-A36X-10 chr1:154201143 C>T maps to NM_014847.3 D74D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MB-01A-11D-A20W-10 chr21:43829671 A>G maps to NM_018961.2 R103R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZS-A9CG-01A-11D-A36X-10 chr11:122671896 T>G maps to NM_032873.4 G484G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAW0-01A-11D-A40R-10 chr12:125397888 C>A maps to NM_021009.5 L143L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LG-A9QD-01A-11D-A382-10 chr12:125397156 G>A maps to NM_021009.5 T387T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WQ-A9G7-01A-11D-A36X-10 chr6:29523919 T>A maps to NM_006398.3 K79*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MA-01A-11D-A20W-10 chr10:60123366 A>G did not map to a codon.
Sequencing variant TCGA-CC-5259-01A-31D-A20W-10 chr4:103722608 A>C did not map to a codon.
Sequencing variant TCGA-DD-AADO-01A-11D-A40R-10 chr3:23932095 A>G maps to NM_003341.3 *194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACP-01A-11D-A40R-10 chr2:238925259 T>C maps to NM_080678.1 D89D. 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-G3-A3CJ-01A-11D-A20W-10 chr11:57327821 A>G maps to NM_004223.3 A37A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr1:154527246 G>A maps to NM_017582.6 D184D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9GZ-01A-11D-A38X-10 chr15:76191766 G>A did not map to a codon.
Sequencing variant TCGA-DD-AACZ-01A-11D-A40R-10 chr15:76183288 G>C maps to NM_173469.2 S321S. 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-DD-AAC8-01A-11D-A40R-10 chr1:64676460 T>A maps to ENST00000371077 L93*. 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-2Y-A9H1-01A-11D-A382-10 chr12:109959356 G>T did not map to a codon.
Sequencing variant TCGA-DD-AACL-01A-11D-A40R-10 chr12:109968391 A>T maps to NM_183415.1 R951*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BD-A3ER-01A-11D-A20W-10 chr7:156974969 T>C maps to NM_014671.2 G313G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAEA-01A-11D-A40R-10 chr7:157013402 A>T maps to NM_014671.2 P645P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACQ-01A-11D-A40R-10 chr11:118245933 A>T maps to NM_004788.2 V487V. 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-WX-AA44-01A-11D-A38X-10 chr11:118242362 C>T maps to NM_004788.2 F181F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr1:10190865 G>T maps to NM_001105562.2 G636*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAE3-01A-11D-A40R-10 chr16:23578363 G>T maps to ENST00000219638 E489*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADY-01A-11D-A40R-10 chr23:153714301 C>T did not map to a codon.
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-DD-A3A1-01A-11D-A20W-10 chr7:138944068 A>G maps to NM_173569.3 E286E. 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-DD-A39Y-01A-11D-A20W-10 chr9:86284242 C>T did not map to a codon.
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-2V-A95S-01A-11D-A36X-10 chr1:156021614 G>A maps to NM_020131.3 Q48*. 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-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-CC-A8HU-01A-11D-A35Z-10 chr1:19455516 A>C maps to ENST00000375267 P2986P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A9FW-01A-11D-A36X-10 chr1:19490751 G>A maps to ENST00000375267 S1565S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACK-01A-11D-A40R-10 chr1:19464664 C>A maps to ENST00000375267 R2914R. 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-DD-AACG-01A-11D-A40R-10 chr1:20517359 A>G maps to NM_152376.3 Q102Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr1:26609380 C>T maps to NM_183008.2 T375T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr2:24199876 C>A maps to NM_181713.3 T73T. Only missense variants will be evaluated by CHASM.
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-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-G3-A3CJ-01A-11D-A20W-10 chr13:76143593 A>G did not map to a codon.
Sequencing variant TCGA-DD-AACW-01A-11D-A40R-10 chr1:192992058 G>T maps to ENST00000367450 Y320*. 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-DD-AAD8-01A-11D-A40R-10 chr4:141481161 A>T maps to NM_021833.4 L271*. 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-GJ-A3OU-01A-31D-A382-10 chr2:128877938 C>T maps to NM_020120.3 H294H. 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-ES-A2HT-01A-12D-A183-10 chr13:96530058 C>A maps to NM_020121.3 G1094*. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-G3-A3CG-01A-11D-A20W-10. Mapping will be selected arbitrarily.
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-BC-A3KG-01A-11D-A20W-10 chr2:64112779 A>G maps to NM_006759.3 S211S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACU-01A-11D-A40R-10 chr2:64112929 G>A maps to NM_006759.3 L261L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAEE-01A-11D-A40R-10 chr2:64109685 T>C maps to NM_006759.3 N114N. 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-WJ-A86L-01A-12D-A45V-10 chr2:234580747 T>C maps to ENST00000373460 V56V. 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-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-DD-AADS-01A-11D-A40R-10 chr4:69962792 A>G maps to NM_001074.2 G185G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EE-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-EP-A2KB-01A-11D-A183-10 chr12:100441350 A>G maps to NM_015054.1 H1346H. 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 chr9:6481675 A>G maps to NM_152896.1 E398E. 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-EP-A2KA-01A-11D-A183-10 chr5:176396708 T>C did not map to a codon.
Sequencing variant TCGA-DD-A1ED-01A-11D-A152-10 chr17:19705088 C>A did not map to a codon.
Sequencing variant TCGA-LG-A9QD-01A-11D-A382-10 chr15:75130666 C>A maps to NM_001099436.1 E396*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9H8-01A-11D-A38X-10 chr3:41607591 G>A maps to NM_017886.2 T1050T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MB-01A-11D-A20W-10 chr3:41439686 A>G maps to NM_017886.2 Y1187Y. Only missense variants will be evaluated by CHASM.
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-CC-A7IE-01A-21D-A382-10 chr21:43531614 G>A maps to NM_173568.3 Q761Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BD-A3ER-01A-11D-A20W-10 chr19:17756597 G>A maps to ENST00000428389 D835D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39Y-01A-11D-A20W-10 chr19:17758257 T>C maps to ENST00000428389 T708T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACP-01A-11D-A40R-10 chr19:17759294 G>A maps to ENST00000428389 C675C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr9:35399262 C>A maps to ENST00000396787 P1323P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr9:35389937 A>G maps to ENST00000396787 E993E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAC8-01A-11D-A40R-10 chr9:35403467 A>T maps to ENST00000396787 T1485T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XR-A8TF-01A-11D-A35Z-10 chr9:35399445 G>A did not map to a codon.
Sequencing variant TCGA-BC-A10T-01A-11D-A12Z-10 chr15:54435881 G>A did not map to a codon.
Sequencing variant TCGA-CC-A9FW-01A-11D-A36X-10 chr15:54305559 A>C maps to ENST00000260323 R154R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr15:54529884 A>G maps to ENST00000260323 E1075E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EE-01A-11D-A12Z-10 chr15:54592571 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-DD-AACL-01A-11D-A40R-10 chr15:54919023 A>T did not map to a codon.
Sequencing variant TCGA-DD-AAVX-01A-11D-A40R-10 chr15:54542553 C>T maps to ENST00000260323 G1120G. 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-ZP-A9D1-01A-11D-A382-10 chr15:54305888 A>G maps to ENST00000260323 L263L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZS-A9CG-01A-11D-A36X-10 chr15:54305885 A>G maps to ENST00000260323 E262E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9H1-01A-11D-A382-10 chr17:73831522 C>A maps to ENST00000412096 L605L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr15:91491924 G>A maps to NM_018671.3 L593L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAC9-01A-11D-A40R-10 chr15:91493442 C>T maps to NM_018671.3 A711A. 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-DD-AAEE-01A-11D-A40R-10 chr6:41002765 C>T maps to NM_173561.2 L16L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A3KG-01A-11D-A20W-10 chr8:35606081 G>T maps to ENST00000416672 E607*. 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-AAE7-01A-11D-A40R-10 chr8:35579902 A>T maps to ENST00000416672 T436T. Only missense variants will be evaluated by CHASM.
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-EP-A2KB-01A-11D-A183-10 chr17:73811296 T>C maps to NM_001080419.1 C384C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XR-A8TC-01A-11D-A35Z-10 chr17:73808616 G>A maps to NM_001080419.1 A267A. 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-AAV5-01A-11D-A36X-10 chr13:115067259 A>G maps to NM_023011.2 Q354Q. Only missense variants will be evaluated by CHASM.
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-AACT-01A-11D-A40R-10 chr3:118906776 A>G maps to NM_006952.3 L75L. 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-5C-A9VH-01A-11D-A36X-10 chr23:74494409 G>T did not map to a codon.
Sequencing variant TCGA-CC-A7IJ-01A-11D-A33Q-10 chr23:74494411 C>T did not map to a codon.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr20:33981954 T>C maps to NM_018244.4 R23R. Only missense variants will be evaluated by CHASM.
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-NI-A8LF-01A-11D-A35Z-10 chr7:43921550 C>A maps to NM_001077663.1 E40*. 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-DD-AAD0-01A-11D-A40R-10 chr1:161011956 A>C maps to NM_007122.3 T75T. 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-CC-A3MB-01A-11D-A20W-10 chr11:17522670 T>C maps to NM_153676.3 E769E. 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-DD-AACJ-01A-11D-A40R-10 chr17:72916456 G>A maps to NM_173477.2 H158H. 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-BC-A10W-01A-11D-A12Z-10 chr1:216373308 G>T maps to ENST00000366943 I1157I. 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-AACP-01A-11D-A40R-10 chr1:216420461 G>A maps to ENST00000366943 F758F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAED-01A-12D-A40R-10 chr1:216011439 T>C maps to ENST00000366943 E3088E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAW2-01A-11D-A40P-10 chr1:216019199 G>A maps to ENST00000366943 N3007N. 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-A5SK-01A-11D-A27I-10 chr1:215960063 T>C maps to ENST00000366943 S3445S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A1-01A-11D-A20W-10 chr10:105152184 G>T maps to NM_032747.2 Y10*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5R-AAAM-01A-12D-A40R-10 chr16:84778401 T>C maps to NM_005153.2 T105T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADL-01A-11D-A40R-10 chr16:84779046 A>G maps to NM_005153.2 A320A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A97K-01A-21D-A382-10 chr23:47104421 G>A did not map to a codon.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr23:47098822 G>A did not map to a codon.
Sequencing variant TCGA-DD-A3A0-01A-11D-A20W-10 chr13:27679960 A>G maps to NM_182488.3 L84L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr3:179448451 G>A maps to NM_003940.2 P403P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A3KG-01A-11D-A20W-10 chr12:62696640 T>C maps to ENST00000280377 G96G. 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-2Y-A9GZ-01A-11D-A38X-10 chr21:30409651 T>C maps to NM_006447.2 S168S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACG-01A-11D-A40R-10 chr11:119243743 A>G maps to NM_004205.4 D149D. 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-4R-AA8I-01A-11D-A382-10 chr9:132637021 C>T maps to NM_001008563.3 H636H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADQ-01A-11D-A40R-10 chr9:132638407 G>T did not map to a codon.
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-ES-A2HT-01A-12D-A183-10 chr1:161134676 T>C maps to NM_012475.4 G479G. 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-DD-AACM-01A-11D-A40R-10 chr17:20919116 G>A maps to ENST00000455117 D330D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAW1-01A-11D-A40P-10 chr17:20908263 C>T maps to ENST00000455117 T522T. 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-DD-AAD1-01A-11D-A40R-10 chr1:55619848 T>G maps to NM_015306.2 A585A. 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-DD-AACI-01A-11D-A40R-10 chr23:132161578 A>G did not map to a codon.
Sequencing variant TCGA-WX-AA44-01A-11D-A38X-10 chr23:132160216 T>A did not map to a codon.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr11:113694376 A>G maps to NM_020886.2 C411C. Only missense variants will be evaluated by CHASM.
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-A1ED-01A-11D-A152-10 chr12:109522827 A>G maps to NM_032663.3 P413P. 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-DD-AACI-01A-11D-A40R-10 chr16:23083411 C>A maps to NM_020718.3 S814S. 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-DD-AAEI-01A-11D-A40R-10 chr2:61632842 C>T maps to NM_014709.3 E184E. 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-2Y-A9H2-01A-12D-A382-10 chr2:219374705 G>A maps to NM_020935.2 Q341*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A0-01A-11D-A20W-10 chr2:219353044 A>G maps to NM_020935.2 S524S. 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-A39Y-01A-11D-A20W-10 chr4:144135648 T>C maps to NM_032557.5 Y840Y. 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-DD-A1EE-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-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-2Y-A9H8-01A-11D-A38X-10 chr7:6150811 T>C maps to ENST00000404835 Y16Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADR-01A-11D-A40R-10 chr7:6189722 G>A maps to ENST00000404835 V632V. 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-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-G3-A3CJ-01A-11D-A20W-10 chr17:9586140 T>C maps to NM_153210.3 A369A. 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-DD-AACI-01A-11D-A40R-10 chr11:11944272 A>G maps to ENST00000399455 K414K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GJ-A9DB-01A-11D-A36X-10 chr6:41774614 C>T maps to ENST00000373009 W36*. 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-2Y-A9GU-01A-11D-A382-10 chr23:55514721 A>G did not map to a codon.
Sequencing variant TCGA-DD-A3A0-01A-11D-A20W-10 chr23:55514364 A>G did not map to a codon.
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-DD-AADU-01A-11D-A40R-10 chr17:5041491 C>T maps to NM_004505.2 N334N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MA-01A-11D-A20W-10 chr16:9009381 A>G maps to NM_003470.2 L303L. 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-DD-AAEA-01A-11D-A40R-10 chr15:50757316 A>T maps to NM_005154.3 R205R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3MA-01A-11D-A20W-10 chr23:41088998 A>G did not map to a codon.
Sequencing variant TCGA-DD-A39Y-01A-11D-A20W-10 chr23:41075803 A>G did not map to a codon.
Sequencing variant TCGA-DD-AACD-01A-11D-A40R-10 chr23:41048570 G>A did not map to a codon.
Sequencing variant TCGA-DD-AADE-01A-11D-A40R-10 chr23:41075385 G>T 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-ZS-A9CE-01A-11D-A36X-10 chr23:41022047 G>T did not map to a codon.
Sequencing variant TCGA-BD-A3ER-01A-11D-A20W-10 chr24:14885658 G>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-A2QR-01A-11D-A20W-10 chr24:14928277 A>G did not map to a codon.
Sequencing variant TCGA-FV-A2QR-01A-11D-A20W-10 chr24:14951988 A>G 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-DD-AACZ-01A-11D-A40R-10 chr13:31205171 A>G maps to NM_005800.4 G143G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A1-01A-11D-A20W-10 chr23:129055251 A>G did not map to a codon.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr5:72864402 C>T maps to NM_032175.2 P114P. Only missense variants will be evaluated by CHASM.
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-DD-AACQ-01A-11D-A40R-10 chr12:101745843 A>T maps to NM_014503.2 I1632I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr12:101736357 G>T maps to NM_014503.2 T1412T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr12:101685545 A>G maps to NM_014503.2 K306K. 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-DD-AAD6-01A-11D-A40R-10 chr6:144808682 G>T did not map to a codon.
Sequencing variant TCGA-DD-AADQ-01A-11D-A40R-10 chr6:144863928 A>G did not map to a codon.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr6:144801075 C>T maps to NM_007124.2 Y1155Y. 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-A39X-01A-11D-A20W-10 chr1:7912997 A>G maps to NM_006786.3 P22P. 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-AAVZ-01A-11D-A40R-10 chr24:15447911 C>T did not map to a codon.
Sequencing variant TCGA-G3-A3CG-01A-11D-A20W-10 chr24:15448105 T>C 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-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-5C-A9VG-01A-11D-A36X-10 chr6:31747208 C>A maps to NM_006295.2 R1131R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WQ-A9G7-01A-11D-A36X-10 chr6:31749893 A>C maps to NM_006295.2 T737T. 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-DD-AADM-01A-11D-A40R-10 chr1:213125027 G>A maps to NM_024749.3 L48L. 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-BC-A112-01A-11D-A12Z-10 chr23:7811708 G>C did not map to a codon.
Sequencing variant TCGA-G3-AAV0-01A-11D-A36X-10 chr5:133326694 G>A maps to NM_003374.2 Q90*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9H0-01A-11D-A382-10 chr10:76980581 A>G maps to NM_001184783.1 G161G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACY-01A-11D-A40R-10 chr6:43746273 G>C did not map to a codon.
Sequencing variant TCGA-G3-AAV0-01A-11D-A36X-10 chr11:64005083 C>G maps to NM_003377.3 S201S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAC8-01A-11D-A40R-10 chr10:135053794 G>A maps to NM_014468.2 T254T. Only missense variants will be evaluated by CHASM.
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-DD-AAED-01A-12D-A40R-10 chr3:156983418 C>A maps to NM_001167912.1 G721*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A3KF-01A-11D-A20W-10 chr17:56056597 T>C maps to NM_007146.2 Q351Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A3KF-01A-11D-A20W-10 chr17:56056600 T>C maps to NM_007146.2 Q350Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A26S-01A-11D-A16V-10 chr17:56056600 T>C maps to NM_007146.2 Q350Q. 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-2Y-A9GU-01A-11D-A382-10 chr23:135632967 C>T did not map to a codon.
Sequencing variant TCGA-2Y-A9H9-01A-21D-A38X-10 chr23:135631013 C>G did not map to a codon.
Sequencing variant TCGA-DD-AAVX-01A-11D-A40R-10 chr6:117589349 A>C maps to NM_182645.2 L29L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr3:10191489 A>G maps to NM_000551.2 R161R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAW0-01A-11D-A40R-10 chr3:38043299 C>T maps to NM_015873.3 S476S. Only missense variants will be evaluated by CHASM.
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-DD-A1EE-01A-11D-A12Z-10 chr19:53761996 C>A maps to NM_173856.2 S123S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GJ-A9DB-01A-11D-A36X-10 chr19:53761894 G>T maps to NM_173856.2 G89G. 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-CC-A3MA-01A-11D-A20W-10 chr9:79834894 C>T maps to ENST00000376646 A260A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EE-01A-11D-A12Z-10 chr9:79824388 C>T maps to ENST00000376646 Q146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADR-01A-11D-A40R-10 chr9:79922964 A>G maps to ENST00000376646 Q1355Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAEA-01A-11D-A40R-10 chr9:79862173 G>T did not map to a codon.
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-YA-A8S7-01A-11D-A36X-10 chr9:79971725 A>G maps to ENST00000376646 E2584E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAD5-01A-11D-A40R-10 chr8:100123342 A>T maps to NM_017890.3 R200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADN-01A-11D-A40R-10 chr8:100127974 A>G maps to NM_017890.3 Q270Q. 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-LG-A9QD-01A-11D-A382-10 chr8:100147861 G>T maps to NM_017890.3 T488T. 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-DD-AADA-01A-11D-A40R-10 chr1:12336578 C>T maps to NM_015378.2 L978L. 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-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-DD-AADN-01A-11D-A40R-10 chr15:41191756 C>T maps to NM_020857.2 L247L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr15:41191111 T>C maps to NM_020857.2 L81L. 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-A3KG-01A-11D-A20W-10 chr10:70917886 T>C maps to NM_004896.3 Y157Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr8:145649443 G>A maps to NM_183057.1 G176G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-AAV3-01A-11D-A36X-10 chr12:122734445 G>C maps to NM_022916.4 L249L. 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-BC-A3KF-01A-11D-A20W-10 chr13:52992176 T>C maps to NM_016075.2 E285E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr11:60899318 C>T maps to NM_017966.4 P347P. 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-EP-A2KA-01A-11D-A183-10 chr7:38798050 C>A maps to NM_014396.3 G485*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr7:38781710 A>G maps to NM_014396.3 T711T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5C-A9VH-01A-11D-A36X-10 chr1:150053491 G>T maps to NM_007259.3 V252V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr18:61071041 G>A maps to NM_004869.3 R128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XR-A8TG-01A-11D-A35Z-10 chr18:61067936 C>A did not map to a codon.
Sequencing variant TCGA-DD-AACC-01A-11D-A40R-10 chr6:33231841 G>A maps to NM_022553.4 V521V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WQ-A9G7-01A-11D-A36X-10 chr6:33239412 G>A maps to NM_022553.4 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr17:526907 T>C maps to NM_001128159.2 E327E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9GY-01A-11D-A382-10 chr2:64189526 A>C maps to NM_016516.2 S225S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADC-01A-11D-A40R-10 chr2:64176271 A>G maps to NM_016516.2 L346L. 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-DD-AAVV-01A-11D-A40R-10 chr2:58386636 A>C maps to NM_001130480.2 R446R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GJ-A3OU-01A-31D-A382-10 chr2:58276007 A>G maps to NM_001130480.2 P14P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EE-01A-11D-A12Z-10 chr19:50482383 T>C maps to NM_016440.3 P464P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAE6-01A-11D-A40R-10 chr12:118506350 C>T maps to NM_019086.5 E466E. 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-XR-A8TC-01A-11D-A35Z-10 chr23:65242304 T>A did not map to a codon.
Sequencing variant TCGA-G3-AAV2-01A-11D-A36X-10 chr1:159826323 C>G maps to NM_001013661.1 V254V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACI-01A-11D-A40R-10 chr19:54545062 A>G maps to NM_198481.3 D187D. Only missense variants will be evaluated by CHASM.
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-AACC-01A-11D-A40R-10 chr14:74726417 C>A maps to NM_182894.2 P231P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr14:74706311 A>G maps to NM_182894.2 T16T. 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-AAE6-01A-11D-A40R-10 chr1:1372592 C>T maps to NM_022834.4 A120A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr10:116045926 C>T maps to NM_198496.1 S409S. 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-2Y-A9GT-01A-11D-A382-10 chr2:98779439 G>A did not map to a codon.
Sequencing variant TCGA-DD-AACS-01A-11D-A40R-10 chr2:98852883 G>T maps to NM_144992.4 L820L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAVZ-01A-11D-A40R-10 chr2:98887261 C>A maps to NM_144992.4 I987I. 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-AAVQ-01A-11D-A40R-10 chr11:123989360 C>T maps to NM_014622.4 S197S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CG-01A-11D-A20W-10 chr11:124013280 T>A did not map to a codon.
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-4R-AA8I-01A-11D-A382-10 chr12:6128577 G>A maps to NM_000552.3 R1336*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAW3-01A-11D-A40P-10 chr12:6128398 C>A maps to NM_000552.3 R1395R. 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-ZS-A9CE-01A-11D-A36X-10 chr12:6230346 C>T maps to NM_000552.3 S71S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAW0-01A-11D-A40R-10 chr10:28897313 G>A maps to NM_016628.3 T373T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EG-01A-11D-A20W-10 chr10:88230751 A>G maps to ENST00000342368 H798H. Only missense variants will be evaluated by CHASM.
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-DD-AAE9-01A-11D-A40R-10 chr13:27255211 G>A maps to NM_006646.5 T246T. 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-A3CG-01A-11D-A20W-10 chr12:14954257 T>C maps to NM_016312.2 Q20Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1ED-01A-11D-A152-10 chr7:71142269 G>A maps to NM_022479.1 P493P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACK-01A-11D-A40R-10 chr7:71130559 A>T maps to NM_022479.1 I415I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr7:73108371 C>A maps to ENST00000423497 T231T. 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-ES-A2HS-01A-11D-A183-10 chr2:224760296 C>A maps to NM_020830.3 G217*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A3KG-01A-11D-A20W-10 chr13:52301855 A>G maps to NM_052950.3 S176S. 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-DD-AAVY-01A-11D-A40R-10 chr4:85663027 T>C maps to NM_014991.4 V2040V. 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-CC-A3MB-01A-11D-A20W-10 chr4:10090366 T>C did not map to a codon.
Sequencing variant TCGA-DD-A1EG-01A-11D-A20W-10 chr10:122643321 A>G maps to NM_018117.11 K590K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr23:48458001 A>G did not map to a codon.
Sequencing variant TCGA-DD-A39Y-01A-11D-A20W-10 chr23:48457999 T>C did not map to a codon.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr23:48458756 T>C did not map to a codon.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr17:9490133 A>G maps to NM_145054.4 G130G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CJ-01A-11D-A20W-10 chr17:9489225 C>T maps to NM_145054.4 C69C. 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-5C-A9VH-01A-11D-A36X-10 chr4:39280266 G>C maps to NM_025132.3 L1342L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5R-AAAM-01A-12D-A40R-10 chr4:39229945 C>T maps to NM_025132.3 Y582Y. 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-ZP-A9D1-01A-11D-A382-10 chr4:39201125 A>G maps to NM_025132.3 G145G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr14:102675271 C>T maps to ENST00000454394 H286H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAD1-01A-11D-A40R-10 chr16:735409 C>T maps to ENST00000248142 A752A. 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-DD-A1EG-01A-11D-A20W-10 chr2:128477144 T>C maps to NM_018383.4 G818G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACD-01A-11D-A40R-10 chr2:128466454 C>A maps to NM_018383.4 E1193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr2:20133273 T>C did not map to a codon.
Sequencing variant TCGA-DD-AAD2-01A-11D-A40R-10 chr5:110445991 C>T maps to NM_139281.2 G533G. 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-WQ-A9G7-01A-11D-A36X-10 chr5:110456745 T>C maps to NM_139281.2 Y741Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39Y-01A-11D-A20W-10 chr9:127619899 T>C maps to NM_001045476.1 P312P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9GY-01A-11D-A382-10 chr21:44272434 C>A did not map to a codon.
Sequencing variant TCGA-DD-A3A0-01A-11D-A20W-10 chr21:44282501 A>G maps to NM_018669.4 A152A. Only missense variants will be evaluated by CHASM.
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-DD-AAE7-01A-11D-A40R-10 chr23:117570750 T>A did not map to a codon.
Sequencing variant TCGA-2Y-A9HA-01A-11D-A38X-10 chr23:48932925 C>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-DD-AA3A-01A-11D-A36X-10 chr23:48934305 G>A did not map to a codon.
Sequencing variant TCGA-DD-AACI-01A-11D-A40R-10 chr23:48935319 T>A did not map to a codon.
Sequencing variant TCGA-DD-A39W-01A-11D-A20W-10 chr17:80576975 G>C maps to NM_019613.3 S216*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5C-AAPD-01A-21D-A38X-10 chr1:109538416 G>C maps to NM_001142550.1 G500G. 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-DD-AAC8-01A-11D-A40R-10 chr9:137023030 A>T maps to NM_052821.3 T307T. 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-DD-AAD5-01A-11D-A40R-10 chr3:122133742 A>G maps to NM_019069.3 P211P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr3:49049707 G>T maps to NM_018031.3 R277R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr3:49051270 A>G maps to NM_018031.3 T798T. 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-DD-AAE4-01A-11D-A40R-10 chr7:158734819 C>T maps to NM_018051.4 Q995*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAW2-01A-11D-A40P-10 chr7:158718938 G>T maps to NM_018051.4 T773T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACZ-01A-11D-A40R-10 chr19:36545926 G>A maps to NM_001083961.1 L18L. 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-DD-AACY-01A-11D-A40R-10 chr1:85537688 G>A did not map to a codon.
Sequencing variant TCGA-DD-AAE7-01A-11D-A40R-10 chr1:85551545 A>G maps to NM_145172.3 E191E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9GU-01A-11D-A382-10 chr1:241958511 C>T maps to NM_144625.4 R991*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9HB-01A-11D-A38X-10 chr1:241875157 T>G maps to NM_144625.4 V333V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADS-01A-11D-A40R-10 chr1:241912885 G>A maps to NM_144625.4 E534E. 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-CC-A3MA-01A-11D-A20W-10 chr1:43649296 T>C maps to NM_001195831.1 C170C. 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-A7MB-01A-11D-A33Q-10 chr2:228762990 A>T maps to NM_178821.1 A178A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADD-01A-11D-A40R-10 chr15:53992109 G>A maps to NM_182758.2 C534C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-AAV5-01A-11D-A36X-10 chr11:62601896 A>G did not map to a codon.
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-DD-AACL-01A-11D-A40R-10 chr15:44120477 A>T maps to NM_024908.3 K126*. 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-AADD-01A-11D-A40R-10 chr1:111986673 A>C did not map to a codon.
Sequencing variant TCGA-2Y-A9HA-01A-11D-A38X-10 chr1:67371058 C>T did not map to a codon.
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-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-DD-AAE7-01A-11D-A40R-10 chr3:52304770 A>T maps to NM_025222.3 T72T. 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-EP-A2KA-01A-11D-A183-10 chr19:33647425 T>C maps to NM_173479.3 S325S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9H8-01A-11D-A38X-10 chr16:706395 G>A maps to NM_145294.4 T687T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EG-01A-11D-A20W-10 chr16:705304 A>G did not map to a codon.
Sequencing variant TCGA-DD-AADV-01A-11D-A38X-10 chr16:712037 G>T maps to NM_145294.4 E1338*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAVW-01A-11D-A40R-10 chr16:717525 C>T maps to NM_145294.4 S1728S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr16:711768 G>T maps to NM_145294.4 G1282G. 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-DD-A3A1-01A-11D-A20W-10 chr15:90281278 T>C maps to NM_020212.1 Y591Y. 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-2Y-A9H7-01A-11D-A38X-10 chr8:124449501 C>A maps to NM_018024.1 R146R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A2QR-01A-11D-A20W-10 chr7:141420770 G>A maps to NM_001105558.1 V265V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A3KF-01A-11D-A20W-10 chr20:44334543 A>G maps to NM_172005.1 *94W. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAEH-01A-11D-A40R-10 chr20:44417609 G>A maps to NM_080614.1 C57C. 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-2Y-A9H9-01A-21D-A38X-10 chr20:44168000 A>G maps to ENST00000372665 L16L. 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-DD-AADE-01A-11D-A40R-10 chr4:1952824 C>T maps to NM_133335.3 P636P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A0-01A-11D-A20W-10 chr8:38205329 T>C maps to NM_023034.1 R120R. 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-XR-A8TC-01A-11D-A35Z-10 chr8:38146243 G>A maps to NM_023034.1 Q1088*. 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-DD-AACG-01A-11D-A40R-10 chr7:29874405 C>G maps to NM_001080529.1 P22P. 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-CC-A8HT-01A-11D-A35Z-10 chr20:43355821 G>A maps to NM_003881.2 G209G. 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-AADA-01A-11D-A40R-10 chr19:15547668 C>T maps to ENST00000389282 T848T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr19:15533976 G>A maps to ENST00000389282 H1622H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr12:988758 A>G maps to NM_018979.3 V798V. 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-DD-AAE8-01A-11D-A40R-10 chr9:96054795 T>A maps to ENST00000297954 P1720P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr9:96079836 T>C maps to ENST00000297954 R2221R. 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-ZS-A9CG-01A-11D-A36X-10 chr9:96070794 C>T maps to ENST00000297954 L2186L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr23:54321141 A>T did not map to a codon.
Sequencing variant TCGA-BC-A3KG-01A-11D-A20W-10 chr23:54265312 T>C did not map to a codon.
Sequencing variant TCGA-CC-A8HV-01A-11D-A35Z-10 chr23:54275437 C>A did not map to a codon.
Sequencing variant TCGA-DD-A3A0-01A-11D-A20W-10 chr23:54263831 A>G did not map to a codon.
Sequencing variant TCGA-DD-AAVX-01A-11D-A40R-10 chr23:54321101 A>G did not map to a codon.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr23:54335736 C>A did not map to a codon.
Sequencing variant TCGA-DD-AAVS-01A-11D-A40R-10 chr17:40947048 C>A maps to NM_032387.4 P870P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAEH-01A-11D-A40R-10 chr12:49375113 G>T maps to NM_005430.3 R268R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACD-01A-11D-A40R-10 chr12:49364297 G>A maps to NM_003394.3 P5P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9GT-01A-11D-A382-10 chr11:75907728 C>T maps to NM_004626.2 L39L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADO-01A-11D-A40R-10 chr11:75905678 T>A maps to NM_004626.2 K177*. 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-CC-A9FW-01A-11D-A36X-10 chr1:228238390 C>A maps to ENST00000366753 A116A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAC8-01A-11D-A40R-10 chr1:228246856 C>T maps to ENST00000366753 R250R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr3:55508544 C>T maps to NM_003392.3 A168A. 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-A2KA-01A-11D-A183-10 chr22:46319020 T>C maps to NM_058238.2 K255K. 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-G3-A3CG-01A-11D-A20W-10 chr10:102239647 C>T maps to NM_003393.3 S40S. 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-A3CG-01A-11D-A20W-10 chr8:30938673 A>G maps to NM_000553.4 G377G. 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-2Y-A9GX-01A-11D-A382-10 chr12:108603912 C>T maps to ENST00000261400 G171G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EG-01A-11D-A20W-10 chr12:108589989 A>G maps to ENST00000261400 R127R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAE2-01A-11D-A40R-10 chr12:108600075 C>A maps to ENST00000261400 I131I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACI-01A-11D-A40R-10 chr11:32413560 G>T maps to NM_024426.4 S463S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A3KF-01A-11D-A20W-10 chr5:167871521 A>G maps to NM_001161661.1 E819E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACT-01A-11D-A40R-10 chr5:167833200 A>T did not map to a codon.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr5:167835650 C>A maps to NM_001161661.1 S287*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10W-01A-11D-A12Z-10 chr4:184169910 T>C maps to ENST00000448232 I259I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BD-A3EP-01A-11D-A22F-10 chr4:184233491 A>G did not map to a codon.
Sequencing variant TCGA-DD-A1ED-01A-11D-A152-10 chr4:184129211 A>G maps to ENST00000448232 E116E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACJ-01A-11D-A40R-10 chr4:184180882 T>G did not map to a codon.
Sequencing variant TCGA-2Y-A9H1-01A-11D-A382-10 chr23:10096095 G>A did not map to a codon.
Sequencing variant TCGA-DD-A1EE-01A-11D-A12Z-10 chr23:10085258 G>A did not map to a codon.
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-EP-A2KB-01A-11D-A183-10 chr8:87479043 A>G maps to NM_007013.3 P897P. Only missense variants will be evaluated by CHASM.
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-4R-AA8I-01A-11D-A382-10 chr19:7687716 G>A maps to NM_020196.2 S434S. 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-DD-AAVY-01A-11D-A40R-10 chr22:29196385 G>A maps to ENST00000403532 Q43*. 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-DD-A39Z-01A-11D-A20W-10 chr2:31620566 T>C maps to NM_000379.3 R154R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAC8-01A-11D-A40R-10 chr2:31606663 T>A maps to NM_000379.3 P281P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAVP-01A-11D-A40R-10 chr23:2712584 A>G did not map to a codon.
Sequencing variant TCGA-ZP-A9CV-01A-11D-A382-10 chr23:2724765 C>T did not map to a codon.
Sequencing variant TCGA-CC-A3MA-01A-11D-A20W-10 chr23:123020183 T>C did not map to a codon.
Sequencing variant TCGA-DD-A3A1-01A-11D-A20W-10 chr23:123019617 T>C did not map to a codon.
Sequencing variant TCGA-BD-A3ER-01A-11D-A20W-10 chr2:168101984 T>C maps to NM_152381.5 S1361S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A8HT-01A-11D-A35Z-10 chr2:168103205 A>G maps to NM_152381.5 T1768T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADF-01A-11D-A40R-10 chr2:168100736 G>A maps to NM_152381.5 V945V. 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-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-5R-AA1C-01A-11D-A40R-10 chr8:56015587 T>A maps to NM_052898.1 A180A. Only missense variants will be evaluated by CHASM.
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-AACQ-01A-11D-A40R-10 chr8:56436482 C>A maps to NM_052898.1 S550S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CG-01A-11D-A20W-10 chr8:6681154 T>C maps to NM_207411.4 P175P. 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-DD-AACB-01A-11D-A40R-10 chr8:71646298 T>A maps to NM_001011720.1 C254*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NI-A4U2-01A-11D-A28X-10 chr23:128876094 G>T 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-BC-A3KG-01A-11D-A20W-10 chr13:21442810 T>C maps to NM_022459.4 Q33Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr13:21442735 C>T maps to NM_022459.4 L58L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr6:43526265 G>A maps to NM_020750.2 S428S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADO-01A-11D-A40R-10 chr6:43492931 T>C maps to NM_020750.2 L1029L. 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-G3-A3CG-01A-11D-A20W-10 chr6:43530010 C>T maps to NM_020750.2 A328A. 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-DD-A3A1-01A-11D-A20W-10 chr8:21848319 A>G did not map to a codon.
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-FV-A495-01A-11D-A25V-10 chr12:64833061 G>T maps to NM_007235.3 L924L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAD8-01A-11D-A40R-10 chr1:180804014 A>T maps to NM_004736.3 R380R. 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-GJ-A3OU-01A-31D-A382-10 chr3:142030412 A>T maps to NM_019001.3 S1687S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACI-01A-11D-A40R-10 chr20:21362680 G>A maps to NM_012255.3 Q878Q. 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-ES-A2HT-01A-12D-A183-10 chr16:17235218 G>T maps to NM_022166.3 R460R. 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-ES-A2HT-01A-12D-A183-10 chr11:101984898 G>T maps to NM_001130145.2 G116*. 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-2Y-A9H6-01A-11D-A38X-10 chr3:183446489 G>A maps to NM_018023.4 P221P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39X-01A-11D-A20W-10 chr3:183472103 A>G maps to NM_018023.4 S447S. 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-DD-AADW-01A-11D-A38X-10 chr19:38798280 G>T maps to NM_001039672.2 L217L. 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-DD-AAE9-01A-11D-A40R-10 chr6:43480850 G>A maps to ENST00000506469 L214L. Only missense variants will be evaluated by CHASM.
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-A39X-01A-11D-A20W-10 chr14:75265056 T>C maps to NM_019589.2 S1019S. 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-DD-A3A0-01A-11D-A20W-10 chr10:27408355 A>G maps to NM_139312.1 A535A. 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-ES-A2HS-01A-11D-A183-10 chr11:57413534 A>G maps to NM_145008.2 A101A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YA-A8S7-01A-11D-A36X-10 chr2:135763002 A>G did not map to a codon.
Sequencing variant TCGA-DD-AACI-01A-11D-A40R-10 chr4:69198560 T>C maps to NM_001031732.2 S326S. 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-A39Z-01A-11D-A20W-10 chr5:112920154 T>C maps to NM_022828.3 P1268P. 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-A119-01A-11D-A12Z-10 chr20:61835048 A>G maps to NM_017798.3 P81P. 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-NI-A8LF-01A-11D-A35Z-10 chr1:29070164 C>T maps to NM_016258.2 V461V. 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-AADK-01A-11D-A40R-10 chr23:21875451 G>T did not map to a codon.
Sequencing variant TCGA-DD-A3A0-01A-11D-A20W-10 chr2:98351043 C>T maps to NM_001079.3 S317S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr2:98349775 A>G maps to NM_001079.3 T269T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAEB-01A-11D-A40R-10 chr4:48496258 T>G maps to NM_175619.1 *425E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A8HT-01A-11D-A35Z-10 chr3:167083712 T>C maps to ENST00000307529 Q78Q. 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-DD-AAD5-01A-11D-A40R-10 chr23:2408699 C>A did not map to a codon.
Sequencing variant TCGA-XR-A8TF-01A-11D-A35Z-10 chr23:2408473 T>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-DD-AACZ-01A-11D-A40R-10 chr14:64998590 G>A maps to NM_014950.2 G637G. 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-DD-AACB-01A-11D-A40R-10 chr6:31868140 C>T maps to NM_181842.2 G314G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADA-01A-11D-A40R-10 chr6:31868734 C>T maps to NM_181842.2 V116V. 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-4R-AA8I-01A-11D-A382-10 chr3:114070330 G>A maps to NM_001164342.1 G198G. 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-DD-AAE4-01A-11D-A40R-10 chr14:64954456 G>A maps to NM_006977.2 D164D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EG-01A-11D-A20W-10 chr19:36205962 T>C maps to NM_014383.1 P145P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZS-A9CF-01A-11D-A382-10 chr1:173840091 A>G maps to NM_001122770.1 V243V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr3:141162006 A>G maps to NM_001080412.2 K259K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAW1-01A-11D-A40P-10 chr3:141163167 T>C maps to NM_001080412.2 N646N. 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-DD-AAE9-01A-11D-A40R-10 chr17:7366503 A>C maps to NM_020899.3 P599P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACZ-01A-11D-A40R-10 chr1:22837791 A>T maps to NM_014870.3 K652*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACA-01A-11D-A40R-10 chr1:197157557 T>C maps to NM_194314.2 K470K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAD8-01A-11D-A40R-10 chr20:62378585 C>A maps to NM_025224.2 V489V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr1:6642237 C>T maps to NM_005341.2 L271L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACQ-01A-11D-A40R-10 chr1:6641167 A>T maps to NM_005341.2 R167*. 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-AAE6-01A-11D-A40R-10 chr9:37441537 A>G maps to NM_014872.2 P337P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAVY-01A-11D-A40R-10 chr1:154987492 A>G maps to ENST00000417934 P153P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACL-01A-11D-A40R-10 chr18:45566766 T>A maps to NM_001039360.2 K238*. 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-A1EG-01A-11D-A20W-10 chr6:33423128 T>C maps to NM_152735.3 R84R. 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-DD-AAE4-01A-11D-A40R-10 chr23:64722581 T>A did not map to a codon.
Sequencing variant TCGA-DD-AAE4-01A-11D-A40R-10 chr23:64722583 G>A 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-AADO-01A-11D-A40R-10 chr13:46542148 T>A maps to ENST00000242848 R1271*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAVR-01A-11D-A40R-10 chr13:46563045 A>G maps to ENST00000242848 H377H. 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-2V-A95S-01A-11D-A36X-10 chr19:47575378 C>G did not map to a codon.
Sequencing variant TCGA-BD-A3EP-01A-11D-A22F-10 chr19:47575266 C>G maps to NM_015168.1 P638P. 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-DD-AADG-01A-11D-A40R-10 chr19:47587631 G>T maps to NM_015168.1 C396*. 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-AACX-01A-11D-A40R-10 chr22:41723226 G>T maps to ENST00000351589 A101A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CG-01A-11D-A20W-10 chr2:112989435 T>C maps to NM_032494.2 E274E. 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-XR-A8TD-01A-12D-A38X-10 chr7:138764366 A>C maps to ENST00000464606 T440T. 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-ZS-A9CE-01A-11D-A36X-10 chr23:117959256 C>A did not map to a codon.
Sequencing variant TCGA-2Y-A9GX-01A-11D-A382-10 chr16:87445308 C>A maps to NM_015144.2 T869T. 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-DD-AACO-01A-11D-A40R-10 chr4:25314443 A>C maps to NM_024936.2 R5R. Only missense variants will be evaluated by CHASM.
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-G3-A3CG-01A-11D-A20W-10 chr9:37357123 T>C maps to NM_032226.2 R497R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A1-01A-11D-A20W-10 chr12:122958448 A>G maps to NM_017612.2 S573S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADU-01A-11D-A40R-10 chr5:80604840 A>G maps to NM_032280.2 K204K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GJ-A9DB-01A-11D-A36X-10 chr12:42717862 T>A maps to NM_033114.3 V14V. Only missense variants will be evaluated by CHASM.
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-2Y-A9H9-01A-21D-A38X-10 chr2:207171123 A>G maps to NM_020923.1 A624A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr2:207171519 G>A maps to NM_020923.1 P756P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A0-01A-11D-A20W-10 chr2:207162016 T>C maps to NM_020923.1 R36R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACE-01A-11D-A40R-10 chr2:207174807 A>G maps to NM_020923.1 E1852E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr2:207175356 G>A maps to NM_020923.1 W2035*. 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-CC-5264-01A-01D-A12Z-10 chr5:837586 T>A maps to NM_024786.2 K265*. 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-2Y-A9H8-01A-11D-A38X-10 chr23:74644580 A>T did not map to a codon.
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-AAE6-01A-11D-A40R-10 chr8:17043873 A>G maps to NM_016353.4 A64A. 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-DD-A1EG-01A-11D-A20W-10 chr22:20131138 T>C maps to NM_013373.3 S662S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr23:128975900 T>C did not map to a codon.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr23:128947656 C>T did not map to a codon.
Sequencing variant TCGA-ZS-A9CF-01A-11D-A382-10 chr23:128957707 T>A did not map to a codon.
Sequencing variant TCGA-DD-AAE6-01A-11D-A40R-10 chr2:145156638 G>A maps to NM_014795.3 S705S. 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-4R-AA8I-01A-11D-A382-10 chr2:220073040 A>G maps to NM_138802.1 Q166Q. 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-DD-A39Z-01A-11D-A20W-10 chr12:72004492 A>G maps to NM_144982.4 C1938C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADV-01A-11D-A38X-10 chr12:72004330 T>C maps to NM_144982.4 E1949E. 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-DD-AADO-01A-11D-A40R-10 chr16:72991689 A>G maps to NM_006885.3 N785N. 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-G3-A3CJ-01A-11D-A20W-10 chr16:72829728 T>C maps to NM_006885.3 R2284R. 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-DD-AA3A-01A-11D-A36X-10 chr8:77768189 C>T maps to NM_024721.4 L3011L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAD5-01A-11D-A40R-10 chr8:77768444 A>T maps to NM_024721.4 T3096T. 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-WQ-A9G7-01A-11D-A36X-10 chr8:77617093 T>C maps to NM_024721.4 P257P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WQ-A9G7-01A-11D-A36X-10 chr8:77617132 C>T maps to NM_024721.4 S270S. 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-DD-AACL-01A-11D-A40R-10 chr19:36832051 T>A maps to NM_020917.2 K226*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr19:36853128 T>C maps to NM_020917.2 T7T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9H7-01A-11D-A38X-10 chr5:178358991 C>T maps to NM_030613.2 S226S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A97K-01A-21D-A382-10 chr5:178359426 G>T maps to NM_030613.2 V371V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr17:4995558 G>T maps to NM_153018.2 E254*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAEB-01A-11D-A40R-10 chr19:38126046 G>A maps to NM_014898.2 P465P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WQ-AB4B-01A-11D-A40P-10 chr14:69256294 T>G maps to NM_004926.2 S324S. 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-AADG-01A-11D-A40R-10 chr2:43452452 C>A maps to NM_006887.4 E164*. 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-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-DD-AACG-01A-11D-A40R-10 chr20:50781291 G>A maps to NM_018197.2 C151C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAD5-01A-11D-A40R-10 chr20:50803416 A>C maps to NM_018197.2 T80T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A3KG-01A-11D-A20W-10 chr16:68598369 A>G maps to NM_133458.2 K560K. 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-AAE7-01A-11D-A40R-10 chr16:88555559 A>G maps to NM_153813.2 P89P. 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-ZS-A9CF-01A-11D-A382-10 chr8:106331208 C>A maps to NM_012082.3 R14R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAED-01A-12D-A40R-10 chr5:32417840 T>C maps to NM_016107.3 Q159Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A1-01A-11D-A20W-10 chr19:3821456 A>G maps to NM_015174.1 L504L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39X-01A-11D-A20W-10 chr23:24197776 A>T did not map to a codon.
Sequencing variant TCGA-DD-A39X-01A-11D-A20W-10 chr23:24197778 G>T did not map to a codon.
Sequencing variant TCGA-FV-A3I1-01A-11D-A22F-10 chr23:24229377 C>A did not map to a codon.
Sequencing variant TCGA-G3-A3CJ-01A-11D-A20W-10 chr24:2846063 C>T did not map to a codon.
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-4R-AA8I-01A-11D-A382-10 chr3:15116269 C>T maps to NM_022340.2 P458P. 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-DD-AADF-01A-11D-A40R-10 chr14:68219126 T>A maps to NM_015346.3 A2435A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADL-01A-11D-A40R-10 chr14:68256274 C>T maps to NM_015346.3 L932L. 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-G3-A3CG-01A-11D-A20W-10 chr14:68241772 A>G maps to NM_015346.3 P1760P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAVX-01A-11D-A40R-10 chr10:99509254 A>T maps to NM_001002261.3 T192T. 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-ES-A2HS-01A-11D-A183-10 chr4:2306995 G>A maps to NM_020972.2 S357S. 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-DD-A39Z-01A-11D-A20W-10 chr1:52705074 T>C maps to NM_004799.2 L662L. 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-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-CC-A8HV-01A-11D-A35Z-10 chr8:124267097 T>A maps to NM_007222.3 V363V. 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-G3-AAV6-01A-21D-A36X-10 chr20:39832197 C>T maps to NM_015035.3 Q453Q. 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-CC-A8HS-01A-11D-A35Z-10 chr13:100637725 G>T maps to NM_007129.2 A463A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5C-A9VG-01A-11D-A36X-10 chr23:136649429 G>T did not map to a codon.
Sequencing variant TCGA-DD-AAEG-01A-11D-A38X-10 chr23:136649299 A>T did not map to a codon.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr23:136649846 C>A did not map to a codon.
Sequencing variant TCGA-WQ-A9G7-01A-11D-A36X-10 chr23:136648911 C>T did not map to a codon.
Sequencing variant TCGA-DD-AADN-01A-11D-A40R-10 chr3:147113963 G>T maps to NM_001168379.1 R159R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr19:58102153 T>C maps to NM_001010879.2 C325C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RC-A7SH-01A-11D-A382-10 chr19:57286076 A>G maps to NM_001146326.1 T521T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZS-A9CF-01A-11D-A382-10 chr19:57286538 G>T maps to NM_001146326.1 L367L. Only missense variants will be evaluated by CHASM.
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-DD-AACT-01A-11D-A40R-10 chr23:101139285 T>A did not map to a codon.
Sequencing variant TCGA-G3-AAV2-01A-11D-A36X-10 chr23:101139681 C>T did not map to a codon.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr3:178745433 G>T maps to NM_022470.3 S186*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAVP-01A-11D-A40R-10 chr10:81064988 G>C did not map to a codon.
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-BC-A3KG-01A-11D-A20W-10 chr1:35570357 A>G maps to NM_024772.3 T265T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADI-01A-11D-A40R-10 chr13:20605571 G>A maps to NM_001190965.1 W655*. 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-EP-A2KB-01A-11D-A183-10 chr13:20659970 T>C maps to NM_001190965.1 N1317N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WX-AA44-01A-11D-A38X-10 chr13:20567235 A>G maps to NM_001190965.1 G8G. 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-DD-AACF-01A-11D-A40R-10 chr23:70468642 G>C 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-DD-AACK-01A-11D-A40R-10 chr1:35851191 A>T maps to NM_005095.2 A573A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACQ-01A-11D-A40R-10 chr1:35884116 T>C maps to NM_005095.2 N1461N. Only missense variants will be evaluated by CHASM.
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-CC-A7IE-01A-21D-A382-10 chr13:20399129 T>C maps to NM_001142684.1 T499T. 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-DD-A3A1-01A-11D-A20W-10 chr1:35477607 T>C did not map to a codon.
Sequencing variant TCGA-DD-AACK-01A-11D-A40R-10 chr1:35452800 T>A maps to NM_007167.3 S1294S. 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-G3-A3CG-01A-11D-A20W-10 chr1:42914249 G>A maps to NM_032257.4 H104H. 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-CC-A8HV-01A-11D-A35Z-10 chr20:45905295 C>T maps to ENST00000471951 Q414Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADD-01A-11D-A40R-10 chr12:133732821 C>T maps to NM_015394.4 F330F. 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-AAEE-01A-11D-A40R-10 chr19:19790277 A>G maps to NM_033204.2 T160T. Only missense variants will be evaluated by CHASM.
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-DD-AAVP-01A-11D-A40R-10 chr19:48789078 A>G maps to NM_153608.1 R66R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACI-01A-11D-A40R-10 chr1:247320350 A>G maps to NM_003431.2 S129S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAD0-01A-11D-A40R-10 chr1:247320146 T>C maps to NM_003431.2 E197E. 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-DD-AACL-01A-11D-A40R-10 chr19:58571396 A>T maps to NM_003436.3 T9T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADE-01A-11D-A40R-10 chr12:133683149 T>C maps to NM_003440.2 A429A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAE4-01A-11D-A40R-10 chr12:133682846 G>A maps to NM_003440.2 P328P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAVX-01A-11D-A40R-10 chr12:133682813 T>G maps to NM_003440.2 T317T. 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-DD-AADO-01A-11D-A40R-10 chr2:219508526 T>C maps to NM_001105537.1 S904S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAW1-01A-11D-A40P-10 chr2:219513535 G>T maps to NM_001105537.1 G365G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9GV-01A-11D-A382-10 chr11:9494251 C>T maps to NM_003442.5 G47G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BD-A3EP-01A-11D-A22F-10 chr11:9537863 G>A maps to NM_003442.5 T547T. 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-A3A1-01A-11D-A20W-10 chr3:124996585 A>G maps to NM_021964.2 H217H. 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-DD-AACP-01A-11D-A40R-10 chr19:44500764 A>G maps to NM_003445.2 K252K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A3KG-01A-11D-A20W-10 chr23:47272505 T>C did not map to a codon.
Sequencing variant TCGA-CC-A9FS-01A-11D-A36X-10 chr23:47272151 T>A did not map to a codon.
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-DD-AAW1-01A-11D-A40P-10 chr19:57929404 A>G maps to NM_006959.2 V47V. 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-2Y-A9H5-01A-11D-A382-10 chr17:11881726 T>G maps to NM_144680.2 P399P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr17:11896053 T>C maps to NM_144680.2 Q31Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZS-A9CG-01A-11D-A36X-10 chr17:11881999 G>T maps to NM_144680.2 L308L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr19:44983587 T>C maps to NM_013256.3 T82T. 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-DD-A119-01A-11D-A12Z-10 chr23:47842407 A>G did not map to a codon.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr23:47836309 G>A did not map to a codon.
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-DD-AACC-01A-11D-A40R-10 chr23:152128321 G>T did not map to a codon.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr23:152128426 A>G 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-G3-A3CG-01A-11D-A20W-10 chr23:152113988 C>T 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-4R-AA8I-01A-11D-A382-10 chr16:71509597 A>G maps to NM_006961.3 G284G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr11:3392926 A>G maps to NM_001130520.1 L4L. 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-BC-A3KG-01A-11D-A20W-10 chr3:44684619 T>C maps to NM_006991.3 I666I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A8HV-01A-11D-A35Z-10 chr3:44674044 G>A maps to NM_006991.3 L241L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAC8-01A-11D-A40R-10 chr3:44685445 A>T maps to NM_006991.3 K942*. 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-DD-AAE1-01A-11D-A40R-10 chr11:123600488 C>T maps to NM_003455.2 T149T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr19:22155264 T>C maps to NM_007153.3 G857G. 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-DD-AACG-01A-11D-A40R-10 chr19:22154760 T>C maps to NM_007153.3 G1025G. 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-G3-AAV6-01A-21D-A36X-10 chr19:22170030 C>A maps to NM_007153.3 V71V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAW0-01A-11D-A40R-10 chr19:58152528 A>G maps to NM_006385.3 G238G. 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-2Y-A9H7-01A-11D-A38X-10 chr11:7022370 T>C maps to NM_013249.2 E181E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr20:52198882 G>A maps to NM_006526.2 C161C. 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-ZP-A9D4-01A-11D-A36X-10 chr19:44570688 A>G maps to NM_013361.4 Q236Q. 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-2Y-A9GV-01A-11D-A382-10 chr19:44635630 C>T maps to NM_013362.2 F288F. 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-A3MA-01A-11D-A20W-10 chr19:44679879 T>C maps to NM_001032372.1 G155G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACL-01A-11D-A40R-10 chr19:44676285 G>T maps to NM_001032372.1 E21*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr19:44739560 C>T maps to NM_182490.1 C326C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EG-01A-11D-A20W-10 chr19:44739698 A>G maps to NM_182490.1 R372R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZP-A9D4-01A-11D-A36X-10 chr19:44739934 T>G maps to NM_182490.1 L451*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr19:44933200 T>C maps to NM_014518.2 S585S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WX-AA44-01A-11D-A38X-10 chr19:44934547 A>G maps to NM_014518.2 D136D. 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-4R-AA8I-01A-11D-A382-10 chr19:44791784 A>G maps to NM_004234.4 C601C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A10W-01A-11D-A12Z-10 chr1:244218511 G>A maps to NM_205768.2 W479*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NO-01A-11D-A28X-10 chr1:244218374 C>A maps to NM_205768.2 T433T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11D-01A-11D-A12Z-10 chr10:44052345 G>C maps to NM_001099284.1 L394L. 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-CC-A3MB-01A-11D-A20W-10 chr19:20003477 T>C maps to NM_021047.2 H474H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LG-A9QD-01A-11D-A382-10 chr19:24270140 T>C did not map to a codon.
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-A3MA-01A-11D-A20W-10 chr16:3340152 T>C maps to NM_005741.4 S549S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EE-01A-11D-A12Z-10 chr19:57723566 G>T maps to NM_003417.4 E368*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A2QR-01A-11D-A20W-10 chr19:57723919 C>T maps to NM_003417.4 C485C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr16:31927483 C>T maps to NM_003414.4 G638G. 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-EP-A2KA-01A-11D-A183-10 chr16:31926475 A>G maps to NM_003414.4 K302K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9H6-01A-11D-A38X-10 chr23:152612616 C>T did not map to a codon.
Sequencing variant TCGA-DD-AAEB-01A-11D-A40R-10 chr16:89799790 C>T maps to NM_001113525.1 P417P. 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-AACD-01A-11D-A40R-10 chr7:148892728 G>A maps to NM_003575.2 Q16Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A0-01A-11D-A20W-10 chr19:44590887 A>G maps to NM_001037813.2 R419R. Only missense variants will be evaluated by CHASM.
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-2Y-A9H8-01A-11D-A38X-10 chr17:18565669 A>G maps to NM_001145045.1 Y383Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACJ-01A-11D-A40R-10 chr17:18566383 C>A maps to NM_001145045.1 R145R. 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-G3-A3CJ-01A-11D-A20W-10 chr6:87970225 A>G maps to NM_015021.1 R2293R. 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-AACP-01A-11D-A40R-10 chr19:35435312 A>G maps to NM_001099438.1 V482V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAVP-01A-11D-A40R-10 chr19:35435357 C>T maps to NM_001099438.1 A497A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9H3-01A-11D-A382-10 chr5:150275987 A>G maps to NM_001172831.1 C287C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FV-A2QR-01A-11D-A20W-10 chr5:150275249 T>C maps to NM_001172831.1 G533G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A11B-01A-11D-A12Z-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-GJ-A3OU-01A-31D-A382-10 chr19:9267978 T>C maps to NM_020933.4 F66F. 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-DD-AAD0-01A-11D-A40R-10 chr19:53432593 C>T maps to NM_203307.2 G19G. 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-DD-AAE1-01A-11D-A40R-10 chr19:58639288 G>T maps to NM_024620.3 R528R. 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-DD-A3A1-01A-11D-A20W-10 chr19:54081145 C>T maps to NM_001079907.1 C444C. 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-DD-AACI-01A-11D-A40R-10 chr20:44596975 C>T maps to NM_022095.3 E156E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAD6-01A-11D-A40R-10 chr20:44592540 T>A maps to NM_022095.3 P397P. 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-DD-AADP-01A-11D-A38X-10 chr10:38344425 A>G maps to NM_006954.1 V458V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr10:38344488 T>C maps to NM_006954.1 S479S. 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-A119-01A-11D-A12Z-10 chr10:43089011 A>G maps to NM_006955.1 T462T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EG-01A-11D-A20W-10 chr20:32346564 T>C maps to ENST00000375200 C327C. 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-EP-A2KA-01A-11D-A183-10 chr19:37368100 T>C maps to NM_003419.3 C123C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NI-01A-11D-A27I-10 chr19:53644385 T>A maps to NM_001172674.1 G566G. 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-DD-AAVW-01A-11D-A40R-10 chr3:44692627 G>A maps to NM_003420.3 E23E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr3:44700748 A>G maps to NM_003420.3 K298K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACC-01A-11D-A40R-10 chr19:52472324 C>A maps to NM_021632.3 L25L. 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-2Y-A9GZ-01A-11D-A38X-10 chr10:64159445 C>A maps to NM_014951.2 C374*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADO-01A-11D-A40R-10 chr5:71756335 G>A maps to NM_152625.1 Q330*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CJ-01A-11D-A20W-10 chr10:38407551 A>G maps to NM_003421.2 R491R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1ED-01A-11D-A152-10 chr19:37733878 C>T maps to NM_152604.1 I247I. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-DD-AACF-01A-11D-A40R-10. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-DD-AACF-01A-11D-A40R-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-DD-AACF-01A-11D-A40R-10 chr12:6777074 C>T maps to ENST00000407384 L127L. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-G3-AAUZ-01A-11D-A382-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-G3-AAUZ-01A-11D-A382-10 chr12:6777080 C>T maps to ENST00000407384 L129L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAD1-01A-11D-A40R-10 chr2:180634263 G>A maps to NM_152520.4 P73P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACZ-01A-11D-A40R-10 chr6:27368625 C>T maps to NM_001076781.1 H159H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9HA-01A-11D-A38X-10 chr7:99096408 G>A maps to NM_032164.2 R171R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WQ-A9G7-01A-11D-A36X-10 chr7:99092120 A>G maps to NM_032164.2 H239H. 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-DD-AACQ-01A-11D-A40R-10 chr18:32953552 T>C maps to NM_145756.2 G143G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADM-01A-11D-A40R-10 chr18:32953438 A>C maps to NM_145756.2 L181L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACJ-01A-11D-A40R-10 chr18:32825454 T>A maps to NM_001135178.2 A262A. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-DD-AAW2-01A-11D-A40P-10. Mapping will be selected arbitrarily.
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-ES-A2HS-01A-11D-A183-10 chr18:72516009 T>C maps to NM_001146190.1 C1656C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WX-AA46-01A-11D-A38X-10 chr18:72344755 C>G maps to NM_017757.2 S594*. 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-CC-A3MA-01A-11D-A20W-10 chr23:47307021 T>C did not map to a codon.
Sequencing variant TCGA-DD-A3A0-01A-11D-A20W-10 chr23:47307868 T>C did not map to a codon.
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-DD-AAC8-01A-11D-A40R-10 chr19:53611939 G>T maps to NM_001164309.1 S453*. 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-ZP-A9CY-01A-11D-A382-10 chr19:53612769 T>C maps to NM_001164309.1 S176S. 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-ES-A2HT-01A-12D-A183-10 chr19:37619071 T>A maps to NM_144689.3 C393*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACU-01A-11D-A40R-10 chr16:49660080 C>A maps to NM_015069.2 E1193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr16:49670349 G>T maps to NM_015069.2 R905R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr16:49671523 A>T maps to NM_015069.2 G513G. 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-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-DD-AAD5-01A-11D-A40R-10 chr19:21216317 C>T maps to NM_025189.3 C51C. 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-2Y-A9GU-01A-11D-A382-10 chr19:21350458 T>C maps to NM_133473.2 D103D. 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-ES-A2HS-01A-11D-A183-10 chr1:23688527 G>T maps to NM_001077195.1 T449T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CJ-01A-11D-A20W-10 chr19:11977009 G>A maps to NM_152262.2 E13E. 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-XR-A8TG-01A-11D-A35Z-10 chr19:56669903 G>A maps to NM_018337.2 V113V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NH-01A-11D-A27I-10 chr19:58991840 C>T maps to NM_017908.2 T367T. 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-DD-A3A0-01A-11D-A20W-10 chr23:134481370 A>G did not map to a codon.
Sequencing variant TCGA-DD-AAE9-01A-11D-A40R-10 chr19:44419098 G>A maps to NM_003425.3 P163P. Only missense variants will be evaluated by CHASM.
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-EP-A2KA-01A-11D-A183-10 chr19:57802157 A>G maps to NM_006635.3 G83G. 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-DD-AAEE-01A-11D-A40R-10 chr9:109691841 C>T maps to NM_021224.4 N1883N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr9:109689750 T>C maps to NM_021224.4 P1186P. 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-ES-A2HS-01A-11D-A183-10 chr19:57089653 A>G maps to NM_001001668.3 K619K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADR-01A-11D-A40R-10 chr5:121488329 C>T maps to NM_207317.1 T215T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CJ-01A-11D-A20W-10 chr19:52803706 A>G maps to NM_144684.2 K14K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3K-AAZ8-01A-12D-A38X-10 chr9:114304528 T>C maps to NM_133464.2 T438T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAD5-01A-11D-A40R-10 chr10:44111880 T>C maps to NM_145312.3 Y130Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr19:20308358 C>A maps to ENST00000428290 T274T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A1-01A-11D-A20W-10 chr10:48371473 A>G maps to NM_153034.2 E314E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACI-01A-11D-A40R-10 chr19:11917799 A>T maps to NM_152356.3 I344I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZP-A9D2-01A-11D-A382-10 chr19:21607546 C>T maps to NM_001076678.2 R696*. 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-BC-A10R-01A-11D-A12Z-10 chr7:99227216 C>T maps to NM_145115.2 Y403Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr16:4802990 G>T maps to NM_021646.1 R277R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACG-01A-11D-A40R-10 chr3:44763598 T>A maps to NM_033210.4 T430T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAEK-01A-11D-A40R-10 chr3:44763337 A>G maps to NM_033210.4 R343R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr19:19917870 A>G maps to NM_001099269.2 L4L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZP-A9D1-01A-11D-A382-10 chr19:19906191 A>T maps to NM_001099269.2 T168T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADR-01A-11D-A40R-10 chr19:32845668 C>T maps to NM_014910.4 L645L. 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-AAD0-01A-11D-A40R-10 chr18:74153981 C>A maps to ENST00000443185 L343L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr8:146033089 C>T maps to NM_213605.2 C263C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACG-01A-11D-A40R-10 chr4:10446372 A>T maps to NM_053042.2 L527*. 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-A4NB-01A-12D-A25V-10 chr18:14105584 C>T maps to NM_145287.3 K318K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9GZ-01A-11D-A38X-10 chr18:22775122 C>A did not map to a codon.
Sequencing variant TCGA-CC-A8HT-01A-11D-A35Z-10 chr18:22805354 C>A maps to NM_015461.2 G843*. 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-AAE7-01A-11D-A40R-10 chr19:52919621 C>A maps to NM_032423.2 S506*. 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-EP-A2KB-01A-11D-A183-10 chr18:56586799 G>T maps to NM_018181.4 A427A. 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-MI-A75H-01A-11D-A32G-10 chr19:30935239 G>A maps to NM_014717.1 S257S. 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-WQ-A9G7-01A-11D-A36X-10 chr19:30935509 C>T maps to NM_014717.1 C347C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XR-A8TD-01A-12D-A38X-10 chr19:31048061 A>T did not map to a codon.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr19:58773097 G>T maps to NM_014480.2 G376*. 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-DD-AADI-01A-11D-A40R-10 chr19:57909861 A>T maps to NM_001172773.1 S81S. 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-DD-AADL-01A-11D-A40R-10 chr19:58199256 A>G maps to ENST00000356715 K538K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BD-A3ER-01A-11D-A20W-10 chr19:2834343 C>T maps to NM_001102651.1 L371L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XR-A8TF-01A-11D-A35Z-10 chr19:2877958 A>T maps to NM_024967.1 R335*. 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-AAVP-01A-11D-A40R-10 chr19:9583899 A>G maps to NM_152476.2 L65L. Only missense variants will be evaluated by CHASM.
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-A39X-01A-11D-A20W-10 chr19:9768757 A>G maps to NM_001130032.1 A56A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A3KG-01A-11D-A20W-10 chr19:12638000 T>C maps to NM_144976.3 G307G. 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-ES-A2HT-01A-12D-A183-10 chr19:37210226 C>T maps to ENST00000423498 Q200*. 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-BC-A3KG-01A-11D-A20W-10 chr8:125988659 A>G maps to NM_152412.2 K50K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A3KF-01A-11D-A20W-10 chr19:38229626 T>C maps to NM_001172690.1 G588G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAE7-01A-11D-A40R-10 chr19:38229947 A>G maps to NM_001172690.1 T481T. 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-DD-AADP-01A-11D-A38X-10 chr19:53013918 T>C maps to NM_001099694.1 S95S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADQ-01A-11D-A40R-10 chr19:53014278 A>T maps to NM_001099694.1 S215S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADB-01A-11D-A40R-10 chr19:56895231 C>T maps to NM_144690.1 *518*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr19:56895789 A>G maps to NM_144690.1 V332V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CG-01A-11D-A20W-10 chr19:56896374 T>C maps to NM_144690.1 R137R. 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-AAEA-01A-11D-A40R-10 chr19:58370622 C>T maps to NM_032828.2 S281S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9H7-01A-11D-A38X-10 chr15:85326094 G>T maps to NM_014630.2 V63V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr15:85327555 G>T maps to NM_014630.2 L550L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAC8-01A-11D-A40R-10 chr17:5086890 T>A maps to NM_032530.1 K221*. 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-DD-AAVY-01A-11D-A40R-10 chr19:58489956 T>C maps to NM_025027.3 A697A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A0-01A-11D-A20W-10 chr19:38190281 C>T maps to NM_032689.4 E250E. 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-3K-AAZ8-01A-12D-A38X-10 chr15:64967422 T>C maps to NM_015042.1 A790A. 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-CC-A3MA-01A-11D-A20W-10 chr19:53208849 T>C maps to NM_001161500.1 E486E. 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-DD-A1EE-01A-11D-A12Z-10 chr19:52443517 C>G maps to NM_001031721.3 L24L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACT-01A-11D-A40R-10 chr19:52496687 T>C maps to ENST00000354939 K558K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAE7-01A-11D-A40R-10 chr19:52496612 T>C maps to ENST00000354939 E583E. 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-EP-A2KA-01A-11D-A183-10 chr3:40558018 G>T maps to NM_175888.2 E312*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACT-01A-11D-A40R-10 chr5:16463666 G>A maps to NM_033414.2 H270H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACE-01A-11D-A40R-10 chr19:11727701 A>G maps to NM_145295.3 P128P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr19:55992667 C>T maps to NM_033113.2 Y32Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr16:30795163 C>T maps to NM_001080417.1 W162*. 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-ZP-A9CV-01A-11D-A382-10 chr23:47918451 A>G 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-AAVZ-01A-11D-A40R-10 chr2:71577247 G>A maps to NM_014497.3 V388V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACW-01A-11D-A40R-10 chr3:179047482 A>T maps to NM_016331.1 R46*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr1:40961673 T>C maps to NM_198494.2 S508S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAEA-01A-11D-A40R-10 chr1:91406718 T>C maps to NM_201269.1 T64T. 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-2Y-A9GT-01A-11D-A382-10 chr23:22291148 A>G did not map to a codon.
Sequencing variant TCGA-BC-A3KF-01A-11D-A20W-10 chr16:31088547 T>C maps to NM_014699.3 R301R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A0-01A-11D-A20W-10 chr16:31089057 T>C maps to NM_014699.3 G471G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACK-01A-11D-A40R-10 chr16:31090545 C>T maps to NM_014699.3 Y967Y. Only missense variants will be evaluated by CHASM.
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-DD-AACW-01A-11D-A40R-10 chr1:182025618 G>A maps to NM_001009992.1 C509C. 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-ZP-A9CZ-01A-11D-A382-10 chr1:182026605 T>C maps to NM_001009992.1 V180V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr17:47389291 G>A maps to NM_014897.2 C387C. 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-AAC8-01A-11D-A40R-10 chr19:53668305 A>T maps to NM_024733.3 I479I. 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-ES-A2HT-01A-12D-A183-10 chr19:56953573 G>A maps to ENST00000342634 Q392*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZP-A9CV-01A-11D-A382-10 chr1:247201278 T>C maps to NM_033213.3 E214E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr1:249142189 C>T maps to NM_024836.1 S239S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EA-01A-11D-A12Z-10 chr1:249142603 C>T maps to NM_024836.1 S377S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADC-01A-11D-A40R-10 chr1:249142141 G>C maps to NM_024836.1 G223G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAEG-01A-11D-A38X-10 chr23:46359733 G>A did not map to a codon.
Sequencing variant TCGA-BC-A112-01A-11D-A12Z-10 chr19:23836431 G>A maps to NM_138330.2 R435*. 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-DD-A119-01A-11D-A12Z-10 chr19:22363102 A>G maps to NM_001001411.2 A472A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CJ-01A-11D-A20W-10 chr19:22363756 T>C maps to NM_001001411.2 K254K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9H3-01A-11D-A382-10 chr19:53740800 A>G maps to NM_182609.2 H393H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EG-01A-11D-A20W-10 chr19:53740869 A>G maps to NM_182609.2 T370T. Only missense variants will be evaluated by CHASM.
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-AAE1-01A-11D-A40R-10 chr1:227843475 A>C maps to NM_178549.3 R564R. 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-DD-AACK-01A-11D-A40R-10 chr19:23927687 C>A maps to NM_138286.2 G222*. 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-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-DD-AACP-01A-11D-A40R-10 chr1:151261603 G>A maps to NM_020832.1 V776V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr1:43317024 G>T maps to ENST00000442768 R163R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAD1-01A-11D-A40R-10 chr1:247150826 G>T maps to NM_020394.3 G330G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr1:120166362 G>A maps to NM_001080470.1 G201G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A3KG-01A-11D-A20W-10 chr1:120168498 T>C maps to NM_001080470.1 T75T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A7IE-01A-21D-A382-10 chr8:146067301 A>G maps to ENST00000446747 R280R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADP-01A-11D-A38X-10 chr8:146054919 C>T maps to ENST00000446747 L31L. 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-4R-AA8I-01A-11D-A382-10 chr19:12059372 C>T maps to NM_144566.1 R178R. 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-A3MA-01A-11D-A20W-10 chr19:12059744 A>G maps to NM_144566.1 G302G. 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-EP-A2KA-01A-11D-A183-10 chr19:21476561 G>T maps to NM_021269.2 T402T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BC-A3KF-01A-11D-A20W-10 chr19:12575009 G>A maps to ENST00000428311 R576*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACI-01A-11D-A40R-10 chr19:12575439 G>T maps to ENST00000428311 S432S. 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-DD-AADL-01A-11D-A40R-10 chr23:84526084 G>T did not map to a codon.
Sequencing variant TCGA-G3-A5SJ-01A-11D-A27I-10 chr23:84526389 T>C did not map to a codon.
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-DD-AAEG-01A-11D-A38X-10 chr4:435882 C>T maps to NM_133474.2 T791T. 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-A7M6-01A-11D-A33Q-10 chr7:63796755 C>G maps to NM_001170905.1 V41V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UB-A7MB-01A-11D-A33Q-10 chr7:63808696 A>G maps to NM_001170905.1 R152R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr12:53579802 C>T maps to NM_001004304.3 H105H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr17:80789772 G>A maps to NM_024702.2 N186N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACL-01A-11D-A40R-10 chr23:134425481 A>G did not map to a codon.
Sequencing variant TCGA-DD-AAE7-01A-11D-A40R-10 chr23:134427745 G>T did not map to a codon.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr23:134426380 C>A 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-AACP-01A-11D-A40R-10 chr19:12089203 T>G maps to NM_001012753.1 Y158*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A1-01A-11D-A20W-10 chr19:53911419 A>G maps to NM_001040185.1 Q204Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAVU-01A-11D-A40R-10 chr19:53911920 A>G maps to NM_001040185.1 T371T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9H3-01A-11D-A382-10 chr19:52793823 A>C maps to NM_001010851.2 R260R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAE7-01A-11D-A40R-10 chr19:52793976 T>C maps to NM_001010851.2 S311S. 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-ES-A2HS-01A-11D-A183-10 chr15:90903882 C>A maps to NM_001004309.2 R274R. 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-A39Y-01A-11D-A20W-10 chr16:89294753 T>C maps to NM_182531.2 S658S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A0-01A-11D-A20W-10 chr16:89294114 A>G maps to NM_182531.2 G445G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr16:89294363 A>G maps to NM_182531.2 T528T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CG-01A-11D-A20W-10 chr16:89293511 T>C maps to NM_182531.2 V244V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACV-01A-11D-A40R-10 chr19:40580706 G>A maps to NM_001142577.1 R549*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9H9-01A-21D-A38X-10 chr19:40540677 G>C maps to NM_001005851.2 P696P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADW-01A-11D-A38X-10 chr19:38160323 C>A maps to NM_152605.3 L242L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4R-AA8I-01A-11D-A382-10 chr9:99580288 T>C maps to NM_001001662.1 K672K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A119-01A-11D-A12Z-10 chr9:99580297 T>C maps to NM_001001662.1 T669T. 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-WQ-A9G7-01A-11D-A36X-10 chr19:38028486 A>G maps to NM_001013659.2 R309R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9H3-01A-11D-A382-10 chr19:58806124 A>G maps to NM_021089.2 E317E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1EG-01A-11D-A20W-10 chr19:58797545 A>G maps to NM_021089.2 R88R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A3A0-01A-11D-A20W-10 chr7:127026147 A>G maps to NM_176814.3 S41S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACT-01A-11D-A40R-10 chr2:185801444 C>G maps to NM_194250.1 S441*. 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-DD-A1EG-01A-11D-A20W-10 chr7:88389388 T>C maps to NM_181646.2 S33S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAVR-01A-11D-A40R-10 chr7:88963558 C>T maps to NM_181646.2 S421S. 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-ZP-A9CZ-01A-11D-A382-10 chr7:88966179 T>A maps to NM_181646.2 L1295*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9H9-01A-21D-A38X-10 chr19:53057401 A>G maps to NM_001039886.3 Q411Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACT-01A-11D-A40R-10 chr19:53050790 T>C maps to NM_001039886.3 A30A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAVX-01A-11D-A40R-10 chr19:53058361 T>A maps to NM_001039886.3 G731G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HT-01A-12D-A183-10 chr19:53057389 T>C maps to NM_001039886.3 A407A. 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-4R-AA8I-01A-11D-A382-10 chr19:58384993 G>A maps to NM_001144989.1 I588I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BD-A3EP-01A-11D-A22F-10 chr19:53453989 A>G maps to NM_001031665.1 C346C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A4NO-01A-11D-A28X-10 chr4:146695656 C>G did not map to a codon.
Sequencing variant TCGA-DD-AACI-01A-11D-A40R-10 chr4:146770558 T>C maps to ENST00000508784 P712P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACI-01A-11D-A40R-10 chr4:146770636 G>C maps to ENST00000508784 V686V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A1ED-01A-11D-A152-10 chr13:115089643 T>C maps to NM_032436.2 P109P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-A3CJ-01A-11D-A20W-10 chr19:37398843 T>C maps to NM_001171979.1 R183R. Only missense variants will be evaluated by CHASM.
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-DD-AAEB-01A-11D-A40R-10 chr19:53116800 G>A maps to NM_018300.3 H339H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ED-A5KG-01A-11D-A27I-10 chr19:53116800 G>A maps to NM_018300.3 H339H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9H3-01A-11D-A382-10 chr20:57769709 T>C maps to NM_178457.1 P1212P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Y-A9H9-01A-21D-A38X-10 chr20:57766715 G>T maps to NM_178457.1 L214L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BD-A3EP-01A-11D-A22F-10 chr20:57767831 C>T maps to NM_178457.1 D586D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A9FW-01A-11D-A36X-10 chr20:57769574 C>T maps to NM_178457.1 P1167P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADL-01A-11D-A40R-10 chr20:57767216 G>A maps to NM_178457.1 P381P. 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-DD-AAD0-01A-11D-A40R-10 chr19:57175000 A>G maps to NM_001005850.1 C544C. 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-CC-A3MB-01A-11D-A20W-10 chr19:52658667 G>A maps to NM_001102657.1 G756G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BD-A3EP-01A-11D-A22F-10 chr14:102798158 G>A maps to NM_018335.3 S464S. 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-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-AACU-01A-11D-A40R-10 chr19:12186501 A>T maps to NM_001136501.1 I189I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5C-A9VG-01A-11D-A36X-10 chr19:53854545 G>A maps to NM_138374.1 Q206Q. 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-DD-A39Y-01A-11D-A20W-10 chr19:53855283 G>A maps to NM_138374.1 S452S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAD5-01A-11D-A40R-10 chr19:53856624 A>G maps to NM_138374.1 Q899Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-AAV0-01A-11D-A36X-10 chr19:53855787 A>G maps to NM_138374.1 S620S. 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-DD-AAE3-01A-11D-A40R-10 chr19:21132306 T>C maps to NM_003429.4 L329L. 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-A119-01A-11D-A12Z-10 chr3:32030624 T>C maps to NM_001137674.1 A18A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr7:149545055 T>C maps to NM_001099220.1 A158A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G3-AAV5-01A-11D-A36X-10 chr7:149543297 G>A maps to NM_001099220.1 W65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A3M9-01A-11D-A20W-10 chr19:52887145 A>T maps to NM_001145434.1 K105*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AACL-01A-11D-A40R-10 chr19:52888534 A>T maps to NM_001145434.1 R568*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KA-01A-11D-A183-10 chr19:20228951 G>T maps to ENST00000427401 G412*. 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-WQ-AB4B-01A-11D-A40P-10 chr19:23542678 G>A maps to NM_003430.2 S1034S. 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-DD-AAD0-01A-11D-A40R-10 chr19:20044589 A>T maps to NM_031218.3 K276*. 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-DD-AADU-01A-11D-A40R-10 chr19:22940397 C>T maps to ENST00000397104 K680K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AADV-01A-11D-A38X-10 chr19:22952080 C>A maps to ENST00000397104 E38*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EP-A2KB-01A-11D-A183-10 chr19:22940397 C>T maps to ENST00000397104 K680K. 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-CC-A8HV-01A-11D-A35Z-10 chr11:60641130 C>A maps to NM_207341.2 Y485*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A9FS-01A-11D-A36X-10 chr16:21212846 C>A maps to NM_003460.1 E513*. 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-ZP-A9D1-01A-11D-A382-10 chr1:238048572 A>T maps to NM_021186.3 P401P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAC8-01A-11D-A40R-10 chr7:50132766 T>A maps to NM_007009.2 P8P. 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-G3-AAV4-01A-11D-A382-10 chr7:50121481 G>A maps to NM_007009.2 V74V. 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-UB-AA0U-01A-11D-A382-10 chr2:136026636 T>C maps to NM_032143.2 A427A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A8HT-01A-11D-A35Z-10 chr23:15809110 G>T did not map to a codon.
Sequencing variant TCGA-ES-A2HS-01A-11D-A183-10 chr19:58564801 C>A maps to NM_182572.3 R204R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAE0-01A-11D-A40R-10 chr16:3139522 C>A maps to NM_032805.1 E583*. 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-BC-A3KG-01A-11D-A20W-10 chr1:33960763 C>T maps to NM_145238.3 F940F. 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-ES-A2HT-01A-12D-A183-10 chr7:99661624 A>G maps to NM_145914.2 K269K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-A39Z-01A-11D-A20W-10 chr19:58846296 T>C maps to NM_181846.2 A43A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAE6-01A-11D-A40R-10 chr19:58846305 G>A maps to NM_181846.2 E46E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CC-A9FU-01A-11D-A36X-10 chr15:43661976 C>A maps to NM_152455.3 R45R. 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-DD-AAD3-01A-11D-A40R-10 chr20:44511554 T>A maps to NM_080603.4 L108L. 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-AACN-01A-11D-A40R-10 chr19:13915862 C>T maps to NM_023072.2 Q205*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAED-01A-12D-A40R-10 chr19:13919680 C>A maps to NM_023072.2 I248I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DD-AAEA-01A-11D-A40R-10 chr6:116977887 G>C maps to NM_145062.2 S307*. 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-DD-AACZ-01A-11D-A40R-10 chr10:58119615 T>A did not map to a codon.
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.
Sequencing variant TCGA-DD-AAVX-01A-11D-A40R-10 chr17:4016071 C>T maps to NM_015113.3 R299R. Only missense variants will be evaluated by CHASM.
