5227 NP_001070868 P590L not found in SNVbox database
692 NP_001070868 A559T not found in SNVbox database
1565 NP_001070868 S642P not found in SNVbox database
3233 NP_001070868 T98M not found in SNVbox database
3291 NP_001070868 F388V not found in SNVbox database
3557 NP_001070868 H676L not found in SNVbox database
Sequencing variant TCGA-A4-A7UZ-01A-12D-A34Z-10 chr16:7703910 G>A maps to NM_145891.2 R304R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr12:9000290 C>T maps to NM_144670.3 R610R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5Y0-01A-11D-A31X-10 chr3:137849688 A>C did not map to a codon.
Sequencing variant TCGA-IA-A40Y-01A-11D-A25F-10 chr3:151475279 T>C maps to NM_207365.3 D368D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr1:12711236 G>T maps to NM_001013630.1 V88V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A561-01A-11D-A26P-10 chr2:69757188 G>A maps to NM_014911.3 F274F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7286-01A-11D-2136-08 chr17:79094951 A>T maps to NM_001080395.2 S928S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A6HP-01A-11D-A31X-10 chr9:107578435 C>T maps to NM_005502.3 T1242T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5878-01A-11D-1589-08 chr2:215840567 A>G maps to NM_173076.2 Y1774Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JN-01A-21D-A42J-10 chr7:48278920 C>T maps to NM_152701.3 H327H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5877-01A-11D-1589-08 chr7:48284202 G>A maps to NM_152701.3 L431L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8195-01A-31D-2396-08 chr7:48411808 C>A maps to NM_152701.3 A3616A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-AAVM-01A-11D-A42J-10 chr7:48390270 A>T maps to NM_152701.3 A3412A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A7SL-01A-11D-A34Z-10 chr7:48431544 C>T maps to NM_152701.3 P3894P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WN-A9G9-01A-12D-A36X-10 chr7:48317733 C>T maps to NM_152701.3 Q2315*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5901-01A-11D-1589-08 chr9:139908395 G>C maps to ENST00000355090 V1475V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PJ-A5Z8-01A-11D-A28G-10 chr9:139907276 C>G maps to ENST00000355090 V1686V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A7SQ-01A-12D-A35Z-10 chr9:139905074 G>A maps to ENST00000355090 T2087T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JR-01A-12D-A42J-10 chr16:2329050 G>A maps to NM_001089.2 Y1480Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7732-01A-11D-2136-08 chr1:94548961 G>A maps to NM_000350.2 I268I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7045-01A-31D-1961-08 chr1:94528185 A>T maps to NM_000350.2 A628A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PJ-A5Z9-01A-11D-A28G-10 chr1:94546178 G>A maps to NM_000350.2 I318I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A44B-01A-11D-A25F-10 chr19:1059068 G>T maps to NM_019112.3 G1816G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WN-A9G9-01A-12D-A36X-10 chr19:1054008 C>T maps to NM_019112.3 G1159G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5890-01A-11D-1589-08 chr17:66981099 G>A maps to NM_080283.3 I1435I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JS-01A-21D-A42J-10 chr1:229684984 A>G maps to NM_012089.2 T238T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A856-01A-11D-A34Z-10 chr1:229666003 A>G maps to NM_012089.2 S529S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7838-01A-11D-2136-08 chr7:87051486 A>G maps to NM_018849.2 L756L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr7:20778603 A>G did not map to a codon.
Sequencing variant TCGA-GL-7966-01A-11D-2201-08 chr2:220074989 G>A maps to NM_005689.2 I794I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PK-01A-11D-A382-10 chr16:16215908 C>T maps to ENST00000399408 N1166N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J7-A8I2-01A-12D-A35Z-10 chr16:48180292 G>A maps to NM_033226.2 R15*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A772-01A-11D-A33Q-10 chr17:48755181 G>A maps to NM_003786.3 S1152S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A71U-01A-12D-A33Q-10 chr3:183639162 G>C maps to NM_005688.2 V1413V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A8YI-01A-21D-A36X-10 chr16:16244451 G>C maps to NM_001171.5 S1462S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A7SS-01A-11D-A35Z-10 chr16:16267178 C>A maps to NM_001171.5 G917*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr12:21962861 G>A maps to NM_005691.2 C1413C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PO-01A-11D-A382-10 chr23:153005610 G>T did not map to a codon.
Sequencing variant TCGA-B3-3925-01A-01D-1458-08 chr4:146041305 G>A did not map to a codon.
Sequencing variant TCGA-5P-A9KE-01A-11D-A42J-10 chr6:30558444 G>A maps to NM_001025091.1 L835L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4113-01A-01D-1252-08 chr4:89039326 A>G maps to NM_004827.2 L259L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PP-01A-11D-A42J-10 chr11:119020845 A>T maps to NM_001142505.1 S57S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A7SS-01A-11D-A35Z-10 chr2:44100947 C>T maps to NM_022437.2 R412*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5Y1-01A-11D-A28G-10 chr14:51368557 C>T maps to ENST00000337334 N264N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A8YI-01A-21D-A36X-10 chr13:108882093 G>A maps to NM_032859.2 V176V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47M-01A-11D-A25F-10 chr3:43744052 T>C maps to NM_016006.4 A160A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr3:58242369 A>T maps to NM_020676.5 P19P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4A-A93W-01A-11D-A36X-10 chr3:100565234 T>C maps to ENST00000471714 E575E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JD-01A-11D-A42J-10 chr9:133748373 T>C maps to NM_007313.2 T364T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4114-01A-01D-1252-08 chr9:133748370 C>T maps to NM_007313.2 A363A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J7-A8I2-01A-12D-A35Z-10 chr4:8082455 G>A maps to NM_001130083.1 G176G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A9DD-01A-11D-A36X-10 chr7:150554943 T>C maps to ENST00000416793 D462D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-5560-01A-01D-1589-08 chr17:975900 C>A maps to NM_021962.2 E283*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7840-01A-11D-2136-08 chr3:127396050 C>A maps to NM_172027.2 I228I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8098-01A-11D-2396-08 chr17:35567391 A>G maps to NM_198834.1 P1232P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NI-01A-11D-A26P-10 chr17:35615280 A>T maps to NM_198834.1 I505I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9Q0-01A-12D-A42J-10 chr17:35609952 C>A maps to NM_198834.1 V612V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6792-01A-21D-1961-08 chr12:109692083 C>T maps to NM_001093.3 L2037L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PR-01A-11D-A42J-10 chr12:109687791 C>A maps to NM_001093.3 Y1891*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr12:112183961 T>C maps to NM_001136538.1 A741A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4A-A93X-01A-11D-A36X-10 chr3:132361613 C>T maps to NM_032169.4 L94L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JD-01A-11D-A42J-10 chr10:124793963 A>C maps to NM_001609.3 T45T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E7-01A-31D-A28G-10 chr17:7127678 T>C maps to ENST00000356839 L570L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7996-01A-11D-2201-08 chr15:89398461 C>T maps to NM_013227.3 F882F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5875-01A-11D-1589-08 chr17:7250506 G>A maps to NM_014716.3 W430*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr3:195006525 T>C maps to NM_012287.5 P745P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59R-01A-11D-A26P-10 chr11:44079984 C>T maps to NM_001031854.2 L482L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JO-01A-11D-A42J-10 chr23:15596287 G>A did not map to a codon.
Sequencing variant TCGA-HE-A5NI-01A-11D-A26P-10 chr9:19435059 C>T maps to NM_001010887.2 L161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J7-6720-01A-11D-2136-08 chr14:23549775 T>C maps to NM_014977.3 V314V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8310-01A-11D-2396-08 chr17:40025022 T>C maps to ENST00000401700 E1094E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A856-01A-11D-A34Z-10 chr17:40054089 C>T maps to ENST00000401700 T501T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5DU-01A-11D-A28G-10 chr22:41911895 T>C maps to ENST00000396512 P270P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A656-01A-11D-A31X-10 chr23:23723160 G>A did not map to a codon.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr3:58517531 C>A maps to NM_003500.3 R197R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W8-01A-11D-A28G-10 chr17:48541576 A>G did not map to a codon.
Sequencing variant TCGA-2Z-A9J7-01A-11D-A382-10 chr16:89167634 G>T maps to NM_174917.2 P182P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9K2-01A-11D-A42J-10 chr16:20651869 G>A maps to NM_052956.2 G343G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A48D-01A-11D-A25F-10 chr16:20559487 G>A maps to NM_182617.3 Q332*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7062-01A-11D-1961-08 chr16:20787238 C>T maps to NM_005622.3 L100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9JW-01A-11D-A42J-10 chr12:7476143 C>T maps to NM_001080454.1 F432F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A9DC-01A-11D-A36X-10 chr12:7459268 A>T maps to NM_001080454.1 G114G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9K6-01A-11D-A42J-10 chr20:25004242 T>C maps to NM_032501.2 G222G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F9-A7VF-01A-11D-A33Q-10 chr7:5567772 G>A maps to NM_001101.3 I282I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-A8LB-01A-11D-A35Z-10 chr7:100253149 C>T maps to NM_016188.4 L54L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A83W-01A-11D-A34Z-10 chr19:39214665 C>T maps to NM_004924.3 A547A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9Q0-01A-12D-A42J-10 chr14:58675767 A>G maps to NM_018477.2 V95V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KV-A6GD-01A-11D-A31X-10 chr20:37383624 T>C maps to NM_024855.3 D267D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Y8-A8RY-01A-11D-A36X-10 chr2:148677843 T>A maps to NM_001616.3 A336A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7061-01A-11D-1961-08 chr3:52023048 G>C maps to ENST00000463937 L496L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-7502-01A-11D-2201-08 chr3:52022537 A>C did not map to a codon.
Sequencing variant TCGA-A4-8517-01A-11D-2396-08 chr16:84228708 G>A maps to NM_139174.3 A286A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A8YH-01A-11D-A36X-10 chr1:155034761 G>A maps to NM_207197.1 L822L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9Q1-01A-11D-A42J-10 chr2:9666344 A>G maps to NM_003183.4 A216A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Y8-A898-01A-11D-A34Z-10 chr2:9668055 T>A maps to NM_003183.4 K160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9J5-01A-21D-A382-10 chr7:87785231 C>T maps to NM_021723.3 T606T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr8:24209519 T>C maps to NM_014265.4 H733H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr8:39044453 A>G maps to NM_145004.5 A314A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7836-01A-11D-2136-08 chr8:39068759 C>T maps to NM_145004.5 Q384*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9K3-01A-11D-A42J-10 chr20:3652296 G>C maps to NM_025220.2 L612L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PX-01A-11D-A42J-10 chr19:8661947 G>A maps to NM_030957.2 I321I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AT-A5NU-01A-11D-A28G-10 chr5:33658353 A>G maps to NM_030955.2 S375S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8098-01A-11D-2396-08 chr9:136305498 G>T maps to NM_139025.3 G607G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr15:100871169 G>A maps to NM_139057.2 I180I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr21:28338044 A>T maps to NM_007038.3 A222A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9J6-01A-11D-A382-10 chr5:64755995 C>T did not map to a codon.
Sequencing variant TCGA-G7-6790-01A-11D-1961-08 chr7:45747950 T>C maps to NM_021116.2 A940A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A40U-01A-11D-A25F-10 chr5:7816983 C>T maps to NM_020546.2 P963P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4A-A93W-01A-11D-A36X-10 chr2:25095498 G>A maps to NM_004036.3 F255F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9K3-01A-11D-A42J-10 chr14:24787719 G>T maps to NM_139247.3 R1046R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J7-6720-01A-11D-2136-08 chr14:24793366 C>A maps to NM_139247.3 L649L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A854-01A-11D-A34Z-10 chr3:123038547 G>A maps to NM_183357.2 T743T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JK-01A-11D-A42J-10 chr12:49170999 C>T maps to NM_015270.3 L421L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8310-01A-11D-2396-08 chr8:132052525 G>A maps to NM_001115.2 I18I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Y8-A896-01A-11D-A35Z-10 chr8:132051978 A>G maps to NM_001115.2 L201L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-A5DJ-01A-11D-A26P-10 chr16:4163952 G>A maps to NM_001116.3 C497C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7062-01A-11D-1961-08 chr16:4029167 G>A maps to NM_001116.3 P876P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55Z-01A-11D-A26P-10 chr16:4164713 G>A maps to NM_001116.3 L244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JT-01A-11D-A42J-10 chr2:70931468 G>A maps to NM_001185054.1 F102F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6790-01A-11D-1961-08 chr2:70903900 G>C maps to NM_001185055.1 G556G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9J7-01A-11D-A382-10 chr10:111884028 C>T maps to NM_016824.3 I466I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr10:111878342 A>G did not map to a codon.
Sequencing variant TCGA-HE-A5NF-01A-11D-A26P-10 chr4:100231923 T>C maps to NM_000668.4 K367K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47M-01A-11D-A25F-10 chr4:100057628 G>T maps to ENST00000505590 I209I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9JY-01A-11D-A42J-10 chr2:3523138 C>T maps to NM_018269.3 K40K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9JU-01A-11D-A42J-10 chr20:49510164 T>C maps to NM_181442.1 Q362Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7841-01A-11D-2136-08 chr15:73045221 C>A maps to NM_031284.4 A317A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-7268-01A-11D-2136-08 chr7:44146298 T>C maps to NM_001129.3 P136P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9Q1-01A-11D-A42J-10 chr7:44150558 C>A maps to NM_001129.3 L511L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9KE-01A-11D-A42J-10 chr12:19615596 C>T maps to NM_001114176.1 S275S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A655-01A-11D-A31Z-10 chr4:7811365 T>C maps to NM_001134647.1 S343S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55Z-01A-11D-A26P-10 chr10:116100455 G>A maps to NM_001001936.1 F17F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47M-01A-11D-A25F-10 chr4:88053422 C>T maps to NM_001166693.1 C1058C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5875-01A-11D-1589-08 chr5:132270291 T>G maps to NM_014423.3 S155S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9J5-01A-21D-A382-10 chr18:12340241 A>C maps to NM_006796.2 A646A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JS-01A-21D-A42J-10 chr4:178354475 T>A maps to NM_000027.3 R278*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5878-01A-11D-1589-08 chr15:87217501 A>G did not map to a codon.
Sequencing variant TCGA-UZ-A9PN-01A-11D-A382-10 chr15:87089230 A>G did not map to a codon.
Sequencing variant TCGA-MH-A561-01A-11D-A26P-10 chr1:48999846 A>G maps to NM_032785.3 *504Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5Y1-01A-11D-A28G-10 chr2:228399579 C>G maps to NM_001135187.1 G372G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7287-01A-11D-2136-08 chr1:100327976 C>G maps to ENST00000311030 S154*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr8:41467378 C>T maps to NM_178819.3 S147S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A71V-01A-11D-A33Q-10 chr8:41476268 C>A maps to NM_178819.3 R374R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PV-01A-11D-A42J-10 chr4:84516011 T>C maps to NM_032717.3 H251H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NF-01A-11D-A26P-10 chr1:957702 C>A maps to NM_198576.2 S108S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5885-01A-11D-1589-08 chr23:115303623 T>G did not map to a codon.
Sequencing variant TCGA-MH-A854-01A-11D-A34Z-10 chr1:11808541 G>A maps to NM_001040196.1 Q112Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr5:177642284 C>T maps to NM_153373.2 G358G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8517-01A-11D-2396-08 chr1:110561172 G>A did not map to a codon.
Sequencing variant TCGA-Y8-A896-01A-11D-A35Z-10 chr1:27874120 G>A maps to NM_001029882.2 A1502A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8195-01A-31D-2396-08 chr6:135644422 C>A maps to NM_017651.4 E1069*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PL-01A-11D-A382-10 chr6:135784362 A>G maps to NM_017651.4 H277H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-A4TM-01A-11D-A31X-10 chr11:62301414 C>T maps to NM_001620.1 T158T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9JU-01A-11D-A42J-10 chr14:105408236 G>A maps to NM_138420.2 S4517S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr14:105409721 G>A maps to NM_138420.2 S4022S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A4ZT-01A-11D-A26P-10 chr5:353962 C>T maps to NM_020731.3 L65L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55W-01A-11D-A26P-10 chr5:434927 G>A maps to NM_020731.3 S713S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr15:86269659 C>G maps to NM_006738.4 L2259L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A7SN-01A-11D-A34Z-10 chr15:86122645 C>T maps to NM_006738.4 D449D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Y8-A895-01A-11D-A35Z-10 chr23:49957180 G>T did not map to a codon.
Sequencing variant TCGA-UZ-A9PP-01A-11D-A42J-10 chr19:15483754 G>A maps to NM_005858.2 Y256Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5885-01A-11D-1589-08 chr7:91631867 A>G maps to NM_005751.4 E879E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A9DD-01A-11D-A36X-10 chr6:109954290 G>T maps to NM_001145128.2 I363I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7838-01A-11D-2136-08 chr7:134260619 C>T maps to ENST00000418096 C246C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NI-01A-11D-A26P-10 chr1:19611545 A>G maps to NM_012067.2 F190F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr1:243800912 C>T maps to NM_005465.3 K187K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6134-01A-11D-1961-08 chr9:116151741 G>A maps to ENST00000277315 D268D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A40Y-01A-11D-A25F-10 chr9:116153878 C>T maps to ENST00000277315 E72E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A71W-01A-12D-A34Z-10 chr4:74277772 A>G maps to NM_000477.5 L258L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A8YH-01A-11D-A36X-10 chr15:101438390 G>C did not map to a codon.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr3:125850316 C>A maps to ENST00000273450 A521A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr12:105433492 C>T maps to NM_001034173.3 K681K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2K-A9WE-01A-11D-A382-10 chr9:104187286 A>G maps to NM_000035.3 D279D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7286-01A-11D-2136-08 chr9:101980773 G>A maps to NM_033087.3 I231I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A9DD-01A-11D-A36X-10 chr3:183963294 G>C maps to NM_005787.5 T135T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7840-01A-11D-2136-08 chr11:43905564 T>C maps to NM_139178.3 I72I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A71R-01A-12D-A33Q-10 chr17:18088006 C>T maps to ENST00000261650 P150P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A8YH-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-BQ-5885-01A-11D-1589-08 chr2:73680676 T>C maps to NM_015120.4 N2340N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7839-01A-11D-2136-08 chr2:73827934 T>C maps to NM_015120.4 R3932R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NJ-01A-11D-A26P-10 chr2:73836706 C>T maps to NM_015120.4 Q4158*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Y8-A896-01A-11D-A35Z-10 chr2:73613064 G>A maps to NM_015120.4 E23E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PK-01A-11D-A382-10 chr18:56246258 A>G maps to NM_052947.3 T583T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PP-01A-11D-A42J-10 chr18:56149189 T>C maps to NM_052947.3 K2126K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A6HP-01A-11D-A31X-10 chr15:85407684 G>A maps to NM_020778.4 L1706L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9Q1-01A-11D-A42J-10 chr15:85360355 C>T maps to NM_020778.4 C93C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A69E-01A-11D-A31X-10 chr1:21889673 C>A maps to NM_000478.4 A123A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A854-01A-11D-A34Z-10 chr1:21890579 C>A maps to NM_000478.4 T173T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr2:202626256 G>A maps to NM_020919.3 Q154*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A854-01A-11D-A34Z-10 chr2:202625786 A>T maps to NM_020919.3 A310A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JL-01A-11D-A42J-10 chr2:202507330 C>G did not map to a codon.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr2:203848265 A>G maps to NM_024744.14 Q699Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-5560-01A-01D-1589-08 chr1:110604110 G>T maps to NM_006492.2 P223P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-5155-01A-01D-1589-08 chr17:33520711 C>T maps to NM_152462.2 L205L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Y8-A898-01A-11D-A34Z-10 chr8:11189415 C>T maps to NM_054028.1 F267F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A655-01A-11D-A31Z-10 chr5:33998824 A>G maps to NM_001167595.1 Y220Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-5155-01A-01D-1589-08 chr6:111213403 T>C maps to NM_001634.4 C156C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PR-01A-11D-A42J-10 chr12:96354187 T>C maps to NM_152435.2 A200A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A7SO-01A-11D-A34Z-10 chr3:49756685 G>A maps to NM_198722.2 N71N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9JU-01A-11D-A42J-10 chr23:112065565 A>T did not map to a codon.
Sequencing variant TCGA-B1-A655-01A-11D-A31Z-10 chr1:115221049 A>G maps to NM_000036.2 Y365Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A83S-01A-11D-A34Z-10 chr2:112638234 G>T maps to NM_022662.2 G56G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8518-01A-11D-2396-08 chr12:110813920 T>C maps to NM_016238.2 V520V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JE-01A-11D-A42J-10 chr14:77275537 T>C maps to NM_015305.3 T171T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59R-01A-11D-A26P-10 chr8:41547821 G>A maps to ENST00000415018 L1343L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A7SS-01A-11D-A35Z-10 chr4:114153414 G>A maps to NM_001148.4 E161E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JS-01A-21D-A42J-10 chr10:61824008 G>A maps to NM_020987.2 I4119I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr10:61830132 G>A maps to NM_020987.2 F3502F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr10:61830688 G>C maps to NM_020987.2 S3317*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PM-01A-21D-A382-10 chr10:61956290 A>G maps to NM_020987.2 A594A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Y8-A894-01A-11D-A35Z-10 chr10:61868590 A>T maps to NM_020987.2 L1057*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7840-01A-11D-2136-08 chr15:65223119 T>G did not map to a codon.
Sequencing variant TCGA-SX-A7SL-01A-11D-A34Z-10 chr17:4087142 G>A maps to NM_016376.3 R588*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chr5:139864823 T>C maps to ENST00000253810 H663H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NL-01A-11D-A26P-10 chr5:139876315 A>G maps to ENST00000253810 E819E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5884-01A-11D-1589-08 chr7:92019369 T>C maps to NM_019004.1 Y664Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E7-01A-31D-A28G-10 chr2:241465101 C>T maps to ENST00000401804 Q445Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-AAVM-01A-11D-A42J-10 chr5:72857113 C>T did not map to a codon.
Sequencing variant TCGA-BQ-5888-01A-11D-1589-08 chr16:89345491 G>A maps to NM_013275.4 L2486L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7045-01A-31D-1961-08 chr18:9257290 T>C maps to NM_015208.3 T1342T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr18:9275634 C>A maps to NM_015208.3 A1959A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4A-A93X-01A-11D-A36X-10 chr1:70819812 G>A maps to NM_030816.4 A93A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Y8-A8RY-01A-11D-A36X-10 chr10:5922266 G>A maps to NM_001009941.2 R308*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A7UZ-01A-12D-A34Z-10 chr4:73986055 T>C did not map to a codon.
Sequencing variant TCGA-A4-A48D-01A-11D-A25F-10 chr3:15765924 G>A maps to NM_015199.3 I219I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9J5-01A-21D-A382-10 chr10:37508183 T>C maps to ENST00000374660 L1245L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JS-01A-21D-A42J-10 chr18:14852331 A>G maps to NM_001145029.1 L1344L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7838-01A-11D-2136-08 chr1:145561664 C>T maps to NM_144698.3 T451T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7288-01A-11D-2136-08 chr2:198001336 C>A maps to NM_001195144.1 R80R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr2:197889958 T>C maps to NM_001195144.1 E561E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6789-01A-11D-1961-08 chr6:35051231 C>A maps to NM_015245.2 I982I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59T-01A-21D-A28G-10 chr12:99640157 G>A maps to NM_152788.3 S747S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Y8-A894-01A-11D-A35Z-10 chr12:99478795 G>A maps to NM_152788.3 S844S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JS-01A-21D-A42J-10 chr16:4747049 C>T maps to NM_133450.2 G650G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-AAVM-01A-11D-A42J-10 chr9:101546299 G>A maps to ENST00000375018 H349H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PL-01A-11D-A382-10 chr2:220099755 A>G maps to NM_001042410.1 S471S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5882-01A-11D-1589-08 chr7:36445952 T>C maps to NM_018685.2 N217N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JE-01A-11D-A42J-10 chr2:242149795 T>G maps to NM_001001891.3 L536L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A854-01A-11D-A34Z-10 chr19:17438616 G>A maps to NM_020959.2 L767L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5892-01A-11D-1589-08 chr12:48866683 C>T maps to NM_012404.2 G79G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A9DE-01A-11D-A36X-10 chr15:90349808 G>A maps to NM_001150.2 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A7SQ-01A-12D-A35Z-10 chr15:90349502 C>T maps to NM_001150.2 K104K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A7SU-01A-11D-A35Z-10 chr15:90349682 G>A maps to NM_001150.2 S44S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4116-01A-01D-1252-08 chr4:80992808 C>A did not map to a codon.
Sequencing variant TCGA-WN-AB4C-01A-11D-A42J-10 chr8:124705532 C>T maps to NM_001003954.1 G223G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr4:79516548 A>G maps to NM_005139.2 E166E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr2:201478583 C>T maps to NM_001159.3 S502S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8098-01A-11D-2396-08 chr14:24032847 C>T did not map to a codon.
Sequencing variant TCGA-2Z-A9J8-01A-11D-A42J-10 chr7:100802477 G>T did not map to a codon.
Sequencing variant TCGA-UZ-A9PS-01A-11D-A42J-10 chr19:50304775 C>T maps to NM_014203.2 G561G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JS-01A-21D-A42J-10 chr17:33977775 T>C maps to NM_001030006.1 I588I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9K6-01A-11D-A42J-10 chr19:47341742 C>T maps to NM_004069.3 K130K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JI-01A-11D-A42J-10 chr10:75889697 T>C maps to NM_207012.2 L212L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr10:75898089 T>C maps to NM_207012.2 L16L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A7SS-01A-11D-A35Z-10 chr8:42015583 C>T maps to NM_006803.3 L133L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55Z-01A-11D-A26P-10 chr15:51294807 T>G maps to NM_007347.3 T1121T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr12:99093183 A>C did not map to a codon.
Sequencing variant TCGA-B9-A5W8-01A-11D-A28G-10 chr4:40818109 T>A maps to NM_004307.1 *760L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7288-01A-11D-2136-08 chr19:1468066 C>T maps to NM_005883.2 P1589P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9J3-01A-12D-A382-10 chr18:10487719 C>A maps to ENST00000423585 C461*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7838-01A-11D-2136-08 chr18:10471913 G>A maps to ENST00000423585 Q261Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Y8-A8RZ-01A-11D-A36X-10 chr18:10471922 G>C maps to ENST00000423585 R264R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J7-A8I2-01A-12D-A35Z-10 chr23:55033280 C>T did not map to a codon.
Sequencing variant TCGA-MH-A562-01A-11D-A26P-10 chr11:43350299 A>T maps to NM_001142930.1 G328G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3473-01A-01D-1252-08 chr19:36362559 T>A maps to NM_001024807.1 L195*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7734-01A-11D-2136-08 chr2:21251316 G>A maps to NM_000384.2 Q571*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr2:21260847 G>A maps to NM_000384.2 A173A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr2:21229323 G>T maps to NM_000384.2 T3472T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5885-01A-11D-1589-08 chr22:39482534 C>G maps to NM_021822.3 A329A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PM-01A-21D-A382-10 chr22:39479828 G>A maps to NM_021822.3 E225E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7045-01A-31D-1961-08 chr22:36661664 C>T maps to NM_145343.2 N277N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7062-01A-11D-1961-08 chr22:36055618 C>G maps to NM_030641.3 V336V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7997-01A-11D-2201-08 chr21:27348293 A>C maps to NM_000484.3 P424P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59T-01A-21D-A28G-10 chr21:27328003 G>C maps to NM_000484.3 T508T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JQ-01A-11D-A42J-10 chr12:105582220 A>G maps to NM_018171.3 S488S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-A8LB-01A-11D-A35Z-10 chr12:105582148 C>A maps to NM_018171.3 V512V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7732-01A-11D-2136-08 chr9:32988091 T>A maps to NM_001195248.1 K71*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A854-01A-11D-A34Z-10 chr9:33447467 G>A maps to NM_004925.3 L21L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PV-01A-11D-A42J-10 chr5:115351417 C>G maps to NM_173800.4 V904V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AT-A5NU-01A-11D-A28G-10 chr15:35189881 T>G maps to NM_014691.2 G756G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9J3-01A-12D-A382-10 chr23:66765163 A>T did not map to a codon.
Sequencing variant TCGA-2Z-A9JO-01A-11D-A42J-10 chr23:66765175 A>T did not map to a codon.
Sequencing variant TCGA-2Z-A9JO-01A-11D-A42J-10 chr23:66765178 A>T did not map to a codon.
Sequencing variant TCGA-5P-A9JW-01A-11D-A42J-10 chr23:66765163 A>T did not map to a codon.
Sequencing variant TCGA-5P-A9JW-01A-11D-A42J-10 chr23:66765166 A>T did not map to a codon.
Sequencing variant TCGA-5P-A9JZ-01A-11D-A42J-10 chr23:66765151 T>A did not map to a codon.
Sequencing variant TCGA-B1-A656-01A-11D-A31X-10 chr23:66765166 A>T did not map to a codon.
Sequencing variant TCGA-F9-A8NY-01A-11D-A35Z-10 chr23:66766364 C>T did not map to a codon.
Sequencing variant TCGA-G7-A8LD-01A-11D-A35Z-10 chr23:66765163 A>T did not map to a codon.
Sequencing variant TCGA-GL-A9DC-01A-11D-A36X-10 chr23:66765163 A>T did not map to a codon.
Sequencing variant TCGA-IA-A83T-01A-11D-A34Z-10 chr23:66765166 A>T did not map to a codon.
Sequencing variant TCGA-SX-A71U-01A-12D-A33Q-10 chr23:66765163 A>T did not map to a codon.
Sequencing variant TCGA-UZ-A9PL-01A-11D-A382-10 chr23:66765228 G>C did not map to a codon.
Sequencing variant TCGA-UZ-A9Q1-01A-11D-A42J-10 chr23:66765151 T>A did not map to a codon.
Sequencing variant TCGA-SX-A7SQ-01A-12D-A35Z-10 chr11:72423564 G>A maps to NM_001040118.2 L266L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr4:36152574 G>T maps to NM_015230.2 I948I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5889-01A-11D-1589-08 chr5:141033933 T>C maps to NM_022481.5 P1406P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9JV-01A-12D-A42J-10 chr12:49332834 G>A maps to NM_001659.2 S147S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8517-01A-11D-2396-08 chr12:49334776 T>C maps to NM_001659.2 L34L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chr22:43213793 A>G maps to NM_014570.4 I294I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8517-01A-11D-2396-08 chr20:47628618 C>A maps to NM_006420.2 R1306R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-A4TM-01A-11D-A31X-10 chr20:47587773 C>G maps to NM_006420.2 L436L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-A8LB-01A-11D-A35Z-10 chr20:47585739 G>A maps to NM_006420.2 K372K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr20:47641989 C>T maps to NM_006420.2 Y1632Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JM-01A-12D-A42J-10 chr20:62331970 G>C maps to NM_003224.3 A167A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-AAVM-01A-11D-A42J-10 chr3:121289565 G>A maps to NM_001012659.1 R2R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47N-01A-11D-A25F-10 chr11:46702649 G>A maps to NM_004308.2 F182F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A8YH-01A-11D-A36X-10 chr11:46701794 G>A maps to NM_004308.2 N286N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A57E-01A-11D-A26P-10 chr15:32929466 T>C maps to NM_014783.3 L831L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PS-01A-11D-A42J-10 chr6:129963089 G>T maps to NM_033515.2 R63R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47N-01A-11D-A25F-10 chr10:24873802 T>C maps to NM_020824.3 G1805G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9J2-01A-11D-A382-10 chr1:94650460 G>T maps to NM_004815.3 A692A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Y8-A8RZ-01A-11D-A36X-10 chr1:94639616 G>T maps to NM_004815.3 P1198P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JQ-01A-11D-A42J-10 chr3:119133436 C>T maps to NM_020754.2 D887D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KV-A6GD-01A-11D-A31X-10 chr11:128933814 A>G maps to NM_001142685.1 P275P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chr23:130215817 G>A did not map to a codon.
Sequencing variant TCGA-SX-A7SR-01A-12D-A35Z-10 chr23:11160421 C>T did not map to a codon.
Sequencing variant TCGA-BQ-5891-01A-11D-1589-08 chr12:57869642 G>T maps to ENST00000393797 R499R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A71U-01A-12D-A33Q-10 chr17:79827785 T>G maps to NM_004309.4 T7T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4A-A93X-01A-11D-A36X-10 chr8:1814769 T>G did not map to a codon.
Sequencing variant TCGA-B9-5155-01A-01D-1589-08 chr1:18023595 G>A maps to NM_018125.3 L1187L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A772-01A-11D-A33Q-10 chr1:156911225 C>T did not map to a codon.
Sequencing variant TCGA-SX-A7SR-01A-12D-A35Z-10 chr1:156906701 A>C maps to NM_198236.1 A1512A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7837-01A-11D-2136-08 chr11:73066675 C>G maps to NM_014786.3 A1184A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WN-AB4C-01A-11D-A42J-10 chr11:73022202 T>A maps to NM_014786.3 P840P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4A-A93Y-01A-11D-A36X-10 chr1:16532673 C>T did not map to a codon.
Sequencing variant TCGA-5P-A9JV-01A-12D-A42J-10 chr1:16532448 C>T maps to NM_153213.3 Q476Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7997-01A-11D-2201-08 chr3:56787576 G>C maps to NM_001128615.1 S163S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr23:135825891 A>T did not map to a codon.
Sequencing variant TCGA-BQ-5885-01A-11D-1589-08 chr13:111885552 G>A maps to NM_001113511.1 E245E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9J5-01A-21D-A382-10 chr1:27056348 C>T maps to NM_006015.4 Q449*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8515-01A-11D-2396-08 chr1:27107194 C>A maps to NM_006015.4 S2269*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A83S-01A-11D-A34Z-10 chr1:27056260 G>T maps to NM_006015.4 G419G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A8YI-01A-21D-A36X-10 chr6:157099428 G>A maps to ENST00000367148 Q122Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr6:157527599 G>A maps to ENST00000367148 K1815K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7288-01A-11D-2136-08 chr12:46285792 G>A did not map to a codon.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr12:46246366 C>A maps to NM_152641.2 P1487P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7841-01A-11D-2136-08 chr19:971935 C>G maps to NM_005224.2 G551G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr1:235386543 T>C maps to NM_016374.5 G334G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5901-01A-11D-1589-08 chr2:97216936 G>A maps to NM_212481.1 G224G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JD-01A-11D-A42J-10 chr10:63851118 C>T maps to NM_032199.2 L633L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7734-01A-11D-2136-08 chr10:63852306 C>A maps to NM_032199.2 R1029R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A7SP-01A-11D-A34Z-10 chr3:49005965 G>T did not map to a codon.
Sequencing variant TCGA-Y8-A8S1-01A-11D-A36X-10 chr7:102738802 C>T maps to NM_031905.3 R279*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7840-01A-11D-2136-08 chr10:28270469 T>C maps to NM_018076.2 K287K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E7-01A-31D-A28G-10 chr3:137982981 C>T maps to ENST00000469044 H409H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr7:98990334 C>T maps to NM_005720.2 A275A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A71U-01A-12D-A33Q-10 chr1:183604773 C>A maps to ENST00000294742 S7S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PM-01A-21D-A382-10 chr23:69500416 G>C did not map to a codon.
Sequencing variant TCGA-2Z-A9JN-01A-21D-A42J-10 chr9:140508148 C>G maps to NM_152285.2 S121S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9J1-01A-11D-A382-10 chr5:78135233 G>A maps to NM_000046.3 S386S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7836-01A-11D-2136-08 chr23:2867408 G>A did not map to a codon.
Sequencing variant TCGA-P4-A5E8-01A-11D-A28G-10 chr23:2861168 C>T did not map to a codon.
Sequencing variant TCGA-4A-A93X-01A-11D-A36X-10 chr2:9528625 C>T maps to NM_003887.2 A778A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Y8-A896-01A-11D-A35Z-10 chr2:9496454 C>T maps to NM_003887.2 C436C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7050-01A-11D-1961-08 chr7:150878331 G>T maps to ENST00000422024 A311A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr7:150878301 C>G maps to ENST00000422024 L321L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A7SN-01A-11D-A34Z-10 chr10:5683907 C>T maps to NM_024701.3 A178A. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-2Z-A9JP-01A-11D-A42J-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-B9-4113-01A-01D-1252-08 chr4:177136795 T>C maps to NM_080874.3 Q315Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A656-01A-11D-A31X-10 chr9:132400145 T>A maps to NM_017873.2 K397*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7062-01A-11D-1961-08 chr6:101296248 T>A maps to NM_006828.2 I192I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3468-01A-01D-1252-08 chr1:155408152 T>A maps to ENST00000368346 P1931P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59R-01A-11D-A26P-10 chr1:155313420 G>A maps to ENST00000368346 R2703R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A9DD-01A-11D-A36X-10 chr1:155449728 A>G maps to ENST00000368346 L978L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-AAVM-01A-11D-A42J-10 chr1:155308131 G>A maps to ENST00000368346 Q2856*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A656-01A-11D-A31X-10 chr23:1540610 G>C did not map to a codon.
Sequencing variant TCGA-HE-A5NH-01A-11D-A26P-10 chr8:62460749 C>T maps to NM_004318.3 E548E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JR-01A-12D-A42J-10 chr11:62156670 A>T maps to NM_025080.3 T186T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NI-01A-11D-A26P-10 chr2:25972918 C>T maps to NM_018263.4 E502E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7045-01A-31D-1961-08 chr18:31263417 A>G maps to NM_030632.1 G255G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PR-01A-11D-A42J-10 chr1:1426048 C>T maps to NM_031921.4 Q538*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5Y1-01A-11D-A28G-10 chr17:29220518 A>T maps to NM_024857.3 K1550*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A560-01A-11D-A26P-10 chr17:29162088 T>A maps to NM_024857.3 P330P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9Q1-01A-11D-A42J-10 chr19:3907798 G>C maps to NM_033064.4 T142T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PJ-A8JU-01A-11D-A35Z-10 chr22:39918543 C>A maps to NM_182810.1 I331I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A855-01A-11D-A34Z-10 chr19:50436033 G>T maps to NM_001193646.1 P178P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5885-01A-11D-1589-08 chr12:53931333 A>T maps to NM_001130059.1 A100A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JE-01A-11D-A42J-10 chr16:10525250 T>C maps to NM_024997.2 S258S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7842-01A-11D-2136-08 chr2:234173558 T>C maps to ENST00000392018 T137T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PO-01A-11D-A382-10 chr2:242611646 G>T maps to ENST00000337606 E500*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Y8-A896-01A-11D-A35Z-10 chr2:220090236 G>A maps to NM_024085.3 D90D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr2:216211584 C>A maps to NM_004044.6 S475*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9J1-01A-11D-A382-10 chr11:108192078 G>T maps to NM_000051.3 S2168S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7997-01A-11D-2201-08 chr11:108155201 T>C did not map to a codon.
Sequencing variant TCGA-UZ-A9PS-01A-11D-A42J-10 chr11:108236078 A>T maps to NM_000051.3 V3005V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WN-A9G9-01A-12D-A36X-10 chr11:108143335 T>A did not map to a codon.
Sequencing variant TCGA-G7-A8LB-01A-11D-A35Z-10 chr16:81077146 A>T maps to NM_015251.2 V348V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7061-01A-11D-1961-08 chr12:7046364 C>G maps to NM_001940.3 S645S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7286-01A-11D-2136-08 chr15:25959388 C>G did not map to a codon.
Sequencing variant TCGA-A4-8312-01A-11D-2396-08 chr15:25972304 A>T did not map to a codon.
Sequencing variant TCGA-B1-A47M-01A-11D-A25F-10 chr15:25981204 G>A maps to NM_024490.3 C246C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A6HP-01A-11D-A31X-10 chr13:113474212 G>A did not map to a codon.
Sequencing variant TCGA-B1-7332-01A-11D-2136-08 chr23:138844141 A>G did not map to a codon.
Sequencing variant TCGA-HE-A5NH-01A-11D-A26P-10 chr23:138880881 A>C did not map to a codon.
Sequencing variant TCGA-2Z-A9JE-01A-11D-A42J-10 chr1:160104411 T>G did not map to a codon.
Sequencing variant TCGA-B9-4115-01A-01D-1252-08 chr1:160105303 C>A maps to NM_000702.3 G732G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PP-01A-11D-A42J-10 chr19:42482814 T>A maps to ENST00000441343 K525*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PZ-01A-11D-A42J-10 chr1:160146319 A>C maps to NM_144699.3 R840R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JL-01A-11D-A42J-10 chr23:119504977 T>C did not map to a codon.
Sequencing variant TCGA-5P-A9K0-01A-11D-A42J-10 chr23:119500446 G>C did not map to a codon.
Sequencing variant TCGA-GL-A9DC-01A-11D-A36X-10 chr12:110760812 T>C maps to NM_170665.3 P160P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5885-01A-11D-1589-08 chr3:10387741 G>A maps to NM_001001331.2 L828L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A7SL-01A-11D-A34Z-10 chr3:10400377 T>C maps to NM_001001331.2 P711P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9J1-01A-11D-A382-10 chr23:152826187 C>A did not map to a codon.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr23:152826335 C>T did not map to a codon.
Sequencing variant TCGA-GL-7966-01A-11D-2201-08 chr23:152823736 C>T did not map to a codon.
Sequencing variant TCGA-MH-A856-01A-11D-A34Z-10 chr16:84482188 C>T maps to ENST00000416219 R518R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9J5-01A-21D-A382-10 chr10:7841870 A>T maps to NM_001001973.1 K189*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JD-01A-11D-A42J-10 chr10:7842037 T>C maps to NM_001001973.1 N207N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7828-01A-11D-2136-08 chr23:153657421 C>A did not map to a codon.
Sequencing variant TCGA-Y8-A897-01A-11D-A35Z-10 chr12:124236886 C>T maps to NM_012463.3 Q705*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5877-01A-11D-1589-08 chr5:172410943 C>T maps to NM_003945.3 F27F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A83W-01A-11D-A34Z-10 chr3:113505218 T>C maps to NM_001690.3 D235D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M8-01A-11D-A31X-10 chr23:77268390 T>A did not map to a codon.
Sequencing variant TCGA-UZ-A9Q1-01A-11D-A42J-10 chr23:77254010 C>T did not map to a codon.
Sequencing variant TCGA-B9-4113-01A-01D-1252-08 chr13:52548107 A>T maps to NM_000053.2 A416A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr13:52548875 G>A maps to NM_000053.2 S160S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A9DE-01A-11D-A36X-10 chr20:50217800 C>T maps to NM_006045.1 K1031K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A7UZ-01A-12D-A34Z-10 chr18:77013435 T>G maps to NM_198531.3 L388*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4113-01A-01D-1252-08 chr3:142274791 A>T maps to NM_001184.3 S756S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-7502-01A-11D-2201-08 chr3:142238532 G>A maps to NM_001184.3 L1454L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5887-01A-11D-1961-08 chr12:111923515 C>A did not map to a codon.
Sequencing variant TCGA-GL-A59R-01A-11D-A26P-10 chr12:111926344 A>G maps to NM_002973.3 V885V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A7SR-01A-12D-A35Z-10 chr12:112036793 C>T maps to NM_002973.3 Q175Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4114-01A-01D-1252-08 chr17:42275085 C>A maps to NM_020218.1 E22*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5878-01A-11D-1589-08 chr2:74756586 G>C maps to ENST00000258081 L30L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F9-A7Q0-01A-11D-A35Z-10 chr20:54963210 C>G did not map to a codon.
Sequencing variant TCGA-B9-A8YH-01A-11D-A36X-10 chr7:70239069 C>T maps to NM_015570.2 L629L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M9-01A-11D-A31X-10 chr7:70255843 A>G maps to NM_015570.2 T1214T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EA-01A-11D-A28G-10 chr7:70231265 G>A maps to NM_015570.2 P545P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-A8LD-01A-11D-A35Z-10 chr12:63544412 G>C maps to NM_000706.3 G68G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F9-A8NY-01A-11D-A35Z-10 chr1:206225072 G>T maps to NM_000707.3 P211P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5901-01A-11D-1589-08 chr13:31821209 A>G maps to NM_194318.3 A107A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9Q0-01A-12D-A42J-10 chr12:122691298 A>T maps to NM_030765.2 P167P. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-G7-6792-01A-21D-1961-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-2Z-A9JK-01A-11D-A42J-10 chr1:44447484 G>T maps to ENST00000309519 A175A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8630-01A-11D-2396-08 chr3:118945880 C>T maps to NM_212543.1 Q87Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A48D-01A-11D-A25F-10 chr9:104125252 T>C maps to NM_001701.3 V238V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr6:90660213 G>A maps to NM_001170794.1 P537P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr14:104027516 A>T maps to NM_001015049.2 T36T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PR-01A-11D-A42J-10 chr8:143558842 G>A maps to NM_001702.2 Q440Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9K2-01A-11D-A42J-10 chr1:32198683 G>A maps to NM_001703.2 A1171A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7585-01A-11D-2136-08 chr1:32207415 C>A maps to NM_001703.2 E524*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5875-01A-11D-1589-08 chr1:32203281 G>A maps to NM_001703.2 T949T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4116-01A-01D-1252-08 chr7:97933660 G>A maps to NM_018842.4 T423T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NK-01A-11D-A26P-10 chr22:38483171 G>T maps to NM_025045.4 S406S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7996-01A-11D-2201-08 chr16:1398015 C>G maps to NM_003933.4 Y1084*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V9-A7HT-01A-11D-A33Q-10 chr10:28970451 T>C maps to NM_012342.2 S114S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A48D-01A-11D-A25F-10 chr16:88105727 G>A maps to NM_001173543.1 A466A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3468-01A-01D-1252-08 chr3:52441416 G>C maps to NM_004656.2 A145A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-5155-01A-01D-1589-08 chr1:171553266 C>T maps to ENST00000392078 Q2528*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-A8LB-01A-11D-A35Z-10 chr1:171501479 A>G did not map to a codon.
Sequencing variant TCGA-GL-8500-01A-11D-2396-08 chr19:49464329 T>C maps to NM_004324.3 Y211Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr14:35242929 A>G maps to NM_013448.2 V1000V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5901-01A-11D-1589-08 chr7:72907198 T>C maps to NM_032408.3 G208G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-A8LB-01A-11D-A35Z-10 chr2:160295122 T>A maps to NM_013450.2 P328P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4116-01A-01D-1252-08 chr16:56531662 G>A maps to NM_031885.3 L597L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Y8-A894-01A-11D-A35Z-10 chr23:152988657 C>T did not map to a codon.
Sequencing variant TCGA-2Z-A9JM-01A-12D-A42J-10 chr16:75263501 A>T maps to NM_001170714.1 P886P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4114-01A-01D-1252-08 chr1:94054730 C>T maps to NM_003567.2 Q244Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A7SO-01A-11D-A34Z-10 chr1:94049638 A>G maps to NM_003567.2 D323D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A71R-01A-12D-A33Q-10 chr12:50232320 A>G maps to NM_181708.2 L238L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9JU-01A-11D-A42J-10 chr16:31121524 G>T did not map to a codon.
Sequencing variant TCGA-J7-A8I2-01A-12D-A35Z-10 chr15:80263199 T>G maps to NM_004049.3 R88R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A562-01A-11D-A26P-10 chr20:30253880 A>G maps to NM_138578.1 F191F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JG-01A-11D-A42J-10 chr22:18138482 G>C maps to NM_015367.2 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NK-01A-11D-A26P-10 chr14:23776984 C>A maps to NM_004050.4 T3T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4116-01A-01D-1252-08 chr16:30899186 C>T maps to NM_004765.2 *218*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7058-01A-11D-1961-08 chr1:147086308 A>C maps to NM_004326.2 R152R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8311-01A-11D-2396-08 chr11:118771982 C>T maps to NM_182557.2 Q823Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A6HP-01A-11D-A31X-10 chr11:118773515 C>A maps to NM_182557.2 P312P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7286-01A-11D-2136-08 chr6:136596668 C>T did not map to a codon.
Sequencing variant TCGA-BQ-5878-01A-11D-1589-08 chr6:136596668 C>T did not map to a codon.
Sequencing variant TCGA-IA-A83S-01A-11D-A34Z-10 chr6:136599310 A>G maps to NM_014739.2 P236P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8310-01A-11D-2396-08 chr23:39932879 G>T did not map to a codon.
Sequencing variant TCGA-A4-A5XZ-01A-11D-A31X-10 chr23:39932147 A>G did not map to a codon.
Sequencing variant TCGA-G7-A4TM-01A-11D-A31X-10 chr23:39916462 G>A did not map to a codon.
Sequencing variant TCGA-HE-A5NI-01A-11D-A26P-10 chr23:39923131 G>T did not map to a codon.
Sequencing variant TCGA-UZ-A9PP-01A-11D-A42J-10 chr23:39930897 A>G did not map to a codon.
Sequencing variant TCGA-2Z-A9JK-01A-11D-A42J-10 chr23:129189869 T>G did not map to a codon.
Sequencing variant TCGA-V9-A7HT-01A-11D-A33Q-10 chr22:23653907 C>T maps to NM_004327.3 Y1069Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5892-01A-11D-1589-08 chr5:70800507 C>T maps to NM_018429.2 Q768*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PL-01A-11D-A382-10 chr5:70793234 A>G maps to NM_018429.2 S646S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr14:101012902 G>A maps to NM_020836.3 H37H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr23:18195782 A>T did not map to a codon.
Sequencing variant TCGA-Y8-A8RY-01A-11D-A36X-10 chr6:107390744 A>G maps to NM_001080450.2 G550G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr11:61730353 C>T maps to NM_001139443.1 A516A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PM-01A-21D-A382-10 chr12:70072596 G>A maps to NM_032735.2 I186I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8310-01A-11D-2396-08 chr16:14755822 G>T maps to NM_016561.2 L286L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A57E-01A-11D-A26P-10 chr7:97842055 G>A maps to NM_177455.3 P145P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7286-01A-11D-2136-08 chr23:102004857 G>C did not map to a codon.
Sequencing variant TCGA-B9-A8YI-01A-21D-A36X-10 chr10:60549019 A>G did not map to a codon.
Sequencing variant TCGA-GL-A9DC-01A-11D-A36X-10 chr10:60560752 T>C maps to NM_001080512.1 C654C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr8:22488016 G>A maps to NM_018688.4 L79L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9K2-01A-11D-A42J-10 chr11:102221169 A>G maps to NM_001166.3 P195P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JS-01A-21D-A42J-10 chr2:32740320 T>C maps to NM_016252.3 A3611A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr2:32626578 C>T maps to NM_016252.3 Q436*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PU-01A-11D-A42J-10 chr2:32824825 G>T maps to NM_016252.3 A4617A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Y8-A8RZ-01A-11D-A36X-10 chr2:32702602 C>A maps to NM_016252.3 L2340L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NK-01A-11D-A26P-10 chr23:50658964 C>T did not map to a codon.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr23:50658767 A>T did not map to a codon.
Sequencing variant TCGA-DW-7840-01A-11D-2136-08 chr4:79786782 T>C maps to NM_198892.1 T380T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A7SP-01A-11D-A34Z-10 chr7:34125602 G>A maps to NM_133468.3 G548G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A48D-01A-11D-A25F-10 chr10:88681452 G>A did not map to a codon.
Sequencing variant TCGA-B9-5155-01A-01D-1589-08 chr15:83935686 C>A maps to NM_001717.3 L112L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7997-01A-11D-2201-08 chr9:16419220 A>G maps to NM_017637.5 S1022S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Y8-A8RZ-01A-11D-A36X-10 chr1:151011012 T>C maps to NM_138278.3 D57D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Y8-A8S0-01A-11D-A36X-10 chr4:13602061 C>T maps to NM_148894.2 L2154L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9Q1-01A-11D-A42J-10 chr2:198643754 C>T maps to NM_197970.2 Q67Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9K3-01A-11D-A42J-10 chr1:220232334 C>G did not map to a codon.
Sequencing variant TCGA-P4-AAVM-01A-11D-A42J-10 chr17:65916182 T>C maps to ENST00000321892 V1953V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PP-01A-11D-A42J-10 chr17:65944311 C>T maps to ENST00000321892 Q2732*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Y8-A8RY-01A-11D-A36X-10 chr7:140507810 T>C maps to NM_004333.4 E220E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5ED-01A-11D-A28G-10 chr12:112096634 G>A maps to NM_006768.3 R376*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A655-01A-11D-A31Z-10 chr17:41203098 G>A maps to ENST00000471181 P1793P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A83V-01A-11D-A34Z-10 chr23:154299851 A>G did not map to a codon.
Sequencing variant TCGA-A4-A5Y0-01A-11D-A31X-10 chr6:32944713 G>A did not map to a codon.
Sequencing variant TCGA-B3-4104-01A-01D-1458-08 chr6:32945958 C>G maps to ENST00000395289 P545P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4104-01A-01D-1458-08 chr6:32947798 C>G maps to ENST00000395289 S714*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-7502-01A-11D-2201-08 chr6:32945265 T>C maps to ENST00000395289 A416A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7996-01A-11D-2201-08 chr19:15350518 C>T maps to NM_058243.2 E1132E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A83W-01A-11D-A34Z-10 chr19:15349621 G>A maps to NM_058243.2 Q1318*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9Q1-01A-11D-A42J-10 chr19:15354086 G>A maps to NM_058243.2 Y931Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WN-AB4C-01A-11D-A42J-10 chr16:50373919 C>T maps to NM_001173984.2 K223K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4A-A93X-01A-11D-A36X-10 chr12:125509744 C>T maps to NM_080626.5 H175H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr12:125509639 C>A maps to NM_080626.5 S140S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4114-01A-01D-1252-08 chr11:1466622 C>T maps to NM_003957.2 D304D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A655-01A-11D-A31Z-10 chr21:40665926 G>T maps to NM_018963.3 S214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr23:80001212 G>A did not map to a codon.
Sequencing variant TCGA-4A-A93W-01A-11D-A36X-10 chr11:62474606 G>A maps to NM_001130702.1 Q21*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55Z-01A-11D-A26P-10 chr12:107713244 G>A maps to NM_001018072.1 A176A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Y8-A8S0-01A-11D-A36X-10 chr10:124066781 G>A maps to ENST00000368994 Q291Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5877-01A-11D-1589-08 chr19:1986876 C>G maps to NM_017797.3 P456P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr14:93708870 G>T maps to NM_001002860.2 T1049T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47N-01A-11D-A25F-10 chr6:26384117 T>C maps to NM_001197237.1 L23L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PL-01A-11D-A382-10 chr10:103190123 G>A maps to NM_033637.2 W24*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A7SP-01A-11D-A34Z-10 chr15:40505676 T>C did not map to a codon.
Sequencing variant TCGA-2Z-A9JE-01A-11D-A42J-10 chr10:45473409 C>A maps to NM_007021.3 L23L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr10:45472881 G>A maps to NM_007021.3 L199L. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-2Z-A9JO-01A-11D-A42J-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-MH-A854-01A-11D-A34Z-10 chr10:115922487 T>G maps to NM_018017.2 V180V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-7268-01A-11D-2136-08 chr10:121598083 A>G maps to NM_024834.2 D459D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A6HP-01A-11D-A31X-10 chr10:98741938 T>G maps to NM_015652.2 S264S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9J2-01A-11D-A382-10 chr10:127411635 G>T did not map to a codon.
Sequencing variant TCGA-GL-A4EM-01A-11D-A25F-10 chr10:5781660 C>T maps to NM_017782.4 Q510*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A9DE-01A-11D-A36X-10 chr10:23622019 A>G maps to NM_153714.2 L101L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr10:33134883 C>A maps to ENST00000375025 R509R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A40U-01A-11D-A25F-10 chr10:103789496 C>T maps to NM_024541.2 L104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A83S-01A-11D-A34Z-10 chr10:103769137 A>C maps to NM_024541.2 L316*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7056-01A-11D-1961-08 chr11:111753249 C>T maps to NM_022761.2 T68T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W9-01A-11D-A28G-10 chr11:30352521 C>T maps to NM_152316.1 V9V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A7SS-01A-11D-A35Z-10 chr11:93494796 A>G maps to ENST00000354421 A297A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8098-01A-11D-2396-08 chr11:77580811 G>A maps to NM_024684.2 E59E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E6-01A-11D-A28G-10 chr11:66610491 C>T maps to ENST00000360962 H641H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A40Y-01A-11D-A25F-10 chr12:110207029 G>A maps to NM_032829.2 T432T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5Y1-01A-11D-A28G-10 chr12:21680691 G>C maps to NM_030572.2 R59R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JM-01A-12D-A42J-10 chr12:112654882 C>T maps to NM_001109662.2 L2225L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JS-01A-21D-A42J-10 chr12:112664522 T>C maps to NM_001109662.2 L2126L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8195-01A-31D-2396-08 chr12:112668607 G>A maps to NM_001109662.2 P1901P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A7SM-01A-11D-A34Z-10 chr12:112622149 C>G maps to NM_001109662.2 L3368L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr12:48888592 T>C maps to NM_152319.3 P85P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4114-01A-01D-1252-08 chr12:64615825 G>C maps to ENST00000311915 A64A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-A8LB-01A-11D-A35Z-10 chr12:64615867 G>A maps to ENST00000311915 S50S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9J3-01A-12D-A382-10 chr12:14959530 G>A maps to NM_001013698.2 C28C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PJ-01A-11D-A382-10 chr12:93100475 G>A maps to NM_001037671.3 S23S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AT-A5NU-01A-11D-A28G-10 chr13:42031875 G>A maps to NM_014059.2 A11A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EA-01A-11D-A28G-10 chr13:46946277 G>A maps to NM_025113.2 S111S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5882-01A-11D-1589-08 chr13:39596541 A>T maps to NM_025138.3 Y217*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr14:57075922 C>A maps to NM_017799.3 R246R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NJ-01A-11D-A26P-10 chr14:57960295 T>A maps to NM_018168.2 S46S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8098-01A-11D-2396-08 chr14:45711248 A>C maps to NM_018353.4 L377L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A83T-01A-11D-A34Z-10 chr14:81297496 G>T maps to NM_152446.3 S400*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55W-01A-11D-A26P-10 chr14:91681815 C>T maps to NM_001102368.1 H544H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A71S-01A-11D-A33Q-10 chr14:91642284 G>A maps to NM_001102368.1 L205L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9KC-01A-11D-A42J-10 chr14:77845294 G>T maps to NM_001010860.1 E512*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr14:77844645 G>A maps to NM_001010860.1 K295K. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-B1-5398-01A-02D-1589-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-MH-A560-01A-11D-A26P-10 chr14:60921716 A>T did not map to a codon.
Sequencing variant TCGA-A4-A57E-01A-11D-A26P-10 chr14:65053587 G>A maps to NM_172365.1 K234K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5878-01A-11D-1589-08 chr14:23467860 A>C maps to NM_021944.2 P124P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5889-01A-11D-1589-08 chr15:24923230 T>A maps to NM_018958.2 T739T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E6-01A-11D-A28G-10 chr15:24923446 T>A maps to NM_018958.2 S811S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E7-01A-31D-A28G-10 chr15:24923341 C>T maps to NM_018958.2 A776A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NJ-01A-11D-A26P-10 chr15:75499666 C>T maps to NM_015492.4 C426C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chr15:90138744 T>C maps to NM_152259.3 D601D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PJ-A5Z9-01A-11D-A28G-10 chr15:90167320 G>A maps to NM_152259.3 T1260T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A40U-01A-11D-A25F-10 chr16:81094971 G>A maps to NM_152337.2 Q328*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr16:67168084 T>C maps to NM_025187.3 H155H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A9DE-01A-11D-A36X-10 chr16:9210570 A>G maps to NM_014117.2 P210P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr16:67702136 C>G maps to NM_001012984.2 Y196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A7SQ-01A-12D-A35Z-10 chr17:6555544 G>C maps to ENST00000391428 P104P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JQ-01A-11D-A42J-10 chr17:34185487 G>T maps to NM_152781.2 A327A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55W-01A-11D-A26P-10 chr17:79518168 A>G maps to NM_025161.5 P117P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PK-01A-11D-A382-10 chr17:57289013 G>A maps to NM_018149.6 V534V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A9DC-01A-11D-A36X-10 chr17:7162046 A>G maps to NM_203413.1 V260V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A561-01A-11D-A26P-10 chr17:74729097 C>A maps to ENST00000317409 A120A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chr18:71816321 C>G maps to NM_014177.2 T93T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4104-01A-01D-1458-08 chr19:757668 C>T maps to NM_173481.2 N241N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PN-01A-11D-A382-10 chr19:3544831 C>T maps to NM_021731.2 L465L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A7SQ-01A-12D-A35Z-10 chr19:36497827 G>T maps to ENST00000455847 R326R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9KA-01A-11D-A42J-10 chr19:14004036 C>T did not map to a codon.
Sequencing variant TCGA-A4-7584-01A-11D-2136-08 chr19:13996868 C>G did not map to a codon.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr11:119210070 G>C maps to NM_015645.3 S234S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9J8-01A-11D-A42J-10 chr1:244662359 G>A maps to NM_001130957.1 G136G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JQ-01A-11D-A42J-10 chr1:200869254 G>A maps to NM_018265.2 A153A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A561-01A-11D-A26P-10 chr1:210006561 G>T maps to NM_014388.6 E141*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8098-01A-11D-2396-08 chr1:169806132 C>T maps to NM_018186.2 S535S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PJ-A8JU-01A-11D-A35Z-10 chr1:36773208 G>A did not map to a codon.
Sequencing variant TCGA-B9-A5W9-01A-11D-A28G-10 chr1:24105127 A>G maps to NM_020362.4 Q41Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A657-01A-11D-A31X-10 chr1:182922004 C>G maps to ENST00000287709 A157A. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-G7-7501-01A-11D-2201-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-SX-A7SO-01A-11D-A34Z-10 chr1:75114959 C>A maps to NM_001002912.4 L21L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J7-6720-01A-11D-2136-08 chr1:156309582 G>C did not map to a codon.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr1:11775242 C>T maps to NM_198545.3 F305F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8515-01A-11D-2396-08 chr1:109649720 G>A maps to NM_001122961.1 F62F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9JU-01A-11D-A42J-10 chr1:185106773 C>A maps to NM_030934.4 E493*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A654-01A-11D-A31X-10 chr1:186355193 T>C maps to NM_017847.5 D103D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4A-A93W-01A-11D-A36X-10 chr1:154180024 T>G maps to NM_001098616.1 T222T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7585-01A-11D-2136-08 chr1:150258999 T>A maps to NM_144697.2 T264T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2K-A9WE-01A-11D-A382-10 chr1:150246487 A>G did not map to a codon.
Sequencing variant TCGA-GL-A9DD-01A-11D-A36X-10 chr1:109192979 G>A maps to ENST00000370031 Y203Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E6-01A-11D-A28G-10 chr1:223567035 C>T maps to NM_152610.2 R73R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8630-01A-11D-2396-08 chr1:156706430 T>C maps to NM_015997.3 H438H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5Y1-01A-11D-A28G-10 chr20:31892697 G>A did not map to a codon.
Sequencing variant TCGA-P4-A5E7-01A-31D-A28G-10 chr20:18414379 C>T maps to NM_001099407.1 L259L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6134-01A-11D-1961-08 chr20:2796279 G>T maps to NM_080739.2 L119L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9Q1-01A-11D-A42J-10 chr20:60992326 C>A maps to NM_080833.2 R51R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JM-01A-12D-A42J-10 chr20:20243775 T>A did not map to a codon.
Sequencing variant TCGA-P4-AAVM-01A-11D-A42J-10 chr20:20226856 C>T maps to ENST00000389655 S722S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A48D-01A-11D-A25F-10 chr20:1161647 G>A maps to NM_018354.1 Y205Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PO-01A-11D-A382-10 chr20:270902 A>T maps to NM_153269.1 V22V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55W-01A-11D-A26P-10 chr21:45949792 G>A maps to ENST00000443468 T228T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5903-01A-11D-1589-08 chr21:33651271 C>T maps to NM_018944.2 E18E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E7-01A-31D-A28G-10 chr22:24106286 G>A maps to NM_182520.2 V13V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9K6-01A-11D-A42J-10 chr22:32108918 T>G maps to NM_173566.2 R1636R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr2:27802750 C>A maps to NM_032266.3 P1104P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J7-A8I2-01A-12D-A35Z-10 chr2:27435094 C>T maps to NM_080592.3 H8H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JS-01A-21D-A42J-10 chr2:241835324 C>G maps to NM_001085437.1 A30A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AT-A5NU-01A-11D-A28G-10 chr2:219222407 C>T maps to NM_198559.1 A90A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr2:219222363 C>T maps to NM_198559.1 Q76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Y8-A8RY-01A-11D-A36X-10 chr2:74802618 C>T maps to NM_138804.3 W340*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A7SS-01A-11D-A35Z-10 chr2:26798880 T>C maps to NM_001105519.1 T62T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A71S-01A-11D-A33Q-10 chr2:29295390 G>A maps to NM_001029883.1 S579S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7997-01A-11D-2201-08 chr2:54587527 G>T maps to NM_001100396.1 L231L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9J6-01A-11D-A382-10 chr2:74043788 A>T maps to NM_001080474.1 S813S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4617-01A-01D-1252-08 chr2:74043216 C>A maps to NM_001080474.1 R623R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr3:62317064 T>A maps to NM_020685.3 V81V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Y8-A895-01A-11D-A35Z-10 chr3:11851066 A>T maps to ENST00000444133 P266P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A71S-01A-11D-A33Q-10 chr3:50324198 C>T maps to NM_153215.1 C89C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PJ-A8JU-01A-11D-A35Z-10 chr3:49841864 C>T maps to NM_203370.1 G103G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A7SO-01A-11D-A34Z-10 chr3:49308827 C>A maps to NM_198562.2 E197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8196-01A-11D-2396-08 chr3:48956090 T>A maps to NM_001123040.1 P164P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr4:165878575 T>C maps to NM_153027.1 P134P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A83S-01A-11D-A34Z-10 chr4:3254937 T>C maps to NM_001042690.1 L109L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4A-A93W-01A-11D-A36X-10 chr4:159592803 C>T maps to NM_001008393.2 V50V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-5155-01A-01D-1589-08 chr9:123742456 A>G maps to NM_001735.2 L1188L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr9:123783918 C>G maps to NM_001735.2 L390L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E6-01A-11D-A28G-10 chr5:156770120 C>A maps to NM_001001343.3 E142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NK-01A-11D-A26P-10 chr5:37121779 A>G maps to NM_023073.3 L2988L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PJ-01A-11D-A382-10 chr5:60455869 T>C maps to NM_001048249.3 K43K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-7332-01A-11D-2136-08 chr6:11735820 G>A maps to NM_001143948.1 A180A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F9-A8NY-01A-11D-A35Z-10 chr6:43193849 C>T maps to ENST00000509253 L168L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NJ-01A-11D-A26P-10 chr6:43193767 C>A maps to NM_199184.1 E127*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3466-01A-01D-1252-08 chr6:53989446 T>C maps to ENST00000502396 I143I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9JW-01A-11D-A42J-10 chr6:74161673 A>G maps to NM_138441.2 T77T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-7501-01A-11D-2201-08 chr6:74135069 A>G maps to NM_138441.2 Y483Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9J3-01A-12D-A382-10 chr6:42989440 C>T maps to NM_033112.2 R17*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A7SP-01A-11D-A34Z-10 chr6:42995150 G>C maps to NM_033112.2 L193L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A4EM-01A-11D-A25F-10 chr6:97629853 A>T maps to NM_198468.2 I770I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9J1-01A-11D-A382-10 chr6:121447578 C>A maps to ENST00000275159 V1017V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A69E-01A-11D-A31X-10 chr6:121433800 G>T maps to ENST00000275159 C1099*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5886-01A-11D-1589-08 chr6:121576520 T>A maps to ENST00000275159 V657V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9J5-01A-21D-A382-10 chr6:109480587 A>T maps to NM_173830.4 S313S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7045-01A-31D-1961-08 chr6:2623683 C>A maps to NM_152554.2 E125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PR-01A-11D-A42J-10 chr6:36298149 G>A maps to NM_001010903.4 F106F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chr6:31627424 A>G maps to NM_021184.3 T100T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A71U-01A-12D-A33Q-10 chr6:151907202 C>T maps to ENST00000367290 N424N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JT-01A-11D-A42J-10 chr7:2581811 G>C maps to NM_152743.3 V319V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JT-01A-11D-A42J-10 chr7:39610142 T>C maps to NM_020192.3 V56V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr7:66410207 T>C maps to NM_017994.4 H135H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5892-01A-11D-1589-08 chr7:100087002 C>T maps to ENST00000423930 A553A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr7:48081006 C>A maps to ENST00000430738 L89L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-7501-01A-11D-2201-08 chr7:120629776 C>G maps to NM_024913.4 T34T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A71U-01A-12D-A33Q-10 chr7:120935570 T>C maps to NM_024913.4 Y982Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F9-A7VF-01A-11D-A33Q-10 chr7:89903319 A>T maps to NM_001039706.2 K294*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A83S-01A-11D-A34Z-10 chr8:33364812 G>A maps to NM_001102401.1 N287N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7996-01A-11D-2201-08 chr8:67405942 T>A maps to NM_152765.3 I20I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9JU-01A-11D-A42J-10 chr8:144653907 C>T maps to NM_001100878.1 L177L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PZ-01A-11D-A42J-10 chr8:10555295 G>A maps to NM_001040032.1 E143E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J7-8537-01A-11D-2396-08 chr8:12879057 T>C maps to NM_020844.2 S290S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9KE-01A-11D-A42J-10 chr8:38369905 T>C maps to NM_207412.1 *224*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A8YH-01A-11D-A36X-10 chr9:98684630 C>T maps to NM_001010895.2 Y459Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4A-A93X-01A-11D-A36X-10 chr9:132084553 C>T maps to NM_001012715.3 S154S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A71U-01A-12D-A33Q-10 chr9:112963538 G>A maps to NM_001012993.2 Q137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9K3-01A-11D-A42J-10 chr9:139741256 C>T maps to NM_001080482.2 R797R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4104-01A-01D-1458-08 chr9:34397496 C>T maps to NM_032596.3 P45P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PL-01A-11D-A382-10 chr9:116185620 C>T maps to ENST00000451722 L183L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JD-01A-11D-A42J-10 chr9:111849611 G>A maps to NM_032012.3 L387L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8195-01A-31D-2396-08 chr9:111853339 G>A maps to NM_032012.3 R338*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A7SM-01A-11D-A34Z-10 chr9:111819563 C>T maps to NM_032012.3 L587L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PK-01A-11D-A382-10 chr9:214700 G>T maps to NM_152569.2 Y232*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr9:136333114 G>A maps to NM_017586.2 T131T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4116-01A-01D-1252-08 chr9:90501483 C>T maps to NM_178828.4 T694T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JS-01A-21D-A42J-10 chr9:74586474 A>G maps to NM_182505.3 P88P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PJ-01A-11D-A382-10 chr9:139730243 C>T maps to NM_001173988.1 A253A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-7268-01A-11D-2136-08 chr9:117400850 T>C maps to ENST00000374049 L233L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E8-01A-11D-A28G-10 chr9:15745612 C>T maps to NM_173550.2 D885D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9JY-01A-11D-A42J-10 chr15:63632588 G>A maps to NM_001218.3 T215T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8195-01A-31D-2396-08 chr8:61192347 C>T maps to NM_004056.4 S64S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-3925-01A-01D-1458-08 chr22:24447424 T>A maps to NM_012295.3 I265I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NH-01A-11D-A26P-10 chr20:60967981 C>G maps to NM_031215.2 S326S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-8500-01A-11D-2396-08 chr19:13346024 G>A maps to NM_023035.2 Q1715*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A71V-01A-11D-A33Q-10 chr19:13372412 G>A maps to NM_023035.2 D1371D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9J7-01A-11D-A382-10 chr9:140904504 G>C maps to ENST00000277549 L713L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9JY-01A-11D-A42J-10 chr9:141016004 C>T maps to ENST00000277549 Q2193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr9:140943669 T>C maps to ENST00000277549 L1206L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr12:2566787 G>T maps to NM_199460.2 G225*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NK-01A-11D-A26P-10 chr12:2763056 C>T maps to NM_199460.2 I1425I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JQ-01A-11D-A42J-10 chr3:53699774 T>G maps to NM_001128840.1 Y285*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9JW-01A-11D-A42J-10 chr3:53694258 C>A maps to NM_001128840.1 A241A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JK-01A-11D-A42J-10 chr1:181727892 G>T did not map to a codon.
Sequencing variant TCGA-HE-A5NK-01A-11D-A26P-10 chr1:181701627 G>A maps to ENST00000357570 A802A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7046-01A-11D-1961-08 chr1:201034980 G>T maps to NM_000069.2 G946G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr3:54930839 C>A maps to NM_018398.2 R771R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3468-01A-01D-1252-08 chr17:37331565 C>T maps to NM_000723.3 L559L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M9-01A-11D-A31X-10 chr17:37341118 T>A did not map to a codon.
Sequencing variant TCGA-4A-A93Y-01A-11D-A36X-10 chr16:24358124 C>T maps to NM_006539.3 A94A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9JV-01A-12D-A42J-10 chr16:24372985 C>T maps to NM_006539.3 I250I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5885-01A-11D-1589-08 chr2:27440796 C>A maps to NM_004341.3 Y45*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NL-01A-11D-A26P-10 chr1:159170697 G>T maps to NM_021189.3 E429*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A856-01A-11D-A34Z-10 chr3:62535722 G>A maps to ENST00000383709 D607D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5886-01A-11D-1589-08 chr7:122269334 A>G maps to NM_001167940.1 D278D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PP-01A-11D-A42J-10 chr11:14992663 T>A maps to NM_001741.2 A25A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PS-01A-11D-A42J-10 chr11:14991617 A>T maps to NM_001741.2 S30S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47M-01A-11D-A25F-10 chr14:90870814 C>T maps to NM_006888.4 I126I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F9-A7VF-01A-11D-A33Q-10 chr14:90870769 A>C maps to NM_006888.4 T111T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr4:114434487 G>A maps to ENST00000515496 F314F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr3:48266892 T>C maps to NM_004345.3 L164L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JE-01A-11D-A42J-10 chr1:7811257 G>T did not map to a codon.
Sequencing variant TCGA-Y8-A898-01A-11D-A34Z-10 chr1:7724718 G>T maps to NM_015215.2 L704L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9J1-01A-11D-A382-10 chr5:179150704 G>A maps to ENST00000415618 P516P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr6:17507927 T>C maps to NM_006366.2 T167T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9JZ-01A-11D-A42J-10 chr6:44137018 G>A maps to NM_007058.3 E30E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JL-01A-11D-A42J-10 chr19:39233091 T>A maps to NM_144691.3 G128G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A562-01A-11D-A26P-10 chr19:39226165 G>T maps to NM_144691.3 I534I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JG-01A-11D-A42J-10 chr3:15287045 A>G maps to NM_014296.2 P626P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-5155-01A-01D-1589-08 chr1:230907779 A>G maps to NM_006615.2 R270R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JT-01A-11D-A42J-10 chr19:36631957 C>G maps to NM_001749.2 G15G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-8121-01A-21D-2396-08 chr12:30888128 C>T maps to NM_001002259.1 A194A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6790-01A-11D-1961-08 chr19:5914494 G>T maps to ENST00000394521 L159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A6HP-01A-11D-A31X-10 chr22:37898634 C>G maps to NM_014550.3 R587R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JL-01A-11D-A42J-10 chr11:67186482 C>G maps to NM_001166222.1 A207A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr17:38319004 G>A maps to NM_007359.4 W212*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5Y1-01A-11D-A28G-10 chr15:40913800 A>T maps to NM_170589.3 R473*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PO-01A-11D-A382-10 chr16:2228946 C>T maps to NM_020764.3 Q1385Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4113-01A-01D-1252-08 chr19:15164632 C>T maps to NM_012114.2 H89H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A7SL-01A-11D-A34Z-10 chr11:104819263 C>T maps to NM_001225.3 T307T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WN-AB4C-01A-11D-A42J-10 chr6:90571847 G>A maps to NM_012115.3 L140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M8-01A-11D-A31X-10 chr1:10714627 G>A maps to NM_001079843.1 Y562Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8311-01A-11D-2396-08 chr11:65788965 C>T did not map to a codon.
Sequencing variant TCGA-B9-A44B-01A-11D-A25F-10 chr15:43940127 G>A maps to NM_172095.1 I44I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AT-A5NU-01A-11D-A28G-10 chr19:38850107 A>T did not map to a codon.
Sequencing variant TCGA-B9-A8YH-01A-11D-A36X-10 chr20:54579176 G>A maps to NM_080617.4 V17V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-7268-01A-11D-2136-08 chr4:169931207 G>T maps to NM_032783.4 S11S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr17:46152377 G>A maps to ENST00000442683 L139L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A83V-01A-11D-A34Z-10 chr17:46154300 C>T maps to ENST00000442683 V22V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7841-01A-11D-2136-08 chr7:26251699 A>T did not map to a codon.
Sequencing variant TCGA-MH-A855-01A-11D-A34Z-10 chr17:77807916 T>C maps to NM_003655.2 A508A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E7-01A-31D-A28G-10 chr22:39066950 G>A maps to NM_015373.3 L47L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9JZ-01A-11D-A42J-10 chr4:15539634 T>C maps to NM_001080522.2 D626D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A9DC-01A-11D-A36X-10 chr10:97784669 T>A did not map to a codon.
Sequencing variant TCGA-5P-A9JU-01A-11D-A42J-10 chr10:70550998 C>G maps to NM_018237.2 S1143S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A854-01A-11D-A34Z-10 chr1:89409052 T>A maps to NM_001008661.2 K399*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9J2-01A-11D-A382-10 chr17:42979926 G>A maps to NM_213607.1 P157P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr4:186382304 C>A maps to NM_152775.3 S82S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5891-01A-11D-1589-08 chr22:21989094 C>G maps to NM_152612.2 S248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A71S-01A-11D-A33Q-10 chr7:128441372 C>T maps to NM_022742.3 S160S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A7SL-01A-11D-A34Z-10 chr2:179720164 A>T maps to NM_173648.3 L990*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8630-01A-11D-2396-08 chr7:76866322 C>G maps to NM_020879.2 T72T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A7SQ-01A-12D-A35Z-10 chr7:76922399 C>T maps to NM_020879.2 F849F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-AAVL-01A-11D-A42J-10 chr1:46088724 C>A maps to NM_001114938.2 L186L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JD-01A-11D-A42J-10 chr3:180334121 T>C maps to NM_181426.1 T872T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A855-01A-11D-A34Z-10 chr3:180379789 A>G maps to NM_181426.1 L72L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9K2-01A-11D-A42J-10 chr3:128720758 C>A maps to NM_024768.2 A96A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A57E-01A-11D-A26P-10 chr17:28512532 G>T maps to NM_032141.2 G506G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5881-01A-11D-1589-08 chr3:122102041 A>G maps to NM_001017928.2 C10C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A71R-01A-12D-A33Q-10 chr12:82752071 C>T maps to NM_014167.4 R28R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8098-01A-11D-2396-08 chr11:32676506 T>C maps to NM_001008391.2 K219K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9KH-01A-11D-A42J-10 chr2:132289288 C>T maps to NM_138770.1 D199D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-AAVM-01A-11D-A42J-10 chr11:86125891 A>C maps to NM_001156474.1 R485R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W9-01A-11D-A28G-10 chr11:65658487 C>T maps to NM_006848.2 R78R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A4EM-01A-11D-A25F-10 chr11:60609626 G>T maps to NM_024098.3 R10R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2K-A9WE-01A-11D-A382-10 chr6:13814460 T>C maps to NM_001031713.2 S67S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PJ-01A-11D-A382-10 chr5:169026068 T>G maps to NM_017785.4 L410L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr7:45112358 C>T maps to NM_001029835.2 T281T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7286-01A-11D-2136-08 chr4:78082687 C>T maps to NM_004354.2 R195*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A9DE-01A-11D-A36X-10 chr4:77969740 A>G maps to NM_006835.2 P255P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5882-01A-11D-1589-08 chr5:132084159 C>A maps to NM_001039780.2 S184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4104-01A-01D-1458-08 chr1:1334455 G>A maps to NM_030937.4 L77L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A83T-01A-11D-A34Z-10 chr5:54528320 G>A maps to NM_021147.3 R145R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9KE-01A-11D-A42J-10 chr2:208576634 G>A maps to ENST00000295414 L5L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9KA-01A-11D-A42J-10 chr3:45943246 A>C maps to NM_031200.2 R323R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JM-01A-12D-A42J-10 chr3:132319325 C>T maps to NM_178445.1 L29L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5Y0-01A-11D-A31X-10 chr1:156294857 A>G maps to NM_005998.4 A109A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NJ-01A-11D-A26P-10 chr5:10263418 G>A maps to NM_012073.3 G497G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr2:73471794 G>T maps to NM_006429.3 L190L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9K8-01A-11D-A42J-10 chr22:17072975 C>T maps to NM_014406.4 L155L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F9-A8NY-01A-11D-A35Z-10 chr22:17072540 G>A maps to NM_014406.4 D300D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PV-01A-11D-A42J-10 chr22:17073026 C>T maps to NM_014406.4 T138T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9J3-01A-12D-A382-10 chr12:7528024 T>C maps to ENST00000416109 G961G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W8-01A-11D-A28G-10 chr12:7526000 C>T maps to ENST00000416109 T1225T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A48D-01A-11D-A25F-10 chr6:109690200 C>T maps to NM_006016.4 V149V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5885-01A-11D-1589-08 chr5:66478707 T>G maps to NM_005582.2 R655R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7996-01A-11D-2201-08 chr19:7810713 G>A maps to NM_021155.3 I146I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7584-01A-11D-2136-08 chr19:35828751 C>T maps to NM_001771.3 N271N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A71U-01A-12D-A33Q-10 chr19:45912506 G>A maps to ENST00000423698 K429K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9J2-01A-11D-A382-10 chr11:60891375 C>T maps to NM_014207.3 Q416*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A561-01A-11D-A26P-10 chr1:26646660 G>T did not map to a codon.
Sequencing variant TCGA-HE-A5NJ-01A-11D-A26P-10 chr12:6309730 G>A maps to NM_001769.2 W22*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JD-01A-11D-A42J-10 chr13:49852538 T>A maps to NM_030911.3 A368A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Y8-A896-01A-11D-A35Z-10 chr13:115008768 G>T maps to NM_003903.3 L193L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9J7-01A-11D-A382-10 chr1:43825897 A>G maps to NM_001255.2 V197V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr1:43828620 G>A did not map to a codon.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr9:4706078 A>G maps to NM_017913.2 E327E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr1:22413229 C>G maps to NM_001039802.1 L119L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr1:22413328 C>G maps to NM_001039802.1 V152V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WN-AB4C-01A-11D-A42J-10 chr1:227182593 G>T maps to ENST00000366766 S1688*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9J6-01A-11D-A382-10 chr11:64594521 C>T maps to NM_017525.2 P1463P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F9-A8NY-01A-11D-A35Z-10 chr6:44355566 C>T maps to NM_001253.2 R3*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PJ-01A-11D-A382-10 chr2:174230205 C>G maps to NM_031942.4 R307R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A69E-01A-11D-A31X-10 chr16:68853182 A>C maps to NM_004360.3 T522T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WN-AB4C-01A-11D-A42J-10 chr5:22078620 G>A maps to NM_004061.3 G55G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr10:73406334 C>T maps to ENST00000398860 Y475Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-AAVL-01A-11D-A42J-10 chr10:73567273 C>G maps to ENST00000398860 A2775A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NF-01A-11D-A26P-10 chr14:23524348 T>A maps to NM_022478.3 K139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-5156-01A-01D-1589-08 chr5:31323225 T>G maps to NM_004932.2 T728T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JN-01A-21D-A42J-10 chr16:61687963 C>A maps to NM_001796.2 E650*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8196-01A-11D-2396-08 chr16:61851549 C>T maps to NM_001796.2 G370G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A562-01A-11D-A26P-10 chr16:89760631 C>T maps to NM_052988.4 I220I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A83S-01A-11D-A34Z-10 chr7:90547016 G>T maps to NM_012395.2 G250G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9J5-01A-21D-A382-10 chr2:202698680 A>G maps to ENST00000450471 K239K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6135-01A-11D-1961-08 chr17:30815100 C>T maps to NM_003885.2 L155L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-7502-01A-11D-2201-08 chr17:46058012 C>T maps to NM_176096.1 L378L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A657-01A-11D-A31X-10 chr4:76521461 G>T maps to ENST00000307465 S462*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr4:76529104 T>A maps to ENST00000307465 K231*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Y8-A894-01A-11D-A35Z-10 chr23:18598003 G>T did not map to a codon.
Sequencing variant TCGA-B9-A5W8-01A-11D-A28G-10 chr9:21971183 T>G maps to NM_001195132.1 R58R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6789-01A-11D-1961-08 chr9:21971119 G>A maps to NM_001195132.1 R80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-5561-01A-01D-1589-08 chr9:22006243 G>A maps to NM_004936.3 V53V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JR-01A-12D-A42J-10 chr1:51439794 G>A maps to NM_078626.2 E120E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr16:22360667 C>A maps to NM_001802.1 P146P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr19:33793107 G>T maps to NM_004364.3 A71A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr19:33793119 G>T maps to NM_004364.3 Y67*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9JY-01A-11D-A42J-10 chr9:135939798 C>T maps to NM_001807.3 A28A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8630-01A-11D-2396-08 chr1:22310246 C>T maps to NM_007352.2 L141L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A6HP-01A-11D-A31X-10 chr1:151678721 T>C maps to NM_007185.4 Q368Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4114-01A-01D-1252-08 chr1:151678721 T>C maps to NM_007185.4 Q368Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8517-01A-11D-2396-08 chr22:46765597 A>G maps to NM_014246.1 A2621A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4104-01A-01D-1458-08 chr22:46930991 G>A maps to NM_014246.1 Y692Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NH-01A-11D-A26P-10 chr22:46931729 G>A maps to NM_014246.1 Y446Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-A6W5-01A-12D-A33Q-10 chr1:109801144 G>A maps to NM_001408.2 E1134E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A654-01A-11D-A31X-10 chr3:48699893 G>A maps to NM_001407.2 G58G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Y8-A8S1-01A-11D-A36X-10 chr3:48690464 A>T maps to NM_001407.2 L1868L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J7-8537-01A-11D-2396-08 chr4:104117118 A>C maps to NM_001813.2 V105V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A83T-01A-11D-A34Z-10 chr1:214802435 T>C maps to NM_016343.3 S372S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A560-01A-11D-A26P-10 chr1:214815374 G>T maps to NM_016343.3 E1232*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E6-01A-11D-A28G-10 chr1:214813547 A>T maps to NM_016343.3 K623*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A8YH-01A-11D-A36X-10 chr23:100375403 G>C did not map to a codon.
Sequencing variant TCGA-SX-A7SM-01A-11D-A34Z-10 chr23:100402790 G>T did not map to a codon.
Sequencing variant TCGA-SX-A71R-01A-12D-A33Q-10 chr13:25486721 G>A maps to NM_018451.3 Q148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5876-01A-11D-1589-08 chr22:42342455 C>G maps to NM_024053.3 S34S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A8YI-01A-21D-A36X-10 chr16:67862426 A>G maps to NM_025082.3 H504H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9Q1-01A-11D-A42J-10 chr4:56818347 C>T maps to NM_025009.3 Q18*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A8YI-01A-21D-A36X-10 chr15:49089694 G>T maps to NM_001194998.1 R115R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A83T-01A-11D-A34Z-10 chr15:49030643 C>T maps to NM_001194998.1 T1645T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Y8-A8RY-01A-11D-A36X-10 chr15:49031303 G>A maps to NM_001194998.1 N1425N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A8YH-01A-11D-A36X-10 chr18:13105008 T>C maps to NM_032142.3 F2326F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59T-01A-21D-A28G-10 chr12:88514779 A>C maps to NM_025114.3 Y451*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WN-A9G9-01A-12D-A36X-10 chr2:65299732 C>A maps to NM_015147.2 S501S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PS-01A-11D-A42J-10 chr2:182468797 T>A maps to NM_001030311.2 K83*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Y8-A8RZ-01A-11D-A36X-10 chr6:31916622 A>G maps to ENST00000437789 S853S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A560-01A-11D-A26P-10 chr1:196654323 A>G maps to NM_000186.3 A307A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A7UZ-01A-12D-A34Z-10 chr1:196952180 A>G maps to ENST00000367414 E99E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A71W-01A-12D-A34Z-10 chr7:117232345 C>A maps to NM_000492.3 R709R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Y8-A894-01A-11D-A35Z-10 chr15:57730577 T>C maps to NM_032866.3 N127N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9J6-01A-11D-A382-10 chr2:27324435 G>T maps to ENST00000404694 P343P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr12:6707539 G>A maps to ENST00000309577 Q512*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9KE-01A-11D-A42J-10 chr1:6212474 G>T maps to NM_015557.2 S289S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5878-01A-11D-1589-08 chr1:6204187 G>A maps to NM_015557.2 Y610Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A44B-01A-11D-A25F-10 chr20:40143494 C>A maps to NM_032221.3 T217T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr20:40033766 G>A maps to NM_032221.3 L2538L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PL-01A-11D-A382-10 chr20:40086017 A>T maps to NM_032221.3 Y905*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9J6-01A-11D-A382-10 chr8:61707583 A>G maps to NM_017780.2 K712K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr8:61654761 T>C maps to NM_017780.2 H257H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PO-01A-11D-A382-10 chr14:21875029 G>C maps to NM_001170629.1 L964L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2K-A9WE-01A-11D-A382-10 chr16:53326886 T>C maps to ENST00000219084 P1811P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr1:111862961 C>T maps to NM_201653.2 N435N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8196-01A-11D-2396-08 chr22:51018474 A>C maps to NM_005198.4 V285V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4A-A93W-01A-11D-A36X-10 chr3:433427 A>G maps to NM_006614.2 L954L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr16:89717998 G>C maps to NM_001083314.1 G21G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Y8-A898-01A-11D-A34Z-10 chr16:89715756 A>G did not map to a codon.
Sequencing variant TCGA-B1-A47M-01A-11D-A25F-10 chr2:220404815 A>T maps to NM_024536.5 A539A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F9-A7VF-01A-11D-A33Q-10 chr7:136700127 G>A maps to NM_001006628.1 E172E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr1:154544110 C>A maps to NM_000748.2 S271*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Y8-A896-01A-11D-A35Z-10 chr2:233394850 T>C did not map to a codon.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr14:24775202 G>C maps to NM_014430.2 L159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5877-01A-11D-1589-08 chr15:65490141 G>A maps to NM_003613.3 L828L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A6HP-01A-11D-A31X-10 chr6:139694868 A>G maps to NM_006079.3 H71H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-A8LE-01A-11D-A35Z-10 chr9:130939946 G>T maps to NM_012127.2 P572P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9JV-01A-12D-A42J-10 chr11:46799724 G>T maps to ENST00000415402 A904A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A8YH-01A-11D-A36X-10 chr11:46772904 T>C maps to ENST00000415402 K1771K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr11:46799003 G>C maps to ENST00000415402 V949V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr1:86890014 C>T maps to NM_006536.5 L29L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JD-01A-11D-A42J-10 chr7:143047463 G>T did not map to a codon.
Sequencing variant TCGA-KV-A6GD-01A-11D-A31X-10 chr7:143049048 G>A maps to NM_000083.2 L986L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PV-01A-11D-A42J-10 chr4:170610218 T>A maps to NM_173872.2 I148I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PX-01A-11D-A42J-10 chr23:49846493 A>G did not map to a codon.
Sequencing variant TCGA-MH-A854-01A-11D-A34Z-10 chr16:1507706 C>T maps to ENST00000382745 L242L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PO-01A-11D-A382-10 chr16:3065428 G>A maps to NM_021195.4 A198A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JD-01A-11D-A42J-10 chr17:7164033 A>G maps to NM_001185022.1 L134L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5XZ-01A-11D-A31X-10 chr16:3063764 C>A maps to NM_020982.3 I134I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7045-01A-31D-1961-08 chr14:38724315 C>T maps to NM_175060.1 R304R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5XZ-01A-11D-A31X-10 chr2:71036917 G>A maps to NM_173535.2 S537S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JE-01A-11D-A42J-10 chr21:36042469 A>G maps to ENST00000360731 E261E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PM-01A-21D-A382-10 chr21:36042469 A>G maps to ENST00000360731 E261E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9J1-01A-11D-A382-10 chr5:157285936 C>G did not map to a codon.
Sequencing variant TCGA-PJ-A8JU-01A-11D-A35Z-10 chr5:157214654 T>C maps to NM_001195555.1 *644*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9J3-01A-12D-A382-10 chr7:73752958 G>A maps to NM_003388.4 T101T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr7:73752799 A>T maps to NM_003388.4 S48S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8196-01A-11D-2396-08 chr2:29379235 A>G maps to ENST00000379543 K394K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A7SL-01A-11D-A34Z-10 chr2:29404713 C>A maps to ENST00000379543 T693T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9J8-01A-11D-A42J-10 chr5:178043949 C>G did not map to a codon.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr5:178050362 C>A maps to NM_020666.2 G19*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4103-01A-01D-1458-08 chr4:56301653 A>T maps to NM_004898.2 S823S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M9-01A-11D-A31X-10 chr1:9809528 G>A maps to NM_001009566.1 H325H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A7SR-01A-12D-A35Z-10 chr1:9815299 G>T maps to NM_001009566.1 S104S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KV-A6GD-01A-11D-A31X-10 chr12:7302197 T>C maps to NM_014718.3 D718D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-A4TM-01A-11D-A31X-10 chr9:36209296 C>T maps to NM_007096.3 F173F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A7SN-01A-11D-A34Z-10 chr9:36204094 G>A maps to NM_007096.3 W135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2K-A9WE-01A-11D-A382-10 chr17:57754323 G>C maps to NM_004859.3 L857L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9KE-01A-11D-A42J-10 chr17:57754371 T>C maps to NM_004859.3 P873P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7045-01A-31D-1961-08 chr16:3554720 T>C maps to NM_015041.1 N8N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr16:66612902 G>A maps to NM_052999.3 *287*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5Y1-01A-11D-A28G-10 chr16:66670439 T>A maps to NM_178818.2 A77A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A57E-01A-11D-A26P-10 chr3:32433538 G>C maps to NM_138410.2 L47L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9J7-01A-11D-A382-10 chr5:79033638 A>G maps to NM_153610.3 K3017K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JS-01A-21D-A42J-10 chr5:79034826 T>A maps to NM_153610.3 R3413R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5881-01A-11D-1589-08 chr5:79032747 T>C maps to NM_153610.3 T2720T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A83S-01A-11D-A34Z-10 chr6:154771339 G>A maps to NM_173515.2 I35I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9Q1-01A-11D-A42J-10 chr6:154732218 A>C maps to NM_173515.2 P376P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9KC-01A-11D-A42J-10 chr10:101090292 G>C maps to NM_020348.2 A383A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9K3-01A-11D-A42J-10 chr10:104678740 C>T maps to NM_017649.3 R168R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A7SP-01A-11D-A34Z-10 chr10:104678458 C>A maps to NM_017649.3 I74I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr2:97428004 C>A maps to NM_020184.3 Y423*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9K2-01A-11D-A42J-10 chr19:54652448 C>G maps to NM_014516.3 S459S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PV-01A-11D-A42J-10 chr19:54647752 G>C maps to NM_014516.3 R90R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6790-01A-11D-1961-08 chr9:17332673 G>A maps to NM_017738.2 K530K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7584-01A-11D-2136-08 chr12:41316145 C>T maps to NM_001843.2 Q106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8196-01A-11D-2396-08 chr1:205028741 C>A maps to NM_005076.3 A243A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JS-01A-21D-A42J-10 chr3:3095548 C>A maps to NM_175607.1 S957*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9KC-01A-11D-A42J-10 chr11:99941226 A>T maps to NM_014361.2 K412*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4A-A93W-01A-11D-A36X-10 chr3:1424738 G>A maps to NM_014461.2 R760R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PS-01A-11D-A42J-10 chr3:1424986 G>A maps to NM_014461.2 L804L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr7:147336336 C>A maps to NM_014141.5 A679A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr9:39140599 G>A maps to NM_033655.3 R598*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JK-01A-11D-A42J-10 chr2:125192133 C>G maps to NM_130773.2 L201L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7287-01A-11D-2136-08 chr17:40717243 G>T did not map to a codon.
Sequencing variant TCGA-GL-A4EM-01A-11D-A25F-10 chr9:140158761 G>A maps to NM_015456.3 L283L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9K6-01A-11D-A42J-10 chr16:70543136 C>T maps to NM_015386.2 Q333Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A83W-01A-11D-A34Z-10 chr1:103471850 A>G maps to NM_080629.2 G580G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A561-01A-11D-A26P-10 chr6:75861880 T>C maps to ENST00000322507 A1267A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6790-01A-11D-1961-08 chr8:121237424 A>T maps to NM_021110.1 S612S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PS-01A-11D-A42J-10 chr8:121170480 T>A maps to NM_021110.1 T67T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PJ-A8JU-01A-11D-A35Z-10 chr1:32151314 A>G maps to NM_001856.3 R647R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-3925-01A-01D-1458-08 chr10:105793763 A>G maps to NM_000494.3 A1365A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A9DE-01A-11D-A36X-10 chr10:105793811 T>A maps to NM_000494.3 A1349A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4A-A93X-01A-11D-A36X-10 chr21:46900747 T>C maps to ENST00000359759 G944G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A656-01A-11D-A31X-10 chr6:70646795 A>G maps to NM_001858.4 P289P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KV-A6GD-01A-11D-A31X-10 chr17:48277126 G>A maps to NM_000088.3 C95C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A657-01A-11D-A31X-10 chr8:139707080 C>A maps to NM_152888.1 L878L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8311-01A-11D-2396-08 chr4:109817831 T>C maps to ENST00000333642 T299T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M9-01A-11D-A31X-10 chr2:189867766 C>T maps to NM_000090.3 P844P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JE-01A-11D-A42J-10 chr2:228174024 A>T maps to NM_000091.4 S1582S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-A6W5-01A-12D-A33Q-10 chr2:228172489 A>C maps to NM_000091.4 A1439A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A7SU-01A-11D-A35Z-10 chr5:74677818 T>C maps to NM_001130105.1 E652E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A44B-01A-11D-A25F-10 chr23:107938133 G>A did not map to a codon.
Sequencing variant TCGA-AL-3473-01A-01D-1252-08 chr23:107433649 T>G did not map to a codon.
Sequencing variant TCGA-2Z-A9JS-01A-21D-A42J-10 chr9:137694763 G>T maps to NM_000093.3 E1013*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7585-01A-11D-2136-08 chr9:137734001 G>C did not map to a codon.
Sequencing variant TCGA-AL-3468-01A-01D-1252-08 chr9:137714851 T>C maps to NM_000093.3 P1539P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A9DD-01A-11D-A36X-10 chr2:189916159 T>A maps to NM_000393.3 G939G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WN-A9G9-01A-12D-A36X-10 chr19:10112280 A>G maps to NM_015719.3 D343D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9K3-01A-11D-A42J-10 chr21:47546101 C>T maps to NM_001849.3 D791D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J7-6720-01A-11D-2136-08 chr21:47542787 G>A did not map to a codon.
Sequencing variant TCGA-UZ-A9PR-01A-11D-A42J-10 chr21:47538954 C>T maps to NM_001849.3 G397G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8098-01A-11D-2396-08 chr2:238280360 C>T maps to NM_057165.4 A1227A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr2:238234212 A>T maps to NM_004369.3 V3161V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7056-01A-11D-1961-08 chr3:48602252 G>A maps to NM_000094.3 R2927R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Y8-A896-01A-11D-A35Z-10 chr3:48619023 C>T maps to NM_000094.3 K1588K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9KC-01A-11D-A42J-10 chr1:36564327 T>G maps to NM_005202.2 P318P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A561-01A-11D-A26P-10 chr1:36564105 A>G maps to NM_005202.2 I392I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr6:71003974 G>A maps to NM_001851.4 D197D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A8YI-01A-21D-A36X-10 chr3:15531094 G>T maps to NM_005677.3 C52*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9JY-01A-11D-A42J-10 chr5:115428294 T>A maps to NM_016144.2 I99I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8517-01A-11D-2396-08 chr1:160305058 A>G maps to NM_001098398.1 D94D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F9-A7VF-01A-11D-A33Q-10 chr4:84185396 C>T maps to NM_015697.7 K407K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr6:99823845 T>A maps to NM_017421.3 T233T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A6HP-01A-11D-A31X-10 chr9:131095204 G>A maps to NM_016035.3 P203P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JD-01A-11D-A42J-10 chr14:74422587 T>C maps to NM_182476.1 D146D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PS-01A-11D-A42J-10 chr14:74426188 T>C maps to NM_182476.1 D285D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4A-A93X-01A-11D-A36X-10 chr17:27943973 G>A maps to ENST00000345068 I351I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-7268-01A-11D-2136-08 chr17:14005507 T>A maps to NM_001303.3 L191L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A7SL-01A-11D-A34Z-10 chr19:36641913 G>A maps to ENST00000437291 S99S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7838-01A-11D-2136-08 chr7:129962494 T>C maps to NM_016352.3 H415H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8517-01A-11D-2396-08 chr10:93999657 A>C maps to NM_014912.4 T150T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr5:173370038 T>G maps to NM_030627.2 Y423*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A9DD-01A-11D-A36X-10 chr10:101802228 T>C maps to NM_001308.2 R444R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Y8-A8S0-01A-11D-A36X-10 chr3:131268824 G>T maps to ENST00000502818 S441*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-7173-01A-11D-2136-08 chr14:24545746 G>A maps to NM_006032.2 P382P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A69E-01A-11D-A31X-10 chr16:89650106 T>A maps to NM_014427.4 I195I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5878-01A-11D-1589-08 chr2:207833967 G>C maps to NM_173077.2 L311L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5892-01A-11D-1589-08 chr2:207827298 C>T maps to NM_173077.2 Y246Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr3:98309566 A>T maps to NM_000097.5 A240A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A83S-01A-11D-A34Z-10 chr14:92608526 T>A maps to NM_017437.1 L227L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PS-01A-11D-A42J-10 chr11:61183971 A>G maps to NM_024811.3 H233H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5877-01A-11D-1589-08 chr19:50200611 C>A maps to NM_152359.2 A57A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-8500-01A-11D-2396-08 chr20:2776795 C>G maps to NM_019609.4 L418L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PK-01A-11D-A382-10 chr10:125521472 G>A maps to NM_198148.2 D564D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F9-A4JJ-01A-11D-A25F-10 chr1:207669653 G>C maps to NM_000651.4 P14P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5902-01A-11D-1589-08 chr16:1718162 C>T maps to NM_020825.3 I1101I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-7173-01A-11D-2136-08 chr3:3209359 T>C maps to NM_016302.3 R215R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E8-01A-11D-A28G-10 chr11:46342258 A>G did not map to a codon.
Sequencing variant TCGA-G7-A4TM-01A-11D-A31X-10 chr16:3860636 G>A maps to NM_004380.2 I314I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EA-01A-11D-A28G-10 chr16:3817822 C>A maps to NM_004380.2 E1050*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr16:3779017 C>T maps to NM_004380.2 G2010G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A7UZ-01A-12D-A34Z-10 chr7:30702463 C>T did not map to a codon.
Sequencing variant TCGA-BQ-5889-01A-11D-1589-08 chr2:36583677 C>G maps to NM_016441.2 Y81*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5876-01A-11D-1589-08 chr6:43275359 T>C maps to ENST00000449267 Q106Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6134-01A-11D-1961-08 chr6:43275461 T>C maps to ENST00000449267 V72V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PJ-01A-11D-A382-10 chr6:43275410 A>G maps to ENST00000449267 P89P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A83S-01A-11D-A34Z-10 chr8:75925136 G>A maps to NM_031461.5 P130P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3466-01A-01D-1252-08 chr16:84940196 G>A maps to NM_031476.3 L481L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr17:29119513 C>A maps to NM_015986.3 S301S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9KA-01A-11D-A42J-10 chr4:5838633 C>A did not map to a codon.
Sequencing variant TCGA-IZ-A6M8-01A-11D-A31X-10 chr20:20033151 G>A maps to NM_016652.4 A106A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A7SS-01A-11D-A35Z-10 chr1:17287327 C>T maps to NM_014675.3 L1370L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V9-A7HT-01A-11D-A33Q-10 chr15:91172532 C>T maps to NM_022769.3 S345S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8311-01A-11D-2396-08 chr21:44589373 C>G maps to NM_000394.2 T55T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr20:47691343 A>G maps to NM_001316.2 E363E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5Y1-01A-11D-A28G-10 chr23:1407701 G>T did not map to a codon.
Sequencing variant TCGA-EV-5903-01A-11D-1589-08 chr10:43651226 A>G maps to NM_018590.3 K210K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WN-A9G9-01A-12D-A36X-10 chr8:2910076 C>A maps to NM_033225.5 E2523*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8630-01A-11D-2396-08 chr1:33985174 T>A maps to ENST00000373381 T3573T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WN-AB4C-01A-11D-A42J-10 chr1:34008359 C>A maps to ENST00000373381 S3039S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5893-01A-11D-1589-08 chr8:113249530 G>T maps to NM_198123.1 Y3505*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7836-01A-11D-2136-08 chr8:113697851 T>G maps to NM_198123.1 P755P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NL-01A-11D-A26P-10 chr8:113516206 C>G did not map to a codon.
Sequencing variant TCGA-A4-8310-01A-11D-2396-08 chr17:80202674 C>T maps to NM_001893.3 Q410Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr15:75982865 G>C maps to NM_001897.4 L180L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6792-01A-21D-1961-08 chr20:23548868 G>T maps to NM_080610.2 I73I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-5155-01A-01D-1589-08 chr20:54974309 T>A maps to NM_001033522.1 S311S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9J6-01A-11D-A382-10 chr10:126715158 A>G maps to NM_022802.2 A390A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3468-01A-01D-1252-08 chr10:126715158 A>G maps to NM_022802.2 A390A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A7SN-01A-11D-A34Z-10 chr20:56098331 G>A maps to ENST00000423479 L182L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A7SS-01A-11D-A35Z-10 chr20:56099186 T>C maps to ENST00000423479 K25K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7045-01A-31D-1961-08 chr1:70895505 T>C maps to NM_001902.5 S206S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6790-01A-11D-1961-08 chr5:138266341 C>T maps to ENST00000355078 R731*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A8YI-01A-21D-A36X-10 chr3:41275682 T>G maps to NM_001904.3 P526P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5878-01A-11D-1589-08 chr3:41274904 C>T maps to NM_001904.3 L385L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr5:11117618 C>A maps to NM_001332.2 T740T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2K-A9WE-01A-11D-A382-10 chr17:3563994 T>C maps to NM_001031681.2 T390T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JT-01A-11D-A42J-10 chr17:3563641 G>A maps to NM_001031681.2 P361P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8195-01A-31D-2396-08 chr17:3550807 C>T maps to NM_001031681.2 L44L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-3925-01A-01D-1458-08 chr23:16685794 A>C did not map to a codon.
Sequencing variant TCGA-5P-A9KA-01A-11D-A42J-10 chr7:117375152 T>A maps to NM_033427.2 G1230G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4103-01A-01D-1458-08 chr7:117364733 T>A maps to NM_033427.2 I1438I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9J2-01A-11D-A382-10 chr10:17110183 A>G maps to NM_001081.3 L963L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9J6-01A-11D-A382-10 chr10:17164867 T>C maps to NM_001081.3 E173E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9J7-01A-11D-A382-10 chr10:16967342 T>C maps to NM_001081.3 S2181S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr10:16916467 G>T maps to NM_001081.3 I3047I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr10:16941135 A>G maps to NM_001081.3 P2819P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7840-01A-11D-2136-08 chr10:35324144 G>T maps to NM_001198778.1 I338I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9J8-01A-11D-A42J-10 chr2:225378263 C>A maps to NM_003590.3 E211*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JQ-01A-11D-A42J-10 chr2:225378263 C>A maps to NM_003590.3 E211*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-7173-01A-11D-2136-08 chr2:225449721 G>T maps to NM_003590.3 S2*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5885-01A-11D-1589-08 chr2:225422515 G>A maps to NM_003590.3 Q42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Y8-A8RZ-01A-11D-A36X-10 chr2:225378238 A>G did not map to a codon.
Sequencing variant TCGA-SX-A7SO-01A-11D-A34Z-10 chr13:113893813 G>C maps to NM_001008895.1 R328R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E7-01A-31D-A28G-10 chr7:101882762 G>A maps to ENST00000360264 A1273A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PJ-A8JU-01A-11D-A35Z-10 chr7:101891787 G>A maps to ENST00000360264 R1339R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5903-01A-11D-1589-08 chr2:180810242 A>G maps to NM_020943.2 P780P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V9-A7HT-01A-11D-A33Q-10 chr10:101996699 A>C maps to NM_018294.4 S427S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A562-01A-11D-A26P-10 chr4:49032878 T>G maps to NM_025087.2 S470S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5876-01A-11D-1589-08 chr2:136873380 G>T maps to NM_001008540.1 I43I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4A-A93Y-01A-11D-A36X-10 chr4:105412356 T>C maps to NM_025212.1 L32L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9K6-01A-11D-A42J-10 chr23:19973667 A>C did not map to a codon.
Sequencing variant TCGA-A4-8310-01A-11D-2396-08 chr23:40506302 A>G did not map to a codon.
Sequencing variant TCGA-SX-A71U-01A-12D-A33Q-10 chr23:40496277 A>G did not map to a codon.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr17:61511912 G>A maps to NM_001915.3 N202N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A7SR-01A-12D-A35Z-10 chr17:4060189 C>T maps to NM_144611.3 V203V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8310-01A-11D-2396-08 chr8:143957216 G>A maps to ENST00000377675 S415S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J7-6720-01A-11D-2136-08 chr8:143956728 C>G did not map to a codon.
Sequencing variant TCGA-BQ-5890-01A-11D-1589-08 chr10:96443671 C>A maps to NM_000772.2 G32G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4A-A93W-01A-11D-A36X-10 chr19:41703753 G>C maps to ENST00000301173 L138L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-7173-01A-11D-2136-08 chr7:99328743 T>A maps to ENST00000292414 K35*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A562-01A-11D-A26P-10 chr19:15651479 C>T maps to NM_173483.3 A297A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8310-01A-11D-2396-08 chr5:39390644 A>G maps to NM_001343.2 I121I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8310-01A-11D-2396-08 chr5:39394410 T>C maps to NM_001343.2 E4E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A7SS-01A-11D-A35Z-10 chr5:39383190 A>G maps to NM_001343.2 P290P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JR-01A-12D-A42J-10 chr9:124544632 T>C maps to ENST00000408936 D1142D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A83S-01A-11D-A34Z-10 chr9:124526155 C>T maps to ENST00000408936 Y486Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9KE-01A-11D-A42J-10 chr3:49568720 C>G maps to NM_004393.4 S259S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-7332-01A-11D-2136-08 chr3:49568798 A>G maps to NM_004393.4 A285A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Y8-A8RY-01A-11D-A36X-10 chr11:61490355 C>T maps to NM_006133.2 Y111Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JE-01A-11D-A42J-10 chr11:61111629 G>A maps to NM_015533.3 A375A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7585-01A-11D-2136-08 chr2:136736936 C>A did not map to a codon.
Sequencing variant TCGA-A4-8310-01A-11D-2396-08 chr6:33287890 T>C maps to NM_001350.4 E454E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PN-01A-11D-A382-10 chr6:33289302 C>T maps to NM_001350.4 E83E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3466-01A-01D-1252-08 chr9:121930243 C>T maps to NM_014618.2 S468S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4104-01A-01D-1458-08 chr17:42828062 C>T maps to NM_145663.2 L430L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr5:176895198 C>A maps to ENST00000393565 S55S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A83V-01A-11D-A34Z-10 chr3:137889002 A>G maps to NM_016216.3 S145S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5ED-01A-11D-A28G-10 chr9:37800964 G>T maps to NM_024345.3 P34P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7840-01A-11D-2136-08 chr23:125685497 A>C did not map to a codon.
Sequencing variant TCGA-PJ-A5Z8-01A-11D-A28G-10 chr2:172333420 T>A maps to NM_025000.3 S381S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JG-01A-11D-A42J-10 chr23:27765727 G>A did not map to a codon.
Sequencing variant TCGA-G7-A4TM-01A-11D-A31X-10 chr3:98600600 A>G maps to ENST00000326857 C72C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AT-A5NU-01A-11D-A28G-10 chr6:24357768 A>T maps to NM_016356.3 T70T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9JV-01A-12D-A42J-10 chr16:2301545 G>T maps to NM_001919.3 R8R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr13:36383186 A>G maps to NM_004734.4 Y578Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A83T-01A-11D-A34Z-10 chr3:36779670 C>T maps to NM_033403.1 G160G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr10:115608964 A>G maps to NM_014881.3 R633R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PX-01A-11D-A42J-10 chr1:114454065 C>T maps to NM_022836.3 A284A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7288-01A-11D-2136-08 chr3:53376260 G>T maps to ENST00000480258 R72R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PX-01A-11D-A42J-10 chr12:2061662 A>T maps to NM_152640.3 A481A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5883-01A-11D-1589-08 chr11:126201298 G>T did not map to a codon.
Sequencing variant TCGA-A4-A48D-01A-11D-A25F-10 chr1:155015934 G>T maps to NM_152494.3 L374L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JQ-01A-11D-A42J-10 chr2:74597420 C>T maps to NM_004082.4 K393K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F9-A4JJ-01A-11D-A25F-10 chr16:20871249 G>A maps to NM_173475.2 L291L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8310-01A-11D-2396-08 chr4:52765462 T>C maps to ENST00000451288 N222N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Y8-A898-01A-11D-A34Z-10 chr11:61079363 C>T maps to NM_001923.3 K723K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9K2-01A-11D-A42J-10 chr7:50544330 A>G maps to NM_000790.3 T344T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-A8LC-01A-11D-A35Z-10 chr11:103907570 C>T maps to NM_001001711.2 C7C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8196-01A-11D-2396-08 chr1:15956838 C>T maps to NM_032341.4 F96F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9KC-01A-11D-A42J-10 chr12:49392076 T>A maps to NM_015086.1 G194G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A71U-01A-12D-A33Q-10 chr6:110726038 A>G maps to NM_003649.2 F160F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E7-01A-31D-A28G-10 chr1:162729663 G>A maps to NM_006182.2 V250V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9J1-01A-11D-A382-10 chr12:31242338 C>T maps to NM_030653.3 N265N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PR-01A-11D-A42J-10 chr14:94528899 A>G maps to NM_020414.3 N262N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Y8-A894-01A-11D-A35Z-10 chr14:94545833 C>T maps to NM_020414.3 E85E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A9DC-01A-11D-A36X-10 chr11:125791200 G>C maps to NM_013264.3 G439G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A71V-01A-11D-A33Q-10 chr16:68057033 G>A maps to NM_018380.3 L24L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-7332-01A-11D-2136-08 chr23:41203028 G>T did not map to a codon.
Sequencing variant TCGA-EV-5901-01A-11D-1589-08 chr23:41202003 G>A did not map to a codon.
Sequencing variant TCGA-B9-5155-01A-01D-1589-08 chr6:74119026 G>A maps to NM_018665.2 K412K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JE-01A-11D-A42J-10 chr5:134118719 T>A maps to ENST00000452510 C377*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7058-01A-11D-1961-08 chr17:62500169 T>C maps to NM_004396.3 G124G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5881-01A-11D-1589-08 chr23:23019107 G>A did not map to a codon.
Sequencing variant TCGA-PJ-A5Z8-01A-11D-A28G-10 chr12:113610194 G>A maps to NM_001111322.1 S414S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PO-01A-11D-A382-10 chr12:113602054 C>G maps to NM_001111322.1 L585L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4617-01A-01D-1252-08 chr12:124093347 A>T maps to NM_020936.1 R175*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9JY-01A-11D-A42J-10 chr9:32467856 G>A maps to NM_014314.3 A696A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59R-01A-11D-A26P-10 chr9:32459419 G>T maps to NM_014314.3 C810*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-A8LB-01A-11D-A35Z-10 chr11:118635953 G>T maps to NM_004397.4 T203T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A7SQ-01A-12D-A35Z-10 chr4:169204722 C>A maps to NM_017631.5 V532V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5XZ-01A-11D-A31X-10 chr4:169382990 C>T maps to NM_001012967.1 T155T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JD-01A-11D-A42J-10 chr16:90021580 C>A maps to NM_207514.1 A104A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NK-01A-11D-A26P-10 chr6:49936557 T>C maps to NM_001037729.1 E27E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7055-01A-11D-1961-08 chr6:49931769 G>A maps to NM_001037499.1 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JD-01A-11D-A42J-10 chr9:126143929 C>T maps to NM_020946.1 K937K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A71R-01A-12D-A33Q-10 chr1:197479792 G>A maps to NM_001195215.1 Q709*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A857-01A-11D-A34Z-10 chr1:115130430 G>T maps to ENST00000393274 S858S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5893-01A-11D-1589-08 chr8:142186772 C>T maps to NM_014957.2 F793F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8515-01A-11D-2396-08 chr15:66031103 A>G maps to ENST00000443035 N247N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5893-01A-11D-1589-08 chr15:65983019 C>T maps to ENST00000443035 V1304V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Y8-A896-01A-11D-A35Z-10 chr9:19372143 G>A maps to NM_017925.4 R1665R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E7-01A-31D-A28G-10 chr12:31551283 C>T maps to NM_144973.3 G1027G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-3925-01A-01D-1458-08 chr22:32193640 A>T maps to NM_001136029.1 K275*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5878-01A-11D-1589-08 chr22:32301996 T>G maps to NM_001136029.1 S1479S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5885-01A-11D-1589-08 chr11:75509460 C>T maps to NM_032564.3 P333P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NH-01A-11D-A26P-10 chr22:20077781 G>C did not map to a codon.
Sequencing variant TCGA-IA-A40Y-01A-11D-A25F-10 chr2:234368473 C>T maps to NM_152879.2 V922V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr3:185960323 T>A maps to NM_001346.2 R599*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PO-01A-11D-A382-10 chr4:960304 C>T maps to NM_001347.2 T459T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W9-01A-11D-A28G-10 chr10:99358954 C>T maps to NM_138413.3 L150L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8196-01A-11D-2396-08 chr6:30640453 G>T maps to NM_003587.4 L55L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chr5:54591350 A>G maps to NM_019030.2 D169D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-5561-01A-01D-1589-08 chr3:47882519 C>A maps to NM_138615.2 R174R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-A8LE-01A-11D-A35Z-10 chr17:5354240 C>T maps to ENST00000457531 A529A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NK-01A-11D-A26P-10 chr20:37653977 C>T maps to NM_021931.3 Q593*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr16:72138440 G>T maps to NM_014003.3 A689A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JM-01A-12D-A42J-10 chr2:39050398 T>C maps to NM_198963.1 L1009L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W9-01A-11D-A28G-10 chr2:39088915 T>C maps to NM_198963.1 A212A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9J8-01A-11D-A42J-10 chr23:96171469 A>C did not map to a codon.
Sequencing variant TCGA-WN-AB4C-01A-11D-A42J-10 chr13:60384949 C>T maps to NM_001042517.1 K1045K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4115-01A-01D-1252-08 chr14:95556879 G>T maps to NM_177438.2 A1908A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-5155-01A-01D-1589-08 chr12:51138541 G>T maps to NM_173602.2 G1551*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A9DC-01A-11D-A36X-10 chr19:2717306 C>T maps to NM_145173.3 T166T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A8YI-01A-21D-A36X-10 chr2:233001387 C>T maps to NM_152383.4 C303C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A7SS-01A-11D-A35Z-10 chr1:223176847 A>G maps to NM_032890.2 R703R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A856-01A-11D-A34Z-10 chr11:111899513 A>T did not map to a codon.
Sequencing variant TCGA-Y8-A8RY-01A-11D-A36X-10 chr11:111933141 T>A maps to NM_001931.4 A609A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A83S-01A-11D-A34Z-10 chr3:38101344 T>A did not map to a codon.
Sequencing variant TCGA-UZ-A9PK-01A-11D-A382-10 chr3:38163860 A>G maps to NM_007335.2 Q1742Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A657-01A-11D-A31X-10 chr3:196888576 A>T maps to NM_004087.2 T172T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A83S-01A-11D-A34Z-10 chr17:7106869 G>A maps to NM_001365.3 R169R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A71U-01A-12D-A33Q-10 chr8:1626466 G>T maps to ENST00000357934 T734T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-7332-01A-11D-2136-08 chr1:35365841 G>A maps to NM_001080418.1 T380T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A8YI-01A-21D-A36X-10 chr1:35370205 C>T maps to NM_001080418.1 W260*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F9-A97G-01A-11D-A382-10 chr1:35350631 G>A maps to NM_001080418.1 N649N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PJ-A5Z8-01A-11D-A28G-10 chr1:35331686 C>T maps to NM_001080418.1 L979L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JN-01A-21D-A42J-10 chr6:43422490 G>A maps to NM_206539.1 R25*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7056-01A-11D-1961-08 chr2:172950597 C>A maps to NM_178120.4 R65R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5890-01A-11D-1589-08 chr10:124351861 C>A maps to ENST00000368915 R751R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JJ-01A-11D-A42J-10 chr23:31462640 A>C did not map to a codon.
Sequencing variant TCGA-B9-4617-01A-01D-1252-08 chr23:32867884 C>T did not map to a codon.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr23:31152281 C>G did not map to a codon.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr23:32305750 G>T did not map to a codon.
Sequencing variant TCGA-SX-A7SP-01A-11D-A34Z-10 chr23:32486635 C>G did not map to a codon.
Sequencing variant TCGA-UZ-A9PK-01A-11D-A382-10 chr9:990922 C>G maps to NM_021240.2 S446*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JT-01A-11D-A42J-10 chr5:118480322 A>G maps to NM_005509.4 L853L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M8-01A-11D-A31X-10 chr5:118479555 T>C maps to NM_005509.4 F799F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Y8-A898-01A-11D-A34Z-10 chr5:118484770 T>C maps to NM_005509.4 C1083C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9J2-01A-11D-A382-10 chr15:51799329 C>T did not map to a codon.
Sequencing variant TCGA-B3-4104-01A-01D-1458-08 chr15:51857283 C>A did not map to a codon.
Sequencing variant TCGA-UZ-A9Q1-01A-11D-A42J-10 chr15:51783939 G>A maps to NM_001174116.1 V1596V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7062-01A-11D-1961-08 chr3:52432934 A>G maps to ENST00000273600 V4117V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6789-01A-11D-1961-08 chr3:52422875 C>T maps to ENST00000273600 L3204L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A40U-01A-11D-A25F-10 chr17:76449534 G>T maps to ENST00000389840 V3459V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47O-01A-11D-A25F-10 chr17:7734796 C>G maps to NM_020877.2 S4183S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9K8-01A-11D-A42J-10 chr5:13794139 G>A maps to NM_001369.2 R2639*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59R-01A-11D-A26P-10 chr2:84846835 T>G maps to NM_001370.1 L1200L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8196-01A-11D-2396-08 chr2:84777108 A>T maps to NM_001370.1 L471L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5876-01A-11D-1589-08 chr2:196749320 T>C maps to NM_018897.2 Q1917Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PM-01A-21D-A382-10 chr2:196825318 C>T maps to NM_018897.2 R852R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Y8-A8S1-01A-11D-A36X-10 chr6:38843575 C>A maps to ENST00000327475 T2598T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7056-01A-11D-1961-08 chr17:11520830 G>C maps to NM_001372.3 R336R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E8-01A-11D-A28G-10 chr17:72306226 G>T maps to NM_023036.4 L473L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A71S-01A-11D-A33Q-10 chr16:4504894 A>T maps to NM_005147.4 K475*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7834-01A-11D-2136-08 chr2:220150707 G>T did not map to a codon.
Sequencing variant TCGA-EV-5903-01A-11D-1589-08 chr2:220149458 C>A maps to NM_006736.5 S242*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9JY-01A-11D-A42J-10 chr7:108213746 C>T maps to NM_012328.2 Q208*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9K6-01A-11D-A42J-10 chr7:108213746 C>T maps to NM_012328.2 Q208*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W8-01A-11D-A28G-10 chr7:108212286 G>A maps to NM_012328.2 E39E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A6HP-01A-11D-A31X-10 chr2:183594618 G>T maps to NM_018981.1 V226V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-O9-A75Z-01A-11D-A33Q-10 chr1:6705132 A>G maps to NM_018198.3 D316D. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-B1-A657-01A-11D-A31X-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-IA-A83V-01A-11D-A34Z-10 chr15:41066036 T>A did not map to a codon.
Sequencing variant TCGA-5P-A9JZ-01A-11D-A42J-10 chr5:34945004 G>A maps to NM_194283.3 R339R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7834-01A-11D-2136-08 chr12:49743365 T>C maps to NM_024902.2 L237L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7842-01A-11D-2136-08 chr9:114429093 G>A did not map to a codon.
Sequencing variant TCGA-SX-A7SM-01A-11D-A34Z-10 chr20:62560862 C>T maps to NM_025219.2 S102S. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-EV-5903-01A-11D-1589-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-EV-5903-01A-11D-1589-08 chr2:27503081 A>T maps to ENST00000406962 K103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KV-A6GE-01A-11D-A31X-10 chr11:6592936 G>T maps to NM_144666.2 A4661A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55Z-01A-11D-A26P-10 chr2:25469541 C>T maps to NM_175629.1 W409*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PJ-01A-11D-A382-10 chr2:25461997 C>A did not map to a codon.
Sequencing variant TCGA-A4-8310-01A-11D-2396-08 chr20:31375211 G>A maps to NM_006892.3 P203P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8310-01A-11D-2396-08 chr2:220239738 G>A maps to NM_012100.2 L415L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr23:117731502 A>T did not map to a codon.
Sequencing variant TCGA-UN-AAZ9-01A-11D-A382-10 chr23:117817166 T>G did not map to a codon.
Sequencing variant TCGA-2Z-A9JD-01A-11D-A42J-10 chr5:169127099 C>A maps to NM_004946.2 T405T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-7332-01A-11D-2136-08 chr8:25226180 C>A maps to NM_024940.6 P1126P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PR-01A-11D-A42J-10 chr8:25177161 C>T maps to NM_024940.6 V504V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7288-01A-11D-2136-08 chr1:63119665 T>C maps to ENST00000371140 V103V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M8-01A-11D-A31X-10 chr9:441957 C>T maps to NM_203447.3 V1813V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr13:99540612 C>T did not map to a codon.
Sequencing variant TCGA-UZ-A9PS-01A-11D-A42J-10 chr9:131708202 G>T maps to NM_014908.3 T460T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A7SS-01A-11D-A35Z-10 chr21:34951868 C>A did not map to a codon.
Sequencing variant TCGA-BQ-5891-01A-11D-1589-08 chr6:83862076 A>G maps to NM_015018.2 L2040L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5903-01A-11D-1589-08 chr6:83862019 T>A maps to NM_015018.2 P2021P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JS-01A-21D-A42J-10 chr19:2194548 G>A maps to ENST00000221482 W208*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A9DE-01A-11D-A36X-10 chr19:2210837 G>T maps to ENST00000221482 A445A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NK-01A-11D-A26P-10 chr19:2210829 C>T maps to ENST00000221482 Q443*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PS-01A-11D-A42J-10 chr19:2216296 A>T maps to ENST00000221482 L647L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7732-01A-11D-2136-08 chr11:118969111 C>T did not map to a codon.
Sequencing variant TCGA-B9-A8YI-01A-21D-A36X-10 chr6:30917944 G>A maps to NM_080870.3 L568L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-A8LE-01A-11D-A35Z-10 chr19:38704379 T>C maps to NM_001135155.1 L332L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5876-01A-11D-1589-08 chr11:65113197 G>A maps to NM_006268.3 L233L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PV-01A-11D-A42J-10 chr1:101456155 T>C maps to NM_015958.2 L222L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9K6-01A-11D-A42J-10 chr2:116593769 C>A maps to NM_020868.3 S663*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A71W-01A-12D-A34Z-10 chr2:116497450 G>A maps to NM_020868.3 K278K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5885-01A-11D-1589-08 chr11:66260241 G>A maps to NM_005700.3 A348A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chr12:7867785 T>A maps to NM_199286.2 S30S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr1:98058808 T>A maps to NM_000110.3 K365*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JG-01A-11D-A42J-10 chr10:134011924 A>T maps to NM_006426.2 K210*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9J3-01A-12D-A382-10 chr12:102271584 G>A maps to NM_018370.2 R6R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5891-01A-11D-1589-08 chr5:174870045 G>A maps to NM_000794.3 D19D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7996-01A-11D-2201-08 chr11:113295343 A>G maps to ENST00000355319 D10D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr11:113288846 C>T maps to ENST00000355319 E99E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PR-01A-11D-A42J-10 chr22:31816282 C>T maps to NM_004147.3 L152L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JL-01A-11D-A42J-10 chr18:28712611 T>C maps to NM_024421.2 T719T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Y8-A897-01A-11D-A35Z-10 chr18:65179562 A>G maps to NM_032160.2 H771H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PZ-01A-11D-A42J-10 chr18:28935299 T>A maps to NM_001942.2 Y1047*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55W-01A-11D-A26P-10 chr18:29116285 T>C maps to NM_001943.3 V515V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-AAVL-01A-11D-A42J-10 chr18:28968922 C>T maps to NM_001134453.1 N153N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9J3-01A-12D-A382-10 chr6:7542207 C>T maps to NM_004415.2 A20A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5877-01A-11D-1589-08 chr6:7562979 T>A maps to NM_004415.2 Y231*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7050-01A-11D-1961-08 chr6:7579569 G>T maps to NM_004415.2 S1049S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A7SQ-01A-12D-A35Z-10 chr6:7578719 C>T maps to NM_004415.2 Y1003Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Y8-A895-01A-11D-A35Z-10 chr6:7578082 C>G maps to NM_004415.2 T983T. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-2Z-A9JL-01A-11D-A42J-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-5P-A9JU-01A-11D-A42J-10 chr4:88536435 C>T maps to NM_014208.3 S874S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A8YH-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-MH-A857-01A-11D-A34Z-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr4:88536435 C>T maps to NM_014208.3 S874S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JP-01A-11D-A42J-10 chr6:56494229 A>G maps to ENST00000361203 S1220S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7734-01A-11D-2136-08 chr6:56463336 T>C maps to ENST00000361203 A3744A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-A8LE-01A-11D-A35Z-10 chr6:56489405 T>G maps to ENST00000361203 R1406R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NI-01A-11D-A26P-10 chr6:56501421 C>T maps to ENST00000361203 W787*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6792-01A-21D-1961-08 chr1:205132070 G>A maps to NM_015375.2 L541L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A71S-01A-11D-A33Q-10 chr12:113531443 G>T maps to NM_004416.2 V368V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PJ-A5Z8-01A-11D-A28G-10 chr17:7147901 A>G maps to NM_015343.4 L214L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5877-01A-11D-1589-08 chr15:45445602 G>C maps to NM_175940.1 V1150V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9JU-01A-11D-A42J-10 chr15:45411429 G>A maps to NM_144565.2 L302L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JG-01A-11D-A42J-10 chr19:5786482 A>T maps to NM_020175.2 I519I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A71V-01A-11D-A33Q-10 chr5:172196605 G>T maps to NM_004417.3 S235S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7836-01A-11D-2136-08 chr1:159752040 T>A maps to NM_017823.3 I122I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8098-01A-11D-2396-08 chr1:167096128 A>G maps to NM_001080426.1 T587T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PS-01A-11D-A42J-10 chr8:29195961 G>A maps to NM_001394.5 A212A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Y8-A8RY-01A-11D-A36X-10 chr8:29197703 G>A maps to NM_001394.5 L164L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A9DE-01A-11D-A36X-10 chr19:57665812 A>G maps to NM_001012729.1 S194S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9K0-01A-11D-A42J-10 chr3:183887830 C>T maps to NM_004423.3 S512S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A69E-01A-11D-A31X-10 chr18:46798649 C>G maps to NM_017653.3 L383L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JS-01A-21D-A42J-10 chr12:68051340 G>T maps to NM_006482.2 V218V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PO-01A-11D-A382-10 chr1:206821236 C>A maps to NM_003582.2 R232R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-A5DJ-01A-11D-A26P-10 chr15:55731767 T>C maps to NM_130810.2 K265K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PX-01A-11D-A42J-10 chr13:96293650 C>T maps to NM_198968.2 K165K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JD-01A-11D-A42J-10 chr16:67226968 G>A maps to NM_001950.3 K101K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A7SN-01A-11D-A34Z-10 chr16:67226689 G>A maps to NM_001950.3 Q54Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Y8-A895-01A-11D-A35Z-10 chr8:86119658 G>C did not map to a codon.
Sequencing variant TCGA-BQ-5882-01A-11D-1589-08 chr16:23540827 C>T maps to NM_001083614.1 V449V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5885-01A-11D-1589-08 chr8:25715867 G>A maps to NM_022659.2 L499L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F9-A7VF-01A-11D-A33Q-10 chr10:131757259 G>C maps to ENST00000355311 Y141*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A7SN-01A-11D-A34Z-10 chr1:43637310 C>T maps to NM_001159936.1 K109K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Y8-A898-01A-11D-A34Z-10 chr1:43632513 G>A maps to NM_001159936.1 G285G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9K6-01A-11D-A42J-10 chr10:74920310 T>G did not map to a codon.
Sequencing variant TCGA-P4-AAVL-01A-11D-A42J-10 chr10:74899239 T>C maps to NM_001135752.1 L449L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4617-01A-01D-1252-08 chr1:21585299 G>T maps to NM_001397.2 A216A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-7502-01A-11D-2201-08 chr2:233350796 G>A maps to NM_004826.2 D189D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8515-01A-11D-2396-08 chr6:127611394 T>C maps to NM_001139510.1 R181R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7963-01B-11D-A28G-10 chr1:53362194 T>C maps to ENST00000371522 K292K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9K0-01A-11D-A42J-10 chr1:150483675 T>A did not map to a codon.
Sequencing variant TCGA-UZ-A9PK-01A-11D-A382-10 chr1:150482013 G>T maps to ENST00000369049 T26T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A8YH-01A-11D-A36X-10 chr9:95272294 A>G maps to NM_001393.3 L398L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr6:139167796 C>A maps to NM_001195037.2 R296R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr16:67910483 G>A maps to NM_014329.3 K111K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PS-01A-11D-A42J-10 chr20:33730266 G>T maps to NM_018217.2 V91V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JO-01A-11D-A42J-10 chr12:93171432 A>G maps to NM_003566.3 L1300L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-8121-01A-21D-2396-08 chr17:60484527 T>C maps to NM_001144933.1 H326H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9KE-01A-11D-A42J-10 chr17:28380418 A>T maps to NM_198529.3 K483*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7584-01A-11D-2136-08 chr17:28407884 G>C maps to NM_198529.3 L1104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5891-01A-11D-1589-08 chr13:22088515 C>T maps to NM_152726.2 V213V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4104-01A-01D-1458-08 chr3:19925988 G>C maps to NM_144715.3 L684L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PR-01A-11D-A42J-10 chr23:44008116 A>T did not map to a codon.
Sequencing variant TCGA-MH-A856-01A-11D-A34Z-10 chr19:1295669 C>T maps to NM_001405.2 Y89Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7584-01A-11D-2136-08 chr8:132968017 C>T maps to NM_015137.3 R214R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr14:23828917 G>A maps to NM_005864.2 L257L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9KE-01A-11D-A42J-10 chr17:42949880 G>A maps to NM_004247.3 F309F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JQ-01A-11D-A42J-10 chr23:13588003 G>T did not map to a codon.
Sequencing variant TCGA-MH-A55W-01A-11D-A26P-10 chr5:38418271 C>A maps to ENST00000354891 G533G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9JZ-01A-11D-A42J-10 chr7:55221780 C>T maps to NM_005228.3 Y275Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr19:41306602 T>A maps to NM_053046.2 C42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A71U-01A-12D-A33Q-10 chr2:63175858 A>G maps to NM_015252.3 G661G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7838-01A-11D-2136-08 chr3:184922366 G>A maps to NM_001966.3 I249I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5893-01A-11D-1589-08 chr23:20152120 C>A did not map to a codon.
Sequencing variant TCGA-A4-8098-01A-11D-2396-08 chr2:37365710 G>A maps to NM_001135651.1 S178S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-A5DJ-01A-11D-A26P-10 chr2:88913361 T>C maps to NM_004836.5 V106V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-5156-01A-01D-1589-08 chr1:36354061 G>A maps to NM_012199.2 V20V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7834-01A-11D-2136-08 chr14:67848334 T>C maps to NM_004094.4 Y202Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5886-01A-11D-1589-08 chr23:24089814 C>T did not map to a codon.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr8:109215295 A>T maps to NM_001568.2 I405I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4103-01A-01D-1458-08 chr19:10230529 A>G maps to NM_003755.3 P2P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9J3-01A-12D-A382-10 chr12:53432172 T>C maps to ENST00000438209 S523S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3468-01A-01D-1252-08 chr22:31837940 T>C maps to NM_019843.3 R790R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9K6-01A-11D-A42J-10 chr3:184042784 G>A maps to NM_001194947.1 E920E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5876-01A-11D-1589-08 chr2:100015353 A>C maps to NM_015904.3 T1179T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5889-01A-11D-1589-08 chr2:99978206 A>T maps to NM_015904.3 V281V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A6HP-01A-11D-A31X-10 chr17:12898189 A>G maps to NM_018127.6 C640C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PX-01A-11D-A42J-10 chr23:47497264 C>T did not map to a codon.
Sequencing variant TCGA-MH-A55W-01A-11D-A26P-10 chr1:205588956 C>G maps to NM_021795.2 *406S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Y8-A896-01A-11D-A35Z-10 chr19:18555597 G>A maps to NM_006532.3 A610A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4A-A93W-01A-11D-A36X-10 chr16:67233132 A>G maps to NM_024712.3 G21G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8630-01A-11D-2396-08 chr16:67236621 T>A maps to NM_024712.3 T550T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9J5-01A-21D-A382-10 chr2:85617284 C>A maps to NM_001135023.1 V280V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr7:73474351 C>A maps to ENST00000358929 P552P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F9-A8NY-01A-11D-A35Z-10 chr19:11664883 G>A maps to NM_032377.3 R43R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9KE-01A-11D-A42J-10 chr22:29628293 C>A maps to NM_133455.2 T242T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5886-01A-11D-1589-08 chr22:29627007 G>T did not map to a codon.
Sequencing variant TCGA-UZ-A9PR-01A-11D-A42J-10 chr2:27305966 C>T maps to NM_007046.3 Q510*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Y8-A8RY-01A-11D-A36X-10 chr23:129822851 A>G did not map to a codon.
Sequencing variant TCGA-BQ-5883-01A-11D-1589-08 chr3:40465426 T>A maps to NM_001248.2 T442T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A71U-01A-12D-A33Q-10 chr8:23305328 C>G maps to NM_004901.3 V92V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7288-01A-11D-2136-08 chr20:25201970 T>A maps to ENST00000443525 G349G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A7SN-01A-11D-A34Z-10 chr9:140332421 C>A maps to NM_001033113.1 E81*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9K3-01A-11D-A42J-10 chr22:41527605 T>C maps to NM_001429.3 S499S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A8YH-01A-11D-A36X-10 chr22:41572321 T>C maps to NM_001429.3 P1617P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PK-01A-11D-A382-10 chr22:41542755 T>C maps to NM_001429.3 P689P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F9-A8NY-01A-11D-A35Z-10 chr12:132547083 G>A maps to ENST00000333577 Q2760Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A9DC-01A-11D-A36X-10 chr12:132547080 G>A maps to ENST00000333577 Q2759Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A9DC-01A-11D-A36X-10 chr12:132547083 G>A maps to ENST00000333577 Q2760Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Y8-A896-01A-11D-A35Z-10 chr18:5397278 C>T maps to NM_012307.2 S873S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UN-AAZ9-01A-11D-A382-10 chr5:111602023 A>T maps to NM_022140.3 Y113*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9J3-01A-12D-A382-10 chr1:38192853 G>C maps to NM_001099439.1 P564P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JG-01A-11D-A42J-10 chr4:66535301 G>T maps to NM_004439.5 L53L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A854-01A-11D-A34Z-10 chr4:66201789 A>G maps to NM_004439.5 P904P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A7SS-01A-11D-A35Z-10 chr3:97311465 G>A maps to NM_001080448.2 P799P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47O-01A-11D-A25F-10 chr1:22902756 G>A maps to NM_020526.3 T69T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4113-01A-01D-1252-08 chr1:22927185 A>T maps to NM_020526.3 P807P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr1:22903098 G>T maps to NM_020526.3 L183L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A7SL-01A-11D-A34Z-10 chr1:22903065 T>C maps to NM_020526.3 S172S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9KH-01A-11D-A42J-10 chr7:100410508 C>A maps to NM_004444.4 E660*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WN-A9G9-01A-12D-A36X-10 chr7:100414913 C>A maps to NM_004444.4 G496G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9K2-01A-11D-A42J-10 chr7:142562073 C>T maps to NM_004445.3 S172S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5889-01A-11D-1589-08 chr7:142562310 G>T maps to NM_004445.3 G251G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-A8LD-01A-11D-A35Z-10 chr7:142562073 C>T maps to NM_004445.3 S172S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A7SM-01A-11D-A34Z-10 chr19:15342597 G>A maps to NM_001142886.1 F106F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9JY-01A-11D-A42J-10 chr8:144947043 G>T maps to NM_031308.1 Y126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-7332-01A-11D-2136-08 chr8:144941595 G>A maps to NM_031308.1 D1942D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J7-A8I2-01A-12D-A35Z-10 chr8:144946577 C>A maps to NM_031308.1 E282*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A71S-01A-11D-A33Q-10 chr1:220160680 T>A maps to NM_004446.2 G947G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WN-AB4C-01A-11D-A42J-10 chr1:51929371 A>T maps to NM_001981.2 S158S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr19:16551693 A>G maps to ENST00000455140 G64G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9Q1-01A-11D-A42J-10 chr12:15776127 G>C maps to NM_004447.5 V773V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A7SR-01A-12D-A35Z-10 chr19:55591173 G>A maps to NM_133180.2 L78L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7839-01A-11D-2136-08 chr11:723295 C>A maps to NM_022772.3 S466*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A71S-01A-11D-A33Q-10 chr11:721126 C>A maps to NM_022772.3 P207P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A83V-01A-11D-A34Z-10 chr5:96126037 A>G maps to NM_016442.3 D495D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4114-01A-01D-1252-08 chr17:37876079 A>C maps to NM_004448.2 R647R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9KC-01A-11D-A42J-10 chr12:56481696 T>C maps to NM_001982.2 F244F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5903-01A-11D-1589-08 chr2:212295692 C>A maps to NM_005235.2 E874*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47O-01A-11D-A25F-10 chr12:1372210 T>A maps to NM_178040.2 R833R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-8500-01A-11D-2396-08 chr19:45868314 G>A maps to NM_000400.3 H154H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PM-01A-21D-A382-10 chr19:45867361 G>A maps to NM_000400.3 D277D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-7502-01A-11D-2201-08 chr13:103524733 C>A maps to NM_000123.2 L955L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-O9-A75Z-01A-11D-A33Q-10 chr10:50668439 T>C maps to NM_000124.2 T1347T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A655-01A-11D-A31Z-10 chr23:71427692 G>T did not map to a codon.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr23:71426808 G>C did not map to a codon.
Sequencing variant TCGA-HE-A5NH-01A-11D-A26P-10 chr12:29502994 A>T maps to NM_016570.2 I193I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PR-01A-11D-A42J-10 chr2:54040084 G>C did not map to a codon.
Sequencing variant TCGA-G7-6792-01A-21D-1961-08 chr10:101911986 A>G maps to NM_001100626.1 Y316Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7836-01A-11D-2136-08 chr1:236385228 A>G maps to NM_019891.3 L402L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NL-01A-11D-A26P-10 chr11:124623586 C>T maps to NM_138961.2 V376V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8196-01A-11D-2396-08 chr13:47354150 A>G maps to NM_001984.1 A173A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7288-01A-11D-2136-08 chr12:53685604 A>G maps to NM_012291.4 T1884T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V9-A7HT-01A-11D-A33Q-10 chr2:239040219 C>T maps to NM_194312.2 A955A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr6:152201892 A>G maps to NM_001122741.1 G249G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JD-01A-11D-A42J-10 chr8:95653651 A>T maps to NM_017697.3 K36*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5878-01A-11D-1589-08 chr23:103499099 C>T did not map to a codon.
Sequencing variant TCGA-2Z-A9JG-01A-11D-A42J-10 chr7:158528196 G>A maps to NM_020728.2 G861G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4104-01A-01D-1458-08 chr2:67631298 A>G maps to NM_019002.3 Q495Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Y8-A898-01A-11D-A34Z-10 chr19:51857558 G>A maps to NM_001014763.1 R112*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-5561-01A-01D-1589-08 chr11:128360460 A>T maps to NM_001143820.1 C75*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JI-01A-11D-A42J-10 chr7:13946126 A>G maps to NM_004956.4 D346D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr7:13971322 C>G maps to NM_004956.4 T202T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4114-01A-01D-1252-08 chr4:5721078 G>A maps to NM_153717.2 S93S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A9DE-01A-11D-A36X-10 chr4:5812076 A>C maps to NM_153717.2 R932R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Y8-A895-01A-11D-A35Z-10 chr1:93029240 A>C maps to NM_005665.4 Y692*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AT-A5NU-01A-11D-A28G-10 chr19:7927063 C>T maps to NM_001159944.1 G567G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A71R-01A-12D-A33Q-10 chr17:18284973 C>G maps to NM_001145127.1 Y92*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A655-01A-11D-A31Z-10 chr8:145134931 C>T maps to NM_019037.2 R86R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8517-01A-11D-2396-08 chr4:122724129 G>A maps to NM_001034194.1 K114K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-A4TM-01A-11D-A31X-10 chr4:122722614 C>T maps to NM_001034194.1 R12R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr11:108380879 C>T maps to NM_015065.2 W1785*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59R-01A-11D-A26P-10 chr11:108381025 T>G maps to NM_015065.2 T1736T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PV-01A-11D-A42J-10 chr11:108384988 A>T maps to NM_015065.2 Y415*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47M-01A-11D-A25F-10 chr8:72182013 G>A maps to NM_000503.4 H337H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-5560-01A-01D-1589-08 chr5:176831340 G>A maps to NM_000505.3 L292L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9Q0-01A-12D-A42J-10 chr5:176831332 C>T maps to NM_000505.3 Q294Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A657-01A-11D-A31X-10 chr1:197020001 T>C maps to NM_001994.2 K521K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A8YH-01A-11D-A36X-10 chr1:197026476 G>T maps to NM_001994.2 I308I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5889-01A-11D-1589-08 chr23:154157882 C>T did not map to a codon.
Sequencing variant TCGA-IA-A83S-01A-11D-A34Z-10 chr23:154159621 G>A did not map to a codon.
Sequencing variant TCGA-IA-A83V-01A-11D-A34Z-10 chr16:74808458 C>A maps to NM_024306.4 P65P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9J2-01A-11D-A382-10 chr23:57475116 C>G did not map to a codon.
Sequencing variant TCGA-IA-A83V-01A-11D-A34Z-10 chr1:51253750 C>T maps to NM_007051.2 R96R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5Y1-01A-11D-A28G-10 chr16:1877592 G>T maps to NM_001018104.2 L121L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-7501-01A-11D-2201-08 chr1:207085118 G>C maps to NM_005449.4 P222P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A561-01A-11D-A26P-10 chr9:130707095 G>A maps to NM_001035254.2 I333I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JO-01A-11D-A42J-10 chr23:55172644 C>G did not map to a codon.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr19:1881346 A>G maps to NM_031213.3 R73R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AT-A5NU-01A-11D-A28G-10 chr9:74489540 A>G maps to NM_016014.2 A152A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5893-01A-11D-1589-08 chr8:59059733 C>T maps to NM_147189.2 S315S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7996-01A-11D-2201-08 chr12:47628908 G>T maps to NM_138371.1 L21L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E6-01A-11D-A28G-10 chr2:203500480 A>C maps to NM_173511.3 R191R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Y8-A894-01A-11D-A35Z-10 chr2:208486599 C>T maps to ENST00000272839 E63E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JQ-01A-11D-A42J-10 chr23:133906198 G>A did not map to a codon.
Sequencing variant TCGA-BQ-7058-01A-11D-1961-08 chr23:63412032 A>G did not map to a codon.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr23:63411695 G>A did not map to a codon.
Sequencing variant TCGA-SX-A7SS-01A-11D-A35Z-10 chr23:63412148 T>C did not map to a codon.
Sequencing variant TCGA-Y8-A8RY-01A-11D-A36X-10 chr23:63411063 C>G did not map to a codon.
Sequencing variant TCGA-SX-A7SQ-01A-12D-A35Z-10 chr2:132249823 C>T maps to NM_001085365.1 E42E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A44B-01A-11D-A25F-10 chr1:1179847 G>C maps to NM_001014980.1 S69S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4114-01A-01D-1252-08 chr8:139163999 G>T maps to NM_015912.3 G906G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A71S-01A-11D-A33Q-10 chr8:139165352 A>G maps to NM_015912.3 S455S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8517-01A-11D-2396-08 chr10:61112191 C>A maps to ENST00000442566 L76L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JO-01A-11D-A42J-10 chr11:6236091 G>A maps to NM_032127.3 N769N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-7502-01A-11D-2201-08 chr3:122128620 C>T maps to NM_014367.3 N136N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7584-01A-11D-2136-08 chr8:79578394 G>C maps to NM_016010.2 L4L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AT-A5NU-01A-11D-A28G-10 chr10:102675795 C>T maps to NM_001136123.1 Q61*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5878-01A-11D-1589-08 chr10:102683798 C>T maps to NM_001136123.1 S347S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F9-A8NY-01A-11D-A35Z-10 chr2:97559674 C>T maps to ENST00000417561 E736E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A83T-01A-11D-A34Z-10 chr14:94395092 G>A maps to NM_138344.3 E216E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-7173-01A-11D-2136-08 chr3:150421568 T>C maps to NM_152394.3 E39E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4115-01A-01D-1252-08 chr4:159092401 A>T maps to NM_001128424.1 T42T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A657-01A-11D-A31X-10 chr7:193540 C>T maps to NM_020223.2 A114A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A657-01A-11D-A31X-10 chr7:193560 T>A maps to NM_020223.2 L121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Y8-A897-01A-11D-A35Z-10 chr7:208976 G>A did not map to a codon.
Sequencing variant TCGA-GL-A59R-01A-11D-A26P-10 chr10:88911775 C>G maps to ENST00000298786 S222*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5Y1-01A-11D-A28G-10 chr18:10691259 T>A maps to NM_022068.2 K2325*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PJ-A8JU-01A-11D-A35Z-10 chr18:10680335 T>C maps to NM_022068.2 K2491K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PJ-A8JU-01A-11D-A35Z-10 chr18:10680341 A>T maps to NM_022068.2 Y2489*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr3:58625896 C>A maps to NM_138805.2 T110T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr7:129120721 C>A maps to ENST00000450266 R740R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JJ-01A-11D-A42J-10 chr6:82461741 G>A maps to ENST00000369756 G120G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9KH-01A-11D-A42J-10 chr6:82461741 G>A maps to ENST00000369756 G120G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A560-01A-11D-A26P-10 chr23:34148935 C>T did not map to a codon.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr23:34961453 G>A did not map to a codon.
Sequencing variant TCGA-5P-A9JV-01A-12D-A42J-10 chr23:24382425 G>C did not map to a codon.
Sequencing variant TCGA-A4-8515-01A-11D-2396-08 chr23:24381816 G>T did not map to a codon.
Sequencing variant TCGA-IA-A83V-01A-11D-A34Z-10 chr23:24381465 G>C did not map to a codon.
Sequencing variant TCGA-SX-A7SP-01A-11D-A34Z-10 chr23:24382434 C>G did not map to a codon.
Sequencing variant TCGA-UN-AAZ9-01A-11D-A382-10 chr23:24382383 G>A did not map to a codon.
Sequencing variant TCGA-BQ-5882-01A-11D-1589-08 chr8:130883631 C>A maps to NM_016623.3 E62*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A83W-01A-11D-A34Z-10 chr10:126384766 C>T maps to NM_014661.3 K31K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7585-01A-11D-2136-08 chr1:190067268 A>T maps to NM_199051.1 L727*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55W-01A-11D-A26P-10 chr15:59139572 A>T maps to NM_001040450.1 V482V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7997-01A-11D-2201-08 chr20:49219115 G>A maps to NM_080829.2 L380L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6790-01A-11D-1961-08 chr5:156590093 T>A maps to NM_130899.2 A394A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9J3-01A-12D-A382-10 chr12:100042117 A>C maps to NM_153364.2 R56R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9K0-01A-11D-A42J-10 chr12:100042137 G>T maps to NM_153364.2 V62V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5876-01A-11D-1589-08 chr1:78325732 T>C maps to NM_198549.2 L399L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JN-01A-21D-A42J-10 chr9:131832228 C>G maps to NM_032809.2 V520V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9Q1-01A-11D-A42J-10 chr9:131832214 C>T maps to NM_032809.2 Q516*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9K2-01A-11D-A42J-10 chr5:94783980 T>C maps to NM_152548.2 S346S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A83T-01A-11D-A34Z-10 chr8:124206352 C>T maps to NM_032899.4 I246I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E8-01A-11D-A28G-10 chr20:37570603 G>A maps to NM_030919.2 V192V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-7332-01A-11D-2136-08 chr17:18881907 G>A maps to NM_001039999.2 V357V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9Q1-01A-11D-A42J-10 chr17:18882129 A>G maps to NM_001039999.2 N283N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5893-01A-11D-1589-08 chr8:144809116 G>C maps to NM_198488.3 A838A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A71U-01A-12D-A33Q-10 chr6:17601242 C>A maps to NM_016255.2 G201G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9JU-01A-11D-A42J-10 chr8:124811758 G>A did not map to a codon.
Sequencing variant TCGA-DW-7841-01A-11D-2136-08 chr8:124787417 C>A maps to NM_144963.2 Y63*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Y8-A894-01A-11D-A35Z-10 chr8:124786385 C>T maps to NM_144963.2 R47*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E7-01A-31D-A28G-10 chr2:33813425 T>C maps to ENST00000395190 Q166Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9K6-01A-11D-A42J-10 chr15:38776826 T>A maps to NM_173611.2 G423G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5DU-01A-11D-A28G-10 chr15:38776826 T>A maps to NM_173611.2 G423G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A560-01A-11D-A26P-10 chr15:38776826 T>A maps to NM_173611.2 G423G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WN-A9G9-01A-12D-A36X-10 chr15:38776811 T>A maps to NM_173611.2 G418G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WN-A9G9-01A-12D-A36X-10 chr15:38776814 T>A maps to NM_173611.2 G419G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr16:89874754 C>A maps to NM_000135.2 A181A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JE-01A-11D-A42J-10 chr23:14863247 T>G did not map to a codon.
Sequencing variant TCGA-5P-A9K3-01A-11D-A42J-10 chr23:14862798 G>A did not map to a codon.
Sequencing variant TCGA-IA-A40Y-01A-11D-A25F-10 chr3:10089632 G>A maps to NM_033084.3 S437S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5Y1-01A-11D-A28G-10 chr15:89856163 A>T maps to NM_001113378.1 G1227G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-5156-01A-01D-1589-08 chr2:58431303 A>G maps to NM_001114636.1 S144S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr14:45636323 C>A maps to NM_020937.2 R654R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59T-01A-21D-A28G-10 chr2:163046172 A>G maps to NM_004460.2 D514D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6789-01A-11D-1961-08 chr12:29485565 T>C maps to NM_018099.3 L431L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr12:29469909 T>A maps to NM_018099.3 Y364*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr13:99092298 T>A did not map to a codon.
Sequencing variant TCGA-B9-A44B-01A-11D-A25F-10 chr2:242407763 C>G maps to NM_014808.2 P701P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5903-01A-11D-1589-08 chr2:242433434 G>C maps to NM_014808.2 V1020V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A9DE-01A-11D-A36X-10 chr17:80047167 G>A maps to NM_004104.4 F686F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M8-01A-11D-A31X-10 chr17:80047602 C>G did not map to a codon.
Sequencing variant TCGA-B1-A655-01A-11D-A31Z-10 chr2:207655322 T>C maps to NM_014929.3 S642S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7585-01A-11D-2136-08 chr5:7867620 A>G maps to NM_024091.3 P192P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PJ-01A-11D-A382-10 chr5:7867536 A>G maps to NM_024091.3 I220I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3468-01A-01D-1252-08 chr20:3128939 A>G maps to NM_021826.4 P259P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JS-01A-21D-A42J-10 chr4:187539963 A>G maps to ENST00000260147 N2595N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr4:187630249 C>A maps to ENST00000260147 T244T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr4:187530417 T>A maps to ENST00000260147 I3378I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WN-AB4C-01A-11D-A42J-10 chr4:187509943 A>T maps to ENST00000260147 Y4526*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JE-01A-11D-A42J-10 chr5:150920244 G>A maps to NM_001447.2 R2974R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55Z-01A-11D-A26P-10 chr5:150911352 G>A maps to NM_001447.2 G3202G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JG-01A-11D-A42J-10 chr4:126239707 T>C maps to NM_024582.4 T714T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9KE-01A-11D-A42J-10 chr4:126372769 T>C maps to NM_024582.4 T3533T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7734-01A-11D-2136-08 chr4:126411929 C>A maps to NM_024582.4 I4651I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr4:126369688 G>T maps to NM_024582.4 S2506S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NL-01A-11D-A26P-10 chr4:126239107 T>C maps to NM_024582.4 I514I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8518-01A-11D-2396-08 chr23:150891104 T>G did not map to a codon.
Sequencing variant TCGA-B9-4114-01A-01D-1252-08 chr11:64889267 G>T maps to NM_001997.4 R6R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5Y1-01A-11D-A28G-10 chr19:40330914 G>A maps to NM_001436.3 V112V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PV-01A-11D-A42J-10 chr19:40328471 G>A maps to NM_001436.3 V187V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8517-01A-11D-2396-08 chr14:92349358 G>T maps to ENST00000267620 G364G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr15:48748936 G>T maps to NM_000138.4 I1773I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A657-01A-11D-A31X-10 chr19:8183904 G>A maps to NM_032447.3 D1071D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A71R-01A-12D-A33Q-10 chr9:97329629 A>T maps to NM_003837.2 I209I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AT-A5NU-01A-11D-A28G-10 chr7:102553613 G>A maps to NM_145032.3 F309F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59T-01A-21D-A28G-10 chr3:33415409 C>T maps to NM_012157.3 C218C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WN-AB4C-01A-11D-A42J-10 chr4:15638132 A>G maps to NM_012161.3 P250P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J7-6720-01A-11D-2136-08 chr2:230875428 A>G maps to NM_174899.4 K132K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4A-A93X-01A-11D-A36X-10 chr5:41925545 T>A maps to NM_012176.2 R45R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr17:18653136 T>A maps to ENST00000395665 L258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8312-01A-11D-2396-08 chr9:123527052 G>A maps to NM_012164.3 D383D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J7-A8I2-01A-12D-A35Z-10 chr4:153273873 G>A maps to NM_018315.4 V3V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F9-A97G-01A-11D-A382-10 chr19:12805524 G>T maps to ENST00000380339 L187L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr19:55385757 C>T maps to NM_002000.2 Q5*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7996-01A-11D-2201-08 chr19:40419756 A>G maps to NM_003890.2 H1079H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr19:40366037 C>G maps to NM_003890.2 P4732P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6789-01A-11D-1961-08 chr19:40408647 G>C maps to NM_003890.2 P1397P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A71U-01A-12D-A33Q-10 chr11:72552499 G>A maps to ENST00000409314 N709N. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-PJ-A5Z9-01A-11D-A28G-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr1:157559027 T>C maps to NM_031282.2 P91P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-AAVL-01A-11D-A42J-10 chr1:157548315 T>A maps to NM_031282.2 G459G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V9-A7HT-01A-11D-A33Q-10 chr1:159778130 A>T maps to NM_001004310.2 A72A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A7SQ-01A-12D-A35Z-10 chr1:161695842 C>A maps to NM_001002901.2 P180P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JD-01A-11D-A42J-10 chr1:155279708 C>T maps to NM_001135821.1 A43A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7584-01A-11D-2136-08 chr11:111749724 A>G maps to ENST00000428306 D44D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A656-01A-11D-A31X-10 chr19:4792819 C>A maps to NM_018708.2 A318A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JS-01A-21D-A42J-10 chr5:114860325 A>G maps to NM_020177.2 T511T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A7SN-01A-11D-A34Z-10 chr5:114860102 A>G maps to NM_020177.2 L586L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47M-01A-11D-A25F-10 chr8:124989659 C>T maps to NM_001039112.2 R292*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A71S-01A-11D-A33Q-10 chr11:63978140 G>A maps to NM_178443.2 L73L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NI-01A-11D-A26P-10 chr6:167435949 C>A maps to NM_007045.2 P211P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr4:1806087 G>T maps to NM_000142.4 A369A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8098-01A-11D-2396-08 chr4:1805486 C>T maps to NM_000142.4 D333D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A657-01A-11D-A31X-10 chr5:176520384 A>G maps to NM_022963.2 R370R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A560-01A-11D-A26P-10 chr4:155526042 T>C maps to ENST00000407946 R443R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F9-A4JJ-01A-11D-A25F-10 chr1:241661271 T>G did not map to a codon.
Sequencing variant TCGA-GL-7966-01A-11D-2201-08 chr1:241663811 G>A maps to NM_000143.3 Q439*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5DU-01A-11D-A28G-10 chr6:97051596 A>G maps to NM_020482.4 V36V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AT-A5NU-01A-11D-A28G-10 chr18:34310625 A>G maps to NM_025135.2 G970G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F9-A7VF-01A-11D-A33Q-10 chr23:15364333 T>G did not map to a codon.
Sequencing variant TCGA-G7-A8LE-01A-11D-A35Z-10 chr6:76024128 G>T maps to NM_015687.2 V473V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7584-01A-11D-2136-08 chr4:54266006 G>C did not map to a codon.
Sequencing variant TCGA-SX-A7SR-01A-12D-A35Z-10 chr11:35641395 C>G maps to NM_014344.3 A404A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J7-A8I2-01A-12D-A35Z-10 chr20:1352845 T>G maps to NM_054014.3 P79P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4104-01A-01D-1458-08 chr14:45603574 G>A maps to NM_002013.3 L29L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr12:2909577 T>G maps to NM_002014.3 A289A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chr12:2909051 A>G maps to NM_002014.3 Q236Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A854-01A-11D-A34Z-10 chr19:47260095 C>T maps to NM_024301.4 N463N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WN-A9G9-01A-12D-A36X-10 chr9:108397412 C>A maps to NM_006731.2 Y418*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WN-AB4C-01A-11D-A42J-10 chr17:17117171 T>G did not map to a codon.
Sequencing variant TCGA-EV-5902-01A-11D-1589-08 chr1:152279671 C>A maps to NM_002016.1 G2564*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5887-01A-11D-1961-08 chr17:18149934 G>A maps to NM_002018.2 F1008F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-AAVL-01A-11D-A42J-10 chr14:21543509 C>G maps to NM_018071.3 G490G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JE-01A-11D-A42J-10 chr7:106301195 C>G maps to NM_175884.4 L49L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JL-01A-11D-A42J-10 chr9:84606599 A>T maps to NM_001001670.2 S405S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5903-01A-11D-1589-08 chr9:84605891 G>A maps to NM_001001670.2 S169S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr11:63885634 G>A maps to NM_013280.4 E632E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9K2-01A-11D-A42J-10 chr14:86088352 T>C maps to NM_013231.4 F165F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A83V-01A-11D-A34Z-10 chr13:28942738 T>C maps to NM_001160030.1 S726S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A40Y-01A-11D-A25F-10 chr5:180050942 T>A maps to NM_182925.4 K514*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F9-A8NY-01A-11D-A35Z-10 chr14:76107631 C>T maps to NM_017791.2 L483L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Y8-A895-01A-11D-A35Z-10 chr14:76045629 C>G maps to NM_017791.2 Y105*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9J1-01A-11D-A382-10 chr16:2980630 G>A maps to ENST00000399667 E182E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A657-01A-11D-A31X-10 chr1:240371138 C>T maps to ENST00000406993 P1152P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F9-A4JJ-01A-11D-A25F-10 chr1:240255570 C>G maps to ENST00000406993 G197G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5882-01A-11D-1589-08 chr2:153471510 T>A maps to NM_052905.3 S403S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JO-01A-11D-A42J-10 chr1:171162499 T>C maps to NM_001460.2 S53S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7585-01A-11D-2136-08 chr23:147011650 T>A did not map to a codon.
Sequencing variant TCGA-SX-A71S-01A-11D-A33Q-10 chr23:147014032 T>C did not map to a codon.
Sequencing variant TCGA-HE-A5NI-01A-11D-A26P-10 chr2:216271072 C>T maps to NM_212482.1 R958R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J7-8537-01A-11D-2396-08 chr1:94009755 G>A maps to ENST00000370253 Q414Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8515-01A-11D-2396-08 chr11:47745664 A>G maps to NM_015308.2 A793A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A9DD-01A-11D-A36X-10 chr11:47745676 T>G maps to NM_015308.2 I789I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Y8-A898-01A-11D-A34Z-10 chr6:159653340 G>A maps to NM_032532.2 K599K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr3:171965495 C>A maps to NM_022763.3 T146T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J7-6720-01A-11D-2136-08 chr3:172025191 C>G maps to NM_022763.3 S367S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JP-01A-11D-A42J-10 chr17:33457437 C>T maps to NM_017559.2 Y320Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr4:159756555 G>A did not map to a codon.
Sequencing variant TCGA-G7-6792-01A-21D-1961-08 chr4:159825695 A>G maps to ENST00000379346 *1138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PU-01A-11D-A42J-10 chr2:28634996 G>C maps to NM_005253.3 V221V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9J1-01A-11D-A382-10 chr5:169532984 G>T maps to NM_012188.4 A8A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-A4TM-01A-11D-A31X-10 chr1:42744041 T>A maps to NM_001198850.1 R116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PV-01A-11D-A42J-10 chr16:86612502 C>A maps to NM_005250.2 I58I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A4EM-01A-11D-A25F-10 chr23:70316473 C>T did not map to a codon.
Sequencing variant TCGA-UZ-A9PV-01A-11D-A42J-10 chr23:70316597 C>A did not map to a codon.
Sequencing variant TCGA-BQ-5875-01A-11D-1589-08 chr7:114299728 G>A did not map to a codon.
Sequencing variant TCGA-GL-A9DE-01A-11D-A36X-10 chr6:1313367 G>T maps to NM_033260.3 A143A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9Q0-01A-12D-A42J-10 chr9:130570588 C>A maps to NM_004957.4 S274*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9J6-01A-11D-A382-10 chr1:74671341 A>G maps to NM_003838.3 S537S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F9-A4JJ-01A-11D-A25F-10 chr19:52327624 T>A maps to NM_002030.3 I208I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-5156-01A-01D-1589-08 chr13:39452996 C>G maps to NM_207361.4 T2963T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4103-01A-01D-1458-08 chr14:52182104 G>T maps to ENST00000344768 T304T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WN-AB4C-01A-11D-A42J-10 chr23:131212369 C>T did not map to a codon.
Sequencing variant TCGA-DW-5560-01A-01D-1589-08 chr1:100214267 A>G maps to NM_001013660.2 Y19Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W8-01A-11D-A28G-10 chr4:48536645 A>G maps to NM_015030.1 S2207S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6790-01A-11D-1961-08 chr4:48578145 T>C maps to NM_015030.1 A874A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr2:183699592 G>T maps to NM_001463.3 R321R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr14:44975260 C>T maps to NM_032135.3 A310A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A655-01A-11D-A31Z-10 chr17:79496378 G>A maps to NM_001077182.2 R274R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A9DC-01A-11D-A36X-10 chr17:79495706 C>T maps to NM_001077182.2 P50P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A7SS-01A-11D-A35Z-10 chr17:79503807 G>A maps to NM_001077182.2 R446R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5902-01A-11D-1589-08 chr2:49190327 G>A maps to NM_000145.3 V544V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PJ-A5Z9-01A-11D-A28G-10 chr15:40056079 C>T maps to NM_152597.4 E167E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5Y1-01A-11D-A28G-10 chr2:186671592 C>T maps to NM_173651.2 Q5943*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr3:120122158 A>G maps to NM_007085.4 N208N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55Z-01A-11D-A26P-10 chr4:162307105 T>A maps to NM_020116.3 I779I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7287-01A-11D-2136-08 chr21:47571510 G>T maps to ENST00000397748 I199I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A7SS-01A-11D-A35Z-10 chr5:121187741 C>A maps to NM_177478.1 L28L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6790-01A-11D-1961-08 chr6:37442388 A>G maps to NM_015050.2 L637L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9J7-01A-11D-A382-10 chr1:78432738 C>A maps to ENST00000436586 G134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NK-01A-11D-A26P-10 chr1:78414968 A>G maps to ENST00000436586 A621A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JS-01A-21D-A42J-10 chr15:91424717 C>T maps to NM_002569.2 H665H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PJ-A8JU-01A-11D-A35Z-10 chr10:75535418 C>A maps to NM_173540.2 I485I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Y8-A896-01A-11D-A35Z-10 chr3:180688018 T>C maps to NM_005087.3 D492D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9KC-01A-11D-A42J-10 chr5:39153578 G>T maps to ENST00000263405 P430P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A654-01A-11D-A31X-10 chr3:46000086 G>C maps to NM_024513.2 Y1204*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5885-01A-11D-1589-08 chr3:46009967 C>T maps to NM_024513.2 E286E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5879-01A-11D-1589-08 chr3:197501075 T>C maps to NM_032288.6 T217T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr11:86663407 G>T maps to NM_012193.2 P130P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E6-01A-11D-A28G-10 chr2:202900341 C>G maps to NM_003507.1 Y324*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WN-AB4C-01A-11D-A42J-10 chr10:35929627 C>A maps to NM_031866.2 E244*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-5156-01A-01D-1589-08 chr19:3527658 C>A maps to NM_001136198.1 P167P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A69E-01A-11D-A31X-10 chr14:31081504 G>A maps to NM_017769.3 T531T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A83T-01A-11D-A34Z-10 chr14:31061653 G>C did not map to a codon.
Sequencing variant TCGA-SX-A71W-01A-12D-A34Z-10 chr17:78085900 T>G did not map to a codon.
Sequencing variant TCGA-BQ-5875-01A-11D-1589-08 chr11:77934563 G>A maps to NM_080491.2 D487D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr23:153928304 G>T did not map to a codon.
Sequencing variant TCGA-IA-A40X-01A-11D-A25F-10 chr23:153908428 A>G did not map to a codon.
Sequencing variant TCGA-BQ-5890-01A-11D-1589-08 chr5:161281259 G>A maps to NM_001127648.1 L57L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8196-01A-11D-2396-08 chr4:46312217 A>T maps to ENST00000507069 A177A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-A5DJ-01A-11D-A26P-10 chr23:151532941 C>T did not map to a codon.
Sequencing variant TCGA-B9-A5W8-01A-11D-A28G-10 chr5:161116040 T>C maps to NM_000811.2 N104N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NH-01A-11D-A26P-10 chr4:47427722 C>G maps to NM_000812.3 T371T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5884-01A-11D-1589-08 chr5:160753380 C>G maps to NM_021911.2 L395L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4104-01A-01D-1458-08 chr15:26793189 G>C maps to NM_021912.4 S391*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NL-01A-11D-A26P-10 chr4:46043271 C>T did not map to a codon.
Sequencing variant TCGA-P4-AAVL-01A-11D-A42J-10 chr23:151821370 G>A did not map to a codon.
Sequencing variant TCGA-G7-6790-01A-11D-1961-08 chr2:171687569 C>T maps to NM_000817.2 L139L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A8YI-01A-21D-A36X-10 chr10:26505777 G>T maps to NM_001134366.1 E14*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W9-01A-11D-A28G-10 chr16:88889079 G>A maps to NM_000512.4 V427V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A6HP-01A-11D-A31X-10 chr5:153755928 C>T maps to NM_198321.3 R221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A561-01A-11D-A26P-10 chr12:51758020 G>C maps to NM_007210.3 P311P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr4:174225145 G>A did not map to a codon.
Sequencing variant TCGA-B1-A47N-01A-11D-A25F-10 chr12:132834319 G>A maps to NM_001122636.1 N289N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr16:81388210 C>A maps to NM_022041.3 R162R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9J5-01A-21D-A382-10 chr11:62394376 C>T maps to NM_198335.2 K806K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A48D-01A-11D-A25F-10 chr19:36029206 A>C did not map to a codon.
Sequencing variant TCGA-BQ-5892-01A-11D-1589-08 chr17:9846495 G>A maps to NM_201433.1 Q225*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A7SP-01A-11D-A34Z-10 chr16:90109647 C>T maps to NM_001481.2 A444A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NJ-01A-11D-A26P-10 chr23:48652220 C>T did not map to a codon.
Sequencing variant TCGA-A4-A5DU-01A-11D-A28G-10 chr20:61050058 G>T maps to NM_080473.4 T173T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59T-01A-21D-A28G-10 chr7:92083892 A>G maps to NM_021167.3 R171R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A71V-01A-11D-A33Q-10 chr15:45668862 A>C maps to ENST00000432007 L128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E7-01A-31D-A28G-10 chr22:30685453 C>T maps to NM_001037666.2 R11R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55W-01A-11D-A26P-10 chr7:56046041 G>C did not map to a codon.
Sequencing variant TCGA-2Z-A9J3-01A-12D-A382-10 chr1:89473417 G>A maps to NM_018284.2 L593L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-5156-01A-01D-1589-08 chr4:72620173 G>A maps to ENST00000504199 L425L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr4:72629624 C>A maps to ENST00000504199 G187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7584-01A-11D-2136-08 chr2:109109238 C>T maps to NM_181453.3 T1480T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7585-01A-11D-2136-08 chr12:120599293 C>T maps to NM_006836.1 E812E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5882-01A-11D-1589-08 chr12:120582189 G>T maps to NM_006836.1 I1805I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A71W-01A-12D-A34Z-10 chr6:10529941 C>G maps to NM_145649.4 Y266*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F9-A7VF-01A-11D-A33Q-10 chr9:74828908 T>A did not map to a codon.
Sequencing variant TCGA-Y8-A8RZ-01A-11D-A36X-10 chr10:48426590 C>A maps to NM_004962.2 V472V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5878-01A-11D-1589-08 chr2:20871055 C>T maps to NM_182828.2 D408D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M9-01A-11D-A31X-10 chr10:5855179 C>A maps to NM_001494.3 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr11:76944147 G>C maps to ENST00000376217 A437A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PM-01A-21D-A382-10 chr11:75160941 C>A maps to NM_030792.6 L154L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UN-AAZ9-01A-11D-A382-10 chr12:58006908 T>A maps to NM_001111270.1 G137G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-8500-01A-11D-2396-08 chr8:95262645 G>A maps to NM_181702.2 S261S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55Z-01A-11D-A26P-10 chr2:39008787 C>T maps to NM_024775.9 F86F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A7SL-01A-11D-A34Z-10 chr3:158362455 T>G maps to ENST00000264263 A11A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8098-01A-11D-2396-08 chr5:74026106 G>T maps to NM_032380.3 I568I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PJ-01A-11D-A382-10 chr5:179758508 G>A maps to NM_005110.2 L129L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9JW-01A-11D-A42J-10 chr8:21608371 G>T maps to NM_001495.4 C174*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A656-01A-11D-A31X-10 chr17:34934556 C>T maps to NM_024835.3 C262C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5891-01A-11D-1589-08 chr20:23967128 C>T maps to NM_178311.2 L40L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5879-01A-11D-1589-08 chr17:61995167 G>T maps to NM_000515.3 V136V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55Z-01A-11D-A26P-10 chr2:233659497 T>A maps to ENST00000373566 P463P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr2:233671360 T>A maps to ENST00000373566 P622P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PZ-01A-11D-A42J-10 chr2:233612394 T>C maps to ENST00000373566 L38L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-5156-01A-01D-1589-08 chr7:150325337 G>A maps to ENST00000438845 I186I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A71V-01A-11D-A33Q-10 chr7:150171316 C>T maps to NM_175571.2 I300I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F9-A7VF-01A-11D-A33Q-10 chr12:110390968 G>A maps to NM_057169.3 P390P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PM-01A-21D-A382-10 chr12:110403362 A>G maps to NM_057169.3 L262L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4A-A93X-01A-11D-A36X-10 chr6:90604945 T>C maps to NM_032602.1 D253D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8310-01A-11D-2396-08 chr23:70444363 C>T did not map to a codon.
Sequencing variant TCGA-MH-A55Z-01A-11D-A26P-10 chr1:35223632 C>T maps to NM_005268.2 T234T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A655-01A-11D-A31Z-10 chr10:35896875 C>A maps to NM_153368.2 I145I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PJ-A5Z8-01A-11D-A28G-10 chr2:69207169 A>G maps to NM_019617.3 T161T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7966-01A-11D-2201-08 chr11:134241358 A>G maps to NM_138342.3 T467T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-AAVM-01A-11D-A42J-10 chr16:74491771 G>A maps to NM_012201.5 Q1089*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PL-01A-11D-A382-10 chr16:74505130 C>T maps to NM_012201.5 Q723Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A9DC-01A-11D-A36X-10 chr2:121746957 C>G maps to NM_005270.4 A1156A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A7SM-01A-11D-A34Z-10 chr7:42187972 C>T maps to NM_000168.5 E73E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47M-01A-11D-A25F-10 chr1:53995547 C>T maps to NM_147193.2 P291P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Y8-A896-01A-11D-A35Z-10 chr5:151231123 G>A maps to NM_001146040.1 Q247*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JK-01A-11D-A42J-10 chr23:102979830 A>G did not map to a codon.
Sequencing variant TCGA-MH-A561-01A-11D-A26P-10 chr23:102973933 T>A did not map to a codon.
Sequencing variant TCGA-4A-A93X-01A-11D-A36X-10 chr19:48205407 G>A maps to NM_015711.3 K1473K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AT-A5NU-01A-11D-A28G-10 chr19:48205551 C>T maps to NM_015711.3 P1521P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E6-01A-11D-A28G-10 chr19:48183986 G>T maps to NM_015711.3 L520L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9K2-01A-11D-A42J-10 chr19:48248918 A>C maps to NM_015710.4 R35R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7061-01A-11D-1961-08 chr7:79842141 A>G maps to NM_002069.5 K277K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr20:57415511 C>A maps to NM_016592.2 S117S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9KC-01A-11D-A42J-10 chr5:180670767 G>C maps to NM_006098.4 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7997-01A-11D-2201-08 chr15:52446238 C>T maps to NM_016194.3 G91G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7045-01A-31D-1961-08 chr9:131028576 G>A maps to NM_004486.4 Q197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55W-01A-11D-A26P-10 chr9:131021445 C>T maps to NM_004486.4 Q672Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8515-01A-11D-2396-08 chr3:37369906 A>G maps to NM_001172713.1 K2002K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A83W-01A-11D-A34Z-10 chr3:37365356 A>G maps to NM_001172713.1 K682K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PJ-A8JU-01A-11D-A35Z-10 chr15:75562488 C>T maps to NM_001164404.1 N677N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E7-01A-31D-A28G-10 chr3:121415216 G>A maps to ENST00000393667 Q1385*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8310-01A-11D-2396-08 chr1:150634374 A>T maps to ENST00000369003 G137G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A7SR-01A-12D-A35Z-10 chr1:150621096 A>G maps to ENST00000369003 T208T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4103-01A-01D-1458-08 chr1:204183025 G>T maps to NM_198447.1 S3S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A856-01A-11D-A34Z-10 chr1:155823223 T>G maps to ENST00000368331 I116I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A9DD-01A-11D-A36X-10 chr10:113924281 C>A did not map to a codon.
Sequencing variant TCGA-IZ-A6M8-01A-11D-A31X-10 chr10:113913351 G>A maps to NM_020918.4 R815*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9J1-01A-11D-A382-10 chr19:33600734 C>T maps to NM_018025.2 A466A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JS-01A-21D-A42J-10 chr17:42476883 G>T maps to NM_001002909.2 S854*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-AAVM-01A-11D-A42J-10 chr17:42476062 G>A maps to NM_001002909.2 Q1128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3473-01A-01D-1252-08 chr5:56542172 T>A maps to NM_001127236.2 I182I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A561-01A-11D-A26P-10 chr1:46124747 A>G maps to NM_021639.4 H4H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr12:50503241 C>G maps to NM_005276.2 Y330*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5882-01A-11D-1589-08 chr2:157367410 C>T maps to NM_000408.4 I126I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9K3-01A-11D-A42J-10 chr23:48979990 C>A did not map to a codon.
Sequencing variant TCGA-BQ-5878-01A-11D-1589-08 chr23:48979067 G>A did not map to a codon.
Sequencing variant TCGA-SX-A71S-01A-11D-A33Q-10 chr1:27216293 C>T maps to NM_018066.3 K98K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A656-01A-11D-A31X-10 chr12:110902938 T>C maps to NM_001164373.1 A53A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7584-01A-11D-2136-08 chr2:207040929 G>A maps to NM_005279.3 L348L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PS-01A-11D-A42J-10 chr6:46973598 C>A maps to ENST00000283297 L850L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9KE-01A-11D-A42J-10 chr13:27333949 C>T maps to NM_005288.3 L5L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47N-01A-11D-A25F-10 chr13:27332980 C>T maps to NM_005288.3 A328A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A44B-01A-11D-A25F-10 chr6:142691577 C>T maps to NM_198569.2 V239V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WN-A9G9-01A-12D-A36X-10 chr7:37780738 C>T maps to NM_181791.1 Y248Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A856-01A-11D-A34Z-10 chr2:175330525 G>T maps to NM_152529.5 T457T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UN-AAZ9-01A-11D-A382-10 chr10:25464394 C>T maps to NM_020752.2 Q16*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F9-A4JJ-01A-11D-A25F-10 chr17:4937585 G>T maps to NM_017986.3 T66T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A7SL-01A-11D-A34Z-10 chr23:53106376 A>C did not map to a codon.
Sequencing variant TCGA-A4-A48D-01A-11D-A25F-10 chr12:57389790 C>G maps to NM_007264.3 V266V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr7:107115464 T>A maps to NM_005295.2 S320S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9JU-01A-11D-A42J-10 chr10:125447636 C>T maps to NM_153442.3 G325G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr19:51273913 G>C maps to NM_001506.1 L19L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7837-01A-11D-2136-08 chr19:51274069 T>C maps to NM_001506.1 R71R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr19:51274069 T>C maps to NM_001506.1 R71R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr19:51274075 A>C maps to NM_001506.1 A73A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr19:51274183 C>T maps to NM_001506.1 L109L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5893-01A-11D-1589-08 chr23:41555434 T>A did not map to a codon.
Sequencing variant TCGA-GL-A9DE-01A-11D-A36X-10 chr23:41555846 T>A did not map to a codon.
Sequencing variant TCGA-MH-A561-01A-11D-A26P-10 chr7:124405026 G>A maps to NM_005302.2 R2*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A560-01A-11D-A26P-10 chr1:202097356 C>T maps to NM_004767.3 L373L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A856-01A-11D-A34Z-10 chr2:133174848 G>T maps to NM_001508.2 S78S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr2:105858581 C>G maps to NM_007227.3 P89P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9JZ-01A-11D-A42J-10 chr23:150349200 C>T did not map to a codon.
Sequencing variant TCGA-PJ-A5Z9-01A-11D-A28G-10 chr23:150348664 G>A did not map to a codon.
Sequencing variant TCGA-IZ-8195-01A-31D-2396-08 chr2:54080606 A>G maps to NM_006794.2 S429S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr12:54756648 G>A maps to NM_020370.2 A329A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9J1-01A-11D-A382-10 chr1:145816731 C>T maps to NM_001097612.1 Q37Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9J2-01A-11D-A382-10 chr5:90012404 C>A maps to NM_032119.3 Y3102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5876-01A-11D-1589-08 chr5:89989973 A>T maps to NM_032119.3 T2467T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55W-01A-11D-A26P-10 chr5:89979467 T>C maps to NM_032119.3 D1910D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9J8-01A-11D-A42J-10 chr23:101910026 G>C did not map to a codon.
Sequencing variant TCGA-BQ-5889-01A-11D-1589-08 chr23:101910682 G>C did not map to a codon.
Sequencing variant TCGA-SX-A7SR-01A-12D-A35Z-10 chr23:101909674 T>C did not map to a codon.
Sequencing variant TCGA-B9-4116-01A-01D-1252-08 chr16:19884047 G>A maps to NM_016235.1 D40D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7046-01A-11D-1961-08 chr17:72436052 T>A maps to NM_022036.2 S91S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A83T-01A-11D-A34Z-10 chr17:80013099 T>C maps to ENST00000392357 G237G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JD-01A-11D-A42J-10 chr8:145732380 T>C maps to NM_005309.2 *497R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F9-A7VF-01A-11D-A33Q-10 chr3:113659164 C>G maps to NM_017577.4 L627L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9KH-01A-11D-A42J-10 chr12:52408634 C>T maps to NM_181711.2 A280A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8311-01A-11D-2396-08 chr12:52401015 C>A maps to NM_181711.2 L71L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Y8-A894-01A-11D-A35Z-10 chr12:52401043 C>T maps to NM_181711.2 R81*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A562-01A-11D-A26P-10 chr7:50742287 G>A maps to NM_005311.4 A69A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PJ-A8JU-01A-11D-A35Z-10 chr17:37903001 A>C did not map to a codon.
Sequencing variant TCGA-2Z-A9JD-01A-11D-A42J-10 chr2:11758486 G>A maps to NM_014668.3 Q1162Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4A-A93W-01A-11D-A36X-10 chr2:10105482 C>T maps to NM_198182.2 F361F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F9-A8NY-01A-11D-A35Z-10 chr2:10126280 A>G maps to NM_198182.2 T380T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A7SN-01A-11D-A34Z-10 chr2:10140747 T>C maps to NM_198182.2 I590I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9J1-01A-11D-A382-10 chr5:153144062 A>G maps to NM_001114183.1 T631T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PZ-01A-11D-A42J-10 chr4:158257701 C>A maps to NM_000826.3 C549*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr11:120745882 C>T maps to NM_014619.2 F365F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Y8-A897-01A-11D-A35Z-10 chr16:10031886 G>A maps to NM_000833.3 Y312Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F9-A4JJ-01A-11D-A25F-10 chr23:48840221 C>T did not map to a codon.
Sequencing variant TCGA-Y8-A895-01A-11D-A35Z-10 chr6:146720169 C>T maps to NM_000838.3 G665G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A7SP-01A-11D-A34Z-10 chr5:178418913 A>T maps to NM_000843.3 Y225*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A44B-01A-11D-A25F-10 chr5:148730493 C>T maps to NM_152407.3 F109F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5893-01A-11D-1589-08 chr5:148730748 C>T maps to NM_152407.3 T194T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A40X-01A-11D-A25F-10 chr17:38121979 C>T maps to NM_178171.4 Q14*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9JW-01A-11D-A42J-10 chr16:11980374 A>G maps to NM_002094.3 L402L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A657-01A-11D-A31X-10 chr13:28367052 C>T maps to NM_145657.1 L76L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9JV-01A-12D-A42J-10 chr2:48896943 T>C maps to NM_172311.2 D1058D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A9DC-01A-11D-A36X-10 chr15:59942866 C>A did not map to a codon.
Sequencing variant TCGA-Y8-A8RY-01A-11D-A36X-10 chr11:18382178 T>C maps to NM_005316.3 S495S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr6:30877828 C>T maps to NM_001517.4 A121A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A69E-01A-11D-A31X-10 chr16:27549610 C>T maps to NM_001520.3 E166E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4113-01A-01D-1252-08 chr2:27565919 G>T maps to NM_001521.2 P114P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3466-01A-01D-1252-08 chr10:1043229 G>A maps to NM_012341.2 K181K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7828-01A-11D-2136-08 chr12:54857069 A>G maps to NM_144594.2 D43D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8098-01A-11D-2396-08 chr12:54856510 T>A did not map to a codon.
Sequencing variant TCGA-SX-A7SR-01A-12D-A35Z-10 chr20:42355168 G>A maps to NM_176791.3 L56L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9J1-01A-11D-A382-10 chr1:42628611 C>A maps to NM_033553.2 E105*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7584-01A-11D-2136-08 chr12:14772232 A>C maps to NM_004963.3 A929A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A9DE-01A-11D-A36X-10 chr17:7907254 C>T maps to NM_000180.3 T269T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F9-A97G-01A-11D-A382-10 chr7:65441076 T>C maps to NM_000181.3 Q279Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7732-01A-11D-2136-08 chr23:2772025 T>A did not map to a codon.
Sequencing variant TCGA-A4-A6HP-01A-11D-A31X-10 chr19:49485592 A>G maps to NM_002103.4 F327F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9Q1-01A-11D-A42J-10 chr19:49489289 G>A maps to NM_002103.4 F165F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9K2-01A-11D-A42J-10 chr20:23345061 A>C maps to NM_022482.3 P14P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JR-01A-12D-A42J-10 chr12:48723565 G>A maps to NM_181788.1 A164A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5Y0-01A-11D-A31X-10 chr1:9305535 C>T maps to NM_004285.3 F181F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PK-01A-11D-A382-10 chr9:99246827 A>G maps to NM_014282.2 R304R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7997-01A-11D-2201-08 chr16:1869996 A>G maps to NM_005326.4 N111N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A772-01A-11D-A33Q-10 chr19:35775706 G>T maps to NM_021175.2 E36*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A7SM-01A-11D-A34Z-10 chr1:119925588 A>G maps to ENST00000361035 R74R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr17:39887799 G>A maps to ENST00000310778 L338L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3472-01A-01D-1252-08 chr1:156593854 C>T maps to NM_021817.2 V114V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NK-01A-11D-A26P-10 chr19:19371724 G>A maps to NM_023002.2 S127S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JS-01A-21D-A42J-10 chr11:46637238 T>C maps to NM_173811.3 R183R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr11:46637367 C>A maps to NM_173811.3 G140G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-A8LE-01A-11D-A35Z-10 chr2:172848146 G>T maps to NM_003642.3 E381*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A71S-01A-11D-A33Q-10 chr9:19080608 A>T maps to NM_017645.3 L311*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Y8-A8S0-01A-11D-A36X-10 chr6:135360837 T>C maps to NM_006620.3 L101L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-A8LE-01A-11D-A35Z-10 chr23:153216892 C>G did not map to a codon.
Sequencing variant TCGA-Y8-A894-01A-11D-A35Z-10 chr23:153216352 A>G did not map to a codon.
Sequencing variant TCGA-AL-7173-01A-11D-2136-08 chr22:50684493 A>G maps to NM_032019.5 L560L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A656-01A-11D-A31X-10 chr3:13525051 T>G maps to NM_024827.3 L80L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A561-01A-11D-A26P-10 chr6:114264644 A>C maps to ENST00000398283 A510A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5903-01A-11D-1589-08 chr2:239988462 A>T maps to NM_006037.3 I981I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AT-A5NU-01A-11D-A28G-10 chr23:48676772 A>G did not map to a codon.
Sequencing variant TCGA-EV-5903-01A-11D-1589-08 chr23:48682179 G>A did not map to a codon.
Sequencing variant TCGA-SX-A7SS-01A-11D-A35Z-10 chr23:48661329 A>G did not map to a codon.
Sequencing variant TCGA-2Z-A9JM-01A-12D-A42J-10 chr23:71792526 C>G did not map to a codon.
Sequencing variant TCGA-A4-A57E-01A-11D-A26P-10 chr7:18975516 C>T maps to NM_178425.2 A963A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr23:7023837 T>G did not map to a codon.
Sequencing variant TCGA-B3-3925-01A-01D-1458-08 chr18:44662720 T>C maps to NM_032124.4 E30E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5876-01A-11D-1589-08 chr18:44639348 A>T maps to NM_032124.4 T225T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PR-01A-11D-A42J-10 chr18:44635148 A>C maps to NM_032124.4 Y228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5XZ-01A-11D-A31X-10 chr2:242196032 T>C maps to NM_005336.3 L213L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7584-01A-11D-2136-08 chr16:50112740 G>T maps to NM_182922.2 G285*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-7502-01A-11D-2201-08 chr16:50104087 G>A did not map to a codon.
Sequencing variant TCGA-F9-A7VF-01A-11D-A33Q-10 chr14:31771693 G>A maps to ENST00000389961 Y1751Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7058-01A-11D-1961-08 chr2:37280724 C>A maps to NM_019024.1 E809*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JJ-01A-11D-A42J-10 chr3:124732409 A>G maps to NM_020733.1 S671S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6135-01A-11D-1961-08 chr4:84342847 A>G maps to NM_133636.2 F939F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2K-A9WE-01A-11D-A382-10 chr17:65147176 A>G maps to NM_014877.3 L781L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8630-01A-11D-2396-08 chr17:65074430 G>A maps to NM_014877.3 L1922L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A655-01A-11D-A31Z-10 chr17:65162706 T>C maps to NM_014877.3 Q594Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WN-A9G9-01A-12D-A36X-10 chr17:65163788 A>T maps to NM_014877.3 S518S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chr23:65390504 C>T did not map to a codon.
Sequencing variant TCGA-4A-A93X-01A-11D-A36X-10 chr11:93754629 G>T maps to NM_001098672.1 G32G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9JW-01A-11D-A42J-10 chr15:64047448 C>A maps to ENST00000261887 E537*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7997-01A-11D-2201-08 chr15:64021463 C>T maps to ENST00000261887 W1042*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A8YI-01A-21D-A36X-10 chr15:63991177 A>G maps to ENST00000261887 L1552L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr15:63955401 C>A maps to ENST00000261887 A2894A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-7501-01A-11D-2201-08 chr4:89575197 G>T maps to NM_014606.1 E231*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-A8LB-01A-11D-A35Z-10 chr10:69804159 C>T did not map to a codon.
Sequencing variant TCGA-A4-7734-01A-11D-2136-08 chr4:89410408 C>G maps to NM_016323.2 V685V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8515-01A-11D-2396-08 chr7:35707132 A>G maps to NM_022373.4 G135G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chr17:80382346 T>C maps to NM_173620.2 P54P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9JY-01A-11D-A42J-10 chr4:3443799 G>C maps to ENST00000511533 L24L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8098-01A-11D-2396-08 chr4:3443799 G>C maps to ENST00000511533 L24L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F9-A97G-01A-11D-A382-10 chr4:3443796 C>G maps to ENST00000511533 L23L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A71U-01A-12D-A33Q-10 chr4:3447057 C>A maps to ENST00000511533 Y361*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PO-01A-11D-A382-10 chr4:3443796 C>G maps to ENST00000511533 L23L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A71U-01A-12D-A33Q-10 chr17:79663906 C>A maps to NM_004712.4 A587A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Y8-A8RZ-01A-11D-A36X-10 chr17:79660683 C>T maps to NM_004712.4 L248L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A40Y-01A-11D-A25F-10 chr1:222715412 G>A maps to NM_024746.3 F353F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A48D-01A-11D-A25F-10 chr7:27582615 C>G maps to NM_152740.3 V196V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A7SM-01A-11D-A34Z-10 chr14:62207302 T>G maps to ENST00000394997 L540L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J7-6720-01A-11D-2136-08 chr5:130500844 G>T maps to NM_005340.5 I18I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NJ-01A-11D-A26P-10 chr7:75183808 C>T maps to NM_005338.4 T660T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr7:139258059 C>A maps to NM_022740.4 P1070P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PS-01A-11D-A42J-10 chr7:139305299 T>C maps to NM_022740.4 S543S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A655-01A-11D-A31Z-10 chr11:33374882 T>C maps to NM_005734.3 S1139S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Y8-A895-01A-11D-A35Z-10 chr11:33373177 T>C maps to NM_005734.3 S944S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5Y1-01A-11D-A28G-10 chr6:26056095 T>C maps to NM_005319.3 K187K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-A5DJ-01A-11D-A26P-10 chr6:26217561 G>A maps to NM_021052.2 K120K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Y8-A8RY-01A-11D-A36X-10 chr6:27115068 G>A maps to NM_080596.1 A54A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3466-01A-01D-1252-08 chr6:27775402 C>T maps to NM_003519.3 E94E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7287-01A-11D-2136-08 chr6:26104204 C>G maps to NM_003542.3 G10G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PS-01A-11D-A42J-10 chr6:26204931 T>C maps to NM_003545.3 R20R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5880-01A-11D-1589-08 chr1:41976754 G>C maps to NM_024503.3 P2196P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chr1:42048584 A>T maps to NM_024503.3 L628L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6134-01A-11D-1961-08 chr1:42048764 G>T maps to NM_024503.3 T568T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F9-A7VF-01A-11D-A33Q-10 chr1:41976928 G>T maps to NM_024503.3 A2138A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W9-01A-11D-A28G-10 chr10:71128299 G>A maps to ENST00000439900 L203L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F9-A7VF-01A-11D-A33Q-10 chr19:37853725 C>T maps to NM_181786.2 N343N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr6:32714065 C>T maps to NM_020056.4 C221C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E6-01A-11D-A28G-10 chr6:30459404 T>C maps to NM_005516.5 A326A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PJ-01A-11D-A382-10 chr6:29797429 G>T maps to ENST00000376828 V290V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4617-01A-01D-1252-08 chr17:53398134 G>A maps to NM_002126.4 E261E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9K3-01A-11D-A42J-10 chr1:186072733 C>G maps to NM_031935.2 P3568P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9KH-01A-11D-A42J-10 chr1:186114981 G>T maps to NM_031935.2 V4845V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7584-01A-11D-2136-08 chr1:186083138 G>A maps to NM_031935.2 Q3720Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5876-01A-11D-1589-08 chr1:185984289 G>A did not map to a codon.
Sequencing variant TCGA-BQ-5877-01A-11D-1589-08 chr1:186072769 A>G maps to NM_031935.2 G3580G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A4EM-01A-11D-A25F-10 chr1:186024753 T>A maps to NM_031935.2 V2364V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PU-01A-11D-A42J-10 chr1:186099714 G>A maps to NM_031935.2 E4372E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8195-01A-31D-2396-08 chr15:77759507 C>A maps to NM_018200.2 P103P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M8-01A-11D-A31X-10 chr15:77750832 C>G maps to NM_018200.2 T28T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E7-01A-31D-A28G-10 chr1:24151845 A>G maps to NM_000191.2 A20A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A71U-01A-12D-A33Q-10 chr1:120300025 G>A maps to NM_005518.3 Q296*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A69E-01A-11D-A31X-10 chr19:1082888 G>T maps to NM_012292.2 L856L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A48D-01A-11D-A25F-10 chr16:4557883 G>T maps to NM_001127205.1 V125V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr16:4557976 C>T maps to NM_001127205.1 R156R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6790-01A-11D-1961-08 chr12:121437342 C>T maps to NM_000545.5 Q561*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8311-01A-11D-2396-08 chr17:36099581 T>C maps to NM_000458.2 Q131Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KV-A6GD-01A-11D-A31X-10 chr5:137088930 G>A maps to NM_006805.3 G275G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PN-01A-11D-A382-10 chr5:137088930 G>A maps to NM_006805.3 G275G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A856-01A-11D-A34Z-10 chr7:26235473 T>C maps to NM_031243.2 G250G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr5:177632983 G>A maps to NM_031266.2 L117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A83T-01A-11D-A34Z-10 chr10:70098906 T>C maps to NM_012207.2 G149G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8310-01A-11D-2396-08 chr9:86587098 G>T maps to NM_031262.2 P217P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6790-01A-11D-1961-08 chr9:86585224 T>A maps to NM_031262.2 K405*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A854-01A-11D-A34Z-10 chr19:41774183 C>T maps to NM_007040.3 Q118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7062-01A-11D-1961-08 chr11:62489599 C>A maps to NM_001079559.1 E450*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F9-A8NY-01A-11D-A35Z-10 chr4:83350690 C>T maps to NM_031372.2 R51R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9J7-01A-11D-A382-10 chr14:23744831 C>T maps to NM_020834.2 E535E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A71V-01A-11D-A33Q-10 chr14:23744801 A>G maps to NM_020834.2 D545D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5878-01A-11D-1589-08 chr19:12875720 C>T maps to NM_013312.2 R578R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Y8-A896-01A-11D-A35Z-10 chr7:27135158 G>A maps to NM_005522.4 Q125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-7502-01A-11D-2201-08 chr7:27211694 C>T maps to NM_018951.3 E352E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A9DC-01A-11D-A36X-10 chr7:27224286 G>A maps to NM_005523.5 Y159Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A855-01A-11D-A34Z-10 chr7:27140419 T>A maps to NM_006735.3 V352V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J7-A8I2-01A-12D-A35Z-10 chr17:46622083 G>A maps to NM_002145.3 Q64*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PN-01A-11D-A382-10 chr12:54422349 C>T maps to NM_004503.3 A15A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A83S-01A-11D-A34Z-10 chr2:177017567 A>T maps to NM_014621.2 S222S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4115-01A-01D-1252-08 chr4:84243393 G>A maps to NM_006665.5 Y117Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A560-01A-11D-A26P-10 chr10:100481442 C>T maps to NM_021828.4 P309P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8310-01A-11D-2396-08 chr19:49657888 T>C maps to NM_002152.2 E202E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47O-01A-11D-A25F-10 chr19:49657888 T>C maps to NM_002152.2 E202E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr19:49657888 T>C maps to NM_002152.2 E202E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PJ-A8JU-01A-11D-A35Z-10 chr19:49656859 C>T maps to NM_002152.2 E545E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Y8-A895-01A-11D-A35Z-10 chr2:20840799 A>G maps to NM_022460.3 N113N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-A5DJ-01A-11D-A26P-10 chr4:11401254 C>T maps to NM_005114.2 T125T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9J5-01A-21D-A382-10 chr1:209907853 C>T maps to NM_005525.2 F289F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9Q0-01A-12D-A42J-10 chr6:33173454 G>A maps to NM_014234.3 K173K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WN-AB4C-01A-11D-A42J-10 chr9:115179214 C>T maps to NM_032303.4 Q164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9KE-01A-11D-A42J-10 chr16:67199507 G>T maps to NM_001040667.2 A69A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JS-01A-21D-A42J-10 chr14:102552293 G>A maps to NM_001017963.2 I232I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PO-01A-11D-A382-10 chr10:118434762 G>A maps to NM_025015.2 V519V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F9-A7VF-01A-11D-A33Q-10 chr21:15746237 G>T maps to NM_006948.4 T372T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7732-01A-11D-2136-08 chr6:31779707 G>A maps to NM_005527.3 G14G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr14:65008124 G>A maps to NM_021979.3 L186L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7838-01A-11D-2136-08 chr9:128001453 A>G maps to NM_005347.4 G254G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9Q1-01A-11D-A42J-10 chr11:122930961 A>G maps to NM_006597.3 A142A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9J6-01A-11D-A382-10 chr2:198367836 A>G maps to NM_002157.2 V81V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A6HP-01A-11D-A31X-10 chr2:198365880 A>G maps to NM_002157.2 G29G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F9-A7VF-01A-11D-A33Q-10 chr1:22180782 T>C maps to NM_005529.5 E2114E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9K6-01A-11D-A42J-10 chr23:135593688 T>G did not map to a codon.
Sequencing variant TCGA-B9-4115-01A-01D-1252-08 chr23:135594032 A>T did not map to a codon.
Sequencing variant TCGA-5P-A9JW-01A-11D-A42J-10 chr5:63257505 G>T maps to NM_000524.2 S14*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PR-01A-11D-A42J-10 chr13:47408977 A>G maps to NM_000621.3 C470C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9Q0-01A-12D-A42J-10 chr3:183756383 C>T maps to NM_001145143.1 G319G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9J5-01A-21D-A382-10 chr23:53565804 G>T did not map to a codon.
Sequencing variant TCGA-2Z-A9JJ-01A-11D-A42J-10 chr23:53627270 T>C did not map to a codon.
Sequencing variant TCGA-4A-A93W-01A-11D-A36X-10 chr23:53566666 C>A did not map to a codon.
Sequencing variant TCGA-5P-A9K0-01A-11D-A42J-10 chr23:53619439 C>T did not map to a codon.
Sequencing variant TCGA-B3-8121-01A-21D-2396-08 chr23:53589173 C>T did not map to a codon.
Sequencing variant TCGA-F9-A8NY-01A-11D-A35Z-10 chr23:53616525 A>T did not map to a codon.
Sequencing variant TCGA-GL-A59T-01A-21D-A28G-10 chr23:53584382 A>G did not map to a codon.
Sequencing variant TCGA-SX-A71W-01A-12D-A34Z-10 chr23:53565884 G>A did not map to a codon.
Sequencing variant TCGA-UZ-A9PM-01A-21D-A382-10 chr23:53641605 C>G did not map to a codon.
Sequencing variant TCGA-A4-8517-01A-11D-2396-08 chr3:50357590 C>T maps to NM_033158.4 R110R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9J1-01A-11D-A382-10 chr16:71163575 C>G maps to NM_032821.2 L398L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A7SS-01A-11D-A35Z-10 chr16:71101221 T>C maps to NM_032821.2 E682E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9Q1-01A-11D-A42J-10 chr9:95027350 G>A maps to ENST00000375660 I522I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9K2-01A-11D-A42J-10 chr1:220267812 G>T maps to NM_018060.3 L85L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JQ-01A-11D-A42J-10 chr6:82906098 A>T maps to NM_015525.2 S1030S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9KC-01A-11D-A42J-10 chr19:10394340 G>T maps to NM_000201.2 T172T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A656-01A-11D-A31X-10 chr19:10444568 T>A maps to NM_002162.3 T536T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9K3-01A-11D-A42J-10 chr10:94250352 C>T did not map to a codon.
Sequencing variant TCGA-A4-7288-01A-11D-2136-08 chr15:90634782 A>G did not map to a codon.
Sequencing variant TCGA-A4-7288-01A-11D-2136-08 chr12:6649693 A>G maps to NM_001193457.1 A557A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A44B-01A-11D-A25F-10 chr19:18288014 C>T maps to NM_006332.3 R183R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Y8-A896-01A-11D-A35Z-10 chr10:91162886 C>T maps to NM_001548.3 V285V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7062-01A-11D-1961-08 chr10:91177426 A>G maps to NM_012420.2 Q157Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9J3-01A-12D-A382-10 chr21:34707891 C>T maps to NM_000629.2 L47L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A4ZT-01A-11D-A26P-10 chr21:34725062 G>A did not map to a codon.
Sequencing variant TCGA-DW-7837-01A-11D-2136-08 chr2:27685656 C>A maps to NM_015662.1 G676*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NJ-01A-11D-A26P-10 chr12:110565895 C>T maps to NM_014055.3 R64*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9K0-01A-11D-A42J-10 chr13:21217614 C>G maps to NM_175605.3 P577P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A48D-01A-11D-A25F-10 chr13:21163993 T>C maps to NM_175605.3 A75A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JN-01A-21D-A42J-10 chr15:65621832 T>G maps to NM_004884.3 G700G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4A-A93W-01A-11D-A36X-10 chr15:65676598 G>T maps to NM_020962.1 I1167I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7840-01A-11D-2136-08 chr15:65684504 T>A maps to NM_020962.1 K697*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9J5-01A-21D-A382-10 chr17:47075184 G>A maps to NM_006546.3 K26K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PJ-01A-11D-A382-10 chr6:160467611 T>C maps to NM_000876.2 N662N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F9-A4JJ-01A-11D-A25F-10 chr1:201166404 C>T maps to NM_001164586.1 Y109Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A40Y-01A-11D-A25F-10 chr11:18738380 A>G maps to NM_173588.3 D380D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A7SO-01A-11D-A34Z-10 chr1:117156795 C>T maps to NM_001542.2 V141V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4115-01A-01D-1252-08 chr11:133814178 C>A maps to NM_014987.1 V115V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4116-01A-01D-1252-08 chr11:133805657 C>T did not map to a codon.
Sequencing variant TCGA-SX-A71U-01A-12D-A33Q-10 chr5:140034272 G>T maps to NM_006083.3 E200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A854-01A-11D-A34Z-10 chr23:153770657 G>T did not map to a codon.
Sequencing variant TCGA-2K-A9WE-01A-11D-A382-10 chr17:37985675 C>A maps to NM_012481.3 G43*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-5155-01A-01D-1589-08 chr11:117869596 A>T maps to NM_001558.3 P326P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A7SS-01A-11D-A35Z-10 chr19:18180413 G>A maps to NM_005535.1 D377D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5Y1-01A-11D-A28G-10 chr15:81517937 A>G maps to NM_172217.3 T66T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4116-01A-01D-1252-08 chr13:21295993 C>T maps to NM_138284.1 V170V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55W-01A-11D-A26P-10 chr22:17566095 C>A maps to NM_014339.5 R39R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M8-01A-11D-A31X-10 chr3:57136552 C>T maps to NM_017563.3 S311S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A57E-01A-11D-A26P-10 chr2:113540316 G>T maps to NM_000575.3 S24S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7996-01A-11D-2201-08 chr2:102849532 C>T maps to NM_003854.2 Q416*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NL-01A-11D-A26P-10 chr16:27459982 G>T maps to NM_181079.4 T354T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6135-01A-11D-1961-08 chr19:50393784 C>T maps to NM_172374.1 L304L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A562-01A-11D-A26P-10 chr16:27374133 G>A maps to NM_000418.2 T487T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Y8-A895-01A-11D-A35Z-10 chr16:27374813 C>A maps to NM_000418.2 S714*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JD-01A-11D-A42J-10 chr5:55247358 T>C maps to NM_002184.3 R591R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4104-01A-01D-1458-08 chr23:155232600 G>A did not map to a codon.
Sequencing variant TCGA-WN-AB4C-01A-11D-A42J-10 chr19:15230034 G>C maps to NM_006844.3 L331L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5903-01A-11D-1589-08 chr7:111127298 T>A maps to NM_032549.2 S78S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A560-01A-11D-A26P-10 chr7:111161446 G>A maps to NM_032549.2 F19F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-3925-01A-01D-1458-08 chr2:86371414 T>G maps to NM_006839.2 G751G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A83V-01A-11D-A34Z-10 chr15:75931981 C>T maps to NM_018285.3 E176E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Y8-A8S1-01A-11D-A36X-10 chr18:22020541 G>C maps to NM_018439.3 S150S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7287-01A-11D-2136-08 chr6:76660532 G>A maps to NM_001563.2 L524L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7287-01A-11D-2136-08 chr6:76660635 G>A maps to NM_001563.2 I489I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JO-01A-11D-A42J-10 chr1:62253583 C>G maps to NM_176877.2 P336P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F9-A7Q0-01A-11D-A35Z-10 chr11:61914248 G>C maps to NM_001040694.1 R693R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F9-A7Q0-01A-11D-A35Z-10 chr11:61914278 C>G maps to NM_001040694.1 R703R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NH-01A-11D-A26P-10 chr12:6760400 C>T did not map to a codon.
Sequencing variant TCGA-Y8-A896-01A-11D-A35Z-10 chr2:121107029 C>G maps to NM_002193.2 G268G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7286-01A-11D-2136-08 chr12:57828749 A>C maps to NM_005538.2 P27P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JD-01A-11D-A42J-10 chr15:41313308 T>C maps to NM_017553.1 P1021P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JS-01A-21D-A42J-10 chr15:41387984 T>C maps to NM_017553.1 T95T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr1:38338747 G>A maps to ENST00000373026 L761L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9K6-01A-11D-A42J-10 chr10:121586616 T>C maps to NM_014937.2 L908L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Y8-A894-01A-11D-A35Z-10 chr22:31529897 G>T did not map to a codon.
Sequencing variant TCGA-A4-7288-01A-11D-2136-08 chr17:1400004 G>C maps to NM_016532.3 T352T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KV-A6GD-01A-11D-A31X-10 chr11:71948602 A>G maps to NM_001567.3 P1105P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Y8-A8RY-01A-11D-A36X-10 chr11:71941502 C>A maps to NM_001567.3 V396V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4104-01A-01D-1458-08 chr14:36005047 C>T maps to NM_032594.3 C530C. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-BQ-7059-01A-11D-1961-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-SX-A71S-01A-11D-A33Q-10 chr17:59952338 C>T maps to NM_020748.2 K847K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-7501-01A-11D-2201-08 chr1:153736637 A>G maps to ENST00000428986 L623L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A560-01A-11D-A26P-10 chr1:153740252 G>T maps to ENST00000428986 E733*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5881-01A-11D-1589-08 chr11:62417116 A>G maps to NM_030628.1 S145S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4A-A93X-01A-11D-A36X-10 chr13:51952389 A>T maps to NM_012141.2 V529V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PJ-01A-11D-A382-10 chr13:51961635 A>G maps to NM_012141.2 P260P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A7SN-01A-11D-A34Z-10 chr10:59986849 A>G maps to NM_152230.4 Y109Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JK-01A-11D-A42J-10 chr14:24651546 C>A maps to ENST00000458132 A845A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A772-01A-11D-A33Q-10 chr14:24656089 G>T maps to ENST00000458132 C250*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A6HP-01A-11D-A31X-10 chr13:98667794 A>T maps to NM_002271.4 V797V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PJ-01A-11D-A382-10 chr11:9430090 A>C maps to NM_006391.2 P75P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr12:30790087 C>G maps to NM_006390.3 L841L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A7SS-01A-11D-A35Z-10 chr12:30792465 A>G maps to NM_006390.3 D824D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr2:237272539 C>T maps to ENST00000457693 L592L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-A8LB-01A-11D-A35Z-10 chr7:2625911 C>A maps to NM_152558.3 R299R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5891-01A-11D-1589-08 chr3:51897175 C>A maps to NM_203424.1 A95A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr3:158980471 C>A maps to NM_001197113.1 P97P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PR-01A-11D-A42J-10 chr15:91017792 G>A maps to NM_003870.3 Q884Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9J1-01A-11D-A382-10 chr5:75960918 C>T maps to NM_006633.2 T866T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr5:75888709 G>A maps to NM_006633.2 L289L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A7SN-01A-11D-A34Z-10 chr5:75970432 C>T maps to NM_006633.2 A1142A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A9DD-01A-11D-A36X-10 chr1:156510498 C>A did not map to a codon.
Sequencing variant TCGA-UZ-A9PN-01A-11D-A382-10 chr1:156524142 G>T maps to NM_178229.4 L444L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8515-01A-11D-2396-08 chr3:12957105 C>T maps to ENST00000429247 V716V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr23:53268432 C>G did not map to a codon.
Sequencing variant TCGA-Y8-A897-01A-11D-A35Z-10 chr23:53350188 C>T did not map to a codon.
Sequencing variant TCGA-MH-A55W-01A-11D-A26P-10 chr12:275006 G>A maps to NM_001170738.1 L974L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Y8-A8RZ-01A-11D-A36X-10 chr7:123143384 G>A maps to NM_178827.4 Q189*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JG-01A-11D-A42J-10 chr1:234743068 C>G maps to NM_182972.2 S526S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7997-01A-11D-2201-08 chr1:234744250 G>T maps to NM_182972.2 A330A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PJ-A5Z9-01A-11D-A28G-10 chr1:234743059 G>A maps to NM_182972.2 F529F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7997-01A-11D-2201-08 chr1:209974722 G>A maps to NM_006147.2 P12P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr16:55360381 G>A maps to NM_024335.2 A60A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr5:50683583 G>T did not map to a codon.
Sequencing variant TCGA-P4-AAVL-01A-11D-A42J-10 chr20:13273027 A>G maps to NM_080826.1 E265E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7828-01A-11D-2136-08 chr19:55966663 G>A maps to NM_024710.2 Q144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9KA-01A-11D-A42J-10 chr19:18545728 G>T maps to NM_016368.4 T557T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JP-01A-11D-A42J-10 chr12:2929936 G>A maps to NM_018463.3 L198L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9K0-01A-11D-A42J-10 chr15:68620581 C>T maps to ENST00000423218 Q640Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7828-01A-11D-2136-08 chr5:52366068 C>G maps to NM_002203.3 P738P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A561-01A-11D-A26P-10 chr17:42449791 C>T did not map to a codon.
Sequencing variant TCGA-4A-A93X-01A-11D-A36X-10 chr2:173352754 A>G maps to ENST00000264106 L836L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Y8-A898-01A-11D-A34Z-10 chr2:173335732 T>C maps to ENST00000264106 T225T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr10:15688932 G>A maps to NM_003638.1 D373D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WN-AB4C-01A-11D-A42J-10 chr10:15688923 G>A maps to NM_003638.1 I376I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JE-01A-11D-A42J-10 chr17:3638167 G>T maps to NM_002208.4 Y866*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5886-01A-11D-1589-08 chr16:31371299 G>A maps to NM_000887.3 R207R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KV-A6GD-01A-11D-A31X-10 chr16:31373394 G>A did not map to a codon.
Sequencing variant TCGA-5P-A9JZ-01A-11D-A42J-10 chr10:33199325 C>T maps to ENST00000374956 Q663Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr17:73746315 G>A maps to NM_001005619.1 W1147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3468-01A-01D-1252-08 chr2:160982927 T>C maps to NM_000888.3 E615E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9J7-01A-11D-A382-10 chr7:20403320 A>G maps to NM_002214.2 P63P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9J1-01A-11D-A382-10 chr10:7773958 G>T maps to NM_002216.2 S549S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A83S-01A-11D-A34Z-10 chr10:7683993 G>A maps to ENST00000256861 A65A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9J6-01A-11D-A382-10 chr23:54777683 C>T did not map to a codon.
Sequencing variant TCGA-Y8-A894-01A-11D-A35Z-10 chr5:156671454 C>A maps to NM_005546.3 Y472*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr13:48833063 A>G maps to NM_021999.4 Q232Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr2:231741582 G>C maps to NM_030926.4 A154A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr14:93408016 C>T maps to NM_014216.4 A378A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JN-01A-21D-A42J-10 chr1:226924883 G>A maps to NM_002221.3 S92S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4115-01A-01D-1252-08 chr19:41223384 A>T maps to NM_025194.2 P115P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JJ-01A-11D-A42J-10 chr12:26810811 G>A maps to NM_002223.2 Q674*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JM-01A-12D-A42J-10 chr12:26572029 C>A maps to NM_002223.2 L2354L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-5156-01A-01D-1589-08 chr12:26553126 G>A maps to NM_002223.2 T2488T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A83T-01A-11D-A34Z-10 chr12:26639108 G>C maps to NM_002223.2 P1913P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PV-01A-11D-A42J-10 chr21:35208936 G>A did not map to a codon.
Sequencing variant TCGA-MH-A55W-01A-11D-A26P-10 chr2:24469666 A>G maps to NM_006277.2 P1128P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A7SQ-01A-12D-A35Z-10 chr2:128262337 C>A maps to NM_017969.2 E381*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5894-01A-11D-1589-08 chr20:10621488 C>A maps to NM_000214.2 S1047S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E7-01A-31D-A28G-10 chr20:10653489 A>C maps to NM_000214.2 Y82*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-5155-01A-01D-1589-08 chr14:105621903 C>T maps to NM_002226.3 E261E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59T-01A-21D-A28G-10 chr9:5126751 T>C maps to NM_004972.3 A1120A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A83S-01A-11D-A34Z-10 chr9:5081773 T>A maps to NM_004972.3 G828G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7838-01A-11D-2136-08 chr4:6066675 C>T maps to NM_001099433.1 L454L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-A8LB-01A-11D-A35Z-10 chr5:146991867 C>T did not map to a codon.
Sequencing variant TCGA-IA-A83W-01A-11D-A34Z-10 chr6:15513598 G>A maps to NM_004973.2 L1132L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J7-6720-01A-11D-2136-08 chr14:59965573 T>C maps to ENST00000356057 L210L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59R-01A-11D-A26P-10 chr10:64968539 A>G maps to NM_032776.1 F963F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A856-01A-11D-A34Z-10 chr1:227921687 C>G maps to NM_023007.2 S204S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J7-6720-01A-11D-2136-08 chr8:75227664 G>A maps to NM_020647.2 R190R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A48D-01A-11D-A25F-10 chr14:23444253 G>A maps to NM_032876.4 N433N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A83W-01A-11D-A34Z-10 chr9:744585 T>G maps to NM_015158.2 S1331S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M9-01A-11D-A31X-10 chr16:75678299 A>T maps to NM_001130089.1 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Y8-A897-01A-11D-A35Z-10 chr16:75662550 C>T maps to NM_001130089.1 L565L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5877-01A-11D-1589-08 chr3:20187857 C>T maps to NM_003884.4 Y685Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5889-01A-11D-1589-08 chr11:65480306 T>A did not map to a codon.
Sequencing variant TCGA-SX-A7SU-01A-11D-A35Z-10 chr13:30814595 C>A did not map to a codon.
Sequencing variant TCGA-GL-A9DE-01A-11D-A36X-10 chr1:15428104 G>A maps to NM_201628.2 L538L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W8-01A-11D-A28G-10 chr15:65369366 C>T maps to NM_001101362.2 L72L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A7SQ-01A-12D-A35Z-10 chr11:105923708 C>A maps to NM_198439.2 V569V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7734-01A-11D-2136-08 chr3:42727130 G>A maps to NM_152393.2 Q7Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7841-01A-11D-2136-08 chr13:41767952 G>A maps to NM_032138.4 A147A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5Y1-01A-11D-A28G-10 chr11:30032893 T>C maps to NM_002233.2 R444R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8518-01A-11D-2396-08 chr1:110774915 G>A maps to NM_004978.4 L631L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4617-01A-01D-1252-08 chr1:110768795 G>A maps to NM_004978.4 R605R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9J1-01A-11D-A382-10 chr7:119915438 G>T maps to NM_012281.2 A251A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7734-01A-11D-2136-08 chr1:112524715 C>T maps to ENST00000315987 P211P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9KH-01A-11D-A42J-10 chr20:49626293 G>A maps to NM_002237.3 R194R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A655-01A-11D-A31Z-10 chr18:77659161 G>A maps to NM_012283.1 A249A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Y8-A8S0-01A-11D-A36X-10 chr1:210857405 C>A maps to NM_172362.2 L729L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7837-01A-11D-2136-08 chr14:63483655 C>G maps to NM_139318.3 L30L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PZ-01A-11D-A42J-10 chr14:63468085 C>T maps to NM_139318.3 T132T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7045-01A-31D-1961-08 chr17:61623122 C>T maps to NM_030779.2 L949L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A71R-01A-12D-A33Q-10 chr3:19479827 C>T maps to NM_144633.2 F450F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E7-01A-31D-A28G-10 chr2:95976176 C>T maps to NM_013434.4 I30I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9J3-01A-12D-A382-10 chr2:233633083 T>C maps to NM_002242.4 A300A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55Z-01A-11D-A26P-10 chr2:233633227 A>T maps to NM_002242.4 P252P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-A6W5-01A-12D-A33Q-10 chr21:39671218 C>A maps to NM_170736.1 P12P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-5155-01A-01D-1589-08 chr21:39671713 C>T maps to NM_170736.1 T177T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr17:68129131 C>A maps to NM_018658.1 R302R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-7501-01A-11D-2201-08 chr6:39159333 G>A maps to NM_003740.3 Q278*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5888-01A-11D-1589-08 chr11:65360849 T>C maps to NM_033455.1 G241G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr19:18100535 C>A maps to ENST00000222249 A411A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7996-01A-11D-2201-08 chr1:154841687 G>A maps to NM_002249.4 S251S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47O-01A-11D-A25F-10 chr1:154680664 C>T maps to NM_002249.4 S661S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Y8-A896-01A-11D-A35Z-10 chr1:154842332 C>T maps to NM_002249.4 Q36Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5Y1-01A-11D-A28G-10 chr11:2798239 C>G maps to NM_000218.2 P570P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EA-01A-11D-A28G-10 chr11:2466534 G>T maps to NM_000218.2 A69A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7837-01A-11D-2136-08 chr20:62078165 G>C maps to NM_172107.2 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr20:62070958 G>A maps to NM_172107.2 L307L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F9-A97G-01A-11D-A382-10 chr1:41285145 T>G did not map to a codon.
Sequencing variant TCGA-DW-7836-01A-11D-2136-08 chr6:73904446 C>T maps to NM_001160133.1 Y722Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A7SP-01A-11D-A34Z-10 chr13:50590072 A>T maps to NM_173605.1 S148S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4114-01A-01D-1252-08 chr8:99441266 G>T maps to NM_020697.2 E354*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PJ-A5Z9-01A-11D-A28G-10 chr9:138594139 C>G maps to ENST00000298480 G12G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PV-01A-11D-A42J-10 chr8:36788663 G>A did not map to a codon.
Sequencing variant TCGA-A4-7996-01A-11D-2201-08 chr9:2718278 C>T maps to NM_133497.2 R180R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-A4TM-01A-11D-A31X-10 chr12:109889449 G>T maps to NM_031954.3 R298R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47M-01A-11D-A25F-10 chr17:7256620 C>T maps to NM_001002914.2 D120D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NF-01A-11D-A26P-10 chr13:77460121 C>G maps to NM_138444.3 S54S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7584-01A-11D-2136-08 chr13:45768534 G>A maps to NM_198404.2 D56D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47M-01A-11D-A25F-10 chr4:44450333 A>T maps to NM_198353.2 T69T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4114-01A-01D-1252-08 chr4:44449784 G>A maps to NM_198353.2 L252L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7915-01A-11D-2201-08 chr22:38877224 G>A maps to NM_016657.1 W120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M8-01A-11D-A31X-10 chr1:23380288 G>A maps to NM_001009999.2 L249L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5901-01A-11D-1589-08 chr12:121947831 C>T maps to ENST00000377071 R395R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9J2-01A-11D-A382-10 chr2:86669202 A>G maps to NM_001146688.1 V11V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5878-01A-11D-1589-08 chr5:137715372 T>C maps to NM_016604.3 R227R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr19:5131902 G>C maps to NM_015015.2 P597P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M9-01A-11D-A31X-10 chr1:202701001 A>C maps to ENST00000367264 Y1361*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A9DC-01A-11D-A36X-10 chr23:53223342 C>T did not map to a codon.
Sequencing variant TCGA-BQ-5886-01A-11D-1589-08 chr23:44949020 G>A did not map to a codon.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr23:44870204 G>C did not map to a codon.
Sequencing variant TCGA-SX-A7SP-01A-11D-A34Z-10 chr23:44949072 C>T did not map to a codon.
Sequencing variant TCGA-SX-A7SS-01A-11D-A35Z-10 chr23:44937746 T>G did not map to a codon.
Sequencing variant TCGA-A4-A6HP-01A-11D-A31X-10 chr17:7748925 C>A maps to NM_001080424.1 A18A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5890-01A-11D-1589-08 chr17:7755371 T>G maps to NM_001080424.1 A1423A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A856-01A-11D-A34Z-10 chr4:55979600 C>T maps to NM_002253.2 G282G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5XZ-01A-11D-A31X-10 chr19:10610565 G>T maps to NM_203500.1 G48G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr19:10610177 G>A maps to NM_203500.1 Q178*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A772-01A-11D-A33Q-10 chr7:142658911 T>G maps to NM_000420.2 A17A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A7SN-01A-11D-A34Z-10 chr12:91445295 C>T did not map to a codon.
Sequencing variant TCGA-BQ-5883-01A-11D-1589-08 chr1:19545820 C>T maps to NM_015047.1 K986K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5886-01A-11D-1589-08 chr17:26948414 A>G did not map to a codon.
Sequencing variant TCGA-UZ-A9Q1-01A-11D-A42J-10 chr17:26961607 A>G maps to NM_014680.2 P999P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JR-01A-12D-A42J-10 chr15:64668942 T>A maps to NM_014736.4 K97*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-A4TM-01A-11D-A31X-10 chr17:73487467 G>T maps to ENST00000375248 E446*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55Z-01A-11D-A26P-10 chr3:197408101 G>A maps to NM_014687.1 F776F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5893-01A-11D-1589-08 chr19:34832920 G>A maps to NM_014686.3 L694L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4114-01A-01D-1252-08 chr14:35593086 T>C maps to NM_014672.2 G212G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A9DE-01A-11D-A36X-10 chr1:47144276 C>T maps to NM_014774.2 Q448Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9J1-01A-11D-A382-10 chr12:22622700 T>C maps to ENST00000446597 Q825Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr12:22623803 C>T maps to ENST00000446597 Q800Q. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-MH-A857-01A-11D-A34Z-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-GL-A9DC-01A-11D-A36X-10 chr1:3742941 A>G maps to NM_014704.3 Y749Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JL-01A-11D-A42J-10 chr14:59006808 C>A maps to ENST00000354386 R1537R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3468-01A-01D-1252-08 chr14:58949255 C>T maps to ENST00000354386 L1043L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A655-01A-11D-A31Z-10 chr11:46666906 C>T maps to NM_001142673.1 Q30*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PJ-01A-11D-A382-10 chr17:2594072 T>C did not map to a codon.
Sequencing variant TCGA-GL-7966-01A-11D-2201-08 chr17:6531559 G>A maps to NM_014804.2 Q199*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4617-01A-01D-1252-08 chr18:8825492 T>C maps to ENST00000456698 L1648L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr18:8813134 C>T maps to ENST00000456698 N1240N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7585-01A-11D-2136-08 chr7:36396612 G>A maps to NM_001100425.1 F255F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A656-01A-11D-A31X-10 chr4:154542028 C>A maps to NM_001131007.1 S1230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Y8-A898-01A-11D-A34Z-10 chr4:154478174 G>T maps to NM_001131007.1 G164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9J3-01A-12D-A382-10 chr15:79760701 G>T maps to NM_015206.2 V909V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7585-01A-11D-2136-08 chr4:123156096 G>T maps to NM_015312.3 E1165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5883-01A-11D-1589-08 chr4:123264652 C>G maps to NM_015312.3 G4147G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PX-01A-11D-A42J-10 chr4:123150304 T>A maps to NM_015312.3 T984T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A560-01A-11D-A26P-10 chr7:141365047 A>T maps to NM_001080392.1 P297P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5DU-01A-11D-A28G-10 chr15:81181039 A>T did not map to a codon.
Sequencing variant TCGA-B9-A5W9-01A-11D-A28G-10 chr23:118219439 T>G did not map to a codon.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr23:118223093 A>G did not map to a codon.
Sequencing variant TCGA-G7-A8LB-01A-11D-A35Z-10 chr4:57182298 C>T maps to NM_020722.1 D877D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7840-01A-11D-2136-08 chr10:24835171 T>C maps to NM_019590.3 H1917H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9JY-01A-11D-A42J-10 chr6:138657619 G>T maps to NM_020340.4 V2177V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-7332-01A-11D-2136-08 chr10:70749010 G>C maps to NM_015634.3 A141A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9J5-01A-21D-A382-10 chr15:52901850 T>C maps to NM_019600.2 K420K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JE-01A-11D-A42J-10 chr10:30315193 G>A maps to NM_020848.2 Q1295*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5893-01A-11D-1589-08 chr18:59888684 C>T maps to NM_020854.3 N271N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9J3-01A-12D-A382-10 chr2:226378137 T>C maps to NM_020864.1 H91H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9KA-01A-11D-A42J-10 chr3:108271220 C>A did not map to a codon.
Sequencing variant TCGA-HE-A5NJ-01A-11D-A26P-10 chr9:100128908 C>T maps to ENST00000375206 C1361C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Y8-A8RZ-01A-11D-A36X-10 chr4:1379720 C>A maps to NM_020894.2 S701*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A8YH-01A-11D-A36X-10 chr18:43481031 A>C maps to NM_020964.2 A1525A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A857-01A-11D-A34Z-10 chr18:43534422 T>C maps to NM_020964.2 T315T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JQ-01A-11D-A42J-10 chr19:18378079 G>A maps to NM_001145304.1 A90A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V9-A7HT-01A-11D-A33Q-10 chr19:18377323 T>A maps to NM_001145304.1 T342T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A856-01A-11D-A34Z-10 chr14:77580330 C>T maps to NM_033426.2 S290S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr14:77580237 C>T maps to NM_033426.2 F259F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F9-A4JJ-01A-11D-A25F-10 chr20:36870193 C>T maps to NM_001029864.1 E113E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PU-01A-11D-A42J-10 chr1:11983150 G>A maps to ENST00000376576 L477L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7996-01A-11D-2201-08 chr3:113376112 C>T maps to NM_001009899.2 Q1472Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8518-01A-11D-2396-08 chr3:113376112 C>T maps to NM_001009899.2 Q1472Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-7268-01A-11D-2136-08 chr3:113376679 G>T maps to NM_001009899.2 G1283G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7061-01A-11D-1961-08 chr3:113377558 T>C maps to NM_001009899.2 S990S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr3:113376121 C>T maps to NM_001009899.2 Q1469Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr3:113376127 C>T maps to NM_001009899.2 Q1467Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A71S-01A-11D-A33Q-10 chr3:113376475 G>A maps to NM_001009899.2 P1351P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Y8-A894-01A-11D-A35Z-10 chr3:113377180 T>A maps to NM_001009899.2 A1116A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-7173-01A-11D-2136-08 chr23:73961091 C>T did not map to a codon.
Sequencing variant TCGA-2Z-A9J2-01A-11D-A382-10 chr8:29024952 G>T maps to NM_015254.3 A365A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8517-01A-11D-2396-08 chr8:28991586 C>T maps to NM_015254.3 P918P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F9-A4JJ-01A-11D-A25F-10 chr8:29037679 G>A maps to NM_015254.3 R221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A657-01A-11D-A31X-10 chr17:43009570 C>T maps to ENST00000438933 Q426Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9JU-01A-11D-A42J-10 chr2:241658506 G>A maps to ENST00000373308 S1718S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Y8-A897-01A-11D-A35Z-10 chr2:241689963 C>T maps to ENST00000373308 R953R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9J2-01A-11D-A382-10 chr1:10394604 G>A maps to ENST00000377086 L984L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9J3-01A-12D-A382-10 chr1:10338125 G>T maps to ENST00000377086 E374*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-AAVM-01A-11D-A42J-10 chr1:10420985 G>A did not map to a codon.
Sequencing variant TCGA-Y8-A8RY-01A-11D-A36X-10 chr12:39695382 G>C maps to ENST00000395670 V1611V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JP-01A-11D-A42J-10 chr14:104618785 G>A maps to NM_015656.1 P241P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr9:86485504 T>A maps to NM_017576.1 K896*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5Y0-01A-11D-A31X-10 chr17:51901647 C>T maps to NM_032559.4 V418V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7061-01A-11D-1961-08 chr23:69637855 T>C did not map to a codon.
Sequencing variant TCGA-P4-A5ED-01A-11D-A28G-10 chr23:69595070 G>A did not map to a codon.
Sequencing variant TCGA-F9-A7Q0-01A-11D-A35Z-10 chr5:154395606 G>T maps to NM_001099293.1 E730*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NL-01A-11D-A26P-10 chr5:154395500 G>A maps to NM_001099293.1 Q694Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PO-01A-11D-A382-10 chr12:57968952 G>T maps to NM_004984.2 V601V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NI-01A-11D-A26P-10 chr10:32320042 A>G maps to NM_004521.2 T513T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7585-01A-11D-2136-08 chr2:149835495 C>T maps to NM_004522.1 Q452*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-AAVL-01A-11D-A42J-10 chr6:33365933 G>A maps to NM_002263.3 E47E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7734-01A-11D-2136-08 chr16:57806197 T>C maps to NM_005550.3 V106V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59T-01A-21D-A28G-10 chr10:7811177 C>T did not map to a codon.
Sequencing variant TCGA-A4-A57E-01A-11D-A26P-10 chr4:55570035 C>G maps to NM_000222.2 V301V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5891-01A-11D-1589-08 chr13:33591075 C>T maps to NM_004795.3 N166N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NL-01A-11D-A26P-10 chr4:39435930 G>T maps to NM_175737.3 R309R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PX-01A-11D-A42J-10 chr19:12996545 C>A maps to NM_006563.3 L166L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NH-01A-11D-A26P-10 chr1:44595404 C>G maps to NM_173484.3 P154P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JG-01A-11D-A42J-10 chr7:129760625 T>C maps to NM_014997.3 G171G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NL-01A-11D-A26P-10 chr16:87760466 C>T maps to NM_017566.3 L221L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PP-01A-11D-A42J-10 chr1:18808386 C>A maps to NM_152375.2 G304G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47M-01A-11D-A25F-10 chr1:202866047 G>A maps to NM_021633.2 S291S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A8YI-01A-21D-A36X-10 chr1:173754360 A>G maps to NM_014458.3 T602T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8517-01A-11D-2396-08 chr22:20796431 G>C maps to NM_032775.3 A611A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4A-A93W-01A-11D-A36X-10 chr2:170592247 C>T maps to NM_144711.5 Q242*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5891-01A-11D-1589-08 chr5:136963989 G>A maps to NM_017415.2 N529N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A83W-01A-11D-A34Z-10 chr6:53516722 G>A maps to NM_001003760.4 R526R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A7UZ-01A-12D-A34Z-10 chr23:21674428 A>G did not map to a codon.
Sequencing variant TCGA-2Z-A9JQ-01A-11D-A42J-10 chr16:84690910 C>T maps to NM_024731.2 F166F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A9DC-01A-11D-A36X-10 chr8:124659248 A>G maps to NM_001081675.2 Y452Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr23:86773062 C>G did not map to a codon.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr19:51518765 G>T maps to NM_001077500.1 I195I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr12:10541381 G>A maps to NM_007360.3 R10*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9K0-01A-11D-A42J-10 chr10:135013100 C>T maps to ENST00000368572 S968S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9KA-01A-11D-A42J-10 chr12:123034323 C>A maps to NM_014708.4 L333L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr3:160249254 A>G maps to NM_002268.3 D126D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6792-01A-21D-1961-08 chr12:75895545 T>C maps to NM_007043.6 A320A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9JW-01A-11D-A42J-10 chr12:53069228 G>A maps to NM_006121.3 S561S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9JZ-01A-11D-A42J-10 chr12:53069228 G>A maps to NM_006121.3 S561S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9J1-01A-11D-A382-10 chr17:39657555 G>T maps to NM_153490.2 T443T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PJ-A5Z9-01A-11D-A28G-10 chr17:39658843 T>C maps to NM_153490.2 K342K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NI-01A-11D-A26P-10 chr17:39092458 C>G did not map to a codon.
Sequencing variant TCGA-WN-AB4C-01A-11D-A42J-10 chr17:38858104 C>A maps to NM_019016.2 L232L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8311-01A-11D-2396-08 chr17:38926070 C>A maps to NM_181539.4 E302*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PJ-A8JU-01A-11D-A35Z-10 chr17:38955926 G>A maps to NM_181535.3 G73G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JM-01A-12D-A42J-10 chr12:53183978 G>A maps to ENST00000309505 G579G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9JZ-01A-11D-A42J-10 chr12:53183978 G>A maps to ENST00000309505 G579G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PS-01A-11D-A42J-10 chr12:53188109 C>A maps to ENST00000309505 R217R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9Q1-01A-11D-A42J-10 chr17:39538609 C>T maps to NM_021013.3 K5K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A856-01A-11D-A34Z-10 chr12:52910545 G>A maps to NM_000424.3 A438A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JQ-01A-11D-A42J-10 chr12:52985267 C>A maps to NM_080747.2 E315*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7585-01A-11D-2136-08 chr12:53097169 G>T maps to NM_175078.2 R17R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A48D-01A-11D-A25F-10 chr12:53225245 C>A maps to NM_175834.2 G214G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JL-01A-11D-A42J-10 chr12:52565442 G>A maps to NM_182507.2 T411T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9K6-01A-11D-A42J-10 chr12:52776298 G>A maps to NM_033045.3 F278F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4617-01A-01D-1252-08 chr12:52756664 C>G maps to NM_002283.3 T350T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr21:46057372 C>T maps to NM_181688.1 C13C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7840-01A-11D-2136-08 chr21:46117130 C>T maps to NM_198699.1 S5S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AT-A5NU-01A-11D-A28G-10 chr21:45978022 G>A maps to NM_198696.2 A192A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr21:45978007 G>A maps to NM_198696.2 L197L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PN-01A-11D-A382-10 chr21:46032796 A>T maps to NM_198695.2 *260C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JT-01A-11D-A42J-10 chr21:46101933 G>T maps to NM_181686.1 C35*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A9DE-01A-11D-A36X-10 chr17:39471746 G>A maps to NM_031964.1 C52C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr21:31709824 G>A maps to NM_001077711.1 C54C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr17:39274237 A>G maps to NM_033059.3 C110C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr17:39280068 G>A maps to NM_031854.2 R102R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9Q1-01A-11D-A42J-10 chr17:39240790 C>G maps to ENST00000377731 R111R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Y8-A8S0-01A-11D-A36X-10 chr17:39240793 C>T maps to ENST00000377731 P112P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A83V-01A-11D-A34Z-10 chr11:71293622 G>A maps to ENST00000376535 C87C. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-A4-A772-01A-11D-A33Q-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-2Z-A9J1-01A-11D-A382-10 chr11:71249124 A>G maps to NM_021046.2 G8G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr3:134323199 C>A maps to NM_178554.4 E403*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47M-01A-11D-A25F-10 chr14:50713787 T>C maps to NM_024884.2 R460R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A83S-01A-11D-A34Z-10 chr20:42157989 C>T maps to NM_032107.4 F324F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr19:54872526 C>A maps to NM_002287.3 V120V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JG-01A-11D-A42J-10 chr18:7016661 A>G maps to NM_005559.2 Y939Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5880-01A-11D-1589-08 chr18:7025997 A>G maps to NM_005559.2 P794P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A57E-01A-11D-A26P-10 chr6:129766959 C>T maps to NM_000426.3 A2141A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9KA-01A-11D-A42J-10 chr18:21343468 G>T maps to ENST00000416669 G388G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7838-01A-11D-2136-08 chr18:21451429 G>T maps to ENST00000416669 V1603V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55Z-01A-11D-A26P-10 chr18:21508089 T>C maps to ENST00000416669 F2729F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7287-01A-11D-2136-08 chr6:112454682 G>C maps to NM_001105206.1 L1188L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J7-A8I2-01A-12D-A35Z-10 chr20:60906116 G>A maps to NM_005560.3 I1207I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Y8-A894-01A-11D-A35Z-10 chr7:107577547 T>A maps to NM_002291.2 S1312S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A9DE-01A-11D-A36X-10 chr9:133901738 C>A maps to ENST00000355048 I147I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr13:113964010 C>T maps to NM_005561.3 S79S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F9-A4JJ-01A-11D-A25F-10 chr23:119581841 G>A did not map to a codon.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr3:182870221 G>T maps to NM_014398.3 R277R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A7SR-01A-12D-A35Z-10 chr3:182871610 T>A maps to NM_014398.3 A206A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JO-01A-11D-A42J-10 chr23:37431494 C>T did not map to a codon.
Sequencing variant TCGA-2Z-A9JK-01A-11D-A42J-10 chr8:98788209 G>A maps to ENST00000378722 A128A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NI-01A-11D-A26P-10 chr22:33679189 G>A maps to NM_133642.3 F625F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59T-01A-21D-A28G-10 chr12:50847397 T>C maps to ENST00000429001 Y326Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5903-01A-11D-1589-08 chr10:858886 A>G maps to NM_015155.1 T732T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A656-01A-11D-A31X-10 chr15:71128825 T>C maps to NM_018357.2 G73G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7061-01A-11D-1961-08 chr23:64749563 C>A did not map to a codon.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr6:150005369 G>T maps to NM_004690.2 I285I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr6:149997826 C>G maps to NM_004690.2 G880G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr1:152777876 G>A maps to NM_178351.3 T26T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JM-01A-12D-A42J-10 chr1:152659504 C>T maps to NM_014357.4 G62G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A7SO-01A-11D-A34Z-10 chr1:152681688 G>C maps to NM_178356.2 G46G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Y8-A894-01A-11D-A35Z-10 chr1:152681688 G>C maps to NM_178356.2 G46G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PK-01A-11D-A382-10 chr4:108999438 C>T maps to NM_016269.4 A315A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PX-01A-11D-A42J-10 chr4:1836664 G>T maps to NM_012318.2 A261A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8630-01A-11D-2396-08 chr12:51450185 G>A maps to ENST00000448283 L285L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8311-01A-11D-2396-08 chr11:63273899 G>C maps to NM_001142535.1 T12T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NI-01A-11D-A26P-10 chr10:95549894 T>C maps to NM_005097.2 D157D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A656-01A-11D-A31X-10 chr11:27402258 C>G did not map to a codon.
Sequencing variant TCGA-B1-A655-01A-11D-A31Z-10 chr7:103969250 C>T maps to NM_199000.2 A8A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4A-A93W-01A-11D-A36X-10 chr1:180235628 C>A maps to NM_033343.3 C117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A7SQ-01A-12D-A35Z-10 chr1:180243425 A>G maps to NM_033343.3 T295T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7584-01A-11D-2136-08 chr19:55144005 C>A maps to ENST00000427581 G287G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr19:54783676 C>T maps to ENST00000391747 E125E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A562-01A-11D-A26P-10 chr19:54721051 G>T maps to NM_001081450.1 T603T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A656-01A-11D-A31X-10 chr7:73535229 G>A maps to NM_002314.2 G544G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JS-01A-21D-A42J-10 chr2:109292438 C>T maps to NM_001193484.1 I237I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-8500-01A-11D-2396-08 chr19:2290212 C>T maps to NM_001101391.1 P521P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55W-01A-11D-A26P-10 chr21:15561569 G>A maps to NM_198996.2 Q94*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr21:15554118 C>T maps to NM_198996.2 T222T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A4ZT-01A-11D-A26P-10 chr5:96443095 C>A maps to NM_153234.4 E119*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr12:66522753 G>A maps to NM_032338.3 Q45*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-A6W5-01A-12D-A33Q-10 chr2:97400230 C>T maps to NM_001142292.1 V113V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-A8LE-01A-11D-A35Z-10 chr3:197726165 G>A maps to NM_001136049.2 Q395Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5879-01A-11D-1589-08 chr1:156105084 C>T maps to NM_170707.2 L306L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59R-01A-11D-A26P-10 chr1:156107473 A>C maps to NM_170707.2 S546S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A9DD-01A-11D-A36X-10 chr1:156105103 G>A did not map to a codon.
Sequencing variant TCGA-2K-A9WE-01A-11D-A382-10 chr19:49002399 C>T maps to NM_001080434.1 E671E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A7UZ-01A-12D-A34Z-10 chr5:96315034 G>A maps to NM_005575.2 E71E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M9-01A-11D-A31X-10 chr4:54343068 T>C maps to NM_001126328.1 T581T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6135-01A-11D-1961-08 chr13:28143268 G>A maps to NM_153371.3 G184G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-5156-01A-01D-1589-08 chr9:90744547 T>C maps to NM_001166137.1 *1135W. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A83V-01A-11D-A34Z-10 chr19:19257424 G>A maps to ENST00000410050 C236C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr16:20851090 C>T maps to NM_030941.2 A466A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5878-01A-11D-1589-08 chr16:48385616 T>C maps to NM_031490.2 F821F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A83V-01A-11D-A34Z-10 chr16:48296781 T>C maps to NM_031490.2 T327T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4113-01A-01D-1252-08 chr23:118109100 G>T did not map to a codon.
Sequencing variant TCGA-DW-7838-01A-11D-2136-08 chr2:74761482 G>A maps to NM_032603.2 H633H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JE-01A-11D-A42J-10 chr23:78010829 C>G did not map to a codon.
Sequencing variant TCGA-B1-A47M-01A-11D-A25F-10 chr23:78011380 C>T did not map to a codon.
Sequencing variant TCGA-MH-A55Z-01A-11D-A26P-10 chr23:78010715 C>A did not map to a codon.
Sequencing variant TCGA-EV-5901-01A-11D-1589-08 chr5:1488542 A>T maps to NM_024830.3 T210T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A4EM-01A-11D-A25F-10 chr12:7125632 C>T maps to NM_005768.5 A32A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JD-01A-11D-A42J-10 chr19:14281545 G>A maps to NM_001008701.2 P114P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9J3-01A-12D-A382-10 chr2:11924033 G>A maps to ENST00000396099 L454L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8196-01A-11D-2396-08 chr2:11960559 A>G maps to ENST00000396099 V853V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A83S-01A-11D-A34Z-10 chr18:2927794 G>A maps to NM_014646.2 S545S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A71S-01A-11D-A33Q-10 chr20:39978759 T>C maps to NM_022896.1 P275P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NH-01A-11D-A26P-10 chr8:19811709 C>T maps to NM_000237.2 D207D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9KA-01A-11D-A42J-10 chr4:151935617 T>C maps to NM_006726.3 E59E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5878-01A-11D-1589-08 chr4:151827109 A>T maps to NM_006726.3 L545L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5885-01A-11D-1589-08 chr4:151829519 G>A maps to NM_006726.3 Q487*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-5155-01A-01D-1589-08 chr13:47269133 G>A maps to NM_001164211.1 S409S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-A8LE-01A-11D-A35Z-10 chr11:801090 G>A maps to NM_145886.3 L554L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PK-01A-11D-A382-10 chr6:40399745 C>T maps to NM_020737.1 T369T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5903-01A-11D-1589-08 chr11:66627367 T>A maps to NM_024036.4 L537*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55Z-01A-11D-A26P-10 chr14:42360767 C>T maps to NM_152447.3 S567S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A44B-01A-11D-A25F-10 chr12:57587700 C>T maps to NM_002332.2 G2608G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Y8-A895-01A-11D-A35Z-10 chr12:57600367 C>T maps to NM_002332.2 R3901R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8195-01A-31D-2396-08 chr14:23345116 C>T maps to NM_014045.3 G320G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J7-8537-01A-11D-2396-08 chr2:141607701 G>A maps to NM_018557.2 N1636N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PN-01A-11D-A382-10 chr2:141598581 C>T maps to NM_018557.2 T1673T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9KE-01A-11D-A42J-10 chr2:170062023 A>G maps to NM_004525.2 Y2560Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A48D-01A-11D-A25F-10 chr2:170012841 G>T maps to NM_004525.2 V4031V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A44B-01A-11D-A25F-10 chr2:170055305 A>G maps to NM_004525.2 P2856P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A8YH-01A-11D-A36X-10 chr2:170097723 T>C maps to NM_004525.2 S1273S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5886-01A-11D-1589-08 chr2:170072852 A>G maps to NM_004525.2 T1912T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A561-01A-11D-A26P-10 chr2:170136008 T>A maps to NM_004525.2 K480*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4617-01A-01D-1252-08 chr11:46897383 G>A maps to ENST00000256991 Q1269*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr12:12302075 C>T maps to NM_002336.2 V1002V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8195-01A-31D-2396-08 chr4:3519767 A>G maps to NM_002337.2 T248T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7841-01A-11D-2136-08 chr2:44207046 A>G maps to NM_133259.3 S129S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A71W-01A-12D-A34Z-10 chr2:44139608 T>C maps to NM_133259.3 S1079S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-7173-01A-11D-2136-08 chr12:7023219 A>C maps to NM_006992.3 A308A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A854-01A-11D-A34Z-10 chr11:76371151 G>A maps to NM_001128922.1 V495V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WN-A9G9-01A-12D-A36X-10 chr11:76371484 G>A maps to NM_001128922.1 A384A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4103-01A-01D-1458-08 chr3:196387839 C>T maps to NM_198565.1 P442P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PJ-A5Z8-01A-11D-A28G-10 chr17:62855781 A>T maps to NM_199340.2 I1494I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A57E-01A-11D-A26P-10 chr12:122669245 T>C maps to NM_001098519.1 L111L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7836-01A-11D-2136-08 chr17:48462616 T>A maps to NM_018509.3 K180*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-AAVM-01A-11D-A42J-10 chr9:131669745 G>A maps to NM_001127244.1 L101L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A40X-01A-11D-A25F-10 chr1:90048544 A>G maps to NM_015350.2 K112K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-5155-01A-01D-1589-08 chr1:90179253 T>C maps to NM_032270.4 H375H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NK-01A-11D-A26P-10 chr1:90179187 T>C maps to NM_032270.4 Y353Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr8:86057650 G>T maps to NM_033402.4 E1002*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-7268-01A-11D-2136-08 chr12:85449851 G>T maps to NM_001079910.1 V427V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PK-01A-11D-A382-10 chr3:169539715 A>T maps to NM_001080460.1 K3*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8098-01A-11D-2396-08 chr15:101529602 A>G maps to NM_024652.3 T254T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr12:40758850 A>G maps to NM_198578.3 L2463L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9J5-01A-21D-A382-10 chr20:6031522 G>A maps to NM_152611.3 N254N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8196-01A-11D-2396-08 chr17:42117588 C>T maps to ENST00000411445 K101K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7061-01A-11D-1961-08 chr19:35757259 A>G did not map to a codon.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr19:35758027 C>A maps to NM_205834.2 T435T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4113-01A-01D-1252-08 chr21:47626683 T>G did not map to a codon.
Sequencing variant TCGA-DW-7836-01A-11D-2136-08 chr2:33246141 T>A maps to ENST00000354476 P244P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M8-01A-11D-A31X-10 chr14:75019016 C>G maps to NM_000428.2 G424G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55Z-01A-11D-A26P-10 chr11:65319016 A>T did not map to a codon.
Sequencing variant TCGA-UZ-A9PX-01A-11D-A42J-10 chr19:41117891 T>A did not map to a codon.
Sequencing variant TCGA-AL-3468-01A-01D-1252-08 chr12:6494284 C>T maps to NM_002342.1 I97I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JT-01A-11D-A42J-10 chr15:41804905 G>A maps to NM_002344.5 L120L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4A-A93Y-01A-11D-A36X-10 chr15:41797954 C>T maps to NM_002344.5 S551S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PX-01A-11D-A42J-10 chr6:144179107 T>C maps to NM_032860.3 N253N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A83S-01A-11D-A34Z-10 chr2:160746832 T>C maps to NM_001198759.1 Q231Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KV-A74V-01A-11D-A33Q-10 chr4:4270270 T>A maps to NM_017816.2 K331*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A40X-01A-11D-A25F-10 chr6:5260905 T>A maps to NM_001164840.1 K21*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55Z-01A-11D-A26P-10 chr1:235884163 G>A maps to NM_000081.2 L3119L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr8:20107304 G>A maps to NM_021020.2 A573A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3466-01A-01D-1252-08 chr12:9096394 A>G did not map to a codon.
Sequencing variant TCGA-UZ-A9PM-01A-21D-A382-10 chr1:39901267 T>A maps to ENST00000361689 I3879I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A83T-01A-11D-A34Z-10 chr23:151092974 C>T did not map to a codon.
Sequencing variant TCGA-Y8-A8RZ-01A-11D-A36X-10 chr23:151092150 G>A did not map to a codon.
Sequencing variant TCGA-UZ-A9Q1-01A-11D-A42J-10 chr23:35821035 C>T did not map to a codon.
Sequencing variant TCGA-B9-4617-01A-01D-1252-08 chr23:30261218 G>T did not map to a codon.
Sequencing variant TCGA-AL-A5DJ-01A-11D-A26P-10 chr23:140996145 G>T did not map to a codon.
Sequencing variant TCGA-UZ-A9PS-01A-11D-A42J-10 chr23:140967156 A>G did not map to a codon.
Sequencing variant TCGA-IZ-A6M9-01A-11D-A31X-10 chr23:54841946 C>T did not map to a codon.
Sequencing variant TCGA-UZ-A9PO-01A-11D-A382-10 chr23:54841869 T>G did not map to a codon.
Sequencing variant TCGA-4A-A93W-01A-11D-A36X-10 chr23:75651090 G>A did not map to a codon.
Sequencing variant TCGA-SX-A71S-01A-11D-A33Q-10 chr3:184428919 A>C maps to NM_022149.4 P230P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E6-01A-11D-A28G-10 chr3:65425596 C>T maps to NM_001033057.1 Q409Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A7SR-01A-12D-A35Z-10 chr3:65350345 T>A maps to NM_001033057.1 A1115A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-7173-01A-11D-2136-08 chr7:78131030 C>A maps to NM_012301.3 V276V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PS-01A-11D-A42J-10 chr7:77885344 T>A maps to NM_012301.3 V654V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Y8-A898-01A-11D-A34Z-10 chr7:77764392 C>A maps to NM_012301.3 V992V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A7SN-01A-11D-A34Z-10 chr1:114184617 C>T maps to NM_001142782.1 V482V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-AAVL-01A-11D-A42J-10 chr23:49022720 G>A did not map to a codon.
Sequencing variant TCGA-BQ-5878-01A-11D-1589-08 chr12:10766046 G>T maps to NM_018048.3 R29R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A9DC-01A-11D-A36X-10 chr23:77131065 A>G did not map to a codon.
Sequencing variant TCGA-KV-A6GD-01A-11D-A31X-10 chr2:110873285 G>A maps to NM_005434.4 F28F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M8-01A-11D-A31X-10 chr9:139748711 C>T maps to ENST00000392881 V240V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr5:179192886 G>A maps to NM_014757.4 L292L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-A4TM-01A-11D-A31X-10 chr5:179201052 G>A maps to NM_014757.4 V742V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8195-01A-31D-2396-08 chr5:179193184 G>T maps to NM_014757.4 E392*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A6HP-01A-11D-A31X-10 chr11:95825253 C>T maps to NM_032427.1 Q647Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47N-01A-11D-A25F-10 chr11:95825247 C>T maps to NM_032427.1 Q649Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47N-01A-11D-A25F-10 chr11:95825253 C>T maps to NM_032427.1 Q647Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W8-01A-11D-A28G-10 chr11:95825394 C>T maps to NM_032427.1 Q600Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-A8LD-01A-11D-A35Z-10 chr11:95825256 T>C maps to NM_032427.1 Q646Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Y8-A898-01A-11D-A34Z-10 chr11:95825253 C>T maps to NM_032427.1 Q647Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A40X-01A-11D-A25F-10 chr4:140811101 C>T maps to ENST00000509479 Q496Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A7SQ-01A-12D-A35Z-10 chr15:91453417 G>A maps to NM_006122.2 G491G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F9-A8NY-01A-11D-A35Z-10 chr15:75653704 C>T maps to NM_006715.2 W412*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr23:43590944 A>C did not map to a codon.
Sequencing variant TCGA-Y8-A8S0-01A-11D-A36X-10 chr23:43603408 T>C did not map to a codon.
Sequencing variant TCGA-AL-3466-01A-01D-1252-08 chr23:43655070 C>A did not map to a codon.
Sequencing variant TCGA-BQ-5880-01A-11D-1589-08 chr23:43702914 C>G did not map to a codon.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr23:43655116 C>T did not map to a codon.
Sequencing variant TCGA-G7-A8LB-01A-11D-A35Z-10 chr15:43818608 G>T maps to ENST00000382031 V1884V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9K0-01A-11D-A42J-10 chr17:12028657 C>T maps to ENST00000415385 R298R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8196-01A-11D-2396-08 chr17:12016634 T>C maps to ENST00000415385 S268S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr19:7976337 A>G maps to ENST00000425613 G360G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7837-01A-11D-2136-08 chr5:56177036 T>A maps to NM_005921.1 P769P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PJ-A5Z9-01A-11D-A28G-10 chr5:56170959 G>T maps to NM_005921.1 L596L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PX-01A-11D-A42J-10 chr5:56178644 T>C maps to NM_005921.1 P1206P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9KA-01A-11D-A42J-10 chr19:40721174 G>C maps to NM_002446.3 L947L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7288-01A-11D-2136-08 chr3:185191374 G>A maps to NM_004721.3 G752G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr3:185146746 C>T maps to NM_004721.3 G126G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A9DD-01A-11D-A36X-10 chr23:19389153 A>C did not map to a codon.
Sequencing variant TCGA-SX-A7SS-01A-11D-A35Z-10 chr17:61767095 G>A did not map to a codon.
Sequencing variant TCGA-DW-7840-01A-11D-2136-08 chr6:161470013 C>A maps to NM_005922.2 S237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PL-01A-11D-A382-10 chr6:91296572 G>C maps to NM_145331.1 S10S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr2:102493543 C>A maps to NM_145686.2 I1043I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NI-01A-11D-A26P-10 chr2:102493591 C>G maps to NM_145686.2 V1059V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7834-01A-11D-2136-08 chr23:135314168 T>C did not map to a codon.
Sequencing variant TCGA-2Z-A9J8-01A-11D-A42J-10 chr8:144803995 G>T maps to NM_139021.2 L468L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7732-01A-11D-2136-08 chr8:144801160 A>T did not map to a codon.
Sequencing variant TCGA-SX-A7SL-01A-11D-A34Z-10 chr15:52357195 A>T maps to NM_002748.3 *722L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E6-01A-11D-A28G-10 chr3:50685440 C>G maps to NM_004635.3 G371G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4A-A93W-01A-11D-A36X-10 chr15:42114510 G>A maps to NM_001128608.1 E1046E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7287-01A-11D-2136-08 chr17:44101443 C>G maps to NM_001123066.3 V746V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PU-01A-11D-A42J-10 chr17:44073779 C>A maps to NM_001123066.3 S526*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M9-01A-11D-A31X-10 chr19:8503276 C>T maps to NM_016496.4 S196S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JI-01A-11D-A42J-10 chr2:119727690 T>A maps to NM_006770.3 V67V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55W-01A-11D-A26P-10 chr11:63671475 C>G maps to NM_001039469.2 S511S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PJ-A5Z9-01A-11D-A28G-10 chr12:57894253 G>C maps to NM_004990.2 R414R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7997-01A-11D-2201-08 chr1:46290208 T>C maps to NM_015112.2 D94D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A71S-01A-11D-A33Q-10 chr5:66461903 G>A maps to NM_001164664.1 E2299E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A7SP-01A-11D-A34Z-10 chr1:31191690 C>T maps to NM_002379.3 K185K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JR-01A-12D-A42J-10 chr8:99015911 A>T maps to ENST00000254898 K410*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr8:99019719 C>T maps to ENST00000254898 C488C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JE-01A-11D-A42J-10 chr16:29820994 C>T maps to NM_001042539.1 Q472*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8195-01A-31D-2396-08 chr2:149248039 A>C maps to ENST00000404807 P1613P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr12:57918526 C>A maps to NM_052897.3 S46S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A657-01A-11D-A31X-10 chr3:152163261 C>T maps to NM_021038.3 I247I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7828-01A-11D-2136-08 chr23:131540268 T>A did not map to a codon.
Sequencing variant TCGA-A4-A5Y0-01A-11D-A31X-10 chr18:74700844 C>T maps to NM_001025101.1 P235P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NJ-01A-11D-A26P-10 chr16:84094305 G>C maps to NM_003791.2 V895V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3468-01A-01D-1252-08 chr23:21857903 T>C did not map to a codon.
Sequencing variant TCGA-PJ-A5Z8-01A-11D-A28G-10 chr18:13826447 G>A maps to NM_005913.2 A228A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59R-01A-11D-A26P-10 chr11:119182660 T>A did not map to a codon.
Sequencing variant TCGA-MH-A562-01A-11D-A26P-10 chr11:119185944 C>T maps to NM_006500.2 A32A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A71V-01A-11D-A33Q-10 chr18:29340392 G>A maps to NM_001034172.2 R78*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A44B-01A-11D-A25F-10 chr23:103349336 C>T did not map to a codon.
Sequencing variant TCGA-BQ-5877-01A-11D-1589-08 chr3:183013204 G>A maps to NM_015078.2 Q520*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V9-A7HT-01A-11D-A33Q-10 chr3:183017879 C>T maps to NM_015078.2 R406R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Y8-A895-01A-11D-A35Z-10 chr3:127335804 G>A maps to NM_004526.2 V539V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A7SS-01A-11D-A35Z-10 chr6:52141272 T>A maps to ENST00000419835 G434G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NI-01A-11D-A26P-10 chr6:119245293 T>C did not map to a codon.
Sequencing variant TCGA-B9-4115-01A-01D-1252-08 chr1:85491699 A>G maps to NM_018298.9 N339N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6135-01A-11D-1961-08 chr1:85491893 G>C maps to NM_018298.9 L302L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr8:6302562 T>C maps to NM_024596.3 A440A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4113-01A-01D-1252-08 chr15:94841733 C>T maps to NM_018349.3 S80S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9J3-01A-12D-A382-10 chr6:30680833 A>C maps to NM_014641.2 P295P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A71V-01A-11D-A33Q-10 chr6:30681673 G>C maps to NM_014641.2 S141S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr6:37622576 C>A maps to ENST00000297153 T237T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KV-A6GE-01A-11D-A31X-10 chr6:37622224 G>T maps to ENST00000297153 P269P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PP-01A-11D-A42J-10 chr7:75693751 A>G maps to NM_005918.2 G243G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E7-01A-31D-A28G-10 chr12:68696604 T>A maps to NM_017440.4 I589I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JQ-01A-11D-A42J-10 chr6:90491212 A>G maps to NM_014611.1 D516D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A854-01A-11D-A34Z-10 chr23:70355043 T>G did not map to a codon.
Sequencing variant TCGA-Y8-A894-01A-11D-A35Z-10 chr23:70350037 C>T did not map to a codon.
Sequencing variant TCGA-IA-A83V-01A-11D-A34Z-10 chr3:151148130 G>A maps to NM_053002.4 T2116T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PJ-A8JU-01A-11D-A35Z-10 chr17:60039086 G>T maps to NM_005121.2 I1706I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PR-01A-11D-A42J-10 chr17:60043907 T>A maps to NM_005121.2 A1432A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JT-01A-11D-A42J-10 chr12:116453056 A>G maps to NM_015335.4 S344S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Y8-A895-01A-11D-A35Z-10 chr12:116460357 A>G maps to NM_015335.4 N176N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9JY-01A-11D-A42J-10 chr23:40526004 T>C did not map to a codon.
Sequencing variant TCGA-A4-8311-01A-11D-2396-08 chr22:20920815 G>A maps to NM_001003891.1 Q251Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr17:38182476 C>T maps to NM_014815.3 S639S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J7-8537-01A-11D-2396-08 chr17:38187789 C>G did not map to a codon.
Sequencing variant TCGA-B1-A655-01A-11D-A31Z-10 chr9:134889752 A>G maps to NM_004269.2 A150A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JL-01A-11D-A42J-10 chr1:156444933 G>A maps to NM_005920.2 L324L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M8-01A-11D-A31X-10 chr5:126705694 G>T did not map to a codon.
Sequencing variant TCGA-AL-3468-01A-01D-1252-08 chr19:42872695 T>C maps to ENST00000251268 C2121C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3472-01A-01D-1252-08 chr22:42191443 C>A maps to NM_152513.3 L1188L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7841-01A-11D-2136-08 chr22:42154471 A>C maps to NM_152513.3 G685G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A44B-01A-11D-A25F-10 chr9:36583633 A>G maps to NM_014791.2 A23A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4A-A93X-01A-11D-A36X-10 chr7:15725802 G>A maps to NM_005924.4 H75H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9KC-01A-11D-A42J-10 chr7:15725799 G>A maps to NM_005924.4 H76H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7286-01A-11D-2136-08 chr7:15725808 G>A maps to NM_005924.4 H73H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A654-01A-11D-A31X-10 chr7:15725799 G>A maps to NM_005924.4 H76H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E8-01A-11D-A28G-10 chr7:15725799 G>A maps to NM_005924.4 H76H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9J3-01A-12D-A382-10 chr2:112705127 C>T maps to NM_006343.2 S247S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4A-A93W-01A-11D-A36X-10 chr2:112767643 G>C did not map to a codon.
Sequencing variant TCGA-UZ-A9PP-01A-11D-A42J-10 chr2:112686994 T>G maps to NM_006343.2 P120P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr15:81282036 G>A maps to NM_015154.1 C32C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A7SR-01A-12D-A35Z-10 chr12:95907667 A>T maps to NM_006838.3 G475G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9JW-01A-11D-A42J-10 chr14:21463349 T>A maps to NM_001029991.1 A301A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4115-01A-01D-1252-08 chr10:126477650 A>G maps to NM_212554.2 L84L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr17:60501295 A>G maps to NM_181725.3 A11A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr2:170677783 C>A did not map to a codon.
Sequencing variant TCGA-IA-A83W-01A-11D-A34Z-10 chr15:82337941 C>T maps to NM_032246.3 Q35Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9J7-01A-11D-A382-10 chr15:44106733 C>T maps to NM_005926.2 E194E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A657-01A-11D-A31X-10 chr15:44105506 C>T maps to NM_005926.2 Q222Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5883-01A-11D-1589-08 chr15:44109599 T>G maps to NM_005926.2 G42G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JK-01A-11D-A42J-10 chr8:8747814 G>A maps to NM_004225.2 A918A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A560-01A-11D-A26P-10 chr8:8655001 C>A did not map to a codon.
Sequencing variant TCGA-2Z-A9JE-01A-11D-A42J-10 chr1:12067261 T>A maps to NM_014874.3 L675L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr3:158519841 G>A maps to NM_022736.2 R16R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AT-A5NU-01A-11D-A28G-10 chr17:74738355 G>A did not map to a codon.
Sequencing variant TCGA-BQ-5875-01A-11D-1589-08 chr17:74772620 C>T maps to NM_024311.2 Q395*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7839-01A-11D-2136-08 chr7:141731532 T>G maps to ENST00000475668 V508V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8195-01A-31D-2396-08 chr10:103563516 A>G maps to NM_012215.3 N337N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A71S-01A-11D-A33Q-10 chr10:103577713 G>A maps to NM_012215.3 A22A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A83S-01A-11D-A34Z-10 chr11:12244190 G>A maps to NM_014632.2 Q450Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr11:12316189 C>T maps to NM_032867.2 D404D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A654-01A-11D-A31X-10 chr23:38664367 G>T did not map to a codon.
Sequencing variant TCGA-2Z-A9J2-01A-11D-A382-10 chr19:1255610 T>C maps to NM_177401.4 T349T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7058-01A-11D-1961-08 chr1:67423740 G>C did not map to a codon.
Sequencing variant TCGA-5P-A9KE-01A-11D-A42J-10 chr17:4788850 G>A maps to NM_153827.4 W194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4116-01A-01D-1252-08 chr17:4800539 T>G maps to NM_153827.4 V1319V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A71V-01A-11D-A33Q-10 chr17:4799845 T>C maps to NM_153827.4 D1246D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8517-01A-11D-2396-08 chr22:50926722 G>T maps to NM_017584.5 G120G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7584-01A-11D-2136-08 chr3:69928531 A>T maps to ENST00000448226 K118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-O9-A75Z-01A-11D-A33Q-10 chr10:129904961 G>T maps to NM_002417.4 I1714I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A48D-01A-11D-A25F-10 chr22:40825748 G>A maps to NM_020831.3 L54L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JE-01A-11D-A42J-10 chr16:14355240 G>A maps to NM_014048.3 A1030A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9JW-01A-11D-A42J-10 chr4:185637571 G>A maps to NM_024629.3 N199N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr12:6859056 C>A maps to NM_005439.2 T172T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr14:75516129 T>A maps to NM_001040108.1 K77*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4104-01A-01D-1458-08 chr12:49425838 G>A maps to NM_003482.3 Q4217*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4104-01A-01D-1458-08 chr12:49426525 G>A maps to NM_003482.3 Q3988*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-7502-01A-11D-2201-08 chr12:49433379 C>G maps to NM_003482.3 L2689L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A7SN-01A-11D-A34Z-10 chr12:49445629 A>G maps to NM_003482.3 P612P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PR-01A-11D-A42J-10 chr12:49427987 T>G maps to NM_003482.3 V3534V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4104-01A-01D-1458-08 chr7:151879015 G>A maps to ENST00000355193 Q1977*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9Q1-01A-11D-A42J-10 chr7:151853288 C>T did not map to a codon.
Sequencing variant TCGA-A4-A5XZ-01A-11D-A31X-10 chr19:36229180 A>G did not map to a codon.
Sequencing variant TCGA-BQ-5884-01A-11D-1589-08 chr13:49796386 C>G maps to NM_001507.1 L371L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8195-01A-31D-2396-08 chr16:2258564 C>T maps to NM_022372.4 G271G. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-DZ-6134-01A-11D-1961-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-DZ-6134-01A-11D-1961-08 chr17:40720855 T>C maps to NM_170607.2 D111D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7841-01A-11D-2136-08 chr12:122618011 C>A maps to NM_014938.3 R404R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A48D-01A-11D-A25F-10 chr3:154855892 T>A maps to NM_007289.2 A241A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A655-01A-11D-A31Z-10 chr3:154858035 A>G maps to NM_007289.2 T304T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr11:102573541 C>A maps to NM_022122.2 P187P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PJ-A5Z9-01A-11D-A28G-10 chr10:88703694 G>A maps to NM_024756.2 A282A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9J5-01A-21D-A382-10 chr22:28194899 T>C maps to NM_002430.2 Q544Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A9DD-01A-11D-A36X-10 chr22:28194893 C>T maps to NM_002430.2 Q546Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A9DE-01A-11D-A36X-10 chr22:28194899 T>C maps to NM_002430.2 Q544Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PJ-A8JU-01A-11D-A35Z-10 chr22:28193969 T>C maps to NM_002430.2 P854P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-7268-01A-11D-2136-08 chr14:61434958 T>C maps to NM_002431.3 H274H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5903-01A-11D-1589-08 chr14:61434985 T>C maps to NM_002431.3 L283L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A71V-01A-11D-A33Q-10 chr6:29634001 T>G maps to NM_002433.4 T170T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A9DD-01A-11D-A36X-10 chr7:100844042 G>A maps to NM_178176.2 L31L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4116-01A-01D-1252-08 chr3:49946455 G>A maps to NM_032355.3 L650L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Y8-A894-01A-11D-A35Z-10 chr3:49949381 C>A maps to NM_032355.3 E161*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9K0-01A-11D-A42J-10 chr21:37741432 A>C maps to ENST00000290384 A590A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PJ-01A-11D-A382-10 chr21:37747536 A>G maps to ENST00000290384 V922V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7062-01A-11D-1961-08 chr23:106201625 A>G did not map to a codon.
Sequencing variant TCGA-V9-A7HT-01A-11D-A33Q-10 chr23:106236527 A>C did not map to a codon.
Sequencing variant TCGA-AL-3466-01A-01D-1252-08 chr1:220971316 G>A maps to NM_022746.3 R238R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AT-A5NU-01A-11D-A28G-10 chr1:220960438 G>T maps to NM_022746.3 L51L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JQ-01A-11D-A42J-10 chr7:100210557 G>T maps to NM_023948.4 R48R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A7UZ-01A-12D-A34Z-10 chr1:113236731 C>T maps to NM_020963.3 I411I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Y8-A894-01A-11D-A35Z-10 chr1:113237493 C>A maps to NM_020963.3 V532V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JG-01A-11D-A42J-10 chr22:50591545 A>C maps to NM_018995.2 R989R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9K3-01A-11D-A42J-10 chr22:50555697 G>T maps to NM_018995.2 E458*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JP-01A-11D-A42J-10 chr17:7490748 C>T maps to NM_004870.3 T208T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr11:58978385 A>T maps to NM_001039396.1 G651G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Y8-A898-01A-11D-A34Z-10 chr1:43814557 G>T maps to NM_005373.2 L451L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9KC-01A-11D-A42J-10 chr23:154007572 G>C did not map to a codon.
Sequencing variant TCGA-G7-A8LE-01A-11D-A35Z-10 chr17:41960405 C>G maps to NM_005374.3 T106T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A7SQ-01A-12D-A35Z-10 chr17:41975629 C>T maps to NM_005374.3 K50K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PK-01A-11D-A382-10 chr2:202514862 G>T maps to NM_033066.2 Y469*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5Y1-01A-11D-A28G-10 chr14:67787026 T>C maps to NM_022474.2 L484L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3472-01A-01D-1252-08 chr17:17080726 G>A did not map to a codon.
Sequencing variant TCGA-DW-7836-01A-11D-2136-08 chr10:17891758 C>T maps to NM_002438.2 L414L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-3926-01A-01D-1252-08 chr17:60766322 T>C did not map to a codon.
Sequencing variant TCGA-PJ-A5Z8-01A-11D-A28G-10 chr11:18195096 C>T maps to NM_054032.3 L98L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr19:13875776 C>T maps to NM_001031727.2 L75L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PV-01A-11D-A42J-10 chr1:54671036 G>A maps to NM_016491.3 R200R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A83V-01A-11D-A34Z-10 chr17:73897870 G>T maps to NM_032478.3 V171V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-AAVL-01A-11D-A42J-10 chr15:89010545 C>T maps to NM_022163.3 R21R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A71W-01A-12D-A34Z-10 chr6:43646266 C>T maps to ENST00000372118 K80K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9Q1-01A-11D-A42J-10 chr6:24423169 T>C maps to NM_020662.2 H371H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WN-AB4C-01A-11D-A42J-10 chr6:24405465 T>C maps to NM_020662.2 T87T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr11:10647665 C>G maps to NM_001098579.1 R396R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A83T-01A-11D-A34Z-10 chr11:60470855 C>A maps to NM_031457.1 I75I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NI-01A-11D-A26P-10 chr5:80037367 G>C did not map to a codon.
Sequencing variant TCGA-IZ-8195-01A-31D-2396-08 chr5:80040401 G>A maps to NM_002439.3 K577K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3468-01A-01D-1252-08 chr6:31712028 A>G maps to ENST00000375742 E217E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7287-01A-11D-2136-08 chr23:64936757 G>C did not map to a codon.
Sequencing variant TCGA-B1-A47M-01A-11D-A25F-10 chr8:16021616 A>G maps to ENST00000445506 D276D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7287-01A-11D-2136-08 chr8:9912061 C>T maps to NM_012331.3 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9JW-01A-11D-A42J-10 chr23:131207117 A>C did not map to a codon.
Sequencing variant TCGA-O9-A75Z-01A-11D-A33Q-10 chr16:56660834 G>A maps to NM_175617.3 Q46Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JD-01A-11D-A42J-10 chr12:107372222 A>G maps to NM_025198.3 D90D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7585-01A-11D-2136-08 chr15:65295423 A>C maps to NM_139242.3 V382V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W8-01A-11D-A28G-10 chr16:86565820 G>A maps to NM_001159377.1 D316D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A71R-01A-12D-A33Q-10 chr23:149767103 G>T did not map to a codon.
Sequencing variant TCGA-2Z-A9JM-01A-12D-A42J-10 chr15:31253166 C>G maps to NM_017762.2 S225S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55Z-01A-11D-A26P-10 chr15:31251263 G>C maps to NM_017762.2 S273S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NJ-01A-11D-A26P-10 chr22:30416248 C>T maps to NM_021090.3 C867C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4113-01A-01D-1252-08 chr1:11273602 G>C maps to NM_004958.3 T1046T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JQ-01A-11D-A42J-10 chr10:30615417 C>T maps to ENST00000358107 R439R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9K8-01A-11D-A42J-10 chr1:236959018 C>T maps to NM_000254.2 Q6*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PJ-A8JU-01A-11D-A35Z-10 chr1:236979822 G>A maps to NM_000254.2 V248V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr5:7878201 G>T maps to NM_024010.2 E210*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JQ-01A-11D-A42J-10 chr8:17503479 T>A maps to NM_001001924.2 P1256P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7842-01A-11D-2136-08 chr8:17513392 G>T maps to NM_001001924.2 Y1029*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47O-01A-11D-A25F-10 chr13:29675027 C>T maps to NM_001033602.2 V865V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JJ-01A-11D-A42J-10 chr19:9062896 G>A maps to NM_024690.2 I8183I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr19:9061597 A>G maps to NM_024690.2 P8616P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7734-01A-11D-2136-08 chr19:9064318 A>G maps to NM_024690.2 H7709H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8311-01A-11D-2396-08 chr19:9077785 G>T maps to NM_024690.2 I3220I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5892-01A-11D-1589-08 chr19:9085837 C>A maps to NM_024690.2 E1993*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F9-A7Q0-01A-11D-A35Z-10 chr19:9008206 G>A maps to NM_024690.2 P13115P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A83T-01A-11D-A34Z-10 chr19:9016699 G>A maps to NM_024690.2 D12679D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A83W-01A-11D-A34Z-10 chr19:8993025 G>A maps to NM_024690.2 S13911S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EA-01A-11D-A28G-10 chr19:9058715 G>C maps to NM_024690.2 S9577*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A7UZ-01A-12D-A34Z-10 chr7:100692138 T>C maps to NM_001040105.1 T4183T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5882-01A-11D-1589-08 chr7:100681164 T>C maps to NM_001040105.1 Y2156Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9JU-01A-11D-A42J-10 chr11:1093322 C>T maps to ENST00000441003 T1714T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr11:1099776 T>C maps to ENST00000441003 P2458P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-AAVL-01A-11D-A42J-10 chr11:1093436 G>C maps to ENST00000441003 T1752T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NL-01A-11D-A26P-10 chr11:1264091 C>T maps to ENST00000447027 R1997R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PZ-01A-11D-A42J-10 chr1:45797351 C>T maps to NM_001128425.1 L389L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-3925-01A-01D-1458-08 chr23:3238718 A>G did not map to a codon.
Sequencing variant TCGA-IA-A83T-01A-11D-A34Z-10 chr23:3229193 G>T did not map to a codon.
Sequencing variant TCGA-WN-AB4C-01A-11D-A42J-10 chr23:3242167 T>C did not map to a codon.
Sequencing variant TCGA-BQ-7046-01A-11D-1961-08 chr17:4451583 C>T maps to NM_001105538.1 T526T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9JW-01A-11D-A42J-10 chr20:42315497 G>T maps to NM_002466.2 E96*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A44B-01A-11D-A25F-10 chr20:42328635 C>T maps to NM_002466.2 I301I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Y8-A8S1-01A-11D-A36X-10 chr20:42338683 C>T maps to NM_002466.2 Y529Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Y8-A897-01A-11D-A35Z-10 chr11:47373012 T>C maps to ENST00000399249 A23A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F9-A7VF-01A-11D-A33Q-10 chr13:77732193 A>G maps to NM_015057.4 H2216H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8312-01A-11D-2396-08 chr17:48600412 A>T maps to NM_032133.4 R500R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-A5DJ-01A-11D-A26P-10 chr2:16085780 C>T maps to NM_005378.4 I319I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A656-01A-11D-A31X-10 chr2:16082257 A>G maps to NM_005378.4 L24L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9JY-01A-11D-A42J-10 chr3:38180442 C>A maps to NM_001172567.1 A97A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9JY-01A-11D-A42J-10 chr17:8404182 G>T maps to ENST00000360416 A1235A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9K6-01A-11D-A42J-10 chr17:8438747 C>T maps to ENST00000360416 L617L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3472-01A-01D-1252-08 chr17:10258305 C>G maps to NM_003802.2 L269L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6790-01A-11D-1961-08 chr17:10227378 A>T maps to NM_003802.2 L965*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-7502-01A-11D-2201-08 chr3:108110609 G>A maps to NM_014981.1 S1829S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8515-01A-11D-2396-08 chr17:10433385 G>A maps to NM_017534.5 A901A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6134-01A-11D-1961-08 chr17:10426830 G>A maps to NM_017534.5 I1818I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5879-01A-11D-1589-08 chr17:10554907 G>A maps to NM_002470.2 G142G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5877-01A-11D-1589-08 chr17:10366487 G>A maps to NM_017533.2 R275*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9KE-01A-11D-A42J-10 chr14:23893154 C>A maps to NM_000257.2 L961L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WN-A9G9-01A-12D-A36X-10 chr14:23902758 G>T maps to NM_000257.2 A61A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A772-01A-11D-A33Q-10 chr20:33586407 G>T maps to NM_020884.3 R1365R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7840-01A-11D-2136-08 chr17:10312635 A>T maps to NM_002472.2 T619T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A40Y-01A-11D-A25F-10 chr17:10300167 A>T maps to NM_002472.2 S1438S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-AAVM-01A-11D-A42J-10 chr17:45299171 C>T maps to NM_002476.2 S146S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8098-01A-11D-2396-08 chr20:35177591 C>T maps to NM_006097.3 N153N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-5156-01A-01D-1589-08 chr16:46766186 C>T maps to NM_182493.2 R465R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5876-01A-11D-1589-08 chr5:16764478 G>T maps to NM_012334.2 A402A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5Y1-01A-11D-A28G-10 chr17:18023901 G>C maps to ENST00000205890 R596R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9Q1-01A-11D-A42J-10 chr13:109379840 C>T maps to NM_015011.1 V117V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A7SL-01A-11D-A34Z-10 chr17:27441097 C>A maps to NM_078471.3 A843A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PS-01A-11D-A42J-10 chr17:27447771 C>T maps to NM_078471.3 E530E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9J6-01A-11D-A382-10 chr22:26164197 G>C maps to ENST00000407587 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7585-01A-11D-2136-08 chr22:26423001 C>G maps to ENST00000407587 L2356L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5880-01A-11D-1589-08 chr22:26400726 C>T maps to ENST00000407587 Q2128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NK-01A-11D-A26P-10 chr22:26422671 C>T maps to ENST00000407587 P2246P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A7SQ-01A-12D-A35Z-10 chr22:26286841 G>A maps to ENST00000407587 K1480K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F9-A4JJ-01A-11D-A25F-10 chr12:57440665 G>A maps to NM_005379.2 L174L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-AAVM-01A-11D-A42J-10 chr2:192227006 T>C maps to NM_001130158.1 L225L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7734-01A-11D-2136-08 chr17:1370771 A>C did not map to a codon.
Sequencing variant TCGA-BQ-7061-01A-11D-1961-08 chr15:59501014 G>A maps to NM_004998.2 D465D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9K0-01A-11D-A42J-10 chr15:52699525 C>T maps to ENST00000358212 K303K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-8500-01A-11D-2396-08 chr15:52606370 T>C maps to ENST00000358212 P1813P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-3925-01A-01D-1458-08 chr18:47500736 C>T maps to NM_001080467.2 G435G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr15:52500780 G>T maps to NM_018728.3 L1452L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5902-01A-11D-1589-08 chr11:76867020 C>T maps to NM_000260.3 H118H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8195-01A-31D-2396-08 chr11:76903187 C>T maps to NM_000260.3 N1339N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JS-01A-21D-A42J-10 chr15:72176077 C>G did not map to a codon.
Sequencing variant TCGA-A4-A48D-01A-11D-A25F-10 chr15:72190907 A>G maps to ENST00000424560 P1312P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-3925-01A-01D-1458-08 chr15:72192124 T>G maps to ENST00000424560 R1125R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-A8LD-01A-11D-A35Z-10 chr19:17305946 G>T maps to NM_004145.3 T1237T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A9DE-01A-11D-A36X-10 chr19:17270209 G>A maps to NM_004145.3 K445K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NJ-01A-11D-A26P-10 chr19:17322845 G>A maps to NM_004145.3 T2067T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5902-01A-11D-1589-08 chr1:171605340 G>C maps to NM_000261.1 L413L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr1:59125679 A>G maps to NM_001085487.1 L826L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9J2-01A-11D-A382-10 chr8:41906304 G>T maps to NM_006766.3 S64*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4617-01A-01D-1252-08 chr10:76602896 G>T maps to NM_012330.2 G94G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A7SM-01A-11D-A34Z-10 chr10:76788652 G>A maps to NM_012330.2 E1357E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A655-01A-11D-A31Z-10 chr2:1805512 T>C maps to ENST00000399161 E1077E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NI-01A-11D-A26P-10 chr19:59082639 G>A maps to NM_198055.1 G39G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A656-01A-11D-A31X-10 chr16:48576973 G>A maps to NM_153029.3 P844P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr13:21306118 T>C maps to NM_174928.1 P123P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5Y1-01A-11D-A28G-10 chr23:153198017 C>T did not map to a codon.
Sequencing variant TCGA-UZ-A9PX-01A-11D-A42J-10 chr23:153199831 G>T did not map to a codon.
Sequencing variant TCGA-2Z-A9JL-01A-11D-A42J-10 chr12:112499042 A>G maps to NM_024953.3 N433N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Y8-A897-01A-11D-A35Z-10 chr14:57857992 G>C maps to NM_001011713.2 L106L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9J8-01A-11D-A42J-10 chr4:76841889 C>G did not map to a codon.
Sequencing variant TCGA-B1-A656-01A-11D-A31X-10 chr11:64813974 G>A maps to ENST00000340252 Y592Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5882-01A-11D-1589-08 chr4:164050120 G>A maps to NM_138386.2 P471P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8196-01A-11D-2396-08 chr17:40695934 C>T maps to NM_000263.3 F637F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A40Y-01A-11D-A25F-10 chr13:101881860 T>C maps to NM_052867.2 G503G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A7SM-01A-11D-A34Z-10 chr13:101760141 T>C did not map to a codon.
Sequencing variant TCGA-2Z-A9JT-01A-11D-A42J-10 chr12:76462721 C>A maps to NM_139207.2 E24*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9JW-01A-11D-A42J-10 chr11:2970488 T>G maps to NM_005969.3 *376Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8311-01A-11D-2396-08 chr17:80443513 C>T maps to ENST00000374611 V418V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-A4TM-01A-11D-A31X-10 chr8:18080419 T>C maps to NM_001160176.1 F350F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A71R-01A-12D-A33Q-10 chr17:72768110 A>G maps to NM_015654.3 L159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JR-01A-12D-A42J-10 chr1:201777103 G>T maps to ENST00000367296 A1224A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5890-01A-11D-1589-08 chr1:201781617 G>T maps to ENST00000367296 E1684*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A7SN-01A-11D-A34Z-10 chr11:20065594 A>G maps to ENST00000396087 S1015S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9K8-01A-11D-A42J-10 chr12:78516052 G>A maps to NM_014903.4 P1361P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7584-01A-11D-2136-08 chr12:78604233 C>T maps to NM_014903.4 C2343C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-A8LE-01A-11D-A35Z-10 chr12:78400769 C>A maps to NM_014903.4 V484V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59R-01A-11D-A26P-10 chr12:78591181 G>C did not map to a codon.
Sequencing variant TCGA-SX-A7SN-01A-11D-A34Z-10 chr2:15415751 A>T maps to NM_015909.2 P1860P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-7501-01A-11D-2201-08 chr13:35733739 A>C maps to ENST00000400445 T1144T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AT-A5NU-01A-11D-A28G-10 chr2:203972838 G>A maps to NM_001114132.1 W597*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5890-01A-11D-1589-08 chr3:47032942 G>T maps to NM_015175.1 L230L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PK-01A-11D-A382-10 chr8:90965470 C>T did not map to a codon.
Sequencing variant TCGA-Y8-A8RY-01A-11D-A36X-10 chr17:41341717 T>C maps to NM_005899.3 P198P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7834-01A-11D-2136-08 chr21:22658661 A>T maps to NM_004540.2 R137R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8310-01A-11D-2396-08 chr12:6638742 C>A maps to NM_014865.3 R1213R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59T-01A-21D-A28G-10 chr12:6637491 T>C maps to NM_014865.3 A1099A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W8-01A-11D-A28G-10 chr19:39687742 C>T maps to NM_001001414.1 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F9-A8NY-01A-11D-A35Z-10 chr1:36029000 C>T maps to NM_001014839.1 L528L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A7SP-01A-11D-A34Z-10 chr12:50190028 C>T maps to NM_001037806.3 P538P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7286-01A-11D-2136-08 chr2:24991158 C>T maps to NM_003743.4 L1409L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PJ-A8JU-01A-11D-A35Z-10 chr2:24930360 T>G maps to NM_003743.4 G674G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-A6W5-01A-12D-A33Q-10 chr8:71040936 C>T maps to NM_006540.2 Q1201Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PJ-A8JU-01A-11D-A35Z-10 chr8:71056985 A>G maps to NM_006540.2 P901P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55W-01A-11D-A26P-10 chr20:46254224 G>A maps to NM_181659.2 Q119Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A656-01A-11D-A31X-10 chr10:51585172 G>A maps to NM_001145260.1 K440K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chr10:51586275 A>T maps to NM_001145260.1 V584V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2K-A9WE-01A-11D-A382-10 chr17:15961806 A>C maps to ENST00000395857 V2011V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5Y0-01A-11D-A31X-10 chr17:15971430 T>G maps to ENST00000395857 T1522T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4116-01A-01D-1252-08 chr17:15964733 A>G maps to ENST00000395857 S1969S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr17:16089948 G>C maps to ENST00000395857 S54*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr12:124848290 A>G maps to NM_006312.4 N954N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PS-01A-11D-A42J-10 chr12:124887083 C>T maps to NM_006312.4 Q502Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8310-01A-11D-2396-08 chr17:8350136 T>C maps to ENST00000402554 S157S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4113-01A-01D-1252-08 chr4:115767017 G>A maps to NM_022569.1 I692I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9JW-01A-11D-A42J-10 chr2:240954245 G>A maps to ENST00000404554 V193V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PJ-A5Z9-01A-11D-A28G-10 chr15:41689068 G>A maps to NM_016013.2 H63H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6792-01A-21D-1961-08 chr6:97344646 A>G maps to NM_014165.3 D71D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59T-01A-21D-A28G-10 chr3:179322635 G>A maps to NM_002492.2 S11S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47O-01A-11D-A25F-10 chr9:32571047 G>T maps to NM_002493.3 V61V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-5561-01A-01D-1589-08 chr19:14677077 C>A did not map to a codon.
Sequencing variant TCGA-5P-A9JW-01A-11D-A42J-10 chr8:125562080 T>A maps to NM_005005.2 L163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7288-01A-11D-2136-08 chr11:47605942 G>A maps to NM_004551.2 L235L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-AAVM-01A-11D-A42J-10 chr11:67800584 C>A maps to NM_002496.3 G69G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7045-01A-31D-1961-08 chr21:44317077 T>C maps to NM_021075.3 S30S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JO-01A-11D-A42J-10 chr2:152410530 G>T maps to NM_001164507.1 Y6479*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-5560-01A-01D-1589-08 chr2:152512858 C>T maps to NM_001164507.1 E2101E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr2:152522654 G>T maps to NM_001164507.1 P1660P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59R-01A-11D-A26P-10 chr2:152390039 G>T maps to NM_001164508.1 A7111A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M9-01A-11D-A31X-10 chr2:152382498 G>A maps to NM_001164507.1 V7378V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4104-01A-01D-1458-08 chr10:21309108 G>A maps to NM_213569.2 F62F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JM-01A-12D-A42J-10 chr15:56142778 C>T maps to ENST00000508342 R855R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7734-01A-11D-2136-08 chr15:56208933 G>A maps to ENST00000508342 H32H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5878-01A-11D-1589-08 chr18:55996284 C>A maps to NM_001144967.1 R247R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A71U-01A-12D-A33Q-10 chr18:56050534 A>T maps to NM_001144967.1 K804*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7734-01A-11D-2136-08 chr3:27297797 G>A maps to ENST00000396636 I693I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JE-01A-11D-A42J-10 chr1:211846907 C>A maps to NM_002497.2 G158*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55Z-01A-11D-A26P-10 chr14:75558058 G>A maps to NM_033116.4 R786*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9JW-01A-11D-A42J-10 chr6:31829962 C>T maps to NM_000434.3 Q55Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A656-01A-11D-A31X-10 chr2:233898966 C>T maps to NM_005383.2 L115L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4617-01A-01D-1252-08 chr17:7230248 G>A maps to NM_032442.2 N291N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A57E-01A-11D-A26P-10 chr7:31377934 G>A maps to NM_022728.2 Y316Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9JY-01A-11D-A42J-10 chr10:71332598 T>C maps to NM_020999.3 G67G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr22:30000102 T>G did not map to a codon.
Sequencing variant TCGA-BQ-5875-01A-11D-1589-08 chr22:30038222 C>A maps to NM_181832.2 Y132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5877-01A-11D-1589-08 chr22:30050708 A>T maps to NM_181832.2 K171*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr22:30051665 G>A did not map to a codon.
Sequencing variant TCGA-P4-A5EA-01A-11D-A28G-10 chr22:30057328 G>A did not map to a codon.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr1:204985553 G>T maps to ENST00000367172 E1311*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JR-01A-12D-A42J-10 chr16:69724915 A>T maps to NM_138713.2 P616P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A7SU-01A-11D-A35Z-10 chr16:69687290 C>G maps to NM_138713.2 S322*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PN-01A-11D-A382-10 chr16:68248265 A>G maps to NM_004555.3 S1047S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9KE-01A-11D-A42J-10 chr17:46128720 C>A maps to ENST00000362042 R100R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A7SQ-01A-12D-A35Z-10 chr7:26224562 A>T maps to NM_004289.6 P415P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr10:104156716 C>T maps to NM_001077494.1 D100D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55Z-01A-11D-A26P-10 chr11:129747270 G>A maps to NM_006165.3 D532D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47N-01A-11D-A25F-10 chr9:33319096 C>T maps to NM_002504.4 C626C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3466-01A-01D-1252-08 chr17:47588005 G>T maps to NM_002507.3 V267V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PM-01A-21D-A382-10 chr23:71354533 T>A did not map to a codon.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr3:49463423 C>G maps to NM_032316.3 L105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9K3-01A-11D-A42J-10 chr14:51208397 G>T maps to NM_020921.3 R1784R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5903-01A-11D-1589-08 chr14:51219340 T>A maps to NM_020921.3 T1615T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A854-01A-11D-A34Z-10 chr4:48037630 G>A maps to NM_207330.1 L225L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PJ-A5Z9-01A-11D-A28G-10 chr4:48037861 T>C maps to NM_207330.1 N302N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-7268-01A-11D-2136-08 chr8:99215363 A>T maps to NM_024759.1 I284I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-5561-01A-01D-1589-08 chr9:107531255 T>A maps to NM_018376.2 I128I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59R-01A-11D-A26P-10 chr3:52505968 C>T maps to NM_007184.3 F183F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A854-01A-11D-A34Z-10 chr3:100074090 T>A maps to NM_020202.4 A270A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4116-01A-01D-1252-08 chr20:21376575 G>T maps to NM_033176.1 A346A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9K6-01A-11D-A42J-10 chr4:13543691 G>A maps to NM_001189.3 P309P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PJ-A5Z9-01A-11D-A28G-10 chr4:13545663 G>A maps to NM_001189.3 L125L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PN-01A-11D-A382-10 chr23:5811458 T>G did not map to a codon.
Sequencing variant TCGA-BQ-7058-01A-11D-1961-08 chr17:26490599 A>G maps to NM_016231.4 L261L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5884-01A-11D-1589-08 chr16:3598163 T>C maps to ENST00000448023 L960L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-O9-A75Z-01A-11D-A33Q-10 chr2:32474766 A>G maps to NM_021209.4 S722S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9K0-01A-11D-A42J-10 chr16:57099126 G>A maps to NM_032206.3 V1386V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WN-AB4C-01A-11D-A42J-10 chr17:5461747 G>A maps to NM_033004.3 F756F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JP-01A-11D-A42J-10 chr11:7083572 C>A maps to NM_176822.3 G938G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7837-01A-11D-2136-08 chr19:56539071 C>T maps to NM_153447.4 V491V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5887-01A-11D-1961-08 chr19:55452314 C>T maps to ENST00000446217 S140S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KV-A6GD-01A-11D-A31X-10 chr19:56487642 C>T maps to NM_176811.2 N950N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr11:119051967 T>A did not map to a codon.
Sequencing variant TCGA-P4-A5E8-01A-11D-A28G-10 chr6:142396952 G>A maps to NM_002511.2 F335F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A9DD-01A-11D-A36X-10 chr3:160967298 T>C maps to ENST00000472947 L421L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9JV-01A-12D-A42J-10 chr7:144096176 G>A maps to ENST00000467773 P445P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E6-01A-11D-A28G-10 chr10:96121494 T>C maps to NM_022451.9 K48K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5XZ-01A-11D-A31X-10 chr7:30492405 G>A maps to NM_006092.2 S209S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9K0-01A-11D-A42J-10 chr17:65720228 T>G maps to NM_015462.3 L195*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4A-A93W-01A-11D-A36X-10 chr22:38087325 C>A maps to NM_024313.2 R209R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9KA-01A-11D-A42J-10 chr9:33467721 G>A maps to NM_022917.4 N523N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-A8LD-01A-11D-A35Z-10 chr9:95077664 A>G maps to NM_017948.5 N414N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A7SM-01A-11D-A34Z-10 chr4:2946953 G>A maps to NM_003703.1 L546L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr2:203155145 T>C maps to NM_015934.3 D200D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8517-01A-11D-2396-08 chr19:15303026 G>T maps to NM_000435.2 R141R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NI-01A-11D-A26P-10 chr6:32169042 C>T maps to NM_004557.3 R1330R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr23:100099032 T>C did not map to a codon.
Sequencing variant TCGA-J7-A8I2-01A-12D-A35Z-10 chr11:66190271 C>T maps to NM_178864.3 P186P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr11:108032023 A>G maps to NM_002519.2 S1263S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A857-01A-11D-A34Z-10 chr7:44561796 G>A maps to NM_013389.2 F894F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55Z-01A-11D-A26P-10 chr20:57282246 A>C maps to NM_024663.3 A297A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J7-8537-01A-11D-2396-08 chr17:45669356 A>T maps to NM_006310.3 I432I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A656-01A-11D-A31X-10 chr4:73012853 C>G maps to NM_004885.2 S298S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7963-01B-11D-A28G-10 chr3:132418234 A>T maps to ENST00000393156 I649I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A655-01A-11D-A31Z-10 chr9:35792785 T>C maps to NM_003995.3 S127S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr17:38253600 A>G maps to NM_021724.3 P29P. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-SX-A7SN-01A-11D-A34Z-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-SX-A7SN-01A-11D-A34Z-10 chr17:38249442 A>G maps to NM_021724.3 L580L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-5156-01A-01D-1589-08 chr15:72104833 C>T maps to NM_014249.2 L244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7834-01A-11D-2136-08 chr9:127262608 C>A maps to NM_004959.4 P210P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JM-01A-12D-A42J-10 chr7:107823349 G>A maps to ENST00000379032 F773F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr7:107808821 G>A maps to ENST00000379032 S1071S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8517-01A-11D-2396-08 chr1:52256296 C>A maps to NM_002525.2 E1094*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7834-01A-11D-2136-08 chr21:16337669 A>G maps to NM_003489.3 D948D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9J7-01A-11D-A382-10 chr23:105179165 C>A did not map to a codon.
Sequencing variant TCGA-F9-A8NY-01A-11D-A35Z-10 chr23:105153847 G>C did not map to a codon.
Sequencing variant TCGA-G7-A8LB-01A-11D-A35Z-10 chr23:105199586 G>A did not map to a codon.
Sequencing variant TCGA-B9-A8YI-01A-21D-A36X-10 chr10:33496596 A>G maps to NM_003873.5 F554F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9J3-01A-12D-A382-10 chr2:51255153 G>A maps to ENST00000404971 G86G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PU-01A-11D-A42J-10 chr2:50850544 T>C maps to ENST00000404971 G380G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9K0-01A-11D-A42J-10 chr11:64410175 G>A maps to NM_138734.2 L34L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7585-01A-11D-2136-08 chr5:176696647 C>T maps to NM_022455.4 N1783N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5903-01A-11D-1589-08 chr5:176639041 T>C maps to NM_022455.4 L1214L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5877-01A-11D-1589-08 chr17:44806263 G>A maps to NM_006178.2 Q624Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59R-01A-11D-A26P-10 chr5:6600167 G>A maps to NM_017755.5 T725T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A8YI-01A-21D-A36X-10 chr17:39981891 C>T maps to NM_052935.4 E262E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A772-01A-11D-A33Q-10 chr17:17209882 A>T maps to ENST00000379552 S98S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7287-01A-11D-2136-08 chr1:156843560 C>T maps to NM_002529.3 F329F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NF-01A-11D-A26P-10 chr1:156851383 C>T maps to NM_002529.3 L781L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JQ-01A-11D-A42J-10 chr19:49404085 T>C maps to NM_006184.5 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7836-01A-11D-2136-08 chr1:27271885 T>C maps to NM_006600.2 N249N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7839-01A-11D-2136-08 chr23:51075839 C>T did not map to a codon.
Sequencing variant TCGA-IA-A83S-01A-11D-A34Z-10 chr23:51076121 A>T did not map to a codon.
Sequencing variant TCGA-DW-7839-01A-11D-2136-08 chr23:51239273 G>A did not map to a codon.
Sequencing variant TCGA-GL-A9DE-01A-11D-A36X-10 chr11:71720099 A>G maps to ENST00000393695 H1663H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7834-01A-11D-2136-08 chr1:229631731 G>T maps to NM_018230.2 I294I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr11:47837536 A>G maps to NM_015231.1 S492S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2K-A9WE-01A-11D-A382-10 chr9:131761489 G>T maps to NM_015354.1 T1185T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9J3-01A-12D-A382-10 chr9:131731687 T>C maps to NM_015354.1 S269S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5903-01A-11D-1589-08 chr9:131755474 G>A did not map to a codon.
Sequencing variant TCGA-B9-A8YI-01A-21D-A36X-10 chr3:13383245 A>G did not map to a codon.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr19:50412995 C>T maps to NM_012346.4 T23T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5890-01A-11D-1589-08 chr16:56792501 T>C maps to NM_014669.3 L78L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9J1-01A-11D-A382-10 chr7:23221709 C>T maps to ENST00000413919 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NJ-01A-11D-A26P-10 chr15:41669494 C>T maps to NM_016359.3 Q409*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr23:102337710 C>T did not map to a codon.
Sequencing variant TCGA-IA-A83S-01A-11D-A34Z-10 chr23:108779140 G>A did not map to a codon.
Sequencing variant TCGA-4A-A93W-01A-11D-A36X-10 chr14:24868617 G>T maps to NM_025081.2 E56*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5878-01A-11D-1589-08 chr12:121465529 C>A maps to NM_003733.2 E250*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9J5-01A-21D-A382-10 chr1:228506774 G>A maps to NM_001098623.1 E4774E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-A6W5-01A-12D-A33Q-10 chr1:228468060 A>G maps to NM_001098623.1 V2615V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5902-01A-11D-1589-08 chr1:228473854 G>C maps to NM_001098623.1 R3027R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55Z-01A-11D-A26P-10 chr1:228469851 G>T maps to NM_001098623.1 E2806*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A854-01A-11D-A34Z-10 chr1:228461690 C>T maps to NM_001098623.1 S1786S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A7SM-01A-11D-A34Z-10 chr1:228558812 A>G maps to NM_001098623.1 V6778V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9Q0-01A-12D-A42J-10 chr1:228528465 G>A maps to NM_001098623.1 A5858A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A4EM-01A-11D-A25F-10 chr23:128678969 T>G did not map to a codon.
Sequencing variant TCGA-HE-A5NH-01A-11D-A26P-10 chr9:131256868 T>C maps to NM_153435.1 A675A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PK-01A-11D-A382-10 chr19:464230 A>G maps to NM_182577.2 P161P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AT-A5NU-01A-11D-A28G-10 chr23:123637523 G>T did not map to a codon.
Sequencing variant TCGA-BQ-5876-01A-11D-1589-08 chr23:123518586 G>C did not map to a codon.
Sequencing variant TCGA-EV-5902-01A-11D-1589-08 chr23:123519704 G>T did not map to a codon.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr23:123680888 T>A did not map to a codon.
Sequencing variant TCGA-A4-A5Y1-01A-11D-A28G-10 chr4:183713662 C>T maps to NM_001080477.1 V1946V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9J3-01A-12D-A382-10 chr23:13779313 C>A did not map to a codon.
Sequencing variant TCGA-A4-8517-01A-11D-2396-08 chr7:44747233 T>C maps to ENST00000444676 N965N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PN-01A-11D-A382-10 chr20:61443935 C>A maps to NM_007346.2 A323A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A8YH-01A-11D-A36X-10 chr6:72011550 C>T maps to NM_024576.3 S385S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7287-01A-11D-2136-08 chr23:70782730 C>T did not map to a codon.
Sequencing variant TCGA-Y8-A896-01A-11D-A35Z-10 chr23:70756179 A>C did not map to a codon.
Sequencing variant TCGA-A4-7996-01A-11D-2201-08 chr9:127572162 C>T maps to NM_182487.2 Y477Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4A-A93Y-01A-11D-A36X-10 chr1:161953623 G>T maps to ENST00000451379 Y699*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A40Y-01A-11D-A25F-10 chr1:161989777 C>G maps to ENST00000451379 S123S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9J7-01A-11D-A382-10 chr8:145112995 G>A maps to ENST00000360660 A335A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr7:128415146 C>T maps to NM_001708.2 K138K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5894-01A-11D-1589-08 chr6:47754338 C>A maps to ENST00000489301 I73I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr10:13160993 C>T maps to NM_021980.4 Q245*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A7SQ-01A-12D-A35Z-10 chr11:6867587 T>C maps to ENST00000379831 A229A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A7SP-01A-11D-A34Z-10 chr11:7949414 G>C maps to NM_001004461.1 G265G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr1:158576302 C>T maps to NM_001004478.1 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8196-01A-11D-2396-08 chr14:20666033 C>T maps to NM_001005503.1 T180T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F9-A7VF-01A-11D-A33Q-10 chr14:20711301 G>T maps to NM_001004479.1 G118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55W-01A-11D-A26P-10 chr1:247836181 C>A maps to NM_001005487.1 T54T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-8500-01A-11D-2396-08 chr9:35869822 C>T maps to NM_001004487.1 T192T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PJ-A8JU-01A-11D-A35Z-10 chr17:3119720 C>T maps to NM_014565.2 D269D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UN-AAZ9-01A-11D-A382-10 chr17:3119720 C>T maps to NM_014565.2 D269D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5893-01A-11D-1589-08 chr9:125391499 G>A maps to NM_001004450.1 F105F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A71U-01A-12D-A33Q-10 chr9:125424668 T>G maps to ENST00000373686 V275V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A655-01A-11D-A31Z-10 chr9:125315954 C>T maps to NM_001004457.1 T169T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NK-01A-11D-A26P-10 chr11:6789369 G>T maps to NM_001004490.1 I273I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7836-01A-11D-2136-08 chr1:248129595 A>G maps to NM_001004491.1 G321G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Y8-A896-01A-11D-A35Z-10 chr11:74800263 T>C maps to NM_001005285.1 V165V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5887-01A-11D-1961-08 chr1:247751787 T>C maps to NM_001001915.1 L43L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr1:248112584 G>A maps to NM_001001963.1 L142L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WN-A9G9-01A-12D-A36X-10 chr1:248112663 C>T maps to NM_001001963.1 R169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E6-01A-11D-A28G-10 chr1:248309354 G>A maps to NM_001004690.1 R302R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PV-01A-11D-A42J-10 chr1:248436731 G>A maps to NM_001004695.1 R129*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JD-01A-11D-A42J-10 chr1:248738034 A>C maps to NM_001001821.1 S8S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A69E-01A-11D-A31X-10 chr1:248059781 G>A maps to NM_001001957.2 K298K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-O9-A75Z-01A-11D-A33Q-10 chr1:248059781 G>A maps to NM_001001957.2 K298K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9J2-01A-11D-A382-10 chr11:55371657 C>T maps to NM_001004700.1 L64L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr11:49974075 C>A maps to NM_001001955.2 I34I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A7SL-01A-11D-A34Z-10 chr11:49974861 T>C maps to NM_001001955.2 I296I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A57E-01A-11D-A26P-10 chr11:48347235 C>T maps to NM_001004702.1 Y248Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9K6-01A-11D-A42J-10 chr14:22133688 C>T maps to NM_001001912.1 H131H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A44B-01A-11D-A25F-10 chr15:102346641 G>T maps to NM_001005326.1 L240L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A83T-01A-11D-A34Z-10 chr15:22369315 C>G maps to NM_001004719.2 T247T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A71S-01A-11D-A33Q-10 chr11:4661415 T>C maps to NM_001004751.2 A132A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9JV-01A-12D-A42J-10 chr11:4703536 G>T maps to NM_030774.3 L135L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A7SO-01A-11D-A34Z-10 chr11:4936638 T>A maps to NM_001005238.1 T85T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9J2-01A-11D-A382-10 chr11:5443618 G>T maps to NM_001004757.2 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-A5DJ-01A-11D-A26P-10 chr11:4869478 A>T maps to NM_001004758.1 G320G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A9DC-01A-11D-A36X-10 chr11:4869826 G>A maps to NM_001004758.1 A204A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A855-01A-11D-A34Z-10 chr11:5067976 C>G maps to NM_001001916.2 A74A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr11:6048448 A>G maps to NM_001001917.2 L162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2K-A9WE-01A-11D-A382-10 chr11:6023640 G>A maps to NM_001005179.2 D246D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F9-A7VF-01A-11D-A33Q-10 chr11:56000202 G>A maps to NM_001004746.1 L153L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr1:158735809 G>A maps to NM_001005185.1 I221I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7966-01A-11D-2201-08 chr1:158517502 A>T maps to NM_001005189.1 I131I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chr19:14991894 G>A maps to NM_030901.1 V91V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9J6-01A-11D-A382-10 chr19:9226307 G>A maps to ENST00000293614 L44L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5885-01A-11D-1589-08 chr11:124310918 C>T maps to NM_012378.1 P21P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-7502-01A-11D-2201-08 chr11:124180473 G>T maps to NM_001002917.1 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3473-01A-01D-1252-08 chr11:124135726 C>T maps to ENST00000341493 A300A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A7SU-01A-11D-A35Z-10 chr11:55889938 C>T maps to NM_001005201.1 L31L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5880-01A-11D-1589-08 chr11:55904465 C>T maps to NM_001004064.1 S243S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5877-01A-11D-1589-08 chr2:201790561 C>A maps to NM_006190.4 E382*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A71V-01A-11D-A33Q-10 chr3:125266347 T>C maps to NM_022776.4 V581V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4A-A93W-01A-11D-A36X-10 chr18:21761234 G>T maps to NM_080597.2 S562S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9JY-01A-11D-A42J-10 chr11:3111821 G>C maps to NM_020896.3 L788L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A83W-01A-11D-A34Z-10 chr11:3114203 C>T maps to NM_020896.3 E675E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W8-01A-11D-A28G-10 chr16:83994294 G>A maps to NM_013370.3 W192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7045-01A-31D-1961-08 chr4:109571837 C>T maps to ENST00000512478 F9F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A83T-01A-11D-A34Z-10 chr2:26781379 G>A maps to NM_194248.2 I20I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E7-01A-31D-A28G-10 chr17:72942795 G>A maps to NM_178233.1 A282A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9Q1-01A-11D-A42J-10 chr5:76926469 C>T maps to NM_032109.2 L199L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NF-01A-11D-A26P-10 chr1:20233030 T>C maps to NM_015207.1 N314N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PS-01A-11D-A42J-10 chr1:20220909 A>G maps to NM_015207.1 V140V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JR-01A-12D-A42J-10 chr4:146063414 A>T maps to ENST00000447906 P585P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E6-01A-11D-A28G-10 chr15:31818595 G>A maps to ENST00000382902 S283S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A8YH-01A-11D-A36X-10 chr12:29639177 C>A did not map to a codon.
Sequencing variant TCGA-5P-A9K0-01A-11D-A42J-10 chr2:42990745 G>A maps to NM_148962.4 L192L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7963-01B-11D-A28G-10 chr2:42990998 C>A maps to NM_148962.4 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr8:107718928 T>C maps to NM_001198533.1 L394L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A4ZT-01A-11D-A26P-10 chr3:8809351 G>T maps to NM_000916.3 I174I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A7SP-01A-11D-A34Z-10 chr12:121659898 T>A maps to NM_002560.2 I119I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WN-AB4C-01A-11D-A42J-10 chr23:78216601 G>A did not map to a codon.
Sequencing variant TCGA-2Z-A9J1-01A-11D-A382-10 chr23:1584747 G>C did not map to a codon.
Sequencing variant TCGA-GL-A59R-01A-11D-A26P-10 chr10:74810905 G>A maps to NM_000917.3 Q269*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6792-01A-21D-1961-08 chr8:101719225 C>G did not map to a codon.
Sequencing variant TCGA-PJ-A8JU-01A-11D-A35Z-10 chr8:101717892 A>G maps to NM_002568.3 V537V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5Y1-01A-11D-A28G-10 chr13:25671121 C>T maps to NM_030979.2 Y262Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A44B-01A-11D-A25F-10 chr13:25671121 C>T maps to NM_030979.2 Y262Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-7268-01A-11D-2136-08 chr1:40029529 C>T maps to NM_001135653.1 L506L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-5561-01A-01D-1589-08 chr1:17609567 G>A maps to NM_016233.2 V663V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9JU-01A-11D-A42J-10 chr1:17721467 T>C maps to NM_207421.3 S453S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PO-01A-11D-A382-10 chr19:42804226 C>T maps to NM_001145940.1 V101V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7838-01A-11D-2136-08 chr23:110366493 G>A did not map to a codon.
Sequencing variant TCGA-SX-A7SL-01A-11D-A34Z-10 chr23:110385395 G>A did not map to a codon.
Sequencing variant TCGA-DW-7834-01A-11D-2136-08 chr4:169433374 G>A maps to NM_001166108.1 R240R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Y8-A898-01A-11D-A34Z-10 chr4:169842682 A>G did not map to a codon.
Sequencing variant TCGA-2Z-A9JP-01A-11D-A42J-10 chr12:56718076 C>T did not map to a codon.
Sequencing variant TCGA-BQ-7050-01A-11D-1961-08 chr12:56720459 T>C maps to NM_001127460.2 P401P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A83S-01A-11D-A34Z-10 chr12:56720417 G>A maps to NM_001127460.2 N415N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JG-01A-11D-A42J-10 chr13:28794513 A>G maps to NM_175854.7 P333P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A4EM-01A-11D-A25F-10 chr11:93911575 C>G maps to NM_015368.3 Y121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9K8-01A-11D-A42J-10 chr22:50615491 G>A maps to NM_052839.3 S117S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-3925-01A-01D-1458-08 chr10:135193908 C>T maps to NM_152911.2 G196G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A560-01A-11D-A26P-10 chr5:78941012 C>T maps to NM_173797.3 V273V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59T-01A-21D-A28G-10 chr1:176525850 G>A maps to NM_020318.2 G131G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7286-01A-11D-2136-08 chr20:49367022 T>C maps to NM_032521.2 *373R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-5561-01A-01D-1589-08 chr4:75937686 G>C maps to NM_015393.3 P32P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9K2-01A-11D-A42J-10 chr16:14704667 T>G did not map to a codon.
Sequencing variant TCGA-B1-A656-01A-11D-A31X-10 chr16:14678280 T>C did not map to a codon.
Sequencing variant TCGA-GL-A59T-01A-21D-A28G-10 chr3:122437695 A>G maps to NM_017554.2 T1566T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr3:122436992 C>G maps to NM_017554.2 S1359*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8098-01A-11D-2396-08 chr13:25029239 T>C maps to NM_006437.3 T891T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4104-01A-01D-1458-08 chr22:44564536 C>T maps to NM_001003828.1 T391T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8310-01A-11D-2396-08 chr23:150828199 G>T did not map to a codon.
Sequencing variant TCGA-Y8-A8S0-01A-11D-A36X-10 chr2:242077490 C>T maps to ENST00000358649 T251T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4A-A93W-01A-11D-A36X-10 chr20:21695395 C>T maps to NM_006192.3 F520F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8195-01A-31D-2396-08 chr2:223066672 C>T maps to NM_181459.3 Q470Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4A-A93X-01A-11D-A36X-10 chr7:154738246 G>T maps to NM_007349.3 C1036*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4A-A93X-01A-11D-A36X-10 chr3:52598064 C>T did not map to a codon.
Sequencing variant TCGA-4A-A93X-01A-11D-A36X-10 chr3:52643767 G>A maps to ENST00000296302 R710*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7058-01A-11D-1961-08 chr3:52584608 A>T maps to ENST00000296302 Y1575*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7061-01A-11D-1961-08 chr3:52651554 C>T did not map to a codon.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr11:66636375 G>T maps to NM_022172.2 Y321*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr2:70314949 A>G maps to NM_006196.3 V25V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PS-01A-11D-A42J-10 chr2:70315517 G>T maps to NM_006196.3 E215*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F9-A4JJ-01A-11D-A25F-10 chr23:91133624 C>A did not map to a codon.
Sequencing variant TCGA-BQ-5877-01A-11D-1589-08 chr10:55626410 G>A maps to NM_001142763.1 A1241A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5878-01A-11D-1589-08 chr10:55583105 G>C maps to NM_001142763.1 L1467L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-3925-01A-01D-1458-08 chr4:138450854 G>A maps to NM_019035.3 H796H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F9-A7VF-01A-11D-A33Q-10 chr4:138452945 C>T maps to NM_019035.3 Q99Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A7SN-01A-11D-A34Z-10 chr13:61986119 C>T maps to NM_022843.3 Q704Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A857-01A-11D-A34Z-10 chr5:140236455 G>T maps to NM_018901.2 E275*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A9DC-01A-11D-A36X-10 chr5:140256289 C>T maps to NM_018903.2 S411S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AT-A5NU-01A-11D-A28G-10 chr5:140176264 C>A maps to NM_018905.2 T572T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3473-01A-01D-1252-08 chr5:140188709 C>T maps to NM_018907.2 R646R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr5:140222315 G>C maps to NM_018911.2 P470P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8196-01A-11D-2396-08 chr5:140223200 G>A maps to NM_018911.2 P765P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7828-01A-11D-2136-08 chr5:140307712 A>G maps to NM_018898.3 Q412Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Y8-A896-01A-11D-A35Z-10 chr5:140431588 C>T maps to NM_013340.2 F178F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JL-01A-11D-A42J-10 chr5:140573696 G>C maps to NM_018930.3 L524L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7840-01A-11D-2136-08 chr5:140605206 G>C maps to NM_018934.2 A710A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PN-01A-11D-A382-10 chr5:140626522 C>T maps to NM_018935.2 F459F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F9-A7Q0-01A-11D-A35Z-10 chr5:140476410 A>C maps to NM_018936.2 A679A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Y8-A894-01A-11D-A35Z-10 chr5:140476410 A>C maps to NM_018936.2 A679A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5886-01A-11D-1589-08 chr5:140481177 T>C maps to NM_018937.2 Y315Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr5:140502470 G>T maps to NM_018938.2 T297T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WN-A9G9-01A-12D-A36X-10 chr5:140554080 C>T maps to NM_018940.2 N555N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JE-01A-11D-A42J-10 chr5:140712542 G>A maps to NM_018912.2 R764R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-5156-01A-01D-1589-08 chr5:140712437 A>G maps to NM_018912.2 G729G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5891-01A-11D-1589-08 chr5:140711927 G>A maps to NM_018912.2 A559A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A7SM-01A-11D-A34Z-10 chr5:140710445 C>G maps to NM_018912.2 R65R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8196-01A-11D-2396-08 chr5:140811804 G>A maps to NM_003735.2 E493E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-O9-A75Z-01A-11D-A33Q-10 chr5:140811390 G>T maps to NM_003735.2 S355S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-A8LE-01A-11D-A35Z-10 chr5:140718666 C>G maps to NM_018915.2 S43S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8098-01A-11D-2396-08 chr5:140724209 A>T maps to NM_018916.3 K204*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8517-01A-11D-2396-08 chr5:140724919 G>T maps to NM_018916.3 L440L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A71R-01A-12D-A33Q-10 chr5:140736032 A>T maps to NM_018917.2 V422V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A655-01A-11D-A31Z-10 chr5:140745639 C>T maps to NM_018918.2 S581S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7841-01A-11D-2136-08 chr5:140753887 C>T maps to NM_018919.2 R80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A7SS-01A-11D-A35Z-10 chr5:140751853 C>A maps to NM_018924.2 T631T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JE-01A-11D-A42J-10 chr5:140769787 C>T maps to NM_003736.2 C779C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9J2-01A-11D-A382-10 chr5:140797587 A>C maps to NM_018927.2 L54L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6135-01A-11D-1961-08 chr5:140856168 C>A maps to NM_002588.2 P162P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8098-01A-11D-2396-08 chr11:82877723 A>G maps to NM_015885.3 K595K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8196-01A-11D-2396-08 chr11:82877726 A>G maps to NM_015885.3 R596R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NL-01A-11D-A26P-10 chr20:56140805 C>A maps to NM_002591.3 P605P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A83S-01A-11D-A34Z-10 chr20:56137812 C>A maps to NM_002591.3 I156I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9JW-01A-11D-A42J-10 chr7:82465002 G>A maps to NM_033026.5 V4743V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47O-01A-11D-A25F-10 chr7:82544314 A>G maps to NM_033026.5 S4329S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7045-01A-31D-1961-08 chr7:82532015 A>G maps to NM_033026.5 P4493P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2K-A9WE-01A-11D-A382-10 chr14:71493570 A>G maps to NM_014982.2 Q1146Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A83S-01A-11D-A34Z-10 chr14:71524367 C>G maps to NM_014982.2 L1593L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JS-01A-21D-A42J-10 chr5:95761538 A>G maps to NM_000439.4 N127N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Y8-A8RZ-01A-11D-A36X-10 chr20:17462588 C>T maps to NM_002594.2 A597A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4103-01A-01D-1458-08 chr3:195974372 G>A maps to NM_005017.2 L117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A655-01A-11D-A31Z-10 chr17:79865646 A>G did not map to a codon.
Sequencing variant TCGA-A4-A6HP-01A-11D-A31X-10 chr10:112655818 A>G maps to NM_014456.4 K441K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9J1-01A-11D-A382-10 chr3:33894164 A>G maps to NM_001162429.1 G614G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7734-01A-11D-2136-08 chr9:125582791 G>A maps to NM_005388.4 Q160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8196-01A-11D-2396-08 chr7:31877506 C>T maps to NM_001191057.1 K353K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JL-01A-11D-A42J-10 chr19:10578236 G>T maps to NM_001111307.1 G867G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr10:95380725 C>A maps to NM_006204.3 R238R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WN-A9G9-01A-12D-A36X-10 chr15:85652312 A>C maps to NM_002605.2 R356R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PN-01A-11D-A382-10 chr11:35006232 T>C maps to NM_003477.2 D380D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A7SL-01A-11D-A34Z-10 chr3:122880181 T>C maps to NM_006810.3 A453A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6134-01A-11D-1961-08 chr2:10927528 A>T maps to ENST00000381611 L397L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JO-01A-11D-A42J-10 chr16:20371930 G>A maps to NM_174924.1 L489L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr16:20376784 G>A maps to NM_174924.1 N398N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W8-01A-11D-A28G-10 chr5:131602210 C>T maps to NM_003687.3 H100H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5DU-01A-11D-A28G-10 chr8:94934632 C>T maps to NM_001161778.1 Q175*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Y8-A898-01A-11D-A34Z-10 chr1:13910572 G>T maps to NM_006474.4 S91S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-A8LB-01A-11D-A35Z-10 chr16:70190775 G>C maps to NM_017990.3 G878G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr5:31983431 C>G maps to NM_178140.2 T216T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr5:32108144 G>A maps to NM_178140.2 L2808L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E6-01A-11D-A28G-10 chr10:119134717 G>T maps to NM_173791.3 I7I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3468-01A-01D-1252-08 chr3:73432827 C>T maps to NM_015009.1 A963A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4113-01A-01D-1252-08 chr12:41585334 C>T maps to NM_001164595.1 R242*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7842-01A-11D-2136-08 chr1:160181402 C>A maps to ENST00000368075 L44L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Y8-A897-01A-11D-A35Z-10 chr1:156878560 C>T maps to NM_001080471.1 C410C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5892-01A-11D-1589-08 chr6:4128066 T>A did not map to a codon.
Sequencing variant TCGA-BQ-5884-01A-11D-1589-08 chr1:32100868 T>C maps to NM_012392.3 P93P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7834-01A-11D-2136-08 chr1:32100954 C>A maps to NM_012392.3 G65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7841-01A-11D-2136-08 chr17:4575081 C>T maps to ENST00000301396 E1212E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr17:8047042 T>G maps to NM_002616.2 P871P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UN-AAZ9-01A-11D-A382-10 chr17:8045217 G>A maps to NM_002616.2 Q1169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr2:239184525 A>C maps to NM_022817.2 S102S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-A8LD-01A-11D-A35Z-10 chr2:239164454 C>T maps to NM_022817.2 K721K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A4EM-01A-11D-A25F-10 chr2:239162230 G>A maps to NM_022817.2 T811T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A856-01A-11D-A34Z-10 chr2:239155117 T>A maps to NM_022817.2 P1222P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr7:92151472 A>G maps to NM_000466.2 N72N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5885-01A-11D-1589-08 chr7:92119226 T>C did not map to a codon.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr1:2341813 A>C maps to NM_153818.1 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8311-01A-11D-2396-08 chr1:10678474 G>A did not map to a codon.
Sequencing variant TCGA-UZ-A9PZ-01A-11D-A42J-10 chr8:77896128 G>A maps to NM_001172087.1 Q96*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3466-01A-01D-1252-08 chr3:48577176 C>A maps to NM_004567.2 E136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3472-01A-01D-1252-08 chr21:45743722 C>T maps to NM_002626.4 I524I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JL-01A-11D-A42J-10 chr12:48536587 A>T maps to NM_001166686.1 S630S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5875-01A-11D-1589-08 chr12:48538848 C>A maps to NM_001166686.1 A747A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9J3-01A-12D-A382-10 chr5:176827427 C>T maps to NM_001029886.2 V50V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F9-A8NY-01A-11D-A35Z-10 chr23:77225037 G>A did not map to a codon.
Sequencing variant TCGA-5P-A9K0-01A-11D-A42J-10 chr6:41704736 G>A maps to NM_002630.3 N340N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A40Y-01A-11D-A25F-10 chr19:15587342 G>T maps to NM_052890.3 T46T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4114-01A-01D-1252-08 chr1:153279660 G>C maps to NM_052891.1 Y46*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2K-A9WE-01A-11D-A382-10 chr1:33841053 G>T maps to ENST00000419414 C29*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F9-A97G-01A-11D-A382-10 chr3:169831154 A>T maps to NM_024947.3 I782I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JL-01A-11D-A42J-10 chr13:50087268 A>C maps to NM_001040443.1 S97S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JM-01A-12D-A42J-10 chr17:27234649 A>T maps to NM_001033561.1 C833*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Y8-A8RY-01A-11D-A36X-10 chr17:27251299 C>T maps to NM_001033561.1 E114E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A8YI-01A-21D-A36X-10 chr23:46898380 C>G did not map to a codon.
Sequencing variant TCGA-MH-A856-01A-11D-A34Z-10 chr4:129793110 T>A maps to NM_199320.2 P741P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9J2-01A-11D-A382-10 chr9:96421818 C>T maps to NM_005392.3 L422L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PZ-01A-11D-A42J-10 chr9:96435950 G>C maps to NM_005392.3 L811L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JP-01A-11D-A42J-10 chr8:133823300 A>G maps to ENST00000395386 A287A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A8YH-01A-11D-A36X-10 chr6:64395140 G>A maps to NM_015153.2 P506P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PJ-A8JU-01A-11D-A35Z-10 chr6:79655790 C>T maps to NM_017934.5 E1519E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7732-01A-11D-2136-08 chr23:71829513 C>T did not map to a codon.
Sequencing variant TCGA-B9-7268-01A-11D-2136-08 chr23:71822084 T>C did not map to a codon.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr23:71886082 G>A did not map to a codon.
Sequencing variant TCGA-PJ-A5Z9-01A-11D-A28G-10 chr23:71802351 G>A did not map to a codon.
Sequencing variant TCGA-A4-8312-01A-11D-2396-08 chr23:18972369 A>G did not map to a codon.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr23:18919657 C>A did not map to a codon.
Sequencing variant TCGA-F9-A8NY-01A-11D-A35Z-10 chr12:76424605 G>A maps to NM_007350.3 Q306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A7SQ-01A-12D-A35Z-10 chr12:76424939 C>T maps to NM_007350.3 Q194Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9J1-01A-11D-A382-10 chr11:118498945 C>T maps to NM_015157.2 L469L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9JY-01A-11D-A42J-10 chr11:605691 C>T maps to ENST00000264555 P474P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A71U-01A-12D-A33Q-10 chr9:131702759 C>A maps to NM_001100876.1 I190I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A654-01A-11D-A31X-10 chr10:60936660 C>A maps to NM_032439.3 P16P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr4:25235820 C>A maps to NM_018323.3 S12S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NF-01A-11D-A26P-10 chr22:21119516 C>T maps to NM_058004.2 W757*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5876-01A-11D-1589-08 chr15:68479998 T>C maps to NM_016166.1 S594S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A8YI-01A-21D-A36X-10 chr4:514957 A>C maps to NM_001127178.1 R410R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-7501-01A-11D-2201-08 chr1:207105816 C>G maps to NM_002644.3 R664R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4115-01A-01D-1252-08 chr1:27121058 C>T maps to NM_017837.2 F178F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4116-01A-01D-1252-08 chr3:196675119 A>T maps to NM_025163.2 L216L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PZ-01A-11D-A42J-10 chr19:49950662 C>T maps to NM_017916.2 S181S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9KE-01A-11D-A42J-10 chr11:17124354 G>T maps to NM_002645.2 S1235S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-A5DJ-01A-11D-A26P-10 chr12:18478008 C>T maps to NM_004570.4 L417L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5902-01A-11D-1589-08 chr3:138456587 T>C maps to NM_006219.1 V254V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9K0-01A-11D-A42J-10 chr1:9781588 G>A maps to ENST00000361110 L657L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr5:67576766 T>G maps to ENST00000396611 T283T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5902-01A-11D-1589-08 chr5:67588177 A>G maps to ENST00000396611 G336G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4104-01A-01D-1458-08 chr19:18279616 G>A maps to NM_005027.2 T630T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9JU-01A-11D-A42J-10 chr2:209150549 T>C maps to NM_015040.3 D238D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E8-01A-11D-A28G-10 chr7:99972036 C>T maps to NM_013439.2 T145T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5878-01A-11D-1589-08 chr10:23003186 G>A maps to NM_005028.4 F23F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8098-01A-11D-2396-08 chr17:65665780 T>C did not map to a codon.
Sequencing variant TCGA-B1-A657-01A-11D-A31X-10 chr11:67267650 G>A maps to NM_004910.2 P294P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5890-01A-11D-1589-08 chr11:67265786 G>A maps to NM_004910.2 S497S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5876-01A-11D-1589-08 chr12:123479958 C>T maps to NM_020845.2 Q677Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7061-01A-11D-1961-08 chr17:6375989 C>T maps to NM_031220.3 Q472Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-A4TM-01A-11D-A31X-10 chr11:94341804 C>T maps to NM_152431.2 D632D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8311-01A-11D-2396-08 chr16:2155891 A>G maps to NM_001009944.2 L2613L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-5156-01A-01D-1589-08 chr16:2155891 A>G maps to NM_001009944.2 L2613L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr16:2155891 A>G maps to NM_001009944.2 L2613L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WN-AB4C-01A-11D-A42J-10 chr7:47832363 A>T maps to NM_138295.3 L2796*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PS-01A-11D-A42J-10 chr16:81219236 C>A maps to NM_052892.3 L619L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F9-A7VF-01A-11D-A33Q-10 chr5:137271568 C>G maps to ENST00000230643 Y585*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JL-01A-11D-A42J-10 chr22:46658025 G>T maps to NM_006071.1 V398V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59T-01A-21D-A28G-10 chr22:46654193 G>A maps to NM_006071.1 Q1676*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9JW-01A-11D-A42J-10 chr6:51889837 G>C maps to NM_138694.3 L1590L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7996-01A-11D-2201-08 chr6:51930864 A>G maps to NM_138694.3 S263S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5890-01A-11D-1589-08 chr6:51882413 G>A maps to NM_138694.3 F1798F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A40Y-01A-11D-A25F-10 chr6:51889789 G>A maps to NM_138694.3 V1606V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Y8-A8S1-01A-11D-A36X-10 chr6:51924821 G>A maps to NM_138694.3 F379F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7734-01A-11D-2136-08 chr8:110420392 G>C maps to ENST00000426474 G643G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr8:110451258 G>A maps to ENST00000426474 K1298K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr9:131482022 C>A maps to NM_013355.3 P728P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JN-01A-21D-A42J-10 chr12:32949083 G>T maps to NM_004572.3 T816T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A772-01A-11D-A33Q-10 chr12:33003715 A>T maps to NM_004572.3 T454T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9J6-01A-11D-A382-10 chr2:159477604 A>G maps to NM_003628.3 P128P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A772-01A-11D-A33Q-10 chr2:159488406 T>A maps to NM_003628.3 T432T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JD-01A-11D-A42J-10 chr11:63342506 G>A maps to NM_001128203.1 V133V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr9:26925950 C>A maps to NM_001031689.2 V247V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Y8-A8S0-01A-11D-A36X-10 chr21:42551432 G>A maps to NM_182832.2 P41P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr20:30784821 C>A maps to NM_002657.3 T308T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NI-01A-11D-A26P-10 chr20:8608960 T>G maps to NM_015192.2 L89L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PR-01A-11D-A42J-10 chr20:8626783 C>T maps to NM_015192.2 N140N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-3925-01A-01D-1458-08 chr15:40594159 T>A maps to NM_004573.2 K194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A656-01A-11D-A31X-10 chr11:64034707 C>T maps to NM_000932.2 Q1156*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr10:95849075 A>G maps to NM_001165979.1 V75V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-AAVM-01A-11D-A42J-10 chr16:81965132 C>G maps to NM_002661.2 S871S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M8-01A-11D-A31X-10 chr1:2418422 G>A maps to NM_014638.2 G298G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9J7-01A-11D-A382-10 chr23:205413 A>C did not map to a codon.
Sequencing variant TCGA-BQ-5889-01A-11D-1589-08 chr3:111432756 C>T maps to ENST00000312791 P216P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr3:171394618 G>A maps to NM_002662.3 F667F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr3:171395428 G>A maps to NM_002662.3 T641T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9K3-01A-11D-A42J-10 chr14:105395667 C>T maps to NM_138790.2 Q165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W8-01A-11D-A28G-10 chr8:145001216 C>T maps to NM_201380.2 A1428A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5875-01A-11D-1589-08 chr8:144998456 C>T maps to NM_201380.2 L2017L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A856-01A-11D-A34Z-10 chr8:144997604 G>A maps to NM_201380.2 D2301D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-AAVM-01A-11D-A42J-10 chr8:144997631 C>G maps to NM_201380.2 A2292A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PX-01A-11D-A42J-10 chr8:144995291 G>T maps to NM_201380.2 S3036S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J7-A8I2-01A-12D-A35Z-10 chr2:179358604 G>T maps to NM_019091.3 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9J3-01A-12D-A382-10 chr19:49341322 G>T maps to NM_020904.2 L676L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F9-A97G-01A-11D-A382-10 chr11:16812447 C>A maps to ENST00000448080 S984S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4A-A93X-01A-11D-A36X-10 chr7:30092324 G>A maps to ENST00000440706 R239R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55Z-01A-11D-A26P-10 chr7:30094388 T>C maps to ENST00000440706 T313T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-AAVM-01A-11D-A42J-10 chr8:96167019 T>A maps to NM_024613.3 *250K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F9-A97G-01A-11D-A382-10 chr14:65208229 C>G maps to ENST00000394691 L665L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9K3-01A-11D-A42J-10 chr1:6529205 C>T maps to NM_198681.2 E792E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9Q1-01A-11D-A42J-10 chr1:6556603 C>T maps to NM_198681.2 K31K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4116-01A-01D-1252-08 chr17:40821476 C>A maps to NM_024927.4 E726*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-AAVL-01A-11D-A42J-10 chr17:40823572 G>T maps to NM_024927.4 T360T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NK-01A-11D-A26P-10 chr9:19126157 C>A maps to NM_001122.2 V60V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NI-01A-11D-A26P-10 chr19:4511772 G>A maps to NM_001080400.1 V719V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W9-01A-11D-A28G-10 chr4:128813595 T>C maps to NM_014264.4 Y705Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4A-A93W-01A-11D-A36X-10 chr3:145806424 A>T maps to NM_182943.2 L318*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7288-01A-11D-2136-08 chr3:145803002 A>T maps to NM_182943.2 V395V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PM-01A-21D-A382-10 chr3:145841933 A>G maps to NM_182943.2 Y64Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7584-01A-11D-2136-08 chr4:155465647 T>C maps to NM_002669.2 K181K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr4:155470081 T>C maps to NM_002669.2 V5V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr23:114883785 G>C did not map to a codon.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr3:146167109 C>T maps to ENST00000497985 K249K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3472-01A-01D-1252-08 chr20:44534918 G>A maps to NM_006227.2 D231D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A561-01A-11D-A26P-10 chr20:44539885 C>T maps to NM_006227.2 K35K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A9DC-01A-11D-A36X-10 chr1:208390904 G>A maps to NM_025179.3 Y121Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5Y1-01A-11D-A28G-10 chr23:153700939 C>T did not map to a codon.
Sequencing variant TCGA-2Z-A9J5-01A-21D-A382-10 chr7:131815330 G>T maps to NM_020911.1 I1864I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9J5-01A-21D-A382-10 chr3:48464320 G>A maps to NM_001130082.1 H381H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7062-01A-11D-1961-08 chr3:48459372 C>A maps to NM_001130082.1 T1107T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A71U-01A-12D-A33Q-10 chr3:48463584 A>G maps to NM_001130082.1 A483A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Y8-A898-01A-11D-A34Z-10 chr3:48461648 T>A maps to NM_001130082.1 P682P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A9DE-01A-11D-A36X-10 chr22:50722098 G>A maps to NM_012401.2 D834D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PJ-A5Z8-01A-11D-A28G-10 chr22:50716443 T>C did not map to a codon.
Sequencing variant TCGA-A4-8098-01A-11D-2396-08 chr23:153037077 G>C did not map to a codon.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr12:94613896 C>A maps to NM_005761.1 R554R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KV-A6GE-01A-11D-A31X-10 chr3:129281630 A>G maps to NM_015103.2 L1608L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A40Y-01A-11D-A25F-10 chr6:89859123 T>A maps to NM_001010853.1 A202A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A40U-01A-11D-A25F-10 chr1:156209391 A>C maps to NM_007221.3 *206C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A657-01A-11D-A31X-10 chr15:74325642 G>A maps to NM_033238.2 K515K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr15:74327952 G>A maps to NM_033239.2 R717R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A656-01A-11D-A31X-10 chr23:152937047 G>C did not map to a codon.
Sequencing variant TCGA-G7-6790-01A-11D-1961-08 chr23:152937463 A>T did not map to a codon.
Sequencing variant TCGA-5P-A9K8-01A-11D-A42J-10 chr6:160239628 C>T maps to NM_173516.1 D389D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A57E-01A-11D-A26P-10 chr10:118357346 T>C maps to NM_006229.2 D194D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-A5DJ-01A-11D-A26P-10 chr6:36238385 G>A maps to ENST00000457797 A50A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A772-01A-11D-A33Q-10 chr23:7894061 C>G did not map to a codon.
Sequencing variant TCGA-UZ-A9PP-01A-11D-A42J-10 chr23:7868820 A>G did not map to a codon.
Sequencing variant TCGA-A4-8098-01A-11D-2396-08 chr19:7615222 G>A maps to NM_001166111.1 A627A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F9-A8NY-01A-11D-A35Z-10 chr9:140356048 G>T maps to NM_001098537.1 S1260S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NH-01A-11D-A26P-10 chr2:55863461 C>T maps to NM_033109.3 S754S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NI-01A-11D-A26P-10 chr6:89793800 T>C maps to NM_006813.2 P290P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8098-01A-11D-2396-08 chr5:74981181 G>C maps to NM_001099271.1 S419S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JD-01A-11D-A42J-10 chr19:14063933 G>T maps to NM_001146254.1 T5T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W9-01A-11D-A28G-10 chr19:14044011 G>A maps to NM_024825.3 L349L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9J1-01A-11D-A382-10 chr7:131241028 G>C maps to NM_001018111.2 P30P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6790-01A-11D-1961-08 chr3:127379598 T>A maps to NM_015720.2 L243*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47M-01A-11D-A25F-10 chr1:151381039 G>A maps to NM_015100.3 S693S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A44B-01A-11D-A25F-10 chr23:24744125 T>A did not map to a codon.
Sequencing variant TCGA-HE-A5NJ-01A-11D-A26P-10 chr23:24750525 T>A did not map to a codon.
Sequencing variant TCGA-Y8-A8RZ-01A-11D-A36X-10 chr12:133252403 A>G maps to ENST00000455752 A341A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9J5-01A-21D-A382-10 chr15:89870190 A>G maps to NM_002693.2 L513L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PS-01A-11D-A42J-10 chr15:89861980 C>G did not map to a codon.
Sequencing variant TCGA-2Z-A9JT-01A-11D-A42J-10 chr10:103343262 A>C did not map to a codon.
Sequencing variant TCGA-UZ-A9PP-01A-11D-A42J-10 chr2:86297160 G>A maps to NM_015425.3 Q616*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JQ-01A-11D-A42J-10 chr9:37500882 G>T maps to NM_022490.1 L311L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E7-01A-31D-A28G-10 chr17:7404999 G>A maps to NM_000937.4 K767K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chr4:57891053 A>G maps to NM_000938.1 V989V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NL-01A-11D-A26P-10 chr16:57503975 G>A maps to NM_032940.2 G181G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PM-01A-21D-A382-10 chr16:57499933 G>C did not map to a codon.
Sequencing variant TCGA-BQ-5875-01A-11D-1589-08 chr11:840427 G>A maps to NM_021128.4 L50L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A83S-01A-11D-A34Z-10 chr10:79744980 G>A maps to NM_007055.3 I1063I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-AAVL-01A-11D-A42J-10 chr7:100304639 C>T maps to NM_005837.2 Q63*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A654-01A-11D-A31X-10 chr7:75615289 T>C maps to NM_000941.2 D573D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5876-01A-11D-1589-08 chr22:16287579 G>T maps to NM_001136213.1 C102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Y8-A8RY-01A-11D-A36X-10 chr1:167343521 C>T maps to NM_002697.3 Q194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9K2-01A-11D-A42J-10 chr6:99283831 C>A maps to NM_005604.2 I361I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JQ-01A-11D-A42J-10 chr4:147560483 C>A maps to NM_004575.2 G64G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JS-01A-21D-A42J-10 chr4:147560483 C>A maps to NM_004575.2 G64G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-7332-01A-11D-2136-08 chr4:147561824 C>T maps to NM_004575.2 A365A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-A8LE-01A-11D-A35Z-10 chr4:147560483 C>A maps to NM_004575.2 G64G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A71V-01A-11D-A33Q-10 chr5:145719331 C>T maps to NM_002700.2 G114G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9KE-01A-11D-A42J-10 chr5:93076951 G>C maps to NM_153216.1 A106A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4114-01A-01D-1252-08 chr5:93076681 A>T maps to NM_153216.1 L196L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7838-01A-11D-2136-08 chr7:39446254 C>T maps to NM_007252.3 S314S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E6-01A-11D-A28G-10 chr7:39500161 G>T maps to NM_007252.3 A473A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A7SL-01A-11D-A34Z-10 chr19:10218530 G>C did not map to a codon.
Sequencing variant TCGA-2Z-A9J7-01A-11D-A382-10 chr5:54771138 G>A maps to NM_003711.2 F66F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7061-01A-11D-1961-08 chr6:35392131 A>C maps to NM_006238.4 T218T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A7SR-01A-12D-A35Z-10 chr6:35387919 C>A maps to NM_006238.4 S49S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A657-01A-11D-A31X-10 chr3:12447396 G>C maps to NM_015869.4 R212R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JK-01A-11D-A42J-10 chr4:23886467 A>G maps to NM_013261.3 D47D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PX-01A-11D-A42J-10 chr4:23833338 T>A maps to NM_013261.3 A90A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4116-01A-01D-1252-08 chr12:81661719 A>G maps to NM_003625.2 L1153L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8098-01A-11D-2396-08 chr1:203025586 C>A maps to ENST00000367238 R710R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7839-01A-11D-2136-08 chr12:27787952 T>C maps to NM_003622.3 L59L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JL-01A-11D-A42J-10 chr11:7660961 G>A did not map to a codon.
Sequencing variant TCGA-SX-A71U-01A-12D-A33Q-10 chr12:42768781 T>C maps to NM_016488.6 D139D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7734-01A-11D-2136-08 chr15:64454354 T>C did not map to a codon.
Sequencing variant TCGA-IZ-8196-01A-11D-2396-08 chr5:122359695 T>A maps to NM_000943.4 T171T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F9-A7VF-01A-11D-A33Q-10 chr4:159634383 C>A maps to NM_005038.2 E261*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-AAVL-01A-11D-A42J-10 chr16:4933990 G>C maps to NM_002705.4 S1555S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5DU-01A-11D-A28G-10 chr2:44457730 T>C maps to NM_002706.4 S438S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7585-01A-11D-2136-08 chr17:58740445 G>T maps to NM_003620.3 E451*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A4ZT-01A-11D-A26P-10 chr17:56833453 G>A maps to NM_014906.3 E32E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A4ZT-01A-11D-A26P-10 chr17:56833456 G>C maps to NM_014906.3 P33P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47N-01A-11D-A25F-10 chr17:56833456 G>C maps to NM_014906.3 P33P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NJ-01A-11D-A26P-10 chr17:56833453 G>A maps to NM_014906.3 E32E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NJ-01A-11D-A26P-10 chr17:56833456 G>C maps to NM_014906.3 P33P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NK-01A-11D-A26P-10 chr17:56833453 G>A maps to NM_014906.3 E32E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NK-01A-11D-A26P-10 chr17:56833456 G>C maps to NM_014906.3 P33P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NK-01A-11D-A26P-10 chr17:56833489 G>A maps to NM_014906.3 E44E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NL-01A-11D-A26P-10 chr17:56833453 G>A maps to NM_014906.3 E32E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NL-01A-11D-A26P-10 chr17:56833456 G>C maps to NM_014906.3 P33P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A40U-01A-11D-A25F-10 chr17:56833456 G>C maps to NM_014906.3 P33P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PO-01A-11D-A382-10 chr17:56833453 G>A maps to NM_014906.3 E32E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PO-01A-11D-A382-10 chr17:56833456 G>C maps to NM_014906.3 P33P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PO-01A-11D-A382-10 chr17:56833489 G>A maps to NM_014906.3 E44E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chr3:52282682 C>T maps to NM_144641.2 L154L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WN-AB4C-01A-11D-A42J-10 chr11:67168587 A>G maps to NM_001008709.1 F57F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9K3-01A-11D-A42J-10 chr12:80182550 A>G maps to NM_001143885.1 S893S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WN-AB4C-01A-11D-A42J-10 chr1:202464696 G>C did not map to a codon.
Sequencing variant TCGA-Y8-A8S0-01A-11D-A36X-10 chr1:202418131 C>G maps to ENST00000367270 S561S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3468-01A-01D-1252-08 chr19:55603616 G>C maps to NM_017607.2 L711L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PK-01A-11D-A382-10 chr19:49376933 A>T maps to NM_014330.3 I148I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A657-01A-11D-A31X-10 chr1:204379051 A>G maps to NM_032833.3 I496I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7062-01A-11D-1961-08 chr20:37536821 G>T maps to NM_015568.2 E394*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A7SU-01A-11D-A35Z-10 chr3:195250520 C>T maps to NM_006241.4 E124E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JN-01A-21D-A42J-10 chr8:8998921 C>T maps to NM_024607.2 S80S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9K0-01A-11D-A42J-10 chr23:49126753 T>A did not map to a codon.
Sequencing variant TCGA-UZ-A9PN-01A-11D-A382-10 chr23:49143254 G>A did not map to a codon.
Sequencing variant TCGA-SX-A7SM-01A-11D-A34Z-10 chr1:28157384 G>C maps to NM_014110.4 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F9-A8NY-01A-11D-A35Z-10 chr7:94540402 T>G maps to NM_001166160.1 A326A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-AAVM-01A-11D-A42J-10 chr8:30651546 T>A maps to NM_001009552.1 G208G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A83W-01A-11D-A34Z-10 chr8:26220332 G>A maps to NM_001177591.1 R267R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr3:135825107 T>C maps to NM_002718.4 A1091A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-AAVL-01A-11D-A42J-10 chr14:35579745 A>G maps to NM_017917.2 D92D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr14:102323021 G>A did not map to a codon.
Sequencing variant TCGA-GL-A9DE-01A-11D-A36X-10 chr18:9570629 A>T maps to NM_001042388.1 T366T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PS-01A-11D-A42J-10 chr14:94722853 T>C maps to NM_058237.1 D641D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A7SR-01A-12D-A35Z-10 chr9:127916019 A>T maps to NM_001123355.1 L191*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JG-01A-11D-A42J-10 chr1:244849927 T>A maps to NM_016076.3 I24I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A71S-01A-11D-A33Q-10 chr6:32122817 G>T maps to NM_138717.1 G71G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A57E-01A-11D-A26P-10 chr1:12835788 C>T maps to NM_001080830.1 R131*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59T-01A-21D-A28G-10 chr11:82560213 T>C maps to NM_199418.2 P287P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PJ-A5Z8-01A-11D-A28G-10 chr21:43241556 C>T maps to NM_022115.3 L1008L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JP-01A-11D-A42J-10 chr1:3334462 C>G maps to NM_022114.3 S921S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J7-8537-01A-11D-2396-08 chr1:3334450 C>T maps to NM_022114.3 D917D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9K2-01A-11D-A42J-10 chr4:121828664 G>A maps to NM_018699.2 D47D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9J1-01A-11D-A382-10 chr1:203452749 G>T maps to NM_201348.1 L146L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A40Y-01A-11D-A25F-10 chr2:44566371 G>A maps to NM_001171603.1 R295*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A40Y-01A-11D-A25F-10 chr2:44566450 A>G maps to NM_001171603.1 N268N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Y8-A897-01A-11D-A35Z-10 chr2:44549876 T>C maps to NM_001171603.1 T671T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KV-A6GD-01A-11D-A31X-10 chr20:47361657 G>A maps to NM_020820.3 I106I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JK-01A-11D-A42J-10 chr1:186276989 T>A maps to NM_005807.3 A713A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A8YH-01A-11D-A36X-10 chr1:186277769 T>C maps to NM_005807.3 I973I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr20:62197378 G>A maps to NM_001037335.2 I932I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PZ-01A-11D-A42J-10 chr20:62195230 G>A maps to NM_001037335.2 G1648G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr12:42858292 G>A maps to NM_153026.2 Q515*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-AAVM-01A-11D-A42J-10 chr12:42853999 G>A maps to NM_153026.2 L703L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M8-01A-11D-A31X-10 chr9:71628288 G>A maps to NM_002732.3 Y240Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr9:71628294 G>A maps to NM_002732.3 P238P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4116-01A-01D-1252-08 chr7:151262971 C>T did not map to a codon.
Sequencing variant TCGA-B9-A44B-01A-11D-A25F-10 chr7:106799966 T>A maps to NM_002736.2 Y399*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-8500-01A-11D-2396-08 chr16:23848698 C>T maps to NM_002738.6 G59G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NI-01A-11D-A26P-10 chr3:53220040 A>T maps to NM_212539.1 K362*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A7SQ-01A-12D-A35Z-10 chr11:6341514 C>T maps to NM_145040.2 L64L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3468-01A-01D-1252-08 chr2:46372318 T>C maps to NM_005400.2 N560N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9JV-01A-12D-A42J-10 chr19:54385762 C>T maps to NM_002739.3 G5G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-A8LE-01A-11D-A35Z-10 chr10:6557091 C>T maps to NM_006257.2 S2S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9JZ-01A-11D-A42J-10 chr19:11558372 A>G maps to ENST00000436195 E323E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4114-01A-01D-1252-08 chr19:11558372 A>G maps to ENST00000436195 E323E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F9-A97G-01A-11D-A382-10 chr19:11558369 G>A maps to ENST00000436195 E322E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-7501-01A-11D-2201-08 chr19:11558369 G>A maps to ENST00000436195 E322E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59T-01A-21D-A28G-10 chr19:11558369 G>A maps to ENST00000436195 E322E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A9DC-01A-11D-A36X-10 chr19:11558366 G>A maps to ENST00000436195 E321E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A7SU-01A-11D-A35Z-10 chr19:11558369 G>A maps to ENST00000436195 E322E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PP-01A-11D-A42J-10 chr19:11558366 G>A maps to ENST00000436195 E321E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5XZ-01A-11D-A31X-10 chr1:2066776 C>T maps to NM_002744.4 R137R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JT-01A-11D-A42J-10 chr2:37501807 A>T maps to NM_005813.3 S469S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A562-01A-11D-A26P-10 chr4:82061796 A>T maps to NM_006259.1 A478A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-5560-01A-01D-1589-08 chr2:179306335 C>T did not map to a codon.
Sequencing variant TCGA-AL-7173-01A-11D-2136-08 chr23:3544549 G>C did not map to a codon.
Sequencing variant TCGA-P4-A5E6-01A-11D-A28G-10 chr1:107599741 C>T maps to NM_018137.2 V135V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KV-A6GE-01A-11D-A31X-10 chr16:68386312 G>A did not map to a codon.
Sequencing variant TCGA-BQ-5878-01A-11D-1589-08 chr20:33762616 A>T maps to NM_006404.3 P61P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3468-01A-01D-1252-08 chr1:214178605 C>T maps to NM_002763.3 S608S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9Q0-01A-12D-A42J-10 chr1:150325323 C>A maps to NM_004698.2 R641R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A7SM-01A-11D-A34Z-10 chr12:50025230 C>G maps to NM_001031698.1 P22P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5890-01A-11D-1589-08 chr20:62642771 G>C maps to NM_012469.3 T480T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A44B-01A-11D-A25F-10 chr12:49690228 C>T maps to ENST00000451891 A207A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr23:12840842 C>G did not map to a codon.
Sequencing variant TCGA-SX-A7SQ-01A-12D-A35Z-10 chr17:18770618 A>G maps to NM_002767.2 K48K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr19:50097990 G>C maps to NM_020719.1 S133S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NK-01A-11D-A26P-10 chr16:30666136 G>A maps to NM_024031.2 L282L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8195-01A-31D-2396-08 chr19:42814765 C>T maps to NM_199285.2 P315P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PJ-A5Z8-01A-11D-A28G-10 chr19:42814044 C>A maps to NM_199285.2 P103P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9K0-01A-11D-A42J-10 chr3:138724831 A>G maps to NM_001134659.1 D93D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9JV-01A-12D-A42J-10 chr3:138739038 G>C maps to NM_001013650.2 Y155*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PR-01A-11D-A42J-10 chr11:32858351 G>A maps to NM_024081.4 V84V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5879-01A-11D-1589-08 chr4:119273491 A>T maps to NM_003619.3 A128A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A655-01A-11D-A31Z-10 chr6:84233612 C>T maps to NM_153362.2 S151S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8098-01A-11D-2396-08 chr16:31098020 C>T maps to NM_001039503.2 Q147Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7834-01A-11D-2136-08 chr8:10390472 G>A maps to NM_198464.3 W219*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5888-01A-11D-1589-08 chr19:841047 C>T maps to NM_002777.3 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9KH-01A-11D-A42J-10 chr9:79465476 G>A maps to NM_015225.2 S82S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47M-01A-11D-A25F-10 chr9:79325025 G>A maps to NM_015225.2 Q722*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3472-01A-01D-1252-08 chr5:139193772 T>C maps to NM_032289.2 D280D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5878-01A-11D-1589-08 chr5:139197068 C>T maps to NM_032289.2 N340N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Y8-A894-01A-11D-A35Z-10 chr2:113956436 C>A maps to NM_012455.2 P915P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J7-6720-01A-11D-2136-08 chr19:43585216 A>T maps to ENST00000449000 Y82*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7058-01A-11D-1961-08 chr19:43237191 G>T maps to NM_021016.3 I151I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A562-01A-11D-A26P-10 chr19:43689068 C>A maps to ENST00000270059 E99*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr1:151372077 G>A maps to NM_002796.2 L5L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9J5-01A-21D-A382-10 chr7:103008256 G>T did not map to a codon.
Sequencing variant TCGA-B9-5155-01A-01D-1589-08 chr7:103002481 G>T maps to NM_002803.2 V123V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7834-01A-11D-2136-08 chr19:40478460 A>G maps to NM_006503.2 T107T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9K2-01A-11D-A42J-10 chr17:30806378 T>C maps to NM_002815.2 P341P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NI-01A-11D-A26P-10 chr17:65362548 G>C maps to NM_002816.3 P29P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7996-01A-11D-2201-08 chr2:162227814 T>C maps to NM_005805.4 I148I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr9:123591453 T>C maps to NM_005047.2 E198E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5901-01A-11D-1589-08 chr3:64004273 C>A did not map to a codon.
Sequencing variant TCGA-B3-A6W5-01A-12D-A33Q-10 chr21:40555299 C>T maps to NM_003720.2 T4T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Y8-A8RY-01A-11D-A36X-10 chr18:12720514 C>T maps to NM_020232.4 P138P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-7502-01A-11D-2201-08 chr1:28477259 G>A maps to NM_001164721.1 N91N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4A-A93W-01A-11D-A36X-10 chr7:99023209 T>C maps to NM_001198879.1 L364L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A654-01A-11D-A31X-10 chr7:99022429 G>A maps to NM_001198879.1 L624L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6134-01A-11D-1961-08 chr7:99022813 G>A maps to NM_001198879.1 A496A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-5155-01A-01D-1589-08 chr9:98229470 C>A maps to NM_000264.3 V829V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PX-01A-11D-A42J-10 chr23:23353162 G>A did not map to a codon.
Sequencing variant TCGA-5P-A9JY-01A-11D-A42J-10 chr1:11585335 G>T maps to NM_020780.1 V860V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A71U-01A-12D-A33Q-10 chr1:11561255 C>T maps to NM_020780.1 T69T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PJ-A8JU-01A-11D-A35Z-10 chr10:89720836 A>T maps to NM_000314.4 K330*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9Q1-01A-11D-A42J-10 chr10:89653782 T>A maps to NM_000314.4 Y27*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3473-01A-01D-1252-08 chr1:78959186 G>A maps to NM_000959.3 A253A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4A-A93W-01A-11D-A36X-10 chr20:48129709 G>A maps to NM_000961.3 D371D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PO-01A-11D-A382-10 chr19:49926467 C>A did not map to a codon.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr8:141745381 C>T maps to NM_005607.4 R688R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Y8-A897-01A-11D-A35Z-10 chr8:141669755 A>G maps to NM_005607.4 L1012L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9Q1-01A-11D-A42J-10 chr20:62168574 C>T maps to NM_005975.2 A31A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7839-01A-11D-2136-08 chr6:43044270 T>G maps to NM_002821.3 P15P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PO-01A-11D-A382-10 chr19:50357982 C>T maps to NM_017432.3 G128G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9J3-01A-12D-A382-10 chr10:17645618 A>T maps to NM_014241.3 T141T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9KA-01A-11D-A42J-10 chr9:21008119 A>G maps to NM_001010915.3 P172P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr7:77267950 G>T maps to NM_002835.3 A728A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9Q1-01A-11D-A42J-10 chr7:77256522 T>A maps to NM_002835.3 T509T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chr1:214556992 G>A maps to NM_005401.4 A735A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A7SR-01A-12D-A35Z-10 chr14:88945295 T>A maps to NM_007039.3 K827*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Y8-A896-01A-11D-A35Z-10 chr14:88935277 G>C maps to NM_007039.3 A1126A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7732-01A-11D-2136-08 chr1:114402064 A>G maps to NM_015967.5 S35S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5879-01A-11D-1589-08 chr20:2998528 C>T maps to NM_002836.3 V337V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JL-01A-11D-A42J-10 chr12:71016215 G>T maps to NM_001109754.1 S221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NK-01A-11D-A26P-10 chr12:71002987 G>A maps to NM_001109754.1 T280T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PV-01A-11D-A42J-10 chr12:71016226 A>G maps to NM_001109754.1 I217I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A560-01A-11D-A26P-10 chr1:198678921 C>T maps to ENST00000271610 N380N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PU-01A-11D-A42J-10 chr9:8460469 A>G maps to NM_002839.3 G1272G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9J3-01A-12D-A382-10 chr10:129846026 G>C did not map to a codon.
Sequencing variant TCGA-B3-3925-01A-01D-1458-08 chr10:129859260 C>A maps to NM_006504.4 I190I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr1:44063521 C>T maps to NM_002840.3 I639I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9JZ-01A-11D-A42J-10 chr19:55710165 C>T maps to NM_002842.3 W512*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A9DE-01A-11D-A36X-10 chr19:55718204 A>C maps to NM_002842.3 T68T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5888-01A-11D-1589-08 chr18:8379244 G>A maps to NM_001105244.1 R1231R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NH-01A-11D-A26P-10 chr18:8378411 G>T maps to NM_001105244.1 R1204R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A40U-01A-11D-A25F-10 chr18:8314789 C>T maps to NM_001105244.1 R952*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PO-01A-11D-A382-10 chr18:8380302 C>T maps to NM_001105244.1 Q1266*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PJ-A8JU-01A-11D-A35Z-10 chr2:220173976 G>A maps to NM_002846.3 S26S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chr20:41100969 G>A maps to ENST00000373198 L462L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9KA-01A-11D-A42J-10 chr7:121616252 C>T maps to NM_002851.2 D161D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5882-01A-11D-1589-08 chr7:121651530 C>T maps to NM_002851.2 L811L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5888-01A-11D-1589-08 chr7:121681009 G>A maps to NM_002851.2 V1926V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55Z-01A-11D-A26P-10 chr8:144902838 T>C maps to NM_078480.1 Q115Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4116-01A-01D-1252-08 chr3:110830988 G>A maps to NM_015480.1 W91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7841-01A-11D-2136-08 chr5:159520918 G>A maps to NM_001130864.1 V246V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E7-01A-31D-A28G-10 chr10:134218415 C>T maps to NM_138499.3 L138L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JT-01A-11D-A42J-10 chr12:120660780 T>G maps to NM_001080855.1 S126S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr12:120653398 G>A maps to NM_001080855.1 G299G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JS-01A-21D-A42J-10 chr1:158911892 A>C maps to NM_152501.3 R236R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5889-01A-11D-1589-08 chr1:158912062 T>G maps to NM_152501.3 A292A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A83S-01A-11D-A34Z-10 chr9:133768990 T>A maps to NM_198180.1 R79*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A7SN-01A-11D-A34Z-10 chr3:49114323 G>A maps to NM_198880.1 Q43*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PR-01A-11D-A42J-10 chr3:49114435 T>C maps to NM_198880.1 L5L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5882-01A-11D-1589-08 chr17:74288034 G>A maps to NM_032134.1 Q759*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A7SS-01A-11D-A35Z-10 chr17:74288746 C>T maps to NM_032134.1 Q521Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4113-01A-01D-1252-08 chr11:32954929 C>A maps to NM_001076786.1 S580*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9J6-01A-11D-A382-10 chr19:10823828 G>A maps to NM_031209.2 V365V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A772-01A-11D-A33Q-10 chr3:113795726 C>T maps to ENST00000485050 T240T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8098-01A-11D-2396-08 chr16:570231 C>T maps to NM_014700.3 R657R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8311-01A-11D-2396-08 chr16:568987 G>A maps to NM_014700.3 T562T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JS-01A-21D-A42J-10 chr9:123954484 T>A maps to NM_016322.3 K24*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KV-A6GD-01A-11D-A31X-10 chr2:238494740 C>A maps to NM_022449.3 V19V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JT-01A-11D-A42J-10 chr12:72167771 T>C maps to NM_014999.2 L121L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A9DE-01A-11D-A36X-10 chr12:72176412 G>A maps to NM_014999.2 E170E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3473-01A-01D-1252-08 chr15:55516127 T>A maps to NM_183235.1 V142V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr17:72736998 C>A maps to NM_001006638.2 T62T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8517-01A-11D-2396-08 chr11:87908438 G>A maps to NM_022337.2 Y38Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9KC-01A-11D-A42J-10 chr3:133557103 C>T did not map to a codon.
Sequencing variant TCGA-B9-5155-01A-01D-1589-08 chr15:63548781 A>T maps to NM_016530.2 R135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47M-01A-11D-A25F-10 chr19:42461227 G>T maps to NM_006423.2 G137G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-8500-01A-11D-2396-08 chr9:125751641 C>T maps to NM_012197.3 V219V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E7-01A-31D-A28G-10 chr14:24734892 C>T maps to NM_182836.1 P544P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8630-01A-11D-2396-08 chr5:131953818 A>G maps to NM_005732.3 A1074A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr5:131976366 T>C maps to NM_005732.3 L1208L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr12:110969391 A>G maps to NM_152442.3 K416K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A6HP-01A-11D-A31X-10 chr7:4841356 G>A maps to NM_018059.4 G923G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PZ-01A-11D-A42J-10 chr1:155110119 T>C maps to NM_018845.3 P122P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JR-01A-12D-A42J-10 chr11:36615487 A>T maps to NM_000536.3 T77T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9JV-01A-12D-A42J-10 chr17:17701401 A>T maps to ENST00000395776 K1714*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-A8LB-01A-11D-A35Z-10 chr17:17697104 G>A maps to ENST00000395776 Q281Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4114-01A-01D-1252-08 chr5:34757667 C>T maps to NM_001145521.1 A44A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A9DC-01A-11D-A36X-10 chr5:34688328 G>A maps to NM_001145525.1 P7P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A9DE-01A-11D-A36X-10 chr18:9535919 G>A maps to NM_006788.3 K651K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E7-01A-31D-A28G-10 chr14:36143778 A>C maps to NM_194301.2 P1081P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-AAVL-01A-11D-A42J-10 chr9:135975748 A>C maps to NM_006266.2 A825A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9K6-01A-11D-A42J-10 chr1:178863073 T>A maps to NM_152663.3 L449*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5891-01A-11D-1589-08 chr16:67840334 C>T maps to NM_020850.1 L35L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9KA-01A-11D-A42J-10 chr5:170289054 G>A maps to NM_022897.3 Q6Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5877-01A-11D-1589-08 chr2:109392303 T>C maps to NM_006267.4 I2803I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7058-01A-11D-1961-08 chr2:109379712 T>C maps to NM_006267.4 N906N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9KA-01A-11D-A42J-10 chr9:6012697 G>T maps to NM_012416.2 T970T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A71U-01A-12D-A33Q-10 chr6:13639867 T>C maps to NM_005493.2 P484P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A655-01A-11D-A31Z-10 chr1:21936723 G>C maps to NM_001145658.1 V360V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr17:2898694 C>A maps to NM_015085.4 R327R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59T-01A-21D-A28G-10 chr9:134505711 C>T did not map to a codon.
Sequencing variant TCGA-Y8-A895-01A-11D-A35Z-10 chr7:22200163 G>A maps to ENST00000344041 Q347*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V9-A7HT-01A-11D-A33Q-10 chr3:25637914 A>T maps to NM_000965.3 A385A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AT-A5NU-01A-11D-A28G-10 chr5:167937679 G>T maps to NM_002887.3 E481*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JT-01A-11D-A42J-10 chr5:86665668 A>G maps to NM_002890.1 E550E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A7SS-01A-11D-A35Z-10 chr1:178063785 T>C maps to ENST00000263528 L35L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7061-01A-11D-1961-08 chr15:79264260 G>A maps to NM_002891.4 R1226*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9J8-01A-11D-A42J-10 chr19:38905688 G>A maps to ENST00000405332 C344C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A856-01A-11D-A34Z-10 chr19:38903683 C>T maps to ENST00000405332 V475V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A9DE-01A-11D-A36X-10 chr12:65078564 A>C did not map to a codon.
Sequencing variant TCGA-2Z-A9JG-01A-11D-A42J-10 chr8:53596455 A>G maps to NM_014781.4 S63S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr23:16864058 A>G did not map to a codon.
Sequencing variant TCGA-GL-A59R-01A-11D-A26P-10 chr18:20562276 G>A maps to ENST00000360790 R175R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A7UZ-01A-12D-A34Z-10 chr16:53504376 C>T maps to NM_005611.3 S776S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JI-01A-11D-A42J-10 chr23:47030581 G>T did not map to a codon.
Sequencing variant TCGA-B9-A8YH-01A-11D-A36X-10 chr23:47030584 T>G did not map to a codon.
Sequencing variant TCGA-G7-A8LC-01A-11D-A35Z-10 chr23:47030581 G>T did not map to a codon.
Sequencing variant TCGA-WN-A9G9-01A-12D-A36X-10 chr23:47044732 G>C did not map to a codon.
Sequencing variant TCGA-2Z-A9J2-01A-11D-A382-10 chr20:34240508 A>G maps to NM_001198838.1 A912A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8196-01A-11D-2396-08 chr8:94747483 A>G maps to NM_203390.2 H385H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8196-01A-11D-2396-08 chr1:110882977 T>C maps to NM_022768.4 P317P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9K0-01A-11D-A42J-10 chr3:51431289 T>C maps to NM_013286.4 L820L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F9-A7VF-01A-11D-A33Q-10 chr3:51431070 C>A maps to NM_013286.4 I747I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PX-01A-11D-A42J-10 chr3:51429621 C>A maps to NM_013286.4 R264R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr12:114385204 G>A maps to NM_016196.3 F447F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr14:23374813 C>G did not map to a codon.
Sequencing variant TCGA-B9-5155-01A-01D-1589-08 chr6:17292211 G>A maps to NM_001143942.1 G191G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5889-01A-11D-1589-08 chr5:145613181 C>T maps to NM_018989.1 G340G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PP-01A-11D-A42J-10 chr5:145583373 T>C maps to NM_018989.1 L16L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4617-01A-01D-1252-08 chr11:66411449 T>A maps to NM_001198845.1 A289A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7584-01A-11D-2136-08 chr2:238722325 G>T did not map to a codon.
Sequencing variant TCGA-A4-7915-01A-11D-2201-08 chr11:66444484 G>A maps to NM_031492.2 F22F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W8-01A-11D-A28G-10 chr3:50147867 T>C maps to NM_005778.2 P445P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55W-01A-11D-A26P-10 chr3:50155813 T>A maps to NM_005778.2 Y791*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Y8-A897-01A-11D-A35Z-10 chr3:50103676 T>G maps to NM_005777.2 P895P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A654-01A-11D-A31X-10 chr23:129546640 A>T did not map to a codon.
Sequencing variant TCGA-IA-A83V-01A-11D-A34Z-10 chr12:7276770 C>A did not map to a codon.
Sequencing variant TCGA-BQ-5881-01A-11D-1589-08 chr20:43940943 C>T maps to NM_014276.2 R176R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4A-A93W-01A-11D-A36X-10 chr9:125612010 G>C maps to NM_001100588.1 T1157T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A40Y-01A-11D-A25F-10 chr13:50134122 G>C maps to NM_018191.3 L125L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JO-01A-11D-A42J-10 chr15:91500568 T>A maps to NM_033544.2 A131A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5887-01A-11D-1961-08 chr4:76439475 T>C maps to NM_015436.2 E7E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr6:31922208 T>C maps to ENST00000375425 S258S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5880-01A-11D-1589-08 chr14:68157016 G>A maps to NM_016026.3 G192G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7996-01A-11D-2201-08 chr11:65423174 A>G maps to NM_021975.3 A339A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7286-01A-11D-2136-08 chr7:103234872 G>C maps to ENST00000428762 P1202P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-5155-01A-01D-1589-08 chr20:30064535 G>A maps to NM_014012.4 L96L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PJ-A5Z9-01A-11D-A28G-10 chr23:153200790 G>T did not map to a codon.
Sequencing variant TCGA-Y8-A8S0-01A-11D-A36X-10 chr23:153207004 A>G did not map to a codon.
Sequencing variant TCGA-2Z-A9JT-01A-11D-A42J-10 chr7:150068584 G>A maps to NM_001099695.1 L142L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NK-01A-11D-A26P-10 chr7:150069171 C>A maps to NM_001099695.1 S338*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A57E-01A-11D-A26P-10 chr6:139235872 G>T maps to ENST00000367663 A582A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-7173-01A-11D-2136-08 chr1:8415615 G>T maps to NM_012102.3 P1510P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4116-01A-01D-1252-08 chr4:39325031 C>T maps to ENST00000381897 E216E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F9-A7Q0-01A-11D-A35Z-10 chr17:33348797 C>T maps to NM_001017368.1 Q61Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5882-01A-11D-1589-08 chr1:175914296 A>G maps to NM_022457.5 L730L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A561-01A-11D-A26P-10 chr1:175996825 T>C did not map to a codon.
Sequencing variant TCGA-BQ-7061-01A-11D-1961-08 chr12:107154994 T>A maps to ENST00000357881 T661T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5889-01A-11D-1589-08 chr6:117241540 T>C maps to NM_173560.3 D417D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UN-AAZ9-01A-11D-A382-10 chr6:117237248 G>A did not map to a codon.
Sequencing variant TCGA-B1-A47M-01A-11D-A25F-10 chr3:101284213 C>T maps to NM_017819.2 Q197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5903-01A-11D-1589-08 chr23:109695934 T>G did not map to a codon.
Sequencing variant TCGA-G7-A8LB-01A-11D-A35Z-10 chr23:109694785 C>T did not map to a codon.
Sequencing variant TCGA-PJ-A8JU-01A-11D-A35Z-10 chr23:109694813 G>A did not map to a codon.
Sequencing variant TCGA-SX-A7SR-01A-12D-A35Z-10 chr23:109697328 T>C did not map to a codon.
Sequencing variant TCGA-DW-7839-01A-11D-2136-08 chr23:71351212 T>C did not map to a codon.
Sequencing variant TCGA-2Z-A9JL-01A-11D-A42J-10 chr1:183775570 A>G maps to NM_015149.3 K65K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-7268-01A-11D-2136-08 chr5:73136426 T>C maps to NM_001080479.2 S423S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5880-01A-11D-1589-08 chr9:35751269 G>A maps to ENST00000456972 Q205Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3468-01A-01D-1252-08 chr2:107049612 A>G maps to ENST00000304514 H778H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A44B-01A-11D-A25F-10 chr2:107073431 G>A maps to ENST00000304514 L134L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A655-01A-11D-A31Z-10 chr5:176798988 C>T maps to ENST00000398128 P539P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A8YI-01A-21D-A36X-10 chr5:176799073 T>C maps to ENST00000398128 *568R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8310-01A-11D-2396-08 chr6:153332801 A>T maps to NM_012419.4 T180T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr1:192128418 C>T maps to NM_130782.2 S63S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7834-01A-11D-2136-08 chr22:29656764 C>A maps to NM_012265.1 G207G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Y8-A894-01A-11D-A35Z-10 chr17:74473012 C>T maps to NM_024599.5 R367R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PN-01A-11D-A382-10 chr16:727362 G>A maps to NM_003961.1 L286L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr1:25628089 G>A maps to ENST00000357542 V238V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr10:62648932 T>A maps to NM_014836.4 R165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-A4TM-01A-11D-A31X-10 chr1:113244308 C>G maps to NM_175744.4 R145R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5902-01A-11D-1589-08 chr5:38954923 A>C maps to ENST00000296782 Y883*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7061-01A-11D-1961-08 chr12:130919338 G>A maps to NM_015347.4 D714D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A4EM-01A-11D-A25F-10 chr1:41107441 C>T maps to NM_014747.2 K52K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr20:19955385 C>T maps to ENST00000255006 S288S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-A8LB-01A-11D-A35Z-10 chr19:39360597 G>T maps to NM_001195833.1 R443R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A9DE-01A-11D-A36X-10 chr6:7395374 A>G maps to NM_031480.2 L122L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-5156-01A-01D-1589-08 chr14:24805464 G>T maps to NM_006871.3 P491P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59T-01A-21D-A28G-10 chr6:84563844 C>T maps to NM_001009994.1 A68A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A7SP-01A-11D-A34Z-10 chr23:73811366 G>T did not map to a codon.
Sequencing variant TCGA-P4-A5E8-01A-11D-A28G-10 chr16:67683207 C>T maps to NM_001013838.1 D580D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-A8LB-01A-11D-A35Z-10 chr2:86968116 T>C maps to NM_022780.3 D70D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9JZ-01A-11D-A42J-10 chr19:12921201 C>A maps to NM_006397.2 G207G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr17:41180502 C>A maps to NM_005440.4 R164R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F9-A7VF-01A-11D-A33Q-10 chr15:59350657 T>A maps to ENST00000434298 T425T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A7SP-01A-11D-A34Z-10 chr15:59358970 A>C maps to ENST00000434298 R459R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5ED-01A-11D-A28G-10 chr23:106034464 G>A did not map to a codon.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr17:74158076 C>A maps to NM_052916.2 E267*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5882-01A-11D-1589-08 chr16:88765420 C>A maps to NM_178841.3 V166V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5902-01A-11D-1589-08 chr3:196214404 G>T maps to NM_152617.3 A141A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5890-01A-11D-1589-08 chr13:25352541 T>C maps to ENST00000381927 L143L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Y8-A894-01A-11D-A35Z-10 chr1:33429683 G>T maps to NM_153341.2 P201P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A71S-01A-11D-A33Q-10 chr9:104302567 A>G maps to NM_019592.5 E71E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9JY-01A-11D-A42J-10 chr17:78356797 A>G maps to NM_020914.4 T4715T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr17:78293015 C>G maps to NM_020914.4 A1025A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7834-01A-11D-2136-08 chr17:78321575 C>T maps to NM_020914.4 R3196R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6789-01A-11D-1961-08 chr17:78355390 C>G maps to NM_020914.4 G4663G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr7:5781126 G>C maps to NM_207111.2 S174*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E6-01A-11D-A28G-10 chr10:90342857 A>C maps to NM_001031709.2 L30L. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-SX-A7SP-01A-11D-A34Z-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-DW-7838-01A-11D-2136-08 chr2:241516156 C>T maps to NM_018226.3 L341L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A9DD-01A-11D-A36X-10 chr3:78710201 C>T maps to NM_002941.3 K766K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9J5-01A-21D-A382-10 chr3:77617479 A>T maps to ENST00000332191 A622A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7046-01A-11D-1961-08 chr11:124765530 G>A maps to NM_019055.5 T286T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JE-01A-11D-A42J-10 chr2:11333931 A>G maps to NM_004850.3 D1220D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr2:11361481 C>A maps to NM_004850.3 T367T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7061-01A-11D-1961-08 chr6:117706857 T>A maps to NM_002944.2 G764G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chr8:55534828 A>G maps to NM_006269.1 A256A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A7SN-01A-11D-A34Z-10 chr8:55537659 G>A maps to NM_006269.1 E406E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PR-01A-11D-A42J-10 chr8:10468691 T>C maps to NM_178857.5 T972T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J7-8537-01A-11D-2396-08 chr23:46713305 C>G did not map to a codon.
Sequencing variant TCGA-Y8-A895-01A-11D-A35Z-10 chr17:1787151 C>T maps to NM_002945.3 L430L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A654-01A-11D-A31X-10 chr23:96139634 G>A did not map to a codon.
Sequencing variant TCGA-A4-A5DU-01A-11D-A28G-10 chr14:21793035 C>T maps to NM_020366.3 P674P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr14:21769307 C>T maps to NM_020366.3 A134A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7045-01A-31D-1961-08 chr23:153627910 G>A did not map to a codon.
Sequencing variant TCGA-5P-A9KE-01A-11D-A42J-10 chr6:35437953 A>G did not map to a codon.
Sequencing variant TCGA-AL-3472-01A-01D-1252-08 chr9:130213581 G>A maps to NM_000976.2 F5F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr1:6246872 A>T maps to NM_000983.3 Y82*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PN-01A-11D-A382-10 chr19:55897935 A>G did not map to a codon.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr3:52029444 G>A maps to NM_000992.2 N11N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Y8-A8RY-01A-11D-A36X-10 chr23:100650415 T>G did not map to a codon.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr2:217364691 T>A maps to NM_000998.4 A51A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr16:1995883 C>T maps to NM_005061.2 L333L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A7SM-01A-11D-A34Z-10 chr15:66791909 G>T maps to NM_000968.2 G373G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A9DD-01A-11D-A36X-10 chr9:136215841 G>A maps to NM_000972.2 E23E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A854-01A-11D-A34Z-10 chr9:136216881 G>T maps to NM_000972.2 T130T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6789-01A-11D-1961-08 chr18:33606994 C>T maps to NM_018170.3 A219A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-5156-01A-01D-1589-08 chr1:150390093 T>C maps to NM_015203.3 N76N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A83V-01A-11D-A34Z-10 chr1:150337219 T>C maps to NM_015203.3 S10S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9Q1-01A-11D-A42J-10 chr4:152021724 A>C maps to NM_001006.3 R51R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7837-01A-11D-2136-08 chr23:20195137 T>C did not map to a codon.
Sequencing variant TCGA-GL-A9DE-01A-11D-A36X-10 chr11:4144482 C>T maps to NM_001033.3 Q397*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Y8-A894-01A-11D-A35Z-10 chr10:99126539 C>T maps to NM_015179.3 E1058E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9J2-01A-11D-A382-10 chr22:42912115 G>A maps to NM_015703.4 T81T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JD-01A-11D-A42J-10 chr11:6624660 A>T maps to NM_015324.2 P24P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A8YI-01A-21D-A36X-10 chr11:6622764 A>C maps to NM_015324.2 P177P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A44B-01A-11D-A25F-10 chr8:108970371 T>C maps to NM_178565.4 T184T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A561-01A-11D-A26P-10 chr2:74668861 G>T maps to NM_001015055.1 R28R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9J2-01A-11D-A382-10 chr14:101347375 G>A maps to NM_001134888.2 D1250D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JQ-01A-11D-A42J-10 chr19:46000065 C>A maps to NM_005619.3 P6P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KV-A74V-01A-11D-A33Q-10 chr18:67816231 G>T maps to NM_173630.3 L738L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9K6-01A-11D-A42J-10 chr4:71660583 G>A maps to NM_001037442.2 R510R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A83V-01A-11D-A34Z-10 chr21:36206707 C>T maps to NM_001754.4 Q268Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4A-A93Y-01A-11D-A36X-10 chr6:45390444 A>G maps to ENST00000359524 Q126Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6790-01A-11D-1961-08 chr6:45390444 A>G maps to ENST00000359524 Q126Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A7SR-01A-12D-A35Z-10 chr6:45390462 G>A maps to ENST00000359524 Q132Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A7SS-01A-11D-A35Z-10 chr1:25229149 C>T maps to NM_001031680.2 S251S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8515-01A-11D-2396-08 chr9:35560974 G>A maps to NM_001135999.1 L1410L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9J1-01A-11D-A382-10 chr21:30378845 A>T maps to NM_016940.2 V284V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JL-01A-11D-A42J-10 chr9:137323759 G>T maps to NM_002957.4 T351T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr19:39039029 T>C maps to NM_000540.2 R4084R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KV-A6GD-01A-11D-A31X-10 chr19:38948846 C>G maps to NM_000540.2 Y694*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WN-A9G9-01A-12D-A36X-10 chr19:38997148 G>A maps to NM_000540.2 T2885T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4A-A93W-01A-11D-A36X-10 chr1:237713902 C>A maps to NM_001035.2 T1042T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PX-01A-11D-A42J-10 chr1:237550597 C>T maps to NM_001035.2 N198N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4A-A93W-01A-11D-A36X-10 chr1:153507303 C>T maps to NM_014624.3 K47K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5886-01A-11D-1589-08 chr19:3179455 C>T maps to NM_003775.3 L222L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9J7-01A-11D-A382-10 chr11:18254054 A>G maps to NM_006512.3 Y39Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JD-01A-11D-A42J-10 chr11:64811958 C>T maps to ENST00000301885 V324V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-AAVL-01A-11D-A42J-10 chr13:23909167 A>G maps to NM_014363.4 I2949I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9J3-01A-12D-A382-10 chr16:51171130 C>T maps to ENST00000251020 E1289E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7838-01A-11D-2136-08 chr16:51172850 A>G maps to ENST00000251020 H1094H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-A8LE-01A-11D-A35Z-10 chr14:21993090 G>A maps to NM_005407.1 S257S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7045-01A-31D-1961-08 chr20:50405585 G>A maps to NM_020436.3 S852S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5893-01A-11D-1589-08 chr6:147830099 G>A maps to NM_001030060.2 A12A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9J1-01A-11D-A382-10 chr7:92732596 A>T maps to NM_017654.3 C938*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JT-01A-11D-A42J-10 chr2:128774007 G>T maps to NM_001145928.1 I180I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8310-01A-11D-2396-08 chr19:55752902 A>T maps to ENST00000443936 L379*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PM-01A-21D-A382-10 chr22:50876322 G>A maps to ENST00000216061 E611E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr11:68377389 T>A maps to NM_001164160.1 S829S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A71V-01A-11D-A33Q-10 chr19:39409423 A>G maps to NM_017827.3 L263L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A8YI-01A-21D-A36X-10 chr6:148855990 C>T maps to NM_015278.3 H683H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5878-01A-11D-1589-08 chr6:148808751 C>G maps to NM_015278.3 L210L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4A-A93W-01A-11D-A36X-10 chr23:128922423 A>C did not map to a codon.
Sequencing variant TCGA-BQ-5876-01A-11D-1589-08 chr1:100572513 A>C maps to NM_194292.1 V454V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F9-A7Q0-01A-11D-A35Z-10 chr14:51101990 A>T maps to NM_021818.2 Y354*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47M-01A-11D-A25F-10 chr7:66456177 G>C maps to NM_016038.2 L190L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr12:123780520 C>A maps to NM_001167856.1 A1372A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A83S-01A-11D-A34Z-10 chr15:75146984 G>T maps to NM_005697.3 P21P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7838-01A-11D-2136-08 chr3:47456624 C>T maps to NM_012235.2 L1034L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A48D-01A-11D-A25F-10 chr8:27516083 C>T maps to NM_016240.2 Q133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr4:83557888 G>C maps to NM_001037582.2 S219S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr15:51993376 A>G maps to NM_013243.3 G381G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M9-01A-11D-A31X-10 chr3:159606613 A>T maps to NM_001197113.1 P476P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3473-01A-01D-1252-08 chr1:41503103 G>A maps to NM_001031694.2 H526H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JQ-01A-11D-A42J-10 chr3:38892110 G>A maps to ENST00000302328 S1396S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A83T-01A-11D-A34Z-10 chr3:38908835 G>A maps to ENST00000302328 D1309D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr2:166915108 C>T maps to NM_001165963.1 R118R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A44B-01A-11D-A25F-10 chr2:166153544 A>T maps to NM_001040142.1 K96*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7966-01A-11D-2201-08 chr2:166201261 C>G maps to NM_001040142.1 L920L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A562-01A-11D-A26P-10 chr17:62045581 C>T maps to NM_000334.4 K279K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A562-01A-11D-A26P-10 chr17:62045584 C>T maps to NM_000334.4 Q278Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A8YH-01A-11D-A36X-10 chr3:38592251 G>A maps to NM_001099404.1 L1871L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9J3-01A-12D-A382-10 chr2:167142944 C>T maps to ENST00000303354 S502S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PV-01A-11D-A42J-10 chr2:167055907 G>T maps to ENST00000303354 S1748S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A561-01A-11D-A26P-10 chr16:23360138 C>G maps to ENST00000307331 T118T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A4ZT-01A-11D-A26P-10 chr17:45918191 A>G maps to NM_138355.3 P6P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A8YI-01A-21D-A36X-10 chr17:45916948 C>A maps to NM_138355.3 L139L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-7502-01A-11D-2201-08 chr17:45915994 C>A maps to NM_138355.3 S280S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-A8LE-01A-11D-A35Z-10 chr17:45915919 A>G maps to NM_138355.3 L305L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PZ-01A-11D-A42J-10 chr2:120221713 G>A maps to NM_002980.2 Y207Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5890-01A-11D-1589-08 chr6:35213119 G>A maps to ENST00000394681 K855K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4116-01A-01D-1252-08 chr11:65305493 G>A maps to NM_020680.3 W696*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5885-01A-11D-1589-08 chr4:76877178 C>T maps to NM_018115.2 R655R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8517-01A-11D-2396-08 chr1:31347252 G>T maps to NM_014654.3 P351P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7584-01A-11D-2136-08 chr14:50256252 C>T maps to NM_004713.3 Q886Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A560-01A-11D-A26P-10 chr1:243419489 G>A maps to NM_006642.3 P5P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JM-01A-12D-A42J-10 chr1:1163849 G>T maps to NM_016176.3 S108S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A7SR-01A-12D-A35Z-10 chr12:57324029 C>T maps to NM_148897.2 E180E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A7SL-01A-11D-A34Z-10 chr9:139360853 A>G maps to NM_014866.1 D1330D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PL-01A-11D-A382-10 chr9:139368590 G>T maps to NM_014866.1 Y1159*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4115-01A-01D-1252-08 chr5:134002686 G>A did not map to a codon.
Sequencing variant TCGA-GL-A9DD-01A-11D-A36X-10 chr4:83748747 G>T maps to ENST00000505472 S1053*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr3:169706124 C>T maps to NM_003262.3 A236A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47M-01A-11D-A25F-10 chr15:49293278 A>C maps to NM_001193489.1 V681V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NL-01A-11D-A26P-10 chr20:13868445 G>T maps to NM_025229.1 A238A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9KH-01A-11D-A42J-10 chr4:25834645 G>A maps to NM_015187.3 R357*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A857-01A-11D-A34Z-10 chr7:83037687 C>T maps to NM_012431.2 L222L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PL-01A-11D-A382-10 chr2:97532109 C>T maps to NM_017789.4 L56L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr9:92007356 A>T maps to NM_006378.3 Y201*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr2:74906850 C>A maps to NM_004263.3 R610R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9JW-01A-11D-A42J-10 chr5:9052120 C>G maps to NM_003966.2 S903S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4103-01A-01D-1458-08 chr5:9226980 C>T maps to NM_003966.2 S144S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4114-01A-01D-1252-08 chr5:9119219 A>T maps to NM_003966.2 S605S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9J5-01A-21D-A382-10 chr3:122647426 G>A maps to NM_001031702.2 V191V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-8500-01A-11D-2396-08 chr5:115822557 G>A maps to ENST00000257414 C283C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8098-01A-11D-2396-08 chr1:151109385 C>T maps to NM_001178061.1 V307V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7045-01A-31D-1961-08 chr1:151112137 T>C maps to NM_001178061.1 E91E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-A8LB-01A-11D-A35Z-10 chr3:185341840 G>T maps to ENST00000427465 E603*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PU-01A-11D-A42J-10 chr17:7474734 G>A maps to ENST00000321337 Q553Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A9DD-01A-11D-A36X-10 chr3:196613000 A>T maps to NM_152699.4 K317*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr2:242277177 G>C maps to ENST00000391972 L224L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NJ-01A-11D-A26P-10 chr22:19709429 C>T maps to NM_002688.5 C300C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A83V-01A-11D-A34Z-10 chr22:19709804 G>A maps to NM_002688.5 L332L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A40Y-01A-11D-A25F-10 chr23:118797594 T>A did not map to a codon.
Sequencing variant TCGA-MH-A855-01A-11D-A34Z-10 chr23:118809561 T>C did not map to a codon.
Sequencing variant TCGA-B9-4113-01A-01D-1252-08 chr7:35912376 G>A did not map to a codon.
Sequencing variant TCGA-5P-A9JW-01A-11D-A42J-10 chr5:132099511 G>T maps to NM_001098811.1 R140R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A4EM-01A-11D-A25F-10 chr6:122777746 A>G maps to NM_020755.2 L84L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8310-01A-11D-2396-08 chr14:94756789 C>T maps to NM_001100607.1 E47E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A9DE-01A-11D-A36X-10 chr14:95030169 C>A maps to NM_006215.2 V117V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A772-01A-11D-A33Q-10 chr14:95053704 G>A maps to NM_000624.4 Q2Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AT-A5NU-01A-11D-A28G-10 chr23:105280774 A>G did not map to a codon.
Sequencing variant TCGA-5P-A9JY-01A-11D-A42J-10 chr18:61324646 C>T did not map to a codon.
Sequencing variant TCGA-P4-A5ED-01A-11D-A28G-10 chr6:2955760 G>C maps to ENST00000316782 L136L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-7173-01A-11D-2136-08 chr6:2890545 C>A maps to NM_004155.4 E328*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr22:21140327 G>A maps to NM_000185.3 E400E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6134-01A-11D-1961-08 chr7:100780345 G>C maps to NM_000602.3 V384V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9KA-01A-11D-A42J-10 chr6:109319901 T>G maps to NM_014454.1 V262V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J7-A8I2-01A-12D-A35Z-10 chr18:42531806 G>A maps to NM_015559.2 L834L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr18:42533243 C>T maps to NM_015559.2 D1313D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9K3-01A-11D-A42J-10 chr3:47079259 G>A maps to NM_014159.6 Q2416*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5875-01A-11D-1589-08 chr3:47061275 T>A maps to NM_014159.6 K2469*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5890-01A-11D-1589-08 chr3:47143046 T>C did not map to a codon.
Sequencing variant TCGA-PJ-A5Z9-01A-11D-A28G-10 chr3:47164504 G>T maps to NM_014159.6 R541R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KV-A6GD-01A-11D-A31X-10 chr14:99929880 C>T maps to NM_032233.2 E46E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr21:37418116 T>C maps to NM_017438.3 R163R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NF-01A-11D-A26P-10 chr21:37408417 G>C maps to NM_017438.3 T440T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7585-01A-11D-2136-08 chr3:9512541 T>C maps to ENST00000407969 L1061L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PU-01A-11D-A42J-10 chr13:50041998 G>A did not map to a codon.
Sequencing variant TCGA-DW-5561-01A-01D-1589-08 chr19:2248400 G>A maps to NM_007165.4 S417S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9K0-01A-11D-A42J-10 chr2:198272751 T>C maps to NM_012433.2 E403E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-7501-01A-11D-2201-08 chr11:65829381 C>A maps to NM_006842.2 P630P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A4EM-01A-11D-A25F-10 chr11:65835415 G>T did not map to a codon.
Sequencing variant TCGA-IZ-A6M8-01A-11D-A31X-10 chr16:70605580 G>A maps to NM_012426.4 V1173V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7288-01A-11D-2136-08 chr19:19420930 C>T maps to NM_172231.2 K95K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A7SO-01A-11D-A34Z-10 chr19:19408122 G>T maps to NM_172231.2 Y306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5884-01A-11D-1589-08 chr3:52939192 C>A maps to NM_016329.3 E854*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E7-01A-31D-A28G-10 chr10:7214000 G>A maps to NM_001018039.1 P757P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9JY-01A-11D-A42J-10 chr1:35657091 T>C maps to NM_005066.2 G289G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A9DC-01A-11D-A36X-10 chr1:35650119 A>T maps to NM_005066.2 T687T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PL-01A-11D-A382-10 chr1:35656515 A>G maps to NM_005066.2 F366F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KV-A6GD-01A-11D-A31X-10 chr17:56083836 G>T maps to NM_006924.4 Y82*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8195-01A-31D-2396-08 chr21:33057762 A>G maps to NM_020706.2 T748T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A9DD-01A-11D-A36X-10 chr19:45555366 A>C maps to NM_007056.2 R46R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NI-01A-11D-A26P-10 chr23:1714402 G>A did not map to a codon.
Sequencing variant TCGA-MH-A55Z-01A-11D-A26P-10 chr23:1719997 C>T did not map to a codon.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr12:46318585 T>A maps to NM_004719.2 P1277P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Y8-A894-01A-11D-A35Z-10 chr12:46327005 A>G maps to NM_004719.2 F214F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A9DE-01A-11D-A36X-10 chr1:29475200 G>C maps to NM_005626.4 S402S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A8YH-01A-11D-A36X-10 chr20:42088516 C>T maps to NM_006275.5 C121C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A7SQ-01A-12D-A35Z-10 chr20:42089558 C>T maps to NM_006275.5 S297S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr10:81702147 G>C maps to NM_003019.4 P143P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr5:156186310 C>T maps to NM_000337.5 F261F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-7268-01A-11D-2136-08 chr8:8235102 A>T maps to NM_001080826.1 T272T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-7173-01A-11D-2136-08 chr15:77406688 G>A maps to NM_024776.2 L1684L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A562-01A-11D-A26P-10 chr15:77472612 A>T maps to NM_024776.2 T552T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PJ-A5Z8-01A-11D-A28G-10 chr2:201438488 T>G maps to NM_152524.5 S1140S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A7SR-01A-12D-A35Z-10 chr17:2274583 C>A maps to NM_014853.2 G484G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A48D-01A-11D-A25F-10 chr22:40800333 C>T maps to NM_015705.4 L81L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A7SL-01A-11D-A34Z-10 chr22:40803842 G>A maps to NM_015705.4 L525L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9J2-01A-11D-A382-10 chr2:235950615 A>T maps to NM_014521.2 I401I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A48D-01A-11D-A25F-10 chr3:15298470 G>A maps to NM_004844.3 L347L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W8-01A-11D-A28G-10 chr23:19560044 C>A did not map to a codon.
Sequencing variant TCGA-DW-7840-01A-11D-2136-08 chr23:19626145 G>T did not map to a codon.
Sequencing variant TCGA-J7-6720-01A-11D-2136-08 chr4:170028337 A>G maps to NM_020870.3 L720L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F9-A7VF-01A-11D-A33Q-10 chr4:8229478 C>T maps to NM_018986.3 P686P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr4:8230106 C>T maps to NM_018986.3 L896L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PS-01A-11D-A42J-10 chr2:253095 G>A maps to NM_015677.2 S7S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7915-01A-11D-2201-08 chr19:4290584 C>T maps to NM_020209.3 A326A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Y8-A894-01A-11D-A35Z-10 chr13:26621070 C>A maps to NM_001007538.1 G156G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7841-01A-11D-2136-08 chr3:48510781 C>T maps to NM_016479.3 P207P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5Y1-01A-11D-A28G-10 chr17:3514080 G>T maps to NM_013276.2 R404R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A83S-01A-11D-A34Z-10 chr17:3526657 G>A maps to NM_013276.2 Q208*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9KA-01A-11D-A42J-10 chr6:146262785 A>T maps to ENST00000367503 A821A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7966-01A-11D-2201-08 chr5:132161118 C>T maps to NM_001172700.1 P238P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JD-01A-11D-A42J-10 chr4:77660480 T>C maps to NM_020859.3 P385P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PS-01A-11D-A42J-10 chr4:77680808 G>T maps to NM_020859.3 V1770V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JJ-01A-11D-A42J-10 chr23:50350750 G>C did not map to a codon.
Sequencing variant TCGA-B9-4116-01A-01D-1252-08 chr23:50350750 G>C did not map to a codon.
Sequencing variant TCGA-B9-A8YH-01A-11D-A36X-10 chr23:50378466 A>G did not map to a codon.
Sequencing variant TCGA-UZ-A9PK-01A-11D-A382-10 chr16:48395958 G>A maps to NM_001006610.1 S158S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9KA-01A-11D-A42J-10 chr11:117064630 C>T maps to NM_001040455.1 V758V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F9-A7VF-01A-11D-A33Q-10 chr11:407105 A>G maps to NM_021805.2 L228L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9J5-01A-21D-A382-10 chr19:51920172 G>A maps to NM_033130.4 P151P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4114-01A-01D-1252-08 chr11:111590500 C>T maps to NM_015191.1 V423V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47N-01A-11D-A25F-10 chr15:75673956 T>A maps to NM_001145357.1 A1095A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5893-01A-11D-1589-08 chr15:75692464 C>T maps to NM_001145357.1 S590S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chr15:75664532 G>A maps to NM_001145357.1 S1203S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KV-A6GD-01A-11D-A31X-10 chr15:75705129 G>A maps to NM_001145357.1 Q244*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9J1-01A-11D-A382-10 chr19:16974594 C>T maps to NM_015260.1 D489D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A7SP-01A-11D-A34Z-10 chr14:72055983 G>A maps to NM_015556.1 V465V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr1:232649813 A>T maps to NM_020808.3 I424I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JD-01A-11D-A42J-10 chr19:38684202 G>C maps to NM_015073.1 R1541R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7287-01A-11D-2136-08 chr20:1615979 C>A maps to NM_018556.3 A338A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4115-01A-01D-1252-08 chr14:105222012 C>T maps to NM_006427.3 D55D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr17:46239836 C>G maps to NM_003726.3 L324L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PJ-A5Z8-01A-11D-A28G-10 chr1:2238152 G>A maps to NM_003036.3 R712R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A83S-01A-11D-A34Z-10 chr13:103701720 A>G maps to NM_000452.2 T279T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9JY-01A-11D-A42J-10 chr8:82606175 A>G maps to NM_001010893.2 P344P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NJ-01A-11D-A26P-10 chr5:127477531 T>A maps to NM_001046.2 V544V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3472-01A-01D-1252-08 chr20:44670174 C>T maps to NM_001134771.1 I377I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A7SM-01A-11D-A34Z-10 chr20:44670003 T>C maps to NM_001134771.1 H320H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7288-01A-11D-2136-08 chr5:1064224 C>G maps to NM_006598.2 L860L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A8YH-01A-11D-A36X-10 chr5:1087044 A>T maps to NM_006598.2 Y216*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5879-01A-11D-1589-08 chr5:1094289 C>T maps to NM_006598.2 G66G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59T-01A-21D-A28G-10 chr5:1093743 C>A maps to NM_006598.2 V82V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A9DC-01A-11D-A36X-10 chr5:1087134 G>A maps to NM_006598.2 Y186Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr7:122765635 A>G maps to NM_022444.3 P409P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9KH-01A-11D-A42J-10 chr17:6594199 C>T maps to NM_177550.3 P445P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5892-01A-11D-1589-08 chr17:6597516 C>G did not map to a codon.
Sequencing variant TCGA-B3-8121-01A-21D-2396-08 chr1:113460276 G>A maps to NM_003051.3 Q251*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A71V-01A-11D-A33Q-10 chr10:91195919 T>A maps to NM_213606.3 P395P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8518-01A-11D-2396-08 chr2:230910734 G>A maps to NM_152527.4 I369I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F9-A97G-01A-11D-A382-10 chr23:73641735 C>T did not map to a codon.
Sequencing variant TCGA-DW-5560-01A-01D-1589-08 chr17:66267172 A>G maps to NM_004694.4 F376F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A83S-01A-11D-A34Z-10 chr10:61424075 A>G maps to NM_194298.2 L115L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NH-01A-11D-A26P-10 chr6:25811998 C>T did not map to a codon.
Sequencing variant TCGA-B9-A5W9-01A-11D-A28G-10 chr10:119003519 G>T maps to NM_003054.4 E54*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NK-01A-11D-A26P-10 chr1:169446749 G>A maps to NM_006996.2 D150D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A71U-01A-12D-A33Q-10 chr2:228566971 T>C maps to NM_025243.3 L21L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PR-01A-11D-A42J-10 chr8:42275392 G>T maps to NM_006749.3 T629T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A6HP-01A-11D-A31X-10 chr11:63065115 A>T maps to NM_001039752.3 G249G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A48D-01A-11D-A25F-10 chr3:38316202 T>C maps to NM_004256.3 A197A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7963-01B-11D-A28G-10 chr6:160769795 C>T maps to ENST00000392145 A115A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W8-01A-11D-A28G-10 chr5:131647951 A>C maps to NM_003059.2 S164S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5901-01A-11D-1589-08 chr5:131729503 G>A did not map to a codon.
Sequencing variant TCGA-A4-8098-01A-11D-2396-08 chr6:43266248 G>A maps to ENST00000372585 L51L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5894-01A-11D-1589-08 chr20:4854627 C>T maps to NM_203327.1 R352R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9JY-01A-11D-A42J-10 chr15:65943144 G>A maps to NM_004727.2 E886E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9Q0-01A-12D-A42J-10 chr15:65943099 A>G maps to NM_004727.2 E871E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7996-01A-11D-2201-08 chr20:19679324 G>C did not map to a codon.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr7:95818644 C>T maps to NM_001160210.1 E298E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3472-01A-01D-1252-08 chr5:140683029 G>A maps to NM_031947.2 Q135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WN-AB4C-01A-11D-A42J-10 chr6:46626711 T>A maps to NM_004277.3 G104G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr3:39431017 C>T maps to NM_017875.2 G34G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PX-01A-11D-A42J-10 chr19:19217182 C>A maps to NM_178526.3 T162T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M9-01A-11D-A31X-10 chr23:118603719 T>G did not map to a codon.
Sequencing variant TCGA-A4-8311-01A-11D-2396-08 chr4:983982 T>C maps to NM_213613.2 T248T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7584-01A-11D-2136-08 chr17:78197108 C>G maps to NM_173626.3 A162A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NJ-01A-11D-A26P-10 chr5:149361288 T>C maps to NM_000112.3 S711S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7732-01A-11D-2136-08 chr7:103029856 G>A maps to ENST00000354356 A442A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7061-01A-11D-1961-08 chr7:103029510 A>G maps to ENST00000354356 Y486Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr3:48668740 T>C did not map to a codon.
Sequencing variant TCGA-BQ-5880-01A-11D-1589-08 chr6:35949920 C>T maps to NM_052961.3 T334T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A657-01A-11D-A31X-10 chr15:85476452 G>A maps to NM_004213.3 P387P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PZ-01A-11D-A42J-10 chr15:85488364 A>G maps to NM_004213.3 P628P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-A8LE-01A-11D-A35Z-10 chr12:40158611 G>C maps to NM_052885.3 Y498*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9KE-01A-11D-A42J-10 chr4:10022969 C>T maps to NM_020041.2 G28G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A7SQ-01A-12D-A35Z-10 chr9:116021052 G>A maps to NM_001859.3 L94L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4A-A93W-01A-11D-A36X-10 chr20:37356235 G>T maps to NM_080552.2 E178*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47M-01A-11D-A25F-10 chr23:48762074 G>A did not map to a codon.
Sequencing variant TCGA-A4-8311-01A-11D-2396-08 chr5:139947278 T>A maps to NM_080670.2 A175A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PJ-A5Z9-01A-11D-A28G-10 chr1:67519573 C>A maps to NM_015139.2 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr9:99106262 C>A maps to NM_007001.2 G203*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NJ-01A-11D-A26P-10 chr12:69158529 G>T maps to NM_018656.2 G268*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4113-01A-01D-1252-08 chr5:150660716 G>T maps to NM_001145017.1 Y375*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7915-01A-11D-2201-08 chr11:92917686 C>A did not map to a codon.
Sequencing variant TCGA-BQ-5884-01A-11D-1589-08 chr17:79220315 C>T maps to NM_001037984.1 Q800Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A854-01A-11D-A34Z-10 chr3:50254732 G>C maps to NM_006841.4 L204L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr16:84063152 A>G maps to NM_001080442.1 P212P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5884-01A-11D-1589-08 chr12:56630208 C>G maps to NM_001135195.1 L325L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2K-A9WE-01A-11D-A382-10 chr6:33170058 T>A maps to NM_006979.2 S218S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7585-01A-11D-2136-08 chr14:69866097 C>T maps to NM_018375.3 F4F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5902-01A-11D-1589-08 chr2:44508524 G>C did not map to a codon.
Sequencing variant TCGA-SX-A71V-01A-11D-A33Q-10 chr2:190428538 T>A maps to NM_014585.5 V391V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A772-01A-11D-A33Q-10 chr19:10738605 T>C maps to NM_020428.3 H57H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JM-01A-12D-A42J-10 chr1:95322999 C>A maps to NM_001114106.1 I394I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W9-01A-11D-A28G-10 chr1:95330397 T>A maps to NM_001114106.1 S446S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A7SS-01A-11D-A35Z-10 chr5:33954589 A>T maps to NM_016180.3 L303*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chr8:142238283 G>A maps to NM_001080431.1 Q28*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9J5-01A-21D-A382-10 chr17:19458999 G>T maps to ENST00000395585 G246*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A9DC-01A-11D-A36X-10 chr17:19480760 A>G maps to ENST00000395585 K536K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4A-A93X-01A-11D-A36X-10 chr2:162762259 C>T maps to NM_001178015.1 I620I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5880-01A-11D-1589-08 chr4:72429511 T>A maps to NM_001098484.2 S1034S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr4:72332249 C>A maps to NM_001098484.2 T529T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PR-01A-11D-A42J-10 chr4:72423544 T>C maps to NM_001098484.2 C960C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7288-01A-11D-2136-08 chr2:74458395 C>A maps to NM_021196.3 T938T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr2:74458395 C>A maps to NM_021196.3 T938T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A71R-01A-12D-A33Q-10 chr3:27477879 T>C maps to ENST00000454389 A196A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7288-01A-11D-2136-08 chr11:26725401 A>G maps to NM_178498.3 H206H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WN-AB4C-01A-11D-A42J-10 chr16:31500224 A>T maps to ENST00000431354 V435V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9K0-01A-11D-A42J-10 chr19:17986909 C>A maps to NM_000453.2 L231L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A655-01A-11D-A31Z-10 chr2:27427729 G>C maps to NM_021095.2 L268L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E7-01A-31D-A28G-10 chr2:108604762 T>A maps to NM_021815.2 L51*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55Z-01A-11D-A26P-10 chr12:101588896 C>T maps to NM_145913.3 V171V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6789-01A-11D-1961-08 chr23:115573955 G>A did not map to a codon.
Sequencing variant TCGA-A4-A4ZT-01A-11D-A26P-10 chr12:85279277 A>G maps to NM_182767.4 S170S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A40X-01A-11D-A25F-10 chr5:1219217 C>T maps to NM_001003841.2 L458L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5877-01A-11D-1589-08 chr16:55705979 C>T maps to NM_001043.3 T179T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-AAVL-01A-11D-A42J-10 chr16:55719084 C>T maps to NM_001043.3 S225S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-A8LC-01A-11D-A35Z-10 chr5:1420692 G>A maps to NM_001044.4 C306C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KV-A6GD-01A-11D-A31X-10 chr3:14508106 A>G maps to NM_001134367.1 A272A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A6HP-01A-11D-A31X-10 chr23:152958792 T>C did not map to a codon.
Sequencing variant TCGA-BQ-5884-01A-11D-1589-08 chr8:87226721 T>A maps to NM_138817.2 R445*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9J5-01A-21D-A382-10 chr3:170244551 G>A maps to NM_020949.2 L58L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8310-01A-11D-2396-08 chr8:17419588 G>A maps to NM_001164771.1 Q587Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5885-01A-11D-1589-08 chr8:17401958 G>T did not map to a codon.
Sequencing variant TCGA-UZ-A9Q1-01A-11D-A42J-10 chr14:23242824 A>T maps to NM_001126106.1 S510S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A71V-01A-11D-A33Q-10 chr14:23634562 G>A maps to NM_012244.2 L147L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A9DD-01A-11D-A36X-10 chr2:40657411 G>A maps to NM_021097.2 N3N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8312-01A-11D-2396-08 chr14:70527577 C>T maps to NM_183002.1 P621P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4115-01A-01D-1252-08 chr1:27428599 C>T maps to NM_003047.3 L614L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9K0-01A-11D-A42J-10 chr5:483551 G>A maps to NM_004174.2 N326N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7058-01A-11D-1961-08 chr17:72745285 A>T maps to NM_004252.3 K101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5875-01A-11D-1589-08 chr23:46491074 A>T did not map to a codon.
Sequencing variant TCGA-Y8-A897-01A-11D-A35Z-10 chr23:46541772 T>C did not map to a codon.
Sequencing variant TCGA-HE-A5NK-01A-11D-A26P-10 chr20:48431565 T>C maps to ENST00000417961 H16H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Y8-A895-01A-11D-A35Z-10 chr12:21459851 C>A maps to NM_134431.3 G136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr3:133692537 G>C maps to NM_005630.2 S122S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59R-01A-11D-A26P-10 chr20:61300282 G>A maps to NM_016354.3 G626G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8311-01A-11D-2396-08 chr5:101834203 C>A maps to NM_173488.3 L115L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A8YH-01A-11D-A36X-10 chr17:33679952 A>G maps to NM_152270.3 L710L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5888-01A-11D-1589-08 chr17:33679779 G>A maps to NM_152270.3 A767A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9KC-01A-11D-A42J-10 chr17:33768162 A>G maps to NM_144682.5 L715L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A71S-01A-11D-A33Q-10 chr17:33588031 C>A maps to NM_144975.3 S352*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A71V-01A-11D-A33Q-10 chr10:98803146 G>A maps to NM_003061.2 T659T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V9-A7HT-01A-11D-A33Q-10 chr4:20258327 G>C maps to ENST00000273739 T71T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J7-8537-01A-11D-2396-08 chr23:144904237 C>T did not map to a codon.
Sequencing variant TCGA-2Z-A9JD-01A-11D-A42J-10 chr23:142718225 A>C did not map to a codon.
Sequencing variant TCGA-J7-6720-01A-11D-2136-08 chr23:142718335 C>A did not map to a codon.
Sequencing variant TCGA-B9-A44B-01A-11D-A25F-10 chr3:57743530 A>G maps to ENST00000428312 L51L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9Q0-01A-12D-A42J-10 chr5:159831847 C>A maps to NM_006425.4 E478*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr4:146463797 G>A maps to NM_001003688.1 P241P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9KC-01A-11D-A42J-10 chr6:71508430 A>G maps to NM_001044305.1 T189T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A7SN-01A-11D-A34Z-10 chr6:71377782 C>A maps to NM_001044305.1 L19L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PM-01A-21D-A382-10 chr1:40880942 G>T did not map to a codon.
Sequencing variant TCGA-5P-A9K3-01A-11D-A42J-10 chr23:128582333 C>G did not map to a codon.
Sequencing variant TCGA-G7-A8LD-01A-11D-A35Z-10 chr23:128652405 G>A did not map to a codon.
Sequencing variant TCGA-SX-A7SP-01A-11D-A34Z-10 chr23:128614705 A>G did not map to a codon.
Sequencing variant TCGA-BQ-5893-01A-11D-1589-08 chr9:2110311 C>T maps to NM_003070.3 S1117S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A7SU-01A-11D-A35Z-10 chr9:2039784 G>A maps to NM_003070.3 Q225Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A7SU-01A-11D-A35Z-10 chr9:2039808 G>A maps to NM_003070.3 Q233Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W8-01A-11D-A28G-10 chr19:11134285 C>G maps to NM_001128849.1 V984V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PK-01A-11D-A382-10 chr19:11113758 G>T maps to NM_001128849.1 E623*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8312-01A-11D-2396-08 chr2:217279801 C>G maps to NM_014140.3 P125P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A83T-01A-11D-A34Z-10 chr17:38793825 T>C did not map to a codon.
Sequencing variant TCGA-BQ-5880-01A-11D-1589-08 chr23:53407984 A>T did not map to a codon.
Sequencing variant TCGA-MH-A561-01A-11D-A26P-10 chr23:53440301 C>G did not map to a codon.
Sequencing variant TCGA-UZ-A9PX-01A-11D-A42J-10 chr22:45809421 C>G maps to NM_148674.3 V9V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JK-01A-11D-A42J-10 chr9:106882314 A>T maps to NM_001042550.1 R668R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PJ-A8JU-01A-11D-A35Z-10 chr2:17865002 A>C maps to ENST00000381272 Y928*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A7SN-01A-11D-A34Z-10 chr2:17881503 G>A maps to ENST00000381272 Q815*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9K6-01A-11D-A42J-10 chr18:2729382 G>A maps to NM_015295.2 T1008T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8630-01A-11D-2396-08 chr18:2718193 C>T maps to NM_015295.2 Q767*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-5155-01A-01D-1589-08 chr17:18220176 T>C maps to NM_144775.2 D358D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A4ZT-01A-11D-A26P-10 chr16:18849888 A>G maps to ENST00000389467 N2356N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JG-01A-11D-A42J-10 chr1:183495888 C>T maps to ENST00000367537 H200H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JM-01A-12D-A42J-10 chr1:183520231 C>T maps to ENST00000367537 S1116S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-AAVM-01A-11D-A42J-10 chr11:6411959 G>T maps to NM_000543.4 A44A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PS-01A-11D-A42J-10 chr16:68405640 T>C maps to NM_018667.3 Q148Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PR-01A-11D-A42J-10 chr6:123124849 A>C maps to NM_006714.3 R204R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A40Y-01A-11D-A25F-10 chr22:31484746 G>C maps to ENST00000454496 R173R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-7332-01A-11D-2136-08 chr9:33048145 G>C maps to NM_018225.2 Y467*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A8YH-01A-11D-A36X-10 chr1:246670462 G>T maps to NM_001167740.1 R19R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Y8-A895-01A-11D-A35Z-10 chr1:246021811 G>A maps to NM_001167740.1 T354T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JK-01A-11D-A42J-10 chr17:1687737 G>C maps to NM_052928.2 R634R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9Q0-01A-12D-A42J-10 chr14:62229243 C>T maps to NM_003082.3 D22D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A9DE-01A-11D-A36X-10 chr5:121786597 G>T maps to ENST00000379533 E733*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V9-A7HT-01A-11D-A33Q-10 chr5:121780388 G>T maps to ENST00000379533 L565L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NF-01A-11D-A26P-10 chr2:242026824 A>T maps to NM_001080437.1 R1380R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Y8-A894-01A-11D-A35Z-10 chr15:101833252 C>T maps to NM_003090.2 L69L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A7SL-01A-11D-A34Z-10 chr20:16719516 T>C maps to NM_198220.2 N133N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-3925-01A-01D-1458-08 chr8:121587443 G>A maps to NM_021021.3 Q340*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7836-01A-11D-2136-08 chr16:69294138 G>A maps to NM_006750.3 K327K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7966-01A-11D-2201-08 chr15:25207296 C>T maps to NM_022804.2 H17H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PJ-A8JU-01A-11D-A35Z-10 chr15:25207340 C>A maps to NM_022804.2 S32*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PX-01A-11D-A42J-10 chr15:25207311 A>G maps to NM_022804.2 E22E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PU-01A-11D-A42J-10 chr14:78203381 A>G maps to NM_012245.2 S190S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A657-01A-11D-A31X-10 chr23:70280927 G>T did not map to a codon.
Sequencing variant TCGA-2Z-A9JS-01A-21D-A42J-10 chr6:86303310 G>T maps to NM_153816.3 S42S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9KC-01A-11D-A42J-10 chr2:27596783 G>C maps to NM_014748.2 G126G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5876-01A-11D-1589-08 chr11:130785819 T>A maps to NM_014758.2 T5T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5ED-01A-11D-A28G-10 chr5:122154606 T>G maps to NM_003100.2 L367L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A71S-01A-11D-A33Q-10 chr1:151665955 A>G maps to ENST00000458013 K525K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6135-01A-11D-1961-08 chr16:12618620 C>T maps to NM_001080530.2 N362N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7045-01A-31D-1961-08 chr14:35062275 A>T maps to NM_152233.2 S243S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A48D-01A-11D-A25F-10 chr6:158330821 T>G maps to NM_016224.3 T277T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr6:107955223 G>T maps to NM_018013.3 P392P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NF-01A-11D-A26P-10 chr17:36508825 C>A maps to NM_014598.2 T233T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A772-01A-11D-A33Q-10 chr9:138589407 C>G maps to NM_001101677.1 S137S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4A-A93W-01A-11D-A36X-10 chr13:36744691 C>T maps to ENST00000511166 T488T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JT-01A-11D-A42J-10 chr21:34926408 T>C maps to NM_138927.1 N1624N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PJ-01A-11D-A382-10 chr21:34927347 A>T maps to NM_138927.1 R1937R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Y8-A896-01A-11D-A35Z-10 chr10:97143752 T>C maps to NM_001034954.1 S509S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9Q1-01A-11D-A42J-10 chr8:22432204 C>T maps to NM_005775.4 F660F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5884-01A-11D-1589-08 chr2:39285903 C>T maps to NM_005633.3 W85*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-3925-01A-01D-1458-08 chr22:38374015 C>T maps to NM_006941.3 Q185Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JS-01A-21D-A42J-10 chr2:174820711 G>A maps to NM_003111.4 I176I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A71S-01A-11D-A33Q-10 chr2:174820132 C>T maps to NM_003111.4 Q369Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5880-01A-11D-1589-08 chr7:21468914 G>A maps to NM_003112.3 Q44Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A4EM-01A-11D-A25F-10 chr7:21469334 T>C maps to NM_003112.3 T184T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E6-01A-11D-A28G-10 chr2:171572791 G>A maps to NM_001003845.2 P25P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E8-01A-11D-A28G-10 chr17:45925060 G>A maps to NM_199262.2 P245P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NI-01A-11D-A26P-10 chr12:53722358 C>T maps to NM_001173467.1 R289R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9JY-01A-11D-A42J-10 chr7:20824955 C>G maps to NM_182700.4 G160G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7839-01A-11D-2136-08 chr7:20824955 C>G maps to NM_182700.4 G160G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9JY-01A-11D-A42J-10 chr17:4871089 G>A maps to NM_004890.2 L4L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A561-01A-11D-A26P-10 chr17:49067111 G>T maps to ENST00000376407 V914V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9JY-01A-11D-A42J-10 chr5:151043687 G>T maps to NM_003118.2 I281I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9J2-01A-11D-A382-10 chr13:24797768 G>A maps to ENST00000424834 V271V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr1:217975147 G>T maps to NM_138796.2 E321*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4104-01A-01D-1458-08 chr17:48628384 G>A maps to NM_022827.2 Q470Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9JV-01A-12D-A42J-10 chr5:94994605 A>T maps to NM_031952.3 V162V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PX-01A-11D-A42J-10 chr6:34508953 G>T maps to NM_012391.1 P147P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9JZ-01A-11D-A42J-10 chr2:220342165 A>G maps to NM_005876.4 S1576S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-5561-01A-01D-1589-08 chr2:220338576 C>A maps to NM_005876.4 R1467R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NH-01A-11D-A26P-10 chr2:220349150 C>T maps to NM_005876.4 S2322S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4116-01A-01D-1252-08 chr17:7324266 C>A maps to NM_199339.2 V91V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NI-01A-11D-A26P-10 chr1:16260462 T>G maps to NM_015001.2 V2576V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4A-A93X-01A-11D-A36X-10 chr13:46288258 C>T maps to NM_152719.1 Q367*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-A8LD-01A-11D-A35Z-10 chr13:46287522 G>A maps to NM_152719.1 V121V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A9DC-01A-11D-A36X-10 chr19:49132773 G>A maps to NM_020126.3 W570*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8196-01A-11D-2396-08 chr2:228860229 G>C maps to NM_001142644.1 S1543S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3468-01A-01D-1252-08 chr23:57021006 G>C did not map to a codon.
Sequencing variant TCGA-B9-4113-01A-01D-1252-08 chr15:41146020 C>T maps to NM_181642.2 G285G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr19:38774303 G>T maps to NM_021102.3 R48R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PJ-01A-11D-A382-10 chr16:89920722 G>T maps to NM_032451.1 P225P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5878-01A-11D-1589-08 chr5:136328173 G>A maps to NM_004598.3 G235G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JE-01A-11D-A42J-10 chr4:1165760 G>T maps to NM_012445.3 S33S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A9DD-01A-11D-A36X-10 chr4:1165649 A>T maps to NM_012445.3 S70S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7286-01A-11D-2136-08 chr2:139308571 A>G maps to NM_001001664.2 A100A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J7-A8I2-01A-12D-A35Z-10 chr15:51014330 C>T maps to NM_032802.3 S439S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-7268-01A-11D-2136-08 chr1:153004964 C>T maps to NM_003125.2 P48P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55Z-01A-11D-A26P-10 chr12:56862410 C>T maps to NM_207344.3 C12C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr9:131339497 T>C maps to NM_001130438.2 A292A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr9:131370473 C>A maps to NM_001130438.2 T1470T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NI-01A-11D-A26P-10 chr9:131386740 G>A maps to NM_001130438.2 K1989K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8517-01A-11D-2396-08 chr2:54851999 C>T maps to NM_003128.2 L414L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9J3-01A-12D-A382-10 chr15:42163670 G>C maps to ENST00000320955 G1783G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8517-01A-11D-2396-08 chr9:94821489 G>A maps to NM_006415.2 L221L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A854-01A-11D-A34Z-10 chr14:78021666 A>G maps to NM_004863.2 S384S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PL-01A-11D-A382-10 chr14:78028817 C>G maps to NM_004863.2 L257L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8311-01A-11D-2396-08 chr2:45616664 G>C maps to NM_018079.4 G924G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JR-01A-12D-A42J-10 chr16:30732249 C>T maps to NM_006662.2 G1068G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8312-01A-11D-2396-08 chr16:30718523 G>T maps to NM_006662.2 R109R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr16:30735226 A>C maps to NM_006662.2 A1494A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NF-01A-11D-A26P-10 chr16:30734927 T>C maps to NM_006662.2 L1395L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EA-01A-11D-A28G-10 chr16:30744760 A>G maps to NM_006662.2 E2096E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A7SQ-01A-12D-A35Z-10 chr17:36714572 C>A maps to NM_025248.2 V697V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-A6W5-01A-12D-A33Q-10 chr22:42274012 C>T maps to NM_004599.2 V549V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-5155-01A-01D-1589-08 chr5:112200370 A>G maps to NM_003135.1 R81R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A9DC-01A-11D-A36X-10 chr11:126134971 G>T maps to NM_003139.3 T469T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F9-A97G-01A-11D-A382-10 chr1:24972472 A>G did not map to a codon.
Sequencing variant TCGA-4A-A93X-01A-11D-A36X-10 chr16:2814198 G>T maps to NM_016333.3 E1224*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5877-01A-11D-1589-08 chr16:2817458 T>C maps to NM_016333.3 S2310S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Y8-A898-01A-11D-A34Z-10 chr16:2819138 C>T maps to NM_016333.3 S2625S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7584-01A-11D-2136-08 chr1:54870253 C>T maps to NM_145716.2 W62*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr2:182765432 T>C maps to NM_001130445.1 L172L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A8YI-01A-21D-A36X-10 chr12:109212090 T>A did not map to a codon.
Sequencing variant TCGA-A4-8517-01A-11D-2396-08 chr7:149502568 C>A maps to NM_198455.2 G2795G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-AAVL-01A-11D-A42J-10 chr7:149518599 C>T maps to NM_198455.2 T4227T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PJ-A5Z8-01A-11D-A28G-10 chr7:149518181 C>T maps to NM_198455.2 C4179C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JE-01A-11D-A42J-10 chr11:57102552 T>A maps to NM_003146.2 K15*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KV-A6GD-01A-11D-A31X-10 chr11:57100281 C>A maps to NM_003146.2 T195T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-A8LE-01A-11D-A35Z-10 chr22:37603059 G>T maps to NM_001051.2 A261A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Y8-A897-01A-11D-A35Z-10 chr16:1129707 C>T maps to NM_001053.3 P280P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8630-01A-11D-2396-08 chr1:1480324 C>T maps to NM_014188.2 R94R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5879-01A-11D-1589-08 chr23:48123288 G>A did not map to a codon.
Sequencing variant TCGA-B3-4104-01A-01D-1458-08 chr8:53028900 C>T maps to NM_014682.2 L979L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr8:53092685 G>T maps to NM_014682.2 T91T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A857-01A-11D-A34Z-10 chr3:98512535 G>T maps to ENST00000493584 V362V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JQ-01A-11D-A42J-10 chr15:92987896 C>A maps to NM_006011.3 R194R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PL-01A-11D-A382-10 chr15:92987940 G>A maps to NM_006011.3 S208S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr18:44284578 G>T maps to NM_013305.4 C60*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J7-8537-01A-11D-2396-08 chr10:17495607 C>T maps to NM_001004470.1 A50A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-7502-01A-11D-2201-08 chr3:52554290 C>A maps to NM_015136.2 C1828*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A854-01A-11D-A34Z-10 chr3:52548198 C>T maps to NM_015136.2 S1172S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PS-01A-11D-A42J-10 chr3:52551366 C>T maps to NM_015136.2 G1507G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A7SQ-01A-12D-A35Z-10 chr12:104160112 G>T maps to NM_017564.9 *2552L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PN-01A-11D-A382-10 chr12:104056743 C>T maps to NM_017564.9 R664*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6790-01A-11D-1961-08 chr17:37368583 C>T maps to NM_198993.3 K399K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NJ-01A-11D-A26P-10 chr17:37373421 G>A maps to NM_198993.3 N134N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PJ-A8JU-01A-11D-A35Z-10 chr3:136096519 A>G maps to NM_005862.2 N784N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4A-A93X-01A-11D-A36X-10 chr23:123205103 C>T did not map to a codon.
Sequencing variant TCGA-A4-7287-01A-11D-2136-08 chr23:123197833 C>A did not map to a codon.
Sequencing variant TCGA-B3-4104-01A-01D-1458-08 chr23:123176468 C>T did not map to a codon.
Sequencing variant TCGA-BQ-5890-01A-11D-1589-08 chr23:123200036 T>C did not map to a codon.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr23:123202455 C>T did not map to a codon.
Sequencing variant TCGA-IA-A83T-01A-11D-A34Z-10 chr23:123229292 T>A did not map to a codon.
Sequencing variant TCGA-2Z-A9J3-01A-12D-A382-10 chr2:152980338 A>C maps to NM_005843.4 S430S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5884-01A-11D-1589-08 chr12:56742946 C>T maps to NM_005419.3 Q480Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr17:40459442 C>A maps to NM_003152.3 Y568*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr20:47741018 T>A maps to NM_017453.2 K239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PJ-A8JU-01A-11D-A35Z-10 chr20:47732329 T>C maps to NM_017453.2 G569G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5Y1-01A-11D-A28G-10 chr8:74464270 A>G maps to NM_001164380.1 Y502Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JQ-01A-11D-A42J-10 chr8:23702288 A>G maps to NM_003155.2 S246S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A854-01A-11D-A34Z-10 chr7:87910334 A>C maps to NM_024636.2 Y348*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55W-01A-11D-A26P-10 chr5:171471933 T>G maps to NM_005990.3 P953P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-5155-01A-01D-1589-08 chr19:1220438 A>T maps to NM_000455.4 K178*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NH-01A-11D-A26P-10 chr2:220470427 G>T maps to NM_052902.2 L250L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PJ-A5Z9-01A-11D-A28G-10 chr10:134036391 C>T maps to NM_173575.2 K364K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-7502-01A-11D-2201-08 chr2:219556969 C>G maps to NM_015690.3 L623L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Y8-A8S1-01A-11D-A36X-10 chr8:80567257 G>A maps to NM_007029.3 E147E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PJ-A5Z8-01A-11D-A28G-10 chr15:74281092 A>G maps to NM_004809.3 F147F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6135-01A-11D-1961-08 chr2:48818888 C>A maps to NM_172311.2 S676S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JS-01A-21D-A42J-10 chr10:70652347 A>G maps to NM_001130161.2 T942T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PJ-A8JU-01A-11D-A35Z-10 chr10:70645489 C>A maps to NM_001130161.2 A646A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9J1-01A-11D-A382-10 chr19:47226539 G>A maps to NM_001039877.1 D539D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A40U-01A-11D-A25F-10 chr16:732018 G>T did not map to a codon.
Sequencing variant TCGA-Y8-A894-01A-11D-A35Z-10 chr6:144508307 G>T maps to NM_003764.3 E182*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PJ-01A-11D-A382-10 chr9:102691076 C>A maps to NM_017919.2 I47I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr16:31046333 C>A maps to NM_004604.3 S117S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A8YH-01A-11D-A36X-10 chr14:53224473 G>C maps to NM_145251.3 V118V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E7-01A-31D-A28G-10 chr2:84652538 C>T maps to NM_003849.3 K338K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A8YI-01A-21D-A36X-10 chr12:118852237 A>C maps to NM_022491.2 *329C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V9-A7HT-01A-11D-A33Q-10 chr8:70515846 C>T maps to NM_001128206.1 N401N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4A-A93W-01A-11D-A36X-10 chr2:108999667 T>C maps to NM_006588.2 A171A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8311-01A-11D-2396-08 chr22:39138451 G>A maps to ENST00000405018 L329L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5903-01A-11D-1589-08 chr14:21821860 C>T did not map to a codon.
Sequencing variant TCGA-2Z-A9JO-01A-11D-A42J-10 chr17:27005194 A>C maps to NM_003170.3 R367R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M9-01A-11D-A31X-10 chr17:27014485 G>T maps to NM_003170.3 L1001L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4103-01A-01D-1458-08 chr22:24581139 C>A maps to NM_019601.3 A287A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PR-01A-11D-A42J-10 chr23:48558806 A>G did not map to a codon.
Sequencing variant TCGA-5P-A9KC-01A-11D-A42J-10 chr11:67926522 A>C maps to NM_017635.3 T430T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4A-A93Y-01A-11D-A36X-10 chr17:30315476 G>T maps to NM_015355.2 E388*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PX-01A-11D-A42J-10 chr9:113241923 C>T maps to ENST00000374463 L826L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A71S-01A-11D-A33Q-10 chr10:29769499 A>G maps to NM_021738.2 Y1781Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A7UZ-01A-12D-A34Z-10 chr1:115488959 T>C maps to NM_003176.2 Y735Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-A6W5-01A-12D-A33Q-10 chr1:115453122 G>A did not map to a codon.
Sequencing variant TCGA-4A-A93Y-01A-11D-A36X-10 chr20:58445039 T>G did not map to a codon.
Sequencing variant TCGA-SX-A7SU-01A-11D-A35Z-10 chr6:10935325 C>T maps to NM_001040274.2 P573P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-7268-01A-11D-2136-08 chr12:102125408 T>C maps to ENST00000449403 Q204Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-5155-01A-01D-1589-08 chr1:85656154 T>C maps to NM_032184.1 V342V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9KA-01A-11D-A42J-10 chr19:46324743 C>T did not map to a codon.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chr23:47432307 G>C did not map to a codon.
Sequencing variant TCGA-UZ-A9Q0-01A-12D-A42J-10 chr6:152462386 C>T maps to NM_182961.2 E8399E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9J3-01A-12D-A382-10 chr14:64548158 A>G did not map to a codon.
Sequencing variant TCGA-5P-A9KA-01A-11D-A42J-10 chr14:64494495 T>C maps to NM_182914.2 L2233L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A40Y-01A-11D-A25F-10 chr14:64519116 T>G maps to NM_182914.2 L2829*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PU-01A-11D-A42J-10 chr14:64669617 C>T maps to NM_182914.2 S6046S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9Q0-01A-12D-A42J-10 chr14:64595264 G>A maps to NM_182914.2 Q4671Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4116-01A-01D-1252-08 chr6:158449968 A>T maps to NM_003898.3 S132S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chr6:158450004 C>T maps to NM_003898.3 V144V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Y8-A897-01A-11D-A35Z-10 chr6:158504534 G>A maps to NM_003898.3 R980R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A7UZ-01A-12D-A34Z-10 chr7:105752600 G>A maps to NM_006754.2 I36I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A7SL-01A-11D-A34Z-10 chr20:43995568 T>A maps to NM_033542.3 T95T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7840-01A-11D-2136-08 chr1:210267874 T>C maps to NM_001146261.1 S262S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9J3-01A-12D-A382-10 chr14:62536435 T>G maps to NM_031914.2 S213S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9Q1-01A-11D-A42J-10 chr1:202572219 C>G maps to NM_177402.4 L124L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A7UZ-01A-12D-A34Z-10 chr11:64897358 C>T maps to NM_172230.2 A479A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A40U-01A-11D-A25F-10 chr22:39814794 G>A maps to NM_006116.2 L203L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9KC-01A-11D-A42J-10 chr10:123842716 T>C maps to NM_206862.2 F234F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A71V-01A-11D-A33Q-10 chr4:7056601 T>C maps to NM_152293.2 L362L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W8-01A-11D-A28G-10 chr23:70618523 G>A did not map to a codon.
Sequencing variant TCGA-BQ-5876-01A-11D-1589-08 chr23:70643917 T>C did not map to a codon.
Sequencing variant TCGA-P4-A5ED-01A-11D-A28G-10 chr9:32633309 G>A maps to NM_153809.2 G756G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7963-01B-11D-A28G-10 chr7:99707630 G>A maps to ENST00000472509 D465D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JK-01A-11D-A42J-10 chr23:100533090 C>T did not map to a codon.
Sequencing variant TCGA-G7-A8LD-01A-11D-A35Z-10 chr6:42025250 G>A maps to NM_138572.2 P163P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5884-01A-11D-1589-08 chr2:160086334 C>A maps to NM_033394.2 P1466P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7585-01A-11D-2136-08 chr17:61490919 G>T maps to ENST00000389520 A1241A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A7SQ-01A-12D-A35Z-10 chr17:61497659 C>T maps to ENST00000389520 V1449V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PJ-01A-11D-A382-10 chr2:162087644 A>G maps to NM_004180.2 S228S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9Q1-01A-11D-A42J-10 chr12:53899549 C>T maps to NM_134323.1 L287L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Y8-A895-01A-11D-A35Z-10 chr7:38305037 T>C maps to ENST00000443402 S80S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7915-01A-11D-2201-08 chr1:6639490 C>T maps to NM_138697.3 A791A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JN-01A-21D-A42J-10 chr1:19181459 G>A maps to NM_152232.2 S168S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-5156-01A-01D-1589-08 chr1:19166251 C>G maps to NM_152232.2 L787L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7966-01A-11D-2201-08 chr5:9629373 G>A maps to NM_019599.2 F257F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7288-01A-11D-2136-08 chr12:11139401 C>A maps to NM_176890.2 G20*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47N-01A-11D-A25F-10 chr7:27856558 A>T maps to ENST00000409980 R687*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5885-01A-11D-1589-08 chr7:27856086 T>C maps to ENST00000409980 N652N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-5561-01A-01D-1589-08 chr12:72288465 A>T maps to NM_022771.4 K237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A71U-01A-12D-A33Q-10 chr12:72274295 T>C maps to NM_022771.4 G84G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Y8-A895-01A-11D-A35Z-10 chr17:77987193 C>T maps to NM_019020.2 G51G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55W-01A-11D-A26P-10 chr4:26585818 T>C maps to NM_018317.2 L2L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7997-01A-11D-2201-08 chr20:419912 G>T maps to ENST00000246077 V290V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9JU-01A-11D-A42J-10 chr3:100025387 G>A did not map to a codon.
Sequencing variant TCGA-GL-A59T-01A-21D-A28G-10 chr16:2550435 G>T maps to ENST00000434757 L490L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A6HP-01A-11D-A31X-10 chr17:18541948 A>G maps to NM_001039397.2 Y88Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PM-01A-21D-A382-10 chr15:78316563 G>T maps to NM_144572.1 T468T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A57E-01A-11D-A26P-10 chr13:75923414 C>A maps to ENST00000431480 L433L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A9DD-01A-11D-A36X-10 chr13:75898482 A>T maps to ENST00000431480 L696L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A71V-01A-11D-A33Q-10 chr13:75869071 G>T maps to ENST00000431480 I1079I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NF-01A-11D-A26P-10 chr3:17550056 A>G maps to NM_001134381.1 Y2Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5885-01A-11D-1589-08 chr2:101670696 G>A maps to NM_001102426.1 F153F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55W-01A-11D-A26P-10 chr4:141600811 G>A maps to NM_015130.2 S182S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8518-01A-11D-2396-08 chr5:179320252 C>G maps to NM_198868.2 L264L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J7-6720-01A-11D-2136-08 chr5:179326224 C>T maps to NM_198868.2 E104E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PL-01A-11D-A382-10 chr6:42713427 G>T maps to NM_003192.2 R128R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr17:80885834 G>C maps to NM_005993.4 R888R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8630-01A-11D-2396-08 chr4:106967780 G>A maps to NM_001163436.1 G876G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4114-01A-01D-1252-08 chr23:9652169 T>C did not map to a codon.
Sequencing variant TCGA-PJ-A5Z9-01A-11D-A28G-10 chr23:9683002 C>T did not map to a codon.
Sequencing variant TCGA-5P-A9K2-01A-11D-A42J-10 chr6:170871003 G>A maps to NM_003194.4 Q60Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8312-01A-11D-2396-08 chr6:170871090 G>A maps to NM_003194.4 Q89Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-A5DJ-01A-11D-A26P-10 chr6:170871003 G>A maps to NM_003194.4 Q60Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7963-01B-11D-A28G-10 chr6:170871003 G>A maps to NM_003194.4 Q60Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-7501-01A-11D-2201-08 chr6:170871003 G>A maps to NM_003194.4 Q60Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-A8LB-01A-11D-A35Z-10 chr6:170871003 G>A maps to NM_003194.4 Q60Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M9-01A-11D-A31X-10 chr6:170871003 G>A maps to NM_003194.4 Q60Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JO-01A-11D-A42J-10 chr7:45148710 T>C maps to ENST00000404564 S53S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A57E-01A-11D-A26P-10 chr12:114841565 G>A maps to NM_000192.3 F46F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59T-01A-21D-A28G-10 chr17:37821722 G>A did not map to a codon.
Sequencing variant TCGA-4A-A93W-01A-11D-A36X-10 chr23:102864301 G>C did not map to a codon.
Sequencing variant TCGA-B1-A655-01A-11D-A31Z-10 chr23:102841990 A>G did not map to a codon.
Sequencing variant TCGA-IZ-A6M9-01A-11D-A31X-10 chr23:102841928 A>T did not map to a codon.
Sequencing variant TCGA-F9-A4JJ-01A-11D-A25F-10 chr18:44560192 G>A maps to NM_016427.2 D481D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8517-01A-11D-2396-08 chr2:27373230 A>T maps to NM_175769.2 K155*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8630-01A-11D-2396-08 chr18:52921811 A>G maps to ENST00000398339 I524I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KV-A6GD-01A-11D-A31X-10 chr2:85361149 C>G maps to NM_031283.2 R87R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr10:114912174 C>A maps to NM_030756.4 P392P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7996-01A-11D-2201-08 chr1:152082278 C>T maps to NM_007113.2 R1138R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A44B-01A-11D-A25F-10 chr6:35086063 T>G maps to NM_001093728.1 T511T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr14:90429931 G>A maps to NM_018319.3 L158L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A7SQ-01A-12D-A35Z-10 chr10:115947803 C>T maps to NM_198795.1 Q72*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4104-01A-01D-1458-08 chr1:154493834 G>A maps to NM_001098475.1 V83V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47M-01A-11D-A25F-10 chr9:100227198 T>G maps to NM_014290.2 P506P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PL-01A-11D-A382-10 chr6:35443199 C>T maps to ENST00000357281 E406E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NL-01A-11D-A26P-10 chr7:97847036 C>T maps to ENST00000379795 E1119E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8630-01A-11D-2396-08 chr17:6703553 C>A did not map to a codon.
Sequencing variant TCGA-PJ-A5Z9-01A-11D-A28G-10 chr1:36552573 C>T maps to NM_014466.2 N225N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A57E-01A-11D-A26P-10 chr14:20846266 G>C maps to NM_007110.4 A1879A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chr14:20845480 G>A maps to NM_007110.4 L2016L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9K2-01A-11D-A42J-10 chr10:70404539 T>A maps to NM_030625.2 L685*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr4:106157460 G>T maps to ENST00000513237 E809*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NI-01A-11D-A26P-10 chr2:74320720 G>T maps to ENST00000409262 G972G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9K8-01A-11D-A42J-10 chr23:70099887 C>T did not map to a codon.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr23:69898663 C>T did not map to a codon.
Sequencing variant TCGA-Y8-A894-01A-11D-A35Z-10 chr23:69844742 A>C did not map to a codon.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr8:30694448 T>C maps to NM_031271.3 Q2734Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Y8-A8S1-01A-11D-A36X-10 chr8:30700776 T>C maps to NM_031271.3 R1919R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A71U-01A-12D-A33Q-10 chr17:80320407 G>T maps to NM_207459.3 E128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PS-01A-11D-A42J-10 chr17:62271047 G>T maps to NM_018469.3 R683R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A8YH-01A-11D-A36X-10 chr7:100238448 G>A maps to NM_003227.3 C111C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JR-01A-12D-A42J-10 chr8:133895242 T>C maps to NM_003235.4 C358C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A9DD-01A-11D-A36X-10 chr8:133953674 C>A maps to NM_003235.4 P1707P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9KC-01A-11D-A42J-10 chr13:95230408 T>C maps to NM_014305.2 S225S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9JU-01A-11D-A42J-10 chr1:92182199 C>T maps to NM_003243.4 E544E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A7SN-01A-11D-A34Z-10 chr18:3457643 T>C maps to NM_170695.2 H304H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A7SQ-01A-12D-A35Z-10 chr14:24718614 C>G maps to NM_000359.2 V786V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A856-01A-11D-A34Z-10 chr2:85554383 C>T maps to ENST00000409015 E157E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A48D-01A-11D-A25F-10 chr15:39886355 C>A maps to NM_003246.2 Y1108*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7050-01A-11D-1961-08 chr15:39882094 C>G maps to NM_003246.2 P672P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A657-01A-11D-A31X-10 chr1:155175048 C>T maps to NM_007112.3 A115A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59T-01A-21D-A28G-10 chr1:155172113 G>A maps to NM_007112.3 R346*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PX-01A-11D-A42J-10 chr5:79375048 C>T maps to NM_003248.4 R827*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A9DD-01A-11D-A36X-10 chr2:88474888 G>A maps to NM_018271.3 T180T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8311-01A-11D-2396-08 chr23:122756984 T>A did not map to a codon.
Sequencing variant TCGA-A4-8517-01A-11D-2396-08 chr23:122755200 T>A did not map to a codon.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr23:122801089 A>G did not map to a codon.
Sequencing variant TCGA-P4-A5EA-01A-11D-A28G-10 chr23:122757674 T>C did not map to a codon.
Sequencing variant TCGA-SX-A7SN-01A-11D-A34Z-10 chr23:122766883 T>C did not map to a codon.
Sequencing variant TCGA-5P-A9K2-01A-11D-A42J-10 chr1:36751971 T>G maps to NM_005119.3 S47S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A560-01A-11D-A26P-10 chr7:11675887 G>A maps to ENST00000423059 R297R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E8-01A-11D-A28G-10 chr2:39964199 C>G did not map to a codon.
Sequencing variant TCGA-SX-A71V-01A-11D-A33Q-10 chr10:121339522 C>G did not map to a codon.
Sequencing variant TCGA-SX-A7SL-01A-11D-A34Z-10 chr21:32638850 G>A maps to NM_003253.2 G146G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W8-01A-11D-A28G-10 chr5:134785314 G>C maps to NM_001099221.1 V105V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-3925-01A-01D-1458-08 chr4:90035226 G>T maps to NM_145715.2 E368*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JJ-01A-11D-A42J-10 chr23:47445923 T>G did not map to a codon.
Sequencing variant TCGA-2Z-A9JQ-01A-11D-A42J-10 chr17:76869984 C>A maps to NM_003255.4 A49A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr14:24709983 G>C maps to NM_001099274.1 A234A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5882-01A-11D-1589-08 chr1:168168188 G>A maps to NM_152902.3 T215T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Y8-A894-01A-11D-A35Z-10 chr6:43466744 T>C maps to NM_001146016.1 T2T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-8121-01A-21D-2396-08 chr15:30008819 A>G maps to NM_003257.3 S1399S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M8-01A-11D-A31X-10 chr15:30019081 T>G maps to NM_003257.3 T738T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JO-01A-11D-A42J-10 chr16:66547632 C>G did not map to a codon.
Sequencing variant TCGA-DW-7841-01A-11D-2136-08 chr17:27052950 G>T maps to NM_138463.3 S55S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F9-A8NY-01A-11D-A35Z-10 chr19:2987355 C>T maps to NM_001143986.1 Q182*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EA-01A-11D-A28G-10 chr4:166996129 T>C maps to ENST00000507499 H786H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr9:35711015 C>T maps to NM_006289.3 K1361K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A7SS-01A-11D-A35Z-10 chr9:35697809 G>T maps to NM_006289.3 S2535*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7841-01A-11D-2136-08 chr15:63097948 C>A maps to NM_015059.2 R2210R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Y8-A895-01A-11D-A35Z-10 chr4:38799492 A>T maps to NM_003263.3 Y320*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9K8-01A-11D-A42J-10 chr4:187006025 A>G maps to NM_003265.2 *905*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47M-01A-11D-A25F-10 chr1:223286360 G>A maps to NM_003268.5 L5L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PO-01A-11D-A382-10 chr23:12905653 A>G did not map to a codon.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr5:170736389 G>A maps to NM_021025.2 A7A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr20:30723908 A>G maps to NM_014742.3 L54L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-A8LB-01A-11D-A35Z-10 chr20:30720848 C>T maps to NM_014742.3 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M8-01A-11D-A31X-10 chr20:30730876 C>T maps to NM_014742.3 F207F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NF-01A-11D-A26P-10 chr12:66546146 T>C maps to ENST00000286424 L119L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A4EM-01A-11D-A25F-10 chr9:75355126 T>C did not map to a codon.
Sequencing variant TCGA-SX-A7SO-01A-11D-A34Z-10 chr20:2517942 G>A maps to NM_080751.2 K21K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59R-01A-11D-A26P-10 chr19:54669260 G>T maps to NM_001145303.1 S285S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9JU-01A-11D-A42J-10 chr16:19474682 T>A maps to NM_001105248.1 I410I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A7SO-01A-11D-A34Z-10 chr17:76118810 C>A maps to NM_007267.6 E368*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3473-01A-01D-1252-08 chr16:19073097 A>T did not map to a codon.
Sequencing variant TCGA-J7-8537-01A-11D-2396-08 chr16:19051690 C>A maps to NM_024847.3 I420I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9KC-01A-11D-A42J-10 chr17:76130533 G>A maps to NM_152468.4 T292T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A9DE-01A-11D-A36X-10 chr3:129390023 A>T maps to NM_001017395.3 S220S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chr5:140021511 G>A maps to ENST00000252100 L124L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JO-01A-11D-A42J-10 chr16:69117518 G>A maps to NM_024562.1 L1080L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Y8-A8RZ-01A-11D-A36X-10 chr19:10945666 T>C maps to NM_006858.2 G136G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WN-AB4C-01A-11D-A42J-10 chr1:93621898 A>G maps to NM_016040.4 I143I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7045-01A-31D-1961-08 chr17:42089523 C>T maps to NM_032376.2 L182L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3473-01A-01D-1252-08 chr17:41365848 C>T maps to NM_145041.1 L72L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8098-01A-11D-2396-08 chr2:98413328 T>A maps to NM_015348.1 A997A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4A-A93X-01A-11D-A36X-10 chr11:60703542 G>T maps to NM_017870.3 E747*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4113-01A-01D-1252-08 chr12:130184818 C>G maps to NM_133448.2 L168L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F9-A97G-01A-11D-A382-10 chr17:32956192 G>A maps to NM_207313.1 R346R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A83T-01A-11D-A34Z-10 chr11:67232159 G>A maps to NM_025124.2 H171H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JD-01A-11D-A42J-10 chr7:142983808 T>C maps to NM_153345.1 L180L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PL-01A-11D-A382-10 chr19:42817620 C>T maps to ENST00000406159 Y31Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A7SS-01A-11D-A35Z-10 chr19:5739404 A>T maps to NM_152784.3 S176S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PR-01A-11D-A42J-10 chr19:36037599 G>T maps to NM_032635.2 V78V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5893-01A-11D-1589-08 chr19:36230749 G>C maps to NM_024660.2 A194A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2K-A9WE-01A-11D-A382-10 chr3:152058399 C>T maps to NM_001123228.1 L98L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A8YI-01A-21D-A36X-10 chr4:83424055 T>G maps to NM_001080506.1 P53P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A7SS-01A-11D-A35Z-10 chr4:38990468 A>C did not map to a codon.
Sequencing variant TCGA-Y8-A8RZ-01A-11D-A36X-10 chr11:62556680 A>T maps to NM_199337.2 R95*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Y8-A895-01A-11D-A35Z-10 chr19:55889459 G>C maps to NM_139172.1 T141T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-AAVM-01A-11D-A42J-10 chr1:9658628 C>G maps to NM_001130924.2 A184A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Y8-A896-01A-11D-A35Z-10 chr10:63188775 T>C maps to NM_178505.6 R171R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8311-01A-11D-2396-08 chr23:15682859 A>G did not map to a codon.
Sequencing variant TCGA-P4-AAVM-01A-11D-A42J-10 chr1:32560491 C>T maps to NM_018056.2 D345D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-A8LE-01A-11D-A35Z-10 chr3:100295845 C>A maps to ENST00000403410 S287*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7288-01A-11D-2136-08 chr11:129724697 A>G maps to NM_138788.3 A124A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Y8-A898-01A-11D-A34Z-10 chr17:57917268 A>G maps to NM_030938.3 K406K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr12:64174891 T>G maps to NM_014254.1 L88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A7SQ-01A-12D-A35Z-10 chr1:15545966 C>T maps to NM_018022.2 L164L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9JZ-01A-11D-A42J-10 chr1:1850653 G>C maps to NM_178545.3 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9KE-01A-11D-A42J-10 chr1:1850653 G>C maps to NM_178545.3 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5XZ-01A-11D-A31X-10 chr1:1850653 G>C maps to NM_178545.3 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7963-01B-11D-A28G-10 chr1:1850653 G>C maps to NM_178545.3 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5882-01A-11D-1589-08 chr1:45120713 G>T maps to NM_024587.2 V117V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JE-01A-11D-A42J-10 chr1:226040424 G>A maps to NM_014698.2 L615L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-5156-01A-01D-1589-08 chr8:94797544 T>C maps to NM_153704.5 Y409Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JG-01A-11D-A42J-10 chr17:7758983 C>G maps to NM_203411.1 A144A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A9DD-01A-11D-A36X-10 chr17:26646333 C>A maps to NM_014573.2 P23P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A6HP-01A-11D-A31X-10 chr3:69072459 T>C maps to NM_007114.2 Q1050Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4116-01A-01D-1252-08 chr3:69096706 T>C maps to NM_007114.2 T383T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5878-01A-11D-1589-08 chr3:69101210 G>A maps to NM_007114.2 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A7SP-01A-11D-A34Z-10 chr3:69092927 G>A maps to NM_007114.2 A517A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A9DE-01A-11D-A36X-10 chr17:28656424 G>A maps to NM_206832.1 R69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5878-01A-11D-1589-08 chr3:33135654 C>T maps to NM_001039770.2 A11A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5892-01A-11D-1589-08 chr4:68777128 C>T maps to NM_182606.3 K399K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59T-01A-21D-A28G-10 chr4:68930402 C>A maps to NM_207407.2 G339*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Y8-A8RY-01A-11D-A36X-10 chr11:117789217 C>T maps to ENST00000413475 V118V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5891-01A-11D-1589-08 chr21:19685346 T>G maps to NM_002772.2 R694R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PR-01A-11D-A42J-10 chr21:19701537 A>G maps to NM_002772.2 I576I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JS-01A-21D-A42J-10 chr22:37462119 T>C maps to ENST00000381792 *825W. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6792-01A-21D-1961-08 chr19:2421952 G>T maps to NM_182973.1 P718P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3472-01A-01D-1252-08 chr12:29670367 A>G maps to NM_001193451.1 L721L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8515-01A-11D-2396-08 chr12:83290129 G>A maps to NM_152588.1 L396L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A772-01A-11D-A33Q-10 chr13:101287286 G>T maps to NM_032813.2 T455T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-A8LB-01A-11D-A35Z-10 chr20:8000100 C>A maps to NM_021156.2 E54*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A71S-01A-11D-A33Q-10 chr18:60052146 C>T maps to NM_003839.2 R577R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9JY-01A-11D-A42J-10 chr1:1141897 C>A maps to NM_004195.2 L18L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W9-01A-11D-A28G-10 chr6:47254096 G>A maps to NM_014452.3 Q111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A71S-01A-11D-A33Q-10 chr1:12170172 G>T maps to NM_001243.3 G196G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A855-01A-11D-A34Z-10 chr3:172232752 A>G maps to ENST00000382750 C56C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A7SS-01A-11D-A35Z-10 chr3:172224317 A>G maps to ENST00000382750 H270H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8517-01A-11D-2396-08 chr5:150444533 C>G maps to NM_006058.3 G41G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A9DC-01A-11D-A36X-10 chr5:150443285 C>T maps to NM_006058.3 Q53Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A8YI-01A-21D-A36X-10 chr8:9564427 T>C maps to NM_003747.2 A459A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9J1-01A-11D-A382-10 chr10:93593659 T>A maps to NM_025235.3 Y442*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7061-01A-11D-1961-08 chr1:175086171 G>C maps to NM_022093.1 V739V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PR-01A-11D-A42J-10 chr1:175087823 C>T maps to NM_022093.1 T838T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55Z-01A-11D-A26P-10 chr5:72183031 T>G maps to NM_002270.3 L429*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JM-01A-12D-A42J-10 chr19:12816353 G>T maps to NM_001136196.1 V605V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7963-01B-11D-A28G-10 chr7:5352625 A>T maps to NM_001080495.2 S2632S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4A-A93W-01A-11D-A36X-10 chr16:24801495 G>A maps to NM_014494.2 E511E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A83T-01A-11D-A34Z-10 chr16:24801624 C>G maps to NM_014494.2 G554G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JL-01A-11D-A42J-10 chr22:40521833 G>T maps to NM_001024843.1 E5*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9K0-01A-11D-A42J-10 chr2:218683235 A>G maps to NM_022648.4 A1169A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-7268-01A-11D-2136-08 chr2:218712983 G>C maps to NM_022648.4 P627P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E7-01A-31D-A28G-10 chr2:218678510 C>G maps to NM_022648.4 P1482P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A8YH-01A-11D-A36X-10 chr17:38634838 G>A maps to NM_032865.5 Q658*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr6:32016287 C>T maps to ENST00000375244 A3299A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PS-01A-11D-A42J-10 chr20:43580552 C>T maps to NM_006809.4 R157R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A7SQ-01A-12D-A35Z-10 chr1:161197091 T>C maps to NM_032174.4 Y76Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Y8-A896-01A-11D-A35Z-10 chr3:25675376 T>C maps to ENST00000264331 K327K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7834-01A-11D-2136-08 chr17:18212207 A>G maps to NM_004618.3 H76H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W9-01A-11D-A28G-10 chr3:133331388 C>T maps to NM_007027.3 L1293L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E8-01A-11D-A28G-10 chr1:179815211 A>C maps to NM_145034.4 L469L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WN-A9G9-01A-12D-A36X-10 chr9:132569639 C>T maps to NM_014506.1 L213L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4104-01A-01D-1458-08 chr17:7579414 C>T maps to NM_001126112.1 W91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JG-01A-11D-A42J-10 chr15:43769941 A>C maps to NM_001141980.1 P268P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4113-01A-01D-1252-08 chr15:43724400 G>A maps to NM_001141980.1 L1222L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A44B-01A-11D-A25F-10 chr15:43771710 T>C maps to NM_001141980.1 E224E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E8-01A-11D-A28G-10 chr15:43748236 G>A maps to NM_001141980.1 Q857*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr1:223984098 A>G maps to NM_001031685.2 N714N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WN-A9G9-01A-12D-A36X-10 chr20:45315709 C>T maps to NM_033550.3 Q148Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JL-01A-11D-A42J-10 chr2:1507789 C>T maps to NM_000547.5 G819G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J7-A8I2-01A-12D-A35Z-10 chr2:1481208 C>T maps to NM_000547.5 L391L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9K0-01A-11D-A42J-10 chr13:103301429 G>A maps to ENST00000376052 K934K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6134-01A-11D-1961-08 chr16:67424232 C>G maps to NM_016140.2 L125L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KV-A6GD-01A-11D-A31X-10 chr1:186316561 A>G maps to NM_003292.2 D935D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JQ-01A-11D-A42J-10 chr21:10959745 T>C maps to NM_199261.2 S76S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E6-01A-11D-A28G-10 chr9:139794875 C>G maps to ENST00000359662 A90A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JL-01A-11D-A42J-10 chr3:42240710 C>T maps to NM_001042646.1 L386L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A656-01A-11D-A31X-10 chr3:42218378 G>A maps to NM_001042646.1 E120E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4114-01A-01D-1252-08 chr2:202262966 G>A maps to NM_015049.2 F197F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4115-01A-01D-1252-08 chr3:36873054 C>T maps to NM_014831.2 L2629L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A6HP-01A-11D-A31X-10 chr16:3712966 G>A maps to NM_016292.2 A570A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F9-A7VF-01A-11D-A33Q-10 chr16:3727497 C>G did not map to a codon.
Sequencing variant TCGA-KV-A6GE-01A-11D-A31X-10 chr21:45502875 G>A maps to NM_003274.4 W644*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F9-A8NY-01A-11D-A35Z-10 chr8:140743456 G>T maps to NM_031466.5 G1196G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8311-01A-11D-2396-08 chr6:41129013 C>T maps to NM_018965.2 V126V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A71S-01A-11D-A33Q-10 chr6:42204005 C>A maps to NM_033502.2 P1001P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UN-AAZ9-01A-11D-A382-10 chr3:129695839 G>A maps to NM_007117.3 E170E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PJ-A8JU-01A-11D-A35Z-10 chr12:72962371 T>C maps to NM_013381.2 T644T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47M-01A-11D-A25F-10 chr2:12858615 C>A maps to NM_021643.3 I61I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5902-01A-11D-1589-08 chr11:5717509 C>T maps to NM_006074.4 P16P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7837-01A-11D-2136-08 chr7:138145433 G>A maps to NM_015905.2 A47A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chr11:119988940 G>A maps to NM_012101.3 F539F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9KE-01A-11D-A42J-10 chr1:114942183 G>A maps to NM_015906.3 T1005T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A71S-01A-11D-A33Q-10 chr1:115006035 G>T maps to NM_015906.3 S263*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-5156-01A-01D-1589-08 chr5:114515695 G>A maps to NM_018700.3 I13I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr6:25967010 G>C maps to NM_006355.2 T87T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9K3-01A-11D-A42J-10 chr7:99516790 G>A maps to NM_033017.3 R78R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A40U-01A-11D-A25F-10 chr3:140401753 G>A maps to NM_152616.4 K264K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A71V-01A-11D-A33Q-10 chr3:140397259 C>T maps to NM_152616.4 C63C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7286-01A-11D-2136-08 chr5:180687082 G>T maps to NM_032765.2 A244A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr15:45048564 G>C did not map to a codon.
Sequencing variant TCGA-A4-8098-01A-11D-2396-08 chr10:104415048 G>A maps to NM_030912.2 T293T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7834-01A-11D-2136-08 chr10:104404880 C>T maps to NM_030912.2 Y169Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PS-01A-11D-A42J-10 chr2:230633434 A>G maps to ENST00000389044 S1941S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PS-01A-11D-A42J-10 chr2:230663700 T>C maps to ENST00000389044 T1097T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A69E-01A-11D-A31X-10 chr5:908119 C>T maps to NM_004237.3 T230T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A83S-01A-11D-A34Z-10 chr3:142443573 G>A did not map to a codon.
Sequencing variant TCGA-HE-A5NL-01A-11D-A26P-10 chr20:33623073 A>C maps to NM_015638.2 L301L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AT-A5NU-01A-11D-A28G-10 chr5:135561910 T>A maps to NM_020389.2 R691R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A71R-01A-12D-A33Q-10 chr15:31327764 A>T maps to NM_002420.4 L873*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A561-01A-11D-A26P-10 chr21:45825793 C>T maps to ENST00000397932 I888I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A655-01A-11D-A31Z-10 chr19:49674875 C>T maps to NM_017636.3 L300L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59R-01A-11D-A26P-10 chr19:49714006 G>T maps to NM_017636.3 T1123T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F9-A4JJ-01A-11D-A25F-10 chr11:2432684 C>T maps to ENST00000452833 A895A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A83T-01A-11D-A34Z-10 chr15:50978725 A>G did not map to a codon.
Sequencing variant TCGA-A4-A57E-01A-11D-A26P-10 chr7:142606702 G>A maps to NM_019841.4 S616S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Y8-A895-01A-11D-A35Z-10 chr7:98562255 C>A maps to ENST00000359863 T2271T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Y8-A896-01A-11D-A35Z-10 chr7:98576478 C>T maps to ENST00000359863 C2855C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9KE-01A-11D-A42J-10 chr9:135781380 G>A maps to NM_000368.4 G528G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9KA-01A-11D-A42J-10 chr16:2112990 C>G maps to NM_000548.3 A460A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5884-01A-11D-1589-08 chr16:2122848 G>A did not map to a codon.
Sequencing variant TCGA-MH-A854-01A-11D-A34Z-10 chr16:2098729 T>C maps to NM_000548.3 F38F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JP-01A-11D-A42J-10 chr13:45148239 T>C maps to NM_183422.2 V657V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7585-01A-11D-2136-08 chr2:99720472 C>A maps to NM_025244.2 E190*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3472-01A-01D-1252-08 chr2:99689478 A>C did not map to a codon.
Sequencing variant TCGA-2Z-A9JD-01A-11D-A42J-10 chr18:72999614 C>A maps to NM_005786.4 S706S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47M-01A-11D-A25F-10 chr18:72999467 C>A maps to NM_005786.4 A657A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-O9-A75Z-01A-11D-A33Q-10 chr19:31768682 G>A maps to NM_020856.2 S672S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-7173-01A-11D-2136-08 chr1:115601515 G>A maps to NM_005725.4 T144T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W7-01A-11D-A31X-10 chr7:128804349 C>A maps to NM_178562.3 A133A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47N-01A-11D-A25F-10 chr23:53114043 C>A did not map to a codon.
Sequencing variant TCGA-SX-A71U-01A-12D-A33Q-10 chr23:53112144 G>C did not map to a codon.
Sequencing variant TCGA-SX-A71U-01A-12D-A33Q-10 chr19:19625678 G>T maps to NM_032037.2 I186I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5886-01A-11D-1589-08 chr6:43226955 C>G maps to NM_032538.1 V399V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A83S-01A-11D-A34Z-10 chr6:43250878 C>T maps to NM_032538.1 Q801*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9J7-01A-11D-A382-10 chr2:3392179 C>G maps to NM_016030.5 P262P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-7173-01A-11D-2136-08 chr2:3483102 G>A maps to NM_016030.5 V693V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Y8-A896-01A-11D-A35Z-10 chr9:130480051 G>A did not map to a codon.
Sequencing variant TCGA-BQ-5877-01A-11D-1589-08 chr10:75037056 G>A maps to NM_145170.3 Q891*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PX-01A-11D-A42J-10 chr10:75051506 C>T maps to NM_145170.3 L707L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PX-01A-11D-A42J-10 chr2:166737186 A>T did not map to a codon.
Sequencing variant TCGA-UZ-A9PX-01A-11D-A42J-10 chr1:156551344 C>T maps to NM_001105669.2 F63F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E7-01A-31D-A28G-10 chr2:74718486 G>A maps to NM_022492.4 Q223Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Y8-A896-01A-11D-A35Z-10 chr2:20101506 G>T maps to NM_001008237.1 R37R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7288-01A-11D-2136-08 chr8:109462082 A>G maps to NM_014673.3 E24E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5882-01A-11D-1589-08 chr8:109489021 C>T maps to NM_014673.3 T201T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5903-01A-11D-1589-08 chr8:109462687 A>T maps to NM_014673.3 A62A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9JV-01A-12D-A42J-10 chr5:94814017 T>A maps to NM_014639.3 A1447A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A7SQ-01A-12D-A35Z-10 chr9:15225958 A>G maps to NM_152574.2 D109D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5875-01A-11D-1589-08 chr2:47300863 C>T maps to ENST00000394850 G817G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A7SS-01A-11D-A35Z-10 chr14:91142992 G>A maps to NM_001010854.1 D342D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4103-01A-01D-1458-08 chr22:43442516 C>G maps to NM_012263.4 L347L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A7SU-01A-11D-A35Z-10 chr2:219619109 T>A maps to NM_014640.4 *1200K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JQ-01A-11D-A42J-10 chr2:179435105 A>T maps to NM_133378.4 V22683V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9KE-01A-11D-A42J-10 chr2:179466286 T>A maps to NM_133378.4 V15911V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr2:179411555 A>G maps to NM_133378.4 D28965D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A8YI-01A-21D-A36X-10 chr2:179604479 T>G maps to NM_133437.3 R4323R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5878-01A-11D-1589-08 chr2:179452052 C>T maps to NM_133378.4 G18727G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5882-01A-11D-1589-08 chr2:179575503 G>A maps to NM_133378.4 G8196G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr2:179611916 T>C maps to ENST00000375038 L5072L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-5560-01A-01D-1589-08 chr2:179433842 G>C maps to NM_133378.4 Y23104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr2:179430005 G>T maps to NM_133378.4 T24383T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6790-01A-11D-1961-08 chr2:179419673 A>G maps to NM_133378.4 D26936D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr2:179425265 A>G maps to NM_133378.4 Y25963Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-7501-01A-11D-2201-08 chr2:179567315 C>A maps to NM_133378.4 E8856*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-A8LB-01A-11D-A35Z-10 chr2:179476841 G>A maps to NM_133378.4 R14198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr2:179599139 A>G maps to NM_133378.4 F3893F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A40X-01A-11D-A25F-10 chr2:179615957 C>T maps to ENST00000375038 T3725T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PJ-01A-11D-A382-10 chr2:179469795 G>A maps to NM_133378.4 V15468V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PL-01A-11D-A382-10 chr2:179474202 A>T maps to NM_133378.4 T14710T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PL-01A-11D-A382-10 chr2:179611760 T>A maps to ENST00000375038 G5124G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PP-01A-11D-A42J-10 chr2:179644086 T>A maps to NM_133378.4 K1278*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr19:54937847 A>G did not map to a codon.
Sequencing variant TCGA-DZ-6135-01A-11D-1961-08 chr13:19751147 C>G maps to NM_006001.1 P325P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7838-01A-11D-2136-08 chr2:132236968 G>A maps to NM_080386.2 R105R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9K3-01A-11D-A42J-10 chr20:57599618 T>C maps to NM_030773.3 N379N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr17:40765684 C>T maps to NM_001070.4 A209A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EA-01A-11D-A28G-10 chr1:151552138 A>G maps to NM_020127.2 K313K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr6:158873217 C>A maps to NM_020245.3 T259T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-7502-01A-11D-2201-08 chr6:139563746 T>C maps to ENST00000358430 A657A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PV-01A-11D-A42J-10 chr6:139563668 G>T maps to ENST00000358430 V683V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5890-01A-11D-1589-08 chr9:113013694 T>C maps to NM_003329.2 V24V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A71S-01A-11D-A33Q-10 chr14:52899032 T>A maps to NM_020784.2 K823*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7058-01A-11D-1961-08 chr6:7889003 A>C maps to NM_030810.3 T299T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WN-AB4C-01A-11D-A42J-10 chr12:104681124 G>T did not map to a codon.
Sequencing variant TCGA-BQ-5876-01A-11D-1589-08 chr15:41854917 T>G did not map to a codon.
Sequencing variant TCGA-B9-7268-01A-11D-2136-08 chr7:66532280 C>A maps to NM_018264.2 R389R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7966-01A-11D-2201-08 chr15:70987422 C>T maps to NM_018003.2 K78K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NI-01A-11D-A26P-10 chr15:70991968 G>A maps to NM_018003.2 R37*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8098-01A-11D-2396-08 chr23:47069021 T>G did not map to a codon.
Sequencing variant TCGA-B1-A47N-01A-11D-A25F-10 chr4:68534338 T>C maps to NM_018227.5 T241T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7045-01A-31D-1961-08 chr9:138839742 T>C maps to NM_016172.2 Q114Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A83V-01A-11D-A34Z-10 chr6:90047952 A>T maps to NM_016021.2 T133T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9J3-01A-12D-A382-10 chr17:74391895 C>T maps to NM_022066.3 K952K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4A-A93X-01A-11D-A36X-10 chr17:74391862 C>T maps to NM_022066.3 A963A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-AAVM-01A-11D-A42J-10 chr17:74449136 G>A maps to NM_022066.3 A29A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9Q0-01A-12D-A42J-10 chr17:74398142 A>G did not map to a codon.
Sequencing variant TCGA-A4-8517-01A-11D-2396-08 chr7:156963037 T>A maps to NM_014671.2 L79*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chr11:118250227 C>T maps to NM_004788.2 Q554*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-5561-01A-01D-1589-08 chr1:11346094 G>C maps to NM_013319.2 L308L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A8YI-01A-21D-A36X-10 chr23:153713965 C>T did not map to a codon.
Sequencing variant TCGA-B9-4114-01A-01D-1252-08 chr20:3090942 G>A maps to NM_014948.2 L479L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7288-01A-11D-2136-08 chr15:43299482 C>A did not map to a codon.
Sequencing variant TCGA-BQ-5891-01A-11D-1589-08 chr6:42657390 G>A maps to NM_015255.2 E1703E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JR-01A-12D-A42J-10 chr1:19491315 G>A maps to ENST00000375267 T1496T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-A8LB-01A-11D-A35Z-10 chr8:103273472 A>T maps to NM_015902.4 P2619P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A8YI-01A-21D-A36X-10 chr10:99330069 C>A maps to NM_024954.3 G158G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr10:99327794 G>A maps to NM_024954.3 K65K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A854-01A-11D-A34Z-10 chr17:42288678 C>A maps to NM_014233.2 V356V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A8YI-01A-21D-A36X-10 chr1:26608864 A>G maps to NM_183008.2 G496G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7963-01B-11D-A28G-10 chr1:26608864 A>G maps to NM_183008.2 G496G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A7SR-01A-12D-A35Z-10 chr11:73715619 G>T maps to NM_003356.3 P184P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5882-01A-11D-1589-08 chr2:128918713 C>A maps to NM_020120.3 I899I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5881-01A-11D-1589-08 chr2:234637942 G>A maps to NM_019093.2 Q57Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A71U-01A-12D-A33Q-10 chr2:234622287 T>G maps to NM_019078.1 P217P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5875-01A-11D-1589-08 chr2:234580747 T>C maps to ENST00000373460 V56V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4103-01A-01D-1458-08 chr4:69978198 A>G maps to NM_001074.2 L445L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A561-01A-11D-A26P-10 chr6:34825519 C>T maps to NM_017754.3 Y531Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A71S-01A-11D-A33Q-10 chr5:176395810 A>T maps to ENST00000377219 L315L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7997-01A-11D-2201-08 chr12:132405712 C>G maps to NM_003565.2 A1010A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7966-01A-11D-2201-08 chr12:132395296 C>T maps to NM_003565.2 S300S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A7SR-01A-12D-A35Z-10 chr17:19720215 C>T maps to NM_014683.3 Q314Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5XZ-01A-11D-A31X-10 chr15:75132622 C>T maps to NM_001099436.1 R216R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JS-01A-21D-A42J-10 chr21:43505509 T>A maps to NM_173568.3 L197L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Y8-A896-01A-11D-A35Z-10 chr21:43529754 C>T maps to NM_173568.3 Q535*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Y8-A895-01A-11D-A35Z-10 chr19:17740111 G>A maps to ENST00000428389 L1318L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NH-01A-11D-A26P-10 chr15:54557622 T>A maps to ENST00000260323 V1249V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A656-01A-11D-A31X-10 chr5:176305474 G>A did not map to a codon.
Sequencing variant TCGA-A4-7997-01A-11D-2201-08 chr10:73055665 C>T maps to NM_170744.3 L758L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7058-01A-11D-1961-08 chr8:35541183 C>T maps to ENST00000416672 T230T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JQ-01A-11D-A42J-10 chr17:73818651 T>A maps to NM_001080419.1 A720A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9JV-01A-12D-A42J-10 chr10:11985131 T>C maps to NM_015542.2 E1070E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A69E-01A-11D-A31X-10 chr23:118977250 T>C did not map to a codon.
Sequencing variant TCGA-MH-A561-01A-11D-A26P-10 chr23:118985466 C>G did not map to a codon.
Sequencing variant TCGA-UZ-A9PO-01A-11D-A382-10 chr7:48146602 G>C maps to NM_003364.2 L190L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr2:158971731 A>G maps to NM_001135098.1 R157R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9J7-01A-11D-A382-10 chr22:30163498 C>T maps to ENST00000406782 Q38*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PO-01A-11D-A382-10 chr16:21974186 C>T maps to NM_003366.2 A165A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A562-01A-11D-A26P-10 chr1:229771820 G>A maps to NM_014777.2 Q487Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A4EM-01A-11D-A25F-10 chr1:215820885 G>T maps to ENST00000366943 I4923I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A69E-01A-11D-A31X-10 chr19:17366409 G>A maps to NM_031941.3 A492A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2K-A9WE-01A-11D-A382-10 chr16:84796614 G>A maps to NM_005153.2 E525E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PK-01A-11D-A382-10 chr23:47103933 G>A did not map to a codon.
Sequencing variant TCGA-A4-8517-01A-11D-2396-08 chr3:179426710 C>A maps to NM_003940.2 A257A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr12:62795033 T>A maps to ENST00000280377 T914T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9J6-01A-11D-A382-10 chr9:132625463 G>T did not map to a codon.
Sequencing variant TCGA-SX-A7SM-01A-11D-A34Z-10 chr9:132638510 C>T maps to NM_001008563.3 F801F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9JY-01A-11D-A42J-10 chr1:55604355 A>G maps to NM_015306.2 H951H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7996-01A-11D-2201-08 chr1:55612676 A>G maps to NM_015306.2 Y725Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WN-A9G9-01A-12D-A36X-10 chr1:55603532 G>T maps to NM_015306.2 A991A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr21:17138431 C>G maps to ENST00000285681 Y80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5879-01A-11D-1589-08 chr23:132160220 A>C did not map to a codon.
Sequencing variant TCGA-Y8-A8RZ-01A-11D-A36X-10 chr19:57642199 A>G maps to NM_020903.2 K719K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5890-01A-11D-1589-08 chr16:23083423 G>T maps to NM_020718.3 T810T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7840-01A-11D-2136-08 chr2:61493233 C>T maps to NM_014709.3 K1834K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-A8LD-01A-11D-A35Z-10 chr2:61522308 C>T maps to NM_014709.3 E1457E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8195-01A-31D-2396-08 chr2:85875074 T>G maps to NM_006590.2 L529*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5902-01A-11D-1589-08 chr3:49362338 T>C maps to NM_003363.3 L207L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A7SQ-01A-12D-A35Z-10 chr7:6196543 C>T maps to ENST00000404835 V1267V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KV-A6GE-01A-11D-A31X-10 chr6:99894084 T>C maps to NM_001080481.1 R521R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A9DC-01A-11D-A36X-10 chr11:11924348 A>G maps to ENST00000399455 K234K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E6-01A-11D-A28G-10 chr1:22073614 A>G maps to NM_032236.5 N312N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A9DD-01A-11D-A36X-10 chr4:120190930 A>G maps to NM_019050.2 L458L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr10:11523767 C>G did not map to a codon.
Sequencing variant TCGA-B9-5156-01A-01D-1589-08 chr23:40999923 C>A did not map to a codon.
Sequencing variant TCGA-B9-A69E-01A-11D-A31X-10 chr23:41043809 C>T did not map to a codon.
Sequencing variant TCGA-A4-A7UZ-01A-12D-A34Z-10 chr23:129058816 G>A did not map to a codon.
Sequencing variant TCGA-BQ-5892-01A-11D-1589-08 chr23:129045743 C>T did not map to a codon.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr13:52603704 G>C maps to NM_021645.5 V255V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NK-01A-11D-A26P-10 chr5:72864378 T>A maps to NM_032175.2 L106L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PX-01A-11D-A42J-10 chr17:49357808 T>C maps to NM_016001.2 S391S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr12:101693786 C>A maps to NM_014503.2 T541T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PS-01A-11D-A42J-10 chr6:144744728 C>A maps to NM_007124.2 V93V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V9-A7HT-01A-11D-A33Q-10 chr6:144811283 C>A maps to NM_007124.2 T1404T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Y8-A8RZ-01A-11D-A36X-10 chr6:144806573 C>T maps to NM_007124.2 T1247T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A71U-01A-12D-A33Q-10 chr12:6574107 C>T did not map to a codon.
Sequencing variant TCGA-UZ-A9PM-01A-21D-A382-10 chr23:155171619 G>T did not map to a codon.
Sequencing variant TCGA-2Z-A9JL-01A-11D-A42J-10 chr1:116228126 C>T maps to NM_001172412.1 I431I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JM-01A-12D-A42J-10 chr1:116206832 G>T maps to NM_001172412.1 L252L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E6-01A-11D-A28G-10 chr16:4432671 T>C maps to NM_138440.2 C598C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5Y1-01A-11D-A28G-10 chr10:118893698 C>T maps to NM_001112704.1 L275L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A48D-01A-11D-A25F-10 chr5:82808190 A>C maps to NM_004385.4 R340R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-8121-01A-21D-2396-08 chr5:82850837 G>A maps to NM_004385.4 W3239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A83V-01A-11D-A34Z-10 chr5:82817376 T>A maps to NM_004385.4 S1084S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A562-01A-11D-A26P-10 chr5:82815684 G>A maps to NM_004385.4 L520L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr9:35061056 A>G maps to NM_007126.3 D438D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JT-01A-11D-A42J-10 chr8:67546978 T>C maps to NM_025054.4 E1142E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A40X-01A-11D-A25F-10 chr23:7811789 C>T did not map to a codon.
Sequencing variant TCGA-Y8-A894-01A-11D-A35Z-10 chr23:135630874 G>C did not map to a codon.
Sequencing variant TCGA-B1-A47M-01A-11D-A25F-10 chr1:156268770 C>T maps to NM_001004319.2 W70*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E6-01A-11D-A28G-10 chr10:17278344 T>G maps to NM_003380.3 L442L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A48D-01A-11D-A25F-10 chr3:42577628 C>T maps to NM_004624.3 G410G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47M-01A-11D-A25F-10 chr7:158828653 T>C maps to ENST00000402066 L407L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7996-01A-11D-2201-08 chr19:53762786 C>T maps to NM_173856.2 R387*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A655-01A-11D-A31Z-10 chr3:51452312 T>G did not map to a codon.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr3:51457621 C>G maps to ENST00000273612 R934R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5875-01A-11D-1589-08 chr9:79955423 T>A maps to ENST00000376646 A2328A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Y8-A8RY-01A-11D-A36X-10 chr8:100836127 T>C maps to NM_017890.3 T3109T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JL-01A-11D-A42J-10 chr15:62277126 T>C maps to NM_020821.2 P550P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5Y1-01A-11D-A28G-10 chr15:62155702 C>A maps to NM_020821.2 E3630*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5876-01A-11D-1589-08 chr1:12327037 T>C maps to NM_015378.2 T565T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5903-01A-11D-1589-08 chr1:12304649 T>C maps to NM_015378.2 V141V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7842-01A-11D-2136-08 chr11:134115447 C>T maps to NM_052875.3 T325T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9JU-01A-11D-A42J-10 chr15:42456664 A>G maps to ENST00000348544 A650A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8517-01A-11D-2396-08 chr15:42462023 G>T maps to ENST00000348544 P388P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5901-01A-11D-1589-08 chr2:64199371 T>A maps to NM_016516.2 K129*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KV-A6GE-01A-11D-A31X-10 chr12:118506350 C>T maps to NM_019086.5 E466E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9JU-01A-11D-A42J-10 chr23:65253394 G>A did not map to a codon.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chr14:68118140 C>T maps to NM_006370.2 L220L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JQ-01A-11D-A42J-10 chr2:98844792 C>T maps to NM_144992.4 S716S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A44B-01A-11D-A25F-10 chr7:49815192 C>T maps to NM_198570.3 D54D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-3925-01A-01D-1458-08 chr2:215440517 G>T maps to NM_001080500.2 E215*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3466-01A-01D-1252-08 chr11:61026691 C>A maps to NM_152718.2 E775*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JG-01A-11D-A42J-10 chr12:6103202 G>T maps to NM_000552.3 V2141V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7997-01A-11D-2201-08 chr12:6138618 G>A maps to NM_000552.3 H952H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr12:6143880 G>T maps to NM_000552.3 P886P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A71S-01A-11D-A33Q-10 chr12:6120942 G>C maps to NM_000552.3 T1894T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Y8-A8S0-01A-11D-A36X-10 chr10:28824567 T>A maps to NM_016628.3 P52P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A8YI-01A-21D-A36X-10 chr1:27742556 A>C maps to NM_006990.2 P153P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr1:27739178 A>G maps to NM_006990.2 C237C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-A4TM-01A-11D-A31X-10 chr1:27736339 A>G maps to NM_006990.2 P395P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr12:14943405 A>G maps to NM_016312.2 P431P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NI-01A-11D-A26P-10 chr7:73249147 A>C maps to NM_152559.2 S221S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JS-01A-21D-A42J-10 chr4:85716132 C>T did not map to a codon.
Sequencing variant TCGA-P4-A5ED-01A-11D-A28G-10 chr4:85675020 T>C maps to NM_014991.4 Q1856Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A7SS-01A-11D-A35Z-10 chr4:85731168 G>T maps to NM_014991.4 S739*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9JW-01A-11D-A42J-10 chr14:55451546 T>C maps to NM_007086.3 G600G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A4ZT-01A-11D-A26P-10 chr4:10099337 A>G maps to NM_017491.3 I185I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NF-01A-11D-A26P-10 chr10:122664156 G>A did not map to a codon.
Sequencing variant TCGA-AT-A5NU-01A-11D-A28G-10 chr17:9501595 C>A maps to NM_145054.4 I194I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A71S-01A-11D-A33Q-10 chr4:177098621 A>G maps to NM_170710.4 R1222R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4A-A93X-01A-11D-A36X-10 chr19:991091 G>A maps to NM_024100.3 R251R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PS-01A-11D-A42J-10 chr19:984376 C>T maps to NM_024100.3 A8A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Y8-A898-01A-11D-A34Z-10 chr4:39218826 T>C maps to NM_025132.3 A441A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Y8-A8S0-01A-11D-A36X-10 chr4:39233428 T>G maps to NM_025132.3 A665A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4114-01A-01D-1252-08 chr14:102675937 T>C maps to ENST00000454394 D508D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A4EM-01A-11D-A25F-10 chr14:102689210 T>A maps to NM_181291.1 T579T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2K-A9WE-01A-11D-A382-10 chr2:128528414 T>A maps to NM_018383.4 R47R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr2:128526505 C>A did not map to a codon.
Sequencing variant TCGA-GL-A9DD-01A-11D-A36X-10 chr5:76758981 A>G maps to NM_018268.2 L96L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr23:117526749 T>G did not map to a codon.
Sequencing variant TCGA-MH-A854-01A-11D-A34Z-10 chr23:117526784 G>C did not map to a codon.
Sequencing variant TCGA-2Z-A9J2-01A-11D-A382-10 chr3:113125860 G>A maps to NM_001164496.1 T306T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6135-01A-11D-1961-08 chr5:140049031 T>C maps to NM_017706.4 H315H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A8YI-01A-21D-A36X-10 chr1:241823861 C>A maps to NM_144625.4 S59*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4103-01A-01D-1458-08 chr12:122413566 T>C maps to NM_144668.4 I994I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WN-AB4C-01A-11D-A42J-10 chr12:122389411 C>T maps to NM_144668.4 H432H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-A8LD-01A-11D-A35Z-10 chr8:124109585 A>C maps to NM_145647.3 R246R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr5:37381725 C>T maps to NM_018034.2 D38D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8515-01A-11D-2396-08 chr17:1633710 G>A maps to NM_001163809.1 K1235K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E6-01A-11D-A28G-10 chr16:707786 C>T maps to NM_145294.4 P833P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8311-01A-11D-2396-08 chr7:134873247 C>T maps to NM_014149.3 E606E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PX-01A-11D-A42J-10 chr15:90260170 T>C maps to NM_020212.1 P262P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WN-AB4C-01A-11D-A42J-10 chr1:27631606 C>T maps to ENST00000319394 Q587*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-5155-01A-01D-1589-08 chr7:141408684 A>T maps to NM_001105558.1 K43*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr4:6303093 C>T maps to NM_006005.3 F524F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7996-01A-11D-2201-08 chr17:38416824 G>A maps to NM_133264.4 Q34Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7838-01A-11D-2136-08 chr17:38420805 A>G maps to NM_133264.4 P126P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59R-01A-11D-A26P-10 chr17:66440667 C>T maps to NM_017983.5 L132L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-7332-01A-11D-2136-08 chr19:15558956 C>T maps to ENST00000389282 K54K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9JU-01A-11D-A42J-10 chr12:1005250 A>G maps to NM_001184985.1 A2126A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A9DD-01A-11D-A36X-10 chr12:1017828 G>C maps to NM_001184985.1 T2600T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7997-01A-11D-2201-08 chr23:54259339 A>T did not map to a codon.
Sequencing variant TCGA-DW-5561-01A-01D-1589-08 chr23:54319392 A>T did not map to a codon.
Sequencing variant TCGA-DW-7834-01A-11D-2136-08 chr17:44845985 C>T maps to NM_030753.3 V256V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-AAVM-01A-11D-A42J-10 chr3:13860791 G>A maps to NM_004625.3 N233N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr17:6012934 C>G maps to NM_015253.1 P286P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-A6W5-01A-12D-A33Q-10 chr5:167881044 A>G maps to NM_001161661.1 G866G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59T-01A-21D-A28G-10 chr23:10062248 A>T did not map to a codon.
Sequencing variant TCGA-MH-A55W-01A-11D-A26P-10 chr23:10066561 A>C did not map to a codon.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr2:31595112 G>T maps to NM_000379.3 R613R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7966-01A-11D-2201-08 chr2:168105758 G>A maps to NM_152381.5 R2619R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr8:56435873 C>G maps to NM_052898.1 A347A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9J1-01A-11D-A382-10 chr23:100183148 C>T did not map to a codon.
Sequencing variant TCGA-MH-A854-01A-11D-A34Z-10 chr13:21370347 C>G maps to NM_022459.4 V888V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr6:43541218 G>C maps to NM_020750.2 V75V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JK-01A-11D-A42J-10 chr12:64825464 T>A maps to NM_007235.3 L708L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W8-01A-11D-A28G-10 chr12:64808727 C>A maps to NM_007235.3 A34A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr5:82406898 G>T maps to NM_022406.2 G64G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JK-01A-11D-A42J-10 chr3:142137717 C>T maps to NM_019001.3 Q393Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-8500-01A-11D-2396-08 chr3:38404483 C>G maps to NM_005108.3 V89V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8310-01A-11D-2396-08 chr16:17202724 C>A maps to NM_022166.3 E903*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F9-A97G-01A-11D-A382-10 chr17:48433615 G>T maps to NM_022167.2 R492R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KV-A6GD-01A-11D-A31X-10 chr11:102100554 G>T maps to NM_001130145.2 G467*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr1:33246689 G>T maps to NM_003680.3 R367R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Y8-A894-01A-11D-A35Z-10 chr23:67731817 T>A did not map to a codon.
Sequencing variant TCGA-A4-A5Y1-01A-11D-A28G-10 chr14:75248110 G>A maps to NM_019589.2 W455*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A71S-01A-11D-A33Q-10 chr14:75265566 T>C maps to NM_019589.2 P1189P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JQ-01A-11D-A42J-10 chr2:135779306 A>T maps to NM_025052.3 L39*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A7SM-01A-11D-A34Z-10 chr2:135744887 G>A maps to NM_025052.3 V518V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A7SP-01A-11D-A34Z-10 chr4:69197865 G>A maps to NM_001031732.2 L359L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PO-01A-11D-A382-10 chr4:69203169 T>C did not map to a codon.
Sequencing variant TCGA-F9-A97G-01A-11D-A382-10 chr7:75959109 A>T maps to NM_012479.3 A176A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JK-01A-11D-A42J-10 chr22:32352565 C>T maps to NM_003405.3 A176A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-5561-01A-01D-1589-08 chr22:32352659 C>T maps to NM_003405.3 L208L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4A-A93W-01A-11D-A36X-10 chr1:155646419 A>C maps to ENST00000368339 V219V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5882-01A-11D-1589-08 chr23:21875587 G>A did not map to a codon.
Sequencing variant TCGA-2Z-A9JO-01A-11D-A42J-10 chr2:98354317 C>T maps to NM_001079.3 V527V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9K0-01A-11D-A42J-10 chr3:167086363 T>A did not map to a codon.
Sequencing variant TCGA-GL-A9DE-01A-11D-A36X-10 chr23:2407031 A>C did not map to a codon.
Sequencing variant TCGA-GL-A59R-01A-11D-A26P-10 chr8:81412102 T>C maps to NM_001105539.1 S449S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr3:101390911 C>A maps to NM_014415.3 S152S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JT-01A-11D-A42J-10 chr6:33283497 G>T maps to NM_001145338.1 S399*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-7332-01A-11D-2136-08 chr1:22850846 C>A maps to NM_014870.3 T1145T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4104-01A-01D-1458-08 chr20:62407207 G>A maps to NM_025224.2 L349L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr4:4322598 C>A maps to NM_145291.3 S618S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NI-01A-11D-A26P-10 chr1:203819760 C>T maps to NM_014827.4 L686L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9Q0-01A-12D-A42J-10 chr1:37948518 A>T maps to NM_025079.2 T369T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4116-01A-01D-1252-08 chr16:88653022 G>T maps to ENST00000452588 E207*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-8500-01A-11D-2396-08 chr16:88653084 C>T maps to ENST00000452588 F227F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-A5DJ-01A-11D-A26P-10 chr2:113079399 C>G maps to NM_198581.2 S348S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A4EM-01A-11D-A25F-10 chr5:132342535 T>G maps to ENST00000509437 R62R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chr1:52902540 G>T maps to NM_001009881.2 R1350R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9J2-01A-11D-A382-10 chr23:77913323 C>T did not map to a codon.
Sequencing variant TCGA-HE-A5NK-01A-11D-A26P-10 chr23:77913358 G>A did not map to a codon.
Sequencing variant TCGA-DW-7841-01A-11D-2136-08 chr5:80600584 G>A maps to NM_032280.2 R3R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr2:207171573 G>A maps to NM_020923.1 R774R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-5561-01A-01D-1589-08 chr1:27176924 G>A maps to NM_032283.2 T260T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7963-01B-11D-A28G-10 chr16:85010784 G>A maps to NM_001145548.1 F259F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5902-01A-11D-1589-08 chr23:128963039 G>T did not map to a codon.
Sequencing variant TCGA-B9-5156-01A-01D-1589-08 chr2:145156026 G>A maps to NM_014795.3 F909F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A57E-01A-11D-A26P-10 chr2:220072713 C>T maps to NM_138802.1 L130L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7050-01A-11D-1961-08 chr12:72017887 A>T maps to NM_144982.4 L1501*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9KA-01A-11D-A42J-10 chr16:72991449 G>A maps to NM_006885.3 Y865Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr16:72984697 G>A maps to NM_006885.3 G962G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W9-01A-11D-A28G-10 chr16:72821092 G>T maps to NM_006885.3 T3694T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr16:72992634 T>C maps to NM_006885.3 E470E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr16:72992637 C>T maps to NM_006885.3 E469E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9J2-01A-11D-A382-10 chr8:77776081 A>T maps to NM_024721.4 K3378*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4113-01A-01D-1252-08 chr8:77776649 C>A maps to NM_024721.4 S3567*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A562-01A-11D-A26P-10 chr8:77616433 G>A maps to NM_024721.4 G37G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WN-A9G9-01A-12D-A36X-10 chr8:77775450 T>A maps to NM_024721.4 P3167P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7838-01A-11D-2136-08 chr17:4995908 T>C maps to NM_153018.2 C370C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7050-01A-11D-1961-08 chr19:39898402 T>C maps to NM_003407.2 P15P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4104-01A-01D-1458-08 chr14:69256348 C>G maps to NM_004926.2 L306L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A9DE-01A-11D-A36X-10 chr14:69256831 G>T maps to NM_004926.2 R145R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PS-01A-11D-A42J-10 chr9:115805448 A>G maps to NM_003408.1 H483H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5884-01A-11D-1589-08 chr20:50769884 C>T maps to NM_018197.2 S282S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E6-01A-11D-A28G-10 chr11:58346867 G>A maps to NM_053023.4 A38A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6792-01A-21D-1961-08 chr3:15116215 C>A maps to NM_022340.2 A476A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4115-01A-01D-1252-08 chr14:68282658 C>A maps to NM_015346.3 E8*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E6-01A-11D-A28G-10 chr14:68268850 G>T maps to NM_015346.3 L528L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NL-01A-11D-A26P-10 chr20:62366739 T>A maps to NM_032527.4 P427P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3468-01A-01D-1252-08 chr20:39831714 G>T maps to NM_015035.3 T614T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EA-01A-11D-A28G-10 chr3:147128793 G>T maps to NM_003412.3 E299*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr7:99621200 A>G maps to NM_003439.1 V24V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A7SN-01A-11D-A34Z-10 chr7:99117528 C>T maps to NM_014569.3 S211S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A656-01A-11D-A31X-10 chr23:101152940 A>T did not map to a codon.
Sequencing variant TCGA-GL-8500-01A-11D-2396-08 chr3:178785386 C>A maps to NM_022470.3 E52*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7838-01A-11D-2136-08 chr7:44805817 C>G maps to NM_031449.3 P766P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WN-AB4C-01A-11D-A42J-10 chr7:44801087 G>A maps to NM_031449.3 V427V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A562-01A-11D-A26P-10 chr1:40724032 G>C maps to NM_005857.3 V30V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NI-01A-11D-A26P-10 chr1:35569919 G>C maps to NM_024772.3 V148V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JM-01A-12D-A42J-10 chr23:70472531 T>C did not map to a codon.
Sequencing variant TCGA-J7-A8I2-01A-12D-A35Z-10 chr23:70472978 G>A did not map to a codon.
Sequencing variant TCGA-BQ-5889-01A-11D-1589-08 chr13:20398871 T>C maps to NM_001142684.1 K585K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JD-01A-11D-A42J-10 chr1:35453205 T>C maps to NM_007167.3 Q1159Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JP-01A-11D-A42J-10 chr1:35452998 G>A maps to NM_007167.3 T1228T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PX-01A-11D-A42J-10 chr1:35457923 A>C maps to NM_007167.3 L686*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr3:50379016 C>T maps to NM_015896.2 W412*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-7502-01A-11D-2201-08 chr19:19789580 G>C maps to NM_033204.2 L59L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr19:58945193 T>A maps to NM_003433.3 G539G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W9-01A-11D-A28G-10 chr19:19822256 T>G maps to NM_021030.2 G611G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A7SQ-01A-12D-A35Z-10 chr19:19823846 T>A maps to NM_021030.2 G81G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr11:9519249 T>G maps to NM_003442.5 T290T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9K3-01A-11D-A42J-10 chr8:146157587 G>A maps to NM_006958.2 D195D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A655-01A-11D-A31Z-10 chr3:44612086 T>C maps to NM_018651.2 Y495Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5902-01A-11D-1589-08 chr9:97063237 C>T maps to NM_194320.2 G466G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9J8-01A-11D-A42J-10 chr11:3380632 G>T maps to NM_001130520.1 S535S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-AAVM-01A-11D-A42J-10 chr11:3380398 T>C maps to NM_001130520.1 K613K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9JV-01A-12D-A42J-10 chr3:44670999 G>A maps to NM_006991.3 E118E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A71U-01A-12D-A33Q-10 chr10:45499113 C>T maps to NM_006963.4 Q100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr19:44570871 C>T maps to NM_013361.4 F297F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5875-01A-11D-1589-08 chr19:44635910 A>C maps to NM_013362.2 R382R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A560-01A-11D-A26P-10 chr19:44739324 A>T maps to NM_182490.1 K248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr16:71483579 G>T maps to NM_145911.1 P116P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr17:5009511 A>G maps to NM_014519.2 Y314Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5880-01A-11D-1589-08 chr18:74622685 C>T maps to NM_007345.3 S906S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NK-01A-11D-A26P-10 chr18:74680293 G>T maps to NM_007345.3 *1846L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A48D-01A-11D-A25F-10 chr8:145947049 A>T maps to NM_138367.1 I665I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A9DE-01A-11D-A36X-10 chr8:145947778 T>C maps to NM_138367.1 E422E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr19:24309779 A>G maps to NM_203282.2 E326E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr19:24310236 A>T maps to NM_203282.2 R479*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9K6-01A-11D-A42J-10 chr11:116655622 G>A maps to NM_003904.3 S256S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-AAVL-01A-11D-A42J-10 chr15:56935188 T>C maps to NM_017661.2 K740K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A7SO-01A-11D-A34Z-10 chr15:56968912 A>G maps to NM_017661.2 V455V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A44B-01A-11D-A25F-10 chr1:200376814 T>C maps to NM_012482.3 Q673Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M8-01A-11D-A31X-10 chr1:200378263 C>T maps to NM_012482.3 Q190Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr21:43413769 T>C maps to NM_020727.4 Q145Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A8YI-01A-21D-A36X-10 chr7:99674929 G>A maps to NM_032924.3 D17D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PM-01A-21D-A382-10 chr6:43316085 C>T maps to NM_014345.2 S1016S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NI-01A-11D-A26P-10 chr16:58031773 G>A maps to NM_020807.1 F132F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A9DC-01A-11D-A36X-10 chr19:54080923 C>T maps to NM_001079907.1 L370L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7584-01A-11D-2136-08 chr20:44578918 G>C maps to NM_022095.3 T1142T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr20:25656222 C>A maps to NM_015655.2 S567S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5903-01A-11D-1589-08 chr20:32376705 G>T maps to ENST00000375200 A630A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8630-01A-11D-2396-08 chr5:176471534 G>C did not map to a codon.
Sequencing variant TCGA-A4-7288-01A-11D-2136-08 chr19:53643806 A>G maps to NM_001172674.1 I759I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr5:71739939 G>C maps to NM_152625.1 Y626*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NJ-01A-11D-A26P-10 chr5:71739708 C>T maps to NM_152625.1 R703R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A7SP-01A-11D-A34Z-10 chr10:38406702 T>C maps to NM_003421.2 N208N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7287-01A-11D-2136-08 chr12:54764719 T>C maps to NM_001130967.1 Q275Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9JV-01A-12D-A42J-10 chr3:21465454 C>A maps to NM_024697.2 G318G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A71U-01A-12D-A33Q-10 chr6:27368766 T>C maps to NM_001076781.1 T206T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9K2-01A-11D-A42J-10 chr7:99092212 G>A maps to NM_032164.2 Q209*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5875-01A-11D-1589-08 chr8:28209092 C>A maps to NM_018660.2 P384P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A7SO-01A-11D-A34Z-10 chr7:148851296 G>A maps to NM_170686.2 K95K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A7SP-01A-11D-A34Z-10 chr18:72775889 G>A maps to NM_017757.2 R2071R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr19:58084257 A>G maps to NM_017879.1 S338S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr19:21240181 A>G maps to NM_025189.3 Q356Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr1:23688887 C>A maps to NM_001077195.1 T329T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NH-01A-11D-A26P-10 chr1:23693622 G>A maps to NM_001077195.1 T24T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Y8-A895-01A-11D-A35Z-10 chr19:56671521 T>A maps to NM_018337.2 A312A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A8YH-01A-11D-A36X-10 chr7:149462501 G>A maps to NM_207336.1 S363S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PO-01A-11D-A382-10 chr19:53344637 T>C maps to NM_001008801.1 E303E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9K0-01A-11D-A42J-10 chr19:57088478 T>C maps to NM_001001668.3 L228L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr19:57037031 A>G maps to NM_020813.2 Q532Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7838-01A-11D-2136-08 chr19:50550198 G>T maps to NM_015428.1 L833L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5878-01A-11D-1589-08 chr10:44112495 C>T maps to NM_145312.3 F335F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7841-01A-11D-2136-08 chr19:58867602 C>A maps to NM_198458.1 E467*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4617-01A-01D-1252-08 chr3:44776080 A>G maps to NM_145044.2 G56G. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-Y8-A8S1-01A-11D-A36X-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-Y8-A8S1-01A-11D-A36X-10 chr10:77161117 G>T maps to ENST00000438638 P120P. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-Y8-A8S1-01A-11D-A36X-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-Y8-A8S1-01A-11D-A36X-10 chr10:77161123 G>T maps to ENST00000438638 P122P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A656-01A-11D-A31X-10 chr19:19905759 G>C maps to NM_001099269.2 P312P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Y8-A894-01A-11D-A35Z-10 chr20:62595673 T>C maps to NM_020713.1 K444K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7838-01A-11D-2136-08 chr18:14105674 T>C maps to NM_145287.3 G288G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7838-01A-11D-2136-08 chr18:22805628 G>C maps to NM_015461.2 V751V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JN-01A-21D-A42J-10 chr19:30935836 C>T maps to NM_014717.1 G456G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9KA-01A-11D-A42J-10 chr19:30935606 C>A maps to NM_014717.1 R380R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PO-01A-11D-A382-10 chr19:31039334 A>T maps to NM_014717.1 K937*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Y8-A8S0-01A-11D-A36X-10 chr19:31039522 A>G maps to NM_014717.1 A999A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7840-01A-11D-2136-08 chr19:7083598 T>C maps to NM_024341.2 S379S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-8500-01A-11D-2396-08 chr19:7075687 C>G maps to NM_024341.2 A18A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr19:9453287 A>G maps to NM_032497.1 G387G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9K6-01A-11D-A42J-10 chr19:9763810 A>G maps to NM_001130032.1 N365N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NJ-01A-11D-A26P-10 chr19:2915554 C>T maps to NM_173480.2 F13F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr19:38056036 G>A maps to NM_016536.3 G431G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A69E-01A-11D-A31X-10 chr19:52376954 A>G maps to NM_032679.2 F96F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9K3-01A-11D-A42J-10 chr19:56935541 A>T maps to NM_001159861.1 G505G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5P-A9JU-01A-11D-A42J-10 chr17:5085262 A>T maps to NM_032530.1 C763*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7045-01A-31D-1961-08 chr16:2052643 C>T maps to ENST00000431526 G185G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr19:35250174 C>A maps to NM_001007248.2 E511*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Y8-A895-01A-11D-A35Z-10 chr19:53268926 G>C maps to NM_198457.2 Y694*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr15:64966234 G>T maps to NM_015042.1 G394G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PR-01A-11D-A42J-10 chr15:64972426 C>T maps to NM_015042.1 S1271S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6135-01A-11D-1961-08 chr19:52496291 C>A maps to ENST00000354939 P690P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A7SP-01A-11D-A34Z-10 chr19:52618817 A>T maps to NM_178523.3 R533R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Y8-A8S1-01A-11D-A36X-10 chr3:40528723 C>T maps to NM_001145082.2 F281F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JG-01A-11D-A42J-10 chr16:30795033 G>A maps to NM_001080417.1 P205P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W8-01A-11D-A28G-10 chr16:30794424 G>A maps to NM_001080417.1 G408G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Y8-A895-01A-11D-A35Z-10 chr16:30794004 G>A maps to NM_001080417.1 G548G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55Z-01A-11D-A26P-10 chr2:71607374 T>C maps to NM_014497.3 T763T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A7SQ-01A-12D-A35Z-10 chr2:71661906 G>A maps to NM_014497.3 Q1969Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A71W-01A-12D-A34Z-10 chr12:48736773 T>C maps to NM_152320.2 R433R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7734-01A-11D-2136-08 chr1:91406115 G>A maps to NM_201269.1 F265F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5XZ-01A-11D-A31X-10 chr1:91403568 G>T maps to NM_201269.1 S1054*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr16:31090722 G>A maps to NM_014699.3 E1026E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A657-01A-11D-A31X-10 chr16:31092684 C>T maps to NM_014699.3 T1680T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A7SN-01A-11D-A34Z-10 chr19:52394349 C>A maps to NM_023074.3 G347*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-7332-01A-11D-2136-08 chr17:47388761 A>G maps to NM_014897.2 H407H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3472-01A-01D-1252-08 chr3:88190086 A>T maps to NM_018293.2 R543*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr7:99158260 C>T maps to NM_001083956.1 L27L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3468-01A-01D-1252-08 chr9:40774145 C>A maps to NM_033160.5 E377*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr19:53668283 T>A maps to NM_024733.3 K487*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7997-01A-11D-2201-08 chr19:23927145 A>G maps to NM_138286.2 A402A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8098-01A-11D-2396-08 chr19:23927145 A>G maps to NM_138286.2 A402A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-7268-01A-11D-2136-08 chr1:151259372 C>G maps to NM_020832.1 A202A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SX-A71S-01A-11D-A33Q-10 chr1:151260815 G>T maps to NM_020832.1 R683R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Y8-A8RY-01A-11D-A36X-10 chr16:30616526 G>T maps to NM_138447.1 S187S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5892-01A-11D-1589-08 chr1:43317093 C>A maps to ENST00000442768 L186L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9J1-01A-11D-A382-10 chr19:12575505 A>G maps to ENST00000428311 H410H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8311-01A-11D-2396-08 chr4:437055 A>G maps to NM_133474.2 S400S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PS-01A-11D-A42J-10 chr19:57955391 C>T maps to NM_001023561.2 L292L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JT-01A-11D-A42J-10 chr17:80789568 G>C maps to NM_024702.2 T254T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Y8-A895-01A-11D-A35Z-10 chr6:35262231 G>A did not map to a codon.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr19:53959647 C>A maps to NM_001008401.3 T629T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UZ-A9PN-01A-11D-A382-10 chr15:35275395 A>G maps to NM_014106.3 P80P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4113-01A-01D-1252-08 chr7:149129442 C>T maps to ENST00000440594 E641E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5890-01A-11D-1589-08 chr16:89294016 C>T maps to NM_182531.2 R413*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V9-A7HT-01A-11D-A33Q-10 chr9:99581194 T>C maps to NM_001001662.1 E370E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A9DD-01A-11D-A36X-10 chr7:148767516 A>C maps to NM_152411.3 *783G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A44B-01A-11D-A25F-10 chr19:12502557 C>T maps to NM_001080821.2 T218T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6790-01A-11D-1961-08 chr2:185801067 A>G maps to NM_194250.1 Q315Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9J3-01A-12D-A382-10 chr19:58385868 C>A maps to NM_001144989.1 E297*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A9DC-01A-11D-A36X-10 chr19:11833784 T>G maps to NM_001080493.2 G188G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A656-01A-11D-A31X-10 chr17:33288776 C>A maps to NM_052857.3 L64L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr17:33289280 T>C maps to NM_052857.3 H232H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-7268-01A-11D-2136-08 chr19:52660095 G>A maps to NM_001102657.1 G280G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5903-01A-11D-1589-08 chr19:52659396 G>A maps to NM_001102657.1 L513L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A8YI-01A-21D-A36X-10 chr19:12187707 G>C maps to NM_001136501.1 V591V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47N-01A-11D-A25F-10 chr19:52877550 G>A did not map to a codon.
Sequencing variant TCGA-A4-7286-01A-11D-2136-08 chr22:29445638 C>A maps to NM_032173.2 L390L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7840-01A-11D-2136-08 chr22:29445938 C>G maps to NM_032173.2 L490L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5889-01A-11D-1589-08 chr1:238053764 A>T maps to NM_021186.3 A57A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A855-01A-11D-A34Z-10 chr3:102171979 G>A maps to NM_175056.1 L124L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4116-01A-01D-1252-08 chr23:15841259 C>G did not map to a codon.
Sequencing variant TCGA-UZ-A9PS-01A-11D-A42J-10 chr23:15841226 G>C did not map to a codon.
Sequencing variant TCGA-UZ-A9PS-01A-11D-A42J-10 chr23:15841259 C>G did not map to a codon.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr1:33960784 C>T maps to NM_145238.3 I947I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9J5-01A-21D-A382-10 chr19:58849867 C>T maps to NM_181846.2 Q218*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A6HP-01A-11D-A31X-10 chr15:43653717 T>C maps to NM_152455.3 K704K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F9-A7VF-01A-11D-A33Q-10 chr1:45485774 C>T maps to NM_020883.1 E886E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EA-01A-11D-A28G-10 chr23:57619113 G>C did not map to a codon.
Sequencing variant TCGA-BQ-7056-01A-11D-1961-08 chr1:53287195 T>C maps to NM_024646.2 H710H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr1:53262038 T>C maps to NM_024646.2 A470A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7838-01A-11D-2136-08 chr17:3919675 C>A maps to NM_015113.3 G2696*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2Z-A9JS-01A-21D-A42J-10 chr1:78034103 T>C maps to NM_015534.4 K793K. Only missense variants will be evaluated by CHASM.
