5408 NP_109597 A400S not found in SNVbox database
7093 NP_705833 G785S not found in SNVbox database
1218 NP_705833 F548S not found in SNVbox database
1681 NP_705833 R222H not found in SNVbox database
2491 NP_705833 H299N not found in SNVbox database
Sequencing variant TCGA-L5-A43E-01A-11D-A247-09 chr10:52573790 C>T maps to NM_138932.2 A391A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RF-01A-13D-A33E-09 chr16:7743344 G>T maps to NM_145893.2 E363*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93D-01A-11D-A387-09 chr12:9227281 G>T maps to NM_000014.4 S1210S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr12:9252078 G>A maps to NM_000014.4 D533D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OW-01A-11D-A28B-09 chr12:9265953 A>C did not map to a codon.
Sequencing variant TCGA-L5-A4OU-01A-11D-A28B-09 chr12:9013756 G>C maps to NM_144670.3 R1122R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93E-01A-11D-A37C-09 chr22:43089312 G>A maps to NM_017436.4 V215V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-AAPN-01A-11D-A403-09 chr3:137850069 G>C maps to NM_016161.2 S10*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr12:125626669 C>T maps to NM_023928.3 A638A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6Y0-01B-11D-A33E-09 chr12:125558420 G>T did not map to a codon.
Sequencing variant TCGA-L5-A4OJ-01A-11D-A27G-09 chr2:69732699 C>T did not map to a codon.
Sequencing variant TCGA-LN-A9FQ-01A-31D-A387-09 chr2:219131707 G>T maps to ENST00000444053 G133G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8W8-01B-11D-A37C-09 chr6:44279945 G>A maps to NM_020745.2 R100*. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-R6-A8WC-01A-11D-A37C-09. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-X8-AAAR-01A-11D-A403-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-LN-A8I0-01A-11D-A36J-09 chr4:57220225 A>G maps to NM_181806.2 L454L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GF-01A-11D-A37C-09 chr7:121756942 G>A maps to NM_005763.3 S252S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93E-01A-11D-A37C-09 chr7:121753715 C>A maps to NM_005763.3 E368*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OE-01A-11D-A27G-09 chr7:121773699 G>A maps to NM_005763.3 A27A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A938-01A-11D-A37C-09 chr17:35310465 C>T maps to NM_012138.3 D188D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A4-01A-11D-A27G-09 chr17:79094680 G>A maps to NM_001080395.2 R1019*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8WC-01A-11D-A37C-09 chr17:79094873 C>T maps to NM_001080395.2 A954A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NV-01A-11D-A37C-09 chr9:107646735 C>A maps to NM_005502.3 G92*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A8I1-01A-11D-A36J-09 chr9:107555516 G>A maps to NM_005502.3 A1857A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FP-01A-31D-A387-09 chr9:107581885 C>A maps to NM_005502.3 L1074L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GJ-01A-11D-A37C-09 chr17:67148623 T>A did not map to a codon.
Sequencing variant TCGA-2H-A9GN-01A-11D-A37C-09 chr17:67178854 G>T maps to NM_080282.3 P864P. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-LN-A4MR-01A-11D-A28B-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-R6-A6XG-01B-11D-A33E-09 chr17:67181657 C>T maps to NM_080282.3 P819P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GO-01A-11D-A37C-09 chr2:215848403 C>T maps to NM_173076.2 W1450*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A4QS-01A-11D-A27G-09 chr2:215866354 A>G maps to NM_173076.2 I930I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OJ-01A-11D-A27G-09 chr2:215802331 G>T maps to NM_173076.2 R2482R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OR-01A-11D-A27G-09 chr2:215872567 G>A maps to NM_173076.2 S825S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NF-01A-11D-A37C-09 chr2:215855533 G>T maps to NM_173076.2 T1172T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A4P3-01A-11D-A27G-09 chr7:48520702 C>G maps to NM_152701.3 S4349*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93D-01A-11D-A387-09 chr7:48619924 T>G maps to NM_152701.3 Y4820*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr7:48312958 G>A maps to NM_152701.3 R1232R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NH-01A-11D-A37C-09 chr7:48315874 T>G maps to NM_152701.3 L2204L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NS-01A-12D-A37C-09 chr7:48287987 T>C maps to NM_152701.3 S604S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NT-01A-11D-A37C-09 chr9:139903008 G>A maps to ENST00000355090 S2408S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6Y0-01B-11D-A33E-09 chr9:139916856 C>T maps to ENST00000355090 S201S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EZ-01A-11D-A36J-09 chr9:139915181 C>T maps to ENST00000355090 W440*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GI-01A-11D-A37C-09 chr16:2336798 G>A maps to NM_001089.2 D1058D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr16:2374410 C>T maps to NM_001089.2 P147P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr1:94506866 G>T maps to NM_000350.2 C1140*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49U-01A-31D-A27G-09 chr1:94502904 C>A maps to NM_000350.2 G1203G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A8HZ-01A-11D-A36J-09 chr1:94497395 G>A maps to NM_000350.2 Q1356*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr17:67260953 G>A maps to ENST00000392677 I1080I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q9-A6FW-01A-31D-A31U-09 chr17:67250502 T>C maps to ENST00000392677 G1400G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A8O2-01A-11D-A36J-09 chr17:67109432 C>T maps to NM_080284.2 L657L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NF-01A-11D-A37C-09 chr19:1046339 C>T maps to NM_019112.3 S519S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr17:66872638 C>T maps to NM_007168.2 P1404P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L7-A6VZ-01A-12D-A33E-09 chr17:66871851 T>G maps to NM_007168.2 R1425R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A8-01A-32D-A27G-09 chr17:66873730 C>G maps to NM_007168.2 V1336V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NJ-01A-11D-A36J-09 chr1:229661842 G>T maps to NM_012089.2 C582*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NW-01A-11D-A37C-09 chr2:169869891 G>T maps to NM_003742.2 Y93*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FH-01A-11D-A33E-09 chr7:20766682 G>A maps to NM_001163941.1 E882E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49O-01A-11D-A247-09 chr7:20768052 C>T maps to NM_001163941.1 R948*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6XQ-01B-11D-A33E-09 chr7:20685712 C>A maps to NM_001163941.1 S311S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A97H-01A-11D-A387-09 chr23:74288929 G>T did not map to a codon.
Sequencing variant TCGA-JY-A938-01A-11D-A37C-09 chr12:123424681 G>A maps to NM_203444.2 Y573Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RE-01A-11D-A33E-09 chr16:16103631 G>T did not map to a codon.
Sequencing variant TCGA-R6-A6L6-01B-11D-A33E-09 chr16:16162051 G>T maps to ENST00000399408 E573*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OR-01A-11D-A27G-09 chr6:43400125 G>A maps to NM_033450.2 L93L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OX-01A-21D-A28B-09 chr16:48221194 G>T maps to NM_032583.3 A950A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OU-01A-11D-A28B-09 chr16:48119526 G>A maps to NM_033226.2 R1269*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NJ-01A-11D-A36J-09 chr16:48121856 G>T maps to NM_033226.2 V1205V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6DQ-01B-11D-A31U-09 chr16:48125057 G>A maps to NM_033226.2 S1086S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X8-AAAR-01A-11D-A403-09 chr16:48125075 C>T maps to NM_033226.2 T1080T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZR-A9CJ-01B-11D-A387-09 chr16:48149421 C>T maps to NM_033226.2 S631S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-AAPN-01A-11D-A403-09 chr13:95858834 G>C maps to NM_005845.3 S371*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49Y-01A-11D-A27G-09 chr16:16276744 G>T maps to NM_001171.5 V662V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A3-01A-11D-A27G-09 chr16:16271330 C>T maps to NM_001171.5 Q856Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GQ-01A-11D-A37C-09 chr11:17483279 C>T maps to ENST00000302539 L224L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A5S3-01A-11D-A28B-09 chr11:17416731 C>A maps to ENST00000302539 L1467L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6F8-01A-11D-A33E-09 chr11:17483264 G>T maps to ENST00000302539 T229T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43E-01A-11D-A247-09 chr11:17498305 G>A maps to ENST00000302539 C6C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr11:17414564 G>A maps to ENST00000302539 F1574F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NK-01A-21D-A37C-09 chr11:17434247 G>A maps to ENST00000302539 R842*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NV-01A-11D-A37C-09 chr11:17430051 T>A maps to ENST00000302539 K904*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6F8-01A-11D-A33E-09 chr12:21998615 G>T maps to NM_005691.2 S1006*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49Y-01A-11D-A27G-09 chr12:22012597 G>T maps to NM_005691.2 G809G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-A7RE-01A-11D-A351-09 chr12:22005334 A>G maps to NM_005691.2 T870T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASW-01A-11D-A403-09 chr12:22069891 C>T maps to NM_005691.2 E184E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr23:153009045 C>T did not map to a codon.
Sequencing variant TCGA-2H-A9GR-01A-12D-A37C-09 chr12:39994434 C>T maps to NM_005164.3 W528*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49M-01A-21D-A27G-09 chr12:39967549 G>T maps to NM_005164.3 S657S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EO-01A-11D-A36J-09 chr12:39973421 C>T did not map to a codon.
Sequencing variant TCGA-JY-A6FD-01A-11D-A33E-09 chr7:150912710 G>A maps to NM_005692.3 Y503Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OJ-01A-11D-A27G-09 chr7:150915851 G>T maps to NM_005692.3 V375V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RF-01A-13D-A33E-09 chr3:183907231 G>A did not map to a codon.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr21:43691298 T>C did not map to a codon.
Sequencing variant TCGA-L5-A8NJ-01A-11D-A36J-09 chr4:89034589 G>A maps to NM_004827.2 S353S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NK-01A-21D-A37C-09 chr11:119025272 G>A maps to NM_001142505.1 V176V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3Y9-01A-12D-A247-09 chr2:44065706 G>A maps to NM_022436.2 L38L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NG-01A-11D-A37C-09 chr14:51347289 G>T did not map to a codon.
Sequencing variant TCGA-L5-A8NJ-01A-11D-A36J-09 chr15:89738467 G>A maps to NM_152924.4 E364E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EY-01A-11D-A36J-09 chr15:89695079 G>T maps to NM_152924.4 G123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA7B-01A-31D-A403-09 chr18:19284500 G>A maps to NM_138340.4 V42V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NS-01A-12D-A37C-09 chr3:58242357 G>A maps to NM_020676.5 T15T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OR-01A-11D-A27G-09 chr19:17405572 C>T maps to NM_024527.4 T281T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49L-01A-11D-A247-09 chr19:17411828 C>G maps to NM_024527.4 V199V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49S-01A-11D-A247-09 chr10:27066071 C>T maps to NM_005470.3 A128A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FH-01A-11D-A33E-09 chr9:133760106 G>A maps to NM_007313.2 P829P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr10:116203871 A>G maps to ENST00000277895 L685L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NT-01A-11D-A37C-09 chr4:8108334 G>A maps to NM_001130083.1 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr5:148630031 C>A maps to NM_014945.2 A584A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FE-01A-11D-A33E-09 chr7:150555060 G>T maps to ENST00000416793 L501L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OJ-01A-11D-A27G-09 chr7:150556092 C>T maps to ENST00000416793 L605L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A939-01A-12D-A37C-09 chr6:26598525 G>T maps to NM_013375.2 E158*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A893-01A-11D-A36J-09 chr11:34194799 G>A maps to NM_145804.2 Y433Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8ER-01A-11D-A36J-09 chr11:34186321 G>A maps to NM_145804.2 P633P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NI-01A-11D-A37C-09 chr18:47320774 G>T maps to NM_006111.2 S151*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr17:35557398 G>T maps to NM_198834.1 R1362R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A8I0-01A-11D-A36J-09 chr17:35581951 A>T maps to NM_198834.1 I1145I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EQ-01A-11D-A36J-09 chr17:35545291 G>A maps to NM_198834.1 L1567L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EU-01A-11D-A36J-09 chr17:35633932 G>T maps to NM_198834.1 A265A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A4P3-01A-11D-A27G-09 chr12:109673409 G>A did not map to a codon.
Sequencing variant TCGA-IG-A5B8-01A-11D-A28B-09 chr12:109647043 C>T maps to NM_001093.3 I1045I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OP-01A-11D-A27G-09 chr12:109629444 G>T maps to NM_001093.3 L724L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr12:109634880 C>T maps to NM_001093.3 H850H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8Q7-01A-11D-A37C-09 chr12:109610095 G>A maps to NM_001093.3 W351*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49S-01A-11D-A247-09 chr3:132277826 T>C maps to NM_032169.4 T777T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EU-01A-11D-A36J-09 chr3:128616489 C>T maps to NM_014049.4 A190A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88V-01A-11D-A351-09 chr10:124810674 G>A maps to NM_001609.3 A367A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A97H-01A-11D-A387-09 chr17:7127298 G>T maps to ENST00000356839 E495*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GQ-01A-11D-A37C-09 chr15:89398110 C>T maps to NM_013227.3 G765G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EO-01A-11D-A36J-09 chr15:89391160 C>A maps to NM_013227.3 R542R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FR-01A-11D-A387-09 chr17:43216518 C>T maps to NM_001135706.1 P273P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XP-A8T8-01A-11D-A36J-09 chr17:43213936 C>T maps to NM_001135706.1 P53P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GR-01A-12D-A37C-09 chr17:31350877 C>T did not map to a codon.
Sequencing variant TCGA-R6-A8WC-01A-11D-A37C-09 chr17:31439043 G>T maps to NM_183377.1 G250G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OE-01A-11D-A27G-09 chr2:220396514 C>T maps to NM_018674.4 N333N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZR-A9CJ-01B-11D-A387-09 chr4:156764859 G>A maps to NM_017419.2 H278H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OJ-01A-11D-A27G-09 chr11:44095007 C>T maps to NM_032592.3 R120R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA7B-01A-31D-A403-09 chr11:44089203 C>T maps to NM_032592.3 F9F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OT-01A-11D-A28B-09 chr11:44074967 C>T maps to NM_001031854.2 R321*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A5B8-01A-11D-A28B-09 chr16:67693164 C>A maps to NM_001082486.1 E240*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FP-01A-31D-A387-09 chr17:61557762 G>T maps to NM_000789.3 E241*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6XQ-01B-11D-A33E-09 chr17:61564013 C>A maps to NM_000789.3 R719R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NQ-01A-11D-A36J-09 chr23:15584414 G>A did not map to a codon.
Sequencing variant TCGA-R6-A8WG-01A-11D-A37C-09 chr23:15603631 G>T did not map to a codon.
Sequencing variant TCGA-VR-AA7B-01A-31D-A403-09 chr23:15618925 C>T did not map to a codon.
Sequencing variant TCGA-L5-A8NG-01A-11D-A37C-09 chr7:100490295 C>T maps to NM_000665.3 L404L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6DN-01B-11D-A31U-09 chr7:100490406 C>T maps to NM_000665.3 S367S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FH-01A-11D-A33E-09 chr14:23548782 A>T maps to NM_014977.3 S645S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88Z-01A-11D-A36J-09 chr1:55065064 C>A maps to NM_015547.3 I287I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NL-01A-12D-A37C-09 chr1:55070050 G>A maps to NM_015547.3 L395L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NS-01A-12D-A37C-09 chr1:55059687 C>T maps to NM_015547.3 F149F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49U-01A-31D-A27G-09 chr1:55064995 G>A maps to NM_015547.3 L264L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8WG-01A-11D-A37C-09 chr6:24687915 A>T maps to NM_001160094.1 R3*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93D-01A-11D-A387-09 chr1:6378591 C>A maps to NM_007274.3 V224V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GQ-01A-11D-A37C-09 chr23:23722810 C>T did not map to a codon.
Sequencing variant TCGA-IG-A51D-01A-11D-A27G-09 chr17:73975070 C>T maps to NM_004035.6 E28E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZR-A9CJ-01B-11D-A387-09 chr17:73947650 C>A maps to NM_004035.6 E318*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RF-01A-13D-A33E-09 chr2:111542370 G>A maps to NM_001142807.1 A46A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA7B-01A-31D-A403-09 chr19:51294950 G>A maps to NM_033068.2 E114E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASX-01A-11D-A387-09 chr22:51183124 C>T maps to NM_001097.2 S252S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RE-A7BO-01A-11D-A33E-09 chr12:6748124 G>T maps to NM_032489.2 R502R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OM-01A-11D-A27G-09 chr23:70824009 T>C did not map to a codon.
Sequencing variant TCGA-L5-A4OP-01A-11D-A27G-09 chr23:70823924 C>T did not map to a codon.
Sequencing variant TCGA-L5-A88Z-01A-11D-A36J-09 chr23:70832393 C>T did not map to a codon.
Sequencing variant TCGA-XP-A8T7-01A-11D-A36J-09 chr23:70823522 C>T did not map to a codon.
Sequencing variant TCGA-2H-A9GO-01A-11D-A37C-09 chr19:6147598 C>T maps to NM_030924.3 L70L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A5B8-01A-11D-A28B-09 chr16:89167109 C>T maps to NM_174917.2 L7L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88Z-01A-11D-A36J-09 chr16:89199545 G>T maps to NM_174917.2 V414V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A893-01A-11D-A36J-09 chr4:185681561 G>T maps to NM_001995.2 Y577*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-AAPN-01A-11D-A403-09 chr23:108911422 G>C did not map to a codon.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr10:114181708 C>T maps to NM_016234.3 H520H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NR-01A-11D-A37C-09 chr10:114158682 C>T maps to NM_016234.3 Q117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A4-01A-11D-A27G-09 chr16:20702456 G>A maps to NM_052956.2 H18H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GK-01A-11D-A37C-09 chr16:20480933 C>T maps to NM_001010845.2 V163V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr16:20491947 A>C maps to NM_001010845.2 G445G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NE-01A-11D-A37C-09 chr16:20488698 T>G maps to NM_001010845.2 T369T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NE-01A-11D-A37C-09 chr16:20557787 A>C maps to NM_182617.3 T369T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43E-01A-11D-A247-09 chr16:20448477 C>T maps to NM_017888.2 N471N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RE-A7BO-01A-11D-A33E-09 chr16:20448661 C>A maps to NM_017888.2 V503V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3I8-01A-11D-A247-09 chr20:24993468 G>A maps to NM_032501.2 T562T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49U-01A-31D-A27G-09 chr20:33508849 G>A maps to NM_001076552.2 W408*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GM-01A-11D-A37C-09 chr12:81648633 A>G did not map to a codon.
Sequencing variant TCGA-LN-A8I1-01A-11D-A36J-09 chr12:81537016 G>A maps to NM_024560.2 G304G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FO-01A-11D-A387-09 chr12:81624850 T>C maps to NM_024560.2 P510P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NW-01A-11D-A37C-09 chr1:229568158 G>A maps to NM_001100.3 G158G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8Q7-01A-11D-A37C-09 chr1:229567269 G>T maps to NM_001100.3 S370S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93E-01A-11D-A37C-09 chr10:90697871 G>A maps to NM_001141945.1 A312A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NT-01A-11D-A37C-09 chr5:56778213 G>T maps to NM_001017992.2 T107T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A2-01A-31D-A27G-09 chr5:56777528 G>T maps to NM_001017992.2 R336R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93C-01A-11D-A387-09 chr3:179305770 G>A maps to NM_004301.3 K421K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NG-01A-11D-A37C-09 chr7:100253446 G>A maps to NM_016188.4 Y27Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A97I-01A-11D-A387-09 chr1:18152455 C>T maps to NM_030812.2 S181S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr1:18152878 C>A maps to NM_030812.2 S322S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FP-01A-31D-A387-09 chr19:8808652 C>A maps to NM_178525.3 L133L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49U-01A-31D-A27G-09 chr1:236914837 C>A maps to NM_001103.2 I575I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A5B8-01A-11D-A28B-09 chr19:39208682 G>A maps to NM_004924.3 Q420Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GG-01A-11D-A37C-09 chr2:65467071 C>G maps to NM_001005386.2 T45T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr7:152549323 C>T maps to NM_020445.4 G355G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr7:152550625 C>T maps to NM_020445.4 Y375Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr12:100598717 G>A maps to NM_022496.3 S23S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A4P3-01A-11D-A27G-09 chr23:127185304 A>C did not map to a codon.
Sequencing variant TCGA-L5-A43I-01A-11D-A247-09 chr23:127185453 T>C did not map to a codon.
Sequencing variant TCGA-LN-A5U7-01A-11D-A31U-09 chr23:127185460 C>G did not map to a codon.
Sequencing variant TCGA-R6-A6XQ-01B-11D-A33E-09 chr2:158637046 C>A maps to NM_001111067.2 E45*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA4D-01A-11D-A37C-09 chr2:158617467 G>A maps to NM_001111067.2 F396F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X8-AAAR-01A-11D-A403-09 chr2:158634690 G>T maps to NM_001111067.2 G165G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88S-01A-11D-A36J-09 chr2:158397599 A>G did not map to a codon.
Sequencing variant TCGA-LN-A4MR-01A-11D-A28B-09 chr2:158390537 C>T maps to NM_145259.2 G458G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FE-01A-11D-A33E-09 chr2:148657053 C>T maps to NM_001616.3 S97S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8WC-01A-11D-A37C-09 chr11:67410227 G>T maps to NM_080658.1 P309P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OR-01A-11D-A27G-09 chr20:43251251 C>T maps to NM_000022.2 P274P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RF-01A-13D-A33E-09 chr4:123333899 T>C maps to NM_139243.3 L395L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr4:123333869 A>G maps to NM_139243.3 S385S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASX-01A-11D-A387-09 chr16:84230516 C>T maps to NM_139174.3 L645L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FD-01A-11D-A33E-09 chr15:58925537 C>A maps to NM_001110.2 E345*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88V-01A-11D-A351-09 chr10:127734652 C>A maps to NM_003474.4 E659*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NQ-01A-11D-A36J-09 chr10:127726812 C>T maps to NM_003474.4 P785P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr1:155032744 T>C maps to NM_207197.1 L711L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FE-01A-11D-A33E-09 chr8:39506019 G>T maps to NM_014237.2 E402*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EP-01A-31D-A403-09 chr8:39463836 C>T maps to NM_014237.2 I48I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EU-01A-11D-A36J-09 chr8:39534971 C>T maps to NM_014237.2 A516A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OU-01A-11D-A28B-09 chr8:39645737 C>T maps to NM_001464.3 L225L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q9-A6FW-01A-31D-A31U-09 chr14:70925691 C>T maps to NM_003813.2 D492D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-A7RE-01A-11D-A351-09 chr7:87795158 G>T maps to NM_021723.3 E697*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HY-01A-12D-A351-09 chr2:207406858 G>T did not map to a codon.
Sequencing variant TCGA-VR-A8EX-01A-11D-A36J-09 chr2:207452096 C>T maps to NM_003812.2 Q596*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A5S3-01A-11D-A28B-09 chr8:24193158 G>A maps to NM_021777.3 R524R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88Z-01A-11D-A36J-09 chr4:175899048 G>A maps to NM_014269.4 T791T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L7-A6VZ-01A-12D-A33E-09 chr4:175897650 T>G maps to NM_014269.4 T325T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A8HZ-01A-11D-A36J-09 chr1:120438559 G>T maps to NM_021794.2 R134R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8ER-01A-11D-A36J-09 chr1:120438760 G>A maps to NM_021794.2 Q67*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A9VB-01A-21D-A37C-09 chr8:39079205 C>T maps to NM_145004.5 C437C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GH-01A-11D-A37C-09 chr8:24348309 A>G did not map to a codon.
Sequencing variant TCGA-L5-A4OE-01A-11D-A27G-09 chr8:24356794 C>A maps to ENST00000380789 S630*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr8:24359014 G>T maps to ENST00000380789 E712*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NR-01A-11D-A37C-09 chr8:24326333 G>T did not map to a codon.
Sequencing variant TCGA-2H-A9GH-01A-11D-A37C-09 chr21:28210406 A>G maps to NM_006988.3 L799L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZR-A9CJ-01B-11D-A387-09 chr21:28212007 C>T maps to NM_006988.3 A642A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43C-01A-11D-A247-09 chr19:8651465 C>A maps to NM_030957.2 P793P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NK-01A-21D-A37C-09 chr5:33637835 C>T maps to NM_030955.2 G578G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASW-01A-11D-A403-09 chr5:33637694 G>T maps to NM_030955.2 P625P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EY-01A-11D-A36J-09 chr5:33561130 C>T did not map to a codon.
Sequencing variant TCGA-VR-A8EP-01A-31D-A403-09 chr9:136321338 T>C did not map to a codon.
Sequencing variant TCGA-VR-A8EZ-01A-11D-A36J-09 chr9:136307650 G>T maps to NM_139025.3 G700G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RE-01A-11D-A33E-09 chr10:72517716 G>C did not map to a codon.
Sequencing variant TCGA-IG-A5S3-01A-11D-A28B-09 chr10:72498629 G>A maps to NM_139155.2 S547S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3Y9-01A-12D-A247-09 chr11:130318900 C>T maps to NM_139055.2 F11F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GO-01A-11D-A37C-09 chr5:5242180 A>C maps to NM_139056.2 R847R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A4QS-01A-11D-A27G-09 chr5:5239959 T>C maps to NM_139056.2 T815T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr5:5140805 G>A maps to NM_139056.2 A34A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RE-01A-11D-A33E-09 chr16:77353778 C>T maps to NM_199355.2 A833A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L7-A56G-01A-21D-A27G-09 chr16:77323160 C>A maps to NM_199355.2 E1184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A8I0-01A-11D-A36J-09 chr16:77327043 G>A maps to NM_199355.2 Q1040*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4ON-01A-11D-A27G-09 chr5:129015551 A>T maps to NM_133638.3 R862*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8WG-01A-11D-A37C-09 chr5:129015551 A>C maps to NM_133638.3 R862R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GJ-01A-11D-A37C-09 chr5:178634591 C>T maps to NM_014244.4 L271L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3YB-01A-11D-A247-09 chr5:178541071 G>C maps to NM_014244.4 L1144L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NH-01A-11D-A37C-09 chr5:178585826 G>A maps to NM_014244.4 C343C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NQ-01A-11D-A36J-09 chr5:178566958 C>T maps to NM_014244.4 P569P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NR-01A-11D-A37C-09 chr5:178540975 T>C maps to NM_014244.4 P1176P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASX-01A-11D-A387-09 chr5:178540956 G>A maps to NM_014244.4 R1183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RF-01A-13D-A33E-09 chr12:43925974 G>A maps to ENST00000389420 N159N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43I-01A-11D-A247-09 chr12:43819397 T>A maps to ENST00000389420 V1401V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6XQ-01B-11D-A33E-09 chr12:43777765 A>T maps to ENST00000389420 C1489*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NS-01A-12D-A37C-09 chr15:79056070 G>A maps to ENST00000258883 C1573C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GH-01A-11D-A37C-09 chr3:64589619 C>T maps to NM_182920.1 W1242*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OH-01A-11D-A27G-09 chr3:64532484 G>T maps to NM_182920.1 Y1671*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr3:64672615 G>A maps to NM_182920.1 Y48Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OR-01A-11D-A27G-09 chr3:64644327 C>T maps to NM_182920.1 T273T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GO-01A-11D-A37C-09 chr9:18777698 C>T maps to NM_001040272.4 R1158*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3I8-01A-11D-A247-09 chr9:18775841 G>A maps to NM_001040272.4 P833P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A4-01A-11D-A27G-09 chr9:18795490 C>T maps to NM_001040272.4 Y1258Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6XG-01B-11D-A33E-09 chr9:18770776 G>T maps to NM_001040272.4 E799*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OJ-01A-11D-A27G-09 chr9:136405771 G>T maps to ENST00000393061 V264V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NV-01A-11D-A37C-09 chr15:84611716 G>A maps to NM_207517.2 T791T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FB-01A-11D-A33E-09 chr7:938840 G>A maps to NM_006869.2 L309L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6XG-01B-11D-A33E-09 chr17:29271983 G>A maps to ENST00000394782 E196E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6XG-01B-11D-A33E-09 chr1:154558300 G>A maps to ENST00000292205 C1124C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6XG-01B-11D-A33E-09 chr10:1405542 G>A maps to NM_018702.2 R253*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr1:33562405 C>T maps to ENST00000373441 A284A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NI-01A-11D-A37C-09 chr1:33560274 C>G maps to ENST00000373441 G238G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GQ-01A-11D-A37C-09 chr14:78399574 G>A maps to NM_020421.3 K471K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FD-01A-11D-A33E-09 chr14:78399709 C>T maps to NM_020421.3 C516C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6Y2-01B-11D-A33E-09 chr14:78325583 G>T maps to NM_020421.3 E129*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49M-01A-21D-A27G-09 chr7:140378975 C>T maps to NM_052853.3 Q368*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XP-A8T8-01A-11D-A36J-09 chr7:140380865 C>T maps to NM_052853.3 Q412*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASV-01A-11D-A387-09 chr19:41209521 G>A maps to NM_024876.3 P241P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6F8-01A-11D-A33E-09 chr8:145616375 G>T maps to NM_174922.3 E196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S8-A6BW-01A-11D-A31U-09 chr8:145616196 G>T maps to NM_174922.3 E162*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASW-01A-11D-A403-09 chr7:45747986 G>A maps to NM_021116.2 A952A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43C-01A-11D-A247-09 chr1:167844396 G>A maps to NM_018417.4 C478C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NV-01A-11D-A37C-09 chr1:167873230 T>C did not map to a codon.
Sequencing variant TCGA-JY-A93E-01A-11D-A37C-09 chr5:7802383 G>A maps to NM_020546.2 P894P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OS-01A-11D-A28B-09 chr5:7520984 G>A maps to NM_020546.2 P181P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XP-A8T6-01A-11D-A36J-09 chr5:7817052 C>T maps to NM_020546.2 A986A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8W8-01B-11D-A37C-09 chr2:25061487 G>A maps to NM_004036.3 R453R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr12:49168285 G>A maps to NM_015270.3 L728L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3Y9-01A-12D-A247-09 chr16:50345981 G>A maps to NM_001114.3 K828K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A8-01A-32D-A27G-09 chr16:50334757 C>T maps to NM_001114.3 N403N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FH-01A-11D-A33E-09 chr8:131922078 G>A maps to NM_001115.2 D505D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43I-01A-11D-A247-09 chr8:132051964 C>T maps to NM_001115.2 S205S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NT-01A-11D-A37C-09 chr8:132051793 G>A maps to NM_001115.2 L262L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XP-A8T6-01A-11D-A36J-09 chr8:132052131 G>T maps to NM_001115.2 R150R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr16:4039069 C>T maps to NM_001116.3 P745P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASW-01A-11D-A403-09 chr18:908308 C>T maps to NM_001117.3 L96L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4MR-01A-11D-A28B-09 chr2:70890766 C>T maps to NM_001185054.1 T657T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EY-01A-11D-A36J-09 chr2:70910896 C>T maps to NM_001185054.1 V317V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NH-01A-11D-A37C-09 chr4:100205627 C>T maps to NM_000667.3 S165S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NL-01A-12D-A37C-09 chr4:100130051 G>A maps to NM_001102470.1 L201L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr4:100131400 T>C maps to NM_001102470.1 G135G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GI-01A-11D-A37C-09 chr4:100349748 C>T maps to NM_000673.4 V65V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A4P3-01A-11D-A27G-09 chr4:100334316 G>T maps to NM_000673.4 V383V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr4:100334324 G>T maps to NM_000673.4 R381R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A5B8-01A-11D-A28B-09 chr8:67355080 T>C did not map to a codon.
Sequencing variant TCGA-R6-A6XG-01B-11D-A33E-09 chr8:67356899 G>T maps to NM_144650.2 V90V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A8I0-01A-11D-A36J-09 chr18:77896382 T>C maps to NM_014913.3 P1029P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A5U7-01A-11D-A31U-09 chr10:64565448 G>A maps to NM_032804.5 P210P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA4D-01A-11D-A37C-09 chr1:203134553 C>T maps to NM_001048230.1 C169C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GJ-01A-11D-A37C-09 chr22:24836613 G>A maps to NM_000675.4 S132S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A4P3-01A-11D-A27G-09 chr13:114098800 G>T maps to NM_138430.3 G106G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3YA-01A-11D-A247-09 chr8:26721736 G>A maps to ENST00000356368 S250S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A939-01A-12D-A37C-09 chr8:26721787 C>T maps to ENST00000356368 T233T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GH-01A-11D-A37C-09 chr10:112838071 G>A maps to NM_000681.3 L106L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88W-01A-11D-A351-09 chr4:3769692 C>T maps to NM_000683.3 R454*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GM-01A-11D-A37C-09 chr22:26063735 C>A maps to NM_005160.3 R158R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NG-01A-11D-A37C-09 chr20:60882436 G>A maps to NM_175573.1 G184G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q9-A6FW-01A-31D-A31U-09 chr20:60882433 G>A maps to NM_175573.1 L183L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43I-01A-11D-A247-09 chr7:44153727 T>C maps to NM_001129.3 P1115P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XP-A8T6-01A-11D-A36J-09 chr7:44152675 C>T maps to NM_001129.3 L886L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr4:7870446 C>A did not map to a codon.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr4:7776484 C>T maps to NM_001134647.1 A681A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L7-A56G-01A-21D-A27G-09 chr4:7845039 C>T maps to NM_001134647.1 S124S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EW-01A-11D-A36J-09 chr10:116073778 G>A maps to NM_001001936.1 Q215*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GF-01A-11D-A37C-09 chr23:148037968 G>T did not map to a codon.
Sequencing variant TCGA-JY-A93C-01A-11D-A387-09 chr23:147891442 G>A did not map to a codon.
Sequencing variant TCGA-L5-A88S-01A-11D-A36J-09 chr23:148044440 G>T did not map to a codon.
Sequencing variant TCGA-L5-A8NG-01A-11D-A37C-09 chr23:148039912 A>T did not map to a codon.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr23:148069011 G>A did not map to a codon.
Sequencing variant TCGA-LN-A4A4-01A-11D-A27G-09 chr23:148035141 C>T did not map to a codon.
Sequencing variant TCGA-V5-AASW-01A-11D-A403-09 chr23:148048400 A>G did not map to a codon.
Sequencing variant TCGA-VR-A8EU-01A-11D-A36J-09 chr23:148038117 C>T did not map to a codon.
Sequencing variant TCGA-ZR-A9CJ-01B-11D-A387-09 chr23:148039900 A>C did not map to a codon.
Sequencing variant TCGA-2H-A9GJ-01A-11D-A37C-09 chr2:100210283 C>T maps to NM_001025108.1 A638A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43I-01A-11D-A247-09 chr2:100623363 G>A maps to NM_001025108.1 A226A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6Y2-01B-11D-A33E-09 chr2:100217960 G>T maps to NM_001025108.1 S461*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASW-01A-11D-A403-09 chr2:100623712 A>G maps to NM_001025108.1 T153T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EZ-01A-11D-A36J-09 chr2:100623661 A>G maps to NM_001025108.1 T170T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GF-01A-11D-A37C-09 chr18:12356719 C>T maps to NM_006796.2 E379E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FD-01A-11D-A33E-09 chr18:12353076 C>T maps to NM_006796.2 K415K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr18:12329671 G>A maps to NM_006796.2 G762G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RE-01A-11D-A33E-09 chr2:64796809 A>G maps to ENST00000422803 G756G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr4:178355570 A>G maps to NM_000027.3 T257T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6F8-01A-11D-A33E-09 chr2:236706514 C>T maps to NM_001037131.1 A262A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6L4-01A-11D-A31U-09 chr2:236706457 C>T maps to NM_001037131.1 C243C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RF-01A-13D-A33E-09 chr10:75435610 C>T maps to NM_001144000.1 P269P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GG-01A-11D-A37C-09 chr15:86822974 C>T maps to NM_152336.2 Y681Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NS-01A-12D-A37C-09 chr15:87099467 G>T maps to NM_152336.2 L957L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6Y2-01B-11D-A33E-09 chr15:86807973 G>T maps to NM_152336.2 V478V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EQ-01A-11D-A36J-09 chr15:86838514 C>A maps to NM_152336.2 V704V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A8JD-01A-11D-A36J-09 chr15:86822893 T>C maps to NM_152336.2 A654A. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-L5-A4OI-01A-11D-A27G-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-LN-A49X-01A-31D-A27G-09 chr1:49511429 C>T maps to NM_032785.3 P140P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49W-01A-11D-A27G-09 chr2:27280242 G>A maps to NM_021831.5 G536G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8Q7-01A-11D-A37C-09 chr2:27275948 C>A maps to NM_021831.5 A41A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A9-01A-11D-A28B-09 chr7:141301070 T>A maps to NM_018238.3 T96T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A51D-01A-11D-A27G-09 chr1:100316651 G>A maps to ENST00000311030 L19L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EQ-01A-11D-A36J-09 chr1:100382218 G>A maps to ENST00000311030 P1472P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr6:32138783 C>A maps to NM_032741.4 G88G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6DN-01B-11D-A31U-09 chr21:45401009 C>T maps to NM_001037553.1 G328G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XP-A8T8-01A-11D-A36J-09 chr8:41469725 C>A maps to NM_178819.3 I243I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NU-01A-11D-A36J-09 chr4:84508431 C>A maps to NM_032717.3 I168I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FP-01A-31D-A387-09 chr15:78805448 C>T maps to NM_001013619.2 Q7*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GR-01A-12D-A37C-09 chr2:178378594 C>T maps to NM_003659.3 C552C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NJ-01A-11D-A36J-09 chr1:957613 C>T maps to NM_198576.2 L79L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HX-01A-11D-A33E-09 chr1:987190 G>T maps to NM_198576.2 E1883*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A4P3-01A-11D-A27G-09 chr9:88292465 G>T maps to ENST00000395847 T107T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FD-01A-11D-A33E-09 chr9:88257807 C>A maps to ENST00000395847 P412P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A893-01A-11D-A36J-09 chr9:88247680 C>T maps to ENST00000395847 T637T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49V-01A-11D-A247-09 chr9:88292465 G>T maps to ENST00000395847 T107T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NJ-01A-11D-A36J-09 chr3:148459670 C>T maps to NM_032049.2 A283A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A4QS-01A-11D-A27G-09 chr23:115303886 A>C did not map to a codon.
Sequencing variant TCGA-VR-A8Q7-01A-11D-A37C-09 chr23:115304320 T>C did not map to a codon.
Sequencing variant TCGA-IC-A6RE-01A-11D-A33E-09 chr2:241813452 G>C maps to NM_000030.2 S218S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88Z-01A-11D-A36J-09 chr5:35013130 C>T maps to NM_031900.3 A372A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XP-A8T6-01A-11D-A36J-09 chr4:109667931 C>T maps to NM_031279.3 Q386Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-A7RE-01A-11D-A351-09 chr1:247013636 G>A maps to ENST00000428671 L1929L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-AAPN-01A-11D-A403-09 chr1:247076621 T>C maps to ENST00000428671 A194A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8W8-01B-11D-A37C-09 chr20:32873244 C>G did not map to a codon.
Sequencing variant TCGA-L5-A8NT-01A-11D-A37C-09 chr7:129040213 C>T maps to NM_015328.3 Q303*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A4QS-01A-11D-A27G-09 chr1:27878146 G>A maps to NM_001029882.2 P160P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93C-01A-11D-A387-09 chr1:27877291 C>T maps to NM_001029882.2 P445P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93D-01A-11D-A387-09 chr1:27874813 C>T maps to NM_001029882.2 P1271P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OX-01A-21D-A28B-09 chr1:27876273 C>A maps to NM_001029882.2 G785*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A4-01A-11D-A27G-09 chr1:27875977 C>T maps to NM_001029882.2 R883R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EQ-01A-11D-A36J-09 chr1:27874531 G>A maps to NM_001029882.2 C1365C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NF-01A-11D-A37C-09 chr6:135784407 T>C maps to NM_017651.4 E262E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GF-01A-11D-A37C-09 chr11:62284500 C>T maps to NM_001620.1 T5796T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3QL-01A-11D-A247-09 chr11:62292798 G>A maps to NM_001620.1 F3030F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A97H-01A-11D-A387-09 chr11:62284237 G>T maps to NM_001620.1 S5884*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OU-01A-11D-A28B-09 chr11:62299593 C>T maps to NM_001620.1 E765E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NG-01A-11D-A37C-09 chr11:62293281 A>T maps to NM_001620.1 V2869V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49M-01A-21D-A27G-09 chr11:62289858 C>G maps to NM_001620.1 L4010L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49M-01A-21D-A27G-09 chr11:62299162 G>T maps to NM_001620.1 S909*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6L4-01A-11D-A31U-09 chr11:62295471 C>T maps to NM_001620.1 L2139L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8W5-01B-11D-A37C-09 chr11:62285777 G>A maps to NM_001620.1 Q5371*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GL-01A-12D-A37C-09 chr14:105408716 G>T maps to NM_138420.2 V4357V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr14:105412924 G>A maps to NM_138420.2 L2955L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr14:105412928 T>G maps to NM_138420.2 A2953A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OE-01A-11D-A27G-09 chr14:105418202 G>A maps to NM_138420.2 A1195A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A2-01A-31D-A27G-09 chr14:105404774 T>C maps to NM_138420.2 R5671R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A8I1-01A-11D-A36J-09 chr14:105406676 C>A maps to NM_138420.2 G5037G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FP-01A-31D-A387-09 chr14:105418586 C>A maps to NM_138420.2 P1067P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XP-A8T6-01A-11D-A36J-09 chr14:105418556 A>G maps to NM_138420.2 L1077L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49L-01A-11D-A247-09 chr5:432960 A>G maps to NM_020731.3 E359E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A5U6-01A-11D-A28B-09 chr5:344028 G>T maps to NM_020731.3 P8P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FB-01A-11D-A33E-09 chr3:186333472 G>T did not map to a codon.
Sequencing variant TCGA-V5-A7RE-01A-11D-A351-09 chr3:186333526 C>T maps to ENST00000273784 C89C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43E-01A-11D-A247-09 chr23:129270035 C>T did not map to a codon.
Sequencing variant TCGA-LN-A7HV-01A-21D-A351-09 chr6:106967344 C>G maps to NM_001624.2 T346T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EZ-01A-11D-A36J-09 chr6:106967401 G>A maps to NM_001624.2 E365E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA7D-01A-11D-A403-09 chr6:106960341 C>T maps to NM_001624.2 D42D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NW-01A-11D-A37C-09 chr1:159036017 C>T maps to NM_004833.1 T166T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8Q7-01A-11D-A37C-09 chr1:159032496 G>T maps to NM_004833.1 A339A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FB-01A-11D-A33E-09 chr21:45706438 G>T did not map to a codon.
Sequencing variant TCGA-L5-A891-01A-11D-A36J-09 chr1:4832540 G>A maps to NM_018836.3 L373L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NI-01A-11D-A37C-09 chr1:4832492 T>C maps to NM_018836.3 S357S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASX-01A-11D-A387-09 chr1:4772619 G>A maps to NM_018836.3 T230T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L7-A56G-01A-21D-A27G-09 chr1:77748055 G>T maps to NM_174858.1 E20*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GM-01A-11D-A37C-09 chr13:42887234 G>T maps to NM_016248.2 E1776*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HX-01A-11D-A33E-09 chr6:151672916 G>T maps to NM_005100.3 E1131*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-A7RE-01A-11D-A351-09 chr6:151626943 C>T maps to NM_005100.3 S75S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49U-01A-31D-A27G-09 chr15:86262364 C>T maps to NM_006738.4 Y2024Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GK-01A-11D-A37C-09 chr12:4736753 G>A maps to NM_006422.2 P438P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NL-01A-12D-A37C-09 chr12:4736243 C>T maps to NM_006422.2 K608K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S8-A6BW-01A-11D-A31U-09 chr12:4737280 G>T maps to NM_006422.2 R263R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A893-01A-11D-A36J-09 chr23:49957182 T>G did not map to a codon.
Sequencing variant TCGA-L5-A8NR-01A-11D-A37C-09 chr23:49957518 C>T did not map to a codon.
Sequencing variant TCGA-LN-A49Y-01A-11D-A27G-09 chr23:49958205 G>C did not map to a codon.
Sequencing variant TCGA-S8-A6BV-01A-21D-A31U-09 chr23:49958694 T>C did not map to a codon.
Sequencing variant TCGA-S8-A6BW-01A-11D-A31U-09 chr23:49958406 C>T did not map to a codon.
Sequencing variant TCGA-VR-A8EZ-01A-11D-A36J-09 chr23:49961617 C>T did not map to a codon.
Sequencing variant TCGA-2H-A9GG-01A-11D-A37C-09 chr14:33291545 C>A maps to NM_004274.4 C1509*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FH-01A-11D-A33E-09 chr14:33293330 G>A maps to NM_004274.4 L2104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A893-01A-11D-A36J-09 chr14:33291430 C>A maps to NM_004274.4 S1471*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr14:33293132 T>C maps to NM_004274.4 C2038C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S8-A6BV-01A-21D-A31U-09 chr19:15512281 G>T maps to NM_014371.2 R165R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr7:91695842 G>T maps to NM_005751.4 E2105*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-AAPN-01A-11D-A403-09 chr7:91630581 G>T maps to NM_005751.4 E451*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASX-01A-11D-A387-09 chr6:109867150 G>A maps to NM_001145128.2 N1048N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49S-01A-11D-A247-09 chr9:117139228 T>C maps to NM_030767.4 R286R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4MR-01A-11D-A28B-09 chr1:46035626 G>A maps to NM_153326.1 *326*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FH-01A-11D-A33E-09 chr1:19633578 G>T maps to NM_003689.2 G235G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A51D-01A-11D-A27G-09 chr14:105236686 G>T maps to NM_001014432.1 G478G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A5U7-01A-11D-A31U-09 chr14:105241541 G>T maps to NM_001014432.1 T146T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASX-01A-11D-A387-09 chr14:105246425 C>T maps to NM_001014432.1 A58A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GF-01A-11D-A37C-09 chr19:40761156 G>A maps to NM_001626.3 T65T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NT-01A-11D-A37C-09 chr1:243801020 C>T maps to NM_005465.3 L151L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GH-01A-11D-A37C-09 chr23:55041309 C>T did not map to a codon.
Sequencing variant TCGA-L5-A8NR-01A-11D-A37C-09 chr23:55041348 A>G did not map to a codon.
Sequencing variant TCGA-2H-A9GK-01A-11D-A37C-09 chr3:105086284 G>A maps to NM_001627.2 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A4QS-01A-11D-A27G-09 chr10:97380871 G>T maps to NM_002860.3 A461A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASX-01A-11D-A387-09 chr10:97386500 G>A maps to NM_002860.3 R371*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA7D-01A-11D-A403-09 chr10:97366617 C>T maps to NM_002860.3 L763L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NJ-01A-11D-A36J-09 chr9:75567890 A>C maps to NM_000689.3 L9*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93F-01A-21D-A37C-09 chr9:38396959 C>T maps to NM_000692.3 G405G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EW-01A-11D-A36J-09 chr9:38396392 C>G maps to NM_000692.3 L216L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr3:125831671 G>A maps to ENST00000273450 R722*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NS-01A-12D-A37C-09 chr12:105440748 T>G did not map to a codon.
Sequencing variant TCGA-LN-A5U7-01A-11D-A31U-09 chr17:19646638 G>A maps to NM_000691.4 I100I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FR-01A-11D-A387-09 chr11:67786318 G>A maps to NM_001161473.1 P116P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X8-AAAR-01A-11D-A403-09 chr11:67789290 C>T maps to NM_001161473.1 C299C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A8I1-01A-11D-A36J-09 chr1:19199389 G>T maps to NM_003748.3 I547I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6F8-01A-11D-A33E-09 chr5:125885970 G>T maps to NM_001182.3 V444V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr9:104189796 G>A maps to NM_000035.3 N169N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8WC-01A-11D-A37C-09 chr17:26901109 A>G maps to NM_005165.2 R258R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr16:5128868 G>A maps to NM_019109.4 T284T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A5U5-01A-21D-A28B-09 chr16:5121960 G>A maps to NM_019109.4 A37A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FO-01A-11D-A387-09 chr16:5125387 G>A did not map to a codon.
Sequencing variant TCGA-L5-A8NE-01A-11D-A37C-09 chr12:38714843 C>T maps to NM_001013620.3 Y417Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NV-01A-11D-A37C-09 chr22:50301592 C>T did not map to a codon.
Sequencing variant TCGA-2H-A9GK-01A-11D-A37C-09 chr23:110951377 G>A did not map to a codon.
Sequencing variant TCGA-IC-A6RF-01A-13D-A33E-09 chr23:110928198 G>T did not map to a codon.
Sequencing variant TCGA-JY-A93D-01A-11D-A387-09 chr23:110952266 T>A did not map to a codon.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr23:110987995 A>T did not map to a codon.
Sequencing variant TCGA-V5-AASV-01A-11D-A387-09 chr23:110988001 T>A did not map to a codon.
Sequencing variant TCGA-LN-A9FQ-01A-31D-A387-09 chr3:125648299 G>C maps to NM_001195223.1 L173L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A6-01A-11D-A27G-09 chr13:37563686 A>T maps to NM_013338.4 Y127*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NW-01A-11D-A37C-09 chr1:63867954 G>A maps to ENST00000263440 Q66Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XP-A8T8-01A-11D-A36J-09 chr11:111708221 G>T maps to ENST00000428306 R706R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GI-01A-11D-A37C-09 chr2:29420534 C>A maps to NM_004304.3 G1316*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6XG-01B-11D-A33E-09 chr14:78140429 C>A maps to NM_006020.2 E299*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NK-01A-21D-A37C-09 chr11:43904226 C>T maps to NM_139178.3 R9*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GH-01A-11D-A37C-09 chr2:73646441 G>T maps to NM_015120.4 L214L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A6QS-01A-12D-A33E-09 chr2:73800517 G>T maps to NM_015120.4 V3837V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FG-01A-11D-A33E-09 chr2:73677769 C>A maps to NM_015120.4 G1371G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr2:73676527 C>T maps to NM_015120.4 S957S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NF-01A-11D-A37C-09 chr2:73676803 C>T maps to NM_015120.4 Y1049Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GF-01A-11D-A37C-09 chr17:6899504 G>A maps to NM_000697.2 Q23Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A97I-01A-11D-A387-09 chr17:6904969 C>G maps to NM_000697.2 S334*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FP-01A-31D-A387-09 chr17:6901871 C>A maps to NM_000697.2 R128R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A891-01A-11D-A36J-09 chr17:7976504 C>T maps to NM_001139.2 L629L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49V-01A-11D-A247-09 chr10:45907710 C>A maps to NM_000698.2 I168I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NN-01A-11D-A37C-09 chr13:31338240 T>A maps to NM_001629.2 *162K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93D-01A-11D-A387-09 chr2:233323429 G>T maps to NM_001631.3 V424V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6Y2-01B-11D-A33E-09 chr2:233322333 C>T maps to NM_001631.3 Y236Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8ER-01A-11D-A36J-09 chr2:233322348 C>T maps to NM_001631.3 S241S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NH-01A-11D-A37C-09 chr4:113345107 T>C maps to NM_025144.3 L162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FH-01A-11D-A33E-09 chr18:56184190 C>A maps to NM_052947.3 G1963G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93F-01A-21D-A37C-09 chr18:56202660 C>T maps to NM_052947.3 Q1586Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88S-01A-11D-A36J-09 chr18:56202528 A>G maps to NM_052947.3 P1630P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OO-01A-11D-A27G-09 chr15:85406097 C>T maps to NM_020778.4 P1656P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88S-01A-11D-A36J-09 chr15:85400869 G>T maps to NM_020778.4 L1169L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr1:21894730 G>A maps to NM_000478.4 P261P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr2:233245387 C>T maps to NM_001632.3 D307D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NG-01A-11D-A37C-09 chr2:233243908 G>A did not map to a codon.
Sequencing variant TCGA-LN-A49X-01A-31D-A27G-09 chr2:233245014 G>A maps to NM_001632.3 W259*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASX-01A-11D-A387-09 chr3:46721931 C>T maps to NM_147129.3 A512A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GI-01A-11D-A37C-09 chr2:202352530 G>T maps to NM_001168221.1 S1756*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8W8-01B-11D-A37C-09 chr2:202436682 C>A maps to NM_001168221.1 E272*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr11:44331252 C>T maps to NM_021926.3 P120P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-A7RC-01B-11D-A403-09 chr17:33520816 G>A maps to NM_152462.2 I170I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93D-01A-11D-A387-09 chr17:7386175 G>C maps to NM_001102614.1 V291V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASX-01A-11D-A387-09 chr5:33989464 C>A maps to NM_001167595.1 V294V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA7D-01A-11D-A403-09 chr4:71467238 C>A maps to NM_016519.4 T133T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88T-01A-11D-A351-09 chr9:116840417 C>T maps to NM_001633.3 T24T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EZ-01A-11D-A36J-09 chr9:116823764 G>A maps to NM_001633.3 C264C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A5B8-01A-11D-A28B-09 chr11:46563841 C>T maps to ENST00000458649 L575L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OE-01A-11D-A27G-09 chr11:46563772 G>C maps to ENST00000458649 S598S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NL-01A-12D-A37C-09 chr11:46515708 C>A maps to ENST00000458649 R795R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49K-01A-11D-A247-09 chr11:46563799 A>G maps to ENST00000458649 P589P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A938-01A-11D-A37C-09 chr6:111208745 C>G maps to NM_001634.4 S50*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RE-01A-11D-A33E-09 chr23:11316829 G>A did not map to a codon.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr23:11316885 G>A did not map to a codon.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr16:56396934 C>T maps to NM_001144.4 A606A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FP-01A-31D-A387-09 chr16:56396853 C>G maps to NM_001144.4 A633A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8ER-01A-11D-A36J-09 chr19:2250423 C>T maps to NM_000479.3 Y167Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NH-01A-11D-A37C-09 chr11:118083140 G>T maps to NM_001098526.1 S60*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8ER-01A-11D-A36J-09 chr3:49755551 G>A maps to NM_198722.2 S449S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RF-01A-13D-A33E-09 chr23:112048234 G>T did not map to a codon.
Sequencing variant TCGA-IG-A3Y9-01A-12D-A247-09 chr23:112058656 G>A did not map to a codon.
Sequencing variant TCGA-IG-A3YA-01A-11D-A247-09 chr23:112058875 G>A did not map to a codon.
Sequencing variant TCGA-JY-A6FD-01A-11D-A33E-09 chr23:112058940 G>T did not map to a codon.
Sequencing variant TCGA-L5-A8NL-01A-12D-A37C-09 chr23:112058795 C>T did not map to a codon.
Sequencing variant TCGA-LN-A49M-01A-21D-A27G-09 chr23:112024178 G>A did not map to a codon.
Sequencing variant TCGA-LN-A4A8-01A-32D-A27G-09 chr23:112065832 C>G did not map to a codon.
Sequencing variant TCGA-LN-A9FP-01A-31D-A387-09 chr23:112059027 C>A did not map to a codon.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr11:94602624 C>T maps to NM_130847.2 T917T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NQ-01A-11D-A36J-09 chr3:134089687 C>T maps to ENST00000514516 L254L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASX-01A-11D-A387-09 chr3:134090251 C>T maps to ENST00000514516 S66S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A8JE-01A-11D-A37C-09 chr1:115219976 C>T maps to NM_000036.2 R494R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6XQ-01B-11D-A33E-09 chr7:38431351 G>T maps to NM_001635.3 Y625*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88W-01A-11D-A351-09 chr1:104297201 T>C maps to NM_001008218.1 H320H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr1:104297162 G>A maps to NM_001008218.1 A307A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA7I-01A-11D-A403-09 chr1:104234014 C>T maps to NM_001008219.1 R334R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HY-01A-12D-A351-09 chr1:104114304 T>C maps to ENST00000305865 S27S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FD-01A-11D-A33E-09 chr2:112529997 G>C maps to NM_022662.2 S1880*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OJ-01A-11D-A27G-09 chr2:112605343 G>T maps to NM_022662.2 Y583*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASX-01A-11D-A387-09 chr9:140075322 G>A maps to NM_013366.3 Y509Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EU-01A-11D-A36J-09 chr12:121790047 C>T maps to NM_016237.4 P32P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OX-01A-21D-A28B-09 chr12:110824210 C>T maps to NM_016238.2 L280L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GH-01A-11D-A37C-09 chr8:108509536 G>A maps to NM_001146.3 Q84*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EP-01A-31D-A403-09 chr8:108296964 G>A maps to NM_001146.3 R384*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GQ-01A-11D-A37C-09 chr20:853725 G>A maps to NM_015985.2 N463N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43C-01A-11D-A247-09 chr20:865892 C>T maps to NM_015985.2 A221A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA7B-01A-31D-A403-09 chr20:858913 G>A maps to NM_015985.2 L370L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A8JE-01A-11D-A37C-09 chr8:41566346 C>T maps to ENST00000415018 E649E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GF-01A-11D-A37C-09 chr4:114158192 G>A maps to NM_001148.4 A178A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GK-01A-11D-A37C-09 chr4:114274918 A>G maps to NM_001148.4 K1715K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FA-01A-11D-A33E-09 chr4:114253157 A>C maps to NM_001148.4 P1052P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43I-01A-11D-A247-09 chr4:114275425 G>T maps to NM_001148.4 S1884S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OE-01A-11D-A27G-09 chr4:114276415 G>A maps to NM_001148.4 P2214P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88V-01A-11D-A351-09 chr4:114278180 G>T maps to NM_001148.4 E2803*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NH-01A-11D-A37C-09 chr4:114275200 G>A maps to NM_001148.4 A1809A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NS-01A-12D-A37C-09 chr4:114209581 A>G maps to NM_001148.4 G739G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49L-01A-11D-A247-09 chr4:114279790 G>A maps to NM_001148.4 A3339A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASW-01A-11D-A403-09 chr4:114203967 G>A maps to NM_001148.4 G673G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EU-01A-11D-A36J-09 chr4:114209642 G>T did not map to a codon.
Sequencing variant TCGA-2H-A9GR-01A-12D-A37C-09 chr10:61829129 C>A maps to NM_020987.2 G3837*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88S-01A-11D-A36J-09 chr10:61834167 G>T maps to NM_020987.2 P2157P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6Y2-01B-11D-A33E-09 chr10:61833326 A>G maps to NM_020987.2 L2438L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA7D-01A-11D-A403-09 chr10:61830486 C>T maps to NM_020987.2 Q3384Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A6QS-01A-12D-A33E-09 chr2:190561096 T>C did not map to a codon.
Sequencing variant TCGA-IG-A50L-01A-11D-A27G-09 chr17:4080499 G>T maps to NM_016376.3 S900*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr17:4071195 G>A maps to NM_016376.3 C1130C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EO-01A-11D-A36J-09 chr19:17396581 C>T maps to NM_152363.4 V543V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6F8-01A-11D-A33E-09 chr12:133306802 C>A maps to NM_015114.1 E649*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OH-01A-11D-A27G-09 chr12:133306305 G>T maps to NM_015114.1 L814L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr2:241494372 C>T maps to ENST00000401804 V82V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr2:241465732 G>A maps to ENST00000401804 H361H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43H-01A-11D-A247-09 chr7:16655487 G>A maps to NM_020319.2 R138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr7:16640463 C>T maps to NM_020319.2 K416K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NE-01A-11D-A37C-09 chr5:72849285 T>C maps to NM_023039.4 E277E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A938-01A-11D-A37C-09 chr18:9281048 C>A maps to NM_015208.3 I2038I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OJ-01A-11D-A27G-09 chr18:9258859 C>T maps to NM_015208.3 D1865D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OU-01A-11D-A28B-09 chr18:9279563 T>G maps to NM_015208.3 T1975T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A8-01A-32D-A27G-09 chr1:70819707 G>C maps to NM_030816.4 L128L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RE-A7BO-01A-11D-A33E-09 chr11:67067564 C>A maps to NM_207354.2 R348R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XP-A8T6-01A-11D-A36J-09 chr11:67068774 C>T maps to NM_207354.2 L418L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49V-01A-11D-A247-09 chr10:5920182 C>T maps to NM_001009941.2 K332K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A97I-01A-11D-A387-09 chr10:99338346 C>T maps to NM_020349.2 A174A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FP-01A-31D-A387-09 chr10:99338019 G>T maps to NM_020349.2 T98T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93E-01A-11D-A37C-09 chr19:4217406 C>T maps to ENST00000262970 A840A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr10:27368032 G>A maps to NM_014915.2 L266L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49N-01A-11D-A247-09 chr19:33134494 G>A maps to NM_032139.2 L190L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr18:21218905 A>G maps to NM_173505.2 G79G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3YB-01A-11D-A247-09 chr10:37507905 A>T did not map to a codon.
Sequencing variant TCGA-LN-A49U-01A-31D-A27G-09 chr10:37486224 A>C maps to ENST00000374660 P940P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GQ-01A-11D-A37C-09 chr18:14764087 T>C maps to NM_001145029.1 N408N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RE-01A-11D-A33E-09 chr18:14760617 G>T did not map to a codon.
Sequencing variant TCGA-IG-A51D-01A-11D-A27G-09 chr18:14763793 G>T maps to NM_001145029.1 V310V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A97I-01A-11D-A387-09 chr18:14850251 C>G maps to NM_001145029.1 V1026V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43E-01A-11D-A247-09 chr18:14851758 A>G maps to NM_001145029.1 A1153A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A2-01A-31D-A27G-09 chr18:14784463 T>A maps to NM_001145029.1 P534P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HV-01A-21D-A351-09 chr18:14852214 A>G maps to NM_001145029.1 Q1305Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6KZ-01A-11D-A31U-09 chr18:14851600 C>T maps to NM_001145029.1 L1101L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NU-01A-11D-A36J-09 chr5:94005955 G>T maps to NM_032290.3 E545*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RE-A7BO-01A-11D-A33E-09 chr5:93979037 T>G maps to NM_032290.3 T164T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RE-A7BO-01A-11D-A33E-09 chr5:94024233 G>A maps to NM_032290.3 L715L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A625-01A-11D-A31U-09 chr1:145563080 C>T maps to NM_144698.3 C923C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A8O2-01A-11D-A36J-09 chr2:97830161 C>G maps to NM_001164315.1 S496*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr2:97899537 C>T maps to NM_001164315.1 D1367D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NE-01A-11D-A37C-09 chr2:97866071 G>A maps to NM_001164315.1 V919V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GF-01A-11D-A37C-09 chr11:82935966 G>A maps to ENST00000260047 T483T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr11:82935966 G>A maps to ENST00000260047 T483T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OJ-01A-11D-A27G-09 chr2:197986193 G>A maps to NM_001195144.1 N256N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NW-01A-11D-A37C-09 chr4:125591790 G>A maps to NM_020337.2 R881*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A939-01A-12D-A37C-09 chr12:56649606 G>A maps to NM_173595.3 R141R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NK-01A-21D-A37C-09 chr5:55422897 G>A maps to NM_024669.2 S216S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A625-01A-11D-A31U-09 chr23:118893518 C>T did not map to a codon.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr23:118893450 C>T did not map to a codon.
Sequencing variant TCGA-L5-A43E-01A-11D-A247-09 chr6:90312803 G>A maps to ENST00000339746 A92A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XP-A8T7-01A-11D-A36J-09 chr6:35048805 G>T maps to NM_015245.2 L860L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NL-01A-12D-A37C-09 chr12:99640517 C>A maps to NM_152788.3 G627G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-A7RC-01B-11D-A403-09 chr12:99201654 T>C maps to NM_181670.2 G261G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OU-01A-11D-A28B-09 chr16:4751503 G>A maps to NM_133450.2 S350S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr9:101552503 G>A maps to ENST00000375018 G248G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6XG-01B-11D-A33E-09 chr9:101552790 G>T maps to ENST00000375018 R153R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A51D-01A-11D-A27G-09 chr12:5915250 G>T maps to ENST00000356134 Y316*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr12:5687597 G>T maps to ENST00000356134 R775R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-AAPN-01A-11D-A403-09 chr12:5672623 C>G maps to ENST00000356134 L947L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6Y0-01B-11D-A33E-09 chr11:26619954 G>C maps to NM_031418.2 L497L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr12:101488062 G>A maps to ENST00000392977 T577T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FO-01A-11D-A387-09 chr12:101505401 C>G maps to ENST00000392977 V788V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-A7RB-01A-11D-A351-09 chr12:101510522 T>C maps to ENST00000392977 S839S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RE-01A-11D-A33E-09 chr11:22301154 G>T maps to NM_213599.2 V862V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3QL-01A-11D-A247-09 chr11:22294477 C>T maps to NM_213599.2 S726S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NN-01A-11D-A37C-09 chr11:22279254 G>A maps to NM_213599.2 T454T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr11:428561 G>A maps to NM_001012302.2 A366A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6Y2-01B-11D-A33E-09 chr11:420817 G>A maps to NM_001012302.2 S511S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EO-01A-11D-A36J-09 chr11:432005 C>T maps to NM_001012302.2 S133S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GI-01A-11D-A37C-09 chr15:69080147 G>A maps to NM_006305.3 T55T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GJ-01A-11D-A37C-09 chr9:100774734 A>G maps to NM_006401.2 E223E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FP-01A-31D-A387-09 chr15:90347794 G>T maps to NM_001150.2 A317A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GH-01A-11D-A37C-09 chr4:169086461 C>G maps to NM_007193.3 L155L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NK-01A-21D-A37C-09 chr4:122599639 G>C maps to NM_001154.3 S135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NN-01A-11D-A37C-09 chr4:122607521 G>T maps to NM_001154.3 L5L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NF-01A-11D-A37C-09 chr1:150960780 G>T maps to NM_003568.2 P272P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FH-01A-11D-A33E-09 chr7:36552784 A>T maps to NM_001177506.1 Y640*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OR-01A-11D-A27G-09 chr7:36657927 A>G maps to NM_001177506.1 V242V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OT-01A-11D-A28B-09 chr17:40997483 G>T maps to NM_009590.2 E281*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EY-01A-11D-A36J-09 chr17:41003956 C>T maps to NM_003734.2 C199C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GK-01A-11D-A37C-09 chr2:201473731 C>T maps to NM_001159.3 S311S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A9-01A-11D-A28B-09 chr2:201457903 G>C maps to NM_001159.3 L27L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA4D-01A-11D-A37C-09 chr2:201473839 C>T maps to NM_001159.3 S347S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49P-01A-11D-A247-09 chr16:71773197 G>T maps to ENST00000423132 S705S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A625-01A-11D-A31U-09 chr19:50303388 C>A maps to NM_014203.2 A479A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FG-01A-11D-A33E-09 chr19:50285876 C>A maps to NM_014203.2 R123R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EY-01A-11D-A36J-09 chr19:50302584 G>T maps to NM_014203.2 E323*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NL-01A-12D-A37C-09 chr11:994157 G>A maps to ENST00000332231 T624T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr11:992534 C>T maps to ENST00000332231 Y435Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8W8-01B-11D-A37C-09 chr17:33953663 G>A maps to NM_001030006.1 R247R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GL-01A-12D-A37C-09 chr3:183896815 C>G maps to ENST00000411763 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OP-01A-11D-A27G-09 chr15:83358147 G>T maps to NM_004644.3 A57A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6L4-01A-11D-A31U-09 chr15:83331461 T>C maps to NM_004644.3 Q920Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GO-01A-11D-A37C-09 chr19:2111746 C>T maps to ENST00000355272 Q956Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93D-01A-11D-A387-09 chr19:2118608 C>T maps to ENST00000355272 V568V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88Z-01A-11D-A36J-09 chr5:115205740 G>C maps to NM_001284.2 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GH-01A-11D-A37C-09 chr15:51240353 G>A maps to NM_007347.3 E438E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FH-01A-11D-A33E-09 chr15:51285651 G>T maps to NM_007347.3 E726*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OE-01A-11D-A27G-09 chr15:51289590 C>T maps to NM_007347.3 G805G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49R-01A-11D-A247-09 chr15:51250985 T>C maps to NM_007347.3 L616L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr12:99109236 G>A maps to NM_181861.1 Q997Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q9-A6FU-01A-11D-A31U-09 chr12:99065329 G>A maps to NM_181861.1 E542E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr9:72131556 G>A maps to NM_001163.3 Y190Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GJ-01A-11D-A37C-09 chr15:29346719 C>A maps to NM_005503.3 R211R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49M-01A-21D-A27G-09 chr15:29400540 C>T maps to NM_005503.3 I662I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASX-01A-11D-A387-09 chr15:29346542 C>T maps to NM_005503.3 H152H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OJ-01A-11D-A27G-09 chr19:3752886 C>T maps to NM_004886.3 P371P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NG-01A-11D-A37C-09 chr10:26856356 G>A maps to NM_019043.3 E647E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GG-01A-11D-A37C-09 chr5:112178799 A>G maps to NM_001127510.2 G2503G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr5:112154721 G>A maps to NM_001127510.2 S331S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A891-01A-11D-A36J-09 chr5:112177095 G>A maps to NM_001127510.2 Q1935Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A4P3-01A-11D-A27G-09 chr18:10488019 G>A maps to ENST00000423585 W561*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A891-01A-11D-A36J-09 chr18:10487666 G>T maps to ENST00000423585 E444*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8ER-01A-11D-A36J-09 chr23:55030233 A>T did not map to a codon.
Sequencing variant TCGA-XP-A8T7-01A-11D-A36J-09 chr23:55033866 G>A did not map to a codon.
Sequencing variant TCGA-LN-A9FP-01A-31D-A387-09 chr11:43342369 G>C did not map to a codon.
Sequencing variant TCGA-L5-A8NG-01A-11D-A37C-09 chr2:68765197 C>T maps to NM_173545.2 G333G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr11:57003869 G>T maps to NM_005161.4 V203V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A5-01A-21D-A27G-09 chr11:116706853 C>T maps to NM_000039.1 L158L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GF-01A-11D-A37C-09 chr2:21234672 G>T maps to NM_000384.2 R1689R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A4P3-01A-11D-A27G-09 chr2:21238335 G>A maps to NM_000384.2 L1138L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93D-01A-11D-A387-09 chr2:21242611 C>T maps to NM_000384.2 P994P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43I-01A-11D-A247-09 chr2:21232669 A>T maps to NM_000384.2 L2357*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr2:21260128 T>C did not map to a codon.
Sequencing variant TCGA-L5-A8NL-01A-12D-A37C-09 chr2:21239324 G>T maps to NM_000384.2 L1106L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NW-01A-11D-A37C-09 chr2:21235440 C>T maps to NM_000384.2 S1433S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6L4-01A-11D-A31U-09 chr2:21252654 G>T maps to NM_000384.2 V491V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8Q7-01A-11D-A37C-09 chr2:21233394 C>A maps to NM_000384.2 L2115L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XP-A8T6-01A-11D-A36J-09 chr2:21230477 G>A maps to NM_000384.2 Q3088*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FB-01A-11D-A33E-09 chr16:28507081 G>T maps to NM_018690.2 G240G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-A7RC-01B-11D-A403-09 chr22:39388093 C>A maps to ENST00000402182 P358P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr22:39421259 C>T maps to NM_152426.3 A132A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EX-01A-11D-A36J-09 chr22:39479861 C>T maps to NM_021822.3 N236N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FA-01A-11D-A33E-09 chr11:116703478 G>T did not map to a codon.
Sequencing variant TCGA-Z6-A8JE-01A-11D-A37C-09 chr3:195306287 G>A maps to ENST00000421243 F43F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NS-01A-12D-A37C-09 chr17:64216828 C>T maps to NM_000042.2 T149T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6XG-01B-11D-A33E-09 chr22:36661571 C>T maps to NM_145343.2 Y246Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GM-01A-11D-A37C-09 chr22:36537958 G>T maps to NM_145640.2 S166S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6Y0-01B-11D-A33E-09 chr22:36122763 G>T maps to NM_030642.1 G217*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FB-01A-11D-A33E-09 chr6:31625025 G>T maps to NM_019101.2 R98R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr21:27264105 C>T maps to NM_000484.3 A713A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8ER-01A-11D-A36J-09 chr17:58524942 C>A maps to NM_006380.2 *586L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OH-01A-11D-A27G-09 chr3:57281446 G>T maps to NM_012096.2 E216*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr12:105600898 C>T maps to NM_018171.3 A187A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GF-01A-11D-A37C-09 chr16:88876150 C>T maps to NM_000485.2 E166E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr16:88876195 C>T maps to NM_000485.2 L151L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A9VB-01A-21D-A37C-09 chr1:154296216 C>T maps to NM_080429.2 N214N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A5B8-01A-11D-A28B-09 chr5:115298658 G>C maps to NM_173800.4 L115L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FG-01A-11D-A33E-09 chr5:115298448 G>A maps to NM_173800.4 P45P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88Z-01A-11D-A36J-09 chr15:35222463 G>A maps to NM_014691.2 L337L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GK-01A-11D-A37C-09 chr23:66863159 G>A did not map to a codon.
Sequencing variant TCGA-JY-A6FA-01A-11D-A33E-09 chr23:66765278 C>A did not map to a codon.
Sequencing variant TCGA-JY-A93F-01A-21D-A37C-09 chr23:66765194 G>A did not map to a codon.
Sequencing variant TCGA-L5-A8NJ-01A-11D-A36J-09 chr23:66765160 A>T did not map to a codon.
Sequencing variant TCGA-LN-A9FP-01A-31D-A387-09 chr23:66931398 A>G did not map to a codon.
Sequencing variant TCGA-M9-A5M8-01A-11D-A28B-09 chr23:66905891 T>C did not map to a codon.
Sequencing variant TCGA-R6-A6KZ-01A-11D-A31U-09 chr23:66765187 A>T did not map to a codon.
Sequencing variant TCGA-R6-A6KZ-01A-11D-A31U-09 chr23:66765190 A>T did not map to a codon.
Sequencing variant TCGA-R6-A6XG-01B-11D-A33E-09 chr23:66766358 C>T did not map to a codon.
Sequencing variant TCGA-V5-A7RB-01A-11D-A351-09 chr23:66905923 C>G did not map to a codon.
Sequencing variant TCGA-Z6-AAPN-01A-11D-A403-09 chr23:66766355 T>C did not map to a codon.
Sequencing variant TCGA-L5-A4OJ-01A-11D-A27G-09 chr23:47426459 A>C did not map to a codon.
Sequencing variant TCGA-L5-A8NT-01A-11D-A37C-09 chr23:47426443 G>A did not map to a codon.
Sequencing variant TCGA-LN-A49W-01A-11D-A27G-09 chr23:47424690 C>A did not map to a codon.
Sequencing variant TCGA-L5-A8NF-01A-11D-A37C-09 chr11:72438098 C>A maps to NM_001040118.2 G25G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FD-01A-11D-A33E-09 chr4:36230810 G>A maps to NM_015230.2 Q100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr4:36160351 C>A maps to NM_015230.2 E918*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NN-01A-11D-A37C-09 chr4:36212334 G>A maps to NM_015230.2 S388S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A3-01A-11D-A27G-09 chr4:36214867 G>T maps to NM_015230.2 S346S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A9-01A-11D-A28B-09 chr4:36130236 C>G maps to NM_015230.2 T1186T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GG-01A-11D-A37C-09 chr5:141041787 G>A maps to NM_022481.5 G945G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NW-01A-11D-A37C-09 chr7:127231307 G>A maps to NM_001662.3 L166L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6XG-01B-11D-A33E-09 chr7:127231141 G>T maps to NM_001662.3 T152T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A8O2-01A-11D-A36J-09 chr20:47649630 C>T maps to NM_006420.2 L1751L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NS-01A-12D-A37C-09 chr20:47605927 G>A maps to NM_006420.2 P880P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A2-01A-31D-A27G-09 chr20:47538533 C>T maps to NM_006420.2 C36C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49Y-01A-11D-A27G-09 chr14:68113431 G>C maps to NM_001172.3 L198L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EQ-01A-11D-A36J-09 chr14:68086727 C>T maps to NM_001172.3 Q12*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RF-01A-13D-A33E-09 chr3:121305140 G>T maps to NM_001012659.1 V214V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A8O2-01A-11D-A36J-09 chr4:148786094 G>A maps to NM_024605.3 E195E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6XQ-01B-11D-A33E-09 chr15:32920993 G>T maps to NM_014783.3 E310*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HV-01A-21D-A351-09 chr10:32101633 C>A did not map to a codon.
Sequencing variant TCGA-L5-A8NN-01A-11D-A37C-09 chr11:110501394 C>T maps to NM_020809.2 R103R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RE-A7BO-01A-11D-A33E-09 chr11:110450893 T>G maps to NM_020809.2 R926R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GM-01A-11D-A37C-09 chr10:24886904 G>T maps to NM_020824.3 R1056R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A8JD-01A-11D-A36J-09 chr10:24959282 G>T maps to NM_020824.3 S36*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EX-01A-11D-A36J-09 chr4:86916531 C>A maps to NM_001025616.2 T575T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A8JD-01A-11D-A36J-09 chr4:86916189 G>A maps to NM_001025616.2 R461R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8WC-01A-11D-A37C-09 chr2:69046253 G>T did not map to a codon.
Sequencing variant TCGA-L5-A893-01A-11D-A36J-09 chr18:6887183 A>G maps to ENST00000400091 Q494Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NR-01A-11D-A37C-09 chr18:6882173 T>C maps to ENST00000400091 D443D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8Q7-01A-11D-A37C-09 chr18:6912057 G>T did not map to a codon.
Sequencing variant TCGA-JY-A938-01A-11D-A37C-09 chr1:161022153 C>T did not map to a codon.
Sequencing variant TCGA-L5-A8NV-01A-11D-A37C-09 chr3:119101231 G>A maps to NM_020754.2 A175A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49O-01A-11D-A247-09 chr3:119101243 C>G maps to NM_020754.2 L179L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93C-01A-11D-A387-09 chr11:128843256 C>T maps to NM_001142685.1 P1034P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93C-01A-11D-A387-09 chr11:128910852 G>A maps to NM_001142685.1 Q325*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A893-01A-11D-A36J-09 chr11:128840478 G>T maps to NM_001142685.1 S1529S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NR-01A-11D-A37C-09 chr11:128843097 A>C maps to NM_001142685.1 S1087S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NR-01A-11D-A37C-09 chr11:128844306 G>A maps to NM_001142685.1 L915L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EQ-01A-11D-A36J-09 chr11:128840139 C>T maps to NM_001142685.1 E1642E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RE-01A-11D-A33E-09 chr23:130218355 T>A did not map to a codon.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr23:130217936 G>A did not map to a codon.
Sequencing variant TCGA-L5-A8NU-01A-11D-A36J-09 chr23:130218355 T>C did not map to a codon.
Sequencing variant TCGA-LN-A49U-01A-31D-A27G-09 chr23:130222714 C>G did not map to a codon.
Sequencing variant TCGA-R6-A6L6-01B-11D-A33E-09 chr23:130220590 G>A did not map to a codon.
Sequencing variant TCGA-V5-A7RC-01B-11D-A403-09 chr23:130217913 C>G did not map to a codon.
Sequencing variant TCGA-VR-AA7B-01A-31D-A403-09 chr23:130217774 G>A did not map to a codon.
Sequencing variant TCGA-JY-A93C-01A-11D-A387-09 chr8:145773257 C>T maps to NM_025251.1 A404A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr8:145773077 C>T maps to NM_025251.1 P464P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OG-01A-11D-A27G-09 chr14:32563111 G>A maps to NM_001030055.1 L1079L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NE-01A-11D-A37C-09 chr14:32559919 C>T maps to NM_001030055.1 I15I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88T-01A-11D-A351-09 chr23:11682516 G>A did not map to a codon.
Sequencing variant TCGA-LN-A9FP-01A-31D-A387-09 chr23:11204401 C>A did not map to a codon.
Sequencing variant TCGA-VR-A8Q7-01A-11D-A37C-09 chr23:11206969 C>A did not map to a codon.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr12:57871262 C>T maps to ENST00000393797 P316P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NL-01A-12D-A37C-09 chr12:57869648 C>T maps to ENST00000393797 W497*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GR-01A-12D-A37C-09 chr8:1900949 G>A maps to ENST00000398564 V1184V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3I8-01A-11D-A247-09 chr8:1853762 C>T maps to ENST00000398564 L641L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8WG-01A-11D-A37C-09 chr8:1905069 G>T maps to ENST00000398564 G1251*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XP-A8T7-01A-11D-A36J-09 chr8:1893810 C>T maps to ENST00000398564 N1154N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NQ-01A-11D-A36J-09 chr1:156911689 G>T maps to NM_198236.1 R1140R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-A7RE-01A-11D-A351-09 chr11:120328460 C>T maps to NM_015313.2 R741*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43M-01A-11D-A247-09 chr17:8222387 G>A maps to NM_173728.3 P699P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NL-01A-12D-A37C-09 chr17:8215790 C>G maps to NM_173728.3 S145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr17:8222396 T>G maps to NM_173728.3 S702S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NQ-01A-11D-A36J-09 chr11:73020555 G>A maps to NM_014786.3 G291G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q9-A6FU-01A-11D-A31U-09 chr19:7505005 C>T maps to NM_001130955.1 S60S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93C-01A-11D-A387-09 chr1:16534231 G>A maps to NM_153213.3 S245S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr7:143884144 C>T maps to NM_001003702.2 L444L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr5:148980675 G>A maps to NM_001001669.2 P64P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A5S3-01A-11D-A28B-09 chr7:144062631 C>G maps to NM_005435.3 S957*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A8HZ-01A-11D-A36J-09 chr23:135772772 A>T did not map to a codon.
Sequencing variant TCGA-RE-A7BO-01A-11D-A33E-09 chr23:135761793 C>A did not map to a codon.
Sequencing variant TCGA-LN-A49S-01A-11D-A247-09 chr23:62875449 C>G did not map to a codon.
Sequencing variant TCGA-R6-A8W5-01B-11D-A37C-09 chr23:62857923 G>T did not map to a codon.
Sequencing variant TCGA-Z6-A8JE-01A-11D-A37C-09 chr23:62944428 G>T did not map to a codon.
Sequencing variant TCGA-2H-A9GF-01A-11D-A37C-09 chr1:27057971 C>A maps to NM_006015.4 Y560*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GR-01A-12D-A37C-09 chr1:27100323 C>T maps to NM_006015.4 Q1346*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FH-01A-11D-A33E-09 chr1:27099396 C>T maps to NM_006015.4 Q1212*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OE-01A-11D-A27G-09 chr1:27057933 C>T maps to NM_006015.4 Q548*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OJ-01A-11D-A27G-09 chr1:27101251 C>T maps to NM_006015.4 Q1512*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49M-01A-21D-A27G-09 chr1:27087878 C>T maps to NM_006015.4 N722N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6Y2-01B-11D-A33E-09 chr1:27023559 C>G maps to NM_006015.4 Y222*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4ON-01A-11D-A27G-09 chr6:157525060 G>C maps to ENST00000367148 T1692T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49P-01A-11D-A247-09 chr6:157469896 A>T maps to ENST00000367148 G884G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q9-A6FU-01A-11D-A31U-09 chr6:157528370 C>T maps to ENST00000367148 S2072S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6KZ-01A-11D-A31U-09 chr6:157522153 C>T maps to ENST00000367148 Q1516*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA7I-01A-11D-A403-09 chr6:157527314 C>T maps to ENST00000367148 L1720L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49O-01A-11D-A247-09 chr12:46230370 G>T did not map to a codon.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr15:74883533 C>T maps to ENST00000395077 A308A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3QL-01A-11D-A247-09 chr14:58831579 C>T maps to NM_002892.3 L925L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6XQ-01B-11D-A33E-09 chr1:235383151 G>C maps to NM_016374.5 S513S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NE-01A-11D-A37C-09 chr10:63816991 A>G maps to NM_032199.2 E321E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8WG-01A-11D-A37C-09 chr3:49008110 G>A maps to NM_006321.2 Q248Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EX-01A-11D-A36J-09 chr23:100241807 A>G did not map to a codon.
Sequencing variant TCGA-L5-A8NI-01A-11D-A37C-09 chr3:93762077 G>T maps to NM_182896.2 E340*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A891-01A-11D-A36J-09 chr2:235405122 G>A maps to ENST00000339728 N36N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NQ-01A-11D-A36J-09 chr2:235405080 C>T maps to ENST00000339728 E50E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A8I1-01A-11D-A36J-09 chr3:5164158 G>T maps to ENST00000438743 A55A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6Y0-01B-11D-A33E-09 chr8:66539512 G>A maps to NM_018120.4 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EU-01A-11D-A36J-09 chr7:102716312 A>T maps to NM_031905.3 K77*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OJ-01A-11D-A27G-09 chr6:109286188 G>T maps to NM_032131.4 V764V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A4P3-01A-11D-A27G-09 chr10:28270508 G>T maps to NM_018076.2 G274G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49W-01A-11D-A27G-09 chr3:137991874 C>T maps to ENST00000469044 L516L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-M9-A5M8-01A-11D-A28B-09 chr23:100807919 C>T did not map to a codon.
Sequencing variant TCGA-L5-A8NW-01A-11D-A37C-09 chr23:100911644 G>T did not map to a codon.
Sequencing variant TCGA-IC-A6RE-01A-11D-A33E-09 chr23:100880908 G>T did not map to a codon.
Sequencing variant TCGA-LN-A49P-01A-11D-A247-09 chr23:101858367 T>G did not map to a codon.
Sequencing variant TCGA-VR-AA7B-01A-31D-A403-09 chr23:100871257 C>T did not map to a codon.
Sequencing variant TCGA-IC-A6RF-01A-13D-A33E-09 chr10:124214281 G>T maps to NM_001099667.1 A13A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A893-01A-11D-A36J-09 chr11:13378284 G>T did not map to a codon.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr12:27573423 G>T maps to NM_020183.3 G624*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OE-01A-11D-A27G-09 chr3:9843355 C>A maps to NM_001198793.1 I82I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NG-01A-11D-A37C-09 chr3:169485220 C>T maps to NM_032487.4 *373*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A9-01A-11D-A28B-09 chr3:169486005 T>C maps to NM_032487.4 P111P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A8I1-01A-11D-A36J-09 chr15:52844184 C>A maps to NM_006628.4 P95P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A8O2-01A-11D-A36J-09 chr23:69497287 C>T did not map to a codon.
Sequencing variant TCGA-JY-A938-01A-11D-A37C-09 chr23:69496297 C>T did not map to a codon.
Sequencing variant TCGA-L5-A43H-01A-11D-A247-09 chr11:74995294 A>T maps to NM_004041.3 Y47*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NW-01A-11D-A37C-09 chr11:74977318 C>T did not map to a codon.
Sequencing variant TCGA-L5-A8NW-01A-11D-A37C-09 chr11:74994329 C>T did not map to a codon.
Sequencing variant TCGA-V5-AASW-01A-11D-A403-09 chr11:74985187 G>A maps to NM_004041.3 R282*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FP-01A-31D-A387-09 chr17:4619266 G>C did not map to a codon.
Sequencing variant TCGA-LN-A4MQ-01A-11D-A28B-09 chr9:140508650 G>A maps to NM_152285.2 V201V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49O-01A-11D-A247-09 chr19:18119839 C>A maps to NM_015683.1 T134T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FH-01A-11D-A33E-09 chr22:51065260 C>T did not map to a codon.
Sequencing variant TCGA-VR-A8EQ-01A-11D-A36J-09 chr5:78181609 G>T maps to NM_000046.3 P313P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FH-01A-11D-A33E-09 chr23:2838660 G>T did not map to a codon.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr23:2828791 G>T did not map to a codon.
Sequencing variant TCGA-LN-A5U7-01A-11D-A31U-09 chr23:2861175 C>T did not map to a codon.
Sequencing variant TCGA-2H-A9GH-01A-11D-A37C-09 chr23:3002338 A>T did not map to a codon.
Sequencing variant TCGA-L5-A43M-01A-11D-A247-09 chr23:3030500 G>C did not map to a codon.
Sequencing variant TCGA-L5-A8NS-01A-12D-A37C-09 chr23:2990156 A>C did not map to a codon.
Sequencing variant TCGA-L5-A8NV-01A-11D-A37C-09 chr23:2990073 T>C did not map to a codon.
Sequencing variant TCGA-R6-A8WG-01A-11D-A37C-09 chr23:3021929 C>T did not map to a codon.
Sequencing variant TCGA-IG-A6QS-01A-12D-A33E-09 chr17:66416460 C>T maps to NM_014960.3 L479L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NT-01A-11D-A37C-09 chr4:114899597 A>G maps to NM_024590.3 T131T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OU-01A-11D-A28B-09 chr5:94918844 T>G maps to NM_198150.2 S214S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HX-01A-11D-A33E-09 chr1:231124098 G>T maps to NM_022786.1 E70*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49S-01A-11D-A247-09 chr23:25028417 C>T did not map to a codon.
Sequencing variant TCGA-L5-A4OH-01A-11D-A27G-09 chr8:131191523 G>T maps to NM_018482.2 Y244*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr2:9491024 G>A did not map to a codon.
Sequencing variant TCGA-L5-A8NK-01A-21D-A37C-09 chr2:9528533 G>T maps to NM_003887.2 E748*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49X-01A-31D-A27G-09 chr2:9517086 C>T maps to NM_003887.2 T599T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-A7RE-01A-11D-A351-09 chr2:9474923 G>A maps to NM_003887.2 L248L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6Y2-01B-11D-A33E-09 chr7:150883937 G>T maps to ENST00000422024 R139R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A8JD-01A-11D-A36J-09 chr23:15320923 A>C did not map to a codon.
Sequencing variant TCGA-IG-A3Y9-01A-12D-A247-09 chr23:63445263 C>A did not map to a codon.
Sequencing variant TCGA-IG-A50L-01A-11D-A27G-09 chr23:63444299 G>T did not map to a codon.
Sequencing variant TCGA-L5-A4OJ-01A-11D-A27G-09 chr23:63444239 A>C did not map to a codon.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr17:42249534 C>T maps to NM_080863.4 V141V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA4G-01A-11D-A37C-09 chr1:76397721 A>G maps to NM_080868.2 F85F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49X-01A-31D-A27G-09 chr14:94401049 C>T maps to ENST00000434324 P620P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HY-01A-12D-A351-09 chr14:94413849 C>A maps to ENST00000434324 T299T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FP-01A-31D-A387-09 chr14:94405564 G>C maps to ENST00000434324 G502G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA7B-01A-31D-A403-09 chr15:101170230 C>T maps to NM_198243.2 F267F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6Y0-01B-11D-A33E-09 chr23:15287930 G>A did not map to a codon.
Sequencing variant TCGA-LN-A9FO-01A-11D-A387-09 chr22:30189407 G>T maps to NM_032204.3 Y620*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NR-01A-11D-A37C-09 chr6:101095201 A>T maps to NM_006828.2 P1126P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RE-01A-11D-A33E-09 chr1:155448919 T>C maps to ENST00000368346 K1247K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43M-01A-11D-A247-09 chr23:1748765 G>A did not map to a codon.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr23:1761873 A>G did not map to a codon.
Sequencing variant TCGA-L5-A8NR-01A-11D-A37C-09 chr23:1755353 C>T did not map to a codon.
Sequencing variant TCGA-LN-A49U-01A-31D-A27G-09 chr23:1743286 G>A did not map to a codon.
Sequencing variant TCGA-VR-AA4D-01A-11D-A37C-09 chr23:1743259 C>T did not map to a codon.
Sequencing variant TCGA-V5-A7RE-01A-11D-A351-09 chr23:1537980 C>T did not map to a codon.
Sequencing variant TCGA-VR-A8EW-01A-11D-A36J-09 chr19:12856258 C>T maps to NM_004317.2 S126S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RE-01A-11D-A33E-09 chr17:3397734 C>A maps to NM_000049.2 I242I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6Y0-01B-11D-A33E-09 chr14:104558979 C>T maps to NM_001080464.1 P31P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr16:29912621 C>T maps to NM_181718.3 S110S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr22:26830126 C>T maps to NM_020437.4 D182D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NQ-01A-11D-A36J-09 chr22:26830126 C>T maps to NM_020437.4 D182D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GK-01A-11D-A37C-09 chr1:197091056 G>C maps to NM_018136.4 L1286L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OG-01A-11D-A27G-09 chr1:197060161 G>A maps to NM_018136.4 R3152*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OQ-01A-11D-A27G-09 chr1:197057451 G>T maps to NM_018136.4 G3365G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93C-01A-11D-A387-09 chr2:70187812 T>C maps to NM_152792.2 E336E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FG-01A-11D-A33E-09 chr17:79954649 G>A maps to ENST00000306729 S287S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43I-01A-11D-A247-09 chr17:79970143 G>A maps to ENST00000306729 T446T. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-L5-A4OO-01A-11D-A27G-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-LN-A49W-01A-11D-A27G-09 chr3:130732924 A>G maps to ENST00000514044 H697H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GM-01A-11D-A37C-09 chr1:176903417 C>T maps to ENST00000281881 A855A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NJ-01A-11D-A36J-09 chr1:177030252 C>T maps to ENST00000281881 S144S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA7I-01A-11D-A403-09 chr1:176926900 C>A maps to ENST00000281881 P608P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-AAPN-01A-11D-A403-09 chr1:177000020 C>T maps to ENST00000281881 V311V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4ON-01A-11D-A27G-09 chr9:120053712 G>A maps to ENST00000313400 H174H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OT-01A-11D-A28B-09 chr9:119738454 G>T maps to ENST00000313400 Y563*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A51D-01A-11D-A27G-09 chr20:31024729 C>T maps to ENST00000375687 V1405V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr20:31021422 C>T maps to ENST00000375687 P474P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASV-01A-11D-A387-09 chr20:31022591 C>T maps to ENST00000375687 R693*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FP-01A-31D-A387-09 chr2:25994387 G>C maps to NM_018263.4 S142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GK-01A-11D-A37C-09 chr18:31318534 T>C maps to NM_030632.1 T389T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GM-01A-11D-A37C-09 chr18:31311979 G>T maps to NM_030632.1 E310*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GR-01A-12D-A37C-09 chr18:31323951 A>G maps to NM_030632.1 E1380E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NN-01A-11D-A37C-09 chr18:31326084 C>T maps to NM_030632.1 S2091S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A5-01A-21D-A27G-09 chr18:31323087 G>A maps to NM_030632.1 E1092E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S8-A6BW-01A-11D-A31U-09 chr18:31319195 G>T maps to NM_030632.1 E610*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GR-01A-12D-A37C-09 chr8:124357204 T>C maps to NM_014109.3 T879T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RE-01A-11D-A33E-09 chr8:124333403 T>C maps to NM_014109.3 Q1381Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NT-01A-11D-A37C-09 chr8:124392779 C>T maps to NM_014109.3 R103R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HY-01A-12D-A351-09 chr8:124358391 T>C maps to NM_014109.3 V822V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GL-01A-12D-A37C-09 chr2:24046175 G>A maps to NM_017552.1 Q695*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FG-01A-11D-A33E-09 chr2:24090760 G>T maps to NM_017552.1 R378R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GM-01A-11D-A37C-09 chr1:1459345 T>G did not map to a codon.
Sequencing variant TCGA-LN-A49K-01A-11D-A247-09 chr1:1412669 C>T maps to NM_031921.4 A74A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EZ-01A-11D-A36J-09 chr1:1396168 C>T maps to NM_001039211.2 F284F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6XQ-01B-11D-A33E-09 chr17:29214208 G>T did not map to a codon.
Sequencing variant TCGA-R6-A8W8-01B-11D-A37C-09 chr17:29196272 G>T maps to NM_024857.3 S1107S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr19:3913845 C>T maps to NM_033064.4 C319C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XP-A8T8-01A-11D-A36J-09 chr22:39917509 C>T maps to NM_182810.1 F20F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6F8-01A-11D-A33E-09 chr12:53918508 G>A maps to NM_001130059.1 R333*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FH-01A-11D-A33E-09 chr12:53926320 G>T maps to NM_001130059.1 G260G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FG-01A-11D-A33E-09 chr16:10575952 T>A maps to NM_024997.2 I632I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GK-01A-11D-A37C-09 chr3:11399889 A>G did not map to a codon.
Sequencing variant TCGA-JY-A93F-01A-21D-A37C-09 chr11:293645 C>T maps to ENST00000409479 F538F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OQ-01A-11D-A27G-09 chr11:292903 G>T maps to ENST00000409479 E393*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr11:63398664 G>T maps to NM_015459.3 G462G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KH-A6WC-01A-11D-A33E-09 chr11:108186795 G>T maps to NM_000051.3 E2052*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A893-01A-11D-A36J-09 chr11:108106560 G>T maps to NM_000051.3 E166*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L7-A6VZ-01A-12D-A33E-09 chr11:108155035 G>T maps to NM_000051.3 E1277*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49N-01A-11D-A247-09 chr11:108203580 T>C maps to NM_000051.3 Y2627Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NI-01A-11D-A37C-09 chr16:81076085 G>A did not map to a codon.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr12:7045896 G>A maps to NM_001940.3 Q489Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr15:25959229 C>T maps to NM_024490.3 P645P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr15:26107955 C>A maps to NM_024490.3 L96L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6KZ-01A-11D-A31U-09 chr15:25959046 C>T maps to NM_024490.3 A706A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3Y9-01A-12D-A247-09 chr5:160114973 C>G maps to NM_025153.2 G36G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NU-01A-11D-A36J-09 chr5:159996678 G>A maps to NM_025153.2 H1254H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8W8-01B-11D-A37C-09 chr5:160059357 G>T maps to NM_025153.2 T466T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EX-01A-11D-A36J-09 chr5:159992804 C>T maps to NM_025153.2 Q1347Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GH-01A-11D-A37C-09 chr4:47548681 G>T maps to NM_020453.3 E480*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FP-01A-31D-A387-09 chr4:47562980 G>T maps to NM_020453.3 E853*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8WG-01A-11D-A37C-09 chr4:47514679 T>C maps to NM_020453.3 S41S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GI-01A-11D-A37C-09 chr3:182584150 G>A maps to NM_014616.1 W513*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr3:182635843 C>T maps to NM_014616.1 N1162N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FH-01A-11D-A33E-09 chr23:138865368 T>C did not map to a codon.
Sequencing variant TCGA-L5-A43C-01A-11D-A247-09 chr23:138856966 G>A did not map to a codon.
Sequencing variant TCGA-L5-A893-01A-11D-A36J-09 chr23:138884447 G>T did not map to a codon.
Sequencing variant TCGA-L5-A8NE-01A-11D-A37C-09 chr23:138897120 G>T did not map to a codon.
Sequencing variant TCGA-LN-A5U7-01A-11D-A31U-09 chr23:138864829 T>C did not map to a codon.
Sequencing variant TCGA-L5-A8NU-01A-11D-A36J-09 chr13:25280562 C>T maps to NM_001185085.1 Q717*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NQ-01A-11D-A36J-09 chr19:19760548 C>T did not map to a codon.
Sequencing variant TCGA-L5-A8NS-01A-12D-A37C-09 chr19:19757090 G>C maps to NM_020410.2 T1057T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A5-01A-21D-A27G-09 chr19:19758015 T>A maps to NM_020410.2 G1009G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4MR-01A-11D-A28B-09 chr19:19766337 T>C maps to NM_020410.2 E465E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A97H-01A-11D-A387-09 chr1:17323610 C>A maps to NM_022089.2 E367*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr1:17316762 C>T maps to NM_022089.2 A757A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NF-01A-11D-A37C-09 chr3:193081987 G>A maps to NM_198505.2 L49L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NT-01A-11D-A37C-09 chr3:193082018 G>A maps to NM_198505.2 V38V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-A7RE-01A-11D-A351-09 chr3:193039502 C>A maps to NM_198505.2 E628*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A1-01A-21D-A27G-09 chr1:116931579 C>T maps to NM_000701.7 F231F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA7B-01A-31D-A403-09 chr1:116926722 G>T maps to NM_000701.7 E34*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A9-01A-11D-A28B-09 chr1:160093830 G>A maps to NM_000702.3 K160K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FP-01A-31D-A387-09 chr19:42492162 C>A maps to ENST00000441343 L94L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr1:160125038 G>A did not map to a codon.
Sequencing variant TCGA-L5-A893-01A-11D-A36J-09 chr1:160134009 G>T maps to NM_144699.3 L281L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43I-01A-11D-A247-09 chr1:169100708 T>A maps to NM_001677.3 C276*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A9VB-01A-21D-A37C-09 chr1:169094266 A>G maps to NM_001677.3 E124E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6KZ-01A-11D-A31U-09 chr23:119509234 G>T did not map to a codon.
Sequencing variant TCGA-L5-A4OF-01A-11D-A27G-09 chr17:3839573 G>T maps to NM_174953.1 Y837*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NV-01A-11D-A37C-09 chr12:89992490 T>G maps to ENST00000428670 G1127G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A51D-01A-11D-A27G-09 chr3:10382386 G>T maps to NM_001001331.2 G973G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93E-01A-11D-A37C-09 chr3:10370803 G>A maps to NM_001001331.2 R1142R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8WC-01A-11D-A37C-09 chr3:10400461 C>T maps to NM_001001331.2 P683P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S8-A6BV-01A-21D-A31U-09 chr3:10491047 G>T maps to NM_001001331.2 L60L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-A7RE-01A-11D-A351-09 chr3:10401654 G>T maps to NM_001001331.2 S604S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GQ-01A-11D-A37C-09 chr23:152835147 G>A did not map to a codon.
Sequencing variant TCGA-L5-A4OP-01A-11D-A27G-09 chr23:152845486 C>A did not map to a codon.
Sequencing variant TCGA-L5-A8NK-01A-21D-A37C-09 chr23:152815519 C>A did not map to a codon.
Sequencing variant TCGA-LN-A9FQ-01A-31D-A387-09 chr23:152818512 G>T did not map to a codon.
Sequencing variant TCGA-V5-A7RB-01A-11D-A351-09 chr23:152845532 T>G did not map to a codon.
Sequencing variant TCGA-JY-A6FE-01A-11D-A33E-09 chr1:203708867 G>T maps to NM_001684.3 L1168L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OH-01A-11D-A27G-09 chr1:203677034 G>T maps to NM_001001396.1 E454*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NK-01A-21D-A37C-09 chr1:203652485 A>G maps to NM_001001396.1 V51V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RF-01A-13D-A33E-09 chr16:84485636 G>T maps to ENST00000416219 E591*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93D-01A-11D-A387-09 chr19:36050723 G>A maps to NM_000704.2 L347L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43E-01A-11D-A247-09 chr19:36051292 G>A maps to NM_000704.2 I253I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A893-01A-11D-A36J-09 chr19:36041946 G>A maps to NM_000704.2 P984P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NG-01A-11D-A37C-09 chr19:36050027 C>T maps to NM_000704.2 A374A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FG-01A-11D-A33E-09 chr19:1244156 C>A maps to NM_001687.4 A119A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A97I-01A-11D-A387-09 chr12:54063705 G>A maps to NM_005176.5 S79S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8WG-01A-11D-A37C-09 chr14:50790661 G>T did not map to a codon.
Sequencing variant TCGA-L5-A8NI-01A-11D-A37C-09 chr23:153660198 A>G did not map to a codon.
Sequencing variant TCGA-VR-A8EU-01A-11D-A36J-09 chr23:153662699 G>A did not map to a codon.
Sequencing variant TCGA-R6-A6L6-01B-11D-A33E-09 chr23:40448251 G>C did not map to a codon.
Sequencing variant TCGA-2H-A9GH-01A-11D-A37C-09 chr17:40642554 C>T maps to NM_001130020.1 N365N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASX-01A-11D-A387-09 chr17:40666415 C>T maps to NM_001130020.1 T787T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NS-01A-12D-A37C-09 chr12:124229214 C>G maps to NM_012463.3 L466L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr7:149572716 C>T maps to NM_001100592.1 A94A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NE-01A-11D-A37C-09 chr3:113499970 G>T maps to NM_001690.3 E53*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GJ-01A-11D-A37C-09 chr13:52511785 C>T maps to NM_000053.2 V1243V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43C-01A-11D-A247-09 chr4:42445669 C>T maps to NM_006095.2 W1012*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NF-01A-11D-A37C-09 chr4:42526845 G>A maps to NM_006095.2 R581*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A1-01A-21D-A27G-09 chr4:42425656 C>G maps to NM_006095.2 L1063L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RF-01A-13D-A33E-09 chr13:26411317 G>T maps to NM_016529.4 P924P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6XG-01B-11D-A33E-09 chr13:26104740 G>T maps to NM_016529.4 L121L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A6-01A-11D-A27G-09 chr18:55334328 A>G maps to NM_005603.4 D760D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88Z-01A-11D-A36J-09 chr19:1785539 G>A maps to NM_138813.2 P1107P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A2-01A-31D-A27G-09 chr19:1809674 C>T maps to NM_138813.2 K123K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FA-01A-11D-A33E-09 chr15:50226247 G>C maps to NM_024837.2 L473L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A3-01A-11D-A27G-09 chr15:50366376 C>A maps to NM_024837.2 E12*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FG-01A-11D-A33E-09 chr20:50287675 C>T maps to NM_006045.1 S386S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NR-01A-11D-A37C-09 chr20:50245526 C>A maps to NM_006045.1 E585*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S8-A6BW-01A-11D-A31U-09 chr20:50244140 C>A maps to NM_006045.1 E615*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-A7RC-01B-11D-A403-09 chr18:76856505 G>A maps to NM_198531.3 L50L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OU-01A-11D-A28B-09 chr3:142272729 A>C maps to NM_001184.3 A823A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NQ-01A-11D-A36J-09 chr3:142218486 C>A maps to NM_001184.3 E1788*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A8-01A-32D-A27G-09 chr3:142168306 T>A maps to NM_001184.3 L2633L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GJ-01A-11D-A37C-09 chr20:3543939 C>T maps to NM_139321.2 N572N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GI-01A-11D-A37C-09 chr10:117059699 T>C maps to NM_207303.2 L858L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OH-01A-11D-A27G-09 chr10:117226742 G>T maps to NM_207303.2 T1159T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A3-01A-11D-A27G-09 chr10:117075176 G>T maps to NM_207303.2 E990*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-A7RB-01A-11D-A351-09 chr10:117040911 T>C maps to NM_207303.2 C716C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RE-01A-11D-A33E-09 chr23:76776324 C>T did not map to a codon.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr23:76891500 G>T did not map to a codon.
Sequencing variant TCGA-L5-A8NL-01A-12D-A37C-09 chr23:76920218 A>G did not map to a codon.
Sequencing variant TCGA-VR-A8EW-01A-11D-A36J-09 chr23:76855036 T>C did not map to a codon.
Sequencing variant TCGA-JY-A6FG-01A-11D-A33E-09 chr6:16328463 G>A maps to NM_000332.3 S26S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GG-01A-11D-A37C-09 chr16:28844773 C>G maps to NM_148414.1 S657*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA7B-01A-31D-A403-09 chr16:28845926 G>T maps to NM_148414.1 T782T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43I-01A-11D-A247-09 chr7:105248337 C>T maps to NM_138495.1 K726K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49S-01A-11D-A247-09 chr7:105401874 G>T maps to NM_152749.3 I130I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A9-01A-11D-A28B-09 chr7:105254707 C>T maps to NM_020725.1 A691A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43E-01A-11D-A247-09 chr17:42274606 G>T maps to NM_020218.1 I115I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr17:42275065 G>A maps to NM_020218.1 V28V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA7D-01A-11D-A403-09 chr20:54959345 C>T maps to NM_198437.1 Q118Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FA-01A-11D-A33E-09 chr19:57744877 G>A maps to NM_001015878.1 V162V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43E-01A-11D-A247-09 chr7:70231113 C>T maps to NM_015570.2 R495*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NR-01A-11D-A37C-09 chr7:69064800 C>T maps to NM_015570.2 S54S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S8-A6BV-01A-21D-A31U-09 chr7:69755385 A>G maps to NM_001127232.1 A231A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3YA-01A-11D-A247-09 chr12:58204169 G>T maps to NM_006576.3 I241I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NS-01A-12D-A37C-09 chr7:32584373 C>T maps to NM_015060.1 R95*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OJ-01A-11D-A27G-09 chr12:63541336 G>T maps to NM_000706.3 G353G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49M-01A-21D-A27G-09 chr23:153171020 A>G did not map to a codon.
Sequencing variant TCGA-IG-A5S3-01A-11D-A28B-09 chr23:69454559 G>A did not map to a codon.
Sequencing variant TCGA-L5-A88Z-01A-11D-A36J-09 chr23:69455665 A>G did not map to a codon.
Sequencing variant TCGA-R6-A8WC-01A-11D-A37C-09 chr23:69459687 C>T did not map to a codon.
Sequencing variant TCGA-V5-A7RB-01A-11D-A351-09 chr23:69455947 T>G did not map to a codon.
Sequencing variant TCGA-L5-A43H-01A-11D-A247-09 chr23:69262135 G>A did not map to a codon.
Sequencing variant TCGA-LN-A49M-01A-21D-A27G-09 chr23:69263823 C>G did not map to a codon.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr17:63531799 C>T maps to NM_004655.3 S727S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8Q7-01A-11D-A37C-09 chr17:63532604 G>A maps to NM_004655.3 S658S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr19:41727119 C>T maps to NM_021913.3 F126F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88V-01A-11D-A351-09 chr19:41754708 T>C maps to NM_021913.3 A565A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NS-01A-12D-A37C-09 chr3:28378342 C>T maps to NM_022461.3 W158*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A5U7-01A-11D-A31U-09 chr3:160804341 A>G maps to NM_033168.2 L67L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A5U5-01A-21D-A28B-09 chr13:31860935 G>T maps to NM_194318.3 V348V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GF-01A-11D-A37C-09 chr11:134253579 G>A maps to NM_054025.2 F205F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr6:71666060 G>A maps to NM_080742.2 D24D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NI-01A-11D-A37C-09 chr19:17922891 G>A maps to NM_014256.3 Q360Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr12:122691379 G>A maps to NM_030765.2 T194T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr2:232263176 C>T maps to NM_145236.2 N249N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr12:58025801 C>T maps to NM_001478.3 A38A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OR-01A-11D-A27G-09 chr12:663074 C>T maps to NM_173593.3 N662N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NQ-01A-11D-A36J-09 chr11:373227 G>A maps to NM_178537.4 S191S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NR-01A-11D-A37C-09 chr11:372928 C>T maps to NM_178537.4 H142H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3YC-01A-11D-A247-09 chr18:29210977 G>T maps to NM_004775.3 Y240*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6DQ-01B-11D-A31U-09 chr18:29218604 A>G did not map to a codon.
Sequencing variant TCGA-VR-A8EQ-01A-11D-A36J-09 chr18:29264293 G>A maps to NM_004775.3 I32I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr8:104225195 C>A maps to ENST00000297574 A105A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A9VB-01A-21D-A37C-09 chr21:42629161 G>A maps to NM_012105.3 A404A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NN-01A-11D-A37C-09 chr21:30714988 C>T maps to NM_206866.1 P682P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RE-A7BO-01A-11D-A33E-09 chr21:30715102 G>T maps to NM_206866.1 G720G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASX-01A-11D-A387-09 chr6:90642384 C>T maps to NM_001170794.1 A756A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6XG-01B-11D-A33E-09 chr9:33256870 G>T maps to NM_004323.5 L271L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr8:143603441 C>T maps to NM_001702.2 R1047R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FP-01A-31D-A387-09 chr8:143618430 C>T maps to NM_001702.2 H1218H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-A7RB-01A-11D-A351-09 chr8:143562930 G>A maps to NM_001702.2 S663S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A9VB-01A-21D-A37C-09 chr8:143623434 G>C maps to NM_001702.2 P1280P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A8-01A-32D-A27G-09 chr1:32205213 G>C maps to NM_001703.2 P730P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88V-01A-11D-A351-09 chr6:70034886 A>C maps to NM_001704.2 R980R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NH-01A-11D-A37C-09 chr6:70042867 A>G maps to NM_001704.2 G1052G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NW-01A-11D-A37C-09 chr6:69684704 A>C maps to NM_001704.2 R526R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49Y-01A-11D-A27G-09 chr6:70049227 G>T maps to NM_001704.2 A1097A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q9-A6FW-01A-31D-A31U-09 chr6:69772888 C>T maps to NM_001704.2 T799T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GO-01A-11D-A37C-09 chr17:79077393 G>A maps to NM_017451.2 Q245Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr17:79077330 G>A maps to NM_017451.2 P224P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NJ-01A-11D-A36J-09 chr17:79059482 G>A maps to NM_017451.2 T103T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr7:97937011 G>A maps to NM_018842.4 D384D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A4P3-01A-11D-A27G-09 chr16:1393011 C>G maps to NM_003933.4 A455A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FE-01A-11D-A33E-09 chr16:1391466 C>T maps to NM_003933.4 P271P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GL-01A-12D-A37C-09 chr6:33541884 G>A maps to ENST00000360661 Q157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49Y-01A-11D-A27G-09 chr4:102951370 C>T maps to NM_017935.4 R617*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93E-01A-11D-A37C-09 chr3:52439266 G>A maps to NM_004656.2 S325S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6Y0-01B-11D-A33E-09 chr2:215593432 C>G maps to NM_000465.2 V767V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EZ-01A-11D-A36J-09 chr2:215646172 G>T maps to NM_000465.2 S142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43M-01A-11D-A247-09 chr9:135458333 G>T maps to NM_020064.3 S50S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A50L-01A-11D-A27G-09 chr1:91182353 C>A maps to NM_020063.1 S133S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NS-01A-12D-A37C-09 chr1:91182392 C>T maps to NM_020063.1 P120P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GH-01A-11D-A37C-09 chr6:31599780 G>T maps to NM_080686.2 E1111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A4QS-01A-11D-A27G-09 chr9:134358094 A>C did not map to a codon.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr9:134319641 G>A maps to NM_013318.3 G180G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49V-01A-11D-A247-09 chr9:134321902 C>G maps to NM_013318.3 S243S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GQ-01A-11D-A37C-09 chr1:171482242 T>C maps to ENST00000392078 P74P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FQ-01A-31D-A387-09 chr1:171514801 C>T maps to ENST00000392078 Q1650*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-A7RB-01A-11D-A351-09 chr1:171505350 C>T maps to ENST00000392078 Q743*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EO-01A-11D-A36J-09 chr1:171511111 G>T maps to ENST00000392078 E1503*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-AAPN-01A-11D-A403-09 chr6:31615558 C>T maps to ENST00000404765 Q199Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FH-01A-11D-A33E-09 chr6:31631628 C>T did not map to a codon.
Sequencing variant TCGA-VR-A8EY-01A-11D-A36J-09 chr6:31664811 T>G did not map to a codon.
Sequencing variant TCGA-L5-A4OF-01A-11D-A27G-09 chr7:72856561 G>A maps to NM_032408.3 A1472A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NJ-01A-11D-A36J-09 chr7:72892290 G>T maps to NM_032408.3 S500S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8WG-01A-11D-A37C-09 chr7:72873922 T>C maps to NM_032408.3 E1125E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA4D-01A-11D-A37C-09 chr7:72873970 G>A maps to NM_032408.3 L1109L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr12:57000029 C>T did not map to a codon.
Sequencing variant TCGA-R6-A8WG-01A-11D-A37C-09 chr12:57007890 G>T maps to NM_013449.3 V256V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43C-01A-11D-A247-09 chr11:66283013 C>T maps to NM_024649.4 R146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OR-01A-11D-A27G-09 chr11:66297344 C>T maps to NM_024649.4 R465R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EZ-01A-11D-A36J-09 chr12:76740690 C>T maps to NM_024685.3 S358S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OF-01A-11D-A27G-09 chr4:122780221 G>T maps to NM_176824.1 I151I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr7:33296863 C>T maps to NM_198428.2 C153C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49N-01A-11D-A247-09 chr3:107492013 C>T maps to NM_001142568.1 D482D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OR-01A-11D-A27G-09 chr19:45314531 C>T maps to NM_005581.3 R45*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49N-01A-11D-A247-09 chr19:45322032 G>T maps to NM_005581.3 S410S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-A7RE-01A-11D-A351-09 chr19:45322679 C>T maps to NM_005581.3 R517R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr7:107221265 G>T maps to NM_001008405.2 G17*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93F-01A-21D-A37C-09 chr23:152967490 G>A did not map to a codon.
Sequencing variant TCGA-L5-A4OJ-01A-11D-A27G-09 chr16:75263636 G>A maps to NM_001170714.1 I841I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NS-01A-12D-A37C-09 chr20:52645407 T>C maps to NM_003657.2 K82K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RE-01A-11D-A33E-09 chr17:59152323 T>G maps to ENST00000407086 S721S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A8I0-01A-11D-A36J-09 chr17:59067399 C>T maps to ENST00000407086 H430H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S8-A6BV-01A-21D-A31U-09 chr17:59115361 C>T maps to ENST00000407086 D655D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A97I-01A-11D-A387-09 chr20:49434785 C>T maps to NM_198799.2 L73L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EO-01A-11D-A36J-09 chr19:49309923 G>T maps to NM_001190.3 G50G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49U-01A-31D-A27G-09 chr12:50236729 G>T maps to NM_181708.2 L47L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NE-01A-11D-A37C-09 chr3:165547507 T>G maps to NM_000055.2 S438S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NE-01A-11D-A37C-09 chr3:165548671 A>C maps to NM_000055.2 G50G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A5U6-01A-11D-A28B-09 chr3:165548073 G>A maps to NM_000055.2 L250L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A8I1-01A-11D-A36J-09 chr3:165503942 C>T maps to NM_000055.2 L558L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6L4-01A-11D-A31U-09 chr3:165547692 C>A maps to NM_000055.2 E377*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OE-01A-11D-A27G-09 chr19:41928276 T>C did not map to a codon.
Sequencing variant TCGA-V5-AASV-01A-11D-A387-09 chr6:80880997 G>A did not map to a codon.
Sequencing variant TCGA-IC-A6RE-01A-11D-A33E-09 chr14:99640660 T>A maps to NM_138576.2 K838*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FB-01A-11D-A33E-09 chr14:99723817 C>T maps to NM_138576.2 E139E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr18:60985683 C>T maps to NM_000633.2 L72L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93F-01A-21D-A37C-09 chr12:122468609 A>T maps to NM_020993.3 K33*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr12:122492853 A>C maps to NM_020993.3 R195R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HW-01A-22D-A351-09 chr16:30903910 C>T maps to NM_004765.2 E146E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RF-01A-13D-A33E-09 chr1:147084714 T>C maps to NM_004326.2 R29R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93D-01A-11D-A387-09 chr1:147095862 G>A maps to NM_004326.2 P1128P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A893-01A-11D-A36J-09 chr1:147091362 G>T maps to NM_004326.2 E468*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49V-01A-11D-A247-09 chr1:147096222 G>A maps to NM_004326.2 T1248T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HX-01A-11D-A33E-09 chr1:147091532 A>G maps to NM_004326.2 E524E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q9-A6FW-01A-31D-A31U-09 chr1:147091475 C>T maps to NM_004326.2 H505H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A938-01A-11D-A37C-09 chr11:118772249 C>T maps to NM_182557.2 A734A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr11:118772426 A>G maps to NM_182557.2 R675R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88W-01A-11D-A351-09 chr11:118773128 C>T maps to NM_182557.2 G441G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RE-01A-11D-A33E-09 chr6:136599655 A>G maps to NM_014739.2 S121S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NH-01A-11D-A37C-09 chr6:136599171 G>T maps to NM_014739.2 R283R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A3-01A-11D-A27G-09 chr6:136596730 G>T maps to NM_014739.2 A597A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XP-A8T6-01A-11D-A36J-09 chr6:136596727 G>A maps to NM_014739.2 S598S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A8-01A-32D-A27G-09 chr16:81324180 G>C maps to NM_017429.2 *548S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NQ-01A-11D-A36J-09 chr23:39914676 G>C did not map to a codon.
Sequencing variant TCGA-V5-AASX-01A-11D-A387-09 chr23:39922264 C>T did not map to a codon.
Sequencing variant TCGA-IG-A4P3-01A-11D-A27G-09 chr11:27679709 G>T maps to NM_001143810.1 R216R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FG-01A-11D-A33E-09 chr5:70791146 G>T maps to NM_018429.2 E571*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NS-01A-12D-A37C-09 chr5:70782417 G>T maps to NM_018429.2 E393*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3Y9-01A-12D-A247-09 chr23:18221838 A>C did not map to a codon.
Sequencing variant TCGA-L5-A8NJ-01A-11D-A36J-09 chr23:18220000 T>C did not map to a codon.
Sequencing variant TCGA-LN-A49R-01A-11D-A247-09 chr23:18189222 G>A did not map to a codon.
Sequencing variant TCGA-VR-AA4G-01A-11D-A37C-09 chr23:18221726 G>T did not map to a codon.
Sequencing variant TCGA-IG-A3Y9-01A-12D-A247-09 chr6:107391609 G>C maps to NM_001080450.2 S262*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OX-01A-21D-A28B-09 chr1:49208309 G>T maps to NM_024603.2 I293I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A9-01A-11D-A28B-09 chr1:49227055 C>A maps to NM_024603.2 E105*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-AAPN-01A-11D-A403-09 chr1:49227055 C>A maps to NM_024603.2 E105*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6XG-01B-11D-A33E-09 chr6:56880027 C>A maps to NM_152731.2 L132L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FA-01A-11D-A33E-09 chr23:102317849 T>G did not map to a codon.
Sequencing variant TCGA-L5-A8NH-01A-11D-A37C-09 chr23:102318196 C>A did not map to a codon.
Sequencing variant TCGA-2H-A9GI-01A-11D-A37C-09 chr16:14738313 C>T maps to NM_016561.2 C37C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EQ-01A-11D-A36J-09 chr23:152773853 G>A did not map to a codon.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr7:97841873 C>A maps to NM_177455.3 R85R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HZ-01A-31D-A351-09 chr3:5025109 C>T maps to NM_003670.2 P324P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88V-01A-11D-A351-09 chr10:60577320 G>A did not map to a codon.
Sequencing variant TCGA-L5-A8NG-01A-11D-A37C-09 chr10:60562849 T>C maps to NM_001080512.1 L677L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-A7RB-01A-11D-A351-09 chr10:60560030 G>A maps to NM_001080512.1 P601P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA4D-01A-11D-A37C-09 chr10:60273031 C>T maps to NM_001080512.1 S43S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr12:32480648 C>T maps to NM_001714.2 Y420Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OJ-01A-11D-A27G-09 chr9:95482725 G>A maps to NM_001003800.1 G306G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NQ-01A-11D-A36J-09 chr11:102201959 G>T maps to NM_182962.1 E438*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GF-01A-11D-A37C-09 chr2:32740344 T>C maps to NM_016252.3 S3619S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GO-01A-11D-A37C-09 chr2:32695335 C>T maps to NM_016252.3 Q2150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6F8-01A-11D-A33E-09 chr2:32693540 G>A maps to NM_016252.3 L1939L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RE-A7BO-01A-11D-A33E-09 chr2:32640224 G>T maps to NM_016252.3 L622L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93F-01A-21D-A37C-09 chr10:97960770 G>T maps to NM_013314.3 P326P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr10:97975101 G>A maps to NM_013314.3 P217P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EQ-01A-11D-A36J-09 chr7:43832404 C>T maps to NM_000712.3 Q116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L7-A6VZ-01A-12D-A33E-09 chr8:22037292 G>T maps to NM_006129.4 R304R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NT-01A-11D-A37C-09 chr23:50659105 C>A did not map to a codon.
Sequencing variant TCGA-LN-A4A9-01A-11D-A28B-09 chr23:50654012 C>G did not map to a codon.
Sequencing variant TCGA-R6-A6XG-01B-11D-A33E-09 chr23:50659504 G>A did not map to a codon.
Sequencing variant TCGA-S8-A6BV-01A-21D-A31U-09 chr23:50659037 C>T did not map to a codon.
Sequencing variant TCGA-XP-A8T6-01A-11D-A36J-09 chr20:6750871 C>T maps to NM_001200.2 F33F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NJ-01A-11D-A36J-09 chr6:55739326 T>G maps to NM_021073.2 R113R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HY-01A-12D-A351-09 chr6:7880461 G>A maps to NM_001718.4 P476P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RF-01A-13D-A33E-09 chr7:34014312 G>T did not map to a codon.
Sequencing variant TCGA-L5-A8NF-01A-11D-A37C-09 chr7:34118667 C>T maps to NM_133468.3 G426G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZR-A9CJ-01B-11D-A387-09 chr4:96052396 G>T maps to ENST00000440890 G300G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GM-01A-11D-A37C-09 chr2:203420070 C>T maps to NM_001204.6 S561S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FG-01A-11D-A33E-09 chr23:15549480 T>A did not map to a codon.
Sequencing variant TCGA-V5-A7RB-01A-11D-A351-09 chr23:15543484 C>A did not map to a codon.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr9:16436055 A>T maps to NM_017637.5 T712T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr10:133787442 G>T maps to NM_004052.2 S17S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XP-A8T7-01A-11D-A36J-09 chr10:133784443 C>A maps to NM_004052.2 E105*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FH-01A-11D-A33E-09 chr3:112996961 C>T maps to ENST00000273395 D521D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KH-A6WC-01A-11D-A33E-09 chr3:112997067 G>T maps to ENST00000273395 G557*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GM-01A-11D-A37C-09 chr4:13606488 G>A maps to NM_148894.2 Q679*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RE-01A-11D-A33E-09 chr4:13605187 T>A maps to NM_148894.2 T1112T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A939-01A-12D-A37C-09 chr4:13615148 C>T maps to NM_148894.2 E437E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr4:13601799 G>A maps to NM_148894.2 R2242*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NR-01A-11D-A37C-09 chr4:13604827 A>G maps to NM_148894.2 N1232N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EZ-01A-11D-A36J-09 chr4:13604638 C>T maps to NM_148894.2 S1295S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FG-01A-11D-A33E-09 chr1:149871804 G>T maps to NM_016074.3 E65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr1:149871914 C>T maps to NM_016074.3 V101V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93E-01A-11D-A37C-09 chr2:74362705 C>A maps to NM_001035505.1 L83L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FP-01A-31D-A387-09 chr20:31606540 C>A maps to NM_025227.1 T256T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA4D-01A-11D-A37C-09 chr22:32810403 A>G maps to NM_174932.2 L470L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6Y2-01B-11D-A33E-09 chr1:220236121 G>T maps to NM_006085.4 R217R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OW-01A-11D-A28B-09 chr17:65941985 C>T maps to ENST00000321892 Q2514*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FR-01A-11D-A387-09 chr7:140481411 C>A maps to NM_004333.4 G466*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HW-01A-22D-A351-09 chr12:112123539 G>A maps to NM_006768.3 P19P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A8I0-01A-11D-A36J-09 chr12:112093422 G>T maps to NM_006768.3 R420R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-M9-A5M8-01A-11D-A28B-09 chr12:112119529 C>T maps to NM_006768.3 P118P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GF-01A-11D-A37C-09 chr17:41276050 G>A maps to ENST00000471181 I21I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NI-01A-11D-A37C-09 chr17:41203113 G>T maps to ENST00000471181 I1788I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GJ-01A-11D-A37C-09 chr13:32971138 G>A maps to NM_000059.3 P3202P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FA-01A-11D-A33E-09 chr13:32906494 G>T maps to NM_000059.3 E294*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A891-01A-11D-A36J-09 chr13:32912070 T>A maps to NM_000059.3 A1193A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88S-01A-11D-A36J-09 chr22:50217248 C>T maps to ENST00000342989 L239L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NI-01A-11D-A37C-09 chr16:50353168 C>A maps to NM_001173984.2 E638*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr5:137495861 G>A maps to NM_139199.1 Q810*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A9-01A-11D-A28B-09 chr5:137498824 G>C maps to NM_139199.1 S694*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GK-01A-11D-A37C-09 chr5:889727 C>T maps to NM_001009877.2 W94*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NV-01A-11D-A37C-09 chr1:92428478 G>T maps to ENST00000347608 V68V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49Y-01A-11D-A27G-09 chr8:37702673 C>T maps to NM_018310.3 E198E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S8-A6BW-01A-11D-A31U-09 chr7:97921977 G>T maps to NM_001159491.1 T91T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88S-01A-11D-A36J-09 chr12:125509843 T>C maps to NM_080626.5 S208S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RE-A7BO-01A-11D-A33E-09 chr12:125509681 C>T maps to NM_080626.5 F154F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OE-01A-11D-A27G-09 chr17:59934421 G>A maps to NM_032043.2 Q126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EW-01A-11D-A36J-09 chr17:59885974 A>G maps to NM_032043.2 A257A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A97H-01A-11D-A387-09 chr3:9783053 G>A maps to NM_001003694.1 R595R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr3:9785475 G>A maps to NM_001003694.1 R842R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A8JD-01A-11D-A36J-09 chr3:9781321 C>T maps to NM_001003694.1 C413C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NS-01A-12D-A37C-09 chr6:36196794 G>A maps to NM_015695.2 K1132K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6F8-01A-11D-A33E-09 chr21:40587220 C>A maps to NM_018963.3 E1243*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3Y9-01A-12D-A247-09 chr23:80001093 C>G did not map to a codon.
Sequencing variant TCGA-IG-A3YA-01A-11D-A247-09 chr23:79940989 C>G did not map to a codon.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr23:79932173 T>C did not map to a codon.
Sequencing variant TCGA-L5-A4OH-01A-11D-A27G-09 chr23:79936908 G>T did not map to a codon.
Sequencing variant TCGA-L5-A4OJ-01A-11D-A27G-09 chr23:79939515 T>C did not map to a codon.
Sequencing variant TCGA-L5-A4OJ-01A-11D-A27G-09 chr23:79947626 T>A did not map to a codon.
Sequencing variant TCGA-IG-A50L-01A-11D-A27G-09 chr1:32846839 T>C maps to NM_001143888.1 P146P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8W8-01B-11D-A37C-09 chr1:32846845 C>T maps to NM_001143888.1 S144S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA4G-01A-11D-A37C-09 chr19:581391 G>C maps to NM_001728.2 L290L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43I-01A-11D-A247-09 chr3:49699192 C>T maps to NM_003458.3 L3305L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NS-01A-12D-A37C-09 chr1:55464885 C>T maps to NM_057176.2 I9I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EQ-01A-11D-A36J-09 chr1:55474126 G>T maps to NM_057176.2 L263L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-AAPN-01A-11D-A403-09 chr10:93768817 C>G maps to NM_003972.2 S1319*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GR-01A-12D-A37C-09 chr15:83687548 A>T maps to NM_025238.3 C400*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr15:83699021 A>G maps to NM_025238.3 F307F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RE-01A-11D-A33E-09 chr12:107713691 G>A maps to NM_001018072.1 P325P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A5B8-01A-11D-A28B-09 chr12:108051485 C>T maps to NM_001018072.1 S1102S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NJ-01A-11D-A36J-09 chr12:108029075 C>T maps to NM_001018072.1 S882S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GR-01A-12D-A37C-09 chr16:3642791 G>T maps to NM_032444.2 T745T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FP-01A-31D-A387-09 chr16:3640929 C>A maps to NM_032444.2 V903V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A5U7-01A-11D-A31U-09 chr10:124096187 C>A maps to ENST00000368994 C482*. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-L5-A4OI-01A-11D-A27G-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-VR-A8EX-01A-11D-A36J-09 chr14:105716549 C>T maps to NM_033271.2 L333L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NU-01A-11D-A36J-09 chr14:93723587 G>A maps to NM_001002860.2 R521*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49Y-01A-11D-A27G-09 chr21:18981447 A>G maps to NM_001130914.1 I5I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q9-A6FW-01A-31D-A31U-09 chr23:100614295 T>C did not map to a codon.
Sequencing variant TCGA-R6-A6XG-01B-11D-A33E-09 chr23:100611042 G>T did not map to a codon.
Sequencing variant TCGA-IG-A3QL-01A-11D-A247-09 chr6:26505211 G>T maps to NM_001732.2 E163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NG-01A-11D-A37C-09 chr6:26509197 C>T maps to NM_001732.2 F459F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6XG-01B-11D-A33E-09 chr6:26466200 C>T maps to NM_007049.3 R319*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OH-01A-11D-A27G-09 chr6:26408017 G>T maps to NM_007048.5 E185*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A51D-01A-11D-A27G-09 chr6:26452497 G>A maps to NM_006994.4 P538P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93D-01A-11D-A387-09 chr5:180424393 C>A maps to NM_197975.2 I193I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A625-01A-11D-A31U-09 chr2:111398881 G>T did not map to a codon.
Sequencing variant TCGA-L5-A8NV-01A-11D-A37C-09 chr2:111419340 C>T maps to NM_004336.3 Q345Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FD-01A-11D-A33E-09 chr15:40504782 C>T maps to ENST00000412359 C837C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A893-01A-11D-A36J-09 chr6:105573324 A>C maps to NM_007073.4 T160T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49M-01A-21D-A27G-09 chr17:56400113 C>T maps to NM_004758.2 L406L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HX-01A-11D-A33E-09 chr17:56383219 G>T maps to NM_004758.2 S1744*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A893-01A-11D-A36J-09 chr10:21435418 T>G maps to NM_001010896.2 R7R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NE-01A-11D-A37C-09 chr10:96971632 A>T did not map to a codon.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr10:127409790 G>T maps to ENST00000356792 G43*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A2-01A-31D-A27G-09 chr10:21805719 A>G maps to NM_207371.3 H344H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8W5-01B-11D-A37C-09 chr10:21805227 G>T maps to NM_207371.3 L508L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EQ-01A-11D-A36J-09 chr10:21804408 G>A maps to NM_207371.3 Y781Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EQ-01A-11D-A36J-09 chr10:21806550 G>T maps to NM_207371.3 L67L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8ER-01A-11D-A36J-09 chr10:21805719 A>G maps to NM_207371.3 H344H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASX-01A-11D-A387-09 chr10:5789016 C>G maps to NM_017782.4 A1211A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93D-01A-11D-A387-09 chr10:104569774 G>T maps to NM_001083913.1 E107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr10:72541635 G>T maps to NM_152710.2 T66T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NR-01A-11D-A37C-09 chr10:99969225 C>A maps to ENST00000314594 S452*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A8JE-01A-11D-A37C-09 chr10:71391540 C>T maps to ENST00000395055 D56D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6F8-01A-11D-A33E-09 chr10:50916524 C>A maps to NM_182554.2 T112T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EP-01A-31D-A403-09 chr10:50902629 C>A maps to NM_001042427.1 A88A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr10:23611348 G>A maps to NM_153714.2 L150L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GJ-01A-11D-A37C-09 chr10:33018339 G>T maps to ENST00000375025 E261*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GF-01A-11D-A37C-09 chr10:50530730 C>T maps to NM_001135196.1 S47S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OU-01A-11D-A28B-09 chr10:50531189 T>C maps to NM_001135196.1 A200A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASX-01A-11D-A387-09 chr10:50532635 T>G maps to NM_001135196.1 P682P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8W8-01B-11D-A37C-09 chr10:105974082 G>T maps to ENST00000389588 S173*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49V-01A-11D-A247-09 chr10:118425179 G>A maps to ENST00000388884 S71S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8W5-01B-11D-A37C-09 chr10:120085670 G>A maps to NM_022063.2 R180*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8WC-01A-11D-A37C-09 chr10:128193536 G>A maps to NM_001004298.2 Q78*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASV-01A-11D-A387-09 chr11:111753211 C>A maps to NM_022761.2 R56R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OX-01A-21D-A28B-09 chr11:64068304 C>T maps to NM_001039496.1 H66H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NK-01A-21D-A37C-09 chr11:76237669 G>A maps to ENST00000393457 G663G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3I8-01A-11D-A247-09 chr11:556251 G>A maps to NM_173573.2 F399F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-A7RB-01A-11D-A351-09 chr11:558685 C>T maps to NM_173573.2 W80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GF-01A-11D-A37C-09 chr11:33565592 C>A maps to ENST00000389726 S531S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NT-01A-11D-A37C-09 chr11:128772513 T>A maps to NM_145013.1 R126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49K-01A-11D-A247-09 chr11:30358339 T>A maps to NM_152316.1 *261K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A6-01A-11D-A27G-09 chr11:30352584 T>A maps to NM_152316.1 T30T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr11:71822268 A>G maps to NM_014042.2 F18F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L7-A6VZ-01A-12D-A33E-09 chr11:122817346 G>A maps to NM_024806.2 T592T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q9-A6FU-01A-11D-A31U-09 chr11:36669654 G>T maps to NM_138787.2 E150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6L6-01B-11D-A33E-09 chr11:66555628 A>G did not map to a codon.
Sequencing variant TCGA-Z6-AAPN-01A-11D-A403-09 chr11:66555678 C>G maps to ENST00000360962 S191*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA4G-01A-11D-A37C-09 chr11:82643984 G>T maps to NM_145018.3 P535P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88Z-01A-11D-A36J-09 chr11:63585505 C>T maps to NM_138471.1 D119D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8W5-01B-11D-A37C-09 chr11:109294748 G>T maps to NM_207645.3 R130R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GQ-01A-11D-A37C-09 chr11:61541624 C>T maps to NM_001127392.1 H434H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FA-01A-11D-A33E-09 chr11:61545850 G>T did not map to a codon.
Sequencing variant TCGA-L5-A8NW-01A-11D-A37C-09 chr11:61547318 G>T maps to NM_001127392.1 S751S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A939-01A-12D-A37C-09 chr12:91348411 C>T maps to NM_152638.2 S36S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr12:91348468 A>G maps to NM_152638.2 G17G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FB-01A-11D-A33E-09 chr12:32136924 G>A maps to NM_018169.3 S1012S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NJ-01A-11D-A36J-09 chr12:32135419 G>T maps to NM_018169.3 E511*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NW-01A-11D-A37C-09 chr12:32134930 C>T maps to NM_018169.3 Q348*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6Y0-01B-11D-A33E-09 chr12:32136171 T>C maps to NM_018169.3 A761A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A8HZ-01A-11D-A36J-09 chr12:13529162 C>A maps to ENST00000318426 L59L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GK-01A-11D-A37C-09 chr12:40114980 C>T maps to NM_001031748.2 C629C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L7-A6VZ-01A-12D-A33E-09 chr12:40040182 C>A maps to NM_001031748.2 P85P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6XG-01B-11D-A33E-09 chr12:40076538 G>T maps to NM_001031748.2 G271G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FP-01A-31D-A387-09 chr12:103872153 G>C maps to NM_001099336.1 T17T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49L-01A-11D-A247-09 chr12:102558359 C>T maps to NM_017915.3 R214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EP-01A-31D-A403-09 chr12:102558364 G>A maps to NM_017915.3 E215E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L7-A6VZ-01A-12D-A33E-09 chr12:88380087 C>A did not map to a codon.
Sequencing variant TCGA-2H-A9GJ-01A-11D-A37C-09 chr12:112685314 C>A maps to NM_001109662.2 E1258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A51D-01A-11D-A27G-09 chr12:112654171 G>A maps to NM_001109662.2 N2291N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OM-01A-11D-A27G-09 chr12:112717041 T>C maps to NM_001109662.2 S415S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OT-01A-11D-A28B-09 chr12:112622686 G>T maps to NM_001109662.2 L3189L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NF-01A-11D-A37C-09 chr12:112757111 C>T maps to NM_001109662.2 E60E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49Y-01A-11D-A27G-09 chr12:112673434 T>A maps to NM_001109662.2 G1694G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A8I1-01A-11D-A36J-09 chr12:112688860 G>T maps to NM_001109662.2 S1038S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FQ-01A-31D-A387-09 chr12:112641529 G>A maps to NM_001109662.2 S2600S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EZ-01A-11D-A36J-09 chr12:112622968 C>T maps to NM_001109662.2 V3095V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA4D-01A-11D-A37C-09 chr12:112690233 G>T maps to NM_001109662.2 R1010R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A938-01A-11D-A37C-09 chr12:64724795 G>A maps to NM_001170633.1 N144N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49W-01A-11D-A27G-09 chr12:97051987 G>C did not map to a codon.
Sequencing variant TCGA-R6-A6Y2-01B-11D-A33E-09 chr12:97102426 G>T maps to ENST00000342887 L615L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49Y-01A-11D-A27G-09 chr12:80615871 C>T maps to NM_173591.3 I103I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HY-01A-12D-A351-09 chr12:80714313 G>A maps to NM_173591.3 R1296R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FG-01A-11D-A33E-09 chr12:64609597 C>T maps to ENST00000311915 E127E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr12:48578354 C>T maps to NM_001013635.3 P150P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr12:48578459 G>T maps to NM_001013635.3 L185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NR-01A-11D-A37C-09 chr12:48578102 C>T maps to NM_001013635.3 D66D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr13:46946505 A>G maps to NM_025113.2 T35T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GH-01A-11D-A37C-09 chr13:39587468 G>A maps to NM_025138.3 G640G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S8-A6BV-01A-21D-A31U-09 chr13:39587522 T>C maps to NM_025138.3 P622P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6Y2-01B-11D-A33E-09 chr13:73320212 A>C maps to ENST00000377815 S350S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OH-01A-11D-A27G-09 chr13:37269256 G>C maps to NM_203451.2 V14V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A891-01A-11D-A36J-09 chr14:57960296 G>C maps to NM_018168.2 S46*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GQ-01A-11D-A37C-09 chr14:90420306 G>T maps to NM_145231.2 L38L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GH-01A-11D-A37C-09 chr14:77873848 G>T maps to NM_001113475.1 A163A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NV-01A-11D-A37C-09 chr14:77861024 G>T maps to NM_001113475.1 I343I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XP-A8T7-01A-11D-A36J-09 chr14:77873058 G>T maps to NM_138791.1 G230G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A4P3-01A-11D-A27G-09 chr14:59942613 G>T maps to NM_144581.1 G304G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A893-01A-11D-A36J-09 chr14:78174464 C>A maps to NM_031210.4 S4*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HY-01A-12D-A351-09 chr14:52466444 G>A maps to NM_016039.2 K131K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NG-01A-11D-A37C-09 chr14:99183560 A>C maps to NM_182560.2 R110R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3YB-01A-11D-A247-09 chr14:60936308 G>T maps to NM_174978.2 S206*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43I-01A-11D-A247-09 chr14:77493049 G>T maps to NM_024496.2 R362R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-A7RB-01A-11D-A351-09 chr14:77491801 G>A maps to NM_024496.2 G778G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RE-01A-11D-A33E-09 chr14:74206048 G>A maps to NM_001043318.1 F221F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6XQ-01B-11D-A33E-09 chr14:95932291 G>T maps to NM_152592.3 Y201*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6F8-01A-11D-A33E-09 chr14:103573187 C>A maps to NM_001077594.1 T511T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OW-01A-11D-A28B-09 chr14:105959064 G>T maps to ENST00000392523 L193L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OE-01A-11D-A27G-09 chr15:24923938 C>A maps to NM_018958.2 G975G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6KZ-01A-11D-A31U-09 chr15:24923215 A>G maps to NM_018958.2 Q734Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-AAPN-01A-11D-A403-09 chr15:24921664 A>T maps to NM_018958.2 S217S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A938-01A-11D-A37C-09 chr15:93015518 G>A maps to NM_153040.2 A47A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RE-A7BO-01A-11D-A33E-09 chr15:93015605 A>G maps to NM_153040.2 Q76Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA7I-01A-11D-A403-09 chr15:49867237 G>A maps to NM_152647.2 S205S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8W5-01B-11D-A37C-09 chr15:75498676 G>T maps to NM_015492.4 S96S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr15:36984337 C>T maps to NM_001130010.1 N146N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr15:90163023 G>A maps to NM_152259.3 P1035P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A9-01A-11D-A28B-09 chr15:90163008 T>C maps to NM_152259.3 Y1030Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A97H-01A-11D-A387-09 chr15:34646054 G>T maps to ENST00000438749 E343*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8WG-01A-11D-A37C-09 chr15:40544553 G>T maps to NM_001039905.1 R140R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93C-01A-11D-A387-09 chr16:67697102 G>A maps to NM_032140.1 I334I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A893-01A-11D-A36J-09 chr16:31519196 C>T maps to NM_022744.2 A101A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-AAPN-01A-11D-A403-09 chr16:19628043 C>T maps to NM_020314.5 Q469*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93E-01A-11D-A37C-09 chr16:67166781 T>C maps to NM_025187.3 L140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KH-A6WC-01A-11D-A33E-09 chr16:9210600 G>T maps to NM_014117.2 S220S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43C-01A-11D-A247-09 chr16:85743839 G>A maps to NM_206967.2 D34D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8W5-01B-11D-A37C-09 chr16:49430392 C>T maps to NM_144602.2 R152*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RE-A7BO-01A-11D-A33E-09 chr16:49407921 A>G maps to NM_144602.2 E24E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr16:67700902 G>A maps to NM_001012984.2 P10P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88Z-01A-11D-A36J-09 chr16:67702160 G>A maps to NM_001012984.2 L204L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A50L-01A-11D-A27G-09 chr16:19718329 T>A maps to NM_001012991.2 K427*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-AAPN-01A-11D-A403-09 chr16:1476217 C>T maps to NM_001010878.1 R135R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8ER-01A-11D-A36J-09 chr17:72956019 C>A maps to NM_030630.2 E322*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93E-01A-11D-A37C-09 chr17:37885786 G>T maps to NM_032339.3 C112*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A1-01A-21D-A27G-09 chr17:37886005 C>A maps to NM_032339.3 E66*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GJ-01A-11D-A37C-09 chr17:17962264 C>T maps to NM_024052.4 Y230Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A8JD-01A-11D-A36J-09 chr17:29231386 G>C maps to NM_024683.3 L64L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49N-01A-11D-A247-09 chr17:43334551 G>A maps to NM_152343.2 C12C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GF-01A-11D-A37C-09 chr17:10609814 G>A maps to NM_020233.4 W221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L7-A6VZ-01A-12D-A33E-09 chr17:42225281 G>T maps to NM_024032.3 V37V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GQ-01A-11D-A37C-09 chr17:79205687 G>A maps to NM_144679.2 S220S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NT-01A-11D-A37C-09 chr17:79210791 G>A maps to NM_144679.2 H67H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A97H-01A-11D-A387-09 chr17:45422436 G>T maps to NM_152347.4 G164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49M-01A-21D-A27G-09 chr17:45451873 C>G maps to NM_152347.4 S305*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr17:80401903 G>A maps to NM_001193657.1 A180A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49M-01A-21D-A27G-09 chr17:34185296 G>C maps to NM_152781.2 L353L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr17:8135520 A>G maps to NM_025099.5 A695A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NR-01A-11D-A37C-09 chr17:8133260 G>T maps to NM_025099.5 R987R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NS-01A-12D-A37C-09 chr17:57290841 C>T maps to NM_018149.6 D886D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A8HZ-01A-11D-A36J-09 chr17:57289729 G>A maps to NM_018149.6 P596P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-AAPN-01A-11D-A403-09 chr17:57288494 G>A maps to NM_018149.6 V361V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A8O2-01A-11D-A36J-09 chr17:7330414 G>T maps to NM_175734.4 E369*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NF-01A-11D-A37C-09 chr17:30665253 A>T maps to NM_022344.2 L155*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3Y9-01A-12D-A247-09 chr17:72588748 T>A maps to NM_152460.2 T188T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr17:72588241 G>A maps to NM_152460.2 A19A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3Y9-01A-12D-A247-09 chr17:35746183 C>T maps to NM_173625.3 Q213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KH-A6WC-01A-11D-A33E-09 chr17:3721642 C>A maps to NM_001114118.1 L408L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49V-01A-11D-A247-09 chr17:3719428 T>G maps to NM_001114118.1 P482P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3QL-01A-11D-A247-09 chr18:34376767 T>A maps to NM_015476.2 *301C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A8JE-01A-11D-A37C-09 chr18:33552862 G>T maps to NM_031446.3 S31S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OE-01A-11D-A27G-09 chr18:43796526 A>G maps to NM_145055.3 S227S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FD-01A-11D-A33E-09 chr18:30803177 A>C maps to NM_001105528.1 L608L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FG-01A-11D-A33E-09 chr18:30926331 G>T maps to NM_001105528.1 L167L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OT-01A-11D-A28B-09 chr18:30928926 A>G maps to NM_001105528.1 S128S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43E-01A-11D-A247-09 chr19:757290 C>T maps to NM_173481.2 D115D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GK-01A-11D-A37C-09 chr19:3624102 C>T maps to NM_021231.1 P75P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-AAPN-01A-11D-A403-09 chr19:16770257 C>G maps to ENST00000358726 L23L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A893-01A-11D-A36J-09 chr19:36494297 G>A maps to ENST00000455847 R564*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L7-A6VZ-01A-12D-A33E-09 chr19:55673608 C>T maps to ENST00000301249 P192P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OG-01A-11D-A27G-09 chr19:44251856 G>A maps to NM_019108.2 Q140*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FP-01A-31D-A387-09 chr19:17379660 G>T maps to NM_014173.2 E16*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3YB-01A-11D-A247-09 chr19:10200372 T>C did not map to a codon.
Sequencing variant TCGA-R6-A8WC-01A-11D-A37C-09 chr1:22970665 C>T maps to NM_172369.3 Y50Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q9-A6FU-01A-11D-A31U-09 chr10:16562629 G>A maps to NM_001010908.1 F145F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASV-01A-11D-A387-09 chr10:16556664 G>T maps to NM_001010908.1 Y210*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6F8-01A-11D-A33E-09 chr17:77043770 G>T maps to ENST00000392445 S159S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NQ-01A-11D-A36J-09 chr5:159776453 C>T maps to NM_031908.4 G238G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZR-A9CJ-01B-11D-A387-09 chr5:159776420 G>A maps to NM_031908.4 A249A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A938-01A-11D-A37C-09 chr22:37578335 G>A maps to NM_182486.1 R243R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43E-01A-11D-A247-09 chr13:24465622 G>A maps to NM_001007537.1 N269N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GK-01A-11D-A37C-09 chr1:244640840 A>G did not map to a codon.
Sequencing variant TCGA-L5-A893-01A-11D-A36J-09 chr1:244780850 T>G maps to NM_001130957.1 S837S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A8O2-01A-11D-A36J-09 chr1:172414299 T>C did not map to a codon.
Sequencing variant TCGA-L5-A4OT-01A-11D-A28B-09 chr1:200878068 G>T did not map to a codon.
Sequencing variant TCGA-L5-A891-01A-11D-A36J-09 chr1:200878411 T>C maps to NM_018265.2 P367P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6Y0-01B-11D-A33E-09 chr1:200868724 G>T maps to NM_018265.2 A145A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr1:210006626 C>T maps to NM_014388.6 H162H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr1:210016855 G>A maps to NM_014388.6 T614T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A4QT-01A-21D-A27G-09 chr1:162343861 G>T maps to NM_182581.3 G254G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EU-01A-11D-A36J-09 chr1:162344172 G>A maps to NM_182581.3 R151*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA7B-01A-31D-A403-09 chr1:36785718 C>T maps to NM_001162530.1 V485V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A938-01A-11D-A37C-09 chr1:220863884 G>A maps to NM_024709.4 A47A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6L4-01A-11D-A31U-09 chr1:179504086 T>C maps to NM_144696.4 S1007S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3Y9-01A-12D-A247-09 chr1:170959079 T>C maps to NM_001163629.1 L322L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A97I-01A-11D-A387-09 chr1:170959001 A>T maps to NM_001163629.1 K296*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A893-01A-11D-A36J-09 chr1:170958994 G>T did not map to a codon.
Sequencing variant TCGA-L5-A8NN-01A-11D-A37C-09 chr1:170934322 C>A maps to NM_001163629.1 S136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EY-01A-11D-A36J-09 chr1:170967361 G>T maps to NM_001163629.1 E515*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OH-01A-11D-A27G-09 chr1:231374737 G>T maps to ENST00000421623 T105T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A6QS-01A-12D-A33E-09 chr1:26161543 C>T maps to NM_024037.1 K338K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NH-01A-11D-A37C-09 chr1:26185815 G>A maps to NM_024037.1 C11C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XP-A8T7-01A-11D-A36J-09 chr1:16719935 C>T maps to NM_001114600.1 S105S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A2-01A-31D-A27G-09 chr1:53163914 G>T maps to NM_023077.2 C28*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4MR-01A-11D-A28B-09 chr1:27278223 G>C maps to NM_152365.2 Y216*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A4P3-01A-11D-A27G-09 chr1:75112383 G>T maps to NM_001002912.4 A70A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A6QS-01A-12D-A33E-09 chr1:75086593 G>T maps to NM_001002912.4 S275*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93D-01A-11D-A387-09 chr1:75102067 G>A maps to NM_001002912.4 Q167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88T-01A-11D-A351-09 chr1:75038471 A>G maps to NM_001002912.4 I974I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88T-01A-11D-A351-09 chr1:75086433 G>T maps to NM_001002912.4 G328G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OE-01A-11D-A27G-09 chr1:55273284 C>A maps to NM_001110533.1 A93A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A8-01A-32D-A27G-09 chr1:156314404 C>T maps to NM_144627.3 L23L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A893-01A-11D-A36J-09 chr1:231004078 C>T maps to NM_032800.2 R60R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A7DP-01A-31D-A33E-09 chr1:185114694 G>T maps to NM_030934.4 T177T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr1:185151133 T>A maps to NM_001105518.1 P361P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr1:28208866 C>T maps to NM_001105556.1 G344G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EX-01A-11D-A36J-09 chr1:85725157 C>T maps to NM_198077.3 E53E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49P-01A-11D-A247-09 chr1:151022912 G>T did not map to a codon.
Sequencing variant TCGA-VR-A8ER-01A-11D-A36J-09 chr1:233113959 C>T maps to NM_032324.1 Q186*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FA-01A-11D-A33E-09 chr1:223567257 G>T maps to NM_152610.2 P147P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S8-A6BW-01A-11D-A31U-09 chr1:223568088 G>C maps to NM_152610.2 L424L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GG-01A-11D-A37C-09 chr1:209956262 C>T maps to NM_152485.2 E239E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A1-01A-21D-A27G-09 chr1:153610908 A>G maps to NM_015607.2 A68A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93F-01A-21D-A37C-09 chr1:60506761 G>T maps to NM_152377.2 T128T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RE-01A-11D-A33E-09 chr1:34663140 T>A maps to NM_001134734.1 C212*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-A7RE-01A-11D-A351-09 chr1:34663155 G>A maps to NM_001134734.1 K217K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6Y0-01B-11D-A33E-09 chr20:55108438 C>G maps to NM_001013646.2 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8W8-01B-11D-A37C-09 chr20:2796201 G>T maps to NM_080739.2 L93L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GK-01A-11D-A37C-09 chr20:34571993 C>T maps to ENST00000373973 D166D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr20:34599097 T>C maps to ENST00000373973 N396N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NR-01A-11D-A37C-09 chr20:30605786 G>A maps to ENST00000300415 L96L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FP-01A-31D-A387-09 chr20:61167652 C>A maps to NM_178463.3 V41V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GH-01A-11D-A37C-09 chr20:31671357 C>T maps to NM_182519.2 R119*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KH-A6WC-01A-11D-A33E-09 chr20:3268357 G>T maps to NM_001009984.1 A802A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OR-01A-11D-A27G-09 chr20:3299047 C>T did not map to a codon.
Sequencing variant TCGA-LN-A5U7-01A-11D-A31U-09 chr20:3240607 G>A maps to NM_001009984.1 G980G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A5B8-01A-11D-A28B-09 chr20:20269494 C>G maps to ENST00000389655 L1016L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA4G-01A-11D-A37C-09 chr20:20258011 C>A maps to ENST00000389655 I905I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OJ-01A-11D-A27G-09 chr20:3804697 G>T maps to NM_018347.1 S119S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EU-01A-11D-A36J-09 chr20:13765854 C>T maps to NM_024120.4 F47F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FP-01A-31D-A387-09 chr20:31767423 C>A maps to NM_080574.2 I220I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FP-01A-31D-A387-09 chr20:18794791 G>T maps to NM_178483.2 P111P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GQ-01A-11D-A37C-09 chr21:45950994 T>C maps to ENST00000443468 P188P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr21:45947291 T>G maps to ENST00000443468 T346T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49Y-01A-11D-A27G-09 chr21:45950949 C>A maps to ENST00000443468 R203R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GK-01A-11D-A37C-09 chr21:47734719 G>C maps to NM_058180.3 A173A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49S-01A-11D-A247-09 chr22:20049071 C>T maps to NM_152906.4 N157N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OS-01A-11D-A28B-09 chr22:32788228 C>A maps to NM_014306.4 E470*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OE-01A-11D-A27G-09 chr22:32110193 C>A maps to NM_173566.2 E1211*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr22:24984228 C>T maps to NM_207644.2 S125S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NE-01A-11D-A37C-09 chr22:46643006 C>T maps to NM_207327.4 P75P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASX-01A-11D-A387-09 chr22:32546458 G>A maps to NM_001010859.1 V167V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GR-01A-12D-A37C-09 chr21:43327822 C>T maps to NM_015500.1 T363T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L7-A56G-01A-21D-A27G-09 chr11:118981760 G>A did not map to a codon.
Sequencing variant TCGA-L5-A88V-01A-11D-A351-09 chr11:73789403 C>T maps to ENST00000334126 K1453K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A893-01A-11D-A36J-09 chr2:26999240 G>T maps to NM_017877.3 G179G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr2:75916351 C>A did not map to a codon.
Sequencing variant TCGA-JY-A93F-01A-21D-A37C-09 chr2:26672861 A>T did not map to a codon.
Sequencing variant TCGA-M9-A5M8-01A-11D-A28B-09 chr2:26654870 G>A maps to NM_145038.2 V295V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OF-01A-11D-A27G-09 chr2:106690369 C>T maps to NM_032411.2 A52A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr2:70387882 G>A maps to NM_017880.1 R464*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A8JD-01A-11D-A36J-09 chr2:70377610 C>T maps to NM_017880.1 E534E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NS-01A-12D-A37C-09 chr2:99454592 C>T maps to NM_207362.2 E76E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FP-01A-31D-A387-09 chr2:99454682 C>A maps to NM_207362.2 P46P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49S-01A-11D-A247-09 chr2:37468804 C>T maps to NM_144736.4 Q165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GI-01A-11D-A37C-09 chr2:219227597 C>T maps to NM_198559.1 T201T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NQ-01A-11D-A36J-09 chr2:29297064 G>A maps to NM_001029883.1 F21F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OJ-01A-11D-A27G-09 chr2:209045467 C>T did not map to a codon.
Sequencing variant TCGA-LN-A9FP-01A-31D-A387-09 chr2:209049740 G>T maps to NM_001099334.2 G19G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NH-01A-11D-A37C-09 chr2:242815413 G>A maps to NM_173821.2 P569P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NR-01A-11D-A37C-09 chr2:242811961 C>T maps to NM_173821.2 A18A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NT-01A-11D-A37C-09 chr2:242815164 C>T maps to NM_173821.2 G486G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L7-A6VZ-01A-12D-A33E-09 chr2:85049136 G>A maps to ENST00000409520 H474H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EX-01A-11D-A36J-09 chr2:85051237 G>A maps to ENST00000409520 A391A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A3-01A-11D-A27G-09 chr19:6693003 C>T maps to NM_000064.2 L1107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4MR-01A-11D-A28B-09 chr19:6697513 C>T maps to NM_000064.2 K879K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EQ-01A-11D-A36J-09 chr19:6684427 C>T maps to NM_000064.2 K1381K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EP-01A-31D-A403-09 chr12:8212672 C>A maps to NM_004054.2 G37*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZR-A9CJ-01B-11D-A387-09 chr12:8211652 G>A maps to NM_004054.2 R377*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A5U6-01A-11D-A28B-09 chr3:119452301 T>A maps to NM_033364.3 G431G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NK-01A-21D-A37C-09 chr3:10146305 G>T maps to NM_001164839.1 C51*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6F8-01A-11D-A33E-09 chr3:99886580 G>T did not map to a codon.
Sequencing variant TCGA-L5-A8NK-01A-21D-A37C-09 chr3:118865477 C>T maps to NM_152539.2 R148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A8I1-01A-11D-A36J-09 chr3:88199285 C>T maps to NM_173824.3 A28A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GO-01A-11D-A37C-09 chr3:43121489 G>A maps to NM_032806.4 V478V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FA-01A-11D-A33E-09 chr3:43121237 G>T maps to NM_032806.4 C562*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NV-01A-11D-A37C-09 chr3:56707744 G>A maps to ENST00000447900 Q114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GN-01A-11D-A37C-09 chr4:57842620 G>T maps to NM_032313.2 I377I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr4:37592204 A>G maps to NM_018302.2 V176V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr4:113539991 T>A maps to NM_018392.4 V402V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S8-A6BV-01A-21D-A31U-09 chr4:113508883 G>T maps to NM_018392.4 S1110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88W-01A-11D-A351-09 chr4:8448311 A>G maps to NM_152544.2 E243E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr4:121958468 G>A maps to NM_024574.3 H219H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NK-01A-21D-A37C-09 chr4:87809348 C>A maps to NM_144645.3 E49*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GL-01A-12D-A37C-09 chr4:98480235 A>G maps to NM_174952.2 I451I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93D-01A-11D-A387-09 chr4:165878494 G>A maps to NM_153027.1 T107T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr4:165878446 C>A maps to NM_153027.1 R91R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr4:184605468 G>T maps to NM_021942.4 G460*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HX-01A-11D-A33E-09 chr4:184601285 G>T maps to NM_021942.4 G327*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49V-01A-11D-A247-09 chr4:5981915 C>T maps to ENST00000324058 E51E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A4QS-01A-11D-A27G-09 chr19:47823631 C>T maps to ENST00000355085 R200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr19:47824041 G>A maps to ENST00000355085 T336T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FG-01A-11D-A33E-09 chr5:134782216 C>T maps to NM_130848.2 W194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GO-01A-11D-A37C-09 chr5:32789564 T>C maps to NM_024563.3 L20L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A891-01A-11D-A36J-09 chr5:175740725 G>T maps to ENST00000443967 L570L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4MQ-01A-11D-A28B-09 chr5:139622994 G>A maps to NM_032412.3 *98*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GF-01A-11D-A37C-09 chr5:43494613 T>C maps to NM_198566.2 T414T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L7-A6VZ-01A-12D-A33E-09 chr5:43492872 G>T maps to NM_198566.2 G478G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GF-01A-11D-A37C-09 chr5:93856417 G>T maps to ENST00000513200 R169R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A4-01A-11D-A27G-09 chr5:43039890 C>T maps to NM_001014279.2 A86A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GJ-01A-11D-A37C-09 chr5:154202945 C>T did not map to a codon.
Sequencing variant TCGA-LN-A49N-01A-11D-A247-09 chr5:156770148 G>A maps to NM_001001343.3 C132C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NW-01A-11D-A37C-09 chr5:172537684 A>G maps to NM_153607.2 S526S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GI-01A-11D-A37C-09 chr5:37176060 C>T maps to NM_023073.3 G1976G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr5:37224364 G>T maps to NM_023073.3 I857I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NW-01A-11D-A37C-09 chr5:37206492 A>G maps to NM_023073.3 S985S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XP-A8T7-01A-11D-A36J-09 chr5:37183046 G>A maps to NM_023073.3 L1746L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NS-01A-12D-A37C-09 chr5:60455835 G>A maps to NM_001048249.3 Q55*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8W8-01B-11D-A37C-09 chr5:179267904 C>T maps to NM_016175.3 S168S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr5:125971899 G>T maps to NM_207408.1 V124V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8WG-01A-11D-A37C-09 chr5:7835548 C>T maps to NM_001089584.1 L70L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GF-01A-11D-A37C-09 chr5:159821726 G>T maps to NM_022090.3 A257A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A5U7-01A-11D-A31U-09 chr5:159821567 T>C maps to NM_022090.3 L310L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L7-A56G-01A-21D-A27G-09 chr5:41160289 G>C maps to NM_001115131.1 G546G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HX-01A-11D-A33E-09 chr5:41199894 G>T maps to NM_001115131.1 C140*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA7D-01A-11D-A403-09 chr6:11768589 G>T maps to NM_001143948.1 V78V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49W-01A-11D-A27G-09 chr6:34574628 C>T maps to NM_024294.2 T188T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RE-A7BO-01A-11D-A33E-09 chr6:165715285 T>C maps to NM_144980.3 E175E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4ON-01A-11D-A27G-09 chr6:54095681 T>G maps to ENST00000502396 S963S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr6:88120370 G>A maps to NM_001031743.2 V59V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OP-01A-11D-A27G-09 chr6:88173823 A>G maps to NM_001031743.2 P575P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr6:97676825 T>A maps to NM_198468.2 R661R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GM-01A-11D-A37C-09 chr6:99729192 C>A maps to NM_032511.2 L359L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GL-01A-12D-A37C-09 chr6:121577238 T>A maps to ENST00000275159 A642A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8WG-01A-11D-A37C-09 chr6:121642777 C>T did not map to a codon.
Sequencing variant TCGA-L5-A8NR-01A-11D-A37C-09 chr6:127837153 G>A maps to NM_001012279.2 R202R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A51D-01A-11D-A27G-09 chr6:133108701 T>C maps to NM_052831.2 P124P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RE-01A-11D-A33E-09 chr6:118786714 A>C maps to NM_001042475.2 A757A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr6:118887390 G>A maps to NM_001042475.2 S107S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q9-A6FW-01A-31D-A31U-09 chr6:118887414 A>C maps to NM_001042475.2 T99T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FO-01A-11D-A387-09 chr6:36290145 G>T maps to NM_001010903.4 S515S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NI-01A-11D-A37C-09 chr6:43970523 G>A maps to NM_153246.4 A130A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NW-01A-11D-A37C-09 chr6:112420501 G>T maps to NM_001033564.1 G6*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4MR-01A-11D-A28B-09 chr6:31692524 C>T maps to NM_025260.2 L182L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RE-01A-11D-A33E-09 chr6:31626854 C>G maps to NM_021184.3 P290P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OJ-01A-11D-A27G-09 chr6:151857457 T>G maps to ENST00000367290 T21T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NI-01A-11D-A37C-09 chr5:40934521 A>C maps to NM_000587.2 G78G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A6-01A-11D-A27G-09 chr7:31732093 A>T maps to NM_006658.4 S13S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GR-01A-12D-A37C-09 chr7:6639484 G>A maps to NM_024067.2 L202L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASX-01A-11D-A387-09 chr7:6631455 G>C maps to NM_024067.2 V124V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GO-01A-11D-A37C-09 chr7:2579268 G>A maps to NM_152743.3 F502F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NR-01A-11D-A37C-09 chr7:23349146 G>A maps to NM_138446.1 E230E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49R-01A-11D-A247-09 chr7:25191223 T>C maps to NM_138811.3 V225V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NL-01A-12D-A37C-09 chr7:142636711 C>T maps to NM_178829.4 G23G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XP-A8T6-01A-11D-A36J-09 chr7:39611881 G>A maps to NM_020192.3 L86L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GO-01A-11D-A37C-09 chr7:129847881 G>A maps to NM_145268.3 W44*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93C-01A-11D-A387-09 chr7:100084521 C>T maps to ENST00000423930 I49I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-A7RE-01A-11D-A351-09 chr7:100084482 C>T maps to ENST00000423930 P36P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L7-A6VZ-01A-12D-A33E-09 chr7:100816687 G>A maps to NM_198571.2 F142F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr7:120704314 G>A maps to NM_024913.4 Q188Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49S-01A-11D-A247-09 chr7:120906459 G>A maps to NM_024913.4 L830L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FP-01A-31D-A387-09 chr7:120907295 C>A maps to NM_024913.4 I887I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HX-01A-11D-A33E-09 chr7:89894641 G>T maps to NM_001039706.2 S128S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FP-01A-31D-A387-09 chr7:89900934 C>T maps to NM_001039706.2 Q210*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A8JD-01A-11D-A36J-09 chr7:6370416 T>C maps to NM_001037163.1 E123E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr1:57378167 G>A maps to NM_000562.2 L491L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6XQ-01B-11D-A33E-09 chr1:57378298 G>T did not map to a codon.
Sequencing variant TCGA-L5-A8NH-01A-11D-A37C-09 chr1:57431534 G>T maps to NM_000066.2 G29G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NT-01A-11D-A37C-09 chr1:57415410 G>T maps to NM_000066.2 Y227*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HX-01A-11D-A33E-09 chr8:69699680 G>T maps to NM_052958.2 E487*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RE-A7BO-01A-11D-A33E-09 chr8:33361279 C>A maps to NM_001102401.1 P367P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A97H-01A-11D-A387-09 chr8:67793085 G>T maps to NM_173518.4 E238*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A8I0-01A-11D-A36J-09 chr8:67796184 C>T maps to NM_173518.4 C343C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr8:99102177 A>G maps to NM_173549.2 P311P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr8:22458525 G>T maps to ENST00000450780 E119*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GF-01A-11D-A37C-09 chr8:144652707 C>T maps to NM_001100878.1 P280P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RE-01A-11D-A33E-09 chr8:144654592 G>A maps to NM_001100878.1 Q98*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A4P3-01A-11D-A27G-09 chr8:12879454 C>T maps to NM_020844.2 L423L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NI-01A-11D-A37C-09 chr8:12878967 T>C maps to NM_020844.2 T260T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OG-01A-11D-A27G-09 chr8:27922179 G>A maps to ENST00000341513 A260A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NQ-01A-11D-A36J-09 chr8:27925048 G>T maps to ENST00000341513 I231I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3Y9-01A-12D-A247-09 chr5:39341297 G>T maps to NM_001737.3 C142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EO-01A-11D-A36J-09 chr9:132084745 G>A maps to NM_001012715.3 W218*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43M-01A-11D-A247-09 chr9:104238318 G>T maps to NM_032342.1 S352S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NR-01A-11D-A37C-09 chr9:35045583 C>T maps to NM_203299.2 S986S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr9:130925725 C>T maps to NM_024112.3 Y28Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr9:140147121 G>A maps to ENST00000388931 S167S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EY-01A-11D-A36J-09 chr9:34381091 C>T maps to NM_032596.3 S170S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GL-01A-12D-A37C-09 chr9:132375865 G>A maps to NM_199350.3 S297S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr9:111698644 T>C maps to NM_017832.3 I63I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43I-01A-11D-A247-09 chr9:86554641 A>T maps to NM_032307.3 Y270*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A1-01A-21D-A27G-09 chr9:86570358 C>T maps to NM_032307.3 A178A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8WG-01A-11D-A37C-09 chr9:4661988 G>T maps to ENST00000454239 L29L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93F-01A-21D-A37C-09 chr9:71155463 G>A maps to NM_153237.1 A89A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A97H-01A-11D-A387-09 chr9:90503679 G>T maps to NM_178828.4 S1426S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49U-01A-31D-A27G-09 chr9:90502182 G>A maps to NM_178828.4 Q927Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6L4-01A-11D-A31U-09 chr9:90502632 A>C maps to NM_178828.4 S1077S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NQ-01A-11D-A36J-09 chr9:114510479 C>T did not map to a codon.
Sequencing variant TCGA-R6-A6Y2-01B-11D-A33E-09 chr9:114454720 G>T maps to NM_173521.3 S1115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93F-01A-21D-A37C-09 chr9:135763818 C>T maps to ENST00000372136 Q164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NI-01A-11D-A37C-09 chr9:15723678 G>T maps to NM_173550.2 E476*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A4-01A-11D-A27G-09 chr9:15744550 C>G maps to NM_173550.2 S777*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A5B8-01A-11D-A28B-09 chr1:150236221 T>C maps to NM_012113.1 L298L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NS-01A-12D-A37C-09 chr1:150235228 T>G maps to NM_012113.1 Y174*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EQ-01A-11D-A36J-09 chr8:86389488 C>T maps to NM_000067.2 S216S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49S-01A-11D-A247-09 chr16:66887277 G>C did not map to a codon.
Sequencing variant TCGA-LN-A49S-01A-11D-A247-09 chr8:61178528 C>T maps to NM_004056.4 Q124Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49V-01A-11D-A247-09 chr8:61121436 T>C maps to NM_004056.4 A260A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EY-01A-11D-A36J-09 chr8:61135294 C>A maps to NM_004056.4 V217V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASX-01A-11D-A387-09 chr9:35676358 C>A maps to NM_001216.2 G271G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GN-01A-11D-A37C-09 chr2:231657971 A>G maps to NM_001130850.1 R108R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NF-01A-11D-A37C-09 chr13:49951207 G>A maps to NM_001079670.1 N57N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OE-01A-11D-A27G-09 chr22:24451335 C>T maps to NM_012295.3 T269T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NE-01A-11D-A37C-09 chr22:24561507 C>T maps to NM_012295.3 R1641*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NN-01A-11D-A37C-09 chr22:24479284 C>T maps to NM_012295.3 Y951Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RE-01A-11D-A33E-09 chr12:121104684 C>G maps to NM_001033677.1 V365V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6DN-01B-11D-A31U-09 chr12:121098878 C>T maps to NM_001033677.1 D315D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OJ-01A-11D-A27G-09 chr1:65145404 G>T maps to ENST00000371073 R1124R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XP-A8T6-01A-11D-A36J-09 chr1:65143952 G>A maps to ENST00000371073 V1068V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GN-01A-11D-A37C-09 chr19:13616886 G>T maps to NM_023035.2 S51*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3Y9-01A-12D-A247-09 chr19:13397431 G>T maps to NM_023035.2 V1150V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FB-01A-11D-A33E-09 chr19:13441079 C>T maps to NM_023035.2 Q442Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FE-01A-11D-A33E-09 chr19:13342532 G>T maps to NM_023035.2 C1801*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93D-01A-11D-A387-09 chr19:13441141 G>T maps to NM_023035.2 R422R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KH-A6WC-01A-11D-A33E-09 chr19:13441097 G>T maps to NM_023035.2 P436P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OU-01A-11D-A28B-09 chr19:13414638 G>A maps to NM_023035.2 G683G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EZ-01A-11D-A36J-09 chr19:13470460 G>A maps to NM_023035.2 Q313*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XP-A8T6-01A-11D-A36J-09 chr19:13368365 C>A did not map to a codon.
Sequencing variant TCGA-2H-A9GI-01A-11D-A37C-09 chr9:140773592 G>A maps to ENST00000277549 T124T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4MR-01A-11D-A28B-09 chr9:141016130 G>T maps to ENST00000277549 E2235*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FB-01A-11D-A33E-09 chr12:2778184 G>T maps to NM_199460.2 L1618L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr12:2693756 G>A maps to NM_199460.2 E771E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A893-01A-11D-A36J-09 chr12:2706456 T>G did not map to a codon.
Sequencing variant TCGA-LN-A9FP-01A-31D-A387-09 chr12:2760888 G>T maps to NM_199460.2 G1391G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6KZ-01A-11D-A31U-09 chr12:2224507 C>T maps to NM_199460.2 I56I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RE-A7BO-01A-11D-A33E-09 chr12:2659136 C>T maps to NM_199460.2 S473S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S8-A6BW-01A-11D-A31U-09 chr12:2690839 C>G maps to NM_199460.2 L660L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OR-01A-11D-A27G-09 chr3:53766989 G>A did not map to a codon.
Sequencing variant TCGA-LN-A9FP-01A-31D-A387-09 chr3:53766861 G>T maps to NM_001128840.1 E832*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GG-01A-11D-A37C-09 chr1:181752855 G>C maps to ENST00000357570 T1802T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GO-01A-11D-A37C-09 chr1:181701789 C>A maps to ENST00000357570 L856L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A939-01A-12D-A37C-09 chr1:181684508 G>T maps to ENST00000357570 G403*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OO-01A-11D-A27G-09 chr1:181453095 C>T maps to ENST00000357570 F72F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OR-01A-11D-A27G-09 chr1:181745355 A>G maps to ENST00000357570 R1753R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49Y-01A-11D-A27G-09 chr1:181685206 G>T maps to ENST00000357570 R419R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49Y-01A-11D-A27G-09 chr1:181688894 G>A maps to ENST00000357570 V549V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A8-01A-32D-A27G-09 chr1:181767729 C>T maps to ENST00000357570 A2234A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FP-01A-31D-A387-09 chr1:181767766 G>T maps to ENST00000357570 E2247*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6Y2-01B-11D-A33E-09 chr1:181701651 C>G maps to ENST00000357570 P810P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RE-A7BO-01A-11D-A33E-09 chr1:181740472 G>A maps to ENST00000357570 R1642R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XP-A8T8-01A-11D-A36J-09 chr1:181724428 G>A maps to ENST00000357570 V1295V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GI-01A-11D-A37C-09 chr23:49069169 T>C did not map to a codon.
Sequencing variant TCGA-IC-A6RE-01A-11D-A33E-09 chr23:49088265 C>T did not map to a codon.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr23:49087003 G>A did not map to a codon.
Sequencing variant TCGA-L5-A4OP-01A-11D-A27G-09 chr23:49076163 T>G did not map to a codon.
Sequencing variant TCGA-L5-A4OR-01A-11D-A27G-09 chr23:49082517 G>A did not map to a codon.
Sequencing variant TCGA-L5-A8NF-01A-11D-A37C-09 chr23:49063211 C>T did not map to a codon.
Sequencing variant TCGA-Z6-A8JD-01A-11D-A36J-09 chr23:49076201 C>G did not map to a codon.
Sequencing variant TCGA-L5-A88S-01A-11D-A36J-09 chr17:48694852 G>T maps to NM_018896.3 L1692L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NI-01A-11D-A37C-09 chr17:48646257 C>T maps to NM_018896.3 V90V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RE-A7BO-01A-11D-A33E-09 chr17:48678462 G>T maps to NM_018896.3 V1281V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NL-01A-12D-A37C-09 chr16:1250519 C>T maps to NM_021098.2 N356N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr16:1259363 C>T maps to NM_021098.2 I1232I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6KZ-01A-11D-A31U-09 chr16:1245070 C>A maps to NM_021098.2 C133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8ER-01A-11D-A36J-09 chr16:1256130 C>T maps to NM_021098.2 D877D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FP-01A-31D-A387-09 chr22:39996622 A>T maps to NM_021096.3 T149T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EY-01A-11D-A36J-09 chr22:40036970 C>A maps to NM_021096.3 C280*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZR-A9CJ-01B-11D-A387-09 chr22:40036988 C>A maps to NM_021096.3 L286L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q9-A6FW-01A-31D-A31U-09 chr1:201063083 G>A maps to NM_000069.2 Y108Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6Y0-01B-11D-A33E-09 chr1:201047062 G>T maps to NM_000069.2 P521P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3YC-01A-11D-A247-09 chr7:81964468 G>A maps to NM_000722.2 N92N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr7:81637039 C>T maps to NM_000722.2 P465P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A8-01A-32D-A27G-09 chr7:81714151 G>T maps to NM_000722.2 R197R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q9-A6FW-01A-31D-A31U-09 chr7:81765971 G>A maps to NM_000722.2 Y125Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OW-01A-11D-A28B-09 chr3:54798377 T>C maps to NM_018398.2 T460T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr12:2019082 C>A maps to NM_172364.4 E159*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASX-01A-11D-A387-09 chr12:1995135 G>A maps to NM_172364.4 R355*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OJ-01A-11D-A27G-09 chr17:37342800 G>T maps to NM_000723.3 S192S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NJ-01A-11D-A36J-09 chr10:18827126 T>C maps to NM_201596.2 L441L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49M-01A-21D-A27G-09 chr12:49217549 C>G maps to NM_000725.2 V85V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-M9-A5M8-01A-11D-A28B-09 chr12:49221666 C>T maps to NM_000725.2 P480P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr17:64881305 C>T maps to NM_145811.2 P259P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XP-A8T8-01A-11D-A36J-09 chr19:54485598 G>A maps to NM_031895.5 S258S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HX-01A-11D-A33E-09 chr2:27447237 C>A maps to NM_004341.3 L378L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FR-01A-11D-A387-09 chr2:27456546 C>T maps to NM_004341.3 S1090S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A8O2-01A-11D-A36J-09 chr11:115080345 T>G maps to NM_014333.3 T342T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OT-01A-11D-A28B-09 chr3:85961682 A>G maps to NM_153184.3 L223L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GF-01A-11D-A37C-09 chr1:159162425 C>T maps to NM_021189.3 S130S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NQ-01A-11D-A36J-09 chr1:159163318 C>T maps to NM_021189.3 L197L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A8JD-01A-11D-A36J-09 chr19:44130330 G>A maps to NM_145296.1 N203N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASW-01A-11D-A403-09 chr3:62499334 G>T maps to NM_183394.2 S876S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZR-A9CJ-01B-11D-A387-09 chr3:62385091 C>A maps to ENST00000383709 E1356*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FD-01A-11D-A33E-09 chr8:91078167 C>T maps to NM_004929.2 K136K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49U-01A-31D-A27G-09 chr11:15096642 C>T maps to NM_000728.3 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FE-01A-11D-A33E-09 chr17:46937762 G>T maps to ENST00000448105 G390*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NE-01A-11D-A37C-09 chr17:46919215 C>T maps to ENST00000448105 I49I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A8O2-01A-11D-A36J-09 chr7:93108801 A>T maps to NM_001164737.1 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S8-A6BV-01A-21D-A31U-09 chr2:188211036 A>C maps to NM_005795.4 S420S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49X-01A-31D-A27G-09 chr7:134625934 G>A maps to NM_033138.3 S493S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr10:105218337 C>T maps to NM_001001412.3 L57L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XP-A8T8-01A-11D-A36J-09 chr10:105215357 C>T maps to NM_001001412.3 T234T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr10:105209410 G>A maps to NM_015916.4 A96A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A3-01A-11D-A27G-09 chr14:90866416 G>A maps to NM_006888.4 Q4Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A5B8-01A-11D-A28B-09 chr19:47111560 G>T maps to NM_005184.2 E48*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NS-01A-12D-A37C-09 chr10:5567314 C>A maps to NM_005185.2 A89A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6Y0-01B-11D-A33E-09 chr15:68486373 G>T maps to NM_033429.2 T190T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8W8-01B-11D-A37C-09 chr10:12867591 C>T maps to NM_153498.2 A314A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NI-01A-11D-A37C-09 chr1:209784836 G>T maps to NM_020439.2 R285R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EX-01A-11D-A36J-09 chr1:209782331 G>T maps to NM_020439.2 G215*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EQ-01A-11D-A36J-09 chr5:110730419 G>A maps to NM_001744.4 K133K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HZ-01A-31D-A351-09 chr17:3786461 A>G maps to ENST00000381771 P174P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr9:138710462 C>A did not map to a codon.
Sequencing variant TCGA-S8-A6BW-01A-11D-A31U-09 chr9:138703424 G>A maps to ENST00000409386 I1524I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASX-01A-11D-A387-09 chr9:138742206 G>A maps to ENST00000409386 L314L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49U-01A-31D-A27G-09 chr1:200826892 A>G maps to ENST00000236925 K1392K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HX-01A-11D-A33E-09 chr1:200817687 T>G maps to ENST00000236925 G608G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASX-01A-11D-A387-09 chr1:200817240 C>A maps to ENST00000236925 I459I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OJ-01A-11D-A27G-09 chr1:7792536 C>T maps to NM_015215.2 R982*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A8HZ-01A-11D-A36J-09 chr1:7798314 G>T maps to NM_015215.2 G1319*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NQ-01A-11D-A36J-09 chr17:4883116 G>T maps to NM_015099.3 P500P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A8HZ-01A-11D-A36J-09 chr17:4885087 T>A maps to NM_015099.3 P150P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A50L-01A-11D-A27G-09 chr12:67705480 A>G maps to NM_018448.3 T1123T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49R-01A-11D-A247-09 chr12:67700045 A>T maps to NM_018448.3 S866S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OJ-01A-11D-A27G-09 chr3:12858854 G>A maps to NM_001162499.1 V808V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OJ-01A-11D-A27G-09 chr5:179147422 A>G maps to ENST00000415618 G383G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr6:17507509 C>T maps to NM_006366.2 S137S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NH-01A-11D-A37C-09 chr6:44137710 C>T maps to NM_007058.3 L136L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8WC-01A-11D-A37C-09 chr2:30954230 T>A maps to ENST00000295055 G654G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GF-01A-11D-A37C-09 chr1:223958168 C>T maps to NM_001748.4 D615D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A891-01A-11D-A36J-09 chr11:76823744 C>T maps to ENST00000360841 I176I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GF-01A-11D-A37C-09 chr23:110496349 C>G did not map to a codon.
Sequencing variant TCGA-JY-A93D-01A-11D-A387-09 chr23:110494491 T>G did not map to a codon.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr23:110495578 A>G did not map to a codon.
Sequencing variant TCGA-L5-A8NH-01A-11D-A37C-09 chr23:110495607 T>A did not map to a codon.
Sequencing variant TCGA-LN-A4A5-01A-21D-A27G-09 chr23:110495710 C>A did not map to a codon.
Sequencing variant TCGA-R6-A6DQ-01B-11D-A31U-09 chr23:110496390 G>A did not map to a codon.
Sequencing variant TCGA-S8-A6BW-01A-11D-A31U-09 chr23:110489962 C>T did not map to a codon.
Sequencing variant TCGA-R6-A6Y0-01B-11D-A33E-09 chr1:230898515 G>T maps to NM_006615.2 E174*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A8I1-01A-11D-A36J-09 chr19:36632053 C>T maps to NM_001749.2 G47G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EY-01A-11D-A36J-09 chr19:36632053 C>T maps to NM_001749.2 G47G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OE-01A-11D-A27G-09 chr11:34119304 C>T maps to NM_005898.4 R688*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q9-A6FW-01A-31D-A31U-09 chr11:34098006 G>A maps to NM_005898.4 R197R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49L-01A-11D-A247-09 chr12:30873756 T>A maps to NM_001002259.1 S712S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NI-01A-11D-A37C-09 chr12:75719045 C>T maps to NM_032606.3 W54*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43M-01A-11D-A247-09 chr5:35921207 C>T maps to NM_144647.3 A5A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88V-01A-11D-A351-09 chr1:113212705 G>A maps to NM_006135.2 W271*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6KZ-01A-11D-A31U-09 chr22:37906322 C>A maps to NM_014550.3 E269*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A6QS-01A-12D-A33E-09 chr7:2946382 G>T maps to NM_032415.4 A1118A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A5U7-01A-11D-A31U-09 chr7:2962952 G>T maps to NM_032415.4 S652*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr17:78176099 C>T maps to NM_024110.2 N700N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-AAPN-01A-11D-A403-09 chr5:40852461 C>G maps to NM_032587.3 S343*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FB-01A-11D-A33E-09 chr13:111287077 G>A maps to NM_018210.2 V202V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA7B-01A-31D-A403-09 chr11:67186431 A>G maps to NM_001166222.1 A190A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr11:3028166 G>A maps to NM_001014437.2 S697S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6L4-01A-11D-A31U-09 chr17:38318022 C>T maps to NM_007359.4 Y105Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EY-01A-11D-A36J-09 chr17:38324561 T>C maps to NM_007359.4 P619P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49M-01A-21D-A27G-09 chr7:94184820 T>A maps to NM_022900.4 Y715*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RE-A7BO-01A-11D-A33E-09 chr7:94162521 C>A maps to NM_022900.4 S155S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GF-01A-11D-A37C-09 chr23:41519765 C>T did not map to a codon.
Sequencing variant TCGA-JY-A6FD-01A-11D-A33E-09 chr23:41524634 G>T did not map to a codon.
Sequencing variant TCGA-R6-A6XQ-01B-11D-A33E-09 chr23:41446169 G>T did not map to a codon.
Sequencing variant TCGA-IG-A97H-01A-11D-A387-09 chr16:2236813 C>T maps to NM_020764.3 Q314Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FB-01A-11D-A33E-09 chr16:2240119 G>A maps to NM_020764.3 S66S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A625-01A-11D-A31U-09 chr17:73502695 C>T maps to NM_020753.3 L195L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A8JD-01A-11D-A36J-09 chr17:73497976 G>A maps to NM_020753.3 Q1060*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XP-A8T8-01A-11D-A36J-09 chr11:104897031 C>A maps to NM_033292.2 E390*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KH-A6WC-01A-11D-A33E-09 chr19:15164351 G>T maps to NM_012114.2 R29R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49M-01A-21D-A27G-09 chr19:15164701 G>T maps to NM_012114.2 L112L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RF-01A-13D-A33E-09 chr11:104872775 G>A maps to NM_001136112.1 D245D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6Y0-01B-11D-A33E-09 chr11:104874036 T>C maps to NM_001136112.1 E182E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NN-01A-11D-A37C-09 chr4:110610547 G>A maps to NM_001226.3 Q274*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A1-01A-21D-A27G-09 chr4:110624545 G>A maps to NM_001226.3 S2S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q9-A6FW-01A-31D-A31U-09 chr10:115481449 G>T maps to NM_033338.4 A129A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NI-01A-11D-A37C-09 chr1:160165778 C>T maps to NM_001231.4 S248S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OH-01A-11D-A27G-09 chr1:116280872 A>G maps to NM_001232.3 I168I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NW-01A-11D-A37C-09 chr1:116283354 G>T maps to NM_001232.3 L138L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FQ-01A-31D-A387-09 chr3:121994702 G>A maps to NM_001178065.1 G474G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GF-01A-11D-A37C-09 chr20:55027467 G>A maps to NM_020356.3 S412S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93D-01A-11D-A387-09 chr20:55012569 A>G maps to NM_020356.3 Q129Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A4P3-01A-11D-A27G-09 chr1:10715780 G>A maps to NM_001079843.1 S530S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93E-01A-11D-A37C-09 chr1:10725215 G>A maps to NM_001079843.1 G143G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr1:10715750 G>A maps to NM_001079843.1 H540H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A893-01A-11D-A36J-09 chr1:10718605 G>C maps to NM_001079843.1 A456A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A1-01A-21D-A27G-09 chr1:10715741 G>A maps to NM_001079843.1 H543H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FO-01A-11D-A387-09 chr1:10707928 C>T maps to NM_001079843.1 S1142S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6XQ-01B-11D-A33E-09 chr1:10709146 G>A maps to NM_001079843.1 D1046D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr11:65793343 G>A maps to NM_053054.3 H169H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EW-01A-11D-A36J-09 chr11:65793202 G>A maps to NM_053054.3 G216G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3QL-01A-11D-A247-09 chr15:43931875 G>A maps to NM_172095.1 Q228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8WC-01A-11D-A37C-09 chr15:43931193 G>A maps to NM_172095.1 I250I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A5B8-01A-11D-A28B-09 chr5:134343645 G>A did not map to a codon.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr5:134347237 G>A maps to NM_178019.2 V374V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FG-01A-11D-A33E-09 chr19:38845407 C>T maps to NM_021185.4 F352F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GK-01A-11D-A37C-09 chr7:116199130 C>A maps to NM_001753.4 I109I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88W-01A-11D-A351-09 chr7:116139909 C>G maps to NM_001233.3 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OO-01A-11D-A27G-09 chr16:88947726 G>A maps to NM_005187.5 S458S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49Y-01A-11D-A27G-09 chr16:88947723 G>A maps to NM_005187.5 S459S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8WC-01A-11D-A37C-09 chr16:88945830 C>T maps to NM_005187.5 S503S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A891-01A-11D-A36J-09 chr11:119169164 C>G maps to NM_005188.2 A783A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93D-01A-11D-A387-09 chr3:105421028 G>T maps to NM_170662.3 S623*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OT-01A-11D-A28B-09 chr16:49315181 A>G maps to NM_004352.3 S65S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr16:49315199 G>A maps to NM_004352.3 S59S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6XG-01B-11D-A33E-09 chr20:54579077 C>T maps to NM_080617.4 T50T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NH-01A-11D-A37C-09 chr7:26246029 G>T maps to NM_016587.2 E23*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GI-01A-11D-A37C-09 chr17:77808432 G>A maps to NM_003655.2 S336S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NK-01A-21D-A37C-09 chr17:77770321 G>C maps to NM_020649.2 L29L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr1:52826166 G>A maps to NM_032449.2 R178*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HX-01A-11D-A33E-09 chr1:52826726 G>A maps to NM_032449.2 G132G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FB-01A-11D-A33E-09 chr4:15529095 G>A maps to NM_001080522.2 Q392Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NN-01A-11D-A37C-09 chr4:15565107 C>T maps to NM_001080522.2 R1049*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EQ-01A-11D-A36J-09 chr4:15477592 G>T maps to NM_001080522.2 E13*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FA-01A-11D-A33E-09 chr10:97786971 C>T maps to NM_001159747.1 I281I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49X-01A-31D-A27G-09 chr3:42906440 T>C maps to NM_001296.4 A149A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49S-01A-11D-A247-09 chr16:57546751 G>A maps to NM_033212.3 L518L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr19:15122080 C>T maps to NM_173482.2 N148N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NV-01A-11D-A37C-09 chr19:15132448 G>T maps to NM_173482.2 G355*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FR-01A-11D-A387-09 chr2:219890845 G>A maps to NM_194302.2 C749C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASX-01A-11D-A387-09 chr2:219874717 G>A maps to NM_194302.2 S1466S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NG-01A-11D-A37C-09 chr4:110606474 G>A maps to NM_017918.4 Q295Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EX-01A-11D-A36J-09 chr4:110605696 G>A maps to NM_017918.4 W237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NH-01A-11D-A37C-09 chr5:114606914 C>A maps to NM_001040440.2 E443*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NW-01A-11D-A37C-09 chr19:48821778 G>A maps to NM_144577.3 S38S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93E-01A-11D-A37C-09 chr3:46965111 G>A maps to NM_144716.3 P110P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49X-01A-31D-A27G-09 chr19:18047331 G>T maps to NM_001136203.1 E35*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EU-01A-11D-A36J-09 chr19:18054448 G>A maps to NM_001136203.1 L199L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NW-01A-11D-A37C-09 chr5:216925 C>T maps to NM_145265.2 R13R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr7:31618021 G>T maps to NM_194300.2 G382*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr7:31682909 T>C maps to NM_194300.2 C642C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RE-A7BO-01A-11D-A33E-09 chr7:31592727 G>A maps to NM_194300.2 A30A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6F8-01A-11D-A33E-09 chr3:42787489 G>T maps to NM_144719.3 I250I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43I-01A-11D-A247-09 chr7:92902024 C>T maps to NM_017667.2 R261*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XP-A8T8-01A-11D-A36J-09 chr7:92932770 G>T did not map to a codon.
Sequencing variant TCGA-XP-A8T7-01A-11D-A36J-09 chr16:57732911 C>T maps to NM_032269.5 H118H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43H-01A-11D-A247-09 chr3:123634432 A>G maps to NM_022757.4 P644P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA7D-01A-11D-A403-09 chr2:179736883 C>T maps to NM_173648.3 A685A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A2-01A-31D-A27G-09 chr2:74701783 C>T maps to ENST00000393965 P714P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FH-01A-11D-A33E-09 chr17:16593965 C>A maps to NM_014695.1 L84L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr17:18528580 G>A did not map to a codon.
Sequencing variant TCGA-2H-A9GQ-01A-11D-A37C-09 chr17:20768733 T>C maps to NM_001004306.1 V220V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93D-01A-11D-A387-09 chr17:20799141 G>A maps to NM_001004306.1 H64H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A5B8-01A-11D-A28B-09 chr7:76891436 G>A did not map to a codon.
Sequencing variant TCGA-Q9-A6FU-01A-11D-A31U-09 chr7:76903893 A>T maps to NM_020879.2 V455V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A6QS-01A-12D-A33E-09 chr10:106139942 C>A maps to NM_001008723.1 R444R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HY-01A-12D-A351-09 chr2:159028671 G>A maps to NM_138803.3 Q577*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GK-01A-11D-A37C-09 chr4:24833261 C>T maps to NM_001130726.2 L277L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88S-01A-11D-A36J-09 chr4:24838107 G>A maps to NM_001130726.2 Q229*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OT-01A-11D-A28B-09 chr2:197511189 G>T maps to NM_001080539.1 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A891-01A-11D-A36J-09 chr19:11532476 C>T maps to NM_145045.4 K486K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A2-01A-31D-A27G-09 chr19:11537523 C>A maps to NM_145045.4 L231L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OT-01A-11D-A28B-09 chr19:49912534 C>T maps to NM_144688.4 R381*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASW-01A-11D-A403-09 chr19:49900948 G>T maps to NM_144688.4 G148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A8JD-01A-11D-A36J-09 chr22:30772436 G>A maps to NM_001017437.2 Q654Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KH-A6WC-01A-11D-A33E-09 chr4:77303785 G>T maps to NM_001042784.1 I297I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OE-01A-11D-A27G-09 chr4:77288832 C>A maps to NM_001042784.1 E482*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OR-01A-11D-A27G-09 chr4:77250092 G>A maps to NM_001042784.1 D986D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GO-01A-11D-A37C-09 chr19:11461551 C>T maps to ENST00000427879 Q214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GH-01A-11D-A37C-09 chr23:133378940 T>C did not map to a codon.
Sequencing variant TCGA-V5-A7RE-01A-11D-A351-09 chr23:133379046 A>G did not map to a codon.
Sequencing variant TCGA-VR-A8EU-01A-11D-A36J-09 chr23:133379618 G>T did not map to a codon.
Sequencing variant TCGA-L5-A4OE-01A-11D-A27G-09 chr1:159862984 G>T maps to NM_012337.2 L38L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L7-A6VZ-01A-12D-A33E-09 chr23:49105332 G>T did not map to a codon.
Sequencing variant TCGA-LN-A8I1-01A-11D-A36J-09 chr23:49106137 C>T did not map to a codon.
Sequencing variant TCGA-Q9-A6FU-01A-11D-A31U-09 chr23:49104663 T>A did not map to a codon.
Sequencing variant TCGA-VR-A8EP-01A-31D-A403-09 chr23:49098511 C>G did not map to a codon.
Sequencing variant TCGA-IG-A5B8-01A-11D-A28B-09 chr1:3673348 G>A maps to NM_152492.2 K202K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NQ-01A-11D-A36J-09 chr1:3677927 G>T maps to NM_152492.2 L265L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A4-01A-11D-A27G-09 chr1:3677910 G>T maps to NM_152492.2 E260*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HY-01A-12D-A351-09 chr1:3680268 G>T did not map to a codon.
Sequencing variant TCGA-JY-A6FE-01A-11D-A33E-09 chr1:43110362 G>T did not map to a codon.
Sequencing variant TCGA-2H-A9GL-01A-12D-A37C-09 chr3:126138543 C>T maps to ENST00000505024 L267L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NK-01A-21D-A37C-09 chr3:126139000 G>C maps to ENST00000505024 R338R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr12:96271998 G>T maps to NM_182496.2 S423*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FA-01A-11D-A33E-09 chr3:180334632 A>C maps to NM_181426.1 L796*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-M9-A5M8-01A-11D-A28B-09 chr17:78032413 G>T maps to NM_017950.2 T427T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8ET-01A-11D-A403-09 chr17:78032329 G>A maps to NM_017950.2 L399L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-AAPN-01A-11D-A403-09 chr17:78013861 G>A maps to NM_017950.2 P115P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NF-01A-11D-A37C-09 chr17:8638851 C>T maps to NM_144681.2 Q190Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GO-01A-11D-A37C-09 chr17:63632092 C>A did not map to a codon.
Sequencing variant TCGA-JY-A6FB-01A-11D-A33E-09 chr17:64024487 G>C maps to NM_145036.3 V513V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49W-01A-11D-A27G-09 chr17:61831839 T>C maps to NM_020198.2 E329E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S8-A6BW-01A-11D-A31U-09 chr3:113187974 G>T maps to NM_144718.3 S241*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GR-01A-12D-A37C-09 chr17:80141647 A>T did not map to a codon.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr17:80121089 G>A maps to ENST00000445854 R676*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NR-01A-11D-A37C-09 chr17:80146216 C>T maps to ENST00000445854 L310L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A5-01A-21D-A27G-09 chr12:123282747 G>T did not map to a codon.
Sequencing variant TCGA-LN-A4MR-01A-11D-A28B-09 chr12:123286163 G>T maps to NM_201435.3 E491*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GQ-01A-11D-A37C-09 chr12:111296452 A>G maps to NM_152591.1 K81K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr12:111321963 C>T maps to NM_152591.1 A328A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GJ-01A-11D-A37C-09 chr16:3085277 G>A maps to NM_001103175.1 R74*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NT-01A-11D-A37C-09 chr16:3078432 C>T maps to NM_001103175.1 S425S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OG-01A-11D-A27G-09 chr3:56600709 A>G maps to NM_001141947.1 S211S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4MR-01A-11D-A28B-09 chr11:93141458 G>A maps to NM_181645.3 E463E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XP-A8T8-01A-11D-A36J-09 chr5:150563966 C>T maps to NM_015621.2 T217T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88V-01A-11D-A351-09 chr11:32675583 C>A did not map to a codon.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr11:32675521 A>G did not map to a codon.
Sequencing variant TCGA-ZR-A9CJ-01B-11D-A387-09 chr11:32697567 C>A did not map to a codon.
Sequencing variant TCGA-2H-A9GH-01A-11D-A37C-09 chr1:100606485 G>T maps to NM_019083.2 G194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A4P3-01A-11D-A27G-09 chr1:100609661 G>T maps to NM_019083.2 V260V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr19:46914705 A>G maps to NM_032040.3 A454A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FG-01A-11D-A33E-09 chr3:112324431 C>T maps to ENST00000447230 S906S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr3:112358575 G>A maps to ENST00000447230 R70R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HY-01A-12D-A351-09 chr3:112358593 C>T maps to ENST00000447230 R64R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A8O2-01A-11D-A36J-09 chr11:86120397 G>A maps to NM_001156474.1 P403P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8ET-01A-11D-A403-09 chr11:86123433 C>T maps to NM_001156474.1 S408S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A9VB-01A-21D-A37C-09 chr11:86108773 A>G maps to NM_001156474.1 E249E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A50L-01A-11D-A27G-09 chr11:96104184 G>A maps to NM_024725.3 Q401*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr11:96117596 G>A maps to NM_024725.3 N105N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OP-01A-11D-A27G-09 chr11:96098164 A>G maps to NM_024725.3 N453N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EQ-01A-11D-A36J-09 chr11:96098236 C>T maps to NM_024725.3 L429L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NI-01A-11D-A37C-09 chr11:85593711 T>C maps to NM_173556.3 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OE-01A-11D-A27G-09 chr2:56570087 C>T maps to NM_001080433.1 Q439*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OW-01A-11D-A28B-09 chr11:60609945 C>T maps to NM_024098.3 Q117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GI-01A-11D-A37C-09 chr11:66360162 G>A maps to NM_018219.2 N108N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L7-A6VZ-01A-12D-A33E-09 chr2:55591106 C>T maps to ENST00000436346 A155A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EZ-01A-11D-A36J-09 chr2:55529025 G>A maps to ENST00000436346 Q1552*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6XQ-01B-11D-A33E-09 chr11:64111515 G>T maps to NM_032251.5 L501L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A8JE-01A-11D-A37C-09 chr11:64110767 C>T maps to NM_032251.5 L394L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A939-01A-12D-A37C-09 chr14:91770136 T>C maps to NM_001080414.2 Q1181Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NG-01A-11D-A37C-09 chr14:91739931 G>T maps to NM_001080414.2 A1708A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RE-A7BO-01A-11D-A33E-09 chr14:91780029 G>T maps to NM_001080414.2 R710R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S8-A6BV-01A-21D-A31U-09 chr14:91774799 T>C maps to NM_001080414.2 A967A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NK-01A-21D-A37C-09 chr12:28515423 C>T maps to NM_018318.3 L210L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GJ-01A-11D-A37C-09 chr12:124427301 G>T maps to NM_025140.1 S71*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NQ-01A-11D-A36J-09 chr2:118732777 G>A maps to NM_019044.4 R246*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6L6-01B-11D-A33E-09 chr19:4262015 C>T maps to NM_018074.4 R205*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L7-A6VZ-01A-12D-A33E-09 chr5:169015513 G>T maps to NM_017785.4 E32*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NF-01A-11D-A37C-09 chr6:31112958 G>A maps to NM_001105564.1 G620G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88W-01A-11D-A351-09 chr9:36170953 G>A maps to NM_005893.2 R485R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GG-01A-11D-A37C-09 chr11:6281229 G>A maps to NM_176875.2 P24P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GQ-01A-11D-A37C-09 chr16:57394439 G>A maps to NM_002990.4 W55*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EX-01A-11D-A36J-09 chr17:34199417 C>T maps to NM_002985.2 W80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GR-01A-12D-A37C-09 chr7:45067377 G>T maps to NM_001029835.2 G25G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A8O2-01A-11D-A36J-09 chr7:45113867 G>T did not map to a codon.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr13:37014166 C>A maps to NM_003914.3 T315T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FP-01A-31D-A387-09 chr14:20779822 C>A maps to NM_182849.1 A240A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A97H-01A-11D-A387-09 chr23:50090672 G>T did not map to a codon.
Sequencing variant TCGA-ZR-A9CJ-01B-11D-A387-09 chr23:50052651 C>T did not map to a codon.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr11:69466016 C>A maps to NM_053056.2 C285*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HX-01A-11D-A33E-09 chr15:43481478 G>T did not map to a codon.
Sequencing variant TCGA-2H-A9GM-01A-11D-A37C-09 chr19:30303881 C>T maps to NM_001238.1 Q40*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S8-A6BV-01A-21D-A31U-09 chr19:30312916 T>C maps to NM_001238.1 R240R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr16:2499296 G>T maps to NM_001761.2 V411V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr16:2499425 C>T maps to NM_001761.2 A454A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8WG-01A-11D-A37C-09 chr14:99976509 C>T maps to ENST00000437596 L398L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A51D-01A-11D-A27G-09 chr3:156868142 G>T maps to NM_020307.2 T234T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HX-01A-11D-A33E-09 chr1:1330815 G>C maps to NM_030937.4 L184L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6Y2-01B-11D-A33E-09 chr2:135676489 G>T maps to NM_058241.2 P22P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49U-01A-31D-A27G-09 chr10:35805449 G>A did not map to a codon.
Sequencing variant TCGA-2H-A9GH-01A-11D-A37C-09 chr3:46245366 G>A maps to NM_001295.2 T146T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q9-A6FW-01A-31D-A31U-09 chr3:46245393 G>A maps to NM_001295.2 H137H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6XQ-01B-11D-A33E-09 chr3:46401260 G>T maps to NM_001123041.2 V345V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6DN-01B-11D-A31U-09 chr6:167550104 T>C maps to NM_004367.5 F129F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88S-01A-11D-A36J-09 chr17:38711548 G>A maps to NM_001838.3 L194L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43H-01A-11D-A247-09 chr3:132320086 C>T maps to NM_178445.1 D282D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49M-01A-21D-A27G-09 chr12:69980552 C>T maps to NM_006431.2 I33I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA7I-01A-11D-A403-09 chr12:69986781 C>T maps to NM_006431.2 D259D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FP-01A-31D-A387-09 chr1:156279013 C>A maps to NM_005998.4 G538G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr5:10256196 C>T maps to NM_012073.3 S154S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr2:73478541 G>A maps to NM_006429.3 L464L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OE-01A-11D-A27G-09 chr2:73476150 C>T maps to NM_006429.3 N272N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NJ-01A-11D-A36J-09 chr21:30445905 C>T maps to NM_006585.2 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43E-01A-11D-A247-09 chr22:17072054 G>A maps to NM_014406.4 D462D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RF-01A-13D-A33E-09 chr6:74497120 C>T maps to NM_133493.3 V834V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OH-01A-11D-A27G-09 chr6:74497117 A>G maps to NM_133493.3 T833T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NR-01A-11D-A37C-09 chr6:74530286 A>C maps to NM_133493.3 R1388R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A625-01A-11D-A31U-09 chr5:140012198 C>A maps to NM_001174105.1 E124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr1:145704301 G>A maps to NM_007053.2 R39*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OE-01A-11D-A27G-09 chr12:7655083 G>T maps to NM_004244.4 T41T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A6-01A-11D-A27G-09 chr12:7639545 G>T maps to NM_004244.4 S696*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6XG-01B-11D-A33E-09 chr12:7647721 C>A maps to NM_004244.4 G459*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OJ-01A-11D-A27G-09 chr12:7527242 G>A maps to ENST00000416109 S1078S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OX-01A-21D-A28B-09 chr19:43857881 C>T maps to NM_020406.2 L6L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-A7RB-01A-11D-A351-09 chr1:158227470 T>C maps to NM_001763.2 C325C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6KZ-01A-11D-A31U-09 chr1:158299214 C>A maps to NM_001764.2 L277L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr1:158152020 G>A maps to NM_001766.3 V176V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S8-A6BV-01A-21D-A31U-09 chr1:158151870 C>T maps to NM_001766.3 N126N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43I-01A-11D-A247-09 chr1:158325246 G>C maps to NM_030893.3 V171V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OW-01A-11D-A28B-09 chr1:158324299 T>A maps to NM_030893.3 T64T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-M9-A5M8-01A-11D-A28B-09 chr1:158324284 G>C maps to NM_030893.3 L59L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43H-01A-11D-A247-09 chr2:71062832 G>C did not map to a codon.
Sequencing variant TCGA-VR-AA4D-01A-11D-A37C-09 chr2:71058195 G>T maps to NM_015717.3 V324V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA7B-01A-31D-A403-09 chr2:71061151 C>T did not map to a codon.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr19:35823798 G>A maps to NM_001771.3 W128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HX-01A-11D-A33E-09 chr19:35832674 G>T maps to NM_001771.3 L614L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EU-01A-11D-A36J-09 chr19:35832387 G>A maps to NM_001771.3 L550L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FG-01A-11D-A33E-09 chr1:160811228 G>A maps to NM_001166663.1 D147D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr1:167408610 C>T maps to NM_198053.2 A63A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93C-01A-11D-A387-09 chr11:66082733 G>A maps to NM_020404.2 Q589*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EZ-01A-11D-A36J-09 chr11:66082523 G>A maps to NM_020404.2 L659L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6DN-01B-11D-A31U-09 chr12:6554290 C>T maps to NM_001242.4 C10C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8ER-01A-11D-A36J-09 chr12:6559345 C>A maps to NM_001242.4 L92L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A9VB-01A-21D-A37C-09 chr12:6554269 G>A maps to NM_001242.4 R3R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr17:72539040 G>A maps to NM_006678.3 S162S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RE-A7BO-01A-11D-A33E-09 chr17:72700794 G>A maps to ENST00000412086 T68T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A2-01A-31D-A27G-09 chr17:41926112 C>A maps to NM_145273.3 G77G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FG-01A-11D-A33E-09 chr19:51728474 G>T maps to NM_001772.3 G13G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NJ-01A-11D-A36J-09 chr19:51729309 G>T maps to NM_001772.3 E224*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr7:80286010 G>A maps to NM_001127444.1 T92T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A4-01A-11D-A27G-09 chr7:80302673 A>C maps to NM_001127444.1 V401V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8WC-01A-11D-A37C-09 chr19:45911840 G>T maps to ENST00000423698 S207S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GF-01A-11D-A37C-09 chr12:6926357 C>T maps to NM_000616.4 L340L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A8-01A-32D-A27G-09 chr12:6924123 G>A maps to NM_000616.4 K191K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FQ-01A-31D-A387-09 chr23:135738562 G>A did not map to a codon.
Sequencing variant TCGA-ZR-A9CJ-01B-11D-A387-09 chr23:135738536 G>A did not map to a codon.
Sequencing variant TCGA-L5-A8NH-01A-11D-A37C-09 chr11:60885645 G>A did not map to a codon.
Sequencing variant TCGA-JY-A6FH-01A-11D-A33E-09 chr1:157804257 A>C maps to NM_005894.2 P219P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q9-A6FU-01A-11D-A31U-09 chr1:157805730 G>T maps to NM_005894.2 L90L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GG-01A-11D-A37C-09 chr12:56119599 G>T maps to NM_001780.4 V216V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OS-01A-11D-A28B-09 chr12:56121048 A>G maps to NM_001780.4 A47A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43H-01A-11D-A247-09 chr17:7483025 C>T maps to NM_001251.2 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OR-01A-11D-A27G-09 chr2:87017721 C>T maps to ENST00000456996 Q85Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr20:23065104 G>T maps to NM_012072.3 G575G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88S-01A-11D-A36J-09 chr20:23066169 C>T maps to NM_012072.3 A220A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RE-A7BO-01A-11D-A33E-09 chr19:14515275 G>T maps to NM_078481.2 E511*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NJ-01A-11D-A36J-09 chr23:149963743 G>A did not map to a codon.
Sequencing variant TCGA-R6-A6KZ-01A-11D-A31U-09 chr1:100908534 G>T maps to NM_033312.2 E168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6Y0-01B-11D-A33E-09 chr9:99284789 G>T maps to NM_033331.2 L447L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A5B8-01A-11D-A28B-09 chr17:45234324 G>A maps to NM_001114091.1 R266*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49R-01A-11D-A247-09 chr17:45214645 T>C maps to NM_001114091.1 Q601Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8WG-01A-11D-A37C-09 chr17:45216209 A>C maps to NM_001114091.1 V539V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASX-01A-11D-A387-09 chr17:45216209 A>C maps to NM_001114091.1 V539V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EZ-01A-11D-A36J-09 chr17:45199822 T>C maps to NM_001114091.1 Q799Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NK-01A-21D-A37C-09 chr6:110501658 G>T maps to NM_015891.2 A4A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49V-01A-11D-A247-09 chr6:110541036 C>T maps to NM_015891.2 S435S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49Y-01A-11D-A27G-09 chr14:103435035 C>A maps to NM_006035.3 R671R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-A7RC-01B-11D-A403-09 chr14:103450048 C>T maps to NM_006035.3 P245P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EO-01A-11D-A36J-09 chr14:103440403 C>T maps to NM_006035.3 G530G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-AAPN-01A-11D-A403-09 chr17:71282204 C>T maps to NM_012121.4 K145K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43M-01A-11D-A247-09 chr22:19496145 G>A maps to NM_001178010.1 L415L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4MQ-01A-11D-A28B-09 chr6:44394256 G>A maps to NM_001253.2 P563P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GM-01A-11D-A37C-09 chr1:91967308 A>G maps to NM_001134420.1 P12P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr1:91978779 G>T maps to NM_001134420.1 L246L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FB-01A-11D-A33E-09 chr7:21948029 G>A maps to NM_018719.4 S133S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A8I0-01A-11D-A36J-09 chr7:21945183 G>A maps to NM_018719.4 T329T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X8-AAAR-01A-11D-A403-09 chr16:68849429 G>T maps to NM_004360.3 E445*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A50L-01A-11D-A27G-09 chr5:24487993 A>G maps to NM_006727.3 N715N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A625-01A-11D-A31U-09 chr5:24491784 T>C maps to NM_006727.3 Q592Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FD-01A-11D-A33E-09 chr5:24498599 A>C maps to NM_006727.3 A474A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OH-01A-11D-A27G-09 chr5:24511518 G>A maps to NM_006727.3 R307*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A8-01A-32D-A27G-09 chr5:24488068 A>G maps to NM_006727.3 I690I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EZ-01A-11D-A36J-09 chr5:24491685 C>G maps to NM_006727.3 L625L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GR-01A-12D-A37C-09 chr16:65026863 G>A maps to NM_001797.2 Y199Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A938-01A-11D-A37C-09 chr5:22078695 A>C maps to NM_004061.3 T30T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43E-01A-11D-A247-09 chr5:21752211 G>A maps to NM_004061.3 F673F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NU-01A-11D-A36J-09 chr5:21751950 T>C maps to NM_004061.3 E760E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49M-01A-21D-A27G-09 chr5:21842383 G>A maps to NM_004061.3 Q234*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RE-A7BO-01A-11D-A33E-09 chr5:21783578 A>G maps to NM_004061.3 D427D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EZ-01A-11D-A36J-09 chr16:83065786 G>T maps to ENST00000268613 V110V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6KZ-01A-11D-A31U-09 chr8:95189940 G>C maps to NM_001144663.1 A53A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OR-01A-11D-A27G-09 chr5:19571716 T>C maps to NM_004934.3 Q408Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FO-01A-11D-A387-09 chr5:19721492 G>T maps to NM_004934.3 L202L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8W5-01B-11D-A37C-09 chr5:19503155 G>A maps to NM_004934.3 F525F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3I8-01A-11D-A247-09 chr18:64211431 G>A maps to NM_021153.2 Y330Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88V-01A-11D-A351-09 chr18:25570059 C>A did not map to a codon.
Sequencing variant TCGA-LN-A49Y-01A-11D-A27G-09 chr18:25543356 G>T maps to NM_001792.3 A826A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FR-01A-11D-A387-09 chr18:59170237 C>T maps to NM_031891.2 Y238Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OF-01A-11D-A27G-09 chr20:44803570 C>T maps to NM_021248.1 A687A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NJ-01A-11D-A36J-09 chr20:44845597 G>A maps to NM_021248.1 R235R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GM-01A-11D-A37C-09 chr10:73558898 C>T maps to ENST00000398860 Y2367Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr10:73562687 C>A maps to ENST00000398860 R2511R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NQ-01A-11D-A36J-09 chr10:73492056 C>T maps to ENST00000398860 L1348L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FP-01A-31D-A387-09 chr10:73571508 T>A maps to ENST00000398860 A3111A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EQ-01A-11D-A36J-09 chr14:23518386 C>T maps to NM_022478.3 A603A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A4QS-01A-11D-A27G-09 chr20:58587736 A>G maps to NM_177980.2 K817K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RF-01A-13D-A33E-09 chr16:68712180 G>T did not map to a codon.
Sequencing variant TCGA-2H-A9GI-01A-11D-A37C-09 chr20:60427901 T>C maps to NM_001794.2 P275P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A7DP-01A-31D-A33E-09 chr20:60498709 C>T maps to NM_001794.2 L526L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A1-01A-21D-A27G-09 chr20:60498648 C>A maps to NM_001794.2 P505P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FP-01A-31D-A387-09 chr20:60499457 G>T maps to NM_001794.2 T565T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q9-A6FU-01A-11D-A31U-09 chr20:60470102 G>T maps to NM_001794.2 T396T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RF-01A-13D-A33E-09 chr16:66426284 G>T maps to NM_001795.3 G406*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q9-A6FW-01A-31D-A31U-09 chr16:66420989 G>A maps to NM_001795.3 S163S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NJ-01A-11D-A36J-09 chr5:31323177 C>G maps to NM_004932.2 V712V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-A7RE-01A-11D-A351-09 chr16:61851477 C>T maps to NM_001796.2 P394P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6Y0-01B-11D-A33E-09 chr5:26902613 G>A maps to NM_016279.3 Y408Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A9VB-01A-21D-A37C-09 chr5:26906169 G>A maps to NM_016279.3 Q237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FH-01A-11D-A33E-09 chr10:85971433 G>T maps to NM_033100.2 E506*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OE-01A-11D-A27G-09 chr7:105621431 G>T maps to NM_152750.4 E90*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr7:105664828 C>T maps to NM_152750.4 P693P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A2-01A-31D-A27G-09 chr11:617431 G>A maps to NM_021924.4 S819S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8ER-01A-11D-A36J-09 chr16:89761400 G>T maps to NM_052988.4 L285L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49U-01A-31D-A27G-09 chr1:1634943 G>C maps to NM_024011.2 L677L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3I8-01A-11D-A247-09 chr7:40027386 C>T maps to NM_003718.4 A467A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XP-A8T6-01A-11D-A36J-09 chr23:47088142 C>G did not map to a codon.
Sequencing variant TCGA-R6-A6Y0-01B-11D-A33E-09 chr12:96704832 G>T maps to NM_002595.4 S180S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49R-01A-11D-A247-09 chr1:205498557 G>T did not map to a codon.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr6:110953272 T>C maps to NM_015076.3 P202P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OG-01A-11D-A27G-09 chr6:110991737 G>A maps to NM_015076.3 R71*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8W5-01B-11D-A37C-09 chr12:56364967 G>A maps to NM_001798.3 W243*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OJ-01A-11D-A27G-09 chr12:123746285 G>T maps to NM_004642.2 S115S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OH-01A-11D-A27G-09 chr17:73998124 G>T maps to NM_001258.2 E73*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3YA-01A-11D-A247-09 chr17:30815537 G>T maps to NM_003885.2 R300R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA7D-01A-11D-A403-09 chr9:123165254 C>G maps to NM_018249.4 L1712L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NG-01A-11D-A37C-09 chr5:68565056 A>G maps to NM_001799.3 S217S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr6:20955678 G>T maps to NM_017774.3 E258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93F-01A-21D-A37C-09 chr14:50808937 G>A maps to ENST00000356146 C794C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RE-A7BO-01A-11D-A33E-09 chr23:18668593 T>C did not map to a codon.
Sequencing variant TCGA-VR-AA7B-01A-31D-A403-09 chr23:18622886 G>T did not map to a codon.
Sequencing variant TCGA-2H-A9GO-01A-11D-A37C-09 chr9:21971015 G>T maps to NM_001195132.1 P114P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OO-01A-11D-A27G-09 chr9:21974694 G>T maps to NM_001195132.1 Y44*. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-L5-A8NG-01A-11D-A37C-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-LN-A8I1-01A-11D-A36J-09 chr9:21971207 C>T did not map to a codon.
Sequencing variant TCGA-M9-A5M8-01A-11D-A28B-09 chr9:21970898 A>G did not map to a codon.
Sequencing variant TCGA-R6-A6DQ-01B-11D-A31U-09 chr9:21974669 T>G maps to NM_058197.4 R53R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XP-A8T7-01A-11D-A36J-09 chr9:21968241 C>T did not map to a codon.
Sequencing variant TCGA-L5-A8NU-01A-11D-A36J-09 chr5:133747416 G>A maps to NM_080656.2 F43F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XP-A8T6-01A-11D-A36J-09 chr10:14879873 C>T maps to NM_001029954.2 T24T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr5:115152082 G>A maps to NM_001801.2 T4T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OJ-01A-11D-A27G-09 chr23:139865772 G>T did not map to a codon.
Sequencing variant TCGA-V5-AASX-01A-11D-A387-09 chr23:139866464 C>T did not map to a codon.
Sequencing variant TCGA-VR-AA7B-01A-31D-A403-09 chr23:139866522 C>A did not map to a codon.
Sequencing variant TCGA-V5-AASX-01A-11D-A387-09 chr16:22358783 G>A maps to NM_001802.1 S289S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr17:72999571 G>A maps to NM_014603.2 P267P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-A7RC-01B-11D-A403-09 chr17:15522727 G>T maps to ENST00000261644 V33V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FD-01A-11D-A33E-09 chr4:85525395 G>T maps to NM_001263.3 E40*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A4QS-01A-11D-A27G-09 chr6:31084611 G>A maps to NM_001264.4 H260H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr13:28539138 C>T maps to NM_001265.3 T185T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3I8-01A-11D-A247-09 chr6:4954288 G>A maps to ENST00000328908 *599*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49M-01A-21D-A27G-09 chr6:4943929 C>T maps to ENST00000328908 F478F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6XQ-01B-11D-A33E-09 chr16:80646528 G>T maps to NM_152342.2 V404V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3QL-01A-11D-A247-09 chr19:51981880 G>A maps to NM_001080405.1 E56E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FH-01A-11D-A33E-09 chr19:51986385 C>G maps to NM_001080405.1 L324L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OX-01A-21D-A28B-09 chr19:42312911 C>T maps to NM_001815.2 V162V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q9-A6FW-01A-31D-A31U-09 chr19:42126966 C>T maps to NM_001817.2 P192P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FR-01A-11D-A387-09 chr19:42221563 C>T maps to NM_004363.2 V383V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A5B8-01A-11D-A28B-09 chr19:42265340 C>G maps to NM_002483.4 L203L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZR-A9CJ-01B-11D-A387-09 chr14:23586974 C>T maps to NM_001805.2 P189P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6DQ-01B-11D-A31U-09 chr2:37455899 C>A maps to NM_005760.2 E146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EY-01A-11D-A36J-09 chr22:17978485 C>T maps to ENST00000400579 D109D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr22:17600400 G>A maps to NM_031890.3 S539S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A97I-01A-11D-A387-09 chr9:135940033 G>A maps to NM_001807.3 L78L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NR-01A-11D-A37C-09 chr9:135947057 C>A maps to NM_001807.3 P726P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49S-01A-11D-A247-09 chr9:135942473 G>T did not map to a codon.
Sequencing variant TCGA-V5-A7RB-01A-11D-A351-09 chr9:135940526 C>A maps to NM_001807.3 G150G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43I-01A-11D-A247-09 chr12:51723602 G>A maps to NM_001971.5 G208G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OJ-01A-11D-A27G-09 chr1:15813779 G>T maps to ENST00000442979 G251*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A8I0-01A-11D-A36J-09 chr1:15807633 C>A maps to ENST00000442979 T57T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NF-01A-11D-A37C-09 chr1:22333433 C>G maps to NM_005747.4 A142A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NN-01A-11D-A37C-09 chr1:22333418 T>C maps to NM_005747.4 D137D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XP-A8T8-01A-11D-A36J-09 chr1:22332268 C>T maps to NM_005747.4 N114N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3QL-01A-11D-A247-09 chr10:11299728 A>C maps to NM_006561.3 G144G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr10:11207538 C>T maps to NM_006561.3 P55P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NR-01A-11D-A37C-09 chr10:11363230 C>A maps to NM_006561.3 T392T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASW-01A-11D-A403-09 chr10:11356186 C>T maps to NM_006561.3 A354A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASX-01A-11D-A387-09 chr10:11330402 G>A maps to NM_006561.3 Q288Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FP-01A-31D-A387-09 chr1:151679696 G>C maps to NM_007185.4 Y282*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6F8-01A-11D-A33E-09 chr15:72580942 G>T maps to NM_052840.4 A370A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HX-01A-11D-A33E-09 chr15:72608241 G>T maps to NM_052840.4 R97R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A7DP-01A-31D-A33E-09 chr22:46759903 G>T maps to NM_014246.1 G3008G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FG-01A-11D-A33E-09 chr22:46787548 G>A maps to NM_014246.1 V2043V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XP-A8T6-01A-11D-A36J-09 chr22:46787668 G>A maps to NM_014246.1 C2003C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OR-01A-11D-A27G-09 chr1:109795271 C>T maps to NM_001408.2 G857G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8ER-01A-11D-A36J-09 chr1:109814988 G>T maps to NM_001408.2 S2672S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OG-01A-11D-A27G-09 chr3:48698501 G>A maps to NM_001407.2 P522P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NE-01A-11D-A37C-09 chr3:48697919 A>C maps to NM_001407.2 R716R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-A7RB-01A-11D-A351-09 chr3:48694698 C>T maps to NM_001407.2 V1277V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FA-01A-11D-A33E-09 chr11:788360 G>A maps to NM_016564.3 L72L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FP-01A-31D-A387-09 chr2:27015646 C>T maps to NM_001809.3 F78F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A5B8-01A-11D-A28B-09 chr4:68378267 A>C maps to NM_001812.2 T488T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GG-01A-11D-A37C-09 chr4:104080028 G>T maps to NM_001813.2 T872T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OW-01A-11D-A28B-09 chr1:214813615 T>C maps to NM_016343.3 N645N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NH-01A-11D-A37C-09 chr1:214814804 A>T maps to NM_016343.3 K1042*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FP-01A-31D-A387-09 chr1:214814240 G>T maps to NM_016343.3 E854*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NL-01A-12D-A37C-09 chr23:100395678 G>T did not map to a codon.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr23:100364891 C>T did not map to a codon.
Sequencing variant TCGA-L5-A4OG-01A-11D-A27G-09 chr13:25480206 G>A maps to NM_018451.3 Q657*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8Q7-01A-11D-A37C-09 chr13:25480756 C>T maps to NM_018451.3 L473L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NW-01A-11D-A37C-09 chr5:64814370 C>T maps to NM_022145.3 L247L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NG-01A-11D-A37C-09 chr16:81058367 G>T maps to NM_001100624.1 G228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49S-01A-11D-A247-09 chr2:25038426 G>T maps to NM_024322.2 G132G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A5S3-01A-11D-A28B-09 chr16:67866356 C>A did not map to a codon.
Sequencing variant TCGA-L5-A88Z-01A-11D-A36J-09 chr16:67863986 A>G maps to NM_025082.3 P289P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NS-01A-12D-A37C-09 chr16:67866140 G>A maps to NM_025082.3 I93I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FD-01A-11D-A33E-09 chr9:123903794 C>T maps to NM_007018.4 L874L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OT-01A-11D-A28B-09 chr9:123929933 C>T maps to NM_007018.4 L1941L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88S-01A-11D-A36J-09 chr5:122717866 G>A maps to NM_153223.3 Q681*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASX-01A-11D-A387-09 chr4:56884023 G>C did not map to a codon.
Sequencing variant TCGA-LN-A7HW-01A-22D-A351-09 chr11:117282841 G>T maps to NM_014956.4 L1447L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A8I1-01A-11D-A36J-09 chr11:117244543 C>A maps to NM_014956.4 G410G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-AAPN-01A-11D-A403-09 chr11:117257945 A>G maps to NM_014956.4 P584P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49W-01A-11D-A27G-09 chr18:13030461 A>G did not map to a codon.
Sequencing variant TCGA-LN-A49M-01A-21D-A27G-09 chr20:34090591 G>A maps to NM_007186.3 L1465L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FP-01A-31D-A387-09 chr20:34055252 G>T maps to NM_007186.3 E242*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr1:179993622 T>C maps to NM_014810.4 V1152V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A4-01A-11D-A27G-09 chr1:180064684 C>T maps to NM_014810.4 Q2847*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6XG-01B-11D-A33E-09 chr9:80858445 C>T maps to NM_001098802.1 D224D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8W5-01B-11D-A37C-09 chr3:101474333 C>T maps to ENST00000327230 H263H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EQ-01A-11D-A36J-09 chr3:101451487 C>T maps to ENST00000327230 Q240*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A5U7-01A-11D-A31U-09 chr9:131196802 G>A maps to NM_016174.4 A482A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43M-01A-11D-A247-09 chr22:47103868 C>A maps to NM_022766.5 G196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NS-01A-12D-A37C-09 chr22:47108184 T>G maps to NM_022766.5 R129R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GI-01A-11D-A37C-09 chr16:55860154 G>A maps to NM_001025195.1 R105*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr16:55857577 G>A maps to NM_001025195.1 H141H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr16:56996988 C>T maps to NM_000078.2 G62G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49S-01A-11D-A247-09 chr6:31914955 C>A maps to ENST00000437789 I659I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GH-01A-11D-A37C-09 chr1:196659304 A>G maps to NM_000186.3 K424K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GL-01A-12D-A37C-09 chr1:196643017 T>A maps to NM_000186.3 P92P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OS-01A-11D-A28B-09 chr1:196706672 G>T maps to NM_000186.3 E889*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NK-01A-21D-A37C-09 chr1:196706630 C>T maps to NM_000186.3 Q875*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q9-A6FU-01A-11D-A31U-09 chr1:196683031 C>T maps to NM_000186.3 Q502*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6XQ-01B-11D-A33E-09 chr1:196682863 G>T did not map to a codon.
Sequencing variant TCGA-L5-A8NW-01A-11D-A37C-09 chr1:196757397 T>A maps to NM_021023.5 S161S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GR-01A-12D-A37C-09 chr1:196965227 T>C maps to ENST00000367414 H313H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NW-01A-11D-A37C-09 chr1:196953133 T>C maps to ENST00000367414 S123S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8W8-01B-11D-A37C-09 chr1:196964905 A>C maps to ENST00000367414 R247R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49L-01A-11D-A247-09 chr11:65623714 T>A did not map to a codon.
Sequencing variant TCGA-L5-A8NI-01A-11D-A37C-09 chr23:47485919 T>A did not map to a codon.
Sequencing variant TCGA-LN-A4MR-01A-11D-A28B-09 chr23:47486319 G>A did not map to a codon.
Sequencing variant TCGA-2H-A9GH-01A-11D-A37C-09 chr7:117180246 T>C maps to NM_000492.3 S321S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A6QS-01A-12D-A33E-09 chr3:88105057 G>T maps to NM_001195308.1 P23P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NJ-01A-11D-A36J-09 chr1:151509273 C>T maps to NM_020770.2 D1125D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NT-01A-11D-A37C-09 chr1:151506464 G>A maps to NM_020770.2 R919R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4MR-01A-11D-A28B-09 chr1:151491112 C>T maps to NM_020770.2 R40*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASW-01A-11D-A403-09 chr1:151491489 C>T maps to NM_020770.2 S165S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A6-01A-11D-A27G-09 chr15:57730211 C>T maps to NM_032866.3 F5F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A9-01A-11D-A28B-09 chr2:27324149 C>A maps to ENST00000404694 E439*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A51D-01A-11D-A27G-09 chr19:4409548 G>T maps to NM_005483.2 P251P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3Y9-01A-12D-A247-09 chr21:37775141 C>T maps to NM_005441.2 L250L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XP-A8T8-01A-11D-A36J-09 chr21:37781695 T>C maps to NM_005441.2 P284P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RE-01A-11D-A33E-09 chr10:50870764 G>T maps to NM_020549.4 L638L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HY-01A-12D-A351-09 chr10:50835781 G>A maps to NM_020549.4 T354T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RF-01A-13D-A33E-09 chr3:14163428 C>A maps to NM_144636.2 G17*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HX-01A-11D-A33E-09 chr3:126633521 G>T did not map to a codon.
Sequencing variant TCGA-L5-A8NR-01A-11D-A37C-09 chr5:98233974 A>G maps to NM_001270.2 P450P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OG-01A-11D-A27G-09 chr15:93522502 G>T maps to NM_001271.3 G956*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NH-01A-11D-A37C-09 chr15:93485156 C>A maps to NM_001271.3 V266V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XP-A8T7-01A-11D-A36J-09 chr15:93540190 A>G maps to NM_001271.3 K1200K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3YA-01A-11D-A247-09 chr12:6707387 C>T maps to ENST00000309577 Q562Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FD-01A-11D-A33E-09 chr1:6188557 C>T did not map to a codon.
Sequencing variant TCGA-LN-A4MR-01A-11D-A28B-09 chr1:6202186 C>T did not map to a codon.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr20:40054757 G>A maps to NM_032221.3 S1368S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GR-01A-12D-A37C-09 chr8:61655224 C>T maps to NM_017780.2 Q412*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3QL-01A-11D-A247-09 chr8:61765095 A>T maps to NM_017780.2 V1978V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A891-01A-11D-A36J-09 chr8:61778110 T>C maps to NM_017780.2 N2871N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NK-01A-21D-A37C-09 chr8:61778005 G>T maps to NM_017780.2 P2836P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q9-A6FU-01A-11D-A31U-09 chr8:61743024 G>T maps to NM_017780.2 E1223*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S8-A6BW-01A-11D-A31U-09 chr8:61777888 C>G maps to NM_017780.2 P2797P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr14:21899049 C>T maps to NM_001170629.1 Q251Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OW-01A-11D-A28B-09 chr14:21899010 G>A maps to NM_001170629.1 A264A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASV-01A-11D-A387-09 chr14:21897311 C>A maps to NM_001170629.1 L342L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XP-A8T8-01A-11D-A36J-09 chr14:21896332 T>C maps to NM_001170629.1 S432S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A3-01A-11D-A27G-09 chr16:53262984 A>G maps to ENST00000219084 Q753Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EQ-01A-11D-A36J-09 chr3:53856659 C>T maps to NM_018397.4 W238*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NT-01A-11D-A37C-09 chr12:133438074 G>A maps to NM_001161344.1 P255P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6XQ-01B-11D-A33E-09 chr12:133434057 G>T maps to NM_001161344.1 P345P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr14:93392963 C>T maps to NM_001275.3 I36I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EO-01A-11D-A36J-09 chr20:5904464 G>T maps to NM_001819.2 E559*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FD-01A-11D-A33E-09 chr1:111860634 C>A maps to NM_201653.2 T211T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88V-01A-11D-A351-09 chr23:72804365 A>G did not map to a codon.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr23:72783225 T>C did not map to a codon.
Sequencing variant TCGA-LN-A9FP-01A-31D-A387-09 chr11:67837675 G>C maps to NM_001277.2 P283P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr3:439986 G>T maps to NM_006614.2 E1058*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OE-01A-11D-A27G-09 chr23:85218944 C>A did not map to a codon.
Sequencing variant TCGA-L5-A4OP-01A-11D-A27G-09 chr23:85218845 C>T did not map to a codon.
Sequencing variant TCGA-R6-A6XG-01B-11D-A33E-09 chr23:85212892 T>C did not map to a codon.
Sequencing variant TCGA-2H-A9GG-01A-11D-A37C-09 chr1:241797459 C>A maps to NM_001821.3 E537*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A97I-01A-11D-A387-09 chr1:241797238 A>G maps to NM_001821.3 P610P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A4QS-01A-11D-A27G-09 chr14:24682714 A>G maps to NM_014169.3 H20H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HW-01A-22D-A351-09 chr9:33266058 G>T maps to NM_016410.5 E41*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6F8-01A-11D-A33E-09 chr8:23104384 G>A maps to NM_152272.3 L59L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88W-01A-11D-A351-09 chr7:29440272 C>T maps to NM_004067.2 Y135Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA4G-01A-11D-A37C-09 chr21:19635168 G>A maps to NM_024944.2 L232L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6XQ-01B-11D-A33E-09 chr15:41571029 C>A maps to NM_007236.4 T159T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6Y0-01B-11D-A33E-09 chr16:23767767 C>T maps to NM_022097.2 Q138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A5U6-01A-11D-A28B-09 chr7:150934476 G>A maps to NM_019015.1 L343L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A4QS-01A-11D-A27G-09 chr3:184106420 T>C maps to NM_003741.2 D867D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr3:184104413 G>A maps to NM_003741.2 A689A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NW-01A-11D-A37C-09 chr3:184104326 G>A maps to NM_003741.2 A660A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GO-01A-11D-A37C-09 chr7:136700023 A>T maps to NM_001006628.1 K138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A6-01A-11D-A27G-09 chr7:136700550 C>T maps to NM_001006628.1 G313G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3YC-01A-11D-A247-09 chr1:240072403 C>T maps to NM_000740.2 F551F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FB-01A-11D-A33E-09 chr1:240072322 C>A maps to NM_000740.2 T524T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L7-A6VZ-01A-12D-A33E-09 chr1:240071723 G>T maps to NM_000740.2 E325*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZR-A9CJ-01B-11D-A387-09 chr1:240072259 T>G maps to NM_000740.2 T503T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A5B8-01A-11D-A28B-09 chr11:46407354 C>T maps to NM_000741.2 K251K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NJ-01A-11D-A36J-09 chr11:3690540 G>T maps to NM_020402.2 R83R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6F8-01A-11D-A33E-09 chr20:61992442 G>A maps to NM_000744.5 R25R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr8:42611063 C>T maps to NM_004198.3 S426S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6Y2-01B-11D-A33E-09 chr8:42612090 G>T maps to NM_004198.3 P118P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-A7RE-01A-11D-A351-09 chr8:42611498 A>G maps to NM_004198.3 S281S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OG-01A-11D-A27G-09 chr15:32460328 C>T maps to NM_001190455.1 D422D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-AAPN-01A-11D-A403-09 chr4:40356242 G>T maps to NM_017581.2 L382L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L7-A6VZ-01A-12D-A33E-09 chr17:7350938 G>T maps to NM_000747.2 E194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q9-A6FW-01A-31D-A31U-09 chr17:7359953 G>A maps to NM_000747.2 W473*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FH-01A-11D-A33E-09 chr1:154542073 C>A maps to NM_000748.2 L67L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr1:154544174 C>T maps to NM_000748.2 L292L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L7-A6VZ-01A-12D-A33E-09 chr1:154542804 C>A maps to NM_000748.2 S109S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZR-A9CJ-01B-11D-A387-09 chr1:154544294 G>A maps to NM_000748.2 A332A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49U-01A-31D-A27G-09 chr8:42586881 C>T maps to NM_000749.3 T144T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OH-01A-11D-A27G-09 chr2:233390933 G>T maps to NM_000751.1 G3G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GR-01A-12D-A37C-09 chr2:233410317 G>A maps to NM_005199.4 S482S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A4P3-01A-11D-A27G-09 chr11:45671710 G>T maps to NM_003654.4 R255R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OE-01A-11D-A27G-09 chr11:45671279 C>T maps to NM_003654.4 S398S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8WC-01A-11D-A37C-09 chr2:101014406 G>T maps to NM_004854.3 G130G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8Q7-01A-11D-A37C-09 chr2:101010093 G>A maps to NM_004854.3 N228N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A9-01A-11D-A28B-09 chr12:104995744 G>T maps to NM_018413.5 L60L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr7:2473032 C>T maps to NM_018641.3 S253S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S8-A6BW-01A-11D-A31U-09 chr3:126261327 C>T maps to NM_152889.1 I311I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A8JD-01A-11D-A36J-09 chr3:126260799 G>A maps to NM_152889.1 P135P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NE-01A-11D-A37C-09 chr10:125805568 A>G maps to NM_015892.3 L54L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr10:125804219 C>T maps to NM_015892.3 P254P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FP-01A-31D-A387-09 chr3:142840872 G>T maps to NM_004267.3 T405T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASX-01A-11D-A387-09 chr3:142840239 C>T maps to NM_004267.3 Y194Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr10:73768015 C>T maps to NM_004273.4 H409H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L7-A56G-01A-21D-A27G-09 chr10:73768108 G>A maps to NM_004273.4 V440V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OH-01A-11D-A27G-09 chr16:71571170 C>T maps to NM_001166395.1 N197N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X8-AAAR-01A-11D-A403-09 chr16:71571632 C>T maps to NM_001166395.1 G351G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FB-01A-11D-A33E-09 chr16:75563652 G>T maps to NM_024533.3 L210L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43I-01A-11D-A247-09 chr16:75563604 C>T maps to NM_024533.3 P226P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93F-01A-21D-A37C-09 chr23:46434206 A>C did not map to a codon.
Sequencing variant TCGA-L5-A4OW-01A-11D-A28B-09 chr23:46433544 C>T did not map to a codon.
Sequencing variant TCGA-L5-A8NH-01A-11D-A37C-09 chr23:46433671 G>A did not map to a codon.
Sequencing variant TCGA-IG-A97I-01A-11D-A387-09 chr19:34263466 C>T maps to NM_022467.3 R258R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr19:34263895 G>A maps to NM_022467.3 Q401Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-A7RC-01B-11D-A403-09 chr19:34263697 C>T maps to NM_022467.3 C335C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8WC-01A-11D-A37C-09 chr16:845704 G>A maps to ENST00000317063 Q941Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr10:101953782 T>C maps to NM_001278.3 G644G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L7-A56G-01A-21D-A27G-09 chr2:96934193 G>T did not map to a codon.
Sequencing variant TCGA-L5-A4OU-01A-11D-A28B-09 chr15:78401610 T>C maps to NM_006383.2 R104R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A8-01A-32D-A27G-09 chr19:42790977 C>G maps to NM_015125.3 V41V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A9-01A-11D-A28B-09 chr19:42796613 C>T maps to NM_015125.3 L1057L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OW-01A-11D-A28B-09 chr18:12254814 G>A did not map to a codon.
Sequencing variant TCGA-VR-A8ET-01A-11D-A403-09 chr18:12264412 G>A maps to ENST00000342845 T131T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6F8-01A-11D-A33E-09 chr14:24777025 G>A maps to NM_014430.2 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GF-01A-11D-A37C-09 chr16:11000761 C>T maps to NM_000246.3 S471S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93F-01A-21D-A37C-09 chr16:11001371 C>T maps to NM_000246.3 L675L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KH-A6WC-01A-11D-A33E-09 chr16:11004058 C>A maps to NM_000246.3 S944*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr15:65499357 G>A maps to NM_003613.3 I62I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-A7RE-01A-11D-A351-09 chr15:65489145 T>G maps to NM_003613.3 R1160R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EQ-01A-11D-A36J-09 chr15:65490735 G>T maps to NM_003613.3 R630R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A4QT-01A-21D-A27G-09 chr19:19656498 C>T maps to NM_153221.2 L1049L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A8I0-01A-11D-A36J-09 chr19:19654601 C>A maps to NM_153221.2 P416P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-M9-A5M8-01A-11D-A28B-09 chr19:19654084 C>T maps to NM_153221.2 R336*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASV-01A-11D-A387-09 chr19:19653754 G>A maps to NM_153221.2 G317G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A4QS-01A-11D-A27G-09 chr10:60029031 C>T did not map to a codon.
Sequencing variant TCGA-IG-A8O2-01A-11D-A36J-09 chr9:130928601 T>G maps to NM_012127.2 T857T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EX-01A-11D-A36J-09 chr9:130941327 C>T maps to NM_012127.2 Q386Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43M-01A-11D-A247-09 chr11:46776436 C>A did not map to a codon.
Sequencing variant TCGA-LN-A4A6-01A-11D-A27G-09 chr11:46810290 T>C maps to ENST00000415402 P636P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43C-01A-11D-A247-09 chr9:91930117 A>G maps to NM_001827.1 Q31Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr2:122125239 T>C maps to NM_015282.2 S1270S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FE-01A-11D-A33E-09 chr3:33580286 G>T maps to ENST00000359576 G1193G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6L4-01A-11D-A31U-09 chr1:86919121 C>T maps to NM_006536.5 S742S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6F8-01A-11D-A33E-09 chr7:143027863 G>T did not map to a codon.
Sequencing variant TCGA-L7-A56G-01A-21D-A27G-09 chr3:184075626 G>A maps to NM_004366.4 I211I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FP-01A-31D-A387-09 chr23:10180565 G>T did not map to a codon.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr23:49806966 G>T did not map to a codon.
Sequencing variant TCGA-LN-A8I1-01A-11D-A36J-09 chr1:11894292 C>T maps to ENST00000376496 S509S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GK-01A-11D-A37C-09 chr16:1515267 C>A maps to ENST00000382745 P71P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6Y2-01B-11D-A33E-09 chr16:1497473 G>T maps to ENST00000382745 S723S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FP-01A-31D-A387-09 chr1:16357019 G>T maps to NM_004070.3 L491L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A6QS-01A-12D-A33E-09 chr13:96230261 T>C maps to NM_182848.3 Y225Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GK-01A-11D-A37C-09 chr21:31538833 A>G maps to NM_012131.2 A34A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GO-01A-11D-A37C-09 chr3:137742602 C>T maps to NM_016369.3 S108S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A6-01A-11D-A27G-09 chr3:137729264 T>A maps to NM_016369.3 Y66*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr23:106171567 G>A did not map to a codon.
Sequencing variant TCGA-R6-A6Y2-01B-11D-A33E-09 chr22:19511943 G>T maps to NM_003277.3 P30P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-A7RC-01B-11D-A403-09 chr16:3065854 C>A maps to NM_021195.4 V56V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A8HZ-01A-11D-A36J-09 chr21:31587979 G>T maps to NM_199328.2 S88S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93C-01A-11D-A387-09 chr3:98240277 C>T maps to NM_001040182.1 L20L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NG-01A-11D-A37C-09 chr12:10167209 C>T maps to NM_001129998.1 S93S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49X-01A-31D-A27G-09 chr14:38724770 C>A maps to NM_175060.1 E153*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6L6-01B-11D-A33E-09 chr14:38724780 G>A maps to NM_175060.1 T149T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OO-01A-11D-A27G-09 chr16:69988451 C>T maps to NM_182619.2 N144N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NS-01A-12D-A37C-09 chr12:10151695 G>A maps to NM_016509.3 Q2*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr3:45077349 C>T maps to NM_003278.2 N181N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8Q7-01A-11D-A37C-09 chr12:8276479 T>G maps to NM_016184.3 T2T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FR-01A-11D-A387-09 chr2:71044149 G>T maps to NM_173535.2 I121I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GK-01A-11D-A37C-09 chr12:8628755 T>C maps to NM_001007033.1 S135S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GR-01A-12D-A37C-09 chr12:10280445 T>A did not map to a codon.
Sequencing variant TCGA-R6-A6XG-01B-11D-A33E-09 chr12:10218212 G>T maps to NM_207345.2 A236A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A938-01A-11D-A37C-09 chr4:141317265 A>G maps to NM_004362.2 N326N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OM-01A-11D-A27G-09 chr4:141321589 G>A maps to NM_004362.2 F205F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A1-01A-21D-A27G-09 chr9:139890206 C>G maps to NM_004669.2 A12A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr7:73770922 C>T maps to NM_003388.4 S329S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6XG-01B-11D-A33E-09 chr7:73791016 G>A maps to NM_003388.4 K762K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A939-01A-12D-A37C-09 chr2:29356671 G>A maps to ENST00000379543 S173S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XP-A8T7-01A-11D-A36J-09 chr1:155238111 G>T maps to ENST00000368361 R176R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-A7RC-01B-11D-A403-09 chr15:74922199 C>T maps to NM_001130028.1 H631H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6Y2-01B-11D-A33E-09 chr5:178032349 C>A maps to NM_020666.2 E390*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr8:1728666 C>T maps to NM_018941.3 F265F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NQ-01A-11D-A36J-09 chr8:1728585 G>T maps to NM_018941.3 L238L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NK-01A-21D-A37C-09 chr4:10492147 C>T maps to NM_052964.2 R410R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6XG-01B-11D-A33E-09 chr11:72004485 G>T maps to NM_030813.3 I683I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3Y9-01A-12D-A247-09 chr19:45476364 C>A maps to NM_001294.2 I69I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FB-01A-11D-A33E-09 chr19:45489735 G>A maps to NM_001294.2 V232V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A8I0-01A-11D-A36J-09 chr5:1341902 G>A maps to NM_030782.3 H112H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A8JD-01A-11D-A36J-09 chr5:1344845 G>A maps to NM_030782.3 S37S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-AAPN-01A-11D-A403-09 chr5:1330462 G>A maps to NM_030782.3 L338L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A8HZ-01A-11D-A36J-09 chr15:65471356 T>C maps to NM_006660.3 S91S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GH-01A-11D-A37C-09 chr3:150690294 G>A maps to NM_001195794.1 H67H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FB-01A-11D-A33E-09 chr4:17524613 G>A maps to NM_001079827.2 P127P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A97I-01A-11D-A387-09 chr1:36214020 G>C maps to NM_022111.3 V819V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A9VB-01A-21D-A37C-09 chr3:140185548 G>T maps to NM_022131.2 A440A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr12:7310094 C>T maps to NM_014718.3 S846S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A50L-01A-11D-A27G-09 chr22:19175594 C>T maps to NM_007098.3 Q1444Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A5U7-01A-11D-A31U-09 chr22:19207486 G>A maps to NM_007098.3 S942S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HW-01A-22D-A351-09 chr22:19210296 G>A maps to NM_007098.3 I776I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S8-A6BW-01A-11D-A31U-09 chr22:19222151 C>A maps to NM_007098.3 L349L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A8I1-01A-11D-A36J-09 chr6:123377006 C>T maps to NM_001010852.2 I244I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NU-01A-11D-A36J-09 chr3:28357822 G>C did not map to a codon.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr16:66612867 C>T maps to NM_052999.3 P275P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NQ-01A-11D-A36J-09 chr3:32398869 G>T maps to NM_178868.3 L51L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA7I-01A-11D-A403-09 chr3:32409470 G>T maps to NM_178868.3 A143A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A4P3-01A-11D-A27G-09 chr5:79095324 C>T maps to NM_153610.3 F4032F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43C-01A-11D-A247-09 chr5:79025230 T>C maps to NM_153610.3 L215L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NS-01A-12D-A37C-09 chr5:79084823 G>A maps to NM_153610.3 L3862L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49R-01A-11D-A247-09 chr5:79025178 C>A maps to NM_153610.3 T197T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EO-01A-11D-A36J-09 chr5:79031680 G>T maps to NM_153610.3 E2365*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EX-01A-11D-A36J-09 chr5:79030184 C>G maps to NM_153610.3 S1866*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8Q7-01A-11D-A37C-09 chr5:79030464 A>G maps to NM_153610.3 Q1959Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A51D-01A-11D-A27G-09 chr8:88297027 T>C maps to NM_173538.2 Y298Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q9-A6FU-01A-11D-A31U-09 chr8:88296976 G>T maps to NM_173538.2 S281S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HZ-01A-31D-A351-09 chr18:72183587 G>A maps to NM_018235.2 R343R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FE-01A-11D-A33E-09 chr23:150906968 C>A did not map to a codon.
Sequencing variant TCGA-LN-A9FP-01A-31D-A387-09 chr23:150909340 C>A did not map to a codon.
Sequencing variant TCGA-L5-A8NN-01A-11D-A37C-09 chr2:99013127 C>T maps to NM_001298.2 R499*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93E-01A-11D-A37C-09 chr16:57996892 C>T maps to NM_001297.4 T122T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49V-01A-11D-A247-09 chr16:57965771 C>T maps to NM_001297.4 T461T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93E-01A-11D-A37C-09 chr8:87751943 C>T maps to NM_019098.4 E50E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NQ-01A-11D-A36J-09 chr8:87588199 A>C maps to NM_019098.4 P754P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GN-01A-11D-A37C-09 chr23:21534648 C>G did not map to a codon.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr23:21627458 C>T did not map to a codon.
Sequencing variant TCGA-L5-A8NI-01A-11D-A37C-09 chr23:21624944 C>T did not map to a codon.
Sequencing variant TCGA-VR-A8EP-01A-31D-A403-09 chr23:21670528 G>C did not map to a codon.
Sequencing variant TCGA-LN-A4A4-01A-11D-A27G-09 chr19:1036245 G>A did not map to a codon.
Sequencing variant TCGA-L5-A88Z-01A-11D-A36J-09 chr10:104809564 G>T maps to NM_017649.3 E575*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GO-01A-11D-A37C-09 chr2:97427929 G>T maps to NM_020184.3 S398S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EX-01A-11D-A36J-09 chr5:154244790 G>T maps to NM_004779.4 E53*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RE-01A-11D-A33E-09 chr7:155301717 C>T maps to NM_001103176.1 K5K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6Y0-01B-11D-A33E-09 chr7:155301588 C>A maps to NM_001103176.1 A48A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L7-A6VZ-01A-12D-A33E-09 chr12:56705096 G>T maps to NM_014255.5 R102R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr6:42905913 C>T maps to NM_006586.3 C194C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A939-01A-12D-A37C-09 chr7:99717418 G>T maps to NM_152755.1 E18*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-AAPN-01A-11D-A403-09 chr6:88854984 C>T maps to NM_016083.4 S3S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A5U5-01A-21D-A28B-09 chr1:24201570 G>T maps to NM_001841.2 C179*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GO-01A-11D-A37C-09 chr2:68544420 A>T maps to NM_015463.2 G66G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FB-01A-11D-A33E-09 chr2:68544288 C>A maps to NM_015463.2 P110P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GH-01A-11D-A37C-09 chr1:246810501 G>A maps to NM_152609.2 L333L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OX-01A-21D-A28B-09 chr17:40956371 G>T maps to NM_173478.2 V125V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GG-01A-11D-A37C-09 chr11:58391894 G>A maps to NM_000614.3 W168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr9:34557905 G>T maps to NM_147164.1 P132P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OO-01A-11D-A27G-09 chr9:17330767 C>T maps to NM_017738.2 R494*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NJ-01A-11D-A36J-09 chr9:17457655 A>G maps to NM_017738.2 S1083S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr9:17457610 A>G maps to NM_017738.2 A1068A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HY-01A-12D-A351-09 chr12:41408075 C>T maps to NM_001843.2 N720N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KH-A6WC-01A-11D-A33E-09 chr1:205033528 C>T maps to NM_005076.3 C440C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr1:205031074 C>T maps to NM_005076.3 G352G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NV-01A-11D-A37C-09 chr1:205039133 C>T maps to NM_005076.3 N792N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49W-01A-11D-A27G-09 chr1:205042859 G>T maps to NM_005076.3 A1030A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A4QS-01A-11D-A27G-09 chr3:74347114 T>C maps to NM_020872.1 A798A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FH-01A-11D-A33E-09 chr3:74385745 A>C maps to NM_020872.1 T476T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L7-A6VZ-01A-12D-A33E-09 chr3:74419074 A>C maps to NM_020872.1 G242G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RE-A7BO-01A-11D-A33E-09 chr3:74414719 T>C maps to NM_020872.1 L360L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NK-01A-21D-A37C-09 chr3:3067915 G>C maps to NM_175607.1 L539L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XP-A8T7-01A-11D-A36J-09 chr3:3085369 G>T maps to NM_175607.1 S931S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GG-01A-11D-A37C-09 chr11:99931942 G>T did not map to a codon.
Sequencing variant TCGA-L5-A4OJ-01A-11D-A27G-09 chr11:100061923 C>T maps to NM_014361.2 Y549Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NG-01A-11D-A37C-09 chr11:100061872 A>G maps to NM_014361.2 P532P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASV-01A-11D-A387-09 chr11:100064337 G>T maps to NM_014361.2 L609L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NG-01A-11D-A37C-09 chr3:1425019 T>C maps to NM_014461.2 S815S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OH-01A-11D-A27G-09 chr17:40849293 G>T maps to NM_003632.2 V1159V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OX-01A-21D-A28B-09 chr17:40841640 C>T maps to NM_003632.2 H577H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr17:40845372 C>T maps to NM_003632.2 N937N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A938-01A-11D-A37C-09 chr7:147926792 C>T maps to NM_014141.5 D1101D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43E-01A-11D-A247-09 chr7:147675016 A>T maps to NM_014141.5 G773G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A893-01A-11D-A36J-09 chr7:147600655 G>T did not map to a codon.
Sequencing variant TCGA-V5-A7RE-01A-11D-A351-09 chr7:148080840 C>T maps to NM_014141.5 A1192A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OR-01A-11D-A27G-09 chr9:39288004 A>C maps to NM_033655.3 T19T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43E-01A-11D-A247-09 chr16:76482820 A>G maps to NM_033401.3 E299E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr2:125192202 G>A maps to NM_130773.2 Q224Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASW-01A-11D-A403-09 chr2:125204489 G>A maps to NM_130773.2 T298T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASX-01A-11D-A387-09 chr2:125192142 G>A maps to NM_130773.2 V204V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr17:7839716 C>T maps to NM_001037144.4 R210*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OH-01A-11D-A27G-09 chr7:51096449 G>T maps to ENST00000395542 G863G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49R-01A-11D-A247-09 chr7:51096149 G>C maps to ENST00000395542 V963V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S8-A6BW-01A-11D-A31U-09 chr7:51096640 G>A maps to ENST00000395542 R800*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49X-01A-31D-A27G-09 chr1:230822766 A>G maps to NM_007357.2 Q489Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NQ-01A-11D-A36J-09 chr16:70551569 C>A maps to NM_015386.2 E110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49L-01A-11D-A247-09 chr16:70546282 G>C maps to NM_015386.2 L199L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr7:107188597 G>T maps to NM_006348.3 Y156*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A2-01A-31D-A27G-09 chr7:106897226 G>A maps to NM_006348.3 Q598*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OX-01A-21D-A28B-09 chr16:23415146 C>T maps to NM_153603.3 G557G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A893-01A-11D-A36J-09 chr16:23400366 C>T maps to NM_153603.3 P729P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49Y-01A-11D-A27G-09 chr16:23464261 A>G maps to NM_153603.3 N18N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA7D-01A-11D-A403-09 chr16:23421668 G>T maps to NM_153603.3 T474T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4ON-01A-11D-A27G-09 chr16:69368467 G>A maps to NM_032382.4 L457L. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-2H-A9GQ-01A-11D-A37C-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-KH-A6WC-01A-11D-A33E-09 chr6:116441236 C>A maps to NM_000493.3 *681L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FP-01A-31D-A387-09 chr6:116441946 G>T maps to NM_000493.3 A444A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93E-01A-11D-A37C-09 chr1:103364236 G>T maps to NM_080629.2 G1423G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr1:103488444 G>A maps to NM_080629.2 D378D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6KZ-01A-11D-A31U-09 chr1:103380334 T>C maps to NM_080629.2 E1295E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S8-A6BW-01A-11D-A31U-09 chr1:103440439 C>A did not map to a codon.
Sequencing variant TCGA-V5-A7RC-01B-11D-A403-09 chr1:103364293 G>T maps to NM_080629.2 T1404T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A8JD-01A-11D-A36J-09 chr1:103444648 G>T maps to NM_080629.2 G886G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A9-01A-11D-A28B-09 chr6:33147583 T>C did not map to a codon.
Sequencing variant TCGA-Z6-A9VB-01A-21D-A37C-09 chr6:33138675 C>A maps to NM_080680.2 G1129*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr6:75836148 G>A maps to ENST00000322507 D2126D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FP-01A-31D-A387-09 chr6:75843645 C>T maps to ENST00000322507 W1864*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8WC-01A-11D-A37C-09 chr6:75831040 C>A maps to ENST00000322507 E2355*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EQ-01A-11D-A36J-09 chr6:75834918 G>A maps to ENST00000322507 S2177S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-AAPN-01A-11D-A403-09 chr6:75893759 G>A maps to ENST00000322507 V366V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA7D-01A-11D-A403-09 chr10:71678828 G>A maps to ENST00000356340 G347G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RE-01A-11D-A33E-09 chr8:121301869 T>G maps to NM_021110.1 T1367T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A4QS-01A-11D-A27G-09 chr8:121381665 T>A maps to NM_021110.1 G1751G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KH-A6WC-01A-11D-A33E-09 chr8:121243716 G>T maps to NM_021110.1 G737*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NN-01A-11D-A37C-09 chr8:121256239 A>G maps to NM_021110.1 G824G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8W5-01B-11D-A37C-09 chr8:121344397 G>T maps to NM_021110.1 G1560*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr9:101706452 C>T maps to NM_001855.3 N7N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A5-01A-21D-A27G-09 chr9:101811973 C>T maps to NM_001855.3 G932G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA7I-01A-11D-A403-09 chr9:101818558 A>C maps to NM_001855.3 T1070T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A9VB-01A-21D-A37C-09 chr9:101706527 G>T maps to NM_001855.3 A32A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XP-A8T8-01A-11D-A36J-09 chr1:32133199 C>T maps to NM_001856.3 G1111G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FD-01A-11D-A33E-09 chr10:105830295 G>C maps to NM_000494.3 L165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6XQ-01B-11D-A33E-09 chr10:105801270 T>A maps to NM_000494.3 P859P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A9VB-01A-21D-A37C-09 chr10:105837198 G>A maps to NM_000494.3 S61S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GJ-01A-11D-A37C-09 chr21:46925781 C>T maps to ENST00000359759 L1455L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8W5-01B-11D-A37C-09 chr21:46895448 G>A maps to ENST00000359759 T681T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EZ-01A-11D-A36J-09 chr21:46914473 C>T maps to ENST00000359759 R1205*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EQ-01A-11D-A36J-09 chr7:94039078 C>T maps to NM_000089.3 R327R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88V-01A-11D-A351-09 chr20:61926503 G>A maps to ENST00000326996 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OR-01A-11D-A27G-09 chr8:139774710 T>G did not map to a codon.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr8:139706797 G>A maps to NM_152888.1 Q885*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EQ-01A-11D-A36J-09 chr8:139658916 A>G maps to NM_152888.1 A1152A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OT-01A-11D-A28B-09 chr5:177689226 G>A maps to ENST00000390654 D222D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RE-01A-11D-A33E-09 chr1:86249801 G>T maps to NM_152890.5 G1405G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HY-01A-12D-A351-09 chr1:86512549 G>T maps to NM_152890.5 G636G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88V-01A-11D-A351-09 chr4:110223106 G>A maps to ENST00000333642 A23A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4ON-01A-11D-A27G-09 chr9:117063405 G>A did not map to a codon.
Sequencing variant TCGA-JY-A6F8-01A-11D-A33E-09 chr12:48391418 G>T maps to NM_001844.4 P167P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr12:48378777 G>A maps to NM_001844.4 N611N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-A7RE-01A-11D-A351-09 chr12:48378876 C>A did not map to a codon.
Sequencing variant TCGA-2H-A9GQ-01A-11D-A37C-09 chr2:189870167 T>A maps to NM_000090.3 G1008G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OH-01A-11D-A27G-09 chr2:189860904 G>A did not map to a codon.
Sequencing variant TCGA-VR-A8EU-01A-11D-A36J-09 chr2:189854838 C>T maps to NM_000090.3 P236P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A4P3-01A-11D-A27G-09 chr13:111102087 G>T maps to NM_001846.2 G381*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr2:228128619 A>G maps to NM_000091.4 S425S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4MR-01A-11D-A28B-09 chr2:228111450 C>T maps to NM_000091.4 I146I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OH-01A-11D-A27G-09 chr2:227983418 G>T maps to ENST00000396625 S144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NQ-01A-11D-A36J-09 chr2:227872751 G>A maps to ENST00000396625 I1597I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GL-01A-12D-A37C-09 chr23:107858206 A>G did not map to a codon.
Sequencing variant TCGA-JY-A6FH-01A-11D-A33E-09 chr23:107920801 G>T did not map to a codon.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr23:107929266 C>T did not map to a codon.
Sequencing variant TCGA-L5-A4OQ-01A-11D-A27G-09 chr23:107802334 G>T did not map to a codon.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr23:107898610 T>C did not map to a codon.
Sequencing variant TCGA-L5-A8NR-01A-11D-A37C-09 chr23:107840673 C>A did not map to a codon.
Sequencing variant TCGA-R6-A8WG-01A-11D-A37C-09 chr23:107923919 C>T did not map to a codon.
Sequencing variant TCGA-VR-AA4D-01A-11D-A37C-09 chr23:107924124 A>G did not map to a codon.
Sequencing variant TCGA-2H-A9GO-01A-11D-A37C-09 chr23:107413218 C>A did not map to a codon.
Sequencing variant TCGA-IG-A3Y9-01A-12D-A247-09 chr23:107400266 C>T did not map to a codon.
Sequencing variant TCGA-JY-A93E-01A-11D-A37C-09 chr23:107464498 G>A did not map to a codon.
Sequencing variant TCGA-LN-A4A4-01A-11D-A27G-09 chr23:107431879 C>T did not map to a codon.
Sequencing variant TCGA-R6-A6L6-01B-11D-A33E-09 chr23:107422507 G>T did not map to a codon.
Sequencing variant TCGA-Z6-A8JE-01A-11D-A37C-09 chr23:107408225 G>C did not map to a codon.
Sequencing variant TCGA-2H-A9GJ-01A-11D-A37C-09 chr9:137582860 G>T maps to NM_000093.3 P71P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GK-01A-11D-A37C-09 chr9:137715272 C>A maps to NM_000093.3 G1552G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GL-01A-12D-A37C-09 chr9:137697035 G>C maps to NM_000093.3 G1078G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OU-01A-11D-A28B-09 chr9:137704470 C>A maps to NM_000093.3 G1255G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L7-A6VZ-01A-12D-A33E-09 chr9:137620554 G>T maps to NM_000093.3 E276*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-A7RB-01A-11D-A351-09 chr9:137708900 T>G maps to NM_000093.3 G1384G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EY-01A-11D-A36J-09 chr9:137658325 G>A maps to NM_000093.3 P705P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A893-01A-11D-A36J-09 chr2:189949925 G>T maps to NM_000393.3 S253*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49S-01A-11D-A247-09 chr2:189917477 C>T maps to NM_000393.3 P904P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A5U7-01A-11D-A31U-09 chr2:189933523 A>T maps to NM_000393.3 S415S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S8-A6BV-01A-21D-A31U-09 chr2:189945769 C>A did not map to a codon.
Sequencing variant TCGA-IG-A3YC-01A-11D-A247-09 chr19:10083615 C>T maps to NM_015719.3 E1251E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OR-01A-11D-A27G-09 chr19:10091480 C>G did not map to a codon.
Sequencing variant TCGA-L5-A8NF-01A-11D-A37C-09 chr19:10077031 C>T maps to NM_015719.3 A1580A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr21:47423638 C>T maps to NM_001848.2 G933G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FA-01A-11D-A33E-09 chr21:47545376 A>C maps to ENST00000413758 P162P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43E-01A-11D-A247-09 chr21:47546098 C>T maps to NM_001849.3 S790S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NQ-01A-11D-A36J-09 chr21:47542072 G>A did not map to a codon.
Sequencing variant TCGA-V5-AASX-01A-11D-A387-09 chr21:47536709 C>T maps to NM_001849.3 N327N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3I8-01A-11D-A247-09 chr2:238280600 G>A maps to NM_004369.3 D1353D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93E-01A-11D-A37C-09 chr2:238263550 G>A maps to NM_004369.3 P2206P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OG-01A-11D-A27G-09 chr2:238283178 G>T maps to NM_004369.3 A1185A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HV-01A-21D-A351-09 chr2:238259799 T>A maps to NM_004369.3 R2263R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASX-01A-11D-A387-09 chr2:238275717 G>A maps to NM_004369.3 D1704D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-AAPN-01A-11D-A403-09 chr2:238261194 C>G maps to NM_004369.3 L2241L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GR-01A-12D-A37C-09 chr3:130103861 A>C maps to ENST00000312481 R506R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RE-01A-11D-A33E-09 chr3:130114046 A>C maps to ENST00000312481 R1103R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RE-01A-11D-A33E-09 chr3:130114054 T>A maps to ENST00000312481 A1105A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A4P3-01A-11D-A27G-09 chr3:130110052 G>T maps to ENST00000312481 V816V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FD-01A-11D-A33E-09 chr3:130188258 C>T maps to ENST00000312481 R2471*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XP-A8T7-01A-11D-A36J-09 chr3:130107706 C>T maps to ENST00000312481 Q716*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NG-01A-11D-A37C-09 chr3:130287170 G>T maps to NM_001102608.1 V708V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A5-01A-21D-A27G-09 chr3:130325810 G>T did not map to a codon.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr3:48616351 G>A maps to NM_000094.3 D1808D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OS-01A-11D-A28B-09 chr3:48606261 C>T maps to NM_000094.3 K2571K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88Z-01A-11D-A36J-09 chr6:70965093 C>G did not map to a codon.
Sequencing variant TCGA-L5-A4OJ-01A-11D-A27G-09 chr1:40779927 G>T maps to NM_001852.3 G66G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr8:120101973 A>G maps to NM_006438.3 G68G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-AAPN-01A-11D-A403-09 chr18:346688 C>A maps to NM_130386.2 L311L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93E-01A-11D-A37C-09 chr13:76104339 C>T maps to NM_203497.2 K39K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NV-01A-11D-A37C-09 chr11:36300160 G>A maps to NM_014186.3 L61L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49S-01A-11D-A247-09 chr19:18899659 G>A maps to NM_000095.2 C197C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6DQ-01B-11D-A31U-09 chr22:19956207 C>T maps to NM_001135162.1 D255D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OJ-01A-11D-A27G-09 chr1:160283885 G>T maps to NM_001098398.1 R246R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OX-01A-21D-A28B-09 chr1:160305049 G>A maps to NM_001098398.1 R97R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GR-01A-12D-A37C-09 chr11:14510126 G>T maps to NM_001144061.1 R204R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr11:14486550 C>T maps to NM_001144061.1 P772P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OR-01A-11D-A27G-09 chr11:14490267 T>G maps to NM_001144061.1 R702R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49U-01A-31D-A27G-09 chr11:14498548 T>C maps to NM_001144061.1 G457G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GL-01A-12D-A37C-09 chr7:99688229 G>T maps to NM_006833.4 E147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49U-01A-31D-A27G-09 chr7:99688532 C>T maps to NM_006833.4 V165V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6F8-01A-11D-A33E-09 chr12:54741804 C>A maps to NM_016057.1 P139P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A7DP-01A-31D-A33E-09 chr12:56661665 G>T maps to NM_144576.3 G75*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FH-01A-11D-A33E-09 chr12:120966889 G>T maps to NM_032314.3 R19R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr16:30198369 C>T maps to NM_007074.3 N154N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-A7RB-01A-11D-A351-09 chr11:67207668 C>T maps to NM_020441.2 T309T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93D-01A-11D-A387-09 chr9:100887123 G>A maps to NM_052820.3 R504*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6F8-01A-11D-A33E-09 chr16:4409312 G>T maps to NM_024535.3 S775*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A891-01A-11D-A36J-09 chr16:4455541 G>A maps to NM_024535.3 Q172*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr17:14095521 G>A maps to NM_001303.3 T304T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FR-01A-11D-A387-09 chr17:14063219 C>T maps to NM_001303.3 N217N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GO-01A-11D-A37C-09 chr5:85913913 C>T maps to NM_001867.2 V14V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EU-01A-11D-A36J-09 chr3:148925177 G>A maps to NM_000096.3 L336L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GQ-01A-11D-A37C-09 chr16:19559291 C>T maps to NM_014711.4 N952N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RF-01A-13D-A33E-09 chr16:19547486 G>T maps to NM_014711.4 E166*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93F-01A-21D-A37C-09 chr7:129906762 G>A maps to NM_001869.2 G14G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GO-01A-11D-A37C-09 chr7:129933070 C>A maps to NM_016352.3 G17G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88S-01A-11D-A36J-09 chr7:129946697 T>A maps to NM_016352.3 P221P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RF-01A-13D-A33E-09 chr7:129986352 G>A maps to NM_080385.4 T9T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43C-01A-11D-A247-09 chr7:130007802 C>A maps to NM_080385.4 Y365*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OE-01A-11D-A27G-09 chr7:129989931 C>A maps to NM_080385.4 I105I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr19:17062997 A>G maps to ENST00000443236 G820G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASX-01A-11D-A387-09 chr3:148552395 G>T maps to NM_001871.2 E87*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A3-01A-11D-A27G-09 chr17:28772819 A>G maps to NM_001304.4 K885K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NQ-01A-11D-A36J-09 chr5:173372060 C>A maps to NM_030627.2 C458*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr5:175306034 C>T maps to NM_001008220.1 H52H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr20:34218839 C>A maps to NM_003915.5 V331V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NT-01A-11D-A37C-09 chr16:57153172 C>T maps to NM_152727.5 L192L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OU-01A-11D-A28B-09 chr3:131268913 T>G maps to ENST00000502818 G411G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OH-01A-11D-A27G-09 chr6:36711497 G>T maps to NM_020939.1 R511R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A8-01A-32D-A27G-09 chr6:36730752 C>A maps to NM_020939.1 E266*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6L4-01A-11D-A31U-09 chr6:36790833 G>A maps to NM_020939.1 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr16:89657607 G>A maps to NM_014427.4 A489A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FH-01A-11D-A33E-09 chr12:39047738 G>T maps to NM_153634.2 S547*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OE-01A-11D-A27G-09 chr12:39155951 C>T maps to NM_153634.2 K214K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FB-01A-11D-A33E-09 chr2:211515162 G>T did not map to a codon.
Sequencing variant TCGA-L5-A4OW-01A-11D-A28B-09 chr8:145624695 C>G maps to NM_013291.2 S454S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NJ-01A-11D-A36J-09 chr8:145618984 G>A maps to NM_013291.2 L1348L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EZ-01A-11D-A36J-09 chr8:145626337 G>A maps to NM_013291.2 H173H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8WC-01A-11D-A37C-09 chr12:69652799 C>T maps to ENST00000266679 S412S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-A7RC-01B-11D-A403-09 chr12:69656278 G>A maps to ENST00000266679 R569R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-A7RC-01B-11D-A403-09 chr12:69656281 T>C maps to ENST00000266679 D570D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-A7RC-01B-11D-A403-09 chr12:69656320 C>T maps to ENST00000266679 R583R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A97I-01A-11D-A387-09 chr22:51010649 G>T maps to NM_152245.2 I480I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8W8-01B-11D-A37C-09 chr19:50208473 T>C maps to NM_152359.2 L295L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GF-01A-11D-A37C-09 chr23:88008519 T>C did not map to a codon.
Sequencing variant TCGA-L5-A43I-01A-11D-A247-09 chr23:88009050 G>C did not map to a codon.
Sequencing variant TCGA-LN-A49Y-01A-11D-A27G-09 chr23:88008706 A>G did not map to a codon.
Sequencing variant TCGA-R6-A6KZ-01A-11D-A31U-09 chr23:88009208 T>G did not map to a codon.
Sequencing variant TCGA-VR-A8EX-01A-11D-A36J-09 chr20:2777868 G>T maps to NM_019609.4 L267L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GR-01A-12D-A37C-09 chr10:125506302 G>A maps to NM_198148.2 Q750*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GQ-01A-11D-A37C-09 chr4:8605847 G>A maps to NM_001014447.2 G214G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6F8-01A-11D-A33E-09 chr4:8620211 C>T maps to NM_001014447.2 N520N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A8-01A-32D-A27G-09 chr4:8620226 C>G maps to NM_001014447.2 V525V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OW-01A-11D-A28B-09 chr1:207755262 G>T maps to NM_000651.4 G1739G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A1-01A-21D-A27G-09 chr1:207872576 G>T maps to NM_175710.1 G396*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S8-A6BV-01A-21D-A31U-09 chr1:207648205 G>A maps to NM_001006658.2 G787G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6XQ-01B-11D-A33E-09 chr16:1676114 G>A maps to NM_020825.3 W163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EW-01A-11D-A36J-09 chr16:1716164 G>A maps to NM_020825.3 T948T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NG-01A-11D-A37C-09 chr9:131862206 G>A maps to NM_000755.3 Y341Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr1:197390733 C>T maps to NM_201253.2 I592I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OJ-01A-11D-A27G-09 chr1:197297561 C>T maps to NM_201253.2 C27C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FP-01A-31D-A387-09 chr1:197316468 G>T did not map to a codon.
Sequencing variant TCGA-VR-AA7B-01A-31D-A403-09 chr1:197404163 C>T maps to NM_201253.2 N1057N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49U-01A-31D-A27G-09 chr9:126133014 G>A maps to NM_173689.5 P561P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3Y9-01A-12D-A247-09 chr7:65617256 C>A maps to NM_014478.4 V120V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3Y9-01A-12D-A247-09 chr7:65617266 C>T maps to NM_014478.4 L124L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49M-01A-21D-A27G-09 chr7:65617253 C>T maps to NM_014478.4 T119T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OT-01A-11D-A28B-09 chr1:152487999 C>T maps to NM_019060.2 C47C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr9:35733096 C>T maps to NM_006368.4 D78D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49M-01A-21D-A27G-09 chr7:137686397 C>T maps to NM_194071.2 L18L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GQ-01A-11D-A37C-09 chr16:3824651 A>T maps to NM_004380.2 L734*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FE-01A-11D-A33E-09 chr16:3820587 G>A maps to NM_004380.2 Q955*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OJ-01A-11D-A27G-09 chr16:3789595 G>T maps to NM_004380.2 C1421*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49K-01A-11D-A247-09 chr16:3807901 G>A maps to NM_004380.2 R1173*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A4-01A-11D-A27G-09 chr16:3781438 G>A maps to NM_004380.2 V1642V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8WC-01A-11D-A37C-09 chr22:50320931 C>T maps to NM_001135101.1 L396L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L7-A6VZ-01A-12D-A33E-09 chr5:76264602 G>T maps to NM_001882.3 G288*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-AAPN-01A-11D-A403-09 chr17:43907862 C>A maps to NM_001145146.1 Y241*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A938-01A-11D-A37C-09 chr2:36744518 C>T maps to NM_016441.2 H680H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EX-01A-11D-A36J-09 chr2:36668612 G>T maps to NM_016441.2 E240*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr4:1388568 C>T maps to NM_175918.3 A90A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GM-01A-11D-A37C-09 chr6:49700906 C>T did not map to a codon.
Sequencing variant TCGA-LN-A4A6-01A-11D-A27G-09 chr22:21272498 C>T maps to NM_005207.3 L93L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA7B-01A-31D-A403-09 chr20:6011943 C>T maps to NM_019095.4 Y196Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr4:5843032 A>G did not map to a codon.
Sequencing variant TCGA-L5-A4OU-01A-11D-A28B-09 chr4:5838625 A>G maps to NM_001014809.1 L440L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OT-01A-11D-A28B-09 chr20:20033127 A>C maps to NM_016652.4 G114G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr1:17265553 C>T maps to NM_014675.3 R509*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr1:159683860 C>T maps to NM_000567.2 P43P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GK-01A-11D-A37C-09 chr10:99677287 C>A maps to NM_018058.4 V228V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FB-01A-11D-A33E-09 chr10:99655677 G>T maps to NM_018058.4 S427S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OR-01A-11D-A27G-09 chr10:99770905 G>A maps to NM_018058.4 I71I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X8-AAAR-01A-11D-A403-09 chr19:18882280 C>T maps to NM_001098482.1 S466S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93F-01A-21D-A37C-09 chr15:91181742 G>A maps to NM_022769.3 P444P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OU-01A-11D-A28B-09 chr15:91172646 T>C maps to NM_022769.3 S383S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A4P3-01A-11D-A27G-09 chr12:107391314 G>T maps to NM_004075.3 I481I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6KZ-01A-11D-A31U-09 chr12:107399003 G>T maps to NM_004075.3 S97*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr11:45891124 G>T maps to NM_021117.3 T338T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OP-01A-11D-A27G-09 chr11:45892000 C>T maps to NM_021117.3 I510I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NJ-01A-11D-A36J-09 chr21:44589331 G>A maps to NM_000394.2 S41S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr22:27024394 G>A did not map to a codon.
Sequencing variant TCGA-L5-A8NF-01A-11D-A37C-09 chr3:97617779 G>A maps to ENST00000182096 K637K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GH-01A-11D-A37C-09 chr13:20978791 A>T maps to NM_015974.2 T276T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NG-01A-11D-A37C-09 chr13:20987430 G>C maps to NM_015974.2 L243L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8W8-01B-11D-A37C-09 chr1:75172867 T>A maps to NM_001889.3 G217G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6L4-01A-11D-A31U-09 chr1:115275389 T>C maps to NM_001130523.1 K310K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-AAPN-01A-11D-A403-09 chr20:47704603 C>T maps to NM_001316.2 L594L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HY-01A-12D-A351-09 chr5:149459675 G>A maps to NM_005211.3 C177C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A51D-01A-11D-A27G-09 chr23:1409283 G>T did not map to a codon.
Sequencing variant TCGA-JY-A6FB-01A-11D-A33E-09 chr23:1428407 G>A did not map to a codon.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr23:1424390 C>T did not map to a codon.
Sequencing variant TCGA-LN-A4A1-01A-21D-A27G-09 chr23:1409388 C>G did not map to a codon.
Sequencing variant TCGA-LN-A5U7-01A-11D-A31U-09 chr23:1419477 G>A did not map to a codon.
Sequencing variant TCGA-IG-A3Y9-01A-12D-A247-09 chr22:37326489 G>A maps to ENST00000262825 V264V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr22:37328883 C>T maps to ENST00000262825 R370*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6DN-01B-11D-A31U-09 chr22:37334388 G>T maps to ENST00000262825 E853*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OH-01A-11D-A27G-09 chr1:36934835 G>T maps to NM_156039.3 L499L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RE-01A-11D-A33E-09 chr8:19362934 G>T maps to NM_018371.4 V137V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FD-01A-11D-A33E-09 chr8:2954437 G>T maps to NM_033225.5 Y2357*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L7-A6VZ-01A-12D-A33E-09 chr8:2976016 C>A maps to NM_033225.5 E2112*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49N-01A-11D-A247-09 chr8:3200962 C>A maps to NM_033225.5 G1162*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6DN-01B-11D-A31U-09 chr8:2975918 A>T did not map to a codon.
Sequencing variant TCGA-2H-A9GK-01A-11D-A37C-09 chr1:34164353 G>A maps to ENST00000373381 V1268V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GR-01A-12D-A37C-09 chr1:34042989 G>A maps to ENST00000373381 N2454N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A4QS-01A-11D-A27G-09 chr1:34037134 G>A maps to ENST00000373381 R2612*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FH-01A-11D-A33E-09 chr1:34066492 T>C maps to ENST00000373381 T2236T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NG-01A-11D-A37C-09 chr1:34076779 G>T maps to ENST00000373381 P2028P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S8-A6BV-01A-21D-A31U-09 chr1:34042917 G>A maps to ENST00000373381 S2478S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GF-01A-11D-A37C-09 chr8:113249506 G>T maps to NM_198123.1 P3513P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RE-01A-11D-A33E-09 chr8:113318413 G>T maps to NM_198123.1 S2631S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A4P3-01A-11D-A27G-09 chr8:113504785 G>T maps to NM_198123.1 S1737*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr8:113529437 C>T maps to NM_198123.1 A1527A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OG-01A-11D-A27G-09 chr8:113516027 C>A maps to NM_198123.1 E1692*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr8:113349855 C>A maps to NM_198123.1 G2253*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HV-01A-21D-A351-09 chr8:114031350 C>T maps to NM_198123.1 L325L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HY-01A-12D-A351-09 chr8:113563013 C>A maps to NM_198123.1 E1484*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6KZ-01A-11D-A31U-09 chr8:113348959 T>G maps to NM_198123.1 R2314R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S8-A6BV-01A-21D-A31U-09 chr8:114186074 G>A maps to NM_198123.1 D195D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A9VB-01A-21D-A37C-09 chr8:113267519 T>A maps to NM_198123.1 A3333A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GQ-01A-11D-A37C-09 chr13:37678733 C>T maps to NM_145203.5 P220P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FH-01A-11D-A33E-09 chr13:37678391 C>T maps to NM_145203.5 V334V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HX-01A-11D-A33E-09 chr6:31637231 C>T maps to ENST00000375885 F187F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3QL-01A-11D-A247-09 chr15:75981215 C>T maps to NM_001897.4 A730A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NJ-01A-11D-A36J-09 chr15:75979739 C>T maps to NM_001897.4 T1222T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NK-01A-21D-A37C-09 chr15:75981845 C>T maps to NM_001897.4 L520L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XP-A8T7-01A-11D-A36J-09 chr3:47604143 G>T maps to ENST00000383738 G549G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A5S3-01A-11D-A28B-09 chr8:67986505 G>T maps to ENST00000389042 E43*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NW-01A-11D-A37C-09 chr8:68044183 A>G did not map to a codon.
Sequencing variant TCGA-LN-A8I0-01A-11D-A36J-09 chr8:68092095 A>G did not map to a codon.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr2:166535345 C>T maps to ENST00000409420 R313*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OP-01A-11D-A27G-09 chr20:18123480 C>G maps to NM_020536.4 L59L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NJ-01A-11D-A36J-09 chr20:18123369 G>T maps to NM_020536.4 S22S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GI-01A-11D-A37C-09 chr20:23728461 T>C maps to NM_001898.2 Q139Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A9VB-01A-21D-A37C-09 chr20:23731293 T>C maps to NM_001898.2 V70V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GG-01A-11D-A37C-09 chr20:23804665 T>C maps to NM_001322.2 Q139Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NR-01A-11D-A37C-09 chr20:23473635 C>T maps to NM_005492.2 A91A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A891-01A-11D-A36J-09 chr23:100088346 C>G did not map to a codon.
Sequencing variant TCGA-L5-A8NH-01A-11D-A37C-09 chr23:100081701 C>T did not map to a codon.
Sequencing variant TCGA-L5-A8NK-01A-21D-A37C-09 chr23:100079172 G>A did not map to a codon.
Sequencing variant TCGA-L5-A4ON-01A-11D-A27G-09 chr23:120008880 G>T did not map to a codon.
Sequencing variant TCGA-L5-A8NH-01A-11D-A37C-09 chr23:120008761 C>T did not map to a codon.
Sequencing variant TCGA-R6-A8WC-01A-11D-A37C-09 chr23:120009284 G>A did not map to a codon.
Sequencing variant TCGA-LN-A9FQ-01A-31D-A387-09 chr23:153881745 G>A did not map to a codon.
Sequencing variant TCGA-2H-A9GL-01A-12D-A37C-09 chr18:19996549 T>A maps to NM_172241.2 K409*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6F8-01A-11D-A33E-09 chr18:19996487 T>C maps to NM_172241.2 A429A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OH-01A-11D-A27G-09 chr14:39790260 G>T did not map to a codon.
Sequencing variant TCGA-LN-A7HZ-01A-31D-A351-09 chr6:132031716 G>T maps to NM_001145659.1 L147L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A893-01A-11D-A36J-09 chr10:126678146 C>T maps to NM_022802.2 A966A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NE-01A-11D-A37C-09 chr10:126682491 T>C maps to NM_022802.2 L821L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4MQ-01A-11D-A28B-09 chr10:126678086 C>T maps to NM_022802.2 *986*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6Y2-01B-11D-A33E-09 chr10:126715317 G>A maps to NM_022802.2 G337G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88Z-01A-11D-A36J-09 chr1:85020792 C>A maps to NM_004388.2 R349R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA4G-01A-11D-A37C-09 chr1:85040023 C>T maps to NM_004388.2 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr18:77474866 C>T maps to NM_004715.3 S469S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr18:77496372 G>T maps to NM_004715.3 E867*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49X-01A-31D-A27G-09 chr18:77496417 C>T maps to NM_004715.3 Q882*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6KZ-01A-11D-A31U-09 chr18:77477872 G>A maps to NM_004715.3 P758P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A893-01A-11D-A36J-09 chr3:37988614 C>T maps to NM_001008392.1 C49C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6L6-01B-11D-A33E-09 chr5:138145893 G>T did not map to a codon.
Sequencing variant TCGA-2H-A9GI-01A-11D-A37C-09 chr2:80646692 A>G maps to ENST00000402739 Q419Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93C-01A-11D-A387-09 chr2:80782890 G>T maps to ENST00000402739 R538R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NR-01A-11D-A37C-09 chr10:68040263 T>C maps to NM_013266.2 T616T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RE-A7BO-01A-11D-A33E-09 chr10:69366708 A>C maps to NM_013266.2 T66T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A51D-01A-11D-A27G-09 chr9:111741737 C>T maps to NM_003798.2 E308E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr3:41275789 T>C did not map to a codon.
Sequencing variant TCGA-L5-A8NR-01A-11D-A37C-09 chr3:41266204 C>T maps to NM_001904.3 Q68*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8W5-01B-11D-A37C-09 chr3:41277241 G>T maps to NM_001904.3 E571*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A938-01A-11D-A37C-09 chr20:36500360 G>A maps to NM_030877.3 P546P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6Y2-01B-11D-A33E-09 chr20:36488709 G>T maps to NM_030877.3 G523*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EU-01A-11D-A36J-09 chr20:36322544 G>T maps to NM_030877.3 L7L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NN-01A-11D-A37C-09 chr11:57575737 C>T maps to NM_001085458.1 Q689*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6Y2-01B-11D-A33E-09 chr11:57576891 C>T maps to NM_001085458.1 R797*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GO-01A-11D-A37C-09 chr5:11732319 G>A maps to NM_001332.2 G34G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NK-01A-21D-A37C-09 chr5:11082915 G>A maps to NM_001332.2 L894L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A8I1-01A-11D-A36J-09 chr5:10981939 G>T maps to NM_001332.2 S1121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6KZ-01A-11D-A31U-09 chr5:11411747 G>T maps to NM_001332.2 I113I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASX-01A-11D-A387-09 chr5:11384849 C>T maps to NM_001332.2 A368A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HX-01A-11D-A33E-09 chr17:3560043 G>T maps to NM_001031681.2 A212A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NI-01A-11D-A37C-09 chr11:10790025 C>T maps to NM_014633.3 S699S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr16:67965002 G>A maps to NM_001907.2 Q52*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S8-A6BV-01A-21D-A31U-09 chr1:206331025 C>T maps to ENST00000361052 F349F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OH-01A-11D-A27G-09 chr11:66335084 G>T maps to NM_003793.3 R121R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FP-01A-31D-A387-09 chr14:25043994 G>C maps to NM_001911.2 G75G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XP-A8T6-01A-11D-A36J-09 chr1:150727557 T>C maps to NM_004079.4 T106T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA7B-01A-31D-A403-09 chr11:70277334 G>A maps to NM_001184740.1 S368S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6XQ-01B-11D-A33E-09 chr7:117432022 G>T maps to NM_033427.2 T409T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A939-01A-12D-A37C-09 chr1:112998845 C>T maps to NM_018704.2 I244I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6F8-01A-11D-A33E-09 chr16:88779038 C>T maps to ENST00000378384 L226L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FH-01A-11D-A33E-09 chr10:16932469 G>A maps to NM_001081.3 N2885N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA7B-01A-31D-A403-09 chr10:16878336 C>T maps to NM_001081.3 S3359S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NL-01A-12D-A37C-09 chr7:148480982 G>T did not map to a codon.
Sequencing variant TCGA-V5-A7RE-01A-11D-A351-09 chr2:225371634 C>T maps to NM_003590.3 E323E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A938-01A-11D-A37C-09 chr13:113898808 C>A maps to NM_001008895.1 I438I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NU-01A-11D-A36J-09 chr23:119668404 G>T did not map to a codon.
Sequencing variant TCGA-R6-A6KZ-01A-11D-A31U-09 chr23:119672584 G>T did not map to a codon.
Sequencing variant TCGA-JY-A6FD-01A-11D-A33E-09 chr6:43016151 G>T maps to NM_001168370.1 R745R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88T-01A-11D-A351-09 chr6:43013044 G>T maps to NM_001168370.1 R1070R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88W-01A-11D-A351-09 chr6:43005593 C>T maps to NM_001168370.1 V1727V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6Y0-01B-11D-A33E-09 chr6:43014653 G>A maps to NM_001168370.1 R871R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GK-01A-11D-A37C-09 chr6:43168190 C>T maps to ENST00000354495 I1134I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RE-01A-11D-A33E-09 chr6:43160939 G>T maps to ENST00000354495 G794G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A893-01A-11D-A36J-09 chr6:43152425 G>A maps to ENST00000354495 A126A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6XQ-01B-11D-A33E-09 chr6:43181533 G>T maps to ENST00000354495 E1858*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XP-A8T7-01A-11D-A36J-09 chr6:43154798 G>T maps to ENST00000354495 V451V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GJ-01A-11D-A37C-09 chr6:33385900 C>T maps to NM_001014433.2 W21*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43I-01A-11D-A247-09 chr7:101821909 G>A maps to ENST00000360264 Q341Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93E-01A-11D-A37C-09 chr12:111747998 C>T maps to NM_015267.3 D471D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A9-01A-11D-A28B-09 chr12:111748076 C>T maps to NM_015267.3 F497F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EQ-01A-11D-A36J-09 chr12:111731319 G>A maps to NM_015267.3 G169G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EQ-01A-11D-A36J-09 chr12:111748305 C>A maps to NM_015267.3 R574R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA4G-01A-11D-A37C-09 chr2:180843002 T>A maps to NM_020943.2 S165S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88Z-01A-11D-A36J-09 chr10:101995433 G>A maps to NM_018294.4 Q488*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A8I0-01A-11D-A36J-09 chr10:102016225 T>C maps to NM_018294.4 K99K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93E-01A-11D-A37C-09 chr11:107299550 T>C maps to NM_152434.2 L469L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OJ-01A-11D-A27G-09 chr11:107300161 G>A maps to NM_152434.2 Q266*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr4:49063826 A>T did not map to a codon.
Sequencing variant TCGA-L5-A8NN-01A-11D-A37C-09 chr4:48996763 G>T maps to NM_025087.2 G214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A8-01A-32D-A27G-09 chr4:49034649 G>T maps to NM_025087.2 E526*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XP-A8T8-01A-11D-A36J-09 chr4:49030702 G>T maps to NM_025087.2 E442*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A5U5-01A-21D-A28B-09 chr16:57416010 G>A maps to NM_002996.3 Q87Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4MR-01A-11D-A28B-09 chr21:18938007 T>C maps to NM_001338.3 *366Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NU-01A-11D-A36J-09 chr2:219029247 C>A maps to NM_000634.2 L229L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GN-01A-11D-A37C-09 chr2:219000351 C>A maps to NM_001168298.1 L276L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OE-01A-11D-A27G-09 chr2:218999902 G>T maps to NM_001168298.1 E127*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A8-01A-32D-A27G-09 chr2:218999542 G>T maps to NM_001168298.1 E7*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A7DP-01A-31D-A33E-09 chr23:70836448 G>T did not map to a codon.
Sequencing variant TCGA-L5-A88V-01A-11D-A351-09 chr23:70837154 A>C did not map to a codon.
Sequencing variant TCGA-LN-A4MR-01A-11D-A28B-09 chr2:136872987 G>A maps to NM_001008540.1 P174P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XP-A8T8-01A-11D-A36J-09 chr23:144909317 C>A did not map to a codon.
Sequencing variant TCGA-XP-A8T6-01A-11D-A36J-09 chr23:35974233 C>A did not map to a codon.
Sequencing variant TCGA-IG-A5B8-01A-11D-A28B-09 chr23:75397536 G>A did not map to a codon.
Sequencing variant TCGA-JY-A6FG-01A-11D-A33E-09 chr23:75395329 A>G did not map to a codon.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr23:45051220 G>A did not map to a codon.
Sequencing variant TCGA-L5-A4OH-01A-11D-A27G-09 chr23:45060030 G>T did not map to a codon.
Sequencing variant TCGA-2H-A9GJ-01A-11D-A37C-09 chr23:106466058 C>T did not map to a codon.
Sequencing variant TCGA-2H-A9GJ-01A-11D-A37C-09 chr23:134303612 C>A did not map to a codon.
Sequencing variant TCGA-L5-A8NJ-01A-11D-A36J-09 chr23:118678376 T>G did not map to a codon.
Sequencing variant TCGA-VR-AA7B-01A-31D-A403-09 chr23:105855927 G>T did not map to a codon.
Sequencing variant TCGA-2H-A9GM-01A-11D-A37C-09 chr23:36122689 A>G did not map to a codon.
Sequencing variant TCGA-IG-A3I8-01A-11D-A247-09 chr23:36162681 G>C did not map to a codon.
Sequencing variant TCGA-IG-A3QL-01A-11D-A247-09 chr23:36117944 T>G did not map to a codon.
Sequencing variant TCGA-L5-A43I-01A-11D-A247-09 chr23:36103548 A>T did not map to a codon.
Sequencing variant TCGA-L5-A8NR-01A-11D-A37C-09 chr1:110038826 G>A maps to NM_001134400.1 V234V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-AAPN-01A-11D-A403-09 chr18:71920819 C>A maps to NM_148923.2 *135L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA4D-01A-11D-A37C-09 chr17:7762920 G>T maps to NM_144607.4 T226T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3Y9-01A-12D-A247-09 chr11:7690912 C>T maps to NM_016229.3 R67R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q9-A6FU-01A-11D-A31U-09 chr22:43027453 G>A maps to NM_001171660.1 I85I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OQ-01A-11D-A27G-09 chr1:54640441 G>A maps to NM_001031672.2 G266G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L7-A6VZ-01A-12D-A33E-09 chr1:54644956 G>T maps to NM_001031672.2 I203I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A4P3-01A-11D-A27G-09 chr23:37655245 G>T did not map to a codon.
Sequencing variant TCGA-JY-A93D-01A-11D-A387-09 chr23:37655264 T>C did not map to a codon.
Sequencing variant TCGA-JY-A93D-01A-11D-A387-09 chr23:37655340 C>T did not map to a codon.
Sequencing variant TCGA-IC-A6RE-01A-11D-A33E-09 chr15:22945047 G>T maps to NM_014608.2 T373T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93C-01A-11D-A387-09 chr15:22940817 G>A maps to NM_014608.2 S361S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NS-01A-12D-A37C-09 chr15:22998466 G>A maps to NM_014608.2 K1053K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8W8-01B-11D-A37C-09 chr15:22933759 C>T maps to NM_014608.2 Q227*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RE-A7BO-01A-11D-A33E-09 chr15:22946995 C>T maps to NM_014608.2 Y423Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A97H-01A-11D-A387-09 chr5:156787306 C>G maps to ENST00000442283 L970L. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-JY-A938-01A-11D-A37C-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr5:156786062 G>T maps to ENST00000442283 V933V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88Z-01A-11D-A36J-09 chr5:156727796 T>C maps to ENST00000442283 S154S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FO-01A-11D-A387-09 chr5:156727760 G>T maps to ENST00000442283 R142R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-AAPN-01A-11D-A403-09 chr5:156752514 C>G maps to ENST00000442283 L642L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GH-01A-11D-A37C-09 chr23:83128495 T>G did not map to a codon.
Sequencing variant TCGA-2H-A9GK-01A-11D-A37C-09 chr23:83129283 A>C did not map to a codon.
Sequencing variant TCGA-L5-A4OG-01A-11D-A27G-09 chr23:83129382 A>C did not map to a codon.
Sequencing variant TCGA-L5-A4OW-01A-11D-A28B-09 chr23:83124909 C>T did not map to a codon.
Sequencing variant TCGA-L5-A8NE-01A-11D-A37C-09 chr23:83129078 A>C did not map to a codon.
Sequencing variant TCGA-L5-A8NU-01A-11D-A36J-09 chr23:83127966 T>G did not map to a codon.
Sequencing variant TCGA-X8-AAAR-01A-11D-A403-09 chr23:83128458 T>A did not map to a codon.
Sequencing variant TCGA-Z6-AAPN-01A-11D-A403-09 chr23:83128290 C>G did not map to a codon.
Sequencing variant TCGA-Z6-AAPN-01A-11D-A403-09 chr23:83129460 C>G did not map to a codon.
Sequencing variant TCGA-L5-A43I-01A-11D-A247-09 chr9:105767542 A>G maps to NM_001340.3 K210K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6Y2-01B-11D-A33E-09 chr9:105767542 A>G maps to NM_001340.3 K210K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88W-01A-11D-A351-09 chr16:50818238 G>T did not map to a codon.
Sequencing variant TCGA-VR-A8EP-01A-31D-A403-09 chr16:50785663 T>C maps to ENST00000311559 G218G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GQ-01A-11D-A37C-09 chr8:143958290 C>T maps to ENST00000377675 L273L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr8:143995766 G>A maps to NM_000498.3 I289I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A1-01A-21D-A27G-09 chr8:143998572 C>T maps to NM_000498.3 K99K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OP-01A-11D-A27G-09 chr15:51510760 T>A maps to NM_031226.2 L240L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49M-01A-21D-A27G-09 chr15:75014784 G>C maps to NM_000499.3 V218V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A893-01A-11D-A36J-09 chr6:32007599 G>C maps to NM_000500.5 L242L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GR-01A-12D-A37C-09 chr2:72359391 C>T maps to NM_019885.2 L501L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q9-A6FW-01A-31D-A31U-09 chr2:127950790 C>T maps to NM_001001665.3 W294*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GR-01A-12D-A37C-09 chr19:41597813 G>A did not map to a codon.
Sequencing variant TCGA-IG-A51D-01A-11D-A27G-09 chr19:41597722 C>T maps to NM_000766.3 F247F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FA-01A-11D-A33E-09 chr19:41510045 C>T maps to NM_000767.4 V104V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EU-01A-11D-A36J-09 chr22:42523616 G>A maps to NM_000106.4 I335I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6L4-01A-11D-A31U-09 chr10:135342130 G>A maps to NM_000773.3 A108A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HV-01A-21D-A351-09 chr19:41626274 C>T maps to NM_000774.3 R120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EW-01A-11D-A36J-09 chr19:41622164 A>G maps to NM_000774.3 S24S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A97I-01A-11D-A387-09 chr4:108866174 C>T maps to NM_183075.2 F180F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A8I1-01A-11D-A36J-09 chr7:1024634 G>C maps to NM_017781.2 T129T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A5B8-01A-11D-A28B-09 chr6:46607322 G>C maps to NM_016593.3 L132L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6KZ-01A-11D-A31U-09 chr14:100184389 G>T did not map to a codon.
Sequencing variant TCGA-S8-A6BV-01A-21D-A31U-09 chr1:47280895 G>T maps to NM_001099772.1 E345*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L7-A6VZ-01A-12D-A33E-09 chr19:15990452 G>A maps to NM_001082.3 F425F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RE-01A-11D-A33E-09 chr19:15648358 G>A maps to NM_173483.3 L145L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6XG-01B-11D-A33E-09 chr19:15658972 C>A maps to NM_173483.3 R397R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASX-01A-11D-A387-09 chr19:15648457 C>T maps to NM_173483.3 S178S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr19:15769133 T>C maps to NM_000896.2 H392H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FD-01A-11D-A33E-09 chr8:65536984 A>T maps to NM_004820.3 G78G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NR-01A-11D-A37C-09 chr1:86048535 C>T maps to NM_001554.4 D319D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr2:10199033 G>A maps to NM_001037160.2 Y141Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4ON-01A-11D-A27G-09 chr23:77528872 G>C did not map to a codon.
Sequencing variant TCGA-LN-A49S-01A-11D-A247-09 chr13:49281210 G>T maps to NM_020377.2 L86L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NE-01A-11D-A37C-09 chr19:48978118 G>T maps to NM_017457.4 E241*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A9-01A-11D-A28B-09 chr19:48976632 C>T maps to NM_017457.4 L144L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q9-A6FU-01A-11D-A31U-09 chr19:48976575 G>T maps to NM_017457.4 V125V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49U-01A-31D-A27G-09 chr7:6210571 G>C maps to ENST00000396741 L200L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A51D-01A-11D-A27G-09 chr22:24743078 C>G maps to NM_015330.2 S893*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93F-01A-21D-A37C-09 chr17:20108049 G>T maps to NM_001033553.1 E230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A3-01A-11D-A27G-09 chr21:27852732 C>T maps to ENST00000435845 A64A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A97H-01A-11D-A387-09 chr14:59787246 G>T maps to NM_014992.1 E129*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6XG-01B-11D-A33E-09 chr6:39846261 G>A maps to ENST00000398904 R481R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A939-01A-12D-A37C-09 chr9:124535011 T>C maps to ENST00000408936 P735P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93D-01A-11D-A387-09 chr9:124535155 C>T maps to ENST00000408936 A783A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A4-01A-11D-A27G-09 chr9:124535314 G>A maps to ENST00000408936 A836A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6XQ-01B-11D-A33E-09 chr9:124530737 C>A maps to ENST00000408936 S575S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A9VB-01A-21D-A37C-09 chr9:124534909 G>A maps to ENST00000408936 P701P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A939-01A-12D-A37C-09 chr13:72255963 G>T maps to ENST00000359684 V311V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43E-01A-11D-A247-09 chr23:85969600 T>G did not map to a codon.
Sequencing variant TCGA-L5-A43I-01A-11D-A247-09 chr23:85906158 A>C did not map to a codon.
Sequencing variant TCGA-L5-A8NV-01A-11D-A37C-09 chr23:86069836 G>A did not map to a codon.
Sequencing variant TCGA-LN-A9FP-01A-31D-A387-09 chr23:85994825 A>T did not map to a codon.
Sequencing variant TCGA-LN-A9FP-01A-31D-A387-09 chr23:86071036 A>G did not map to a codon.
Sequencing variant TCGA-VR-A8EU-01A-11D-A36J-09 chr23:86069758 G>A did not map to a codon.
Sequencing variant TCGA-2H-A9GO-01A-11D-A37C-09 chr14:59113545 C>T maps to NM_016651.5 H735H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GN-01A-11D-A37C-09 chr19:47152182 G>A maps to NM_145056.2 I482I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6XG-01B-11D-A33E-09 chr19:47151904 C>T maps to NM_145056.2 W575*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASV-01A-11D-A387-09 chr3:49570286 C>A maps to NM_004393.4 G781G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6F8-01A-11D-A33E-09 chr11:61511390 G>A maps to NM_006133.2 T853T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A8JD-01A-11D-A36J-09 chr11:61496470 C>T maps to NM_006133.2 L280L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GM-01A-11D-A37C-09 chr7:6452616 C>T maps to NM_139179.3 L492L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NT-01A-11D-A37C-09 chr7:6464412 C>A maps to NM_139179.3 V370V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr11:61109364 C>T maps to NM_015533.3 D212D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GR-01A-12D-A37C-09 chr13:106142219 C>A maps to NM_001161812.1 T56T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q9-A6FW-01A-31D-A31U-09 chr13:106124927 G>T maps to NM_172370.3 E59*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GM-01A-11D-A37C-09 chr9:90321180 C>T maps to NM_004938.2 T1065T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RE-A7BO-01A-11D-A33E-09 chr9:90220078 G>T maps to NM_004938.2 L91L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OR-01A-11D-A27G-09 chr15:64275754 G>A maps to NM_014326.3 T97T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8ET-01A-11D-A403-09 chr15:64200717 G>T did not map to a codon.
Sequencing variant TCGA-LN-A7HX-01A-11D-A33E-09 chr4:100784192 G>T maps to NM_014395.2 L188L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GR-01A-12D-A37C-09 chr1:159176206 T>G maps to NM_001122951.2 S328S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GK-01A-11D-A37C-09 chr6:33289322 G>A maps to NM_001350.4 Q77*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8W8-01B-11D-A37C-09 chr9:121929457 C>T maps to NM_014618.2 L730L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EU-01A-11D-A36J-09 chr9:121929724 C>T maps to NM_014618.2 S641S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93D-01A-11D-A387-09 chr17:42828477 C>A maps to NM_145663.2 R569R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr9:136507450 C>T maps to NM_000787.3 P203P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88S-01A-11D-A36J-09 chr2:120125867 C>A maps to NM_001178017.1 G99G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A8I0-01A-11D-A36J-09 chr5:176885169 A>T maps to ENST00000393565 A601A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XP-A8T8-01A-11D-A36J-09 chr5:176887454 G>T maps to ENST00000393565 P311P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3Y9-01A-12D-A247-09 chr12:45410228 G>C maps to NM_001004329.2 S287*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A5S3-01A-11D-A28B-09 chr12:45417493 G>T maps to NM_001004329.2 S228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A893-01A-11D-A36J-09 chr12:45444437 T>C maps to NM_001004329.2 Q91Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A625-01A-11D-A31U-09 chr9:34089556 G>T maps to NM_015397.3 I352I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GL-01A-12D-A37C-09 chr23:125685849 T>C did not map to a codon.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr23:125686219 G>A did not map to a codon.
Sequencing variant TCGA-R6-A8W8-01B-11D-A37C-09 chr23:125686170 C>A did not map to a codon.
Sequencing variant TCGA-VR-A8EP-01A-31D-A403-09 chr23:125685868 T>C did not map to a codon.
Sequencing variant TCGA-VR-AA7B-01A-31D-A403-09 chr23:125685530 C>T did not map to a codon.
Sequencing variant TCGA-VR-AA7D-01A-11D-A403-09 chr23:125685997 G>A did not map to a codon.
Sequencing variant TCGA-VR-AA7I-01A-11D-A403-09 chr23:125685221 T>C did not map to a codon.
Sequencing variant TCGA-X8-AAAR-01A-11D-A403-09 chr23:125685284 T>G did not map to a codon.
Sequencing variant TCGA-2H-A9GF-01A-11D-A37C-09 chr23:125299489 C>T did not map to a codon.
Sequencing variant TCGA-2H-A9GH-01A-11D-A37C-09 chr23:125298804 C>A did not map to a codon.
Sequencing variant TCGA-JY-A93C-01A-11D-A387-09 chr23:125298845 C>A did not map to a codon.
Sequencing variant TCGA-L5-A43E-01A-11D-A247-09 chr23:125298765 T>G did not map to a codon.
Sequencing variant TCGA-LN-A49Y-01A-11D-A27G-09 chr23:125299264 C>A did not map to a codon.
Sequencing variant TCGA-R6-A8W8-01B-11D-A37C-09 chr23:125298722 C>T did not map to a codon.
Sequencing variant TCGA-VR-A8EX-01A-11D-A36J-09 chr23:125298881 C>A did not map to a codon.
Sequencing variant TCGA-VR-AA7B-01A-31D-A403-09 chr23:125299585 C>T did not map to a codon.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr8:104427645 C>A maps to NM_015420.6 S143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6Y0-01B-11D-A33E-09 chr8:104427571 T>C maps to NM_015420.6 T118T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GM-01A-11D-A37C-09 chr4:41984855 C>T maps to NM_001029955.3 L349L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OF-01A-11D-A27G-09 chr4:41984591 G>C maps to NM_001029955.3 G261G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3QL-01A-11D-A247-09 chr8:88885725 C>G maps to NM_152418.3 L158L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49M-01A-21D-A27G-09 chr8:88886082 G>A maps to NM_152418.3 F39F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EO-01A-11D-A36J-09 chr8:88885798 G>T maps to NM_152418.3 S134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A891-01A-11D-A36J-09 chr14:69522073 G>A maps to NM_003861.2 I443I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A8JE-01A-11D-A37C-09 chr14:69520681 T>C maps to NM_003861.2 T907T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr1:168034904 G>A maps to ENST00000367840 R839R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr1:168034883 C>T maps to ENST00000367840 G832G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GO-01A-11D-A37C-09 chr17:61666410 C>A maps to NM_005828.3 A302A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A8I0-01A-11D-A36J-09 chr23:27998246 C>T did not map to a codon.
Sequencing variant TCGA-LN-A9FP-01A-31D-A387-09 chr23:27998865 C>A did not map to a codon.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr23:27765038 C>T did not map to a codon.
Sequencing variant TCGA-L5-A8NJ-01A-11D-A36J-09 chr23:27766866 G>T did not map to a codon.
Sequencing variant TCGA-Q9-A6FU-01A-11D-A31U-09 chr23:27765401 G>A did not map to a codon.
Sequencing variant TCGA-XP-A8T7-01A-11D-A36J-09 chr23:27766026 G>A did not map to a codon.
Sequencing variant TCGA-JY-A93C-01A-11D-A387-09 chr6:117859865 C>T maps to ENST00000338728 Q282*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RE-A7BO-01A-11D-A33E-09 chr3:98527010 C>A maps to ENST00000326857 A528A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RE-01A-11D-A33E-09 chr18:51025731 T>A maps to NM_005215.3 S1321S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3Y9-01A-12D-A247-09 chr18:50976873 G>A maps to NM_005215.3 P1078P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FB-01A-11D-A33E-09 chr18:51025707 G>T maps to NM_005215.3 L1313L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OQ-01A-11D-A27G-09 chr18:50961529 A>C maps to NM_005215.3 G1060G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NG-01A-11D-A37C-09 chr18:50936958 C>T maps to NM_005215.3 R1025*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49S-01A-11D-A247-09 chr18:51025707 G>C maps to NM_005215.3 L1313L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HX-01A-11D-A33E-09 chr18:50731605 G>T maps to NM_005215.3 E532*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6XQ-01B-11D-A33E-09 chr18:50866152 G>A maps to NM_005215.3 W745*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43C-01A-11D-A247-09 chr11:31327825 C>A maps to NM_181807.2 G182*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NG-01A-11D-A37C-09 chr11:31312304 A>T maps to NM_181807.2 S283S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FQ-01A-31D-A387-09 chr11:31349671 A>G maps to NM_181807.2 D52D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A8O2-01A-11D-A36J-09 chr6:24205235 G>T maps to NM_016356.3 V339V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GK-01A-11D-A37C-09 chr11:6647157 C>A maps to NM_003737.2 E2242*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RF-01A-13D-A33E-09 chr11:6648764 G>T maps to NM_003737.2 L1835L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FA-01A-11D-A33E-09 chr11:6648068 G>T maps to NM_003737.2 R2067R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6XG-01B-11D-A33E-09 chr11:6651815 G>A maps to NM_003737.2 R1403R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr4:155411313 G>A maps to NM_001142552.1 R398R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OO-01A-11D-A27G-09 chr4:155241543 T>C maps to NM_017639.3 L1214L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NK-01A-21D-A37C-09 chr4:155219048 G>A maps to NM_017639.3 F1684F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NK-01A-21D-A37C-09 chr4:155254136 T>A maps to NM_017639.3 K576*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NK-01A-21D-A37C-09 chr4:155411595 C>T maps to NM_001142552.1 A304A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr4:155412141 G>A maps to NM_001142552.1 T122T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6DQ-01B-11D-A31U-09 chr4:155278438 G>A maps to NM_017639.3 V244V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49M-01A-21D-A27G-09 chr16:2296895 C>T maps to NM_001919.3 E86E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GH-01A-11D-A37C-09 chr13:36362404 G>A maps to NM_004734.4 T692T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-AAPN-01A-11D-A403-09 chr13:36410270 C>T maps to NM_004734.4 S376S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A4P3-01A-11D-A27G-09 chr4:151153529 G>A maps to NM_001040261.4 V464V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr3:36756895 G>T maps to NM_033403.1 R624R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L7-A6VZ-01A-12D-A33E-09 chr10:115596895 C>A maps to NM_014881.3 G963*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6Y2-01B-11D-A33E-09 chr10:115612802 G>T maps to NM_014881.3 R47R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GO-01A-11D-A37C-09 chr10:14974897 G>C maps to NM_001033855.1 L245L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43H-01A-11D-A247-09 chr10:14995952 G>A maps to NM_001033855.1 F19F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RE-A7BO-01A-11D-A33E-09 chr1:155005214 G>T maps to NM_144622.2 R157R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A5S3-01A-11D-A28B-09 chr13:95114433 G>A maps to NM_001129889.1 D291D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6XG-01B-11D-A33E-09 chr13:95092238 A>G maps to NM_001129889.1 A524A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FQ-01A-31D-A387-09 chr2:74595884 C>T maps to NM_004082.4 V608V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A97H-01A-11D-A387-09 chr12:57927733 A>T did not map to a codon.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr8:30036927 C>A maps to NM_006571.2 S96S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FB-01A-11D-A33E-09 chr23:110644498 C>A did not map to a codon.
Sequencing variant TCGA-L5-A4OS-01A-11D-A28B-09 chr23:110576329 C>A did not map to a codon.
Sequencing variant TCGA-V5-A7RB-01A-11D-A351-09 chr23:110653399 C>T did not map to a codon.
Sequencing variant TCGA-VR-A8EQ-01A-11D-A36J-09 chr23:110653363 G>A did not map to a codon.
Sequencing variant TCGA-LN-A4MR-01A-11D-A28B-09 chr6:31696814 G>A maps to NM_013974.1 Q42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6Y2-01B-11D-A33E-09 chr11:61068327 G>A maps to NM_001923.3 L1098L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NH-01A-11D-A37C-09 chr11:47254426 C>T maps to NM_000107.2 Y173Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HZ-01A-31D-A351-09 chr14:53570520 G>A maps to NM_001160148.1 Q298*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GH-01A-11D-A37C-09 chr11:103908167 G>T maps to NM_001001711.2 L206L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GJ-01A-11D-A37C-09 chr11:103908639 G>T maps to NM_001001711.2 G364*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49L-01A-11D-A247-09 chr10:74034858 C>T maps to NM_019058.2 F204F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr12:49391698 C>A maps to NM_015086.1 L320L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XP-A8T7-01A-11D-A36J-09 chr1:20982213 C>A maps to NM_005216.4 T154T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L7-A56G-01A-21D-A27G-09 chr6:30862387 C>T maps to NM_013994.2 Q485*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EU-01A-11D-A36J-09 chr2:15757365 A>G did not map to a codon.
Sequencing variant TCGA-VR-AA4G-01A-11D-A37C-09 chr2:15768941 G>T maps to NM_004939.1 L618L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A8HZ-01A-11D-A36J-09 chr12:31256768 G>A maps to NM_030653.3 *907*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RE-A7BO-01A-11D-A33E-09 chr12:31250906 C>A maps to NM_030653.3 V617V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XP-A8T6-01A-11D-A36J-09 chr22:38884007 G>T maps to NM_001098504.1 T520T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6Y0-01B-11D-A33E-09 chr2:118578864 G>T maps to NM_006773.3 E215*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3Y9-01A-12D-A247-09 chr16:70390093 G>A maps to NM_018332.3 L79L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA7B-01A-31D-A403-09 chr16:70404230 G>T maps to NM_018332.3 E376*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6DN-01B-11D-A31U-09 chr16:70363250 C>T maps to NM_007242.4 L222L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S8-A6BV-01A-21D-A31U-09 chr14:94528650 G>A maps to NM_020414.3 I345I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EZ-01A-11D-A36J-09 chr14:94517536 T>G maps to NM_020414.3 *860Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HV-01A-21D-A351-09 chr23:134715017 T>A did not map to a codon.
Multiple mappings detected for codon TCGA-LN-A5U5-01A-21D-A28B-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-IG-A3Y9-01A-12D-A247-09 chr23:41206954 G>C did not map to a codon.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr23:41201774 C>T did not map to a codon.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr23:41202034 C>T did not map to a codon.
Sequencing variant TCGA-LN-A49V-01A-11D-A247-09 chr23:41198320 C>T did not map to a codon.
Sequencing variant TCGA-LN-A49V-01A-11D-A247-09 chr24:15029442 G>T did not map to a codon.
Sequencing variant TCGA-XP-A8T8-01A-11D-A36J-09 chr5:176943361 G>A maps to NM_016222.2 D75D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FA-01A-11D-A33E-09 chr17:62499110 C>A maps to NM_004396.3 E306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GL-01A-12D-A37C-09 chr10:70696799 C>T maps to NM_024045.1 H568H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HW-01A-22D-A351-09 chr10:70700817 G>A maps to NM_024045.1 G586G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XP-A8T8-01A-11D-A36J-09 chr10:70696733 A>T maps to NM_024045.1 R546R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GI-01A-11D-A37C-09 chr12:132624260 C>T maps to NM_175066.3 R631R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q9-A6FU-01A-11D-A31U-09 chr12:132626102 G>A maps to NM_175066.3 G348G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93F-01A-21D-A37C-09 chr12:113603799 T>C maps to NM_001111322.1 P484P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NI-01A-11D-A37C-09 chr7:44608557 G>T maps to NM_019082.2 R443R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S8-A6BW-01A-11D-A31U-09 chr9:32459469 G>A maps to NM_014314.3 Q794*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GQ-01A-11D-A37C-09 chr4:169342928 C>T maps to NM_001012967.1 V792V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NI-01A-11D-A37C-09 chr8:91057129 C>T maps to NM_001359.1 G264G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A893-01A-11D-A36J-09 chr19:42721105 C>T maps to NM_133328.2 L18L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-A7RC-01B-11D-A403-09 chr6:35280401 G>T did not map to a codon.
Sequencing variant TCGA-L5-A4OJ-01A-11D-A27G-09 chr16:90027486 G>T maps to NM_207514.1 R282R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FH-01A-11D-A33E-09 chr8:7340203 A>G maps to NM_152251.3 N40N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RE-01A-11D-A33E-09 chr6:49986803 G>A maps to NM_001037497.1 D30D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OW-01A-11D-A28B-09 chr20:29960723 A>T maps to NM_054112.2 G41G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A9-01A-11D-A28B-09 chr20:30037841 A>G maps to NM_153324.2 Q23Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A891-01A-11D-A36J-09 chr9:126220095 G>T maps to NM_020946.1 A358A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RE-A7BO-01A-11D-A33E-09 chr9:126433581 G>T maps to NM_020946.1 V147V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X8-AAAR-01A-11D-A403-09 chr9:126144355 G>A maps to NM_020946.1 G795G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NK-01A-21D-A37C-09 chr1:197552365 G>A maps to NM_001195215.1 F355F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr19:6475731 G>A maps to NM_024898.2 H270H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43E-01A-11D-A247-09 chr7:140273780 G>A maps to NM_015689.3 R425*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49M-01A-21D-A27G-09 chr7:140269452 G>C maps to NM_015689.3 S511*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XP-A8T7-01A-11D-A36J-09 chr7:140244497 G>T maps to NM_015689.3 S749S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A891-01A-11D-A36J-09 chr9:19352541 G>T maps to NM_017925.4 E1269*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6KZ-01A-11D-A31U-09 chr9:19336363 C>T maps to NM_017925.4 Q660*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6XG-01B-11D-A33E-09 chr9:19346067 C>A maps to NM_017925.4 R816R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EQ-01A-11D-A36J-09 chr9:19324505 G>T did not map to a codon.
Sequencing variant TCGA-L5-A4OG-01A-11D-A27G-09 chr12:31595785 A>G maps to NM_144973.3 I645I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q9-A6FU-01A-11D-A31U-09 chr12:31540554 G>T maps to NM_144973.3 I1269I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EQ-01A-11D-A36J-09 chr22:32289686 G>T maps to NM_001136029.1 E1376*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA7B-01A-31D-A403-09 chr22:32215188 C>T maps to NM_001136029.1 R616R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88T-01A-11D-A351-09 chr12:16109897 G>C maps to NM_015954.2 V20V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93C-01A-11D-A387-09 chr22:24180921 C>G maps to NM_001135751.1 P45P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GL-01A-12D-A37C-09 chr15:89070881 G>A maps to NM_017996.3 Q418*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3YB-01A-11D-A247-09 chr15:89074850 G>T maps to NM_017996.3 S40*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49O-01A-11D-A247-09 chr15:89074354 A>G maps to NM_017996.3 H205H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93E-01A-11D-A37C-09 chr1:3775329 C>T maps to ENST00000430539 L55L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49U-01A-31D-A27G-09 chr9:117165568 C>T maps to NM_015404.3 A823A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q9-A6FU-01A-11D-A31U-09 chr2:179325073 G>A did not map to a codon.
Sequencing variant TCGA-LN-A9FP-01A-31D-A387-09 chr23:69421793 C>A did not map to a codon.
Sequencing variant TCGA-LN-A49R-01A-11D-A247-09 chr22:19052581 T>C did not map to a codon.
Sequencing variant TCGA-R6-A8WC-01A-11D-A37C-09 chr7:14722291 G>A maps to NM_004080.2 V307V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NQ-01A-11D-A36J-09 chr2:234355360 G>A maps to NM_152879.2 W446*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A2-01A-31D-A27G-09 chr2:234367024 G>A maps to NM_152879.2 Q892Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XP-A8T7-01A-11D-A36J-09 chr3:185929634 C>T maps to NM_001346.2 S622S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NW-01A-11D-A37C-09 chr13:42764661 G>T did not map to a codon.
Sequencing variant TCGA-2H-A9GR-01A-12D-A37C-09 chr7:137339487 G>T maps to NM_004717.2 S243*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3QL-01A-11D-A247-09 chr7:137374663 C>T maps to NM_004717.2 E162E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A5U6-01A-11D-A28B-09 chr7:137374665 C>A maps to NM_004717.2 E162*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A8HZ-01A-11D-A36J-09 chr7:137269971 C>A maps to NM_004717.2 E516*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RE-A7BO-01A-11D-A33E-09 chr7:137128841 T>C maps to NM_004717.2 P922P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A6QS-01A-12D-A33E-09 chr23:50122992 G>A did not map to a codon.
Sequencing variant TCGA-IG-A97H-01A-11D-A387-09 chr23:50146072 A>G did not map to a codon.
Sequencing variant TCGA-L5-A88V-01A-11D-A351-09 chr23:50165515 G>T did not map to a codon.
Sequencing variant TCGA-LN-A4MQ-01A-11D-A28B-09 chr23:50163451 C>A did not map to a codon.
Sequencing variant TCGA-Q9-A6FU-01A-11D-A31U-09 chr23:50133336 G>C did not map to a codon.
Sequencing variant TCGA-RE-A7BO-01A-11D-A33E-09 chr23:50213278 C>T did not map to a codon.
Sequencing variant TCGA-Q9-A6FW-01A-31D-A31U-09 chr2:74154135 C>T maps to NM_080916.1 H33H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr3:93780331 G>A maps to NM_001195643.1 I8I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OO-01A-11D-A27G-09 chr12:49485079 G>A maps to NM_021044.2 D132D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr14:24766023 G>A maps to NM_001136050.2 R72*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr17:27228277 G>A maps to NM_144683.3 L138L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OF-01A-11D-A27G-09 chr14:24435042 T>C did not map to a codon.
Sequencing variant TCGA-L5-A4OR-01A-11D-A27G-09 chr17:9680522 C>T maps to ENST00000330255 P187P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A6-01A-11D-A27G-09 chr23:2184835 C>T did not map to a codon.
Sequencing variant TCGA-L5-A43M-01A-11D-A247-09 chr4:24531251 G>T maps to NM_001358.2 R748R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A8O2-01A-11D-A36J-09 chr5:54589921 G>A maps to NM_019030.2 R235*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A8I1-01A-11D-A36J-09 chr3:47889695 A>G maps to NM_138615.2 V771V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NW-01A-11D-A37C-09 chr19:47861290 G>T maps to NM_014681.5 E396*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA7I-01A-11D-A403-09 chr20:37650517 C>T maps to NM_021931.3 I511I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr2:39089426 G>A maps to NM_198963.1 N144N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A891-01A-11D-A36J-09 chr17:40262782 G>A maps to NM_024119.2 G173G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93F-01A-21D-A37C-09 chr17:41571169 C>T maps to NM_004941.1 V376V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FO-01A-11D-A387-09 chr17:41582145 C>T maps to NM_004941.1 Q561*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HY-01A-12D-A351-09 chr1:182850530 A>G maps to NM_001357.4 L919L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8WG-01A-11D-A37C-09 chr1:182828172 A>G did not map to a codon.
Sequencing variant TCGA-2H-A9GF-01A-11D-A37C-09 chr23:96354738 C>T did not map to a codon.
Sequencing variant TCGA-IG-A3I8-01A-11D-A247-09 chr23:96013191 C>T did not map to a codon.
Sequencing variant TCGA-IG-A3Y9-01A-12D-A247-09 chr23:96502802 G>C did not map to a codon.
Sequencing variant TCGA-IG-A6QS-01A-12D-A33E-09 chr23:96396711 A>G did not map to a codon.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr23:96173527 C>A did not map to a codon.
Sequencing variant TCGA-LN-A49P-01A-11D-A247-09 chr23:96212976 G>T did not map to a codon.
Sequencing variant TCGA-LN-A7HW-01A-22D-A351-09 chr23:96684667 G>T did not map to a codon.
Sequencing variant TCGA-R6-A6KZ-01A-11D-A31U-09 chr23:96192268 A>T did not map to a codon.
Sequencing variant TCGA-R6-A8W8-01B-11D-A37C-09 chr23:95993590 C>T did not map to a codon.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr13:60565347 T>A maps to NM_001042517.1 G435G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NK-01A-21D-A37C-09 chr14:95570226 G>T maps to NM_177438.2 S1169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OE-01A-11D-A27G-09 chr20:61522366 G>T maps to NM_033081.2 I1162I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FQ-01A-31D-A387-09 chr20:61513658 G>A maps to NM_033081.2 R1217*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KH-A6WC-01A-11D-A33E-09 chr5:61689847 C>T maps to NM_014473.2 P199P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4MR-01A-11D-A28B-09 chr21:47970532 C>T maps to ENST00000318711 L906L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FO-01A-11D-A387-09 chr21:47954535 A>G maps to ENST00000318711 T527T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NR-01A-11D-A37C-09 chr12:51102284 G>A maps to NM_173602.2 A863A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X8-AAAR-01A-11D-A403-09 chr12:51097963 G>T maps to NM_173602.2 V789V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NW-01A-11D-A37C-09 chr10:355975 G>A maps to NM_014974.2 H1327H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S8-A6BV-01A-21D-A31U-09 chr10:408571 G>C maps to NM_014974.2 T884T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A4P3-01A-11D-A27G-09 chr13:73335786 G>T maps to NM_014953.3 T836T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HW-01A-22D-A351-09 chr13:73333932 C>A maps to NM_014953.3 *959Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A97I-01A-11D-A387-09 chr15:66610848 G>T maps to NM_001143688.1 E353*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A50L-01A-11D-A27G-09 chr2:233113981 G>T maps to NM_152383.4 E451*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA4G-01A-11D-A37C-09 chr2:233198623 G>T maps to NM_152383.4 L695L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43C-01A-11D-A247-09 chr1:231830163 C>T maps to NM_001164537.1 A220A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RF-01A-13D-A33E-09 chr1:223116505 C>A maps to NM_032890.2 S114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EU-01A-11D-A36J-09 chr1:223116620 G>A maps to NM_032890.2 P152P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OW-01A-11D-A28B-09 chr23:154002913 T>C did not map to a codon.
Sequencing variant TCGA-R6-A8WC-01A-11D-A37C-09 chr23:154005129 G>A did not map to a codon.
Sequencing variant TCGA-L5-A8NQ-01A-11D-A36J-09 chr11:65546630 G>A maps to NM_138368.3 L388L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A8HZ-01A-11D-A36J-09 chr10:54074702 C>T maps to NM_012242.2 D88D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43I-01A-11D-A247-09 chr8:12947940 G>A maps to NM_182643.2 T1298T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OH-01A-11D-A27G-09 chr8:12960300 G>T maps to NM_182643.2 R522R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr8:12973134 T>C maps to NM_182643.2 L460L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASV-01A-11D-A387-09 chr8:13357529 C>T maps to NM_182643.2 W17*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EQ-01A-11D-A36J-09 chr8:12947788 G>T maps to NM_182643.2 S1349*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OR-01A-11D-A27G-09 chr3:38101296 A>G maps to NM_007335.2 P209P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NL-01A-12D-A37C-09 chr3:38103732 C>T maps to NM_007335.2 N249N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EZ-01A-11D-A36J-09 chr3:38164059 C>T maps to NM_007337.2 S1767S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X8-AAAR-01A-11D-A403-09 chr3:38158134 G>T maps to NM_007335.2 E1350*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr11:83770364 G>T maps to NM_001142699.1 G304G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49W-01A-11D-A27G-09 chr11:83962298 A>T maps to NM_001142699.1 T185T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GL-01A-12D-A37C-09 chr10:79566670 C>A maps to NM_004747.3 R1604R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr10:79579659 C>T maps to NM_004747.3 P1173P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr18:3534564 G>A maps to NM_004746.2 A702A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FG-01A-11D-A33E-09 chr1:35334650 G>A maps to NM_001080418.1 G680G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49K-01A-11D-A247-09 chr1:35334317 G>T maps to NM_001080418.1 C791*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EQ-01A-11D-A36J-09 chr1:35370006 C>T maps to NM_001080418.1 S326S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A8I0-01A-11D-A36J-09 chr20:35154318 G>T maps to ENST00000339266 L890L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NJ-01A-11D-A36J-09 chr14:55646412 G>A maps to NM_014750.4 N236N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6XQ-01B-11D-A33E-09 chr14:55615074 T>C maps to NM_014750.4 E845E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6Y0-01B-11D-A33E-09 chr14:101200908 G>A maps to NM_003836.5 P276P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43M-01A-11D-A247-09 chr19:39994765 A>G maps to NM_016941.3 E236E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EO-01A-11D-A36J-09 chr17:48072323 G>T maps to NM_005220.2 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OO-01A-11D-A27G-09 chr17:48050512 G>A maps to NM_138281.2 P120P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A8-01A-32D-A27G-09 chr7:96635387 A>G maps to NM_005222.3 Q33Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6Y2-01B-11D-A33E-09 chr1:44684855 C>T maps to NM_019100.4 R283R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FP-01A-31D-A387-09 chr1:46978147 C>A maps to NM_147192.2 L377L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GM-01A-11D-A37C-09 chr23:32472938 C>T did not map to a codon.
Sequencing variant TCGA-IC-A6RE-01A-11D-A33E-09 chr23:32328221 A>C did not map to a codon.
Sequencing variant TCGA-IG-A4QS-01A-11D-A27G-09 chr23:32381008 A>C did not map to a codon.
Sequencing variant TCGA-JY-A6F8-01A-11D-A33E-09 chr23:32486680 G>T did not map to a codon.
Sequencing variant TCGA-JY-A6FG-01A-11D-A33E-09 chr23:31676246 G>T did not map to a codon.
Sequencing variant TCGA-JY-A93C-01A-11D-A387-09 chr23:32862922 G>T did not map to a codon.
Sequencing variant TCGA-JY-A93D-01A-11D-A387-09 chr23:31224763 C>T did not map to a codon.
Sequencing variant TCGA-JY-A93E-01A-11D-A37C-09 chr23:32328388 G>T did not map to a codon.
Sequencing variant TCGA-L5-A891-01A-11D-A36J-09 chr23:32536192 A>G did not map to a codon.
Sequencing variant TCGA-L5-A891-01A-11D-A36J-09 chr23:32834619 A>T did not map to a codon.
Sequencing variant TCGA-L5-A8NT-01A-11D-A37C-09 chr23:31341747 G>A did not map to a codon.
Sequencing variant TCGA-L5-A8NW-01A-11D-A37C-09 chr23:31152221 T>G did not map to a codon.
Sequencing variant TCGA-L7-A56G-01A-21D-A27G-09 chr23:32486662 C>T did not map to a codon.
Sequencing variant TCGA-LN-A49R-01A-11D-A247-09 chr23:32472791 A>T did not map to a codon.
Sequencing variant TCGA-LN-A49Y-01A-11D-A27G-09 chr23:32490335 G>T did not map to a codon.
Sequencing variant TCGA-LN-A7HX-01A-11D-A33E-09 chr23:32382798 T>C did not map to a codon.
Sequencing variant TCGA-LN-A9FP-01A-31D-A387-09 chr23:32481652 C>A did not map to a codon.
Sequencing variant TCGA-R6-A6L6-01B-11D-A33E-09 chr23:31525457 C>T did not map to a codon.
Sequencing variant TCGA-R6-A6Y2-01B-11D-A33E-09 chr23:32509575 C>A did not map to a codon.
Sequencing variant TCGA-XP-A8T8-01A-11D-A36J-09 chr23:32613896 C>T did not map to a codon.
Sequencing variant TCGA-VR-A8EX-01A-11D-A36J-09 chr9:916803 C>A maps to NM_021951.2 Y288*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FE-01A-11D-A33E-09 chr9:22451251 C>A maps to NM_022160.2 S286*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49V-01A-11D-A247-09 chr5:118556216 G>C maps to NM_005509.4 L2667L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FO-01A-11D-A387-09 chr5:118484612 G>T maps to NM_005509.4 E1031*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q9-A6FW-01A-31D-A31U-09 chr5:118454597 C>T maps to NM_005509.4 L278L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8WC-01A-11D-A37C-09 chr15:51839581 C>T maps to NM_001174116.1 W197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8WG-01A-11D-A37C-09 chr15:51828603 T>C maps to NM_001174116.1 R691R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GN-01A-11D-A37C-09 chr3:52428675 C>A maps to ENST00000273600 R3672R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A5B8-01A-11D-A28B-09 chr3:52414132 C>T maps to ENST00000273600 L2530L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr3:52431014 C>T maps to ENST00000273600 S3978S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6XG-01B-11D-A33E-09 chr3:52406927 G>T maps to ENST00000273600 G2282*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3I8-01A-11D-A247-09 chr12:124256178 A>G maps to NM_207437.3 L49L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3YB-01A-11D-A247-09 chr12:124364179 G>T did not map to a codon.
Sequencing variant TCGA-IG-A5B8-01A-11D-A28B-09 chr12:124343711 C>T maps to NM_207437.3 Q2098*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FA-01A-11D-A33E-09 chr12:124419179 C>A maps to NM_207437.3 S4379*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43M-01A-11D-A247-09 chr12:124352661 G>T maps to NM_207437.3 L2387L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr12:124335571 G>A maps to NM_207437.3 L1962L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OJ-01A-11D-A27G-09 chr12:124330607 G>T maps to NM_207437.3 T1789T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88Z-01A-11D-A36J-09 chr12:124403416 G>T maps to NM_207437.3 L3691L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr12:124325933 G>A maps to NM_207437.3 A1616A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NR-01A-11D-A37C-09 chr12:124401080 C>T maps to NM_207437.3 R3482R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A1-01A-21D-A27G-09 chr12:124332584 G>A maps to NM_207437.3 A1846A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4ON-01A-11D-A27G-09 chr7:21779254 G>A maps to NM_003777.3 P2633P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NQ-01A-11D-A36J-09 chr7:21603810 C>G maps to NM_003777.3 L330L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L7-A6VZ-01A-12D-A33E-09 chr7:21938962 C>T maps to NM_003777.3 D4360D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A4-01A-11D-A27G-09 chr7:21750322 T>C did not map to a codon.
Sequencing variant TCGA-R6-A8WC-01A-11D-A37C-09 chr7:21583081 G>A maps to NM_003777.3 T73T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A9VB-01A-21D-A37C-09 chr7:21657234 A>G did not map to a codon.
Sequencing variant TCGA-IG-A3Y9-01A-12D-A247-09 chr3:57399534 C>T maps to NM_178504.4 L1967L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49Y-01A-11D-A27G-09 chr3:57431005 G>A maps to NM_178504.4 L1417L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A939-01A-12D-A37C-09 chr17:76562800 A>G maps to ENST00000389840 R488R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NK-01A-21D-A37C-09 chr17:76502822 G>T maps to ENST00000389840 S1590S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GO-01A-11D-A37C-09 chr17:7721352 C>T maps to NM_020877.2 N3442N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FE-01A-11D-A33E-09 chr16:20981173 C>A maps to NM_017539.1 E2800*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OG-01A-11D-A27G-09 chr16:20981192 G>C maps to NM_017539.1 G2793G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88T-01A-11D-A351-09 chr16:21136658 G>T maps to NM_017539.1 S414*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr16:21136675 G>A maps to NM_017539.1 C408C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NS-01A-12D-A37C-09 chr16:20952733 G>T maps to NM_017539.1 I3881I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A9-01A-11D-A28B-09 chr16:21152625 G>T maps to NM_017539.1 S172S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6XG-01B-11D-A33E-09 chr16:21098316 C>A maps to NM_017539.1 T910T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S8-A6BW-01A-11D-A31U-09 chr16:21139068 G>A maps to NM_017539.1 Q383*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KH-A6WC-01A-11D-A33E-09 chr5:13839570 C>A maps to NM_001369.2 E1926*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OH-01A-11D-A27G-09 chr5:13769167 G>T maps to NM_001369.2 A3266A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OJ-01A-11D-A27G-09 chr5:13736027 G>T maps to NM_001369.2 G3823G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OT-01A-11D-A28B-09 chr5:13729593 A>T maps to NM_001369.2 L3946*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OX-01A-21D-A28B-09 chr5:13868095 A>C maps to NM_001369.2 S1280S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NH-01A-11D-A37C-09 chr5:13845020 C>T maps to NM_001369.2 A1732A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NN-01A-11D-A37C-09 chr5:13885263 C>T maps to NM_001369.2 T939T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49M-01A-21D-A27G-09 chr5:13883155 G>T maps to NM_001369.2 R1011R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HY-01A-12D-A351-09 chr5:13719066 T>C maps to NM_001369.2 T4141T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GG-01A-11D-A37C-09 chr2:84806757 A>T maps to NM_001370.1 T728T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GH-01A-11D-A37C-09 chr2:84897534 T>C maps to NM_001370.1 T2130T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NF-01A-11D-A37C-09 chr2:84940367 C>G maps to NM_001370.1 P3176P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A8-01A-32D-A27G-09 chr2:84912582 G>C maps to NM_001370.1 L2350L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A8I0-01A-11D-A36J-09 chr2:85046516 C>T maps to NM_001370.1 C4154C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GM-01A-11D-A37C-09 chr2:196765008 C>A maps to NM_018897.2 L1515L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OT-01A-11D-A28B-09 chr2:196753008 C>T maps to NM_018897.2 S1793S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A3-01A-11D-A27G-09 chr2:196749415 G>A maps to NM_018897.2 R1886*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EW-01A-11D-A36J-09 chr2:196799410 T>C maps to NM_018897.2 V1125V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A8JD-01A-11D-A36J-09 chr2:196671472 C>T maps to NM_018897.2 R3389R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GQ-01A-11D-A37C-09 chr6:38704934 A>G maps to ENST00000327475 A273A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA7I-01A-11D-A403-09 chr6:38854596 G>T maps to ENST00000327475 E2752*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FE-01A-11D-A33E-09 chr17:11797758 G>A maps to NM_001372.3 T3784T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OG-01A-11D-A27G-09 chr17:11783506 A>T maps to NM_001372.3 K3531*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HX-01A-11D-A33E-09 chr17:11809042 C>A maps to NM_001372.3 S3889*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FR-01A-11D-A387-09 chr17:11523026 G>T maps to NM_001372.3 E427*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8W5-01B-11D-A37C-09 chr17:11778483 G>T maps to NM_001372.3 T3487T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EY-01A-11D-A36J-09 chr17:11648202 C>T maps to NM_001372.3 D2067D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FD-01A-11D-A33E-09 chr17:72301521 C>T maps to NM_023036.4 G384G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FP-01A-31D-A387-09 chr16:4496969 G>T maps to NM_005147.4 G360G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A5U7-01A-11D-A31U-09 chr19:14628954 C>T maps to NM_006145.1 E69E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr2:220149369 G>T maps to NM_006736.5 L212L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8W8-01B-11D-A37C-09 chr2:220149624 G>A maps to NM_006736.5 G297G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S8-A6BW-01A-11D-A31U-09 chr3:128181533 G>A maps to NM_153330.2 S185S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43H-01A-11D-A247-09 chr10:22209876 C>A maps to NM_022365.3 L129L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GH-01A-11D-A37C-09 chr2:183621087 C>T maps to NM_018981.1 N567N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3I8-01A-11D-A247-09 chr10:69571380 C>T maps to NM_021800.2 L66L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6XG-01B-11D-A33E-09 chr3:132221269 A>T maps to NM_015268.3 L1558L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X8-AAAR-01A-11D-A403-09 chr3:132175634 G>T maps to NM_015268.3 V436V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S8-A6BW-01A-11D-A31U-09 chr13:43659933 A>G maps to NM_013238.2 T114T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GK-01A-11D-A37C-09 chr1:15870906 C>T maps to NM_015291.2 G196G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr3:180705809 C>T did not map to a codon.
Sequencing variant TCGA-LN-A7HX-01A-11D-A33E-09 chr7:102957428 C>T maps to NM_014377.1 E425E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A5B8-01A-11D-A28B-09 chr11:31392294 G>C did not map to a codon.
Sequencing variant TCGA-L5-A8NT-01A-11D-A37C-09 chr11:31436405 G>T maps to NM_181706.4 E54*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr2:25180753 C>T maps to NM_016544.2 W110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NE-01A-11D-A37C-09 chr1:65878665 C>G maps to ENST00000371069 A957A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49K-01A-11D-A247-09 chr17:40149134 G>T maps to NM_003315.3 R97R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A891-01A-11D-A36J-09 chr23:153631068 A>G did not map to a codon.
Sequencing variant TCGA-LN-A49U-01A-31D-A27G-09 chr23:153631449 C>T did not map to a codon.
Sequencing variant TCGA-LN-A49U-01A-31D-A27G-09 chr23:153633250 C>G did not map to a codon.
Sequencing variant TCGA-L5-A8NF-01A-11D-A37C-09 chr3:58178416 G>T maps to NM_004944.2 S305S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OO-01A-11D-A27G-09 chr2:230450598 G>A maps to NM_139072.3 L274L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L7-A6VZ-01A-12D-A33E-09 chr11:6565415 G>T maps to NM_144666.2 E1232*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr9:131016962 T>C maps to ENST00000372923 P855P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FD-01A-11D-A33E-09 chr10:101658498 C>G did not map to a codon.
Sequencing variant TCGA-L5-A4OJ-01A-11D-A27G-09 chr10:101637037 G>T maps to ENST00000342239 S1559*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FA-01A-11D-A33E-09 chr19:10254518 T>C maps to NM_001130823.1 K1013K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr19:10254536 G>A maps to NM_001130823.1 Y1007Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A8-01A-32D-A27G-09 chr19:10270335 G>A maps to NM_001130823.1 F426F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XP-A8T6-01A-11D-A36J-09 chr19:10265091 C>A maps to NM_001130823.1 T632T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GH-01A-11D-A37C-09 chr2:25463509 G>A maps to NM_175629.1 Y724Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43C-01A-11D-A247-09 chr2:25462039 G>A maps to NM_175629.1 H789H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43I-01A-11D-A247-09 chr20:31376727 C>T maps to NM_006892.3 A241A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OP-01A-11D-A27G-09 chr1:94343391 C>T maps to NM_014597.4 A33A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GO-01A-11D-A37C-09 chr10:129207589 C>T maps to ENST00000398025 F1471F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43E-01A-11D-A247-09 chr10:129213427 G>T maps to ENST00000398025 E1526*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8WG-01A-11D-A37C-09 chr10:128830466 G>T maps to ENST00000398025 E578*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EX-01A-11D-A36J-09 chr2:225751205 C>T maps to NM_014689.2 E153E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A5B8-01A-11D-A28B-09 chr23:117758548 A>G did not map to a codon.
Sequencing variant TCGA-JY-A93C-01A-11D-A387-09 chr23:117700053 G>A did not map to a codon.
Sequencing variant TCGA-L5-A8NH-01A-11D-A37C-09 chr23:117814624 G>T did not map to a codon.
Sequencing variant TCGA-L5-A8NR-01A-11D-A37C-09 chr23:117712575 C>T did not map to a codon.
Sequencing variant TCGA-V5-AASW-01A-11D-A403-09 chr23:117773510 G>A did not map to a codon.
Sequencing variant TCGA-VR-A8ER-01A-11D-A36J-09 chr23:117819758 G>A did not map to a codon.
Sequencing variant TCGA-L5-A8NJ-01A-11D-A36J-09 chr5:169108823 T>C maps to NM_004946.2 L183L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NW-01A-11D-A37C-09 chr5:169097601 G>T did not map to a codon.
Sequencing variant TCGA-R6-A6L4-01A-11D-A31U-09 chr5:169108759 T>C maps to NM_004946.2 L161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-A7RB-01A-11D-A351-09 chr5:169423169 T>C did not map to a codon.
Sequencing variant TCGA-VR-AA7D-01A-11D-A403-09 chr5:169412884 G>T maps to NM_004946.2 V984V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43C-01A-11D-A247-09 chr3:51352436 G>T maps to NM_004947.4 G1094*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NF-01A-11D-A37C-09 chr3:51349977 C>T maps to NM_004947.4 T1055T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A2-01A-31D-A27G-09 chr3:50927458 G>A maps to NM_004947.4 G55G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A8JD-01A-11D-A36J-09 chr3:51413180 G>A maps to NM_004947.4 P1805P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FB-01A-11D-A33E-09 chr7:111428767 C>T maps to ENST00000428084 L1117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A3-01A-11D-A27G-09 chr7:111509683 G>T maps to ENST00000428084 Y685*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q9-A6FW-01A-31D-A31U-09 chr7:111509628 C>G did not map to a codon.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr8:25230153 G>T maps to NM_024940.6 E1202*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HV-01A-21D-A351-09 chr8:25261195 T>A maps to NM_024940.6 S1683S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8WG-01A-11D-A37C-09 chr8:25220657 G>A did not map to a codon.
Sequencing variant TCGA-IG-A51D-01A-11D-A27G-09 chr9:399174 C>T maps to NM_203447.3 I1050I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OE-01A-11D-A27G-09 chr9:325712 C>A maps to NM_203447.3 L290L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr9:289569 C>T maps to NM_203447.3 I131I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr9:328098 C>T maps to NM_203447.3 A324A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FQ-01A-31D-A387-09 chr9:399159 G>T maps to NM_203447.3 A1045A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8W5-01B-11D-A37C-09 chr16:57507546 G>A maps to NM_018110.3 I280I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GN-01A-11D-A37C-09 chr20:53205283 C>T maps to NM_018431.3 I116I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RE-01A-11D-A33E-09 chr9:131709252 A>G maps to NM_014908.3 F110F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3YC-01A-11D-A247-09 chr6:31939107 G>T maps to NM_005510.3 G115G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RE-A7BO-01A-11D-A33E-09 chr6:83839954 G>T maps to NM_015018.2 G819*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASX-01A-11D-A387-09 chr6:83847208 C>T maps to NM_015018.2 Q1150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XP-A8T7-01A-11D-A36J-09 chr6:83847133 G>T maps to NM_015018.2 E1125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6F8-01A-11D-A33E-09 chr21:37602975 G>T maps to NM_005128.2 E632*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr21:37661366 G>A maps to NM_005128.2 T2126T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-A7RE-01A-11D-A351-09 chr21:37617443 C>T maps to NM_005128.2 L1056L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A8I1-01A-11D-A36J-09 chr19:2217007 C>T maps to ENST00000221482 G821G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A6QS-01A-12D-A33E-09 chr11:118971799 G>T maps to NM_001382.3 L70L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X8-AAAR-01A-11D-A403-09 chr16:89702745 G>T maps to NM_004413.3 V104V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49X-01A-31D-A27G-09 chr16:68023257 G>A maps to NM_022355.2 I346I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OO-01A-11D-A27G-09 chr14:73141062 C>T maps to NM_012074.3 P252P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49M-01A-21D-A27G-09 chr9:130698039 C>T maps to NM_003863.3 V72V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A4QS-01A-11D-A27G-09 chr2:116447469 G>A maps to NM_020868.3 A183A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49L-01A-11D-A247-09 chr2:116525871 G>T did not map to a codon.
Sequencing variant TCGA-LN-A7HX-01A-11D-A33E-09 chr2:116485403 G>T maps to NM_020868.3 E197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8W5-01B-11D-A37C-09 chr2:116447261 G>T did not map to a codon.
Sequencing variant TCGA-L5-A8NW-01A-11D-A37C-09 chr2:162881325 C>T maps to NM_001935.3 W337*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8W8-01B-11D-A37C-09 chr2:162875299 C>T maps to NM_001935.3 R453R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NN-01A-11D-A37C-09 chr7:154595587 C>T maps to NM_130797.2 N474N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43I-01A-11D-A247-09 chr19:4714336 A>G maps to ENST00000357909 N102N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NH-01A-11D-A37C-09 chr19:4703928 G>A maps to ENST00000357909 G325G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43C-01A-11D-A247-09 chr12:7869564 G>A maps to NM_199286.2 K124K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49N-01A-11D-A247-09 chr1:168698181 G>T maps to NM_001937.4 C77*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr12:64062104 G>A maps to NM_173812.4 R23R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA4G-01A-11D-A37C-09 chr19:32968497 G>T maps to NM_001172774.1 G590*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr1:98060678 C>T maps to NM_000110.3 T298T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49W-01A-11D-A27G-09 chr1:97658622 A>C did not map to a codon.
Sequencing variant TCGA-LN-A7HW-01A-22D-A351-09 chr8:105405212 G>T maps to NM_001385.2 I414I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NR-01A-11D-A37C-09 chr5:146795410 C>T maps to NM_001197294.1 E227E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6F8-01A-11D-A33E-09 chr2:27150119 G>T did not map to a codon.
Sequencing variant TCGA-L5-A4OR-01A-11D-A27G-09 chr2:74746272 G>A maps to NM_133637.2 R631*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr5:174869160 G>A maps to NM_000794.3 D314D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NI-01A-11D-A37C-09 chr11:113285183 C>A did not map to a codon.
Sequencing variant TCGA-VR-AA7I-01A-11D-A403-09 chr11:113295304 G>A maps to ENST00000355319 N23N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OS-01A-11D-A28B-09 chr4:9784945 G>A maps to NM_000798.4 E431E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EW-01A-11D-A36J-09 chr22:31799190 G>A did not map to a codon.
Sequencing variant TCGA-IG-A4QS-01A-11D-A27G-09 chr10:50599278 C>T maps to NM_001080520.1 S26S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A6QS-01A-12D-A33E-09 chr23:100515127 G>T did not map to a codon.
Sequencing variant TCGA-IG-A97I-01A-11D-A387-09 chr23:100497357 G>T did not map to a codon.
Sequencing variant TCGA-JY-A6FE-01A-11D-A33E-09 chr23:100507654 G>T did not map to a codon.
Sequencing variant TCGA-L5-A893-01A-11D-A36J-09 chr23:100509875 G>A did not map to a codon.
Sequencing variant TCGA-R6-A8WG-01A-11D-A37C-09 chr23:100503182 C>A did not map to a codon.
Sequencing variant TCGA-Z6-A9VB-01A-21D-A37C-09 chr23:100509526 G>T did not map to a codon.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr18:28711574 G>T maps to NM_024421.2 T823T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A8I0-01A-11D-A36J-09 chr18:28662347 G>T maps to ENST00000438199 I386I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A4-01A-11D-A27G-09 chr18:28588319 G>T maps to NM_001941.3 R479R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8W8-01B-11D-A37C-09 chr18:28586984 G>A maps to NM_001941.3 T592T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S8-A6BW-01A-11D-A31U-09 chr18:28604444 C>T maps to NM_001941.3 A215A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88W-01A-11D-A351-09 chr21:41424026 G>T maps to NM_001389.3 R1681R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A4-01A-11D-A27G-09 chr21:41648174 C>T maps to NM_001389.3 Q735Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q9-A6FW-01A-31D-A31U-09 chr21:41446993 G>T maps to NM_001389.3 R1620R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A7DP-01A-31D-A33E-09 chr11:117340691 G>T maps to NM_020693.2 P1046P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88Z-01A-11D-A36J-09 chr11:117352704 G>A maps to NM_020693.2 N904N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NJ-01A-11D-A36J-09 chr11:117387275 G>A maps to NM_020693.2 D623D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NR-01A-11D-A37C-09 chr11:117389187 G>A maps to NM_020693.2 N561N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A8HZ-01A-11D-A36J-09 chr11:117329509 G>A maps to NM_020693.2 G1236G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-AAPN-01A-11D-A403-09 chr11:117387200 G>A maps to NM_020693.2 S648S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NJ-01A-11D-A36J-09 chr6:116757007 T>G maps to NM_013352.2 T459T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8W5-01B-11D-A37C-09 chr18:65180051 G>T maps to NM_032160.2 V608V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GK-01A-11D-A37C-09 chr18:28934606 G>A maps to NM_001942.2 S816S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GR-01A-12D-A37C-09 chr18:29055706 G>T maps to NM_001944.2 V828V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RE-A7BO-01A-11D-A33E-09 chr6:7579555 C>A maps to NM_004415.2 R1045R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A5B8-01A-11D-A28B-09 chr4:88534006 G>A maps to NM_014208.3 G223G. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-LN-A4MR-01A-11D-A28B-09. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-LN-A4MR-01A-11D-A28B-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-2H-A9GN-01A-11D-A37C-09 chr6:56374517 A>G maps to ENST00000361203 L6101L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GQ-01A-11D-A37C-09 chr6:56490034 G>T maps to ENST00000361203 R1373R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3I8-01A-11D-A247-09 chr6:56494091 T>C maps to ENST00000361203 Q1266Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr6:56335021 G>A maps to ENST00000361203 G7222G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NI-01A-11D-A37C-09 chr6:56437022 T>C maps to ENST00000361203 E4321E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NR-01A-11D-A37C-09 chr6:56485365 G>A maps to ENST00000281662 R1720*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49S-01A-11D-A247-09 chr6:56426279 G>C maps to ENST00000361203 L4501L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6KZ-01A-11D-A31U-09 chr6:56365978 C>A maps to ENST00000361203 E6388*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6Y0-01B-11D-A33E-09 chr6:56371272 G>A maps to ENST00000361203 Q6267*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EX-01A-11D-A36J-09 chr6:56417400 G>A maps to ENST00000361203 Q5186*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EZ-01A-11D-A36J-09 chr6:56492823 G>T maps to ENST00000361203 T1326T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RE-01A-11D-A33E-09 chr1:205138756 C>A maps to NM_015375.2 S286S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93C-01A-11D-A387-09 chr1:205117393 C>T maps to NM_015375.2 K847K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8W5-01B-11D-A37C-09 chr1:205156710 G>T maps to NM_015375.2 V163V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FE-01A-11D-A33E-09 chr18:32418784 C>A maps to NM_001390.4 R417R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NF-01A-11D-A37C-09 chr18:32395956 C>T maps to NM_001390.4 R230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A891-01A-11D-A36J-09 chr2:25851214 G>A maps to NM_021907.3 R63*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93F-01A-21D-A37C-09 chr6:15533519 G>A maps to NM_032122.4 D206D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr15:49935657 A>G maps to NM_001144955.1 L266L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FH-01A-11D-A33E-09 chr7:76131709 C>A maps to NM_020892.2 L442L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93E-01A-11D-A37C-09 chr7:76111981 C>T maps to NM_020892.2 L142L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr7:76131625 C>T maps to NM_020892.2 I414I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A8I0-01A-11D-A36J-09 chr7:76110026 G>A maps to NM_020892.2 Q67Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NR-01A-11D-A37C-09 chr3:122288126 A>G maps to NM_138287.3 S397S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HW-01A-22D-A351-09 chr15:45444574 C>T maps to NM_175940.1 F1095F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr15:45405203 G>A maps to NM_014080.4 H47H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q9-A6FU-01A-11D-A31U-09 chr15:45399057 G>C maps to NM_014080.4 T601T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3I8-01A-11D-A247-09 chr15:45406922 C>T maps to NM_207581.3 L40L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8W5-01B-11D-A37C-09 chr17:80016124 C>A maps to NM_022156.3 G430*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NV-01A-11D-A37C-09 chr16:68112717 T>C maps to NM_017803.3 P437P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NF-01A-11D-A37C-09 chr1:161719719 G>T maps to NM_007240.1 A43A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NF-01A-11D-A37C-09 chr1:161721523 C>A maps to NM_007240.1 P137P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NW-01A-11D-A37C-09 chr10:76854631 G>T maps to ENST00000356369 R262R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RE-01A-11D-A33E-09 chr2:183960175 T>C maps to NM_080876.3 V148V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8WC-01A-11D-A37C-09 chr6:345904 C>T maps to ENST00000457386 R80R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr8:33449610 G>A maps to NM_024025.1 R186*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A50L-01A-11D-A27G-09 chr1:167096072 G>T maps to NM_001080426.1 E569*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A8O2-01A-11D-A36J-09 chr1:167096644 G>A maps to NM_001080426.1 A759A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L7-A6VZ-01A-12D-A33E-09 chr1:167095829 G>T maps to NM_001080426.1 E488*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FQ-01A-31D-A387-09 chr1:167096344 G>T maps to NM_001080426.1 L659L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EX-01A-11D-A36J-09 chr8:29195865 G>A maps to NM_001394.5 C244C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZR-A9CJ-01B-11D-A387-09 chr8:29195865 G>T maps to NM_001394.5 C244*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GL-01A-12D-A37C-09 chr12:89745660 C>T maps to NM_001946.2 S52S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q9-A6FU-01A-11D-A31U-09 chr12:89745615 C>T maps to NM_001946.2 Q67Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8WG-01A-11D-A37C-09 chr23:152914770 T>G did not map to a codon.
Sequencing variant TCGA-L5-A88Z-01A-11D-A36J-09 chr19:57672114 G>A maps to NM_001012729.1 Q26*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3QL-01A-11D-A247-09 chr1:1275450 G>A maps to ENST00000378888 D292D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GM-01A-11D-A37C-09 chr17:7130507 G>A maps to NM_004422.2 L482L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GI-01A-11D-A37C-09 chr3:183887839 C>T maps to NM_004423.3 A515A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NE-01A-11D-A37C-09 chr18:46889555 G>A maps to NM_017653.3 Q157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GF-01A-11D-A37C-09 chr14:102467316 G>A maps to NM_001376.4 L1367L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3Y9-01A-12D-A247-09 chr14:102499767 C>T maps to NM_001376.4 L3454L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A5B8-01A-11D-A28B-09 chr14:102449795 C>A maps to NM_001376.4 I437I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A97I-01A-11D-A387-09 chr14:102486373 C>T maps to NM_001376.4 L2830L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A938-01A-11D-A37C-09 chr14:102449488 A>G maps to NM_001376.4 R365R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OU-01A-11D-A28B-09 chr14:102510642 G>A maps to NM_001376.4 P4239P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88Z-01A-11D-A36J-09 chr14:102471557 G>T maps to NM_001376.4 R1806R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NR-01A-11D-A37C-09 chr14:102493003 C>T maps to NM_001376.4 L2911L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FQ-01A-31D-A387-09 chr14:102472349 G>T maps to NM_001376.4 V1853V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8WG-01A-11D-A37C-09 chr14:102500660 G>A did not map to a codon.
Sequencing variant TCGA-Z6-AAPN-01A-11D-A403-09 chr14:102483492 C>T maps to NM_001376.4 C2639C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NS-01A-12D-A37C-09 chr7:95616415 T>C maps to NM_004411.4 D281D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49L-01A-11D-A247-09 chr7:95457367 G>A did not map to a codon.
Sequencing variant TCGA-Z6-AAPN-01A-11D-A403-09 chr7:95705493 C>T maps to NM_004411.4 L562L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49L-01A-11D-A247-09 chr2:172585300 C>A maps to NM_001378.1 V444V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q9-A6FW-01A-31D-A31U-09 chr16:66776397 C>A maps to NM_006141.2 E158*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OE-01A-11D-A27G-09 chr11:103040911 G>T maps to NM_001080463.1 G1682*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OT-01A-11D-A28B-09 chr11:103106511 G>T maps to NM_001080463.1 E3227*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NH-01A-11D-A37C-09 chr11:103104820 G>T maps to NM_001080463.1 E3167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6DN-01B-11D-A31U-09 chr11:103047021 G>A maps to NM_001080463.1 T1911T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8WC-01A-11D-A37C-09 chr11:103107244 G>T maps to NM_001080463.1 E3266*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-A7RB-01A-11D-A351-09 chr11:103022953 A>G maps to NM_001080463.1 K1012K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EZ-01A-11D-A36J-09 chr11:103027454 G>A maps to NM_001080463.1 L1361L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6Y2-01B-11D-A33E-09 chr20:33122441 C>A maps to ENST00000374846 I82I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93F-01A-21D-A37C-09 chr23:37700358 C>A did not map to a codon.
Sequencing variant TCGA-JY-A6FG-01A-11D-A33E-09 chr21:38845004 C>A maps to NM_001396.3 C10*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FP-01A-31D-A387-09 chr21:38878462 G>A maps to NM_001396.3 R536R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3YC-01A-11D-A247-09 chr19:40319119 G>A maps to NM_004714.1 G208G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HY-01A-12D-A351-09 chr12:4705421 G>A maps to NM_003845.1 V130V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OQ-01A-11D-A27G-09 chr2:71755482 G>A maps to NM_001130987.1 K444K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr2:71681136 G>A maps to NM_001130981.1 R3R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49V-01A-11D-A247-09 chr2:71827928 C>A maps to NM_001130987.1 S1285*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A8-01A-32D-A27G-09 chr2:71753403 C>A maps to NM_001130987.1 R402R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A8-01A-32D-A27G-09 chr2:71892348 C>T maps to NM_001130987.1 F1744F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A8JE-01A-11D-A37C-09 chr2:71801356 C>T maps to NM_001130987.1 G1086G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GL-01A-12D-A37C-09 chr2:207530607 T>G maps to NM_001093730.1 R376R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A9-01A-11D-A28B-09 chr3:137822804 G>C maps to NM_173543.2 S3S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HW-01A-22D-A351-09 chr20:32264555 G>A maps to NM_005225.2 L432L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FG-01A-11D-A33E-09 chr8:86119672 G>A maps to ENST00000256117 L189L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GM-01A-11D-A37C-09 chr12:77421831 G>A maps to NM_203394.2 G657G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88V-01A-11D-A351-09 chr5:158139189 G>A maps to NM_024007.3 N507N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4ON-01A-11D-A27G-09 chr8:25898182 G>A maps to NM_022659.2 V119V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NL-01A-12D-A37C-09 chr8:25890599 C>T did not map to a codon.
Sequencing variant TCGA-L5-A8NU-01A-11D-A36J-09 chr10:131757220 C>T maps to ENST00000355311 L154L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A51D-01A-11D-A27G-09 chr3:73111573 A>G maps to NM_018029.3 A114A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GI-01A-11D-A37C-09 chr3:184005668 C>T maps to NM_014693.3 D554D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93C-01A-11D-A387-09 chr3:183995995 C>T maps to NM_014693.3 N333N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8WC-01A-11D-A37C-09 chr3:184008604 T>C maps to NM_014693.3 G715G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49S-01A-11D-A247-09 chr2:233347865 G>T maps to NM_004826.2 V510V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr6:139165649 C>T maps to NM_001195037.2 R233*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93D-01A-11D-A387-09 chr23:65822516 A>C did not map to a codon.
Sequencing variant TCGA-IC-A6RF-01A-13D-A33E-09 chr16:67912945 T>C maps to NM_014329.3 P458P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93E-01A-11D-A37C-09 chr16:67913138 G>T did not map to a codon.
Sequencing variant TCGA-LN-A4A1-01A-21D-A27G-09 chr16:67911273 C>T maps to NM_014329.3 F202F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EY-01A-11D-A36J-09 chr16:67913015 G>T maps to NM_014329.3 E482*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EZ-01A-11D-A36J-09 chr16:67910486 C>G maps to NM_014329.3 A112A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HZ-01A-31D-A351-09 chr14:21238743 C>T maps to NM_022360.4 I145I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FB-01A-11D-A33E-09 chr3:5244834 G>T did not map to a codon.
Sequencing variant TCGA-IG-A51D-01A-11D-A27G-09 chr20:33719586 C>T did not map to a codon.
Sequencing variant TCGA-JY-A939-01A-12D-A37C-09 chr5:83402503 C>T maps to NM_005711.3 W205*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr5:83239318 T>C maps to NM_005711.3 R454R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NJ-01A-11D-A36J-09 chr5:83433071 T>C maps to NM_005711.3 R152R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASW-01A-11D-A403-09 chr20:57899498 G>A maps to NM_207034.1 Q234Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RE-01A-11D-A33E-09 chr4:148406991 A>G maps to NM_001957.3 Q53Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XP-A8T8-01A-11D-A36J-09 chr11:85966329 G>T did not map to a codon.
Sequencing variant TCGA-R6-A6Y2-01B-11D-A33E-09 chr8:144662313 C>T maps to NM_032378.4 G591G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASX-01A-11D-A387-09 chr8:144662316 G>A maps to NM_032378.4 D590D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A4-01A-11D-A27G-09 chr19:3982326 G>A maps to NM_001961.3 F236F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6Y2-01B-11D-A33E-09 chr19:3982031 G>A maps to NM_001961.3 N270N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr7:36194796 A>G maps to NM_030636.2 T288T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NV-01A-11D-A37C-09 chr7:36194610 G>A maps to NM_030636.2 L226L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OE-01A-11D-A27G-09 chr8:49647686 C>T maps to NM_024593.3 K8K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49P-01A-11D-A247-09 chr8:49643125 G>A maps to NM_024593.3 R98*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OJ-01A-11D-A27G-09 chr17:28295947 A>G maps to NM_198529.3 P110P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8WG-01A-11D-A37C-09 chr22:44112834 G>A maps to NM_022785.3 Q259*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OE-01A-11D-A27G-09 chr11:65638796 C>T maps to NM_016938.3 K66K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GN-01A-11D-A37C-09 chr19:1295852 C>T maps to NM_001405.2 Y150Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EW-01A-11D-A36J-09 chr19:1299898 C>T maps to NM_001405.2 L199L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NK-01A-21D-A37C-09 chr1:155057656 C>G maps to ENST00000505139 P68P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FD-01A-11D-A33E-09 chr5:106763017 G>A maps to NM_001962.2 H106H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6DQ-01B-11D-A31U-09 chr23:68060495 G>A did not map to a codon.
Sequencing variant TCGA-L5-A43E-01A-11D-A247-09 chr8:132952791 G>A maps to NM_015137.3 L19L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88W-01A-11D-A351-09 chr8:132991104 A>T maps to NM_015137.3 G446G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FD-01A-11D-A33E-09 chr4:110897166 G>T did not map to a codon.
Sequencing variant TCGA-VR-AA7B-01A-31D-A403-09 chr4:110915910 C>T maps to NM_001963.4 L960L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3YA-01A-11D-A247-09 chr23:13621507 G>T did not map to a codon.
Sequencing variant TCGA-IG-A5B8-01A-11D-A28B-09 chr5:38438417 C>T maps to ENST00000354891 F775F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NT-01A-11D-A37C-09 chr5:38258921 G>A maps to ENST00000354891 A22A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EX-01A-11D-A36J-09 chr5:38338852 C>T maps to ENST00000354891 S87S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A5S3-01A-11D-A28B-09 chr7:55273279 G>A maps to NM_005228.3 A1201A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OJ-01A-11D-A27G-09 chr19:41306596 G>T maps to NM_053046.2 L40L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OH-01A-11D-A27G-09 chr10:64575780 G>T maps to NM_001136178.1 T3T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49R-01A-11D-A247-09 chr10:64575630 T>G maps to NM_001136178.1 G53G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S8-A6BV-01A-21D-A31U-09 chr2:73519307 G>A maps to NM_001965.3 I349I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OJ-01A-11D-A27G-09 chr2:63176033 G>T maps to NM_015252.3 E720*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EP-01A-31D-A403-09 chr2:63176059 C>T maps to NM_015252.3 I728I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NV-01A-11D-A37C-09 chr11:64627629 C>T maps to NM_006795.2 Q227Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FQ-01A-31D-A387-09 chr19:48244235 C>T maps to NM_014601.3 L393L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NJ-01A-11D-A36J-09 chr2:31489488 A>G maps to NM_014600.2 K509K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X8-AAAR-01A-11D-A403-09 chr2:31467220 A>G maps to NM_014600.2 G103G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GI-01A-11D-A37C-09 chr15:42192878 G>A maps to NM_139265.3 P530P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RE-01A-11D-A33E-09 chr15:42264524 G>A maps to NM_139265.3 A56A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GF-01A-11D-A37C-09 chr9:140728898 C>T maps to NM_024757.4 F1213F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49V-01A-11D-A247-09 chr9:140611420 G>T maps to NM_024757.4 L143L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EQ-01A-11D-A36J-09 chr9:140611615 G>A maps to NM_024757.4 P208P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA4D-01A-11D-A37C-09 chr9:140710454 C>T maps to NM_024757.4 C1105C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A5B8-01A-11D-A28B-09 chr6:31847869 G>C maps to ENST00000395728 V1265V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XP-A8T8-01A-11D-A36J-09 chr11:125448943 C>T maps to ENST00000278903 Q198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S8-A6BV-01A-21D-A31U-09 chr19:40022957 C>G maps to NM_152361.1 *162S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88V-01A-11D-A351-09 chr12:104698037 C>A maps to NM_001008394.1 S109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A97H-01A-11D-A387-09 chr24:22751374 A>G did not map to a codon.
Sequencing variant TCGA-KH-A6WC-01A-11D-A33E-09 chr2:37368814 C>T maps to NM_001135651.1 T90T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr15:40309341 C>T maps to NM_001013703.2 Q1322*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr15:40241360 C>T maps to NM_001013703.2 S135S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A5B8-01A-11D-A28B-09 chr12:124111667 C>T maps to NM_001414.3 L135L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EW-01A-11D-A36J-09 chr12:124107309 T>A did not map to a codon.
Sequencing variant TCGA-L5-A8NL-01A-12D-A37C-09 chr3:183855471 C>T maps to NM_003907.2 R129*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88W-01A-11D-A351-09 chr1:36379441 G>A did not map to a codon.
Sequencing variant TCGA-IG-A5S3-01A-11D-A28B-09 chr23:24075596 C>T did not map to a codon.
Sequencing variant TCGA-L5-A8NV-01A-11D-A37C-09 chr23:24091267 G>T did not map to a codon.
Sequencing variant TCGA-Z6-A8JE-01A-11D-A37C-09 chr10:120801700 G>T maps to NM_003750.2 R1111R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FB-01A-11D-A33E-09 chr7:2412353 T>C maps to ENST00000314800 A578A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NH-01A-11D-A37C-09 chr8:117658785 C>T maps to ENST00000411422 P309P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A2-01A-31D-A27G-09 chr15:44846785 A>G maps to NM_003758.2 P110P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GM-01A-11D-A37C-09 chr3:186503673 C>T maps to ENST00000440191 I118I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GO-01A-11D-A37C-09 chr3:184041273 G>T maps to NM_001194947.1 E730*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr3:184045616 G>T did not map to a codon.
Sequencing variant TCGA-L5-A8NV-01A-11D-A37C-09 chr3:184045114 T>C maps to NM_001194947.1 P1187P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GQ-01A-11D-A37C-09 chr1:21299503 C>T maps to NM_001198801.1 E138E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8WG-01A-11D-A37C-09 chr1:21205815 C>T maps to NM_001198801.1 T854T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GQ-01A-11D-A37C-09 chr2:99977777 T>C maps to NM_015904.3 D138D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A97H-01A-11D-A387-09 chr2:99977011 G>A maps to NM_015904.3 K82K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NW-01A-11D-A37C-09 chr2:99978107 G>T maps to NM_015904.3 A248A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr9:23704940 A>G maps to ENST00000359598 S182S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr9:23692566 C>T maps to ENST00000359598 T384T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S8-A6BW-01A-11D-A31U-09 chr9:23731091 G>T maps to ENST00000359598 Y115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GR-01A-12D-A37C-09 chr1:50572047 A>C maps to NM_001144775.1 R15R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FP-01A-31D-A387-09 chr1:50661317 C>T maps to NM_021952.3 P198P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-AAPN-01A-11D-A403-09 chr13:41515339 G>A maps to NM_172373.3 Q325*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OH-01A-11D-A27G-09 chr1:201981120 G>A maps to NM_004433.4 W67*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GF-01A-11D-A37C-09 chr11:34502401 A>G maps to NM_198381.1 V206V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A5B8-01A-11D-A28B-09 chr11:34515143 G>A maps to NM_198381.1 F89F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OS-01A-11D-A28B-09 chr22:37769431 G>A maps to NM_052906.3 L715L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RE-01A-11D-A33E-09 chr23:47498580 G>A did not map to a codon.
Sequencing variant TCGA-V5-A7RB-01A-11D-A351-09 chr23:47498708 T>C did not map to a codon.
Sequencing variant TCGA-L5-A4OW-01A-11D-A28B-09 chr19:18557180 G>T maps to NM_006532.3 R548R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NN-01A-11D-A37C-09 chr15:44066532 G>A maps to NM_025165.2 H295H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GO-01A-11D-A37C-09 chr7:37354504 T>C maps to NM_014800.9 E47E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93D-01A-11D-A387-09 chr7:37251020 G>T maps to NM_014800.9 Y352*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43I-01A-11D-A247-09 chr7:36934565 G>A maps to NM_014800.9 S498S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NE-01A-11D-A37C-09 chr7:37382288 C>A maps to NM_014800.9 P2P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6Y2-01B-11D-A33E-09 chr7:36934484 C>T maps to NM_014800.9 Q525Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr20:45014791 G>A maps to ENST00000439931 T216T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49Y-01A-11D-A27G-09 chr11:107518315 G>T maps to NM_018712.3 L181L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr7:73470748 G>A maps to ENST00000358929 P433P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FP-01A-31D-A387-09 chr7:73474213 A>T maps to ENST00000358929 A506A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EZ-01A-11D-A36J-09 chr7:73456950 C>G maps to ENST00000358929 G80G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A8JD-01A-11D-A36J-09 chr5:60053362 C>T maps to NM_024930.2 W203*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A4QS-01A-11D-A27G-09 chr18:33750036 G>A maps to ENST00000442325 W761*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6L4-01A-11D-A31U-09 chr18:33750129 C>T maps to ENST00000442325 S792S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr8:27987106 T>C maps to NM_018091.5 L236L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr11:31561257 G>T maps to ENST00000395934 L103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GL-01A-12D-A37C-09 chr1:79387435 C>T maps to NM_022159.3 W373*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GL-01A-12D-A37C-09 chr1:79404881 A>C maps to NM_022159.3 T129T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OS-01A-11D-A28B-09 chr1:79411959 T>G maps to NM_022159.3 I108I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NG-01A-11D-A37C-09 chr23:153609156 G>T did not map to a codon.
Sequencing variant TCGA-VR-A8EY-01A-11D-A36J-09 chr23:153609471 G>T did not map to a codon.
Sequencing variant TCGA-VR-A8EY-01A-11D-A36J-09 chr17:48452976 A>G maps to NM_001166131.1 K136K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr7:101194403 C>T maps to ENST00000397927 R337*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EZ-01A-11D-A36J-09 chr18:2891504 G>T maps to NM_032048.2 T460T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FH-01A-11D-A33E-09 chr14:100380521 G>T maps to NM_001008707.1 E520*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HX-01A-11D-A33E-09 chr14:100361060 G>T maps to NM_001008707.1 E234*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88Z-01A-11D-A36J-09 chr19:46124821 G>A maps to NM_001193268.1 D506D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr2:42490437 T>C maps to NM_019063.3 T211T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr2:42511824 C>T maps to NM_019063.3 G331G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A2-01A-31D-A27G-09 chr2:42508023 G>A maps to NM_019063.3 R234R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A2-01A-31D-A27G-09 chr14:89124636 G>A maps to ENST00000380664 G1257G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8Q7-01A-11D-A37C-09 chr19:6937658 G>T maps to ENST00000381407 T887T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FH-01A-11D-A33E-09 chr19:14761999 C>A maps to NM_032571.3 A198A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NL-01A-12D-A37C-09 chr19:14774281 A>G maps to NM_032571.3 Y49Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L7-A6VZ-01A-12D-A33E-09 chr10:119305282 G>T maps to NM_004098.3 E183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OH-01A-11D-A27G-09 chr2:119600698 G>T maps to NM_001426.3 R332R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A938-01A-11D-A37C-09 chr4:71509220 C>G maps to NM_031889.2 S693*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49U-01A-31D-A27G-09 chr4:71508639 A>T maps to NM_031889.2 G499G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FH-01A-11D-A33E-09 chr12:48111403 G>T maps to NM_001172439.1 R93R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FP-01A-31D-A387-09 chr17:77082109 G>A maps to NM_001042573.1 E637E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr1:8927292 G>A maps to NM_001428.2 N109N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4MR-01A-11D-A28B-09 chr1:8928110 C>T maps to NM_001428.2 L82L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6Y2-01B-11D-A33E-09 chr1:8921451 G>T maps to NM_001428.2 A424A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GK-01A-11D-A37C-09 chr13:43900626 G>T maps to NM_001127615.1 T357T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88V-01A-11D-A351-09 chr13:43900599 C>T maps to NM_001127615.1 S366S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr23:129804064 G>A did not map to a codon.
Sequencing variant TCGA-L5-A8NR-01A-11D-A37C-09 chr23:129822856 G>A did not map to a codon.
Sequencing variant TCGA-LN-A8I0-01A-11D-A36J-09 chr23:129803956 C>T did not map to a codon.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr4:111397884 C>T maps to NM_001977.3 H105H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8WG-01A-11D-A37C-09 chr4:111431405 T>C maps to NM_001977.3 F400F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASX-01A-11D-A387-09 chr6:132172306 C>T maps to NM_006208.2 F152F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GM-01A-11D-A37C-09 chr6:131973680 G>T did not map to a codon.
Sequencing variant TCGA-JY-A6FA-01A-11D-A33E-09 chr6:132059219 A>G maps to NM_005021.3 E739E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr6:132043496 T>C maps to NM_005021.3 N566N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NS-01A-12D-A37C-09 chr6:46107440 C>T maps to NM_014936.4 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A8HZ-01A-11D-A36J-09 chr6:46135852 G>T maps to NM_021572.4 P49P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6XG-01B-11D-A33E-09 chr6:46135471 T>C maps to NM_021572.4 S176S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr17:77710925 T>C maps to NM_178543.3 P371P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88Z-01A-11D-A36J-09 chr10:97607214 G>T maps to NM_001098175.1 E283*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EY-01A-11D-A36J-09 chr10:97604275 G>T maps to NM_001098175.1 E160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NW-01A-11D-A37C-09 chr9:139944963 C>T maps to NM_203468.1 P267P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OO-01A-11D-A27G-09 chr8:23306282 G>T maps to NM_004901.3 R60R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8W5-01B-11D-A37C-09 chr8:23290606 G>T maps to NM_004901.3 V561V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FO-01A-11D-A387-09 chr14:74440670 C>T maps to NM_001249.2 G265G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr3:27761749 G>A maps to ENST00000449599 F316F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr22:41513395 A>G maps to NM_001429.3 P100P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49V-01A-11D-A247-09 chr22:41568667 G>A did not map to a codon.
Sequencing variant TCGA-LN-A9FO-01A-11D-A387-09 chr22:41558784 T>A did not map to a codon.
Sequencing variant TCGA-L7-A6VZ-01A-12D-A33E-09 chr12:132512791 G>T maps to ENST00000333577 T1816T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L7-A6VZ-01A-12D-A33E-09 chr12:132514631 G>T maps to ENST00000333577 E1931*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49X-01A-31D-A27G-09 chr12:132512559 A>G did not map to a codon.
Sequencing variant TCGA-R6-A6XG-01B-11D-A33E-09 chr12:132512804 G>T maps to ENST00000333577 G1821*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-A7RE-01A-11D-A351-09 chr12:132547140 G>A maps to ENST00000333577 Q2779Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASX-01A-11D-A387-09 chr12:132547140 G>A maps to ENST00000333577 Q2779Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr2:46608779 G>A maps to NM_001430.4 P697P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6DN-01B-11D-A31U-09 chr2:46583906 C>T maps to NM_001430.4 C138C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FG-01A-11D-A33E-09 chr1:29365938 G>A did not map to a codon.
Sequencing variant TCGA-JY-A6FE-01A-11D-A33E-09 chr20:34778582 G>T maps to NM_012156.2 V388V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4MQ-01A-11D-A28B-09 chr20:34797648 C>T maps to NM_012156.2 F636F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA4G-01A-11D-A37C-09 chr6:131186735 C>G maps to NM_001431.3 L923L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3YC-01A-11D-A247-09 chr18:5428400 G>T maps to NM_012307.2 R326R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4ON-01A-11D-A27G-09 chr18:5394762 T>C maps to NM_012307.2 K1061K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88V-01A-11D-A351-09 chr18:5478308 G>T maps to NM_012307.2 V104V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49M-01A-21D-A27G-09 chr18:5406960 C>A maps to NM_012307.2 E722*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q9-A6FW-01A-31D-A31U-09 chr18:5406796 G>A maps to NM_012307.2 I776I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-A7RB-01A-11D-A351-09 chr18:5489095 C>T maps to NM_012307.2 A29A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93D-01A-11D-A387-09 chr5:111504483 C>T maps to NM_022140.3 V628V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GG-01A-11D-A37C-09 chr9:112017825 G>A maps to NM_019114.3 S378S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49Y-01A-11D-A27G-09 chr2:120922455 G>A maps to NM_020909.3 E644E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A9-01A-11D-A28B-09 chr2:120925514 A>G maps to NM_020909.3 G689G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HX-01A-11D-A33E-09 chr10:32575674 G>T maps to NM_025209.2 T446T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A893-01A-11D-A36J-09 chr7:143088618 C>T maps to NM_005232.4 T954T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NJ-01A-11D-A36J-09 chr7:143095514 G>A maps to NM_005232.4 L455L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6L6-01B-11D-A33E-09 chr7:143094700 C>T maps to NM_005232.4 L555L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3QL-01A-11D-A247-09 chr1:38185712 C>A maps to NM_001099439.1 A810A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr1:38219905 C>T maps to NM_001099439.1 P329P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr1:38227206 G>A maps to NM_001099439.1 C240C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A97H-01A-11D-A387-09 chr1:16464459 G>A maps to NM_004431.3 S400S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88W-01A-11D-A351-09 chr1:16459851 C>A maps to NM_004431.3 E626*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A4-01A-11D-A27G-09 chr1:16460075 G>A maps to NM_004431.3 Y588Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A9VB-01A-21D-A37C-09 chr1:16458591 C>T maps to NM_004431.3 L764L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FD-01A-11D-A33E-09 chr3:89462300 A>G maps to NM_005233.5 P591P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93E-01A-11D-A37C-09 chr2:222290753 G>T maps to NM_004438.3 P985P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GM-01A-11D-A37C-09 chr4:66280140 C>T maps to NM_004439.5 T516T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr4:66535354 G>A maps to NM_004439.5 R36*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L7-A6VZ-01A-12D-A33E-09 chr4:66467470 A>G maps to NM_004439.5 S266S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A1-01A-21D-A27G-09 chr4:66197757 G>T maps to NM_004439.5 R981R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASX-01A-11D-A387-09 chr4:66230834 G>T maps to NM_004439.5 G712G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NJ-01A-11D-A36J-09 chr3:97466311 C>T maps to NM_001080448.2 V1058V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6KZ-01A-11D-A31U-09 chr3:97124069 T>C maps to NM_001080448.2 A561A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA4G-01A-11D-A37C-09 chr3:97356913 T>G maps to NM_001080448.2 A924A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GF-01A-11D-A37C-09 chr3:134825425 T>C maps to NM_004441.4 P314P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GF-01A-11D-A37C-09 chr3:134851748 C>T maps to NM_004441.4 G385G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RE-01A-11D-A33E-09 chr3:134960051 A>G maps to NM_004441.4 S803S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FH-01A-11D-A33E-09 chr3:134884808 G>T did not map to a codon.
Sequencing variant TCGA-L5-A4OS-01A-11D-A28B-09 chr3:134881020 C>T maps to NM_004441.4 D528D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr3:134670232 C>T maps to NM_004441.4 Y48Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NS-01A-12D-A37C-09 chr3:134977895 G>A maps to NM_004441.4 K963K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FQ-01A-31D-A387-09 chr7:100417901 G>T maps to NM_004444.4 T275T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A891-01A-11D-A36J-09 chr7:142562097 T>C maps to NM_004445.3 A180A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GM-01A-11D-A37C-09 chr19:15341893 C>T maps to NM_001142886.1 S165S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6Y0-01B-11D-A33E-09 chr19:15342089 G>A maps to NM_001142886.1 D149D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OH-01A-11D-A27G-09 chr1:92498097 G>T maps to NM_173567.4 E90*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3QL-01A-11D-A247-09 chr3:37033712 G>A maps to NM_014805.3 L286L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3Y9-01A-12D-A247-09 chr3:37033359 G>C maps to NM_014805.3 V403V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr19:56203121 G>A maps to NM_001130071.1 S341S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OW-01A-11D-A28B-09 chr17:19216545 C>T maps to NM_014964.4 G367G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A8I1-01A-11D-A36J-09 chr17:48618873 G>T maps to NM_017957.2 T468T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NJ-01A-11D-A36J-09 chr19:11491846 G>A maps to NM_000121.3 S208S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr8:144942927 C>T maps to NM_031308.1 L1498L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr8:144947010 G>A maps to NM_031308.1 I137I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4ON-01A-11D-A27G-09 chr8:144940782 G>A maps to NM_031308.1 D2213D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49Y-01A-11D-A27G-09 chr8:144947156 G>T maps to NM_031308.1 R89R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XP-A8T6-01A-11D-A36J-09 chr8:144945771 C>T maps to NM_031308.1 E550E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A8O2-01A-11D-A36J-09 chr1:220160601 T>A maps to NM_004446.2 K974*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6F8-01A-11D-A33E-09 chr1:220195819 T>C maps to NM_004446.2 K328K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88T-01A-11D-A351-09 chr1:220160716 G>T maps to NM_004446.2 L935L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49X-01A-31D-A27G-09 chr1:51906101 G>A maps to NM_001981.2 N319N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NR-01A-11D-A37C-09 chr19:16528890 C>T maps to ENST00000455140 T325T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A7DP-01A-31D-A33E-09 chr12:15784374 C>T did not map to a codon.
Sequencing variant TCGA-Q9-A6FU-01A-11D-A31U-09 chr12:15811042 C>T maps to NM_004447.5 L357L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A4P3-01A-11D-A27G-09 chr11:721937 G>T maps to NM_022772.3 E311*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr1:110300958 G>T maps to NM_139053.1 P233P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA4D-01A-11D-A37C-09 chr1:110294816 T>G did not map to a codon.
Sequencing variant TCGA-VR-A8Q7-01A-11D-A37C-09 chr13:43537396 T>C maps to NM_001002264.1 R161R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OJ-01A-11D-A27G-09 chr5:96253164 G>T did not map to a codon.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr23:48687784 G>A did not map to a codon.
Sequencing variant TCGA-L7-A6VZ-01A-12D-A33E-09 chr5:65349237 G>T maps to ENST00000506030 E698*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A8JE-01A-11D-A37C-09 chr5:65350088 C>A maps to ENST00000506030 Y981*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr12:56495023 C>T maps to NM_001982.2 R1127R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43C-01A-11D-A247-09 chr2:212288963 C>A maps to NM_005235.2 E928*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OJ-01A-11D-A27G-09 chr2:212251632 T>C maps to NM_005235.2 R1142R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6XG-01B-11D-A33E-09 chr2:212812172 C>A maps to NM_005235.2 G135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GM-01A-11D-A37C-09 chr3:56330139 C>T maps to ENST00000460849 E327E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr3:56330172 G>T maps to ENST00000460849 G316G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A8I0-01A-11D-A36J-09 chr2:128036798 G>T maps to NM_000122.1 V560V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4MR-01A-11D-A28B-09 chr16:14029601 C>A did not map to a codon.
Sequencing variant TCGA-2H-A9GI-01A-11D-A37C-09 chr10:50681582 G>T maps to NM_000124.2 L883L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr10:50684357 T>C did not map to a codon.
Sequencing variant TCGA-LN-A8HZ-01A-11D-A36J-09 chr10:50678882 T>C maps to NM_000124.2 Q1041Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NI-01A-11D-A37C-09 chr23:71427368 C>T did not map to a codon.
Sequencing variant TCGA-L5-A88S-01A-11D-A36J-09 chr5:60183320 G>T maps to NM_000082.3 C356*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr21:39947606 C>T maps to NM_001136154.1 P6P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X8-AAAR-01A-11D-A403-09 chr21:39947584 C>T did not map to a codon.
Sequencing variant TCGA-L5-A88Z-01A-11D-A36J-09 chr2:54040156 G>A maps to NM_015701.3 K391K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A5-01A-21D-A27G-09 chr1:43308660 G>T maps to NM_018538.3 E396*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FD-01A-11D-A33E-09 chr9:5787516 G>T maps to NM_024896.2 T821T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GH-01A-11D-A37C-09 chr17:62130145 C>T maps to NM_001433.3 E749E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OE-01A-11D-A27G-09 chr17:62131645 G>T maps to NM_001433.3 Y639*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GL-01A-12D-A37C-09 chr1:236433177 G>C maps to NM_019891.3 Y73*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FB-01A-11D-A33E-09 chr1:8074193 C>T maps to NM_018948.3 P155P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RE-01A-11D-A33E-09 chr7:64452675 A>C maps to NM_001007253.3 T243T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GQ-01A-11D-A37C-09 chr6:11104019 G>C maps to NM_207582.2 T508T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GQ-01A-11D-A37C-09 chr12:53666580 G>A maps to NM_012291.4 P482P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A5S3-01A-11D-A28B-09 chr12:53668780 G>T maps to NM_012291.4 E563*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OH-01A-11D-A27G-09 chr12:53681811 G>T maps to NM_012291.4 L1411L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XP-A8T6-01A-11D-A36J-09 chr12:53682997 G>T maps to NM_012291.4 R1611R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr1:6504566 G>A maps to NM_031475.2 R339R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3I8-01A-11D-A247-09 chr14:64727212 G>A maps to NM_001437.2 A302A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr14:64723981 G>A maps to NM_001437.2 P351P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NJ-01A-11D-A36J-09 chr16:68265591 C>T maps to NM_024939.2 L435L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49L-01A-11D-A247-09 chr1:216741435 C>G maps to NM_001438.2 V198V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8W8-01B-11D-A37C-09 chr1:216692713 A>T maps to NM_001438.2 A304A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S8-A6BW-01A-11D-A31U-09 chr1:216896592 C>A maps to NM_001438.2 E17*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NG-01A-11D-A37C-09 chr23:103498836 C>T did not map to a codon.
Sequencing variant TCGA-L5-A8NK-01A-21D-A37C-09 chr23:103495089 G>C did not map to a codon.
Sequencing variant TCGA-LN-A7HX-01A-11D-A33E-09 chr23:103499091 C>A did not map to a codon.
Sequencing variant TCGA-R6-A8W5-01B-11D-A37C-09 chr23:103499075 G>A did not map to a codon.
Sequencing variant TCGA-JY-A6FD-01A-11D-A33E-09 chr7:158527117 G>T maps to NM_020728.2 T877T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GQ-01A-11D-A37C-09 chr3:138191617 C>A maps to NM_031913.3 P718P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A2-01A-31D-A27G-09 chr3:138183219 C>T maps to NM_031913.3 Q317*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GF-01A-11D-A37C-09 chr2:67632364 C>T maps to NM_019002.3 Q851*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43I-01A-11D-A247-09 chr2:67630791 T>G maps to NM_019002.3 T326T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr2:67626313 A>G maps to NM_019002.3 T79T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OU-01A-11D-A28B-09 chr2:67631301 T>C maps to NM_019002.3 N496N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NW-01A-11D-A37C-09 chr2:67630381 G>T maps to NM_019002.3 E190*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93D-01A-11D-A387-09 chr4:159629655 G>T maps to NM_004453.2 G611*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S8-A6BV-01A-21D-A31U-09 chr12:22824228 G>T maps to NM_018638.4 E331*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr11:128359269 G>A maps to NM_001143820.1 C150C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A4P3-01A-11D-A27G-09 chr7:13950873 G>A maps to NM_004956.4 S287S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A939-01A-12D-A37C-09 chr17:41607044 C>T did not map to a codon.
Sequencing variant TCGA-L5-A8NN-01A-11D-A37C-09 chr17:41622355 C>T maps to NM_001079675.1 T63T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8WG-01A-11D-A37C-09 chr17:41622934 G>T maps to NM_001079675.1 T17T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EQ-01A-11D-A36J-09 chr12:12022496 C>T maps to NM_001987.4 L201L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr4:5809990 C>T maps to NM_153717.2 H875H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A5U7-01A-11D-A31U-09 chr4:5743441 G>A did not map to a codon.
Sequencing variant TCGA-L5-A4OG-01A-11D-A27G-09 chr4:5617214 C>A maps to NM_147127.4 L921L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6KZ-01A-11D-A31U-09 chr4:5664868 G>A maps to NM_147127.4 S370S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NJ-01A-11D-A36J-09 chr1:93091469 C>A maps to NM_005665.4 E501*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NQ-01A-11D-A36J-09 chr14:100604119 C>T maps to NM_016337.2 Q359*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GH-01A-11D-A37C-09 chr17:74004778 G>A maps to NM_001988.2 Q1503*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NW-01A-11D-A37C-09 chr17:74005673 C>T maps to NM_001988.2 P1204P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASV-01A-11D-A387-09 chr17:74006237 G>T maps to NM_001988.2 T1016T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RF-01A-13D-A33E-09 chr7:27284772 C>T maps to NM_001989.3 S178S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GG-01A-11D-A37C-09 chr1:242016686 A>G maps to NM_006027.4 G103G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4MR-01A-11D-A28B-09 chr4:56736999 G>T maps to NM_018261.3 E254*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FQ-01A-31D-A387-09 chr4:56734598 C>T maps to NM_018261.3 I171I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A893-01A-11D-A36J-09 chr6:610146 C>T maps to NM_018303.4 T231T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NE-01A-11D-A37C-09 chr6:572546 G>T maps to NM_018303.4 S472S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A5B8-01A-11D-A28B-09 chr16:67223571 G>C maps to NM_178516.3 S3*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93E-01A-11D-A37C-09 chr16:67219281 C>T maps to NM_178516.3 A536A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GL-01A-12D-A37C-09 chr14:57696599 C>T did not map to a codon.
Sequencing variant TCGA-KH-A6WC-01A-11D-A33E-09 chr14:57710887 C>A maps to ENST00000340918 E154*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA4D-01A-11D-A37C-09 chr10:94714401 C>T maps to NM_019053.4 D514D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A50L-01A-11D-A27G-09 chr1:231471715 C>T maps to NM_175876.3 E592E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88S-01A-11D-A36J-09 chr1:11137656 C>T did not map to a codon.
Sequencing variant TCGA-R6-A6DQ-01B-11D-A31U-09 chr19:41898856 G>A maps to NM_020158.3 Y59Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FE-01A-11D-A33E-09 chr3:45046821 G>A maps to NM_015004.3 S177S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OX-01A-21D-A28B-09 chr11:108382045 A>T maps to NM_015065.2 T1396T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NT-01A-11D-A37C-09 chr11:108382591 G>T maps to NM_015065.2 C1214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88Z-01A-11D-A36J-09 chr8:118811970 G>A maps to NM_000127.2 R741*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RE-01A-11D-A33E-09 chr8:72234486 A>G maps to NM_000503.4 S73S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A893-01A-11D-A36J-09 chr6:133846295 A>G maps to ENST00000452339 K587K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GF-01A-11D-A37C-09 chr6:65301178 C>T maps to ENST00000370616 Q1527Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GR-01A-12D-A37C-09 chr6:65301484 A>C maps to ENST00000370616 T1425T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A6QS-01A-12D-A33E-09 chr6:64791749 G>T maps to ENST00000370616 Y2190*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FH-01A-11D-A33E-09 chr6:66205227 G>T maps to ENST00000370616 R26R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43E-01A-11D-A247-09 chr6:65523281 A>G maps to ENST00000370616 T1144T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43E-01A-11D-A247-09 chr6:66115231 A>G maps to ENST00000370616 P297P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OG-01A-11D-A27G-09 chr6:65300260 A>G maps to ENST00000370616 T1833T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr6:64430614 A>G maps to ENST00000370616 F3125F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr6:65622632 A>T maps to ENST00000370616 C795*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A8I1-01A-11D-A36J-09 chr6:65301787 G>T maps to ENST00000370616 L1324L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A9VB-01A-21D-A37C-09 chr17:40870595 A>T maps to ENST00000264646 L272L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NH-01A-11D-A37C-09 chr7:148524335 C>A maps to NM_004456.3 R216R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RF-01A-13D-A33E-09 chr1:197026308 G>T maps to NM_001994.2 A335A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr1:197021827 T>C maps to NM_001994.2 P497P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A3-01A-11D-A27G-09 chr11:46751010 G>A maps to NM_000506.3 G518G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4MR-01A-11D-A28B-09 chr11:46749671 G>A maps to NM_000506.3 E419E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88V-01A-11D-A351-09 chr1:95005862 A>T maps to NM_001993.4 I54I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GG-01A-11D-A37C-09 chr23:154227788 A>T did not map to a codon.
Sequencing variant TCGA-IG-A50L-01A-11D-A27G-09 chr23:154158116 T>C did not map to a codon.
Sequencing variant TCGA-JY-A93D-01A-11D-A387-09 chr23:154158655 G>T did not map to a codon.
Sequencing variant TCGA-L5-A4OF-01A-11D-A27G-09 chr23:154158691 C>G did not map to a codon.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr23:154194907 C>T did not map to a codon.
Sequencing variant TCGA-L5-A4OW-01A-11D-A28B-09 chr23:154158671 A>T did not map to a codon.
Sequencing variant TCGA-L5-A4OX-01A-21D-A28B-09 chr23:154158007 C>T did not map to a codon.
Sequencing variant TCGA-LN-A49K-01A-11D-A247-09 chr23:138643809 C>T did not map to a codon.
Sequencing variant TCGA-V5-A7RE-01A-11D-A351-09 chr23:138643756 T>C did not map to a codon.
Sequencing variant TCGA-LN-A8I0-01A-11D-A36J-09 chr16:74752978 G>A maps to NM_024306.4 Y231Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FE-01A-11D-A33E-09 chr23:57458420 C>G did not map to a codon.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr23:57318977 C>T did not map to a codon.
Sequencing variant TCGA-L5-A8NH-01A-11D-A37C-09 chr23:57313371 A>G did not map to a codon.
Sequencing variant TCGA-XP-A8T6-01A-11D-A36J-09 chr2:88427515 G>A maps to NM_001443.1 Y7Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A51D-01A-11D-A27G-09 chr8:82439329 G>T maps to NM_001105281.1 S91S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4MR-01A-11D-A28B-09 chr11:70049639 C>T maps to NM_003824.3 F25F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FQ-01A-31D-A387-09 chr16:1877559 C>T maps to NM_001018104.2 D110D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OG-01A-11D-A27G-09 chr2:96078478 C>T maps to NM_016044.2 V283V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EO-01A-11D-A36J-09 chr3:138329849 C>T maps to NM_001033030.1 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EP-01A-31D-A403-09 chr3:138340278 T>C maps to NM_001033030.1 D37D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A8I1-01A-11D-A36J-09 chr12:50282985 C>G did not map to a codon.
Sequencing variant TCGA-L5-A8NQ-01A-11D-A36J-09 chr9:130710473 G>T maps to NM_001035254.2 I164I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr23:55172585 G>A did not map to a codon.
Sequencing variant TCGA-L5-A8NE-01A-11D-A37C-09 chr23:55172585 G>A did not map to a codon.
Sequencing variant TCGA-2H-A9GJ-01A-11D-A37C-09 chr5:14601227 G>T maps to NM_019018.2 L73L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6XQ-01B-11D-A33E-09 chr5:14607501 G>T maps to NM_019018.2 E188*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49X-01A-31D-A27G-09 chr5:14693027 C>A maps to NM_138348.4 Y310*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A8I0-01A-11D-A36J-09 chr5:14687650 A>T maps to NM_138348.4 K164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A97H-01A-11D-A387-09 chr10:14816270 G>T maps to NM_031453.2 S131*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OJ-01A-11D-A27G-09 chr10:14709634 G>T maps to NM_031453.2 S156*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GN-01A-11D-A37C-09 chr19:1880935 T>C maps to NM_031213.3 T148T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NT-01A-11D-A37C-09 chr8:59059538 C>T maps to NM_147189.2 V250V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NW-01A-11D-A37C-09 chr11:58919795 G>T maps to NM_198847.2 E219*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NW-01A-11D-A37C-09 chr11:58919899 C>T maps to NM_198847.2 T253T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49L-01A-11D-A247-09 chr11:58920608 C>T maps to NM_198847.2 Q490*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A97I-01A-11D-A387-09 chr3:57647251 A>T maps to NM_152678.2 P180P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A8-01A-32D-A27G-09 chr3:57619035 G>A maps to NM_152678.2 R437*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A8O2-01A-11D-A36J-09 chr22:50752257 G>C maps to NM_001001794.3 L396L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NE-01A-11D-A37C-09 chr17:47810055 C>A maps to NM_030802.3 E75*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NI-01A-11D-A37C-09 chr2:208489021 A>G maps to ENST00000272839 F26F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EQ-01A-11D-A36J-09 chr9:96324519 G>T maps to ENST00000333936 V1021V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NV-01A-11D-A37C-09 chr6:170704668 T>C did not map to a codon.
Sequencing variant TCGA-L5-A8NG-01A-11D-A37C-09 chr23:54117832 C>T did not map to a codon.
Sequencing variant TCGA-Q9-A6FU-01A-11D-A31U-09 chr23:54143072 C>T did not map to a codon.
Sequencing variant TCGA-R6-A6L6-01B-11D-A33E-09 chr23:54114226 G>T did not map to a codon.
Sequencing variant TCGA-V5-A7RB-01A-11D-A351-09 chr23:54161519 C>T did not map to a codon.
Sequencing variant TCGA-VR-A8EO-01A-11D-A36J-09 chr23:54186037 G>T did not map to a codon.
Sequencing variant TCGA-L5-A4OJ-01A-11D-A27G-09 chr23:133906175 G>T did not map to a codon.
Sequencing variant TCGA-VR-AA7D-01A-11D-A403-09 chr23:133938242 G>T did not map to a codon.
Sequencing variant TCGA-L5-A8NF-01A-11D-A37C-09 chr23:63410679 G>T did not map to a codon.
Sequencing variant TCGA-R6-A6DQ-01B-11D-A31U-09 chr23:63412560 G>T did not map to a codon.
Sequencing variant TCGA-S8-A6BV-01A-21D-A31U-09 chr23:63410421 G>T did not map to a codon.
Sequencing variant TCGA-VR-A8EW-01A-11D-A36J-09 chr23:63410561 G>T did not map to a codon.
Sequencing variant TCGA-VR-AA7B-01A-31D-A403-09 chr23:63413071 T>C did not map to a codon.
Sequencing variant TCGA-LN-A49W-01A-11D-A27G-09 chr2:131520724 C>T maps to NM_001105195.1 S360S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A939-01A-12D-A37C-09 chr13:51854620 C>A maps to NM_145019.2 G326G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr13:51825748 C>T maps to NM_145019.2 S118S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A7DP-01A-31D-A33E-09 chr2:225266458 G>T maps to NM_001122779.1 A9A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GF-01A-11D-A37C-09 chr9:130287349 G>T maps to NM_022833.2 G136G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RE-01A-11D-A33E-09 chr3:184056193 G>A maps to NM_144635.4 W36*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr3:184062460 G>A maps to NM_144635.4 P268P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr1:16385003 G>A maps to NM_182623.2 T257T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A4P3-01A-11D-A27G-09 chr23:92964879 G>T did not map to a codon.
Sequencing variant TCGA-L5-A893-01A-11D-A36J-09 chr23:92964530 G>A did not map to a codon.
Sequencing variant TCGA-L5-A43I-01A-11D-A247-09 chr8:139149480 G>A maps to NM_015912.3 V1308V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr8:139144925 C>G maps to NM_015912.3 L1377L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr8:139163951 G>T maps to NM_015912.3 G922G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr8:139209857 G>A maps to NM_015912.3 R242*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-A7RC-01B-11D-A403-09 chr8:139180270 C>A maps to NM_015912.3 L375L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA7B-01A-31D-A403-09 chr8:139144976 A>C maps to NM_015912.3 T1360T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA7B-01A-31D-A403-09 chr8:139255188 G>C maps to NM_015912.3 S222*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NG-01A-11D-A37C-09 chr4:89708958 T>A maps to NM_014883.2 R406*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49P-01A-11D-A247-09 chr4:89859292 A>G maps to NM_014883.2 Y235Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASX-01A-11D-A387-09 chr4:89941734 G>T maps to NM_014883.2 P101P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OX-01A-21D-A28B-09 chr8:53477669 G>A maps to NM_207413.3 P49P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EO-01A-11D-A36J-09 chr5:79817925 C>T maps to NM_205548.1 Q214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OX-01A-21D-A28B-09 chr5:177161917 T>G maps to ENST00000425383 V227V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OR-01A-11D-A27G-09 chr5:175528579 C>T maps to NM_001079529.2 A220A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OX-01A-21D-A28B-09 chr5:175530245 A>C maps to NM_001079529.2 V227V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OH-01A-11D-A27G-09 chr9:18928736 G>T maps to NM_153707.2 G246G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EO-01A-11D-A36J-09 chr9:18928886 G>T maps to NM_153707.2 L196L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr23:68725687 A>G did not map to a codon.
Sequencing variant TCGA-IC-A6RE-01A-11D-A33E-09 chr11:6243799 C>A maps to NM_032127.3 E355*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L7-A6VZ-01A-12D-A33E-09 chr10:116615068 G>T maps to NM_020940.3 L639L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A6QS-01A-12D-A33E-09 chr8:21953881 C>A maps to NM_022749.5 P53P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NU-01A-11D-A36J-09 chr8:21959805 C>T maps to NM_022749.5 L658L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4MR-01A-11D-A28B-09 chr3:122121697 A>C maps to NM_014367.3 T42T. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-R6-A6XQ-01B-11D-A33E-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr1:179783146 G>A maps to NM_173509.2 T109T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OJ-01A-11D-A27G-09 chr1:179783227 C>T maps to NM_173509.2 S136S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A3-01A-11D-A27G-09 chr8:79609677 G>T maps to NM_016010.2 G181*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A8I0-01A-11D-A36J-09 chr14:75537780 G>T maps to NM_024643.2 E169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A97H-01A-11D-A387-09 chr11:73130982 G>T maps to ENST00000064778 T80T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASW-01A-11D-A403-09 chr11:73122546 C>T maps to ENST00000064778 P113P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GK-01A-11D-A37C-09 chr5:74135904 G>A maps to NM_015566.1 L76L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OT-01A-11D-A28B-09 chr2:187559025 C>A maps to NM_177454.3 I42I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A5U5-01A-21D-A28B-09 chr2:187559025 C>A maps to NM_177454.3 I42I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q9-A6FW-01A-31D-A31U-09 chr2:187627400 G>T maps to NM_177454.3 E778*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A4QS-01A-11D-A27G-09 chr5:99921887 A>G maps to NM_198507.1 *191*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88W-01A-11D-A351-09 chr10:126523240 G>T maps to NM_032182.3 E317*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88S-01A-11D-A36J-09 chr10:102721631 A>T did not map to a codon.
Sequencing variant TCGA-2H-A9GN-01A-11D-A37C-09 chr2:97595016 G>T maps to ENST00000417561 V521V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OH-01A-11D-A27G-09 chr2:29255901 G>T maps to NM_199280.2 A705A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93C-01A-11D-A387-09 chr14:94394681 G>A maps to NM_138344.3 A79A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OH-01A-11D-A27G-09 chr6:119301427 G>A maps to NM_024581.4 R726*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HX-01A-11D-A33E-09 chr6:119345269 C>A maps to NM_024581.4 E290*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OJ-01A-11D-A27G-09 chr12:49993826 C>A maps to NM_032130.2 R532R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GI-01A-11D-A37C-09 chr19:35719355 G>T maps to NM_152481.1 P76P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GN-01A-11D-A37C-09 chr7:30893032 C>T maps to ENST00000509504 C8C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OG-01A-11D-A27G-09 chr9:72006644 C>T maps to NM_001127608.1 A426A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FP-01A-31D-A387-09 chr16:10864158 G>C maps to NM_001079512.2 G204G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8WG-01A-11D-A37C-09 chr10:86132007 G>A maps to ENST00000372088 S400S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OO-01A-11D-A27G-09 chr4:2674071 T>G maps to ENST00000324666 Y477*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A8JD-01A-11D-A36J-09 chr4:2696768 G>A maps to ENST00000324666 E772E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OU-01A-11D-A28B-09 chr3:150387186 A>C maps to NM_152394.3 G465G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OT-01A-11D-A28B-09 chr10:128974386 G>A maps to NM_001039762.2 P91P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-A7RB-01A-11D-A351-09 chr10:128974404 G>A maps to NM_001039762.2 R85R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A625-01A-11D-A31U-09 chr23:103432908 C>G did not map to a codon.
Sequencing variant TCGA-L5-A8NN-01A-11D-A37C-09 chr23:103420451 A>G did not map to a codon.
Sequencing variant TCGA-R6-A8WC-01A-11D-A37C-09 chr3:68588031 G>T did not map to a codon.
Sequencing variant TCGA-XP-A8T6-01A-11D-A36J-09 chr1:113269298 C>T maps to NM_001004440.1 D169D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A9VB-01A-21D-A37C-09 chr1:179019498 A>C maps to NM_014864.3 R155R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GQ-01A-11D-A37C-09 chr9:97082711 C>T maps to NM_017561.1 A382A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr10:49207769 G>A maps to ENST00000342763 A16A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr6:116836791 G>A maps to NM_153711.2 A190A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EQ-01A-11D-A36J-09 chr6:116833248 C>T maps to NM_153711.2 S130S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr6:116783244 C>T maps to NM_001010919.1 Y51Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GH-01A-11D-A37C-09 chr18:10671604 T>C maps to NM_022068.2 E2726E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr18:10752834 G>T maps to NM_022068.2 L1297L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr18:10759834 G>A maps to NM_022068.2 L1150L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A5-01A-21D-A27G-09 chr18:10681729 G>A maps to NM_022068.2 A2456A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EW-01A-11D-A36J-09 chr18:10760965 T>C maps to NM_022068.2 G1106G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A891-01A-11D-A36J-09 chr3:58639451 G>T maps to NM_138805.2 R24R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA7D-01A-11D-A403-09 chr3:58635040 C>T did not map to a codon.
Sequencing variant TCGA-JY-A6FA-01A-11D-A33E-09 chr1:110589334 C>T maps to NM_033088.2 Q484*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr1:20879657 G>A maps to NM_207334.2 E64E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49M-01A-21D-A27G-09 chr1:27333124 G>A maps to NM_052943.3 S196S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EP-01A-31D-A403-09 chr1:27333124 G>A maps to NM_052943.3 S196S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XP-A8T6-01A-11D-A36J-09 chr1:27332674 C>T maps to NM_052943.3 L346L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A51D-01A-11D-A27G-09 chr23:79698218 G>A did not map to a codon.
Sequencing variant TCGA-L5-A4OX-01A-21D-A28B-09 chr23:79698477 T>G did not map to a codon.
Sequencing variant TCGA-LN-A9FO-01A-11D-A387-09 chr23:79698375 C>A did not map to a codon.
Sequencing variant TCGA-2H-A9GF-01A-11D-A37C-09 chr23:34149724 C>T did not map to a codon.
Sequencing variant TCGA-JY-A938-01A-11D-A37C-09 chr23:34148742 A>G did not map to a codon.
Sequencing variant TCGA-L5-A43E-01A-11D-A247-09 chr23:34148881 C>T did not map to a codon.
Sequencing variant TCGA-L5-A4OW-01A-11D-A28B-09 chr23:34149454 C>T did not map to a codon.
Sequencing variant TCGA-Z6-A9VB-01A-21D-A37C-09 chr23:34149758 G>T did not map to a codon.
Sequencing variant TCGA-ZR-A9CJ-01B-11D-A387-09 chr23:34148794 G>A did not map to a codon.
Sequencing variant TCGA-2H-A9GL-01A-12D-A37C-09 chr23:37029015 C>T did not map to a codon.
Sequencing variant TCGA-IG-A3YA-01A-11D-A247-09 chr23:37027956 G>A did not map to a codon.
Sequencing variant TCGA-JY-A6F8-01A-11D-A33E-09 chr23:37027450 C>A did not map to a codon.
Sequencing variant TCGA-L5-A4OE-01A-11D-A27G-09 chr23:37027001 C>T did not map to a codon.
Sequencing variant TCGA-L5-A4OE-01A-11D-A27G-09 chr23:37028718 C>T did not map to a codon.
Sequencing variant TCGA-L5-A4OJ-01A-11D-A27G-09 chr23:37028365 C>T did not map to a codon.
Sequencing variant TCGA-L5-A8NE-01A-11D-A37C-09 chr23:37026950 G>C did not map to a codon.
Sequencing variant TCGA-2H-A9GM-01A-11D-A37C-09 chr13:37603913 G>T maps to NM_001014286.2 V327V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NK-01A-21D-A37C-09 chr2:16769366 G>C maps to NM_030797.3 V7V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A8I0-01A-11D-A36J-09 chr2:16745362 C>A did not map to a codon.
Sequencing variant TCGA-V5-A7RB-01A-11D-A351-09 chr23:153677072 G>C did not map to a codon.
Sequencing variant TCGA-2H-A9GK-01A-11D-A37C-09 chr5:137680946 C>T maps to NM_001135647.1 S190S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GL-01A-12D-A37C-09 chr11:114577403 T>C maps to NM_182495.5 L478L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4ON-01A-11D-A27G-09 chr11:114550456 T>C maps to NM_182495.5 I35I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA7D-01A-11D-A403-09 chr17:644587 G>T maps to NM_024792.1 T184T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NL-01A-12D-A37C-09 chr1:177250183 C>A maps to NM_021165.2 C624*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NR-01A-11D-A37C-09 chr1:177250516 A>G maps to NM_021165.2 K735K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA7D-01A-11D-A403-09 chr1:177247738 G>T maps to NM_021165.2 R351R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KH-A6WC-01A-11D-A33E-09 chr1:190067407 G>T maps to NM_199051.1 R681R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6KZ-01A-11D-A31U-09 chr1:190068038 G>A maps to NM_199051.1 S470S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA4D-01A-11D-A37C-09 chr1:190067355 G>T maps to NM_199051.1 S698*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A5U5-01A-21D-A28B-09 chr1:150978595 C>T maps to NM_001163258.1 T12T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6L6-01B-11D-A33E-09 chr15:59064347 G>T maps to NM_001040450.1 E252*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GG-01A-11D-A37C-09 chr16:67574523 C>T maps to NM_001193523.1 R260*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FG-01A-11D-A33E-09 chr6:24809942 A>T did not map to a codon.
Sequencing variant TCGA-L5-A8NH-01A-11D-A37C-09 chr6:24843686 G>T maps to NM_014722.2 C441*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GJ-01A-11D-A37C-09 chr20:49232600 G>A maps to NM_080829.2 Q92*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RF-01A-13D-A33E-09 chr20:49218950 G>A maps to NM_080829.2 H435H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FH-01A-11D-A33E-09 chr20:49208888 G>T maps to NM_080829.2 R853R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43E-01A-11D-A247-09 chr20:49225463 G>A maps to NM_080829.2 P219P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4ON-01A-11D-A27G-09 chr20:49226214 G>A maps to NM_080829.2 R153R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GQ-01A-11D-A37C-09 chr23:119402111 G>T did not map to a codon.
Sequencing variant TCGA-L5-A8NJ-01A-11D-A36J-09 chr23:119438338 G>T did not map to a codon.
Sequencing variant TCGA-Q9-A6FU-01A-11D-A31U-09 chr13:114498173 C>T maps to NM_182614.2 C102C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr1:212799736 C>T maps to NM_153606.3 H506H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OE-01A-11D-A27G-09 chr5:156590081 G>T maps to NM_130899.2 L398L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3Y9-01A-12D-A247-09 chr12:100043169 G>A maps to NM_153364.2 E240E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3QL-01A-11D-A247-09 chr7:128370052 C>T maps to NM_032599.2 S317S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FE-01A-11D-A33E-09 chr1:120839838 T>C maps to NM_001100910.1 S2S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A51D-01A-11D-A27G-09 chr9:131823530 G>T maps to NM_032809.2 G306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GM-01A-11D-A37C-09 chr9:40702723 C>T maps to NM_001083124.1 G127G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RE-01A-11D-A33E-09 chr9:40702807 G>A maps to NM_001083124.1 P155P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OO-01A-11D-A27G-09 chr9:43627999 C>A maps to NM_001145196.1 L229L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A5U7-01A-11D-A31U-09 chr9:43628645 G>T maps to NM_001145196.1 S99*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A1-01A-21D-A27G-09 chr1:28087090 G>T maps to NM_001143912.1 *342L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OH-01A-11D-A27G-09 chr9:134136472 G>T maps to NM_033387.3 T196T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49Y-01A-11D-A27G-09 chr15:59808890 C>A maps to NM_152450.2 A278A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASW-01A-11D-A403-09 chr2:38201272 C>T maps to NM_144713.3 V359V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88V-01A-11D-A351-09 chr6:54806541 C>T maps to NM_001010872.1 R925*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A1-01A-21D-A27G-09 chr6:54735247 C>G maps to NM_001010872.1 V68V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASW-01A-11D-A403-09 chr20:33875492 G>A maps to NM_178468.4 L363L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FG-01A-11D-A33E-09 chr22:40391300 C>A maps to NM_138435.2 G85G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A5B8-01A-11D-A28B-09 chr17:18907092 G>A maps to NM_001039999.2 Q88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NK-01A-21D-A37C-09 chr17:18907092 G>A maps to NM_001039999.2 Q88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HY-01A-12D-A351-09 chr17:18874830 G>A maps to NM_001039999.2 T771T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XP-A8T6-01A-11D-A36J-09 chr16:5147683 G>A maps to NM_201400.2 R19R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NQ-01A-11D-A36J-09 chr8:12283439 A>G maps to NM_001137610.1 Y317Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OU-01A-11D-A28B-09 chr11:71498635 C>T maps to NM_018172.2 R18R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EQ-01A-11D-A36J-09 chr12:8376110 G>A maps to NM_018088.3 S122S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A9VB-01A-21D-A37C-09 chr12:8376137 C>T maps to NM_018088.3 Q113Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A4P3-01A-11D-A27G-09 chr8:94738685 C>G maps to ENST00000452913 S241*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-AAPN-01A-11D-A403-09 chr16:85141484 C>G maps to ENST00000393246 L131L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93E-01A-11D-A37C-09 chr19:38895989 G>T maps to NM_174905.3 E188*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FR-01A-11D-A387-09 chr23:8761713 A>C did not map to a codon.
Sequencing variant TCGA-RE-A7BO-01A-11D-A33E-09 chr23:8761751 C>A did not map to a codon.
Sequencing variant TCGA-IG-A3Y9-01A-12D-A247-09 chr23:8997385 C>G did not map to a codon.
Sequencing variant TCGA-2H-A9GL-01A-12D-A37C-09 chr23:13058885 T>C did not map to a codon.
Sequencing variant TCGA-Q9-A6FU-01A-11D-A31U-09 chr23:14883003 G>T did not map to a codon.
Sequencing variant TCGA-R6-A6DQ-01B-11D-A31U-09 chr23:14862006 G>C did not map to a codon.
Sequencing variant TCGA-R6-A8WC-01A-11D-A37C-09 chr23:14882979 T>C did not map to a codon.
Sequencing variant TCGA-VR-AA7B-01A-31D-A403-09 chr23:14863280 G>C did not map to a codon.
Sequencing variant TCGA-Z6-A8JD-01A-11D-A36J-09 chr23:14863401 C>G did not map to a codon.
Sequencing variant TCGA-L5-A8NJ-01A-11D-A36J-09 chr9:97869548 G>T maps to NM_000136.2 V444V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A9-01A-11D-A28B-09 chr9:97869386 A>T maps to NM_000136.2 A498A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q9-A6FW-01A-31D-A31U-09 chr3:10107132 G>T maps to NM_033084.3 E742*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-AAPN-01A-11D-A403-09 chr3:10131996 C>T maps to NM_033084.3 F1235F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr11:22646527 G>A maps to NM_022725.3 L277L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EX-01A-11D-A36J-09 chr15:89859687 T>C maps to NM_001113378.1 *1329Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RE-01A-11D-A33E-09 chr14:45628399 C>T maps to NM_020937.2 Q500*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A939-01A-12D-A37C-09 chr14:45658088 G>T maps to NM_020937.2 E1622*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43E-01A-11D-A247-09 chr14:45645572 C>T maps to NM_020937.2 Q1206*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OQ-01A-11D-A27G-09 chr14:45623961 C>T maps to NM_020937.2 L416L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr14:45644287 T>C maps to NM_020937.2 Y777Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-A7RC-01B-11D-A403-09 chr14:45606437 T>C maps to NM_020937.2 Y225Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8WG-01A-11D-A37C-09 chr12:29464814 G>A did not map to a codon.
Sequencing variant TCGA-VR-A8EU-01A-11D-A36J-09 chr12:29423408 C>G maps to NM_018099.3 G9G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HX-01A-11D-A33E-09 chr13:99063028 G>T maps to NM_005766.2 V548V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GM-01A-11D-A37C-09 chr2:242312705 G>T did not map to a codon.
Sequencing variant TCGA-IC-A6RE-01A-11D-A33E-09 chr2:242343250 C>T maps to NM_014808.2 C64C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NL-01A-12D-A37C-09 chr19:13041424 C>T did not map to a codon.
Sequencing variant TCGA-L5-A4OR-01A-11D-A27G-09 chr2:223507594 G>T maps to NM_005687.3 R82R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr2:223507640 G>A maps to NM_005687.3 D66D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6L4-01A-11D-A31U-09 chr1:172634915 C>T maps to NM_000639.1 C202C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EX-01A-11D-A36J-09 chr1:172634773 C>G maps to NM_000639.1 S155*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KH-A6WC-01A-11D-A33E-09 chr17:80039883 C>G did not map to a codon.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr17:80046082 C>T maps to NM_004104.4 T898T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OG-01A-11D-A27G-09 chr17:80046281 G>A maps to NM_004104.4 A859A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr17:80041179 C>A maps to NM_004104.4 G1821G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A893-01A-11D-A36J-09 chr17:80041188 G>T maps to NM_004104.4 I1818I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NW-01A-11D-A37C-09 chr17:80048946 T>C did not map to a codon.
Sequencing variant TCGA-LN-A9FP-01A-31D-A387-09 chr17:80043513 G>A maps to NM_004104.4 L1322L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A9VB-01A-21D-A37C-09 chr17:80038422 G>A maps to NM_004104.4 I2290I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EQ-01A-11D-A36J-09 chr2:170402727 C>T maps to NM_024622.3 K567K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8W8-01B-11D-A37C-09 chr5:7867767 C>T maps to NM_024091.3 K143K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GR-01A-12D-A37C-09 chr20:3128912 A>T maps to NM_021826.4 Y268*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FH-01A-11D-A33E-09 chr4:187540344 C>A maps to ENST00000260147 L2468L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OF-01A-11D-A27G-09 chr4:187628344 G>A maps to ENST00000260147 I879I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OJ-01A-11D-A27G-09 chr4:187629118 C>T maps to ENST00000260147 S621S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88T-01A-11D-A351-09 chr4:187538271 T>A maps to ENST00000260147 K2991*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88Z-01A-11D-A36J-09 chr4:187554966 G>A maps to ENST00000260147 Y1398Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A9-01A-11D-A28B-09 chr4:187524843 G>C maps to ENST00000260147 L3615L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FB-01A-11D-A33E-09 chr5:150946026 G>T maps to NM_001447.2 P822P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr5:150923670 A>G maps to NM_001447.2 Y2339Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-A7RC-01B-11D-A403-09 chr5:150946898 G>T maps to NM_001447.2 R532R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA7B-01A-31D-A403-09 chr5:150948296 G>A maps to NM_001447.2 Q66*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GR-01A-12D-A37C-09 chr11:92534683 A>G maps to ENST00000298047 Q2835Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A5B8-01A-11D-A28B-09 chr11:92538329 C>T maps to ENST00000298047 R2970*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A97I-01A-11D-A387-09 chr11:92085865 C>A maps to ENST00000298047 Y196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr11:92577335 C>T maps to ENST00000298047 H3601H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88W-01A-11D-A351-09 chr11:92532139 T>C maps to ENST00000298047 Y1987Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NJ-01A-11D-A36J-09 chr11:92577767 G>C maps to ENST00000298047 G3745G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RE-A7BO-01A-11D-A33E-09 chr11:92534122 C>T maps to ENST00000298047 A2648A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA4D-01A-11D-A37C-09 chr11:92568180 C>A maps to ENST00000298047 P3339P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3YA-01A-11D-A247-09 chr4:126371927 C>T maps to NM_024582.4 Q3253*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A4QS-01A-11D-A27G-09 chr4:126336174 A>G maps to NM_024582.4 Q2019Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr4:126408619 G>T maps to NM_024582.4 G4313*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OW-01A-11D-A28B-09 chr4:126373294 A>C maps to NM_024582.4 T3708T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NK-01A-21D-A37C-09 chr4:126242131 C>A maps to NM_024582.4 L1522L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NN-01A-11D-A37C-09 chr4:126238184 G>T maps to NM_024582.4 G207*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NR-01A-11D-A37C-09 chr4:126238057 C>T maps to NM_024582.4 I164I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HX-01A-11D-A33E-09 chr4:126336312 T>C maps to NM_024582.4 I2065I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6XG-01B-11D-A33E-09 chr4:126402847 C>T maps to NM_024582.4 G4257G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZR-A9CJ-01B-11D-A387-09 chr4:126336052 T>C maps to NM_024582.4 L1979L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GO-01A-11D-A37C-09 chr23:150885854 C>A did not map to a codon.
Sequencing variant TCGA-L5-A4OJ-01A-11D-A27G-09 chr23:150884595 C>A did not map to a codon.
Sequencing variant TCGA-Z6-AAPN-01A-11D-A403-09 chr23:150884667 G>C did not map to a codon.
Sequencing variant TCGA-X8-AAAR-01A-11D-A403-09 chr19:40328461 C>A maps to NM_001436.3 E191*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GO-01A-11D-A37C-09 chr1:16101327 G>A maps to NM_001024215.1 G309G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OG-01A-11D-A27G-09 chr1:16101255 C>T maps to NM_017556.2 S285S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NT-01A-11D-A37C-09 chr3:13671356 C>T maps to NM_001165035.1 C960C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HY-01A-12D-A351-09 chr3:13670420 G>A maps to NM_001165035.1 T862T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8W8-01B-11D-A37C-09 chr3:13670519 C>T maps to NM_001165035.1 H895H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GF-01A-11D-A37C-09 chr15:48779551 G>A maps to NM_000138.4 C1140C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GR-01A-12D-A37C-09 chr15:48784700 A>T maps to NM_000138.4 C937*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4MR-01A-11D-A28B-09 chr15:48936864 C>T maps to NM_000138.4 V34V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S8-A6BV-01A-21D-A31U-09 chr15:48773942 G>A maps to NM_000138.4 C1291C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GF-01A-11D-A37C-09 chr5:127654613 G>A maps to NM_001999.3 C1517C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr5:127638704 G>A maps to NM_001999.3 C1959C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NE-01A-11D-A37C-09 chr5:127642854 G>T maps to NM_001999.3 T1798T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NF-01A-11D-A37C-09 chr5:127674676 G>A maps to NM_001999.3 C1140C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NW-01A-11D-A37C-09 chr5:127595296 G>C maps to NM_001999.3 L2863L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-A7RB-01A-11D-A351-09 chr5:127647075 C>A maps to NM_001999.3 G1664*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XP-A8T6-01A-11D-A36J-09 chr5:127728954 G>T maps to NM_001999.3 G446G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FH-01A-11D-A33E-09 chr19:8210811 G>A maps to NM_032447.3 C120C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr19:8145953 G>A maps to NM_032447.3 V2462V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49Y-01A-11D-A27G-09 chr19:8161810 G>T maps to NM_032447.3 C1789*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OJ-01A-11D-A27G-09 chr9:97355868 G>T maps to NM_003837.2 S47*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OX-01A-21D-A28B-09 chr9:97329653 G>C maps to NM_003837.2 V201V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-AAPN-01A-11D-A403-09 chr9:97346897 G>A maps to NM_003837.2 C129C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr16:30680548 C>T maps to ENST00000356166 A842A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GR-01A-12D-A37C-09 chr7:102604100 G>T maps to NM_145032.3 S201S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88V-01A-11D-A351-09 chr3:33406163 G>A maps to NM_012157.3 R81R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43H-01A-11D-A247-09 chr17:37437665 C>T maps to NM_032875.2 V224V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASX-01A-11D-A387-09 chr17:37441732 C>T maps to NM_032875.2 L164L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HZ-01A-31D-A351-09 chr6:99322297 C>G maps to NM_012160.3 P574P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NK-01A-21D-A37C-09 chr5:15937133 G>T maps to NM_012304.3 E439*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FA-01A-11D-A33E-09 chr2:48035282 C>A maps to NM_001190274.1 E920*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8ET-01A-11D-A403-09 chr8:28309932 C>A maps to NM_172366.2 E190*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr10:5957463 G>T maps to NM_032807.3 E550*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NR-01A-11D-A37C-09 chr11:33792356 T>A maps to NM_012175.3 R42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93C-01A-11D-A387-09 chr16:87380785 G>A maps to NM_024735.3 N161N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A893-01A-11D-A36J-09 chr16:87367613 G>A maps to NM_024735.3 G425G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr16:87364977 G>T maps to NM_024735.3 V512V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A50L-01A-11D-A27G-09 chr17:6684107 G>T maps to NM_153230.2 P307P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NQ-01A-11D-A36J-09 chr17:6683202 G>T maps to NM_153230.2 E6*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6F8-01A-11D-A33E-09 chr2:73495954 G>A maps to ENST00000295133 R329R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GK-01A-11D-A37C-09 chr8:101146146 T>C maps to NM_001029860.3 L670L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr8:101153206 A>G maps to NM_001029860.3 D425D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NR-01A-11D-A37C-09 chr8:101154373 C>T maps to NM_001029860.3 S36S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr19:46215925 G>A maps to NM_001080469.1 S276S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NW-01A-11D-A37C-09 chr17:37107881 G>A maps to NM_001008777.2 L190L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr22:32881116 G>A maps to NM_012179.3 L236L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr17:18647919 C>T maps to ENST00000395665 I121I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FQ-01A-31D-A387-09 chr5:171305016 C>A maps to NM_012300.2 V302V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr9:123550233 T>C maps to NM_012164.3 A101A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EZ-01A-11D-A36J-09 chr9:139837094 G>T maps to NM_018998.2 G193G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GN-01A-11D-A37C-09 chr4:153332738 G>A maps to NM_033632.2 Q73*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XP-A8T7-01A-11D-A36J-09 chr4:153250882 G>A maps to NM_033632.2 R393*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NG-01A-11D-A37C-09 chr19:12800369 A>G maps to ENST00000380339 T437T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88T-01A-11D-A351-09 chr1:207133113 G>T maps to NM_001170631.1 R495R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EQ-01A-11D-A36J-09 chr14:75182771 C>T maps to NM_015962.4 Q88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93E-01A-11D-A37C-09 chr19:40433434 G>T maps to NM_003890.2 Y278*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr19:40392610 C>T maps to NM_003890.2 P2631P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OE-01A-11D-A27G-09 chr19:40398360 C>T maps to NM_003890.2 A2202A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OJ-01A-11D-A27G-09 chr19:40364340 C>T maps to NM_003890.2 S4767S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A891-01A-11D-A36J-09 chr19:40398135 C>T maps to NM_003890.2 A2277A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NR-01A-11D-A37C-09 chr19:40408701 G>A maps to NM_003890.2 P1379P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6L4-01A-11D-A31U-09 chr19:40421094 C>T maps to NM_003890.2 V942V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASX-01A-11D-A387-09 chr19:40408617 T>C maps to NM_003890.2 S1407S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43H-01A-11D-A247-09 chr1:161641284 C>T maps to NM_004001.4 S79S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6DN-01B-11D-A31U-09 chr1:161641440 T>C did not map to a codon.
Sequencing variant TCGA-VR-A8EX-01A-11D-A36J-09 chr1:161642864 A>G maps to NM_004001.4 T164T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6F8-01A-11D-A33E-09 chr19:50028825 G>A maps to NM_004107.4 L328L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GQ-01A-11D-A37C-09 chr19:17898536 C>T maps to NM_015122.2 S843S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A6QS-01A-12D-A33E-09 chr19:17893855 C>A maps to NM_015122.2 T656T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6Y2-01B-11D-A33E-09 chr19:17883315 G>T maps to NM_015122.2 L215L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GM-01A-11D-A37C-09 chr5:72377779 G>A maps to NM_138782.2 T717T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr5:141028580 G>A maps to ENST00000354789 N174N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6L4-01A-11D-A31U-09 chr1:157771259 T>G maps to NM_052938.4 R332R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4ON-01A-11D-A27G-09 chr1:157737294 T>C maps to NM_030764.3 P296P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA7I-01A-11D-A403-09 chr1:157740415 T>C maps to NM_030764.3 G31G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GR-01A-12D-A37C-09 chr1:157667002 A>G maps to NM_052939.3 S257S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A939-01A-12D-A37C-09 chr1:157665149 C>T maps to NM_052939.3 Q460Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr1:157660324 T>C did not map to a codon.
Sequencing variant TCGA-IG-A3I8-01A-11D-A247-09 chr1:157551429 G>A maps to NM_031282.2 T380T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A891-01A-11D-A36J-09 chr1:157490828 C>T maps to NM_031281.2 E831E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA7B-01A-31D-A403-09 chr1:157512736 C>T maps to NM_031281.2 L345L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FE-01A-11D-A33E-09 chr1:161695654 G>T maps to NM_001002901.2 E118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NK-01A-21D-A37C-09 chr1:161693353 C>T maps to NM_001002901.2 R84*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASX-01A-11D-A387-09 chr1:155288466 G>A maps to NM_001135821.1 Q232Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NT-01A-11D-A37C-09 chr19:10421304 G>A maps to NM_001031734.2 L137L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93D-01A-11D-A387-09 chr11:111749780 G>A maps to ENST00000428306 Q26*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OH-01A-11D-A27G-09 chr11:111746107 G>T maps to NM_138378.1 I471I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XP-A8T6-01A-11D-A36J-09 chr5:114879142 G>A maps to NM_020177.2 L16L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GQ-01A-11D-A37C-09 chr11:61563117 C>T maps to NM_004111.4 G95G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A8I0-01A-11D-A36J-09 chr11:61562991 G>A maps to NM_004111.4 L53L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6KZ-01A-11D-A31U-09 chr11:61563400 C>T maps to NM_004111.4 L190L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GR-01A-12D-A37C-09 chr7:19184961 G>A maps to NM_152898.2 C8C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L7-A6VZ-01A-12D-A33E-09 chr7:19184739 G>A maps to NM_152898.2 R82R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XP-A8T6-01A-11D-A36J-09 chr20:6091159 T>A did not map to a codon.
Sequencing variant TCGA-LN-A7HW-01A-22D-A351-09 chr11:63978611 C>G maps to NM_178443.2 L161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49Y-01A-11D-A27G-09 chr15:91434331 C>T maps to NM_002005.3 L481L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NW-01A-11D-A37C-09 chr7:121942248 G>T maps to NM_001024613.2 C410*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr3:62358147 G>A maps to NM_018008.3 G132G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FH-01A-11D-A33E-09 chr19:35941155 G>A maps to NM_005306.2 R180R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6F8-01A-11D-A33E-09 chr19:35850415 G>T maps to NM_005304.3 V208V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93D-01A-11D-A387-09 chr4:155507461 C>T maps to NM_000508.3 W373*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GR-01A-12D-A37C-09 chr4:155487150 G>A maps to NM_005141.4 L102L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A891-01A-11D-A36J-09 chr23:54482154 C>T did not map to a codon.
Sequencing variant TCGA-L5-A4OT-01A-11D-A28B-09 chr12:32729380 C>T maps to NM_139241.2 G30G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA7B-01A-31D-A403-09 chr12:32772732 G>A maps to NM_139241.2 E480E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A6QS-01A-12D-A33E-09 chr3:14974653 G>T maps to NM_152536.3 E1457*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6L6-01B-11D-A33E-09 chr3:14860754 G>A maps to NM_152536.3 S59S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr12:95501370 G>T maps to NM_018351.3 R1101R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HV-01A-21D-A351-09 chr12:95604834 G>T maps to NM_018351.3 I75I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EY-01A-11D-A36J-09 chr12:95546718 G>T maps to NM_018351.3 I879I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr5:44310591 G>A maps to NM_004465.1 A122A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RF-01A-13D-A33E-09 chr3:192125874 G>A maps to NM_021032.4 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OJ-01A-11D-A27G-09 chr23:137715090 T>G did not map to a codon.
Sequencing variant TCGA-L5-A4OT-01A-11D-A28B-09 chr23:137785180 A>C did not map to a codon.
Sequencing variant TCGA-L5-A8NG-01A-11D-A37C-09 chr23:137939762 T>G did not map to a codon.
Sequencing variant TCGA-Q9-A6FU-01A-11D-A31U-09 chr23:137717718 C>T did not map to a codon.
Sequencing variant TCGA-L5-A8NQ-01A-11D-A36J-09 chr8:21905657 G>T maps to NM_003867.2 L183L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASX-01A-11D-A387-09 chr5:170883661 G>A maps to NM_003862.2 P159P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GR-01A-12D-A37C-09 chr12:4479907 C>T maps to NM_020638.2 T119T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88V-01A-11D-A351-09 chr12:4479523 G>A maps to NM_020638.2 F247F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93C-01A-11D-A387-09 chr4:81196109 G>T maps to NM_004464.3 G135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA7D-01A-11D-A403-09 chr4:81188196 C>T maps to NM_004464.3 G73G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88V-01A-11D-A351-09 chr15:49776662 C>T maps to NM_002009.3 Q183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NV-01A-11D-A37C-09 chr8:38285888 T>A maps to NM_001174067.1 T174T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93E-01A-11D-A37C-09 chr10:123245030 C>T maps to ENST00000351936 V711V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr10:123279621 G>A maps to ENST00000351936 V289V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A50L-01A-11D-A27G-09 chr5:176519412 G>T maps to NM_213647.1 V273V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A625-01A-11D-A31U-09 chr4:155528019 G>A maps to ENST00000407946 G330G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q9-A6FW-01A-31D-A31U-09 chr1:60139733 G>T maps to NM_001113411.1 E505*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OE-01A-11D-A27G-09 chr7:76826237 G>T maps to NM_006682.2 T226T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XP-A8T6-01A-11D-A36J-09 chr3:59997127 T>C did not map to a codon.
Sequencing variant TCGA-IG-A4P3-01A-11D-A27G-09 chr23:135291419 G>A did not map to a codon.
Sequencing variant TCGA-JY-A6F8-01A-11D-A33E-09 chr23:135288565 G>C did not map to a codon.
Sequencing variant TCGA-IG-A6QS-01A-12D-A33E-09 chr1:38464973 G>T maps to NM_004468.3 A37A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RE-01A-11D-A33E-09 chr6:97058455 T>C maps to NM_020482.4 T171T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A8O2-01A-11D-A36J-09 chr16:67268057 C>T maps to NM_013241.2 K516K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6F8-01A-11D-A33E-09 chr16:67263791 C>A maps to NM_013241.2 E1106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49S-01A-11D-A247-09 chr16:67265980 G>C maps to NM_013241.2 L721L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X8-AAAR-01A-11D-A403-09 chr18:34310635 G>T maps to NM_025135.2 E974*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X8-AAAR-01A-11D-A403-09 chr9:133779537 G>A maps to NM_001145106.1 D433D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A4P3-01A-11D-A27G-09 chr6:110112717 C>T maps to NM_014845.5 Q774*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EZ-01A-11D-A36J-09 chr6:110083317 A>C maps to NM_014845.5 R432R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OS-01A-11D-A28B-09 chr2:71014834 C>T maps to NM_001004311.3 A110A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NF-01A-11D-A37C-09 chr2:164467537 C>T maps to NM_018086.2 P268P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr7:50513031 G>A maps to NM_022116.3 R652*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NW-01A-11D-A37C-09 chr6:76018614 T>A did not map to a codon.
Sequencing variant TCGA-L5-A4OE-01A-11D-A27G-09 chr3:99568550 C>A maps to NM_001042459.1 E657*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43C-01A-11D-A247-09 chr19:56104859 C>T maps to NM_032836.2 A149A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-A7RE-01A-11D-A351-09 chr17:39969527 C>A maps to NM_021939.3 S81*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93E-01A-11D-A37C-09 chr9:115940967 G>A maps to ENST00000446284 S701S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A939-01A-12D-A37C-09 chr7:72742618 G>A maps to NM_003602.3 S33S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A97I-01A-11D-A387-09 chr2:179330498 A>G maps to ENST00000350591 *258Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q9-A6FU-01A-11D-A31U-09 chr7:33014252 T>C maps to NM_007270.3 N82N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6Y0-01B-11D-A33E-09 chr1:154960624 G>T maps to NM_025207.4 L139L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GR-01A-12D-A37C-09 chr1:152280794 T>G maps to NM_002016.1 A2189A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3QL-01A-11D-A247-09 chr1:152283350 G>T maps to NM_002016.1 S1337S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A51D-01A-11D-A27G-09 chr1:152278185 G>T maps to NM_002016.1 S3059*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43I-01A-11D-A247-09 chr1:152277404 C>T maps to NM_002016.1 P3319P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A5U7-01A-11D-A31U-09 chr1:152284592 A>G maps to NM_002016.1 S923S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EU-01A-11D-A36J-09 chr1:152284118 T>C maps to NM_002016.1 S1081S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XP-A8T8-01A-11D-A36J-09 chr1:152277312 G>C maps to NM_002016.1 S3350*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NT-01A-11D-A37C-09 chr1:152327618 G>A maps to NM_001014342.2 Y881Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr17:18150066 G>A maps to NM_002018.2 G964G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EO-01A-11D-A36J-09 chr17:78397413 C>T maps to NM_173627.3 N166N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EQ-01A-11D-A36J-09 chr17:78399374 G>A maps to NM_173627.3 L223L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NG-01A-11D-A37C-09 chr9:84609275 G>C maps to NM_001001670.2 V1297V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NR-01A-11D-A37C-09 chr9:84607805 T>C maps to NM_001001670.2 T807T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8ER-01A-11D-A36J-09 chr9:84606905 C>T maps to NM_001001670.2 L507L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EW-01A-11D-A36J-09 chr9:84607397 C>A maps to NM_001001670.2 S671S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3QL-01A-11D-A247-09 chr23:153590884 G>T did not map to a codon.
Sequencing variant TCGA-LN-A49M-01A-21D-A27G-09 chr23:153589758 C>A did not map to a codon.
Sequencing variant TCGA-Q9-A6FU-01A-11D-A31U-09 chr23:153581173 G>A did not map to a codon.
Sequencing variant TCGA-Q9-A6FW-01A-31D-A31U-09 chr23:153588525 C>T did not map to a codon.
Sequencing variant TCGA-JY-A6FD-01A-11D-A33E-09 chr3:58145285 G>T maps to NM_001164317.1 S2329S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88W-01A-11D-A351-09 chr7:128486430 C>T maps to NM_001458.4 G1347G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NS-01A-12D-A37C-09 chr7:128470942 C>T maps to NM_001458.4 R84R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NS-01A-12D-A37C-09 chr7:128498573 T>C maps to NM_001458.4 P2725P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NV-01A-11D-A37C-09 chr7:128488920 G>A maps to NM_001458.4 P1604P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr6:30697903 G>A maps to NM_005803.2 S383S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KH-A6WC-01A-11D-A33E-09 chr17:27208317 G>T maps to ENST00000394906 I385I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr17:27211322 C>A maps to ENST00000394906 E103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8W8-01B-11D-A37C-09 chr17:27207850 G>T maps to ENST00000394906 T431T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GI-01A-11D-A37C-09 chr11:63885043 C>T maps to NM_013280.4 G435G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr14:86089810 C>T maps to NM_013231.4 S651S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L7-A6VZ-01A-12D-A33E-09 chr14:86088428 C>A maps to NM_013231.4 R191R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr13:28893667 G>A maps to NM_002019.4 R1060*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49U-01A-31D-A27G-09 chr13:28908258 T>G maps to NM_002019.4 S832S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8WC-01A-11D-A37C-09 chr13:29012408 G>A maps to NM_002019.4 L154L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EX-01A-11D-A36J-09 chr13:28964124 G>T maps to NM_002019.4 R593R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A97H-01A-11D-A387-09 chr13:28623674 C>T did not map to a codon.
Sequencing variant TCGA-L5-A8NK-01A-21D-A37C-09 chr13:28626731 G>A maps to NM_004119.2 S188S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6L6-01B-11D-A33E-09 chr13:28623600 G>T maps to NM_004119.2 S319*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EX-01A-11D-A36J-09 chr13:28602426 T>A did not map to a codon.
Sequencing variant TCGA-VR-AA7I-01A-11D-A403-09 chr19:49979701 G>A maps to NM_001459.2 W74*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GO-01A-11D-A37C-09 chr5:180058728 C>T maps to NM_182925.4 E36E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GR-01A-12D-A37C-09 chr5:180048196 G>A maps to NM_182925.4 S692S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-A7RE-01A-11D-A351-09 chr1:213032240 G>A maps to NM_014053.2 L149L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr14:76045398 G>A maps to NM_017791.2 S28S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA4G-01A-11D-A37C-09 chr15:33261258 G>A maps to NM_001103184.2 L658L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GJ-01A-11D-A37C-09 chr1:240519209 T>C maps to ENST00000330178 G96G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GK-01A-11D-A37C-09 chr1:240371276 T>G maps to ENST00000406993 P1198P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr1:240256443 G>A maps to ENST00000406993 T488T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NW-01A-11D-A37C-09 chr1:240371435 T>C maps to ENST00000406993 P1251P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A2-01A-31D-A27G-09 chr1:240370835 G>T maps to ENST00000406993 L1051L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A5U6-01A-11D-A28B-09 chr1:240370784 G>T maps to ENST00000406993 L1034L. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-R6-A6L6-01B-11D-A33E-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-VR-A8EQ-01A-11D-A36J-09 chr1:240255870 C>T maps to ENST00000406993 V297V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X8-AAAR-01A-11D-A403-09 chr1:240256707 G>A maps to ENST00000406993 P576P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A8JD-01A-11D-A36J-09 chr1:240371345 C>A maps to ENST00000406993 P1221P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr17:43319735 T>C maps to NM_005892.3 T638T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NI-01A-11D-A37C-09 chr17:43319298 C>G maps to NM_005892.3 A557A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RF-01A-13D-A33E-09 chr12:50044559 G>T maps to NM_175736.4 A633A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FD-01A-11D-A33E-09 chr12:50044989 G>T maps to NM_175736.4 G586G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OO-01A-11D-A27G-09 chr12:50050233 G>T maps to NM_175736.4 R280R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43H-01A-11D-A247-09 chr1:171252320 G>T maps to NM_002021.1 E408*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A5B8-01A-11D-A28B-09 chr1:171165873 G>A maps to NM_001460.2 Q136Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XP-A8T8-01A-11D-A36J-09 chr1:171154890 T>C maps to NM_001460.2 S13S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A7DP-01A-31D-A33E-09 chr23:147010264 C>A did not map to a codon.
Sequencing variant TCGA-L5-A8NH-01A-11D-A37C-09 chr23:147011713 C>G did not map to a codon.
Sequencing variant TCGA-2H-A9GF-01A-11D-A37C-09 chr23:147084797 G>A did not map to a codon.
Sequencing variant TCGA-L5-A4OW-01A-11D-A28B-09 chr23:147088343 T>C did not map to a codon.
Sequencing variant TCGA-2H-A9GG-01A-11D-A37C-09 chr2:216284106 G>A maps to NM_212482.1 D559D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6F8-01A-11D-A33E-09 chr2:216237006 G>A maps to NM_212482.1 F2113F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FH-01A-11D-A33E-09 chr2:216279652 G>T maps to NM_212482.1 I616I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NH-01A-11D-A37C-09 chr2:216264039 G>A maps to NM_212482.1 T1096T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L7-A6VZ-01A-12D-A33E-09 chr2:216248102 G>T maps to NM_212482.1 T1666T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HY-01A-12D-A351-09 chr2:216269250 C>T maps to NM_212482.1 Q1038Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FP-01A-31D-A387-09 chr2:216249640 G>A maps to NM_212482.1 I1557I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASX-01A-11D-A387-09 chr11:47744590 A>T maps to NM_015308.2 P914P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GF-01A-11D-A37C-09 chr6:159659684 C>T maps to NM_032532.2 R1390*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6DQ-01B-11D-A31U-09 chr6:159660604 C>T maps to NM_032532.2 R1413*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A4QS-01A-11D-A27G-09 chr3:172050928 G>T maps to NM_022763.3 V535V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6XQ-01B-11D-A33E-09 chr5:131008398 C>A maps to NM_133372.2 E580*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A51D-01A-11D-A27G-09 chr4:159789785 C>A maps to ENST00000379346 P689P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RE-01A-11D-A33E-09 chr11:49227683 A>G maps to NM_004476.1 T53T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RF-01A-13D-A33E-09 chr11:49204789 A>G maps to NM_004476.1 Y277Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43I-01A-11D-A247-09 chr11:49204789 A>G maps to NM_004476.1 Y277Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OW-01A-11D-A28B-09 chr11:49208203 C>A maps to NM_004476.1 G211*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NQ-01A-11D-A36J-09 chr11:49204789 A>G maps to NM_004476.1 Y277Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NW-01A-11D-A37C-09 chr11:49175864 A>T maps to NM_004476.1 A601A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49M-01A-21D-A27G-09 chr11:49204789 A>G maps to NM_004476.1 Y277Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49U-01A-31D-A27G-09 chr11:49204789 A>G maps to NM_004476.1 Y277Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EY-01A-11D-A36J-09 chr11:49204789 A>G maps to NM_004476.1 Y277Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZR-A9CJ-01B-11D-A387-09 chr11:49204789 A>G maps to NM_004476.1 Y277Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4ON-01A-11D-A27G-09 chr11:89421811 T>G maps to NM_153696.2 A223A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NJ-01A-11D-A36J-09 chr11:71907013 C>T maps to NM_016729.2 C189C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6XG-01B-11D-A33E-09 chr11:94039704 C>A maps to NM_001080486.1 C55*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93E-01A-11D-A37C-09 chr20:22563117 G>A maps to NM_021784.4 Y254Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OO-01A-11D-A27G-09 chr20:22563090 G>A maps to NM_021784.4 C263C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-A7RC-01B-11D-A403-09 chr19:46375505 G>T maps to NM_004497.2 L81L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NS-01A-12D-A37C-09 chr9:79634683 C>T maps to NM_001013735.1 D38D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr16:86602227 C>T maps to NM_005251.2 S429S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6Y2-01B-11D-A33E-09 chr9:70917938 C>T maps to NM_199135.4 D24D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr9:70177788 G>A maps to NM_001126334.1 G65G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RE-01A-11D-A33E-09 chr6:1390985 C>T maps to NM_001452.1 H268H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NQ-01A-11D-A36J-09 chr6:1390655 C>T maps to NM_001452.1 F158F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NT-01A-11D-A37C-09 chr14:29237108 C>T maps to NM_005249.3 Y208Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49U-01A-31D-A27G-09 chr8:145701070 C>T maps to NM_003923.2 R23R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EX-01A-11D-A36J-09 chr17:74136020 C>A maps to NM_001454.3 T152T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8Q7-01A-11D-A37C-09 chr17:74134093 C>T maps to NM_001454.3 A202A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A9VB-01A-21D-A37C-09 chr17:74133964 G>A maps to NM_001454.3 T245T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FD-01A-11D-A33E-09 chr12:8201389 C>T maps to NM_018416.2 F441F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NK-01A-21D-A37C-09 chr7:4800866 C>T maps to ENST00000450194 T601T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A8I1-01A-11D-A36J-09 chr7:4798960 G>A maps to ENST00000450194 Q455Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OW-01A-11D-A28B-09 chr3:138665330 G>A maps to NM_023067.3 S78S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A891-01A-11D-A36J-09 chr12:2968142 A>G maps to NM_202002.1 P689P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FP-01A-31D-A387-09 chr14:89629021 C>T maps to NM_001085471.1 K403K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FD-01A-11D-A33E-09 chr3:71015090 G>T maps to NM_032682.4 T613T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A938-01A-11D-A37C-09 chr3:71064749 G>A maps to NM_032682.4 C308C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6KZ-01A-11D-A31U-09 chr3:71247108 A>C maps to NM_001012505.1 V97V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HX-01A-11D-A33E-09 chr7:114269984 A>G maps to NM_148898.3 Q199Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASV-01A-11D-A387-09 chr7:114329834 A>T did not map to a codon.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr23:49108165 G>A did not map to a codon.
Sequencing variant TCGA-2H-A9GK-01A-11D-A37C-09 chr6:41555241 G>T maps to NM_001012426.1 R288R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OU-01A-11D-A28B-09 chr11:118850228 C>A maps to NM_181721.2 P154P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NQ-01A-11D-A36J-09 chr23:55650498 G>A did not map to a codon.
Sequencing variant TCGA-LN-A4A2-01A-31D-A27G-09 chr23:55650455 G>C did not map to a codon.
Sequencing variant TCGA-IG-A4QT-01A-21D-A27G-09 chr11:126147445 G>T maps to NM_017547.3 G441G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-A7RC-01B-11D-A403-09 chr11:126145249 C>A maps to NM_017547.3 P220P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GL-01A-12D-A37C-09 chr20:30432967 G>A maps to NM_004118.3 P126P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NL-01A-12D-A37C-09 chr20:30432415 G>A maps to NM_004118.3 S310S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NG-01A-11D-A37C-09 chr9:130566931 C>T maps to NM_004957.4 F113F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XP-A8T6-01A-11D-A36J-09 chr9:130570535 G>A maps to NM_004957.4 V256V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OP-01A-11D-A27G-09 chr1:74670699 C>T maps to NM_003838.3 V323V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA4D-01A-11D-A37C-09 chr19:52249968 G>A maps to NM_002029.3 F93F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NK-01A-21D-A37C-09 chr19:52272699 G>T maps to NM_001005738.1 L263L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OS-01A-11D-A28B-09 chr4:79345575 T>C did not map to a codon.
Sequencing variant TCGA-L5-A8NS-01A-12D-A37C-09 chr4:79340101 G>A did not map to a codon.
Sequencing variant TCGA-LN-A8HZ-01A-11D-A36J-09 chr4:79343065 G>T maps to NM_025074.6 T1530T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6DN-01B-11D-A31U-09 chr4:79295322 G>A maps to NM_025074.6 G1023G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OT-01A-11D-A28B-09 chr9:14857574 A>G maps to ENST00000380880 D268D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NJ-01A-11D-A36J-09 chr9:14848681 G>C maps to ENST00000380880 P417P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASX-01A-11D-A387-09 chr9:14756393 A>C maps to ENST00000380880 S1798S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GK-01A-11D-A37C-09 chr13:39451334 G>T maps to NM_207361.4 G2876*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GN-01A-11D-A37C-09 chr13:39264039 C>T maps to NM_207361.4 H853H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4ON-01A-11D-A27G-09 chr13:39262882 T>C maps to NM_207361.4 L468L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NG-01A-11D-A37C-09 chr13:39263253 A>G maps to NM_207361.4 S591S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8WG-01A-11D-A37C-09 chr13:39452382 C>T maps to NM_207361.4 P2928P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FP-01A-31D-A387-09 chr4:190883075 G>C maps to NM_004477.2 T243T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GK-01A-11D-A37C-09 chr10:135439802 C>T maps to ENST00000443774 S62S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49O-01A-11D-A247-09 chr6:168479698 G>A maps to NM_024919.3 R26*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93C-01A-11D-A387-09 chr9:86153074 G>A maps to NM_174938.4 S24S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FB-01A-11D-A33E-09 chr10:13702381 C>T maps to NM_018027.3 W611*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q9-A6FW-01A-31D-A31U-09 chr10:13699152 G>A maps to NM_018027.3 G812G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8W5-01B-11D-A37C-09 chr10:13696432 G>T maps to NM_018027.3 I1011I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6DN-01B-11D-A31U-09 chr3:69242852 C>A maps to NM_015123.1 E554*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EP-01A-31D-A403-09 chr3:69230095 C>G maps to NM_015123.1 L935L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3Y9-01A-12D-A247-09 chr14:52187043 C>T maps to ENST00000344768 S432S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GL-01A-12D-A37C-09 chr23:131212755 T>A did not map to a codon.
Sequencing variant TCGA-JY-A6F8-01A-11D-A33E-09 chr23:131261853 G>C did not map to a codon.
Sequencing variant TCGA-VR-A8EQ-01A-11D-A36J-09 chr23:131233529 C>T did not map to a codon.
Sequencing variant TCGA-R6-A6Y2-01B-11D-A33E-09 chr11:65172423 G>A maps to NM_031904.3 S387S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A97I-01A-11D-A387-09 chr9:37744830 C>T maps to NM_014907.2 I934I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3YA-01A-11D-A247-09 chr10:49440311 A>C maps to NM_001018071.3 Y338*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr10:49440275 G>A maps to NM_001018071.3 N350N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OT-01A-11D-A28B-09 chr23:12734449 T>C did not map to a codon.
Sequencing variant TCGA-V5-AASX-01A-11D-A387-09 chr23:12734818 C>T did not map to a codon.
Sequencing variant TCGA-VR-A8Q7-01A-11D-A37C-09 chr23:12734447 A>G did not map to a codon.
Sequencing variant TCGA-2H-A9GK-01A-11D-A37C-09 chr1:100176453 G>T maps to NM_001013660.2 S511*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NS-01A-12D-A37C-09 chr13:32798405 G>C maps to NM_023037.2 L1600L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NW-01A-11D-A37C-09 chr13:32709286 G>A maps to NM_023037.2 T348T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A5S3-01A-11D-A28B-09 chr4:48559129 G>T maps to NM_015030.1 G1377G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A939-01A-12D-A37C-09 chr4:48636315 C>A maps to NM_015030.1 E38*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OH-01A-11D-A27G-09 chr4:48567033 G>T maps to NM_015030.1 G1119G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NF-01A-11D-A37C-09 chr4:48591841 T>C maps to NM_015030.1 R520R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6XQ-01B-11D-A33E-09 chr14:44974441 C>T maps to NM_032135.3 E583E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EQ-01A-11D-A36J-09 chr14:44974801 T>C maps to NM_032135.3 K463K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A891-01A-11D-A36J-09 chr15:83437777 A>T maps to NM_001007122.2 P469P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OJ-01A-11D-A27G-09 chr2:49195943 A>C maps to NM_000145.3 T249T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OT-01A-11D-A28B-09 chr2:49191061 C>A maps to NM_000145.3 E300*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RE-A7BO-01A-11D-A33E-09 chr2:49191062 T>C maps to NM_000145.3 Q299Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GO-01A-11D-A37C-09 chr2:186673391 A>G maps to NM_173651.2 K6542K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3QL-01A-11D-A247-09 chr2:186604131 C>T maps to NM_173651.2 L142L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93C-01A-11D-A387-09 chr2:186664502 C>G maps to NM_173651.2 Y3579*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr2:186666047 G>A maps to NM_173651.2 E4094E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NV-01A-11D-A37C-09 chr2:186666038 G>A maps to NM_173651.2 W4091*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A5U7-01A-11D-A31U-09 chr2:186669758 T>C maps to NM_173651.2 G5331G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FP-01A-31D-A387-09 chr2:186656427 C>A maps to NM_173651.2 S1611*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XP-A8T6-01A-11D-A36J-09 chr2:186655867 T>C maps to NM_173651.2 A1424A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OG-01A-11D-A27G-09 chr5:52779521 C>T maps to NM_013409.1 L156L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NS-01A-12D-A37C-09 chr5:52779493 A>G maps to NM_013409.1 L146L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HV-01A-21D-A351-09 chr5:132585212 G>A maps to NM_015082.1 T261T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NT-01A-11D-A37C-09 chr21:47574183 G>A maps to ENST00000397748 D39D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FQ-01A-31D-A387-09 chr23:31090037 C>T did not map to a codon.
Sequencing variant TCGA-R6-A6DQ-01B-11D-A31U-09 chr5:121188110 C>T maps to NM_177478.1 D151D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6Y2-01B-11D-A33E-09 chr5:121188035 G>A maps to NM_177478.1 A126A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L7-A6VZ-01A-12D-A33E-09 chr16:53860210 G>T maps to NM_001080432.2 G187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FR-01A-11D-A387-09 chr23:48340857 G>T did not map to a codon.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr7:2275110 G>A maps to NM_013393.1 D129D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A5U7-01A-11D-A31U-09 chr7:2279080 C>T maps to NM_013393.1 A90A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49L-01A-11D-A247-09 chr16:71319538 C>A maps to NM_018348.5 A95A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A8JD-01A-11D-A36J-09 chr6:37414119 G>A maps to NM_015050.2 R113R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NW-01A-11D-A37C-09 chr9:133470943 C>T maps to NM_003934.1 Y53Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6DQ-01B-11D-A31U-09 chr9:133510069 G>A maps to NM_003934.1 P509P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A938-01A-11D-A37C-09 chr1:24172587 G>A maps to NM_000147.4 S412S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43I-01A-11D-A247-09 chr16:70497527 C>T maps to NM_145059.2 L29L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OJ-01A-11D-A27G-09 chr16:70501298 G>T maps to NM_145059.2 R169R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-A7RC-01B-11D-A403-09 chr16:70502786 C>T maps to NM_145059.2 A233A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr23:44401201 G>A did not map to a codon.
Sequencing variant TCGA-L5-A43I-01A-11D-A247-09 chr15:91422671 A>C did not map to a codon.
Sequencing variant TCGA-L5-A8NE-01A-11D-A37C-09 chr15:91420845 G>A did not map to a codon.
Sequencing variant TCGA-L5-A4OP-01A-11D-A27G-09 chr16:31201635 T>A maps to NM_004960.3 G403G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6DN-01B-11D-A31U-09 chr16:31199659 G>T maps to NM_004960.3 G272*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A4-01A-11D-A27G-09 chr19:5867205 G>A maps to NM_002034.2 D177D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A5-01A-21D-A27G-09 chr19:5867037 G>A maps to NM_002034.2 D233D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FG-01A-11D-A33E-09 chr14:66188718 C>T maps to NM_178155.1 G354G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A8JE-01A-11D-A37C-09 chr11:6502988 G>T maps to NM_012192.3 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6Y2-01B-11D-A33E-09 chr19:35612192 C>T maps to NM_001136010.1 Y47Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GN-01A-11D-A37C-09 chr5:39202765 G>T maps to ENST00000263405 T108T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr5:39153686 C>T maps to ENST00000263405 T394T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NQ-01A-11D-A36J-09 chr5:39202036 C>T maps to ENST00000263405 P351P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FD-01A-11D-A33E-09 chr3:46021322 C>T did not map to a codon.
Sequencing variant TCGA-V5-AASW-01A-11D-A403-09 chr12:130648662 C>T maps to NM_007197.3 N392N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KH-A6WC-01A-11D-A33E-09 chr17:42636366 G>T maps to NM_001466.3 S437S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43C-01A-11D-A247-09 chr17:42635994 C>T maps to NM_001466.3 D313D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr8:28420372 C>T maps to NM_017412.3 R616*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OS-01A-11D-A28B-09 chr11:86662615 G>A maps to NM_012193.2 P394P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8WC-01A-11D-A37C-09 chr11:86662288 C>T maps to NM_012193.2 T503T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RE-01A-11D-A33E-09 chr2:208632692 G>A maps to NM_003468.3 F257F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NK-01A-21D-A37C-09 chr7:72849458 G>C maps to NM_003508.2 L374L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FG-01A-11D-A33E-09 chr19:3530788 G>T did not map to a codon.
Sequencing variant TCGA-L5-A8NQ-01A-11D-A36J-09 chr19:3525966 G>A maps to NM_001136198.1 W57*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASV-01A-11D-A387-09 chr5:151183520 C>T maps to NM_198395.1 R424*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XP-A8T7-01A-11D-A36J-09 chr4:76587142 G>A maps to NM_203505.2 L23L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6L6-01B-11D-A33E-09 chr17:42153233 G>T maps to NM_138387.3 V288V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93E-01A-11D-A37C-09 chr17:78086726 C>T maps to NM_001079804.1 C647C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OE-01A-11D-A27G-09 chr17:78090817 G>T maps to NM_001079804.1 G747G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93F-01A-21D-A37C-09 chr23:153925437 C>T did not map to a codon.
Sequencing variant TCGA-L5-A8NL-01A-12D-A37C-09 chr23:153906515 T>G did not map to a codon.
Sequencing variant TCGA-VR-A8EX-01A-11D-A36J-09 chr23:153944370 C>T did not map to a codon.
Sequencing variant TCGA-RE-A7BO-01A-11D-A33E-09 chr22:17488926 G>T maps to NM_001037814.1 P26P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-AAPN-01A-11D-A403-09 chr22:17488986 G>A maps to NM_001037814.1 P6P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASW-01A-11D-A403-09 chr12:10370693 G>T maps to NM_031412.2 V41V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4ON-01A-11D-A27G-09 chr6:29581139 G>A maps to NM_001470.2 N482N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HX-01A-11D-A33E-09 chr6:29588991 G>T maps to NM_001470.2 I403I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OX-01A-21D-A28B-09 chr9:101340351 G>A maps to NM_005458.7 C108C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FD-01A-11D-A33E-09 chr5:161317973 C>A maps to NM_001127648.1 Y258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA7I-01A-11D-A403-09 chr5:161317916 T>G maps to NM_001127648.1 V239V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A4P3-01A-11D-A27G-09 chr4:46252360 A>C maps to ENST00000507069 Y500*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-M9-A5M8-01A-11D-A28B-09 chr23:151424444 C>T did not map to a codon.
Sequencing variant TCGA-L5-A4OJ-01A-11D-A27G-09 chr15:27193247 C>A maps to NM_000810.3 Y419*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8W8-01B-11D-A37C-09 chr5:161128571 C>T maps to NM_000811.2 S385S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93F-01A-21D-A37C-09 chr4:47408861 G>T maps to NM_000812.3 G333G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FQ-01A-31D-A387-09 chr4:47427816 C>T maps to NM_000812.3 Q403*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X8-AAAR-01A-11D-A403-09 chr4:47163448 C>A maps to NM_000812.3 R142R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr15:26806288 G>A maps to NM_021912.4 N290N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NK-01A-21D-A37C-09 chr15:27018790 C>T did not map to a codon.
Sequencing variant TCGA-R6-A6Y2-01B-11D-A33E-09 chr15:26792963 A>C maps to NM_021912.4 V466V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8Q7-01A-11D-A37C-09 chr15:26806323 C>A did not map to a codon.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr1:1961474 G>A maps to NM_000815.4 T371T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OJ-01A-11D-A27G-09 chr23:151143044 G>T did not map to a codon.
Sequencing variant TCGA-L5-A88T-01A-11D-A351-09 chr23:151130907 A>C did not map to a codon.
Sequencing variant TCGA-LN-A49V-01A-11D-A247-09 chr23:151138168 C>A did not map to a codon.
Sequencing variant TCGA-L5-A8NH-01A-11D-A37C-09 chr5:170224475 G>A maps to NM_014211.2 T155T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EZ-01A-11D-A36J-09 chr19:13065135 C>T maps to NM_052850.2 K185K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OU-01A-11D-A28B-09 chr23:49161347 C>T did not map to a codon.
Sequencing variant TCGA-LN-A9FP-01A-31D-A387-09 chr23:49161382 C>G did not map to a codon.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr4:870337 G>T maps to NM_005255.2 A678A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6XQ-01B-11D-A33E-09 chr4:862465 C>T maps to NM_005255.2 P752P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr22:30951275 G>A maps to NM_004861.1 N312N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr2:242743355 C>T maps to NM_022134.2 D324D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OE-01A-11D-A27G-09 chr7:99757844 C>A maps to NM_024637.4 L389L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A50L-01A-11D-A27G-09 chr14:88431852 T>C maps to NM_000153.2 V343V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA7B-01A-31D-A403-09 chr17:73759428 C>T maps to ENST00000437911 T179T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr5:153796474 G>A maps to NM_198321.3 Q585Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NQ-01A-11D-A36J-09 chr5:153677528 C>T maps to NM_198321.3 P97P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A939-01A-12D-A37C-09 chr9:101589032 G>T did not map to a codon.
Sequencing variant TCGA-JY-A938-01A-11D-A37C-09 chr1:230203083 C>T maps to NM_004481.3 I19I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FG-01A-11D-A33E-09 chr2:166611181 G>T maps to NM_004482.3 G527G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FE-01A-11D-A33E-09 chr2:158115476 G>T maps to NM_014568.1 E295*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GI-01A-11D-A37C-09 chr12:51748201 G>A maps to NM_007210.3 C610C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6F8-01A-11D-A33E-09 chr12:4830037 G>A maps to NM_017417.1 V65V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NG-01A-11D-A37C-09 chr12:4870248 C>T maps to NM_017417.1 A433A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr12:4848346 T>C maps to NM_017417.1 Y176Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6F8-01A-11D-A33E-09 chr12:132905552 G>A maps to NM_001122636.1 N79N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49X-01A-31D-A27G-09 chr14:69805401 T>C maps to NM_020692.2 S334S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GR-01A-12D-A37C-09 chr3:16237302 A>C maps to NM_054110.4 T192T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88Z-01A-11D-A36J-09 chr3:16254212 G>T maps to NM_054110.4 L445L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A8HZ-01A-11D-A36J-09 chr3:16237380 G>T maps to NM_054110.4 V218V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A8I1-01A-11D-A36J-09 chr3:16250102 G>A maps to NM_054110.4 W335*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EX-01A-11D-A36J-09 chr11:11398889 C>T maps to NM_198516.2 R272R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr4:173150832 G>A maps to NM_001034845.2 G55G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6Y0-01B-11D-A33E-09 chr4:172735820 G>T maps to NM_001034845.2 L30L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr17:74073034 C>T maps to NM_003857.2 R229R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GQ-01A-11D-A37C-09 chr19:1399820 G>T maps to NM_138924.1 R100R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr16:81410848 T>C maps to NM_022041.3 L510L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NR-01A-11D-A37C-09 chr15:42622791 G>T maps to NM_198141.2 G555*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GO-01A-11D-A37C-09 chr19:36033271 G>T maps to NM_014364.4 V167V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr19:36034635 C>T maps to NM_014364.4 L321L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NS-01A-12D-A37C-09 chr19:36027766 A>G maps to NM_014364.4 P40P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GL-01A-12D-A37C-09 chr9:128112612 G>T maps to NM_015635.2 A1140A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FB-01A-11D-A33E-09 chr9:128124956 G>T maps to NM_015635.2 E1466*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NI-01A-11D-A37C-09 chr9:130106618 G>T did not map to a codon.
Sequencing variant TCGA-IC-A6RF-01A-13D-A33E-09 chr21:34877880 G>T maps to NM_001136006.1 V904V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HX-01A-11D-A33E-09 chr21:34894555 G>T maps to NM_001136006.1 I444I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S8-A6BV-01A-21D-A31U-09 chr21:34876757 G>T maps to NM_001136006.1 T934T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93C-01A-11D-A387-09 chr9:89561663 C>A maps to NM_002048.2 E11*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FR-01A-11D-A387-09 chr11:22747881 G>T maps to NM_005256.3 S104S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GI-01A-11D-A37C-09 chr17:34074128 G>A maps to NM_139285.2 R331*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NS-01A-12D-A37C-09 chr17:34072682 G>A maps to NM_139285.2 N611N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6KZ-01A-11D-A31U-09 chr17:34077214 G>A maps to NM_139285.2 Q170*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8W8-01B-11D-A37C-09 chr17:34077290 C>T maps to NM_139285.2 V144V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A4P3-01A-11D-A27G-09 chr12:100994179 G>T maps to NM_174942.1 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A5S3-01A-11D-A28B-09 chr13:114541096 G>A maps to ENST00000357389 F178F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GL-01A-12D-A37C-09 chr17:9837515 G>A maps to NM_201433.1 D284D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49V-01A-11D-A247-09 chr17:9862554 C>T maps to NM_201433.1 S163S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RE-01A-11D-A33E-09 chr23:48652483 C>G did not map to a codon.
Sequencing variant TCGA-LN-A4A8-01A-32D-A27G-09 chr23:48650411 G>A did not map to a codon.
Sequencing variant TCGA-V5-AASW-01A-11D-A403-09 chr3:128199936 C>T maps to NM_032638.4 P456P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4ON-01A-11D-A27G-09 chr10:8097680 G>T maps to NM_001002295.1 G21G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A5B8-01A-11D-A28B-09 chr8:11615866 G>A maps to NM_002052.3 K404K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S8-A6BV-01A-21D-A31U-09 chr19:19603234 C>T maps to ENST00000404158 T149T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A97H-01A-11D-A387-09 chr15:45657032 C>T maps to ENST00000432007 W388*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EX-01A-11D-A36J-09 chr15:45654375 C>A maps to ENST00000432007 L454L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NS-01A-12D-A37C-09 chr22:30681877 C>T maps to ENST00000434291 L439L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X8-AAAR-01A-11D-A403-09 chr1:155207370 T>C did not map to a codon.
Sequencing variant TCGA-L5-A4ON-01A-11D-A27G-09 chr9:35737849 A>G maps to NM_020944.2 A800A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASX-01A-11D-A387-09 chr3:81720027 C>T maps to ENST00000264326 Q130Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XP-A8T6-01A-11D-A36J-09 chr10:104119145 C>T maps to NM_004193.2 Y377Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6KZ-01A-11D-A31U-09 chr1:89573944 G>A maps to NM_004120.3 F563F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49X-01A-31D-A27G-09 chr1:89843994 G>T maps to NM_198460.2 E150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NF-01A-11D-A37C-09 chr1:89618083 C>T maps to NM_207398.2 E164E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EZ-01A-11D-A36J-09 chr1:89617966 G>T maps to NM_207398.2 A203A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OQ-01A-11D-A27G-09 chr2:237074958 G>T maps to NM_001485.2 G215G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr7:127223204 G>A maps to NM_024523.5 R397R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93F-01A-21D-A37C-09 chr2:109087534 G>T maps to NM_181453.3 E584*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A5U6-01A-11D-A28B-09 chr2:109087995 G>A maps to NM_181453.3 E737E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6Y0-01B-11D-A33E-09 chr2:109086105 G>T did not map to a codon.
Sequencing variant TCGA-VR-AA7I-01A-11D-A403-09 chr2:109086171 A>G maps to NM_181453.3 K129K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A8JE-01A-11D-A37C-09 chr2:109067568 G>A did not map to a codon.
Sequencing variant TCGA-L5-A8NR-01A-11D-A37C-09 chr19:13004318 G>T maps to NM_000159.2 S119S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A893-01A-11D-A36J-09 chr21:34110575 C>A maps to NM_016631.3 E797*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A8I0-01A-11D-A36J-09 chr21:34120807 A>G did not map to a codon.
Sequencing variant TCGA-IG-A5B8-01A-11D-A28B-09 chr14:55310766 G>T maps to NM_001024024.1 R241R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93C-01A-11D-A387-09 chr14:55312529 C>T maps to NM_001024024.1 T194T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93D-01A-11D-A387-09 chr6:53363688 T>G maps to NM_001498.3 I593I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A5B8-01A-11D-A28B-09 chr6:10876177 C>T maps to NM_004752.3 K176K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NQ-01A-11D-A36J-09 chr6:10877412 C>T maps to NM_004752.3 L101L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr6:10557096 C>T maps to NM_001491.2 N147N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6XG-01B-11D-A33E-09 chr15:59911752 G>T maps to NM_004751.2 *439L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XP-A8T6-01A-11D-A36J-09 chr15:59911072 C>T maps to NM_004751.2 D212D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FG-01A-11D-A33E-09 chr9:74825649 A>G maps to ENST00000238018 T144T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NG-01A-11D-A37C-09 chr16:19522216 C>A maps to NM_016641.3 E163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A4QT-01A-21D-A27G-09 chr10:48438446 C>T maps to NM_004962.2 R88R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6DN-01B-11D-A31U-09 chr10:48416384 C>T maps to NM_016204.1 T103T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3YC-01A-11D-A247-09 chr12:7842644 G>A maps to NM_020634.1 S308S. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-2H-A9GL-01A-12D-A37C-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-2H-A9GL-01A-12D-A37C-09 chr20:34022030 C>T maps to ENST00000374375 F25F. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-JY-A6FB-01A-11D-A33E-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-JY-A6FB-01A-11D-A33E-09 chr20:34022108 G>T maps to ENST00000374375 T51T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NH-01A-11D-A37C-09 chr8:97157144 G>A maps to NM_001001557.2 F338F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88V-01A-11D-A351-09 chr2:20870854 C>T maps to NM_182828.2 H341H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88T-01A-11D-A351-09 chr5:132197853 G>T maps to NM_005260.3 I264I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EU-01A-11D-A36J-09 chr5:132200008 G>T maps to NM_005260.3 R73R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93D-01A-11D-A387-09 chr23:153668792 G>A did not map to a codon.
Sequencing variant TCGA-L5-A88S-01A-11D-A36J-09 chr17:57334522 G>T maps to NM_182569.3 L136L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EQ-01A-11D-A36J-09 chr17:650985 C>T maps to NM_015721.2 S99S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GN-01A-11D-A37C-09 chr3:158408048 C>T maps to ENST00000264263 N688N. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-LN-A4MR-01A-11D-A28B-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-Z6-AAPN-01A-11D-A403-09 chr3:158363490 C>G maps to ENST00000264263 S52*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A5B8-01A-11D-A28B-09 chr2:69575384 G>T maps to ENST00000357308 I309I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8W8-01B-11D-A37C-09 chr2:69556816 A>T maps to ENST00000357308 P532P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OR-01A-11D-A27G-09 chr10:117885012 G>A maps to NM_005264.4 L163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93E-01A-11D-A37C-09 chr8:21552005 G>A maps to NM_001495.4 N414N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A6-01A-11D-A27G-09 chr5:137600202 G>A maps to NM_001496.3 N42N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr22:38019410 G>A maps to ENST00000381756 T246T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NS-01A-12D-A37C-09 chr22:38014498 C>T maps to ENST00000381756 D100D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A9-01A-11D-A28B-09 chr8:63948273 A>G maps to NM_003878.2 Y55Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88V-01A-11D-A351-09 chr19:38877400 G>A maps to NM_152657.3 P167P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49L-01A-11D-A247-09 chr19:38876737 G>T maps to NM_152657.3 G388G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A51D-01A-11D-A27G-09 chr17:34937809 G>T maps to NM_024835.3 E353*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A9-01A-11D-A28B-09 chr17:34916661 A>T maps to NM_024835.3 K160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr20:33451229 C>T maps to NM_178026.2 A97A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A9-01A-11D-A28B-09 chr17:61994788 G>A maps to NM_000515.3 N178N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3YC-01A-11D-A247-09 chr17:61958787 C>T maps to NM_002059.3 R34R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr17:61958421 T>C maps to NM_002059.3 T86T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A97I-01A-11D-A387-09 chr10:85901339 G>A maps to ENST00000436406 V28V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A5B8-01A-11D-A28B-09 chr5:42718721 G>A maps to NM_000163.2 E371E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OT-01A-11D-A28B-09 chr5:42700004 G>T maps to NM_000163.2 V173V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A5U7-01A-11D-A31U-09 chr5:42719318 A>G maps to NM_000163.2 E570E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HY-01A-12D-A351-09 chr7:31003736 G>C maps to NM_000823.3 P18P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43E-01A-11D-A247-09 chr3:172165867 G>A maps to NM_198407.2 G112G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88S-01A-11D-A36J-09 chr11:59604767 C>T maps to NM_005142.2 T250T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RF-01A-13D-A33E-09 chr2:233651858 G>T did not map to a codon.
Sequencing variant TCGA-JY-A6FA-01A-11D-A33E-09 chr2:233671333 C>A maps to ENST00000373566 P613P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A8I0-01A-11D-A36J-09 chr2:233681604 G>T maps to ENST00000373566 E767*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A8I0-01A-11D-A36J-09 chr2:233681730 C>T maps to ENST00000373566 R809*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6DQ-01B-11D-A31U-09 chr2:233655986 C>A maps to ENST00000373566 P393P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr7:150417406 C>T maps to NM_130759.3 Y105Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8WG-01A-11D-A37C-09 chr7:150389658 G>T maps to NM_015660.2 V95V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88V-01A-11D-A351-09 chr7:150269568 C>A maps to ENST00000430830 I151I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EZ-01A-11D-A36J-09 chr7:150325469 G>T maps to ENST00000438845 T142T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OE-01A-11D-A27G-09 chr7:150217464 G>T maps to NM_153236.3 E135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OT-01A-11D-A28B-09 chr7:150174549 G>A maps to NM_175571.2 A560A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3Y9-01A-12D-A247-09 chr16:85711916 G>A maps to NM_016095.2 I153I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A4-01A-11D-A27G-09 chr16:85712253 C>T maps to NM_016095.2 P108P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49P-01A-11D-A247-09 chr8:41393950 C>T maps to NM_032336.2 Q57*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A8-01A-32D-A27G-09 chr12:110383085 C>A maps to NM_057169.3 S570S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A8-01A-32D-A27G-09 chr6:121768355 C>T maps to NM_000165.3 V121V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr13:20716932 G>A maps to NM_021954.3 A165A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EW-01A-11D-A36J-09 chr13:20717061 G>T maps to NM_021954.3 P122P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A939-01A-12D-A37C-09 chr1:147230637 G>A maps to NM_005266.5 R237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A893-01A-11D-A36J-09 chr1:147230836 G>T maps to NM_005266.5 G170G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6Y0-01B-11D-A33E-09 chr1:147380795 G>A maps to NM_005267.4 R238R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASV-01A-11D-A387-09 chr1:147381176 C>A maps to NM_005267.4 A365A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3Y9-01A-12D-A247-09 chr1:39340429 G>A maps to NM_030772.4 F447F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASX-01A-11D-A387-09 chr23:70443601 G>T did not map to a codon.
Sequencing variant TCGA-L5-A4OG-01A-11D-A27G-09 chr13:20796938 C>T maps to NM_001110221.2 T227T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr13:20797450 G>A maps to NM_001110221.2 Q57*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NT-01A-11D-A37C-09 chr1:228346574 G>A maps to NM_020435.2 S372S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49U-01A-31D-A27G-09 chr1:228346301 C>T maps to NM_020435.2 L281L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A9-01A-11D-A28B-09 chr15:35044810 G>T maps to NM_020660.1 R278R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OG-01A-11D-A27G-09 chr23:30739004 C>T did not map to a codon.
Sequencing variant TCGA-2H-A9GQ-01A-11D-A37C-09 chr4:80329141 C>T maps to NM_033214.2 T71T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93E-01A-11D-A37C-09 chr3:141944228 C>T maps to NM_001039547.2 G23G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GK-01A-11D-A37C-09 chr9:86368198 G>A maps to NM_025211.3 L272L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3YA-01A-11D-A247-09 chr23:100656623 T>C did not map to a codon.
Sequencing variant TCGA-VR-A8EX-01A-11D-A36J-09 chr3:33065805 T>C maps to NM_000404.2 V360V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A625-01A-11D-A31U-09 chr11:134188556 A>G maps to NM_001080407.2 G604G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6F8-01A-11D-A33E-09 chr11:134183871 G>T maps to NM_001080407.2 L539L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A891-01A-11D-A36J-09 chr11:134183295 C>T maps to NM_001080407.2 R503*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASW-01A-11D-A403-09 chr11:134147677 C>T maps to NM_001080407.2 P78P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L7-A6VZ-01A-12D-A33E-09 chr9:6554685 G>A maps to NM_000170.2 G766G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A891-01A-11D-A36J-09 chr16:74516994 T>C maps to NM_012201.5 L533L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XP-A8T7-01A-11D-A36J-09 chr16:74496520 G>T maps to NM_012201.5 R933R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A4P3-01A-11D-A27G-09 chr12:57864971 G>T maps to NM_005269.2 E817*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OR-01A-11D-A27G-09 chr12:57864850 C>T maps to NM_005269.2 T776T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6Y0-01B-11D-A33E-09 chr12:57858935 G>T maps to NM_005269.2 G144G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XP-A8T6-01A-11D-A36J-09 chr12:57865570 G>A maps to NM_005269.2 V1016V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3I8-01A-11D-A247-09 chr7:42005958 G>A maps to NM_000168.5 R904R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr7:42085010 G>A maps to NM_000168.5 I266I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A3-01A-11D-A27G-09 chr7:42004062 G>A maps to NM_000168.5 S1536S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A9-01A-11D-A28B-09 chr7:42017205 G>C maps to NM_000168.5 S588*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6DQ-01B-11D-A31U-09 chr7:42006012 C>T maps to NM_000168.5 P886P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A5B8-01A-11D-A28B-09 chr8:144358343 C>G maps to NM_138465.3 V167V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr8:144358904 C>T maps to NM_138465.3 G354G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3Y9-01A-12D-A247-09 chr12:75728516 G>A maps to ENST00000378695 L3L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A7DP-01A-31D-A33E-09 chr12:75816821 A>G maps to NM_152436.1 K241K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6DN-01B-11D-A31U-09 chr12:75804236 G>T maps to ENST00000378692 R86R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6Y2-01B-11D-A33E-09 chr9:3856150 G>T maps to NM_001042413.1 I777I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S8-A6BW-01A-11D-A31U-09 chr17:679086 C>A maps to ENST00000397393 E315*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASX-01A-11D-A387-09 chr23:48629451 G>A did not map to a codon.
Sequencing variant TCGA-LN-A9FP-01A-31D-A387-09 chr6:39047378 G>T maps to NM_002062.3 G361G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GH-01A-11D-A37C-09 chr17:9791262 C>T maps to NM_004246.1 A433A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A2-01A-31D-A27G-09 chr17:9760838 C>T maps to NM_004246.1 N237N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NW-01A-11D-A37C-09 chr23:14599303 G>T did not map to a codon.
Sequencing variant TCGA-LN-A49M-01A-21D-A27G-09 chr23:14627270 A>T did not map to a codon.
Sequencing variant TCGA-XP-A8T6-01A-11D-A36J-09 chr4:175565061 G>T maps to NM_006529.2 R424R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RE-01A-11D-A33E-09 chr4:158091618 T>C maps to NM_001166060.1 S411S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A8HZ-01A-11D-A36J-09 chr4:158065088 G>A maps to NM_001166060.1 A294A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A9VB-01A-21D-A37C-09 chr4:158041815 T>C did not map to a codon.
Sequencing variant TCGA-JY-A6FA-01A-11D-A33E-09 chr10:131964814 C>T maps to NM_006541.4 Q175*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr12:56881844 G>T maps to NM_013267.2 R20R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA7B-01A-31D-A403-09 chr12:129431942 G>A maps to ENST00000442111 K240K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49O-01A-11D-A247-09 chr19:17692129 C>T maps to NM_024656.2 V582V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr19:48184448 G>A maps to NM_015711.3 P674P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EU-01A-11D-A36J-09 chr10:88854346 G>A maps to NM_005271.3 R60R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3I8-01A-11D-A247-09 chr23:120182346 C>A did not map to a codon.
Sequencing variant TCGA-L5-A4OM-01A-11D-A27G-09 chr23:120181833 G>A did not map to a codon.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr23:120182540 G>A did not map to a codon.
Sequencing variant TCGA-LN-A49V-01A-11D-A247-09 chr23:120182378 G>T did not map to a codon.
Sequencing variant TCGA-VR-AA7B-01A-31D-A403-09 chr11:58478151 G>C maps to NM_201648.2 L133L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-A7RB-01A-11D-A351-09 chr11:58604840 G>C maps to NM_145016.3 T72T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EZ-01A-11D-A36J-09 chr11:58607018 C>A maps to NM_145016.3 E23*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GR-01A-12D-A37C-09 chr1:29018136 T>G maps to NM_006582.2 A94A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49O-01A-11D-A247-09 chr1:29030773 G>A maps to NM_006582.2 Q277Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A4P3-01A-11D-A27G-09 chr20:62223483 G>C maps to NM_012384.3 L281L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FG-01A-11D-A33E-09 chr20:62250678 G>A maps to NM_012384.3 D24D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8W8-01B-11D-A37C-09 chr19:19745735 G>A maps to NM_016573.2 G584G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GI-01A-11D-A37C-09 chr6:24780904 A>G maps to NM_015895.3 P22P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GG-01A-11D-A37C-09 chr6:16247146 C>T maps to NM_006877.3 N54N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NI-01A-11D-A37C-09 chr6:16290813 C>T maps to NM_006877.3 T273T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr3:155655420 T>C maps to NM_003875.2 G674G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr17:63052563 T>A maps to NM_006572.4 K50*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L7-A6VZ-01A-12D-A33E-09 chr17:63052435 C>T maps to NM_006572.4 V92V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EZ-01A-11D-A36J-09 chr17:63010776 A>T maps to NM_006572.4 L244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NE-01A-11D-A37C-09 chr19:3151743 C>T maps to NM_002068.2 Y175Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A8JD-01A-11D-A36J-09 chr19:3162842 G>T maps to NM_002068.2 T317T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr3:50294247 C>T maps to NM_002070.2 S229S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EZ-01A-11D-A36J-09 chr1:110134704 C>T maps to NM_006496.2 C305C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A5S3-01A-11D-A28B-09 chr9:80646046 G>A maps to NM_002072.3 D35D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6L6-01B-11D-A33E-09 chr9:80409501 G>A maps to NM_002072.3 V204V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A4QS-01A-11D-A27G-09 chr20:57430198 C>T maps to NM_080425.2 Q627*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OU-01A-11D-A28B-09 chr20:57429276 C>T maps to NM_080425.2 D319D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L7-A6VZ-01A-12D-A33E-09 chr20:57466892 C>A maps to NM_001077488.1 R38R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RE-A7BO-01A-11D-A33E-09 chr20:57430179 C>T maps to NM_080425.2 F620F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A9VB-01A-21D-A37C-09 chr20:57428514 C>T maps to NM_080425.2 G65G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NS-01A-12D-A37C-09 chr1:110152712 G>A maps to NM_005272.3 I84I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr1:1720537 G>A maps to NM_002074.2 D290D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A97H-01A-11D-A387-09 chr22:19808146 C>T maps to NM_053004.2 T76T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NK-01A-21D-A37C-09 chr7:100276333 C>T maps to NM_005273.3 H311H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OE-01A-11D-A27G-09 chr14:52417394 C>T did not map to a codon.
Sequencing variant TCGA-L5-A4OG-01A-11D-A27G-09 chr14:52417395 G>A did not map to a codon.
Sequencing variant TCGA-JY-A938-01A-11D-A37C-09 chr1:235715519 C>T maps to NM_004485.3 A39A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZR-A9CJ-01B-11D-A387-09 chr7:93540125 A>C maps to NM_021955.3 R41R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FA-01A-11D-A33E-09 chr1:38034504 G>T maps to NM_013285.2 A605A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EZ-01A-11D-A36J-09 chr1:38040039 C>T maps to NM_013285.2 L440L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RF-01A-13D-A33E-09 chr23:54578108 C>T did not map to a codon.
Sequencing variant TCGA-VR-AA7B-01A-31D-A403-09 chr23:54584944 G>T did not map to a codon.
Sequencing variant TCGA-VR-A8EW-01A-11D-A36J-09 chr5:141385742 G>T maps to NM_005471.4 I125I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A8HZ-01A-11D-A36J-09 chr12:102183822 G>A maps to NM_024312.4 P72P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A8JD-01A-11D-A36J-09 chr16:1412295 C>T maps to NM_032520.4 L167L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OS-01A-11D-A28B-09 chr8:25279130 C>T maps to NM_001083111.1 T65T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GO-01A-11D-A37C-09 chr9:131030439 C>G did not map to a codon.
Sequencing variant TCGA-R6-A6Y2-01B-11D-A33E-09 chr9:131020086 C>A maps to NM_004486.4 G838*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L7-A6VZ-01A-12D-A33E-09 chr3:37381676 G>A maps to NM_001172713.1 G2168G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-M9-A5M8-01A-11D-A28B-09 chr14:93275648 A>G maps to NM_005113.2 L259L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GF-01A-11D-A37C-09 chr15:72953681 C>T maps to NM_018652.4 H214H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-A7RB-01A-11D-A351-09 chr8:41355026 G>C did not map to a codon.
Sequencing variant TCGA-R6-A8W5-01B-11D-A37C-09 chr10:99619285 C>T maps to NM_001010917.1 S28S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr15:34820021 C>T maps to NM_001023567.4 A541A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A4QS-01A-11D-A27G-09 chr3:121383819 G>A maps to ENST00000393667 Q3210*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A625-01A-11D-A31U-09 chr3:121400678 A>G maps to ENST00000393667 L2910L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FH-01A-11D-A33E-09 chr3:121395811 G>A maps to ENST00000393667 L3035L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8WC-01A-11D-A37C-09 chr3:121410778 G>A maps to ENST00000393667 R2478*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49R-01A-11D-A247-09 chr9:88650484 C>T maps to ENST00000376023 P280P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A8O2-01A-11D-A36J-09 chr5:32126581 C>T maps to NM_022130.3 Q211Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43H-01A-11D-A247-09 chr5:32143865 A>G maps to NM_022130.3 L116L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GG-01A-11D-A37C-09 chr1:155735240 C>T maps to ENST00000368331 E1341E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GI-01A-11D-A37C-09 chr1:155734856 G>T maps to ENST00000368331 T1469T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A938-01A-11D-A37C-09 chr1:155753817 T>C maps to ENST00000368331 V617V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q9-A6FW-01A-31D-A31U-09 chr16:20327344 T>C maps to NM_001007240.1 Q481Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A893-01A-11D-A36J-09 chr3:194118888 C>T maps to NM_004488.2 A41A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-A7RB-01A-11D-A351-09 chr3:194117360 G>A maps to NM_004488.2 R551*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RE-01A-11D-A33E-09 chr8:145139754 T>C maps to NM_003801.3 L381L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA4G-01A-11D-A37C-09 chr10:113913355 G>A maps to NM_020918.4 C813C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6XG-01B-11D-A33E-09 chr2:96691727 G>A maps to NM_207328.2 G396G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HW-01A-22D-A351-09 chr19:33609991 C>T maps to NM_018025.2 F830F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6F8-01A-11D-A33E-09 chr1:156565511 G>T maps to NM_015590.3 P207P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-A7RB-01A-11D-A351-09 chr17:42475360 G>A maps to NM_001002909.2 Q1362*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XP-A8T7-01A-11D-A36J-09 chr5:56510007 A>G maps to NM_001127236.2 P17P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3Y9-01A-12D-A247-09 chr1:46099806 C>G maps to NM_021639.4 V282V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OG-01A-11D-A27G-09 chr23:132795820 C>T did not map to a codon.
Sequencing variant TCGA-2H-A9GG-01A-11D-A37C-09 chr13:92797094 A>T maps to NM_004466.4 R472*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NI-01A-11D-A37C-09 chr13:94680140 G>A maps to NM_005708.3 L290L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A8I0-01A-11D-A36J-09 chr13:94482728 C>A maps to NM_005708.3 A214A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EO-01A-11D-A36J-09 chr13:94482414 C>T maps to NM_005708.3 R110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZR-A9CJ-01B-11D-A387-09 chr13:94482416 A>G maps to NM_005708.3 R110R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A4P3-01A-11D-A27G-09 chr2:157426010 C>G maps to NM_000408.4 L479L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A939-01A-12D-A37C-09 chr2:157436297 C>T maps to NM_000408.4 Q686*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr2:157407141 T>C maps to NM_000408.4 C285C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OO-01A-11D-A27G-09 chr2:157426714 A>G maps to NM_000408.4 P531P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NL-01A-12D-A37C-09 chr11:64702839 G>A maps to NM_130769.3 C31C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43H-01A-11D-A247-09 chr19:34890654 C>T maps to NM_000175.3 G502G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OG-01A-11D-A27G-09 chr6:24450082 G>A maps to NM_001503.2 N460N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8ER-01A-11D-A36J-09 chr6:24448364 G>T maps to NM_001503.2 C506*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GK-01A-11D-A37C-09 chr4:176622759 T>G maps to NM_005277.3 R66R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q9-A6FW-01A-31D-A31U-09 chr4:176594833 A>G maps to NM_005277.3 A128A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49M-01A-21D-A27G-09 chr1:27216260 G>A maps to NM_018066.3 F109F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OG-01A-11D-A27G-09 chr23:136112588 G>A did not map to a codon.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr23:136113357 G>A did not map to a codon.
Sequencing variant TCGA-LN-A4A1-01A-21D-A27G-09 chr9:132816282 C>T maps to NM_001136557.1 L24L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A1-01A-21D-A27G-09 chr12:123200612 G>A maps to NM_006018.2 A224A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6L6-01B-11D-A33E-09 chr6:46984421 C>A maps to ENST00000283297 E233*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GN-01A-11D-A37C-09 chr23:135430820 T>G did not map to a codon.
Sequencing variant TCGA-2H-A9GN-01A-11D-A37C-09 chr23:135445723 G>T did not map to a codon.
Sequencing variant TCGA-IG-A4P3-01A-11D-A27G-09 chr23:135429031 C>T did not map to a codon.
Sequencing variant TCGA-JY-A6FD-01A-11D-A33E-09 chr23:135430354 T>C did not map to a codon.
Sequencing variant TCGA-L5-A43I-01A-11D-A247-09 chr23:135428494 G>T did not map to a codon.
Sequencing variant TCGA-L5-A8NR-01A-11D-A37C-09 chr23:135432566 T>G did not map to a codon.
Sequencing variant TCGA-L5-A8NR-01A-11D-A37C-09 chr23:135439882 A>G did not map to a codon.
Sequencing variant TCGA-LN-A4MR-01A-11D-A28B-09 chr23:135429364 C>T did not map to a codon.
Sequencing variant TCGA-Q9-A6FU-01A-11D-A31U-09 chr23:135432292 G>T did not map to a codon.
Sequencing variant TCGA-R6-A6Y2-01B-11D-A33E-09 chr23:135427223 G>T did not map to a codon.
Sequencing variant TCGA-VR-AA7B-01A-31D-A403-09 chr23:135430242 C>T did not map to a codon.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr2:26535918 C>T maps to NM_001145168.1 A515A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A938-01A-11D-A37C-09 chr6:47682564 C>A maps to NM_153838.3 I528I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A939-01A-12D-A37C-09 chr6:46839652 G>T maps to NM_015234.4 I446I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6L6-01B-11D-A33E-09 chr13:27333601 G>A maps to NM_005288.3 V121V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A9VB-01A-21D-A37C-09 chr13:27333514 C>T maps to NM_005288.3 S150S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A4P3-01A-11D-A27G-09 chr8:37698774 G>A maps to NM_032777.9 L973L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr8:37692813 C>T maps to NM_032777.9 G577G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr8:37696505 C>T maps to NM_032777.9 G764G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3YC-01A-11D-A247-09 chr6:142723826 T>C maps to NM_198569.2 N605N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L7-A6VZ-01A-12D-A33E-09 chr6:142715087 G>T maps to NM_198569.2 E473*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FO-01A-11D-A387-09 chr14:59930819 C>T maps to NM_022571.5 L375L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OT-01A-11D-A28B-09 chr14:53066828 A>C did not map to a codon.
Sequencing variant TCGA-LN-A49X-01A-31D-A27G-09 chr7:37780567 C>A maps to NM_181791.1 A191A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-A7RB-01A-11D-A351-09 chr7:37780846 C>A maps to NM_181791.1 V284V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EO-01A-11D-A36J-09 chr17:72363871 C>A maps to NM_181790.1 S76S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49L-01A-11D-A247-09 chr7:1098154 C>A did not map to a codon.
Sequencing variant TCGA-L5-A4OG-01A-11D-A27G-09 chr3:154146546 T>C maps to NM_001038705.1 E286E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A8O2-01A-11D-A36J-09 chr11:67219229 C>T maps to NM_206997.1 P322P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NL-01A-12D-A37C-09 chr1:6313984 G>A maps to NM_207370.2 I193I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr1:9165715 C>T maps to NM_024980.4 R207R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FE-01A-11D-A33E-09 chr10:25887176 G>T maps to NM_020752.2 P874P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KH-A6WC-01A-11D-A33E-09 chr10:25883265 G>T maps to NM_020752.2 L646L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43E-01A-11D-A247-09 chr10:25888058 A>T maps to NM_020752.2 R1168R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6Y2-01B-11D-A33E-09 chr10:25887230 G>T maps to NM_020752.2 G892G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-A7RB-01A-11D-A351-09 chr10:25883307 G>C maps to NM_020752.2 G660G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OE-01A-11D-A27G-09 chr1:168066340 G>A maps to NM_153832.1 S168S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OE-01A-11D-A27G-09 chr2:128408920 G>A maps to NM_005291.2 P232P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88Z-01A-11D-A36J-09 chr8:145583535 G>T maps to NM_024531.3 S128S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NQ-01A-11D-A36J-09 chr23:53105818 G>T did not map to a codon.
Sequencing variant TCGA-L5-A4OE-01A-11D-A27G-09 chr23:78426728 G>T did not map to a codon.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr23:78427237 C>T did not map to a codon.
Sequencing variant TCGA-2H-A9GQ-01A-11D-A37C-09 chr17:36484879 T>C maps to ENST00000398597 A1525A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A1-01A-21D-A27G-09 chr17:36483730 G>T maps to ENST00000398597 S1908S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZR-A9CJ-01B-11D-A387-09 chr17:36499227 G>A maps to ENST00000398597 L149L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-AAPN-01A-11D-A403-09 chr13:95271748 A>C maps to NM_180989.4 P238P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A939-01A-12D-A37C-09 chr8:142367888 C>A maps to NM_005293.2 L45L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr8:142367057 G>A maps to NM_005293.2 S322S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr8:142367351 C>T maps to NM_005293.2 S224S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HX-01A-11D-A33E-09 chr9:125796991 G>T maps to NM_005294.1 V49V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RE-A7BO-01A-11D-A33E-09 chr10:125434381 C>T maps to NM_153442.3 A239A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RE-01A-11D-A33E-09 chr23:41555682 G>A did not map to a codon.
Sequencing variant TCGA-V5-AASW-01A-11D-A403-09 chr2:241569884 C>T maps to NM_001195381.1 S203S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RE-01A-11D-A33E-09 chr7:124404499 G>A maps to NM_005302.2 S177S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr7:124387325 G>A maps to NM_005302.2 N365N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A9VB-01A-21D-A37C-09 chr1:202097549 G>T maps to NM_004767.3 E438*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OG-01A-11D-A27G-09 chr2:133175427 C>T maps to NM_001508.2 S271S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6XG-01B-11D-A33E-09 chr2:133402989 G>A maps to NM_001508.2 P391P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OJ-01A-11D-A27G-09 chr19:46094359 G>T maps to NM_005282.2 P255P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NW-01A-11D-A37C-09 chr19:46095040 G>A maps to NM_005282.2 I28I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49Y-01A-11D-A27G-09 chr11:60620688 G>A maps to NM_004778.2 F169F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6XG-01B-11D-A33E-09 chr2:105858479 C>A maps to NM_007227.3 V55V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8W8-01B-11D-A37C-09 chr23:150348679 G>A did not map to a codon.
Sequencing variant TCGA-VR-AA7B-01A-31D-A403-09 chr1:174417613 C>G maps to NM_005684.4 S122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93C-01A-11D-A387-09 chr2:231775308 G>A maps to NM_005683.3 I123I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GQ-01A-11D-A37C-09 chr16:57691340 C>T maps to NM_005682.5 Y408Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OH-01A-11D-A27G-09 chr23:19027871 G>T did not map to a codon.
Sequencing variant TCGA-IG-A5B8-01A-11D-A28B-09 chr19:47844097 C>T maps to NM_018485.1 S14S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZR-A9CJ-01B-11D-A387-09 chr4:8584356 G>A maps to NM_080819.2 P256P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NG-01A-11D-A37C-09 chr11:94113380 G>A maps to NM_016540.3 P402P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RE-A7BO-01A-11D-A33E-09 chr11:94113932 G>A maps to NM_016540.3 D218D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43E-01A-11D-A247-09 chr3:151012364 G>A maps to NM_023915.3 I223I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GF-01A-11D-A37C-09 chr1:101004650 C>A maps to NM_022049.2 I43I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FP-01A-31D-A387-09 chr16:57717927 C>A maps to NM_170776.4 A322A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr5:90119241 G>A maps to NM_032119.3 R5399R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NS-01A-12D-A37C-09 chr5:89989975 C>A maps to NM_032119.3 S2468*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49K-01A-11D-A247-09 chr5:89981639 G>T maps to NM_032119.3 A2106A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA7I-01A-11D-A403-09 chr5:90144560 C>T maps to NM_032119.3 F5709F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GF-01A-11D-A37C-09 chr23:101909621 C>G did not map to a codon.
Sequencing variant TCGA-JY-A6FA-01A-11D-A33E-09 chr23:101909993 G>A did not map to a codon.
Sequencing variant TCGA-VR-A8EW-01A-11D-A36J-09 chr23:101912225 C>G did not map to a codon.
Sequencing variant TCGA-IG-A4QS-01A-11D-A27G-09 chr23:101971322 G>A did not map to a codon.
Sequencing variant TCGA-LN-A9FO-01A-11D-A387-09 chr23:101970761 G>T did not map to a codon.
Sequencing variant TCGA-Z6-A8JE-01A-11D-A37C-09 chr16:19883969 G>A maps to NM_016235.1 G66G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OH-01A-11D-A27G-09 chr6:117127865 G>T maps to NM_148963.2 S334S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OJ-01A-11D-A27G-09 chr6:117114294 G>T maps to NM_148963.2 L597L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NU-01A-11D-A36J-09 chr6:117127658 G>A maps to NM_148963.2 L403L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr4:90169280 C>A maps to NM_198281.2 G661*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A51D-01A-11D-A27G-09 chr17:80011220 C>T maps to NM_212492.1 Y75Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88W-01A-11D-A351-09 chr17:80011790 A>G maps to NM_212492.1 E98E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HY-01A-12D-A351-09 chr17:80013948 C>T maps to NM_212492.1 Q343*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8W8-01B-11D-A37C-09 chr9:139243167 G>T maps to NM_001145638.1 T409T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KH-A6WC-01A-11D-A33E-09 chr1:109465145 C>A maps to NM_013296.4 C516*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q9-A6FW-01A-31D-A31U-09 chr6:28501886 G>A maps to NM_001509.2 T203T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A97I-01A-11D-A387-09 chr11:123465505 G>A maps to ENST00000456860 W142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FA-01A-11D-A33E-09 chr11:123480971 G>T maps to ENST00000456860 V479V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FH-01A-11D-A33E-09 chr11:123483490 C>T maps to ENST00000456860 R512*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49O-01A-11D-A247-09 chr5:125821383 C>A maps to NM_023927.2 S326*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A9-01A-11D-A28B-09 chr22:47022731 T>C maps to NM_015124.2 G12G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A9-01A-11D-A28B-09 chr22:47072524 C>G maps to NM_015124.2 S531*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93D-01A-11D-A387-09 chr22:40356068 G>T maps to NM_004810.2 E61*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A4P3-01A-11D-A27G-09 chr12:52404908 G>T maps to NM_181711.2 L146L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A97H-01A-11D-A387-09 chr2:11761096 G>T maps to NM_014668.3 E1371*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-M9-A5M8-01A-11D-A28B-09 chr2:11774343 G>A maps to NM_014668.3 L1693L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6XQ-01B-11D-A33E-09 chr2:11767136 G>A maps to NM_014668.3 T1452T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S8-A6BW-01A-11D-A31U-09 chr2:11742611 C>T maps to NM_014668.3 L870L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EQ-01A-11D-A36J-09 chr2:11720942 C>T maps to NM_014668.3 R296*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49S-01A-11D-A247-09 chr15:33022941 C>G maps to NM_013372.6 T17T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASX-01A-11D-A387-09 chr1:240656361 G>A maps to NM_022469.3 P138P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NU-01A-11D-A36J-09 chr5:153149891 G>T maps to NM_001114183.1 R729R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49L-01A-11D-A247-09 chr5:153175033 A>G did not map to a codon.
Sequencing variant TCGA-R6-A6DN-01B-11D-A31U-09 chr5:153190784 A>C maps to NM_001114183.1 *907Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-A7RE-01A-11D-A351-09 chr23:122616851 G>A did not map to a codon.
Sequencing variant TCGA-VR-AA7I-01A-11D-A403-09 chr23:122318471 G>T did not map to a codon.
Sequencing variant TCGA-X8-AAAR-01A-11D-A403-09 chr23:122536893 G>A did not map to a codon.
Sequencing variant TCGA-Z6-A8JD-01A-11D-A36J-09 chr23:122318456 G>A did not map to a codon.
Sequencing variant TCGA-Z6-AAPN-01A-11D-A403-09 chr23:122613988 C>T did not map to a codon.
Sequencing variant TCGA-JY-A6FH-01A-11D-A33E-09 chr11:105797614 G>T maps to NM_000829.3 E666*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A51D-01A-11D-A27G-09 chr10:87379697 G>A maps to NM_017551.2 G762G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FG-01A-11D-A33E-09 chr10:87966133 G>A maps to NM_017551.2 Y169Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NG-01A-11D-A37C-09 chr10:87407033 A>C maps to NM_017551.2 A706A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NS-01A-12D-A37C-09 chr10:87482893 G>A maps to NM_017551.2 G621G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FB-01A-11D-A33E-09 chr4:94693642 C>A maps to NM_001510.2 S1006S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OW-01A-11D-A28B-09 chr4:94137896 C>T maps to NM_001510.2 N266N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FG-01A-11D-A33E-09 chr6:101847188 C>A maps to NM_021956.4 V12V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43C-01A-11D-A247-09 chr6:102376296 G>A maps to NM_021956.4 E625E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OH-01A-11D-A27G-09 chr6:101847170 G>A maps to NM_021956.4 P6P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49M-01A-21D-A27G-09 chr6:102337691 C>T maps to NM_021956.4 L568L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GO-01A-11D-A37C-09 chr1:37356629 T>G maps to NM_000831.3 R61R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RF-01A-13D-A33E-09 chr1:37271816 G>T maps to NM_000831.3 Y734*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A893-01A-11D-A36J-09 chr1:37267538 G>A maps to NM_000831.3 V891V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NQ-01A-11D-A36J-09 chr1:37270659 C>A maps to NM_000831.3 G831G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q9-A6FW-01A-31D-A31U-09 chr1:37271876 C>T maps to NM_000831.3 K714K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8WC-01A-11D-A37C-09 chr1:37325591 G>T maps to NM_000831.3 P271P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FB-01A-11D-A33E-09 chr11:120744854 C>T maps to NM_014619.2 G329G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A8I1-01A-11D-A36J-09 chr11:120831695 G>T maps to NM_014619.2 V651V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6DQ-01B-11D-A31U-09 chr11:120856617 C>T maps to NM_014619.2 S840S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASX-01A-11D-A387-09 chr11:120531107 C>T maps to NM_014619.2 I27I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OJ-01A-11D-A27G-09 chr19:42525544 G>T maps to NM_002088.3 G593G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr19:42509893 G>A maps to NM_002088.3 Y748Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6DQ-01B-11D-A31U-09 chr19:42509908 G>A maps to NM_002088.3 L743L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NW-01A-11D-A37C-09 chr9:140056470 C>T maps to ENST00000371546 N542N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6F8-01A-11D-A33E-09 chr16:9858547 C>A maps to NM_000833.3 G951G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OQ-01A-11D-A27G-09 chr16:9943749 G>A maps to NM_000833.3 S397S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6L4-01A-11D-A31U-09 chr16:9923492 A>C maps to NM_000833.3 S598S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6XG-01B-11D-A33E-09 chr16:9857431 A>G maps to NM_000833.3 N1323N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA4D-01A-11D-A37C-09 chr16:9923300 C>T maps to NM_000833.3 V662V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43E-01A-11D-A247-09 chr12:13769498 C>G maps to NM_000834.3 L406L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr12:13764668 A>G maps to NM_000834.3 A590A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49Y-01A-11D-A27G-09 chr12:13716393 G>A maps to NM_000834.3 L1260L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6XQ-01B-11D-A33E-09 chr12:13768093 G>T maps to NM_000834.3 V536V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q9-A6FW-01A-31D-A31U-09 chr17:72846346 C>A maps to NM_000835.3 E497*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NL-01A-12D-A37C-09 chr19:48917814 C>T maps to NM_000836.2 C462C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EP-01A-31D-A403-09 chr19:48922911 G>A maps to NM_000836.2 S644S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NV-01A-11D-A37C-09 chr9:104449447 G>T maps to NM_133445.2 S245*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FO-01A-11D-A387-09 chr9:104499883 G>A maps to NM_133445.2 D126D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A8I1-01A-11D-A36J-09 chr19:1004829 C>T maps to NM_138690.1 L444L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr12:66990678 G>A maps to ENST00000359742 S28S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HX-01A-11D-A33E-09 chr3:14567436 G>A maps to ENST00000507975 D111D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OW-01A-11D-A28B-09 chr23:48834840 T>C did not map to a codon.
Sequencing variant TCGA-LN-A5U7-01A-11D-A31U-09 chr23:48847120 G>T did not map to a codon.
Sequencing variant TCGA-2H-A9GQ-01A-11D-A37C-09 chr4:3030967 C>T maps to NM_182982.2 P367P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NI-01A-11D-A37C-09 chr4:3030926 G>T did not map to a codon.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr10:121189929 G>T maps to NM_005308.2 G193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A8JE-01A-11D-A37C-09 chr10:121182725 G>T maps to NM_005308.2 E130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr19:47423885 C>T maps to NM_004491.4 Q652*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GF-01A-11D-A37C-09 chr6:146755847 C>T maps to NM_000838.3 S1167S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr6:146351348 G>A maps to NM_000838.3 T232T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OU-01A-11D-A28B-09 chr6:146351240 T>G maps to NM_000838.3 T196T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A8HZ-01A-11D-A36J-09 chr3:51746592 G>T maps to NM_000839.3 V185V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93E-01A-11D-A37C-09 chr7:86468291 G>T maps to NM_000840.2 E488*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OW-01A-11D-A28B-09 chr7:86493637 G>A maps to NM_000840.2 R869R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NR-01A-11D-A37C-09 chr7:86394586 G>C maps to NM_000840.2 G42G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr6:34003758 G>A maps to NM_000841.1 Q710*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr6:34059792 C>T maps to NM_000841.1 S201S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OJ-01A-11D-A27G-09 chr5:178410024 G>T maps to NM_000843.3 G774G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HZ-01A-31D-A351-09 chr5:178413398 G>T maps to NM_000843.3 S619*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A893-01A-11D-A36J-09 chr3:6903326 C>T maps to NM_181874.2 Y84Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49Y-01A-11D-A27G-09 chr3:7188295 C>A maps to NM_181874.2 S226*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASV-01A-11D-A387-09 chr3:6903374 G>T maps to NM_181874.2 T100T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EU-01A-11D-A36J-09 chr3:7188221 C>T maps to NM_181874.2 P201P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6F8-01A-11D-A33E-09 chr7:126173068 G>T maps to NM_001127323.1 T789T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A9VB-01A-21D-A37C-09 chr7:126173578 G>A maps to NM_001127323.1 R619R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OU-01A-11D-A28B-09 chr17:42427871 C>T maps to NM_002087.2 H175H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NW-01A-11D-A37C-09 chr17:42426906 C>T maps to NM_002087.2 C84C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OF-01A-11D-A27G-09 chr23:16170439 G>T did not map to a codon.
Sequencing variant TCGA-IG-A97H-01A-11D-A387-09 chr19:48956266 C>T maps to NM_031485.3 R442R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3YB-01A-11D-A247-09 chr4:43032467 C>T maps to NM_001080476.2 R262*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A97I-01A-11D-A387-09 chr4:42965094 C>T maps to NM_001080476.2 R191*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8WG-01A-11D-A37C-09 chr4:43022412 C>T maps to NM_001080476.2 Q224*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A4P3-01A-11D-A27G-09 chr8:130789632 C>T maps to NM_031415.2 E67E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6F8-01A-11D-A33E-09 chr17:3629164 G>T maps to NM_031965.2 E646*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93D-01A-11D-A387-09 chr3:119624621 G>A maps to NM_002093.3 Q265*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OW-01A-11D-A28B-09 chr9:124080950 C>A maps to NM_000177.4 V379V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A9VB-01A-21D-A37C-09 chr7:142962172 C>T maps to NM_001143679.1 R124R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A9-01A-11D-A28B-09 chr22:24300540 C>A maps to NM_000854.3 G152G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A9-01A-11D-A28B-09 chr22:24325165 G>T maps to NM_000854.3 G152G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EX-01A-11D-A36J-09 chr2:48848394 G>A maps to NM_172311.2 P775P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88Z-01A-11D-A36J-09 chr3:120500158 G>T maps to NM_005513.2 E388*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A9-01A-11D-A28B-09 chr11:18361124 C>G maps to NM_005316.3 P176P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FD-01A-11D-A33E-09 chr6:158613033 C>T maps to NM_207118.2 L21L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASX-01A-11D-A387-09 chr6:158613098 C>T maps to NM_207118.2 H42H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q9-A6FW-01A-31D-A31U-09 chr7:74133240 A>G maps to NM_032999.2 E308E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4MR-01A-11D-A28B-09 chr16:27481556 G>A maps to NM_001520.3 D1562D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FD-01A-11D-A33E-09 chr2:27566339 G>A maps to NM_001521.2 Q28*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FG-01A-11D-A33E-09 chr2:27551708 A>G did not map to a codon.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr2:27558465 T>C maps to NM_001521.2 P525P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EQ-01A-11D-A36J-09 chr2:197629381 G>A maps to NM_012086.2 R856*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A938-01A-11D-A37C-09 chr9:135553981 C>T maps to NM_012204.2 R326*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NR-01A-11D-A37C-09 chr9:135555135 C>T maps to NM_012204.2 R710R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FH-01A-11D-A33E-09 chr9:135933249 G>T maps to NM_001122823.1 T488T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6Y2-01B-11D-A33E-09 chr9:135906457 G>T maps to NM_001122823.1 R20R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FH-01A-11D-A33E-09 chr6:43594098 G>A maps to NM_019096.3 Q88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GG-01A-11D-A37C-09 chr10:1053055 G>A maps to NM_012341.2 R367R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A939-01A-12D-A37C-09 chr10:1052987 G>T maps to NM_012341.2 E345*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HW-01A-22D-A351-09 chr20:60775766 C>A maps to NM_015666.3 G285G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NL-01A-12D-A37C-09 chr20:42355078 C>A maps to NM_176791.3 E86*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RE-A7BO-01A-11D-A33E-09 chr20:42354941 C>T maps to NM_176791.3 T131T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A51D-01A-11D-A27G-09 chr1:42620499 C>T maps to NM_007102.2 C80C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RF-01A-13D-A33E-09 chr11:106558334 C>T maps to ENST00000282249 S744S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q9-A6FW-01A-31D-A31U-09 chr4:156638420 T>C maps to NM_001130684.1 D561D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr12:14832636 G>A maps to NM_004963.3 R262*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A5B8-01A-11D-A28B-09 chr17:7910833 C>T maps to NM_000180.3 G518G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FG-01A-11D-A33E-09 chr23:108641817 G>A did not map to a codon.
Sequencing variant TCGA-L5-A43E-01A-11D-A247-09 chr23:108708490 G>T did not map to a codon.
Sequencing variant TCGA-R6-A6KZ-01A-11D-A31U-09 chr23:108638590 A>C did not map to a codon.
Sequencing variant TCGA-VR-A8EU-01A-11D-A36J-09 chr4:44688649 T>A maps to NM_021927.2 I286I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr7:65439349 G>A maps to NM_000181.3 P441P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A6QS-01A-12D-A33E-09 chr12:42499823 G>T maps to NM_173601.1 I220I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GI-01A-11D-A37C-09 chr23:2773101 G>A did not map to a codon.
Sequencing variant TCGA-L5-A88Z-01A-11D-A36J-09 chr23:2799151 C>T did not map to a codon.
Sequencing variant TCGA-LN-A9FQ-01A-31D-A387-09 chr23:2777905 G>A did not map to a codon.
Sequencing variant TCGA-VR-A8EU-01A-11D-A36J-09 chr4:145038045 C>T maps to NM_002099.6 T106T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GO-01A-11D-A37C-09 chr19:49490516 C>T maps to NM_002103.4 P142P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A8JD-01A-11D-A36J-09 chr19:49484890 C>A maps to NM_002103.4 V355V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr20:23347638 G>T did not map to a codon.
Sequencing variant TCGA-R6-A8WG-01A-11D-A37C-09 chr20:23349537 A>T maps to NM_022482.3 S533S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A8JE-01A-11D-A37C-09 chr20:23345550 C>G maps to NM_022482.3 L177L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6DQ-01B-11D-A31U-09 chr5:54405874 C>T maps to NM_006144.3 C218C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr5:54326288 G>A maps to NM_002104.2 V80V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr12:48723223 G>A maps to NM_181788.1 S50S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OE-01A-11D-A27G-09 chr3:129268028 C>A maps to NM_153833.1 P188P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93C-01A-11D-A387-09 chr23:154113572 C>T did not map to a codon.
Sequencing variant TCGA-IG-A3QL-01A-11D-A247-09 chr5:134705830 C>T maps to NM_138610.2 A58A. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-L5-A8NN-01A-11D-A37C-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-R6-A8W8-01B-11D-A37C-09 chr23:103268122 G>T did not map to a codon.
Sequencing variant TCGA-L5-A4OM-01A-11D-A27G-09 chr1:226252078 C>T maps to NM_002107.3 R9R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A5U5-01A-21D-A28B-09 chr12:31945088 G>C maps to NM_001013699.2 T4T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6XG-01B-11D-A33E-09 chr10:115340368 C>T maps to NM_004132.3 D252D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GI-01A-11D-A37C-09 chr2:26502880 A>G maps to NM_000183.2 K277K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GN-01A-11D-A37C-09 chr12:96379930 A>G maps to NM_002108.2 H353H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A5B8-01A-11D-A28B-09 chr12:96389544 C>T maps to NM_002108.2 V48V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NK-01A-21D-A37C-09 chr12:96380980 G>C maps to NM_002108.2 L305L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NJ-01A-11D-A36J-09 chr5:153857301 G>A maps to NM_004821.2 G89G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HX-01A-11D-A33E-09 chr20:7894902 G>T maps to NM_017545.2 G151G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr17:39890493 C>T maps to ENST00000310778 T131T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NH-01A-11D-A37C-09 chr17:39884551 C>T maps to ENST00000310778 S367S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FB-01A-11D-A33E-09 chr1:156594236 C>A maps to NM_021817.2 A178A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EY-01A-11D-A36J-09 chr5:140070829 G>T maps to NM_002109.3 G20G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GQ-01A-11D-A37C-09 chr19:52222713 G>A maps to NM_001523.2 R149R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6XG-01B-11D-A33E-09 chr19:52222983 G>A maps to NM_001523.2 Y59Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RE-A7BO-01A-11D-A33E-09 chr19:52217192 G>A maps to NM_001523.2 S408S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49M-01A-21D-A27G-09 chr8:122626753 G>A maps to NM_005328.2 L418L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49M-01A-21D-A27G-09 chr8:122626767 G>A maps to NM_005328.2 Q414*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A8O2-01A-11D-A36J-09 chr16:69147348 C>T maps to NM_005329.2 C214C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6L6-01B-11D-A33E-09 chr14:23417123 T>A maps to NM_017815.2 K221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A5S3-01A-11D-A28B-09 chr19:36111188 C>A maps to NM_015302.1 L537L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NQ-01A-11D-A36J-09 chr19:36106011 G>A maps to NM_015302.1 Q96Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4MR-01A-11D-A28B-09 chr19:36110934 C>A maps to NM_015302.1 V476V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr9:19058187 G>A maps to NM_017645.3 P859P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FQ-01A-31D-A387-09 chr23:152721027 G>A did not map to a codon.
Sequencing variant TCGA-VR-AA4D-01A-11D-A37C-09 chr5:156535949 C>T maps to NM_032782.3 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NV-01A-11D-A37C-09 chr1:154245865 A>G maps to NM_006118.3 E36E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S8-A6BW-01A-11D-A31U-09 chr11:5248188 C>A maps to NM_000518.4 V21V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88S-01A-11D-A36J-09 chr11:5290890 G>T maps to NM_005330.3 Y36*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NE-01A-11D-A37C-09 chr11:5290749 C>T maps to NM_005330.3 K83K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RE-A7BO-01A-11D-A33E-09 chr11:5290788 A>C maps to NM_005330.3 T70T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8WG-01A-11D-A37C-09 chr11:5269621 T>G maps to ENST00000440157 A142A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GL-01A-12D-A37C-09 chr11:5274578 G>C maps to ENST00000399563 T129T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6Y0-01B-11D-A33E-09 chr11:5275626 A>C maps to ENST00000399563 T75T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A5S3-01A-11D-A28B-09 chr6:135357716 T>C maps to NM_001145207.1 K626K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A939-01A-12D-A37C-09 chr23:11139817 G>A did not map to a codon.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr23:11135399 A>T did not map to a codon.
Sequencing variant TCGA-2H-A9GM-01A-11D-A37C-09 chr23:153222952 A>G did not map to a codon.
Sequencing variant TCGA-IG-A3YC-01A-11D-A247-09 chr23:153220289 C>A did not map to a codon.
Sequencing variant TCGA-JY-A6FD-01A-11D-A33E-09 chr23:153219808 A>G did not map to a codon.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr23:153220902 C>T did not map to a codon.
Sequencing variant TCGA-L5-A8NQ-01A-11D-A36J-09 chr23:153221702 G>A did not map to a codon.
Sequencing variant TCGA-L5-A88S-01A-11D-A36J-09 chr16:3073310 G>A maps to NM_017885.2 F68F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A5U7-01A-11D-A31U-09 chr12:104458352 C>T maps to NM_013320.2 S5S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RE-A7BO-01A-11D-A33E-09 chr12:104492153 A>T maps to NM_013320.2 K592*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GG-01A-11D-A37C-09 chr5:45262094 A>T maps to NM_021072.2 L867L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RE-01A-11D-A33E-09 chr5:45262547 A>T maps to NM_021072.2 T716T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A51D-01A-11D-A27G-09 chr5:45262429 G>A maps to NM_021072.2 Q756*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88T-01A-11D-A351-09 chr5:45645327 G>A maps to NM_021072.2 R270*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6DN-01B-11D-A31U-09 chr5:45262334 G>A maps to NM_021072.2 S787S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-A7RE-01A-11D-A351-09 chr5:45262168 G>A maps to NM_021072.2 R843*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A8JD-01A-11D-A36J-09 chr5:45262501 G>A maps to NM_021072.2 Q732*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OT-01A-11D-A28B-09 chr15:73617464 G>A maps to NM_005477.2 F603F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XP-A8T7-01A-11D-A36J-09 chr1:32084942 C>T maps to NM_001525.2 I50I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GJ-01A-11D-A37C-09 chr6:55039442 G>T maps to NM_001526.3 E20*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr6:55145210 T>C maps to NM_001526.3 A358A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-A7RC-01B-11D-A403-09 chr1:32768244 G>T maps to NM_004964.2 G25*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EQ-01A-11D-A36J-09 chr1:32782360 G>A maps to NM_004964.2 E86E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr3:13546119 T>C maps to NM_024827.3 P327P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NG-01A-11D-A37C-09 chr6:114277792 G>A maps to ENST00000398283 G210G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr5:141005622 C>T maps to NM_003883.3 S312S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GL-01A-12D-A37C-09 chr2:240085518 G>A maps to NM_006037.3 S197S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3YB-01A-11D-A247-09 chr17:42162042 G>T maps to NM_001015053.1 R730R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EX-01A-11D-A36J-09 chr17:42160015 T>A maps to NM_001015053.1 V849V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr23:48681612 G>T did not map to a codon.
Sequencing variant TCGA-L5-A8NL-01A-12D-A37C-09 chr23:48676793 G>A did not map to a codon.
Sequencing variant TCGA-M9-A5M8-01A-11D-A28B-09 chr23:48664041 G>A did not map to a codon.
Sequencing variant TCGA-2H-A9GJ-01A-11D-A37C-09 chr7:18687496 C>A maps to NM_178425.2 I375I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43I-01A-11D-A247-09 chr7:18788704 C>T maps to NM_178425.2 R663*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr7:18869171 G>T did not map to a codon.
Sequencing variant TCGA-L5-A88T-01A-11D-A351-09 chr7:19015466 A>C maps to NM_178425.2 R1021R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6Y2-01B-11D-A33E-09 chr7:18788725 C>T maps to NM_178425.2 R670*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NL-01A-12D-A37C-09 chr15:50544899 G>T maps to NM_002112.3 R287R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88T-01A-11D-A351-09 chr15:91475175 T>C did not map to a codon.
Sequencing variant TCGA-LN-A4A9-01A-11D-A28B-09 chr23:6995435 G>A did not map to a codon.
Sequencing variant TCGA-LN-A5U7-01A-11D-A31U-09 chr18:44639383 G>A maps to NM_032124.4 Q214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A8HZ-01A-11D-A36J-09 chr9:116136523 C>T maps to NM_031219.2 G37G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FG-01A-11D-A33E-09 chr2:242181873 C>A did not map to a codon.
Sequencing variant TCGA-JY-A6FG-01A-11D-A33E-09 chr23:83724052 C>A did not map to a codon.
Sequencing variant TCGA-L5-A893-01A-11D-A36J-09 chr23:83724242 T>G did not map to a codon.
Sequencing variant TCGA-L5-A8NK-01A-21D-A37C-09 chr23:83599382 G>T did not map to a codon.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr23:83616577 G>T did not map to a codon.
Sequencing variant TCGA-L5-A8NW-01A-11D-A37C-09 chr23:83599351 T>A did not map to a codon.
Sequencing variant TCGA-RE-A7BO-01A-11D-A33E-09 chr23:83599321 T>C did not map to a codon.
Sequencing variant TCGA-LN-A49M-01A-21D-A27G-09 chr1:236740142 C>T maps to NM_018072.5 L954L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8W8-01B-11D-A37C-09 chr14:73987651 G>A maps to ENST00000334988 Q278*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OG-01A-11D-A27G-09 chr2:37276983 G>A maps to NM_019024.1 G836G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASX-01A-11D-A387-09 chr2:37255141 G>A maps to NM_019024.1 I1259I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OH-01A-11D-A27G-09 chr17:58121220 G>T maps to NM_022070.4 A1083A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr8:145267981 G>A maps to NM_001099281.1 P409P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OO-01A-11D-A27G-09 chr8:145245829 G>T maps to NM_032450.2 E236*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A1-01A-21D-A27G-09 chr5:41015518 C>T maps to ENST00000296803 V983V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6L6-01B-11D-A33E-09 chr5:41018509 G>C maps to ENST00000296803 S900*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OR-01A-11D-A27G-09 chr14:31647369 G>A maps to NM_015382.2 A77A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A8I1-01A-11D-A36J-09 chr10:93250955 G>A did not map to a codon.
Sequencing variant TCGA-L5-A4OO-01A-11D-A27G-09 chr7:43351451 C>T maps to NM_015052.3 R40*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr7:43484921 G>A maps to NM_015052.3 T717T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6DQ-01B-11D-A31U-09 chr7:43506044 G>T did not map to a codon.
Sequencing variant TCGA-R6-A6L6-01B-11D-A33E-09 chr7:43360232 G>T did not map to a codon.
Sequencing variant TCGA-IG-A3YB-01A-11D-A247-09 chr2:197184301 C>A maps to NM_020760.1 E438*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr2:197184626 A>G maps to NM_020760.1 D329D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OU-01A-11D-A28B-09 chr3:124739729 T>C maps to NM_020733.1 R386R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EP-01A-31D-A403-09 chr12:66703556 T>G maps to NM_033647.2 L283L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FD-01A-11D-A33E-09 chr9:100692386 T>C maps to NM_018437.3 T430T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A4QS-01A-11D-A27G-09 chr23:65486414 T>G did not map to a codon.
Sequencing variant TCGA-L5-A4OW-01A-11D-A28B-09 chr23:65413354 A>C did not map to a codon.
Sequencing variant TCGA-L7-A6VZ-01A-12D-A33E-09 chr23:65428032 G>A did not map to a codon.
Sequencing variant TCGA-LN-A49L-01A-11D-A247-09 chr23:65411971 A>T did not map to a codon.
Sequencing variant TCGA-V5-A7RB-01A-11D-A351-09 chr23:65415043 G>T did not map to a codon.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr11:93844769 C>T maps to NM_001098672.1 N1092N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GJ-01A-11D-A37C-09 chr15:63918206 G>A maps to ENST00000261887 L4418L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RE-01A-11D-A33E-09 chr15:64005603 G>A maps to ENST00000261887 Q1471*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NJ-01A-11D-A36J-09 chr15:63991148 G>A maps to ENST00000261887 R1561R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NJ-01A-11D-A36J-09 chr15:64027048 C>G did not map to a codon.
Sequencing variant TCGA-R6-A8W5-01B-11D-A37C-09 chr15:63961884 A>G maps to ENST00000261887 S2686S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA7D-01A-11D-A403-09 chr15:64026960 G>A maps to ENST00000261887 Q870*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A8JE-01A-11D-A37C-09 chr15:64021786 G>T maps to ENST00000261887 S977*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A51D-01A-11D-A27G-09 chr15:28361835 C>A maps to NM_004667.4 V4528V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FB-01A-11D-A33E-09 chr15:28408275 G>A maps to NM_004667.4 S3570S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NK-01A-21D-A37C-09 chr15:28501403 G>A maps to NM_004667.4 S859S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XP-A8T7-01A-11D-A36J-09 chr15:28514545 C>A maps to NM_004667.4 G432*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L7-A6VZ-01A-12D-A33E-09 chr4:89576390 G>T maps to NM_014606.1 E282*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49R-01A-11D-A247-09 chr4:89601386 G>T maps to NM_014606.1 T780T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OH-01A-11D-A27G-09 chr4:89338610 G>T maps to NM_017912.3 L531L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr7:35675004 C>T maps to NM_022373.4 Q227Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-M9-A5M8-01A-11D-A28B-09 chr3:193854763 C>T maps to NM_005524.2 S73S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr1:40092235 C>T maps to NM_014571.3 A310A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4MR-01A-11D-A28B-09 chr1:40092513 G>A maps to NM_014571.3 R218*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6XG-01B-11D-A33E-09 chr1:145416450 C>T maps to NM_213653.3 Q266*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FO-01A-11D-A387-09 chr1:91727918 G>A maps to NM_001017975.3 L1373L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93F-01A-21D-A37C-09 chr4:3443799 G>C maps to ENST00000511533 L24L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43C-01A-11D-A247-09 chr4:3446080 C>T maps to ENST00000511533 G214G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XP-A8T7-01A-11D-A36J-09 chr4:3443799 G>C maps to ENST00000511533 L24L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NQ-01A-11D-A36J-09 chr17:79667620 G>T maps to NM_004712.4 A669A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8W8-01B-11D-A37C-09 chr17:79662868 G>A maps to NM_004712.4 A411A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EO-01A-11D-A36J-09 chr17:79662970 C>T maps to NM_004712.4 S445S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GR-01A-12D-A37C-09 chr3:42740346 G>T maps to NM_020707.3 G112G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OT-01A-11D-A28B-09 chr10:94454488 C>T maps to NM_002729.4 D259D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FH-01A-11D-A33E-09 chr1:222717195 G>A maps to NM_024746.3 P219P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93D-01A-11D-A387-09 chr1:222712024 G>A maps to NM_024746.3 L514L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-AAPN-01A-11D-A403-09 chr1:222717195 G>T maps to NM_024746.3 P219P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NI-01A-11D-A37C-09 chr1:100547617 G>C maps to NM_033055.2 L442L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr9:97203356 C>T maps to NM_032558.2 H162H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FO-01A-11D-A387-09 chr17:1961208 G>T maps to NM_001098202.1 E428*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RE-01A-11D-A33E-09 chr22:21800740 G>T maps to NM_015094.2 T519T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GQ-01A-11D-A37C-09 chr14:62193490 A>G maps to ENST00000394997 L176L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FE-01A-11D-A33E-09 chr19:46832498 C>G maps to NM_152795.2 P492P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49Y-01A-11D-A27G-09 chr7:75186054 C>A maps to NM_005338.4 E548*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A8I0-01A-11D-A36J-09 chr7:75182802 G>T maps to NM_005338.4 A748A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GH-01A-11D-A37C-09 chr7:139268761 G>A maps to NM_022740.4 H922H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr11:33308838 C>A maps to NM_005734.3 P293P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NR-01A-11D-A37C-09 chr22:19384324 G>T maps to NM_003325.3 T213T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EZ-01A-11D-A36J-09 chr16:30006910 C>A maps to NM_003609.3 E6*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZR-A9CJ-01B-11D-A387-09 chr6:27835244 C>T maps to NM_005322.2 K21K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FO-01A-11D-A387-09 chr6:26056023 C>T maps to NM_005319.3 K211K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RF-01A-13D-A33E-09 chr6:26124547 C>T maps to NM_003512.3 R30*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A6-01A-11D-A27G-09 chr6:27833152 G>A maps to NM_003511.2 Q7Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EX-01A-11D-A36J-09 chr6:27860561 C>T maps to NM_003514.2 E122E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A8HZ-01A-11D-A36J-09 chr6:26124065 G>A maps to NM_003526.2 Q23*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49Y-01A-11D-A27G-09 chr6:26184244 C>T maps to NM_003523.2 I74I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3Y9-01A-12D-A247-09 chr6:27114568 T>C maps to NM_080593.2 E3E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr6:27806813 C>A maps to NM_003520.3 S125S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3YC-01A-11D-A247-09 chr6:26031994 C>T maps to NM_003537.3 E98E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49X-01A-31D-A27G-09 chr6:26032005 C>A maps to NM_003537.3 E95*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6DN-01B-11D-A31U-09 chr6:26045793 C>T maps to NM_003531.2 I52I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HW-01A-22D-A351-09 chr6:26271356 G>A maps to NM_003534.2 Q86*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43I-01A-11D-A247-09 chr6:27777904 C>T maps to NM_003536.2 R18R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NW-01A-11D-A37C-09 chr6:26027468 G>A maps to NM_003544.2 R4R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A8JE-01A-11D-A37C-09 chr6:26104466 C>T maps to NM_003542.3 L98L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43I-01A-11D-A247-09 chr6:26205069 G>A maps to NM_003545.3 V66V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-A7RE-01A-11D-A351-09 chr6:27798994 C>G maps to NM_003541.2 *104S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49X-01A-31D-A27G-09 chr1:149398804 C>G maps to NM_001024599.3 S125S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A9VB-01A-21D-A37C-09 chr12:14923991 C>T maps to NM_175054.2 K9K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88V-01A-11D-A351-09 chr6:12126084 G>A maps to NM_002114.2 W2019*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NN-01A-11D-A37C-09 chr6:12130056 C>T maps to NM_002114.2 N2047N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49R-01A-11D-A247-09 chr6:12125355 C>T maps to NM_002114.2 D1776D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A2-01A-31D-A27G-09 chr6:12125242 G>T maps to NM_002114.2 E1739*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HV-01A-21D-A351-09 chr6:12161990 G>A maps to NM_002114.2 R2269R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HW-01A-22D-A351-09 chr6:12164526 C>T maps to NM_002114.2 L2664L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FO-01A-11D-A387-09 chr6:143081379 T>C maps to NM_006734.3 R2015R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OW-01A-11D-A28B-09 chr1:42049976 G>A maps to NM_024503.3 F164F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8W5-01B-11D-A37C-09 chr1:41979410 G>A maps to NM_024503.3 D1827D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EQ-01A-11D-A36J-09 chr1:42046255 T>G maps to NM_024503.3 R1405R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A7DP-01A-31D-A33E-09 chr2:234749813 G>A maps to NM_018410.3 Q538*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-AAPN-01A-11D-A403-09 chr2:75104435 C>G maps to NM_000189.4 S340*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NR-01A-11D-A37C-09 chr5:176308316 G>T maps to NM_002115.2 Y871*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8W5-01B-11D-A37C-09 chr5:176314482 G>T maps to NM_002115.2 P523P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GF-01A-11D-A37C-09 chr10:71026452 A>G maps to NM_025130.3 K898K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OP-01A-11D-A27G-09 chr19:37853617 G>T maps to NM_181786.2 G307G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASX-01A-11D-A387-09 chr6:29912283 T>G maps to ENST00000376806 S301S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A8JE-01A-11D-A37C-09 chr6:29910768 G>A maps to ENST00000376806 G103G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93F-01A-21D-A37C-09 chr6:31323324 C>A maps to ENST00000428231 E292*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASX-01A-11D-A387-09 chr6:31323207 C>A maps to ENST00000428231 G331*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FP-01A-31D-A387-09 chr6:32917463 G>A maps to NM_006120.3 F192F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FG-01A-11D-A33E-09 chr6:32975250 G>A maps to NM_002119.3 N150N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93D-01A-11D-A387-09 chr6:33043880 G>T maps to NM_002121.4 V21V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A8O2-01A-11D-A36J-09 chr6:29691239 C>T did not map to a codon.
Sequencing variant TCGA-L5-A8NR-01A-11D-A37C-09 chr6:29795962 G>A maps to ENST00000376828 P76P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GR-01A-12D-A37C-09 chr21:38139567 C>T maps to NM_000411.5 P490P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93D-01A-11D-A387-09 chr1:221055545 G>A maps to NM_021958.3 T271T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XP-A8T6-01A-11D-A36J-09 chr20:30126008 C>T maps to NM_178581.1 L104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GM-01A-11D-A37C-09 chr1:185878593 G>T maps to NM_031935.2 V249V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RE-01A-11D-A33E-09 chr1:186083995 T>C maps to NM_031935.2 H3774H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3Y9-01A-12D-A247-09 chr1:185902923 C>G maps to NM_031935.2 S599*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A5B8-01A-11D-A28B-09 chr1:186050411 G>A maps to NM_031935.2 L2891L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr1:185951460 C>A maps to NM_031935.2 P910P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49R-01A-11D-A247-09 chr1:186092110 G>A maps to NM_031935.2 K4086K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A6-01A-11D-A27G-09 chr1:185985348 C>T maps to NM_031935.2 I1723I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HX-01A-11D-A33E-09 chr1:185902945 C>G maps to NM_031935.2 L606L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A8HZ-01A-11D-A36J-09 chr1:186113435 G>T maps to NM_031935.2 E4686*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6KZ-01A-11D-A31U-09 chr1:186031029 C>T maps to NM_031935.2 Q2454*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6XG-01B-11D-A33E-09 chr1:186017921 A>T maps to NM_031935.2 A2176A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASX-01A-11D-A387-09 chr1:186088916 C>G maps to NM_031935.2 V3999V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASX-01A-11D-A387-09 chr1:186097327 C>A maps to NM_031935.2 S4270*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASW-01A-11D-A403-09 chr15:77759474 G>A maps to NM_018200.2 K92K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GH-01A-11D-A37C-09 chr4:174253278 C>T maps to NM_002129.3 E194E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr4:174254085 G>A maps to NM_002129.3 G119G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A893-01A-11D-A36J-09 chr23:150156359 G>A did not map to a codon.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr23:150155676 G>A did not map to a codon.
Sequencing variant TCGA-VR-A8EP-01A-31D-A403-09 chr1:34329980 G>C maps to NM_145205.4 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-A7RC-01B-11D-A403-09 chr5:74639789 G>C did not map to a codon.
Sequencing variant TCGA-S8-A6BW-01A-11D-A31U-09 chr21:40720241 C>T maps to NM_004965.6 A34A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GR-01A-12D-A37C-09 chr23:80371810 T>G did not map to a codon.
Sequencing variant TCGA-IG-A3YA-01A-11D-A247-09 chr23:80371789 G>T did not map to a codon.
Sequencing variant TCGA-L5-A4OH-01A-11D-A27G-09 chr23:80371789 G>T did not map to a codon.
Sequencing variant TCGA-L5-A8NS-01A-12D-A37C-09 chr23:80370664 T>C did not map to a codon.
Sequencing variant TCGA-LN-A49K-01A-11D-A247-09 chr23:80371789 G>T did not map to a codon.
Sequencing variant TCGA-JY-A6FD-01A-11D-A33E-09 chr22:35659856 C>G maps to NM_001003681.2 Y83*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GK-01A-11D-A37C-09 chr19:1083035 G>T maps to NM_012292.2 S905S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OG-01A-11D-A27G-09 chr19:1068534 C>T maps to NM_012292.2 H71H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr19:1073741 C>T maps to NM_012292.2 S240S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr10:124907929 G>A maps to NM_005519.1 P12P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88V-01A-11D-A351-09 chr10:124895956 C>T maps to NM_001105574.1 R131*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NR-01A-11D-A37C-09 chr10:124896928 G>T maps to NM_001105574.1 L252L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NH-01A-11D-A37C-09 chr16:1748983 C>T maps to ENST00000382711 S214S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8WC-01A-11D-A37C-09 chr16:1735556 T>C maps to ENST00000382711 P82P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FA-01A-11D-A33E-09 chr12:121431998 C>G maps to NM_000545.5 S249*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FA-01A-11D-A33E-09 chr12:121432188 C>G maps to NM_000545.5 L312L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GI-01A-11D-A37C-09 chr20:43048460 G>A maps to ENST00000338692 L309L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FG-01A-11D-A33E-09 chr20:43057080 C>T maps to ENST00000338692 L442L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49O-01A-11D-A247-09 chr20:43058229 G>A maps to ENST00000338692 P480P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A1-01A-21D-A27G-09 chr20:43052980 T>C maps to NM_178850.1 L406L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4MR-01A-11D-A28B-09 chr5:137089437 T>C maps to NM_006805.3 K106K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NW-01A-11D-A37C-09 chr12:54675945 G>T maps to NM_031157.2 E118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FH-01A-11D-A33E-09 chr5:179045244 G>T maps to NM_005520.2 R206R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-AAPN-01A-11D-A403-09 chr5:179047894 G>C maps to NM_005520.2 S132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASX-01A-11D-A387-09 chr10:70097636 G>A maps to NM_012207.2 G45G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr9:86586595 G>A maps to NM_031262.2 Y333Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6DQ-01B-11D-A31U-09 chr9:86587851 G>T maps to NM_031262.2 C184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A97H-01A-11D-A387-09 chr19:8536250 C>T maps to NM_005968.3 Q313*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EU-01A-11D-A36J-09 chr4:83350555 T>C maps to NM_031372.2 Q96Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q9-A6FU-01A-11D-A31U-09 chr19:12876824 C>G maps to NM_013312.2 L505L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6Y0-01B-11D-A33E-09 chr19:12881825 C>A maps to NM_013312.2 A274A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-AAPN-01A-11D-A403-09 chr19:12882119 G>C maps to NM_013312.2 S205*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L7-A6VZ-01A-12D-A33E-09 chr8:42823326 G>A maps to NM_032410.3 A364A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8WC-01A-11D-A37C-09 chr4:57522151 G>A maps to NM_032495.5 T23T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GM-01A-11D-A37C-09 chr7:27135318 G>A maps to NM_005522.4 H71H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NR-01A-11D-A37C-09 chr7:27134094 C>G maps to NM_005522.4 G324G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6Y0-01B-11D-A33E-09 chr7:27135318 G>A maps to NM_005522.4 H71H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49N-01A-11D-A247-09 chr7:27148112 C>T maps to NM_153631.2 K251K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8WC-01A-11D-A37C-09 chr7:27170322 G>T maps to NM_002141.4 S10S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NI-01A-11D-A37C-09 chr17:46621975 C>A maps to NM_002145.3 E100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr17:46628043 G>A maps to NM_002146.4 G316G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EZ-01A-11D-A36J-09 chr17:46627743 A>G maps to NM_002146.4 P416P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OW-01A-11D-A28B-09 chr17:46690706 G>T maps to NM_024016.3 R197R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GL-01A-12D-A37C-09 chr12:54350292 C>T maps to NM_173860.1 N264N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A97I-01A-11D-A387-09 chr12:54394502 G>A maps to NM_006897.1 L177L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-A7RB-01A-11D-A351-09 chr12:54396371 G>T maps to NM_006897.1 E233*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A8O2-01A-11D-A36J-09 chr2:176982184 G>A maps to NM_002148.3 Q208Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr2:176996150 C>T maps to NM_019558.3 I228I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A9VB-01A-21D-A37C-09 chr1:21083670 C>A maps to NM_016287.3 S323S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NU-01A-11D-A36J-09 chr1:33354762 G>A maps to NM_002143.2 A88A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr1:45793176 C>T maps to NM_032756.2 A119A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RE-A7BO-01A-11D-A33E-09 chr10:100185456 G>C maps to NM_000195.2 A392A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GN-01A-11D-A37C-09 chr3:148877871 G>T maps to NM_032383.3 E638*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NS-01A-12D-A37C-09 chr3:148857971 G>A maps to NM_032383.3 S133S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NW-01A-11D-A37C-09 chr3:148868388 C>T maps to NM_032383.3 N389N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A97H-01A-11D-A387-09 chr22:26860749 C>T maps to NM_022081.4 Q282Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A97H-01A-11D-A387-09 chr11:18327773 C>T maps to NM_181507.1 R244R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93C-01A-11D-A387-09 chr11:18303558 A>G maps to NM_181507.1 L1089L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NT-01A-11D-A37C-09 chr10:100503679 G>A maps to NM_021828.4 S248S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6F8-01A-11D-A33E-09 chr11:6461929 G>A maps to NM_000613.2 G38G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr11:6461397 G>T maps to NM_000613.2 I111I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr8:21984703 G>A maps to NM_005144.4 P417P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NQ-01A-11D-A36J-09 chr19:49657885 C>T maps to NM_002152.2 E203E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L7-A6VZ-01A-12D-A33E-09 chr19:49658060 G>T maps to NM_002152.2 S145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GK-01A-11D-A37C-09 chr5:175110524 C>T maps to NM_001131055.1 L97L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA4G-01A-11D-A37C-09 chr5:175110301 C>A maps to NM_001131055.1 T22T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GK-01A-11D-A37C-09 chr1:152192298 A>T maps to NM_001009931.1 S602S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RE-01A-11D-A33E-09 chr1:152191662 A>C maps to NM_001009931.1 A814A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3YA-01A-11D-A247-09 chr1:152195672 G>T maps to NM_001009931.1 A19A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr1:152187978 G>A maps to NM_001009931.1 H2042H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OH-01A-11D-A27G-09 chr1:152195672 G>T maps to NM_001009931.1 A19A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr1:152187630 G>A maps to NM_001009931.1 R2158R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr1:152189040 G>A maps to NM_001009931.1 R1688R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr1:152192465 G>A maps to NM_001009931.1 R547*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OW-01A-11D-A28B-09 chr1:152188212 G>A maps to NM_001009931.1 Y1964Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NN-01A-11D-A37C-09 chr1:152186613 C>G maps to NM_001009931.1 S2497S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49W-01A-11D-A27G-09 chr1:152187117 G>A maps to NM_001009931.1 G2329G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASW-01A-11D-A403-09 chr1:152186613 C>G maps to NM_001009931.1 S2497S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XP-A8T7-01A-11D-A36J-09 chr1:152186613 C>G maps to NM_001009931.1 S2497S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HV-01A-21D-A351-09 chr1:87538710 C>T maps to NM_012262.3 D73D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GR-01A-12D-A37C-09 chr4:11401401 C>T maps to NM_005114.2 L76L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X8-AAAR-01A-11D-A403-09 chr4:11401464 C>T maps to NM_005114.2 P55P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FB-01A-11D-A33E-09 chr17:14248497 G>A maps to NM_006041.1 S236S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr16:25703776 G>A maps to NM_006040.2 P13P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L7-A6VZ-01A-12D-A33E-09 chr16:25703881 G>A maps to NM_006040.2 L48L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NE-01A-11D-A37C-09 chr23:132090939 G>T did not map to a codon.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr23:131762902 C>T did not map to a codon.
Sequencing variant TCGA-IG-A8O2-01A-11D-A36J-09 chr13:96743466 C>T maps to NM_153456.2 N117N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA7D-01A-11D-A403-09 chr13:97485217 C>T maps to NM_153456.2 R394R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A5B8-01A-11D-A28B-09 chr16:67470641 C>T maps to NM_000196.3 L318L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8WG-01A-11D-A37C-09 chr16:67470653 A>T maps to NM_000196.3 V322V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OE-01A-11D-A27G-09 chr17:40706596 G>A maps to NM_000413.2 A238A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASV-01A-11D-A387-09 chr23:53459302 G>A did not map to a codon.
Sequencing variant TCGA-IG-A8O2-01A-11D-A36J-09 chr11:43859884 G>A maps to NM_016142.2 L185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OJ-01A-11D-A27G-09 chr11:43772500 A>G maps to NM_016142.2 A67A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FQ-01A-31D-A387-09 chr19:49316482 C>A maps to NM_016246.2 G254G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49M-01A-21D-A27G-09 chr16:84163980 G>T maps to NM_031463.4 L92L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A5U7-01A-11D-A31U-09 chr6:122752626 C>A maps to NM_004506.3 S428*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NL-01A-12D-A37C-09 chr12:104335267 A>G maps to NM_003299.1 T391T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr10:118434561 A>C maps to NM_025015.2 R586R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OG-01A-11D-A27G-09 chr10:14912594 G>A did not map to a codon.
Sequencing variant TCGA-LN-A7HY-01A-12D-A351-09 chr6:31783685 C>T maps to NM_005345.5 I51I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49U-01A-31D-A27G-09 chr6:31797493 G>A maps to NM_005346.4 K589K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3I8-01A-11D-A247-09 chr14:65009114 C>T maps to NM_021979.3 D516D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3Y9-01A-12D-A247-09 chr14:65009363 G>A maps to NM_021979.3 Q599Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RF-01A-13D-A33E-09 chr5:137895633 C>T maps to NM_004134.6 L443L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A8HZ-01A-11D-A36J-09 chr5:137892471 A>G maps to NM_004134.6 P604P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6DQ-01B-11D-A31U-09 chr11:111784265 G>T maps to NM_001541.3 E66*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-A7RE-01A-11D-A351-09 chr17:40275104 G>A maps to NM_033194.2 V79V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A5U6-01A-11D-A28B-09 chr19:55790904 T>G maps to NM_012267.4 S24S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr1:22168101 G>A maps to NM_005529.5 H3086H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NW-01A-11D-A37C-09 chr1:22168801 G>A maps to NM_005529.5 A2994A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A5U7-01A-11D-A31U-09 chr1:22178377 G>A maps to NM_005529.5 A2304A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8WC-01A-11D-A37C-09 chr1:22201216 A>G maps to NM_005529.5 C1140C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A6QS-01A-12D-A33E-09 chr13:31725822 G>T maps to NM_006644.2 R196R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr13:31722126 G>T maps to NM_006644.2 P449P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A5S3-01A-11D-A28B-09 chr11:20385842 C>T maps to NM_001098520.1 S54S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr11:20388802 T>C maps to NM_001098520.1 G127G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GG-01A-11D-A37C-09 chr23:135585058 G>C did not map to a codon.
Sequencing variant TCGA-LN-A4A4-01A-11D-A27G-09 chr23:135594150 T>C did not map to a codon.
Sequencing variant TCGA-2H-A9GF-01A-11D-A37C-09 chr5:63256865 G>A maps to NM_000524.2 R227R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GG-01A-11D-A37C-09 chr5:63256805 G>T maps to NM_000524.2 A247A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr6:78172235 G>A maps to NM_000863.1 S295S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XP-A8T7-01A-11D-A36J-09 chr6:78172543 C>A maps to NM_000863.1 E193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr6:87726134 C>T maps to NM_000865.2 C361C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OP-01A-11D-A27G-09 chr23:114082576 C>T did not map to a codon.
Sequencing variant TCGA-IG-A3Y9-01A-12D-A247-09 chr11:113856797 C>T maps to NM_213621.3 V208V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EQ-01A-11D-A36J-09 chr11:113853940 C>T maps to NM_213621.3 S164S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GN-01A-11D-A37C-09 chr11:113803806 C>T maps to NM_006028.3 Q230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RE-A7BO-01A-11D-A33E-09 chr3:183772515 C>T maps to NM_130770.2 G25G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A5U5-01A-21D-A28B-09 chr3:183818348 G>A maps to NM_182589.2 V63V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6Y0-01B-11D-A33E-09 chr7:154863167 G>T maps to NM_024012.2 E187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr2:74757417 C>A maps to NM_013247.4 A95A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GQ-01A-11D-A37C-09 chr4:8271835 C>T maps to NM_053044.3 L47L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr4:8293254 C>T maps to NM_053044.3 S289S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASV-01A-11D-A387-09 chr4:8272042 G>A maps to NM_053044.3 T116T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NV-01A-11D-A37C-09 chr8:38840023 G>A maps to NM_153692.3 A374A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A4P3-01A-11D-A27G-09 chr4:3189557 G>T maps to NM_002111.6 E1724*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EX-01A-11D-A36J-09 chr4:3136264 C>T maps to NM_002111.6 F877F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A51D-01A-11D-A27G-09 chr21:33340685 C>G maps to NM_014586.1 T333T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FG-01A-11D-A33E-09 chr21:33370906 G>T maps to NM_014586.1 E519*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-A7RE-01A-11D-A351-09 chr6:656674 C>T maps to NM_148959.3 A90A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GF-01A-11D-A37C-09 chr23:53562354 C>T did not map to a codon.
Sequencing variant TCGA-2H-A9GK-01A-11D-A37C-09 chr23:53565334 C>T did not map to a codon.
Sequencing variant TCGA-IG-A3QL-01A-11D-A247-09 chr23:53641612 G>T did not map to a codon.
Sequencing variant TCGA-JY-A93D-01A-11D-A387-09 chr23:53630390 G>T did not map to a codon.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr23:53576404 C>T did not map to a codon.
Sequencing variant TCGA-L5-A4OG-01A-11D-A27G-09 chr23:53635827 A>T did not map to a codon.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr23:53577970 C>A did not map to a codon.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr23:53587250 C>T did not map to a codon.
Sequencing variant TCGA-L5-A4OJ-01A-11D-A27G-09 chr23:53575166 C>T did not map to a codon.
Sequencing variant TCGA-L5-A4OJ-01A-11D-A27G-09 chr23:53596599 G>T did not map to a codon.
Sequencing variant TCGA-L5-A4OJ-01A-11D-A27G-09 chr23:53658550 G>T did not map to a codon.
Sequencing variant TCGA-L5-A4OW-01A-11D-A28B-09 chr23:53602121 T>A did not map to a codon.
Sequencing variant TCGA-L5-A893-01A-11D-A36J-09 chr23:53561024 T>C did not map to a codon.
Sequencing variant TCGA-L5-A8NJ-01A-11D-A36J-09 chr23:53661226 G>T did not map to a codon.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr23:53570859 G>A did not map to a codon.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr23:53600795 C>T did not map to a codon.
Sequencing variant TCGA-L5-A8NT-01A-11D-A37C-09 chr23:53602168 C>T did not map to a codon.
Sequencing variant TCGA-LN-A49R-01A-11D-A247-09 chr23:53579694 G>T did not map to a codon.
Sequencing variant TCGA-LN-A4A5-01A-21D-A27G-09 chr23:53573488 A>C did not map to a codon.
Sequencing variant TCGA-Q9-A6FU-01A-11D-A31U-09 chr23:53575128 T>C did not map to a codon.
Sequencing variant TCGA-R6-A6XG-01B-11D-A33E-09 chr23:53600756 T>A did not map to a codon.
Sequencing variant TCGA-VR-A8EW-01A-11D-A36J-09 chr23:53631640 G>T did not map to a codon.
Sequencing variant TCGA-IG-A625-01A-11D-A31U-09 chr3:50357377 G>A maps to NM_033158.4 F181F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6Y0-01B-11D-A33E-09 chr7:123508662 C>G maps to NM_012269.2 L112L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EZ-01A-11D-A36J-09 chr7:123516965 C>T maps to NM_012269.2 N401N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr16:70889080 G>A maps to NM_032821.2 S4130S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49Y-01A-11D-A27G-09 chr16:70891650 G>T maps to NM_032821.2 I4083I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-A7RE-01A-11D-A351-09 chr16:71009106 C>T maps to NM_032821.2 Q1567Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XP-A8T8-01A-11D-A36J-09 chr16:70995940 C>T maps to NM_032821.2 W1962*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NN-01A-11D-A37C-09 chr11:118918723 G>C maps to NM_001130991.1 R815R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GO-01A-11D-A37C-09 chr2:9618380 A>G maps to NM_001039613.1 S55S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr9:95009782 G>T maps to ENST00000375660 G891G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A2-01A-31D-A27G-09 chr1:220318981 C>T maps to NM_018060.3 L961L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RE-01A-11D-A33E-09 chr4:88731762 T>G maps to NM_004967.3 T84T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FD-01A-11D-A33E-09 chr4:88732896 C>T maps to NM_004967.3 Y263Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr6:82935220 C>A maps to NM_015525.2 P266P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASX-01A-11D-A387-09 chr6:82924425 G>C maps to NM_015525.2 L574L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EP-01A-31D-A403-09 chr7:8260924 G>C maps to ENST00000422063 L120L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GI-01A-11D-A37C-09 chr19:10394883 G>A maps to NM_000201.2 S271S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A5B8-01A-11D-A28B-09 chr19:10395226 G>A maps to NM_000201.2 L358L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OJ-01A-11D-A27G-09 chr17:62082506 G>T maps to NM_001099789.1 S96S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr19:10403405 G>A maps to NM_003259.3 A360A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49W-01A-11D-A27G-09 chr19:10403908 G>A maps to NM_003259.3 T484T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FO-01A-11D-A387-09 chr19:10403824 G>A maps to NM_003259.3 L456L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43I-01A-11D-A247-09 chr10:94234655 G>T maps to NM_004969.3 L686L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NS-01A-12D-A37C-09 chr10:94223527 G>A maps to NM_004969.3 Y907Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6XG-01B-11D-A33E-09 chr20:2639429 A>C maps to NM_006899.2 S375S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OG-01A-11D-A27G-09 chr23:153052254 C>G did not map to a codon.
Sequencing variant TCGA-LN-A49S-01A-11D-A247-09 chr23:153051694 G>A did not map to a codon.
Sequencing variant TCGA-VR-A8EZ-01A-11D-A36J-09 chr10:1088604 C>T maps to NM_004508.2 R168R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RF-01A-13D-A33E-09 chr23:148571893 G>A did not map to a codon.
Sequencing variant TCGA-IG-A5B8-01A-11D-A28B-09 chr19:13264137 C>G maps to NM_004907.2 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OR-01A-11D-A27G-09 chr1:181058829 G>C maps to NM_016545.4 G264G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A8HZ-01A-11D-A36J-09 chr12:6660124 A>G maps to NM_001193457.1 R272R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A4-01A-11D-A27G-09 chr1:79107492 G>T maps to NM_006820.2 *453L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6Y2-01B-11D-A33E-09 chr10:91066976 C>T maps to NM_001547.4 R422*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6L4-01A-11D-A31U-09 chr11:308206 G>A maps to NM_006435.2 V5V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A97H-01A-11D-A387-09 chr9:21187113 G>A maps to NM_021068.2 S139S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6Y0-01B-11D-A33E-09 chr6:137540465 C>T did not map to a codon.
Sequencing variant TCGA-VR-AA7D-01A-11D-A403-09 chr21:34787210 G>T maps to ENST00000381995 L49L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FG-01A-11D-A33E-09 chr16:1621405 A>G did not map to a codon.
Sequencing variant TCGA-L5-A88W-01A-11D-A351-09 chr16:1568309 G>A maps to NM_014714.3 L1363L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A938-01A-11D-A37C-09 chr2:27679394 G>A maps to NM_015662.1 D1118D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr2:27695197 G>A maps to NM_015662.1 T481T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-AAPN-01A-11D-A403-09 chr2:27683888 G>A maps to NM_015662.1 F838F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NS-01A-12D-A37C-09 chr17:26656250 G>C maps to NM_174887.2 S128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FP-01A-31D-A387-09 chr20:42242549 G>C maps to NM_016004.2 A182A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6Y0-01B-11D-A33E-09 chr9:27056330 G>T did not map to a codon.
Sequencing variant TCGA-R6-A8W8-01B-11D-A37C-09 chr9:27060612 C>T maps to NM_025103.2 Q550*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FG-01A-11D-A33E-09 chr3:160037577 T>C maps to ENST00000483754 Q480Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OU-01A-11D-A28B-09 chr15:65623957 G>A maps to NM_004884.3 A396A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr15:65702607 G>A maps to NM_020962.1 N157N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HY-01A-12D-A351-09 chr15:65703487 C>T maps to NM_020962.1 Q97Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A97I-01A-11D-A387-09 chr15:99500553 C>G maps to NM_000875.3 P1329P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6KZ-01A-11D-A31U-09 chr15:99434635 G>A maps to NM_000875.3 A241A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASV-01A-11D-A387-09 chr15:99434833 C>T maps to NM_000875.3 C307C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A50L-01A-11D-A27G-09 chr6:160481679 C>T maps to NM_000876.2 R1065*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OT-01A-11D-A28B-09 chr6:160505028 G>T maps to NM_000876.2 E1961*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49M-01A-21D-A27G-09 chr6:160501185 C>G maps to NM_000876.2 V1904V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA4D-01A-11D-A37C-09 chr6:160523574 C>T maps to NM_000876.2 P2289P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XP-A8T8-01A-11D-A36J-09 chr6:160430067 A>T maps to NM_000876.2 R106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GI-01A-11D-A37C-09 chr16:1841563 C>T maps to NM_001146006.1 T323T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr16:1840900 C>G maps to NM_001146006.1 G544G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-AAPN-01A-11D-A403-09 chr16:1841182 G>C maps to NM_001146006.1 L450L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KH-A6WC-01A-11D-A33E-09 chr19:46627240 G>T maps to NM_207393.1 P84P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NH-01A-11D-A37C-09 chr1:201181076 A>G maps to NM_001164586.1 P2352P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EZ-01A-11D-A36J-09 chr1:201163372 G>A maps to NM_001164586.1 Q33Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A8JE-01A-11D-A37C-09 chr11:68701367 G>A maps to NM_002180.2 S508S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43H-01A-11D-A247-09 chr22:23235888 C>T maps to ENST00000410090 L73L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RE-01A-11D-A33E-09 chr23:130417079 T>G did not map to a codon.
Sequencing variant TCGA-L5-A4OE-01A-11D-A27G-09 chr23:130416536 G>T did not map to a codon.
Sequencing variant TCGA-L5-A8NU-01A-11D-A36J-09 chr23:130409497 A>C did not map to a codon.
Sequencing variant TCGA-R6-A6XQ-01B-11D-A33E-09 chr23:130417198 G>T did not map to a codon.
Sequencing variant TCGA-L5-A4OH-01A-11D-A27G-09 chr3:151174849 G>T maps to NM_178822.4 I96I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr3:151164702 A>G maps to NM_178822.4 I1022I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OU-01A-11D-A28B-09 chr3:151164486 A>G maps to NM_178822.4 I1094I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6Y2-01B-11D-A33E-09 chr3:118649027 G>A maps to NM_152538.2 S48S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OJ-01A-11D-A27G-09 chr11:18739478 C>T maps to NM_173588.3 L324L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6XQ-01B-11D-A33E-09 chr11:18727655 C>T maps to NM_173588.3 K1206K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3YA-01A-11D-A247-09 chr1:117142807 A>T maps to NM_001542.2 L615*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OS-01A-11D-A28B-09 chr1:117127483 G>A maps to NM_001542.2 H897H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A8JD-01A-11D-A36J-09 chr1:117156525 G>A maps to NM_001542.2 L231L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A891-01A-11D-A36J-09 chr16:21655703 G>A maps to NM_005849.2 L147L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OU-01A-11D-A28B-09 chr1:159898627 G>A maps to NM_001135050.1 D850D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FE-01A-11D-A33E-09 chr11:133789697 G>T maps to NM_014987.1 R1308R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49U-01A-31D-A27G-09 chr11:133796852 C>A maps to NM_014987.1 G589*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6F8-01A-11D-A33E-09 chr9:111640375 C>A maps to NM_003640.3 G1252*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88S-01A-11D-A36J-09 chr9:111688830 C>T maps to NM_003640.3 Q146Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZR-A9CJ-01B-11D-A387-09 chr9:111665945 T>A maps to NM_003640.3 S549S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EO-01A-11D-A36J-09 chr1:206653840 C>T maps to NM_014002.3 S464S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A4P3-01A-11D-A27G-09 chr11:117863956 G>T maps to NM_001558.3 V123V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OH-01A-11D-A27G-09 chr11:117859095 G>T did not map to a codon.
Sequencing variant TCGA-VR-A8EQ-01A-11D-A36J-09 chr11:117859095 G>T did not map to a codon.
Sequencing variant TCGA-2H-A9GK-01A-11D-A37C-09 chr9:34657095 G>A maps to NM_001142784.1 W132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A51D-01A-11D-A27G-09 chr5:158749445 C>T maps to NM_002187.2 T146T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49Y-01A-11D-A27G-09 chr19:18170808 G>T maps to NM_005535.1 G626G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EQ-01A-11D-A36J-09 chr23:117900498 G>T did not map to a codon.
Sequencing variant TCGA-L5-A4OJ-01A-11D-A27G-09 chr23:114242550 A>C did not map to a codon.
Sequencing variant TCGA-L5-A893-01A-11D-A36J-09 chr23:114239843 G>T did not map to a codon.
Sequencing variant TCGA-V5-AASX-01A-11D-A387-09 chr23:114245243 G>C did not map to a codon.
Sequencing variant TCGA-L5-A8NQ-01A-11D-A36J-09 chr15:81558084 C>T maps to NM_172217.3 L169L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr5:148754054 G>A maps to NM_014443.2 S140S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A8-01A-32D-A27G-09 chr22:17578724 C>T maps to NM_014339.5 L68L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA7D-01A-11D-A403-09 chr22:17586490 G>A maps to NM_014339.5 P314P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GH-01A-11D-A37C-09 chr3:9971728 A>T maps to NM_153461.2 K463*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NH-01A-11D-A37C-09 chr3:9975156 G>A maps to NM_153461.2 A752A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q9-A6FW-01A-31D-A31U-09 chr3:9970019 C>T maps to NM_153461.2 A374A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr3:57132269 G>A maps to NM_017563.3 D487D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr1:207010075 C>T maps to NM_153758.2 H61H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OT-01A-11D-A28B-09 chr1:207014365 T>C maps to NM_153758.2 C165C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88T-01A-11D-A351-09 chr1:207010151 G>A did not map to a codon.
Sequencing variant TCGA-L5-A8NR-01A-11D-A37C-09 chr1:206972298 G>A maps to NM_153758.2 V20V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6Y2-01B-11D-A33E-09 chr2:113539199 G>A maps to NM_000575.3 I100I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NQ-01A-11D-A36J-09 chr2:113788673 C>G maps to NM_173178.1 L24L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8ER-01A-11D-A36J-09 chr2:102632363 G>T maps to NM_004633.3 E122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RF-01A-13D-A33E-09 chr23:29417386 G>T did not map to a codon.
Sequencing variant TCGA-L5-A88Z-01A-11D-A36J-09 chr23:29301301 A>T did not map to a codon.
Sequencing variant TCGA-L5-A8NH-01A-11D-A37C-09 chr23:29938111 A>C did not map to a codon.
Sequencing variant TCGA-L5-A8NI-01A-11D-A37C-09 chr23:29973906 G>A did not map to a codon.
Sequencing variant TCGA-L5-A8NN-01A-11D-A37C-09 chr23:29973624 C>T did not map to a codon.
Sequencing variant TCGA-LN-A49Y-01A-11D-A27G-09 chr23:29301328 C>A did not map to a codon.
Sequencing variant TCGA-L5-A88S-01A-11D-A36J-09 chr23:105011644 T>G did not map to a codon.
Sequencing variant TCGA-LN-A49Y-01A-11D-A27G-09 chr23:104992961 A>C did not map to a codon.
Sequencing variant TCGA-R6-A6L4-01A-11D-A31U-09 chr23:105011434 C>A did not map to a codon.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr2:102851426 G>A maps to NM_003854.2 S456S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88S-01A-11D-A36J-09 chr2:102835497 G>T maps to NM_003854.2 V270V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XP-A8T8-01A-11D-A36J-09 chr2:102808450 T>C maps to NM_003854.2 T120T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OF-01A-11D-A27G-09 chr3:136699395 G>A maps to NM_144717.3 A59A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA4G-01A-11D-A37C-09 chr16:27460099 C>T maps to NM_181079.4 Y393Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EQ-01A-11D-A36J-09 chr1:24465106 G>T maps to NM_021258.2 G47G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA4D-01A-11D-A37C-09 chr1:24447324 G>T maps to NM_021258.2 G565G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L7-A6VZ-01A-12D-A33E-09 chr6:137468891 G>T maps to NM_052962.2 Y203*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASW-01A-11D-A403-09 chr6:137476102 C>T maps to NM_052962.2 T149T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88W-01A-11D-A351-09 chr1:67724811 A>G did not map to a codon.
Sequencing variant TCGA-R6-A6Y2-01B-11D-A33E-09 chr14:23844854 G>A maps to NM_022789.3 R100R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88W-01A-11D-A351-09 chr16:28511193 C>T maps to NM_145659.3 E170E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EZ-01A-11D-A36J-09 chr16:28511193 C>T maps to NM_145659.3 E170E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EZ-01A-11D-A36J-09 chr16:28511196 T>C maps to NM_145659.3 E169E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GN-01A-11D-A37C-09 chr19:14160007 C>T maps to NM_004843.2 A428A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49S-01A-11D-A247-09 chr19:14157365 G>T maps to NM_004843.2 G359G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr19:39760219 C>T maps to NM_172138.1 D121D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93E-01A-11D-A37C-09 chr10:6063543 G>A maps to NM_000417.2 H160H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr23:70330526 G>A did not map to a codon.
Sequencing variant TCGA-V5-A7RB-01A-11D-A351-09 chr23:70330006 G>T did not map to a codon.
Sequencing variant TCGA-Z6-A8JD-01A-11D-A36J-09 chr23:70327738 C>G did not map to a codon.
Sequencing variant TCGA-IG-A5S3-01A-11D-A28B-09 chr5:131398417 G>A maps to NM_000588.3 T131T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NR-01A-11D-A37C-09 chr5:55164733 T>G maps to NM_139017.4 T90T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr16:70690942 C>T maps to NM_152456.2 D107D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NR-01A-11D-A37C-09 chr23:1497626 C>T did not map to a codon.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr7:22767196 C>T maps to NM_000600.3 R52*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88S-01A-11D-A36J-09 chr5:55256371 T>A maps to NM_002184.3 T277T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GR-01A-12D-A37C-09 chr8:79652242 A>G maps to NM_000880.3 A74A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93F-01A-21D-A37C-09 chr8:79710312 T>C maps to NM_000880.3 Q47Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GL-01A-12D-A37C-09 chr5:35876524 T>G maps to NM_002185.2 T439T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FB-01A-11D-A33E-09 chr5:35873731 G>T maps to NM_002185.2 E230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6XG-01B-11D-A33E-09 chr5:35876107 T>G maps to NM_002185.2 P300P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RF-01A-13D-A33E-09 chr5:135228157 G>T maps to NM_000590.1 G119G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A893-01A-11D-A36J-09 chr23:155234143 A>C did not map to a codon.
Sequencing variant TCGA-LN-A49X-01A-31D-A27G-09 chr23:155233446 C>T did not map to a codon.
Sequencing variant TCGA-LN-A7HZ-01A-31D-A351-09 chr23:155239803 C>G did not map to a codon.
Sequencing variant TCGA-R6-A8WC-01A-11D-A37C-09 chr23:155234212 C>A did not map to a codon.
Sequencing variant TCGA-L5-A8NK-01A-21D-A37C-09 chr19:10789846 C>T maps to NM_017620.2 T242T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8Q7-01A-11D-A37C-09 chr11:6631754 C>T maps to NM_001014795.1 L424L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GF-01A-11D-A37C-09 chr7:110303711 T>C maps to NM_032549.2 K158K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr7:110303714 C>T maps to NM_032549.2 Q157Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OW-01A-11D-A28B-09 chr17:43922682 G>A maps to NM_175882.2 Q137Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XP-A8T6-01A-11D-A36J-09 chr17:43923000 T>C maps to NM_175882.2 D243D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A891-01A-11D-A36J-09 chr18:22008834 G>T maps to NM_018439.3 V56V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93E-01A-11D-A37C-09 chr7:128034541 C>T maps to NM_000883.3 Q554Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93E-01A-11D-A37C-09 chr7:128036729 G>A maps to NM_000883.3 A395A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FA-01A-11D-A33E-09 chr3:100963356 C>T maps to NM_016247.2 G606G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A938-01A-11D-A37C-09 chr3:100962489 A>C maps to NM_016247.2 T895T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NF-01A-11D-A37C-09 chr1:62579861 T>C maps to NM_176877.2 P1533P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A8O2-01A-11D-A36J-09 chr11:61897830 C>A maps to NM_001040694.1 R278R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FG-01A-11D-A33E-09 chr14:105180910 C>T maps to ENST00000252520 L1138L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GO-01A-11D-A37C-09 chr13:111372024 C>T maps to NM_005537.3 R339*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr7:120606728 T>C maps to NM_019071.2 A138A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A97H-01A-11D-A387-09 chr2:242662677 A>G maps to NM_032329.4 K224K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GM-01A-11D-A37C-09 chr7:41729787 G>T maps to NM_002192.2 C247*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A8HZ-01A-11D-A36J-09 chr2:121106885 C>T maps to NM_002193.2 D220D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49S-01A-11D-A247-09 chr2:74683271 C>G maps to ENST00000452361 S138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OR-01A-11D-A27G-09 chr2:206911273 G>A maps to NM_017759.4 Q343*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NU-01A-11D-A36J-09 chr2:99172217 C>A maps to NM_001134224.1 S595*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NV-01A-11D-A37C-09 chr10:134591285 G>T maps to NM_005539.3 R363R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OJ-01A-11D-A27G-09 chr1:38406366 G>T maps to ENST00000373026 A128A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FD-01A-11D-A33E-09 chr9:139327462 G>T maps to NM_019892.3 G408G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93E-01A-11D-A37C-09 chr9:139324164 G>A maps to NM_019892.3 Q633*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49Y-01A-11D-A27G-09 chr10:121565956 C>T maps to NM_014937.2 Q469*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EU-01A-11D-A36J-09 chr17:1412529 G>T maps to NM_016532.3 R166R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A4P3-01A-11D-A27G-09 chr11:71941178 G>T maps to NM_001567.3 V318V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RE-01A-11D-A33E-09 chr7:155090009 C>T maps to ENST00000344756 H5H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A8I0-01A-11D-A36J-09 chr7:155094455 G>A did not map to a codon.
Sequencing variant TCGA-2H-A9GR-01A-12D-A37C-09 chr9:5185503 G>T maps to NM_007179.2 C33*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A9-01A-11D-A28B-09 chr9:5185533 C>T maps to NM_007179.2 L23L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EQ-01A-11D-A36J-09 chr14:36004315 C>A maps to NM_032594.3 I286I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FD-01A-11D-A33E-09 chr19:7172393 G>T maps to NM_000208.2 S392*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr1:156814635 C>A did not map to a codon.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr1:156814955 G>A maps to NM_014215.2 Y783Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FP-01A-31D-A387-09 chr1:156815774 G>C maps to NM_014215.2 G649G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr7:1534465 G>T maps to ENST00000389470 P760P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XP-A8T7-01A-11D-A36J-09 chr7:1533525 G>C maps to ENST00000389470 S772S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HZ-01A-31D-A351-09 chr13:51948407 T>C maps to NM_012141.2 K680K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EU-01A-11D-A36J-09 chr1:212120047 C>T did not map to a codon.
Sequencing variant TCGA-JY-A6F8-01A-11D-A33E-09 chr8:95888447 G>T did not map to a codon.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr8:28628530 G>A maps to NM_018250.3 L544L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6F8-01A-11D-A33E-09 chr9:103035176 G>T maps to NM_014425.2 E535*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A4P3-01A-11D-A27G-09 chr3:48726144 G>T maps to ENST00000395509 S304*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FB-01A-11D-A33E-09 chr3:48732631 G>A maps to ENST00000395509 C31C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FH-01A-11D-A33E-09 chr3:48726154 G>T maps to ENST00000395509 R301R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RE-A7BO-01A-11D-A33E-09 chr3:48732763 G>T maps to ENST00000443964 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GI-01A-11D-A37C-09 chr6:33694506 C>T did not map to a codon.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr6:33696072 G>T maps to NM_054111.4 T68T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6XQ-01B-11D-A33E-09 chr6:33690742 G>T maps to NM_054111.4 I329I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr14:24654088 G>A maps to ENST00000458132 S502S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6XG-01B-11D-A33E-09 chr14:24657938 C>A maps to ENST00000458132 E19*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A891-01A-11D-A36J-09 chr13:98645241 G>T maps to NM_002271.4 E274*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-A7RE-01A-11D-A351-09 chr12:30805928 A>G maps to NM_006390.3 F682F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GQ-01A-11D-A37C-09 chr1:46165854 C>T maps to NM_005897.2 W513*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3Y9-01A-12D-A247-09 chr1:46193359 G>A maps to NM_005897.2 Q331*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KH-A6WC-01A-11D-A33E-09 chr1:46179998 G>T maps to NM_005897.2 L483L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NE-01A-11D-A37C-09 chr1:46193438 C>T maps to NM_005897.2 W304*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr2:237240169 C>T maps to ENST00000457693 A743A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GG-01A-11D-A37C-09 chr7:2623315 G>T maps to NM_152558.3 R249R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FG-01A-11D-A33E-09 chr7:2625839 A>G did not map to a codon.
Sequencing variant TCGA-L5-A43H-01A-11D-A247-09 chr7:2645632 T>C did not map to a codon.
Sequencing variant TCGA-L5-A88Z-01A-11D-A36J-09 chr7:2645595 C>T maps to NM_152558.3 S610S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8WG-01A-11D-A37C-09 chr7:2622227 G>C maps to NM_152558.3 L215L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8WC-01A-11D-A37C-09 chr3:51864627 G>A maps to NM_001085479.1 A92A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NQ-01A-11D-A36J-09 chr15:90992789 G>C did not map to a codon.
Sequencing variant TCGA-IG-A4P3-01A-11D-A27G-09 chr5:75888709 G>A maps to NM_006633.2 L289L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6DQ-01B-11D-A31U-09 chr5:75970312 C>T maps to NM_006633.2 N1102N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FD-01A-11D-A33E-09 chr23:53268413 G>C did not map to a codon.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr23:53285055 C>G did not map to a codon.
Sequencing variant TCGA-L5-A4OJ-01A-11D-A27G-09 chr23:53263496 G>A did not map to a codon.
Sequencing variant TCGA-L5-A4OW-01A-11D-A28B-09 chr23:53349733 C>T did not map to a codon.
Sequencing variant TCGA-L5-A8NL-01A-12D-A37C-09 chr23:53279887 C>A did not map to a codon.
Sequencing variant TCGA-L5-A88S-01A-11D-A36J-09 chr7:123150075 A>G maps to NM_178827.4 L137L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A2-01A-31D-A27G-09 chr7:123097573 G>C maps to NM_178827.4 S685*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OW-01A-11D-A28B-09 chr23:153281952 G>C did not map to a codon.
Sequencing variant TCGA-Z6-A9VB-01A-21D-A37C-09 chr23:153282027 G>A did not map to a codon.
Sequencing variant TCGA-VR-A8EW-01A-11D-A36J-09 chr6:79577391 G>T maps to NM_001010844.1 T33T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43C-01A-11D-A247-09 chr3:10255051 C>T maps to NM_001570.3 H230H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OH-01A-11D-A27G-09 chr3:10283812 G>T maps to NM_001570.3 S593S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NS-01A-12D-A37C-09 chr3:10261452 C>T maps to NM_001570.3 I331I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4MQ-01A-11D-A28B-09 chr3:10255057 G>A maps to NM_001570.3 K232K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr12:44180242 T>A maps to NM_016123.3 I410I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A97I-01A-11D-A387-09 chr15:78790409 G>A maps to NM_004136.2 S939S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr15:78762886 T>C maps to NM_004136.2 L215L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49W-01A-11D-A27G-09 chr15:78730684 C>T maps to NM_004136.2 D2D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88T-01A-11D-A351-09 chr5:131821979 G>T maps to NM_002198.2 Y210*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr1:234743088 G>A maps to NM_182972.2 Q520*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A5U7-01A-11D-A31U-09 chr19:50163081 G>A maps to NM_001571.5 P369P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-A7RE-01A-11D-A351-09 chr6:393166 C>T maps to NM_002460.3 G5G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6Y2-01B-11D-A33E-09 chr1:209963068 G>T maps to NM_006147.2 C374*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr14:24632611 A>G maps to NM_006084.4 P130P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43C-01A-11D-A247-09 chr19:44223000 G>A maps to NM_019612.3 S97S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NJ-01A-11D-A36J-09 chr19:44222749 G>T maps to NM_019612.3 E14*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A3-01A-11D-A27G-09 chr19:44223369 G>A maps to NM_019612.3 P220P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RE-01A-11D-A33E-09 chr19:44099418 G>A maps to NM_001007561.2 I24I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr13:110435019 C>T maps to NM_003749.2 P1127P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8W5-01B-11D-A37C-09 chr13:110436618 C>A maps to NM_003749.2 S594S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93F-01A-21D-A37C-09 chr23:107976166 C>T did not map to a codon.
Sequencing variant TCGA-R6-A6L6-01B-11D-A33E-09 chr23:107976117 C>A did not map to a codon.
Sequencing variant TCGA-VR-A8EW-01A-11D-A36J-09 chr23:107976075 C>A did not map to a codon.
Sequencing variant TCGA-VR-A8Q7-01A-11D-A37C-09 chr23:107977529 G>A did not map to a codon.
Sequencing variant TCGA-2H-A9GI-01A-11D-A37C-09 chr5:3600783 G>T maps to NM_024337.3 P458P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr5:3599697 C>T maps to NM_024337.3 G212G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr5:3599712 C>T maps to NM_024337.3 A217A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88V-01A-11D-A351-09 chr5:3599748 C>T maps to NM_024337.3 D229D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NJ-01A-11D-A36J-09 chr5:3599409 T>C maps to NM_024337.3 A116A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6L4-01A-11D-A31U-09 chr5:3599409 T>G maps to NM_024337.3 A116A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GH-01A-11D-A37C-09 chr5:2749613 G>T maps to NM_033267.4 T179T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93D-01A-11D-A387-09 chr5:1878121 G>A maps to NM_016358.2 L507L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OH-01A-11D-A27G-09 chr16:55361257 G>T maps to NM_024335.2 L118L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8ET-01A-11D-A403-09 chr16:55362816 C>T maps to NM_024335.2 C309C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr15:76633629 C>A maps to NM_145805.1 A317A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49V-01A-11D-A247-09 chr15:76632668 G>A maps to NM_145805.1 T188T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FQ-01A-31D-A387-09 chr15:76630257 C>T maps to NM_145805.1 C66C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6L6-01B-11D-A33E-09 chr15:76633521 C>T maps to NM_145805.1 I281I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FO-01A-11D-A387-09 chr15:74467243 G>T maps to NM_201526.1 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZR-A9CJ-01B-11D-A387-09 chr15:74426477 C>T maps to NM_001130137.1 N461N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6L6-01B-11D-A33E-09 chr14:77951087 G>T maps to NM_199296.2 R106R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NR-01A-11D-A37C-09 chr19:55966409 G>A maps to NM_024710.2 S177S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HY-01A-12D-A351-09 chr19:55966406 T>C maps to NM_024710.2 E178E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NG-01A-11D-A37C-09 chr22:35481478 G>A maps to NM_001008494.1 R177R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASV-01A-11D-A387-09 chr22:35480443 G>A maps to NM_001008494.1 Q150Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A8JE-01A-11D-A37C-09 chr22:35481508 G>T maps to NM_001008494.1 S187S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GL-01A-12D-A37C-09 chr20:33068498 T>C maps to ENST00000262650 S679S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q9-A6FU-01A-11D-A31U-09 chr20:33049898 C>T maps to ENST00000262650 Q474*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43H-01A-11D-A247-09 chr16:47345167 T>C maps to NM_030790.3 L351L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FG-01A-11D-A33E-09 chr5:52206092 C>T maps to NM_181501.1 C567C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NV-01A-11D-A37C-09 chr5:52145256 C>T maps to NM_181501.1 S40S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XP-A8T7-01A-11D-A36J-09 chr1:145532151 G>T maps to NM_003637.3 E266*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr15:68695276 G>A maps to ENST00000423218 H48H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NN-01A-11D-A37C-09 chr15:68649616 G>T maps to ENST00000423218 G207G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA7B-01A-31D-A403-09 chr17:42462406 C>G maps to NM_000419.3 S236S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FP-01A-31D-A387-09 chr17:48151810 G>T did not map to a codon.
Sequencing variant TCGA-VR-A8EQ-01A-11D-A36J-09 chr17:48148780 G>A maps to NM_002204.2 Q286Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XP-A8T6-01A-11D-A36J-09 chr17:48157712 C>T maps to NM_002204.2 R932*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GN-01A-11D-A37C-09 chr2:182363437 G>T maps to NM_000885.4 V543V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NR-01A-11D-A37C-09 chr2:182322979 C>T maps to NM_000885.4 P85P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA4G-01A-11D-A37C-09 chr12:54795802 G>A maps to NM_002205.2 P736P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93D-01A-11D-A387-09 chr12:56091594 G>A maps to ENST00000347027 G475G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3Y9-01A-12D-A247-09 chr10:15688953 C>T maps to NM_003638.1 V366V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A1-01A-21D-A27G-09 chr10:15573107 C>A maps to NM_003638.1 E975*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A891-01A-11D-A36J-09 chr3:37785458 C>T maps to NM_002207.2 D789D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RE-A7BO-01A-11D-A33E-09 chr3:37792002 T>C maps to NM_002207.2 S828S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49Y-01A-11D-A27G-09 chr16:31426245 C>G maps to ENST00000444228 P755P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EZ-01A-11D-A36J-09 chr16:31424552 C>G maps to ENST00000444228 S677*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FA-01A-11D-A33E-09 chr16:30495432 G>A did not map to a codon.
Sequencing variant TCGA-LN-A49V-01A-11D-A247-09 chr16:30522254 G>A maps to NM_002209.2 S891S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8W8-01B-11D-A37C-09 chr16:30490733 G>A maps to NM_002209.2 L176L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASW-01A-11D-A403-09 chr16:30531227 C>A maps to NM_002209.2 Y1093*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr16:31336607 G>T maps to NM_001145808.1 G797G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93E-01A-11D-A37C-09 chr2:187532500 G>T maps to NM_002210.3 E811*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NF-01A-11D-A37C-09 chr2:187529244 G>T maps to NM_002210.3 G650G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A8HZ-01A-11D-A36J-09 chr2:187529331 G>T maps to NM_002210.3 L679L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NE-01A-11D-A37C-09 chr16:31374553 G>A maps to NM_000887.3 A523A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NE-01A-11D-A37C-09 chr16:31391151 T>C maps to NM_000887.3 A981A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NF-01A-11D-A37C-09 chr16:31390951 C>A maps to NM_000887.3 A951A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49R-01A-11D-A247-09 chr16:31373950 C>G maps to NM_000887.3 A412A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A8O2-01A-11D-A36J-09 chr10:33214828 G>A maps to ENST00000374956 F252F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A6QS-01A-12D-A33E-09 chr23:70523686 A>T did not map to a codon.
Sequencing variant TCGA-RE-A7BO-01A-11D-A33E-09 chr23:70524099 G>T did not map to a codon.
Sequencing variant TCGA-LN-A49V-01A-11D-A247-09 chr21:46320285 G>A maps to NM_000211.3 N282N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6L6-01B-11D-A33E-09 chr21:46320387 C>T maps to NM_000211.3 E248E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr17:73732133 C>T maps to NM_001005619.1 R554*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FP-01A-31D-A387-09 chr17:73747157 C>T maps to NM_001005619.1 Y1253Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OW-01A-11D-A28B-09 chr3:124483297 G>A maps to NM_002213.3 I748I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A893-01A-11D-A36J-09 chr2:160994053 G>T maps to NM_000888.3 C517*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr13:102220153 C>T maps to NM_004791.1 Q141*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GL-01A-12D-A37C-09 chr3:52818318 G>A maps to NM_002215.2 T411T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NG-01A-11D-A37C-09 chr10:7759657 C>T maps to NM_002216.2 F179F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr10:7763613 G>A maps to NM_002216.2 A247A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A7DP-01A-31D-A33E-09 chr3:52831208 C>T maps to NM_002217.3 L159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43I-01A-11D-A247-09 chr10:7621716 C>A did not map to a codon.
Sequencing variant TCGA-2H-A9GI-01A-11D-A37C-09 chr5:156608059 G>T maps to NM_005546.3 S24S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88W-01A-11D-A351-09 chr5:156649946 C>T maps to NM_005546.3 L190L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NE-01A-11D-A37C-09 chr5:156608050 T>G maps to NM_005546.3 T21T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49Y-01A-11D-A27G-09 chr5:156679677 C>A maps to NM_005546.3 S618*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A1-01A-21D-A27G-09 chr5:156671416 C>T maps to NM_005546.3 L460L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A625-01A-11D-A31U-09 chr20:3194686 G>A maps to NM_033453.2 G82G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr14:93429192 G>A maps to NM_014216.4 D122D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RE-A7BO-01A-11D-A33E-09 chr14:93412700 G>T maps to NM_014216.4 A292A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr15:41794043 C>T maps to NM_002220.1 G266G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EX-01A-11D-A36J-09 chr15:41793749 G>A maps to NM_002220.1 G193G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93C-01A-11D-A387-09 chr1:226923580 G>A maps to NM_002221.3 Q527*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NJ-01A-11D-A36J-09 chr1:226827314 C>A maps to NM_002221.3 T832T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6KZ-01A-11D-A31U-09 chr1:226825420 G>T maps to NM_002221.3 R862R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RE-01A-11D-A33E-09 chr19:41223894 C>A maps to NM_025194.2 S285S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RE-01A-11D-A33E-09 chr3:4704811 A>G maps to ENST00000356617 Q488Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OX-01A-21D-A28B-09 chr3:4712574 G>A maps to ENST00000356617 G719G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A9-01A-11D-A28B-09 chr3:4687129 T>C maps to ENST00000356617 D224D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3I8-01A-11D-A247-09 chr12:26774190 G>T maps to NM_002223.2 Y1109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KH-A6WC-01A-11D-A33E-09 chr6:33662730 C>A maps to ENST00000374316 R2606R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49S-01A-11D-A247-09 chr6:33653185 C>T maps to ENST00000374316 F1786F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FR-01A-11D-A387-09 chr6:33659404 G>C maps to ENST00000374316 G2413G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8WC-01A-11D-A37C-09 chr6:33646232 G>A maps to ENST00000374316 T1228T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr10:106074318 G>A maps to NM_033397.2 A497A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OS-01A-11D-A28B-09 chr10:106074540 G>A maps to NM_033397.2 T423T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OJ-01A-11D-A27G-09 chr2:24432862 G>T maps to NM_006277.2 R1433R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X8-AAAR-01A-11D-A403-09 chr2:24427240 G>T maps to NM_006277.2 Y1603*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49S-01A-11D-A247-09 chr15:40703767 C>T maps to NM_002225.3 L192L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6XG-01B-11D-A33E-09 chr2:128261066 G>A maps to NM_017969.2 T435T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A8JD-01A-11D-A36J-09 chr20:10653640 G>T maps to NM_000214.2 S32*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RE-01A-11D-A33E-09 chr14:105609379 G>A maps to NM_002226.3 S1123S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr9:5044448 C>A maps to NM_004972.3 R133R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A8JD-01A-11D-A36J-09 chr4:6082039 C>G did not map to a codon.
Sequencing variant TCGA-2H-A9GR-01A-12D-A37C-09 chr5:147021268 A>G did not map to a codon.
Sequencing variant TCGA-LN-A9FP-01A-31D-A387-09 chr5:147040584 G>T maps to NM_014790.3 R185R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49L-01A-11D-A247-09 chr11:134014717 G>A maps to NM_032801.3 P192P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6DN-01B-11D-A31U-09 chr14:75904635 C>T maps to NM_001135049.1 Q16*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88S-01A-11D-A36J-09 chr10:64958354 T>C maps to NM_032776.1 K1803K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6XG-01B-11D-A33E-09 chr10:64967531 C>T maps to NM_032776.1 Q1299Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OM-01A-11D-A27G-09 chr15:42127813 G>A maps to NM_005090.3 W167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FB-01A-11D-A33E-09 chr15:42138473 C>A maps to NM_005090.3 T789T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OX-01A-21D-A28B-09 chr15:42136010 T>C did not map to a codon.
Sequencing variant TCGA-VR-A8EP-01A-31D-A403-09 chr15:42137202 T>C maps to NM_005090.3 L623L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A6QS-01A-12D-A33E-09 chr5:78573803 C>A maps to NM_152405.4 A368A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FG-01A-11D-A33E-09 chr8:75171618 C>T did not map to a codon.
Sequencing variant TCGA-L5-A4ON-01A-11D-A27G-09 chr20:42744352 C>T maps to NM_020433.4 A654A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OX-01A-21D-A28B-09 chr20:42744490 C>T maps to NM_020433.4 T608T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr16:87723990 G>T maps to NM_020655.2 V675V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A8HZ-01A-11D-A36J-09 chr16:87717864 G>C maps to NM_020655.2 R426R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6F8-01A-11D-A33E-09 chr14:24040364 G>T maps to NM_032452.2 P525P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A8-01A-32D-A27G-09 chr14:24041032 C>T maps to NM_032452.2 L416L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RF-01A-13D-A33E-09 chr19:2252588 C>T maps to NM_144616.3 P245P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FA-01A-11D-A33E-09 chr19:2254446 G>A maps to NM_144616.3 P48P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3QL-01A-11D-A247-09 chr14:23450544 C>A maps to NM_032876.4 E311*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RF-01A-13D-A33E-09 chr19:12903517 G>T maps to NM_002229.2 S311S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FH-01A-11D-A33E-09 chr23:8536273 G>T did not map to a codon.
Sequencing variant TCGA-IG-A4P3-01A-11D-A27G-09 chr3:124438116 G>T maps to NM_001024660.3 E2921*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr3:124117634 C>T maps to NM_001024660.3 Q753*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A6QS-01A-12D-A33E-09 chr9:711981 G>T maps to NM_015158.2 E406*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr9:742404 C>T maps to NM_015158.2 N1299N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A893-01A-11D-A36J-09 chr9:730133 G>T maps to NM_015158.2 E928*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr9:738310 C>T maps to NM_015158.2 H1120H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43I-01A-11D-A247-09 chr1:62740568 C>A maps to NM_181712.4 L69L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr1:62739569 G>A maps to NM_181712.4 N402N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A8I0-01A-11D-A36J-09 chr16:75670404 G>T maps to NM_001130089.1 I171I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GM-01A-11D-A37C-09 chr3:20153120 C>T maps to NM_003884.4 C295C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q9-A6FW-01A-31D-A31U-09 chr1:15441058 C>T maps to NM_201628.2 D752D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A4P3-01A-11D-A27G-09 chr10:102824319 C>T maps to NM_030929.4 P245P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr2:170371229 C>T maps to ENST00000419050 C357C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NN-01A-11D-A37C-09 chr3:127642563 C>T maps to NM_207335.2 V220V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OJ-01A-11D-A27G-09 chr11:105923577 C>G maps to NM_198439.2 *613S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZR-A9CJ-01B-11D-A387-09 chr3:42733463 G>A maps to NM_152393.2 V615V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GK-01A-11D-A37C-09 chr13:41706584 C>T maps to NM_152903.4 R21R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S8-A6BV-01A-21D-A31U-09 chr13:41705090 G>A maps to NM_152903.4 C519C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EO-01A-11D-A36J-09 chr13:41705905 C>A maps to NM_152903.4 E248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OR-01A-11D-A27G-09 chr1:111215784 C>G maps to NM_002232.3 T549T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OU-01A-11D-A28B-09 chr1:111216093 A>T maps to NM_002232.3 G446G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A893-01A-11D-A36J-09 chr1:111216789 G>A maps to NM_002232.3 R214R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A8JE-01A-11D-A37C-09 chr1:111215885 G>A maps to NM_002232.3 R516*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XP-A8T7-01A-11D-A36J-09 chr11:30033502 C>A maps to NM_002233.2 L241L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GN-01A-11D-A37C-09 chr12:5153504 G>A maps to NM_002234.2 V64V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88Z-01A-11D-A36J-09 chr12:5155088 C>T maps to NM_002234.2 S592S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6L6-01B-11D-A33E-09 chr12:5153933 C>T maps to NM_002234.2 D207D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GF-01A-11D-A37C-09 chr12:4919746 C>T maps to NM_002235.3 S180S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr12:4919977 C>A maps to NM_002235.3 S257S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASX-01A-11D-A387-09 chr12:4920697 C>T maps to NM_002235.3 G497G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88W-01A-11D-A351-09 chr3:155861166 C>A maps to NM_003471.3 S67*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr1:6150468 C>T maps to NM_003636.3 R146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A5S3-01A-11D-A28B-09 chr20:48098774 G>A maps to NM_004975.2 N81N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A1-01A-21D-A27G-09 chr20:47991181 G>A maps to NM_004975.2 L305L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr8:73849362 C>T maps to NM_004770.2 T591T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NT-01A-11D-A37C-09 chr8:73480107 G>T maps to NM_004770.2 E47*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49W-01A-11D-A27G-09 chr8:73849587 G>A maps to NM_004770.2 T666T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FR-01A-11D-A387-09 chr8:73849089 G>A maps to NM_004770.2 S500S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr12:75601160 G>A maps to NM_139137.2 P201P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43C-01A-11D-A247-09 chr19:50826652 G>A maps to NM_004977.2 V519V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NF-01A-11D-A37C-09 chr19:50826457 C>T maps to NM_004977.2 P584P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NQ-01A-11D-A36J-09 chr1:110765752 C>G maps to NM_004978.4 T282T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6L4-01A-11D-A31U-09 chr23:48826499 C>T did not map to a codon.
Sequencing variant TCGA-IG-A3YA-01A-11D-A247-09 chr7:119914700 G>A maps to NM_012281.2 V5V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93D-01A-11D-A387-09 chr7:119915138 C>T maps to NM_012281.2 D151D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OE-01A-11D-A27G-09 chr7:119915537 C>T maps to NM_012281.2 D284D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OH-01A-11D-A27G-09 chr1:112524364 G>T maps to ENST00000315987 L328L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q9-A6FW-01A-31D-A31U-09 chr1:112525096 G>A maps to ENST00000315987 F84F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FO-01A-11D-A387-09 chr23:108868054 G>T did not map to a codon.
Sequencing variant TCGA-R6-A8W5-01B-11D-A37C-09 chr18:77624215 C>T maps to NM_012283.1 S183S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr2:42671595 C>T maps to NM_133329.5 T263T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FB-01A-11D-A33E-09 chr16:84256560 G>A maps to NM_172347.2 S274S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49W-01A-11D-A27G-09 chr1:211093141 C>G maps to NM_172362.2 G434G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GJ-01A-11D-A37C-09 chr7:150648578 G>T maps to NM_000238.2 T634T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A4QS-01A-11D-A27G-09 chr7:150648206 G>A maps to NM_000238.2 S649S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FD-01A-11D-A33E-09 chr7:150642566 C>T maps to NM_000238.2 P1122P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NU-01A-11D-A36J-09 chr7:150647325 G>A maps to NM_000238.2 L776L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6XQ-01B-11D-A33E-09 chr7:150648626 G>T maps to NM_000238.2 T618T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GK-01A-11D-A37C-09 chr12:49950969 C>T maps to NM_012284.1 S860S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3YB-01A-11D-A247-09 chr17:40321668 C>G maps to NM_012285.2 G472G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A8I0-01A-11D-A36J-09 chr14:63246447 G>T maps to NM_139318.3 R673R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NJ-01A-11D-A36J-09 chr17:61601569 C>T maps to NM_030779.2 C49C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FE-01A-11D-A33E-09 chr2:163292017 G>T maps to NM_033272.2 G548G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GG-01A-11D-A37C-09 chr17:21319343 G>A maps to NM_021012.4 A230A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A5U5-01A-21D-A28B-09 chr17:21319868 C>T maps to NM_021012.4 S405S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8W8-01B-11D-A37C-09 chr17:21319232 G>A maps to NM_021012.4 T193T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EY-01A-11D-A36J-09 chr17:21319091 C>T maps to NM_021012.4 Y146Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASW-01A-11D-A403-09 chr17:68171794 C>T maps to NM_000891.2 D205D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OE-01A-11D-A27G-09 chr11:128781330 G>T maps to NM_000890.3 E55*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr11:128781287 G>A maps to NM_000890.3 T40T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A8I1-01A-11D-A36J-09 chr11:128786560 G>T maps to NM_000890.3 E399*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XP-A8T6-01A-11D-A36J-09 chr21:39086838 G>T maps to NM_002240.2 T207T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6XQ-01B-11D-A33E-09 chr12:21926468 G>A maps to NM_004982.2 R28*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43I-01A-11D-A247-09 chr1:160054575 C>T maps to NM_004983.2 D252D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GH-01A-11D-A37C-09 chr1:233749940 C>T maps to NM_002245.3 S8S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NQ-01A-11D-A36J-09 chr1:233749985 C>T maps to NM_002245.3 F23F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-AAPN-01A-11D-A403-09 chr14:90650757 C>G maps to NM_022054.2 S213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93C-01A-11D-A387-09 chr20:43379100 C>T maps to ENST00000372861 F205F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43E-01A-11D-A247-09 chr20:43379388 C>T maps to ENST00000372861 R301R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6XG-01B-11D-A33E-09 chr10:78799284 C>T did not map to a codon.
Sequencing variant TCGA-R6-A8W8-01B-11D-A37C-09 chr10:78839252 G>A maps to NM_001161352.1 Q527*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A9VB-01A-21D-A37C-09 chr3:178962476 G>A maps to NM_171828.1 Q87*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr12:70824402 G>A maps to NM_014505.4 A201A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A4P3-01A-11D-A27G-09 chr1:154794624 G>T maps to NM_002249.4 I323I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OE-01A-11D-A27G-09 chr1:154794591 G>T maps to NM_002249.4 I334I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L7-A6VZ-01A-12D-A33E-09 chr1:154842332 C>T maps to NM_002249.4 Q36Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr11:2610022 G>A maps to NM_000218.2 T444T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HV-01A-21D-A351-09 chr11:2869031 C>A maps to NM_000218.2 T610T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88Z-01A-11D-A36J-09 chr20:62103552 C>T maps to NM_172107.2 P88P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A3-01A-11D-A27G-09 chr20:62045496 G>A maps to NM_172107.2 C525C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6F8-01A-11D-A33E-09 chr8:133492449 C>T maps to NM_004519.2 L110L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6F8-01A-11D-A33E-09 chr8:133492539 C>T maps to NM_004519.2 R80R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A2-01A-31D-A27G-09 chr8:133492506 G>C maps to NM_004519.2 T91T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6KZ-01A-11D-A31U-09 chr8:133184937 G>T maps to NM_004519.2 G349G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OT-01A-11D-A28B-09 chr6:73830210 T>C maps to NM_001160133.1 V377V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L7-A6VZ-01A-12D-A33E-09 chr6:73900332 G>T maps to NM_001160133.1 E558*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XP-A8T6-01A-11D-A36J-09 chr6:73751727 C>T maps to NM_001160133.1 R187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GM-01A-11D-A37C-09 chr8:99441034 G>T maps to NM_020697.2 V276V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49W-01A-11D-A27G-09 chr8:99441484 C>T maps to NM_020697.2 A426A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XP-A8T6-01A-11D-A36J-09 chr8:99440686 G>A maps to NM_020697.2 K160K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OE-01A-11D-A27G-09 chr2:18112841 C>A maps to NM_002252.3 I189I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RE-01A-11D-A33E-09 chr1:196300369 A>C maps to NM_198503.2 P673P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FD-01A-11D-A33E-09 chr8:36671819 C>T maps to NM_001031836.2 T276T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FH-01A-11D-A33E-09 chr8:36694411 G>T maps to NM_001031836.2 V489V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr8:36793350 T>G maps to NM_001031836.2 P1121P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A8I1-01A-11D-A36J-09 chr8:36721956 G>T maps to NM_001031836.2 G643*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASX-01A-11D-A387-09 chr8:36780045 G>T maps to NM_001031836.2 G879*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GL-01A-12D-A37C-09 chr8:110980793 A>G maps to NM_014379.2 C342C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A5B8-01A-11D-A28B-09 chr8:110986467 G>A maps to NM_014379.2 F50F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OH-01A-11D-A27G-09 chr8:110986368 G>T maps to NM_014379.2 A83A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OH-01A-11D-A27G-09 chr8:110986410 G>T maps to NM_014379.2 A69A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr8:110980378 G>A maps to NM_014379.2 R481*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6F8-01A-11D-A33E-09 chr13:77460103 G>T maps to NM_138444.3 L60L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASV-01A-11D-A387-09 chr11:77727683 G>A maps to NM_023930.3 N241N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GR-01A-12D-A37C-09 chr5:143853370 G>A maps to NM_020768.3 T327T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A5B8-01A-11D-A28B-09 chr5:143853448 G>C maps to NM_020768.3 L353L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NQ-01A-11D-A36J-09 chr5:143586747 C>G maps to NM_020768.3 L157L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43I-01A-11D-A247-09 chr17:73045403 T>C maps to NM_015353.1 T143T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA7B-01A-31D-A403-09 chr1:215793773 G>A maps to NM_016121.3 R754R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3Y9-01A-12D-A247-09 chr13:45768276 G>A maps to NM_198404.2 F142F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FB-01A-11D-A33E-09 chr16:2752445 C>T maps to NM_018992.3 Y214Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NQ-01A-11D-A36J-09 chr7:66103972 C>T maps to NM_153033.3 N208N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RF-01A-13D-A33E-09 chr4:44449988 G>T maps to NM_198353.2 A184A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr4:44177099 G>A maps to NM_198353.2 Q377*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr4:44449817 G>A maps to NM_198353.2 I241I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49Y-01A-11D-A27G-09 chr13:103443451 C>A maps to NM_024089.2 T294T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GI-01A-11D-A37C-09 chr11:108352841 G>T maps to NM_153705.4 G264G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A97I-01A-11D-A387-09 chr1:23395625 G>A maps to NM_001009999.2 L465L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OW-01A-11D-A28B-09 chr11:67012682 G>A maps to NM_012308.2 K529K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RF-01A-13D-A33E-09 chr12:121951121 G>T maps to ENST00000377071 R377R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43C-01A-11D-A247-09 chr12:121951163 G>T maps to ENST00000377071 C363*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FG-01A-11D-A33E-09 chr2:86716721 A>T maps to NM_001146688.1 G1171G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93F-01A-21D-A37C-09 chr2:86705839 A>G maps to NM_001146688.1 S766S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A5B8-01A-11D-A28B-09 chr5:137761146 G>A maps to NM_016604.3 W1429*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93E-01A-11D-A37C-09 chr1:44132177 C>T maps to NM_014663.2 T243T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88S-01A-11D-A36J-09 chr19:5144078 C>T maps to NM_015015.2 H884H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L7-A6VZ-01A-12D-A33E-09 chr19:5144036 C>A maps to NM_015015.2 S870S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6DN-01B-11D-A31U-09 chr19:5132014 G>T maps to NM_015015.2 E635*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr11:94758855 T>C maps to NM_001161630.1 L45L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A5B8-01A-11D-A28B-09 chr12:431718 G>A maps to NM_001042603.1 R764*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EQ-01A-11D-A36J-09 chr12:419112 G>A maps to NM_001042603.1 T1078T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HX-01A-11D-A33E-09 chr1:202742368 T>C maps to ENST00000367264 K151K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FO-01A-11D-A387-09 chr23:53223825 G>A did not map to a codon.
Sequencing variant TCGA-Q9-A6FU-01A-11D-A31U-09 chr23:53246369 G>A did not map to a codon.
Sequencing variant TCGA-IG-A51D-01A-11D-A27G-09 chr23:44950109 G>A did not map to a codon.
Sequencing variant TCGA-IG-A625-01A-11D-A31U-09 chr23:44941833 A>T did not map to a codon.
Sequencing variant TCGA-L5-A4OE-01A-11D-A27G-09 chr23:44949972 C>A did not map to a codon.
Sequencing variant TCGA-L5-A8NG-01A-11D-A37C-09 chr23:44941851 A>T did not map to a codon.
Sequencing variant TCGA-L5-A8NI-01A-11D-A37C-09 chr23:44922978 G>A did not map to a codon.
Sequencing variant TCGA-R6-A6Y2-01B-11D-A33E-09 chr23:44920584 G>A did not map to a codon.
Sequencing variant TCGA-VR-A8EU-01A-11D-A36J-09 chr23:44949997 A>T did not map to a codon.
Sequencing variant TCGA-JY-A939-01A-12D-A37C-09 chr4:55956187 T>A maps to NM_002253.2 K1043*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43C-01A-11D-A247-09 chr4:55970999 G>T maps to NM_002253.2 P599P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr19:10610580 C>T maps to NM_203500.1 T43T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASX-01A-11D-A387-09 chr6:62995778 C>T maps to NM_152688.2 S25S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GI-01A-11D-A37C-09 chr8:136619223 T>C maps to NM_006558.1 A278A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A5U6-01A-11D-A28B-09 chr19:6417018 G>A maps to NM_003685.2 N387N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OM-01A-11D-A27G-09 chr9:2829812 C>A maps to NM_014878.4 L271L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OM-01A-11D-A27G-09 chr9:2834110 C>T maps to NM_014878.4 L120L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr9:2834089 A>G maps to NM_014878.4 S127S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49L-01A-11D-A247-09 chr1:19559219 A>T maps to NM_015047.1 Y560*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FE-01A-11D-A33E-09 chr17:26959177 G>T maps to NM_014680.2 V1295V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr17:26962453 G>A maps to NM_014680.2 G717G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6Y2-01B-11D-A33E-09 chr17:26961607 A>G maps to NM_014680.2 P999P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FH-01A-11D-A33E-09 chr5:141309599 C>A maps to NM_014773.3 S206S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93C-01A-11D-A387-09 chr5:141309192 G>A maps to NM_014773.3 R153R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EU-01A-11D-A36J-09 chr16:85687978 G>A maps to NM_014615.2 S174S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43I-01A-11D-A247-09 chr17:73482013 G>A maps to ENST00000375248 G69G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr17:73487188 G>A maps to ENST00000375248 T402T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr17:73490810 C>T maps to ENST00000375248 I843I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8WC-01A-11D-A37C-09 chr6:42832451 G>A maps to NM_015349.1 E836E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RE-01A-11D-A33E-09 chr14:105359958 G>T maps to ENST00000453495 E1416*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49V-01A-11D-A247-09 chr14:105359963 C>T maps to ENST00000453495 D1417D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A8O2-01A-11D-A36J-09 chr6:24564463 C>T maps to NM_014809.3 S799S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NG-01A-11D-A37C-09 chr6:24566911 G>A maps to NM_014809.3 S735S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8WC-01A-11D-A37C-09 chr6:24566863 G>A maps to NM_014809.3 S751S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NK-01A-21D-A37C-09 chr1:35919199 G>C maps to NM_024874.4 S624*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FB-01A-11D-A33E-09 chr19:34818995 G>A maps to NM_014686.3 S348S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A4P3-01A-11D-A27G-09 chr20:36625250 G>T maps to NM_014657.1 I966I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A51D-01A-11D-A27G-09 chr20:36640850 C>G maps to NM_014657.1 L456L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GN-01A-11D-A37C-09 chr7:4824611 G>A maps to ENST00000450194 P999P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43E-01A-11D-A247-09 chr7:4823398 C>T maps to ENST00000450194 G908G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88Z-01A-11D-A36J-09 chr7:4824678 C>T maps to ENST00000450194 R1022*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A5B8-01A-11D-A28B-09 chr16:15715631 G>C maps to NM_014647.3 S866*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A8JD-01A-11D-A36J-09 chr16:15714338 G>A maps to NM_014647.3 L897L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A4P3-01A-11D-A27G-09 chr1:43916149 G>A maps to NM_015284.2 *2534*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FG-01A-11D-A33E-09 chr1:47157528 C>T maps to NM_014774.2 K220K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NK-01A-21D-A37C-09 chr1:47154134 C>A maps to NM_014774.2 E293*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A51D-01A-11D-A27G-09 chr1:3755526 C>A did not map to a codon.
Sequencing variant TCGA-Z6-AAPN-01A-11D-A403-09 chr1:3756339 C>T maps to NM_014704.3 R189R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A625-01A-11D-A31U-09 chr13:42161712 C>A maps to NM_015058.1 E1736*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A4P3-01A-11D-A27G-09 chr14:58979345 G>T did not map to a codon.
Sequencing variant TCGA-L5-A8NS-01A-12D-A37C-09 chr14:58896141 G>A maps to ENST00000354386 V99V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GN-01A-11D-A37C-09 chr9:138379217 C>T maps to NM_014811.3 S954S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OE-01A-11D-A27G-09 chr9:138378131 C>A maps to NM_014811.3 C592*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NS-01A-12D-A37C-09 chr9:138378542 G>A maps to NM_014811.3 T729T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49L-01A-11D-A247-09 chr9:138377489 G>A maps to NM_014811.3 Q378Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8W8-01B-11D-A37C-09 chr9:138379061 C>T maps to NM_014811.3 A902A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FH-01A-11D-A33E-09 chr11:46690364 G>T maps to NM_001142673.1 E418*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A938-01A-11D-A37C-09 chr12:55359871 G>A maps to NM_001098815.1 S137S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GI-01A-11D-A37C-09 chr1:39878347 C>A maps to NM_015038.1 S804*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HX-01A-11D-A33E-09 chr6:97001213 C>G maps to NM_015323.4 V740V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XP-A8T6-01A-11D-A36J-09 chr6:96986511 G>A maps to NM_015323.4 L328L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3Y9-01A-12D-A247-09 chr18:8813074 G>C maps to ENST00000456698 L1220L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr18:8825002 G>A maps to ENST00000456698 T1484T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q9-A6FW-01A-31D-A31U-09 chr18:8793057 C>T maps to ENST00000306329 L671L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OH-01A-11D-A27G-09 chr19:19448016 G>A maps to NM_015329.3 A133A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr1:155903597 G>T maps to NM_014949.2 L27L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A97H-01A-11D-A387-09 chr5:5462675 A>C maps to NM_015325.1 R1077R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4MR-01A-11D-A28B-09 chr5:5465102 G>T maps to NM_015325.1 E1886*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OJ-01A-11D-A27G-09 chr18:29487485 G>T maps to NM_014939.3 C442*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASX-01A-11D-A387-09 chr18:29454466 G>A maps to NM_014939.3 L643L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49N-01A-11D-A247-09 chr15:79750679 A>T maps to NM_015206.2 R731*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A9VB-01A-21D-A37C-09 chr15:79749997 C>T maps to NM_015206.2 T503T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HY-01A-12D-A351-09 chr12:105551050 G>T maps to NM_015275.1 E955*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93F-01A-21D-A37C-09 chr4:123147860 G>A did not map to a codon.
Sequencing variant TCGA-VR-A8EQ-01A-11D-A36J-09 chr7:141364999 C>T maps to NM_001080392.1 V313V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NW-01A-11D-A37C-09 chr9:34371717 G>A maps to NM_020702.3 R408R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OW-01A-11D-A28B-09 chr5:175777627 G>A maps to NM_020444.3 A149A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr15:81217985 C>T maps to NM_018689.1 A770A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A4QS-01A-11D-A27G-09 chr23:118221264 C>G did not map to a codon.
Sequencing variant TCGA-L5-A4OM-01A-11D-A27G-09 chr23:118219375 G>T did not map to a codon.
Sequencing variant TCGA-L5-A4OW-01A-11D-A28B-09 chr23:118222390 A>C did not map to a codon.
Sequencing variant TCGA-L5-A4OW-01A-11D-A28B-09 chr23:118222579 T>C did not map to a codon.
Sequencing variant TCGA-LN-A49W-01A-11D-A27G-09 chr23:118257579 G>A did not map to a codon.
Sequencing variant TCGA-Q9-A6FW-01A-31D-A31U-09 chr23:118223625 G>A did not map to a codon.
Sequencing variant TCGA-VR-AA7B-01A-31D-A403-09 chr23:118221020 C>T did not map to a codon.
Sequencing variant TCGA-XP-A8T6-01A-11D-A36J-09 chr23:118221249 C>A did not map to a codon.
Sequencing variant TCGA-JY-A6FE-01A-11D-A33E-09 chr10:24762671 A>G maps to NM_019590.3 K454K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6DQ-01B-11D-A31U-09 chr10:24835060 G>T maps to NM_019590.3 P1880P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GO-01A-11D-A37C-09 chr6:138599612 C>T maps to NM_020340.4 D718D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A97I-01A-11D-A387-09 chr6:138550973 G>A maps to NM_020340.4 V135V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FP-01A-31D-A387-09 chr17:44144913 C>A did not map to a codon.
Sequencing variant TCGA-V5-AASV-01A-11D-A387-09 chr17:44248370 A>T maps to NM_015443.3 L380*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6DN-01B-11D-A31U-09 chr2:97302701 G>C maps to ENST00000421845 T57T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A939-01A-12D-A37C-09 chr1:109743446 C>A maps to NM_020775.3 G966G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A8JE-01A-11D-A37C-09 chr7:86569421 T>A maps to NM_001142749.2 K251*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A8JE-01A-11D-A37C-09 chr18:34740345 T>A did not map to a codon.
Sequencing variant TCGA-L5-A8NG-01A-11D-A37C-09 chr11:101833019 C>T maps to NM_020802.2 S418S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S8-A6BW-01A-11D-A31U-09 chr3:113697806 C>T maps to NM_020817.1 T786T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GH-01A-11D-A37C-09 chr14:94008859 C>A maps to ENST00000393153 R525R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OE-01A-11D-A27G-09 chr14:94088105 G>T maps to ENST00000393153 S1531S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GN-01A-11D-A37C-09 chr8:95538800 G>A maps to NM_015496.3 C557C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A2-01A-31D-A27G-09 chr8:95547193 A>G maps to NM_015496.3 C119C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NV-01A-11D-A37C-09 chr4:186085252 A>G maps to NM_020827.1 N467N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A5U7-01A-11D-A31U-09 chr4:186111978 T>C maps to NM_020827.1 V124V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6Y2-01B-11D-A33E-09 chr4:186084008 G>T maps to NM_020827.1 S514S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4ON-01A-11D-A27G-09 chr10:30316553 C>T maps to NM_020848.2 E841E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A893-01A-11D-A36J-09 chr10:30336522 G>T maps to NM_020848.2 R73R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FE-01A-11D-A33E-09 chr12:13224299 C>G maps to NM_020853.1 A498A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr18:59922663 C>T maps to NM_020854.3 R617*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A50L-01A-11D-A27G-09 chr2:226516199 T>A maps to NM_020864.1 P627P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr2:226446861 C>T maps to NM_020864.1 P243P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A6-01A-11D-A27G-09 chr2:226447050 C>T maps to NM_020864.1 F306F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NG-01A-11D-A37C-09 chr9:100077197 A>G maps to ENST00000375206 E438E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FP-01A-31D-A387-09 chr4:1343539 G>T maps to NM_020894.2 L109L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr9:35106612 C>T maps to NM_025182.2 G327G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr9:35106612 C>T maps to NM_025182.2 G327G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FE-01A-11D-A33E-09 chr7:138603426 C>T maps to NM_001164665.1 W315*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93F-01A-21D-A37C-09 chr7:138603523 A>T maps to NM_001164665.1 L283*. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-LN-A7HX-01A-11D-A33E-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-L5-A8NK-01A-21D-A37C-09 chr10:118671343 G>T maps to NM_001127211.1 S439*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A8O2-01A-11D-A36J-09 chr1:180904862 G>A maps to NM_020950.1 A606A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NG-01A-11D-A37C-09 chr1:180897673 C>T maps to NM_020950.1 S390S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OH-01A-11D-A27G-09 chr18:43529452 G>A maps to NM_020964.2 I498I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NK-01A-21D-A37C-09 chr18:43496414 G>A maps to NM_020964.2 N1124N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8W5-01B-11D-A37C-09 chr18:43496129 G>T maps to NM_020964.2 P1142P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA7B-01A-31D-A403-09 chr22:44681531 G>T maps to NM_001099294.1 Y125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EP-01A-31D-A403-09 chr19:18368267 C>A maps to NM_001145304.1 E1276*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EW-01A-11D-A36J-09 chr13:45602137 A>G maps to NM_018559.2 *341*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NS-01A-12D-A37C-09 chr14:77572080 C>T maps to NM_033426.2 S10S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NQ-01A-11D-A36J-09 chr20:36855582 G>A maps to NM_001029864.1 L675L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EQ-01A-11D-A36J-09 chr20:36869863 T>A maps to NM_001029864.1 P223P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6DQ-01B-11D-A31U-09 chr9:20944646 T>C maps to NM_017794.3 V1143V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A4QS-01A-11D-A27G-09 chr2:61345224 C>T maps to NM_001129993.1 R668*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FG-01A-11D-A33E-09 chr6:111580923 G>T maps to NM_153369.2 L7L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FB-01A-11D-A33E-09 chr6:30653318 G>T maps to NM_133471.3 A159A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A8I0-01A-11D-A36J-09 chr6:30652835 T>C maps to NM_133471.3 E320E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88Z-01A-11D-A36J-09 chr9:115422316 C>A maps to NM_133465.2 R707R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NS-01A-12D-A37C-09 chr8:22473233 C>T maps to NM_021174.5 Q473*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr1:11983511 C>T maps to ENST00000376576 T356T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr3:113376115 C>T maps to NM_001009899.2 Q1471Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr3:113376121 C>T maps to NM_001009899.2 Q1469Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NF-01A-11D-A37C-09 chr3:113378492 G>T maps to NM_001009899.2 S679*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8WC-01A-11D-A37C-09 chr3:113376115 C>T maps to NM_001009899.2 Q1471Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GR-01A-12D-A37C-09 chr23:73963952 A>C did not map to a codon.
Sequencing variant TCGA-IG-A50L-01A-11D-A27G-09 chr23:73963733 T>C did not map to a codon.
Sequencing variant TCGA-JY-A93C-01A-11D-A387-09 chr23:73961538 G>T did not map to a codon.
Sequencing variant TCGA-JY-A93F-01A-21D-A37C-09 chr23:73960194 G>T did not map to a codon.
Sequencing variant TCGA-L5-A4ON-01A-11D-A27G-09 chr23:73960101 C>G did not map to a codon.
Sequencing variant TCGA-L5-A4OW-01A-11D-A28B-09 chr23:73961266 T>A did not map to a codon.
Sequencing variant TCGA-L5-A891-01A-11D-A36J-09 chr23:73963509 G>C did not map to a codon.
Sequencing variant TCGA-L5-A893-01A-11D-A36J-09 chr23:73961053 T>C did not map to a codon.
Sequencing variant TCGA-R6-A6XG-01B-11D-A33E-09 chr23:73962148 G>T did not map to a codon.
Sequencing variant TCGA-VR-A8EZ-01A-11D-A36J-09 chr23:73962183 A>G did not map to a codon.
Sequencing variant TCGA-2H-A9GO-01A-11D-A37C-09 chr9:5922827 G>T maps to NM_001017969.2 T1056T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43E-01A-11D-A247-09 chr2:8890382 C>T maps to NM_020738.2 A1091A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr2:8934032 G>A maps to NM_020738.2 R395*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A6-01A-11D-A27G-09 chr2:8919883 G>A maps to NM_020738.2 Q764*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HX-01A-11D-A33E-09 chr2:8943199 C>A maps to NM_020738.2 E221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L7-A6VZ-01A-12D-A33E-09 chr9:116857591 G>A maps to ENST00000259410 L301L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A3-01A-11D-A27G-09 chr6:17849621 G>T maps to NM_022113.4 G272G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GK-01A-11D-A37C-09 chr8:29023208 C>T maps to NM_015254.3 E413E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr8:29035023 G>T maps to NM_015254.3 G264G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NI-01A-11D-A37C-09 chr8:28929563 G>A maps to NM_015254.3 T1597T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr8:28974482 G>A maps to NM_015254.3 C1234C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q9-A6FU-01A-11D-A31U-09 chr8:28997677 G>A maps to NM_015254.3 R839*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GG-01A-11D-A37C-09 chr3:44847375 G>A maps to NM_020242.2 L623L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88W-01A-11D-A351-09 chr3:44819650 C>T maps to NM_020242.2 C97C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3YA-01A-11D-A247-09 chr1:20998479 G>A maps to NM_020816.2 G891G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NJ-01A-11D-A36J-09 chr1:21016692 G>T maps to NM_020816.2 R457R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49U-01A-31D-A27G-09 chr1:21042066 G>A maps to NM_020816.2 F99F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8ER-01A-11D-A36J-09 chr17:43013492 G>T maps to ENST00000438933 R74R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EU-01A-11D-A36J-09 chr17:72346552 G>A maps to NM_153209.3 L409L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GN-01A-11D-A37C-09 chr2:241725749 A>C did not map to a codon.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr2:241725900 G>A maps to ENST00000373308 R153R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6F8-01A-11D-A33E-09 chr1:10364186 G>T maps to NM_183416.3 E982*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OT-01A-11D-A28B-09 chr1:10397522 T>A maps to ENST00000377086 T1118T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OR-01A-11D-A27G-09 chr5:137518142 G>T maps to NM_005733.2 T169T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASW-01A-11D-A403-09 chr5:137519020 C>T maps to NM_005733.2 C332C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A5B8-01A-11D-A28B-09 chr10:91492753 C>G maps to ENST00000416354 S829*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A4-01A-11D-A27G-09 chr12:39735382 C>T maps to ENST00000395670 E615E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A97I-01A-11D-A387-09 chr1:200967541 G>A maps to NM_017596.2 L683L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6Y2-01B-11D-A33E-09 chr1:200959450 C>A maps to NM_017596.2 E949*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XP-A8T8-01A-11D-A36J-09 chr16:29814197 C>T maps to NM_007317.1 T463T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NH-01A-11D-A37C-09 chr15:69732684 T>C maps to NM_138555.1 N642N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RE-01A-11D-A33E-09 chr9:34311338 T>A maps to NM_194313.2 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KH-A6WC-01A-11D-A33E-09 chr6:168439398 C>T maps to NM_030615.2 L162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NJ-01A-11D-A36J-09 chr14:104641615 C>T maps to NM_015656.1 R831*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RE-A7BO-01A-11D-A33E-09 chr14:104638925 G>T maps to NM_015656.1 S447S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6F8-01A-11D-A33E-09 chr1:245849383 C>T maps to NM_018012.3 S1033S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr1:245849620 C>T maps to NM_018012.3 G1112G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-M9-A5M8-01A-11D-A28B-09 chr1:245849059 G>A maps to NM_018012.3 T925T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr9:86452377 G>T maps to NM_017576.1 V1248V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EX-01A-11D-A36J-09 chr9:86504110 G>A maps to NM_017576.1 R623*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GI-01A-11D-A37C-09 chr17:51900496 C>T maps to NM_032559.4 Q35*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FB-01A-11D-A33E-09 chr17:51901323 G>A maps to NM_032559.4 T310T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OU-01A-11D-A28B-09 chr17:51901054 C>A maps to NM_032559.4 R221R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NE-01A-11D-A37C-09 chr17:51901449 C>T maps to NM_032559.4 V352V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NN-01A-11D-A37C-09 chr20:30898257 C>T maps to NM_004798.3 S226S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EY-01A-11D-A36J-09 chr20:30917957 G>T maps to NM_004798.3 V661V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A8O2-01A-11D-A36J-09 chr2:26203715 G>C maps to NM_002254.6 R357R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A893-01A-11D-A36J-09 chr2:26203514 G>T maps to NM_002254.6 G424G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6Y2-01B-11D-A33E-09 chr2:26152859 C>A maps to NM_002254.6 R693R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43I-01A-11D-A247-09 chr23:69521773 G>C did not map to a codon.
Sequencing variant TCGA-L5-A4OG-01A-11D-A27G-09 chr23:69615564 A>C did not map to a codon.
Sequencing variant TCGA-L5-A4OP-01A-11D-A27G-09 chr23:69595950 T>A did not map to a codon.
Sequencing variant TCGA-LN-A4A1-01A-21D-A27G-09 chr23:69594098 A>T did not map to a codon.
Sequencing variant TCGA-Q9-A6FU-01A-11D-A31U-09 chr10:32311946 G>A maps to NM_004521.2 G581G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A51D-01A-11D-A27G-09 chr2:149854939 C>T maps to NM_004522.1 S709S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RE-01A-11D-A33E-09 chr3:47287001 C>T did not map to a codon.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr6:33374230 C>T maps to NM_002263.3 L599L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49M-01A-21D-A27G-09 chr6:33374169 C>T maps to NM_002263.3 L578L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A4P3-01A-11D-A27G-09 chr16:57798132 G>T maps to NM_005550.3 V513V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FE-01A-11D-A33E-09 chr16:57793061 C>T maps to NM_001130100.1 *827*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HY-01A-12D-A351-09 chr19:55329984 C>A maps to ENST00000355608 R96R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr1:158064152 C>T maps to ENST00000368173 I606I. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-JY-A6FB-01A-11D-A33E-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-JY-A6FB-01A-11D-A33E-09 chr11:126310352 C>A maps to ENST00000239597 S297S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr11:126299147 G>A maps to NM_032531.3 R578*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NS-01A-12D-A37C-09 chr11:126343241 G>A maps to NM_032531.3 R185*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EZ-01A-11D-A36J-09 chr11:126294540 G>T maps to NM_032531.3 S757S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr4:55561888 C>T maps to NM_000222.2 G93G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NG-01A-11D-A37C-09 chr4:55592079 G>T maps to NM_000222.2 P468P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FA-01A-11D-A33E-09 chr13:33635153 A>C maps to NM_004795.3 G646G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NW-01A-11D-A37C-09 chr13:33635917 G>T did not map to a codon.
Sequencing variant TCGA-R6-A6KZ-01A-11D-A31U-09 chr4:39408704 C>T maps to NM_175737.3 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A2-01A-31D-A27G-09 chr19:12995818 C>T maps to NM_006563.3 S323S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EW-01A-11D-A36J-09 chr8:103663829 G>A maps to NM_005655.2 Q244*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZR-A9CJ-01B-11D-A387-09 chr19:1854586 G>A maps to NM_031918.3 P210P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr1:44595029 C>T maps to NM_173484.3 N29N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OE-01A-11D-A27G-09 chr4:38690447 C>A maps to NM_016531.5 S100S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr4:38690546 G>A maps to NM_016531.5 R133R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NG-01A-11D-A37C-09 chr4:38696527 G>T did not map to a codon.
Sequencing variant TCGA-L5-A43C-01A-11D-A247-09 chr2:207988663 C>T maps to NM_003709.2 T189T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A2-01A-31D-A27G-09 chr2:207988642 A>G maps to NM_003709.2 S196S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q9-A6FU-01A-11D-A31U-09 chr23:56295888 C>T did not map to a codon.
Sequencing variant TCGA-R6-A6DN-01B-11D-A31U-09 chr23:56291803 T>C did not map to a codon.
Sequencing variant TCGA-VR-A8EQ-01A-11D-A36J-09 chr23:56291945 C>A did not map to a codon.
Sequencing variant TCGA-V5-AASX-01A-11D-A387-09 chr14:50190639 A>G maps to NM_172193.2 Q151Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RF-01A-13D-A33E-09 chr7:129756387 G>T maps to NM_014997.3 G119G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA7D-01A-11D-A403-09 chr14:50244591 G>A maps to NM_014315.2 V129V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8Q7-01A-11D-A37C-09 chr1:18809628 C>T maps to NM_152375.2 C718C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A939-01A-12D-A37C-09 chr22:50987857 C>T maps to NM_138433.3 Y421Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A51D-01A-11D-A27G-09 chr13:70514336 C>T maps to NM_020866.2 E283E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RE-A7BO-01A-11D-A33E-09 chr13:70514282 G>T maps to NM_020866.2 C301*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A7DP-01A-31D-A33E-09 chr17:40004469 G>T maps to NM_152467.3 E580*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6Y0-01B-11D-A33E-09 chr17:40001401 G>T maps to NM_152467.3 E237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NS-01A-12D-A37C-09 chr1:202887394 A>G maps to NM_021633.2 F157F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A4QS-01A-11D-A27G-09 chr23:117033236 T>C did not map to a codon.
Sequencing variant TCGA-L5-A893-01A-11D-A36J-09 chr23:117043736 G>A did not map to a codon.
Sequencing variant TCGA-VR-A8EQ-01A-11D-A36J-09 chr23:117033205 A>C did not map to a codon.
Sequencing variant TCGA-2H-A9GO-01A-11D-A37C-09 chr23:24006109 C>G did not map to a codon.
Sequencing variant TCGA-R6-A8WG-01A-11D-A37C-09 chr23:24024585 T>C did not map to a codon.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr1:900525 G>A maps to NM_198317.2 P628P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A893-01A-11D-A36J-09 chr1:897048 C>T maps to NM_198317.2 H136H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43E-01A-11D-A247-09 chr3:47371500 G>C maps to NM_025010.4 V154V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A8HZ-01A-11D-A36J-09 chr3:47384289 C>T maps to NM_025010.4 G436G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FP-01A-31D-A387-09 chr4:166149970 G>T maps to NM_001161521.1 L59L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr1:173703091 C>A maps to NM_014458.3 A88A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XP-A8T6-01A-11D-A36J-09 chr2:170591805 T>A maps to NM_144711.5 Y94*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GO-01A-11D-A37C-09 chr19:18779955 G>A maps to NM_018316.1 T583T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A5B8-01A-11D-A28B-09 chr14:45403679 G>T maps to ENST00000355081 C341*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8W5-01B-11D-A37C-09 chr14:45400590 G>A maps to ENST00000355081 Y513Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A8I1-01A-11D-A36J-09 chr2:239049953 C>T maps to NM_198582.3 L187L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EY-01A-11D-A36J-09 chr2:239054438 C>T maps to NM_198582.3 S372S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GI-01A-11D-A37C-09 chr6:53516582 C>T maps to NM_001003760.4 W573*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93D-01A-11D-A387-09 chr6:97423885 C>T maps to NM_052904.3 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NL-01A-12D-A37C-09 chr6:97423984 C>T maps to NM_052904.3 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA7I-01A-11D-A403-09 chr6:97578787 T>C maps to NM_052904.3 T523T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93D-01A-11D-A387-09 chr8:124663966 G>A maps to NM_001081675.2 S400S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr8:124664404 G>T maps to NM_001081675.2 T254T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-A7RE-01A-11D-A351-09 chr8:124664818 G>A maps to NM_001081675.2 F116F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EU-01A-11D-A36J-09 chr8:124664836 G>A maps to NM_001081675.2 A110A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr23:86772932 C>T did not map to a codon.
Sequencing variant TCGA-LN-A9FO-01A-11D-A387-09 chr23:86873035 A>T did not map to a codon.
Sequencing variant TCGA-Z6-AAPN-01A-11D-A403-09 chr23:86880712 C>G did not map to a codon.
Sequencing variant TCGA-JY-A6FA-01A-11D-A33E-09 chr3:183209897 G>C maps to NM_130446.2 Y561*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr3:183245686 C>T maps to NM_130446.2 A135A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q9-A6FW-01A-31D-A31U-09 chr3:183273291 G>A maps to NM_130446.2 D50D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EO-01A-11D-A36J-09 chr9:21333628 A>G maps to NM_018847.2 A410A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OE-01A-11D-A27G-09 chr19:51322530 G>A maps to NM_002257.2 G236G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HX-01A-11D-A33E-09 chr19:51324990 G>T maps to NM_002257.2 L61L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NS-01A-12D-A37C-09 chr19:51530734 C>T maps to NM_144947.1 S13S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HW-01A-22D-A351-09 chr19:51330299 G>A maps to NM_017509.2 N105N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A625-01A-11D-A31U-09 chr19:51379817 G>A maps to NM_005551.3 P99P. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-R6-A6Y2-01B-11D-A33E-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-VR-A8EY-01A-11D-A36J-09 chr19:51483658 G>A maps to NM_005046.2 P102P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NL-01A-12D-A37C-09 chr2:48737156 C>T maps to NM_001135629.2 R697*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASX-01A-11D-A387-09 chr2:48698302 C>T maps to NM_001135629.2 I325I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NE-01A-11D-A37C-09 chr12:10464126 C>A maps to ENST00000381908 S76S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RE-A7BO-01A-11D-A33E-09 chr3:186457203 G>T did not map to a codon.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr12:123082349 C>T maps to NM_014708.4 G1476G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49M-01A-21D-A27G-09 chr12:123030787 G>A maps to NM_014708.4 K245K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HV-01A-21D-A351-09 chr12:123036166 G>T did not map to a codon.
Sequencing variant TCGA-R6-A6XQ-01B-11D-A33E-09 chr3:122146487 A>T maps to NM_002264.3 V442V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NK-01A-21D-A37C-09 chr1:152732306 G>A maps to NM_001025231.1 V81V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XP-A8T7-01A-11D-A36J-09 chr19:47986767 C>T maps to NM_007059.2 T100T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-M9-A5M8-01A-11D-A28B-09 chr22:29490306 C>T maps to NM_032045.4 G53G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr19:10668529 C>T maps to NM_023008.3 K473K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KH-A6WC-01A-11D-A33E-09 chr7:91865793 G>A maps to NM_194456.1 R140*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8WC-01A-11D-A37C-09 chr12:53069171 G>A maps to NM_006121.3 S580S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93D-01A-11D-A387-09 chr17:39659586 G>T maps to NM_153490.2 I229I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HV-01A-21D-A351-09 chr17:39659227 C>T maps to NM_153490.2 E286E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OW-01A-11D-A28B-09 chr17:39742710 G>A maps to NM_000526.4 L126L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49M-01A-21D-A27G-09 chr17:39777079 G>A maps to NM_000422.2 Q338*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GH-01A-11D-A37C-09 chr17:38854885 C>A maps to NM_019016.2 E460*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RE-01A-11D-A33E-09 chr17:38938664 T>G maps to NM_181537.3 G27G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NF-01A-11D-A37C-09 chr17:38933253 G>A maps to NM_181537.3 S459S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OJ-01A-11D-A27G-09 chr17:39616469 G>T maps to NM_002278.3 S413S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NR-01A-11D-A37C-09 chr17:39622042 G>C maps to NM_002278.3 L230L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49M-01A-21D-A27G-09 chr17:39505615 G>C maps to NM_004138.2 S138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EW-01A-11D-A36J-09 chr17:39521426 C>A maps to ENST00000394004 L293L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3YA-01A-11D-A247-09 chr17:39538435 G>A maps to NM_021013.3 C63C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RE-01A-11D-A33E-09 chr12:53202110 C>T maps to NM_002272.2 R438R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr17:39135255 G>A maps to NM_182497.3 T332T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49W-01A-11D-A27G-09 chr12:52882149 G>T maps to NM_005554.3 I462I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr12:52841134 C>A maps to NM_005555.3 G512*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RE-A7BO-01A-11D-A33E-09 chr12:52841341 G>A maps to NM_005555.3 G480G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GL-01A-12D-A37C-09 chr12:52865857 G>C maps to NM_173086.4 L249L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L7-A6VZ-01A-12D-A33E-09 chr12:52862908 G>A maps to NM_173086.4 G544G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GG-01A-11D-A37C-09 chr12:52635269 G>A maps to NM_005556.3 L236L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6F8-01A-11D-A33E-09 chr12:52984741 G>A maps to NM_080747.2 Q323*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RE-01A-11D-A33E-09 chr12:53162829 C>A maps to NM_015848.4 G528G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FP-01A-31D-A387-09 chr12:53165003 C>A did not map to a codon.
Sequencing variant TCGA-RE-A7BO-01A-11D-A33E-09 chr12:53292542 G>T maps to NM_002273.3 Y374*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GG-01A-11D-A37C-09 chr12:52585449 C>A maps to NM_182507.2 L79L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A9VB-01A-21D-A37C-09 chr12:52800028 C>T maps to NM_033033.3 R11R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OR-01A-11D-A27G-09 chr12:52710768 G>A maps to NM_002282.3 S263S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RF-01A-13D-A33E-09 chr12:52757080 G>A maps to NM_002283.3 D300D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93F-01A-21D-A37C-09 chr12:52757173 G>A maps to NM_002283.3 A269A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S8-A6BV-01A-21D-A31U-09 chr12:52755283 T>G did not map to a codon.
Sequencing variant TCGA-L5-A4OS-01A-11D-A28B-09 chr12:52695792 C>G maps to NM_002284.3 P31P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A893-01A-11D-A36J-09 chr17:39727650 C>T maps to NM_000226.3 Q198Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OE-01A-11D-A27G-09 chr21:46057783 C>A maps to NM_181688.1 V150V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr21:46117508 C>T maps to NM_198699.1 C131C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q9-A6FU-01A-11D-A31U-09 chr21:45978577 G>T maps to NM_198696.2 S7S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA4D-01A-11D-A37C-09 chr21:46000434 G>A maps to NM_198694.2 S7S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X8-AAAR-01A-11D-A403-09 chr21:46021042 C>T maps to ENST00000380102 S174S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GN-01A-11D-A37C-09 chr21:32253807 G>A maps to NM_175858.2 S12S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93D-01A-11D-A387-09 chr21:32253564 G>T maps to NM_175858.2 S93S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A8I1-01A-11D-A36J-09 chr21:31797972 G>A maps to NM_181622.1 H86H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93D-01A-11D-A387-09 chr21:31869188 A>G maps to NM_181610.1 N80N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L7-A6VZ-01A-12D-A33E-09 chr21:31869392 G>T maps to ENST00000433652 G12G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OG-01A-11D-A27G-09 chr21:31874222 G>T maps to NM_181611.1 C62*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L7-A6VZ-01A-12D-A33E-09 chr21:32410729 C>A maps to NM_001099219.1 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HW-01A-22D-A351-09 chr21:31988817 G>T maps to ENST00000399871 G38G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GL-01A-12D-A37C-09 chr21:31655244 A>G maps to NM_001085455.1 P2P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr21:31655067 G>A maps to NM_001085455.1 C61C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GO-01A-11D-A37C-09 chr21:31692194 T>C maps to NM_203405.1 T53T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6L6-01B-11D-A33E-09 chr17:39156015 G>C maps to NM_031959.2 V30V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3YC-01A-11D-A247-09 chr17:39324397 G>A maps to NM_033187.1 V9V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-M9-A5M8-01A-11D-A28B-09 chr17:39240565 G>A maps to ENST00000377731 R36R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A8HZ-01A-11D-A36J-09 chr17:39261660 C>G maps to NM_001146041.1 G7G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A9-01A-11D-A28B-09 chr11:1606185 A>G maps to NM_001005922.1 G98G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A9-01A-11D-A28B-09 chr11:1606197 T>G maps to NM_001005922.1 G94G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A5B8-01A-11D-A28B-09 chr11:71276875 A>G maps to ENST00000422553 K138K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43H-01A-11D-A247-09 chr11:1628955 C>T maps to ENST00000359229 K270K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr11:1651171 C>T maps to NM_001001480.2 G34G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4MR-01A-11D-A28B-09 chr11:1651711 A>G maps to NM_001001480.2 Q214Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-AAPN-01A-11D-A403-09 chr11:71238746 C>G maps to NM_001012503.1 S134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-M9-A5M8-01A-11D-A28B-09 chr17:39382933 C>T maps to NM_031961.2 Q10*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-M9-A5M8-01A-11D-A28B-09 chr17:39411664 C>T maps to NM_030975.2 Q10*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FO-01A-11D-A387-09 chr17:25931750 G>T maps to ENST00000268763 A482A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A939-01A-12D-A37C-09 chr12:117977584 C>T maps to ENST00000339824 P542P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A5U7-01A-11D-A31U-09 chr12:117914381 G>A maps to ENST00000339824 R823R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HY-01A-12D-A351-09 chr12:117977635 C>T maps to ENST00000339824 T525T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A50L-01A-11D-A27G-09 chr23:153130786 C>T did not map to a codon.
Sequencing variant TCGA-JY-A6FH-01A-11D-A33E-09 chr23:153130277 G>T did not map to a codon.
Sequencing variant TCGA-L5-A88Z-01A-11D-A36J-09 chr23:153132168 T>C did not map to a codon.
Sequencing variant TCGA-L7-A6VZ-01A-12D-A33E-09 chr23:153134316 G>A did not map to a codon.
Sequencing variant TCGA-LN-A5U6-01A-11D-A28B-09 chr23:153134085 G>A did not map to a codon.
Sequencing variant TCGA-VR-A8EQ-01A-11D-A36J-09 chr23:153134085 G>A did not map to a codon.
Sequencing variant TCGA-JY-A93D-01A-11D-A387-09 chr1:62676045 G>T maps to NM_019079.4 E534*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RE-A7BO-01A-11D-A33E-09 chr1:62676525 G>T maps to NM_019079.4 E694*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr14:50735880 C>T maps to NM_024884.2 P302P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A50L-01A-11D-A27G-09 chr20:42157354 C>A maps to NM_032107.4 A285A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OH-01A-11D-A27G-09 chr22:41605729 G>T maps to NM_031488.4 E19*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NK-01A-21D-A37C-09 chr22:41623139 G>T maps to NM_031488.4 V545V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NF-01A-11D-A37C-09 chr6:130415491 G>T maps to NM_032438.2 A572A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr18:6093419 G>T maps to NM_173464.3 S436*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A4-01A-11D-A27G-09 chr18:6311609 G>A maps to NM_173464.3 N5N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GR-01A-12D-A37C-09 chr12:55026094 C>T maps to NM_033277.1 Q61Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43C-01A-11D-A247-09 chr18:7043224 C>T did not map to a codon.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr18:6975947 A>G maps to NM_005559.2 G2159G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OE-01A-11D-A27G-09 chr18:6965421 A>G maps to NM_005559.2 L2354L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OW-01A-11D-A28B-09 chr18:6950864 G>T maps to NM_005559.2 G2771G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr18:7024413 C>T maps to NM_005559.2 W818*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L7-A6VZ-01A-12D-A33E-09 chr18:6993682 T>C maps to NM_005559.2 Q1655Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8WG-01A-11D-A37C-09 chr18:7012080 G>A maps to NM_005559.2 R1140R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GO-01A-11D-A37C-09 chr6:129635906 C>T maps to NM_000426.3 T1173T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A5B8-01A-11D-A28B-09 chr6:129724964 G>C did not map to a codon.
Sequencing variant TCGA-L5-A8NS-01A-12D-A37C-09 chr6:129807651 C>T maps to NM_000426.3 L2595L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49K-01A-11D-A247-09 chr6:129785572 G>T maps to NM_000426.3 L2377L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49W-01A-11D-A27G-09 chr18:21329507 G>T maps to ENST00000416669 E228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3YA-01A-11D-A247-09 chr6:112508789 G>T maps to NM_001105206.1 C276*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A97I-01A-11D-A387-09 chr20:60886989 G>A maps to NM_005560.3 Y3207Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88V-01A-11D-A351-09 chr20:60912700 C>T maps to NM_005560.3 T703T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GN-01A-11D-A37C-09 chr7:107569651 T>G did not map to a codon.
Sequencing variant TCGA-VR-A8EW-01A-11D-A36J-09 chr7:107638865 G>A maps to NM_002291.2 L95L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93E-01A-11D-A37C-09 chr3:49160627 C>T maps to NM_002292.3 Q1387Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FP-01A-31D-A387-09 chr3:49161854 G>A maps to NM_002292.3 S1100S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A5B8-01A-11D-A28B-09 chr1:209800281 C>T maps to NM_000228.2 L509L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GH-01A-11D-A37C-09 chr1:183087274 G>T maps to NM_002293.3 E662*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr1:183196722 G>A maps to NM_005562.2 P453P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr9:133946902 G>T maps to ENST00000355048 T1034T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASW-01A-11D-A403-09 chr9:133932370 G>A maps to ENST00000355048 P665P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3QL-01A-11D-A247-09 chr23:119589254 G>T did not map to a codon.
Sequencing variant TCGA-XP-A8T7-01A-11D-A36J-09 chr3:182871573 G>A maps to NM_014398.3 Q219*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A4P3-01A-11D-A27G-09 chr4:17600161 C>G maps to NM_015907.2 L387L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NQ-01A-11D-A36J-09 chr4:17586669 G>T maps to NM_015907.2 T205T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6XG-01B-11D-A33E-09 chr22:33712228 C>T maps to NM_133642.3 Q431Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASW-01A-11D-A403-09 chr15:71128816 G>A maps to NM_018357.2 N76N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GQ-01A-11D-A37C-09 chr3:45530291 C>T maps to NM_015340.3 S409S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3YB-01A-11D-A247-09 chr3:45500279 G>T maps to NM_015340.3 E218*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OM-01A-11D-A27G-09 chr3:45557697 G>A maps to NM_015340.3 G658G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RF-01A-13D-A33E-09 chr23:64738219 A>G did not map to a codon.
Sequencing variant TCGA-IG-A4QS-01A-11D-A27G-09 chr23:64743981 G>T did not map to a codon.
Sequencing variant TCGA-L5-A4OU-01A-11D-A28B-09 chr17:37074944 C>T maps to NM_006148.2 Q234*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A8JE-01A-11D-A37C-09 chr15:101013167 G>T maps to ENST00000394113 L244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RF-01A-13D-A33E-09 chr16:28997468 C>A maps to NM_014387.3 P59P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XP-A8T7-01A-11D-A36J-09 chr6:149997780 G>T maps to NM_004690.2 R896R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HX-01A-11D-A33E-09 chr13:21562127 G>T maps to NM_014572.2 Y597*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A5B8-01A-11D-A28B-09 chr1:203743775 G>A maps to NM_017773.3 Q388Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NI-01A-11D-A37C-09 chr1:203740066 T>C did not map to a codon.
Sequencing variant TCGA-Z6-A8JE-01A-11D-A37C-09 chr11:111430915 C>G maps to ENST00000375615 V294V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93D-01A-11D-A387-09 chr2:30457269 G>A did not map to a codon.
Sequencing variant TCGA-LN-A4A2-01A-31D-A27G-09 chr20:36982827 G>A maps to NM_004139.2 S171S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr1:225592357 G>T maps to NM_194442.1 R512R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OJ-01A-11D-A27G-09 chr10:102988554 G>A maps to NM_006562.4 D6D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A8JE-01A-11D-A37C-09 chr2:74725122 G>C maps to NM_001009812.1 L172L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4MQ-01A-11D-A28B-09 chr15:68124643 G>T maps to ENST00000380035 E874*. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-LN-A9FP-01A-31D-A387-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-L5-A88V-01A-11D-A351-09 chr1:152636847 C>T maps to NM_178430.2 P89P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NT-01A-11D-A37C-09 chr1:152538408 G>T maps to NM_178435.2 C92*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FB-01A-11D-A33E-09 chr1:152681754 C>A maps to NM_178356.2 S68S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49M-01A-21D-A27G-09 chr16:25186293 G>T maps to ENST00000380963 L311L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A891-01A-11D-A36J-09 chr9:130913919 A>G maps to ENST00000373013 K95K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr4:18023329 A>G maps to NM_001166139.1 A15A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49Y-01A-11D-A27G-09 chr13:46718647 C>A maps to NM_002298.4 T394T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GI-01A-11D-A37C-09 chr2:136567303 A>C maps to NM_002299.2 T871T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49W-01A-11D-A27G-09 chr2:136566568 C>T maps to NM_002299.2 Q1116Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A8-01A-32D-A27G-09 chr2:136570211 C>G maps to NM_002299.2 L674L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6Y0-01B-11D-A33E-09 chr2:136564730 G>T maps to NM_002299.2 G1380G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA7D-01A-11D-A403-09 chr2:136564748 G>T maps to NM_002299.2 Y1374*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6Y2-01B-11D-A33E-09 chr15:66850359 G>T maps to NM_207338.2 A240A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FP-01A-31D-A387-09 chr10:88466293 T>A maps to NM_007078.2 P301P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43I-01A-11D-A247-09 chr12:21788571 G>A maps to NM_002300.6 S303S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr16:75147876 G>A maps to NM_153486.3 P295P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A891-01A-11D-A36J-09 chr16:75149179 C>T maps to NM_153486.3 L81L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8W5-01B-11D-A37C-09 chr16:75146325 G>A maps to NM_153486.3 G484G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GO-01A-11D-A37C-09 chr19:11231049 G>A maps to NM_000527.4 V664V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93E-01A-11D-A37C-09 chr19:11240345 G>A maps to NM_000527.4 S849S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OM-01A-11D-A27G-09 chr11:36119943 C>T maps to NM_174902.2 S129S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88T-01A-11D-A351-09 chr23:140271052 G>A did not map to a codon.
Sequencing variant TCGA-L5-A88T-01A-11D-A351-09 chr13:53298170 C>T maps to NM_007015.2 E143E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A893-01A-11D-A36J-09 chr3:156570673 G>T maps to NM_001004316.2 G56*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FP-01A-31D-A387-09 chr6:33752153 G>T maps to NM_181336.3 L276L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NN-01A-11D-A37C-09 chr19:54969280 G>T did not map to a codon.
Sequencing variant TCGA-LN-A49N-01A-11D-A247-09 chr19:54968054 G>C maps to ENST00000431846 L562L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EQ-01A-11D-A36J-09 chr19:54963326 G>T maps to ENST00000431846 P32P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A8-01A-32D-A27G-09 chr19:54973716 G>A maps to NM_198988.1 N353N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GH-01A-11D-A37C-09 chr1:66102028 T>A maps to NM_002303.5 L943L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASX-01A-11D-A387-09 chr1:66102028 T>G maps to NM_002303.5 L943L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EX-01A-11D-A36J-09 chr1:66058441 T>C maps to NM_002303.5 P199P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OE-01A-11D-A27G-09 chr3:189688651 C>A maps to NM_018192.3 E616*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FD-01A-11D-A33E-09 chr12:51450146 G>T maps to ENST00000448283 R272R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OQ-01A-11D-A27G-09 chr7:2565991 C>T maps to NM_001040167.1 H312H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93D-01A-11D-A387-09 chr22:37966317 C>A maps to NM_006498.2 L117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A8JD-01A-11D-A36J-09 chr17:76969203 C>G maps to NM_005567.3 V159V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A4-01A-11D-A27G-09 chr1:236704980 C>T maps to NM_201545.1 L165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A51D-01A-11D-A27G-09 chr17:18390983 C>T maps to NM_001040078.2 F119F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A97H-01A-11D-A387-09 chr17:18396130 T>C maps to NM_001040078.2 S294S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GL-01A-12D-A37C-09 chr4:25028543 G>T maps to NM_018176.3 S96*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EO-01A-11D-A36J-09 chr4:25005843 G>A maps to NM_018176.3 V289V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43C-01A-11D-A247-09 chr1:202245466 G>A maps to NM_001017403.1 P154P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASV-01A-11D-A387-09 chr1:202276456 G>T did not map to a codon.
Sequencing variant TCGA-VR-A8EO-01A-11D-A36J-09 chr6:63995556 G>T maps to NM_016571.2 R89R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88W-01A-11D-A351-09 chr1:206776494 G>C maps to NM_006893.2 L198L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EX-01A-11D-A36J-09 chr19:49519432 G>C maps to NM_000894.2 L106L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A8I1-01A-11D-A36J-09 chr2:48915636 C>T maps to NM_000233.3 W433*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6DN-01B-11D-A31U-09 chr2:48925916 G>A maps to NM_000233.3 Q235*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XP-A8T7-01A-11D-A36J-09 chr2:48921376 C>G maps to NM_000233.3 V311V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43E-01A-11D-A247-09 chr7:103969418 C>T maps to NM_199000.2 G64G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASX-01A-11D-A387-09 chr7:103969250 C>T maps to NM_199000.2 A8A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XP-A8T7-01A-11D-A36J-09 chr7:103969247 T>C maps to NM_199000.2 A7A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3Y9-01A-12D-A247-09 chr6:35782461 C>G maps to NM_182548.3 L184L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HZ-01A-31D-A351-09 chr6:35773671 C>T maps to NM_182548.3 S75S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OJ-01A-11D-A27G-09 chr10:126185529 G>T maps to NM_022126.3 G156G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8W8-01B-11D-A37C-09 chr10:126301883 C>T maps to NM_022126.3 N256N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GF-01A-11D-A37C-09 chr17:35300238 C>T maps to NM_005568.3 T344T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6XG-01B-11D-A33E-09 chr1:75602807 C>T maps to NM_001001933.1 D43D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RE-01A-11D-A33E-09 chr5:38510728 T>C maps to NM_002310.5 K276K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RE-01A-11D-A33E-09 chr5:38510734 T>C maps to NM_002310.5 Q274Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OO-01A-11D-A27G-09 chr5:38484941 G>T maps to NM_002310.5 I842I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8Q7-01A-11D-A37C-09 chr5:38490351 C>A maps to NM_002310.5 G703*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A97H-01A-11D-A387-09 chr19:48665526 G>T maps to NM_000234.1 P33P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88S-01A-11D-A36J-09 chr19:48630557 G>A maps to NM_000234.1 F660F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HX-01A-11D-A33E-09 chr19:48640269 G>T maps to NM_000234.1 I442I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr17:33326422 G>A maps to NM_013975.3 T737T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A1-01A-21D-A27G-09 chr13:108863309 C>A maps to NM_001098268.1 G103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A51D-01A-11D-A27G-09 chr19:55085969 C>T maps to NM_001130917.1 H91H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FD-01A-11D-A33E-09 chr19:55086219 C>A maps to NM_001130917.1 L125L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NQ-01A-11D-A36J-09 chr19:55087565 C>A maps to NM_001130917.1 L415L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr19:54802011 C>T maps to ENST00000251375 A392A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q9-A6FU-01A-11D-A31U-09 chr19:54848412 T>G maps to NM_012276.3 G318G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4MR-01A-11D-A28B-09 chr19:54823233 G>T maps to NM_021250.2 I103I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FP-01A-31D-A387-09 chr19:54744788 C>A maps to ENST00000245620 G291G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr19:55179120 G>A maps to ENST00000391733 T360T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-AAPN-01A-11D-A403-09 chr19:55175697 C>T maps to ENST00000391733 S139S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EO-01A-11D-A36J-09 chr19:54761021 C>T did not map to a codon.
Sequencing variant TCGA-RE-A7BO-01A-11D-A33E-09 chr12:50598455 G>T maps to NM_001113546.1 S248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASX-01A-11D-A387-09 chr3:45637429 G>C maps to NM_014240.2 S353S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FP-01A-31D-A387-09 chr19:36243134 G>A maps to NM_019104.1 E31E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8WC-01A-11D-A37C-09 chr19:36245291 A>G did not map to a codon.
Sequencing variant TCGA-JY-A6FE-01A-11D-A33E-09 chr12:81242082 C>A maps to NM_004664.2 E74*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A8O2-01A-11D-A36J-09 chr15:77907090 C>G maps to NM_032808.5 R386R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93D-01A-11D-A387-09 chr15:77907462 G>T maps to NM_032808.5 G262G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XP-A8T8-01A-11D-A36J-09 chr1:151773857 T>C maps to NM_001004432.2 P441P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NN-01A-11D-A37C-09 chr10:90438383 C>G maps to NM_001198829.1 A391A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49N-01A-11D-A247-09 chr3:185252681 G>C maps to NM_139248.2 L96L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XP-A8T6-01A-11D-A36J-09 chr21:15554180 C>T did not map to a codon.
Sequencing variant TCGA-2H-A9GL-01A-12D-A37C-09 chr10:90528547 G>C did not map to a codon.
Sequencing variant TCGA-IC-A6RE-01A-11D-A33E-09 chr5:96430718 A>G maps to NM_153234.4 S194S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NK-01A-21D-A37C-09 chr5:96460289 C>T maps to NM_153234.4 Q42Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GG-01A-11D-A37C-09 chr15:75112433 C>T maps to NM_021819.2 S256S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EZ-01A-11D-A36J-09 chr15:75116810 G>A maps to NM_021819.2 V481V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6Y0-01B-11D-A33E-09 chr5:176765594 G>T maps to NM_006816.2 L109L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GJ-01A-11D-A37C-09 chr5:36137523 G>A maps to NM_001007527.1 Q130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43M-01A-11D-A247-09 chr16:920851 G>T maps to ENST00000262301 S370*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q9-A6FW-01A-31D-A31U-09 chr16:920017 G>A maps to ENST00000262301 S427S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EY-01A-11D-A36J-09 chr16:920751 G>A maps to ENST00000262301 V403V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GI-01A-11D-A37C-09 chr22:50942068 C>T maps to NM_033200.2 W625*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NV-01A-11D-A37C-09 chr22:50942260 C>T maps to NM_033200.2 T597T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49W-01A-11D-A27G-09 chr22:50944765 G>T maps to NM_033200.2 A181A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6L6-01B-11D-A33E-09 chr22:50942047 G>T maps to NM_033200.2 P632P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FE-01A-11D-A33E-09 chr5:126113415 C>T maps to NM_005573.3 G72G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q9-A6FW-01A-31D-A31U-09 chr19:2431819 G>A maps to NM_032737.2 G537G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FE-01A-11D-A33E-09 chr11:33881096 G>T maps to NM_005574.3 C163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr12:16713447 G>A maps to ENST00000441439 C95C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FP-01A-31D-A387-09 chr1:87805311 T>A maps to NM_006769.3 L110L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RE-01A-11D-A33E-09 chr1:201869081 C>T maps to NM_012134.2 E353E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49V-01A-11D-A247-09 chr1:201915357 G>A maps to NM_012134.2 D37D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NN-01A-11D-A37C-09 chr7:123302461 C>T maps to NM_207163.1 N274N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A97H-01A-11D-A387-09 chr7:97820970 C>A maps to NM_014916.3 P398P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr19:49003053 G>T maps to NM_001080434.1 P453P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8Q7-01A-11D-A37C-09 chr19:49002993 C>T maps to NM_001080434.1 P473P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HY-01A-12D-A351-09 chr1:165322386 G>T maps to NM_177398.3 A63A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8ER-01A-11D-A36J-09 chr1:165218761 G>A maps to NM_177398.3 R127*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GI-01A-11D-A37C-09 chr9:129453222 G>T maps to NM_001174147.1 V145V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OJ-01A-11D-A27G-09 chr9:129455487 C>T maps to NM_001174147.1 S209S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FE-01A-11D-A33E-09 chr5:96332091 A>G did not map to a codon.
Sequencing variant TCGA-S8-A6BW-01A-11D-A31U-09 chr5:96341826 G>T maps to NM_005575.2 L612L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EW-01A-11D-A36J-09 chr5:96339189 C>T maps to NM_005575.2 Y575Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6F8-01A-11D-A33E-09 chr4:54373550 G>A maps to NM_001126328.1 S236S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49O-01A-11D-A247-09 chr4:54362372 G>T maps to NM_001126328.1 P389P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L7-A6VZ-01A-12D-A33E-09 chr13:28141832 G>T maps to NM_153371.3 R267R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6DN-01B-11D-A31U-09 chr19:19261544 C>T maps to ENST00000409447 T47T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6F8-01A-11D-A33E-09 chr16:48368152 G>T maps to NM_031490.2 E608*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EZ-01A-11D-A36J-09 chr8:12592792 A>G did not map to a codon.
Sequencing variant TCGA-2H-A9GH-01A-11D-A37C-09 chr23:118148248 T>C did not map to a codon.
Sequencing variant TCGA-L5-A4ON-01A-11D-A27G-09 chr8:23186065 G>A maps to NM_002318.2 R327*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RF-01A-13D-A33E-09 chr10:100020862 G>T maps to NM_032211.6 R160R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OH-01A-11D-A27G-09 chr10:100012167 G>T maps to NM_032211.6 S631S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6L6-01B-11D-A33E-09 chr6:160969600 G>T maps to NM_005577.2 C1688*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr9:113704387 G>T maps to NM_057159.2 R36R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X8-AAAR-01A-11D-A403-09 chr19:19737604 C>T maps to NM_004720.5 L163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A6QS-01A-12D-A33E-09 chr1:85279549 G>A maps to NM_012152.2 V347V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8ER-01A-11D-A36J-09 chr12:6729478 G>T maps to ENST00000435659 G312G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93E-01A-11D-A37C-09 chr16:55608566 C>T maps to NM_017839.4 R414*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GN-01A-11D-A37C-09 chr15:34655018 G>A maps to NM_153613.2 L255L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A939-01A-12D-A37C-09 chr15:34651937 A>G maps to NM_153613.2 A417A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OF-01A-11D-A27G-09 chr19:14274195 C>A maps to NM_001008701.2 L144L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr19:14288526 G>A maps to NM_001008701.2 L34L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6Y0-01B-11D-A33E-09 chr1:82409085 C>A maps to ENST00000370717 Y277*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8WC-01A-11D-A37C-09 chr4:62599269 C>A maps to ENST00000506720 S466*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr2:11964847 T>C maps to ENST00000396099 S910S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-A7RC-01B-11D-A403-09 chr2:11927287 G>T maps to ENST00000396099 G552G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FO-01A-11D-A387-09 chr20:39986952 G>T maps to NM_022896.1 G757*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-AAPN-01A-11D-A403-09 chr8:19813422 G>T maps to NM_000237.2 E283*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A50L-01A-11D-A27G-09 chr17:56329697 C>T maps to NM_006151.2 S312S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A939-01A-12D-A37C-09 chr19:11470600 C>T maps to NM_001170635.1 S95S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FD-01A-11D-A33E-09 chr19:821507 G>A maps to NM_024888.1 L18L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FP-01A-31D-A387-09 chr19:815234 G>T maps to NM_024888.1 A118A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GK-01A-11D-A37C-09 chr1:99772253 T>G maps to NM_014839.4 T660T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr4:155665741 G>A maps to NM_004744.3 T88T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GG-01A-11D-A37C-09 chr4:151935671 G>A maps to NM_006726.3 I41I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A6QS-01A-12D-A33E-09 chr4:151247050 C>A did not map to a codon.
Sequencing variant TCGA-L5-A88W-01A-11D-A351-09 chr4:151604719 C>T maps to NM_006726.3 W1968*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A1-01A-21D-A27G-09 chr4:151791716 C>T maps to NM_006726.3 Q803Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A97I-01A-11D-A387-09 chr13:47224408 G>T maps to NM_001164211.1 L127L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NH-01A-11D-A37C-09 chr13:47263313 C>T maps to NM_001164211.1 R333*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A5U6-01A-11D-A28B-09 chr23:114422838 G>T did not map to a codon.
Sequencing variant TCGA-LN-A7HX-01A-11D-A33E-09 chr23:114398258 C>T did not map to a codon.
Sequencing variant TCGA-2H-A9GR-01A-12D-A37C-09 chr7:100183597 C>T maps to NM_002319.3 V42V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88V-01A-11D-A351-09 chr7:100180050 G>C maps to NM_002319.3 P84P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NK-01A-21D-A37C-09 chr11:804100 G>T maps to NM_145886.3 V96V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A8O2-01A-11D-A36J-09 chr6:40399643 G>A maps to NM_020737.1 S403S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr19:36431205 C>T maps to NM_024509.1 C293C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A8JE-01A-11D-A37C-09 chr14:42357020 C>G maps to NM_152447.3 S398*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OG-01A-11D-A27G-09 chr19:4538425 C>T maps to NM_052972.2 L190L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RE-01A-11D-A33E-09 chr3:66434523 G>A maps to NM_015541.2 D654D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr3:66433684 G>T maps to NM_015541.2 R738R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NT-01A-11D-A37C-09 chr3:66444596 G>A maps to NM_015541.2 D445D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA7D-01A-11D-A403-09 chr3:66436585 G>A maps to NM_015541.2 V536V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A891-01A-11D-A36J-09 chr12:59270233 G>A maps to NM_153377.3 D896D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43C-01A-11D-A247-09 chr10:85991793 C>A maps to NM_015613.2 L587L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43M-01A-11D-A247-09 chr10:85992507 C>T maps to NM_015613.2 P349P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6F8-01A-11D-A33E-09 chr4:110791308 G>A maps to NM_198506.2 K423K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr12:57605983 C>T maps to NM_002332.2 G4478G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L7-A6VZ-01A-12D-A33E-09 chr12:57571245 C>A maps to NM_002332.2 P1411P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8ET-01A-11D-A403-09 chr12:57579401 C>T maps to NM_002332.2 H2184H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr6:150141773 G>A maps to NM_032832.5 R472*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RE-01A-11D-A33E-09 chr8:105509675 A>C maps to NM_013437.4 T368T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GK-01A-11D-A37C-09 chr2:141214095 A>G maps to NM_018557.2 T3297T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GR-01A-12D-A37C-09 chr2:141459349 T>A maps to NM_018557.2 R2123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RE-01A-11D-A33E-09 chr2:141986842 T>C maps to NM_018557.2 R253R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RE-01A-11D-A33E-09 chr2:142012178 A>G maps to NM_018557.2 C125C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3Y9-01A-12D-A247-09 chr2:141143522 G>T maps to NM_018557.2 P3490P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A4QS-01A-11D-A27G-09 chr2:141208224 A>G maps to NM_018557.2 R3323R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FG-01A-11D-A33E-09 chr2:141299444 C>T maps to NM_018557.2 R2430R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43E-01A-11D-A247-09 chr2:141597655 T>G did not map to a codon.
Sequencing variant TCGA-L5-A4OG-01A-11D-A27G-09 chr2:141762949 A>G maps to NM_018557.2 A819A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr2:141201959 T>C maps to NM_018557.2 P3411P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4ON-01A-11D-A27G-09 chr2:141459344 G>A maps to NM_018557.2 T2124T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OR-01A-11D-A27G-09 chr2:141130628 A>G maps to NM_018557.2 C3572C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OW-01A-11D-A28B-09 chr2:141458110 A>C maps to NM_018557.2 A2169A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49Y-01A-11D-A27G-09 chr2:141816619 T>A maps to NM_018557.2 R414*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A9-01A-11D-A28B-09 chr2:141128843 A>G maps to NM_018557.2 T3593T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6XQ-01B-11D-A33E-09 chr2:141598620 T>C maps to NM_018557.2 S1660S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8WG-01A-11D-A37C-09 chr2:141291617 T>C maps to NM_018557.2 G2578G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RE-A7BO-01A-11D-A33E-09 chr2:141739816 A>T maps to NM_018557.2 S933S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASX-01A-11D-A387-09 chr2:141272282 A>G maps to NM_018557.2 H2736H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EQ-01A-11D-A36J-09 chr2:141660603 A>G maps to NM_018557.2 Y1217Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EW-01A-11D-A36J-09 chr2:142567878 G>A maps to NM_018557.2 C58C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93E-01A-11D-A37C-09 chr2:170034502 C>T maps to NM_004525.2 T3401T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NV-01A-11D-A37C-09 chr2:170177380 C>T maps to NM_004525.2 A31A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49K-01A-11D-A247-09 chr2:170030639 G>A maps to NM_004525.2 C3601C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A1-01A-21D-A27G-09 chr2:170027100 A>G maps to NM_004525.2 H3780H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZR-A9CJ-01B-11D-A387-09 chr2:170025141 C>A maps to NM_004525.2 E3848*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NI-01A-11D-A37C-09 chr19:33696341 G>A maps to NM_002333.3 A222A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93E-01A-11D-A37C-09 chr11:46890563 G>A maps to ENST00000256991 I1649I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NK-01A-21D-A37C-09 chr11:46911918 G>T maps to ENST00000256991 A653A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A6QS-01A-12D-A33E-09 chr11:68181295 C>G maps to NM_002335.2 L881L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FG-01A-11D-A33E-09 chr11:68183886 G>A maps to NM_002335.2 L973L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr11:68131292 G>A maps to NM_002335.2 W255*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93F-01A-21D-A37C-09 chr2:44190728 G>A maps to NM_133259.3 Q496*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GF-01A-11D-A37C-09 chr6:53747765 T>C maps to NM_018214.4 N146N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8W8-01B-11D-A37C-09 chr5:195432 G>T maps to NM_001080478.1 E504*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S8-A6BW-01A-11D-A31U-09 chr5:191775 C>T maps to NM_001080478.1 S41S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93E-01A-11D-A37C-09 chr6:25500403 T>C maps to NM_017640.5 L446L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr6:25435802 G>T maps to NM_017640.5 L114L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr6:25495431 T>C maps to NM_017640.5 P438P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6L6-01B-11D-A33E-09 chr6:25605047 G>A maps to NM_017640.5 G1187G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GH-01A-11D-A37C-09 chr14:24524823 G>T maps to NM_138360.3 R226R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GL-01A-12D-A37C-09 chr14:24524273 G>A did not map to a codon.
Sequencing variant TCGA-L5-A8NT-01A-11D-A37C-09 chr9:26996480 G>A maps to NM_022901.2 T204T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3QL-01A-11D-A247-09 chr12:7016542 G>A maps to NM_201650.2 E185E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HX-01A-11D-A33E-09 chr10:134174992 G>T maps to NM_030626.2 L401L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NH-01A-11D-A37C-09 chr15:99892670 C>T maps to NM_144598.2 C230C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NU-01A-11D-A36J-09 chr15:99796291 G>T maps to NM_144598.2 E44*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6Y2-01B-11D-A33E-09 chr11:76371079 G>T maps to NM_001128922.1 L519L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3QL-01A-11D-A247-09 chr3:196387350 G>A maps to NM_198565.1 L279L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NW-01A-11D-A37C-09 chr3:196388262 G>T maps to NM_198565.1 S583S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8ET-01A-11D-A403-09 chr3:196386810 C>T maps to NM_198565.1 G99G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NN-01A-11D-A37C-09 chr16:67380181 C>A maps to NM_018296.5 L74L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EW-01A-11D-A36J-09 chr17:44632541 G>A maps to NM_001006607.2 W1628*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XP-A8T7-01A-11D-A36J-09 chr17:44626125 G>A maps to NM_001006607.2 G1207G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S8-A6BW-01A-11D-A31U-09 chr17:62893153 C>T maps to NM_199340.2 A74A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A5U7-01A-11D-A31U-09 chr1:70671211 C>T maps to NM_017768.4 L4L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NS-01A-12D-A37C-09 chr1:46746101 G>C maps to ENST00000254454 P607P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA4G-01A-11D-A37C-09 chr1:46746080 C>T maps to ENST00000254454 L614L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49S-01A-11D-A247-09 chr12:122677395 C>T maps to NM_001098519.1 V398V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr17:17891351 C>T maps to NM_031294.3 D128D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93F-01A-21D-A37C-09 chr11:40137316 G>A maps to NM_020929.1 R176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8WC-01A-11D-A37C-09 chr11:40136996 C>A maps to NM_020929.1 L282L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EO-01A-11D-A36J-09 chr16:84182610 G>T did not map to a codon.
Sequencing variant TCGA-JY-A93D-01A-11D-A387-09 chr11:56949645 T>C maps to NM_001005210.2 D93D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49W-01A-11D-A27G-09 chr8:133595956 C>A maps to ENST00000250173 E404*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A625-01A-11D-A31U-09 chr4:52862197 C>T maps to NM_001024611.1 T330T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A891-01A-11D-A36J-09 chr4:52861276 C>T maps to NM_001024611.1 Q637Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr1:70225991 G>A maps to NM_020794.2 Q35Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EX-01A-11D-A36J-09 chr1:70225960 C>A maps to NM_020794.2 S25*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8W8-01B-11D-A37C-09 chr1:90049549 G>A maps to NM_015350.2 L447L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43E-01A-11D-A247-09 chr1:90180084 C>T maps to NM_032270.4 I652I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr1:90400756 A>G maps to NM_001134479.1 S710S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93C-01A-11D-A387-09 chr8:86044117 C>T maps to NM_033402.4 D630D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OW-01A-11D-A28B-09 chr3:37100290 G>T maps to NM_006309.2 I620I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GG-01A-11D-A37C-09 chr12:85450310 G>A maps to NM_001079910.1 Q580Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GK-01A-11D-A37C-09 chr12:85517860 T>C maps to NM_001079910.1 L1191L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GN-01A-11D-A37C-09 chr12:85517974 G>T maps to NM_001079910.1 E1229*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A7DP-01A-31D-A33E-09 chr12:85521700 G>T maps to NM_001079910.1 E1367*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A9-01A-11D-A28B-09 chr12:85449855 G>T maps to NM_001079910.1 E429*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6F8-01A-11D-A33E-09 chr1:74540390 T>C maps to NM_001105659.1 K317K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NW-01A-11D-A37C-09 chr3:169540620 C>T maps to NM_001080460.1 N304N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NE-01A-11D-A37C-09 chr15:101549049 T>A maps to NM_024652.3 R257R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA7I-01A-11D-A403-09 chr15:101591973 G>T maps to NM_024652.3 P1166P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GF-01A-11D-A37C-09 chr12:40646756 T>G maps to NM_198578.3 S409S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NF-01A-11D-A37C-09 chr12:40634304 G>T maps to NM_198578.3 E198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NI-01A-11D-A37C-09 chr12:40753151 A>T maps to NM_198578.3 R2312*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NJ-01A-11D-A36J-09 chr12:40681183 C>T maps to NM_198578.3 I844I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr12:40740636 T>C maps to NM_198578.3 Y2064Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA7B-01A-31D-A403-09 chr12:40689289 G>A maps to NM_198578.3 E980E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GQ-01A-11D-A37C-09 chr3:3886721 G>T maps to NM_020873.5 E133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A893-01A-11D-A36J-09 chr1:204587950 G>A maps to NM_201630.1 I390I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NN-01A-11D-A37C-09 chr7:110763329 C>T maps to NM_018334.4 R168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RE-A7BO-01A-11D-A33E-09 chr7:110762846 C>A maps to NM_018334.4 R7R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OH-01A-11D-A27G-09 chr20:6022627 C>T maps to NM_152611.3 P421P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr2:80530815 G>A maps to NM_178839.4 C43C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OR-01A-11D-A27G-09 chr2:80530482 G>A maps to NM_178839.4 P154P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A8HZ-01A-11D-A36J-09 chr2:80530053 G>T maps to NM_178839.4 P297P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZR-A9CJ-01B-11D-A387-09 chr2:80530904 G>A maps to NM_178839.4 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49M-01A-21D-A27G-09 chr10:68857427 C>T maps to NM_178011.3 L540L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8W5-01B-11D-A37C-09 chr10:68687288 C>T maps to NM_178011.3 I205I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EZ-01A-11D-A36J-09 chr10:68687864 G>A maps to NM_178011.3 P397P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OF-01A-11D-A27G-09 chr2:77746304 G>A maps to NM_001134745.1 N230N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OP-01A-11D-A27G-09 chr2:76975988 G>A maps to NM_001134745.1 I535I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RE-A7BO-01A-11D-A33E-09 chr9:130236143 C>A maps to NM_001005374.2 I228I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A4-01A-11D-A27G-09 chr3:54959123 G>T maps to NM_020678.2 A42A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EX-01A-11D-A36J-09 chr3:54958910 C>T maps to NM_020678.2 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZR-A9CJ-01B-11D-A387-09 chr12:1937325 G>T maps to NM_001163926.1 P4P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93E-01A-11D-A37C-09 chr7:102109465 C>T maps to NM_152892.1 I395I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49M-01A-21D-A27G-09 chr1:36859679 C>G maps to NM_032881.1 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FO-01A-11D-A387-09 chr20:60704985 G>A maps to NM_144703.2 Q191Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6KZ-01A-11D-A31U-09 chr20:60705583 A>G did not map to a codon.
Sequencing variant TCGA-JY-A6F8-01A-11D-A33E-09 chr11:1908054 G>T maps to ENST00000381758 E399*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GL-01A-12D-A37C-09 chr19:35758273 T>G maps to NM_205834.2 G517G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GH-01A-11D-A37C-09 chr21:47635093 C>G maps to NM_002340.5 P337P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8W5-01B-11D-A37C-09 chr12:96412681 C>T did not map to a codon.
Sequencing variant TCGA-LN-A49M-01A-21D-A27G-09 chr14:24785315 C>G maps to NM_181657.3 L153L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FE-01A-11D-A33E-09 chr2:33484652 A>C did not map to a codon.
Sequencing variant TCGA-R6-A6L4-01A-11D-A31U-09 chr2:33482361 G>T maps to ENST00000354476 E727*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EW-01A-11D-A36J-09 chr2:33488448 T>C maps to ENST00000354476 T870T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr14:74995694 G>A maps to NM_000428.2 G706G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88T-01A-11D-A351-09 chr14:75022359 C>T maps to NM_000428.2 Q289Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NT-01A-11D-A37C-09 chr14:75052600 C>T maps to NM_000428.2 P262P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49V-01A-11D-A247-09 chr14:74974790 G>A maps to NM_000428.2 D1220D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr11:65320668 C>T maps to NM_001130144.2 Q343Q. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-V5-A7RB-01A-11D-A351-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-Z6-A8JE-01A-11D-A37C-09 chr19:41111455 G>T maps to ENST00000308370 A263A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A893-01A-11D-A36J-09 chr12:6499471 G>A maps to NM_002342.1 Q332Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NF-01A-11D-A37C-09 chr15:41805205 G>T maps to NM_002344.5 I52I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A50L-01A-11D-A27G-09 chr6:144179138 G>T maps to NM_032860.3 E264*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GL-01A-12D-A37C-09 chr11:24759803 C>T maps to NM_001009909.2 Q97*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43I-01A-11D-A247-09 chr11:25098873 G>C did not map to a codon.
Sequencing variant TCGA-L5-A8NR-01A-11D-A37C-09 chr11:25071621 A>G maps to NM_001009909.2 Q268Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A8JD-01A-11D-A36J-09 chr11:24518815 G>A maps to NM_001009909.2 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FG-01A-11D-A33E-09 chr6:31638954 G>A maps to ENST00000375873 T46T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GR-01A-12D-A37C-09 chr2:160663487 A>T maps to NM_001198759.1 P1662P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OJ-01A-11D-A27G-09 chr2:160692030 G>A maps to NM_001198759.1 C1211C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NV-01A-11D-A37C-09 chr2:160661722 G>A maps to NM_002349.3 Y1667Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8WC-01A-11D-A37C-09 chr2:160735802 G>A maps to NM_001198759.1 D494D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8WC-01A-11D-A37C-09 chr6:6589068 C>T maps to NM_004271.3 S34S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6KZ-01A-11D-A31U-09 chr1:160784258 C>T maps to ENST00000263285 V260V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A4-01A-11D-A27G-09 chr2:99901178 T>G maps to NM_174898.2 P146P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A9-01A-11D-A28B-09 chr2:99858935 G>T maps to NM_175735.3 S177*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GQ-01A-11D-A37C-09 chr8:56879418 G>A maps to NM_002350.2 E312E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6Y0-01B-11D-A33E-09 chr8:143857077 G>A maps to NM_023946.2 N29N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A9VB-01A-21D-A37C-09 chr8:143832526 G>A maps to NM_205545.1 I40I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NV-01A-11D-A37C-09 chr1:219347270 C>T maps to NM_138794.3 I13I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49M-01A-21D-A27G-09 chr1:151134279 C>T maps to NM_212551.4 K159K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A4P3-01A-11D-A27G-09 chr1:235897833 G>T maps to NM_000081.2 C2828*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6F8-01A-11D-A33E-09 chr1:235878570 G>T maps to NM_000081.2 S3238S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr1:235897833 G>T maps to NM_000081.2 C2828*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OU-01A-11D-A28B-09 chr1:235827306 G>A maps to NM_000081.2 P3748P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S8-A6BV-01A-21D-A31U-09 chr1:235972610 G>A maps to NM_000081.2 R503*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A8O2-01A-11D-A36J-09 chr22:21341810 C>T maps to NM_006767.3 T113T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr22:21347193 G>A did not map to a codon.
Sequencing variant TCGA-LN-A4A5-01A-21D-A27G-09 chr22:21348235 C>T maps to NM_006767.3 H459H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr8:20110343 G>A maps to NM_021020.2 Y366Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3Y9-01A-12D-A247-09 chr10:102762381 G>C maps to NM_032429.2 V29V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASX-01A-11D-A387-09 chr10:102763854 C>T maps to NM_032429.2 R334*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A51D-01A-11D-A27G-09 chr13:36049876 C>T maps to NM_005584.4 Q133Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NT-01A-11D-A37C-09 chr13:36049600 C>T maps to NM_005584.4 A225A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EQ-01A-11D-A36J-09 chr13:36050158 G>A maps to NM_005584.4 S39S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6F8-01A-11D-A33E-09 chr1:39765984 T>A maps to ENST00000361689 L867*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A939-01A-12D-A37C-09 chr1:39906713 G>T maps to ENST00000361689 E4104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OJ-01A-11D-A27G-09 chr1:39906683 G>T maps to ENST00000361689 E4094*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6XG-01B-11D-A33E-09 chr1:39800560 C>T maps to ENST00000289893 S1207S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6XQ-01B-11D-A33E-09 chr1:39715765 C>A maps to ENST00000361689 G121G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EW-01A-11D-A36J-09 chr1:39893940 G>A maps to ENST00000361689 R3533R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA7B-01A-31D-A403-09 chr1:39835765 C>T maps to ENST00000361689 Q2273*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GK-01A-11D-A37C-09 chr20:15843406 C>T maps to ENST00000310348 F221F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr4:120982059 C>T maps to NM_002358.3 T138T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3Y9-01A-12D-A247-09 chr1:11735183 G>A maps to ENST00000376669 D196D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4MQ-01A-11D-A28B-09 chr19:504757 G>A maps to NM_130760.2 A314A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr11:47310954 G>A maps to NM_003682.3 A909A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NI-01A-11D-A37C-09 chr11:47307014 C>T maps to NM_003682.3 L809L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OW-01A-11D-A28B-09 chr8:145160669 G>A did not map to a codon.
Sequencing variant TCGA-LN-A49L-01A-11D-A247-09 chr8:145160881 C>A maps to NM_032272.4 S65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8WC-01A-11D-A37C-09 chr22:38610596 C>T maps to NM_012323.3 R69R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr7:1579725 C>T maps to NM_002360.3 R62R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88T-01A-11D-A351-09 chr19:35800942 C>T maps to NM_002361.3 S466S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NW-01A-11D-A37C-09 chr23:152482747 G>A did not map to a codon.
Sequencing variant TCGA-2H-A9GK-01A-11D-A37C-09 chr23:151303609 C>A did not map to a codon.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr23:151303083 C>A did not map to a codon.
Sequencing variant TCGA-L5-A4OJ-01A-11D-A27G-09 chr23:151304072 C>T did not map to a codon.
Sequencing variant TCGA-L5-A8NI-01A-11D-A37C-09 chr23:151303877 T>C did not map to a codon.
Sequencing variant TCGA-2H-A9GG-01A-11D-A37C-09 chr23:148797717 G>T did not map to a codon.
Sequencing variant TCGA-IG-A4QS-01A-11D-A27G-09 chr23:151900432 T>G did not map to a codon.
Sequencing variant TCGA-JY-A93E-01A-11D-A37C-09 chr23:151900212 C>T did not map to a codon.
Sequencing variant TCGA-IC-A6RE-01A-11D-A33E-09 chr23:151092793 G>C did not map to a codon.
Sequencing variant TCGA-IG-A97I-01A-11D-A387-09 chr23:151092504 C>A did not map to a codon.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr23:151283729 G>A did not map to a codon.
Sequencing variant TCGA-L5-A8NQ-01A-11D-A36J-09 chr23:151869921 C>T did not map to a codon.
Sequencing variant TCGA-XP-A8T7-01A-11D-A36J-09 chr23:151870171 C>A did not map to a codon.
Sequencing variant TCGA-IC-A6RE-01A-11D-A33E-09 chr23:149013829 C>T did not map to a codon.
Sequencing variant TCGA-R6-A6L6-01B-11D-A33E-09 chr23:149013843 C>A did not map to a codon.
Sequencing variant TCGA-LN-A49P-01A-11D-A247-09 chr23:148664812 G>A did not map to a codon.
Sequencing variant TCGA-R6-A8W8-01B-11D-A37C-09 chr23:30269481 A>G did not map to a codon.
Sequencing variant TCGA-L5-A4OX-01A-21D-A28B-09 chr23:27840073 T>A did not map to a codon.
Sequencing variant TCGA-R6-A6XG-01B-11D-A33E-09 chr23:27839519 G>T did not map to a codon.
Sequencing variant TCGA-2H-A9GR-01A-12D-A37C-09 chr23:35820810 T>C did not map to a codon.
Sequencing variant TCGA-RE-A7BO-01A-11D-A33E-09 chr23:26157599 A>C did not map to a codon.
Sequencing variant TCGA-L5-A893-01A-11D-A36J-09 chr23:30237368 G>T did not map to a codon.
Sequencing variant TCGA-RE-A7BO-01A-11D-A33E-09 chr23:30236801 A>C did not map to a codon.
Sequencing variant TCGA-Z6-A8JE-01A-11D-A37C-09 chr23:30236788 C>G did not map to a codon.
Sequencing variant TCGA-2H-A9GO-01A-11D-A37C-09 chr23:30254367 C>T did not map to a codon.
Sequencing variant TCGA-L5-A8NR-01A-11D-A37C-09 chr23:30254477 A>G did not map to a codon.
Sequencing variant TCGA-Z6-A8JE-01A-11D-A37C-09 chr23:30254353 C>T did not map to a codon.
Sequencing variant TCGA-2H-A9GN-01A-11D-A37C-09 chr23:30261120 C>T did not map to a codon.
Sequencing variant TCGA-L5-A8NJ-01A-11D-A36J-09 chr23:30261074 A>G did not map to a codon.
Sequencing variant TCGA-LN-A4A9-01A-11D-A28B-09 chr23:30260668 C>T did not map to a codon.
Sequencing variant TCGA-VR-AA7I-01A-11D-A403-09 chr23:30261126 T>G did not map to a codon.
Sequencing variant TCGA-IC-A6RF-01A-13D-A33E-09 chr23:26212569 G>T did not map to a codon.
Sequencing variant TCGA-IG-A3I8-01A-11D-A247-09 chr23:26213164 G>C did not map to a codon.
Sequencing variant TCGA-LN-A49V-01A-11D-A247-09 chr23:26213136 G>T did not map to a codon.
Sequencing variant TCGA-LN-A49Y-01A-11D-A27G-09 chr23:26212333 A>C did not map to a codon.
Sequencing variant TCGA-VR-AA7B-01A-31D-A403-09 chr23:26212542 G>T did not map to a codon.
Sequencing variant TCGA-JY-A93F-01A-21D-A37C-09 chr23:140993739 G>T did not map to a codon.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr23:140994823 C>A did not map to a codon.
Sequencing variant TCGA-L5-A4OX-01A-21D-A28B-09 chr23:140993850 A>C did not map to a codon.
Sequencing variant TCGA-L5-A4OX-01A-21D-A28B-09 chr23:140996373 T>G did not map to a codon.
Sequencing variant TCGA-L5-A8NT-01A-11D-A37C-09 chr23:140995191 G>C did not map to a codon.
Sequencing variant TCGA-LN-A8I1-01A-11D-A36J-09 chr23:140994967 A>T did not map to a codon.
Sequencing variant TCGA-LN-A8I1-01A-11D-A36J-09 chr23:140994983 C>T did not map to a codon.
Sequencing variant TCGA-LN-A8I1-01A-11D-A36J-09 chr23:140995005 A>C did not map to a codon.
Sequencing variant TCGA-V5-A7RC-01B-11D-A403-09 chr23:140994087 C>A did not map to a codon.
Sequencing variant TCGA-VR-A8EY-01A-11D-A36J-09 chr23:140993813 C>G did not map to a codon.
Sequencing variant TCGA-VR-AA7I-01A-11D-A403-09 chr23:140994795 C>T did not map to a codon.
Sequencing variant TCGA-Z6-A8JE-01A-11D-A37C-09 chr23:140996199 C>T did not map to a codon.
Sequencing variant TCGA-LN-A49M-01A-21D-A27G-09 chr23:141290895 G>A did not map to a codon.
Sequencing variant TCGA-LN-A49R-01A-11D-A247-09 chr23:141291731 G>A did not map to a codon.
Sequencing variant TCGA-R6-A6DQ-01B-11D-A31U-09 chr23:141290891 A>C did not map to a codon.
Sequencing variant TCGA-2H-A9GI-01A-11D-A37C-09 chr23:140985395 T>G did not map to a codon.
Sequencing variant TCGA-LN-A4A2-01A-31D-A27G-09 chr23:140985577 C>A did not map to a codon.
Sequencing variant TCGA-LN-A4A6-01A-11D-A27G-09 chr23:140983064 C>T did not map to a codon.
Sequencing variant TCGA-LN-A4A6-01A-11D-A27G-09 chr23:140985272 G>C did not map to a codon.
Sequencing variant TCGA-Q9-A6FU-01A-11D-A31U-09 chr23:140985177 A>T did not map to a codon.
Sequencing variant TCGA-Q9-A6FW-01A-31D-A31U-09 chr23:140984911 G>A did not map to a codon.
Sequencing variant TCGA-R6-A8WG-01A-11D-A37C-09 chr23:140984506 G>T did not map to a codon.
Sequencing variant TCGA-V5-AASV-01A-11D-A387-09 chr23:140984537 G>A did not map to a codon.
Sequencing variant TCGA-VR-A8EQ-01A-11D-A36J-09 chr23:140983146 A>G did not map to a codon.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr23:51639753 C>T did not map to a codon.
Sequencing variant TCGA-L5-A4OW-01A-11D-A28B-09 chr23:51644981 T>G did not map to a codon.
Sequencing variant TCGA-L5-A8NG-01A-11D-A37C-09 chr23:51644890 C>T did not map to a codon.
Sequencing variant TCGA-V5-AASX-01A-11D-A387-09 chr23:54842000 C>A did not map to a codon.
Sequencing variant TCGA-2H-A9GI-01A-11D-A37C-09 chr23:75650294 A>G did not map to a codon.
Sequencing variant TCGA-JY-A6FB-01A-11D-A33E-09 chr23:75648430 C>T did not map to a codon.
Sequencing variant TCGA-L5-A43E-01A-11D-A247-09 chr23:75649100 G>A did not map to a codon.
Sequencing variant TCGA-L5-A8NG-01A-11D-A37C-09 chr23:75650470 A>C did not map to a codon.
Sequencing variant TCGA-L5-A8NJ-01A-11D-A36J-09 chr23:75649974 T>C did not map to a codon.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr23:75650000 C>A did not map to a codon.
Sequencing variant TCGA-VR-AA4G-01A-11D-A37C-09 chr23:75648923 C>T did not map to a codon.
Sequencing variant TCGA-2H-A9GK-01A-11D-A37C-09 chr23:75004856 G>C did not map to a codon.
Sequencing variant TCGA-JY-A93E-01A-11D-A37C-09 chr23:75003937 C>A did not map to a codon.
Sequencing variant TCGA-JY-A93E-01A-11D-A37C-09 chr23:75004271 T>G did not map to a codon.
Sequencing variant TCGA-L5-A4OP-01A-11D-A27G-09 chr23:75004083 T>G did not map to a codon.
Sequencing variant TCGA-L5-A4OT-01A-11D-A28B-09 chr23:75004140 A>C did not map to a codon.
Sequencing variant TCGA-L5-A8NG-01A-11D-A37C-09 chr23:75004001 T>G did not map to a codon.
Sequencing variant TCGA-R6-A8W8-01B-11D-A37C-09 chr23:75003411 G>A did not map to a codon.
Sequencing variant TCGA-2H-A9GQ-01A-11D-A37C-09 chr23:55479334 C>T did not map to a codon.
Sequencing variant TCGA-VR-A8EQ-01A-11D-A36J-09 chr23:55479466 A>G did not map to a codon.
Sequencing variant TCGA-IG-A4P3-01A-11D-A27G-09 chr15:23890264 G>C maps to NM_019066.4 S875S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OE-01A-11D-A27G-09 chr15:23889870 G>A maps to NM_019066.4 Q1007*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OH-01A-11D-A27G-09 chr15:23889631 G>T maps to NM_019066.4 A1086A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49Y-01A-11D-A27G-09 chr15:23889958 C>T maps to NM_019066.4 R977R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6L4-01A-11D-A31U-09 chr15:23890549 C>T maps to NM_019066.4 P780P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OE-01A-11D-A27G-09 chr1:114226110 A>G maps to NM_001142782.1 K1307K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A9VB-01A-21D-A37C-09 chr1:113933939 C>T maps to NM_001142782.1 R95R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A8JD-01A-11D-A36J-09 chr23:77112966 T>A did not map to a codon.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr9:139753252 C>A maps to ENST00000392881 T1051T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GF-01A-11D-A37C-09 chr5:179192382 C>T maps to NM_014757.4 G124G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RF-01A-13D-A33E-09 chr11:95825421 C>T maps to NM_032427.1 Q591Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3QL-01A-11D-A247-09 chr11:96074768 G>A maps to NM_032427.1 A97A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A7DP-01A-31D-A33E-09 chr11:95825364 C>T maps to NM_032427.1 Q610Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FQ-01A-31D-A387-09 chr11:95825370 C>T maps to NM_032427.1 Q608Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GL-01A-12D-A37C-09 chr4:140811437 G>T maps to ENST00000509479 P384P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NL-01A-12D-A37C-09 chr4:140811107 C>T maps to ENST00000509479 Q494Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HW-01A-22D-A351-09 chr4:140811077 C>T maps to ENST00000509479 Q504Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6Y0-01B-11D-A33E-09 chr4:140812012 G>A maps to ENST00000509479 R193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GL-01A-12D-A37C-09 chr23:149638883 C>A did not map to a codon.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr23:149638718 G>A did not map to a codon.
Sequencing variant TCGA-L5-A88S-01A-11D-A36J-09 chr23:149680830 G>T did not map to a codon.
Sequencing variant TCGA-L5-A8NQ-01A-11D-A36J-09 chr23:149638835 C>G did not map to a codon.
Sequencing variant TCGA-L5-A8NS-01A-12D-A37C-09 chr23:149639631 T>C did not map to a codon.
Sequencing variant TCGA-VR-A8EY-01A-11D-A36J-09 chr23:149639248 G>T did not map to a codon.
Sequencing variant TCGA-ZR-A9CJ-01B-11D-A387-09 chr23:149639338 G>T did not map to a codon.
Sequencing variant TCGA-L5-A4OR-01A-11D-A27G-09 chr6:119501085 G>A maps to NM_005907.2 D620D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43E-01A-11D-A247-09 chr19:12775734 G>A maps to NM_000528.3 A167A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6XG-01B-11D-A33E-09 chr4:6596272 C>T maps to NM_015274.1 Q291*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NJ-01A-11D-A36J-09 chr15:75660484 C>T maps to NM_006715.2 E52E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A8I1-01A-11D-A36J-09 chr4:103571708 G>T maps to NM_005908.3 T618T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EQ-01A-11D-A36J-09 chr4:103578862 C>T maps to NM_005908.3 W560*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RE-A7BO-01A-11D-A33E-09 chr6:96034470 T>C maps to NM_024641.2 T52T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA7B-01A-31D-A403-09 chr6:96053780 G>T maps to NM_024641.2 G297*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-A7RC-01B-11D-A403-09 chr1:38261478 G>A maps to NM_001113482.1 V207V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr12:12483848 G>A maps to NM_018050.2 P136P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GK-01A-11D-A37C-09 chr23:43571183 C>T did not map to a codon.
Sequencing variant TCGA-L5-A891-01A-11D-A36J-09 chr23:43587476 C>G did not map to a codon.
Sequencing variant TCGA-R6-A6KZ-01A-11D-A31U-09 chr23:43591034 G>A did not map to a codon.
Sequencing variant TCGA-L5-A8NG-01A-11D-A37C-09 chr23:43702991 A>C did not map to a codon.
Sequencing variant TCGA-Z6-AAPN-01A-11D-A403-09 chr23:43661489 C>T did not map to a codon.
Sequencing variant TCGA-IG-A3YB-01A-11D-A247-09 chr5:71495634 C>T maps to NM_005909.3 S2151S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A938-01A-11D-A37C-09 chr5:71482490 C>A maps to NM_005909.3 T140T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43C-01A-11D-A247-09 chr5:71403399 C>T maps to NM_005909.3 S14S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr5:71494171 C>T maps to NM_005909.3 R1664*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NK-01A-21D-A37C-09 chr5:71493384 G>A maps to NM_005909.3 P1401P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6L6-01B-11D-A33E-09 chr5:71482532 C>A maps to NM_005909.3 S154S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49L-01A-11D-A247-09 chr20:33147158 C>T maps to NM_181509.1 I39I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GL-01A-12D-A37C-09 chr2:210595013 C>T maps to NM_002374.3 R1793*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A939-01A-12D-A37C-09 chr2:210557511 T>G maps to NM_002374.3 T206T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NL-01A-12D-A37C-09 chr2:210557838 T>C maps to NM_002374.3 S315S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4MQ-01A-11D-A28B-09 chr2:210559467 A>T maps to NM_002374.3 V858V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XP-A8T6-01A-11D-A36J-09 chr2:210517947 G>A maps to NM_002374.3 P18P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A893-01A-11D-A36J-09 chr15:66779569 C>T maps to NM_002755.3 Y300Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASX-01A-11D-A387-09 chr17:12028637 C>T maps to ENST00000415385 R292*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GL-01A-12D-A37C-09 chr15:68061971 G>A maps to NM_145160.1 S389S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GG-01A-11D-A37C-09 chr17:67515467 A>G maps to NM_002758.3 T87T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3I8-01A-11D-A247-09 chr5:56189380 A>G maps to NM_005921.1 P1471P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EZ-01A-11D-A36J-09 chr5:56161770 C>A maps to NM_005921.1 S423*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EZ-01A-11D-A36J-09 chr5:56179412 A>G maps to NM_005921.1 E1242E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A97H-01A-11D-A387-09 chr19:40718832 G>T maps to NM_002446.3 T558T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OG-01A-11D-A27G-09 chr11:65380855 G>A maps to NM_002419.3 G124G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FG-01A-11D-A33E-09 chr12:53877410 G>T maps to NM_001193511.1 L485L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KH-A6WC-01A-11D-A33E-09 chr3:185165696 G>T maps to NM_004721.3 V324V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr3:185184612 G>A did not map to a codon.
Sequencing variant TCGA-IG-A97I-01A-11D-A387-09 chr23:19390938 T>C did not map to a codon.
Sequencing variant TCGA-Q9-A6FU-01A-11D-A31U-09 chr23:19391655 G>C did not map to a codon.
Sequencing variant TCGA-Q9-A6FU-01A-11D-A31U-09 chr23:19418721 T>A did not map to a codon.
Sequencing variant TCGA-XP-A8T7-01A-11D-A36J-09 chr17:61744307 C>A maps to NM_203351.1 S161S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A8O2-01A-11D-A36J-09 chr6:161494610 C>T maps to NM_005922.2 D688D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FG-01A-11D-A33E-09 chr6:161514015 G>A maps to NM_005922.2 A1092A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NH-01A-11D-A37C-09 chr6:161470618 G>T maps to NM_005922.2 E439*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49P-01A-11D-A247-09 chr6:161470624 G>T maps to NM_005922.2 E441*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr6:137019799 G>T maps to NM_005923.3 T211T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4MR-01A-11D-A28B-09 chr6:137019721 G>A maps to NM_005923.3 L237L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6DN-01B-11D-A31U-09 chr6:136932474 G>A maps to NM_005923.3 D822D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49V-01A-11D-A247-09 chr1:27685090 G>T maps to NM_004672.3 Y865*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GR-01A-12D-A37C-09 chr6:91246094 G>A maps to NM_145331.1 S439S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FQ-01A-31D-A387-09 chr6:91246114 C>A maps to NM_145331.1 G433*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6XG-01B-11D-A33E-09 chr6:91266318 T>A maps to NM_145331.1 T169T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HY-01A-12D-A351-09 chr10:30739242 C>T maps to NM_005204.2 H187H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S8-A6BW-01A-11D-A31U-09 chr10:30749674 C>T maps to NM_005204.2 L438L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NK-01A-21D-A37C-09 chr14:71204981 C>T maps to NM_033141.2 E608E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EQ-01A-11D-A36J-09 chr2:102448249 C>A maps to NM_145686.2 P192P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49K-01A-11D-A247-09 chr11:75299015 C>T maps to NM_033063.1 T510T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49M-01A-21D-A27G-09 chr23:20030482 G>A did not map to a codon.
Sequencing variant TCGA-LN-A7HX-01A-11D-A33E-09 chr23:20043082 C>A did not map to a codon.
Sequencing variant TCGA-LN-A8HZ-01A-11D-A36J-09 chr23:20030524 C>G did not map to a codon.
Sequencing variant TCGA-IG-A50L-01A-11D-A27G-09 chr23:135313963 T>C did not map to a codon.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr4:156281334 T>G maps to NM_001039580.1 A345A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49P-01A-11D-A247-09 chr4:156274405 G>T maps to NM_001039580.1 A489A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HX-01A-11D-A33E-09 chr4:156283236 A>G maps to NM_001039580.1 S255S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A8I1-01A-11D-A36J-09 chr22:22123603 G>T maps to NM_138957.2 I324I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6L4-01A-11D-A31U-09 chr4:86938392 A>T maps to NM_138982.2 G461G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FB-01A-11D-A33E-09 chr8:144801008 C>T maps to NM_139021.2 I117I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FB-01A-11D-A33E-09 chr8:144801011 C>T maps to NM_139021.2 F118F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FB-01A-11D-A33E-09 chr8:144802412 C>T maps to NM_139021.2 L245L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A8I1-01A-11D-A36J-09 chr14:55529949 G>A maps to NM_144578.3 S211S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RE-A7BO-01A-11D-A33E-09 chr14:55529589 C>A maps to NM_144578.3 S91S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A2-01A-31D-A27G-09 chr16:30129093 C>T maps to NM_002746.2 K224K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HZ-01A-31D-A351-09 chr16:30129433 G>A maps to NM_002746.2 T198T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A8JD-01A-11D-A36J-09 chr18:48256222 G>A maps to NM_002747.3 *588*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S8-A6BW-01A-11D-A31U-09 chr10:49628337 C>T maps to NM_139049.1 I197I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NF-01A-11D-A37C-09 chr11:45925665 T>C maps to NM_005456.2 P540P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93E-01A-11D-A37C-09 chr16:1779534 G>A maps to NM_015133.3 Q186Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NF-01A-11D-A37C-09 chr16:1818619 C>T maps to NM_015133.3 F1294F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr16:1797088 C>T maps to NM_015133.3 T268T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A938-01A-11D-A37C-09 chr5:179668156 T>C did not map to a codon.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr9:128347904 G>A maps to NM_001006617.1 S200S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A50L-01A-11D-A27G-09 chr1:206858690 C>G maps to NM_032960.2 P39P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RE-01A-11D-A33E-09 chr12:112321522 G>T maps to NM_139078.1 E267*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr15:42115239 G>T maps to NM_001128608.1 G1146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6L4-01A-11D-A31U-09 chr17:44060542 G>C did not map to a codon.
Sequencing variant TCGA-Z6-A9VB-01A-21D-A37C-09 chr17:44061258 G>A maps to NM_001123066.3 P363P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L7-A6VZ-01A-12D-A33E-09 chr17:60813486 G>C maps to NM_152598.2 S581*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HX-01A-11D-A33E-09 chr17:60865947 G>A maps to NM_152598.2 R35*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NS-01A-12D-A37C-09 chr19:8503351 G>T maps to NM_016496.4 A221A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A4QS-01A-11D-A27G-09 chr2:217148413 G>C maps to NM_020814.2 V185V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr2:217142512 G>A maps to NM_020814.2 I249I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NN-01A-11D-A37C-09 chr2:217124264 G>T maps to NM_020814.2 R335R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XP-A8T6-01A-11D-A36J-09 chr2:217234788 G>A maps to NM_020814.2 H65H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GF-01A-11D-A37C-09 chr5:10405768 C>A maps to NM_005885.2 R478R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A97I-01A-11D-A387-09 chr5:10410317 G>T maps to NM_005885.2 E541*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FD-01A-11D-A33E-09 chr5:10382026 A>G maps to NM_005885.2 A102A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FE-01A-11D-A33E-09 chr10:45953908 C>T maps to NM_145021.4 Q218Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A5S3-01A-11D-A28B-09 chr2:119727699 G>T maps to NM_006770.3 L70L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A4QS-01A-11D-A27G-09 chr1:220825477 A>G maps to NM_018650.3 E574E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NI-01A-11D-A37C-09 chr1:220752751 C>T maps to NM_018650.3 S36S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA7D-01A-11D-A403-09 chr1:220835504 G>A maps to NM_018650.3 L795L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93D-01A-11D-A387-09 chr11:63670094 C>A maps to NM_001039469.2 T419T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr11:63665753 T>C did not map to a codon.
Sequencing variant TCGA-L5-A893-01A-11D-A36J-09 chr14:103932742 G>T maps to ENST00000335102 E344*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GM-01A-11D-A37C-09 chr2:198571904 G>T maps to NM_138395.3 R592R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NF-01A-11D-A37C-09 chr5:68715894 C>A maps to NM_001038603.2 S228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49Y-01A-11D-A27G-09 chr5:68715943 G>T maps to NM_001038603.2 G244G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HX-01A-11D-A33E-09 chr16:71674800 G>A maps to NM_001017967.2 V368V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GH-01A-11D-A37C-09 chr6:160328868 C>A maps to NM_002377.2 S294S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OE-01A-11D-A27G-09 chr3:186943174 C>A maps to NM_001879.5 E560*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A2-01A-31D-A27G-09 chr1:11105561 C>T maps to NM_006610.2 A149A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A939-01A-12D-A37C-09 chr1:46496276 A>G did not map to a codon.
Sequencing variant TCGA-JY-A939-01A-12D-A37C-09 chr1:46501456 C>T maps to NM_015112.2 Q1706*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OH-01A-11D-A27G-09 chr1:46497073 C>T maps to NM_015112.2 R1002*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NI-01A-11D-A37C-09 chr1:46499768 C>A maps to NM_015112.2 R1233R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6F8-01A-11D-A33E-09 chr5:66430446 G>T maps to NM_001164664.1 E775*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NR-01A-11D-A37C-09 chr5:66385996 C>T maps to NM_001164664.1 S257S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3YA-01A-11D-A247-09 chr10:27459381 T>C maps to NM_001172303.1 S498S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NS-01A-12D-A37C-09 chr2:85770070 C>T maps to NM_005911.4 F333F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49O-01A-11D-A247-09 chr5:162943689 C>T maps to NM_013283.3 C231C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8ET-01A-11D-A403-09 chr19:3779410 G>T maps to NM_002378.3 A323A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NE-01A-11D-A37C-09 chr2:20205631 G>A maps to NM_002381.4 G221G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NU-01A-11D-A36J-09 chr5:138658284 A>C did not map to a codon.
Sequencing variant TCGA-S8-A6BW-01A-11D-A31U-09 chr5:138661311 G>T maps to ENST00000394800 E826*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr20:3845275 T>C maps to NM_020746.3 P333P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr2:149221352 G>T maps to ENST00000404807 E88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASW-01A-11D-A403-09 chr2:149247653 A>C maps to ENST00000404807 R1485R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GK-01A-11D-A37C-09 chr14:36777396 T>A did not map to a codon.
Sequencing variant TCGA-L7-A6VZ-01A-12D-A33E-09 chr10:54529048 C>A maps to NM_000242.2 E111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A97H-01A-11D-A387-09 chr5:89770100 C>T maps to NM_203406.1 A3A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-A7RE-01A-11D-A351-09 chr5:89756983 C>A maps to NM_203406.1 *280Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr13:97995457 T>A maps to ENST00000376673 T176T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RE-A7BO-01A-11D-A33E-09 chr6:20131396 G>A maps to NM_001080480.1 T151T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NV-01A-11D-A37C-09 chr2:9008632 G>A maps to NM_138799.2 D310D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6DN-01B-11D-A31U-09 chr19:54687560 C>T maps to NM_024298.3 L112L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A5-01A-21D-A27G-09 chr18:74696751 C>T maps to NM_001025101.1 T283T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr16:84108234 G>A maps to NM_003791.2 N520N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3QL-01A-11D-A247-09 chr23:21896253 G>T did not map to a codon.
Sequencing variant TCGA-L5-A4OO-01A-11D-A27G-09 chr23:21861367 G>T did not map to a codon.
Sequencing variant TCGA-L5-A4OW-01A-11D-A28B-09 chr23:21869645 C>T did not map to a codon.
Sequencing variant TCGA-LN-A4A5-01A-21D-A27G-09 chr23:21861335 G>A did not map to a codon.
Sequencing variant TCGA-VR-AA7B-01A-31D-A403-09 chr18:13884644 G>T maps to NM_000529.2 I291I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93E-01A-11D-A37C-09 chr20:54824549 C>T maps to ENST00000371389 H254H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GK-01A-11D-A37C-09 chr18:58038874 G>T maps to NM_005912.2 R236R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NU-01A-11D-A36J-09 chr18:58038661 T>C maps to NM_005912.2 Q307Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A3-01A-11D-A27G-09 chr18:58038994 G>T maps to NM_005912.2 C196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-AAPN-01A-11D-A403-09 chr18:58038943 G>C maps to NM_005912.2 V213V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3I8-01A-11D-A247-09 chr18:13826393 C>T maps to NM_005913.2 L210L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr11:119182248 G>T maps to NM_006500.2 V466V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3Y9-01A-12D-A247-09 chr9:37888331 C>T maps to NM_033412.3 L72L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6Y0-01B-11D-A33E-09 chr23:103349670 C>T did not map to a codon.
Sequencing variant TCGA-L5-A8NE-01A-11D-A37C-09 chr3:182737953 G>T maps to NM_020166.3 G647G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93D-01A-11D-A387-09 chr23:138667260 A>G did not map to a codon.
Sequencing variant TCGA-L5-A4OX-01A-21D-A28B-09 chr23:138678768 C>T did not map to a codon.
Sequencing variant TCGA-L5-A8NS-01A-12D-A37C-09 chr23:138678709 T>C did not map to a codon.
Sequencing variant TCGA-LN-A4A5-01A-21D-A27G-09 chr13:113724462 G>A maps to NM_001112732.1 R381R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3QL-01A-11D-A247-09 chr3:182948801 G>A maps to NM_015078.2 R622R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OE-01A-11D-A27G-09 chr3:183097170 G>T maps to NM_015078.2 I63I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A5-01A-21D-A27G-09 chr3:182941139 C>G maps to NM_015078.2 L765L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA7B-01A-31D-A403-09 chr3:182933847 G>C maps to NM_015078.2 S802*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S8-A6BV-01A-21D-A31U-09 chr22:41077866 C>T maps to NM_005297.3 Q402*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XP-A8T8-01A-11D-A36J-09 chr6:100391009 G>A maps to NM_032503.2 A134A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A891-01A-11D-A36J-09 chr10:13214404 A>T maps to NM_182751.2 K127*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6Y0-01B-11D-A33E-09 chr10:13213246 G>T maps to NM_182751.2 T111T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GJ-01A-11D-A37C-09 chr20:5958592 A>C maps to NM_032485.4 V489V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A6QS-01A-12D-A33E-09 chr1:85422174 G>T maps to NM_153259.2 Y168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NQ-01A-11D-A36J-09 chr1:85506833 C>T maps to NM_018298.9 Q85Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GF-01A-11D-A37C-09 chr8:6293567 G>T did not map to a codon.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr8:6289043 T>C maps to NM_024596.3 I86I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49M-01A-21D-A27G-09 chr8:6289087 C>G maps to NM_024596.3 S101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8W8-01B-11D-A37C-09 chr12:49956844 C>T maps to NM_001012300.1 A261A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8W5-01B-11D-A37C-09 chr5:94230446 G>T maps to NM_024717.4 V582V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr15:94858853 C>T maps to NM_018349.3 R209*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49V-01A-11D-A247-09 chr6:30671586 C>T maps to NM_014641.2 V1791V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FB-01A-11D-A33E-09 chr7:114619651 G>T maps to NM_199072.4 L212L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43M-01A-11D-A247-09 chr6:37623624 G>A maps to ENST00000297153 R144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OJ-01A-11D-A27G-09 chr6:37626177 C>T maps to ENST00000297153 T75T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NN-01A-11D-A37C-09 chr6:37622642 C>T maps to ENST00000297153 Q215Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASX-01A-11D-A387-09 chr6:37618131 G>A maps to ENST00000297153 R454R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KH-A6WC-01A-11D-A33E-09 chr14:47613426 C>A maps to NM_001113498.2 E216*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OX-01A-21D-A28B-09 chr14:47351259 C>T maps to NM_001113498.2 V801V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49P-01A-11D-A247-09 chr14:47342645 T>C maps to NM_001113498.2 G914G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A8JD-01A-11D-A36J-09 chr14:47504274 G>T maps to NM_001113498.2 T586T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HZ-01A-31D-A351-09 chr12:68720466 G>T maps to NM_017440.4 T156T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HY-01A-12D-A351-09 chr12:69229655 G>A maps to NM_002392.3 Q244Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6F8-01A-11D-A33E-09 chr1:204515936 G>T maps to NM_002393.3 G279*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KH-A6WC-01A-11D-A33E-09 chr6:90422465 G>T maps to NM_014611.1 R2420R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OE-01A-11D-A27G-09 chr6:90362716 G>A maps to NM_014611.1 I5273I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88T-01A-11D-A351-09 chr6:90365588 G>A maps to NM_014611.1 S5128S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A2-01A-31D-A27G-09 chr6:90459387 C>T maps to NM_014611.1 A1163A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S8-A6BW-01A-11D-A31U-09 chr6:90398429 C>T maps to NM_014611.1 V3707V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EX-01A-11D-A36J-09 chr6:90438847 T>A maps to NM_014611.1 L1717L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GO-01A-11D-A37C-09 chr6:42980730 C>T maps to NM_014623.2 E113E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NI-01A-11D-A37C-09 chr6:42980661 A>T did not map to a codon.
Sequencing variant TCGA-JY-A93D-01A-11D-A387-09 chr3:168819858 G>T maps to NM_004991.3 R920R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RE-01A-11D-A33E-09 chr23:153296570 C>A did not map to a codon.
Sequencing variant TCGA-JY-A6F8-01A-11D-A33E-09 chr23:153295921 G>T did not map to a codon.
Sequencing variant TCGA-JY-A93F-01A-21D-A37C-09 chr23:153295832 G>A did not map to a codon.
Sequencing variant TCGA-Z6-AAPN-01A-11D-A403-09 chr23:153295861 C>G did not map to a codon.
Sequencing variant TCGA-LN-A4MR-01A-11D-A28B-09 chr17:37566024 G>A maps to NM_004774.3 Q817*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HZ-01A-31D-A351-09 chr17:37566856 G>A maps to NM_004774.3 N539N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GF-01A-11D-A37C-09 chr23:70342373 G>T did not map to a codon.
Sequencing variant TCGA-2H-A9GJ-01A-11D-A37C-09 chr23:70361120 A>G did not map to a codon.
Sequencing variant TCGA-JY-A6FD-01A-11D-A33E-09 chr23:70339932 G>T did not map to a codon.
Sequencing variant TCGA-L5-A4OE-01A-11D-A27G-09 chr23:70346288 G>T did not map to a codon.
Sequencing variant TCGA-IG-A4P3-01A-11D-A27G-09 chr3:151105596 G>T did not map to a codon.
Sequencing variant TCGA-JY-A939-01A-12D-A37C-09 chr12:116401222 C>T maps to NM_015335.4 S2163S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr12:116418611 T>C maps to NM_015335.4 K1769K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RE-01A-11D-A33E-09 chr23:40523689 G>A did not map to a codon.
Sequencing variant TCGA-IG-A97H-01A-11D-A387-09 chr23:40541947 C>A did not map to a codon.
Sequencing variant TCGA-S8-A6BW-01A-11D-A31U-09 chr23:40513745 G>A did not map to a codon.
Sequencing variant TCGA-L5-A8NS-01A-12D-A37C-09 chr22:20909316 C>T maps to NM_001003891.1 G111G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EW-01A-11D-A36J-09 chr11:57472549 A>G maps to ENST00000431606 D123D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A50L-01A-11D-A27G-09 chr6:131927729 G>T maps to ENST00000403834 S425*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A938-01A-11D-A37C-09 chr17:38189431 C>T maps to NM_014815.3 A233A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NV-01A-11D-A37C-09 chr17:38187473 G>A maps to NM_014815.3 L364L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EZ-01A-11D-A36J-09 chr17:38178914 C>T maps to NM_014815.3 P805P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OU-01A-11D-A28B-09 chr19:50338428 C>T maps to NM_030973.3 R557*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FB-01A-11D-A33E-09 chr13:48654028 G>T maps to NM_014166.2 G197G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GQ-01A-11D-A37C-09 chr5:88018582 A>T maps to NM_002397.4 P420P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RF-01A-13D-A33E-09 chr5:88057049 C>T maps to NM_002397.4 R118R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A939-01A-12D-A37C-09 chr5:88100420 G>A maps to NM_002397.4 I84I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43H-01A-11D-A247-09 chr5:88027680 C>T maps to NM_002397.4 L225L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr16:3304659 C>T maps to NM_000243.2 G136G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49U-01A-31D-A27G-09 chr15:66249959 C>T maps to NM_032445.2 Q404Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FD-01A-11D-A33E-09 chr1:3431143 G>A maps to ENST00000452816 Q350*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93D-01A-11D-A387-09 chr1:3425795 C>T maps to ENST00000452816 P532P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OF-01A-11D-A27G-09 chr19:42841021 G>T maps to ENST00000251268 L436L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr19:42838220 C>T maps to ENST00000251268 R138R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L7-A6VZ-01A-12D-A33E-09 chr19:42872626 G>T maps to ENST00000251268 L2098L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASX-01A-11D-A387-09 chr19:42874501 C>T maps to ENST00000251268 D2332D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88Z-01A-11D-A36J-09 chr22:42180663 C>T maps to NM_152513.3 A1074A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NS-01A-12D-A37C-09 chr17:41738714 G>C maps to NM_004527.3 S63*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49Y-01A-11D-A27G-09 chr17:41738713 T>A maps to NM_004527.3 S63S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZR-A9CJ-01B-11D-A387-09 chr17:41738608 G>T maps to NM_004527.3 V98V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr7:15652020 C>T maps to NM_005924.4 A302A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FQ-01A-31D-A387-09 chr7:15725592 C>T maps to NM_005924.4 A145A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-A7RC-01B-11D-A403-09 chr7:15725802 G>A maps to NM_005924.4 H75H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3QL-01A-11D-A247-09 chr6:46787379 C>T maps to NM_005588.2 H165H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OW-01A-11D-A28B-09 chr2:112722828 C>T maps to NM_006343.2 S273S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr15:90320196 G>A maps to NM_001039958.1 G203G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RE-01A-11D-A33E-09 chr7:116422131 T>C maps to NM_001127500.1 L1223L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NN-01A-11D-A37C-09 chr17:81052283 G>A maps to NM_001004431.1 E300E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XP-A8T7-01A-11D-A36J-09 chr14:21462708 A>T maps to NM_001029991.1 S235S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OE-01A-11D-A27G-09 chr10:126454173 C>A maps to NM_212554.2 E135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GF-01A-11D-A37C-09 chr1:171753184 C>T maps to NM_015935.4 G153G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NL-01A-12D-A37C-09 chr1:171753484 C>G maps to NM_015935.4 A253A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GN-01A-11D-A37C-09 chr4:119609097 C>T maps to NM_020961.2 D29D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr4:119626836 T>C maps to NM_020961.2 V309V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr1:156051671 G>A maps to NM_001093725.1 L40L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8W5-01B-11D-A37C-09 chr15:82335814 C>A maps to NM_032246.3 G466*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GK-01A-11D-A37C-09 chr19:1556851 C>T maps to NM_001174118.1 P222P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NN-01A-11D-A37C-09 chr15:44107235 C>T maps to NM_005926.2 V112V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A8JD-01A-11D-A36J-09 chr5:153432772 C>T maps to NM_005927.4 Q197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr2:228195473 G>A maps to NM_020194.4 P57P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RE-01A-11D-A33E-09 chr3:196753570 C>T maps to NM_005929.5 E88E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OE-01A-11D-A27G-09 chr3:196748332 C>T maps to NM_005929.5 A218A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OS-01A-11D-A28B-09 chr3:179107818 G>T maps to NM_033540.2 L680L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FD-01A-11D-A33E-09 chr22:37875508 G>A maps to NM_002405.3 N145N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NK-01A-21D-A37C-09 chr11:119212575 G>A maps to NM_031433.2 S502S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GL-01A-12D-A37C-09 chr2:24239738 C>T maps to ENST00000338315 I124I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6Y0-01B-11D-A33E-09 chr1:205555335 G>A did not map to a codon.
Sequencing variant TCGA-LN-A49O-01A-11D-A247-09 chr12:53647344 C>T maps to NM_001170790.1 C349C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A5U7-01A-11D-A31U-09 chr2:191301210 C>G maps to NM_017694.3 V152V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NV-01A-11D-A37C-09 chr17:8702342 C>T maps to NM_152599.3 P32P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RE-01A-11D-A33E-09 chr4:128886249 G>C maps to NM_152778.2 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASV-01A-11D-A387-09 chr4:128841925 G>T maps to NM_152778.2 I472I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GO-01A-11D-A37C-09 chr2:103335283 C>T maps to NM_032718.3 G340G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FE-01A-11D-A33E-09 chr2:103353148 C>A maps to NM_032718.3 G41*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A5S3-01A-11D-A28B-09 chr15:42058226 A>C maps to ENST00000219905 P2698P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A97I-01A-11D-A387-09 chr15:42003262 C>T maps to ENST00000219905 L934L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NF-01A-11D-A37C-09 chr15:42042213 G>T maps to ENST00000219905 E2186*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EQ-01A-11D-A36J-09 chr15:42042414 G>T maps to ENST00000219905 E2253*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A8JD-01A-11D-A36J-09 chr15:42057138 G>A maps to ENST00000219905 P2649P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93F-01A-21D-A37C-09 chr7:141764223 T>G maps to ENST00000475668 L1462L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93F-01A-21D-A37C-09 chr7:141764226 T>C maps to ENST00000475668 C1463C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HZ-01A-31D-A351-09 chr7:141705416 T>C maps to ENST00000475668 V29V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FP-01A-31D-A387-09 chr7:141720843 C>A maps to ENST00000475668 L173L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-A7RE-01A-11D-A351-09 chr7:141739971 G>T did not map to a codon.
Sequencing variant TCGA-IG-A8O2-01A-11D-A36J-09 chr22:39883405 C>T maps to NM_001098270.1 C18C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6L6-01B-11D-A33E-09 chr22:39884527 C>T maps to NM_001098270.1 F392F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OW-01A-11D-A28B-09 chr2:135199369 C>T maps to NM_002410.3 A637A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EX-01A-11D-A36J-09 chr2:135076307 G>T maps to NM_002410.3 E191*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FB-01A-11D-A33E-09 chr7:22532993 G>A maps to ENST00000441815 Y329Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A8O2-01A-11D-A36J-09 chr3:127411060 C>A maps to NM_007283.5 G308*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49V-01A-11D-A247-09 chr16:4714708 G>A did not map to a codon.
Sequencing variant TCGA-LN-A9FO-01A-11D-A387-09 chr1:222791506 C>A maps to NM_198551.2 R19R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XP-A8T7-01A-11D-A36J-09 chr1:222805565 C>T maps to NM_198551.2 Q1077*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OE-01A-11D-A27G-09 chr6:109765474 G>A maps to NM_022765.3 V1041V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OF-01A-11D-A27G-09 chr6:109766170 C>T maps to NM_022765.3 W970*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A8I1-01A-11D-A36J-09 chr11:12247736 G>T maps to NM_014632.2 E570*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZR-A9CJ-01B-11D-A387-09 chr11:12241962 G>A maps to NM_014632.2 A388A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GI-01A-11D-A37C-09 chr22:18310413 G>A maps to NM_015241.2 S1063S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88Z-01A-11D-A36J-09 chr11:12315445 A>G maps to NM_032867.2 K156K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49L-01A-11D-A247-09 chr22:38333777 G>T maps to NM_033386.2 E817*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A8JE-01A-11D-A37C-09 chr22:38313799 C>T maps to NM_033386.2 Q142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr7:1484823 C>T maps to NM_182924.3 S294S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASX-01A-11D-A387-09 chr7:1498893 G>A maps to NM_182924.3 I23I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FH-01A-11D-A33E-09 chr23:10535075 C>A did not map to a codon.
Sequencing variant TCGA-L5-A4OJ-01A-11D-A27G-09 chr23:10437870 G>T did not map to a codon.
Sequencing variant TCGA-LN-A4A3-01A-11D-A27G-09 chr23:10417676 G>A did not map to a codon.
Sequencing variant TCGA-JY-A6FD-01A-11D-A33E-09 chr23:107084037 G>A did not map to a codon.
Sequencing variant TCGA-L5-A4OJ-01A-11D-A27G-09 chr23:107159334 C>A did not map to a codon.
Sequencing variant TCGA-L5-A893-01A-11D-A36J-09 chr23:107170087 C>A did not map to a codon.
Sequencing variant TCGA-S8-A6BV-01A-21D-A31U-09 chr23:107148758 C>A did not map to a codon.
Sequencing variant TCGA-L5-A4OQ-01A-11D-A27G-09 chr19:1255010 C>A maps to NM_177401.4 I269I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A4QS-01A-11D-A27G-09 chr1:67424599 C>T maps to NM_001077700.2 Q190*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6Y0-01B-11D-A33E-09 chr22:24237105 G>T maps to NM_002415.1 E86*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NE-01A-11D-A37C-09 chr17:4800530 C>T maps to NM_153827.4 S1316S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr7:7612168 T>C maps to NM_019005.3 C21C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EP-01A-31D-A403-09 chr13:24383996 G>A maps to NM_005932.3 Q574*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6XQ-01B-11D-A33E-09 chr2:99790474 G>T maps to NM_138798.1 T52T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OX-01A-21D-A28B-09 chr3:70014296 C>T maps to ENST00000448226 V493V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-A7RC-01B-11D-A403-09 chr3:69987139 G>T maps to ENST00000448226 G174G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OF-01A-11D-A27G-09 chr1:226413488 C>A maps to NM_031944.1 I225I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FG-01A-11D-A33E-09 chr10:129910412 C>T maps to NM_002417.4 S651S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OO-01A-11D-A27G-09 chr10:129908756 C>T maps to NM_002417.4 P767P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NG-01A-11D-A37C-09 chr10:129904469 C>T maps to NM_002417.4 K1878K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NR-01A-11D-A37C-09 chr10:129907607 C>T maps to NM_002417.4 R832R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49N-01A-11D-A247-09 chr10:129908756 C>T maps to NM_002417.4 P767P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6L6-01B-11D-A33E-09 chr16:14311144 G>T did not map to a codon.
Sequencing variant TCGA-2H-A9GN-01A-11D-A37C-09 chr7:131149110 G>T maps to NM_013255.4 E578*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A6-01A-11D-A27G-09 chr19:2046657 T>A maps to NM_199054.2 L28L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-A7RE-01A-11D-A351-09 chr7:140158881 G>A maps to NM_013446.3 H232H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49Y-01A-11D-A27G-09 chr15:23811870 C>A maps to NM_005664.3 C314*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43I-01A-11D-A247-09 chr12:121131924 G>T maps to NM_014730.2 L89L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OE-01A-11D-A27G-09 chr3:158289109 C>T maps to NM_022443.4 S7S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FP-01A-31D-A387-09 chr4:185637643 C>T maps to NM_024629.3 E175E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RF-01A-13D-A33E-09 chr3:37061852 G>T maps to NM_000249.3 E313*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A97H-01A-11D-A387-09 chr11:118343154 G>T maps to NM_001197104.1 R427R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OH-01A-11D-A27G-09 chr11:118354911 G>T maps to NM_001197104.1 P1367P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OP-01A-11D-A27G-09 chr11:118352584 C>T maps to NM_001197104.1 R1264*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GL-01A-12D-A37C-09 chr12:49445149 G>C maps to NM_003482.3 P772P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A625-01A-11D-A31U-09 chr12:49433517 T>A maps to NM_003482.3 K2679*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93F-01A-21D-A37C-09 chr12:49425502 G>A maps to NM_003482.3 Q4329*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KH-A6WC-01A-11D-A33E-09 chr12:49427263 G>A maps to NM_003482.3 Q3742*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43E-01A-11D-A247-09 chr12:49426582 G>A maps to NM_003482.3 Q3969*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88W-01A-11D-A351-09 chr12:49441853 T>G did not map to a codon.
Sequencing variant TCGA-LN-A5U5-01A-21D-A28B-09 chr12:49426915 G>A maps to NM_003482.3 Q3858*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HZ-01A-31D-A351-09 chr12:49435699 C>T maps to NM_003482.3 L2061L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASW-01A-11D-A403-09 chr12:49446705 C>T maps to NM_003482.3 V368V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EU-01A-11D-A36J-09 chr12:49416551 G>A maps to NM_003482.3 Q5387*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-AAPN-01A-11D-A403-09 chr12:49427917 C>A maps to NM_003482.3 E3558*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OQ-01A-11D-A27G-09 chr7:151848558 T>A maps to ENST00000355193 K4269*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NG-01A-11D-A37C-09 chr7:151851096 C>A maps to ENST00000355193 E4149*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NK-01A-21D-A37C-09 chr7:151873958 G>C maps to ENST00000355193 S2860*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr7:151882651 T>C maps to ENST00000355193 A1691A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HZ-01A-31D-A351-09 chr7:151947036 C>T maps to ENST00000355193 A579A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FP-01A-31D-A387-09 chr7:151878491 T>A maps to ENST00000355193 T2151T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8Q7-01A-11D-A37C-09 chr7:151962133 G>T maps to ENST00000355193 C391*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XP-A8T7-01A-11D-A36J-09 chr7:151878415 G>A maps to ENST00000355193 Q2177*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr19:36210770 A>C maps to NM_014727.1 P174P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88S-01A-11D-A36J-09 chr19:36218096 C>T maps to NM_014727.1 N1348N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr19:36227709 G>T maps to NM_014727.1 E2427*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr19:36227816 G>A maps to NM_014727.1 A2434A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA7D-01A-11D-A403-09 chr19:36212414 C>T maps to NM_014727.1 H722H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RF-01A-13D-A33E-09 chr7:104717407 A>T did not map to a codon.
Sequencing variant TCGA-V5-AASW-01A-11D-A403-09 chr7:104717848 C>T maps to NM_182931.2 Q367*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6F8-01A-11D-A33E-09 chr9:20413889 G>T maps to NM_004529.2 L318L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr9:20414366 G>A maps to NM_004529.2 S159S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASW-01A-11D-A403-09 chr9:20414312 G>A maps to NM_004529.2 S177S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FG-01A-11D-A33E-09 chr6:168323557 C>T maps to ENST00000400822 H969H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OG-01A-11D-A27G-09 chr6:168347465 G>T maps to ENST00000400822 G1138G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NL-01A-12D-A37C-09 chr6:168265352 G>C maps to ENST00000400822 A76A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr6:168347573 C>T maps to ENST00000400822 N1174N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93D-01A-11D-A387-09 chr2:238402113 C>T maps to NM_024101.5 A15A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3QL-01A-11D-A247-09 chr7:73013936 G>A maps to NM_032951.2 L330L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EO-01A-11D-A36J-09 chr7:73008266 C>T maps to NM_032951.2 L829L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EY-01A-11D-A36J-09 chr7:73008639 G>A maps to NM_032951.2 L802L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A8JD-01A-11D-A36J-09 chr7:73030404 G>A maps to NM_032951.2 I132I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OR-01A-11D-A27G-09 chr1:45974674 G>T maps to NM_015506.2 E213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HV-01A-21D-A351-09 chr17:53471787 C>T maps to NM_012329.2 W208*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GQ-01A-11D-A37C-09 chr3:154802111 C>T maps to NM_007289.2 Y52Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr1:2530094 G>T maps to NM_033467.3 A392A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GJ-01A-11D-A37C-09 chr11:102662185 G>A maps to NM_002421.3 H358H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr11:102666261 A>G maps to NM_002421.3 A234A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-M9-A5M8-01A-11D-A28B-09 chr11:102667491 T>A maps to NM_002421.3 G176G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NQ-01A-11D-A36J-09 chr22:24121531 G>A maps to NM_005940.3 L89L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A5U6-01A-11D-A28B-09 chr22:24124521 C>T maps to NM_005940.3 P395P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-A7RC-01B-11D-A403-09 chr11:102743836 G>T maps to ENST00000326227 Y36*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A4P3-01A-11D-A27G-09 chr11:102822857 A>G maps to NM_002427.3 L228L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A8JE-01A-11D-A37C-09 chr11:102815027 G>A maps to NM_002427.3 R461R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GQ-01A-11D-A37C-09 chr14:23306079 C>A maps to NM_004995.2 L18L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NF-01A-11D-A37C-09 chr8:89339429 G>A maps to NM_005941.4 I2I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49V-01A-11D-A247-09 chr12:132335614 G>A maps to NM_016155.4 V536V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-A7RE-01A-11D-A351-09 chr12:56233465 C>A maps to NM_002429.4 E194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OE-01A-11D-A27G-09 chr16:55513423 G>A maps to NM_004530.4 T11T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EX-01A-11D-A36J-09 chr20:33862199 C>A maps to NM_006690.3 R576R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A8JD-01A-11D-A36J-09 chr20:33851657 C>T maps to NM_006690.3 S294S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NE-01A-11D-A37C-09 chr16:3100088 G>T maps to NM_022468.4 R104R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NH-01A-11D-A37C-09 chr16:3100008 G>T did not map to a codon.
Sequencing variant TCGA-L7-A6VZ-01A-12D-A33E-09 chr16:3107374 C>A maps to NM_022468.4 P301P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6XQ-01B-11D-A33E-09 chr16:3097522 G>A maps to NM_022468.4 A69A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6XG-01B-11D-A33E-09 chr11:5010966 G>T maps to NM_021801.3 R63R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A97H-01A-11D-A387-09 chr11:102562550 G>A maps to NM_022122.2 S496S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr20:44639803 C>T maps to NM_004994.2 N224N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr20:44640818 C>T maps to NM_004994.2 C347C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8ER-01A-11D-A36J-09 chr20:44637669 G>T maps to NM_004994.2 L35L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RE-01A-11D-A33E-09 chr10:88717280 C>T maps to NM_024756.2 L6L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EW-01A-11D-A36J-09 chr10:88702245 G>A maps to NM_024756.2 N765N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EZ-01A-11D-A36J-09 chr10:88703784 C>T maps to NM_024756.2 L252L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A8-01A-32D-A27G-09 chr14:61275046 C>T maps to NM_002431.3 F107F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GK-01A-11D-A37C-09 chr1:158815415 A>C maps to NM_002432.1 R204R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A97H-01A-11D-A387-09 chr1:158815480 C>T maps to NM_002432.1 Y225Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6XG-01B-11D-A33E-09 chr1:158815571 T>C maps to NM_002432.1 L256L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-AAPN-01A-11D-A403-09 chr17:2290287 C>A maps to NM_020310.2 V552V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GR-01A-12D-A37C-09 chr7:156803026 A>G maps to NM_005515.3 N6N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GJ-01A-11D-A37C-09 chr14:93650311 G>A maps to NM_022151.4 I92I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A8JE-01A-11D-A37C-09 chr11:1501648 C>T maps to NM_001172223.1 T113T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr4:71840884 G>A maps to ENST00000396051 W102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A5U5-01A-21D-A28B-09 chr4:71840983 G>T maps to ENST00000396051 T135T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr2:74392408 A>G maps to NM_018221.3 I115I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OJ-01A-11D-A27G-09 chr9:27455332 G>A maps to NM_024761.3 N72N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NR-01A-11D-A37C-09 chr1:47078810 G>A maps to NM_145279.4 A113A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6KZ-01A-11D-A31U-09 chr1:47078648 C>T maps to NM_145279.4 P167P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FG-01A-11D-A33E-09 chr18:33795864 C>T maps to NM_017947.2 V574V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NE-01A-11D-A37C-09 chr18:33779984 G>T maps to NM_017947.2 L213L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A4QS-01A-11D-A27G-09 chr6:39880115 G>T maps to ENST00000425303 A291A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EQ-01A-11D-A36J-09 chr6:39880680 C>T maps to ENST00000425303 W275*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49O-01A-11D-A247-09 chr6:29637969 A>G maps to NM_206811.3 G204G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NV-01A-11D-A37C-09 chr7:100843571 C>T maps to NM_178176.2 S77S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EP-01A-31D-A403-09 chr7:100843773 G>C maps to NM_178176.2 V44V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GG-01A-11D-A37C-09 chr12:62931428 G>A maps to ENST00000393630 A687A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RF-01A-13D-A33E-09 chr12:62949800 C>A maps to ENST00000393630 R1081R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OO-01A-11D-A27G-09 chr3:108698359 A>T did not map to a codon.
Sequencing variant TCGA-LN-A5U6-01A-11D-A28B-09 chr3:108751661 A>C maps to NM_014429.3 L490L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A8JE-01A-11D-A37C-09 chr21:37705975 T>C maps to ENST00000290384 T24T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A5B8-01A-11D-A28B-09 chr23:106228368 G>T did not map to a codon.
Sequencing variant TCGA-VR-A8EY-01A-11D-A36J-09 chr23:106224143 C>G did not map to a codon.
Sequencing variant TCGA-VR-A8EW-01A-11D-A36J-09 chr1:2290083 G>T maps to NM_024848.1 V272V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FE-01A-11D-A33E-09 chr8:57025929 G>T maps to NM_005372.1 P204P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr8:57026409 C>T maps to NM_005372.1 P44P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RE-01A-11D-A33E-09 chr1:220953533 A>G maps to NM_017898.3 P279P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A938-01A-11D-A37C-09 chr23:14933838 G>T did not map to a codon.
Sequencing variant TCGA-L5-A8NQ-01A-11D-A36J-09 chr23:14921097 G>C did not map to a codon.
Sequencing variant TCGA-R6-A8WC-01A-11D-A37C-09 chr23:14891843 G>T did not map to a codon.
Sequencing variant TCGA-VR-A8EZ-01A-11D-A36J-09 chr23:14891656 G>T did not map to a codon.
Sequencing variant TCGA-VR-AA7B-01A-31D-A403-09 chr23:14921104 G>C did not map to a codon.
Sequencing variant TCGA-Z6-A8JD-01A-11D-A36J-09 chr23:14929397 G>T did not map to a codon.
Sequencing variant TCGA-2H-A9GK-01A-11D-A37C-09 chr1:113231691 G>A maps to NM_020963.3 R91R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OQ-01A-11D-A27G-09 chr1:113234374 C>T maps to NM_020963.3 Q309*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A5U7-01A-11D-A31U-09 chr9:13221475 C>A maps to ENST00000319217 T257T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EX-01A-11D-A36J-09 chr11:58980157 G>A maps to NM_001039396.1 R61*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A6QS-01A-12D-A33E-09 chr13:20237215 G>T maps to ENST00000414242 G657*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43M-01A-11D-A247-09 chr15:75190055 C>T maps to NM_002435.1 A419A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A9-01A-11D-A28B-09 chr1:43804212 G>A maps to NM_005373.2 R71R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A97I-01A-11D-A387-09 chr17:56357256 G>A maps to ENST00000340482 L123L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A4-01A-11D-A27G-09 chr17:56350189 G>T maps to ENST00000340482 R603R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6DQ-01B-11D-A31U-09 chr14:67787831 G>A maps to NM_022474.2 S532S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GH-01A-11D-A37C-09 chr10:28378762 A>G maps to NM_173496.3 F320F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr21:33684111 G>A maps to ENST00000445271 A110A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3Y9-01A-12D-A247-09 chr3:138121104 C>T maps to NM_001085049.1 I207I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EZ-01A-11D-A36J-09 chr10:17865241 G>T maps to NM_002438.2 V77V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OP-01A-11D-A27G-09 chr17:60743590 C>T maps to NM_006039.3 Y219Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NT-01A-11D-A37C-09 chr17:60741943 C>T maps to NM_006039.3 Q52*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6L6-01B-11D-A33E-09 chr11:68772955 G>A maps to NM_145015.4 Y274Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GO-01A-11D-A37C-09 chr11:18158958 G>A maps to NM_054031.3 A70A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X8-AAAR-01A-11D-A403-09 chr11:18158961 C>T maps to NM_054031.3 A71A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FR-01A-11D-A387-09 chr11:18195432 G>A maps to NM_054032.3 P210P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EW-01A-11D-A36J-09 chr17:45904114 G>T maps to NM_145255.3 Y140*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-AAPN-01A-11D-A403-09 chr8:121455467 A>G maps to NM_014078.5 S36S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FE-01A-11D-A33E-09 chr6:44081843 G>T maps to NM_032111.2 I58I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr8:55055255 G>T maps to NM_014175.3 E155*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OE-01A-11D-A27G-09 chr3:131188617 C>A did not map to a codon.
Sequencing variant TCGA-Q9-A6FW-01A-31D-A31U-09 chr2:99802707 C>A maps to ENST00000424491 G44G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A938-01A-11D-A37C-09 chr19:10367464 C>A maps to NM_146387.1 R137R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S8-A6BW-01A-11D-A31U-09 chr19:10370425 C>T maps to NM_146387.1 S291S. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-L5-A8NQ-01A-11D-A36J-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-L5-A8NT-01A-11D-A37C-09 chr19:3765203 C>T maps to NM_172251.2 S53S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NK-01A-21D-A37C-09 chr15:89018445 G>A maps to NM_022839.3 Q129Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93D-01A-11D-A387-09 chr1:174987552 C>T did not map to a codon.
Sequencing variant TCGA-IG-A3I8-01A-11D-A247-09 chr1:36923528 G>A maps to NM_031280.3 R147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OJ-01A-11D-A27G-09 chr7:56022766 G>T maps to ENST00000426595 G192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NQ-01A-11D-A36J-09 chr7:56022735 C>T maps to ENST00000426595 F181F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A8I0-01A-11D-A36J-09 chr6:43655403 C>G did not map to a codon.
Sequencing variant TCGA-R6-A6DQ-01B-11D-A31U-09 chr6:43642961 C>A maps to ENST00000372118 P215P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A939-01A-12D-A37C-09 chr9:138392961 C>T maps to NM_016034.3 D54D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OH-01A-11D-A27G-09 chr9:138395441 G>T maps to NM_016034.3 L118L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88Z-01A-11D-A36J-09 chr9:138395957 T>C maps to NM_016034.3 A290A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NG-01A-11D-A37C-09 chr9:138395456 G>A maps to NM_016034.3 T123T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NQ-01A-11D-A36J-09 chr3:139062879 C>T maps to NM_020191.2 L4L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASW-01A-11D-A403-09 chr7:43906347 G>A maps to NM_032014.2 R152*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GJ-01A-11D-A37C-09 chr5:44812021 G>T maps to NM_016640.3 V251V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OH-01A-11D-A27G-09 chr5:68524114 G>T maps to NM_033281.5 L65L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GF-01A-11D-A37C-09 chr2:95770415 C>T maps to NM_031902.3 L244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OH-01A-11D-A27G-09 chr2:95766222 G>T maps to NM_031902.3 P309P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8WC-01A-11D-A37C-09 chr2:95780885 G>A maps to NM_031902.3 Q68*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr6:24415277 G>T maps to NM_020662.2 G202G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr1:19585040 C>T maps to NM_016183.3 R188R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RE-A7BO-01A-11D-A33E-09 chr11:10650358 G>T maps to NM_001098579.1 L188L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FQ-01A-31D-A387-09 chr11:60229936 C>T maps to NM_152866.2 L30L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NT-01A-11D-A37C-09 chr11:60557949 G>T maps to NM_206893.3 E48*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NW-01A-11D-A37C-09 chr11:60565960 C>T maps to NM_206893.3 G232G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A50L-01A-11D-A27G-09 chr11:60268515 A>G did not map to a codon.
Sequencing variant TCGA-L7-A6VZ-01A-12D-A33E-09 chr11:60310033 G>T maps to NM_001012417.2 E149*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43M-01A-11D-A247-09 chr11:60543106 C>T maps to NM_001098835.1 S214S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A8I1-01A-11D-A36J-09 chr11:59939660 G>A maps to NM_152852.1 D239D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L7-A6VZ-01A-12D-A33E-09 chr2:17998336 C>T maps to NM_001105569.1 R184R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3Y9-01A-12D-A247-09 chr5:79950578 C>G maps to NM_002439.3 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A5S3-01A-11D-A28B-09 chr1:76346961 G>T maps to NM_002440.2 E605*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43M-01A-11D-A247-09 chr1:76280728 A>G maps to NM_002440.2 Q241Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OS-01A-11D-A28B-09 chr1:76333263 T>C maps to NM_002440.2 D432D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A9VB-01A-21D-A37C-09 chr2:48026990 C>T maps to NM_000179.2 P623P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OO-01A-11D-A27G-09 chr17:38285496 G>T did not map to a codon.
Sequencing variant TCGA-LN-A4A5-01A-21D-A27G-09 chr3:135871404 T>C maps to NM_018133.3 L106L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr23:11783862 G>A did not map to a codon.
Sequencing variant TCGA-L5-A4OO-01A-11D-A27G-09 chr2:234775169 C>T did not map to a codon.
Sequencing variant TCGA-IG-A5B8-01A-11D-A28B-09 chr16:812751 G>T maps to NM_013404.4 L24L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3YB-01A-11D-A247-09 chr16:820092 G>A maps to NM_001025190.1 H964H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr16:830601 C>T maps to NM_001025190.1 A133A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GI-01A-11D-A37C-09 chr23:64956698 G>A did not map to a codon.
Sequencing variant TCGA-2H-A9GI-01A-11D-A37C-09 chr23:64956742 A>G did not map to a codon.
Sequencing variant TCGA-L5-A4OE-01A-11D-A27G-09 chr23:64949487 G>A did not map to a codon.
Sequencing variant TCGA-L5-A4OG-01A-11D-A27G-09 chr23:64959698 C>T did not map to a codon.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr23:64955271 G>T did not map to a codon.
Sequencing variant TCGA-L5-A893-01A-11D-A36J-09 chr23:64958408 C>G did not map to a codon.
Sequencing variant TCGA-V5-AASV-01A-11D-A387-09 chr23:64956742 A>G did not map to a codon.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr8:16012653 C>A did not map to a codon.
Sequencing variant TCGA-L5-A8NQ-01A-11D-A36J-09 chr8:15998555 T>G did not map to a codon.
Sequencing variant TCGA-V5-A7RE-01A-11D-A351-09 chr8:16012633 A>G maps to ENST00000445506 G297G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NS-01A-12D-A37C-09 chr12:65702436 T>C did not map to a codon.
Sequencing variant TCGA-LN-A4A1-01A-21D-A27G-09 chr3:49725037 G>C maps to NM_020998.3 P102P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GO-01A-11D-A37C-09 chr3:49935599 G>A maps to NM_002447.2 T588T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6Y2-01B-11D-A33E-09 chr3:49932734 C>A maps to NM_002447.2 E1046*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43I-01A-11D-A247-09 chr2:190922214 G>T maps to NM_005259.2 I299I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49S-01A-11D-A247-09 chr1:155582928 A>G maps to NM_018116.2 P396P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NW-01A-11D-A37C-09 chr4:4864563 C>T maps to NM_002448.3 R202R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6KZ-01A-11D-A31U-09 chr16:56693024 C>T maps to ENST00000394501 A46A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NL-01A-12D-A37C-09 chr16:56703816 C>T maps to NM_005951.2 C7C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8WG-01A-11D-A37C-09 chr8:121483103 G>T maps to NM_022045.3 L364L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93F-01A-21D-A37C-09 chr1:38280974 G>T maps to NM_005955.2 R699R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASW-01A-11D-A403-09 chr1:93575871 C>T maps to NM_007358.3 L31L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OJ-01A-11D-A27G-09 chr15:65295575 G>T maps to NM_139242.3 R332R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr6:151331084 C>T maps to NM_015440.3 G752G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NS-01A-12D-A37C-09 chr4:75041019 A>G maps to NM_001144978.1 L117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NF-01A-11D-A37C-09 chr1:11852370 G>C maps to ENST00000376585 Y573*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FO-01A-11D-A387-09 chr1:11861266 C>T maps to ENST00000376585 L183L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49U-01A-31D-A27G-09 chr2:55470217 T>C did not map to a codon.
Sequencing variant TCGA-Z6-A8JD-01A-11D-A36J-09 chr2:55489518 T>C maps to NM_002453.2 K88K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr11:68517735 C>T maps to NM_004923.3 A131A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A625-01A-11D-A31U-09 chr23:149818272 C>T did not map to a codon.
Sequencing variant TCGA-LN-A4MQ-01A-11D-A28B-09 chr23:149898658 G>A did not map to a codon.
Sequencing variant TCGA-IG-A51D-01A-11D-A27G-09 chr15:31266645 C>T maps to NM_017762.2 K115K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OE-01A-11D-A27G-09 chr1:149907007 G>T maps to NM_001145862.1 S113S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NK-01A-21D-A37C-09 chr1:149902815 G>A maps to NM_001145862.1 L444L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A9VB-01A-21D-A37C-09 chr1:149904174 G>A maps to NM_001145862.1 R345*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FP-01A-31D-A387-09 chr3:9726927 G>A maps to NM_001077525.2 E387E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6DN-01B-11D-A31U-09 chr11:95582864 C>T maps to NM_016156.5 R322R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr22:30415780 C>T maps to NM_021090.3 G711G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49Y-01A-11D-A27G-09 chr22:30414034 C>T maps to NM_021090.3 T598T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XP-A8T8-01A-11D-A36J-09 chr22:30387631 G>T maps to NM_021090.3 E145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6F8-01A-11D-A33E-09 chr13:25832790 C>A maps to NM_004685.3 E256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GO-01A-11D-A37C-09 chr8:17159668 C>T maps to NM_004686.4 L538L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr8:17161979 C>T maps to NM_004686.4 R467R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88W-01A-11D-A351-09 chr23:63569872 G>T did not map to a codon.
Sequencing variant TCGA-V5-AASX-01A-11D-A387-09 chr8:11162417 C>T maps to NM_015458.3 V162V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A9VB-01A-21D-A37C-09 chr4:187455430 C>T maps to NM_005958.3 T155T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GL-01A-12D-A37C-09 chr11:92714994 G>T maps to NM_005959.3 A202A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q9-A6FW-01A-31D-A31U-09 chr6:74190468 C>T maps to NM_001123226.1 R401*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EW-01A-11D-A36J-09 chr1:11181416 C>A maps to NM_004958.3 P2273P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr1:236972026 T>G maps to NM_000254.2 S121S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8WC-01A-11D-A37C-09 chr1:237026803 C>T maps to NM_000254.2 H785H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49Y-01A-11D-A27G-09 chr5:7897310 C>T maps to NM_024010.2 Q662*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GR-01A-12D-A37C-09 chr8:125568579 G>A maps to NM_014751.4 R433*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA4D-01A-11D-A37C-09 chr8:125716369 C>T did not map to a codon.
Sequencing variant TCGA-IG-A6QS-01A-12D-A33E-09 chr4:100534267 G>T maps to ENST00000511045 G757*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S8-A6BV-01A-21D-A31U-09 chr4:100521875 C>T maps to ENST00000511045 L435L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A8HZ-01A-11D-A36J-09 chr13:29600335 G>T maps to NM_001033602.2 E511*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FP-01A-31D-A387-09 chr13:29599323 G>T maps to NM_001033602.2 L173L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GI-01A-11D-A37C-09 chr19:9049752 A>G maps to NM_024690.2 S10626S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GJ-01A-11D-A37C-09 chr19:9049461 A>G maps to NM_024690.2 A10723A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GL-01A-12D-A37C-09 chr19:9086330 T>A maps to NM_024690.2 T1828T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GM-01A-11D-A37C-09 chr19:9066961 A>G maps to NM_024690.2 P6828P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GR-01A-12D-A37C-09 chr19:9068269 A>G maps to NM_024690.2 T6392T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RE-01A-11D-A33E-09 chr19:9046662 T>C maps to NM_024690.2 P11656P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3Y9-01A-12D-A247-09 chr19:9084624 G>C maps to NM_024690.2 S2397*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A4P3-01A-11D-A27G-09 chr19:9075970 T>A maps to NM_024690.2 P3825P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A50L-01A-11D-A27G-09 chr19:9090485 A>T maps to NM_024690.2 S443S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A5B8-01A-11D-A28B-09 chr19:9089300 G>A maps to NM_024690.2 L838L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FB-01A-11D-A33E-09 chr19:9059173 C>T maps to NM_024690.2 P9424P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A938-01A-11D-A37C-09 chr19:8961960 G>T maps to NM_024690.2 C14472*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OJ-01A-11D-A27G-09 chr19:9089864 G>A maps to NM_024690.2 S650S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OQ-01A-11D-A27G-09 chr19:9069913 G>T maps to NM_024690.2 I5844I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OR-01A-11D-A27G-09 chr19:9048222 T>C maps to NM_024690.2 E11136E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OT-01A-11D-A28B-09 chr19:9059053 A>C maps to NM_024690.2 T9464T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NQ-01A-11D-A36J-09 chr19:9085586 G>T maps to NM_024690.2 G2076G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L7-A6VZ-01A-12D-A33E-09 chr19:9067009 A>T maps to NM_024690.2 T6812T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HY-01A-12D-A351-09 chr19:9045687 T>C maps to NM_024690.2 T11981T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HZ-01A-31D-A351-09 chr19:9085943 G>T maps to NM_024690.2 I1957I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-M9-A5M8-01A-11D-A28B-09 chr19:9063580 C>T maps to NM_024690.2 E7955E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6DN-01B-11D-A31U-09 chr19:9070672 T>A maps to NM_024690.2 G5591G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6XG-01B-11D-A33E-09 chr19:9059053 A>C maps to NM_024690.2 T9464T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6Y0-01B-11D-A33E-09 chr19:8976799 G>T maps to NM_024690.2 S14089*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RE-A7BO-01A-11D-A33E-09 chr19:9072973 C>T maps to NM_024690.2 T4824T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-A7RB-01A-11D-A351-09 chr19:9073600 A>C maps to NM_024690.2 T4615T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EX-01A-11D-A36J-09 chr19:9064267 C>T maps to NM_024690.2 A7726A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EX-01A-11D-A36J-09 chr19:9084034 C>A maps to NM_024690.2 E2594*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XP-A8T8-01A-11D-A36J-09 chr19:9071104 C>T maps to NM_024690.2 S5447S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr7:100685145 T>G maps to NM_001040105.1 V3483V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NU-01A-11D-A36J-09 chr7:100696338 C>T maps to NM_001040105.1 Y4392Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S8-A6BV-01A-21D-A31U-09 chr7:100677375 C>T maps to NM_001040105.1 S893S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GF-01A-11D-A37C-09 chr11:1085958 C>T maps to ENST00000441003 D933D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A50L-01A-11D-A27G-09 chr11:1093844 G>A maps to ENST00000441003 T1888T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93D-01A-11D-A387-09 chr11:1103845 C>T maps to ENST00000441003 T2715T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93F-01A-21D-A37C-09 chr11:1096385 C>T maps to ENST00000441003 Y2137Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NQ-01A-11D-A36J-09 chr11:1079733 G>C maps to ENST00000441003 V317V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OH-01A-11D-A27G-09 chr6:30954062 G>T maps to NM_001010909.2 V37V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OU-01A-11D-A28B-09 chr6:30955325 T>G maps to NM_001010909.2 T458T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FH-01A-11D-A33E-09 chr3:195490952 G>T maps to NM_018406.5 P4669P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GM-01A-11D-A37C-09 chr11:1256434 C>T maps to ENST00000447027 C920C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GN-01A-11D-A37C-09 chr11:1269836 C>T maps to ENST00000447027 V3912V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RE-01A-11D-A33E-09 chr11:1274133 C>T maps to ENST00000447027 V5050V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RF-01A-13D-A33E-09 chr11:1256531 G>T did not map to a codon.
Sequencing variant TCGA-IG-A625-01A-11D-A31U-09 chr11:1265735 C>T maps to ENST00000447027 S2545S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NL-01A-12D-A37C-09 chr11:1280191 C>A maps to ENST00000447027 G5541G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr11:1273603 C>T maps to ENST00000447027 A4968A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XP-A8T8-01A-11D-A36J-09 chr11:1269980 C>T maps to ENST00000447027 T3960T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GH-01A-11D-A37C-09 chr11:1025813 G>A maps to NM_005961.2 I930I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GQ-01A-11D-A37C-09 chr11:1031202 G>A maps to NM_005961.2 D180D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HY-01A-12D-A351-09 chr11:1027329 G>A maps to NM_005961.2 C723C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A97H-01A-11D-A387-09 chr23:105451395 C>T did not map to a codon.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr23:105451231 G>T did not map to a codon.
Sequencing variant TCGA-LN-A49L-01A-11D-A247-09 chr23:105450625 C>G did not map to a codon.
Sequencing variant TCGA-R6-A8W5-01B-11D-A37C-09 chr23:105450128 A>C did not map to a codon.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr9:113457776 A>G maps to ENST00000189978 S151S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49S-01A-11D-A247-09 chr9:113459654 C>T maps to ENST00000189978 N179N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASW-01A-11D-A403-09 chr6:8015899 C>T maps to NM_201280.2 A182A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A97H-01A-11D-A387-09 chr16:88721684 G>T maps to NM_002461.1 P273P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A8I1-01A-11D-A36J-09 chr12:110019328 G>T maps to NM_001114185.1 P167P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr16:29855903 C>T maps to NM_017458.3 I575I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OP-01A-11D-A27G-09 chr16:29857511 G>A maps to NM_017458.3 A724A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S8-A6BW-01A-11D-A31U-09 chr16:29859259 C>T maps to NM_017458.3 Q878*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EO-01A-11D-A36J-09 chr16:29853262 G>A maps to NM_017458.3 S488S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GK-01A-11D-A37C-09 chr21:42748940 C>T maps to NM_002463.1 F36F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr21:42749720 C>T maps to NM_002463.1 P85P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49R-01A-11D-A247-09 chr2:70148869 C>G maps to NM_002357.2 S59*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RE-01A-11D-A33E-09 chr23:3240212 G>T did not map to a codon.
Sequencing variant TCGA-IC-A6RE-01A-11D-A33E-09 chr23:3240216 G>T did not map to a codon.
Sequencing variant TCGA-IG-A7DP-01A-31D-A33E-09 chr23:3242901 C>A did not map to a codon.
Sequencing variant TCGA-L5-A4OE-01A-11D-A27G-09 chr23:3228850 C>T did not map to a codon.
Sequencing variant TCGA-L5-A8NF-01A-11D-A37C-09 chr23:3238107 A>G did not map to a codon.
Sequencing variant TCGA-L5-A8NF-01A-11D-A37C-09 chr23:3240439 G>A did not map to a codon.
Sequencing variant TCGA-L5-A8NV-01A-11D-A37C-09 chr23:3241681 G>A did not map to a codon.
Sequencing variant TCGA-LN-A4A6-01A-11D-A27G-09 chr23:3228542 C>T did not map to a codon.
Sequencing variant TCGA-RE-A7BO-01A-11D-A33E-09 chr23:3241799 T>G did not map to a codon.
Sequencing variant TCGA-VR-A8EQ-01A-11D-A36J-09 chr23:3235677 G>A did not map to a codon.
Sequencing variant TCGA-VR-A8EQ-01A-11D-A36J-09 chr23:3242384 C>T did not map to a codon.
Sequencing variant TCGA-JY-A6FD-01A-11D-A33E-09 chr6:135521338 T>C did not map to a codon.
Sequencing variant TCGA-L5-A8NN-01A-11D-A37C-09 chr6:135518457 G>A maps to NM_001130173.1 S521S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3Y9-01A-12D-A247-09 chr8:67485682 G>T maps to NM_001080416.2 S510*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NQ-01A-11D-A36J-09 chr12:102061573 G>T maps to NM_002465.2 L807L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93D-01A-11D-A387-09 chr19:50944199 G>A maps to NM_004533.3 P212P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49K-01A-11D-A247-09 chr19:50951587 G>A maps to NM_004533.3 W471*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NN-01A-11D-A37C-09 chr11:47353665 G>A maps to ENST00000399249 N1257N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8Q7-01A-11D-A37C-09 chr11:47362784 G>A maps to ENST00000399249 L601L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GF-01A-11D-A37C-09 chr8:128751155 C>T maps to NM_002467.4 F231F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6F8-01A-11D-A33E-09 chr8:128750894 C>T maps to NM_002467.4 I144I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FG-01A-11D-A33E-09 chr13:77657219 T>G maps to NM_015057.4 S3661S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OJ-01A-11D-A27G-09 chr13:77807342 G>T maps to NM_015057.4 A895A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-A7RE-01A-11D-A351-09 chr1:40363556 G>A maps to NM_001033082.2 D224D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A8HZ-01A-11D-A36J-09 chr2:16085954 G>A maps to NM_005378.4 S377S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OQ-01A-11D-A27G-09 chr3:38180160 C>T maps to NM_001172567.1 P3P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr3:38182017 C>T maps to NM_001172567.1 G214G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A891-01A-11D-A36J-09 chr12:81101965 G>A maps to NM_002469.2 K156K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-A7RC-01B-11D-A403-09 chr12:81101623 C>A maps to NM_002469.2 S42S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GL-01A-12D-A37C-09 chr17:10404069 C>A did not map to a codon.
Sequencing variant TCGA-L5-A4OE-01A-11D-A27G-09 chr17:10402364 G>A maps to NM_005963.3 Q1304*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NQ-01A-11D-A36J-09 chr17:10416982 G>A maps to NM_005963.3 F255F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EY-01A-11D-A36J-09 chr17:10401140 G>C maps to NM_005963.3 L1425L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NF-01A-11D-A37C-09 chr17:8381681 G>A maps to ENST00000360416 R1894*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EX-01A-11D-A36J-09 chr17:8445445 G>T maps to ENST00000360416 C528*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3QL-01A-11D-A247-09 chr16:15835387 G>A maps to NM_001040114.1 L938L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NJ-01A-11D-A36J-09 chr16:15839071 G>A maps to NM_001040114.1 Q819*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49U-01A-31D-A27G-09 chr16:15854504 T>C maps to NM_001040114.1 K387K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S8-A6BV-01A-21D-A31U-09 chr16:15844129 G>A maps to NM_001040114.1 S648S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASV-01A-11D-A387-09 chr16:15818260 G>A maps to NM_001040114.1 S1381S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3Y9-01A-12D-A247-09 chr17:10206758 C>G maps to NM_003802.2 L1841L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NR-01A-11D-A37C-09 chr17:10212568 C>T maps to NM_003802.2 V1717V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6XG-01B-11D-A33E-09 chr3:108127150 G>T maps to NM_014981.1 V1552V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA7B-01A-31D-A403-09 chr3:108163546 C>T maps to NM_014981.1 L885L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NE-01A-11D-A37C-09 chr17:10426980 G>A maps to NM_017534.5 A1768A. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-L5-A8NI-01A-11D-A37C-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-LN-A4A8-01A-32D-A27G-09 chr17:10451185 G>A maps to NM_017534.5 R18*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FP-01A-31D-A387-09 chr17:10432018 G>T maps to NM_017534.5 V1244V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6KZ-01A-11D-A31U-09 chr17:10428383 T>G did not map to a codon.
Sequencing variant TCGA-S8-A6BV-01A-21D-A31U-09 chr17:10427168 C>A maps to NM_017534.5 L1736L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EQ-01A-11D-A36J-09 chr17:10432982 G>C maps to NM_017534.5 L1005L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EY-01A-11D-A36J-09 chr17:10428869 C>A maps to NM_017534.5 E1479*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KH-A6WC-01A-11D-A33E-09 chr17:10543028 C>A maps to NM_002470.2 E925*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr17:10546238 G>A maps to NM_002470.2 F495F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A4P3-01A-11D-A27G-09 chr17:10355269 G>T maps to NM_017533.2 V1242V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43E-01A-11D-A247-09 chr17:10362573 G>A maps to NM_017533.2 I527I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr17:10348448 A>G maps to NM_017533.2 A1770A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8WG-01A-11D-A37C-09 chr17:10367851 G>T maps to NM_017533.2 Y195*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASW-01A-11D-A403-09 chr17:10348310 G>T maps to NM_017533.2 I1816I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GI-01A-11D-A37C-09 chr14:23863429 G>A maps to NM_002471.3 S844S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FB-01A-11D-A33E-09 chr14:23874913 G>A maps to NM_002471.3 D89D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NN-01A-11D-A37C-09 chr14:23863420 C>T maps to NM_002471.3 T847T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6DN-01B-11D-A31U-09 chr14:23862682 G>T maps to NM_002471.3 I991I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GI-01A-11D-A37C-09 chr14:23890229 G>A maps to NM_000257.2 N1091N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A5-01A-21D-A27G-09 chr14:23898238 A>G maps to NM_000257.2 N444N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43I-01A-11D-A247-09 chr20:33586547 G>A maps to NM_020884.3 V1382V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A1-01A-21D-A27G-09 chr20:33567244 G>A maps to NM_020884.3 E90E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA7D-01A-11D-A403-09 chr20:33568834 G>C did not map to a codon.
Sequencing variant TCGA-IG-A4P3-01A-11D-A27G-09 chr17:10299897 C>G maps to NM_002472.2 T1500T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr17:10318469 A>G maps to NM_002472.2 G256G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NN-01A-11D-A37C-09 chr17:10304047 G>T maps to NM_002472.2 R1132R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HX-01A-11D-A33E-09 chr17:10301804 G>T maps to NM_002472.2 Y1378*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FP-01A-31D-A387-09 chr17:10296407 G>A maps to NM_002472.2 I1762I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OE-01A-11D-A27G-09 chr22:36700135 G>T maps to NM_002473.4 A765A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A1-01A-21D-A27G-09 chr22:36690173 C>T maps to NM_002473.4 V1267V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OH-01A-11D-A27G-09 chr7:101259546 G>T maps to NM_138403.4 A162A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NW-01A-11D-A37C-09 chr7:44178519 T>C maps to ENST00000457314 *198W. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49M-01A-21D-A27G-09 chr6:16129564 T>C maps to NM_013262.3 Y4Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr3:123419011 C>T maps to NM_053025.3 K1101K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr3:123453041 G>A maps to NM_053025.3 T267T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NV-01A-11D-A37C-09 chr3:123375991 C>T maps to NM_053025.3 T1423T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GH-01A-11D-A37C-09 chr20:30409337 A>G maps to NM_033118.3 P190P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q9-A6FW-01A-31D-A31U-09 chr20:30414508 C>T maps to NM_033118.3 F358F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A5B8-01A-11D-A28B-09 chr16:46761261 C>A maps to NM_182493.2 R600R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EZ-01A-11D-A36J-09 chr6:2693021 G>T maps to NM_001012418.3 L77L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A4-01A-11D-A27G-09 chr3:169496706 C>T maps to NM_018657.4 Q140*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HV-01A-21D-A351-09 chr3:169496699 A>G maps to NM_018657.4 E137E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49W-01A-11D-A27G-09 chr5:16670917 G>C maps to NM_012334.2 S1867*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EX-01A-11D-A36J-09 chr5:16670646 C>T maps to NM_012334.2 L1957L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NG-01A-11D-A37C-09 chr17:18022797 C>T maps to ENST00000205890 G228G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr17:18058716 C>T maps to ENST00000205890 G2810G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49M-01A-21D-A27G-09 chr17:18023040 C>T maps to ENST00000205890 Y309Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr13:109792621 G>A maps to NM_015011.1 R1332R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EY-01A-11D-A36J-09 chr13:109793188 C>T maps to NM_015011.1 V1521V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr17:27424354 C>T maps to NM_078471.3 R1372R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6XQ-01B-11D-A33E-09 chr17:27423863 G>T maps to NM_078471.3 R1434R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GR-01A-12D-A37C-09 chr22:26399251 T>A maps to ENST00000407587 C2105*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3YB-01A-11D-A247-09 chr22:26164785 C>T maps to ENST00000407587 D303D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A2-01A-31D-A27G-09 chr22:26299711 G>T maps to ENST00000407587 E1690*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A9-01A-11D-A28B-09 chr22:26298603 C>A maps to ENST00000407587 A1618A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6XG-01B-11D-A33E-09 chr22:26231268 T>C maps to ENST00000407587 L1025L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6Y0-01B-11D-A33E-09 chr17:34852181 G>T maps to NM_001163735.1 P942P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A8JD-01A-11D-A36J-09 chr12:57423251 G>C maps to NM_005379.2 L948L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6Y0-01B-11D-A33E-09 chr2:192267360 C>T maps to NM_001130158.1 R825*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RF-01A-13D-A33E-09 chr17:1386152 A>C did not map to a codon.
Sequencing variant TCGA-ZR-A9CJ-01B-11D-A387-09 chr17:1382888 G>A maps to NM_001080779.1 T339T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S8-A6BW-01A-11D-A31U-09 chr17:30821800 G>A maps to NM_015194.1 F999F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-AAPN-01A-11D-A403-09 chr17:30981620 G>T maps to NM_015194.1 L788L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HY-01A-12D-A351-09 chr19:8587612 C>G maps to NM_012335.3 P985P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3QL-01A-11D-A247-09 chr10:26417468 T>A did not map to a codon.
Sequencing variant TCGA-L5-A4OE-01A-11D-A27G-09 chr10:26315324 G>T maps to NM_017433.4 E273*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A8JD-01A-11D-A36J-09 chr10:26482173 A>C maps to NM_017433.4 P1493P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr2:171371458 A>G maps to NM_138995.3 P1133P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NS-01A-12D-A37C-09 chr2:171262125 C>T maps to NM_138995.3 Q835*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OJ-01A-11D-A27G-09 chr15:52668562 G>T maps to ENST00000358212 R801R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88S-01A-11D-A36J-09 chr18:47402067 T>A maps to NM_001080467.2 K1176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NG-01A-11D-A37C-09 chr18:47518678 C>T maps to NM_001080467.2 E245E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr18:47500880 G>T maps to NM_001080467.2 T387T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-AAPN-01A-11D-A403-09 chr15:52527915 C>T maps to NM_018728.3 Q971Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8ET-01A-11D-A403-09 chr6:76545673 G>T did not map to a codon.
Sequencing variant TCGA-IG-A6QS-01A-12D-A33E-09 chr11:76915259 C>T maps to NM_000260.3 T1822T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6DQ-01B-11D-A31U-09 chr11:76893002 G>T maps to NM_000260.3 E971*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RE-A7BO-01A-11D-A33E-09 chr11:76874014 C>T maps to NM_000260.3 I557I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8ET-01A-11D-A403-09 chr11:76917247 G>A did not map to a codon.
Sequencing variant TCGA-L5-A88Z-01A-11D-A36J-09 chr2:128327485 G>A did not map to a codon.
Sequencing variant TCGA-LN-A4A2-01A-31D-A27G-09 chr2:128370115 C>T maps to ENST00000389524 P1086P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4MR-01A-11D-A28B-09 chr2:128350401 C>T maps to ENST00000389524 R676*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NS-01A-12D-A37C-09 chr15:72193555 C>T maps to ENST00000424560 L1042L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HV-01A-21D-A351-09 chr15:72192086 T>C maps to ENST00000424560 E1137E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49S-01A-11D-A247-09 chr19:17212763 C>T maps to NM_004145.3 D79D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HW-01A-22D-A351-09 chr19:17264846 C>T maps to NM_004145.3 Q357*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6XG-01B-11D-A33E-09 chr1:171605843 C>A maps to NM_000261.1 G246*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88S-01A-11D-A36J-09 chr17:12656132 C>T maps to NM_001146312.1 L510L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A4-01A-11D-A27G-09 chr17:12649385 G>C maps to NM_001146312.1 L374L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASX-01A-11D-A387-09 chr17:12656530 T>C maps to NM_001146312.1 A642A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr11:17741517 G>A maps to NM_002478.4 S63S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EX-01A-11D-A36J-09 chr11:17741338 C>T maps to NM_002478.4 L4L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NK-01A-21D-A37C-09 chr10:95079770 C>A did not map to a codon.
Sequencing variant TCGA-L5-A8NE-01A-11D-A37C-09 chr18:3067395 G>T maps to NM_003803.3 S1641*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA4D-01A-11D-A37C-09 chr18:3134770 G>T maps to NM_003803.3 S754*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GI-01A-11D-A37C-09 chr8:2046715 C>A maps to NM_003970.2 Y781*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93D-01A-11D-A387-09 chr8:2000308 C>G maps to NM_003970.2 S47S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OJ-01A-11D-A27G-09 chr8:2092796 C>T maps to NM_003970.2 D1430D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NW-01A-11D-A37C-09 chr1:24411016 G>A maps to ENST00000330966 S638S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8W8-01B-11D-A37C-09 chr1:24417404 G>T maps to ENST00000330966 V439V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49M-01A-21D-A27G-09 chr10:69961658 G>A maps to NM_032578.2 V1189V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8WC-01A-11D-A37C-09 chr10:69881861 G>T maps to NM_032578.2 E223*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr19:46404932 G>A maps to NM_001012643.2 R33R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OH-01A-11D-A27G-09 chr3:40085744 C>T maps to NM_015460.2 C105C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8WG-01A-11D-A37C-09 chr3:40085744 C>T maps to NM_015460.2 C105C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93F-01A-21D-A37C-09 chr1:59131213 G>T maps to NM_001085487.1 T707T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8ET-01A-11D-A403-09 chr17:47893184 G>T maps to NM_007067.4 G291G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A7DP-01A-31D-A33E-09 chr8:41791381 C>T maps to NM_006766.3 A1452A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A9-01A-11D-A28B-09 chr8:41806772 C>T maps to NM_006766.3 E569E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FB-01A-11D-A33E-09 chr10:76781835 G>A maps to NM_012330.2 E1073E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NE-01A-11D-A37C-09 chr10:76790461 G>A maps to NM_012330.2 T1960T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88W-01A-11D-A351-09 chr20:62844937 G>A maps to NM_004535.2 E523E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EX-01A-11D-A36J-09 chr20:62843470 C>T maps to NM_004535.2 S499S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8Q7-01A-11D-A37C-09 chr20:62871249 G>A maps to NM_004535.2 P1077P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr2:1983000 T>G did not map to a codon.
Sequencing variant TCGA-L5-A4OR-01A-11D-A27G-09 chr2:1890312 G>C maps to ENST00000399161 L903L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EP-01A-31D-A403-09 chr2:1893240 G>A maps to ENST00000399161 D764D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GK-01A-11D-A37C-09 chr19:59081730 G>C maps to NM_198055.1 S187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FH-01A-11D-A33E-09 chr19:59073507 C>T maps to NM_198055.1 Q712Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NR-01A-11D-A37C-09 chr4:40124820 G>T maps to NM_018177.3 E1425*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6Y2-01B-11D-A33E-09 chr5:177547252 G>A maps to NM_015111.1 A135A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NH-01A-11D-A37C-09 chr13:21306194 G>T maps to NM_174928.1 S98*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EZ-01A-11D-A36J-09 chr23:153197546 G>C did not map to a codon.
Sequencing variant TCGA-2H-A9GI-01A-11D-A37C-09 chr4:80246473 A>C maps to NM_032693.2 S186S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A5B8-01A-11D-A28B-09 chr4:80246827 C>T maps to NM_032693.2 P68P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49Y-01A-11D-A27G-09 chr4:80246776 G>T maps to NM_032693.2 G85G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4ON-01A-11D-A27G-09 chr4:140297559 G>A maps to NM_057175.3 P663P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93D-01A-11D-A387-09 chr20:20013262 G>T maps to NM_016100.3 S139S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FA-01A-11D-A33E-09 chr9:88631474 C>A maps to NM_024635.3 Y530*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6F8-01A-11D-A33E-09 chr3:113442353 G>A maps to NM_025146.2 C60C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EX-01A-11D-A36J-09 chr3:113440607 C>T maps to NM_025146.2 *170*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FO-01A-11D-A387-09 chr11:89882265 C>A maps to NM_005467.3 G158G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EW-01A-11D-A36J-09 chr11:89896164 C>T maps to NM_005467.3 Y346Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X8-AAAR-01A-11D-A403-09 chr11:89896508 C>T maps to NM_005467.3 D369D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EX-01A-11D-A36J-09 chr11:64825852 G>A maps to ENST00000340252 T47T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FG-01A-11D-A33E-09 chr3:175165131 G>A maps to NM_207015.2 A402A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-A7RE-01A-11D-A351-09 chr3:175293959 C>T maps to NM_207015.2 D595D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A5B8-01A-11D-A28B-09 chr12:57486238 C>T maps to NM_005967.3 I322I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NK-01A-21D-A37C-09 chr12:57485166 C>T maps to NM_005967.3 Q115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GR-01A-12D-A37C-09 chr12:57113630 C>T maps to NM_001113203.1 P561P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NK-01A-21D-A37C-09 chr12:57111773 A>G maps to NM_001113203.1 P1180P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A51D-01A-11D-A27G-09 chr17:59668535 C>G maps to NM_199290.3 P2P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OH-01A-11D-A27G-09 chr11:71166196 G>T maps to NM_018161.4 G43*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49L-01A-11D-A247-09 chr16:66847532 A>C maps to ENST00000359087 L326*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FD-01A-11D-A33E-09 chr17:42084979 G>C maps to NM_153006.2 L430L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OE-01A-11D-A27G-09 chr9:130829110 C>A maps to NM_197956.3 V90V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49N-01A-11D-A247-09 chr9:130826153 C>T maps to NM_197956.3 T179T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GK-01A-11D-A37C-09 chr13:101762981 A>C maps to NM_052867.2 T784T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GR-01A-12D-A37C-09 chr13:101763023 T>G maps to NM_052867.2 G770G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6F8-01A-11D-A33E-09 chr13:101733970 C>T maps to NM_052867.2 S1264S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FE-01A-11D-A33E-09 chr13:101755520 A>G did not map to a codon.
Sequencing variant TCGA-JY-A938-01A-11D-A37C-09 chr13:101714385 T>A maps to NM_052867.2 I1563I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93E-01A-11D-A37C-09 chr13:102029401 A>G maps to NM_052867.2 F127F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr13:101742265 C>T maps to NM_052867.2 A1107A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OU-01A-11D-A28B-09 chr13:101910907 G>A maps to NM_052867.2 S384S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6Y0-01B-11D-A33E-09 chr13:101717781 G>T maps to NM_052867.2 G1526G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GN-01A-11D-A37C-09 chr19:46417600 G>A maps to NM_001029861.2 N117N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A9VB-01A-21D-A37C-09 chr9:100845270 T>A maps to NM_018946.3 T338T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-AAPN-01A-11D-A403-09 chr9:100839225 G>A maps to NM_018946.3 L125L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASX-01A-11D-A387-09 chr12:76448797 C>T did not map to a codon.
Sequencing variant TCGA-RE-A7BO-01A-11D-A33E-09 chr23:72433665 C>G did not map to a codon.
Sequencing variant TCGA-IG-A3YC-01A-11D-A247-09 chr23:92927198 T>G did not map to a codon.
Sequencing variant TCGA-L5-A4OJ-01A-11D-A27G-09 chr23:92928149 T>C did not map to a codon.
Sequencing variant TCGA-L5-A8NL-01A-12D-A37C-09 chr23:92926985 A>G did not map to a codon.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr23:92927879 G>T did not map to a codon.
Sequencing variant TCGA-RE-A7BO-01A-11D-A33E-09 chr23:92926798 T>G did not map to a codon.
Sequencing variant TCGA-V5-AASX-01A-11D-A387-09 chr23:92926798 T>C did not map to a codon.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr20:23360530 A>C maps to ENST00000431864 T241T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RF-01A-13D-A33E-09 chr7:102760460 G>T maps to ENST00000455523 S241S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NN-01A-11D-A37C-09 chr7:102760609 C>A maps to ENST00000455523 G192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr11:34158540 G>T maps to NM_024662.2 G727*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HV-01A-21D-A351-09 chr16:3533570 C>T maps to NM_024845.2 N182N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NI-01A-11D-A37C-09 chr8:18258115 T>C maps to NM_000015.2 D201D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A8JD-01A-11D-A36J-09 chr17:72769776 G>T maps to NM_015654.3 S43*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4ON-01A-11D-A27G-09 chr1:201618308 G>T maps to ENST00000367296 P171P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OE-01A-11D-A27G-09 chr11:20072879 G>T did not map to a codon.
Sequencing variant TCGA-L5-A4OU-01A-11D-A28B-09 chr11:19970542 A>G maps to ENST00000396087 E877E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A5U6-01A-11D-A28B-09 chr11:20066598 C>A maps to ENST00000396087 G1118G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EW-01A-11D-A36J-09 chr11:20067054 C>T maps to ENST00000396087 N1270N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FD-01A-11D-A33E-09 chr12:78511808 G>T maps to NM_014903.4 L924L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A8-01A-32D-A27G-09 chr12:78400820 A>G maps to NM_014903.4 K501K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8W8-01B-11D-A37C-09 chr12:78362474 C>T maps to NM_014903.4 Q222*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8Q7-01A-11D-A37C-09 chr12:78392115 G>T did not map to a codon.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr2:15614271 C>T maps to NM_015909.2 R506R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GF-01A-11D-A37C-09 chr13:36245076 T>C maps to ENST00000400445 A2930A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43E-01A-11D-A247-09 chr13:35733223 C>T maps to ENST00000400445 N972N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8WG-01A-11D-A37C-09 chr13:35785238 G>T maps to ENST00000400445 V1857V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88W-01A-11D-A351-09 chr2:204058576 C>T maps to NM_001114132.1 D2298D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8ER-01A-11D-A36J-09 chr2:203972213 G>T maps to NM_001114132.1 L418L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OW-01A-11D-A28B-09 chr3:47040459 G>A maps to NM_015175.1 A1132A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr21:22881229 G>A maps to NM_004540.2 L712L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NT-01A-11D-A37C-09 chr21:22849775 G>A maps to NM_004540.2 K687K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GJ-01A-11D-A37C-09 chr12:6635320 C>T maps to NM_014865.3 A812A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A7DP-01A-31D-A33E-09 chr12:6635717 C>T maps to NM_014865.3 Q891*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr12:6630170 C>T maps to NM_014865.3 R537*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr12:6623451 C>T maps to NM_014865.3 Y203Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6KZ-01A-11D-A31U-09 chr12:6624086 G>T did not map to a codon.
Sequencing variant TCGA-2H-A9GH-01A-11D-A37C-09 chr11:134073621 C>T maps to NM_015261.2 L465L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A4P3-01A-11D-A27G-09 chr4:17813842 G>T did not map to a codon.
Sequencing variant TCGA-R6-A6L4-01A-11D-A31U-09 chr4:17839315 A>T maps to NM_022346.3 A786A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr7:158483384 G>A maps to NM_017760.5 R138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49Y-01A-11D-A27G-09 chr2:97008911 G>T maps to NM_015341.3 A155A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A938-01A-11D-A37C-09 chr9:100416156 G>A maps to NM_002486.4 L379L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EZ-01A-11D-A36J-09 chr9:100418316 T>C maps to NM_002486.4 P441P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A938-01A-11D-A37C-09 chr19:39691111 C>A maps to NM_001001414.1 G225G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A939-01A-12D-A37C-09 chr1:36028216 G>A maps to NM_001014839.1 W456*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GO-01A-11D-A37C-09 chr3:172428852 C>A maps to NM_001146276.1 G6G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A6-01A-11D-A27G-09 chr3:172351285 C>T maps to NM_001146276.1 K442K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A8I1-01A-11D-A36J-09 chr1:183543651 G>T maps to NM_001127651.2 S157S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EZ-01A-11D-A36J-09 chr2:106498468 G>A maps to NM_001004720.2 V304V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43I-01A-11D-A247-09 chr12:54925985 T>C maps to NM_005337.4 G938G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NR-01A-11D-A37C-09 chr2:133540075 A>G maps to NM_207363.2 T1436T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FH-01A-11D-A33E-09 chr2:232323097 G>A maps to NM_005381.2 R390*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr2:232326560 G>T maps to NM_005381.2 A101A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8Q7-01A-11D-A37C-09 chr2:232320316 G>A maps to NM_005381.2 F617F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NJ-01A-11D-A36J-09 chr2:24952368 G>A did not map to a codon.
Sequencing variant TCGA-L5-A8NG-01A-11D-A37C-09 chr8:71053577 G>A maps to NM_006540.2 Q957*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OF-01A-11D-A27G-09 chr20:46279841 G>A maps to NM_181659.2 Q1256Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr20:46279856 G>A maps to NM_181659.2 Q1261Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OW-01A-11D-A28B-09 chr20:46279856 G>A maps to NM_181659.2 Q1261Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NS-01A-12D-A37C-09 chr20:46281289 A>T maps to NM_181659.2 K1363*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FO-01A-11D-A387-09 chr20:46279856 G>A maps to NM_181659.2 Q1261Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FB-01A-11D-A33E-09 chr10:51586329 C>T maps to NM_001145260.1 G602G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A4P3-01A-11D-A27G-09 chr20:44691013 G>T maps to NM_020967.2 S555S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-A7RC-01B-11D-A403-09 chr20:44699149 G>T maps to NM_020967.2 R22R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43I-01A-11D-A247-09 chr20:33337957 G>A maps to NM_014071.2 P680P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49W-01A-11D-A27G-09 chr20:33330204 T>C maps to NM_014071.2 Q1285Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HX-01A-11D-A33E-09 chr20:33329256 G>T maps to NM_014071.2 V1601V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8Q7-01A-11D-A37C-09 chr20:33330741 T>C maps to NM_014071.2 G1106G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA4D-01A-11D-A37C-09 chr20:33345406 G>A maps to NM_014071.2 Q382*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A891-01A-11D-A36J-09 chr6:126242132 C>T maps to NM_181782.4 S763S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GL-01A-12D-A37C-09 chr17:16042326 C>T maps to ENST00000395857 K449K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HY-01A-12D-A351-09 chr17:16024423 A>T maps to ENST00000395857 A598A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8WC-01A-11D-A37C-09 chr17:16040726 C>A did not map to a codon.
Sequencing variant TCGA-IC-A6RF-01A-13D-A33E-09 chr12:124870323 G>T maps to NM_006312.4 L662L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FB-01A-11D-A33E-09 chr12:124819755 C>T maps to NM_006312.4 S2119S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr12:124862852 C>T maps to NM_006312.4 V699V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr12:124846744 G>A maps to NM_006312.4 S1008S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr12:124829302 C>T maps to NM_006312.4 S1525S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8WC-01A-11D-A37C-09 chr19:55424097 G>T maps to NM_004829.5 R258R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X8-AAAR-01A-11D-A403-09 chr1:160326958 C>T maps to NM_015331.2 S641S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OU-01A-11D-A28B-09 chr18:2579003 A>G maps to NM_006101.2 L185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49Y-01A-11D-A27G-09 chr18:2590097 G>T maps to NM_006101.2 E318*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NH-01A-11D-A37C-09 chr16:15758646 C>T maps to NM_001143979.1 S4S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NK-01A-21D-A37C-09 chr17:8350155 G>T maps to ENST00000402554 E164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EX-01A-11D-A36J-09 chr9:140110462 G>T maps to NM_001144026.1 R516R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OJ-01A-11D-A27G-09 chr23:43809158 G>T did not map to a codon.
Sequencing variant TCGA-VR-A8Q7-01A-11D-A37C-09 chr5:149900923 C>T maps to NM_001543.4 Y36Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3YB-01A-11D-A247-09 chr10:75563439 G>T maps to NM_003635.3 T678T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FD-01A-11D-A33E-09 chr10:75563502 G>T maps to NM_003635.3 Y657*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49S-01A-11D-A247-09 chr10:75564537 C>T maps to NM_003635.3 Q612Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GO-01A-11D-A37C-09 chr4:119026180 T>C maps to NM_004784.2 L330L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RE-01A-11D-A33E-09 chr4:119036075 T>C maps to NM_004784.2 S395S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OH-01A-11D-A27G-09 chr4:115769396 G>T maps to NM_022569.1 G638G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NI-01A-11D-A37C-09 chr4:115997919 G>T maps to NM_022569.1 L91L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X8-AAAR-01A-11D-A403-09 chr4:115898388 T>C maps to NM_022569.1 A340A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6XG-01B-11D-A33E-09 chr23:119005967 G>T did not map to a codon.
Sequencing variant TCGA-VR-A8EO-01A-11D-A36J-09 chr19:19638874 C>T maps to ENST00000450144 Y125Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A2-01A-31D-A27G-09 chr9:124914552 C>A maps to NM_014222.2 L62L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr15:41688938 C>A maps to NM_016013.2 G107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88S-01A-11D-A36J-09 chr3:49059962 C>T maps to NM_199069.1 Q88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3Y9-01A-12D-A247-09 chr19:14677010 C>T maps to NM_004146.4 E116E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A8O2-01A-11D-A36J-09 chr19:14682779 G>T maps to NM_004146.4 G11G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49Y-01A-11D-A27G-09 chr4:140216937 G>A maps to NM_001184990.1 A5A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88Z-01A-11D-A36J-09 chr1:161180117 C>T maps to NM_004550.4 R269*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GF-01A-11D-A37C-09 chr2:152492779 G>T maps to NM_001164507.1 P3021P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr2:152410371 G>A maps to NM_001164507.1 H6532H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OE-01A-11D-A27G-09 chr2:152409287 G>T maps to NM_001164507.1 I6578I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr2:152420127 T>G maps to NM_001164507.1 R6229R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OQ-01A-11D-A27G-09 chr2:152402930 G>T maps to NM_001164507.1 V6798V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88V-01A-11D-A351-09 chr2:152466582 G>A maps to NM_001164507.1 Q4024*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88W-01A-11D-A351-09 chr2:152436106 G>A maps to NM_001164507.1 S5483S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NN-01A-11D-A37C-09 chr2:152534586 G>T maps to NM_001164507.1 R1124R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-A7RB-01A-11D-A351-09 chr2:152528930 G>A maps to NM_001164507.1 D1417D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA7B-01A-31D-A403-09 chr2:152512795 G>T maps to NM_001164507.1 V2122V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XP-A8T7-01A-11D-A36J-09 chr2:152548622 C>A maps to NM_001164507.1 E686*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A9VB-01A-21D-A37C-09 chr2:152432748 C>T maps to NM_001164507.1 T5608T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3I8-01A-11D-A247-09 chr10:21108358 C>T maps to ENST00000430741 L683L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FA-01A-11D-A33E-09 chr10:21097517 T>A maps to ENST00000430741 G896G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8WG-01A-11D-A37C-09 chr10:21112175 T>C maps to ENST00000430741 E641E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GK-01A-11D-A37C-09 chr8:91893331 C>T maps to NM_022351.4 L111L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3QL-01A-11D-A247-09 chr18:55996355 C>T maps to NM_001144967.1 P270P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FH-01A-11D-A33E-09 chr18:56063467 G>T maps to NM_001144967.1 V965V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr8:24813279 G>T maps to ENST00000221169 T250T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6F8-01A-11D-A33E-09 chr8:24774934 G>T maps to NM_005382.2 E523*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FA-01A-11D-A33E-09 chr8:24776020 G>T maps to NM_005382.2 E885*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OH-01A-11D-A27G-09 chr8:24772310 C>T maps to NM_005382.2 R335R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FO-01A-11D-A387-09 chr8:24771822 C>T maps to NM_005382.2 L173L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NF-01A-11D-A37C-09 chr1:71873191 G>T maps to NM_173808.2 Y334*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EQ-01A-11D-A36J-09 chr15:75646604 G>A maps to NM_024608.2 P287P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49L-01A-11D-A247-09 chr4:170520291 G>A maps to ENST00000507142 R91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-A7RB-01A-11D-A351-09 chr4:170476956 T>A maps to ENST00000507142 A492A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GK-01A-11D-A37C-09 chr3:27337136 C>T maps to ENST00000396636 K425K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FP-01A-31D-A387-09 chr3:27385844 C>A maps to ENST00000396636 E94*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASW-01A-11D-A403-09 chr3:130889731 G>T did not map to a codon.
Sequencing variant TCGA-LN-A8I0-01A-11D-A36J-09 chr1:211846998 G>A maps to NM_002497.2 C127C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NT-01A-11D-A37C-09 chr13:52661569 G>A maps to NM_199289.1 A432A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A891-01A-11D-A36J-09 chr17:27065180 C>T maps to NM_178170.2 F380F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A891-01A-11D-A36J-09 chr17:27065185 C>A maps to NM_178170.2 S382*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A891-01A-11D-A36J-09 chr17:27065758 C>T maps to NM_178170.2 I431I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-AAPN-01A-11D-A403-09 chr9:140344060 G>C maps to NM_001130969.1 L495L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43M-01A-11D-A247-09 chr11:20968943 C>T maps to NM_006157.3 H378H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OR-01A-11D-A27G-09 chr11:20699481 G>A maps to NM_006157.3 V20V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6L6-01B-11D-A33E-09 chr11:20907086 G>T did not map to a codon.
Sequencing variant TCGA-2H-A9GH-01A-11D-A37C-09 chr12:44915836 A>C maps to NM_001145107.1 T757T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OF-01A-11D-A27G-09 chr12:45168613 C>A maps to NM_001145107.1 E354*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NF-01A-11D-A37C-09 chr12:45000976 G>C maps to NM_001145107.1 G596G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NL-01A-12D-A37C-09 chr12:44913814 G>T maps to NM_001145107.1 G841G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GG-01A-11D-A37C-09 chr15:73547070 C>T maps to NM_002499.3 Q665*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASX-01A-11D-A387-09 chr15:73590935 A>C maps to NM_002499.3 P1383P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr1:156640742 G>T maps to NM_006617.1 S1079S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GR-01A-12D-A37C-09 chr18:70526301 T>G maps to NM_153181.2 P75P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GK-01A-11D-A37C-09 chr2:242755704 A>G maps to NM_001167599.1 S21S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A939-01A-12D-A37C-09 chr2:182543464 G>A maps to NM_002500.2 D41D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr10:71332331 G>A maps to NM_020999.3 C156C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr10:71332487 G>A maps to NM_020999.3 D104D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A5B8-01A-11D-A28B-09 chr17:29527460 C>T maps to NM_001042492.2 R304*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NE-01A-11D-A37C-09 chr17:29528503 G>T did not map to a codon.
Sequencing variant TCGA-LN-A49R-01A-11D-A247-09 chr17:29554302 C>T maps to NM_001042492.2 N773N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6L6-01B-11D-A33E-09 chr22:30057295 G>T maps to NM_181832.2 E260*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EY-01A-11D-A36J-09 chr22:30070823 G>T did not map to a codon.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr1:204939849 G>A maps to ENST00000367172 W370*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6L6-01B-11D-A33E-09 chr16:69726421 G>A maps to NM_138713.2 Q898Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8W5-01B-11D-A37C-09 chr16:69726421 G>A maps to NM_138713.2 Q898Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8ER-01A-11D-A36J-09 chr18:77221365 G>A maps to NM_172387.1 P640P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GQ-01A-11D-A37C-09 chr20:50140170 C>T maps to NM_012340.3 P203P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8W5-01B-11D-A37C-09 chr20:50049180 G>A maps to NM_012340.3 A715A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A8HZ-01A-11D-A36J-09 chr16:28975130 C>T maps to NM_032815.3 L403L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X8-AAAR-01A-11D-A403-09 chr12:54686490 C>T maps to NM_001136023.1 Q263Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A939-01A-12D-A37C-09 chr17:46136805 C>T maps to ENST00000362042 R727*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49M-01A-21D-A27G-09 chr17:46134842 C>T maps to ENST00000362042 L336L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49K-01A-11D-A247-09 chr7:26224322 T>C maps to NM_004289.6 T335T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GH-01A-11D-A37C-09 chr9:94171972 C>T maps to NM_005384.2 T348T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr4:103533681 G>A maps to NM_003998.3 A837A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OU-01A-11D-A28B-09 chr4:103514702 G>A maps to NM_003998.3 G396G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZR-A9CJ-01B-11D-A387-09 chr4:103451071 G>C did not map to a codon.
Sequencing variant TCGA-LN-A49V-01A-11D-A247-09 chr10:104161037 C>T maps to NM_001077494.1 R725*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr19:39398217 C>T maps to NM_002503.3 H296H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr6:31515509 C>A maps to NM_005007.3 A13A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XP-A8T6-01A-11D-A36J-09 chr8:145668589 T>G maps to NM_013432.4 R127R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EU-01A-11D-A36J-09 chr11:129739724 G>A maps to NM_006165.3 G1090G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93C-01A-11D-A387-09 chr9:33311167 C>T maps to NM_002504.4 R481*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GJ-01A-11D-A37C-09 chr12:104519903 A>C maps to NM_006166.3 P73P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OP-01A-11D-A27G-09 chr12:104517093 G>A maps to NM_006166.3 I113I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HY-01A-12D-A351-09 chr12:104519954 A>G maps to NM_006166.3 D56D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASX-01A-11D-A387-09 chr1:41236498 G>A maps to ENST00000308733 *459*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NQ-01A-11D-A36J-09 chr2:233785104 G>A maps to NM_019850.2 I239I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43H-01A-11D-A247-09 chr1:115828864 G>A maps to NM_002506.2 P184P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GK-01A-11D-A37C-09 chr15:90814632 C>A maps to NM_001033088.1 L163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A4-01A-11D-A27G-09 chr4:103867842 G>T maps to NM_139173.3 T162T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93F-01A-21D-A37C-09 chr10:115668043 G>T maps to NM_198514.3 E644*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RE-01A-11D-A33E-09 chr23:17746821 G>T did not map to a codon.
Sequencing variant TCGA-Z6-AAPN-01A-11D-A403-09 chr23:17745850 G>C did not map to a codon.
Sequencing variant TCGA-IC-A6RE-01A-11D-A33E-09 chr23:71363113 A>C did not map to a codon.
Sequencing variant TCGA-JY-A93E-01A-11D-A37C-09 chr23:71359667 C>T did not map to a codon.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr23:71354499 C>T did not map to a codon.
Sequencing variant TCGA-LN-A49O-01A-11D-A247-09 chr23:71359228 C>G did not map to a codon.
Sequencing variant TCGA-R6-A8W8-01B-11D-A37C-09 chr23:71357027 G>A did not map to a codon.
Sequencing variant TCGA-VR-A8ER-01A-11D-A36J-09 chr23:71359848 G>T did not map to a codon.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr1:236141178 G>A maps to NM_002508.2 I1244I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-A7RE-01A-11D-A351-09 chr1:236175224 G>A maps to NM_002508.2 P841P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A9-01A-11D-A28B-09 chr14:51239777 G>A maps to NM_020921.3 D234D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49Y-01A-11D-A27G-09 chr9:95888701 G>A maps to NM_004148.3 L98L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr12:772502 G>A maps to NM_016533.4 I54I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3I8-01A-11D-A247-09 chr20:25434170 C>T maps to NM_025176.4 E1355E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3I8-01A-11D-A247-09 chr20:25434212 C>T maps to NM_025176.4 V1341V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49Y-01A-11D-A27G-09 chr5:37014783 G>T did not map to a codon.
Sequencing variant TCGA-RE-A7BO-01A-11D-A33E-09 chr5:36970986 C>G maps to NM_133433.3 S207*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA4D-01A-11D-A37C-09 chr5:37020559 G>T did not map to a codon.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr3:52514213 C>T maps to NM_007184.3 S477S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A8JE-01A-11D-A37C-09 chr8:63492201 G>T maps to NM_173688.2 G53G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OX-01A-21D-A28B-09 chr20:61878932 G>A maps to NM_152864.3 I156I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EY-01A-11D-A36J-09 chr23:119066176 T>C did not map to a codon.
Sequencing variant TCGA-V5-A7RB-01A-11D-A351-09 chr6:28227239 C>T maps to NM_001007531.1 Q31*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr16:50659406 C>T maps to NM_033119.3 C126C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3YC-01A-11D-A247-09 chr5:1034950 C>T maps to NM_033120.2 L169L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-AAPN-01A-11D-A403-09 chr5:1033538 C>T maps to NM_033120.2 L85L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49S-01A-11D-A247-09 chr3:23942370 C>T maps to NM_020345.3 V88V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6F8-01A-11D-A33E-09 chr19:45659085 G>T maps to NM_198478.3 A206A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A893-01A-11D-A36J-09 chr19:45655399 C>T maps to NM_198478.3 P765P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EU-01A-11D-A36J-09 chr19:45656612 G>C maps to NM_198478.3 S361*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A9VB-01A-21D-A37C-09 chr19:45656299 G>A maps to NM_198478.3 Y465Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GO-01A-11D-A37C-09 chr23:118724445 T>C did not map to a codon.
Sequencing variant TCGA-L5-A88V-01A-11D-A351-09 chr23:118723468 G>A did not map to a codon.
Sequencing variant TCGA-IG-A6QS-01A-12D-A33E-09 chr3:42680192 G>T maps to NM_005385.3 G999G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr14:36986896 G>A maps to NM_001079668.2 G264G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NW-01A-11D-A37C-09 chr20:21492908 G>A maps to NM_002509.2 R158R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4ON-01A-11D-A27G-09 chr3:173996811 G>T maps to NM_014932.2 E341*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6DN-01B-11D-A31U-09 chr3:173322864 T>A maps to NM_014932.2 Y159*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FD-01A-11D-A33E-09 chr23:70367645 C>A did not map to a codon.
Sequencing variant TCGA-KH-A6WC-01A-11D-A33E-09 chr23:70386936 C>T did not map to a codon.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr23:70367608 C>T did not map to a codon.
Sequencing variant TCGA-RE-A7BO-01A-11D-A33E-09 chr23:70386973 C>T did not map to a codon.
Sequencing variant TCGA-2H-A9GL-01A-12D-A37C-09 chr23:5827148 A>G did not map to a codon.
Sequencing variant TCGA-L5-A43E-01A-11D-A247-09 chr23:6069062 A>C did not map to a codon.
Sequencing variant TCGA-L5-A4OU-01A-11D-A28B-09 chr23:5821828 G>A did not map to a codon.
Sequencing variant TCGA-R6-A6XG-01B-11D-A33E-09 chr23:6069500 G>A did not map to a codon.
Sequencing variant TCGA-2H-A9GI-01A-11D-A37C-09 chr24:16936228 T>A did not map to a codon.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr24:16952603 G>A did not map to a codon.
Sequencing variant TCGA-L5-A8NH-01A-11D-A37C-09 chr24:16953044 C>A did not map to a codon.
Sequencing variant TCGA-JY-A93F-01A-21D-A37C-09 chr16:3613040 G>A maps to ENST00000448023 L680L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49S-01A-11D-A247-09 chr16:3607658 G>A maps to ENST00000448023 I725I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8WG-01A-11D-A37C-09 chr16:3613530 G>A maps to ENST00000448023 G516G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASW-01A-11D-A403-09 chr16:3602276 C>A maps to ENST00000448023 L804L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NJ-01A-11D-A36J-09 chr2:32475732 A>G maps to NM_021209.4 G400G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASX-01A-11D-A387-09 chr2:32476284 G>A maps to NM_021209.4 L216L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93E-01A-11D-A37C-09 chr16:57101699 C>T maps to NM_032206.3 Q1487*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr16:57113481 C>T maps to NM_032206.3 N1754N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L7-A6VZ-01A-12D-A33E-09 chr16:57054744 C>T maps to NM_032206.3 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3YC-01A-11D-A247-09 chr17:5434002 G>T maps to NM_033004.3 G1106G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A5B8-01A-11D-A28B-09 chr17:5433951 C>T maps to NM_033004.3 V1123V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NE-01A-11D-A37C-09 chr17:5456833 G>A maps to NM_033004.3 L800L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NW-01A-11D-A37C-09 chr19:56320172 G>A maps to NM_145007.3 I601I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6XQ-01B-11D-A33E-09 chr19:54313955 G>T maps to ENST00000391773 P319P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8WC-01A-11D-A37C-09 chr19:54307315 G>C maps to ENST00000391773 T826T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA7B-01A-31D-A403-09 chr19:54308649 G>A maps to ENST00000391773 L767L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49L-01A-11D-A247-09 chr19:56416357 C>T maps to NM_176810.2 K856K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EZ-01A-11D-A36J-09 chr19:56424443 G>A maps to NM_176810.2 Q247*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HZ-01A-31D-A351-09 chr11:7060993 A>G maps to NM_176822.3 Q113Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr19:55494829 C>T maps to NM_017852.3 C588C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EX-01A-11D-A36J-09 chr19:55494604 G>T maps to NM_017852.3 L513L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X8-AAAR-01A-11D-A403-09 chr19:55501999 G>T maps to NM_017852.3 E890*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A8HZ-01A-11D-A36J-09 chr19:56388458 G>T maps to NM_134444.4 E875*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EQ-01A-11D-A36J-09 chr19:56382309 G>A maps to NM_134444.4 L824L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A5B8-01A-11D-A28B-09 chr19:56515192 C>T maps to NM_153447.4 L58L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr19:56538312 C>T maps to NM_153447.4 H238H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA4D-01A-11D-A37C-09 chr19:56538277 G>T did not map to a codon.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr11:285297 C>A maps to NM_138329.1 T891T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GL-01A-12D-A37C-09 chr19:55450464 G>A maps to ENST00000446217 C602C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr19:55450977 C>T maps to ENST00000446217 P431P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr19:55447774 G>A maps to ENST00000446217 T746T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NQ-01A-11D-A36J-09 chr19:55451628 C>T maps to ENST00000446217 T214T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A8-01A-32D-A27G-09 chr19:55452839 G>C maps to ENST00000446217 L108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6L6-01B-11D-A33E-09 chr19:55450532 G>A maps to ENST00000446217 Q580*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S8-A6BV-01A-21D-A31U-09 chr19:56466077 C>A maps to NM_176811.2 I218I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr19:56244869 G>T maps to NM_176820.2 L109L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A5B8-01A-11D-A28B-09 chr11:119050455 C>T maps to NM_024618.2 Q576*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr15:85198626 A>G maps to NM_205858.1 A113A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A4QT-01A-21D-A27G-09 chr3:160951233 G>A maps to ENST00000472947 K108K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GI-01A-11D-A37C-09 chr1:169199981 G>T maps to NM_013330.3 R322R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NL-01A-12D-A37C-09 chr1:183221790 G>T maps to NM_015039.2 I303I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NL-01A-12D-A37C-09 chr1:183387333 C>T maps to NM_015039.2 G23G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A6QS-01A-12D-A33E-09 chr10:15154836 G>T maps to ENST00000378143 P463P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8ET-01A-11D-A403-09 chr5:151784587 G>A maps to NM_020167.4 T29T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OT-01A-11D-A28B-09 chr5:43653169 C>T maps to NM_182977.2 L638L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NJ-01A-11D-A36J-09 chr16:69783467 G>T maps to NM_014062.1 P131P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FP-01A-31D-A387-09 chr16:69788598 C>A maps to NM_014062.1 E32*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-A7RE-01A-11D-A351-09 chr16:69778841 G>A maps to NM_014062.1 S301S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3I8-01A-11D-A247-09 chr7:144096925 G>A maps to ENST00000467773 R360*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EX-01A-11D-A36J-09 chr10:96109876 G>C maps to NM_022451.9 S374*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HX-01A-11D-A33E-09 chr12:132629488 C>T maps to NM_024078.1 Q70*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A939-01A-12D-A37C-09 chr7:30492171 G>A maps to NM_006092.2 D287D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6L4-01A-11D-A31U-09 chr16:50733864 G>A maps to NM_022162.1 R180R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr2:10815950 G>T maps to NM_024894.2 S86S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49Y-01A-11D-A27G-09 chr22:38083950 G>T maps to NM_024313.2 E40*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr9:95077337 G>A maps to NM_017948.5 S523S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6L4-01A-11D-A31U-09 chr9:95076605 C>T maps to NM_017948.5 A767A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8W5-01B-11D-A37C-09 chr10:103919294 G>T maps to ENST00000405356 E287*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A8HZ-01A-11D-A36J-09 chr16:18549918 G>A maps to NM_001004060.1 H383H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6Y2-01B-11D-A33E-09 chr16:16349608 C>A maps to ENST00000263012 T332T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GQ-01A-11D-A37C-09 chr4:2956222 G>A maps to NM_003703.1 G180G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RF-01A-13D-A33E-09 chr4:2956258 G>T maps to NM_003703.1 G168G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FD-01A-11D-A33E-09 chr4:2955330 C>T maps to NM_003703.1 T218T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RE-01A-11D-A33E-09 chr5:175813850 A>T maps to ENST00000451293 Y92*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NS-01A-12D-A37C-09 chr5:175813853 G>T maps to ENST00000451293 P91P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3YA-01A-11D-A247-09 chr12:117703276 G>A maps to ENST00000338101 T660T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FA-01A-11D-A33E-09 chr12:117718601 G>A maps to ENST00000338101 L484L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr12:117655960 G>A maps to ENST00000338101 N1427N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EU-01A-11D-A36J-09 chr12:117672481 G>A maps to ENST00000338101 F1075F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HY-01A-12D-A351-09 chr17:26091135 G>T maps to NM_000625.4 P821P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6XG-01B-11D-A33E-09 chr17:26093543 C>T maps to NM_000625.4 P746P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X8-AAAR-01A-11D-A403-09 chr17:26116635 C>T maps to NM_000625.4 T63T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RE-01A-11D-A33E-09 chr2:169707380 C>G maps to NM_001171631.1 V222V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KH-A6WC-01A-11D-A33E-09 chr9:139397631 A>G did not map to a codon.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr9:139401188 C>A maps to NM_017617.3 E1294*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88T-01A-11D-A351-09 chr9:139410451 G>C maps to NM_017617.3 Y550*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88T-01A-11D-A351-09 chr9:139418431 C>A did not map to a codon.
Sequencing variant TCGA-VR-A8EQ-01A-11D-A36J-09 chr9:139391545 C>T maps to NM_017617.3 S2215S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EQ-01A-11D-A36J-09 chr9:139412279 C>T maps to NM_017617.3 E455E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EY-01A-11D-A36J-09 chr9:139413041 C>T did not map to a codon.
Sequencing variant TCGA-LN-A49W-01A-11D-A27G-09 chr1:120512368 T>A did not map to a codon.
Sequencing variant TCGA-L5-A8NR-01A-11D-A37C-09 chr1:145273433 C>G maps to ENST00000454606 V108V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GM-01A-11D-A37C-09 chr19:15290184 T>A maps to NM_000435.2 P1150P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A938-01A-11D-A37C-09 chr19:15298066 G>A maps to NM_000435.2 I563I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93D-01A-11D-A387-09 chr19:15302298 G>A maps to NM_000435.2 F324F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L7-A56G-01A-21D-A27G-09 chr19:15300180 G>A maps to NM_000435.2 I365I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L7-A56G-01A-21D-A27G-09 chr19:15300207 G>A maps to NM_000435.2 V356V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L7-A56G-01A-21D-A27G-09 chr19:15303191 G>A maps to NM_000435.2 F112F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L7-A6VZ-01A-12D-A33E-09 chr19:15281175 G>T maps to NM_000435.2 R1694R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L7-A6VZ-01A-12D-A33E-09 chr19:15289687 G>T maps to NM_000435.2 C1261*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49X-01A-31D-A27G-09 chr19:15296490 C>T did not map to a codon.
Sequencing variant TCGA-R6-A6Y0-01B-11D-A33E-09 chr19:15302439 C>T maps to NM_000435.2 E277E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-A7RC-01B-11D-A403-09 chr19:15291624 C>T maps to NM_000435.2 W1003*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA7D-01A-11D-A403-09 chr19:15292531 G>A maps to NM_000435.2 R883*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KH-A6WC-01A-11D-A33E-09 chr6:32181561 G>T maps to NM_004557.3 G741G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A8I0-01A-11D-A36J-09 chr6:32183073 G>C maps to NM_004557.3 L650L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49W-01A-11D-A27G-09 chr8:120430328 G>C maps to NM_002514.3 G114G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93F-01A-21D-A37C-09 chr14:27064754 G>A maps to ENST00000449198 D64D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HW-01A-22D-A351-09 chr19:46443969 G>C maps to NM_002516.2 L210L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q9-A6FU-01A-11D-A31U-09 chr23:100105307 C>T did not map to a codon.
Sequencing variant TCGA-L5-A4ON-01A-11D-A27G-09 chr6:155764535 C>T maps to NM_015718.2 A119A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A1-01A-21D-A27G-09 chr6:155743923 G>A maps to NM_015718.2 C404C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A8-01A-32D-A27G-09 chr6:155764430 G>A maps to NM_015718.2 L154L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GK-01A-11D-A37C-09 chr11:89133397 T>C maps to NM_016931.3 K332K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OE-01A-11D-A27G-09 chr11:89177377 C>T maps to NM_016931.3 L124L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NR-01A-11D-A37C-09 chr15:69341355 C>T maps to NM_024505.3 L653L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GI-01A-11D-A37C-09 chr16:2031150 C>A maps to NM_172168.1 V10V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NI-01A-11D-A37C-09 chr16:2029800 T>C maps to NM_172168.1 L235L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OH-01A-11D-A27G-09 chr19:47539367 T>G maps to NM_002517.2 L223L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OH-01A-11D-A27G-09 chr19:47539376 C>A maps to NM_002517.2 T226T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FP-01A-31D-A387-09 chr14:34269168 G>A maps to NM_001164749.1 A552A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NF-01A-11D-A37C-09 chr11:66191635 T>G maps to NM_178864.3 P425P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EY-01A-11D-A36J-09 chr11:66190166 C>T maps to NM_178864.3 F151F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA4G-01A-11D-A37C-09 chr11:108044482 G>A maps to NM_002519.2 Q410*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XP-A8T7-01A-11D-A36J-09 chr11:108058907 T>A did not map to a codon.
Sequencing variant TCGA-2H-A9GQ-01A-11D-A37C-09 chr7:44555411 G>T maps to NM_013389.2 L1289L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr20:57268947 C>T maps to NM_024663.3 C102C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NH-01A-11D-A37C-09 chr20:57282219 G>A maps to NM_024663.3 A288A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93C-01A-11D-A387-09 chr17:45695742 G>T maps to NM_006310.3 E775*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA4D-01A-11D-A37C-09 chr17:45608674 G>T maps to NM_006310.3 L3L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EQ-01A-11D-A36J-09 chr12:53901174 C>T maps to NM_003717.2 Q28Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA4D-01A-11D-A37C-09 chr10:72015105 C>T maps to ENST00000277942 A300A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FP-01A-31D-A387-09 chr3:132441159 C>A maps to ENST00000393156 E14*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A5B8-01A-11D-A28B-09 chr1:5947472 G>A maps to NM_015102.2 V786V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88W-01A-11D-A351-09 chr1:5925320 C>A maps to NM_015102.2 L1219L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NF-01A-11D-A37C-09 chr19:36339236 G>A maps to NM_004646.3 N411N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S8-A6BW-01A-11D-A31U-09 chr19:36339269 G>T maps to NM_004646.3 S400S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XP-A8T7-01A-11D-A36J-09 chr19:36333044 G>A maps to NM_004646.3 L882L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FB-01A-11D-A33E-09 chr16:15045674 G>A maps to NM_006985.2 A282A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NT-01A-11D-A37C-09 chr4:106816880 G>T did not map to a codon.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr2:232790896 G>A maps to NM_024409.1 S21S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OJ-01A-11D-A27G-09 chr1:153659783 G>T maps to NM_000906.3 E682*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49V-01A-11D-A247-09 chr1:153655046 C>T maps to NM_000906.3 P415P. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-L5-A8NJ-01A-11D-A36J-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-JY-A6FB-01A-11D-A33E-09 chr5:32711914 G>T maps to ENST00000265074 P11P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NJ-01A-11D-A36J-09 chr5:32711944 C>T maps to ENST00000265074 A21A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FO-01A-11D-A387-09 chr5:32739000 C>T maps to ENST00000265074 H308H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASW-01A-11D-A403-09 chr5:32724885 C>T maps to ENST00000265074 Y284Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A50L-01A-11D-A27G-09 chr16:139732 G>A maps to ENST00000399953 N443N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr16:162651 C>T maps to ENST00000399953 A172A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OU-01A-11D-A28B-09 chr7:98254300 C>T maps to NM_002523.2 Y237Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A938-01A-11D-A37C-09 chr22:39218703 G>A maps to NM_014293.2 N471N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NU-01A-11D-A36J-09 chr22:39222642 G>A maps to NM_014293.2 T320T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FP-01A-31D-A387-09 chr22:39222663 C>A maps to NM_014293.2 L313L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr7:24324975 C>T maps to NM_000905.3 D39D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49S-01A-11D-A247-09 chr4:164247643 C>T maps to NM_000909.4 K21K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr4:156135405 G>A maps to NM_000910.2 P105P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NU-01A-11D-A36J-09 chr4:156135423 C>G maps to NM_000910.2 T111T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GQ-01A-11D-A37C-09 chr23:30327394 G>A did not map to a codon.
Sequencing variant TCGA-V5-AASV-01A-11D-A387-09 chr23:30326922 C>T did not map to a codon.
Sequencing variant TCGA-R6-A6L4-01A-11D-A31U-09 chr17:38251253 G>A maps to NM_021724.3 H456H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6F8-01A-11D-A33E-09 chr3:24004095 G>T maps to NM_005126.4 L382L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GN-01A-11D-A37C-09 chr19:50885723 C>G maps to NM_007121.4 R416R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A8I1-01A-11D-A36J-09 chr19:50881824 G>A maps to NM_007121.4 Q173Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A1-01A-21D-A27G-09 chr11:47282122 C>T maps to NM_005693.2 Y132Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43C-01A-11D-A247-09 chr12:95434293 G>T maps to NM_003297.2 S404*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr19:19312793 G>T maps to ENST00000420605 A120A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA7D-01A-11D-A403-09 chr6:108497938 C>A maps to ENST00000368983 P201P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr2:157185942 C>T maps to NM_006186.3 P252P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A4QT-01A-21D-A27G-09 chr9:102590531 G>T maps to NM_173200.1 E81*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L7-A6VZ-01A-12D-A33E-09 chr10:115381762 G>T maps to ENST00000369358 V886V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-A7RB-01A-11D-A351-09 chr10:115380371 G>C maps to ENST00000369358 L963L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HX-01A-11D-A33E-09 chr7:107872818 C>T maps to ENST00000379032 R126R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HY-01A-12D-A351-09 chr1:52303156 A>T did not map to a codon.
Sequencing variant TCGA-R6-A6Y2-01B-11D-A33E-09 chr1:52306074 T>C maps to NM_002525.2 E151E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GI-01A-11D-A37C-09 chr8:32617882 A>G maps to NM_013956.3 R414R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A4QS-01A-11D-A27G-09 chr8:32453466 G>T maps to NM_013956.3 G74G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4ON-01A-11D-A27G-09 chr8:32505697 A>G maps to NM_013959.3 Q154Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OT-01A-11D-A28B-09 chr8:32621601 A>G maps to NM_013956.3 Q540Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6DQ-01B-11D-A31U-09 chr8:32621346 G>A maps to NM_013956.3 S455S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EX-01A-11D-A36J-09 chr8:32621460 G>A maps to NM_013956.3 E493E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OT-01A-11D-A28B-09 chr10:84745120 C>T maps to ENST00000404547 S641S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NJ-01A-11D-A36J-09 chr10:84745031 C>T maps to ENST00000404547 Q612*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GR-01A-12D-A37C-09 chr23:105181572 A>G did not map to a codon.
Sequencing variant TCGA-IG-A4QS-01A-11D-A27G-09 chr23:105156739 A>C did not map to a codon.
Sequencing variant TCGA-L5-A88W-01A-11D-A351-09 chr23:105183879 C>G did not map to a codon.
Sequencing variant TCGA-LN-A49Y-01A-11D-A27G-09 chr23:105125724 C>G did not map to a codon.
Sequencing variant TCGA-R6-A6Y0-01B-11D-A33E-09 chr23:105153086 T>G did not map to a codon.
Sequencing variant TCGA-L5-A8NW-01A-11D-A37C-09 chr10:33471650 G>A maps to NM_003873.5 N819N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GI-01A-11D-A37C-09 chr2:206641090 G>A maps to NM_018534.3 A854A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6F8-01A-11D-A33E-09 chr2:206656993 G>T maps to NM_201266.1 E826*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NL-01A-12D-A37C-09 chr2:206592643 G>T maps to NM_201266.1 T340T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A6-01A-11D-A27G-09 chr2:206628609 G>T maps to NM_201266.1 E753*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8W5-01B-11D-A37C-09 chr2:206659484 C>T maps to NM_201266.1 Y833Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NR-01A-11D-A37C-09 chr6:24146172 G>T maps to NM_080723.4 *196L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GJ-01A-11D-A37C-09 chr2:51149817 C>T maps to ENST00000404971 A299A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A4QS-01A-11D-A27G-09 chr2:50850699 A>G maps to ENST00000404971 L329L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A938-01A-11D-A37C-09 chr2:50758383 C>T maps to ENST00000404971 V816V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A939-01A-12D-A37C-09 chr2:51149817 C>T maps to ENST00000404971 A299A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49Y-01A-11D-A27G-09 chr2:50280636 C>A maps to ENST00000404971 L1340L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GI-01A-11D-A37C-09 chr11:64415727 G>A maps to NM_015080.3 C1122C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GI-01A-11D-A37C-09 chr11:64434790 G>T maps to NM_015080.3 R577R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NS-01A-12D-A37C-09 chr11:64402741 C>T did not map to a codon.
Sequencing variant TCGA-LN-A49L-01A-11D-A247-09 chr11:64428407 G>A maps to NM_015080.3 R668*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L7-A6VZ-01A-12D-A33E-09 chr14:80328021 G>A maps to NM_004796.4 P967P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49S-01A-11D-A247-09 chr14:79434616 T>C maps to NM_004796.4 L651L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6Y0-01B-11D-A33E-09 chr14:80328054 G>C maps to NM_004796.4 V978V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8Q7-01A-11D-A37C-09 chr14:80158528 T>C maps to NM_001105250.1 N205N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RF-01A-13D-A33E-09 chr5:176678793 G>T maps to NM_022455.4 E1569*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RF-01A-13D-A33E-09 chr5:176709522 C>T maps to NM_022455.4 R1984*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93F-01A-21D-A37C-09 chr5:176709464 G>A did not map to a codon.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr5:176721679 A>G maps to NM_022455.4 K2437K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4MR-01A-11D-A28B-09 chr5:176719053 G>T maps to NM_022455.4 E2120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASW-01A-11D-A403-09 chr16:27268846 G>A maps to NM_145080.3 H15H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93E-01A-11D-A37C-09 chr10:18903420 G>T maps to NM_182543.2 R181R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3YA-01A-11D-A247-09 chr2:18765854 G>A maps to ENST00000455492 D293D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr17:17250122 C>T maps to ENST00000379552 A189A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4ON-01A-11D-A27G-09 chr11:132205041 G>A did not map to a codon.
Sequencing variant TCGA-IG-A5B8-01A-11D-A28B-09 chr16:2522729 C>T maps to NM_006181.1 R319R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FE-01A-11D-A33E-09 chr12:96063914 G>T maps to NM_021229.3 C506*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FH-01A-11D-A33E-09 chr19:49174222 G>T maps to NM_145807.1 L7L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8WG-01A-11D-A37C-09 chr9:135102325 C>T maps to NM_032536.2 C316C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88T-01A-11D-A351-09 chr9:87325706 G>T did not map to a codon.
Sequencing variant TCGA-L5-A4OJ-01A-11D-A27G-09 chr15:88799255 G>A maps to NM_001012338.1 I43I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8W5-01B-11D-A37C-09 chr15:88799366 G>A maps to NM_001012338.1 C6C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A939-01A-12D-A37C-09 chr20:61340825 G>A maps to NM_002531.2 A89A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NJ-01A-11D-A36J-09 chr20:61386238 G>A did not map to a codon.
Sequencing variant TCGA-L5-A8NS-01A-12D-A37C-09 chr20:61341149 C>T maps to NM_002531.2 A197A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HX-01A-11D-A33E-09 chr20:61389684 C>T maps to NM_002531.2 Y328Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr12:106460762 G>A maps to NM_014840.2 C601C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A6QS-01A-12D-A33E-09 chr7:151057289 G>T maps to ENST00000355851 G253*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OH-01A-11D-A27G-09 chr7:151065970 G>T maps to ENST00000355851 E416*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GM-01A-11D-A37C-09 chr8:110305696 C>T maps to NM_032869.3 L172L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EU-01A-11D-A36J-09 chr8:110308630 G>A maps to NM_032869.3 S147S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3QL-01A-11D-A247-09 chr23:51076023 G>A did not map to a codon.
Sequencing variant TCGA-Z6-A8JE-01A-11D-A37C-09 chr23:51076023 G>A did not map to a codon.
Sequencing variant TCGA-L5-A4OF-01A-11D-A27G-09 chr10:74890582 G>A maps to NM_015901.4 L327L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8Q7-01A-11D-A37C-09 chr3:131102145 T>C maps to NM_152395.2 S183S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3QL-01A-11D-A247-09 chr10:12209760 G>A maps to ENST00000378937 Y213Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6L6-01B-11D-A33E-09 chr16:77759423 G>A maps to NM_001105663.1 L44L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S8-A6BW-01A-11D-A31U-09 chr1:163310158 G>T maps to NM_145697.2 V204V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FA-01A-11D-A33E-09 chr13:45523906 G>T maps to NM_012345.2 S363*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49R-01A-11D-A247-09 chr13:45523974 T>A did not map to a codon.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr11:71730661 A>G maps to ENST00000393695 A160A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3I8-01A-11D-A247-09 chr19:41173888 C>T maps to NM_004756.3 Q438Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93D-01A-11D-A387-09 chr6:17633075 C>A did not map to a codon.
Sequencing variant TCGA-L5-A88V-01A-11D-A351-09 chr6:17675152 G>A maps to ENST00000430136 R279*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49X-01A-31D-A27G-09 chr6:17661925 T>C maps to ENST00000430136 R451R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A50L-01A-11D-A27G-09 chr11:47837041 G>A maps to NM_015231.1 L559L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49W-01A-11D-A27G-09 chr11:47809747 T>C maps to NM_015231.1 E1244E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GN-01A-11D-A37C-09 chr9:131767800 C>T maps to NM_015354.1 L1577L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A5B8-01A-11D-A28B-09 chr9:131748957 G>T did not map to a codon.
Sequencing variant TCGA-JY-A6F8-01A-11D-A33E-09 chr9:131761961 G>T maps to NM_015354.1 E1241*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HW-01A-22D-A351-09 chr9:131768006 C>T maps to NM_015354.1 F1607F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FQ-01A-31D-A387-09 chr9:131733122 G>T maps to NM_015354.1 L333L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6Y0-01B-11D-A33E-09 chr9:131720320 C>A maps to NM_015354.1 A120A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A625-01A-11D-A31U-09 chr7:135261144 A>G maps to NM_015135.2 T157T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8WG-01A-11D-A37C-09 chr7:135303236 G>T maps to NM_015135.2 L1283L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GI-01A-11D-A37C-09 chr3:13429847 G>A maps to NM_024923.2 T213T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr3:13417859 G>A maps to NM_024923.2 Y408Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr3:13359205 C>T maps to NM_024923.2 W1880*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A5-01A-21D-A27G-09 chr3:13373868 G>A maps to NM_024923.2 Q1287*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RF-01A-13D-A33E-09 chr1:154061966 G>T maps to NM_207308.2 S764*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr1:153965411 C>A did not map to a codon.
Sequencing variant TCGA-JY-A6FG-01A-11D-A33E-09 chr17:73204644 G>A maps to NM_024844.3 K19K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OS-01A-11D-A28B-09 chr16:56878424 A>G maps to NM_014669.3 Q788Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8WG-01A-11D-A37C-09 chr16:56839481 C>T maps to NM_014669.3 R143*. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-R6-A8W8-01B-11D-A37C-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-VR-A8Q7-01A-11D-A37C-09 chr16:28549405 C>T maps to NM_001042483.1 G79G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GF-01A-11D-A37C-09 chr6:118024774 T>C maps to NM_138459.3 N233N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3YB-01A-11D-A247-09 chr19:16860995 C>T maps to ENST00000438489 L515L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L7-A56G-01A-21D-A27G-09 chr19:16918781 C>T maps to ENST00000438489 Y1374Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4MR-01A-11D-A28B-09 chr19:16884030 G>A maps to ENST00000438489 Q835Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6L6-01B-11D-A33E-09 chr19:16923593 C>G maps to ENST00000438489 S1442S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OG-01A-11D-A27G-09 chr23:101620154 C>A did not map to a codon.
Sequencing variant TCGA-L5-A4ON-01A-11D-A27G-09 chr23:101624587 C>T did not map to a codon.
Sequencing variant TCGA-L5-A8NF-01A-11D-A37C-09 chr23:101623933 A>G did not map to a codon.
Sequencing variant TCGA-Q9-A6FW-01A-31D-A31U-09 chr23:101615752 C>T did not map to a codon.
Sequencing variant TCGA-LN-A49P-01A-11D-A247-09 chr23:102347946 G>T did not map to a codon.
Sequencing variant TCGA-2H-A9GR-01A-12D-A37C-09 chr23:101093212 T>C did not map to a codon.
Sequencing variant TCGA-VR-A8EY-01A-11D-A36J-09 chr23:101095813 A>G did not map to a codon.
Sequencing variant TCGA-LN-A4MQ-01A-11D-A28B-09 chr17:47656097 C>T maps to ENST00000513748 L65L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6DQ-01B-11D-A31U-09 chr20:23334729 G>T maps to NM_013248.2 E18*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L7-A56G-01A-21D-A27G-09 chr14:24880308 C>T maps to NM_025081.2 C814C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FO-01A-11D-A387-09 chr14:24880347 G>T maps to NM_025081.2 R827R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A5S3-01A-11D-A28B-09 chr23:41332754 G>A did not map to a codon.
Sequencing variant TCGA-R6-A6KZ-01A-11D-A31U-09 chr23:41332759 G>T did not map to a codon.
Sequencing variant TCGA-IG-A4P3-01A-11D-A27G-09 chr12:113385762 G>A maps to NM_006187.2 L296L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RE-01A-11D-A33E-09 chr10:126094006 C>A maps to NM_000274.3 E216*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HY-01A-12D-A351-09 chr10:126097427 C>T maps to NM_000274.3 K102K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8WC-01A-11D-A37C-09 chr10:126090409 T>C did not map to a codon.
Sequencing variant TCGA-L7-A6VZ-01A-12D-A33E-09 chr12:56622933 G>T maps to NM_024068.3 P191P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NR-01A-11D-A37C-09 chr9:138439068 G>A maps to NM_014582.2 T84T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49Y-01A-11D-A27G-09 chr9:138439804 G>C maps to NM_014582.2 L122L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASX-01A-11D-A387-09 chr9:138439762 C>T maps to NM_014582.2 D108D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FD-01A-11D-A33E-09 chr1:228467708 C>T maps to NM_001098623.1 L2528L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93E-01A-11D-A37C-09 chr1:228547657 G>A maps to NM_052843.2 S6355S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FP-01A-31D-A387-09 chr1:228495816 G>T maps to NM_001098623.1 E4158*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASW-01A-11D-A403-09 chr1:228476025 G>A did not map to a codon.
Sequencing variant TCGA-XP-A8T7-01A-11D-A36J-09 chr1:228554145 G>T maps to NM_001098623.1 E6408*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr2:220432508 G>A maps to NM_015311.2 R489*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A97I-01A-11D-A387-09 chr15:28116297 A>C did not map to a codon.
Sequencing variant TCGA-LN-A9FP-01A-31D-A387-09 chr15:28326849 C>A maps to NM_000275.2 G57G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-A7RB-01A-11D-A351-09 chr15:28200321 G>A maps to NM_000275.2 I608I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr4:48851982 C>T maps to NM_001168254.1 Y92Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr5:68805315 C>T maps to NM_002538.2 D133D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr7:5922244 A>G maps to NM_001097622.1 E61E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A5U7-01A-11D-A31U-09 chr4:71062447 G>T maps to NM_017855.3 E31*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr8:103572964 C>T maps to NM_024410.3 C202C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KH-A6WC-01A-11D-A33E-09 chr9:131260844 G>A maps to NM_153435.1 A786A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NQ-01A-11D-A36J-09 chr9:131260854 G>T did not map to a codon.
Sequencing variant TCGA-IG-A4QT-01A-21D-A27G-09 chr1:86842068 C>T maps to ENST00000370567 L219L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NQ-01A-11D-A36J-09 chr1:86820362 C>T maps to ENST00000370567 Q510Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49V-01A-11D-A247-09 chr15:76019671 C>T maps to NM_175881.3 R206*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA4D-01A-11D-A37C-09 chr19:464038 C>A maps to NM_182577.2 L225L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RE-01A-11D-A33E-09 chr23:123657382 C>G did not map to a codon.
Sequencing variant TCGA-IG-A4QS-01A-11D-A27G-09 chr23:123519780 C>T did not map to a codon.
Sequencing variant TCGA-IG-A8O2-01A-11D-A36J-09 chr23:123680762 C>T did not map to a codon.
Sequencing variant TCGA-L5-A4OE-01A-11D-A27G-09 chr23:123838997 G>T did not map to a codon.
Sequencing variant TCGA-L5-A4OG-01A-11D-A27G-09 chr23:123779097 C>T did not map to a codon.
Sequencing variant TCGA-L5-A4OJ-01A-11D-A27G-09 chr23:123514856 C>A did not map to a codon.
Sequencing variant TCGA-L5-A8NJ-01A-11D-A36J-09 chr23:123654588 T>G did not map to a codon.
Sequencing variant TCGA-L5-A8NL-01A-12D-A37C-09 chr23:123631043 C>T did not map to a codon.
Sequencing variant TCGA-R6-A6Y0-01B-11D-A33E-09 chr23:123838993 A>G did not map to a codon.
Sequencing variant TCGA-V5-AASW-01A-11D-A403-09 chr23:124029837 C>T did not map to a codon.
Sequencing variant TCGA-VR-A8EU-01A-11D-A36J-09 chr23:123870826 G>A did not map to a codon.
Sequencing variant TCGA-2H-A9GG-01A-11D-A37C-09 chr5:166712000 C>T maps to NM_001122679.1 S53S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49U-01A-31D-A27G-09 chr5:167517586 C>T maps to NM_001122679.1 F508F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASV-01A-11D-A387-09 chr5:167420176 G>T maps to NM_001122679.1 A392A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GK-01A-11D-A37C-09 chr4:183267984 G>T maps to NM_001080477.1 G138G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88Z-01A-11D-A36J-09 chr4:183714436 C>A maps to NM_001080477.1 I2204I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr4:183714346 C>T maps to NM_001080477.1 R2174R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NV-01A-11D-A37C-09 chr4:183522242 G>T maps to NM_001080477.1 L226L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6KZ-01A-11D-A31U-09 chr4:183651466 C>T maps to NM_001080477.1 D900D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6XG-01B-11D-A33E-09 chr4:183600931 C>T maps to NM_001080477.1 A480A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RE-A7BO-01A-11D-A33E-09 chr4:183674673 G>T maps to NM_001080477.1 G1312*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr11:78369189 G>A maps to NM_001098816.2 F2741F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OH-01A-11D-A27G-09 chr23:13778544 G>T did not map to a codon.
Sequencing variant TCGA-R6-A6Y0-01B-11D-A33E-09 chr23:13767592 T>G did not map to a codon.
Sequencing variant TCGA-Z6-AAPN-01A-11D-A403-09 chr7:44664044 C>T maps to ENST00000444676 Q35*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GF-01A-11D-A37C-09 chr12:123463397 C>T maps to ENST00000228922 G210G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XP-A8T6-01A-11D-A36J-09 chr12:123461500 G>A maps to ENST00000228922 R129R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASX-01A-11D-A387-09 chr20:61444883 G>A maps to NM_007346.2 S639S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A4QS-01A-11D-A27G-09 chr6:72011415 T>C maps to NM_024576.3 T340T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OJ-01A-11D-A27G-09 chr23:70767755 G>T did not map to a codon.
Sequencing variant TCGA-L7-A56G-01A-21D-A27G-09 chr23:70787358 C>T did not map to a codon.
Sequencing variant TCGA-LN-A4A5-01A-21D-A27G-09 chr23:70783038 G>C did not map to a codon.
Sequencing variant TCGA-V5-A7RC-01B-11D-A403-09 chr23:70775169 G>T did not map to a codon.
Sequencing variant TCGA-LN-A5U5-01A-21D-A28B-09 chr10:15091714 C>A maps to NM_018324.2 G38G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3YA-01A-11D-A247-09 chr1:102270447 A>T maps to ENST00000338858 T261T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OF-01A-11D-A27G-09 chr11:7507132 T>C maps to NM_198474.3 S9S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GL-01A-12D-A37C-09 chr9:127549513 C>T maps to NM_182487.2 L117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr1:161953560 G>T maps to ENST00000451379 S720S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L7-A6VZ-01A-12D-A33E-09 chr1:58946791 G>A maps to NM_145243.3 R474*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HW-01A-22D-A351-09 chr1:59004812 C>A maps to NM_145243.3 G52*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93E-01A-11D-A37C-09 chr9:95177604 T>C maps to NM_005014.2 Q365Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A893-01A-11D-A36J-09 chr9:95179780 G>A maps to NM_005014.2 C20C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GK-01A-11D-A37C-09 chr17:29622573 G>T maps to NM_002544.4 S259*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OE-01A-11D-A27G-09 chr17:29622473 C>T maps to NM_002544.4 L292L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr15:53081748 C>T maps to NM_004498.1 P111P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr18:55103826 C>T maps to NM_004852.2 N293N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q9-A6FU-01A-11D-A31U-09 chr6:74079455 G>A maps to NM_001080507.2 S20S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A4P3-01A-11D-A27G-09 chr3:193335054 G>A maps to NM_130837.2 L179L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GR-01A-12D-A37C-09 chr11:132290137 A>T maps to NM_002545.3 A329A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NL-01A-12D-A37C-09 chr23:67273603 G>T did not map to a codon.
Sequencing variant TCGA-Z6-AAPN-01A-11D-A403-09 chr8:145113707 G>A maps to ENST00000360660 R185R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GF-01A-11D-A37C-09 chr23:153421839 G>A did not map to a codon.
Sequencing variant TCGA-Z6-A8JD-01A-11D-A36J-09 chr23:153420168 T>G did not map to a codon.
Sequencing variant TCGA-X8-AAAR-01A-11D-A403-09 chr7:128414668 G>T maps to NM_001708.2 T190T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XP-A8T6-01A-11D-A36J-09 chr6:47779442 T>C maps to ENST00000489301 S344S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OT-01A-11D-A28B-09 chr8:54147610 A>C maps to NM_000912.3 A106A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8W5-01B-11D-A37C-09 chr20:62729950 C>T maps to NM_000913.3 C304C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6F8-01A-11D-A33E-09 chr6:154431488 G>T did not map to a codon.
Sequencing variant TCGA-R6-A6KZ-01A-11D-A31U-09 chr1:203472137 G>A did not map to a codon.
Sequencing variant TCGA-LN-A49L-01A-11D-A247-09 chr10:13151283 G>A maps to NM_021980.4 L54L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FH-01A-11D-A33E-09 chr11:6891758 G>A maps to NM_001004460.1 K258K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASW-01A-11D-A403-09 chr11:6891831 G>T maps to NM_001004460.1 E283*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA7B-01A-31D-A403-09 chr11:6891243 C>T maps to NM_001004460.1 Q87*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6KZ-01A-11D-A31U-09 chr11:6867410 T>C maps to ENST00000379831 S170S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49K-01A-11D-A247-09 chr11:7949462 G>C maps to NM_001004461.1 T249T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr12:55615173 C>T maps to NM_001005280.1 R122R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A4QS-01A-11D-A27G-09 chr11:123886647 T>C maps to NM_001004462.1 L123L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FP-01A-31D-A387-09 chr11:123887126 C>G maps to NM_001004462.1 L282L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A4-01A-11D-A27G-09 chr11:123900745 G>T maps to ENST00000375021 S139S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8WG-01A-11D-A37C-09 chr11:123900724 C>T maps to ENST00000375021 T132T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OW-01A-11D-A28B-09 chr11:123894159 T>G maps to NM_001001953.1 T147T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OP-01A-11D-A27G-09 chr19:15852243 C>T maps to NM_013938.1 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EX-01A-11D-A36J-09 chr19:15904866 G>A maps to NM_001004466.1 G3G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr1:159410054 G>A maps to NM_012351.2 T169T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A893-01A-11D-A36J-09 chr1:159409958 C>A maps to NM_012351.2 I137I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASW-01A-11D-A403-09 chr1:159505478 A>G maps to NM_001004469.1 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA4D-01A-11D-A37C-09 chr1:158435969 T>C maps to NM_001004473.1 L207L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OR-01A-11D-A27G-09 chr1:158390305 G>A maps to NM_001004476.1 V117V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASX-01A-11D-A387-09 chr1:158390341 G>A maps to NM_001004476.1 L105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A891-01A-11D-A36J-09 chr12:56030743 G>A maps to NM_206899.1 L23L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3YA-01A-11D-A247-09 chr11:57995723 G>A maps to NM_001004471.2 S208S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NG-01A-11D-A37C-09 chr11:57995921 G>A maps to NM_001004471.2 R142R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HX-01A-11D-A33E-09 chr1:158449926 C>A maps to NM_001004472.1 S87*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GH-01A-11D-A37C-09 chr1:158549446 T>G maps to NM_001004477.1 A81A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr1:158549365 A>G maps to NM_001004477.1 I108I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HV-01A-21D-A351-09 chr1:158549593 G>C maps to NM_001004477.1 G32G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FA-01A-11D-A33E-09 chr1:158576362 T>A maps to NM_001004478.1 I45I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43H-01A-11D-A247-09 chr1:158577070 G>A maps to NM_001004478.1 V281V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49K-01A-11D-A247-09 chr1:158576617 C>A maps to NM_001004478.1 L130L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASX-01A-11D-A387-09 chr1:158576410 C>A maps to NM_001004478.1 L61L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49R-01A-11D-A247-09 chr6:29394521 A>G maps to NM_013937.2 H299H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GI-01A-11D-A37C-09 chr14:19378217 A>T maps to NM_001013354.1 R209*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-A7RE-01A-11D-A351-09 chr14:20711240 C>G maps to NM_001004479.1 S97S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A6QS-01A-12D-A33E-09 chr1:248004324 A>G maps to NM_001001959.1 L292L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OM-01A-11D-A27G-09 chr1:248005146 G>A maps to NM_001001959.1 Q18*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XP-A8T7-01A-11D-A36J-09 chr1:248004652 C>A maps to NM_001001959.1 P182P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EZ-01A-11D-A36J-09 chr6:29364589 T>A maps to NM_013936.3 T38T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A8JE-01A-11D-A37C-09 chr9:107367330 G>C maps to NM_001004481.1 S193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HW-01A-22D-A351-09 chr9:107298338 G>C maps to NM_001001961.1 L252L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NR-01A-11D-A37C-09 chr9:107331999 C>T maps to NM_001004483.1 I184I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GF-01A-11D-A37C-09 chr9:107379981 G>A maps to NM_001001956.1 F168F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A5B8-01A-11D-A28B-09 chr9:107379582 C>T maps to NM_001001956.1 K301K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NE-01A-11D-A37C-09 chr9:107456707 C>T maps to NM_001004484.1 Y2Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A4P3-01A-11D-A27G-09 chr23:130678782 G>A did not map to a codon.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr23:130678938 C>T did not map to a codon.
Sequencing variant TCGA-LN-A4A9-01A-11D-A28B-09 chr1:248512819 C>T maps to NM_001001918.1 V248V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q9-A6FW-01A-31D-A31U-09 chr17:3119720 C>T maps to NM_014565.2 D269D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A8JD-01A-11D-A36J-09 chr1:247921357 C>G maps to NM_012353.2 V117V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZR-A9CJ-01B-11D-A387-09 chr1:247921594 G>T maps to NM_012353.2 T38T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GG-01A-11D-A37C-09 chr17:2995687 G>A maps to NM_002548.2 A201A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GG-01A-11D-A37C-09 chr17:3030710 G>A maps to ENST00000381953 I83I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OE-01A-11D-A27G-09 chr17:3030173 G>T maps to ENST00000381953 T262T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S8-A6BV-01A-21D-A31U-09 chr19:15198106 C>T maps to NM_001004713.1 T77T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GR-01A-12D-A37C-09 chr9:125273130 C>T maps to ENST00000444856 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49U-01A-31D-A27G-09 chr9:125512920 C>T maps to ENST00000373684 S301S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6Y2-01B-11D-A33E-09 chr9:125289382 G>A maps to ENST00000359439 L65L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GN-01A-11D-A37C-09 chr7:144015711 G>T maps to NM_001005287.1 L165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8W5-01B-11D-A37C-09 chr7:143793131 G>A maps to NM_001004135.1 *311*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A893-01A-11D-A36J-09 chr7:143826276 T>C maps to NM_001001659.1 I24I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr7:143826930 C>T maps to NM_001001659.1 S242S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HV-01A-21D-A351-09 chr7:143747991 G>T maps to NM_012365.1 L166L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OM-01A-11D-A27G-09 chr11:6789645 G>A maps to NM_001004490.1 I181I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88S-01A-11D-A36J-09 chr11:6790089 G>T maps to NM_001004490.1 I33I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HW-01A-22D-A351-09 chr11:74800002 G>T maps to NM_001005285.1 V252V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8WC-01A-11D-A37C-09 chr1:247695138 G>A maps to NM_198074.4 A225A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GL-01A-12D-A37C-09 chr7:143657083 T>C maps to NM_012369.2 T7T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6KZ-01A-11D-A31U-09 chr7:143657734 C>T maps to NM_012369.2 T224T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FA-01A-11D-A33E-09 chr7:143633227 G>A maps to NM_001004685.1 W301*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q9-A6FU-01A-11D-A31U-09 chr1:247752346 T>A maps to NM_001001915.1 L229*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EU-01A-11D-A36J-09 chr1:247752159 C>T maps to NM_001001915.1 L167L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA4G-01A-11D-A37C-09 chr1:248685671 C>A maps to NM_001013355.1 S242*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FP-01A-31D-A387-09 chr1:248201851 G>T maps to NM_001004686.2 G95*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8W5-01B-11D-A37C-09 chr1:248201859 G>A maps to NM_001004686.2 G97G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr1:248224642 T>C maps to NM_001004687.1 V220V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FP-01A-31D-A387-09 chr1:248224699 C>A maps to NM_001004687.1 T239T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6DN-01B-11D-A31U-09 chr1:248224766 A>C maps to NM_001004687.1 R262R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OT-01A-11D-A28B-09 chr1:248112219 A>C maps to NM_001001963.1 R21R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EW-01A-11D-A36J-09 chr1:248112320 C>A maps to NM_001001963.1 L54L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr1:248343302 C>T maps to NM_001004688.1 Q6*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49X-01A-31D-A27G-09 chr1:248343796 G>T maps to NM_001004688.1 G170G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A8JD-01A-11D-A36J-09 chr1:248344135 C>T maps to NM_001004688.1 P283P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EY-01A-11D-A36J-09 chr1:248367306 G>C maps to NM_001004689.1 *313S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NG-01A-11D-A37C-09 chr1:248308865 A>G maps to NM_001004690.1 K139K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A5U7-01A-11D-A31U-09 chr1:248487276 A>G maps to NM_001004691.1 V198V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NN-01A-11D-A37C-09 chr9:35957426 G>T maps to NM_019897.2 I223I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A4QS-01A-11D-A27G-09 chr1:248756468 A>G maps to NM_001004693.1 L201L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93F-01A-21D-A37C-09 chr1:248790144 G>T maps to NM_001001964.1 G95G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OF-01A-11D-A27G-09 chr1:248790423 C>T maps to NM_001001964.1 T2T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GR-01A-12D-A37C-09 chr1:248457938 A>G maps to NM_001004692.1 N314N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L7-A56G-01A-21D-A27G-09 chr1:248457986 G>T maps to NM_001004692.1 A298A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NN-01A-11D-A37C-09 chr1:248616763 C>T maps to NM_001004136.1 I222I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49Y-01A-11D-A27G-09 chr1:248617051 G>T maps to NM_001004136.1 A318A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8WC-01A-11D-A37C-09 chr1:248436537 G>A maps to NM_001004695.1 F193F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93D-01A-11D-A387-09 chr1:248551762 T>G maps to NM_001005471.1 L285*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49X-01A-31D-A27G-09 chr1:248551358 C>T maps to NM_001005471.1 F150F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8WC-01A-11D-A37C-09 chr1:248084897 C>T maps to NM_001005522.1 F193F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RE-A7BO-01A-11D-A33E-09 chr6:29012867 C>A maps to NM_030903.3 G29*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A8-01A-32D-A27G-09 chr1:247655130 G>T maps to NM_001004698.2 A234A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49P-01A-11D-A247-09 chr17:3182034 G>A maps to NM_002551.3 H65H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-AAPN-01A-11D-A403-09 chr17:3324820 G>A maps to NM_012373.2 L320L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GL-01A-12D-A37C-09 chr11:55136270 T>G maps to NM_001005275.1 T304T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FP-01A-31D-A387-09 chr11:55135604 C>A maps to NM_001005275.1 S82S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q9-A6FU-01A-11D-A31U-09 chr11:55135646 C>T maps to NM_001005275.1 F96F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43C-01A-11D-A247-09 chr11:55110723 T>A maps to NM_001005274.1 T16T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A2-01A-31D-A27G-09 chr11:55110882 C>A maps to NM_001005274.1 A69A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HX-01A-11D-A33E-09 chr11:55111056 G>T maps to NM_001005274.1 P127P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NS-01A-12D-A37C-09 chr11:48511186 C>T maps to NM_001005512.2 N281N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GR-01A-12D-A37C-09 chr11:51411645 G>T maps to NM_001005272.3 P250P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88Z-01A-11D-A36J-09 chr11:51412173 G>A maps to NM_001005272.3 T74T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A4QS-01A-11D-A27G-09 chr11:55371555 T>C maps to NM_001004700.1 Q98Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A8O2-01A-11D-A36J-09 chr11:55371597 G>A maps to NM_001004700.1 L84L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GR-01A-12D-A37C-09 chr11:50003725 A>T maps to NM_001005270.2 I104I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NL-01A-12D-A37C-09 chr11:50003815 A>G maps to NM_001005270.2 S74S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EQ-01A-11D-A36J-09 chr11:50003188 C>A maps to NM_001005270.2 V283V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A5U7-01A-11D-A31U-09 chr11:55322498 G>A maps to NM_001001920.1 E239E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FP-01A-31D-A387-09 chr11:55322144 C>T maps to NM_001001920.1 F121F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RE-A7BO-01A-11D-A33E-09 chr11:55322516 T>C maps to NM_001001920.1 T245T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49L-01A-11D-A247-09 chr11:55339984 C>T maps to NM_001004701.2 L128L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GI-01A-11D-A37C-09 chr11:48346845 T>C maps to NM_001004702.1 S118S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NH-01A-11D-A37C-09 chr11:48346873 G>T maps to NM_001004702.1 G128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-AAPN-01A-11D-A403-09 chr11:48346986 C>G maps to NM_001004702.1 L165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A4QS-01A-11D-A27G-09 chr11:51515370 T>C maps to NM_001004703.1 F30F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93D-01A-11D-A387-09 chr11:55433079 T>C maps to NM_001004704.1 A146A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49M-01A-21D-A27G-09 chr11:55432917 C>T maps to NM_001004704.1 L92L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FP-01A-31D-A387-09 chr11:55432965 G>C maps to NM_001004704.1 V108V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A8O2-01A-11D-A36J-09 chr11:59245408 C>T maps to NM_001004705.1 C169C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HV-01A-21D-A351-09 chr11:59245627 C>T maps to NM_001004705.1 S242S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr11:123810340 T>C maps to NM_001001965.1 H6H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RE-01A-11D-A33E-09 chr11:59224555 A>G maps to NM_001004708.1 G41G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q9-A6FU-01A-11D-A31U-09 chr11:59224783 G>A maps to NM_001004708.1 V117V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GO-01A-11D-A37C-09 chr15:102359249 C>G maps to NM_001001674.1 Y287*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GH-01A-11D-A37C-09 chr14:20404046 T>C maps to NM_001004063.2 S74S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49M-01A-21D-A27G-09 chr14:20404052 T>C maps to NM_001004063.2 F76F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49U-01A-31D-A27G-09 chr14:20404130 C>T maps to NM_001004063.2 F102F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A4-01A-11D-A27G-09 chr14:20404270 G>A maps to NM_001004063.2 W149*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49W-01A-11D-A27G-09 chr14:20502223 G>A maps to NM_001004714.1 R232*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A2-01A-31D-A27G-09 chr14:20482509 T>C maps to NM_001004712.1 P281P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S8-A6BW-01A-11D-A31U-09 chr14:20345269 C>T maps to NM_001005501.1 L282L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A5U7-01A-11D-A31U-09 chr15:22368838 G>A maps to NM_001004719.2 E88E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49M-01A-21D-A27G-09 chr14:20295897 C>T maps to NM_001004723.1 C97C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA7D-01A-11D-A403-09 chr14:20296518 G>A maps to NM_001004723.1 K304K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L7-A6VZ-01A-12D-A33E-09 chr15:22383119 T>G maps to NM_001005241.1 A216A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6DQ-01B-11D-A31U-09 chr14:20611971 G>T maps to NM_001004724.1 L26L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88V-01A-11D-A351-09 chr11:55406280 G>T maps to NM_001004124.1 G150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NN-01A-11D-A37C-09 chr11:55406657 C>A maps to NM_001004124.1 I275I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OE-01A-11D-A27G-09 chr14:20216179 G>T maps to NM_172194.1 V198V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49N-01A-11D-A247-09 chr14:20215876 A>G maps to NM_172194.1 G97G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASX-01A-11D-A387-09 chr14:20216086 G>T maps to NM_172194.1 L167L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93F-01A-21D-A37C-09 chr11:48328640 C>T maps to NM_001004725.1 N289N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GI-01A-11D-A37C-09 chr11:55418426 T>C maps to NM_001004059.2 S16S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZR-A9CJ-01B-11D-A387-09 chr11:55419137 T>A maps to NM_001004059.2 T253T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NW-01A-11D-A37C-09 chr11:48286287 G>T maps to NM_001004726.1 V292V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr11:48267011 C>T maps to NM_001004727.1 C119C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XP-A8T6-01A-11D-A36J-09 chr11:4967978 G>A maps to NM_001005329.1 L118L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OT-01A-11D-A28B-09 chr11:4929262 A>T maps to NM_001004749.1 K222*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NJ-01A-11D-A36J-09 chr11:5345082 T>G maps to NM_033180.4 R149R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-A7RE-01A-11D-A351-09 chr11:5322504 G>A maps to NM_033179.2 G224G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NH-01A-11D-A37C-09 chr11:4673818 T>A maps to NM_152430.3 P21P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA4G-01A-11D-A37C-09 chr11:4703782 G>A maps to NM_030774.3 S53S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L7-A6VZ-01A-12D-A33E-09 chr11:4842956 G>A maps to NM_001004753.1 Q114Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr11:4944873 G>A maps to NM_001005237.1 S232S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NS-01A-12D-A37C-09 chr11:4945467 G>A maps to NM_001005237.1 C34C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6Y0-01B-11D-A33E-09 chr11:4944885 G>A maps to NM_001005237.1 L228L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EY-01A-11D-A36J-09 chr11:4944690 G>T maps to NM_001005237.1 I293I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr11:4936758 C>T maps to NM_001005238.1 P45P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49V-01A-11D-A247-09 chr11:4936275 A>G maps to NM_001005238.1 F206F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OT-01A-11D-A28B-09 chr11:5461802 G>C maps to NM_001005288.2 A314A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EZ-01A-11D-A36J-09 chr11:5475293 C>T maps to NM_001004754.2 I192I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASX-01A-11D-A387-09 chr11:5443870 G>A maps to NM_001004757.2 G147G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OS-01A-11D-A28B-09 chr11:4869958 G>T maps to NM_001004758.1 C160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr11:4870354 T>C maps to NM_001004758.1 L28L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OR-01A-11D-A27G-09 chr11:4904055 C>A maps to NM_001004759.1 L336L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GM-01A-11D-A37C-09 chr11:5173188 G>T maps to NM_012375.2 I137I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr11:5173097 G>T maps to NM_012375.2 R168R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A891-01A-11D-A36J-09 chr11:5142748 C>G maps to NM_001005222.2 G20G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A8I0-01A-11D-A36J-09 chr11:5142487 G>A maps to NM_001005222.2 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6Y0-01B-11D-A33E-09 chr11:5142535 G>A maps to NM_001005222.2 F91F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6XG-01B-11D-A33E-09 chr11:5153445 A>G maps to NM_001005160.2 L143L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr11:5603089 A>G maps to NM_001005162.2 S328S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OE-01A-11D-A27G-09 chr11:5510670 C>A maps to NM_001005163.2 G245G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6Y0-01B-11D-A33E-09 chr11:5080749 C>T maps to NM_001005164.2 V36V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-A7RB-01A-11D-A351-09 chr11:5862452 A>G maps to ENST00000379946 A229A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RF-01A-13D-A33E-09 chr11:5878581 C>T maps to NM_001005168.1 E117E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A97I-01A-11D-A387-09 chr11:5878457 G>A maps to NM_001005168.1 L159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88V-01A-11D-A351-09 chr11:5878911 C>T maps to NM_001005168.1 T7T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A4QS-01A-11D-A27G-09 chr11:5565850 T>C maps to NM_001005289.1 G301G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NL-01A-12D-A37C-09 chr11:4608197 T>G maps to NM_001005170.2 S52S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GR-01A-12D-A37C-09 chr11:4510951 C>A maps to NM_001005171.2 V274V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OR-01A-11D-A27G-09 chr11:4470964 G>T maps to NM_001005172.2 L132L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASW-01A-11D-A403-09 chr11:6007248 C>T maps to NM_001005173.2 A304A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8W8-01B-11D-A37C-09 chr11:5809668 C>T maps to NM_001001913.1 V126V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr11:5776884 T>C maps to NM_001005175.2 C305C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A5B8-01A-11D-A28B-09 chr11:6048625 G>T maps to NM_001001917.2 A103A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-A7RE-01A-11D-A351-09 chr11:6048775 C>A maps to NM_001001917.2 L53L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NN-01A-11D-A37C-09 chr11:5969254 C>T maps to NM_001003443.2 R227*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NQ-01A-11D-A36J-09 chr11:5969262 G>C maps to NM_001003443.2 V229V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S8-A6BV-01A-21D-A31U-09 chr11:5758474 A>T maps to NM_001005180.2 A243A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASV-01A-11D-A387-09 chr11:59189982 G>T maps to NM_001001954.1 G148G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3Y9-01A-12D-A247-09 chr11:56756447 G>A maps to NM_001005323.1 Q20Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OS-01A-11D-A28B-09 chr11:59132149 C>A maps to NM_001004729.1 C73*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA4G-01A-11D-A37C-09 chr11:56409726 G>C maps to NM_001002925.1 T63T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OE-01A-11D-A27G-09 chr11:56431988 G>T maps to NM_001004730.1 V276V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr11:56431958 C>T maps to NM_001004730.1 Y266Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NK-01A-21D-A37C-09 chr14:21623200 G>T maps to NM_001004731.1 I328I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr11:58207225 G>T maps to NM_001004733.2 T133T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OU-01A-11D-A28B-09 chr11:58207474 G>A maps to NM_001004733.2 D50D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88Z-01A-11D-A36J-09 chr11:58190659 G>A maps to NM_001005566.2 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HY-01A-12D-A351-09 chr11:58170144 G>A maps to NM_001005469.1 V246V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FP-01A-31D-A387-09 chr11:55541209 C>A maps to NM_001001967.1 C99*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A4QS-01A-11D-A27G-09 chr11:55563201 T>C maps to NM_001004735.1 F57F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NW-01A-11D-A37C-09 chr11:55563642 C>T maps to NM_001004735.1 F204F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OW-01A-11D-A28B-09 chr11:55587683 T>G maps to ENST00000395203 T195T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A8-01A-32D-A27G-09 chr3:97888441 C>G maps to NM_001005515.1 S300*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EX-01A-11D-A36J-09 chr3:98002651 A>G maps to NM_001005482.1 T307T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3QL-01A-11D-A247-09 chr3:97983601 T>C maps to NM_001005479.1 I158I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A625-01A-11D-A31U-09 chr3:97983601 T>C maps to NM_001005479.1 I158I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A5-01A-21D-A27G-09 chr3:97983601 T>C maps to NM_001005479.1 I158I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-AAPN-01A-11D-A403-09 chr11:55703531 G>A maps to NM_006637.1 F115F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OE-01A-11D-A27G-09 chr11:55944156 G>T maps to NM_001005492.1 E22*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OW-01A-11D-A28B-09 chr3:98110009 T>C maps to NM_001005516.1 T167T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GM-01A-11D-A37C-09 chr3:98072885 G>T maps to NM_001005517.1 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HY-01A-12D-A351-09 chr3:98073473 T>C maps to NM_001005517.1 I259I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GR-01A-12D-A37C-09 chr11:55579376 T>G maps to NM_001004738.1 A145A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A4QT-01A-21D-A27G-09 chr11:55579775 C>T maps to NM_001004738.1 Y278Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OT-01A-11D-A28B-09 chr11:55579352 T>G maps to NM_001004738.1 S137S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3I8-01A-11D-A247-09 chr11:55595410 C>A maps to NM_001004739.1 S239S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88V-01A-11D-A351-09 chr11:55595134 C>A maps to NM_001004739.1 C147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6L4-01A-11D-A31U-09 chr11:56310160 A>C maps to NM_001005245.1 T191T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HX-01A-11D-A33E-09 chr11:56230676 C>T maps to NM_001004743.1 A67A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3I8-01A-11D-A247-09 chr11:56185375 C>T maps to NM_001004744.1 E111E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A8I0-01A-11D-A36J-09 chr11:56185549 A>C maps to NM_001004744.1 T53T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NE-01A-11D-A37C-09 chr11:56043854 A>G maps to NM_001004745.1 R247R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NH-01A-11D-A37C-09 chr11:56043713 T>C maps to NM_001004745.1 S200S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA7D-01A-11D-A403-09 chr11:56043398 C>A maps to NM_001004745.1 V95V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GI-01A-11D-A37C-09 chr11:55999980 A>G maps to NM_001004746.1 S227S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RE-01A-11D-A33E-09 chr11:56000496 G>T maps to NM_001004746.1 G55G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OT-01A-11D-A28B-09 chr11:55999980 A>C maps to NM_001004746.1 S227S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OW-01A-11D-A28B-09 chr11:55999980 A>G maps to NM_001004746.1 S227S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49Y-01A-11D-A27G-09 chr11:56000130 G>C maps to NM_001004746.1 P177P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XP-A8T6-01A-11D-A36J-09 chr11:56000004 A>G maps to NM_001004746.1 D219D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GI-01A-11D-A37C-09 chr11:56020013 C>A maps to NM_001004747.1 V113V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49U-01A-31D-A27G-09 chr11:56020397 C>A maps to NM_001004747.1 I241I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q9-A6FU-01A-11D-A31U-09 chr6:29323468 G>A maps to NM_030876.5 F168F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A4P3-01A-11D-A27G-09 chr11:55681209 G>T maps to NM_001001960.1 P283P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93C-01A-11D-A387-09 chr11:6816471 T>C maps to NM_003696.2 G156G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93F-01A-21D-A37C-09 chr11:6816276 G>T maps to NM_003696.2 A221A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S8-A6BV-01A-21D-A31U-09 chr11:6815961 A>G maps to NM_003696.2 N326N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RE-A7BO-01A-11D-A33E-09 chr7:143701313 T>C maps to NM_001005281.1 S75S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EU-01A-11D-A36J-09 chr2:240969561 G>A maps to NM_001005853.1 V95V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A5U5-01A-21D-A28B-09 chr12:55846701 C>T maps to NM_054105.1 A235A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88W-01A-11D-A351-09 chr12:55794947 G>T maps to NM_001005518.1 V212V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr12:55863763 G>T maps to NM_001005499.1 L53L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr12:55820520 C>T maps to NM_001005183.1 Q162*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A893-01A-11D-A36J-09 chr1:247875721 G>T maps to NM_001005286.1 Y112*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OS-01A-11D-A28B-09 chr1:158687130 A>G maps to ENST00000368146 L275L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A8HZ-01A-11D-A36J-09 chr1:158724853 G>A maps to NM_001005184.1 L83L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93D-01A-11D-A387-09 chr11:123676266 G>T maps to NM_001005325.1 S264*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OJ-01A-11D-A27G-09 chr1:158735896 C>T maps to NM_001005185.1 T192T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43C-01A-11D-A247-09 chr1:158746861 G>T maps to NM_001005278.1 A188A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA7D-01A-11D-A403-09 chr14:21109502 C>T maps to NM_001001968.1 L116L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NE-01A-11D-A37C-09 chr11:123813641 T>A maps to NM_001005187.1 R302*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49Y-01A-11D-A27G-09 chr11:123814163 G>A maps to NM_001005187.1 R128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr11:123624443 T>G maps to NM_001005188.1 T261T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr19:14991540 A>G maps to NM_030901.1 G209G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr19:9296597 G>T maps to NM_175883.2 L47L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A97I-01A-11D-A387-09 chr19:9361751 C>T maps to NM_001079935.1 F11F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49O-01A-11D-A247-09 chr11:124440068 G>T maps to NM_001005194.1 T35T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A4-01A-11D-A27G-09 chr11:124413293 G>C maps to NM_001005195.1 S86*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NF-01A-11D-A37C-09 chr11:124252549 G>T maps to NM_001005468.1 S230S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A97H-01A-11D-A387-09 chr11:124266926 A>G maps to NM_001005467.1 F107F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A5-01A-21D-A27G-09 chr11:124266926 A>G maps to NM_001005467.1 F107F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HY-01A-12D-A351-09 chr11:124294377 G>T maps to NM_001005196.1 L130L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-A7RE-01A-11D-A351-09 chr11:124294640 A>G maps to NM_001005196.1 L43L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L7-A6VZ-01A-12D-A33E-09 chr11:124180005 G>T maps to NM_001002917.1 A219A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NE-01A-11D-A37C-09 chr11:124189724 A>T maps to NM_001002918.1 Y123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FP-01A-31D-A387-09 chr11:124190033 G>T maps to NM_001002918.1 R20R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93D-01A-11D-A387-09 chr11:56058493 C>T maps to NM_001005199.1 T15T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L7-A6VZ-01A-12D-A33E-09 chr11:56057869 G>T maps to NM_001005199.1 T223T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A6-01A-11D-A27G-09 chr11:56058415 G>T maps to NM_001005199.1 G41G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A8I0-01A-11D-A36J-09 chr11:56058079 G>A maps to NM_001005199.1 I153I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A4P3-01A-11D-A27G-09 chr11:55890769 A>C maps to NM_001005201.1 R308R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43I-01A-11D-A247-09 chr11:55890576 T>A maps to NM_001005201.1 S243S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OX-01A-21D-A28B-09 chr11:55890582 C>T maps to NM_001005201.1 L245L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49O-01A-11D-A247-09 chr11:55890162 C>G maps to NM_001005201.1 V105V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FH-01A-11D-A33E-09 chr11:56128222 T>G maps to NM_001005205.1 S167S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A891-01A-11D-A36J-09 chr11:56086211 C>T maps to NM_001005202.1 L144L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-AAPN-01A-11D-A403-09 chr11:56086441 C>T maps to NM_001005202.1 L220L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FP-01A-31D-A387-09 chr12:48919788 C>G maps to NM_001005203.2 A125A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A5U7-01A-11D-A31U-09 chr7:141619454 G>A maps to NM_001001656.1 V260V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr16:30965123 G>T maps to NM_152288.2 E283*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GJ-01A-11D-A37C-09 chr6:88372777 T>C maps to NM_181837.2 A584A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NV-01A-11D-A37C-09 chr6:88313146 G>T maps to NM_181837.2 E75*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6XG-01B-11D-A33E-09 chr17:38080378 G>A maps to NM_139280.2 Y26Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr12:58112062 G>A maps to NM_006812.3 E423E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OH-01A-11D-A27G-09 chr18:21761132 G>T maps to NM_080597.2 L596L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr18:21761132 G>T maps to NM_080597.2 L596L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-A7RC-01B-11D-A403-09 chr20:60868921 C>A maps to NM_144498.1 S474S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr7:24932010 C>T maps to NM_015550.2 K27K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr2:179201134 G>A maps to ENST00000392505 S255S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FR-01A-11D-A387-09 chr2:179257142 C>T maps to ENST00000392505 S842S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr17:45885766 T>G did not map to a codon.
Sequencing variant TCGA-2H-A9GF-01A-11D-A37C-09 chr12:76786437 G>A maps to NM_020841.4 S284S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RF-01A-13D-A33E-09 chr12:76881289 C>T maps to NM_020841.4 S14S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-A7RB-01A-11D-A351-09 chr12:76786524 G>A maps to NM_020841.4 C255C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr19:54600284 G>T maps to NM_130771.3 S83S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NS-01A-12D-A37C-09 chr16:83999149 G>T maps to NM_013370.3 L407L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A5B8-01A-11D-A28B-09 chr8:99963844 C>T maps to ENST00000457907 S406S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KH-A6WC-01A-11D-A33E-09 chr8:99962899 G>T maps to ENST00000457907 E346*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FQ-01A-31D-A387-09 chr8:99961212 G>T maps to ENST00000457907 P132P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA4D-01A-11D-A37C-09 chr23:38268007 A>T did not map to a codon.
Sequencing variant TCGA-IG-A51D-01A-11D-A27G-09 chr16:21726331 G>A maps to ENST00000286149 Q463Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GN-01A-11D-A37C-09 chr2:26703131 C>T maps to NM_194248.2 L617L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A4P3-01A-11D-A27G-09 chr2:26703077 G>T maps to NM_194248.2 V635V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr2:26684618 C>T maps to NM_194248.2 A1826A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr2:26741943 C>T maps to NM_194248.2 K87K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OO-01A-11D-A27G-09 chr2:26700313 C>T maps to NM_194248.2 R792R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88T-01A-11D-A351-09 chr2:26725256 A>G maps to NM_194248.2 H207H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr2:26741970 G>A maps to NM_194248.2 I78I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-A7RB-01A-11D-A351-09 chr17:72943296 C>T maps to NM_178233.1 L449L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GK-01A-11D-A37C-09 chr20:16730645 T>C maps to NM_020157.2 V118V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3Y9-01A-12D-A247-09 chr5:76932723 G>A maps to NM_032109.2 F123F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NH-01A-11D-A37C-09 chr11:63764924 C>T maps to ENST00000422031 G278G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NV-01A-11D-A37C-09 chr14:94503805 C>A maps to NM_023112.3 Y28*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr23:48814241 C>T did not map to a codon.
Sequencing variant TCGA-L5-A4OJ-01A-11D-A27G-09 chr23:69283088 G>T did not map to a codon.
Sequencing variant TCGA-2H-A9GM-01A-11D-A37C-09 chr8:92090639 T>C maps to NM_016023.3 I154I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3I8-01A-11D-A247-09 chr8:92097034 T>G maps to NM_016023.3 L304*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43E-01A-11D-A247-09 chr8:92082603 C>T maps to NM_016023.3 L28L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q9-A6FU-01A-11D-A31U-09 chr8:92086057 G>C did not map to a codon.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr15:31776543 C>A maps to ENST00000382902 S585S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NK-01A-21D-A37C-09 chr1:149922095 C>A maps to NM_020205.2 E292*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NR-01A-11D-A37C-09 chr1:149915979 G>A maps to NM_020205.2 R770*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6F8-01A-11D-A33E-09 chr14:57270952 G>A maps to NM_021728.2 R76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A8HZ-01A-11D-A36J-09 chr17:1946157 G>T maps to NM_080822.2 V148V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA4G-01A-11D-A37C-09 chr12:29627997 G>T maps to NM_183378.2 P532P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA7D-01A-11D-A403-09 chr12:29626013 T>C maps to NM_183378.2 P541P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OE-01A-11D-A27G-09 chr11:7718029 A>G maps to NM_198185.2 L375L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A6-01A-11D-A27G-09 chr1:111968030 G>A maps to ENST00000369728 I161I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S8-A6BW-01A-11D-A31U-09 chr1:111957457 C>T maps to ENST00000369728 E619E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XP-A8T7-01A-11D-A36J-09 chr20:18005450 G>A maps to NM_021220.2 C219C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3Y9-01A-12D-A247-09 chr14:23235861 T>C maps to NM_005015.3 G44G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FP-01A-31D-A387-09 chr1:40236195 C>T maps to NM_022120.1 E244E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-AAPN-01A-11D-A403-09 chr1:40236868 G>C maps to NM_022120.1 S20*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A97H-01A-11D-A387-09 chr2:42991001 G>A maps to NM_148962.4 G106G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43I-01A-11D-A247-09 chr13:97639709 C>A maps to NM_080818.3 G102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASX-01A-11D-A387-09 chr13:97639173 G>A maps to NM_080818.3 I280I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OE-01A-11D-A27G-09 chr8:107718694 C>A maps to NM_001198533.1 R316R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr17:3808603 G>A maps to NM_002558.2 V65V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6XG-01B-11D-A33E-09 chr17:3807316 G>T maps to NM_002558.2 G143G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A893-01A-11D-A36J-09 chr17:3592830 G>A maps to ENST00000435558 S236S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GI-01A-11D-A37C-09 chr3:152553639 G>A maps to NM_002563.2 S23S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RE-01A-11D-A33E-09 chr3:152554204 C>T maps to NM_002563.2 R212*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OP-01A-11D-A27G-09 chr23:78216862 C>T did not map to a codon.
Sequencing variant TCGA-LN-A7HY-01A-12D-A351-09 chr23:78216848 C>T did not map to a codon.
Sequencing variant TCGA-RE-A7BO-01A-11D-A33E-09 chr23:78216927 T>A did not map to a codon.
Sequencing variant TCGA-Z6-A8JD-01A-11D-A36J-09 chr23:78216382 T>A did not map to a codon.
Sequencing variant TCGA-Q9-A6FU-01A-11D-A31U-09 chr3:151056000 G>C maps to NM_022788.3 L211L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr11:72946283 G>A maps to NM_176071.1 R360R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3Y9-01A-12D-A247-09 chr23:69478522 G>A did not map to a codon.
Sequencing variant TCGA-L5-A8NG-01A-11D-A37C-09 chr23:1584750 C>T did not map to a codon.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr23:1584893 G>A did not map to a codon.
Sequencing variant TCGA-IG-A4P3-01A-11D-A27G-09 chr8:101719225 C>G did not map to a codon.
Sequencing variant TCGA-JY-A93C-01A-11D-A387-09 chr13:25670410 G>A maps to NM_030979.2 A25A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr13:25671274 G>A maps to NM_030979.2 A313A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EZ-01A-11D-A36J-09 chr13:25671805 T>A maps to NM_030979.2 A490A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A97H-01A-11D-A387-09 chr23:90691326 G>A did not map to a codon.
Sequencing variant TCGA-L5-A4OR-01A-11D-A27G-09 chr23:90690648 T>G did not map to a codon.
Sequencing variant TCGA-L5-A8NR-01A-11D-A37C-09 chr23:90690712 T>G did not map to a codon.
Sequencing variant TCGA-L5-A8NS-01A-12D-A37C-09 chr23:90691006 C>G did not map to a codon.
Sequencing variant TCGA-X8-AAAR-01A-11D-A403-09 chr23:90690685 A>C did not map to a codon.
Sequencing variant TCGA-L5-A8NU-01A-11D-A36J-09 chr14:23792217 G>T maps to NM_004643.3 V159V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr6:163149329 C>A maps to NM_152410.2 T21T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA4D-01A-11D-A37C-09 chr11:66006622 C>T maps to NM_018026.2 D768D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OJ-01A-11D-A27G-09 chr14:105849725 C>T maps to ENST00000458164 P552P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EX-01A-11D-A36J-09 chr1:17597381 G>T maps to NM_016233.2 S280S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FD-01A-11D-A33E-09 chr1:17698738 G>T did not map to a codon.
Sequencing variant TCGA-L5-A8NF-01A-11D-A37C-09 chr1:17720863 G>T maps to NM_207421.3 G417G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NG-01A-11D-A37C-09 chr19:39876774 G>A maps to NM_019088.2 S484S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr17:2576015 G>A maps to NM_000430.3 R212R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr11:117031886 T>C maps to NM_002572.3 L66L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4ON-01A-11D-A27G-09 chr11:117045610 G>A maps to NM_001184748.1 A132A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KH-A6WC-01A-11D-A33E-09 chr23:49458732 C>A did not map to a codon.
Sequencing variant TCGA-JY-A6F8-01A-11D-A33E-09 chr5:43547974 G>T maps to NM_006451.4 S159*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A5U7-01A-11D-A31U-09 chr11:77054945 G>A maps to NM_001128620.1 Q306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8W5-01B-11D-A37C-09 chr23:110389748 C>T did not map to a codon.
Sequencing variant TCGA-VR-AA7B-01A-31D-A403-09 chr23:110406852 C>T did not map to a codon.
Sequencing variant TCGA-JY-A6FG-01A-11D-A33E-09 chr20:9560911 C>A maps to NM_177990.2 S290S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93E-01A-11D-A37C-09 chr4:169604254 G>A did not map to a codon.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr4:169812207 G>T maps to NM_001166108.1 P700P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RF-01A-13D-A33E-09 chr11:35492293 G>A maps to NM_015430.2 N189N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6DQ-01B-11D-A31U-09 chr20:3869971 G>A maps to NM_153638.2 S75S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA4G-01A-11D-A37C-09 chr5:167988396 C>T did not map to a codon.
Sequencing variant TCGA-LN-A4A4-01A-11D-A27G-09 chr11:124489476 C>A maps to NM_052959.2 S275S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A8O2-01A-11D-A36J-09 chr5:78944903 G>A maps to NM_173797.3 P306P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASV-01A-11D-A387-09 chr5:78981026 G>A maps to NM_173797.3 W462*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr16:50257095 G>A maps to NM_001040284.2 R378R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49M-01A-21D-A27G-09 chr16:50261883 T>C maps to NM_001040284.2 T630T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr14:73729127 C>T maps to ENST00000427855 F772F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4MR-01A-11D-A28B-09 chr14:73739371 G>T maps to ENST00000427855 *1279Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A939-01A-12D-A37C-09 chr14:96986548 G>T maps to NM_032632.3 E56*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49Y-01A-11D-A27G-09 chr9:118982240 G>T maps to NM_002581.3 T648T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S8-A6BV-01A-21D-A31U-09 chr9:119109488 G>A did not map to a codon.
Sequencing variant TCGA-IC-A6RF-01A-13D-A33E-09 chr1:176659351 G>T maps to NM_020318.2 L739L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A51D-01A-11D-A27G-09 chr1:176526315 G>A maps to NM_020318.2 A286A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FH-01A-11D-A33E-09 chr1:176564725 C>G maps to NM_020318.2 P662P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr1:176526096 C>T maps to NM_020318.2 S213S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr1:176708820 C>T maps to NM_020318.2 G1286G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EQ-01A-11D-A36J-09 chr1:176526096 C>T maps to NM_020318.2 S213S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GF-01A-11D-A37C-09 chr10:89419749 C>T maps to NM_001015880.1 I4I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93E-01A-11D-A37C-09 chr16:3021711 G>A maps to NM_152341.3 L195L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EX-01A-11D-A36J-09 chr15:69677147 C>T maps to NM_017705.3 F104F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RE-01A-11D-A33E-09 chr10:34601285 C>T maps to NM_001184792.1 K1030K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A5B8-01A-11D-A28B-09 chr10:34626222 G>C maps to NM_019619.3 S850*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FE-01A-11D-A33E-09 chr10:34625162 C>A maps to NM_019619.3 E860*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OF-01A-11D-A27G-09 chr10:34666951 G>A maps to NM_019619.3 L494L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NJ-01A-11D-A36J-09 chr10:34625163 G>A maps to NM_019619.3 D859D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NK-01A-21D-A37C-09 chr10:34400147 C>T maps to NM_019619.3 A1340A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NK-01A-21D-A37C-09 chr10:34649187 C>G did not map to a codon.
Sequencing variant TCGA-V5-AASX-01A-11D-A387-09 chr10:34759144 G>T maps to NM_019619.3 G150G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6DN-01B-11D-A31U-09 chr18:77917938 C>T maps to NM_032510.3 P282P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OP-01A-11D-A27G-09 chr6:161990395 T>C maps to NM_004562.2 G308G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L7-A6VZ-01A-12D-A33E-09 chr6:161969884 C>T did not map to a codon.
Sequencing variant TCGA-LN-A49M-01A-21D-A27G-09 chr3:183602517 G>A maps to NM_018622.5 L39L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A8I0-01A-11D-A36J-09 chr4:75938360 G>T did not map to a codon.
Sequencing variant TCGA-IC-A6RE-01A-11D-A33E-09 chr8:145059730 C>T maps to NM_032789.3 A174A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A2-01A-31D-A27G-09 chr8:145059976 C>G maps to NM_032789.3 S116S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4MR-01A-11D-A28B-09 chr8:145057844 C>A maps to NM_032789.3 E638*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASV-01A-11D-A387-09 chr8:145059487 G>A maps to NM_032789.3 R228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA7I-01A-11D-A403-09 chr7:139746765 G>A maps to NM_022750.2 Q302*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49U-01A-31D-A27G-09 chr3:122447374 T>C maps to NM_017554.2 H1779H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr3:51980258 C>T maps to NM_001003931.2 A399A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA7I-01A-11D-A403-09 chr3:51976713 G>C maps to NM_001003931.2 L3L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GL-01A-12D-A37C-09 chr13:24995334 G>A maps to NM_006437.3 A1699A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OO-01A-11D-A27G-09 chr13:25068764 T>A maps to NM_006437.3 L229L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49W-01A-11D-A27G-09 chr13:25021303 C>T maps to NM_006437.3 R1045R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4MR-01A-11D-A28B-09 chr13:25058792 G>A maps to NM_006437.3 L482L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EU-01A-11D-A36J-09 chr13:25016085 A>G maps to NM_006437.3 F1188F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49K-01A-11D-A247-09 chr5:50093010 G>T maps to ENST00000505697 E507*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NJ-01A-11D-A36J-09 chr3:122274684 C>T maps to NM_031458.2 G146G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49S-01A-11D-A247-09 chr3:122255180 C>T maps to NM_031458.2 K673K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GK-01A-11D-A37C-09 chr1:55224663 G>T maps to NM_152268.3 L57L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EX-01A-11D-A36J-09 chr11:12525934 C>T maps to NM_018222.4 R206*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GK-01A-11D-A37C-09 chr23:150791458 T>G did not map to a codon.
Sequencing variant TCGA-2H-A9GL-01A-12D-A37C-09 chr23:150780177 A>G did not map to a codon.
Sequencing variant TCGA-2H-A9GL-01A-12D-A37C-09 chr23:150842602 A>C did not map to a codon.
Sequencing variant TCGA-L5-A43C-01A-11D-A247-09 chr23:150840899 G>T did not map to a codon.
Sequencing variant TCGA-R6-A6KZ-01A-11D-A31U-09 chr23:150840246 A>C did not map to a codon.
Sequencing variant TCGA-Z6-A8JE-01A-11D-A37C-09 chr23:150840071 G>A did not map to a codon.
Sequencing variant TCGA-L5-A4OE-01A-11D-A27G-09 chr11:59423057 G>T maps to NM_152716.2 P323P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A4QS-01A-11D-A27G-09 chr20:21687511 G>A maps to NM_006192.3 P241P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OS-01A-11D-A28B-09 chr20:21687379 C>T maps to NM_006192.3 R197R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NS-01A-12D-A37C-09 chr11:31815068 G>A maps to NM_001604.4 R331*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EO-01A-11D-A36J-09 chr11:31822341 G>A maps to NM_001604.4 D154D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93C-01A-11D-A387-09 chr1:19071365 C>T maps to NM_001135254.1 L487L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FR-01A-11D-A387-09 chr2:114004338 G>T maps to NM_003466.3 I61I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49Y-01A-11D-A27G-09 chr7:154785467 C>T maps to NM_007349.3 V76V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASV-01A-11D-A387-09 chr7:154774988 T>A maps to NM_007349.3 G126G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A50L-01A-11D-A27G-09 chr3:52651531 G>A maps to ENST00000296302 R522*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A97H-01A-11D-A387-09 chr3:52668637 G>T maps to ENST00000296302 P427P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A938-01A-11D-A37C-09 chr3:52712579 G>A maps to ENST00000296302 R58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-A7RB-01A-11D-A351-09 chr3:52712579 G>T maps to ENST00000296302 R58R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A8JD-01A-11D-A36J-09 chr3:52597510 T>C did not map to a codon.
Sequencing variant TCGA-L5-A8NK-01A-21D-A37C-09 chr1:164789342 A>T maps to NM_002585.2 G344G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GG-01A-11D-A37C-09 chr1:154924333 G>A maps to NM_020524.2 Q39*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3YC-01A-11D-A247-09 chr12:53848619 C>A maps to NM_005016.5 V12V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OE-01A-11D-A27G-09 chr21:47316263 G>T maps to NM_020528.2 L51L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GF-01A-11D-A37C-09 chr13:100861647 G>A maps to NM_000282.3 K177K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3Y9-01A-12D-A247-09 chr13:100861713 C>G maps to NM_000282.3 V199V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A8O2-01A-11D-A36J-09 chr13:100962085 G>T did not map to a codon.
Sequencing variant TCGA-XP-A8T8-01A-11D-A36J-09 chr3:136012596 G>T did not map to a codon.
Sequencing variant TCGA-JY-A93C-01A-11D-A387-09 chr5:141244971 G>A maps to NM_032420.2 D308D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43E-01A-11D-A247-09 chr4:134072758 C>T maps to NM_032961.1 T488T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OE-01A-11D-A27G-09 chr4:134072236 C>T maps to NM_032961.1 G314G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr4:134071771 C>T maps to NM_032961.1 Y159Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OO-01A-11D-A27G-09 chr4:134071342 C>A maps to NM_032961.1 V16V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HZ-01A-31D-A351-09 chr4:134072083 T>C maps to NM_032961.1 S263S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6XG-01B-11D-A33E-09 chr4:134073781 C>T maps to NM_032961.1 S829S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6XG-01B-11D-A33E-09 chr4:134073919 C>A maps to NM_032961.1 S875S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FD-01A-11D-A33E-09 chr23:91642827 G>T did not map to a codon.
Sequencing variant TCGA-JY-A6FG-01A-11D-A33E-09 chr23:91873636 C>A did not map to a codon.
Sequencing variant TCGA-L5-A43C-01A-11D-A247-09 chr23:91134271 G>A did not map to a codon.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr23:91091003 C>T did not map to a codon.
Sequencing variant TCGA-L5-A4OE-01A-11D-A27G-09 chr23:91873444 C>A did not map to a codon.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr23:91133117 C>T did not map to a codon.
Sequencing variant TCGA-L5-A4OO-01A-11D-A27G-09 chr23:91873879 C>T did not map to a codon.
Sequencing variant TCGA-L5-A4OW-01A-11D-A28B-09 chr23:91131911 G>T did not map to a codon.
Sequencing variant TCGA-L5-A8NE-01A-11D-A37C-09 chr23:91132815 A>C did not map to a codon.
Sequencing variant TCGA-L5-A8NI-01A-11D-A37C-09 chr23:91134271 G>A did not map to a codon.
Sequencing variant TCGA-L5-A8NJ-01A-11D-A36J-09 chr23:91873793 C>T did not map to a codon.
Sequencing variant TCGA-L5-A8NV-01A-11D-A37C-09 chr23:91090518 G>T did not map to a codon.
Sequencing variant TCGA-LN-A5U7-01A-11D-A31U-09 chr23:91642779 G>A did not map to a codon.
Sequencing variant TCGA-LN-A7HW-01A-22D-A351-09 chr23:91518125 G>A did not map to a codon.
Sequencing variant TCGA-RE-A7BO-01A-11D-A33E-09 chr23:91134100 T>C did not map to a codon.
Sequencing variant TCGA-VR-AA4G-01A-11D-A37C-09 chr23:91873844 C>T did not map to a codon.
Sequencing variant TCGA-R6-A6Y0-01B-11D-A33E-09 chr24:4968284 C>A did not map to a codon.
Sequencing variant TCGA-L5-A88S-01A-11D-A36J-09 chr5:141335613 C>T maps to NM_016580.2 A601A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASV-01A-11D-A387-09 chr5:141324996 C>A maps to NM_016580.2 T1168T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A8JE-01A-11D-A37C-09 chr5:141334668 G>C maps to NM_016580.2 L916L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RE-01A-11D-A33E-09 chr10:55582820 T>C maps to NM_001142763.1 K1562K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RE-01A-11D-A33E-09 chr10:55955474 T>G maps to NM_001142763.1 R430R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93E-01A-11D-A37C-09 chr10:55581893 C>T maps to NM_001142763.1 Q1871Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr10:55719504 G>A maps to NM_001142763.1 Q1042*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NV-01A-11D-A37C-09 chr10:55912909 A>C maps to NM_001142763.1 T583T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A4-01A-11D-A27G-09 chr10:55892730 T>C maps to NM_001142763.1 P612P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6XG-01B-11D-A33E-09 chr10:56423984 G>T maps to NM_001142763.1 S13*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EW-01A-11D-A36J-09 chr10:55582696 G>A maps to NM_001142763.1 L1604L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GK-01A-11D-A37C-09 chr13:58299064 A>G maps to NM_001040429.2 P1039P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GQ-01A-11D-A37C-09 chr13:58299184 G>T maps to NM_001040429.2 L1079L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A51D-01A-11D-A27G-09 chr13:58208620 G>A maps to NM_001040429.2 T647T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NH-01A-11D-A37C-09 chr13:58208353 G>A maps to NM_001040429.2 G558G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-A7RB-01A-11D-A351-09 chr4:138451538 G>A maps to NM_019035.3 D568D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FD-01A-11D-A33E-09 chr23:99661721 C>T did not map to a codon.
Sequencing variant TCGA-L5-A4OT-01A-11D-A28B-09 chr23:99663100 A>C did not map to a codon.
Sequencing variant TCGA-LN-A49W-01A-11D-A27G-09 chr23:99662989 C>T did not map to a codon.
Sequencing variant TCGA-LN-A4A2-01A-31D-A27G-09 chr23:99661678 C>A did not map to a codon.
Sequencing variant TCGA-R6-A6KZ-01A-11D-A31U-09 chr23:99551695 C>A did not map to a codon.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr4:30723073 G>A maps to NM_001173523.1 A10A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NR-01A-11D-A37C-09 chr13:53422025 G>A maps to NM_002590.2 R182R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GI-01A-11D-A37C-09 chr13:67799671 G>C maps to NM_203487.2 L967L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RE-A7BO-01A-11D-A33E-09 chr13:66878786 T>G maps to NM_203487.2 *1238Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr5:140167668 C>T maps to NM_018900.2 D598D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A1-01A-21D-A27G-09 chr5:140168120 C>A maps to NM_018900.2 S749*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8W5-01B-11D-A37C-09 chr5:140167908 G>A maps to NM_018900.2 A678A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OU-01A-11D-A28B-09 chr5:140236754 T>C maps to NM_018901.2 S374S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr5:140250121 G>A maps to NM_018902.3 A478A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GO-01A-11D-A37C-09 chr5:140255344 C>T maps to NM_018903.2 C96C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4ON-01A-11D-A27G-09 chr5:140257123 C>T maps to NM_018903.2 P689P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr5:140256352 G>A maps to NM_018903.2 S432S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr5:140256976 G>A maps to NM_018903.2 A640A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr5:140262128 C>T maps to NM_018904.2 R92R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OO-01A-11D-A27G-09 chr5:140263490 C>A maps to NM_018904.2 G546G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr5:140176198 G>A maps to NM_018905.2 T550T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OH-01A-11D-A27G-09 chr5:140176801 G>A maps to NM_018905.2 S751S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr5:140175607 G>A maps to NM_018905.2 T353T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49Y-01A-11D-A27G-09 chr5:140176747 G>A maps to NM_018905.2 A733A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6L6-01B-11D-A33E-09 chr5:140174554 G>A maps to NM_018905.2 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr5:140182155 C>T maps to NM_018906.2 S458S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OT-01A-11D-A28B-09 chr5:140182593 C>T maps to NM_018906.2 N604N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NW-01A-11D-A37C-09 chr5:140182827 G>A maps to NM_018906.2 A682A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49X-01A-31D-A27G-09 chr5:140182335 C>T maps to NM_018906.2 Y518Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6Y2-01B-11D-A33E-09 chr5:140187431 C>T maps to NM_018907.2 P220P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RE-A7BO-01A-11D-A33E-09 chr5:140188385 C>T maps to NM_018907.2 R538R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EQ-01A-11D-A36J-09 chr5:140188700 G>T maps to NM_018907.2 P643P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OR-01A-11D-A27G-09 chr5:140201527 G>A maps to NM_018908.2 A56A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A893-01A-11D-A36J-09 chr5:140203585 C>T maps to NM_018908.2 S742S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43H-01A-11D-A247-09 chr5:140209868 G>A maps to NM_018909.2 A731A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OJ-01A-11D-A27G-09 chr5:140216157 C>T maps to NM_018910.2 G730G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-A7RB-01A-11D-A351-09 chr5:140216109 C>T maps to NM_018910.2 T714T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A51D-01A-11D-A27G-09 chr5:140228250 G>A maps to NM_031857.1 A57A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93E-01A-11D-A37C-09 chr5:140229432 C>T maps to NM_031857.1 N451N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A893-01A-11D-A36J-09 chr5:140230269 C>A maps to NM_031857.1 G730G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr5:140229588 G>A maps to NM_031857.1 S503S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49Y-01A-11D-A27G-09 chr5:140229768 G>C maps to NM_031857.1 P563P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FO-01A-11D-A387-09 chr5:140230374 G>A maps to NM_031857.1 Q765Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6DQ-01B-11D-A31U-09 chr5:140229375 G>A maps to NM_031857.1 S432S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A5B8-01A-11D-A28B-09 chr5:140307391 C>G maps to NM_018898.3 L305L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NG-01A-11D-A37C-09 chr5:140306542 C>T maps to NM_018898.3 L22L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NI-01A-11D-A37C-09 chr5:140307981 C>A maps to NM_018898.3 S502*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6Y2-01B-11D-A33E-09 chr5:140307145 G>T maps to NM_018898.3 V223V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A939-01A-12D-A37C-09 chr5:140348786 G>A maps to NM_018899.5 G812G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49Y-01A-11D-A27G-09 chr5:140347250 G>T maps to NM_018899.5 T300T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XP-A8T7-01A-11D-A36J-09 chr5:140347415 C>T maps to NM_018899.5 I355I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A5B8-01A-11D-A28B-09 chr5:140431921 C>G maps to NM_013340.2 L289L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RE-01A-11D-A33E-09 chr5:140581065 C>T maps to NM_018931.2 T573T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr5:140579997 T>C maps to NM_018931.2 G217G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr5:140580048 C>T maps to NM_018931.2 D234D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr5:140580069 A>G maps to NM_018931.2 E241E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A6QS-01A-12D-A33E-09 chr5:140589129 C>T maps to NM_018932.3 G217G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OT-01A-11D-A28B-09 chr5:140589471 T>C maps to NM_018932.3 S331S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OU-01A-11D-A28B-09 chr5:140589228 G>A maps to NM_018932.3 K250K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HY-01A-12D-A351-09 chr5:140588790 G>A maps to NM_018932.3 L104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8WG-01A-11D-A37C-09 chr5:140589507 C>T maps to NM_018932.3 N343N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49Y-01A-11D-A27G-09 chr5:140594186 C>A maps to NM_018933.2 G164G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EU-01A-11D-A36J-09 chr5:140595515 C>G maps to NM_018933.2 L607L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XP-A8T6-01A-11D-A36J-09 chr5:140595491 C>T maps to NM_018933.2 N599N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr5:140604225 C>T maps to NM_018934.2 C383C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4MQ-01A-11D-A28B-09 chr5:140604552 G>A maps to NM_018934.2 P492P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FP-01A-31D-A387-09 chr5:140603151 G>T maps to NM_018934.2 R25R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HV-01A-21D-A351-09 chr5:140627239 T>G maps to NM_018935.2 S698S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6DQ-01B-11D-A31U-09 chr5:140626810 C>T maps to NM_018935.2 N555N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GO-01A-11D-A37C-09 chr5:140562568 C>T maps to NM_020957.1 N145N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr5:140563849 C>T maps to NM_020957.1 C572C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GR-01A-12D-A37C-09 chr5:140476059 C>T maps to NM_018936.2 F562F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FB-01A-11D-A33E-09 chr5:140475147 C>T maps to NM_018936.2 P258P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OE-01A-11D-A27G-09 chr5:140474967 G>T maps to NM_018936.2 L198L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A5U7-01A-11D-A31U-09 chr5:140476236 G>A maps to NM_018936.2 A621A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XP-A8T7-01A-11D-A36J-09 chr5:140476080 C>T maps to NM_018936.2 N569N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49O-01A-11D-A247-09 chr5:140482554 C>T maps to NM_018937.2 F774F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr5:140503235 C>T maps to NM_018938.2 D552D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr5:140503442 C>T maps to NM_018938.2 G621G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NU-01A-11D-A36J-09 chr5:140502329 C>A maps to NM_018938.2 V250V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GR-01A-12D-A37C-09 chr5:140529936 C>T maps to NM_018939.2 S33S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FD-01A-11D-A33E-09 chr5:140530576 G>T maps to NM_018939.2 E247*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49Y-01A-11D-A27G-09 chr5:140531970 G>T maps to NM_018939.2 L711L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X8-AAAR-01A-11D-A403-09 chr5:140531568 G>A maps to NM_018939.2 A577A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S8-A6BV-01A-21D-A31U-09 chr5:140554212 C>T maps to NM_018940.2 N599N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-A7RE-01A-11D-A351-09 chr5:140552743 T>C maps to NM_018940.2 L110L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93D-01A-11D-A387-09 chr5:140559405 G>A maps to NM_019120.2 S597S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OG-01A-11D-A27G-09 chr5:140559729 G>A maps to NM_019120.2 S705S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr5:140559276 C>T maps to NM_019120.2 D554D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NN-01A-11D-A37C-09 chr5:140558871 C>T maps to NM_019120.2 N419N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-A7RC-01B-11D-A403-09 chr5:140559033 C>T maps to NM_019120.2 S473S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr5:140710766 C>T maps to NM_018912.2 L172L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43I-01A-11D-A247-09 chr5:140801606 C>T maps to NM_018914.2 D271D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr5:140801618 C>T maps to NM_018914.2 N275N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NI-01A-11D-A37C-09 chr5:140802464 C>T maps to NM_018914.2 N557N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GF-01A-11D-A37C-09 chr5:140812167 G>T maps to NM_003735.2 P614P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr5:140810541 G>A maps to NM_003735.2 T72T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6XG-01B-11D-A33E-09 chr5:140720763 C>T maps to NM_018915.2 G742G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GM-01A-11D-A37C-09 chr5:140725369 G>A maps to NM_018916.3 K590K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr5:140724853 T>A maps to NM_018916.3 Y418*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr5:140725963 C>T maps to NM_018916.3 S788S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S8-A6BV-01A-21D-A31U-09 chr5:140723815 G>A maps to NM_018916.3 T72T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OW-01A-11D-A28B-09 chr5:140734991 C>T maps to NM_018917.2 F75F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr5:140735561 A>G maps to NM_018917.2 K265K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L7-A6VZ-01A-12D-A33E-09 chr5:140746059 G>A maps to NM_018918.2 K721K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4MQ-01A-11D-A28B-09 chr5:140745553 C>T maps to NM_018918.2 L553L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASX-01A-11D-A387-09 chr5:140744134 C>T maps to NM_018918.2 R80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A4-01A-11D-A27G-09 chr5:140754631 C>T maps to NM_018919.2 R328*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASX-01A-11D-A387-09 chr5:140755518 G>A maps to NM_018919.2 T623T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA7B-01A-31D-A403-09 chr5:140755584 C>T maps to NM_018919.2 A645A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43I-01A-11D-A247-09 chr5:140774173 G>A maps to NM_032088.1 S598S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6XG-01B-11D-A33E-09 chr5:140773786 C>A maps to NM_032088.1 A469A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HX-01A-11D-A33E-09 chr5:140782779 G>A maps to NM_018921.2 A87A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6L6-01B-11D-A33E-09 chr5:140731470 G>A maps to NM_018922.2 V548V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GH-01A-11D-A37C-09 chr5:140741033 C>T maps to NM_018923.2 D444D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FD-01A-11D-A33E-09 chr5:140741729 C>T maps to NM_018923.2 S676S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XP-A8T8-01A-11D-A36J-09 chr5:140741228 G>A maps to NM_018923.2 A509A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NF-01A-11D-A37C-09 chr5:140788746 T>A maps to NM_018926.2 G326G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GG-01A-11D-A37C-09 chr5:140798970 C>T maps to NM_018927.2 F515F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GN-01A-11D-A37C-09 chr5:140798868 C>T maps to NM_018927.2 F481F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FG-01A-11D-A33E-09 chr5:140797860 C>A maps to NM_018927.2 S145S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93E-01A-11D-A37C-09 chr5:140799289 C>T maps to NM_018927.2 R622*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RE-A7BO-01A-11D-A33E-09 chr5:140798757 C>T maps to NM_018927.2 D444D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XP-A8T8-01A-11D-A36J-09 chr5:140797617 C>T maps to NM_018927.2 R64R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GQ-01A-11D-A37C-09 chr5:140856510 C>T maps to NM_002588.2 N276N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FG-01A-11D-A33E-09 chr5:140871074 G>T maps to NM_018929.2 T756T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A938-01A-11D-A37C-09 chr5:140870261 T>C maps to NM_018929.2 D485D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NR-01A-11D-A37C-09 chr2:74733104 C>T maps to NM_032673.2 Q168Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XP-A8T6-01A-11D-A36J-09 chr17:36891778 G>C maps to NM_007144.2 P244P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GL-01A-12D-A37C-09 chr4:737325 G>A maps to NM_006315.4 K109K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49W-01A-11D-A27G-09 chr20:44573646 C>T maps to NM_022104.3 I382I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6F8-01A-11D-A33E-09 chr20:56138619 G>T did not map to a codon.
Sequencing variant TCGA-LN-A49W-01A-11D-A27G-09 chr14:24572369 G>T maps to NM_004563.2 G458G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GI-01A-11D-A37C-09 chr7:82584391 A>C maps to NM_033026.5 S1959S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GR-01A-12D-A37C-09 chr7:82581891 C>A maps to NM_033026.5 E2793*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RE-01A-11D-A33E-09 chr7:82581923 G>T maps to NM_033026.5 S2782*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RE-01A-11D-A33E-09 chr7:82585561 A>C maps to NM_033026.5 A1569A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A4QS-01A-11D-A27G-09 chr7:82764561 A>G maps to NM_033026.5 S768S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FE-01A-11D-A33E-09 chr7:82585186 G>A maps to NM_033026.5 D1694D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43E-01A-11D-A247-09 chr7:82584391 A>C maps to NM_033026.5 S1959S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr7:82791761 G>A maps to NM_033026.5 S49S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OU-01A-11D-A28B-09 chr7:82538207 A>G maps to NM_033026.5 S4474S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OU-01A-11D-A28B-09 chr7:82595623 T>C maps to NM_033026.5 Q1160Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NG-01A-11D-A37C-09 chr7:82595488 A>C maps to NM_033026.5 A1205A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr7:82578943 G>A maps to NM_033026.5 Q3654*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HX-01A-11D-A33E-09 chr7:82579101 G>T maps to NM_033026.5 S3601*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASV-01A-11D-A387-09 chr7:82584499 A>G maps to NM_033026.5 H1923H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASX-01A-11D-A387-09 chr7:82584288 T>A maps to NM_033026.5 R1994*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OP-01A-11D-A27G-09 chr8:17814237 C>G maps to NM_006197.3 S533*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A9-01A-11D-A28B-09 chr6:150123513 G>C maps to NM_005389.2 *286S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OX-01A-21D-A28B-09 chr8:52733120 G>A maps to NM_052937.2 Y288Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NW-01A-11D-A37C-09 chr8:52733081 G>A maps to NM_052937.2 D301D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49O-01A-11D-A247-09 chr8:52733123 A>C maps to NM_052937.2 T287T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OO-01A-11D-A27G-09 chr3:101304300 A>G maps to NM_020357.1 P100P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FG-01A-11D-A33E-09 chr21:47851825 G>A maps to NM_006031.5 L2816L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OE-01A-11D-A27G-09 chr21:47850517 G>T maps to NM_006031.5 E2671*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NF-01A-11D-A37C-09 chr21:47819580 T>C maps to NM_006031.5 D1554D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49Y-01A-11D-A27G-09 chr21:47775525 G>T maps to NM_006031.5 E641*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X8-AAAR-01A-11D-A403-09 chr21:47786666 G>A maps to NM_006031.5 A926A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GL-01A-12D-A37C-09 chr1:233397059 G>T maps to NM_014801.3 S163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3YB-01A-11D-A247-09 chr1:233394197 G>A maps to NM_014801.3 Y470Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr1:233134042 G>A maps to NM_014801.3 G1915G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A891-01A-11D-A36J-09 chr11:65396124 C>T maps to NM_032223.2 I1254I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88V-01A-11D-A351-09 chr3:142561780 T>A maps to NM_013363.3 V186V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EX-01A-11D-A36J-09 chr21:41300927 A>G maps to NM_006198.2 Q27Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-M9-A5M8-01A-11D-A28B-09 chr5:95746476 C>T did not map to a codon.
Sequencing variant TCGA-XP-A8T8-01A-11D-A36J-09 chr5:95728919 G>A maps to NM_000439.4 Q683*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NQ-01A-11D-A36J-09 chr15:101853632 C>A maps to NM_002570.3 E882*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6Y0-01B-11D-A33E-09 chr15:101971640 G>T maps to NM_002570.3 R180R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-A7RE-01A-11D-A351-09 chr15:101906494 G>A maps to NM_002570.3 F587F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GH-01A-11D-A37C-09 chr11:117100473 G>A maps to NM_004716.2 F29F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A50L-01A-11D-A27G-09 chr11:117079692 T>A maps to NM_004716.2 P537P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6Y0-01B-11D-A33E-09 chr11:117077811 C>T maps to NM_004716.2 W617*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NL-01A-12D-A37C-09 chr1:55523164 A>G maps to NM_174936.3 S386S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GO-01A-11D-A37C-09 chr23:24665158 G>A did not map to a codon.
Sequencing variant TCGA-IG-A3I8-01A-11D-A247-09 chr23:24625954 C>T did not map to a codon.
Sequencing variant TCGA-L5-A4OE-01A-11D-A27G-09 chr23:24597491 C>A did not map to a codon.
Sequencing variant TCGA-Z6-A8JE-01A-11D-A37C-09 chr2:242795100 G>A maps to NM_005018.2 T36T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OQ-01A-11D-A27G-09 chr19:33076746 T>C maps to NM_004708.3 P64P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A4P3-01A-11D-A27G-09 chr3:33870404 C>T maps to NM_001162429.1 Q265*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OE-01A-11D-A27G-09 chr3:33868053 C>T maps to NM_001162429.1 Y233Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OJ-01A-11D-A27G-09 chr3:33879703 G>T maps to NM_001162429.1 E361*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A893-01A-11D-A36J-09 chr3:57545405 C>A maps to NM_177966.5 S502*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A51D-01A-11D-A27G-09 chr12:54967205 C>T maps to NM_000924.3 R302*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GI-01A-11D-A37C-09 chr11:72288493 G>A maps to NM_002599.3 Y920Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A8O2-01A-11D-A36J-09 chr12:20774227 A>C did not map to a codon.
Sequencing variant TCGA-L5-A8NW-01A-11D-A37C-09 chr12:20522242 C>T maps to NM_000921.3 R9*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NW-01A-11D-A37C-09 chr12:20522418 G>A maps to NM_000921.3 A67A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S8-A6BW-01A-11D-A31U-09 chr12:20523042 G>A maps to NM_000921.3 L275L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EY-01A-11D-A36J-09 chr12:20786712 G>T did not map to a codon.
Sequencing variant TCGA-2H-A9GK-01A-11D-A37C-09 chr1:66384384 T>C maps to NM_001037341.1 L50L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GK-01A-11D-A37C-09 chr1:66798110 C>T maps to NM_001037339.1 I13I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA7B-01A-31D-A403-09 chr19:18322637 G>A maps to NM_000923.3 R574R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A97I-01A-11D-A387-09 chr5:58271510 C>T maps to NM_001104631.1 K662K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FG-01A-11D-A33E-09 chr1:145075751 C>T maps to NM_022359.5 T37T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr1:145075829 G>T maps to NM_022359.5 R11R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA7D-01A-11D-A403-09 chr1:144916731 C>T maps to NM_014644.4 L541L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NK-01A-21D-A37C-09 chr4:120528238 C>T maps to NM_001083.3 V122V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NF-01A-11D-A37C-09 chr5:149323978 G>A maps to NM_000440.2 C86C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A8I0-01A-11D-A36J-09 chr5:149324056 G>T maps to NM_000440.2 I60I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A7DP-01A-31D-A33E-09 chr4:619585 G>T maps to NM_000283.3 T57T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XP-A8T8-01A-11D-A36J-09 chr4:657650 G>A maps to NM_000283.3 L671L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6XG-01B-11D-A33E-09 chr10:95418859 G>T did not map to a codon.
Sequencing variant TCGA-Z6-A8JE-01A-11D-A37C-09 chr10:95372505 C>T maps to NM_006204.3 A8A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A4P3-01A-11D-A27G-09 chr8:66753635 G>A maps to ENST00000401827 F36F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NG-01A-11D-A37C-09 chr8:66631621 C>T maps to ENST00000401827 W451*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q9-A6FW-01A-31D-A31U-09 chr6:136508213 T>C maps to NM_018945.3 L362L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr21:44190871 C>T maps to NM_002606.2 Y550Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA4G-01A-11D-A37C-09 chr4:55146649 G>A did not map to a codon.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr5:149513314 C>T maps to NM_002609.3 R256R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FH-01A-11D-A33E-09 chr4:96761633 C>T maps to NM_005390.4 H111H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NG-01A-11D-A37C-09 chr4:96761930 T>C maps to NM_005390.4 A210A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASV-01A-11D-A387-09 chr15:44038853 C>T maps to NM_005313.4 I39I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A5B8-01A-11D-A28B-09 chr7:148701242 G>A maps to NM_004911.4 V527V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6L4-01A-11D-A31U-09 chr2:10930910 C>G maps to ENST00000381611 T263T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6XG-01B-11D-A33E-09 chr17:48184156 G>T did not map to a codon.
Sequencing variant TCGA-ZR-A9CJ-01B-11D-A387-09 chr23:24552066 G>T did not map to a codon.
Sequencing variant TCGA-LN-A8I1-01A-11D-A36J-09 chr8:22439043 G>T did not map to a codon.
Sequencing variant TCGA-V5-A7RC-01B-11D-A403-09 chr8:22442537 G>T maps to NM_021630.5 V358V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3Y9-01A-12D-A247-09 chr4:186456519 G>A maps to NM_014476.4 F23F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASX-01A-11D-A387-09 chr4:186427781 G>A maps to NM_014476.4 P229P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NN-01A-11D-A37C-09 chr4:95578594 G>A maps to NM_006457.3 L494L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr5:176918058 G>A maps to NM_005451.3 Q163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FB-01A-11D-A33E-09 chr8:94935235 C>T maps to NM_001161778.1 Q376*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-M9-A5M8-01A-11D-A28B-09 chr16:66919131 C>T maps to NM_020786.2 A315A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3YB-01A-11D-A247-09 chr16:70190706 C>G maps to NM_017990.3 L855L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49M-01A-21D-A27G-09 chr16:70187388 G>A maps to NM_017990.3 E716E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A6-01A-11D-A27G-09 chr4:39915247 C>T maps to NM_001100399.1 W325*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-AAPN-01A-11D-A403-09 chr4:39891929 C>A maps to NM_001100399.1 E609*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NQ-01A-11D-A36J-09 chr13:33275575 G>T did not map to a codon.
Sequencing variant TCGA-L5-A8NS-01A-12D-A37C-09 chr6:107595331 T>C maps to NM_020381.3 P177P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr13:28498618 C>T maps to NM_000209.3 G211G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HY-01A-12D-A351-09 chr22:38061676 C>T maps to ENST00000442465 P539P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr5:31983542 C>T maps to NM_178140.2 G253G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OH-01A-11D-A27G-09 chr23:153069013 G>A did not map to a codon.
Sequencing variant TCGA-L5-A8NR-01A-11D-A37C-09 chr23:153069860 C>T did not map to a codon.
Sequencing variant TCGA-R6-A8W8-01B-11D-A37C-09 chr23:153069775 G>A did not map to a codon.
Sequencing variant TCGA-JY-A93F-01A-21D-A37C-09 chr10:102789898 G>A maps to NM_001195263.1 S26S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FO-01A-11D-A387-09 chr10:102778669 C>T maps to NM_001195263.1 A411A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A97H-01A-11D-A387-09 chr10:119100614 T>C did not map to a codon.
Sequencing variant TCGA-R6-A8W8-01B-11D-A37C-09 chr10:119134123 G>A maps to NM_173791.3 A205A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EQ-01A-11D-A36J-09 chr10:119043841 G>T maps to NM_173791.3 S801*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A9VB-01A-21D-A37C-09 chr10:119043704 G>A maps to NM_173791.3 Q847*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A9VB-01A-21D-A37C-09 chr10:119044394 C>A maps to NM_173791.3 E617*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FA-01A-11D-A33E-09 chr1:47653001 G>T maps to NM_005764.3 C55*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr3:73673853 G>A maps to NM_015009.1 C41C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HY-01A-12D-A351-09 chr3:73433778 G>A maps to NM_015009.1 F646F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA4D-01A-11D-A37C-09 chr3:73453348 C>T maps to NM_015009.1 K372K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X8-AAAR-01A-11D-A403-09 chr3:73433187 G>A maps to NM_015009.1 S843S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OE-01A-11D-A27G-09 chr12:41831754 C>A maps to NM_013377.3 C3*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6L6-01B-11D-A33E-09 chr12:41966629 C>A maps to NM_001164595.1 I683I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EZ-01A-11D-A36J-09 chr12:41903640 G>T maps to NM_001164595.1 E377*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6XQ-01B-11D-A33E-09 chr12:118582593 C>T maps to NM_002567.2 L184L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GR-01A-12D-A37C-09 chr19:57325573 T>C maps to NM_006210.2 E1412E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GR-01A-12D-A37C-09 chr19:57327775 A>C maps to NM_006210.2 T678T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3I8-01A-11D-A247-09 chr19:57325603 G>A maps to NM_006210.2 A1402A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FE-01A-11D-A33E-09 chr19:57325171 G>T maps to NM_006210.2 I1546I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NE-01A-11D-A37C-09 chr19:57326872 A>G maps to NM_006210.2 A979A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr19:57328135 G>A maps to NM_006210.2 G558G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NW-01A-11D-A37C-09 chr19:57325231 A>G maps to NM_006210.2 T1526T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8ER-01A-11D-A36J-09 chr2:64322156 G>T maps to NM_020651.3 G312G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XP-A8T6-01A-11D-A36J-09 chr14:56763775 G>A maps to NM_021255.2 P385P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr11:66239922 C>T maps to NM_145065.2 S146S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NW-01A-11D-A37C-09 chr11:66238736 G>T maps to NM_145065.2 G83G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A5U7-01A-11D-A31U-09 chr11:66235712 C>A maps to NM_145065.2 G38G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XP-A8T6-01A-11D-A36J-09 chr11:66241209 G>A maps to NM_145065.2 E218E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr17:17409599 C>T maps to NM_148172.1 T198T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S8-A6BW-01A-11D-A31U-09 chr8:57358446 C>T maps to NM_001135690.1 V22V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr17:8053367 C>T maps to NM_002616.2 P150P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NF-01A-11D-A37C-09 chr17:8050699 C>A did not map to a codon.
Sequencing variant TCGA-L5-A8NK-01A-21D-A37C-09 chr17:8046066 G>A maps to NM_002616.2 S1053S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr1:7846784 C>T maps to ENST00000377532 N93N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RE-A7BO-01A-11D-A33E-09 chr1:7896000 G>T maps to ENST00000377532 E1132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr22:30977619 G>A maps to NM_014303.2 D214D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88S-01A-11D-A36J-09 chr7:92135589 C>T maps to NM_000466.2 V624V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NF-01A-11D-A37C-09 chr1:145522904 C>T maps to NM_003846.2 R256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr1:10596277 G>T maps to NM_004565.2 T31T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OJ-01A-11D-A27G-09 chr1:10596277 G>T maps to NM_004565.2 T31T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A97I-01A-11D-A387-09 chr11:45936187 G>T maps to NM_057174.2 R170R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASV-01A-11D-A387-09 chr11:45935478 G>A maps to NM_057174.2 L260L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A8O2-01A-11D-A36J-09 chr8:77896249 C>T maps to NM_001172087.1 E55E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q9-A6FU-01A-11D-A31U-09 chr8:77895530 G>C maps to NM_001172087.1 S295*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8ER-01A-11D-A36J-09 chr6:143800300 G>T maps to NM_003630.2 E303*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49P-01A-11D-A247-09 chr3:179592165 G>A maps to NM_016559.1 S225S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HX-01A-11D-A33E-09 chr3:179525561 C>A maps to NM_016559.1 E526*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6Y2-01B-11D-A33E-09 chr3:179592120 C>T maps to NM_016559.1 P240P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3QL-01A-11D-A247-09 chr17:8160281 G>T did not map to a codon.
Sequencing variant TCGA-L7-A6VZ-01A-12D-A33E-09 chr17:8167163 G>T maps to NM_012393.2 L567L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A9VB-01A-21D-A37C-09 chr17:8158845 G>T maps to NM_012393.2 V137V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L7-A56G-01A-21D-A27G-09 chr12:53690037 A>G maps to NM_002624.3 L62L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GN-01A-11D-A37C-09 chr23:54982676 C>T did not map to a codon.
Sequencing variant TCGA-L5-A88V-01A-11D-A351-09 chr23:54961427 G>T did not map to a codon.
Sequencing variant TCGA-JY-A6F8-01A-11D-A33E-09 chr1:207244560 C>T maps to NM_006212.2 L417L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q9-A6FU-01A-11D-A31U-09 chr1:207243746 G>A maps to NM_006212.2 K405K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EQ-01A-11D-A36J-09 chr10:6258136 G>T maps to NM_004566.3 E117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EQ-01A-11D-A36J-09 chr10:6261587 C>T maps to NM_004566.3 D185D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr17:4849206 A>G maps to NM_005022.2 R137R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FP-01A-31D-A387-09 chr11:60971722 C>A maps to NM_001079807.1 P67P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A5U6-01A-11D-A28B-09 chr7:44104882 C>A maps to NM_000290.3 V82V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr2:197712753 G>A maps to NM_024989.3 C623C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-AAPN-01A-11D-A403-09 chr2:197777707 A>G maps to NM_024989.3 L183L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KH-A6WC-01A-11D-A33E-09 chr10:50724703 C>A maps to ENST00000515869 E621*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GL-01A-12D-A37C-09 chr15:34396390 G>A maps to NM_152595.4 K553K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6XG-01B-11D-A33E-09 chr1:230472965 G>T maps to ENST00000321327 L351L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X8-AAAR-01A-11D-A403-09 chr1:230472896 G>T maps to ENST00000321327 P374P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GH-01A-11D-A37C-09 chr8:97797324 T>A maps to ENST00000325141 L67*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NT-01A-11D-A37C-09 chr8:98155408 T>C maps to ENST00000325141 P471P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NL-01A-12D-A37C-09 chr5:114557679 G>T maps to NM_005023.3 A228A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6XQ-01B-11D-A33E-09 chr23:77369396 G>T did not map to a codon.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr6:49754576 A>G maps to NM_138733.4 C108C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr19:15587228 G>A maps to NM_052890.3 C84C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NR-01A-11D-A37C-09 chr1:153317649 G>A maps to NM_020393.2 A116A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-AAPN-01A-11D-A403-09 chr4:37836310 C>T maps to NM_018290.3 A107A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr9:70993120 C>T maps to NM_021965.3 R90*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr15:99512697 T>C maps to NM_001102612.2 V109V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GF-01A-11D-A37C-09 chr11:100996844 G>T maps to NM_000926.4 S561*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr11:100962607 C>A did not map to a codon.
Sequencing variant TCGA-S8-A6BW-01A-11D-A31U-09 chr11:100922293 G>A maps to NM_000926.4 R740*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RE-A7BO-01A-11D-A33E-09 chr23:118374350 G>T did not map to a codon.
Sequencing variant TCGA-Q9-A6FU-01A-11D-A31U-09 chr4:129193572 G>C maps to NM_006320.4 S197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FP-01A-31D-A387-09 chr6:13228204 G>T maps to NM_030948.1 E382*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr20:58422168 G>T did not map to a codon.
Sequencing variant TCGA-LN-A49M-01A-21D-A27G-09 chr20:58342364 G>A maps to NM_080672.3 E222E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6F8-01A-11D-A33E-09 chr5:125960470 G>T maps to NM_032177.3 E374*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KH-A6WC-01A-11D-A33E-09 chr5:125939612 G>T maps to NM_032177.3 E150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FP-01A-31D-A387-09 chr17:47486520 C>A did not map to a codon.
Sequencing variant TCGA-IG-A7DP-01A-31D-A33E-09 chr12:9073600 G>A maps to ENST00000433083 R177R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OJ-01A-11D-A27G-09 chr23:22151692 A>G did not map to a codon.
Sequencing variant TCGA-VR-A8EY-01A-11D-A36J-09 chr23:22117196 C>T did not map to a codon.
Sequencing variant TCGA-JY-A6FG-01A-11D-A33E-09 chr6:33382136 G>T maps to NM_024165.2 L290L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A4P3-01A-11D-A27G-09 chr6:170117958 C>G maps to NM_018288.3 L123L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GO-01A-11D-A37C-09 chr17:27233338 C>T maps to NM_001033561.1 Q959Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EO-01A-11D-A36J-09 chr7:11068426 A>G maps to ENST00000303905 S479S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RF-01A-13D-A33E-09 chr5:133873736 G>T maps to ENST00000448712 S55S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49P-01A-11D-A247-09 chr5:133895549 C>T maps to ENST00000448712 A130A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FD-01A-11D-A33E-09 chr23:46917884 G>A did not map to a codon.
Sequencing variant TCGA-L5-A8NJ-01A-11D-A36J-09 chr23:46887391 G>T did not map to a codon.
Sequencing variant TCGA-L5-A8NN-01A-11D-A37C-09 chr23:46887435 C>T did not map to a codon.
Sequencing variant TCGA-V5-AASX-01A-11D-A387-09 chr23:46857592 C>A did not map to a codon.
Sequencing variant TCGA-Z6-A8JD-01A-11D-A36J-09 chr23:46915567 C>T did not map to a codon.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr4:129783388 T>C maps to NM_024900.3 I504I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EX-01A-11D-A36J-09 chr4:129792507 A>G did not map to a codon.
Sequencing variant TCGA-IC-A6RF-01A-13D-A33E-09 chr9:123632124 G>T maps to NM_015651.1 R155R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8W8-01B-11D-A37C-09 chr9:96428129 G>A maps to NM_005392.3 P700P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49V-01A-11D-A247-09 chr20:34505481 G>A maps to NM_016436.4 V634V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr22:45289354 G>A maps to NM_138415.3 S314S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OR-01A-11D-A27G-09 chr22:45309797 C>T maps to NM_138415.3 T245T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GG-01A-11D-A37C-09 chr6:64421948 G>T maps to NM_015153.2 E1489*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASX-01A-11D-A387-09 chr6:64422151 G>A maps to NM_015153.2 T1556T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NQ-01A-11D-A36J-09 chr23:133547595 G>T did not map to a codon.
Sequencing variant TCGA-L5-A8NW-01A-11D-A37C-09 chr3:52457214 G>A maps to ENST00000454052 W344*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3YB-01A-11D-A247-09 chr23:53970564 A>C did not map to a codon.
Sequencing variant TCGA-L5-A8NN-01A-11D-A37C-09 chr23:54069145 C>T did not map to a codon.
Sequencing variant TCGA-L5-A8NR-01A-11D-A37C-09 chr23:54022144 C>T did not map to a codon.
Sequencing variant TCGA-R6-A6L6-01B-11D-A33E-09 chr23:54040951 G>T did not map to a codon.
Sequencing variant TCGA-VR-A8EW-01A-11D-A36J-09 chr23:54040939 T>C did not map to a codon.
Sequencing variant TCGA-LN-A49L-01A-11D-A247-09 chr6:79655197 C>T maps to NM_017934.5 V1549V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GO-01A-11D-A37C-09 chr23:71933720 C>T did not map to a codon.
Sequencing variant TCGA-IG-A97H-01A-11D-A387-09 chr23:71800901 C>T did not map to a codon.
Sequencing variant TCGA-L5-A88Z-01A-11D-A36J-09 chr23:71856231 G>T did not map to a codon.
Sequencing variant TCGA-LN-A7HW-01A-22D-A351-09 chr23:71876025 G>A did not map to a codon.
Sequencing variant TCGA-V5-AASW-01A-11D-A403-09 chr23:71855003 C>G did not map to a codon.
Sequencing variant TCGA-2H-A9GR-01A-12D-A37C-09 chr23:18936848 G>T did not map to a codon.
Sequencing variant TCGA-JY-A93F-01A-21D-A37C-09 chr23:18915364 C>T did not map to a codon.
Sequencing variant TCGA-L5-A8NE-01A-11D-A37C-09 chr23:18917321 G>A did not map to a codon.
Sequencing variant TCGA-L5-A8NK-01A-21D-A37C-09 chr23:18936847 C>T did not map to a codon.
Sequencing variant TCGA-VR-A8Q7-01A-11D-A37C-09 chr23:18954190 G>C did not map to a codon.
Sequencing variant TCGA-ZR-A9CJ-01B-11D-A387-09 chr23:18912338 G>A did not map to a codon.
Sequencing variant TCGA-IG-A8O2-01A-11D-A36J-09 chr16:47699943 G>A did not map to a codon.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr16:30767569 A>G maps to NM_000294.2 P208P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6XG-01B-11D-A33E-09 chr3:111632383 C>T maps to NM_001134438.1 D518D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8WC-01A-11D-A37C-09 chr3:111688670 C>T maps to NM_001134438.1 L1150L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8ER-01A-11D-A36J-09 chr3:111603467 G>T maps to NM_001134438.1 G182*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A5B8-01A-11D-A28B-09 chr18:60646372 G>T maps to NM_194449.2 R1621R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FB-01A-11D-A33E-09 chr18:60646274 G>T maps to NM_194449.2 E1589*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr18:60645904 C>T maps to NM_194449.2 G1465G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OJ-01A-11D-A27G-09 chr17:47301622 C>A maps to NM_001143804.1 V288V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88Z-01A-11D-A36J-09 chr11:71952304 G>A maps to NM_005169.3 S82S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GM-01A-11D-A37C-09 chr11:608011 C>T maps to ENST00000264555 P852P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FH-01A-11D-A33E-09 chr11:601668 C>T maps to ENST00000264555 R374*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OQ-01A-11D-A27G-09 chr11:597554 G>A maps to ENST00000264555 T293T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88V-01A-11D-A351-09 chr1:114269062 T>C maps to NM_006608.2 G155G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr7:77569844 C>T maps to ENST00000427986 R581*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6Y2-01B-11D-A33E-09 chr10:13322987 G>A maps to NM_006214.3 S317S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NS-01A-12D-A37C-09 chr10:60994183 C>G maps to NM_032439.3 S76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49O-01A-11D-A247-09 chr6:36927006 C>T maps to NM_153370.2 G86G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A891-01A-11D-A36J-09 chr4:25254043 G>T maps to NM_018323.3 E124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FA-01A-11D-A33E-09 chr22:21161743 G>T maps to NM_058004.2 A300A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KH-A6WC-01A-11D-A33E-09 chr22:21083683 G>T maps to NM_058004.2 I1475I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr22:21119498 C>T maps to NM_058004.2 E763E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr22:21161674 C>T maps to NM_058004.2 L323L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49L-01A-11D-A247-09 chr22:21064263 G>C maps to NM_058004.2 V1977V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8WG-01A-11D-A37C-09 chr22:21064215 G>T maps to NM_058004.2 G1993G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A5U5-01A-21D-A28B-09 chr1:151278722 G>A maps to NM_002651.2 P445P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-M9-A5M8-01A-11D-A28B-09 chr18:44424025 C>T maps to NM_004671.2 L344L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GG-01A-11D-A37C-09 chr19:4013273 C>G maps to NM_015897.2 L127L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr19:4033557 C>T maps to NM_015897.2 Y374Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A893-01A-11D-A36J-09 chr11:85685804 G>T maps to ENST00000393343 Y638*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A97I-01A-11D-A387-09 chr2:229890404 G>T maps to NM_017933.4 I230I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49P-01A-11D-A247-09 chr2:229890644 C>T maps to NM_017933.4 G150G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A6-01A-11D-A27G-09 chr1:172411231 T>C maps to NM_153747.1 L177L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XP-A8T8-01A-11D-A36J-09 chr2:46842240 G>T maps to NM_002643.3 I21I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GO-01A-11D-A37C-09 chr9:35091858 C>A maps to NM_032634.2 A675A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8Q7-01A-11D-A37C-09 chr9:35092617 C>T maps to NM_032634.2 P422P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr21:38439661 T>C maps to NM_153681.2 L82L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NR-01A-11D-A37C-09 chr16:633345 C>T maps to NM_148920.1 P665P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr1:207112679 G>A maps to NM_002644.3 Q58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FP-01A-31D-A387-09 chr1:207110473 C>T maps to NM_002644.3 S337S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3YB-01A-11D-A247-09 chr17:26883214 G>A maps to NM_033198.3 R384*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6XQ-01B-11D-A33E-09 chr17:26898141 C>T maps to NM_033198.3 P33P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OF-01A-11D-A27G-09 chr17:34893066 G>A maps to NM_178517.3 L39L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EU-01A-11D-A36J-09 chr3:196460739 A>T maps to NM_001166304.1 V266V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A8O2-01A-11D-A36J-09 chr10:98469468 C>T maps to NM_152309.2 P95P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49K-01A-11D-A247-09 chr11:17190417 C>A maps to NM_002645.2 E291*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A5U5-01A-21D-A28B-09 chr11:17111317 T>C maps to NM_002645.2 K1676K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GK-01A-11D-A37C-09 chr1:204426963 G>T maps to NM_002646.3 S535S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A97I-01A-11D-A387-09 chr18:39637871 A>T maps to ENST00000398870 G764G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A8I0-01A-11D-A36J-09 chr18:39647365 C>T maps to ENST00000398870 F847F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A891-01A-11D-A36J-09 chr1:9778915 C>T maps to ENST00000361110 Y360Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EZ-01A-11D-A36J-09 chr1:9784048 G>T maps to ENST00000361110 E897*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A8I0-01A-11D-A36J-09 chr5:67588171 C>A maps to ENST00000396611 Y334*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FA-01A-11D-A33E-09 chr19:18273932 C>G maps to NM_005027.2 L422L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6XG-01B-11D-A33E-09 chr19:18271373 G>T did not map to a codon.
Sequencing variant TCGA-R6-A6L6-01B-11D-A33E-09 chr1:46511588 C>A did not map to a codon.
Sequencing variant TCGA-L5-A8NS-01A-12D-A37C-09 chr3:130409452 G>A maps to NM_014602.2 L1048L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A8HZ-01A-11D-A36J-09 chr17:8793371 G>A maps to NM_001142633.1 I243I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A4P3-01A-11D-A27G-09 chr17:8731962 G>T maps to NM_001010855.2 R412R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr17:8736326 G>A maps to NM_001010855.2 H227H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49Y-01A-11D-A27G-09 chr17:8736254 C>T maps to NM_001010855.2 L251L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GH-01A-11D-A37C-09 chr2:209190823 G>T maps to NM_015040.3 E1097*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OT-01A-11D-A28B-09 chr2:209212733 C>T maps to NM_015040.3 G1787G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88Z-01A-11D-A36J-09 chr2:209150468 A>T maps to NM_015040.3 T211T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A8I0-01A-11D-A36J-09 chr2:209207314 C>T maps to NM_015040.3 R1657*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OU-01A-11D-A28B-09 chr7:99957138 C>T maps to ENST00000413850 L317L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RE-01A-11D-A33E-09 chr23:48772478 C>T did not map to a codon.
Sequencing variant TCGA-JY-A6FH-01A-11D-A33E-09 chr7:76982275 C>T maps to NM_017439.3 V492V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6Y2-01B-11D-A33E-09 chr7:142832371 G>T maps to NM_002652.2 E61*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OJ-01A-11D-A27G-09 chr19:3656453 G>T maps to NM_012398.2 V190V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A891-01A-11D-A36J-09 chr19:3653584 G>A maps to NM_012398.2 N208N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A9-01A-11D-A28B-09 chr19:3656453 G>A maps to NM_012398.2 V190V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FB-01A-11D-A33E-09 chr23:15474053 C>A did not map to a codon.
Sequencing variant TCGA-LN-A49M-01A-21D-A27G-09 chr23:15403202 G>C did not map to a codon.
Sequencing variant TCGA-2H-A9GN-01A-11D-A37C-09 chr17:10728671 C>A maps to NM_001101387.1 L97L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HW-01A-22D-A351-09 chr17:10728608 C>T maps to NM_001101387.1 Q118Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49X-01A-31D-A27G-09 chr22:28292538 C>T did not map to a codon.
Sequencing variant TCGA-R6-A6Y2-01B-11D-A33E-09 chr17:65628317 C>A maps to NM_012417.2 C142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OJ-01A-11D-A27G-09 chr12:123497205 G>A maps to NM_020845.2 P123P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8W5-01B-11D-A37C-09 chr12:123470822 C>T maps to NM_020845.2 T1267T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FR-01A-11D-A387-09 chr17:6380422 C>T maps to NM_031220.3 P337P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6XQ-01B-11D-A33E-09 chr17:6386931 G>A maps to NM_031220.3 V164V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8WG-01A-11D-A37C-09 chr17:6381944 G>T maps to NM_031220.3 V233V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr4:111543526 G>T maps to NM_000325.5 P30P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6L4-01A-11D-A31U-09 chr4:111543489 G>A maps to NM_000325.5 Q43*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RE-01A-11D-A33E-09 chr12:130833810 T>C maps to NM_004764.4 T254T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NS-01A-12D-A37C-09 chr12:130833903 C>T maps to NM_004764.4 N285N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A8JD-01A-11D-A36J-09 chr12:130847364 C>G maps to NM_004764.4 L675L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr8:22211816 G>A maps to NM_001135721.1 R897R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OM-01A-11D-A27G-09 chr23:68382749 C>A did not map to a codon.
Sequencing variant TCGA-RE-A7BO-01A-11D-A33E-09 chr23:68382726 C>T did not map to a codon.
Sequencing variant TCGA-L5-A4OU-01A-11D-A28B-09 chr16:2158501 C>T maps to NM_001009944.2 A2222A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NF-01A-11D-A37C-09 chr16:2144122 G>A maps to NM_001009944.2 Q3530*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NI-01A-11D-A37C-09 chr16:2164866 G>A maps to NM_001009944.2 H719H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L7-A6VZ-01A-12D-A33E-09 chr16:2161498 C>A maps to NM_001009944.2 V1223V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HW-01A-22D-A351-09 chr16:2160142 G>A maps to NM_001009944.2 A1675A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr7:47852864 G>A maps to NM_138295.3 I2400I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NW-01A-11D-A37C-09 chr7:47979805 G>T maps to NM_138295.3 S90*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EU-01A-11D-A36J-09 chr7:47921600 G>T maps to NM_138295.3 P1116P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A4P3-01A-11D-A27G-09 chr4:88957370 G>T did not map to a codon.
Sequencing variant TCGA-LN-A49U-01A-31D-A27G-09 chr4:88977398 C>T maps to NM_000297.2 F626F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EZ-01A-11D-A36J-09 chr5:137260763 G>A maps to ENST00000230643 K529K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr2:42280449 C>G maps to NM_138370.2 A237A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43C-01A-11D-A247-09 chr22:46653521 C>A maps to NM_006071.1 E1900*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GM-01A-11D-A37C-09 chr6:51524567 A>C maps to NM_138694.3 T3452T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43E-01A-11D-A247-09 chr6:51893045 C>T maps to NM_138694.3 S1156S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OE-01A-11D-A27G-09 chr6:51777374 C>A did not map to a codon.
Sequencing variant TCGA-L5-A4OW-01A-11D-A28B-09 chr6:51935813 G>A maps to NM_138694.3 G219G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NE-01A-11D-A37C-09 chr6:51924833 C>T maps to NM_138694.3 R375R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NF-01A-11D-A37C-09 chr6:51503710 G>T maps to NM_138694.3 Y3814*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FQ-01A-31D-A387-09 chr6:51523790 C>T maps to NM_138694.3 G3711G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q9-A6FU-01A-11D-A31U-09 chr6:51483923 G>A maps to NM_138694.3 F4060F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A8JE-01A-11D-A37C-09 chr6:51824752 T>C maps to NM_138694.3 Q1941Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3I8-01A-11D-A247-09 chr8:110417359 G>C did not map to a codon.
Sequencing variant TCGA-L5-A8NH-01A-11D-A37C-09 chr8:110477199 T>C maps to ENST00000426474 L2713L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A1-01A-21D-A27G-09 chr8:110466968 C>T maps to ENST00000426474 S2254S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FQ-01A-31D-A387-09 chr8:110442219 G>A maps to ENST00000426474 W1061*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6XG-01B-11D-A33E-09 chr8:110527509 G>T maps to ENST00000426474 E3890*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NQ-01A-11D-A36J-09 chr20:43243229 C>T maps to NM_181805.1 F11F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93E-01A-11D-A37C-09 chr1:155261728 C>T did not map to a codon.
Sequencing variant TCGA-V5-AASW-01A-11D-A403-09 chr1:155265485 C>T maps to ENST00000423816 A140A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49M-01A-21D-A27G-09 chr15:72502158 G>A maps to ENST00000419739 L214L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FP-01A-31D-A387-09 chr19:14578587 C>A maps to NM_213560.1 R629R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr21:44433176 G>T did not map to a codon.
Sequencing variant TCGA-L5-A893-01A-11D-A36J-09 chr11:125301194 G>A maps to NM_022062.2 E442E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA7D-01A-11D-A403-09 chr12:32977059 C>T maps to NM_004572.3 A575A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3I8-01A-11D-A247-09 chr2:159526238 C>T maps to NM_003628.3 Y912Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93F-01A-21D-A37C-09 chr2:159488427 G>A maps to NM_003628.3 Q439Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NE-01A-11D-A37C-09 chr2:159514661 C>A maps to NM_003628.3 S643S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A9-01A-11D-A28B-09 chr3:119347679 G>A maps to NM_015900.2 K418K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NF-01A-11D-A37C-09 chr15:42292153 G>T maps to NM_001080490.1 L270L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr15:42437800 C>T maps to ENST00000397272 E586E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A8JD-01A-11D-A36J-09 chr15:42444891 C>A maps to ENST00000397272 E199*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr22:38541584 A>G maps to NM_003560.2 Y95Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr6:144263028 G>A maps to NM_001080951.1 T308T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49S-01A-11D-A247-09 chr8:42038180 G>T maps to NM_000930.3 Y304*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49X-01A-31D-A27G-09 chr8:42037507 C>T maps to NM_000930.3 P433P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FP-01A-31D-A387-09 chr2:28820875 G>T maps to NM_153021.4 G776*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6KZ-01A-11D-A31U-09 chr2:28804939 C>T maps to NM_153021.4 H524H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3Y9-01A-12D-A247-09 chr12:14664607 G>A maps to NM_024829.5 S294S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A7DP-01A-31D-A33E-09 chr12:14656852 G>T maps to NM_024829.5 S505S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GO-01A-11D-A37C-09 chr12:113806983 C>T maps to NM_173542.3 A118A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A9VB-01A-21D-A37C-09 chr12:113806938 G>A maps to NM_173542.3 L103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RE-01A-11D-A33E-09 chr20:8630089 T>G maps to NM_015192.2 S196S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NN-01A-11D-A37C-09 chr15:40594184 G>A maps to NM_004573.2 L185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OS-01A-11D-A28B-09 chr20:9389319 A>T maps to NM_001172646.1 S610S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NF-01A-11D-A37C-09 chr20:9449233 C>T maps to NM_001172646.1 R1089*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FG-01A-11D-A33E-09 chr3:38049855 G>T maps to NM_001130964.1 V656V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93E-01A-11D-A37C-09 chr3:38058148 G>A maps to NM_001130964.1 F108F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HX-01A-11D-A33E-09 chr2:219492939 G>T maps to ENST00000432688 E321*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GL-01A-12D-A37C-09 chr10:96030304 G>T maps to ENST00000371380 S1484S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OJ-01A-11D-A27G-09 chr10:96084762 G>T maps to ENST00000371380 E2279*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HX-01A-11D-A33E-09 chr10:96022422 C>G maps to ENST00000371380 L1329L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XP-A8T7-01A-11D-A36J-09 chr10:95993927 G>A maps to ENST00000371380 V691V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88W-01A-11D-A351-09 chr16:81942085 G>A maps to NM_002661.2 T541T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8WC-01A-11D-A37C-09 chr16:81934351 G>T maps to NM_002661.2 S443S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43M-01A-11D-A247-09 chr3:155212208 G>T maps to ENST00000340059 L652L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L7-A6VZ-01A-12D-A33E-09 chr3:155200037 G>T maps to ENST00000340059 T1267T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A8-01A-32D-A27G-09 chr3:155267677 C>T maps to ENST00000340059 L408L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OU-01A-11D-A28B-09 chr2:198953694 C>T maps to NM_006226.3 V943V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GG-01A-11D-A37C-09 chr3:17051593 T>G maps to NM_001144382.1 Y248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GK-01A-11D-A37C-09 chr23:205430 C>T did not map to a codon.
Sequencing variant TCGA-Q9-A6FU-01A-11D-A31U-09 chr5:41510616 A>T maps to NM_001005473.2 S4S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FB-01A-11D-A33E-09 chr3:171453399 C>A maps to NM_002662.3 E106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q9-A6FU-01A-11D-A31U-09 chr17:4721812 C>T maps to NM_002663.3 Y678Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GR-01A-12D-A37C-09 chr1:242277235 G>T maps to NM_152666.2 I342I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A4P3-01A-11D-A27G-09 chr1:242271124 A>G maps to NM_152666.2 L363L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FB-01A-11D-A33E-09 chr1:242271091 G>A maps to NM_152666.2 R374*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FH-01A-11D-A33E-09 chr1:242253188 G>A maps to NM_152666.2 D526D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-A7RB-01A-11D-A351-09 chr1:242271124 A>G maps to NM_152666.2 L363L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3Y9-01A-12D-A247-09 chr8:144996791 C>T maps to NM_201380.2 E2572E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A5B8-01A-11D-A28B-09 chr8:144995123 G>T maps to NM_201380.2 I3092I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr8:144994399 G>A maps to NM_201380.2 Q3334*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OJ-01A-11D-A27G-09 chr8:144995420 G>A maps to NM_201380.2 P2993P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NG-01A-11D-A37C-09 chr8:144994003 C>A maps to NM_201380.2 E3466*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NI-01A-11D-A37C-09 chr8:145001216 C>T maps to NM_201380.2 A1428A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr8:144994757 G>A maps to NM_201380.2 T3214T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr8:38809685 C>T maps to NM_021623.1 N163N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr2:179350398 T>C maps to NM_019091.3 N24N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA4G-01A-11D-A37C-09 chr2:179355542 T>C did not map to a codon.
Sequencing variant TCGA-LN-A7HY-01A-12D-A351-09 chr12:19496361 G>T maps to ENST00000317589 E783*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49V-01A-11D-A247-09 chr1:204237353 C>T maps to ENST00000367191 A63A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A97I-01A-11D-A387-09 chr11:16872791 G>A maps to ENST00000448080 Y214Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NL-01A-12D-A37C-09 chr11:16877391 C>T maps to ENST00000448080 T125T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49W-01A-11D-A27G-09 chr12:45568028 T>C maps to ENST00000256692 K40K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-AAPN-01A-11D-A403-09 chr12:45567422 C>T maps to ENST00000256692 K242K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49S-01A-11D-A247-09 chr14:65210414 C>T maps to ENST00000394691 V1218V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49V-01A-11D-A247-09 chr14:65197519 C>T maps to ENST00000394691 S190S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FH-01A-11D-A33E-09 chr1:6530818 G>T maps to NM_198681.2 R583R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XP-A8T7-01A-11D-A36J-09 chr1:6533204 G>T maps to NM_198681.2 G352G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NR-01A-11D-A37C-09 chr12:6428023 C>T maps to NM_001144856.1 C463C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49R-01A-11D-A247-09 chr12:6427984 G>A maps to NM_001144856.1 K450K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NV-01A-11D-A37C-09 chr2:43965590 G>T maps to NM_172069.3 E1019*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-A7RB-01A-11D-A351-09 chr17:40823100 G>A maps to NM_024927.4 N444N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A4QS-01A-11D-A27G-09 chr17:43545712 T>C maps to NM_014798.2 V390V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OU-01A-11D-A28B-09 chr17:43530940 G>A maps to NM_014798.2 A759A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HV-01A-21D-A351-09 chr1:16053913 G>A maps to ENST00000420314 P552P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XP-A8T6-01A-11D-A36J-09 chr15:65157915 G>A maps to NM_025201.4 E434E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A1-01A-21D-A27G-09 chr6:161152208 T>G maps to NM_000301.3 V461V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GF-01A-11D-A37C-09 chr15:90208852 C>G maps to NM_002666.4 L510L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FH-01A-11D-A33E-09 chr9:19121076 G>A maps to NM_001122.2 S132S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6Y2-01B-11D-A33E-09 chr19:4847711 G>T maps to NM_005817.4 V275V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-M9-A5M8-01A-11D-A28B-09 chr19:4510467 C>T maps to NM_001080400.1 A1154A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA7B-01A-31D-A403-09 chr19:4512993 A>G maps to NM_001080400.1 S312S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A891-01A-11D-A36J-09 chr19:4529802 G>T maps to NM_001013706.2 S111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q9-A6FU-01A-11D-A31U-09 chr20:21106770 C>T maps to NM_018474.4 L5L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A893-01A-11D-A36J-09 chr5:57750817 G>T maps to NM_006622.2 R596R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49M-01A-21D-A27G-09 chr1:45269889 G>C maps to NM_004073.2 L438L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A4P3-01A-11D-A27G-09 chr4:128811265 G>T maps to NM_014264.4 E569*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GR-01A-12D-A37C-09 chr1:12009873 G>A maps to ENST00000376369 S118S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A2-01A-31D-A27G-09 chr1:12008069 C>T maps to ENST00000376369 T85T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-AAPN-01A-11D-A403-09 chr1:12012750 C>T maps to ENST00000376369 Q227*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OU-01A-11D-A28B-09 chr3:145790410 T>C maps to NM_182943.2 K595K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A4P3-01A-11D-A27G-09 chr23:103040563 G>T did not map to a codon.
Sequencing variant TCGA-JY-A6FA-01A-11D-A33E-09 chr23:49028405 C>T did not map to a codon.
Sequencing variant TCGA-V5-AASW-01A-11D-A403-09 chr4:155458496 G>T maps to NM_002669.2 R476R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q9-A6FU-01A-11D-A31U-09 chr3:142383111 G>A maps to NM_001172312.1 E11E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OW-01A-11D-A28B-09 chr23:114863594 G>T did not map to a codon.
Sequencing variant TCGA-R6-A6Y2-01B-11D-A33E-09 chr17:7296933 C>A maps to NM_020360.2 E77*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FE-01A-11D-A33E-09 chr3:145912919 G>T maps to NM_020353.2 C312*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6F8-01A-11D-A33E-09 chr20:44536518 C>T maps to NM_006227.2 T170T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FB-01A-11D-A33E-09 chr19:17487875 G>T maps to NM_031310.1 L74L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KH-A6WC-01A-11D-A33E-09 chr19:17487776 G>A maps to NM_031310.1 R107R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASV-01A-11D-A387-09 chr19:17476375 C>A maps to NM_031310.1 E300*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GR-01A-12D-A37C-09 chr3:126737154 G>T maps to NM_032242.3 E1227*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr3:126708215 G>A maps to NM_032242.3 T260T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A5U7-01A-11D-A31U-09 chr3:126708350 G>T maps to NM_032242.3 A305A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8WG-01A-11D-A37C-09 chr3:126749108 C>T maps to NM_032242.3 D1695D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-A7RC-01B-11D-A403-09 chr3:126748338 C>T maps to NM_032242.3 I1610I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3Y9-01A-12D-A247-09 chr1:208390940 G>A maps to NM_025179.3 L109L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A50L-01A-11D-A27G-09 chr1:208225787 G>T maps to NM_025179.3 L959L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43E-01A-11D-A247-09 chr1:208390628 G>A maps to NM_025179.3 L213L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NL-01A-12D-A37C-09 chr1:208217904 C>T maps to NM_025179.3 L1274L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49S-01A-11D-A247-09 chr1:208391108 C>T maps to NM_025179.3 L53L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RE-A7BO-01A-11D-A33E-09 chr1:208391186 C>T maps to NM_025179.3 L27L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HY-01A-12D-A351-09 chr23:153697204 A>T did not map to a codon.
Sequencing variant TCGA-Q9-A6FU-01A-11D-A31U-09 chr23:153695950 G>T did not map to a codon.
Sequencing variant TCGA-Q9-A6FU-01A-11D-A31U-09 chr23:153698329 C>T did not map to a codon.
Sequencing variant TCGA-L5-A88Z-01A-11D-A36J-09 chr7:131913110 G>A maps to NM_020911.1 N574N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NT-01A-11D-A37C-09 chr7:131831445 C>T maps to NM_020911.1 R1626R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q9-A6FW-01A-31D-A31U-09 chr7:131853148 G>A maps to NM_020911.1 Y1400Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8WG-01A-11D-A37C-09 chr7:131895860 G>T maps to NM_020911.1 P713P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43I-01A-11D-A247-09 chr3:48465420 A>T maps to NM_001130082.1 Y200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr3:48454261 G>A maps to NM_001130082.1 R1581R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EU-01A-11D-A36J-09 chr3:48456237 C>T maps to NM_001130082.1 R1393R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EU-01A-11D-A36J-09 chr22:50728476 G>A maps to NM_012401.2 N179N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EY-01A-11D-A36J-09 chr22:50728206 G>T maps to NM_012401.2 P269P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr23:153044129 G>A did not map to a codon.
Sequencing variant TCGA-L5-A4OP-01A-11D-A27G-09 chr23:153033155 G>A did not map to a codon.
Sequencing variant TCGA-L5-A4OW-01A-11D-A28B-09 chr23:153038999 C>A did not map to a codon.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr23:153043746 G>A did not map to a codon.
Sequencing variant TCGA-L5-A8NS-01A-12D-A37C-09 chr23:153037062 C>A did not map to a codon.
Sequencing variant TCGA-L5-A8NE-01A-11D-A37C-09 chr12:94562963 C>T maps to NM_005761.1 I366I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4ON-01A-11D-A27G-09 chr3:129288770 G>A maps to NM_015103.2 I1260I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6DN-01B-11D-A31U-09 chr3:129292498 G>A maps to NM_015103.2 H925H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA4G-01A-11D-A37C-09 chr20:56284578 G>A maps to NM_020182.3 V20V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A8JE-01A-11D-A37C-09 chr20:56227195 G>T maps to NM_020182.3 T259T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A5U7-01A-11D-A31U-09 chr16:72159998 C>T maps to NM_031293.2 L707L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A8I0-01A-11D-A36J-09 chr16:72188211 C>T maps to NM_031293.2 L104L. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-2H-A9GK-01A-11D-A37C-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-LN-A4A9-01A-11D-A28B-09 chr22:41980058 T>C maps to NM_002676.2 G126G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A4P3-01A-11D-A27G-09 chr17:15142815 G>T maps to NM_000304.2 Y97*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4MQ-01A-11D-A28B-09 chr17:15134263 G>T maps to NM_000304.2 V151V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FH-01A-11D-A33E-09 chr9:139310794 G>T maps to NM_015160.1 L195L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RE-01A-11D-A33E-09 chr7:102950883 C>A maps to NM_004279.2 S372S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EP-01A-31D-A403-09 chr7:102939016 A>T maps to NM_004279.2 S34S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A2-01A-31D-A27G-09 chr2:190732644 A>G maps to NM_000534.4 K821K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A8JE-01A-11D-A37C-09 chr2:190660631 C>T maps to NM_000534.4 Y90Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FP-01A-31D-A387-09 chr7:6045568 T>C maps to NM_000535.5 V39V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A6QS-01A-12D-A33E-09 chr23:152936412 G>T did not map to a codon.
Sequencing variant TCGA-S8-A6BV-01A-21D-A31U-09 chr6:160239686 G>A did not map to a codon.
Sequencing variant TCGA-2H-A9GQ-01A-11D-A37C-09 chr10:118351286 A>G maps to NM_006229.2 K18K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A893-01A-11D-A36J-09 chr10:118354276 C>T maps to NM_006229.2 C122C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-AAPN-01A-11D-A403-09 chr10:118383541 C>T maps to NM_005396.4 F46F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OW-01A-11D-A28B-09 chr10:118236292 A>G maps to NM_001011709.2 A434A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A8HZ-01A-11D-A36J-09 chr10:118220678 G>T did not map to a codon.
Sequencing variant TCGA-LN-A9FP-01A-31D-A387-09 chr23:152226334 G>C did not map to a codon.
Multiple mappings detected for codon TCGA-L5-A4OW-01A-11D-A28B-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-L5-A4OW-01A-11D-A28B-09 chr17:37826275 G>A maps to NM_002686.3 Q161Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A5-01A-21D-A27G-09 chr14:39650488 G>T maps to NM_002687.3 E526*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GM-01A-11D-A37C-09 chr2:68389785 T>A maps to NM_020143.2 L204*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49M-01A-21D-A27G-09 chr22:44330532 C>T maps to NM_025225.2 F248F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NJ-01A-11D-A36J-09 chr23:7870083 C>T did not map to a codon.
Sequencing variant TCGA-LN-A4A1-01A-21D-A27G-09 chr19:7622120 C>T maps to NM_001166111.1 P1126P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6XG-01B-11D-A33E-09 chr19:7620582 C>T maps to NM_001166111.1 I1019I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr5:74984888 T>C maps to NM_001099271.1 V359V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OE-01A-11D-A27G-09 chr1:53544108 C>A maps to NM_153703.4 R357R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L7-A6VZ-01A-12D-A33E-09 chr7:131191443 G>A maps to NM_001018111.2 C381C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FB-01A-11D-A33E-09 chr3:127379569 G>T maps to NM_015720.2 V233V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A5U7-01A-11D-A31U-09 chr3:127390275 G>C did not map to a codon.
Sequencing variant TCGA-R6-A6Y0-01B-11D-A33E-09 chr3:127387366 G>T maps to NM_015720.2 G430G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NU-01A-11D-A36J-09 chr23:84600955 C>T did not map to a codon.
Sequencing variant TCGA-L7-A6VZ-01A-12D-A33E-09 chr23:84563181 G>C did not map to a codon.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr1:166818616 C>T maps to NM_017542.3 A267A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OH-01A-11D-A27G-09 chr1:151396521 G>T maps to NM_015100.3 R476R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr23:24735596 C>A did not map to a codon.
Sequencing variant TCGA-VR-AA7I-01A-11D-A403-09 chr8:42214741 G>T did not map to a codon.
Sequencing variant TCGA-VR-AA4D-01A-11D-A37C-09 chr7:44155473 T>A maps to NM_006230.2 G346G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OG-01A-11D-A27G-09 chr17:26678701 G>A maps to NM_015584.3 Y248Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OE-01A-11D-A27G-09 chr12:133219195 C>T maps to ENST00000455752 K1619K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NK-01A-21D-A37C-09 chr12:133219480 G>A maps to ENST00000455752 H1554H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L7-A6VZ-01A-12D-A33E-09 chr12:133244226 G>A maps to ENST00000455752 C730C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49Y-01A-11D-A27G-09 chr12:133201571 C>A maps to ENST00000455752 L2225L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X8-AAAR-01A-11D-A403-09 chr12:133233955 G>T maps to ENST00000455752 T1149T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-AAPN-01A-11D-A403-09 chr12:133226307 G>T maps to ENST00000455752 P1253P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RF-01A-13D-A33E-09 chr15:89869958 G>T maps to NM_002693.2 P532P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NK-01A-21D-A37C-09 chr15:89862173 A>T maps to NM_002693.2 A1087A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RE-01A-11D-A33E-09 chr3:121179010 A>C maps to ENST00000393672 R2482R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr3:121208120 G>T maps to ENST00000393672 P1355P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L7-A6VZ-01A-12D-A33E-09 chr3:121230839 G>C maps to ENST00000393672 S638*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49U-01A-31D-A27G-09 chr3:121260275 G>T maps to ENST00000393672 R265R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6Y0-01B-11D-A33E-09 chr3:121207907 T>C maps to ENST00000393672 R1426R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RE-A7BO-01A-11D-A33E-09 chr3:121208591 C>T maps to ENST00000393672 A1198A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A4P3-01A-11D-A27G-09 chr2:86258455 G>T maps to NM_015425.3 C1525*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6F8-01A-11D-A33E-09 chr2:86281400 C>T maps to NM_015425.3 T690T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OH-01A-11D-A27G-09 chr2:86258677 G>T maps to NM_015425.3 P1451P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr2:86302260 G>A maps to NM_015425.3 D501D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NS-01A-12D-A37C-09 chr2:113332934 A>C maps to NM_019014.4 R1013R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-AAPN-01A-11D-A403-09 chr2:113331137 G>A did not map to a codon.
Sequencing variant TCGA-L5-A4OS-01A-11D-A28B-09 chr17:7415273 C>T maps to NM_000937.4 R1416*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49V-01A-11D-A247-09 chr3:184086033 C>T maps to NM_006232.2 F135F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASW-01A-11D-A403-09 chr3:184081315 G>C maps to NM_006232.2 V12V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASW-01A-11D-A403-09 chr3:184081339 G>A maps to NM_006232.2 K20K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A4P3-01A-11D-A27G-09 chr7:102119271 G>C maps to ENST00000393794 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NR-01A-11D-A37C-09 chr10:79753092 G>T maps to NM_007055.3 C883*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OS-01A-11D-A28B-09 chr12:106831540 G>T maps to NM_018082.5 E647*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A891-01A-11D-A36J-09 chr5:89802442 C>T maps to NM_006467.2 D179D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A2-01A-31D-A27G-09 chr16:97515 G>A maps to NM_016310.3 Q81*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr19:621240 G>A maps to NM_005035.3 D819D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A8I0-01A-11D-A36J-09 chr7:72413093 C>T maps to ENST00000434423 T854T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6XQ-01B-11D-A33E-09 chr1:46662689 G>A maps to ENST00000371986 R63*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A8O2-01A-11D-A36J-09 chr13:29242659 G>A maps to NM_015932.5 Q71Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr13:29238657 G>T maps to NM_015932.5 V38V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GI-01A-11D-A37C-09 chr7:76240861 T>A maps to NM_012230.3 K162*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FO-01A-11D-A387-09 chr7:76254992 G>A maps to NM_012230.3 Q25*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA7B-01A-31D-A403-09 chr7:95001649 C>A maps to NM_000940.2 G68*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88S-01A-11D-A36J-09 chr8:99139842 C>T maps to NM_015029.2 R55*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OP-01A-11D-A27G-09 chr23:48368280 G>A did not map to a codon.
Sequencing variant TCGA-2H-A9GG-01A-11D-A37C-09 chr13:38154737 T>A maps to NM_006475.2 K497*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr13:38164538 C>T maps to NM_006475.2 P137P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NL-01A-12D-A37C-09 chr13:38151911 T>C maps to NM_006475.2 K662K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZR-A9CJ-01B-11D-A387-09 chr13:38154785 T>A maps to NM_006475.2 R481*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OT-01A-11D-A28B-09 chr18:14537831 A>G maps to ENST00000444806 L260L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49R-01A-11D-A247-09 chr18:14542752 C>T maps to ENST00000444806 P131P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GN-01A-11D-A37C-09 chr2:132021883 C>T maps to NM_001083538.1 N952N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr2:131985954 G>A did not map to a codon.
Sequencing variant TCGA-V5-AASX-01A-11D-A387-09 chr2:132021598 C>T maps to NM_001083538.1 D857D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr2:130868114 C>T did not map to a codon.
Sequencing variant TCGA-L5-A8NE-01A-11D-A37C-09 chr14:19563511 A>G maps to NM_001005356.2 R342R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49R-01A-11D-A247-09 chr14:19574338 G>T maps to NM_001005356.2 E466*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr14:20002278 C>A maps to ENST00000439503 L466L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A8JE-01A-11D-A37C-09 chr14:20020112 C>T maps to ENST00000439503 R36R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49L-01A-11D-A247-09 chr1:167343526 C>T maps to NM_002697.3 I195I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RE-01A-11D-A33E-09 chr6:99282802 C>A maps to NM_005604.2 I18I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KH-A6WC-01A-11D-A33E-09 chr2:105473303 G>T maps to NM_006236.1 E446*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HX-01A-11D-A33E-09 chr2:105473133 C>G maps to NM_006236.1 S389*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr23:82763399 C>T did not map to a codon.
Sequencing variant TCGA-IG-A5B8-01A-11D-A28B-09 chr4:147561863 C>T maps to NM_004575.2 I378I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASV-01A-11D-A387-09 chr4:147560492 A>C maps to NM_004575.2 G67G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASX-01A-11D-A387-09 chr4:147561443 G>A maps to NM_004575.2 A238A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr5:145719655 G>A maps to NM_002700.2 S222S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr5:145719505 C>T maps to NM_002700.2 A172A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr6:31132948 G>A maps to NM_002701.4 Q258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L7-A6VZ-01A-12D-A33E-09 chr8:128428572 G>A maps to NM_001159542.1 K154K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr5:93076992 G>A maps to NM_153216.1 R93*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A4QS-01A-11D-A27G-09 chr7:39379319 T>C maps to NM_007252.3 P197P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6DQ-01B-11D-A31U-09 chr7:39472857 G>A maps to NM_007252.3 L403L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6L4-01A-11D-A31U-09 chr5:54721116 C>A maps to NM_176895.1 E259*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr9:134183418 C>T maps to NM_032728.3 Y187Y. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-L5-A4OI-01A-11D-A27G-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-Z6-AAPN-01A-11D-A403-09 chr6:35392449 C>T maps to NM_006238.4 F324F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-AAPN-01A-11D-A403-09 chr3:12447447 C>T maps to NM_015869.4 I229I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EQ-01A-11D-A36J-09 chr4:23815506 C>T maps to NM_013261.3 L533L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NQ-01A-11D-A36J-09 chr5:149206270 C>T maps to NM_133263.3 L96L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HV-01A-21D-A351-09 chr23:18845420 C>T did not map to a codon.
Sequencing variant TCGA-L5-A8NT-01A-11D-A37C-09 chr4:76785641 G>A maps to NM_006239.2 N653N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A8JD-01A-11D-A36J-09 chr11:70218319 G>C did not map to a codon.
Sequencing variant TCGA-2H-A9GQ-01A-11D-A37C-09 chr12:81655761 C>T maps to NM_003625.2 *1258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASX-01A-11D-A387-09 chr19:49636265 G>A maps to NM_003660.2 A296A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L7-A6VZ-01A-12D-A33E-09 chr11:7631632 G>T maps to NM_003621.2 E200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q9-A6FW-01A-31D-A31U-09 chr11:7670438 C>T maps to NM_003621.2 D657D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA7D-01A-11D-A403-09 chr12:42778781 A>G maps to NM_016488.6 E184E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93E-01A-11D-A37C-09 chr7:44839009 C>T maps to NM_021130.3 S40S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A938-01A-11D-A37C-09 chr15:64455068 C>G maps to NM_000942.4 G39G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6DN-01B-11D-A31U-09 chr4:159642594 G>T maps to NM_005038.2 P42P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KH-A6WC-01A-11D-A33E-09 chr6:149847909 C>A maps to NM_139126.2 V227V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6L6-01B-11D-A33E-09 chr6:149856808 C>T maps to NM_139126.2 V129V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L7-A6VZ-01A-12D-A33E-09 chr15:43851029 G>T maps to NM_001130858.2 C1116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A51D-01A-11D-A27G-09 chr16:4938210 C>T maps to NM_002705.4 E802E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GI-01A-11D-A37C-09 chr17:58740748 C>T maps to NM_003620.3 R552*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FD-01A-11D-A33E-09 chr17:58700915 C>T maps to NM_003620.3 S169S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NK-01A-21D-A37C-09 chr17:58740433 G>T maps to NM_003620.3 E447*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr22:22287852 G>A maps to NM_014634.3 R219R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EU-01A-11D-A36J-09 chr4:89198298 A>G maps to NM_152542.3 A179A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FD-01A-11D-A33E-09 chr1:161140273 G>T maps to NM_001122764.1 E355*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49Y-01A-11D-A27G-09 chr11:67168162 C>A maps to NM_001008709.1 E150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NR-01A-11D-A37C-09 chr2:29006801 C>T maps to NM_002709.2 Q184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6XQ-01B-11D-A33E-09 chr12:80211230 A>G maps to NM_001143885.1 A394A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NW-01A-11D-A37C-09 chr1:202549678 G>T maps to NM_002481.3 L980L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OP-01A-11D-A27G-09 chr14:104251167 G>A maps to NM_015316.2 R81*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr19:45899676 G>T maps to NM_001142502.1 R244R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A893-01A-11D-A36J-09 chr11:64012400 C>G did not map to a codon.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr11:64014016 C>G maps to NM_138689.2 G43G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93E-01A-11D-A37C-09 chr6:150569881 G>T maps to NM_030949.2 E142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NI-01A-11D-A37C-09 chr6:150569907 G>A maps to NM_030949.2 R150R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A9-01A-11D-A28B-09 chr15:41108161 C>T maps to NM_001130143.1 Q162Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr20:37529286 A>G maps to NM_015568.2 E177E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NQ-01A-11D-A36J-09 chr20:37536770 C>T maps to NM_015568.2 Q377*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HX-01A-11D-A33E-09 chr7:113518435 G>T maps to NM_002711.3 S904*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NJ-01A-11D-A36J-09 chr10:93389700 A>G maps to NM_005398.4 L313L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NV-01A-11D-A37C-09 chr10:93390346 C>A maps to NM_005398.4 A97A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GI-01A-11D-A37C-09 chr20:58514137 C>T maps to NM_006242.3 A283A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FG-01A-11D-A33E-09 chr23:49137872 G>T did not map to a codon.
Sequencing variant TCGA-L5-A8NL-01A-12D-A37C-09 chr7:94881071 A>C did not map to a codon.
Sequencing variant TCGA-R6-A8WG-01A-11D-A37C-09 chr7:94898625 G>T maps to NM_001166160.1 P977P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A5U7-01A-11D-A31U-09 chr11:111635630 T>A did not map to a codon.
Sequencing variant TCGA-LN-A4MQ-01A-11D-A28B-09 chr23:307472 T>C did not map to a codon.
Sequencing variant TCGA-Z6-A8JE-01A-11D-A37C-09 chr23:307470 C>T did not map to a codon.
Sequencing variant TCGA-L5-A43I-01A-11D-A247-09 chr11:64695823 C>T maps to NM_006244.3 L217L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4ON-01A-11D-A27G-09 chr4:102004362 G>T maps to NM_000944.4 A280A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OJ-01A-11D-A27G-09 chr8:22396989 G>T maps to ENST00000397775 E453*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3YC-01A-11D-A247-09 chr9:104356906 G>A maps to NM_147180.2 Y102Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A8I0-01A-11D-A36J-09 chr9:104356840 G>T maps to NM_147180.2 G124G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr18:9547801 C>T maps to NM_001042388.1 A946A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3I8-01A-11D-A247-09 chr14:94710983 C>T maps to NM_058237.1 L427L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A5B8-01A-11D-A28B-09 chr14:94722886 G>C maps to NM_058237.1 V652V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GR-01A-12D-A37C-09 chr10:103899459 G>T maps to NM_015062.3 E399*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NR-01A-11D-A37C-09 chr10:103906471 C>T maps to NM_015062.3 P1241P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A3-01A-11D-A27G-09 chr10:103901474 G>T maps to NM_015062.3 V1070V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NQ-01A-11D-A36J-09 chr17:42018992 C>A maps to NM_002722.3 L10L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NT-01A-11D-A37C-09 chr23:48755852 G>A did not map to a codon.
Sequencing variant TCGA-XP-A8T6-01A-11D-A36J-09 chr23:48759675 A>C did not map to a codon.
Sequencing variant TCGA-JY-A6FE-01A-11D-A33E-09 chr18:77710830 G>T maps to NM_025078.4 P32P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6L6-01B-11D-A33E-09 chr18:77679353 G>T maps to NM_025078.4 Y146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A8O2-01A-11D-A36J-09 chr19:8555252 C>T maps to NM_032152.4 E648E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NR-01A-11D-A37C-09 chr22:22890682 C>A maps to NM_206954.1 E446*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GO-01A-11D-A37C-09 chr1:12885132 T>C maps to NM_001146344.1 Q326Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OR-01A-11D-A27G-09 chr1:12835213 C>T maps to NM_001080830.1 S68S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GN-01A-11D-A37C-09 chr1:13716930 A>C maps to NM_001099851.1 R140R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NU-01A-11D-A36J-09 chr1:12942189 T>C maps to ENST00000376192 E120E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZR-A9CJ-01B-11D-A387-09 chr1:12943146 T>C maps to NM_001009611.2 Q23Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GQ-01A-11D-A37C-09 chr1:13000962 G>A maps to ENST00000415464 S240S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FA-01A-11D-A33E-09 chr1:13001127 C>T maps to ENST00000415464 L185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XP-A8T7-01A-11D-A36J-09 chr12:11506232 G>T maps to NM_005039.3 G268G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43I-01A-11D-A247-09 chr12:11546492 A>G maps to NM_006248.3 S173S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr12:11546378 T>C maps to NM_006248.3 K211K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RE-A7BO-01A-11D-A33E-09 chr12:11546189 A>G maps to NM_006248.3 P274P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S8-A6BV-01A-21D-A31U-09 chr12:11546375 A>G maps to NM_006248.3 P212P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA7B-01A-31D-A403-09 chr12:11546641 G>A maps to NM_006248.3 Q124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A97H-01A-11D-A387-09 chr12:11421032 G>A maps to NM_006249.4 T50T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6KZ-01A-11D-A31U-09 chr12:11461445 A>G maps to NM_002723.3 P157P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OE-01A-11D-A27G-09 chr11:82611354 G>T maps to NM_199418.2 G30G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6F8-01A-11D-A33E-09 chr6:106553657 C>A maps to NM_001198.3 P541P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FA-01A-11D-A33E-09 chr6:106553477 G>A maps to NM_001198.3 P481P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr6:106553729 G>A maps to NM_001198.3 P565P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43I-01A-11D-A247-09 chr11:129800979 A>G maps to NM_020228.2 H487H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88Z-01A-11D-A36J-09 chr11:129814908 T>C did not map to a codon.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr6:100062376 G>A maps to ENST00000359773 L632L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49P-01A-11D-A247-09 chr8:70964527 G>A maps to NM_024504.2 A500A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3Y9-01A-12D-A247-09 chr21:43221624 C>T maps to NM_022115.3 P1433P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88V-01A-11D-A351-09 chr21:43274681 G>A maps to NM_022115.3 G543G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NN-01A-11D-A37C-09 chr21:43256296 G>T maps to NM_022115.3 C767*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NT-01A-11D-A37C-09 chr1:3329151 C>T maps to NM_022114.3 S797S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EX-01A-11D-A36J-09 chr1:3342258 G>A maps to NM_022114.3 G1018G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6F8-01A-11D-A33E-09 chr4:121737721 G>A maps to NM_018699.2 Q251*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FB-01A-11D-A33E-09 chr4:121737989 G>T maps to NM_018699.2 S247*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASV-01A-11D-A387-09 chr4:81122550 C>T maps to NM_001099403.1 N109N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-AAPN-01A-11D-A403-09 chr4:81123143 C>T maps to NM_001099403.1 F176F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A4-01A-11D-A27G-09 chr5:23522918 G>T maps to NM_020227.2 L269L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASV-01A-11D-A387-09 chr5:23526879 T>C maps to NM_020227.2 F561F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XP-A8T8-01A-11D-A36J-09 chr5:23522933 C>T maps to NM_020227.2 G274G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XP-A8T8-01A-11D-A36J-09 chr5:23527044 C>A maps to NM_020227.2 G616G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A9VB-01A-21D-A37C-09 chr5:23522456 G>T maps to NM_020227.2 E185*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-AAPN-01A-11D-A403-09 chr5:23527656 C>T maps to NM_020227.2 L820L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OG-01A-11D-A27G-09 chr23:23685897 G>A did not map to a codon.
Sequencing variant TCGA-JY-A939-01A-12D-A37C-09 chr1:173450516 G>T maps to NM_004905.2 E50*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NG-01A-11D-A37C-09 chr1:173454532 G>T maps to NM_004905.2 E96*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OE-01A-11D-A27G-09 chr1:203452623 C>A maps to NM_201348.1 I104I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A4-01A-11D-A27G-09 chr1:203452623 C>T maps to NM_201348.1 I104I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49X-01A-31D-A27G-09 chr6:105729748 G>T maps to NM_002726.4 L570L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EW-01A-11D-A36J-09 chr2:44553862 C>T maps to NM_001171603.1 A578A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-AAPN-01A-11D-A403-09 chr2:44586683 C>T maps to NM_001171603.1 K57K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6Y2-01B-11D-A33E-09 chr20:47251237 G>A maps to NM_020820.3 Q1415*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GI-01A-11D-A37C-09 chr8:68930086 T>C maps to NM_024870.2 L50L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RE-01A-11D-A33E-09 chr8:68993021 C>T maps to NM_024870.2 D609D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OG-01A-11D-A27G-09 chr8:69058489 A>G maps to NM_024870.2 K1378K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OT-01A-11D-A28B-09 chr8:69020465 T>G maps to NM_024870.2 S946S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88V-01A-11D-A351-09 chr8:68993012 A>T maps to NM_024870.2 G606G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X8-AAAR-01A-11D-A403-09 chr8:69021831 G>T maps to NM_024870.2 V1040V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr1:186276770 C>T maps to NM_005807.3 P640P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr20:62195614 C>T maps to NM_001037335.2 A1520A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NQ-01A-11D-A36J-09 chr20:62194138 G>A maps to NM_001037335.2 L2012L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A1-01A-21D-A27G-09 chr20:62196934 G>A maps to NM_001037335.2 D1080D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A9-01A-11D-A28B-09 chr20:62194953 G>A maps to NM_001037335.2 L1741L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EZ-01A-11D-A36J-09 chr20:62194075 C>T maps to NM_001037335.2 L2033L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A8JD-01A-11D-A36J-09 chr20:62192572 G>A maps to NM_001037335.2 V2336V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93D-01A-11D-A387-09 chr12:57127929 C>T did not map to a codon.
Sequencing variant TCGA-LN-A9FP-01A-31D-A387-09 chr12:57132265 C>A maps to NM_000946.2 E366*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8W5-01B-11D-A37C-09 chr12:57127969 G>A maps to NM_000946.2 L402L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GK-01A-11D-A37C-09 chr6:57512518 T>C maps to NM_000947.2 C449C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GL-01A-12D-A37C-09 chr6:57244770 T>C maps to NM_000947.2 L178L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88V-01A-11D-A351-09 chr14:94187801 G>A maps to NM_178013.3 N150N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NQ-01A-11D-A36J-09 chr5:40771926 G>A maps to NM_206907.3 I149I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HX-01A-11D-A33E-09 chr5:40767572 A>G maps to NM_206907.3 D287D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FO-01A-11D-A387-09 chr5:40775592 G>A maps to NM_206907.3 I94I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr19:14208487 T>C did not map to a codon.
Sequencing variant TCGA-JY-A93D-01A-11D-A387-09 chr9:71628849 G>T maps to NM_002732.3 G53G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NF-01A-11D-A37C-09 chr7:720327 T>C maps to NM_002735.2 S71S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FP-01A-31D-A387-09 chr7:716864 C>A did not map to a codon.
Sequencing variant TCGA-V5-AASX-01A-11D-A387-09 chr7:720336 C>T maps to NM_002735.2 R68R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43C-01A-11D-A247-09 chr16:24192245 C>A maps to NM_002738.6 P510P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49Y-01A-11D-A27G-09 chr16:24135160 C>A maps to NM_002738.6 A308A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FP-01A-31D-A387-09 chr16:24135199 G>T maps to NM_002738.6 T321T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RE-A7BO-01A-11D-A33E-09 chr16:23847615 C>T maps to NM_002738.6 T40T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KH-A6WC-01A-11D-A33E-09 chr3:53215230 G>T maps to NM_212539.1 L108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NQ-01A-11D-A36J-09 chr3:53212437 C>T did not map to a codon.
Sequencing variant TCGA-IG-A51D-01A-11D-A27G-09 chr19:54407956 C>G maps to NM_002739.3 P575P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NS-01A-12D-A37C-09 chr14:61915965 C>G maps to NM_006255.3 S233*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr1:2116390 G>A maps to NM_002744.4 E574E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A5B8-01A-11D-A28B-09 chr14:30068913 G>C maps to NM_002742.2 S672*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93E-01A-11D-A37C-09 chr14:30066912 G>T maps to NM_002742.2 R740R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OH-01A-11D-A27G-09 chr14:30066864 T>G maps to NM_002742.2 R756R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OR-01A-11D-A27G-09 chr14:30066912 G>T maps to NM_002742.2 R740R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NF-01A-11D-A37C-09 chr14:30068313 C>T maps to NM_002742.2 R695R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RE-A7BO-01A-11D-A33E-09 chr14:30068926 C>A maps to NM_002742.2 E668*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NS-01A-12D-A37C-09 chr19:47200419 G>A maps to ENST00000449438 Y437Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HW-01A-22D-A351-09 chr19:47197276 G>A maps to ENST00000449438 F477F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A9VB-01A-21D-A37C-09 chr19:47181823 G>A maps to ENST00000449438 L723L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A9VB-01A-21D-A37C-09 chr19:47207557 G>A maps to ENST00000449438 L253L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49W-01A-11D-A27G-09 chr2:37516570 T>C maps to NM_005813.3 V215V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GQ-01A-11D-A37C-09 chr8:48866997 C>T maps to NM_006904.6 Q136Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A938-01A-11D-A37C-09 chr8:48694816 T>G did not map to a codon.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr8:48691160 G>A maps to NM_006904.6 F3903F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr8:48734353 C>A did not map to a codon.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr8:48767817 G>A maps to NM_006904.6 V2241V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8WC-01A-11D-A37C-09 chr8:48744395 A>G maps to NM_006904.6 V2747V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA7B-01A-31D-A403-09 chr8:48866214 G>C maps to NM_006904.6 S229*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A8JD-01A-11D-A36J-09 chr8:48827891 C>G maps to NM_006904.6 L871L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GG-01A-11D-A37C-09 chr10:53822319 A>G maps to NM_001098512.1 S273S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88Z-01A-11D-A36J-09 chr10:53814275 G>A maps to NM_001098512.1 R250R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NF-01A-11D-A37C-09 chr4:82126023 T>A maps to NM_006259.1 K60*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OH-01A-11D-A27G-09 chr2:179301046 C>T did not map to a codon.
Sequencing variant TCGA-R6-A6KZ-01A-11D-A31U-09 chr11:76063647 A>G maps to NM_004705.2 P182P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GL-01A-12D-A37C-09 chr6:22290492 T>C maps to ENST00000397199 Q135Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OW-01A-11D-A28B-09 chr6:22292814 A>C maps to ENST00000397199 T89T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-A7RB-01A-11D-A351-09 chr10:120354615 G>A maps to NM_004248.2 V47V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43H-01A-11D-A247-09 chr5:35072679 C>T maps to NM_000949.4 W180*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49M-01A-21D-A27G-09 chr16:11370119 C>T maps to ENST00000435245 L36L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GL-01A-12D-A37C-09 chr1:107600102 C>T maps to NM_018137.2 L256L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43I-01A-11D-A247-09 chr12:3692261 G>A maps to NM_019854.3 S289S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr12:3600862 C>A maps to NM_019854.3 T24T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A891-01A-11D-A36J-09 chr20:4705274 G>A maps to NM_012409.2 T26T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A3-01A-11D-A27G-09 chr17:27031778 A>G maps to ENST00000415329 C86C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-A7RE-01A-11D-A351-09 chr17:27030760 C>A maps to ENST00000415329 E304*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr22:18918567 G>A maps to NM_016335.4 S139S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FQ-01A-31D-A387-09 chr19:36303331 G>T maps to NM_021232.1 R177R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZR-A9CJ-01B-11D-A387-09 chr1:110996632 C>T maps to NM_032414.2 S41S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NL-01A-12D-A37C-09 chr2:68882626 C>T maps to NM_138964.2 G367G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8WC-01A-11D-A37C-09 chr20:5294625 G>A maps to NM_144773.2 S130S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASX-01A-11D-A387-09 chr4:71265049 C>T maps to NM_021225.4 F16F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88Z-01A-11D-A36J-09 chr8:37633453 G>T maps to NM_007198.3 E206*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NR-01A-11D-A37C-09 chr11:60669880 A>T maps to NM_014502.4 I173I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OU-01A-11D-A28B-09 chr1:109241943 C>A maps to NM_018061.2 R315R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A97H-01A-11D-A387-09 chr14:45579750 G>T did not map to a codon.
Sequencing variant TCGA-IC-A6RE-01A-11D-A33E-09 chr12:50030497 G>A did not map to a codon.
Sequencing variant TCGA-Q9-A6FU-01A-11D-A31U-09 chr20:62654207 C>T maps to NM_012469.3 Y582Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A938-01A-11D-A37C-09 chr17:1582136 C>T maps to NM_006445.3 L546L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr17:1582091 G>A maps to NM_006445.3 H561H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NS-01A-12D-A37C-09 chr17:1564933 G>C maps to NM_006445.3 L1391L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NF-01A-11D-A37C-09 chr23:106885629 C>T did not map to a codon.
Sequencing variant TCGA-L5-A43M-01A-11D-A247-09 chr23:12837706 G>T did not map to a codon.
Sequencing variant TCGA-LN-A9FR-01A-11D-A387-09 chr23:12837705 G>C did not map to a codon.
Sequencing variant TCGA-VR-A8EZ-01A-11D-A36J-09 chr23:12828230 A>G did not map to a codon.
Sequencing variant TCGA-L5-A8NQ-01A-11D-A36J-09 chr17:74326691 G>A maps to NM_002766.2 F173F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HX-01A-11D-A33E-09 chr19:50117864 G>T maps to NM_020719.1 E1617*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S8-A6BW-01A-11D-A31U-09 chr19:50102743 C>G maps to NM_020719.1 L1298L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr16:30664142 C>T maps to NM_024031.2 A98A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr7:29606190 C>T maps to NM_175887.2 S82S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RE-01A-11D-A33E-09 chr5:120021870 A>C maps to NM_016644.1 R105R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49R-01A-11D-A247-09 chr5:120022337 G>T maps to NM_016644.1 V260V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A8JE-01A-11D-A37C-09 chr19:42814489 A>T maps to NM_199285.2 P223P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GM-01A-11D-A37C-09 chr3:138724342 C>T maps to NM_001134659.1 P256P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6XG-01B-11D-A33E-09 chr3:138739029 G>A maps to NM_001013650.2 D158D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6XG-01B-11D-A33E-09 chr3:138762946 G>A maps to NM_001134657.1 A172A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NI-01A-11D-A37C-09 chr11:36440810 G>A maps to NM_001160167.1 L84L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A5U6-01A-11D-A28B-09 chr19:50093636 G>A maps to NM_000951.2 R200R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OJ-01A-11D-A27G-09 chr23:150869441 T>G did not map to a codon.
Sequencing variant TCGA-L5-A8NK-01A-21D-A37C-09 chr23:150869316 C>T did not map to a codon.
Sequencing variant TCGA-L5-A8NR-01A-11D-A37C-09 chr23:150868620 A>G did not map to a codon.
Sequencing variant TCGA-IC-A6RF-01A-13D-A33E-09 chr6:32117442 C>T maps to NM_030651.3 P205P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA4G-01A-11D-A37C-09 chr6:32118207 C>T maps to NM_030651.3 A165A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6Y0-01B-11D-A33E-09 chr16:29824420 G>T maps to NM_145239.2 E16*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr3:9989595 G>A maps to NM_207351.3 R421*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASW-01A-11D-A403-09 chr9:132481696 G>A maps to NM_016307.3 Q149Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A5U7-01A-11D-A31U-09 chr4:119220047 T>C maps to NM_003619.3 K559K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93E-01A-11D-A37C-09 chr16:2903946 G>T maps to NM_022119.3 Y212*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA7B-01A-31D-A403-09 chr16:2763676 G>T maps to NM_031948.3 I177I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OG-01A-11D-A27G-09 chr9:33796659 T>C maps to NM_007343.3 D77D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OO-01A-11D-A27G-09 chr9:33798036 T>C maps to NM_007343.3 T194T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88V-01A-11D-A351-09 chr9:33798036 T>C maps to NM_007343.3 T194T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49S-01A-11D-A247-09 chr6:84234263 G>T maps to NM_153362.2 A368A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr16:31150581 G>T maps to NM_173502.3 P815P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4ON-01A-11D-A27G-09 chr16:31155122 G>A maps to NM_173502.3 G252G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EQ-01A-11D-A36J-09 chr7:141537834 G>T maps to NM_001008270.2 I85I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43H-01A-11D-A247-09 chr3:46875456 G>A maps to NM_182702.1 G43G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FG-01A-11D-A33E-09 chr15:55964702 G>A maps to NM_173814.4 Q661*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr15:55965575 G>A maps to NM_173814.4 S615S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OE-01A-11D-A27G-09 chr15:56032808 G>A maps to NM_173814.4 V56V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr19:40901306 G>A maps to NM_181882.2 G984G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HW-01A-22D-A351-09 chr10:104176705 C>T maps to NM_002779.3 P30P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A8I0-01A-11D-A36J-09 chr5:139192909 G>T maps to NM_032289.2 E130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6Y0-01B-11D-A33E-09 chr5:139193040 C>T maps to NM_032289.2 C173C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZR-A9CJ-01B-11D-A387-09 chr8:18729695 C>T maps to ENST00000440756 Q226Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr2:113955412 C>T maps to NM_012455.2 P849P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HX-01A-11D-A33E-09 chr2:113940983 C>T maps to NM_012455.2 T317T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XP-A8T8-01A-11D-A36J-09 chr19:43373154 G>A maps to NM_006905.2 N247N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OR-01A-11D-A27G-09 chr19:43523012 A>G maps to ENST00000306308 G212G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4MR-01A-11D-A28B-09 chr19:43579504 C>A did not map to a codon.
Sequencing variant TCGA-L5-A8NV-01A-11D-A37C-09 chr19:43236998 C>A maps to NM_021016.3 E216*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49O-01A-11D-A247-09 chr8:87060699 C>T maps to ENST00000276616 A383A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RE-01A-11D-A33E-09 chr14:58730476 G>T maps to NM_002788.2 E178*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93C-01A-11D-A387-09 chr14:58734208 C>T maps to NM_002788.2 C187C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OJ-01A-11D-A27G-09 chr14:58737134 G>T did not map to a codon.
Sequencing variant TCGA-LN-A49P-01A-11D-A247-09 chr14:58738591 A>G maps to NM_002788.2 E249E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FP-01A-31D-A387-09 chr15:78834885 A>T maps to NM_002789.4 G36G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GK-01A-11D-A37C-09 chr17:36916827 C>T maps to NM_002795.2 Y147Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A4P3-01A-11D-A27G-09 chr17:36909464 C>T maps to NM_002795.2 I22I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr6:32827215 C>T maps to NM_002800.4 S189S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GG-01A-11D-A37C-09 chr19:40485722 G>T did not map to a codon.
Sequencing variant TCGA-2H-A9GK-01A-11D-A37C-09 chr17:61905526 C>T maps to NM_002805.5 S18S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GM-01A-11D-A37C-09 chr17:61905526 C>T maps to NM_002805.5 S18S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GR-01A-12D-A37C-09 chr2:231927339 G>A maps to NM_002807.3 G85G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4MR-01A-11D-A28B-09 chr17:30807534 G>C maps to NM_002815.2 L385L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr17:65337162 G>A maps to NM_002816.3 S389S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HX-01A-11D-A33E-09 chr3:184019769 C>T maps to NM_002808.3 C205C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GR-01A-12D-A37C-09 chr3:64005036 G>A maps to ENST00000492933 L197L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3Y9-01A-12D-A247-09 chr7:1608891 G>A maps to NM_001134340.1 F28F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NH-01A-11D-A37C-09 chr6:31106526 T>C maps to NM_014068.2 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NT-01A-11D-A37C-09 chr18:43585473 G>T maps to NM_024430.3 I126I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q9-A6FU-01A-11D-A31U-09 chr9:72374806 C>G maps to NM_001099666.1 V16V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A938-01A-11D-A37C-09 chr7:99022858 C>T maps to NM_001198879.1 K481K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NV-01A-11D-A37C-09 chr7:99022948 C>T maps to NM_001198879.1 P451P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8WG-01A-11D-A37C-09 chr5:71616207 G>T did not map to a codon.
Sequencing variant TCGA-IG-A3Y9-01A-12D-A247-09 chr2:86361472 C>T maps to NM_017952.5 L534L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A6QS-01A-12D-A33E-09 chr9:98218644 G>T maps to NM_000264.3 L1073L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49R-01A-11D-A247-09 chr9:98242323 T>A maps to NM_000264.3 R332*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EU-01A-11D-A36J-09 chr9:98218580 C>A maps to NM_000264.3 E1095*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EW-01A-11D-A36J-09 chr9:98239985 T>A did not map to a codon.
Sequencing variant TCGA-LN-A5U6-01A-11D-A28B-09 chr1:45292309 C>T maps to NM_003738.4 V942V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NV-01A-11D-A37C-09 chr23:23410815 C>T did not map to a codon.
Sequencing variant TCGA-LN-A7HV-01A-21D-A351-09 chr23:23397966 A>G did not map to a codon.
Sequencing variant TCGA-L5-A4OX-01A-21D-A28B-09 chr1:11561652 C>T maps to NM_020780.1 R202*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NU-01A-11D-A36J-09 chr1:11561237 C>A maps to NM_020780.1 T63T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-A7RC-01B-11D-A403-09 chr1:11580897 C>A maps to NM_020780.1 T785T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-AAPN-01A-11D-A403-09 chr1:11561423 G>A maps to NM_020780.1 A125A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZR-A9CJ-01B-11D-A387-09 chr1:11579484 G>T maps to NM_020780.1 G655*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4MQ-01A-11D-A28B-09 chr10:89692903 C>T maps to NM_000314.4 R130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4MQ-01A-11D-A28B-09 chr10:89717761 A>T maps to NM_000314.4 K263*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88S-01A-11D-A36J-09 chr1:71477990 G>A maps to ENST00000354608 C358C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GH-01A-11D-A37C-09 chr5:40691993 G>A maps to NM_000958.2 W327*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr1:78959097 G>T maps to NM_000959.3 G224*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr1:117504096 G>T maps to NM_020440.2 R482R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EX-01A-11D-A36J-09 chr1:117487301 G>A maps to NM_020440.2 V140V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FP-01A-31D-A387-09 chr19:47124857 G>A maps to NM_000960.3 F280F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A8I0-01A-11D-A36J-09 chr9:125143815 G>A maps to NM_000962.2 K221K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OH-01A-11D-A27G-09 chr1:186645101 G>A maps to NM_000963.2 Y395Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A50L-01A-11D-A27G-09 chr2:209345853 C>T maps to NM_005048.2 T347T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr8:27294937 G>A maps to NM_004103.3 P484P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49U-01A-31D-A27G-09 chr2:232573420 C>G maps to NM_001099285.1 S2*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A4P3-01A-11D-A27G-09 chr6:64289198 G>T maps to NM_003463.3 G123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA7B-01A-31D-A403-09 chr15:65856551 G>C did not map to a codon.
Sequencing variant TCGA-LN-A7HY-01A-12D-A351-09 chr3:123301133 A>T maps to NM_198402.3 A66A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A3-01A-11D-A27G-09 chr20:49195058 C>T maps to NM_002827.2 R199*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49M-01A-21D-A27G-09 chr12:112924298 C>A maps to ENST00000392596 V419V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GR-01A-12D-A37C-09 chr4:87693996 T>G maps to NM_080685.2 A1750A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NL-01A-12D-A37C-09 chr4:87687595 C>T maps to NM_080685.2 L1424L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NR-01A-11D-A37C-09 chr4:87622935 G>T maps to NM_080685.2 E393*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49M-01A-21D-A27G-09 chr4:87686555 G>A maps to NM_080685.2 V1391V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6KZ-01A-11D-A31U-09 chr4:87610244 C>T maps to NM_080685.2 L150L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S8-A6BV-01A-21D-A31U-09 chr4:87672181 C>G maps to NM_080685.2 S1024*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A8JD-01A-11D-A36J-09 chr4:87684272 C>G maps to NM_080685.2 S1316*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OH-01A-11D-A27G-09 chr1:214542827 G>T maps to NM_005401.4 G1081G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr1:214560190 C>T maps to NM_005401.4 S354S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XP-A8T8-01A-11D-A36J-09 chr1:214560235 G>A maps to NM_005401.4 P339P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA7B-01A-31D-A403-09 chr2:131117001 G>A maps to NM_014369.3 T104T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A50L-01A-11D-A27G-09 chr18:12859246 G>T maps to NM_002828.2 R26R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A938-01A-11D-A37C-09 chr9:112153416 C>T did not map to a codon.
Sequencing variant TCGA-JY-A93F-01A-21D-A37C-09 chr9:112225696 A>T maps to NM_002829.3 R6R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GR-01A-12D-A37C-09 chr2:120704129 C>T maps to NM_002830.2 R546*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NH-01A-11D-A37C-09 chr2:120714493 C>G maps to NM_002830.2 Y685*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A51D-01A-11D-A27G-09 chr11:18751320 G>T maps to NM_032781.3 S458S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA4G-01A-11D-A37C-09 chr12:7064024 C>T maps to ENST00000416215 G130G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FO-01A-11D-A387-09 chr15:75809692 C>T maps to NM_002833.2 Q145Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GL-01A-12D-A37C-09 chr20:3005236 C>T maps to NM_002836.3 T528T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OT-01A-11D-A28B-09 chr12:70965007 A>T maps to NM_001109754.1 T1056T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8W8-01B-11D-A37C-09 chr12:70918372 T>C did not map to a codon.
Sequencing variant TCGA-JY-A6F8-01A-11D-A33E-09 chr1:198697519 C>A maps to ENST00000271610 S591*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr9:8449821 G>A maps to NM_002839.3 S1297S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EO-01A-11D-A36J-09 chr9:8341758 G>T maps to NM_002839.3 A1627A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr1:44054631 C>T maps to NM_002840.3 L304L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OH-01A-11D-A27G-09 chr1:44044538 G>T maps to NM_002840.3 A209A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A5-01A-21D-A27G-09 chr1:44019256 G>A maps to NM_002840.3 P62P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6L4-01A-11D-A31U-09 chr3:62188911 G>A maps to NM_002841.3 T481T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASV-01A-11D-A387-09 chr3:62229528 T>C maps to NM_002841.3 P808P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A891-01A-11D-A36J-09 chr19:55715272 G>T maps to NM_002842.3 R255R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A8JE-01A-11D-A37C-09 chr19:55698884 C>A maps to NM_002842.3 L854L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FR-01A-11D-A387-09 chr11:48149404 C>T maps to NM_002843.3 S389S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q9-A6FW-01A-31D-A31U-09 chr11:48161119 C>T maps to NM_002843.3 G745G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GI-01A-11D-A37C-09 chr6:128298109 G>A maps to ENST00000368210 G1285G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-AAPN-01A-11D-A403-09 chr6:128388852 G>T maps to ENST00000368210 V656V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A4QS-01A-11D-A27G-09 chr18:8253276 T>G maps to NM_001105244.1 T873T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr18:8380292 G>T did not map to a codon.
Sequencing variant TCGA-LN-A49U-01A-31D-A27G-09 chr18:8244112 G>A maps to NM_001105244.1 V786V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A8I1-01A-11D-A36J-09 chr18:7955117 G>C did not map to a codon.
Sequencing variant TCGA-V5-AASX-01A-11D-A387-09 chr18:7774150 C>A maps to NM_001105244.1 G26G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA4G-01A-11D-A37C-09 chr18:8314801 C>T maps to NM_001105244.1 Q956*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NK-01A-21D-A37C-09 chr2:220164084 G>C maps to NM_002846.3 T515T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8W5-01B-11D-A37C-09 chr2:220173952 G>A maps to NM_002846.3 A34A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GN-01A-11D-A37C-09 chr7:157475485 C>T maps to NM_002847.3 Q644Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A5B8-01A-11D-A28B-09 chr7:157333461 C>T maps to NM_002847.3 A998A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NN-01A-11D-A37C-09 chr7:157387998 G>A maps to NM_002847.3 H809H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49K-01A-11D-A247-09 chr12:15710403 T>C maps to NM_030667.1 G858G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4MR-01A-11D-A28B-09 chr12:15739973 C>T maps to NM_030667.1 I1133I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASV-01A-11D-A387-09 chr12:15734641 G>T maps to NM_030667.1 T1054T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RE-01A-11D-A33E-09 chr12:71286608 A>G maps to NM_002849.2 S69S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FA-01A-11D-A33E-09 chr12:71148029 C>A maps to NM_002849.2 G227*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A50L-01A-11D-A27G-09 chr19:5214589 C>T maps to NM_002850.3 R1492R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FD-01A-11D-A33E-09 chr19:5244257 G>A maps to NM_002850.3 I408I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OH-01A-11D-A27G-09 chr19:5265127 G>T maps to NM_002850.3 T153T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr19:5239053 C>T maps to NM_002850.3 P575P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NW-01A-11D-A37C-09 chr19:5229534 C>T maps to NM_002850.3 P772P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43I-01A-11D-A247-09 chr20:40739097 G>T maps to ENST00000373198 R1065R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L7-A6VZ-01A-12D-A33E-09 chr20:40864896 T>G maps to ENST00000373198 R791R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6L6-01B-11D-A33E-09 chr20:40877451 G>T maps to ENST00000373198 T748T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49M-01A-21D-A27G-09 chr1:29631862 G>A did not map to a codon.
Sequencing variant TCGA-JY-A6FE-01A-11D-A33E-09 chr7:121679505 A>C did not map to a codon.
Sequencing variant TCGA-L5-A4OT-01A-11D-A28B-09 chr7:121651970 T>G maps to NM_002851.2 T957T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NS-01A-12D-A37C-09 chr7:121650872 C>T maps to NM_002851.2 P591P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EZ-01A-11D-A36J-09 chr17:40557037 G>A maps to NM_012232.5 R280R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OJ-01A-11D-A27G-09 chr2:20508089 G>T maps to ENST00000361078 Y258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OR-01A-11D-A27G-09 chr2:20458105 G>A maps to ENST00000361078 A794A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NK-01A-21D-A37C-09 chr5:139494602 G>A maps to NM_005859.4 K279K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A8O2-01A-11D-A36J-09 chr8:30889848 C>T maps to NM_013357.2 Q150Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NL-01A-12D-A37C-09 chr8:30890163 T>A maps to NM_013357.2 S45S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93E-01A-11D-A37C-09 chr12:44124364 G>T maps to NM_031292.3 C640*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FD-01A-11D-A33E-09 chr11:119545302 C>T maps to NM_203286.1 *353*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FG-01A-11D-A33E-09 chr11:119535969 C>T maps to NM_002855.4 R347R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A8I1-01A-11D-A36J-09 chr11:119549352 G>A maps to NM_002855.4 Q68*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NS-01A-12D-A37C-09 chr12:108102886 G>T did not map to a codon.
Sequencing variant TCGA-IC-A6RE-01A-11D-A33E-09 chr21:45539307 C>G maps to NM_005049.2 S364S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OE-01A-11D-A27G-09 chr21:45528947 C>A maps to NM_005049.2 G34G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8WG-01A-11D-A37C-09 chr21:45537716 G>T maps to NM_005049.2 E285*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NW-01A-11D-A37C-09 chr5:159546080 G>A maps to NM_001130864.1 A105A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FQ-01A-31D-A387-09 chr5:159519670 C>T maps to NM_001130864.1 K662K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OW-01A-11D-A28B-09 chr2:1652614 G>A maps to NM_012293.1 N979N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr2:1652401 G>A maps to NM_012293.1 Y1050Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr2:1677546 A>G maps to NM_012293.1 L296L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q9-A6FU-01A-11D-A31U-09 chr12:133272598 C>T maps to NM_018663.1 L122L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASW-01A-11D-A403-09 chr20:32295571 G>A maps to NM_007238.4 S193S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6F8-01A-11D-A33E-09 chr12:120661549 G>T maps to NM_001080855.1 S109S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr17:79892834 G>A maps to ENST00000432920 A196A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6KZ-01A-11D-A31U-09 chr8:144687986 G>A maps to NM_023078.3 T248T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FG-01A-11D-A33E-09 chr16:31228223 G>A maps to NM_152901.2 G42G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6F8-01A-11D-A33E-09 chr20:25259010 G>T maps to NM_002862.3 T304T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HX-01A-11D-A33E-09 chr20:25262689 G>T maps to NM_002862.3 L475L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FR-01A-11D-A387-09 chr20:25228819 G>T maps to NM_002862.3 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr1:154932070 G>A maps to NM_138300.3 P135P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GG-01A-11D-A37C-09 chr1:158911855 A>C maps to NM_152501.3 T223T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49U-01A-31D-A27G-09 chr17:42030683 G>C maps to NM_004160.4 L56L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NN-01A-11D-A37C-09 chr12:9305469 A>C maps to NM_002864.2 T1357T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4MQ-01A-11D-A28B-09 chr20:3147482 G>A maps to NM_014731.2 T109T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr4:122254189 C>A maps to NM_198179.2 E195*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OR-01A-11D-A27G-09 chr3:49094420 G>T maps to NM_198880.1 G404G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A8I0-01A-11D-A36J-09 chr17:74287107 G>A maps to NM_032134.1 L1068L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A6QS-01A-12D-A33E-09 chr1:180155247 G>T maps to NM_002826.4 V316V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49X-01A-31D-A27G-09 chr1:180166100 C>T maps to NM_002826.4 L725L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RE-A7BO-01A-11D-A33E-09 chr19:10823828 G>T maps to NM_031209.2 V365V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S8-A6BV-01A-21D-A31U-09 chr19:10823276 C>T maps to NM_031209.2 F278F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HX-01A-11D-A33E-09 chr12:57652735 G>T maps to ENST00000438036 Y798*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A9VB-01A-21D-A37C-09 chr12:57663111 G>A maps to ENST00000438036 Q622*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr20:42972025 C>T maps to NM_178491.2 S130S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A2-01A-31D-A27G-09 chr2:26350814 C>T maps to NM_016131.4 R172*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASV-01A-11D-A387-09 chr15:66180063 G>A maps to ENST00000435304 K224K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GQ-01A-11D-A37C-09 chr19:8468390 C>T maps to NM_004218.3 P202P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GR-01A-12D-A37C-09 chr19:8467046 G>A maps to NM_004218.3 W105*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr8:37729769 G>A maps to NM_001002814.2 D850D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr8:37728986 G>T maps to NM_001002814.2 P1111P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A8JD-01A-11D-A36J-09 chr14:65438752 G>A maps to NM_198686.2 I14I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NR-01A-11D-A37C-09 chr1:156035799 G>T maps to NM_020387.2 E48*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NT-01A-11D-A37C-09 chr1:156038210 C>T maps to NM_020387.2 S130S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6L4-01A-11D-A31U-09 chr15:55497768 G>C maps to NM_183235.1 S201*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NW-01A-11D-A37C-09 chr8:61504468 C>T maps to NM_002865.1 R139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8ER-01A-11D-A36J-09 chr8:61496837 C>T maps to NM_002865.1 Y86Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OJ-01A-11D-A27G-09 chr11:82693419 G>T maps to NM_014488.3 S133S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A938-01A-11D-A37C-09 chr6:146870762 T>G maps to NM_006834.3 A138A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A97I-01A-11D-A387-09 chr23:129318276 G>A did not map to a codon.
Sequencing variant TCGA-L5-A4OU-01A-11D-A28B-09 chr17:27041592 A>C maps to ENST00000413526 A268A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A625-01A-11D-A31U-09 chr22:23503090 C>T maps to NM_004914.2 S281S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A5S3-01A-11D-A28B-09 chr5:57913495 C>T maps to NM_138453.2 Y17Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A625-01A-11D-A31U-09 chr5:58021833 A>C maps to NM_138453.2 T86T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A8JE-01A-11D-A37C-09 chr19:11446225 G>T maps to NM_004283.3 Y123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8ER-01A-11D-A36J-09 chr2:135920325 G>T maps to NM_001172435.1 E799*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L7-A6VZ-01A-12D-A33E-09 chr23:102192430 G>C did not map to a codon.
Sequencing variant TCGA-JY-A6FE-01A-11D-A33E-09 chr23:69503402 C>T did not map to a codon.
Sequencing variant TCGA-L5-A8NE-01A-11D-A37C-09 chr17:40282412 G>A maps to NM_201434.1 S36S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NW-01A-11D-A37C-09 chr17:5271754 G>T maps to NM_004703.4 E626*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GK-01A-11D-A37C-09 chr9:127982851 C>T maps to NM_005833.3 S133S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr9:127990264 A>G maps to NM_005833.3 A201A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93C-01A-11D-A387-09 chr9:125838523 G>T maps to NM_012197.3 G752*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S8-A6BV-01A-21D-A31U-09 chr9:125752360 C>T maps to NM_012197.3 A264A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FH-01A-11D-A33E-09 chr1:174190246 A>G maps to NM_014857.3 P92P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A893-01A-11D-A36J-09 chr7:100959717 G>T maps to NM_022777.2 S104S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GG-01A-11D-A37C-09 chr12:50388106 G>T maps to NM_013277.3 G382G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HX-01A-11D-A33E-09 chr5:68689058 G>T maps to NM_133339.1 E434*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EQ-01A-11D-A36J-09 chr5:131893061 G>T maps to NM_005732.3 G16*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NW-01A-11D-A37C-09 chr14:68934956 G>A maps to NM_133509.3 L342L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93D-01A-11D-A387-09 chr8:95390588 G>T maps to NM_012415.2 I778I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A51D-01A-11D-A27G-09 chr1:46733162 T>A maps to NM_003579.3 T308T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr3:51679779 G>T did not map to a codon.
Sequencing variant TCGA-L5-A88V-01A-11D-A351-09 chr11:67165002 G>T maps to NM_004584.2 L383L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A8I0-01A-11D-A36J-09 chr12:110956487 C>T maps to NM_152442.3 S201S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49Y-01A-11D-A27G-09 chr7:4874576 C>A maps to NM_018059.4 A359A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6DQ-01B-11D-A31U-09 chr7:4874576 C>T maps to NM_018059.4 A359A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8WG-01A-11D-A37C-09 chr7:4874714 C>A maps to NM_018059.4 G313G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EX-01A-11D-A36J-09 chr7:4874345 G>T maps to NM_018059.4 P436P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-AAPN-01A-11D-A403-09 chr7:4874537 G>T maps to NM_018059.4 L372L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A9-01A-11D-A28B-09 chr6:150209741 G>A maps to NM_139165.1 I228I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A6QS-01A-12D-A33E-09 chr11:36596846 G>T maps to NM_000448.2 E665*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OU-01A-11D-A28B-09 chr11:36597526 G>A maps to NM_000448.2 K891K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GL-01A-12D-A37C-09 chr11:36615295 G>T maps to NM_000536.3 S141S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA4D-01A-11D-A37C-09 chr11:36615694 G>T maps to NM_000536.3 V8V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A6QS-01A-12D-A33E-09 chr17:17697104 G>A maps to ENST00000395776 Q281Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OJ-01A-11D-A27G-09 chr17:17700182 G>T maps to ENST00000395776 R1307R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OJ-01A-11D-A27G-09 chr5:34808689 G>T maps to NM_001145521.1 A127A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASX-01A-11D-A387-09 chr5:34796082 C>A maps to NM_001145521.1 L69L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr7:39745765 A>G maps to NM_005402.2 E181E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GN-01A-11D-A37C-09 chr18:9517254 C>A maps to NM_006788.3 Y219*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OT-01A-11D-A28B-09 chr20:37121751 C>T maps to NM_020336.2 H122H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EX-01A-11D-A36J-09 chr20:37146210 C>T maps to NM_020336.2 Q372*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L7-A6VZ-01A-12D-A33E-09 chr9:135977459 G>T maps to NM_006266.2 L692L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EW-01A-11D-A36J-09 chr1:178780523 T>C maps to NM_152663.3 Y124Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NR-01A-11D-A37C-09 chr20:32661372 C>T maps to NM_016732.1 I87I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4ON-01A-11D-A27G-09 chr8:85774632 C>A maps to NM_001100391.1 V185V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NS-01A-12D-A37C-09 chr8:85441592 A>T maps to NM_001100391.1 K26*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8W5-01B-11D-A37C-09 chr17:40914460 C>T maps to ENST00000456272 C89C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8Q7-01A-11D-A37C-09 chr22:20109825 C>G maps to NM_002882.2 L64L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr2:109368084 G>A maps to NM_006267.4 V519V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3YB-01A-11D-A247-09 chr19:5918643 G>T maps to NM_007322.2 R446R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NK-01A-21D-A37C-09 chr19:5921257 G>C maps to NM_007322.2 L428L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EU-01A-11D-A36J-09 chr19:5951442 A>G maps to NM_007322.2 P81P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NW-01A-11D-A37C-09 chr5:36269492 T>A maps to NM_001161429.1 G89G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A8I1-01A-11D-A36J-09 chr5:36253801 G>A maps to NM_001161429.1 R397*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93D-01A-11D-A387-09 chr17:2808622 G>A maps to NM_015085.4 R42R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FQ-01A-31D-A387-09 chr17:2930266 C>T maps to NM_015085.4 F670F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr4:99363153 G>A maps to NM_001100426.1 K571K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OU-01A-11D-A28B-09 chr23:131348423 T>C did not map to a codon.
Sequencing variant TCGA-LN-A49S-01A-11D-A247-09 chr23:131348450 T>A did not map to a codon.
Sequencing variant TCGA-LN-A4A2-01A-31D-A27G-09 chr9:134501525 G>A maps to NM_198679.1 Y496Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr4:160260485 C>T maps to NM_014247.2 D677D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NJ-01A-11D-A36J-09 chr4:160265190 G>A maps to NM_014247.2 K925K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8Q7-01A-11D-A37C-09 chr4:160189324 C>A maps to NM_014247.2 I6I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OW-01A-11D-A28B-09 chr12:48142276 C>T maps to NM_001098531.2 L401L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FO-01A-11D-A387-09 chr7:22233042 C>T maps to ENST00000344041 K229K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-AAPN-01A-11D-A403-09 chr5:130764604 G>A maps to ENST00000514667 S1640S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FP-01A-31D-A387-09 chr2:204304270 C>T maps to ENST00000374493 Q1266Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A891-01A-11D-A36J-09 chr17:38508237 G>A maps to NM_001145301.2 P182P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4MQ-01A-11D-A28B-09 chr12:53621212 G>A maps to NM_000966.4 F39F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GJ-01A-11D-A37C-09 chr5:167919692 T>A maps to NM_002887.3 T70T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49U-01A-31D-A27G-09 chr5:86645149 C>T maps to NM_002890.1 Q408*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASW-01A-11D-A403-09 chr3:141259434 C>T maps to ENST00000452898 Q171*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3YB-01A-11D-A247-09 chr13:114793366 C>A maps to ENST00000389544 G162G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NF-01A-11D-A37C-09 chr19:15571891 G>T maps to NM_022904.1 P195P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr9:85637250 G>A maps to NM_152573.2 D223D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A4P3-01A-11D-A27G-09 chr10:43692529 G>T maps to ENST00000374459 S422S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NJ-01A-11D-A36J-09 chr4:82368695 G>A maps to NM_152545.1 Q231*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NU-01A-11D-A36J-09 chr5:179564941 C>T maps to NM_175062.3 A37A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A5B8-01A-11D-A28B-09 chr15:79298643 C>T maps to NM_002891.4 L666L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NR-01A-11D-A37C-09 chr15:79382678 G>A maps to NM_002891.4 F54F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L7-A56G-01A-21D-A27G-09 chr15:79310154 G>T maps to NM_002891.4 S567*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EQ-01A-11D-A36J-09 chr15:79291087 G>A maps to NM_002891.4 L958L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HV-01A-21D-A351-09 chr15:38798039 C>A did not map to a codon.
Sequencing variant TCGA-VR-A8EW-01A-11D-A36J-09 chr15:38852064 T>A maps to NM_005739.3 G59G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OE-01A-11D-A27G-09 chr2:33740274 T>A did not map to a codon.
Sequencing variant TCGA-L5-A4OE-01A-11D-A27G-09 chr2:33745724 C>T maps to NM_170672.2 H114H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L7-A6VZ-01A-12D-A33E-09 chr2:33783811 G>T maps to NM_170672.2 L593L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49Y-01A-11D-A27G-09 chr2:33764168 C>A maps to NM_170672.2 T390T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GO-01A-11D-A37C-09 chr19:38901800 G>A maps to ENST00000405332 P603P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GR-01A-12D-A37C-09 chr19:38905745 A>G maps to ENST00000405332 T325T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49L-01A-11D-A247-09 chr19:38904096 G>A maps to ENST00000405332 F417F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FP-01A-31D-A387-09 chr19:38905514 G>T maps to ENST00000405332 A402A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASW-01A-11D-A403-09 chr19:38909029 C>T did not map to a codon.
Sequencing variant TCGA-VR-A8EP-01A-31D-A403-09 chr19:49230041 C>T maps to NM_017805.2 K709K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr17:34067486 C>T maps to NM_033315.3 Y92Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6XG-01B-11D-A33E-09 chr17:34062292 C>T maps to NM_033315.3 S30S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GK-01A-11D-A37C-09 chr15:65347311 G>A maps to NM_016563.2 T242T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GN-01A-11D-A37C-09 chr20:4776545 G>A maps to NM_014737.2 L68L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NN-01A-11D-A37C-09 chr4:74459298 G>A maps to NM_201431.1 G84G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A97H-01A-11D-A387-09 chr11:562262 G>A maps to NM_003475.3 P103P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XP-A8T7-01A-11D-A36J-09 chr19:10439551 G>T maps to NM_133452.2 G191G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NG-01A-11D-A37C-09 chr18:56939784 G>A maps to NM_013435.2 V117V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FD-01A-11D-A33E-09 chr13:49030485 G>T did not map to a codon.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr13:48916751 G>A maps to NM_000321.2 K94K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A893-01A-11D-A36J-09 chr13:48955537 C>T maps to NM_000321.2 R552*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EP-01A-31D-A403-09 chr13:48947602 C>G maps to NM_000321.2 S397*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RE-01A-11D-A33E-09 chr8:53570012 A>C maps to NM_014781.4 T792T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OP-01A-11D-A27G-09 chr8:53586542 C>T maps to NM_014781.4 Q288Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr8:53554984 T>C maps to NM_014781.4 S1421S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6L6-01B-11D-A33E-09 chr16:24583537 T>C maps to NM_006910.4 S1717S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA7B-01A-31D-A403-09 chr16:24581205 G>A maps to NM_006910.4 E1065E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A8JE-01A-11D-A37C-09 chr23:16887220 G>A did not map to a codon.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr18:20606157 T>C maps to ENST00000360790 P888P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GQ-01A-11D-A37C-09 chr20:35724276 C>A maps to NM_002895.2 E19*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GL-01A-12D-A37C-09 chr23:47044964 G>T did not map to a codon.
Sequencing variant TCGA-JY-A6FH-01A-11D-A33E-09 chr23:47039308 G>A did not map to a codon.
Sequencing variant TCGA-JY-A93F-01A-21D-A37C-09 chr23:47040704 G>A did not map to a codon.
Sequencing variant TCGA-JY-A6FB-01A-11D-A33E-09 chr21:15596827 A>G maps to NM_144770.3 L134L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr8:94746148 G>T maps to NM_203390.2 P830P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A891-01A-11D-A36J-09 chr8:94746685 G>A maps to NM_203390.2 F651F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FG-01A-11D-A33E-09 chr14:73576164 G>T maps to NM_021239.2 E553*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NS-01A-12D-A37C-09 chr13:79940816 G>A maps to ENST00000438737 P363P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GR-01A-12D-A37C-09 chr5:145610440 C>T maps to NM_018989.1 R271*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93E-01A-11D-A37C-09 chr5:145609303 C>T maps to NM_018989.1 D140D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr5:145583378 G>T maps to NM_018989.1 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NI-01A-11D-A37C-09 chr7:127958054 G>T maps to NM_018077.2 A556A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OW-01A-11D-A28B-09 chr23:48433655 G>A did not map to a codon.
Sequencing variant TCGA-L5-A4OE-01A-11D-A27G-09 chr23:106310813 T>C did not map to a codon.
Sequencing variant TCGA-Q9-A6FW-01A-31D-A31U-09 chr2:238726335 A>C maps to NM_001080504.2 S259S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KH-A6WC-01A-11D-A33E-09 chr4:40428046 G>T maps to NM_001098634.1 I552I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88S-01A-11D-A36J-09 chr3:50129548 C>A maps to NM_005778.2 R31R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A5U7-01A-11D-A31U-09 chr3:50098934 C>T maps to NM_005777.2 Y798Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-AAPN-01A-11D-A403-09 chr3:50106178 G>C maps to NM_005777.2 L1000L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NN-01A-11D-A37C-09 chr12:56974966 G>T did not map to a codon.
Sequencing variant TCGA-JY-A6FB-01A-11D-A33E-09 chr23:129546510 G>T did not map to a codon.
Sequencing variant TCGA-L5-A88S-01A-11D-A36J-09 chr23:129536264 T>C did not map to a codon.
Sequencing variant TCGA-LN-A9FP-01A-31D-A387-09 chr23:129545420 G>T did not map to a codon.
Sequencing variant TCGA-L5-A43I-01A-11D-A247-09 chr1:89448840 T>C maps to NM_019610.5 R223R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASX-01A-11D-A387-09 chr1:89449058 T>A maps to NM_019610.5 R151*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RE-01A-11D-A33E-09 chr11:7110518 T>C maps to NM_014469.4 F56F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NF-01A-11D-A37C-09 chr11:7111368 C>T maps to NM_014469.4 R340*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NS-01A-12D-A37C-09 chr11:7110455 C>T maps to NM_014469.4 V35V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q9-A6FU-01A-11D-A31U-09 chr11:7111256 C>T maps to NM_014469.4 Y302Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RE-A7BO-01A-11D-A33E-09 chr11:7111079 C>T maps to NM_014469.4 Y243Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FH-01A-11D-A33E-09 chr10:48388264 G>A maps to NM_002900.2 P871P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr10:48390415 G>A maps to NM_002900.2 H154H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L7-A56G-01A-21D-A27G-09 chr10:48389038 G>A maps to NM_002900.2 P613P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GF-01A-11D-A37C-09 chr1:173933252 T>A maps to NM_172071.2 A563A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6KZ-01A-11D-A31U-09 chr1:173934233 C>A maps to NM_172071.2 L453L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr9:125659701 G>T maps to NM_001100588.1 I29I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A6-01A-11D-A27G-09 chr9:125639796 T>C maps to NM_001100588.1 P426P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASW-01A-11D-A403-09 chr21:35893938 G>A maps to NM_004414.5 S148S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASW-01A-11D-A403-09 chr1:24861730 G>T maps to NM_013441.2 A230A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr4:76407851 G>A maps to NM_015436.2 R228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49X-01A-31D-A27G-09 chr4:76439453 G>A maps to NM_015436.2 R15*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49V-01A-11D-A247-09 chr19:50031851 C>T maps to NM_020650.2 S41S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr1:167653201 C>T maps to NM_052862.3 A24A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HV-01A-21D-A351-09 chr1:167666532 G>A maps to NM_052862.3 A224A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FO-01A-11D-A387-09 chr6:31922590 A>G maps to ENST00000375425 G168G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr14:68157944 G>A maps to NM_016026.3 H122H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49W-01A-11D-A27G-09 chr19:55559826 G>A maps to NM_001145971.1 A176A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EP-01A-31D-A403-09 chr19:55570630 G>T maps to NM_001145971.1 T26T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3I8-01A-11D-A247-09 chr12:21639442 T>C maps to NM_032941.2 S157S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-A7RE-01A-11D-A351-09 chr12:21630862 G>A maps to NM_032941.2 N247N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GQ-01A-11D-A37C-09 chr17:73627066 T>C maps to NM_004259.5 E524E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93D-01A-11D-A387-09 chr17:73626917 C>G did not map to a codon.
Sequencing variant TCGA-L5-A88V-01A-11D-A351-09 chr10:65359024 T>A maps to NM_001001330.2 A133A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3Y9-01A-12D-A247-09 chr2:79349977 G>A maps to NM_002909.4 W111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RE-01A-11D-A33E-09 chr2:61149586 C>T maps to NM_002908.2 Q593*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RE-01A-11D-A33E-09 chr19:45532203 C>A maps to ENST00000221452 C315*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GO-01A-11D-A37C-09 chr4:37640082 C>T maps to NM_001085399.1 L143L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OR-01A-11D-A27G-09 chr7:103338428 C>A maps to ENST00000428762 V338V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OT-01A-11D-A28B-09 chr7:103322621 A>G maps to ENST00000428762 D410D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr7:103629674 G>A maps to ENST00000428762 H43H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A2-01A-31D-A27G-09 chr7:103143466 C>A maps to ENST00000428762 G2829*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q9-A6FW-01A-31D-A31U-09 chr7:103243885 C>T maps to ENST00000428762 P1066P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A8JD-01A-11D-A36J-09 chr7:103155683 G>A maps to ENST00000428762 A2689A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FD-01A-11D-A33E-09 chr1:204131164 G>A maps to NM_000537.3 S75S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NK-01A-21D-A37C-09 chr1:204125332 G>T maps to NM_000537.3 A311A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr23:153209095 C>T did not map to a codon.
Sequencing variant TCGA-XP-A8T6-01A-11D-A36J-09 chr23:153208329 G>A did not map to a codon.
Sequencing variant TCGA-L5-A8NE-01A-11D-A37C-09 chr23:17080641 T>C did not map to a codon.
Sequencing variant TCGA-L5-A43E-01A-11D-A247-09 chr10:43619214 C>T maps to NM_020975.4 T966T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A5B8-01A-11D-A28B-09 chr2:100017706 T>C maps to NM_016316.2 T1251T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NF-01A-11D-A37C-09 chr2:100021023 G>A maps to NM_016316.2 G976G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43I-01A-11D-A247-09 chr6:111685106 G>A maps to NM_002912.3 Y2276Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NH-01A-11D-A37C-09 chr6:111688630 A>G maps to NM_002912.3 P2120P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EY-01A-11D-A36J-09 chr6:111693908 G>T maps to NM_002912.3 S1883S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93E-01A-11D-A37C-09 chr19:1816335 G>A maps to NM_020695.3 H1155H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49V-01A-11D-A247-09 chr19:1823682 C>T maps to NM_020695.3 A706A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASV-01A-11D-A387-09 chr19:1828268 A>C maps to NM_020695.3 P173P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OP-01A-11D-A27G-09 chr9:136282882 G>T maps to NM_020385.2 R28R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EZ-01A-11D-A36J-09 chr3:186507805 G>T maps to NM_181573.2 L348L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GQ-01A-11D-A37C-09 chr12:118463596 C>A maps to NM_007370.4 S209S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GL-01A-12D-A37C-09 chr17:33353416 A>G maps to NM_001017368.1 A52A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4MR-01A-11D-A28B-09 chr17:33348698 T>C maps to NM_001017368.1 T94T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8WC-01A-11D-A37C-09 chr17:80007651 G>A maps to NM_002917.1 I243I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NU-01A-11D-A36J-09 chr22:32588919 C>T maps to NM_001098527.2 L175L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88Z-01A-11D-A36J-09 chr22:32756306 C>T maps to NM_001098535.1 R148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GI-01A-11D-A37C-09 chr3:16419420 C>T maps to NM_015150.1 V210V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49Y-01A-11D-A27G-09 chr3:16419498 G>T maps to NM_015150.1 T184T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr19:14104409 G>A maps to NM_002918.4 P82P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr19:6013116 C>A did not map to a codon.
Sequencing variant TCGA-2H-A9GQ-01A-11D-A37C-09 chr9:3266288 G>A maps to NM_134428.1 A458A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L7-A6VZ-01A-12D-A33E-09 chr9:3270392 G>T maps to NM_134428.1 P445P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A8I0-01A-11D-A36J-09 chr9:3248084 C>A maps to NM_134428.1 E639*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8WG-01A-11D-A37C-09 chr9:3330318 G>T maps to NM_134428.1 G138G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr1:151318679 C>T did not map to a codon.
Sequencing variant TCGA-LN-A9FO-01A-11D-A387-09 chr15:56386364 A>G maps to NM_022841.5 N1187N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RE-01A-11D-A33E-09 chr23:109697819 G>T did not map to a codon.
Sequencing variant TCGA-LN-A4A1-01A-21D-A27G-09 chr23:109697614 T>C did not map to a codon.
Sequencing variant TCGA-JY-A6F8-01A-11D-A33E-09 chr23:71349780 C>T did not map to a codon.
Sequencing variant TCGA-KH-A6WC-01A-11D-A33E-09 chr23:71349975 G>C did not map to a codon.
Sequencing variant TCGA-R6-A6KZ-01A-11D-A31U-09 chr23:71350746 G>A did not map to a codon.
Sequencing variant TCGA-VR-A8EZ-01A-11D-A36J-09 chr23:71350085 T>C did not map to a codon.
Sequencing variant TCGA-2H-A9GR-01A-12D-A37C-09 chr15:93588440 G>A maps to NM_020211.2 F380F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A4QS-01A-11D-A27G-09 chr15:93588422 G>A maps to NM_020211.2 G386G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NE-01A-11D-A37C-09 chr5:98129162 C>A maps to NM_001012761.2 T381T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RE-01A-11D-A33E-09 chr9:35752729 C>A maps to ENST00000456972 P385P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-A7RE-01A-11D-A351-09 chr2:108476267 G>A maps to NM_182588.2 L575L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EQ-01A-11D-A36J-09 chr2:108487760 C>T maps to NM_182588.2 R1101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49M-01A-21D-A27G-09 chr16:320791 G>A maps to NM_183337.1 R340*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NT-01A-11D-A37C-09 chr4:3422408 G>A maps to NM_198229.2 S934S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8ER-01A-11D-A36J-09 chr8:101018283 T>A maps to NM_015668.3 L805L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8ET-01A-11D-A403-09 chr9:116353677 G>T did not map to a codon.
Sequencing variant TCGA-L5-A8NK-01A-21D-A37C-09 chr1:163042229 T>A maps to NM_001102445.2 S127S. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-L5-A8NI-01A-11D-A37C-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-L5-A8NI-01A-11D-A37C-09 chr6:49573530 T>A maps to ENST00000418071 R402*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93C-01A-11D-A387-09 chr7:75511279 G>T maps to NM_001040456.1 V104V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49Y-01A-11D-A27G-09 chr16:109824 C>A did not map to a codon.
Sequencing variant TCGA-IC-A6RF-01A-13D-A33E-09 chr1:156354354 C>A maps to NM_020407.3 P424P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OX-01A-21D-A28B-09 chr1:156347810 C>T maps to NM_020407.3 A135A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L7-A56G-01A-21D-A27G-09 chr1:25718575 C>T maps to NM_020485.4 L181L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93F-01A-21D-A37C-09 chr1:25611164 C>T maps to ENST00000357542 L84L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FB-01A-11D-A33E-09 chr8:22852125 C>T maps to NM_001160036.1 G10G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr8:22862120 A>G maps to NM_001160036.1 Q80Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3YC-01A-11D-A247-09 chr5:95103748 G>T did not map to a codon.
Sequencing variant TCGA-LN-A8HZ-01A-11D-A36J-09 chr12:122219078 C>T maps to NM_019034.2 R82R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OJ-01A-11D-A27G-09 chr23:119293305 C>T did not map to a codon.
Sequencing variant TCGA-R6-A6DN-01B-11D-A31U-09 chr8:144457754 C>T maps to ENST00000422773 G31G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A8JE-01A-11D-A37C-09 chr8:144462881 C>G maps to ENST00000422773 S471*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NJ-01A-11D-A36J-09 chr19:33486950 G>A maps to NM_033103.4 I467I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OJ-01A-11D-A27G-09 chr23:53457372 T>C did not map to a codon.
Sequencing variant TCGA-L5-A8NS-01A-12D-A37C-09 chr23:53457931 G>A did not map to a codon.
Sequencing variant TCGA-L5-A8NU-01A-11D-A36J-09 chr23:53455373 G>T did not map to a codon.
Sequencing variant TCGA-L5-A4OO-01A-11D-A27G-09 chr22:45821832 C>T maps to NM_015653.3 I221I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NN-01A-11D-A37C-09 chr11:209474 G>A maps to NM_021932.4 L67L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FQ-01A-31D-A387-09 chr12:107208703 G>C maps to ENST00000392837 L121L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RE-A7BO-01A-11D-A33E-09 chr12:107254097 G>T maps to ENST00000392837 A453A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6L6-01B-11D-A33E-09 chr17:12823122 C>T maps to NM_014859.4 L147L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RF-01A-13D-A33E-09 chr5:38945020 A>G maps to ENST00000296782 L1619L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FR-01A-11D-A387-09 chr5:38942959 A>C maps to ENST00000296782 L1700*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FH-01A-11D-A33E-09 chr2:152319843 G>T maps to NM_018151.4 G1270G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XP-A8T8-01A-11D-A36J-09 chr2:152325153 G>C did not map to a codon.
Sequencing variant TCGA-L5-A8NH-01A-11D-A37C-09 chr12:130926744 G>T maps to NM_015347.4 S367S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RE-A7BO-01A-11D-A33E-09 chr12:130927080 G>A maps to NM_015347.4 S255S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A9VB-01A-21D-A37C-09 chr12:130926543 G>A maps to NM_015347.4 A434A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88S-01A-11D-A36J-09 chr1:42865150 G>A maps to NM_173642.3 Q80Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A5U6-01A-11D-A28B-09 chr12:8904625 G>A maps to NM_020734.2 T160T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8W5-01B-11D-A37C-09 chr12:8926292 G>T maps to NM_020734.2 T358T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GF-01A-11D-A37C-09 chr6:72889606 T>C maps to NM_014989.4 P267P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GF-01A-11D-A37C-09 chr6:72922920 T>G maps to NM_001168407.1 V32V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GI-01A-11D-A37C-09 chr8:104924381 A>G maps to NM_001100117.2 G598G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GK-01A-11D-A37C-09 chr8:104898168 T>C maps to NM_001100117.2 L448L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GL-01A-12D-A37C-09 chr8:105025816 A>G maps to NM_001100117.2 G1064G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A4QS-01A-11D-A27G-09 chr8:104898168 T>C maps to NM_001100117.2 L448L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OG-01A-11D-A27G-09 chr8:104898168 T>C maps to NM_001100117.2 L448L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OT-01A-11D-A28B-09 chr8:104898095 T>G maps to NM_001100117.2 S423S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OT-01A-11D-A28B-09 chr8:104924381 A>T maps to NM_001100117.2 G598G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88T-01A-11D-A351-09 chr8:104987675 C>T maps to NM_001100117.2 R957*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NL-01A-12D-A37C-09 chr8:104897915 G>A maps to NM_001100117.2 R363R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NQ-01A-11D-A36J-09 chr8:104898095 T>C maps to NM_001100117.2 S423S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6DQ-01B-11D-A31U-09 chr8:105001530 A>T did not map to a codon.
Alternatively spliced codon TCGA-S8-A6BV-01A-21D-A31U-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-VR-A8EP-01A-31D-A403-09 chr8:104898081 C>T maps to NM_001100117.2 Q419*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8W8-01B-11D-A37C-09 chr20:43438825 G>A maps to NM_182970.2 D29D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A5S3-01A-11D-A28B-09 chr11:66103266 G>A maps to NM_004292.2 F116F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EW-01A-11D-A36J-09 chr11:66100108 G>T maps to NM_004292.2 R664R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NQ-01A-11D-A36J-09 chr20:19981578 A>G maps to ENST00000255006 *945W. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA4G-01A-11D-A37C-09 chr20:19956306 C>T maps to ENST00000255006 C595C. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-LN-A4A2-01A-31D-A27G-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-VR-A8EU-01A-11D-A36J-09 chr5:96512995 C>T did not map to a codon.
Sequencing variant TCGA-R6-A6Y0-01B-11D-A33E-09 chr21:43187117 C>G maps to ENST00000352483 V28V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A8-01A-32D-A27G-09 chr23:106145439 G>T did not map to a codon.
Sequencing variant TCGA-XP-A8T7-01A-11D-A36J-09 chr1:40705441 C>T maps to NM_012421.3 Q1690*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EW-01A-11D-A36J-09 chr23:73812329 G>A did not map to a codon.
Sequencing variant TCGA-L5-A4OE-01A-11D-A27G-09 chr9:5335514 C>A maps to NM_006911.2 L98L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FD-01A-11D-A33E-09 chr16:67682605 C>T maps to NM_001013838.1 L486L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49V-01A-11D-A247-09 chr6:151742423 A>T maps to NM_017909.2 S345S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6XQ-01B-11D-A33E-09 chr2:86980657 C>T maps to NM_022780.3 V166V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49R-01A-11D-A247-09 chr5:177565147 G>T maps to NM_022762.3 E10*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A97H-01A-11D-A387-09 chr13:51519600 G>T maps to NM_024570.2 V183V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr5:31431689 C>T maps to NM_013235.4 A1046A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88Z-01A-11D-A36J-09 chr5:31409236 G>A maps to NM_013235.4 D1260D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OE-01A-11D-A27G-09 chr12:49254791 G>T maps to NM_014470.3 I147I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NR-01A-11D-A37C-09 chr12:121004646 C>A maps to ENST00000458409 P640P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NE-01A-11D-A37C-09 chr2:86832516 G>A maps to NM_005667.3 V169V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr15:59368392 C>T maps to ENST00000434298 R643*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FP-01A-31D-A387-09 chr15:59373268 C>T maps to ENST00000434298 Q695*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FQ-01A-31D-A387-09 chr15:59323810 G>T maps to ENST00000434298 E264*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OX-01A-21D-A28B-09 chr23:119005266 G>A did not map to a codon.
Sequencing variant TCGA-Q9-A6FU-01A-11D-A31U-09 chr1:145682021 G>A did not map to a codon.
Sequencing variant TCGA-XP-A8T6-01A-11D-A36J-09 chr8:33406938 G>A maps to NM_024787.2 A114A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr3:49736505 C>T maps to NM_022064.2 S244S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr3:49739822 C>T maps to NM_022064.2 N538N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr23:106031214 G>T did not map to a codon.
Sequencing variant TCGA-L5-A8NJ-01A-11D-A36J-09 chr7:122338318 A>G maps to NM_139175.1 I218I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6F8-01A-11D-A33E-09 chr18:29704765 G>T maps to NM_001191324.1 L210L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A8-01A-32D-A27G-09 chr8:125498687 C>T maps to NM_007218.3 F266F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6F8-01A-11D-A33E-09 chr6:127608468 T>C maps to ENST00000368314 P237P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NQ-01A-11D-A36J-09 chr7:122342264 C>G maps to NM_198085.1 G180G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49S-01A-11D-A247-09 chr7:122342396 G>T maps to NM_198085.1 G136G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GI-01A-11D-A37C-09 chr4:141888805 G>A maps to NM_020724.1 R236*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4ON-01A-11D-A27G-09 chr4:142053866 G>A maps to NM_020724.1 T32T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr21:30338184 A>G did not map to a codon.
Sequencing variant TCGA-V5-AASX-01A-11D-A387-09 chr17:4847880 C>T maps to NM_015528.1 C233C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8Q7-01A-11D-A37C-09 chr17:4846521 C>T maps to NM_015528.1 Y173Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GO-01A-11D-A37C-09 chr3:196199340 G>A maps to NM_152617.3 C355C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr3:196214436 G>A maps to NM_152617.3 R131*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NS-01A-12D-A37C-09 chr11:74547539 T>A maps to NM_001098638.1 L631*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A9-01A-11D-A28B-09 chr11:74546962 C>T maps to NM_001098638.1 Q439*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NS-01A-12D-A37C-09 chr13:25453386 G>A maps to ENST00000381927 P1661P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6Y0-01B-11D-A33E-09 chr13:25378524 G>T maps to ENST00000381927 T683T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8WC-01A-11D-A37C-09 chr8:42720612 G>A maps to NM_030954.3 Y114Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NJ-01A-11D-A36J-09 chr5:63621153 T>C maps to NM_001113561.1 L457L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XP-A8T7-01A-11D-A36J-09 chr5:63509746 G>T maps to NM_001113561.1 L198L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88V-01A-11D-A351-09 chr1:33412074 C>T maps to NM_153341.2 V359V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RE-01A-11D-A33E-09 chr9:104314937 A>T maps to NM_019592.5 K602*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr1:6270327 C>T maps to NM_207396.2 H282H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A7DP-01A-31D-A33E-09 chr17:78320933 G>T maps to NM_020914.4 A2982A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr17:78337440 G>A maps to NM_020914.4 T3916T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OU-01A-11D-A28B-09 chr17:78346352 C>T maps to NM_020914.4 S4239S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NK-01A-21D-A37C-09 chr17:78262163 T>A did not map to a codon.
Sequencing variant TCGA-L5-A8NL-01A-12D-A37C-09 chr17:78272201 G>C maps to NM_020914.4 L747L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49Y-01A-11D-A27G-09 chr17:78261933 G>T maps to NM_020914.4 P243P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A5U7-01A-11D-A31U-09 chr17:78319436 C>T maps to NM_020914.4 S2483S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EY-01A-11D-A36J-09 chr17:78318717 G>T maps to NM_020914.4 E2244*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XP-A8T8-01A-11D-A36J-09 chr17:78353430 G>T maps to NM_020914.4 P4568P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4MQ-01A-11D-A28B-09 chr7:5760758 G>A maps to NM_207111.2 R517*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NQ-01A-11D-A36J-09 chr1:45110738 G>A maps to ENST00000453887 R432R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6Y2-01B-11D-A33E-09 chr1:45116420 G>T maps to ENST00000453887 G560*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-A7RC-01B-11D-A403-09 chr1:45115559 G>A maps to ENST00000453887 S521S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A8-01A-32D-A27G-09 chr2:219529069 G>A maps to NM_022453.2 G330G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XP-A8T8-01A-11D-A36J-09 chr7:156450239 G>T maps to NM_001184997.1 L141L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA7D-01A-11D-A403-09 chr6:30041252 A>G maps to NM_025236.3 D190D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FE-01A-11D-A33E-09 chr16:30779970 C>T maps to NM_014771.2 L671L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NS-01A-12D-A37C-09 chr16:30777482 G>C did not map to a codon.
Sequencing variant TCGA-IG-A3Y9-01A-12D-A247-09 chr12:56600446 C>T maps to NM_194359.1 L246L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4ON-01A-11D-A27G-09 chr17:56435891 G>T maps to NM_017763.4 G415G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OU-01A-11D-A28B-09 chr17:56439976 C>A maps to NM_017763.4 V205V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49S-01A-11D-A247-09 chr17:56438272 G>A maps to NM_017763.4 I240I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A939-01A-12D-A37C-09 chr13:26788998 A>T maps to NM_005977.3 S340S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NI-01A-11D-A37C-09 chr13:26789576 G>T maps to NM_005977.3 R148R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OR-01A-11D-A27G-09 chr6:37342481 C>T maps to NM_003958.3 T375T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr17:58040250 G>A maps to NM_016125.3 L151L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A5B8-01A-11D-A28B-09 chr12:117204677 C>G maps to NM_001109903.1 L229L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OX-01A-21D-A28B-09 chr12:117187990 C>T maps to NM_001109903.1 D143D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49X-01A-31D-A27G-09 chr6:89600275 C>T maps to NM_003800.3 K278K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A4QT-01A-21D-A27G-09 chr10:90122414 G>T maps to NM_001031709.2 L198L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88V-01A-11D-A351-09 chr10:90074273 C>T maps to NM_001031709.2 P275P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FQ-01A-31D-A387-09 chr10:90342041 G>A maps to NM_001031709.2 C47C. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-VR-A8EU-01A-11D-A36J-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-VR-A8EU-01A-11D-A36J-09 chr17:685695 G>A maps to NM_018146.2 A26A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FG-01A-11D-A33E-09 chr2:241513670 C>T maps to NM_018226.3 F129F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93F-01A-21D-A37C-09 chr2:241515025 A>G maps to NM_018226.3 A272A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A6QS-01A-12D-A33E-09 chr1:156027789 C>A maps to NM_014017.3 R85R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NG-01A-11D-A37C-09 chr1:156028129 G>T maps to NM_014017.3 E116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GF-01A-11D-A37C-09 chr3:78680428 T>A maps to NM_002941.3 R1170*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GR-01A-12D-A37C-09 chr3:78685022 G>A maps to NM_002941.3 S1091S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A4P3-01A-11D-A27G-09 chr3:78689029 G>T maps to NM_002941.3 I967I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr3:78685184 A>C maps to NM_002941.3 V1037V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GF-01A-11D-A37C-09 chr3:77595600 A>G maps to ENST00000332191 K349K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A4QS-01A-11D-A27G-09 chr3:77147237 C>T maps to ENST00000332191 G45G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RF-01A-13D-A33E-09 chr11:124740980 G>T maps to NM_022370.3 E369*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NJ-01A-11D-A36J-09 chr11:124735605 C>T maps to NM_022370.3 L45L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49L-01A-11D-A247-09 chr11:124743662 G>C maps to NM_022370.3 V563V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FQ-01A-31D-A387-09 chr11:124739842 G>C did not map to a codon.
Sequencing variant TCGA-IG-A8O2-01A-11D-A36J-09 chr11:124761270 G>A maps to NM_019055.5 L624L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NJ-01A-11D-A36J-09 chr11:124757375 C>T maps to NM_019055.5 L692L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr11:124765467 G>A maps to NM_019055.5 S307S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr18:18622640 A>G maps to NM_005406.2 V235V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3YA-01A-11D-A247-09 chr2:11351834 G>A maps to NM_004850.3 I725I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GF-01A-11D-A37C-09 chr9:115024804 A>G maps to NM_001163790.1 N173N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASW-01A-11D-A403-09 chr9:114989734 C>T maps to NM_001163790.1 Q471Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RF-01A-13D-A33E-09 chr9:94489025 C>T did not map to a codon.
Sequencing variant TCGA-L5-A88Z-01A-11D-A36J-09 chr6:117708160 A>G maps to NM_002944.2 A672A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A1-01A-21D-A27G-09 chr6:117609723 A>T maps to NM_002944.2 P2325P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3YB-01A-11D-A247-09 chr8:55539063 G>T maps to NM_006269.1 G874G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A4QT-01A-21D-A27G-09 chr8:55537882 G>T maps to NM_006269.1 G481*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88V-01A-11D-A351-09 chr8:55542525 G>A maps to NM_006269.1 L2028L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASW-01A-11D-A403-09 chr8:55538982 G>A maps to NM_006269.1 L847L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NL-01A-12D-A37C-09 chr8:10480590 G>A maps to NM_178857.5 R41*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49S-01A-11D-A247-09 chr8:10469642 G>T maps to NM_178857.5 G655G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A8I1-01A-11D-A36J-09 chr8:10470477 G>T maps to NM_178857.5 S377*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA7D-01A-11D-A403-09 chr8:10468841 C>A maps to NM_178857.5 L922L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A8JE-01A-11D-A37C-09 chr8:10464974 A>G maps to NM_178857.5 G2211G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93C-01A-11D-A387-09 chr23:46713482 G>T did not map to a codon.
Sequencing variant TCGA-L5-A8NI-01A-11D-A37C-09 chr23:46713467 T>A did not map to a codon.
Sequencing variant TCGA-L5-A8NK-01A-21D-A37C-09 chr23:46713019 A>G did not map to a codon.
Sequencing variant TCGA-LN-A49S-01A-11D-A247-09 chr23:46696585 C>A did not map to a codon.
Sequencing variant TCGA-L5-A8NE-01A-11D-A37C-09 chr23:96139621 C>T did not map to a codon.
Sequencing variant TCGA-L5-A8NQ-01A-11D-A36J-09 chr23:96139346 C>G did not map to a codon.
Sequencing variant TCGA-LN-A49X-01A-31D-A27G-09 chr23:96140054 A>G did not map to a codon.
Sequencing variant TCGA-JY-A939-01A-12D-A37C-09 chr17:5329554 G>T did not map to a codon.
Sequencing variant TCGA-IG-A5B8-01A-11D-A28B-09 chr15:41816046 C>T maps to NM_015540.2 E786E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88V-01A-11D-A351-09 chr15:41819263 G>T maps to NM_015540.2 V583V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49K-01A-11D-A247-09 chr15:41829176 C>T maps to NM_015540.2 P49P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A8-01A-32D-A27G-09 chr1:92846386 G>T maps to NM_024813.2 E599*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NL-01A-12D-A37C-09 chr12:48090063 C>G maps to NM_024604.2 L180L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L7-A6VZ-01A-12D-A33E-09 chr12:48080645 T>C maps to NM_024604.2 E303E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q9-A6FU-01A-11D-A31U-09 chr1:68914382 C>T maps to NM_000329.2 E6E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FO-01A-11D-A387-09 chr1:84961935 C>T maps to NM_025065.6 F297F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FP-01A-31D-A387-09 chr23:38178136 G>T did not map to a codon.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr14:21816411 G>T maps to NM_020366.3 L1233L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88S-01A-11D-A36J-09 chr16:53652935 C>A did not map to a codon.
Sequencing variant TCGA-LN-A49W-01A-11D-A27G-09 chr12:113334572 G>A maps to NM_001143854.1 V691V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FP-01A-31D-A387-09 chr12:113312941 C>T maps to NM_001143854.1 Q284*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr17:169326 G>T maps to NM_006987.3 R79R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-A7RE-01A-11D-A351-09 chr2:89028848 C>T maps to NM_144563.2 H152H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6KZ-01A-11D-A31U-09 chr23:153627910 G>A did not map to a codon.
Sequencing variant TCGA-R6-A6DQ-01B-11D-A31U-09 chr17:8280944 A>C maps to NM_000987.3 S125S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43C-01A-11D-A247-09 chr3:52027881 T>G maps to NM_000992.2 P121P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A4P3-01A-11D-A27G-09 chr22:39708980 C>G maps to NM_000967.3 L392L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OH-01A-11D-A27G-09 chr3:12877709 G>T maps to ENST00000273223 A115A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NQ-01A-11D-A36J-09 chr19:5691619 C>G maps to NM_015414.3 A102A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASX-01A-11D-A387-09 chr19:5691410 G>T maps to NM_015414.3 E59*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FB-01A-11D-A33E-09 chr15:66791957 T>G maps to NM_000968.2 A357A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6XQ-01B-11D-A33E-09 chr6:42852468 G>T maps to NM_198486.2 E135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EZ-01A-11D-A36J-09 chr3:128341047 G>A maps to NM_002950.3 Q534*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A8-01A-32D-A27G-09 chr6:30312962 G>A maps to ENST00000428040 V5V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FD-01A-11D-A33E-09 chr15:75248375 C>G maps to NM_017793.2 A183A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-AAPN-01A-11D-A403-09 chr1:150444822 A>G maps to NM_015203.3 T1133T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93C-01A-11D-A387-09 chr2:154334953 C>T maps to NM_019845.2 A42A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49M-01A-21D-A27G-09 chr2:154334905 C>T maps to NM_019845.2 Q58Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NT-01A-11D-A37C-09 chr17:45056319 G>A maps to NM_203400.3 G18G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EW-01A-11D-A36J-09 chr11:17098715 G>A maps to NM_001017.2 I50I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A3-01A-11D-A27G-09 chr5:149827254 G>T maps to NM_005617.3 V14V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8W5-01B-11D-A37C-09 chr16:2014593 G>T maps to NM_002952.3 P11P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43C-01A-11D-A247-09 chr12:56436328 C>T maps to NM_001029.3 R42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FB-01A-11D-A33E-09 chr4:152020848 G>A maps to NM_001006.3 K15K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HV-01A-21D-A351-09 chr19:58904398 G>T maps to NM_001009.3 R55R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NH-01A-11D-A37C-09 chr1:26898371 C>T maps to NM_001006665.1 C604C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GO-01A-11D-A37C-09 chr23:83362681 G>A did not map to a codon.
Sequencing variant TCGA-L5-A43C-01A-11D-A247-09 chr23:83352796 A>C did not map to a codon.
Sequencing variant TCGA-LN-A49M-01A-21D-A27G-09 chr23:83361418 C>A did not map to a codon.
Sequencing variant TCGA-R6-A6DN-01B-11D-A31U-09 chr23:83351265 C>T did not map to a codon.
Sequencing variant TCGA-IG-A6QS-01A-12D-A33E-09 chr11:67202558 C>A maps to NM_003952.2 P456P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8WC-01A-11D-A37C-09 chr1:45242354 C>G maps to NM_001012.1 P40P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NV-01A-11D-A37C-09 chr17:78704473 C>T maps to NM_020761.2 Q208*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8W5-01B-11D-A37C-09 chr17:78704397 G>T maps to NM_020761.2 L182L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XP-A8T8-01A-11D-A36J-09 chr17:78765282 T>C maps to NM_020761.2 P288P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3YC-01A-11D-A247-09 chr16:836114 G>A maps to NM_058192.2 P258P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OR-01A-11D-A27G-09 chr23:55744780 G>T did not map to a codon.
Sequencing variant TCGA-L5-A893-01A-11D-A36J-09 chr23:55757974 T>G did not map to a codon.
Sequencing variant TCGA-L5-A8NR-01A-11D-A37C-09 chr23:55755726 T>G did not map to a codon.
Sequencing variant TCGA-LN-A49S-01A-11D-A247-09 chr23:55748669 A>T did not map to a codon.
Sequencing variant TCGA-LN-A4A5-01A-21D-A27G-09 chr1:39317318 G>A maps to NM_022157.2 I289I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr6:90121613 G>A maps to NM_021244.4 D33D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93C-01A-11D-A387-09 chr20:17599255 G>A maps to ENST00000377813 S1248S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr20:17641106 C>A maps to ENST00000377813 G16*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A1-01A-21D-A27G-09 chr20:17639255 T>A maps to ENST00000377813 K633*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A2-01A-31D-A27G-09 chr20:17614112 G>A maps to ENST00000377813 Q868*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GM-01A-11D-A37C-09 chr6:7230279 C>T maps to NM_001003699.3 Q650*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OH-01A-11D-A27G-09 chr6:7230980 G>T maps to NM_001003699.3 S883S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NV-01A-11D-A37C-09 chr11:4142838 T>C maps to NM_001033.3 P294P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr8:103236303 G>A maps to NM_015713.4 R174*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3I8-01A-11D-A247-09 chr16:15159152 G>A maps to NM_018427.3 T543T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3Y9-01A-12D-A247-09 chr1:218480910 G>A maps to NM_016052.3 L214L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr22:42910202 G>A maps to NM_015703.4 S222S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A4P3-01A-11D-A27G-09 chr11:6623316 G>T maps to NM_015324.2 P76P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FP-01A-31D-A387-09 chr3:51969419 C>A maps to NM_004704.3 R303R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3QL-01A-11D-A247-09 chr8:67342178 G>T maps to NM_015169.3 L271L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A625-01A-11D-A31U-09 chr23:18665388 C>T did not map to a codon.
Sequencing variant TCGA-JY-A6FH-01A-11D-A33E-09 chr23:18665447 G>T did not map to a codon.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr1:114319835 G>A maps to NM_018364.3 R552*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49M-01A-21D-A27G-09 chr11:77383153 C>T maps to NM_016578.3 K1228K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NF-01A-11D-A37C-09 chr6:116938140 G>T maps to NM_001010892.2 E119*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XP-A8T6-01A-11D-A36J-09 chr6:116948790 G>T did not map to a codon.
Sequencing variant TCGA-JY-A6FH-01A-11D-A33E-09 chr19:46307821 G>T maps to NM_030785.3 A447A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RE-A7BO-01A-11D-A33E-09 chr19:46317873 G>T maps to NM_030785.3 A187A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NH-01A-11D-A37C-09 chr3:158261201 G>T maps to NM_016625.2 E280*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZR-A9CJ-01B-11D-A387-09 chr3:158261207 G>T maps to NM_016625.2 E282*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6Y2-01B-11D-A33E-09 chr12:122990141 G>A maps to NM_023012.5 Q413*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S8-A6BW-01A-11D-A31U-09 chr10:16796954 G>A maps to NM_012425.3 F105F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr22:23404124 T>C did not map to a codon.
Sequencing variant TCGA-L5-A43M-01A-11D-A247-09 chr20:62321467 C>T maps to ENST00000482936 L724L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XP-A8T8-01A-11D-A36J-09 chr20:62319726 G>A maps to ENST00000482936 L570L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A8I0-01A-11D-A36J-09 chr10:63964712 A>G maps to NM_145307.2 P363P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GF-01A-11D-A37C-09 chr14:101349574 G>A maps to NM_001134888.2 D517D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OJ-01A-11D-A27G-09 chr14:101350669 C>T maps to NM_001134888.2 E152E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4MR-01A-11D-A28B-09 chr14:101347783 C>A maps to NM_001134888.2 R1114R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A8O2-01A-11D-A36J-09 chr14:60193765 C>A maps to NM_021136.2 E546*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A8HZ-01A-11D-A36J-09 chr14:60194150 G>A maps to NM_021136.2 S417S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A938-01A-11D-A37C-09 chr11:63520047 G>A maps to ENST00000377819 V936V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43I-01A-11D-A247-09 chr17:1840386 C>T maps to NM_178568.2 P243P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FQ-01A-31D-A387-09 chr17:1840983 G>A maps to NM_178568.2 N44N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZR-A9CJ-01B-11D-A387-09 chr17:1840005 G>A maps to NM_178568.2 A370A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93C-01A-11D-A387-09 chr3:187416573 G>A maps to NM_001004312.2 Y130Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OE-01A-11D-A27G-09 chr18:67742585 A>T did not map to a codon.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr18:67759941 G>T maps to NM_173630.3 S1334S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L7-A6VZ-01A-12D-A33E-09 chr18:67755341 G>T maps to NM_173630.3 T1395T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A5B8-01A-11D-A28B-09 chr7:87258249 C>T maps to NM_138290.2 I37I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49M-01A-21D-A27G-09 chr7:87436699 G>A maps to NM_138290.2 K340K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6Y0-01B-11D-A33E-09 chr7:87436687 G>T maps to NM_138290.2 L336L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A1-01A-21D-A27G-09 chr8:93017522 G>T maps to NM_175634.2 A187A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43I-01A-11D-A247-09 chr6:45390459 G>A maps to ENST00000359524 Q131Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FQ-01A-31D-A387-09 chr1:155295177 C>G maps to NM_001105203.1 L535L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EU-01A-11D-A36J-09 chr1:155296482 T>C maps to NM_001105203.1 T658T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6F8-01A-11D-A33E-09 chr3:127801414 G>T maps to NM_003707.2 I374I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GL-01A-12D-A37C-09 chr19:49510281 G>T maps to NM_006666.1 A91A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NQ-01A-11D-A36J-09 chr19:49513244 C>T maps to NM_006666.1 I195I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NQ-01A-11D-A36J-09 chr19:49513865 C>G maps to NM_006666.1 S262*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43I-01A-11D-A247-09 chr4:159568032 G>A maps to ENST00000440678 W506*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FB-01A-11D-A33E-09 chr13:32348755 G>T did not map to a codon.
Sequencing variant TCGA-R6-A8WC-01A-11D-A37C-09 chr5:33937726 C>T maps to NM_016568.3 I294I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OR-01A-11D-A27G-09 chr9:137321026 C>T maps to NM_002957.4 T328T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A4QS-01A-11D-A27G-09 chr1:165386425 G>A maps to NM_006917.4 G158G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A5B8-01A-11D-A28B-09 chr1:165377515 C>T maps to NM_006917.4 Q362Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RF-01A-13D-A33E-09 chr19:39025782 G>T maps to NM_000540.2 E3788*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr19:38981337 G>A maps to NM_000540.2 L2031L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49M-01A-21D-A27G-09 chr19:39062662 C>G maps to NM_000540.2 S4584*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6L6-01B-11D-A33E-09 chr19:38954119 G>T maps to NM_000540.2 E879*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8W8-01B-11D-A37C-09 chr19:39052024 G>A maps to NM_000540.2 A4185A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GK-01A-11D-A37C-09 chr1:237777543 C>T maps to NM_001035.2 L1706L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GR-01A-12D-A37C-09 chr1:237604647 A>G maps to NM_001035.2 E345E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A6QS-01A-12D-A33E-09 chr1:237780786 G>T did not map to a codon.
Sequencing variant TCGA-L5-A43E-01A-11D-A247-09 chr1:237886426 G>T did not map to a codon.
Sequencing variant TCGA-L5-A43I-01A-11D-A247-09 chr1:237947620 G>A maps to NM_001035.2 A4203A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OE-01A-11D-A27G-09 chr1:237666610 C>T maps to NM_001035.2 R807*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NW-01A-11D-A37C-09 chr1:237777984 G>T maps to NM_001035.2 E1853*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49L-01A-11D-A247-09 chr1:237753262 C>T maps to NM_001035.2 Q1257*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4MR-01A-11D-A28B-09 chr1:237863702 G>A maps to NM_001035.2 L3101L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HZ-01A-31D-A351-09 chr1:237617835 C>T maps to NM_001035.2 R480*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FR-01A-11D-A387-09 chr1:237811849 C>T maps to NM_001035.2 F2483F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-A7RC-01B-11D-A403-09 chr1:237947386 C>G maps to NM_001035.2 V4125V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-A7RC-01B-11D-A403-09 chr1:237955574 G>T maps to NM_001035.2 L4578L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EQ-01A-11D-A36J-09 chr1:237550621 T>C maps to NM_001035.2 A206A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA4G-01A-11D-A37C-09 chr1:237608789 G>T maps to NM_001035.2 R420R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X8-AAAR-01A-11D-A403-09 chr1:237580415 A>C maps to NM_001035.2 R281R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GR-01A-12D-A37C-09 chr15:33922208 G>A maps to NM_001036.3 K916K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3Y9-01A-12D-A247-09 chr15:34078106 C>T maps to NM_001036.3 L3171L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6F8-01A-11D-A33E-09 chr15:33993250 G>A maps to NM_001036.3 A2151A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FE-01A-11D-A33E-09 chr15:33955035 G>T maps to NM_001036.3 E1769*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FH-01A-11D-A33E-09 chr15:33831635 C>T maps to NM_001036.3 L173L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FH-01A-11D-A33E-09 chr15:33922179 G>T maps to NM_001036.3 E907*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr15:34048505 G>T did not map to a codon.
Sequencing variant TCGA-VR-A8ER-01A-11D-A36J-09 chr15:34105085 G>A maps to NM_001036.3 W3427*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A8JD-01A-11D-A36J-09 chr15:34064134 C>G maps to NM_001036.3 S2944*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49N-01A-11D-A247-09 chr1:153346936 G>T maps to NM_005621.1 T44T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FP-01A-31D-A387-09 chr1:153520322 C>T did not map to a codon.
Sequencing variant TCGA-VR-A8Q7-01A-11D-A37C-09 chr1:101704653 C>T maps to NM_001400.4 S38S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FG-01A-11D-A33E-09 chr19:3179167 C>T maps to NM_003775.3 F126F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NW-01A-11D-A37C-09 chr19:3179261 A>T maps to NM_003775.3 K158*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GR-01A-12D-A37C-09 chr19:10624955 C>T maps to NM_001166215.1 P244P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88Z-01A-11D-A36J-09 chr19:10624598 C>T maps to NM_001166215.1 S363S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43E-01A-11D-A247-09 chr13:23904430 A>C maps to NM_014363.4 A4528A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OG-01A-11D-A27G-09 chr13:23905798 A>C maps to NM_014363.4 T4072T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr13:23910850 G>T maps to NM_014363.4 T2388T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A9VB-01A-21D-A37C-09 chr13:23915308 G>C maps to NM_014363.4 A902A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZR-A9CJ-01B-11D-A387-09 chr13:23908709 A>T maps to NM_014363.4 L3102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OU-01A-11D-A28B-09 chr19:47653534 T>A maps to NM_005500.2 L96*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr19:5653398 C>T maps to ENST00000433404 D498D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OW-01A-11D-A28B-09 chr19:5641935 G>A maps to ENST00000433404 P175P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49L-01A-11D-A247-09 chr2:234224722 G>T maps to NM_000541.4 V26V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GI-01A-11D-A37C-09 chr23:134992320 G>A did not map to a codon.
Sequencing variant TCGA-L5-A8NF-01A-11D-A37C-09 chr23:134987422 C>G did not map to a codon.
Sequencing variant TCGA-Z6-A9VB-01A-21D-A37C-09 chr23:134993791 C>A did not map to a codon.
Sequencing variant TCGA-JY-A6F8-01A-11D-A33E-09 chr16:51175811 T>C maps to ENST00000251020 Q107Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A939-01A-12D-A37C-09 chr16:51173576 G>T maps to ENST00000251020 S852S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49U-01A-31D-A27G-09 chr16:51173801 G>A maps to ENST00000251020 N777N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASX-01A-11D-A387-09 chr16:51173270 G>A maps to ENST00000251020 S954S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NI-01A-11D-A37C-09 chr14:21990863 G>T maps to NM_005407.1 R1000R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GM-01A-11D-A37C-09 chr19:39866395 C>A maps to NM_018028.2 A258A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FH-01A-11D-A33E-09 chr19:39860548 G>T maps to NM_018028.2 E151*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A938-01A-11D-A37C-09 chr19:39860505 A>T maps to NM_018028.2 T136T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88W-01A-11D-A351-09 chr19:39870718 G>A maps to NM_018028.2 Q548Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6F8-01A-11D-A33E-09 chr7:92733037 G>T maps to NM_017654.3 Y791*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr7:92731996 G>A maps to NM_017654.3 N1138N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6KZ-01A-11D-A31U-09 chr7:92734548 T>G maps to NM_017654.3 R288R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NN-01A-11D-A37C-09 chr7:92764138 T>C maps to NM_152703.2 E382E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A97H-01A-11D-A387-09 chr21:15882699 G>A maps to ENST00000285670 F232F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASW-01A-11D-A403-09 chr21:15882675 C>T maps to ENST00000285670 T240T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GI-01A-11D-A37C-09 chr2:128757708 G>A maps to NM_001145928.1 F369F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XP-A8T6-01A-11D-A36J-09 chr2:128699580 T>C maps to NM_001145928.1 *1084W. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr17:73698583 C>T maps to NM_013260.6 R141*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NV-01A-11D-A37C-09 chr19:55743291 T>G maps to ENST00000443936 R790R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZR-A9CJ-01B-11D-A387-09 chr11:68315546 T>C maps to NM_001164160.1 L143L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr10:71921647 G>T maps to NM_020150.4 I8I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A893-01A-11D-A36J-09 chr9:136536778 C>T maps to NM_007101.3 W735*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6XQ-01B-11D-A33E-09 chr9:136559398 C>A maps to NM_007101.3 P634P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EQ-01A-11D-A36J-09 chr9:136536708 G>A maps to NM_007101.3 H758H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6XG-01B-11D-A33E-09 chr17:26723194 G>T maps to ENST00000379061 E687*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S8-A6BV-01A-21D-A31U-09 chr1:109773543 C>T maps to ENST00000369923 V164V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr6:148865155 G>A maps to NM_015278.3 E850E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q9-A6FW-01A-31D-A31U-09 chr6:148711340 C>T maps to NM_015278.3 D76D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA4D-01A-11D-A37C-09 chr6:148792634 A>C maps to NM_015278.3 S170S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NW-01A-11D-A37C-09 chr1:100573415 G>A maps to NM_194292.1 Q336*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GG-01A-11D-A37C-09 chr23:84363283 G>T did not map to a codon.
Sequencing variant TCGA-IG-A3YA-01A-11D-A247-09 chr23:84362458 G>C did not map to a codon.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr23:84363924 G>T did not map to a codon.
Sequencing variant TCGA-LN-A4A1-01A-21D-A27G-09 chr23:84363347 G>T did not map to a codon.
Sequencing variant TCGA-L5-A88V-01A-11D-A351-09 chr14:51107484 G>A maps to NM_021818.2 Y311Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S8-A6BV-01A-21D-A31U-09 chr22:50893822 G>A maps to ENST00000337034 Q1472*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OJ-01A-11D-A27G-09 chr12:123829961 G>A maps to NM_001167856.1 R131R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L7-A6VZ-01A-12D-A33E-09 chr19:1109591 G>A maps to NM_014963.2 S1043S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A5U5-01A-21D-A28B-09 chr19:36018070 C>T maps to NM_001166034.1 G371G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A5U7-01A-11D-A31U-09 chr19:36018325 A>G maps to NM_001166034.1 A286A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OT-01A-11D-A28B-09 chr1:155227350 C>T maps to NM_005698.2 W205*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EP-01A-31D-A403-09 chr19:1924142 C>T maps to NM_079834.2 Q184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3QL-01A-11D-A247-09 chr6:28543363 G>T maps to NM_052923.1 S373*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FG-01A-11D-A33E-09 chr3:47467000 G>A maps to NM_012235.2 F337F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A1-01A-21D-A27G-09 chr3:47469123 C>T maps to NM_012235.2 L148L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S8-A6BW-01A-11D-A31U-09 chr3:47462507 G>A maps to NM_012235.2 L419L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr15:76958033 T>A maps to ENST00000324767 K869*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4ON-01A-11D-A27G-09 chr15:76958127 C>T maps to ENST00000324767 E837E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49M-01A-21D-A27G-09 chr15:77067387 C>T maps to ENST00000324767 V281V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GR-01A-12D-A37C-09 chr8:27779319 G>A maps to NM_173833.5 R228R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6XG-01B-11D-A33E-09 chr12:125348161 G>T maps to NM_005505.4 L35L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-A7RE-01A-11D-A351-09 chr17:1538714 G>A maps to NM_003693.2 S610S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6L6-01B-11D-A33E-09 chr22:20781730 C>T maps to NM_153334.4 S554S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49M-01A-21D-A27G-09 chr13:78191992 C>T maps to NM_144777.2 Q523*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8W8-01B-11D-A37C-09 chr13:78146276 G>T maps to NM_144777.2 P166P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr14:31107413 T>C maps to ENST00000311943 N140N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OS-01A-11D-A28B-09 chr2:224463859 G>C maps to NM_003469.4 V47V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A8I0-01A-11D-A36J-09 chr2:224463670 C>T maps to NM_003469.4 W110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OT-01A-11D-A28B-09 chr15:51975283 A>G maps to NM_013243.3 E48E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S8-A6BV-01A-21D-A31U-09 chr11:62190553 G>A maps to NM_003357.4 L89L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FH-01A-11D-A33E-09 chr3:159606664 C>T maps to NM_001197113.1 T493T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FP-01A-31D-A387-09 chr3:159606730 A>G maps to NM_001197113.1 E515E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A50L-01A-11D-A27G-09 chr7:12644287 G>A maps to NM_001112706.2 K222K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A6QS-01A-12D-A33E-09 chr7:12610420 G>T maps to NM_001112706.2 R3R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OH-01A-11D-A27G-09 chr2:238991975 G>T maps to NM_016510.4 E289*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr2:238991921 C>T maps to NM_016510.4 R271*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3Y9-01A-12D-A247-09 chr23:18275037 C>G did not map to a codon.
Sequencing variant TCGA-L5-A4OW-01A-11D-A28B-09 chr23:18264856 A>C did not map to a codon.
Sequencing variant TCGA-LN-A8I0-01A-11D-A36J-09 chr6:108029192 C>T maps to NM_198081.3 A332A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GI-01A-11D-A37C-09 chr3:38783781 G>A maps to NM_006514.2 I702I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RE-01A-11D-A33E-09 chr3:38913760 A>G maps to ENST00000302328 L1140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49K-01A-11D-A247-09 chr3:38962699 C>A maps to ENST00000302328 L253L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NF-01A-11D-A37C-09 chr2:166848273 C>T maps to NM_001165963.1 P1837P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49N-01A-11D-A247-09 chr2:166872186 G>T maps to NM_001165963.1 G1160G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FP-01A-31D-A387-09 chr2:166847873 C>A maps to NM_001165963.1 E1971*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-A7RB-01A-11D-A351-09 chr2:166850800 C>T maps to NM_001165963.1 V1569V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3YC-01A-11D-A247-09 chr19:35524872 C>T maps to NM_199037.3 S226S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GF-01A-11D-A37C-09 chr2:166198960 T>G maps to NM_001040142.1 V848V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OG-01A-11D-A27G-09 chr2:166245430 C>A maps to NM_001040142.1 I1705I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr2:166171982 G>A maps to NM_001040142.1 A462A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8W8-01B-11D-A37C-09 chr2:166201216 G>A maps to NM_001040142.1 K905K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A4P3-01A-11D-A27G-09 chr2:165996003 G>A maps to NM_006922.3 L712L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NR-01A-11D-A37C-09 chr2:166003484 C>A maps to NM_006922.3 G479*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OF-01A-11D-A27G-09 chr11:123524452 A>G did not map to a codon.
Sequencing variant TCGA-IG-A625-01A-11D-A31U-09 chr17:62022995 C>T maps to NM_000334.4 V1148V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr17:62020366 G>T maps to NM_000334.4 T1369T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NK-01A-21D-A37C-09 chr17:62034632 G>A maps to NM_000334.4 F755F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr17:62045455 G>A maps to NM_000334.4 N321N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L7-A6VZ-01A-12D-A33E-09 chr17:62019123 G>A maps to NM_000334.4 Y1506Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43I-01A-11D-A247-09 chr3:38592534 G>A maps to NM_001099404.1 S1776S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OH-01A-11D-A27G-09 chr3:38591964 G>T maps to NM_001099404.1 S1966S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr3:38622706 G>A maps to NM_001099404.1 C981C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GM-01A-11D-A37C-09 chr2:167334115 C>A maps to NM_002976.2 E31*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A6QS-01A-12D-A33E-09 chr2:167322492 C>T maps to NM_002976.2 L223L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6L6-01B-11D-A33E-09 chr2:167322480 T>G maps to NM_002976.2 V227V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GM-01A-11D-A37C-09 chr12:52080157 T>C maps to NM_014191.2 F134F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr12:52156423 C>T maps to NM_014191.2 D836D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OU-01A-11D-A28B-09 chr12:52162881 C>T maps to NM_014191.2 I1045I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6L4-01A-11D-A31U-09 chr12:52200088 G>T maps to NM_014191.2 E1607*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-AAPN-01A-11D-A403-09 chr12:52056609 G>A maps to NM_014191.2 A3A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FD-01A-11D-A33E-09 chr2:167133513 G>A maps to ENST00000303354 V952V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr2:167055646 G>A maps to ENST00000303354 D1835D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49X-01A-31D-A27G-09 chr2:167056174 G>A maps to ENST00000303354 Y1659Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6XQ-01B-11D-A33E-09 chr2:167083215 T>C did not map to a codon.
Sequencing variant TCGA-VR-AA4D-01A-11D-A37C-09 chr2:167084182 A>G maps to ENST00000303354 V1420V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XP-A8T6-01A-11D-A36J-09 chr2:167056009 G>T maps to ENST00000303354 P1714P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8WG-01A-11D-A37C-09 chr12:6457241 G>A maps to NM_001159576.1 Q662*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RE-A7BO-01A-11D-A33E-09 chr12:6457892 C>A maps to NM_001159576.1 T602T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KH-A6WC-01A-11D-A33E-09 chr22:50962416 C>A maps to NM_001169111.1 E142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr4:141302185 A>G maps to NM_001153484.1 G136G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr17:55058512 C>A maps to NM_021626.2 A49A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49W-01A-11D-A27G-09 chr2:175263170 G>T did not map to a codon.
Sequencing variant TCGA-LN-A49V-01A-11D-A247-09 chr22:43600128 G>A maps to NM_173050.2 F947F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A51D-01A-11D-A27G-09 chr6:35211788 G>A maps to ENST00000394681 Q723Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NS-01A-12D-A37C-09 chr6:35216418 G>A maps to ENST00000394681 L989L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3YC-01A-11D-A247-09 chr11:65304154 C>T maps to NM_020680.3 L584L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6XG-01B-11D-A33E-09 chr11:65299048 G>T maps to NM_020680.3 V337V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49L-01A-11D-A247-09 chr12:100676831 C>A maps to NM_017988.4 V28V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OH-01A-11D-A27G-09 chr1:169838163 G>T maps to NM_181093.2 L214L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr1:169836092 C>A maps to NM_181093.2 V253V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASV-01A-11D-A387-09 chr8:59484764 T>C maps to NM_005625.3 N44N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr20:1293247 G>A maps to NM_080489.4 V181V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6Y0-01B-11D-A33E-09 chr14:50251371 C>G maps to NM_004713.3 L1071L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49X-01A-31D-A27G-09 chr1:243434326 G>T maps to NM_006642.3 E90*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A97I-01A-11D-A387-09 chr11:61213449 C>G maps to NM_017841.2 V136V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4MR-01A-11D-A28B-09 chr11:61205245 C>T maps to NM_017841.2 S62S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GF-01A-11D-A37C-09 chr7:4153769 C>T maps to NM_152744.3 V1229V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GJ-01A-11D-A37C-09 chr7:4050652 C>T maps to NM_152744.3 T729T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GK-01A-11D-A37C-09 chr7:3681695 T>G maps to NM_152744.3 T224T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RF-01A-13D-A33E-09 chr7:3678686 G>T maps to NM_152744.3 V170V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A51D-01A-11D-A27G-09 chr7:4247735 C>G maps to NM_152744.3 Y1740*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A6QS-01A-12D-A33E-09 chr7:4056934 C>T maps to NM_152744.3 A851A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4ON-01A-11D-A27G-09 chr7:4051762 G>A maps to NM_152744.3 P772P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OP-01A-11D-A27G-09 chr7:4188990 C>A maps to NM_152744.3 S1507S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NT-01A-11D-A37C-09 chr7:4056814 T>A maps to NM_152744.3 A811A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-A7RB-01A-11D-A351-09 chr7:4185503 G>A maps to NM_152744.3 W1460*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X8-AAAR-01A-11D-A403-09 chr7:3681695 T>G maps to NM_152744.3 T224T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4MQ-01A-11D-A28B-09 chr17:71375665 G>C maps to NM_001144952.1 Y1595*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XP-A8T8-01A-11D-A36J-09 chr17:71429904 C>A maps to NM_001144952.1 S426S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GJ-01A-11D-A37C-09 chr3:10342967 C>A maps to ENST00000343726 E362*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A9VB-01A-21D-A37C-09 chr3:10357051 G>T maps to ENST00000343726 I85I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr22:30812025 C>T maps to NM_012429.2 G287G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49L-01A-11D-A247-09 chr22:30812055 C>T maps to NM_012429.2 L297L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OR-01A-11D-A27G-09 chr16:5009356 C>A maps to NM_014692.1 V11V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NE-01A-11D-A37C-09 chr16:5058462 G>A maps to NM_014692.1 W538*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NG-01A-11D-A37C-09 chr16:5038250 C>T maps to NM_014692.1 R105R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NR-01A-11D-A37C-09 chr16:5057471 C>T maps to NM_014692.1 R519R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X8-AAAR-01A-11D-A403-09 chr16:5009368 G>T maps to NM_014692.1 P15P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NI-01A-11D-A37C-09 chr9:139350128 C>T maps to NM_014866.1 G1927G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NN-01A-11D-A37C-09 chr9:139369856 G>A maps to NM_014866.1 N737N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HX-01A-11D-A33E-09 chr9:139369031 G>T maps to NM_014866.1 S1012S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FO-01A-11D-A387-09 chr1:177913773 A>C maps to NM_033127.2 T601T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3YB-01A-11D-A247-09 chr14:39532557 G>A maps to NM_006364.2 T456T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NQ-01A-11D-A36J-09 chr14:39502531 C>A maps to NM_006364.2 E737*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A8JD-01A-11D-A36J-09 chr10:121685687 C>T maps to NM_007190.2 C754C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A4P3-01A-11D-A27G-09 chr5:134007576 G>T did not map to a codon.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr5:134050781 C>T maps to NM_021982.1 N932N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FP-01A-31D-A387-09 chr4:110446036 C>T maps to NM_006323.2 Q858*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A8-01A-32D-A27G-09 chr10:75526571 A>T maps to NM_198597.1 V618V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASW-01A-11D-A403-09 chr10:75526865 G>T maps to NM_198597.1 E650*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A5B8-01A-11D-A28B-09 chr4:119649763 G>C maps to ENST00000379735 L971L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr4:119736807 T>C maps to ENST00000379735 R157R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93D-01A-11D-A387-09 chr4:83788383 G>T maps to ENST00000505472 S323*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FO-01A-11D-A387-09 chr4:83799894 C>G maps to ENST00000505472 V130V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GI-01A-11D-A37C-09 chr10:102248620 A>G maps to NM_015490.3 T1094T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr3:127774387 C>T maps to ENST00000464451 T41T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-A7RC-01B-11D-A403-09 chr6:108232547 A>C did not map to a codon.
Sequencing variant TCGA-VR-AA4G-01A-11D-A37C-09 chr18:12955478 A>G maps to NM_001013437.1 V60V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr14:81945991 G>A maps to NM_005065.4 G713G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L7-A6VZ-01A-12D-A33E-09 chr14:81943462 G>T maps to NM_005065.4 Y746*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3YC-01A-11D-A247-09 chr20:13850834 G>A maps to NM_025229.1 G373G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr20:13894523 G>A maps to NM_025229.1 D151D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr4:25780792 C>T maps to NM_015187.3 A830A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GG-01A-11D-A37C-09 chr1:169702095 G>T maps to NM_000450.2 S27S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OO-01A-11D-A27G-09 chr1:169670755 A>G maps to NM_000655.4 V355V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GK-01A-11D-A37C-09 chr1:169588458 T>C did not map to a codon.
Sequencing variant TCGA-L5-A4OJ-01A-11D-A27G-09 chr1:169578895 G>T maps to NM_003005.3 V393V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L7-A56G-01A-21D-A27G-09 chr19:40006040 T>C maps to NM_182704.1 T63T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3YC-01A-11D-A247-09 chr7:83592578 G>T maps to NM_006080.2 S601*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FG-01A-11D-A33E-09 chr7:83591085 T>C maps to NM_006080.2 L639L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88S-01A-11D-A36J-09 chr7:83634709 G>C maps to NM_006080.2 V435V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA7I-01A-11D-A403-09 chr7:80427446 A>G maps to NM_006379.2 I364I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HV-01A-21D-A351-09 chr7:84694821 A>G maps to NM_152754.2 D212D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EZ-01A-11D-A36J-09 chr7:84685161 A>T maps to NM_152754.2 I244I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr3:50222191 C>T maps to NM_004186.3 A467A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OT-01A-11D-A28B-09 chr3:50220413 G>A maps to NM_004186.3 P327P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr3:52474798 G>A maps to NM_020163.1 L323L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NF-01A-11D-A37C-09 chr3:52474807 C>T maps to NM_020163.1 G320G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6Y2-01B-11D-A33E-09 chr3:52476594 G>A maps to NM_020163.1 R107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NU-01A-11D-A36J-09 chr1:156130699 C>T maps to NM_022367.3 D230D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OP-01A-11D-A27G-09 chr15:90771823 C>T maps to NM_198925.2 C821C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NI-01A-11D-A37C-09 chr2:97531627 A>G maps to NM_017789.4 C99C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49S-01A-11D-A247-09 chr2:97530539 C>T maps to NM_017789.4 P288P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RF-01A-13D-A33E-09 chr9:92006181 G>T maps to NM_006378.3 C257*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NH-01A-11D-A37C-09 chr9:92002316 G>A maps to NM_006378.3 V438V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr9:91994101 C>T maps to NM_006378.3 A702A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49U-01A-31D-A27G-09 chr9:91994287 G>T maps to NM_006378.3 A640A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EZ-01A-11D-A36J-09 chr5:9066718 T>A maps to NM_003966.2 K705*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A939-01A-12D-A37C-09 chr3:122631064 G>T maps to NM_001031702.2 L950L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NE-01A-11D-A37C-09 chr5:115823893 T>G did not map to a codon.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr5:115831944 A>G did not map to a codon.
Sequencing variant TCGA-IG-A5B8-01A-11D-A28B-09 chr19:4548163 G>T maps to NM_032108.3 G492G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NW-01A-11D-A37C-09 chr19:4552603 G>T maps to NM_032108.3 G273G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3QL-01A-11D-A247-09 chr1:151109547 C>T maps to NM_001178061.1 V253V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49R-01A-11D-A247-09 chr1:151105027 G>A maps to NM_001178061.1 L941L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OW-01A-11D-A28B-09 chr15:48063700 T>C maps to NM_153618.1 L981L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6XG-01B-11D-A33E-09 chr15:48063589 C>T maps to NM_153618.1 R944*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3Y9-01A-12D-A247-09 chr20:43850641 T>C maps to NM_003008.2 F123F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6DQ-01B-11D-A31U-09 chr20:43851850 G>A maps to NM_003008.2 K526K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A3-01A-11D-A27G-09 chr6:76412675 G>T maps to NM_015571.2 A868A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OF-01A-11D-A27G-09 chr3:101056351 C>T did not map to a codon.
Sequencing variant TCGA-RE-A7BO-01A-11D-A33E-09 chr2:110342896 C>A maps to ENST00000356688 G73G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A51D-01A-11D-A27G-09 chr4:77949785 C>T maps to ENST00000510515 Q330*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HX-01A-11D-A33E-09 chr7:55902219 C>A maps to NM_207366.2 T206T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RE-01A-11D-A33E-09 chr22:42377840 G>T did not map to a codon.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr22:19707860 C>T maps to NM_002688.5 D127D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OP-01A-11D-A27G-09 chr23:118767379 C>A did not map to a codon.
Sequencing variant TCGA-L5-A8NF-01A-11D-A37C-09 chr1:67880929 G>A maps to NM_001018067.1 G363G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OJ-01A-11D-A27G-09 chr15:44084579 C>T maps to ENST00000409960 T2T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NQ-01A-11D-A36J-09 chr11:18014500 G>C maps to NM_012139.2 S221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6DQ-01B-11D-A31U-09 chr6:122768321 C>T maps to NM_020755.2 W313*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HY-01A-12D-A351-09 chr1:31901871 C>G maps to NM_178865.4 L276L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4MR-01A-11D-A28B-09 chr20:43135469 G>A maps to NM_006811.2 Q261*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-A7RB-01A-11D-A351-09 chr20:43138567 G>T maps to NM_006811.2 R193R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A891-01A-11D-A36J-09 chr15:44087924 G>A maps to ENST00000319327 L384L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr14:94956094 G>A maps to NM_173850.2 D305D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A97I-01A-11D-A387-09 chr14:95029842 C>G maps to NM_006215.2 L8L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FD-01A-11D-A33E-09 chr14:94770817 G>T maps to NM_001756.3 I385I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A893-01A-11D-A36J-09 chr23:105280572 A>T did not map to a codon.
Sequencing variant TCGA-2H-A9GI-01A-11D-A37C-09 chr6:2890644 G>A maps to NM_004155.4 Q295*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A50L-01A-11D-A27G-09 chr6:2892150 G>C maps to NM_004155.4 R213R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93E-01A-11D-A37C-09 chr17:1680026 C>T maps to NM_002615.4 Q330*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49S-01A-11D-A247-09 chr11:57373935 C>T maps to ENST00000403558 F358F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8WG-01A-11D-A37C-09 chr19:40928745 G>A maps to NM_013376.3 R236R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4MR-01A-11D-A28B-09 chr19:40947558 C>T maps to NM_203344.2 G143G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q9-A6FW-01A-31D-A31U-09 chr19:40947483 T>C maps to NM_203344.2 P168P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A8JD-01A-11D-A36J-09 chr11:94906419 C>A maps to NM_144665.2 *493L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3I8-01A-11D-A247-09 chr2:179986656 C>G did not map to a codon.
Sequencing variant TCGA-JY-A6FB-01A-11D-A33E-09 chr2:180047846 C>A maps to NM_178123.4 E42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr2:180016103 G>A maps to NM_178123.4 S128S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NK-01A-21D-A37C-09 chr2:180016091 C>T maps to NM_178123.4 L132L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RE-01A-11D-A33E-09 chr9:131455202 G>C maps to NM_001122821.1 L158L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49Y-01A-11D-A27G-09 chr18:42456561 G>A maps to NM_001130110.1 K191K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASX-01A-11D-A387-09 chr18:42531092 C>T maps to NM_015559.2 L596L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RF-01A-13D-A33E-09 chr3:47155364 C>G did not map to a codon.
Sequencing variant TCGA-LN-A4MR-01A-11D-A28B-09 chr4:140454372 G>A maps to NM_030648.2 F106F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr12:123892039 C>T maps to NM_020382.3 C283C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3Y9-01A-12D-A247-09 chr1:150923930 G>A maps to NM_001145415.1 K768K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr1:150917539 C>T maps to NM_001145415.1 R366*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr1:150931755 G>A maps to NM_001145415.1 Q811Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr1:150936217 G>A did not map to a codon.
Sequencing variant TCGA-V5-AASV-01A-11D-A387-09 chr1:150936764 C>T maps to NM_001145415.1 Y1267Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XP-A8T6-01A-11D-A36J-09 chr1:150913896 G>A maps to NM_001145415.1 L180L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NR-01A-11D-A37C-09 chr9:135204701 C>A maps to ENST00000372169 S761S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X8-AAAR-01A-11D-A403-09 chr17:27332848 C>A maps to NM_178860.4 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GI-01A-11D-A37C-09 chr22:26688606 G>A maps to NM_021115.4 K110K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NT-01A-11D-A37C-09 chr22:26688432 G>T maps to NM_021115.4 P52P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49Y-01A-11D-A27G-09 chr16:29909172 C>G did not map to a codon.
Sequencing variant TCGA-VR-A8EZ-01A-11D-A36J-09 chr22:30741013 G>A maps to NM_005877.4 Q187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-AAPN-01A-11D-A403-09 chr22:30730594 C>G maps to NM_005877.4 G790G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6Y0-01B-11D-A33E-09 chr2:198268375 A>T maps to NM_012433.2 L551*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-A7RB-01A-11D-A351-09 chr2:198257071 A>G maps to NM_012433.2 D1290D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L7-A6VZ-01A-12D-A33E-09 chr16:70590173 G>T maps to NM_012426.4 R601R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EX-01A-11D-A36J-09 chr16:70599427 G>T did not map to a codon.
Sequencing variant TCGA-LN-A9FQ-01A-31D-A387-09 chr19:19416841 G>A maps to NM_172231.2 T118T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8W5-01B-11D-A37C-09 chr3:52977501 C>T maps to NM_016329.3 E77E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93D-01A-11D-A387-09 chr10:7326105 G>T maps to NM_001018039.1 R178R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q9-A6FU-01A-11D-A31U-09 chr10:7326112 C>T did not map to a codon.
Sequencing variant TCGA-V5-A7RE-01A-11D-A351-09 chr10:7247840 G>A maps to NM_001018039.1 D460D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GO-01A-11D-A37C-09 chr7:37956031 G>T maps to ENST00000223214 P58P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GI-01A-11D-A37C-09 chr17:56084378 G>A maps to NM_006924.4 G40G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8WC-01A-11D-A37C-09 chr19:19130024 T>C maps to NM_001017392.3 R581R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NI-01A-11D-A37C-09 chr23:1712779 C>T did not map to a codon.
Sequencing variant TCGA-L7-A6VZ-01A-12D-A33E-09 chr23:1712480 G>T did not map to a codon.
Sequencing variant TCGA-L5-A891-01A-11D-A36J-09 chr6:99857221 T>C did not map to a codon.
Sequencing variant TCGA-L5-A8NE-01A-11D-A37C-09 chr12:46322277 G>A maps to NM_004719.2 S402S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6L6-01B-11D-A33E-09 chr6:36569505 A>G maps to NM_003017.4 R134R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GH-01A-11D-A37C-09 chr14:70238179 C>T did not map to a codon.
Sequencing variant TCGA-JY-A6FA-01A-11D-A33E-09 chr1:168200750 G>T did not map to a codon.
Sequencing variant TCGA-JY-A6FD-01A-11D-A33E-09 chr10:81319209 G>A maps to NM_001098668.2 L10L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HY-01A-12D-A351-09 chr2:73215477 C>G did not map to a codon.
Sequencing variant TCGA-L5-A4OT-01A-11D-A28B-09 chr5:155771518 T>A maps to NM_000337.5 T8T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NT-01A-11D-A37C-09 chr5:156186334 G>T maps to NM_000337.5 G269G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49X-01A-31D-A27G-09 chr7:94218010 C>T maps to NM_001099401.1 Q454Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A5U5-01A-21D-A28B-09 chr1:67108533 C>T maps to ENST00000237247 P94P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8WG-01A-11D-A37C-09 chr1:67147756 A>G maps to ENST00000237247 P344P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASW-01A-11D-A403-09 chr8:42958882 G>A maps to NM_032237.3 Q64Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43H-01A-11D-A247-09 chr8:8185258 G>T maps to NM_001080826.1 C1011*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr15:77407252 G>A maps to NM_024776.2 L1496L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr15:77472837 G>A maps to NM_024776.2 V477V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OE-01A-11D-A27G-09 chr2:201436242 G>T maps to NM_152524.5 E392*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NL-01A-12D-A37C-09 chr2:201399804 A>C maps to NM_152524.5 R74R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RE-01A-11D-A33E-09 chr17:2276308 C>T maps to NM_014853.2 R617R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr17:2268624 G>A maps to NM_014853.2 R426R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A8O2-01A-11D-A36J-09 chr19:2762545 G>A maps to NM_003021.3 N198N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43C-01A-11D-A247-09 chr19:2763649 C>G did not map to a codon.
Sequencing variant TCGA-2H-A9GF-01A-11D-A37C-09 chr5:64981211 C>T maps to NM_019072.2 K154K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr10:82331258 G>A maps to NM_207372.2 A140A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93C-01A-11D-A387-09 chr1:21049286 G>A maps to ENST00000444387 Q358*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q9-A6FU-01A-11D-A31U-09 chr1:21050597 C>T maps to ENST00000444387 L273L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A4-01A-11D-A27G-09 chr6:80383497 T>C maps to NM_031469.2 N71N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr22:38046678 G>A maps to NM_018957.3 P515P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-A7RB-01A-11D-A351-09 chr2:235950357 G>C maps to NM_014521.2 V315V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6DN-01B-11D-A31U-09 chr3:15311297 G>T maps to NM_004844.3 A139A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NJ-01A-11D-A36J-09 chr19:4361665 G>A maps to NM_003025.2 G346G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr19:4361752 G>A maps to NM_003025.2 F317F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6Y2-01B-11D-A33E-09 chr19:4363466 C>A maps to NM_003025.2 E210*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6XG-01B-11D-A33E-09 chr9:17747116 C>T maps to NM_003026.2 F33F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GF-01A-11D-A37C-09 chr15:84245417 C>T maps to ENST00000434347 V191V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr15:84237359 G>A maps to ENST00000434347 T97T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6F8-01A-11D-A33E-09 chr1:87181418 A>T maps to ENST00000482504 K29*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93E-01A-11D-A37C-09 chr23:19713765 G>T did not map to a codon.
Sequencing variant TCGA-LN-A5U6-01A-11D-A28B-09 chr23:19568146 G>C did not map to a codon.
Sequencing variant TCGA-Z6-A9VB-01A-21D-A37C-09 chr23:19702015 G>T did not map to a codon.
Sequencing variant TCGA-L5-A88Z-01A-11D-A36J-09 chr5:145442017 C>T maps to NM_152550.3 Y648Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6DN-01B-11D-A31U-09 chr5:145428709 G>A maps to NM_152550.3 R408R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XP-A8T8-01A-11D-A36J-09 chr5:145442254 C>A maps to NM_152550.3 P727P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NK-01A-21D-A37C-09 chr4:8207064 C>T maps to NM_018986.3 P48P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FB-01A-11D-A33E-09 chr5:148407137 G>T maps to NM_024577.3 T719T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GJ-01A-11D-A37C-09 chr19:51165296 G>A maps to ENST00000391814 Y2145Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43E-01A-11D-A247-09 chr19:51217186 C>T maps to ENST00000391814 A220A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NG-01A-11D-A37C-09 chr19:51169687 G>A maps to ENST00000391814 G1851G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA7I-01A-11D-A403-09 chr19:51189601 G>A maps to ENST00000391814 D831D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6XG-01B-11D-A33E-09 chr22:51159737 G>A maps to NM_001080420.1 P1175P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X8-AAAR-01A-11D-A403-09 chr22:51159629 G>T maps to NM_001080420.1 A1139A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8W8-01B-11D-A37C-09 chr8:145154928 G>T maps to NM_030974.3 C140*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASW-01A-11D-A403-09 chr9:91653171 G>A maps to NM_016848.5 P464P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93E-01A-11D-A37C-09 chr15:49127097 C>T maps to NM_203349.3 A535A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88Z-01A-11D-A36J-09 chr16:46617506 A>G maps to NM_024745.4 N538N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA4G-01A-11D-A37C-09 chr16:46650015 T>C maps to NM_024745.4 E146E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RE-01A-11D-A33E-09 chr1:154474132 G>T maps to NM_001010846.2 R124R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49V-01A-11D-A247-09 chr1:154473950 G>A maps to NM_001010846.2 P184P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA4G-01A-11D-A37C-09 chr12:57626050 C>T maps to NM_005412.5 F190F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L7-A6VZ-01A-12D-A33E-09 chr10:112764518 C>A maps to NM_007373.3 S376S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr17:3513904 G>A maps to NM_013276.2 V462V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HX-01A-11D-A33E-09 chr6:146266722 C>A maps to ENST00000367503 G458*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HY-01A-12D-A351-09 chr6:146243863 T>C maps to ENST00000367503 P1222P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FP-01A-31D-A387-09 chr6:146269406 C>T did not map to a codon.
Sequencing variant TCGA-IG-A51D-01A-11D-A27G-09 chr5:132158682 G>A maps to NM_001172700.1 V788V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GJ-01A-11D-A37C-09 chr23:9862634 G>T did not map to a codon.
Sequencing variant TCGA-IG-A4QS-01A-11D-A27G-09 chr23:9900466 G>T did not map to a codon.
Sequencing variant TCGA-JY-A6FG-01A-11D-A33E-09 chr23:9905300 C>T did not map to a codon.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr23:9863380 G>A did not map to a codon.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr23:9900354 G>A did not map to a codon.
Sequencing variant TCGA-L5-A4OJ-01A-11D-A27G-09 chr23:9864213 G>C did not map to a codon.
Sequencing variant TCGA-L5-A4OO-01A-11D-A27G-09 chr23:9900610 G>A did not map to a codon.
Sequencing variant TCGA-L5-A4OR-01A-11D-A27G-09 chr23:9912762 A>T did not map to a codon.
Sequencing variant TCGA-Z6-AAPN-01A-11D-A403-09 chr23:9914722 G>C did not map to a codon.
Sequencing variant TCGA-IC-A6RE-01A-11D-A33E-09 chr4:77652019 C>T maps to NM_020859.3 P173P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88W-01A-11D-A351-09 chr4:77357288 G>T maps to NM_020859.3 L28L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HY-01A-12D-A351-09 chr4:77661902 C>G maps to NM_020859.3 S859S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GM-01A-11D-A37C-09 chr23:50377487 C>A did not map to a codon.
Sequencing variant TCGA-VR-AA4G-01A-11D-A37C-09 chr23:50381300 C>T did not map to a codon.
Sequencing variant TCGA-L5-A4OX-01A-21D-A28B-09 chr3:164712163 A>C maps to NM_001041.3 T1574T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FR-01A-11D-A387-09 chr3:164700807 T>C maps to NM_001041.3 V1743V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FR-01A-11D-A387-09 chr3:164709997 G>A maps to NM_001041.3 Y1650Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S8-A6BW-01A-11D-A31U-09 chr3:164786914 G>A maps to NM_001041.3 F108F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-AAPN-01A-11D-A403-09 chr3:164700086 G>A maps to NM_001041.3 L1787L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OX-01A-21D-A28B-09 chr11:124530642 C>A maps to NM_170601.3 E96*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A6-01A-11D-A27G-09 chr16:48396036 C>T maps to NM_001006610.1 A132A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FP-01A-31D-A387-09 chr3:150460350 C>T maps to NM_005067.5 V184V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr13:46425731 T>C maps to NM_198849.2 V11V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GK-01A-11D-A37C-09 chr3:113303616 G>T did not map to a codon.
Sequencing variant TCGA-R6-A6DN-01B-11D-A31U-09 chr3:113327291 T>C maps to ENST00000393830 G543G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43C-01A-11D-A247-09 chr11:117066609 C>T maps to NM_001040455.1 I805I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A8HZ-01A-11D-A36J-09 chr11:117060947 C>A maps to NM_001040455.1 I520I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-A7RE-01A-11D-A351-09 chr11:117061433 C>A maps to NM_001040455.1 P571P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A5B8-01A-11D-A28B-09 chr20:3674092 C>T did not map to a codon.
Sequencing variant TCGA-L5-A8NV-01A-11D-A37C-09 chr19:52003612 C>T maps to NM_033329.1 L5L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NW-01A-11D-A37C-09 chr19:52147164 G>T maps to NM_001098612.1 L293L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93D-01A-11D-A387-09 chr19:52115504 C>T maps to ENST00000222107 S545S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A6-01A-11D-A27G-09 chr19:52133161 G>A maps to NM_003830.2 S115S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OM-01A-11D-A27G-09 chr19:52034112 C>T maps to NM_001245.5 T176T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8W8-01B-11D-A37C-09 chr19:51645916 C>A maps to NM_014385.2 L97L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FB-01A-11D-A33E-09 chr19:51958906 T>C maps to NM_014442.2 S272S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GL-01A-12D-A37C-09 chr19:51633329 C>T maps to NM_014441.2 H462H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FA-01A-11D-A33E-09 chr21:44840161 C>T maps to NM_173354.3 A308A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr21:44837637 C>T maps to NM_173354.3 R587R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49P-01A-11D-A247-09 chr11:111491116 G>T maps to NM_015191.1 E103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASX-01A-11D-A387-09 chr11:111594546 G>A maps to NM_015191.1 P825P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A4QS-01A-11D-A27G-09 chr6:100841711 G>A maps to ENST00000262901 G407G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NQ-01A-11D-A36J-09 chr6:100841765 C>G did not map to a codon.
Sequencing variant TCGA-L5-A8NU-01A-11D-A36J-09 chr21:38114048 C>T maps to NM_005069.3 Y294Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GI-01A-11D-A37C-09 chr15:75705181 A>G maps to NM_001145357.1 H226H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6Y2-01B-11D-A33E-09 chr14:72117168 G>T maps to NM_015556.1 G646*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RE-01A-11D-A33E-09 chr1:232650208 G>A maps to NM_020808.3 R293*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A938-01A-11D-A37C-09 chr1:232615465 C>T maps to NM_020808.3 T664T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93E-01A-11D-A37C-09 chr1:232561443 G>A maps to NM_020808.3 S1507S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OQ-01A-11D-A27G-09 chr1:232650478 A>G maps to NM_020808.3 L203L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NH-01A-11D-A37C-09 chr1:232581351 G>A maps to NM_020808.3 C1092C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GJ-01A-11D-A37C-09 chr19:38609987 C>T maps to NM_015073.1 P778P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q9-A6FW-01A-31D-A31U-09 chr19:38652938 C>T maps to NM_015073.1 A1236A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HV-01A-21D-A351-09 chr20:1559179 G>T maps to NM_006065.3 Y79*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6DQ-01B-11D-A31U-09 chr19:39370088 C>T maps to NM_012237.3 E333E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3I8-01A-11D-A247-09 chr11:233166 C>T maps to NM_012239.5 P174P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GL-01A-12D-A37C-09 chr12:120750387 G>A maps to NM_012240.2 E209E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr2:45171871 C>T maps to NM_005413.3 T324T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NW-01A-11D-A37C-09 chr2:45169386 C>T maps to NM_005413.3 S48S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8W8-01B-11D-A37C-09 chr2:45171796 G>A maps to NM_005413.3 T299T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OU-01A-11D-A28B-09 chr19:46269142 G>A maps to NM_175875.4 H612H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-A7RC-01B-11D-A403-09 chr14:60976247 C>T maps to ENST00000381716 C103C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A893-01A-11D-A36J-09 chr1:2235374 C>T maps to NM_003036.3 A436A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA4G-01A-11D-A37C-09 chr1:2237625 G>A maps to NM_003036.3 R645R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XP-A8T6-01A-11D-A36J-09 chr1:2160897 G>T maps to NM_003036.3 L231L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6Y0-01B-11D-A33E-09 chr6:31931787 G>A maps to NM_006929.4 Q582Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6Y0-01B-11D-A33E-09 chr6:31937095 G>T maps to NM_006929.4 E1147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A6-01A-11D-A27G-09 chr5:54637599 G>T did not map to a codon.
Sequencing variant TCGA-LN-A49U-01A-31D-A27G-09 chr20:35242775 G>C maps to NM_032214.2 L199L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49U-01A-31D-A27G-09 chr20:35242811 G>C maps to NM_032214.2 L187L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49U-01A-31D-A27G-09 chr1:160465849 C>G did not map to a codon.
Sequencing variant TCGA-2H-A9GK-01A-11D-A37C-09 chr1:159922240 C>A maps to NM_033438.3 E159*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NW-01A-11D-A37C-09 chr1:159923407 C>A maps to NM_033438.3 E28*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EQ-01A-11D-A36J-09 chr13:103718236 G>T maps to NM_000452.2 G121G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OU-01A-11D-A28B-09 chr23:153716992 G>T did not map to a codon.
Sequencing variant TCGA-L5-A8NF-01A-11D-A37C-09 chr8:82606430 C>T maps to NM_001010893.2 R259R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88V-01A-11D-A351-09 chr4:147442806 A>G maps to ENST00000507030 A21A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A2-01A-31D-A27G-09 chr2:219259679 C>A maps to NM_000578.3 T525T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RE-A7BO-01A-11D-A33E-09 chr2:219255997 C>T maps to NM_000578.3 D344D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-AAPN-01A-11D-A403-09 chr12:51393016 C>T maps to NM_001174125.1 R234R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KH-A6WC-01A-11D-A33E-09 chr15:48537004 G>T maps to NM_000338.2 G452G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NU-01A-11D-A36J-09 chr15:48522689 G>A maps to NM_000338.2 W322*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr16:56926016 G>A maps to NM_000339.2 A797A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OO-01A-11D-A27G-09 chr16:56918000 G>A maps to NM_000339.2 A570A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RE-01A-11D-A33E-09 chr20:44685161 T>A maps to NM_001134771.1 P1046P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr20:44669991 G>A maps to NM_001134771.1 T316T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49U-01A-31D-A27G-09 chr20:44674581 C>T maps to NM_001134771.1 C568C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8W8-01B-11D-A37C-09 chr20:44669097 C>T maps to NM_001134771.1 Y256Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-A7RE-01A-11D-A351-09 chr20:44676706 A>C maps to NM_001134771.1 P688P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RE-01A-11D-A33E-09 chr15:34546622 C>A maps to NM_133647.1 L348L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A8HZ-01A-11D-A36J-09 chr15:34567564 C>T maps to NM_133647.1 G99G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A4P3-01A-11D-A27G-09 chr5:1083965 G>T maps to NM_006598.2 L341L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4MR-01A-11D-A28B-09 chr5:1079522 C>T maps to NM_006598.2 T462T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EX-01A-11D-A36J-09 chr5:1079588 C>G maps to NM_006598.2 R440R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-AAPN-01A-11D-A403-09 chr5:1085363 G>A maps to NM_006598.2 F300F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3I8-01A-11D-A247-09 chr3:124854512 C>A maps to NM_001195483.1 G246*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HX-01A-11D-A33E-09 chr3:124826790 G>T maps to NM_001195483.1 T413T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FP-01A-31D-A387-09 chr17:26820660 C>A maps to NM_001145975.1 T366T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XP-A8T7-01A-11D-A36J-09 chr17:26822704 G>A maps to NM_001145975.1 K496K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GM-01A-11D-A37C-09 chr20:45204263 C>T maps to NM_022829.5 W427*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A8JE-01A-11D-A37C-09 chr17:6606341 G>A maps to NM_177550.3 T221T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49R-01A-11D-A247-09 chr18:43310428 G>A maps to NM_001146037.1 Q104Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr13:99362007 G>T maps to NM_005073.3 P322P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A8-01A-32D-A27G-09 chr13:99358507 C>G did not map to a codon.
Sequencing variant TCGA-VR-A8EO-01A-11D-A36J-09 chr17:6945036 G>A maps to NM_153357.1 S459S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88S-01A-11D-A36J-09 chr2:230910800 C>T maps to NM_152527.4 S347S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8W8-01B-11D-A37C-09 chr2:230923852 G>T maps to NM_152527.4 T72T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3Y9-01A-12D-A247-09 chr23:73749128 C>G did not map to a codon.
Sequencing variant TCGA-L5-A8NS-01A-12D-A37C-09 chr23:73641365 G>T did not map to a codon.
Sequencing variant TCGA-V5-AASX-01A-11D-A387-09 chr23:73751335 A>G did not map to a codon.
Sequencing variant TCGA-VR-AA4D-01A-11D-A37C-09 chr23:73751297 A>T did not map to a codon.
Sequencing variant TCGA-R6-A6L6-01B-11D-A33E-09 chr17:80196593 G>T maps to NM_001042423.1 A380A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3QL-01A-11D-A247-09 chr17:73096276 T>A maps to ENST00000450736 L213L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A4P3-01A-11D-A27G-09 chr17:73096681 C>T maps to ENST00000450736 F348F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr22:38474460 G>A maps to NM_013356.2 S483S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FA-01A-11D-A33E-09 chr6:25913641 G>A maps to NM_005835.2 L398L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A51D-01A-11D-A27G-09 chr6:25769403 G>T maps to NM_005495.2 E95*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8W8-01B-11D-A37C-09 chr6:74320148 G>A maps to NM_012434.4 S411S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HV-01A-21D-A351-09 chr11:22387153 G>A maps to NM_020346.2 K270K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EY-01A-11D-A36J-09 chr11:22363298 C>T maps to NM_020346.2 I104I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr19:49934033 G>T maps to NM_020309.3 A475A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A891-01A-11D-A36J-09 chr20:61588798 G>T maps to NM_022082.3 G88G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A8HZ-01A-11D-A36J-09 chr10:119013562 T>C maps to NM_003054.4 F176F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RF-01A-13D-A33E-09 chr10:50818986 C>T maps to NM_003055.2 G67G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A51D-01A-11D-A27G-09 chr10:50818911 G>A maps to NM_003055.2 A42A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr10:50819808 C>T maps to NM_003055.2 G341G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr10:50819742 G>A maps to NM_003055.2 T319T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASX-01A-11D-A387-09 chr10:50820255 G>A maps to NM_003055.2 P490P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A8I1-01A-11D-A36J-09 chr9:4585393 G>T maps to NM_004170.5 E471*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OS-01A-11D-A28B-09 chr5:36686223 G>T maps to NM_004172.4 V494V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49M-01A-21D-A27G-09 chr19:15083544 G>A maps to NM_005071.1 L60L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88S-01A-11D-A36J-09 chr8:42329773 C>T maps to NM_006749.3 R45R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EU-01A-11D-A36J-09 chr8:42297136 T>A maps to NM_006749.3 V255V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88W-01A-11D-A351-09 chr11:64329781 G>T maps to NM_018484.2 T232T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6F8-01A-11D-A33E-09 chr11:64360945 C>T maps to NM_144585.2 F192F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HY-01A-12D-A351-09 chr11:64368306 C>T maps to NM_144585.2 L499L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6DQ-01B-11D-A31U-09 chr11:64359360 C>T maps to NM_144585.2 A111A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NV-01A-11D-A37C-09 chr3:38316549 G>A maps to NM_004256.3 G236G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6Y0-01B-11D-A33E-09 chr3:38318434 C>A maps to NM_004256.3 S460*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GH-01A-11D-A37C-09 chr3:38357956 C>T maps to NM_004803.3 L559L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OH-01A-11D-A27G-09 chr6:110760033 G>T maps to NM_033125.2 P400P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OH-01A-11D-A27G-09 chr6:110777988 G>T maps to NM_033125.2 I95I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OT-01A-11D-A28B-09 chr11:2924610 G>A maps to NM_002555.5 R12R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43M-01A-11D-A247-09 chr6:160679543 G>A maps to NM_003058.3 G82G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FP-01A-31D-A387-09 chr6:160664751 G>T maps to NM_003058.3 Y377*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q9-A6FW-01A-31D-A31U-09 chr11:64981528 C>T maps to ENST00000438990 T62T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OJ-01A-11D-A27G-09 chr11:62850900 G>A maps to NM_001136506.1 L367L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A5B8-01A-11D-A28B-09 chr5:131657979 C>T maps to NM_003059.2 F252F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8W8-01B-11D-A37C-09 chr5:131630482 G>A maps to NM_003059.2 L58L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GK-01A-11D-A37C-09 chr11:62752129 C>T maps to NM_004790.3 G11G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr20:4893540 G>A maps to NM_203327.1 N64N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A2-01A-31D-A27G-09 chr20:4893540 G>A maps to NM_203327.1 N64N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49M-01A-21D-A27G-09 chr15:65943237 C>T maps to NM_004727.2 I917I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-M9-A5M8-01A-11D-A28B-09 chr15:65930492 G>T maps to NM_004727.2 E640*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GF-01A-11D-A37C-09 chr9:19516400 C>T did not map to a codon.
Sequencing variant TCGA-2H-A9GQ-01A-11D-A37C-09 chr9:19528097 G>T maps to NM_020344.2 S506S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RE-01A-11D-A33E-09 chr20:19673906 T>A maps to NM_020689.3 G443G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-A7RC-01B-11D-A403-09 chr17:4841059 G>A maps to NM_003562.4 Y307Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NR-01A-11D-A37C-09 chr2:172641885 C>T maps to NM_003705.3 T645T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NV-01A-11D-A37C-09 chr22:41173082 C>T maps to NM_006358.2 T218T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8W5-01B-11D-A37C-09 chr22:18072878 G>A maps to NM_031481.1 E275E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EO-01A-11D-A36J-09 chr22:18063896 C>T maps to NM_031481.1 Q39*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49X-01A-31D-A27G-09 chr9:130868490 G>T maps to ENST00000373069 G333G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EO-01A-11D-A36J-09 chr9:130864647 G>T did not map to a codon.
Sequencing variant TCGA-L5-A4OT-01A-11D-A28B-09 chr3:66419917 A>C maps to NM_173471.3 A195A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93F-01A-21D-A37C-09 chr8:104427087 C>T maps to NM_030780.3 L26L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A4P3-01A-11D-A27G-09 chr3:140675494 C>G maps to NM_001104647.1 V56V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L7-A56G-01A-21D-A27G-09 chr3:140692767 A>G maps to NM_001104647.1 K221K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A9VB-01A-21D-A37C-09 chr7:87476366 G>A maps to NM_018843.3 Y176Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HZ-01A-31D-A351-09 chr19:6433617 G>A maps to NM_173637.3 A29A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A51D-01A-11D-A27G-09 chr19:19206998 G>A maps to NM_178526.3 S22S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6Y2-01B-11D-A33E-09 chr23:118586028 G>A did not map to a codon.
Sequencing variant TCGA-Z6-AAPN-01A-11D-A403-09 chr11:65144517 G>A maps to NM_182556.2 I123I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NN-01A-11D-A37C-09 chr23:118603755 T>A did not map to a codon.
Sequencing variant TCGA-XP-A8T8-01A-11D-A36J-09 chr23:118604451 A>G did not map to a codon.
Sequencing variant TCGA-2H-A9GO-01A-11D-A37C-09 chr23:1508155 G>A did not map to a codon.
Sequencing variant TCGA-LN-A4A8-01A-32D-A27G-09 chr23:1506280 G>A did not map to a codon.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr4:985262 G>A maps to NM_213613.2 L77L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q9-A6FW-01A-31D-A31U-09 chr4:983910 C>T maps to NM_213613.2 A272A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RF-01A-13D-A33E-09 chr5:149357797 G>T maps to NM_000112.3 G195*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OT-01A-11D-A28B-09 chr7:107423730 G>A maps to NM_000111.2 I346I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A5U7-01A-11D-A31U-09 chr7:107414598 C>A did not map to a codon.
Sequencing variant TCGA-R6-A6L4-01A-11D-A31U-09 chr7:107423292 G>A maps to NM_000111.2 I420I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A5B8-01A-11D-A28B-09 chr7:107334900 G>A maps to NM_000441.1 G439G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L7-A6VZ-01A-12D-A33E-09 chr7:107303845 G>T maps to NM_000441.1 S90S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr6:35944995 A>G maps to NM_052961.3 S386S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49X-01A-31D-A27G-09 chr1:205899088 C>G maps to NM_134325.2 L216L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X8-AAAR-01A-11D-A403-09 chr1:205890900 C>T maps to NM_134325.2 P616P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OH-01A-11D-A27G-09 chr15:50519184 G>T maps to NM_003645.3 G423*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q9-A6FW-01A-31D-A31U-09 chr9:131107436 C>T maps to NM_005094.3 G55G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A938-01A-11D-A37C-09 chr5:128351576 G>T did not map to a codon.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr9:86955494 G>T maps to NM_022127.2 G18G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr6:44201261 G>A maps to ENST00000313248 V535V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49M-01A-21D-A27G-09 chr7:5336606 G>A maps to NM_153247.2 T220T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASW-01A-11D-A403-09 chr1:43396407 C>G maps to NM_006516.2 L135L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GL-01A-12D-A37C-09 chr20:45354892 A>C maps to NM_030777.3 A406A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RE-A7BO-01A-11D-A33E-09 chr6:134350158 C>G maps to NM_145176.2 L268L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A938-01A-11D-A37C-09 chr12:7966968 G>A maps to NM_153449.2 D502D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FP-01A-31D-A387-09 chr12:8077077 C>T maps to NM_006931.2 R332R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A6-01A-11D-A27G-09 chr20:62374232 A>T maps to NM_020062.3 K352*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FO-01A-11D-A387-09 chr9:136337223 G>A maps to NM_017585.3 C481C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FP-01A-31D-A387-09 chr9:136339162 G>T maps to NM_017585.3 S325S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A8JE-01A-11D-A37C-09 chr1:9064925 G>T maps to NM_207420.2 S402*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XP-A8T8-01A-11D-A36J-09 chr4:9982320 G>T maps to NM_020041.2 I192I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A8O2-01A-11D-A36J-09 chr1:220101731 G>T maps to NM_018713.2 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NI-01A-11D-A37C-09 chr1:220089149 G>T maps to NM_018713.2 R367R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6Y2-01B-11D-A33E-09 chr1:26366307 C>T maps to NM_001004434.1 L311L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3YC-01A-11D-A247-09 chr2:27480192 C>T maps to NM_003459.4 G202G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A6QS-01A-12D-A33E-09 chr15:45779786 G>T maps to NM_013309.4 S313*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A2-01A-31D-A27G-09 chr15:45814393 G>A maps to NM_013309.4 D53D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OJ-01A-11D-A27G-09 chr5:68423938 G>T maps to NM_022902.2 E703*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L7-A56G-01A-21D-A27G-09 chr5:68396657 A>G maps to NM_022902.2 L36L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6DN-01B-11D-A31U-09 chr5:68396657 A>G maps to NM_022902.2 L36L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6Y2-01B-11D-A33E-09 chr5:68398887 G>T did not map to a codon.
Sequencing variant TCGA-JY-A93D-01A-11D-A387-09 chr8:118169954 C>A maps to NM_173851.2 I148I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OT-01A-11D-A28B-09 chr8:118174051 T>C maps to NM_173851.2 A216A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8W8-01B-11D-A37C-09 chr8:118183342 G>A maps to NM_173851.2 V300V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4ON-01A-11D-A27G-09 chr4:42080285 G>T maps to NM_006345.3 E536*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr20:37356882 C>A maps to NM_080552.2 S393S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A8HZ-01A-11D-A36J-09 chr5:176812814 C>T maps to NM_003052.4 R25*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HX-01A-11D-A33E-09 chr6:88221147 A>T maps to NM_006416.4 V306V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88T-01A-11D-A351-09 chr23:48762484 C>T did not map to a codon.
Sequencing variant TCGA-2H-A9GH-01A-11D-A37C-09 chr6:44224422 G>T maps to NM_178148.2 T68T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8WG-01A-11D-A37C-09 chr11:45832402 G>T maps to NM_018389.4 L204L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RE-01A-11D-A33E-09 chr1:67519674 G>A maps to NM_015139.2 Q8*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr19:16666160 G>A maps to NM_024881.4 S268S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A6-01A-11D-A27G-09 chr22:31042744 C>T maps to NM_001001479.2 L260L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr6:118596718 C>T maps to NM_001029858.3 S245S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GR-01A-12D-A37C-09 chr11:107673780 G>T maps to NM_017515.4 I295I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RE-A7BO-01A-11D-A33E-09 chr1:234458985 C>T maps to NM_173508.2 R490R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A5S3-01A-11D-A28B-09 chr5:150660710 G>A maps to NM_001145017.1 I377I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A5U7-01A-11D-A31U-09 chr5:150656992 G>T maps to NM_001145017.1 I499I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FD-01A-11D-A33E-09 chr21:43955657 C>A maps to NM_018964.3 L116L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GK-01A-11D-A37C-09 chr11:124954181 T>A maps to NM_198277.2 T364T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FD-01A-11D-A33E-09 chr12:46582818 G>T maps to NM_030674.3 S466S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6XQ-01B-11D-A33E-09 chr17:79225167 C>T maps to NM_138570.2 P730P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93E-01A-11D-A37C-09 chr12:46758905 C>T maps to NM_018976.4 S210S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OP-01A-11D-A27G-09 chr23:48324663 G>T did not map to a codon.
Sequencing variant TCGA-R6-A8W8-01B-11D-A37C-09 chr14:61519065 G>A did not map to a codon.
Sequencing variant TCGA-LN-A49R-01A-11D-A247-09 chr16:58701330 G>A maps to NM_018231.1 G449G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3I8-01A-11D-A247-09 chr16:84050268 G>A maps to NM_001080442.1 A339A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA7I-01A-11D-A403-09 chr16:84070481 G>A maps to NM_001080442.1 S71S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NL-01A-12D-A37C-09 chr10:18276411 C>T maps to NM_001145195.1 Y367Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A5B8-01A-11D-A28B-09 chr8:145637922 C>T maps to NM_130849.2 *648*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49S-01A-11D-A247-09 chr8:145640647 G>A maps to NM_130849.2 F210F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr18:33706270 G>T maps to NM_012319.3 R234R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FA-01A-11D-A33E-09 chr4:103184317 C>T maps to NM_001135146.1 K422K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93C-01A-11D-A387-09 chr4:103228744 G>A maps to NM_001135146.1 L134L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-AAPN-01A-11D-A403-09 chr2:44547730 C>T maps to NM_000341.3 R671*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FD-01A-11D-A33E-09 chr1:205779530 C>T maps to NM_173854.4 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A97H-01A-11D-A387-09 chr3:125741671 C>T maps to NM_001008485.1 L234L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HX-01A-11D-A33E-09 chr3:125775272 G>T maps to NM_001008487.1 C41*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA7D-01A-11D-A403-09 chr17:1479962 G>A maps to ENST00000382147 S496S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A2-01A-31D-A27G-09 chr9:108127762 G>C did not map to a codon.
Sequencing variant TCGA-VR-AA7I-01A-11D-A403-09 chr9:108147755 C>T maps to NM_080546.3 V641V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RE-01A-11D-A33E-09 chr1:95286602 G>A maps to NM_001114106.1 W42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A8JE-01A-11D-A37C-09 chr1:95293098 C>G maps to NM_001114106.1 V105V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OE-01A-11D-A27G-09 chr1:75684272 G>A maps to NM_152697.4 C477C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RE-A7BO-01A-11D-A33E-09 chr1:75684211 G>A maps to NM_152697.4 R498*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-AAPN-01A-11D-A403-09 chr1:75805271 G>A maps to NM_152697.4 A32A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XP-A8T8-01A-11D-A36J-09 chr1:8386004 C>T maps to ENST00000377479 S240S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3QL-01A-11D-A247-09 chr5:33984552 C>A maps to NM_016180.3 E46*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OE-01A-11D-A27G-09 chr5:33947438 A>T maps to NM_016180.3 G399G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NR-01A-11D-A37C-09 chr1:205628415 G>T maps to NM_033102.2 Y536*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr8:142221558 G>C maps to NM_001080431.1 G793G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RE-A7BO-01A-11D-A33E-09 chr8:142231844 G>T maps to NM_001080431.1 Y36*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr9:115652622 C>T maps to NM_033051.3 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NF-01A-11D-A37C-09 chr9:115652721 G>T maps to NM_033051.3 I80I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASX-01A-11D-A387-09 chr9:115652625 C>T maps to NM_033051.3 S112S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NJ-01A-11D-A36J-09 chr13:29278216 A>G maps to NM_001135919.1 I388I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A51D-01A-11D-A27G-09 chr17:19470500 C>T maps to ENST00000395585 I423I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr17:19618054 T>C maps to NM_152908.3 A91A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A8O2-01A-11D-A36J-09 chr12:48173961 C>T maps to NM_017842.2 S113S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L7-A6VZ-01A-12D-A33E-09 chr17:42336629 C>A maps to NM_000342.3 P259P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A51D-01A-11D-A27G-09 chr2:27905114 G>A maps to NM_018158.2 K588K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OJ-01A-11D-A27G-09 chr2:27886963 G>A maps to NM_018158.2 E115E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GF-01A-11D-A37C-09 chr7:150767427 C>T maps to NM_003040.3 R482*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A5B8-01A-11D-A28B-09 chr7:150768591 G>A maps to NM_003040.3 L697L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A8HZ-01A-11D-A36J-09 chr7:150769141 C>T maps to NM_003040.3 F818F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A938-01A-11D-A37C-09 chr2:220501481 G>T maps to NM_201574.2 L834L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A939-01A-12D-A37C-09 chr4:72338535 G>T maps to NM_001098484.2 T584T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43I-01A-11D-A247-09 chr3:27427484 G>C maps to ENST00000454389 L1130L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OH-01A-11D-A27G-09 chr3:27433266 G>A maps to ENST00000454389 F1050F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FP-01A-31D-A387-09 chr12:51865175 C>G maps to NM_001039960.1 Y588*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA4D-01A-11D-A37C-09 chr12:51845972 G>T maps to NM_001039960.1 E115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A9VB-01A-21D-A37C-09 chr12:51890821 C>T maps to NM_001039960.1 R999*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr16:24919406 G>A maps to NM_052944.2 A463A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NV-01A-11D-A37C-09 chr16:24902395 G>T did not map to a codon.
Sequencing variant TCGA-IG-A6QS-01A-12D-A33E-09 chr16:31500245 C>A maps to ENST00000431354 P442P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GK-01A-11D-A37C-09 chr19:17985310 C>T maps to NM_000453.2 Y144Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A939-01A-12D-A37C-09 chr19:17988835 C>T maps to NM_000453.2 I301I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr2:108626717 C>T maps to NM_021815.2 R382*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OW-01A-11D-A28B-09 chr3:11067496 C>T maps to NM_003042.3 Y296Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88W-01A-11D-A351-09 chr12:306028 G>A maps to NM_003044.3 I365I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NF-01A-11D-A37C-09 chr12:305291 C>A maps to NM_003044.3 E442*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93E-01A-11D-A37C-09 chr23:115569090 G>T did not map to a codon.
Sequencing variant TCGA-VR-A8EQ-01A-11D-A36J-09 chr23:115585608 G>A did not map to a codon.
Sequencing variant TCGA-IG-A3QL-01A-11D-A247-09 chr19:49797778 G>A maps to NM_014037.2 L421L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A97I-01A-11D-A387-09 chr1:110737277 C>A maps to NM_001010898.2 S459S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6F8-01A-11D-A33E-09 chr1:110740983 C>A maps to NM_001010898.2 S701*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OT-01A-11D-A28B-09 chr1:110740221 G>A did not map to a codon.
Sequencing variant TCGA-L7-A6VZ-01A-12D-A33E-09 chr5:1244804 C>T maps to NM_182632.2 L527L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A893-01A-11D-A36J-09 chr5:1212592 C>T maps to NM_001003841.2 T219T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NH-01A-11D-A37C-09 chr5:1219076 G>A maps to NM_001003841.2 P411P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RE-A7BO-01A-11D-A33E-09 chr5:1212599 G>T did not map to a codon.
Sequencing variant TCGA-VR-A8EQ-01A-11D-A36J-09 chr16:55731828 C>T maps to NM_001043.3 V427V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RF-01A-13D-A33E-09 chr3:45814026 G>T maps to NM_020208.3 T221T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A5U7-01A-11D-A31U-09 chr3:45817258 A>G maps to NM_020208.3 T192T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GF-01A-11D-A37C-09 chr5:1403038 C>A maps to NM_001044.4 E589*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GK-01A-11D-A37C-09 chr5:1432625 C>T maps to NM_001044.4 S202S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OS-01A-11D-A28B-09 chr17:28548751 A>G maps to ENST00000394821 H117H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr3:14489313 G>T maps to NM_001134367.1 E197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NV-01A-11D-A37C-09 chr3:14508094 G>T maps to NM_001134367.1 P268P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8W8-01B-11D-A37C-09 chr3:14485183 C>T maps to NM_001134367.1 H14H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6Y0-01B-11D-A33E-09 chr5:149580708 G>T maps to NM_014228.3 G261*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FD-01A-11D-A33E-09 chr1:44466462 G>T maps to NM_201649.2 R577R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49Y-01A-11D-A27G-09 chr1:44476524 C>T maps to NM_201649.2 K93K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-AAPN-01A-11D-A403-09 chr1:44474227 G>A maps to NM_201649.2 I202I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NG-01A-11D-A37C-09 chr13:30091409 A>T maps to NM_003045.4 L516L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A9VB-01A-21D-A37C-09 chr13:30096467 G>T maps to NM_003045.4 S392*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GL-01A-12D-A37C-09 chr19:33703262 G>T maps to NM_019849.2 G241G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A8JE-01A-11D-A37C-09 chr4:139100536 G>A maps to ENST00000280612 F426F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93C-01A-11D-A387-09 chr8:87235207 G>A maps to NM_138817.2 L270L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A4P3-01A-11D-A27G-09 chr3:170198909 G>A maps to NM_020949.2 A387A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA7B-01A-31D-A403-09 chr8:17412488 C>T maps to NM_003046.5 L404L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GR-01A-12D-A37C-09 chr23:70147797 G>A did not map to a codon.
Sequencing variant TCGA-IG-A4P3-01A-11D-A27G-09 chr23:70148788 G>C did not map to a codon.
Sequencing variant TCGA-LN-A4A3-01A-11D-A27G-09 chr16:87868077 G>C maps to NM_003486.5 P470P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NI-01A-11D-A37C-09 chr14:23243153 G>T maps to NM_001126106.1 R473R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49S-01A-11D-A247-09 chr14:23245095 G>C maps to NM_001126106.1 S315*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A938-01A-11D-A37C-09 chr19:33355050 G>T maps to NM_014270.4 G143G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FA-01A-11D-A33E-09 chr2:40656142 G>T maps to NM_021097.2 A426A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr2:40657336 G>T maps to NM_021097.2 S28S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6XQ-01B-11D-A33E-09 chr19:47960695 C>T maps to NM_015063.2 P277P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA4G-01A-11D-A37C-09 chr19:47969219 G>T maps to NM_015063.2 V147V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HX-01A-11D-A33E-09 chr14:70512792 C>A maps to NM_183002.1 P885P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43I-01A-11D-A247-09 chr3:111936290 T>A maps to NM_183061.1 S596S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr1:173526481 T>C maps to NM_178527.3 Q404Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RF-01A-13D-A33E-09 chr5:488463 G>A maps to NM_004174.2 F214F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FH-01A-11D-A33E-09 chr5:492103 G>A maps to NM_004174.2 I98I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3Y9-01A-12D-A247-09 chr2:103141508 C>G maps to NM_001011552.3 L615L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A5B8-01A-11D-A28B-09 chr2:103120145 C>T maps to NM_001011552.3 L320L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6XG-01B-11D-A33E-09 chr2:103121711 G>T did not map to a codon.
Sequencing variant TCGA-IG-A3Y9-01A-12D-A247-09 chr16:67292259 G>A maps to NM_004594.2 L512L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OU-01A-11D-A28B-09 chr16:67304974 T>C maps to NM_004594.2 S851S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6DQ-01B-11D-A31U-09 chr16:67286503 C>T maps to NM_004594.2 L83L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XP-A8T6-01A-11D-A36J-09 chr16:67304864 C>T maps to NM_004594.2 L815L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A4P3-01A-11D-A27G-09 chr23:135098865 G>T did not map to a codon.
Sequencing variant TCGA-L5-A4OJ-01A-11D-A27G-09 chr23:135126795 C>T did not map to a codon.
Sequencing variant TCGA-L5-A4OW-01A-11D-A28B-09 chr23:135104756 T>C did not map to a codon.
Sequencing variant TCGA-XP-A8T7-01A-11D-A36J-09 chr23:135106541 G>T did not map to a codon.
Sequencing variant TCGA-ZR-A9CJ-01B-11D-A387-09 chr23:135126631 G>T did not map to a codon.
Sequencing variant TCGA-IG-A3YB-01A-11D-A247-09 chr23:46502751 G>T did not map to a codon.
Sequencing variant TCGA-L5-A4OJ-01A-11D-A27G-09 chr23:46522027 C>T did not map to a codon.
Sequencing variant TCGA-LN-A7HY-01A-12D-A351-09 chr3:143551001 A>C maps to NM_173653.3 T79T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8WG-01A-11D-A37C-09 chr12:21033791 T>C maps to NM_019844.2 N445N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OJ-01A-11D-A27G-09 chr11:74880254 G>T maps to NM_007256.4 L162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr15:92459374 C>T maps to NM_013272.3 C111C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6XQ-01B-11D-A33E-09 chr15:92706313 C>A maps to NM_013272.3 I694I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-AAPN-01A-11D-A403-09 chr20:61300306 C>T maps to NM_016354.3 F634F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OJ-01A-11D-A27G-09 chr5:101583020 G>T maps to NM_180991.4 C582*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A2-01A-31D-A27G-09 chr5:101583041 C>T maps to NM_180991.4 A575A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A625-01A-11D-A31U-09 chr5:101735275 G>T maps to NM_173488.3 I599I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93C-01A-11D-A387-09 chr5:101834431 C>A maps to NM_173488.3 P39P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr5:101834245 A>T maps to NM_173488.3 C101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-M9-A5M8-01A-11D-A28B-09 chr5:101755693 G>T maps to NM_173488.3 G436G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-AAPN-01A-11D-A403-09 chr5:101794129 G>A maps to NM_173488.3 L363L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8WC-01A-11D-A37C-09 chr17:33749082 C>T maps to NM_018042.3 W322*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49N-01A-11D-A247-09 chr17:33806862 G>A maps to ENST00000361112 H151H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA7B-01A-31D-A403-09 chr1:41483369 G>T maps to NM_144990.3 P298P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A7DP-01A-31D-A33E-09 chr10:98806435 G>T maps to NM_003061.2 R610R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GI-01A-11D-A37C-09 chr4:20569202 T>C maps to ENST00000273739 T975T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GO-01A-11D-A37C-09 chr4:20544249 G>T did not map to a codon.
Sequencing variant TCGA-JY-A93E-01A-11D-A37C-09 chr4:20618584 C>T maps to ENST00000273739 N1313N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88Z-01A-11D-A36J-09 chr4:20525669 C>T maps to ENST00000273739 C440C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EZ-01A-11D-A36J-09 chr4:20493432 C>T maps to ENST00000273739 A279A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RE-01A-11D-A33E-09 chr5:168119625 C>A maps to NM_003062.2 L1054L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OX-01A-21D-A28B-09 chr5:168149268 C>T maps to NM_003062.2 L825L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4MQ-01A-11D-A28B-09 chr5:168310286 G>A maps to NM_003062.2 I156I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZR-A9CJ-01B-11D-A387-09 chr13:84454325 G>A maps to NM_052910.1 S439S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GR-01A-12D-A37C-09 chr23:144905920 T>G did not map to a codon.
Sequencing variant TCGA-L5-A4OW-01A-11D-A28B-09 chr23:144905710 T>C did not map to a codon.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr23:144904397 G>T did not map to a codon.
Sequencing variant TCGA-LN-A49P-01A-11D-A247-09 chr23:144905224 C>A did not map to a codon.
Sequencing variant TCGA-LN-A49S-01A-11D-A247-09 chr23:144904329 C>A did not map to a codon.
Sequencing variant TCGA-R6-A8W5-01B-11D-A37C-09 chr23:144905899 G>A did not map to a codon.
Sequencing variant TCGA-V5-A7RC-01B-11D-A403-09 chr23:144905264 C>G did not map to a codon.
Sequencing variant TCGA-L5-A43I-01A-11D-A247-09 chr3:164907801 G>A maps to NM_014926.2 R273*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr3:164906497 C>T maps to NM_014926.2 R707R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NE-01A-11D-A37C-09 chr3:164906580 G>A maps to NM_014926.2 R680*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA7B-01A-31D-A403-09 chr3:164907207 G>A maps to NM_014926.2 L471L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XP-A8T6-01A-11D-A36J-09 chr3:164907745 A>T maps to NM_014926.2 A291A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GI-01A-11D-A37C-09 chr23:142718595 T>G did not map to a codon.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr23:142717788 G>A did not map to a codon.
Sequencing variant TCGA-LN-A9FO-01A-11D-A387-09 chr23:142718077 C>G did not map to a codon.
Sequencing variant TCGA-LN-A9FP-01A-31D-A387-09 chr23:142718474 G>T did not map to a codon.
Sequencing variant TCGA-R6-A8W5-01B-11D-A37C-09 chr23:142716870 G>T did not map to a codon.
Sequencing variant TCGA-V5-A7RC-01B-11D-A403-09 chr23:142718625 C>A did not map to a codon.
Sequencing variant TCGA-XP-A8T6-01A-11D-A36J-09 chr23:142717584 C>A did not map to a codon.
Sequencing variant TCGA-L5-A8NE-01A-11D-A37C-09 chr13:88328306 C>T maps to NM_015567.1 Q222*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NJ-01A-11D-A36J-09 chr13:88330471 G>T maps to NM_015567.1 P943P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr13:88327705 G>A maps to NM_015567.1 W21*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr13:88330072 G>C maps to NM_015567.1 P810P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q9-A6FW-01A-31D-A31U-09 chr13:88328572 G>A maps to NM_015567.1 P310P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6XQ-01B-11D-A33E-09 chr13:86369530 C>A maps to NM_032229.2 A371A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A8HZ-01A-11D-A36J-09 chr10:105762240 C>T maps to NM_014720.2 D435D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8W8-01B-11D-A37C-09 chr10:105762237 T>C maps to NM_014720.2 P434P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RF-01A-13D-A33E-09 chr15:59225695 G>T maps to NM_024755.2 T23T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NI-01A-11D-A37C-09 chr5:159834512 T>C maps to NM_006425.4 K365K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OQ-01A-11D-A27G-09 chr4:146435830 G>A maps to NM_001003688.1 Q22Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OG-01A-11D-A27G-09 chr18:48573436 G>T maps to NM_005359.5 T7T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q9-A6FU-01A-11D-A31U-09 chr18:48604763 T>G maps to NM_005359.5 L529*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6KZ-01A-11D-A31U-09 chr18:48603031 C>T maps to NM_005359.5 R445*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6Y0-01B-11D-A33E-09 chr18:48575670 C>G maps to NM_005359.5 S144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA7D-01A-11D-A403-09 chr18:48603031 C>T maps to NM_005359.5 R445*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-AAPN-01A-11D-A403-09 chr18:48581228 C>G maps to NM_005359.5 S178*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A5B8-01A-11D-A28B-09 chr13:37422853 G>A maps to NM_001127217.2 Q455*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6Y2-01B-11D-A33E-09 chr6:71377798 C>T maps to NM_001044305.1 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93C-01A-11D-A387-09 chr23:128645852 G>T did not map to a codon.
Sequencing variant TCGA-L5-A8NE-01A-11D-A37C-09 chr23:128605258 T>C did not map to a codon.
Sequencing variant TCGA-L5-A8NG-01A-11D-A37C-09 chr23:128633805 A>C did not map to a codon.
Sequencing variant TCGA-IC-A6RE-01A-11D-A33E-09 chr9:2033023 C>T maps to NM_003070.3 R100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49U-01A-31D-A27G-09 chr9:2056794 G>T maps to NM_003070.3 E433*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A8HZ-01A-11D-A36J-09 chr19:11100103 G>A maps to NM_001128849.1 L410L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OG-01A-11D-A27G-09 chr4:144457811 C>T maps to NM_003601.2 L492L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FB-01A-11D-A33E-09 chr2:217315720 G>T maps to NM_014140.3 R668R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49Y-01A-11D-A27G-09 chr2:217280026 G>A maps to NM_014140.3 S200S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6DN-01B-11D-A31U-09 chr2:217280989 C>G maps to NM_014140.3 T274T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6Y0-01B-11D-A33E-09 chr12:56558480 G>T maps to NM_003075.3 P1058P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr7:150938619 G>T maps to NM_003078.3 S286S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr7:150936200 C>T maps to NM_003078.3 V467V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FO-01A-11D-A387-09 chr22:45802660 G>T maps to NM_148674.3 V128V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASW-01A-11D-A403-09 chr22:45745629 T>C maps to NM_148674.3 L1158L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FB-01A-11D-A33E-09 chr9:106887224 G>T maps to NM_001042550.1 E764*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OO-01A-11D-A27G-09 chr9:106857809 C>T maps to NM_001042550.1 L49L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HY-01A-12D-A351-09 chr9:106860800 C>T maps to NM_001042550.1 F131F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6Y2-01B-11D-A33E-09 chr9:106878557 C>A maps to NM_001042550.1 A583A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA4G-01A-11D-A37C-09 chr10:112362580 A>T did not map to a codon.
Sequencing variant TCGA-JY-A6FG-01A-11D-A33E-09 chr3:160138587 C>T maps to NM_005496.3 L640L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GO-01A-11D-A37C-09 chr9:72962953 G>A maps to NM_015110.3 E963E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A50L-01A-11D-A27G-09 chr9:72915085 A>G maps to NM_015110.3 K478K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6Y0-01B-11D-A33E-09 chr9:72892249 A>G maps to NM_015110.3 V135V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NS-01A-12D-A37C-09 chr16:18856782 T>A maps to ENST00000389467 K2063*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASX-01A-11D-A387-09 chr16:18872018 G>A maps to ENST00000389467 L1259L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A8JD-01A-11D-A36J-09 chr1:156231133 G>T maps to NM_015327.2 L699L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OE-01A-11D-A27G-09 chr1:183519018 G>T maps to ENST00000367537 E1029*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NI-01A-11D-A37C-09 chr10:112057440 G>C maps to NM_005871.3 T103T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NI-01A-11D-A37C-09 chr14:70477508 C>T maps to NM_001034852.1 L235L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6KZ-01A-11D-A31U-09 chr11:6412633 C>T maps to NM_000543.4 R113R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GR-01A-12D-A37C-09 chr6:109763197 C>T maps to NM_003080.2 L82L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr6:109764846 C>G maps to NM_003080.2 L337L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GI-01A-11D-A37C-09 chr16:68405586 C>T maps to NM_018667.3 Q166Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49S-01A-11D-A247-09 chr16:68405670 G>T maps to NM_018667.3 L138L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6XQ-01B-11D-A33E-09 chr6:123122526 G>T maps to NM_006714.3 E182*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88T-01A-11D-A351-09 chr1:28271749 C>T maps to NM_014474.2 F23F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASX-01A-11D-A387-09 chr1:28282256 C>T maps to NM_014474.2 F251F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8W5-01B-11D-A37C-09 chr4:71255444 T>G maps to NM_006685.3 P40P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NR-01A-11D-A37C-09 chr12:54576322 G>A maps to NM_014311.1 R124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A8HZ-01A-11D-A36J-09 chr17:62543829 G>A maps to NM_022739.3 V653V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr2:88383894 G>A maps to NM_198274.3 G66G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NV-01A-11D-A37C-09 chr2:88387575 C>T maps to NM_198274.3 I170I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49K-01A-11D-A247-09 chr17:1703985 G>T maps to NM_052928.2 S234S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RE-01A-11D-A33E-09 chr20:48604466 G>A maps to NM_005985.3 L223L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-M9-A5M8-01A-11D-A28B-09 chr8:49833767 G>C maps to NM_003068.3 Y19*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GI-01A-11D-A37C-09 chr6:84265928 G>T maps to NM_014841.2 P889P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88S-01A-11D-A36J-09 chr6:84269885 C>T maps to NM_014841.2 P856P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6F8-01A-11D-A33E-09 chr9:139272096 C>T maps to NM_003086.2 S1394S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr7:127714588 C>T maps to NM_014390.2 G605G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A4QS-01A-11D-A27G-09 chr2:242004958 C>T maps to NM_001080437.1 N986N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KH-A6WC-01A-11D-A33E-09 chr2:242009497 G>T maps to NM_001080437.1 A1157A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A8HZ-01A-11D-A36J-09 chr2:241991850 C>T maps to NM_001080437.1 C683C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA7I-01A-11D-A403-09 chr2:242003534 C>A maps to NM_001080437.1 C864*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43E-01A-11D-A247-09 chr2:96942903 G>A maps to NM_014014.3 Q2003*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88Z-01A-11D-A36J-09 chr2:96944360 G>A maps to NM_014014.3 I1804I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8WC-01A-11D-A37C-09 chr2:96947597 G>A maps to NM_014014.3 L1660L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RE-A7BO-01A-11D-A33E-09 chr2:96952154 G>T maps to NM_014014.3 T1299T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EU-01A-11D-A36J-09 chr2:96944360 G>A maps to NM_014014.3 I1804I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FA-01A-11D-A33E-09 chr19:49604726 C>T maps to NM_003089.4 H158H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6KZ-01A-11D-A31U-09 chr15:101827874 C>T maps to NM_003090.2 S114S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NF-01A-11D-A37C-09 chr19:46191712 G>A maps to NM_004597.5 N38N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-A7RB-01A-11D-A351-09 chr19:46190957 C>T maps to NM_004597.5 V70V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GF-01A-11D-A37C-09 chr15:25223031 C>A maps to NM_022805.2 P176P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NV-01A-11D-A37C-09 chr15:25223557 A>G maps to NM_022805.2 P230P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A8O2-01A-11D-A36J-09 chr8:121644773 G>T maps to NM_021021.3 T302T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr16:69317975 C>T maps to NM_006750.3 R392*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-M9-A5M8-01A-11D-A28B-09 chr8:51617158 G>A did not map to a codon.
Sequencing variant TCGA-R6-A6XG-01B-11D-A33E-09 chr8:51449338 T>C maps to NM_018967.2 S217S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GI-01A-11D-A37C-09 chr2:1271172 T>C maps to NM_018968.3 L372L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr15:64424091 G>A did not map to a codon.
Sequencing variant TCGA-IG-A3YC-01A-11D-A247-09 chr6:86277259 C>T maps to NM_153816.3 P151P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FB-01A-11D-A33E-09 chr5:53839222 G>A maps to NM_001102575.1 Q612Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88V-01A-11D-A351-09 chr5:53814765 G>A maps to NM_052870.2 P328P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GO-01A-11D-A37C-09 chr11:130785516 G>T maps to NM_014758.2 I106I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr16:50707922 C>T maps to NM_182854.2 R115R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr4:186267692 C>T maps to NM_031953.2 C566C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HV-01A-21D-A351-09 chr4:186260594 G>T maps to NM_031953.2 L495L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NE-01A-11D-A37C-09 chr16:12662431 C>T maps to NM_001080530.2 S411S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FQ-01A-31D-A387-09 chr16:12293472 C>T maps to NM_001080530.2 L152L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EQ-01A-11D-A36J-09 chr16:12172756 G>T maps to NM_001080530.2 E78*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-AAPN-01A-11D-A403-09 chr9:115580088 C>G maps to NM_001012994.1 L151L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RE-A7BO-01A-11D-A33E-09 chr3:125170226 G>T maps to NM_003794.2 R409R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-AAPN-01A-11D-A403-09 chr7:2317767 G>A maps to NM_013321.2 F89F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A9-01A-11D-A28B-09 chr1:179304720 A>G maps to NM_003101.4 S86S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA7D-01A-11D-A403-09 chr12:53497989 G>A maps to NM_003578.3 E46E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93D-01A-11D-A387-09 chr6:107955613 C>T maps to NM_018013.3 T522T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OG-01A-11D-A27G-09 chr6:107956646 C>T maps to NM_018013.3 R867*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8WC-01A-11D-A37C-09 chr6:107955277 C>T maps to NM_018013.3 P410P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FE-01A-11D-A33E-09 chr14:55509974 A>C maps to NM_199421.1 S72S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FB-01A-11D-A33E-09 chr18:67992305 C>A maps to NM_004232.3 P134P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A1-01A-21D-A27G-09 chr18:67993380 C>A maps to NM_004232.3 R493R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr21:33040845 C>T maps to NM_000454.4 N140N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GH-01A-11D-A37C-09 chr13:36748632 T>A maps to ENST00000511166 P364P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A4P3-01A-11D-A27G-09 chr13:36744697 G>T maps to ENST00000511166 G486G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FB-01A-11D-A33E-09 chr16:597572 G>A maps to NM_005632.2 P245P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OX-01A-21D-A28B-09 chr16:597227 G>A maps to NM_005632.2 E130E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OE-01A-11D-A27G-09 chr10:97101350 C>A maps to NM_001034954.1 R838R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NH-01A-11D-A37C-09 chr10:97081739 C>T maps to NM_001034954.1 R1226R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NU-01A-11D-A36J-09 chr10:97154773 G>T maps to NM_001034954.1 I427I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FG-01A-11D-A33E-09 chr4:186583258 G>A maps to ENST00000355634 L131L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr4:186545130 G>A maps to ENST00000355634 Y580Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NN-01A-11D-A37C-09 chr4:186598447 G>T maps to NM_001145673.1 T65T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6F8-01A-11D-A33E-09 chr10:108589379 C>T maps to NM_001013031.1 L226L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GO-01A-11D-A37C-09 chr10:106982917 A>T maps to NM_014978.1 R927*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GO-01A-11D-A37C-09 chr11:121476266 G>A maps to NM_003105.5 R1645R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr11:121430340 G>A maps to NM_003105.5 K1008K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8WG-01A-11D-A37C-09 chr1:109856992 G>T maps to NM_002959.4 R791R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EU-01A-11D-A36J-09 chr1:109898039 G>T maps to NM_002959.4 T164T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EX-01A-11D-A36J-09 chr2:39283971 A>T maps to NM_005633.3 S127S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A5B8-01A-11D-A28B-09 chr14:50649279 C>T maps to NM_006939.2 L253L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93D-01A-11D-A387-09 chr22:38369996 C>T maps to NM_006941.3 P302P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GR-01A-12D-A37C-09 chr2:5833993 C>T maps to NM_003108.3 L381L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GO-01A-11D-A37C-09 chr23:139587000 T>A did not map to a codon.
Sequencing variant TCGA-IC-A6RE-01A-11D-A33E-09 chr12:23687308 A>C maps to NM_006940.4 T712T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-A7RB-01A-11D-A351-09 chr12:23908617 T>C maps to NM_006940.4 K174K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASV-01A-11D-A387-09 chr11:16077435 G>T maps to NM_001145819.1 A384A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FA-01A-11D-A33E-09 chr8:10584105 C>T maps to ENST00000354846 L155L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EP-01A-31D-A403-09 chr8:10584081 G>A maps to ENST00000354846 N163N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88Y-01A-11D-A351-09 chr17:70118949 C>A maps to NM_000346.3 Y174*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A1-01A-21D-A27G-09 chr12:53800471 C>T maps to NM_138473.2 P593P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr2:231371094 G>T maps to NM_001080391.1 G650*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A8HZ-01A-11D-A36J-09 chr2:231371133 G>T maps to NM_001080391.1 G663*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GK-01A-11D-A37C-09 chr2:231048322 G>T maps to NM_080424.2 S438*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43H-01A-11D-A247-09 chr2:231065664 A>G maps to NM_080424.2 T355T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr2:231037654 G>A maps to NM_080424.2 C537C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93D-01A-11D-A387-09 chr17:45925507 C>T maps to NM_199262.2 L96L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q9-A6FW-01A-31D-A31U-09 chr17:45924820 G>T maps to NM_199262.2 R325R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88W-01A-11D-A351-09 chr12:53723183 G>A maps to NM_001173467.1 S14S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A938-01A-11D-A37C-09 chr7:20824097 G>A maps to NM_182700.4 S446S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NJ-01A-11D-A36J-09 chr7:20824391 G>T maps to NM_182700.4 A348A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZR-A9CJ-01B-11D-A387-09 chr7:20824505 C>T maps to NM_182700.4 P310P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3Y9-01A-12D-A247-09 chr1:118596627 G>C maps to NM_206996.2 L937L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr1:118539225 G>T maps to NM_206996.2 V1639V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49Y-01A-11D-A27G-09 chr1:118584485 G>T maps to NM_206996.2 V998V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q9-A6FU-01A-11D-A31U-09 chr1:118596716 C>A did not map to a codon.
Sequencing variant TCGA-R6-A6Y0-01B-11D-A33E-09 chr10:22690088 G>C did not map to a codon.
Sequencing variant TCGA-2H-A9GM-01A-11D-A37C-09 chr9:35811297 G>A maps to NM_001039592.1 Q249*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3QL-01A-11D-A247-09 chr17:49091694 C>A maps to ENST00000376407 E371*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr17:49075878 G>A maps to ENST00000376407 S588S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6XQ-01B-11D-A33E-09 chr17:49059941 G>A maps to ENST00000376407 V1061V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49K-01A-11D-A247-09 chr7:123594115 C>T maps to NM_001174046.1 Y164Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-A7RB-01A-11D-A351-09 chr23:140335762 T>C did not map to a codon.
Sequencing variant TCGA-VR-A8EO-01A-11D-A36J-09 chr23:140335649 C>A did not map to a codon.
Sequencing variant TCGA-VR-A8EX-01A-11D-A36J-09 chr23:140335750 C>G did not map to a codon.
Sequencing variant TCGA-VR-AA7B-01A-31D-A403-09 chr23:140336534 T>A did not map to a codon.
Sequencing variant TCGA-IC-A6RF-01A-13D-A33E-09 chr23:144337319 A>T did not map to a codon.
Sequencing variant TCGA-IG-A4QS-01A-11D-A27G-09 chr23:144337249 G>A did not map to a codon.
Sequencing variant TCGA-L5-A8NJ-01A-11D-A36J-09 chr23:144337272 C>A did not map to a codon.
Sequencing variant TCGA-IG-A4P3-01A-11D-A27G-09 chr23:142596675 C>G did not map to a codon.
Sequencing variant TCGA-L5-A43C-01A-11D-A247-09 chr23:142605167 C>T did not map to a codon.
Sequencing variant TCGA-LN-A5U7-01A-11D-A31U-09 chr2:32289127 G>T maps to NM_014946.3 V76V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr1:84991634 T>C maps to ENST00000263717 N163N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A625-01A-11D-A31U-09 chr3:172835310 C>A maps to NM_031955.5 E71*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49K-01A-11D-A247-09 chr3:172643274 T>C maps to NM_031955.5 Q363Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HY-01A-12D-A351-09 chr1:217842376 A>T maps to NM_138796.2 V81V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A8I1-01A-11D-A36J-09 chr4:52943091 C>T maps to NM_145263.2 L302L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EW-01A-11D-A36J-09 chr4:52917942 C>T maps to NM_145263.2 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr20:48522908 G>T maps to NM_006038.3 A270A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6XQ-01B-11D-A33E-09 chr20:48522353 C>A maps to NM_006038.3 T455T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43M-01A-11D-A247-09 chr1:48850998 G>T maps to NM_019073.2 C297*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NS-01A-12D-A37C-09 chr1:48821376 A>G maps to NM_019073.2 L387L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RE-01A-11D-A33E-09 chr2:201284106 C>T maps to ENST00000409151 C119C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A5U7-01A-11D-A31U-09 chr7:99917259 G>A maps to NM_001004351.4 K473K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q9-A6FU-01A-11D-A31U-09 chr20:3758927 G>C maps to NM_015417.4 L214L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GR-01A-12D-A37C-09 chr5:35800170 A>G maps to NM_024867.3 G1644G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NV-01A-11D-A37C-09 chr5:35793298 G>A maps to NM_024867.3 E1531E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EW-01A-11D-A36J-09 chr5:35709101 G>T maps to NM_024867.3 L906L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RE-01A-11D-A33E-09 chr2:220355176 C>T maps to NM_005876.4 R2990*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A939-01A-12D-A37C-09 chr2:220348118 G>A maps to NM_005876.4 R1978R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OX-01A-21D-A28B-09 chr2:220315876 C>T maps to NM_005876.4 Y711Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr2:220349120 G>A maps to NM_005876.4 V2312V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr1:16260996 G>T maps to NM_015001.2 T2754T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A8I0-01A-11D-A36J-09 chr1:16255999 G>T maps to NM_015001.2 G1089*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FP-01A-31D-A387-09 chr15:69238241 G>T maps to NM_145658.3 S123S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3YC-01A-11D-A247-09 chr15:44914419 G>T maps to NM_025137.3 P814P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GM-01A-11D-A37C-09 chr13:36909222 G>A maps to NM_001142294.1 R249*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A4QS-01A-11D-A27G-09 chr13:36909526 A>G maps to NM_001142294.1 T147T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RE-01A-11D-A33E-09 chr2:228860247 G>C maps to NM_001142644.1 L1537L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OE-01A-11D-A27G-09 chr2:228882998 G>A maps to NM_001142644.1 S857S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A5U7-01A-11D-A31U-09 chr2:228996764 T>C maps to NM_001142644.1 E23E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FP-01A-31D-A387-09 chr2:228883670 G>T maps to NM_001142644.1 Y633*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8W5-01B-11D-A37C-09 chr2:228858302 G>A maps to NM_001142644.1 G1556G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASW-01A-11D-A403-09 chr2:228883331 C>T maps to NM_001142644.1 E746E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OJ-01A-11D-A27G-09 chr23:57162330 T>C did not map to a codon.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr23:57146544 T>C did not map to a codon.
Sequencing variant TCGA-L5-A4OG-01A-11D-A27G-09 chr23:57021368 C>T did not map to a codon.
Sequencing variant TCGA-JY-A6FD-01A-11D-A33E-09 chr23:62570562 G>T did not map to a codon.
Sequencing variant TCGA-IC-A6RE-01A-11D-A33E-09 chr5:147513405 G>T maps to NM_001127698.1 E1078*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A938-01A-11D-A37C-09 chr16:89925575 G>T maps to NM_032451.1 E426*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr16:89920953 G>A maps to NM_032451.1 V262V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49X-01A-31D-A27G-09 chr16:28993281 G>T maps to NM_032038.2 L290L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A8I0-01A-11D-A36J-09 chr17:4435943 C>T maps to NM_001124758.1 T300T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A7DP-01A-31D-A33E-09 chr17:4349366 C>A maps to NM_182538.4 R143R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EW-01A-11D-A36J-09 chr20:55904958 C>T maps to ENST00000371258 F12F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FO-01A-11D-A387-09 chr1:32266182 G>T maps to NM_144569.4 A487A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A8I1-01A-11D-A36J-09 chr10:73827479 G>A maps to NM_014767.2 T200T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-AAPN-01A-11D-A403-09 chr4:167713336 C>T maps to NM_016950.2 L234L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-AAPN-01A-11D-A403-09 chr11:14277294 C>T maps to NM_006108.2 Q398*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr4:88903738 C>T maps to NM_001040058.1 N212N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NI-01A-11D-A37C-09 chr2:234959515 G>T did not map to a codon.
Sequencing variant TCGA-VR-AA7B-01A-31D-A403-09 chr12:121220482 G>T maps to NM_139015.3 L159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A8JD-01A-11D-A36J-09 chr12:121205248 C>T maps to NM_139015.3 G307G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GR-01A-12D-A37C-09 chr2:65540838 A>T maps to NM_181784.2 Y351*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-AAPN-01A-11D-A403-09 chr1:153066152 C>T maps to NM_001024209.2 E25E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A6QS-01A-12D-A33E-09 chr4:124323396 A>G maps to NM_199327.1 E217E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OE-01A-11D-A27G-09 chr11:55653116 G>A maps to NM_032681.3 K71K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6L4-01A-11D-A31U-09 chr1:9427594 G>A maps to NM_025106.3 P261P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GJ-01A-11D-A37C-09 chr1:158617432 T>C maps to NM_003126.2 K1264K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GK-01A-11D-A37C-09 chr1:158584080 C>T maps to NM_003126.2 V2268V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3QL-01A-11D-A247-09 chr1:158612699 T>C maps to NM_003126.2 K1503K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6F8-01A-11D-A33E-09 chr1:158604350 A>G maps to NM_003126.2 D1849D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr1:158623216 T>C did not map to a codon.
Sequencing variant TCGA-LN-A49N-01A-11D-A247-09 chr1:158636282 G>T maps to NM_003126.2 T681T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EZ-01A-11D-A36J-09 chr1:158623118 G>T maps to NM_003126.2 R1045R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A9VB-01A-21D-A37C-09 chr1:158612689 G>A maps to NM_003126.2 R1507*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZR-A9CJ-01B-11D-A387-09 chr1:158592922 G>A maps to NM_003126.2 D1990D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A7DP-01A-31D-A33E-09 chr9:131394491 G>T maps to NM_001130438.2 L2283L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A97I-01A-11D-A387-09 chr9:131388229 T>G maps to NM_001130438.2 L2084L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NH-01A-11D-A37C-09 chr9:131370474 G>T maps to NM_001130438.2 E1471*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6KZ-01A-11D-A31U-09 chr9:131344062 G>A maps to NM_001130438.2 A488A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-AAPN-01A-11D-A403-09 chr9:131371526 G>A maps to NM_001130438.2 A1574A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XP-A8T7-01A-11D-A36J-09 chr14:65233374 C>A maps to NM_000347.5 *2138Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93D-01A-11D-A387-09 chr2:54864937 G>T maps to NM_003128.2 E1286*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FP-01A-31D-A387-09 chr2:54880792 G>T maps to NM_003128.2 A1875A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr11:66466465 G>A maps to NM_006946.2 H1288H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr11:66472850 C>T maps to NM_006946.2 A632A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FQ-01A-31D-A387-09 chr11:66467040 G>T maps to NM_006946.2 L1204L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8ER-01A-11D-A36J-09 chr19:41008711 G>T maps to NM_020971.2 E412*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr15:42160631 C>T maps to ENST00000320955 Q2007Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NS-01A-12D-A37C-09 chr15:42169047 G>A maps to ENST00000320955 H1270H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASW-01A-11D-A403-09 chr15:42169050 T>C maps to ENST00000320955 A1269A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EY-01A-11D-A36J-09 chr9:94842355 T>C maps to NM_006415.2 A123A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NJ-01A-11D-A36J-09 chr14:77978709 G>A maps to NM_004863.2 Q536*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A5U7-01A-11D-A31U-09 chr14:78023489 C>T did not map to a codon.
Sequencing variant TCGA-L5-A4OO-01A-11D-A27G-09 chr5:79616604 C>T maps to NM_032567.3 Q191*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43C-01A-11D-A247-09 chr2:45807092 G>T maps to NM_018079.4 G331G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RE-A7BO-01A-11D-A33E-09 chr20:36030929 C>T maps to ENST00000373558 C409C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OG-01A-11D-A27G-09 chr16:30750429 C>T maps to NM_006662.2 P3023P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HV-01A-21D-A351-09 chr16:30720961 A>G maps to NM_006662.2 P254P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EQ-01A-11D-A36J-09 chr16:30750261 G>A maps to NM_006662.2 Q2967Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA7B-01A-31D-A403-09 chr16:30749317 G>T maps to NM_006662.2 E2653*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FG-01A-11D-A33E-09 chr17:17719807 G>A maps to NM_001005291.2 A700A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43H-01A-11D-A247-09 chr12:64536103 G>A maps to NM_020762.2 L970L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NN-01A-11D-A37C-09 chr12:64474128 C>T maps to NM_020762.2 L463L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NH-01A-11D-A37C-09 chr3:9100156 C>T did not map to a codon.
Sequencing variant TCGA-Z6-A8JE-01A-11D-A37C-09 chr3:9097937 G>T maps to NM_014850.2 T368T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93F-01A-21D-A37C-09 chr16:4242708 G>T maps to ENST00000330063 Y727*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr1:11115981 G>T maps to NM_003132.2 G207G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NS-01A-12D-A37C-09 chr20:62178744 G>A maps to NM_080823.2 G24G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6DN-01B-11D-A31U-09 chr20:62172296 G>C maps to NM_080823.2 R447R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OO-01A-11D-A27G-09 chr6:35837646 C>T maps to ENST00000361690 T357T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NJ-01A-11D-A36J-09 chr6:35838067 T>C maps to ENST00000361690 Q343Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HW-01A-22D-A351-09 chr23:153047663 G>A did not map to a codon.
Sequencing variant TCGA-R6-A6Y0-01B-11D-A33E-09 chr23:153047266 G>T did not map to a codon.
Sequencing variant TCGA-L5-A8NE-01A-11D-A37C-09 chr23:38031201 A>C did not map to a codon.
Sequencing variant TCGA-L5-A8NQ-01A-11D-A36J-09 chr23:38079994 C>A did not map to a codon.
Sequencing variant TCGA-L5-A8NR-01A-11D-A37C-09 chr23:38016193 G>T did not map to a codon.
Sequencing variant TCGA-IG-A6QS-01A-12D-A33E-09 chr23:99920276 T>G did not map to a codon.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr22:26884175 C>T maps to NM_001013694.2 Y144Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OE-01A-11D-A27G-09 chr1:24996715 C>A maps to NM_005839.3 P770P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RE-01A-11D-A33E-09 chr16:2817410 T>G maps to NM_016333.3 A2294A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OX-01A-21D-A28B-09 chr16:2814389 C>T maps to NM_016333.3 S1287S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OJ-01A-11D-A27G-09 chr12:119594329 G>T maps to NM_194286.2 R521R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A8O2-01A-11D-A36J-09 chr7:100484426 G>T maps to NM_015908.5 S553S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6DQ-01B-11D-A31U-09 chr20:629462 C>T maps to NM_080725.1 A103A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XP-A8T8-01A-11D-A36J-09 chr20:60736517 C>T maps to NM_198935.1 G86G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49O-01A-11D-A247-09 chr7:141450108 A>T did not map to a codon.
Sequencing variant TCGA-JY-A93F-01A-21D-A37C-09 chr2:182783598 G>T maps to NM_001130445.1 E995*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KH-A6WC-01A-11D-A33E-09 chr17:27963456 G>T maps to NM_033389.2 C570*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FP-01A-31D-A387-09 chr17:28003884 C>T maps to NM_033389.2 T162T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASV-01A-11D-A387-09 chr11:67075316 G>A maps to NM_017857.3 G264G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93F-01A-21D-A37C-09 chr7:149474800 C>A maps to NM_198455.2 G200G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NI-01A-11D-A37C-09 chr7:149511584 G>A maps to NM_198455.2 S3418S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NQ-01A-11D-A36J-09 chr7:149522964 C>T maps to NM_198455.2 P4734P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HX-01A-11D-A33E-09 chr7:149474348 C>A maps to NM_198455.2 A131A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A8I1-01A-11D-A36J-09 chr7:149511901 C>A maps to NM_198455.2 C3487*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EU-01A-11D-A36J-09 chr7:149474896 C>T maps to NM_198455.2 H232H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A8JD-01A-11D-A36J-09 chr7:149477371 C>T maps to NM_198455.2 L481L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GJ-01A-11D-A37C-09 chr6:7290164 C>T did not map to a codon.
Sequencing variant TCGA-Z6-A8JD-01A-11D-A36J-09 chr11:65339075 C>G maps to NM_006396.1 L157L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43M-01A-11D-A247-09 chr14:38678866 G>T maps to NM_001049.2 T91T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49K-01A-11D-A247-09 chr17:71165532 G>T maps to NM_001050.2 V25V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GF-01A-11D-A37C-09 chr22:37603089 G>A maps to NM_001051.2 S251S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr22:37602690 C>T maps to NM_001051.2 G384G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GM-01A-11D-A37C-09 chr16:1129611 C>T maps to NM_001053.3 R248R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4ON-01A-11D-A27G-09 chr16:1129923 C>T maps to NM_001053.3 R352R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A9-01A-11D-A28B-09 chr23:48243538 T>A did not map to a codon.
Sequencing variant TCGA-IG-A3QL-01A-11D-A247-09 chr23:48053591 C>T did not map to a codon.
Sequencing variant TCGA-L5-A8NI-01A-11D-A37C-09 chr22:41223098 C>G did not map to a codon.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr11:130079457 C>T maps to NM_021978.3 G797G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A9-01A-11D-A28B-09 chr8:53084979 T>C maps to NM_014682.2 E147E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8ET-01A-11D-A403-09 chr8:53092685 G>T maps to NM_014682.2 T91T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q9-A6FW-01A-31D-A31U-09 chr16:70417131 G>A maps to NM_006927.3 Y240Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RE-01A-11D-A33E-09 chr11:8751709 G>T maps to NM_005418.3 S376*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FQ-01A-31D-A387-09 chr11:8732409 G>A maps to NM_005418.3 G778G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6DN-01B-11D-A31U-09 chr11:8752017 G>A maps to NM_005418.3 G273G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XP-A8T6-01A-11D-A36J-09 chr11:8719177 G>A maps to NM_005418.3 D982D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OS-01A-11D-A28B-09 chr3:186769079 C>A maps to NM_003032.2 A217A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FE-01A-11D-A33E-09 chr2:107423379 G>T maps to NM_001142351.1 C448*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88V-01A-11D-A351-09 chr2:107459701 G>A maps to NM_001142351.1 A244A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8WG-01A-11D-A37C-09 chr2:107459974 G>T maps to NM_001142351.1 P153P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EZ-01A-11D-A36J-09 chr17:74621942 A>T maps to NM_018414.3 T521T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A9VB-01A-21D-A37C-09 chr17:74625792 C>T maps to NM_018414.3 R44R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S8-A6BV-01A-21D-A31U-09 chr1:76877736 A>C maps to NM_152996.2 S86S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NJ-01A-11D-A36J-09 chr1:77334345 G>A maps to NM_030965.1 A60A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FG-01A-11D-A33E-09 chr9:130656796 G>T maps to NM_013443.3 G97G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6XQ-01B-11D-A33E-09 chr7:116759697 A>T maps to ENST00000323984 G106G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NQ-01A-11D-A36J-09 chr18:55020184 G>A maps to NM_015879.2 E36E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASX-01A-11D-A387-09 chr18:55021740 G>A maps to NM_015879.2 A96A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49W-01A-11D-A27G-09 chr5:100222258 C>T maps to NM_005668.4 V97V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GR-01A-12D-A37C-09 chr3:52547773 C>T maps to NM_015136.2 L1104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr3:52551564 G>T did not map to a codon.
Sequencing variant TCGA-L5-A88S-01A-11D-A36J-09 chr3:52544054 C>T maps to NM_015136.2 S839S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NT-01A-11D-A37C-09 chr3:52556951 G>A maps to NM_015136.2 V2302V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NW-01A-11D-A37C-09 chr3:52555007 C>G maps to NM_015136.2 G1965G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A5U5-01A-21D-A28B-09 chr3:52551964 C>A maps to NM_015136.2 C1569*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RE-A7BO-01A-11D-A33E-09 chr3:52544252 T>C did not map to a codon.
Sequencing variant TCGA-V5-AASX-01A-11D-A387-09 chr3:52550231 C>T maps to NM_015136.2 R1374R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GF-01A-11D-A37C-09 chr12:104131497 T>C maps to NM_017564.9 C1879C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GR-01A-12D-A37C-09 chr12:104098352 C>T maps to NM_017564.9 C1287C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GM-01A-11D-A37C-09 chr3:136141316 G>T maps to NM_005862.2 R658R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A6QS-01A-12D-A33E-09 chr3:136082261 G>T maps to NM_005862.2 T911T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4ON-01A-11D-A27G-09 chr3:136221514 C>T maps to NM_005862.2 K261K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OW-01A-11D-A28B-09 chr23:123176427 C>A did not map to a codon.
Sequencing variant TCGA-L5-A8NJ-01A-11D-A36J-09 chr23:123215373 C>T did not map to a codon.
Sequencing variant TCGA-LN-A49O-01A-11D-A247-09 chr23:123210194 G>T did not map to a codon.
Sequencing variant TCGA-JY-A93E-01A-11D-A37C-09 chr7:66773929 G>A maps to NM_022906.2 G32G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6Y2-01B-11D-A33E-09 chr10:17746458 G>T maps to NM_003473.2 L314L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NW-01A-11D-A37C-09 chr2:153000480 T>A maps to NM_005843.4 T188T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr10:90676486 G>T maps to NM_020799.2 A318A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88V-01A-11D-A351-09 chr19:4333711 C>A maps to ENST00000314714 R92R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49O-01A-11D-A247-09 chr11:72466799 T>C did not map to a codon.
Sequencing variant TCGA-IG-A4P3-01A-11D-A27G-09 chr13:33692349 G>T maps to NM_178007.2 R703R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A8-01A-32D-A27G-09 chr13:33760147 G>T maps to NM_178007.2 P4P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A8JE-01A-11D-A37C-09 chr13:33700298 G>T maps to NM_178007.2 V659V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OJ-01A-11D-A27G-09 chr17:37813293 G>T maps to NM_006804.3 E85*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GK-01A-11D-A37C-09 chr23:67937515 G>T did not map to a codon.
Sequencing variant TCGA-L5-A4OW-01A-11D-A28B-09 chr23:67942428 C>T did not map to a codon.
Sequencing variant TCGA-V5-AASX-01A-11D-A387-09 chr23:67944241 C>T did not map to a codon.
Sequencing variant TCGA-RE-A7BO-01A-11D-A33E-09 chr12:56737902 G>A maps to NM_005419.3 Q707*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NV-01A-11D-A37C-09 chr17:40483491 G>A maps to NM_139276.2 D369D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA4D-01A-11D-A37C-09 chr17:40491334 C>A maps to NM_139276.2 V155V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43H-01A-11D-A247-09 chr2:191919260 C>A did not map to a codon.
Sequencing variant TCGA-2H-A9GQ-01A-11D-A37C-09 chr17:40457644 G>A maps to NM_003152.3 V466V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NK-01A-21D-A37C-09 chr17:40359717 A>G maps to NM_012448.3 P645P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OG-01A-11D-A27G-09 chr20:47734454 G>A maps to NM_017453.2 A456A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q9-A6FW-01A-31D-A31U-09 chr8:74515977 G>A maps to NM_001164380.1 R338*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A5B8-01A-11D-A28B-09 chr8:23702447 G>C maps to NM_003155.2 L193L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A51D-01A-11D-A27G-09 chr7:89859298 T>C maps to NM_152999.3 S378S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6F8-01A-11D-A33E-09 chr1:47717560 G>T maps to NM_001048166.1 I1038I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A51D-01A-11D-A27G-09 chr4:27009195 G>T maps to ENST00000382009 L428L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr19:1220392 C>T maps to NM_000455.4 D162D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A8JD-01A-11D-A36J-09 chr19:1226529 G>T maps to NM_000455.4 E396*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-AAPN-01A-11D-A403-09 chr19:1220639 C>T maps to NM_000455.4 Q220*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FO-01A-11D-A387-09 chr2:220480763 A>G did not map to a codon.
Sequencing variant TCGA-L5-A8NU-01A-11D-A36J-09 chr2:220111884 C>T maps to ENST00000409260 F164F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OJ-01A-11D-A27G-09 chr2:197004397 G>T maps to NM_004226.3 S261*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FQ-01A-31D-A387-09 chr2:197021277 G>T maps to NM_004226.3 R74R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GK-01A-11D-A37C-09 chr2:242437664 C>T maps to NM_006374.3 L339L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q9-A6FW-01A-31D-A31U-09 chr8:99761533 G>T maps to ENST00000354930 V135V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FP-01A-31D-A387-09 chr4:5448433 C>G maps to NM_018401.1 G199G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr10:134036379 C>T maps to NM_173575.2 P368P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6XG-01B-11D-A33E-09 chr11:8478952 G>C maps to NM_030906.2 S211*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L7-A6VZ-01A-12D-A33E-09 chr20:2097324 G>T maps to NM_080836.3 L302L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-AAPN-01A-11D-A403-09 chr2:219557015 G>T maps to NM_015690.3 G639*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OW-01A-11D-A28B-09 chr12:27472323 C>T maps to NM_015000.3 P381P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A6QS-01A-12D-A33E-09 chr2:168931517 G>T maps to NM_013233.2 R406R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FG-01A-11D-A33E-09 chr20:43607119 G>A maps to NM_006282.2 E51E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8ER-01A-11D-A36J-09 chr20:43623729 G>A did not map to a codon.
Sequencing variant TCGA-L7-A6VZ-01A-12D-A33E-09 chr1:36814304 G>A maps to ENST00000373130 L250L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FP-01A-31D-A387-09 chr13:39550709 C>A maps to NM_145286.2 G66*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GH-01A-11D-A37C-09 chr2:48809569 C>T maps to NM_172311.2 R600*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FB-01A-11D-A33E-09 chr2:48808056 C>A maps to NM_172311.2 P95P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88W-01A-11D-A351-09 chr2:48808502 C>G maps to NM_172311.2 S244*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q9-A6FW-01A-31D-A31U-09 chr2:48822434 T>C maps to NM_001198595.1 T734T. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-L5-A4OX-01A-21D-A28B-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-R6-A6L6-01B-11D-A33E-09 chr2:202344885 C>T maps to NM_018571.5 Y415Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EZ-01A-11D-A36J-09 chr9:125898382 G>T maps to NM_018387.4 A570A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NV-01A-11D-A37C-09 chr11:125484061 C>T maps to NM_152713.3 N545N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZR-A9CJ-01B-11D-A387-09 chr11:125489994 G>T maps to NM_152713.3 E685*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NF-01A-11D-A37C-09 chr3:31663634 G>T maps to NM_178862.1 V458V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NL-01A-12D-A37C-09 chr3:31674471 G>T maps to NM_178862.1 E745*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A9VB-01A-21D-A37C-09 chr3:31666480 A>G maps to NM_178862.1 V601V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3Y9-01A-12D-A247-09 chr9:102713412 G>A maps to NM_017919.2 L87L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6XQ-01B-11D-A33E-09 chr9:102730927 C>G maps to NM_017919.2 P294P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NI-01A-11D-A37C-09 chr11:59523090 C>T maps to NM_004177.4 L5L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RF-01A-13D-A33E-09 chr11:62595063 G>T maps to NM_003164.3 R89R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr9:130444702 G>A maps to NM_003165.3 W522*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GI-01A-11D-A37C-09 chr19:7706940 G>A maps to ENST00000441779 Q211Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EX-01A-11D-A36J-09 chr3:120760583 G>T maps to NM_014980.2 E109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GR-01A-12D-A37C-09 chr8:70512985 A>C maps to NM_001128206.1 R295R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43C-01A-11D-A247-09 chr8:70501313 C>T maps to NM_001128206.1 P224P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FP-01A-31D-A387-09 chr20:46313303 C>A maps to NM_001161841.1 A253A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RE-A7BO-01A-11D-A33E-09 chr16:28620134 G>A maps to NM_177529.1 Y14Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASV-01A-11D-A387-09 chr16:28617216 C>T maps to NM_177529.1 A271A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A4-01A-11D-A27G-09 chr16:28603713 C>T maps to NM_001054.3 L215L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A7DP-01A-31D-A33E-09 chr2:108910749 C>T maps to ENST00000437390 R73*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NE-01A-11D-A37C-09 chr4:70707712 T>C maps to NM_005420.2 *295*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HV-01A-21D-A351-09 chr19:48386899 T>C maps to NM_003167.3 P93P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43E-01A-11D-A247-09 chr22:44258217 G>A maps to NM_014351.3 F15F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RE-01A-11D-A33E-09 chr2:37410581 C>A maps to NM_001032377.1 E92*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA4G-01A-11D-A37C-09 chr3:4458862 G>T maps to NM_182760.3 G263G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OJ-01A-11D-A27G-09 chr7:881708 G>T maps to ENST00000456758 R189R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GM-01A-11D-A37C-09 chr22:39132346 C>T maps to ENST00000405018 R714R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EY-01A-11D-A36J-09 chr22:39134597 G>T maps to ENST00000405018 A668A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HW-01A-22D-A351-09 chr20:31584142 G>A maps to NM_080675.3 L138L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93E-01A-11D-A37C-09 chr17:56423630 G>T maps to NM_003168.1 S110S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A5U5-01A-21D-A28B-09 chr19:39963104 C>T maps to NM_003169.3 I669I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FD-01A-11D-A33E-09 chr17:27002161 G>T maps to NM_003170.3 E174*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr17:27002425 C>T maps to NM_003170.3 D182D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6DN-01B-11D-A31U-09 chr17:27026895 C>T maps to NM_003170.3 Q1516*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA7B-01A-31D-A403-09 chr17:27023871 G>A maps to NM_003170.3 K1327K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FD-01A-11D-A33E-09 chr2:27883882 G>T maps to NM_014860.1 I129I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EU-01A-11D-A36J-09 chr2:27880463 T>A maps to NM_014860.1 T164T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RE-01A-11D-A33E-09 chr22:24581897 G>T did not map to a codon.
Sequencing variant TCGA-L5-A4OE-01A-11D-A27G-09 chr22:24583630 G>T maps to NM_019601.3 E662*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr22:24584235 C>T maps to NM_019601.3 L795L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr23:48564744 C>T did not map to a codon.
Sequencing variant TCGA-L5-A891-01A-11D-A36J-09 chr11:67939152 A>T maps to NM_017635.3 L226*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L7-A6VZ-01A-12D-A33E-09 chr11:67939073 G>T maps to NM_017635.3 V252V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49Y-01A-11D-A27G-09 chr19:55858815 G>T maps to NM_032701.3 *463L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FB-01A-11D-A33E-09 chr1:149877571 G>T maps to NM_014849.3 S635S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X8-AAAR-01A-11D-A403-09 chr1:149885041 C>T maps to NM_014849.3 A117A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49L-01A-11D-A247-09 chr15:91832772 A>C maps to NM_014848.4 A577A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X8-AAAR-01A-11D-A403-09 chr15:91832790 G>T maps to NM_014848.4 L583L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49M-01A-21D-A27G-09 chr5:75427798 C>G maps to NM_014979.1 S75*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6KZ-01A-11D-A31U-09 chr9:113168501 C>T maps to ENST00000374463 P3129P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GO-01A-11D-A37C-09 chr10:29782144 G>T maps to NM_021738.2 P1339P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A4P3-01A-11D-A27G-09 chr10:29821900 C>G maps to NM_021738.2 V465V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr10:29820935 C>T maps to NM_021738.2 S668S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6F8-01A-11D-A33E-09 chr7:138363229 G>A maps to NM_001139456.1 I41I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A8JD-01A-11D-A36J-09 chr11:9759810 C>T maps to NM_015055.2 Q378*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NK-01A-21D-A37C-09 chr23:16761849 T>A did not map to a codon.
Sequencing variant TCGA-VR-A8EQ-01A-11D-A36J-09 chr23:16778363 C>T did not map to a codon.
Sequencing variant TCGA-LN-A49Y-01A-11D-A27G-09 chr19:39694849 G>A maps to NM_001080468.2 S15S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A891-01A-11D-A36J-09 chr1:115438066 A>G did not map to a codon.
Sequencing variant TCGA-LN-A5U6-01A-11D-A28B-09 chr1:115537629 T>A maps to NM_003176.2 L974*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49V-01A-11D-A247-09 chr20:58453092 G>T maps to NM_014258.2 S983S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OU-01A-11D-A28B-09 chr6:10955445 G>A maps to NM_001040274.2 L684L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A9-01A-11D-A28B-09 chr6:10930702 C>A maps to NM_001040274.2 S530*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6F8-01A-11D-A33E-09 chr1:85648338 A>G maps to NM_032184.1 A662A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-AAPN-01A-11D-A403-09 chr9:93607823 G>T maps to NM_003177.5 E176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr19:46328448 G>A maps to NM_004819.2 L824L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88V-01A-11D-A351-09 chr19:46330850 G>A maps to NM_004819.2 R700*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OJ-01A-11D-A27G-09 chr23:47435958 G>T did not map to a codon.
Sequencing variant TCGA-L5-A4OJ-01A-11D-A27G-09 chr1:33161293 G>A maps to NM_030786.2 H135H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-A7RC-01B-11D-A403-09 chr1:33149974 C>T maps to NM_030786.2 L414L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GJ-01A-11D-A37C-09 chr6:152577786 G>A maps to NM_182961.2 F6362F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GL-01A-12D-A37C-09 chr6:152631080 C>A maps to NM_182961.2 R5697R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GQ-01A-11D-A37C-09 chr6:152746667 T>C maps to NM_182961.2 E1705E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A4P3-01A-11D-A27G-09 chr6:152792773 G>A maps to NM_182961.2 Y530Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A7DP-01A-31D-A33E-09 chr6:152473129 C>T maps to NM_182961.2 L8092L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93C-01A-11D-A387-09 chr6:152712456 A>C maps to NM_182961.2 T2653T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OG-01A-11D-A27G-09 chr6:152676067 G>C maps to NM_182961.2 S3551*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NG-01A-11D-A37C-09 chr6:152771896 C>T maps to NM_182961.2 V1086V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr6:152826486 G>A maps to NM_182961.2 S209S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NQ-01A-11D-A36J-09 chr6:152784607 G>T maps to NM_182961.2 A659A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NQ-01A-11D-A36J-09 chr6:152831446 G>A maps to NM_182961.2 S154S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NS-01A-12D-A37C-09 chr6:152658134 G>T maps to NM_182961.2 V4123V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L7-A6VZ-01A-12D-A33E-09 chr6:152651068 C>A maps to NM_182961.2 L4917L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FP-01A-31D-A387-09 chr6:152675823 T>C maps to NM_182961.2 A3632A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6L6-01B-11D-A33E-09 chr6:152655225 C>T maps to NM_182961.2 Q4237Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EZ-01A-11D-A36J-09 chr6:152702454 T>A maps to NM_182961.2 R2899*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-AAPN-01A-11D-A403-09 chr6:152730771 G>T maps to NM_182961.2 V2101V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FD-01A-11D-A33E-09 chr14:64532289 G>T maps to NM_182914.2 L3451L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43I-01A-11D-A247-09 chr14:64428291 A>G maps to NM_182914.2 A279A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr14:64450605 T>C did not map to a codon.
Sequencing variant TCGA-IG-A5B8-01A-11D-A28B-09 chr6:33408514 G>A maps to NM_006772.2 P562P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88V-01A-11D-A351-09 chr22:39760252 C>T maps to NM_145738.2 S18S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-A7RE-01A-11D-A351-09 chr19:48878930 G>T maps to NM_012451.3 S131S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr21:34018913 T>C did not map to a codon.
Sequencing variant TCGA-L5-A8NN-01A-11D-A37C-09 chr21:34045677 G>T maps to NM_003895.3 P605P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FP-01A-31D-A387-09 chr21:34003656 G>C maps to NM_003895.3 S1496*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A97H-01A-11D-A387-09 chr6:158487570 G>T maps to NM_003898.3 G541*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NH-01A-11D-A37C-09 chr6:158505198 G>A maps to NM_003898.3 T1067T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q9-A6FU-01A-11D-A31U-09 chr6:158492678 G>A maps to NM_003898.3 A662A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8W5-01B-11D-A37C-09 chr6:158505052 G>T maps to NM_003898.3 E1019*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr15:99672503 T>C maps to ENST00000336292 I1312I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr5:150027557 G>A maps to NM_001166209.1 A151A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr5:150028877 C>T maps to NM_001166209.1 S591S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49P-01A-11D-A247-09 chr5:150029258 C>T maps to NM_001166209.1 S718S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A5U6-01A-11D-A28B-09 chr4:119978553 A>C did not map to a codon.
Sequencing variant TCGA-L5-A43H-01A-11D-A247-09 chr10:75413173 G>A maps to NM_001114133.1 P165P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr10:75407477 C>T maps to NM_001114133.1 T644T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HV-01A-21D-A351-09 chr17:35879083 C>A maps to NM_007247.4 E1302*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OE-01A-11D-A27G-09 chr23:49054187 G>T did not map to a codon.
Sequencing variant TCGA-R6-A8WG-01A-11D-A37C-09 chr23:49050790 G>A did not map to a codon.
Sequencing variant TCGA-L5-A8NU-01A-11D-A36J-09 chr12:33560220 C>A maps to NM_198992.3 E194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A625-01A-11D-A31U-09 chr1:155838230 G>T maps to NM_152280.4 P170P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASX-01A-11D-A387-09 chr14:62536529 G>T maps to NM_031914.2 E245*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr1:202574789 C>T maps to NM_177402.4 G37G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FB-01A-11D-A33E-09 chr19:51135718 C>T maps to NM_001160329.1 S166S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NE-01A-11D-A37C-09 chr19:51132598 C>T maps to NM_001160329.1 E411E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A5U7-01A-11D-A31U-09 chr18:40853826 G>A maps to NM_020783.3 T189T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EQ-01A-11D-A36J-09 chr18:40850379 C>A maps to NM_020783.3 G402*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA7B-01A-31D-A403-09 chr18:40850369 C>T maps to NM_020783.3 W405*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NG-01A-11D-A37C-09 chr19:55686689 C>A maps to NM_003180.2 L186L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A939-01A-12D-A37C-09 chr1:114682355 G>T maps to ENST00000369545 A131A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FD-01A-11D-A33E-09 chr11:61286122 G>T maps to NM_004200.2 A396A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GO-01A-11D-A37C-09 chr11:7335090 A>G maps to NM_175733.3 Q321Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43H-01A-11D-A247-09 chr11:85406270 G>T maps to ENST00000359152 L1770L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A8HZ-01A-11D-A36J-09 chr11:85435273 T>C maps to ENST00000359152 A1266A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-A7RB-01A-11D-A351-09 chr11:85445678 G>A maps to NM_001162953.1 I231I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49K-01A-11D-A247-09 chr23:99956214 C>T did not map to a codon.
Sequencing variant TCGA-LN-A4A6-01A-11D-A27G-09 chr23:99941717 G>T did not map to a codon.
Sequencing variant TCGA-L5-A8NQ-01A-11D-A36J-09 chr6:166578286 C>T did not map to a codon.
Sequencing variant TCGA-L5-A8NI-01A-11D-A37C-09 chr6:132938984 A>G maps to NM_001033080.1 Y120Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A5U7-01A-11D-A31U-09 chr6:132874110 G>T maps to NM_053278.1 E94*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A9-01A-11D-A28B-09 chr22:39824120 C>T maps to NM_006116.2 Q414*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OJ-01A-11D-A27G-09 chr6:149699962 A>C maps to NM_015093.4 S304S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A893-01A-11D-A36J-09 chr23:30873573 G>T did not map to a codon.
Sequencing variant TCGA-L5-A893-01A-11D-A36J-09 chr23:30873599 G>T did not map to a codon.
Sequencing variant TCGA-L5-A4OR-01A-11D-A27G-09 chr17:47917251 C>T maps to NM_170685.2 T90T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93E-01A-11D-A37C-09 chr10:123843280 C>T maps to NM_206862.2 L422L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A891-01A-11D-A36J-09 chr10:123845395 C>T maps to NM_206862.2 A1127A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8Q7-01A-11D-A37C-09 chr10:123987478 C>T maps to NM_206862.2 L2618L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q9-A6FU-01A-11D-A31U-09 chr17:61681892 G>A did not map to a codon.
Sequencing variant TCGA-2H-A9GF-01A-11D-A37C-09 chr2:75425904 T>C maps to NM_001058.3 V52V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A5B8-01A-11D-A28B-09 chr2:75425862 C>T maps to NM_001058.3 V66V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6DQ-01B-11D-A31U-09 chr10:71166847 G>A maps to NM_001057.2 L310L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr4:104640370 G>A maps to NM_001059.2 G154G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A8O2-01A-11D-A36J-09 chr1:166831609 G>A maps to NM_053053.3 Q124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NV-01A-11D-A37C-09 chr1:166831597 T>A maps to NM_053053.3 K128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KH-A6WC-01A-11D-A33E-09 chr4:7055886 C>A maps to NM_152293.2 C123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr4:7056450 G>A maps to NM_152293.2 A311A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6DQ-01B-11D-A31U-09 chr4:7056528 C>T maps to NM_152293.2 S337S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8WC-01A-11D-A37C-09 chr4:7055826 C>T maps to NM_152293.2 P103P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A8JD-01A-11D-A36J-09 chr4:7056572 C>G maps to NM_152293.2 S352*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr3:9825803 G>A maps to NM_006354.2 S338S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GJ-01A-11D-A37C-09 chr23:70678158 G>T did not map to a codon.
Sequencing variant TCGA-IC-A6RF-01A-13D-A33E-09 chr23:70617239 C>T did not map to a codon.
Sequencing variant TCGA-KH-A6WC-01A-11D-A33E-09 chr23:70598240 G>T did not map to a codon.
Sequencing variant TCGA-L5-A8NT-01A-11D-A37C-09 chr23:70601713 G>T did not map to a codon.
Sequencing variant TCGA-R6-A6L4-01A-11D-A31U-09 chr23:70609453 A>T did not map to a codon.
Sequencing variant TCGA-VR-AA7B-01A-31D-A403-09 chr23:70612509 C>T did not map to a codon.
Sequencing variant TCGA-2H-A9GF-01A-11D-A37C-09 chr11:6632680 G>A maps to NM_006284.2 I130I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NE-01A-11D-A37C-09 chr11:6632476 G>A maps to NM_006284.2 A170A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A5B8-01A-11D-A28B-09 chr2:10008429 C>G maps to NM_005680.2 S142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NT-01A-11D-A37C-09 chr16:84216923 A>G maps to NM_005679.2 L112L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA7B-01A-31D-A403-09 chr11:93469858 C>G did not map to a codon.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr9:32630105 G>A maps to NM_153809.2 H1824H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr8:120744195 T>G maps to NM_003184.3 R1190R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KH-A6WC-01A-11D-A33E-09 chr10:8006694 G>T maps to NM_031923.2 E408*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49S-01A-11D-A247-09 chr10:8006228 T>A maps to NM_031923.2 V252V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3Y9-01A-12D-A247-09 chr20:60578928 G>T maps to NM_003185.3 I743I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EZ-01A-11D-A36J-09 chr20:60581598 G>A maps to NM_003185.3 V730V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GJ-01A-11D-A37C-09 chr18:23845279 G>A did not map to a codon.
Sequencing variant TCGA-L5-A4OR-01A-11D-A27G-09 chr1:229738642 C>A maps to NM_014409.3 E91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FD-01A-11D-A33E-09 chr11:62549739 C>A maps to NM_006473.2 I254I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88W-01A-11D-A351-09 chr5:140699107 T>C maps to NM_005642.2 R168R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A97I-01A-11D-A387-09 chr23:100531513 A>G did not map to a codon.
Sequencing variant TCGA-Z6-A9VB-01A-21D-A37C-09 chr23:100531457 C>A did not map to a codon.
Sequencing variant TCGA-RE-A7BO-01A-11D-A33E-09 chr23:77387168 C>T did not map to a codon.
Sequencing variant TCGA-LN-A4A8-01A-32D-A27G-09 chr6:159461855 G>T maps to NM_054114.3 L162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr2:160050799 C>T maps to NM_033394.2 N925N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr2:160076365 C>T maps to NM_033394.2 G1222G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RE-A7BO-01A-11D-A33E-09 chr2:160035290 C>A maps to NM_033394.2 L709L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EO-01A-11D-A36J-09 chr2:160027185 C>T maps to NM_033394.2 N407N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8Q7-01A-11D-A37C-09 chr2:160086368 C>T maps to NM_033394.2 Q1478*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6Y0-01B-11D-A33E-09 chr17:61482568 C>A maps to ENST00000389520 R1066R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NQ-01A-11D-A36J-09 chr2:162061208 C>T maps to NM_004180.2 L78L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NT-01A-11D-A37C-09 chr2:162087606 G>T maps to NM_004180.2 G216*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HX-01A-11D-A33E-09 chr2:162091890 G>T maps to NM_004180.2 S380S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr17:27778670 C>T maps to NM_020791.2 G35G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OX-01A-21D-A28B-09 chr17:27844496 C>A maps to NM_020791.2 P577P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A891-01A-11D-A36J-09 chr17:27822697 C>T maps to NM_020791.2 Q318*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NS-01A-12D-A37C-09 chr17:27794200 G>A maps to NM_020791.2 K57K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr16:29997583 A>G did not map to a codon.
Sequencing variant TCGA-LN-A5U5-01A-21D-A28B-09 chr16:29998793 C>A maps to NM_016151.2 G1067G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49U-01A-31D-A27G-09 chr12:118693354 C>T maps to NM_016281.3 L6L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr6:32818894 C>T maps to NM_000593.5 T352T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EX-01A-11D-A36J-09 chr6:32818768 G>T maps to NM_000593.5 T394T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L7-A56G-01A-21D-A27G-09 chr12:6566731 C>T maps to NM_018009.4 T242T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GH-01A-11D-A37C-09 chr4:16164963 G>A maps to NM_153365.2 D557D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KH-A6WC-01A-11D-A33E-09 chr1:234528169 G>T maps to NM_005646.3 L1563L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X8-AAAR-01A-11D-A403-09 chr1:234563509 A>G maps to NM_005646.3 I1021I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NF-01A-11D-A37C-09 chr1:11080619 C>T maps to NM_007375.3 F226F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L7-A56G-01A-21D-A27G-09 chr1:19180922 C>T maps to NM_152232.2 P347P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-AAPN-01A-11D-A403-09 chr1:19166647 G>T maps to NM_152232.2 I655I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OJ-01A-11D-A27G-09 chr1:1269396 G>A maps to NM_152228.1 P704P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49R-01A-11D-A247-09 chr1:1266823 G>T maps to NM_152228.1 G33G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GO-01A-11D-A37C-09 chr12:10978033 G>A maps to NM_023921.1 L279L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A97I-01A-11D-A387-09 chr7:122634851 G>A maps to NM_016945.2 S279S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A2-01A-31D-A27G-09 chr7:122635286 C>G maps to NM_016945.2 L134L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GL-01A-12D-A37C-09 chr7:141464737 A>G maps to NM_016943.2 P260P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49K-01A-11D-A247-09 chr12:11244633 G>A maps to ENST00000422992 N65N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49K-01A-11D-A247-09 chr12:11244645 T>C maps to ENST00000422992 V61V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASV-01A-11D-A387-09 chr12:11138967 C>T maps to NM_176890.2 G164G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NN-01A-11D-A37C-09 chr12:10954755 C>T maps to NM_023919.2 V138V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A1-01A-21D-A27G-09 chr12:10954347 A>T maps to NM_023919.2 A274A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3QL-01A-11D-A247-09 chr12:10959270 A>G maps to NM_023918.1 L103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S8-A6BV-01A-21D-A31U-09 chr16:71602141 C>A maps to NM_000353.2 E424*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FQ-01A-31D-A387-09 chr3:10291030 C>A maps to NM_014760.3 P49P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-A7RB-01A-11D-A351-09 chr4:38126580 A>T did not map to a codon.
Sequencing variant TCGA-L5-A8NE-01A-11D-A37C-09 chr16:30376899 G>A maps to NM_015527.3 P324P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A3-01A-11D-A27G-09 chr16:30370526 C>T maps to NM_015527.3 S536S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93D-01A-11D-A387-09 chr9:131553893 G>T maps to NM_018201.3 L74L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6XG-01B-11D-A33E-09 chr9:131565638 C>T maps to NM_018201.3 Y218Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GM-01A-11D-A37C-09 chr4:7012498 C>T maps to NM_001113361.1 D546D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GF-01A-11D-A37C-09 chr4:26750060 C>A maps to NM_018317.2 R450R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3Y9-01A-12D-A247-09 chr4:26744168 C>T maps to NM_018317.2 Q423*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FP-01A-31D-A387-09 chr9:100975481 G>T maps to NM_018421.3 R465R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GQ-01A-11D-A37C-09 chr15:74177203 C>T maps to NM_153356.1 L150L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RF-01A-13D-A33E-09 chr15:74181426 G>A maps to NM_153356.1 K332K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A5U7-01A-11D-A31U-09 chr15:74173812 C>A maps to NM_153356.1 S45*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FG-01A-11D-A33E-09 chr6:37281656 C>T maps to NM_017772.2 S385S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A97H-01A-11D-A387-09 chr3:100029350 C>T maps to ENST00000394144 I506I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A8O2-01A-11D-A36J-09 chr23:48417662 G>A did not map to a codon.
Sequencing variant TCGA-2H-A9GK-01A-11D-A37C-09 chr17:15644473 C>A maps to NM_178571.4 A195A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RE-01A-11D-A33E-09 chr15:78317635 G>A maps to NM_144572.1 L351L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GG-01A-11D-A37C-09 chr3:17447963 C>T maps to NM_001134381.1 Q74Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HV-01A-21D-A351-09 chr3:17416136 G>A maps to NM_001134381.1 L246L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FH-01A-11D-A33E-09 chr2:101654014 G>A maps to NM_001102426.1 S462S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GN-01A-11D-A37C-09 chr23:106066576 C>G did not map to a codon.
Sequencing variant TCGA-KH-A6WC-01A-11D-A33E-09 chr23:106109159 G>T did not map to a codon.
Sequencing variant TCGA-XP-A8T8-01A-11D-A36J-09 chr4:141590790 T>C maps to NM_015130.2 K478K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S8-A6BW-01A-11D-A31U-09 chr3:186281914 G>T maps to NM_001134415.1 A68A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A938-01A-11D-A37C-09 chr17:80861310 G>A maps to NM_005993.4 L587L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HV-01A-21D-A351-09 chr1:235612061 A>G maps to NM_003193.3 L523L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A6-01A-11D-A27G-09 chr4:106967750 G>T maps to NM_001163436.1 L886L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr12:64868146 G>T maps to NM_013254.3 G226G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88Z-01A-11D-A36J-09 chr23:9665427 C>T did not map to a codon.
Sequencing variant TCGA-R6-A8WC-01A-11D-A37C-09 chr23:9622335 T>C did not map to a codon.
Sequencing variant TCGA-L5-A4OO-01A-11D-A27G-09 chr24:6939641 C>T did not map to a codon.
Sequencing variant TCGA-L5-A88W-01A-11D-A351-09 chr7:72987737 C>T maps to NM_012453.2 E170E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S8-A6BV-01A-21D-A31U-09 chr16:2024420 C>T maps to NM_006453.2 N78N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3Y9-01A-12D-A247-09 chr6:170871003 G>A maps to NM_003194.4 Q60Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88V-01A-11D-A351-09 chr6:170871042 G>A maps to NM_003194.4 Q73Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L7-A6VZ-01A-12D-A33E-09 chr6:170871033 G>A maps to NM_003194.4 Q70Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OR-01A-11D-A27G-09 chr2:162275467 C>T maps to NM_006593.2 D345D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A8I0-01A-11D-A36J-09 chr2:162280506 C>T maps to NM_006593.2 P606P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr11:124502083 C>T maps to NM_032811.2 Q396*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A4P3-01A-11D-A27G-09 chr7:45139977 G>T maps to ENST00000404564 G625G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr7:45144170 C>T maps to ENST00000404564 T302T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EO-01A-11D-A36J-09 chr22:19770478 C>T maps to NM_005992.1 D351D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GG-01A-11D-A37C-09 chr1:119427567 C>T maps to ENST00000369429 P532P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OE-01A-11D-A27G-09 chr1:119467304 G>T maps to ENST00000369429 L219L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OX-01A-21D-A28B-09 chr1:119427939 A>G maps to ENST00000369429 A408A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HZ-01A-31D-A351-09 chr1:119427369 G>A maps to ENST00000369429 S598S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93E-01A-11D-A37C-09 chr17:59479068 G>T maps to NM_005994.3 V140V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93E-01A-11D-A37C-09 chr17:59482956 G>A maps to NM_005994.3 P482P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6KZ-01A-11D-A31U-09 chr17:59485500 C>T maps to NM_005994.3 P591P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RE-01A-11D-A33E-09 chr23:79286418 T>C did not map to a codon.
Sequencing variant TCGA-L5-A8NR-01A-11D-A37C-09 chr23:79286533 A>T did not map to a codon.
Sequencing variant TCGA-LN-A49Y-01A-11D-A27G-09 chr23:79282339 C>A did not map to a codon.
Sequencing variant TCGA-R6-A6KZ-01A-11D-A31U-09 chr23:79279596 G>T did not map to a codon.
Sequencing variant TCGA-R6-A6L4-01A-11D-A31U-09 chr23:79283494 T>C did not map to a codon.
Sequencing variant TCGA-2H-A9GF-01A-11D-A37C-09 chr17:59533901 G>A maps to ENST00000393853 P17P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NE-01A-11D-A37C-09 chr19:3600440 G>T maps to NM_201636.2 L64L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6XG-01B-11D-A33E-09 chr19:3595871 C>G maps to NM_201636.2 L282L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GN-01A-11D-A37C-09 chr8:54906286 G>A maps to NM_006756.2 D87D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A8JE-01A-11D-A37C-09 chr20:62697887 C>G maps to NM_003195.4 L44L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GR-01A-12D-A37C-09 chr23:101382464 T>G did not map to a codon.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr23:101381877 C>A did not map to a codon.
Sequencing variant TCGA-VR-A8EQ-01A-11D-A36J-09 chr23:101382234 G>A did not map to a codon.
Sequencing variant TCGA-L5-A43C-01A-11D-A247-09 chr23:102842228 T>C did not map to a codon.
Sequencing variant TCGA-XP-A8T7-01A-11D-A36J-09 chr23:102841917 G>T did not map to a codon.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr23:101396160 C>T did not map to a codon.
Sequencing variant TCGA-2H-A9GO-01A-11D-A37C-09 chr8:74858939 G>C maps to NM_005648.2 T88T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EU-01A-11D-A36J-09 chr1:24078324 C>T maps to NM_003198.2 Y436Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GJ-01A-11D-A37C-09 chr18:44560143 G>T maps to NM_016427.2 R498R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GO-01A-11D-A37C-09 chr18:44560411 T>A maps to NM_016427.2 G408G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93E-01A-11D-A37C-09 chr18:44560117 G>T maps to NM_016427.2 R506R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NE-01A-11D-A37C-09 chr18:44560945 A>G maps to NM_016427.2 S230S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FH-01A-11D-A33E-09 chr18:44543315 G>A maps to NM_001100817.1 L352L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FD-01A-11D-A33E-09 chr5:145834807 A>G maps to NM_006706.3 G83G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43H-01A-11D-A247-09 chr5:145834756 C>G maps to NM_006706.3 P66P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OU-01A-11D-A28B-09 chr5:145838889 G>A maps to NM_006706.3 Q294Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43I-01A-11D-A247-09 chr10:132944840 G>A maps to NM_174937.3 L373L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43I-01A-11D-A247-09 chr10:133106471 A>T did not map to a codon.
Sequencing variant TCGA-L5-A8NE-01A-11D-A37C-09 chr10:133107432 T>G maps to NM_174937.3 R158R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6DN-01B-11D-A31U-09 chr6:31129243 C>T maps to NM_007109.2 R87*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GH-01A-11D-A37C-09 chr22:42606751 C>T maps to NM_005650.1 T1520T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NJ-01A-11D-A36J-09 chr2:27375629 C>T maps to NM_175769.2 T180T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EU-01A-11D-A36J-09 chr19:1612272 C>T maps to NM_001136139.1 A582A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93D-01A-11D-A387-09 chr18:53017613 T>C maps to ENST00000398339 K277K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OS-01A-11D-A28B-09 chr5:133473772 C>T maps to ENST00000395029 H155H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6Y0-01B-11D-A33E-09 chr5:133473796 C>T maps to ENST00000395029 Y163Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA7D-01A-11D-A403-09 chr2:85361006 C>A maps to NM_031283.2 S67*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A97H-01A-11D-A387-09 chr10:114911603 G>A maps to NM_030756.4 L351L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr10:114925541 C>T maps to NM_030756.4 L534L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NS-01A-12D-A37C-09 chr10:114849211 C>T maps to NM_001146283.1 P179P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr20:61488859 A>G maps to NM_006602.2 A375A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GF-01A-11D-A37C-09 chr1:152084219 G>A maps to NM_007113.2 L491L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A6-01A-11D-A27G-09 chr1:152082710 C>T maps to NM_007113.2 E994E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-A7RC-01B-11D-A403-09 chr1:152081489 G>T maps to NM_007113.2 C1401*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EY-01A-11D-A36J-09 chr1:152059328 C>A maps to NM_001008536.1 E277*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr12:110350841 C>T maps to NM_032300.4 R367*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA7B-01A-31D-A403-09 chr22:31019042 C>T maps to NM_000355.3 R399*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FB-01A-11D-A33E-09 chr5:149754265 C>A maps to ENST00000451292 P390P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA4D-01A-11D-A37C-09 chr1:45272225 G>A maps to NM_001013632.2 R39*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3I8-01A-11D-A247-09 chr12:111072533 G>T maps to NM_001082538.2 E258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OE-01A-11D-A27G-09 chr12:124171411 C>T maps to NM_024809.3 F198F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NW-01A-11D-A37C-09 chr12:124171534 C>T maps to NM_024809.3 S239S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NG-01A-11D-A37C-09 chr10:97453623 C>T maps to ENST00000371217 V29V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3I8-01A-11D-A247-09 chr4:156831332 G>A maps to NM_005651.2 E196E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GM-01A-11D-A37C-09 chr14:90429604 C>T maps to NM_018319.3 S49S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3Y9-01A-12D-A247-09 chr14:90446925 C>T maps to NM_018319.3 V278V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FQ-01A-31D-A387-09 chr10:115961250 C>T maps to NM_198795.1 I204I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OJ-01A-11D-A27G-09 chr1:154492833 C>T maps to NM_001098475.1 Q66*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8W8-01B-11D-A37C-09 chr1:154517336 C>A maps to NM_001098475.1 A288A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASX-01A-11D-A387-09 chr1:154517280 C>T maps to NM_001098475.1 L270L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr13:61103041 T>C maps to NM_001146070.1 G561G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A4P3-01A-11D-A27G-09 chr1:179659933 G>A maps to ENST00000444136 L988L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GH-01A-11D-A37C-09 chr6:46656365 C>T maps to NM_001010870.2 H167H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A8O2-01A-11D-A36J-09 chr6:46657520 T>C maps to NM_001010870.2 Y552Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RE-01A-11D-A33E-09 chr9:100234624 T>C maps to NM_014290.2 L598L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A939-01A-12D-A37C-09 chr14:104457533 C>T maps to NM_153046.2 R385*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr1:151753979 G>T maps to NM_001083965.1 R70R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6KZ-01A-11D-A31U-09 chr1:151749016 A>G maps to NM_001083965.1 A314A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FH-01A-11D-A33E-09 chr6:35443839 G>T maps to ENST00000357281 G289G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NL-01A-12D-A37C-09 chr12:3104000 C>T maps to NM_003213.3 T23T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA7D-01A-11D-A403-09 chr12:3147204 C>A maps to NM_003213.3 P323P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3YB-01A-11D-A247-09 chr4:48141031 G>A maps to NM_003215.2 L515L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FE-01A-11D-A33E-09 chr4:48169924 C>A maps to NM_003215.2 E181*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49W-01A-11D-A27G-09 chr7:97847084 G>A maps to ENST00000379795 S1103S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HX-01A-11D-A33E-09 chr7:97867826 G>A maps to ENST00000379795 N343N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OP-01A-11D-A27G-09 chr14:102964033 C>T maps to NM_014844.3 P1353P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HY-01A-12D-A351-09 chr14:102880971 G>T did not map to a codon.
Sequencing variant TCGA-IG-A5B8-01A-11D-A28B-09 chr19:14675791 C>T maps to ENST00000436007 L213L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OU-01A-11D-A28B-09 chr4:65170929 A>G maps to NM_001010874.4 T228T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr4:65155448 A>G maps to NM_001010874.4 L271L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49S-01A-11D-A247-09 chr4:65180403 T>C maps to NM_001010874.4 G171G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8W5-01B-11D-A37C-09 chr4:65175642 A>C maps to NM_001010874.4 A186A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr9:27180304 T>A maps to NM_000459.3 C323*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A893-01A-11D-A36J-09 chr9:27185607 C>T maps to NM_000459.3 P436P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NJ-01A-11D-A36J-09 chr9:27229190 T>G maps to NM_000459.3 T1112T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A5U7-01A-11D-A31U-09 chr9:27158009 G>T maps to NM_000459.3 V78V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZR-A9CJ-01B-11D-A387-09 chr9:27169600 C>A maps to NM_000459.3 S201*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93E-01A-11D-A37C-09 chr17:6704114 G>A maps to NM_053285.1 Q334*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6XQ-01B-11D-A33E-09 chr17:6733587 G>T maps to NM_053285.1 R36R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OE-01A-11D-A27G-09 chr1:36551585 C>A maps to NM_014466.2 I144I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A6QS-01A-12D-A33E-09 chr2:95539264 G>T maps to NM_144705.2 E167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GK-01A-11D-A37C-09 chr16:1550700 G>T did not map to a codon.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr16:1550421 C>T maps to NM_016111.3 H359H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A4QT-01A-21D-A27G-09 chr14:20851739 G>T maps to NM_007110.4 G1258G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88S-01A-11D-A36J-09 chr14:20844364 T>C maps to NM_007110.4 E2049E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A5U5-01A-21D-A28B-09 chr16:58018604 G>A maps to NM_199046.2 A172A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OH-01A-11D-A27G-09 chr5:1278869 C>T maps to NM_198253.2 R724R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA7I-01A-11D-A403-09 chr5:1272326 C>T maps to NM_198253.2 P785P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FG-01A-11D-A33E-09 chr10:70332884 G>T maps to NM_030625.2 G264*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GG-01A-11D-A37C-09 chr4:106157774 A>G maps to ENST00000513237 Q913Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A8-01A-32D-A27G-09 chr4:106157096 C>T maps to ENST00000513237 D687D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6Y0-01B-11D-A33E-09 chr4:106155749 C>A maps to ENST00000513237 S238S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GF-01A-11D-A37C-09 chr2:74275329 G>A maps to ENST00000409262 S669S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GM-01A-11D-A37C-09 chr2:74327580 G>A maps to ENST00000409262 P1129P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A8HZ-01A-11D-A36J-09 chr2:74274964 C>T maps to ENST00000409262 Q548*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FP-01A-31D-A387-09 chr2:74275074 G>T maps to ENST00000409262 L584L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S8-A6BW-01A-11D-A31U-09 chr2:74327952 C>T maps to ENST00000409262 P1253P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49K-01A-11D-A247-09 chr9:103065970 G>A maps to NM_017746.3 L873L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RE-01A-11D-A33E-09 chr23:69902539 A>C did not map to a codon.
Sequencing variant TCGA-LN-A49M-01A-21D-A27G-09 chr23:69871377 C>T did not map to a codon.
Sequencing variant TCGA-LN-A4A9-01A-11D-A28B-09 chr23:69964045 A>G did not map to a codon.
Sequencing variant TCGA-V5-AASV-01A-11D-A387-09 chr23:69898667 C>T did not map to a codon.
Sequencing variant TCGA-2H-A9GK-01A-11D-A37C-09 chr23:104464870 T>C did not map to a codon.
Sequencing variant TCGA-IG-A51D-01A-11D-A27G-09 chr23:104464793 G>A did not map to a codon.
Sequencing variant TCGA-L5-A8NF-01A-11D-A37C-09 chr23:104463917 G>A did not map to a codon.
Sequencing variant TCGA-L5-A88Z-01A-11D-A36J-09 chr17:56676582 G>C maps to ENST00000240361 S714*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GF-01A-11D-A37C-09 chr8:30694694 A>G maps to NM_031271.3 F2652F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OG-01A-11D-A27G-09 chr8:30700452 A>G maps to NM_031271.3 D2027D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr8:30701436 T>C maps to NM_031271.3 T1699T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA4D-01A-11D-A37C-09 chr8:30694785 G>T maps to NM_031271.3 S2622*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A97H-01A-11D-A387-09 chr15:56720603 G>T maps to NM_198524.1 E380*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OT-01A-11D-A28B-09 chr15:56686978 G>T maps to NM_198524.1 E259*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NL-01A-12D-A37C-09 chr3:133476750 G>T maps to NM_001063.3 E337*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43H-01A-11D-A247-09 chr6:10402727 C>A maps to ENST00000379613 E296*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASV-01A-11D-A387-09 chr6:50791202 G>A maps to ENST00000263046 P64P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NR-01A-11D-A37C-09 chr20:55204644 C>T maps to NM_003222.3 C15C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93C-01A-11D-A387-09 chr6:50696968 T>A maps to NM_172238.3 L276*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr6:50712910 T>C maps to NM_172238.3 H325H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OJ-01A-11D-A27G-09 chr6:50683160 G>A maps to NM_172238.3 S124S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88V-01A-11D-A351-09 chr16:4311925 G>A maps to NM_003223.2 R127*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HX-01A-11D-A33E-09 chr12:51566124 G>T maps to NM_005653.4 S27S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA7B-01A-31D-A403-09 chr2:121995272 G>T maps to NM_014553.2 S310*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OE-01A-11D-A27G-09 chr23:48889016 C>A did not map to a codon.
Sequencing variant TCGA-JY-A6F8-01A-11D-A33E-09 chr7:115590970 G>T maps to NM_012252.2 R158R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A97I-01A-11D-A387-09 chr3:100432639 G>T maps to NM_001007565.2 V37V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NR-01A-11D-A37C-09 chr22:26892715 G>A maps to NM_012143.2 Q526*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASV-01A-11D-A387-09 chr22:26888020 C>T maps to NM_012143.2 W824*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A6-01A-11D-A27G-09 chr19:54617836 G>T maps to NM_013342.3 C89*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NG-01A-11D-A37C-09 chr7:100238620 C>T maps to NM_003227.3 T88T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GR-01A-12D-A37C-09 chr8:134042139 C>T maps to NM_003235.4 R2371*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A891-01A-11D-A36J-09 chr8:133920542 C>T maps to NM_003235.4 F1320F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NU-01A-11D-A36J-09 chr8:133883695 C>A maps to NM_003235.4 Y126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr16:31488291 G>A maps to NM_001042454.2 A360A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6KZ-01A-11D-A31U-09 chr16:31485022 A>G maps to NM_001042454.2 S50S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93C-01A-11D-A387-09 chr1:218607749 C>A maps to NM_001135599.2 I266I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49N-01A-11D-A247-09 chr3:30691946 C>G maps to NM_001024847.2 S175*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A5U6-01A-11D-A28B-09 chr3:30713298 G>A maps to NM_001024847.2 K233K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A4P3-01A-11D-A27G-09 chr1:92193263 G>C maps to NM_003243.4 V279V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XP-A8T6-01A-11D-A36J-09 chr2:105886007 T>A maps to NM_004257.4 P709P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6F8-01A-11D-A33E-09 chr23:89177776 G>T did not map to a codon.
Sequencing variant TCGA-L5-A891-01A-11D-A36J-09 chr23:89177106 C>T did not map to a codon.
Sequencing variant TCGA-LN-A8I1-01A-11D-A36J-09 chr23:89177503 G>A did not map to a codon.
Sequencing variant TCGA-R6-A8W5-01B-11D-A37C-09 chr23:89177238 A>C did not map to a codon.
Sequencing variant TCGA-LN-A9FQ-01A-31D-A387-09 chr14:24724340 C>T maps to NM_000359.2 A588A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr20:36789861 G>A maps to NM_004613.2 Y50Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FO-01A-11D-A387-09 chr20:2312956 G>T did not map to a codon.
Sequencing variant TCGA-L5-A4OQ-01A-11D-A27G-09 chr3:44955210 C>G maps to NM_003241.3 T683T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GH-01A-11D-A37C-09 chr20:2384434 C>T maps to NM_198994.2 R434R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OG-01A-11D-A27G-09 chr20:2413134 G>A did not map to a codon.
Sequencing variant TCGA-L5-A4ON-01A-11D-A27G-09 chr20:2375224 C>T maps to NM_198994.2 S45S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NJ-01A-11D-A36J-09 chr20:2375945 T>G maps to NM_198994.2 T96T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HZ-01A-31D-A351-09 chr20:2378610 C>T maps to NM_198994.2 S197S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr2:85555049 G>T maps to ENST00000409015 V12V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88W-01A-11D-A351-09 chr16:67877020 C>T maps to NM_020457.2 I188I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GJ-01A-11D-A37C-09 chr2:242541322 G>T maps to NM_015963.5 P534P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8W5-01B-11D-A37C-09 chr2:242545862 C>T maps to NM_015963.5 V422V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASW-01A-11D-A403-09 chr2:242573178 C>G maps to NM_015963.5 S131S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr22:21355662 G>A maps to NM_030573.2 L40L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A97I-01A-11D-A387-09 chr6:169648853 C>T maps to NM_003247.2 Q89Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr6:169634946 G>A maps to NM_003247.2 A511A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr6:169639772 G>A maps to NM_003247.2 C350C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EU-01A-11D-A36J-09 chr6:169622426 C>T maps to NM_003247.2 T1046T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NG-01A-11D-A37C-09 chr5:79351797 T>C maps to NM_003248.4 A161A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NE-01A-11D-A37C-09 chr1:151824836 C>T maps to NM_182578.3 L74L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A5S3-01A-11D-A28B-09 chr2:88474918 A>G maps to NM_018271.3 G190G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NH-01A-11D-A37C-09 chr2:88478332 G>A maps to NM_018271.3 P201P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8W5-01B-11D-A37C-09 chr2:88482531 C>T maps to NM_018271.3 A339A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NJ-01A-11D-A36J-09 chr23:122754755 A>C did not map to a codon.
Sequencing variant TCGA-L5-A8NL-01A-12D-A37C-09 chr23:122802070 G>T did not map to a codon.
Sequencing variant TCGA-L5-A8NQ-01A-11D-A36J-09 chr23:122799633 C>G did not map to a codon.
Sequencing variant TCGA-L5-A4OQ-01A-11D-A27G-09 chr3:63823666 G>T maps to NM_025075.2 R113R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr19:2807602 C>T maps to NM_003249.3 C350C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA7B-01A-31D-A403-09 chr3:184091253 A>G maps to NM_000460.2 S115S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NJ-01A-11D-A36J-09 chr13:52952184 G>T maps to NM_018676.3 S640S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EO-01A-11D-A36J-09 chr15:72057375 G>T maps to NM_024817.2 G869G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr7:11676256 A>G maps to ENST00000423059 C174C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NI-01A-11D-A37C-09 chr7:11676142 G>A maps to ENST00000423059 S212S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49N-01A-11D-A247-09 chr7:11486944 C>T maps to ENST00000423059 Q904Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FG-01A-11D-A33E-09 chr2:138033558 C>A maps to ENST00000272643 G821G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NI-01A-11D-A37C-09 chr2:137872720 A>G maps to ENST00000272643 K409K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NR-01A-11D-A37C-09 chr2:138208593 G>T did not map to a codon.
Sequencing variant TCGA-LN-A8HZ-01A-11D-A36J-09 chr2:137814517 C>A maps to ENST00000272643 S223*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NS-01A-12D-A37C-09 chr14:24026197 G>T maps to NM_024328.3 E78*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-A7RE-01A-11D-A351-09 chr16:20749249 G>T maps to ENST00000431224 L231L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A893-01A-11D-A36J-09 chr11:134118701 C>T did not map to a codon.
Sequencing variant TCGA-IG-A3QL-01A-11D-A247-09 chr21:32525395 G>A maps to NM_003253.2 L1076L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3Y9-01A-12D-A247-09 chr21:32638327 G>A maps to NM_003253.2 Q321*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43E-01A-11D-A247-09 chr21:32624334 C>T maps to NM_003253.2 A378A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr21:32508317 G>A maps to NM_003253.2 T1272T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4ON-01A-11D-A27G-09 chr21:32537341 G>A maps to NM_003253.2 T976T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NN-01A-11D-A37C-09 chr21:32492817 G>T maps to NM_003253.2 S1548S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6Y0-01B-11D-A33E-09 chr21:32537326 G>T maps to NM_003253.2 T981T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49M-01A-21D-A27G-09 chr1:43783284 C>T maps to NM_005424.2 L891L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4MR-01A-11D-A28B-09 chr11:65124655 C>T maps to NM_145719.2 Y459Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NW-01A-11D-A37C-09 chr5:149375695 G>A maps to NM_030953.2 S72S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6L4-01A-11D-A31U-09 chr5:149375788 G>T maps to NM_030953.2 P41P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4ON-01A-11D-A27G-09 chr16:3350226 G>A maps to NM_033208.3 R130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NL-01A-12D-A37C-09 chr16:3349696 G>T maps to NM_033208.3 S306S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A9-01A-11D-A28B-09 chr16:3348997 G>A maps to NM_033208.3 F539F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3I8-01A-11D-A247-09 chr3:114018534 C>A maps to ENST00000481065 V228V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OJ-01A-11D-A27G-09 chr5:156375475 G>A maps to NM_138379.2 H265H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GI-01A-11D-A37C-09 chr12:56817447 C>T maps to NM_003920.3 E670E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FB-01A-11D-A33E-09 chr12:56815968 G>A maps to NM_003920.3 S815S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NG-01A-11D-A37C-09 chr12:56815245 T>C maps to NM_003920.3 T919T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASV-01A-11D-A387-09 chr12:56817429 C>T maps to NM_003920.3 E676E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A8JE-01A-11D-A37C-09 chr12:56814439 G>A maps to NM_003920.3 L1047L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A9VB-01A-21D-A37C-09 chr12:56817447 C>T maps to NM_003920.3 E670E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EW-01A-11D-A36J-09 chr23:48751195 C>T did not map to a codon.
Sequencing variant TCGA-LN-A5U7-01A-11D-A31U-09 chr17:900387 G>A maps to NM_013337.2 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6Y2-01B-11D-A33E-09 chr19:7998369 G>T maps to NM_006351.3 R257R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-M9-A5M8-01A-11D-A28B-09 chr22:33255309 G>A maps to NM_000362.4 W194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NW-01A-11D-A37C-09 chr1:32049125 C>T maps to NM_022164.2 L178L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EY-01A-11D-A36J-09 chr9:71869137 G>T maps to NM_004817.3 E1141*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FG-01A-11D-A33E-09 chr19:3734313 T>C maps to NM_014428.1 S322S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NL-01A-12D-A37C-09 chr3:53262290 C>T did not map to a codon.
Sequencing variant TCGA-LN-A4A9-01A-11D-A28B-09 chr3:53264541 G>C maps to ENST00000423516 T354T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OP-01A-11D-A27G-09 chr23:153543621 T>A did not map to a codon.
Sequencing variant TCGA-LN-A4A8-01A-32D-A27G-09 chr4:164394763 C>T maps to NM_032136.4 S41S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GK-01A-11D-A37C-09 chr9:84230980 C>A maps to NM_005077.3 L278L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr9:84208173 G>A maps to NM_005077.3 H449H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A5U5-01A-21D-A28B-09 chr9:84268948 A>C maps to NM_005077.3 T79T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FA-01A-11D-A33E-09 chr19:3025059 C>G maps to NM_003260.4 L84L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6Y2-01B-11D-A33E-09 chr15:70343731 G>A maps to NM_005078.2 Q737*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FB-01A-11D-A33E-09 chr9:82336770 C>A maps to ENST00000376537 R684R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OW-01A-11D-A28B-09 chr9:82335073 C>T maps to ENST00000376537 R600R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A5U6-01A-11D-A28B-09 chr9:82336709 C>T maps to ENST00000376537 G663G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6KZ-01A-11D-A31U-09 chr9:82267548 C>T maps to ENST00000376537 L144L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6Y2-01B-11D-A33E-09 chr9:82336677 G>T maps to ENST00000376537 G653*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A8I1-01A-11D-A36J-09 chr19:2987130 C>T maps to NM_001143986.1 L146L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GF-01A-11D-A37C-09 chr17:60673966 G>T maps to ENST00000326270 R516R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X8-AAAR-01A-11D-A403-09 chr17:60689901 G>A maps to ENST00000326270 A765A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GR-01A-12D-A37C-09 chr4:166976338 A>C maps to ENST00000507499 R569R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr4:166946528 C>T maps to ENST00000507499 G368G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NH-01A-11D-A37C-09 chr4:166929125 T>G maps to ENST00000507499 P281P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49X-01A-31D-A27G-09 chr10:98144479 G>A maps to NM_012465.3 P686P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A5B8-01A-11D-A28B-09 chr9:35706803 G>C maps to NM_006289.3 V1683V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NW-01A-11D-A37C-09 chr9:35713961 T>C maps to NM_006289.3 L1079L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A8I0-01A-11D-A36J-09 chr9:35707163 G>A maps to NM_006289.3 L1620L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GK-01A-11D-A37C-09 chr15:63004276 G>C did not map to a codon.
Sequencing variant TCGA-2H-A9GM-01A-11D-A37C-09 chr15:63000912 C>T maps to NM_015059.2 G795G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A891-01A-11D-A36J-09 chr15:63111819 G>T maps to NM_015059.2 G2293*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A893-01A-11D-A36J-09 chr15:63014550 G>T did not map to a codon.
Sequencing variant TCGA-LN-A4A5-01A-21D-A27G-09 chr15:63042647 C>G maps to NM_015059.2 L1389L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88V-01A-11D-A351-09 chr4:38774955 T>C maps to NM_030956.3 K752K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93C-01A-11D-A387-09 chr4:154625405 C>T maps to NM_003264.3 H449H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A4QS-01A-11D-A27G-09 chr9:120475581 T>C maps to NM_138554.3 S392S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XP-A8T6-01A-11D-A36J-09 chr23:12905424 A>T did not map to a codon.
Sequencing variant TCGA-L5-A893-01A-11D-A36J-09 chr23:12937424 T>C did not map to a codon.
Sequencing variant TCGA-XP-A8T8-01A-11D-A36J-09 chr23:12938287 T>C did not map to a codon.
Sequencing variant TCGA-IC-A6RF-01A-13D-A33E-09 chr10:102896594 G>A maps to NM_005521.3 L306L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KH-A6WC-01A-11D-A33E-09 chr2:228228649 G>T maps to NM_024795.3 P160P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6F8-01A-11D-A33E-09 chr8:105367334 G>T maps to NM_030788.2 L420L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FB-01A-11D-A33E-09 chr14:24662055 G>A maps to NM_006405.5 V255V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A3-01A-11D-A27G-09 chr14:24661560 G>T maps to NM_006405.5 G323G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6Y2-01B-11D-A33E-09 chr13:100153988 C>G maps to NM_004800.1 P43P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q9-A6FW-01A-31D-A31U-09 chr20:30734619 C>A maps to NM_014742.3 R306R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FO-01A-11D-A387-09 chr12:66539652 T>C maps to ENST00000286424 Q191Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FP-01A-31D-A387-09 chr20:2605000 C>A maps to NM_080751.2 L755L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A4P3-01A-11D-A27G-09 chr15:81644085 G>T maps to ENST00000454937 S344S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr19:54668188 C>T maps to NM_001145303.1 T370T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L7-A56G-01A-21D-A27G-09 chr16:19485598 G>A did not map to a codon.
Sequencing variant TCGA-VR-AA4G-01A-11D-A37C-09 chr16:19451842 G>A maps to NM_001105248.1 P161P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA7D-01A-11D-A403-09 chr16:19475198 C>T maps to NM_001105248.1 V446V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OS-01A-11D-A28B-09 chr17:76120757 G>C maps to NM_007267.6 L246L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GK-01A-11D-A37C-09 chr16:19041667 G>T maps to NM_024847.3 L278L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GJ-01A-11D-A37C-09 chr3:129547038 C>T maps to NM_001017395.3 R61R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49P-01A-11D-A247-09 chr3:129373822 G>C maps to NM_001017395.3 A545A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A5B8-01A-11D-A28B-09 chr1:165737459 C>T maps to NM_019026.3 L39L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GK-01A-11D-A37C-09 chr1:20067392 C>A maps to NM_181719.4 E307*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NK-01A-21D-A37C-09 chr1:20097815 C>T maps to NM_181719.4 P113P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NJ-01A-11D-A36J-09 chr5:140023718 C>T maps to ENST00000252100 S386S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49Y-01A-11D-A27G-09 chr16:69007949 C>T maps to NM_024562.1 D907D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A9-01A-11D-A28B-09 chr16:68900992 T>C maps to NM_024562.1 D288D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GF-01A-11D-A37C-09 chr19:10943820 G>A maps to NM_006858.2 F178F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XP-A8T8-01A-11D-A36J-09 chr19:10945728 C>A maps to NM_006858.2 E116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GQ-01A-11D-A37C-09 chr9:103271285 G>T did not map to a codon.
Sequencing variant TCGA-LN-A4A2-01A-31D-A27G-09 chr2:192863842 C>A maps to NM_016192.2 E210*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FG-01A-11D-A33E-09 chr17:42092300 G>T maps to NM_032376.2 S7*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GH-01A-11D-A37C-09 chr17:7339828 G>A maps to NM_178518.2 T177T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A4P3-01A-11D-A27G-09 chr17:72781706 C>T maps to NM_017728.3 V44V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3Y9-01A-12D-A247-09 chr17:79288253 G>C maps to NM_178520.3 L3L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S8-A6BV-01A-21D-A31U-09 chr11:60689318 C>G maps to NM_024092.2 A138A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr3:10015328 G>T maps to NM_018447.2 L159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NW-01A-11D-A37C-09 chr12:44782038 G>T maps to NM_032256.1 G377*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr14:105995578 C>T maps to NM_025268.2 Y136Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L7-A6VZ-01A-12D-A33E-09 chr4:4242076 G>T maps to ENST00000382753 T123T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr4:1719362 G>T maps to NM_001127266.1 L240L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A891-01A-11D-A36J-09 chr2:98377309 T>A maps to NM_015348.1 K1653*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EQ-01A-11D-A36J-09 chr12:125834008 C>T maps to NM_052907.2 R22*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GG-01A-11D-A37C-09 chr12:129822244 A>T maps to NM_133448.2 S411S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OE-01A-11D-A27G-09 chr12:129558776 G>A maps to NM_133448.2 A981A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EU-01A-11D-A36J-09 chr12:129559151 C>T maps to NM_133448.2 T856T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NS-01A-12D-A37C-09 chr17:32963117 G>C maps to NM_207313.1 V600V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FH-01A-11D-A33E-09 chr19:42821920 G>T maps to ENST00000406159 G335*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6F8-01A-11D-A33E-09 chr19:5757894 C>A maps to NM_152784.3 T440T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NI-01A-11D-A37C-09 chr19:5754153 G>T maps to NM_152784.3 L392L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8WC-01A-11D-A37C-09 chr19:5748201 A>G maps to NM_152784.3 K280K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S8-A6BW-01A-11D-A31U-09 chr19:5724872 G>C maps to NM_152784.3 G42G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FQ-01A-31D-A387-09 chr3:152058399 C>T maps to NM_001123228.1 L98L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8ER-01A-11D-A36J-09 chr2:85826345 G>T maps to NM_001031738.2 G223G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A8I1-01A-11D-A36J-09 chr4:122682831 C>A maps to NM_152399.2 E25*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA7B-01A-31D-A403-09 chr2:135215727 C>G maps to NM_030923.4 V228V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43I-01A-11D-A247-09 chr2:62728352 T>C maps to NM_198276.2 E196E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3Y9-01A-12D-A247-09 chr5:138860384 C>A maps to NM_198282.2 L170L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q9-A6FU-01A-11D-A31U-09 chr4:941565 A>G maps to NM_032326.2 T13T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KH-A6WC-01A-11D-A33E-09 chr7:150490640 G>T maps to NM_014020.3 G121G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OW-01A-11D-A28B-09 chr7:150491084 C>T maps to NM_014020.3 L93L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OW-01A-11D-A28B-09 chr4:148555366 C>T maps to NM_018241.2 Q367*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr16:8889940 C>T maps to NM_015421.3 R170R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L7-A6VZ-01A-12D-A33E-09 chr16:8890319 G>T maps to NM_015421.3 S44*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A8O2-01A-11D-A36J-09 chr16:50063690 A>T maps to NM_153261.4 I68I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A51D-01A-11D-A27G-09 chr7:15427132 G>A maps to NM_001004320.1 F285F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6DN-01B-11D-A31U-09 chr7:15425154 A>T maps to NM_001004320.1 S330S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NW-01A-11D-A37C-09 chr7:19765274 G>T maps to NM_152774.3 S107S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RE-01A-11D-A33E-09 chr6:130761773 G>T maps to NM_052913.2 V69V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A4P3-01A-11D-A27G-09 chr18:5890235 G>T maps to NM_001080209.1 A609A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88Z-01A-11D-A36J-09 chr15:72700131 G>A maps to NM_001080462.1 P240P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NI-01A-11D-A37C-09 chr15:72691088 C>G maps to NM_001080462.1 L59L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GR-01A-12D-A37C-09 chr1:212551020 G>T maps to NM_001198862.1 A283A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8WG-01A-11D-A37C-09 chr2:27261401 T>C did not map to a codon.
Sequencing variant TCGA-JY-A93E-01A-11D-A37C-09 chr11:62558223 C>T maps to NM_001080501.2 R160R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A4P3-01A-11D-A27G-09 chr6:75974997 G>A maps to NM_018247.3 Y134Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EX-01A-11D-A36J-09 chr6:75965913 G>A maps to NM_018247.3 I330I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FG-01A-11D-A33E-09 chr23:100349692 G>T did not map to a codon.
Sequencing variant TCGA-LN-A49K-01A-11D-A247-09 chr2:120194907 C>T maps to NM_183240.2 L155L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93C-01A-11D-A387-09 chr3:44905742 C>T maps to NM_144638.1 L83L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EW-01A-11D-A36J-09 chr23:34648475 G>A did not map to a codon.
Sequencing variant TCGA-LN-A7HW-01A-22D-A351-09 chr1:1849757 G>T maps to NM_178545.3 R95R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93D-01A-11D-A387-09 chr1:95614299 C>T maps to NM_152487.2 G66G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FD-01A-11D-A33E-09 chr1:25785137 G>T maps to NM_018202.4 V303V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A8JD-01A-11D-A36J-09 chr1:54518837 G>T maps to ENST00000371338 L8L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HZ-01A-31D-A351-09 chr19:18729256 C>T maps to NM_012109.2 S285S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A5B8-01A-11D-A28B-09 chr1:55457721 G>A maps to NM_182532.1 P193P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GL-01A-12D-A37C-09 chr1:226055627 C>T maps to NM_014698.2 L158L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr1:226040371 C>T maps to NM_014698.2 A632A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA4D-01A-11D-A37C-09 chr8:94792885 C>T maps to NM_153704.5 Y260Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A9VB-01A-21D-A37C-09 chr8:94821159 C>T maps to NM_153704.5 D844D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr8:74891017 C>T maps to NM_017866.5 R80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4MR-01A-11D-A28B-09 chr8:74891031 G>T maps to NM_017866.5 T84T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3Y9-01A-12D-A247-09 chr8:133759305 G>C maps to ENST00000395406 L123L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NW-01A-11D-A37C-09 chr1:156255724 G>C maps to NM_032323.2 L236L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NV-01A-11D-A37C-09 chr11:18722742 T>C maps to NM_153347.1 H95H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6KZ-01A-11D-A31U-09 chr9:35846964 C>T maps to ENST00000360192 V629V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NI-01A-11D-A37C-09 chr9:136385395 G>A maps to NM_001080483.2 C50C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S8-A6BV-01A-21D-A31U-09 chr9:136389831 C>T maps to NM_001080483.2 A45A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GF-01A-11D-A37C-09 chr20:24523763 C>T maps to NM_024893.1 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GH-01A-11D-A37C-09 chr20:24523981 G>A maps to NM_024893.1 V83V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GL-01A-12D-A37C-09 chr20:24565586 C>T maps to NM_024893.1 C192C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A51D-01A-11D-A27G-09 chr19:41889781 C>T maps to NM_001098825.1 C125C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49S-01A-11D-A247-09 chr17:7259741 G>T maps to NM_198154.1 L155L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A3-01A-11D-A27G-09 chr3:69088133 C>T maps to NM_007114.2 E618E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A8JD-01A-11D-A36J-09 chr3:69088141 C>A maps to NM_007114.2 E616*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RE-01A-11D-A33E-09 chr23:154736753 C>A did not map to a codon.
Sequencing variant TCGA-LN-A4A1-01A-21D-A27G-09 chr4:68812228 A>G maps to NM_182606.3 I24I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A97I-01A-11D-A387-09 chr4:69096946 T>C maps to NM_182502.3 L220L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NR-01A-11D-A37C-09 chr21:19775825 T>C maps to NM_002772.2 V38V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NI-01A-11D-A37C-09 chr21:43809062 T>C maps to ENST00000380399 K183K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49Y-01A-11D-A27G-09 chr11:113569744 C>A maps to NM_030770.2 L70L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49Y-01A-11D-A27G-09 chr22:37485697 C>A maps to ENST00000381792 L252L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XP-A8T6-01A-11D-A36J-09 chr19:2399191 G>A did not map to a codon.
Sequencing variant TCGA-Z6-A8JD-01A-11D-A36J-09 chr19:2425185 C>T maps to NM_182973.1 I934I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GK-01A-11D-A37C-09 chr23:101770004 A>C did not map to a codon.
Sequencing variant TCGA-L5-A8NW-01A-11D-A37C-09 chr12:29786081 T>A maps to NM_001193451.1 K376*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6L4-01A-11D-A31U-09 chr12:29670401 A>C maps to NM_001193451.1 A709A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A6-01A-11D-A27G-09 chr12:83289682 A>G maps to NM_152588.1 G247G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A893-01A-11D-A36J-09 chr12:88586396 A>T maps to NM_181783.3 K575*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6XG-01B-11D-A33E-09 chr18:66348307 T>G maps to NM_019022.3 S315S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr9:117848230 G>T maps to NM_002160.2 S593S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OX-01A-21D-A28B-09 chr9:117849340 G>A maps to NM_002160.2 S223S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49M-01A-21D-A27G-09 chr5:118729074 G>A maps to NM_014350.2 *199*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8WC-01A-11D-A37C-09 chr15:51350296 G>A maps to NM_207381.2 N220N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr8:23054711 C>T maps to NM_003844.3 P340P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A97H-01A-11D-A387-09 chr8:23006035 G>A maps to NM_003840.3 A95A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A9-01A-11D-A28B-09 chr8:119945473 G>A maps to NM_002546.3 D32D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8WC-01A-11D-A37C-09 chr8:119945383 G>A maps to NM_002546.3 C62C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr1:2489214 G>A maps to NM_003820.2 P40P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q9-A6FU-01A-11D-A31U-09 chr13:24200844 G>C did not map to a codon.
Sequencing variant TCGA-XP-A8T7-01A-11D-A36J-09 chr13:24242194 G>A maps to NM_018647.2 V271V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6L6-01B-11D-A33E-09 chr12:6442548 C>T maps to NM_001065.3 G152G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A8JD-01A-11D-A36J-09 chr1:12252970 G>A maps to NM_001066.2 T201T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A891-01A-11D-A36J-09 chr1:6522066 G>T maps to ENST00000355862 P305P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NK-01A-21D-A37C-09 chr1:1147000 T>C maps to NM_003327.3 G256G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NK-01A-21D-A37C-09 chr1:12164491 C>T maps to NM_001243.3 R109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr1:12195643 G>T did not map to a codon.
Sequencing variant TCGA-Z6-A9VB-01A-21D-A37C-09 chr1:12164485 G>T maps to NM_001243.3 E107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XP-A8T7-01A-11D-A36J-09 chr13:43148537 G>A maps to NM_003701.3 P33P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A1-01A-21D-A27G-09 chr17:7452583 G>A maps to NM_172089.3 L38L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FH-01A-11D-A33E-09 chr9:117568160 G>T maps to NM_005118.2 L44L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6L6-01B-11D-A33E-09 chr1:173155951 G>T maps to NM_003326.3 I85I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr9:117692514 C>T maps to NM_001244.2 P23P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RF-01A-13D-A33E-09 chr5:150411869 G>A maps to NM_006058.3 P618P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A5U5-01A-21D-A28B-09 chr5:150443228 C>A maps to NM_006058.3 L72L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q9-A6FW-01A-31D-A31U-09 chr3:195593866 C>A maps to NM_001010938.1 L1049L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NK-01A-21D-A37C-09 chr8:9437893 G>T did not map to a codon.
Sequencing variant TCGA-2H-A9GQ-01A-11D-A37C-09 chr11:57085348 G>A maps to NM_033396.2 S247S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88V-01A-11D-A351-09 chr11:57068025 C>T maps to NM_033396.2 K1726K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NS-01A-12D-A37C-09 chr11:57088070 A>T maps to NM_033396.2 G70G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GK-01A-11D-A37C-09 chr1:175092722 C>T maps to NM_022093.1 G946G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A939-01A-12D-A37C-09 chr1:175049323 G>A maps to NM_022093.1 L270L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr1:175097223 C>T maps to NM_022093.1 G1034G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A2-01A-31D-A27G-09 chr1:175066782 C>T maps to NM_022093.1 R607*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr20:44453470 C>T maps to NM_003279.2 T2T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X8-AAAR-01A-11D-A403-09 chr20:44453233 C>T maps to NM_003279.2 G33G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6F8-01A-11D-A33E-09 chr1:74954929 G>T maps to NM_001112808.2 E828*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93E-01A-11D-A37C-09 chr1:74954919 C>A maps to NM_001112808.2 L824L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43I-01A-11D-A247-09 chr1:74715141 G>T did not map to a codon.
Sequencing variant TCGA-LN-A4A3-01A-11D-A27G-09 chr1:74819775 A>G maps to NM_001112808.2 K481K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FP-01A-31D-A387-09 chr11:1955825 G>A maps to ENST00000397301 K188K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASW-01A-11D-A403-09 chr5:72178964 G>T maps to NM_002270.3 T352T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NH-01A-11D-A37C-09 chr7:128645133 A>T maps to ENST00000471166 L211*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EZ-01A-11D-A36J-09 chr7:128694794 G>T maps to ENST00000471166 L10L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GF-01A-11D-A37C-09 chr1:175375751 C>A maps to NM_003285.2 L33L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3YB-01A-11D-A247-09 chr1:175293655 C>A did not map to a codon.
Sequencing variant TCGA-LN-A49R-01A-11D-A247-09 chr1:175372315 G>A maps to NM_003285.2 C312C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S8-A6BV-01A-21D-A31U-09 chr1:175299279 G>A maps to NM_003285.2 Y1241Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA4D-01A-11D-A37C-09 chr1:175372432 C>T maps to NM_003285.2 K273K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GR-01A-12D-A37C-09 chr7:5410840 G>A maps to NM_001080495.2 P1128P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A51D-01A-11D-A27G-09 chr7:5391651 C>T maps to NM_001080495.2 L1756L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FA-01A-11D-A33E-09 chr7:5414007 C>A maps to NM_001080495.2 G969G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49M-01A-21D-A27G-09 chr7:5427354 C>T maps to NM_001080495.2 L700L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X8-AAAR-01A-11D-A403-09 chr7:5410471 G>A maps to NM_001080495.2 P1251P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A9VB-01A-21D-A37C-09 chr16:24788374 A>G maps to NM_014494.2 P95P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A4P3-01A-11D-A27G-09 chr17:76083022 G>T maps to NM_001142640.1 P1214P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GI-01A-11D-A37C-09 chr2:218678419 G>A maps to NM_022648.4 Q1513*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA7D-01A-11D-A403-09 chr2:218750791 G>A maps to NM_022648.4 Q214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr7:47408139 C>T maps to NM_022748.11 Q701Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NQ-01A-11D-A36J-09 chr7:47408373 G>C maps to NM_022748.11 V623V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-AAPN-01A-11D-A403-09 chr7:47323458 G>A maps to NM_022748.11 C1311C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GH-01A-11D-A37C-09 chr6:32011607 G>A maps to ENST00000375244 I3816I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A4QS-01A-11D-A27G-09 chr6:32064957 G>C maps to ENST00000375244 G224G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KH-A6WC-01A-11D-A33E-09 chr6:32049951 C>A maps to ENST00000375244 R1199R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88W-01A-11D-A351-09 chr17:17783044 G>T maps to NM_001082968.1 R225R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L7-A6VZ-01A-12D-A33E-09 chr17:17810777 G>T maps to NM_001082968.1 I40I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OE-01A-11D-A27G-09 chr14:58874105 G>T maps to NM_207377.2 E109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EQ-01A-11D-A36J-09 chr14:58875293 T>A maps to NM_207377.2 P151P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr22:39078976 A>G maps to NM_020243.4 Q110Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OJ-01A-11D-A27G-09 chr20:43572201 G>T maps to NM_006809.4 V239V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8ER-01A-11D-A36J-09 chr3:100105092 C>T maps to NM_014820.3 E198E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A6-01A-11D-A27G-09 chr8:144400202 G>C maps to NM_052963.1 L400L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A8JD-01A-11D-A36J-09 chr8:144403487 G>A maps to NM_052963.1 L343L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NS-01A-12D-A37C-09 chr17:38567941 T>C maps to ENST00000357601 K308K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-M9-A5M8-01A-11D-A28B-09 chr17:38562641 G>A maps to ENST00000357601 I685I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-M9-A5M8-01A-11D-A28B-09 chr17:38562680 G>A maps to ENST00000357601 I672I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-M9-A5M8-01A-11D-A28B-09 chr17:38563098 G>A maps to ENST00000357601 I610I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NG-01A-11D-A37C-09 chr17:18181535 G>A maps to NM_004618.3 S760S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA7D-01A-11D-A403-09 chr17:18217911 C>T did not map to a codon.
Alternatively spliced codon TCGA-LN-A4A4-01A-11D-A27G-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-XP-A8T6-01A-11D-A36J-09 chr22:22328813 G>A maps to NM_003935.3 H39H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GN-01A-11D-A37C-09 chr3:133339081 T>C maps to NM_007027.3 R1096R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EQ-01A-11D-A36J-09 chr1:179886639 C>T maps to ENST00000398836 L341L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASW-01A-11D-A403-09 chr1:179820406 G>T maps to NM_145034.4 I42I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EO-01A-11D-A36J-09 chr1:179057074 G>T maps to NM_022371.3 T223T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93D-01A-11D-A387-09 chr20:42602017 C>T maps to ENST00000348077 D46D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OX-01A-21D-A28B-09 chr16:52484427 G>T maps to ENST00000407228 R147R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GH-01A-11D-A37C-09 chr17:7578211 G>A maps to NM_001126112.1 R213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GK-01A-11D-A37C-09 chr17:7578262 G>A maps to NM_001126112.1 R196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3YC-01A-11D-A247-09 chr17:7578492 C>T maps to NM_001126112.1 W146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A4QS-01A-11D-A27G-09 chr17:7578211 G>A maps to NM_001126112.1 R213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A97H-01A-11D-A387-09 chr17:7578290 T>A did not map to a codon.
Sequencing variant TCGA-JY-A6F8-01A-11D-A33E-09 chr17:7578262 G>A maps to NM_001126112.1 R196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FA-01A-11D-A33E-09 chr17:7578256 C>A maps to NM_001126112.1 E198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FD-01A-11D-A33E-09 chr17:7577021 G>A maps to NM_001126112.1 R306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A939-01A-12D-A37C-09 chr17:7577497 C>T did not map to a codon.
Sequencing variant TCGA-JY-A93E-01A-11D-A37C-09 chr17:7577021 G>A maps to NM_001126112.1 R306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OG-01A-11D-A27G-09 chr17:7579413 C>T maps to NM_001126112.1 W91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OJ-01A-11D-A27G-09 chr17:7578256 C>A maps to NM_001126112.1 E198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OM-01A-11D-A27G-09 chr17:7578369 C>T did not map to a codon.
Sequencing variant TCGA-L5-A4OW-01A-11D-A28B-09 chr17:7578430 G>A maps to NM_001126112.1 Q167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88S-01A-11D-A36J-09 chr17:7576896 G>A maps to NM_001126112.1 Q317*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A891-01A-11D-A36J-09 chr17:7574002 G>A maps to NM_001126112.1 R342*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NV-01A-11D-A37C-09 chr17:7578262 G>A maps to NM_001126112.1 R196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49M-01A-21D-A27G-09 chr17:7578211 G>A maps to NM_001126112.1 R213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49N-01A-11D-A247-09 chr17:7577527 G>T maps to NM_001126112.1 I251I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49P-01A-11D-A247-09 chr17:7577609 T>C did not map to a codon.
Sequencing variant TCGA-LN-A49R-01A-11D-A247-09 chr17:7578369 C>A did not map to a codon.
Sequencing variant TCGA-LN-A49S-01A-11D-A247-09 chr17:7574002 G>A maps to NM_001126112.1 R342*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49U-01A-31D-A27G-09 chr17:7579314 G>T maps to NM_001126112.1 C124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A2-01A-31D-A27G-09 chr17:7578555 T>A did not map to a codon.
Sequencing variant TCGA-LN-A4A3-01A-11D-A27G-09 chr17:7577057 C>A maps to NM_001126112.1 E294*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A4-01A-11D-A27G-09 chr17:7577497 C>T did not map to a codon.
Sequencing variant TCGA-LN-A7HY-01A-12D-A351-09 chr17:7578178 C>A maps to NM_001126112.1 E224*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A8HZ-01A-11D-A36J-09 chr17:7574034 T>G did not map to a codon.
Sequencing variant TCGA-LN-A9FO-01A-11D-A387-09 chr17:7578238 C>A maps to NM_001126112.1 E204*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FP-01A-31D-A387-09 chr17:7577057 C>A maps to NM_001126112.1 E294*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FP-01A-31D-A387-09 chr17:7579311 C>A maps to NM_001126112.1 T125T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FQ-01A-31D-A387-09 chr17:7577021 G>A maps to NM_001126112.1 R306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FR-01A-11D-A387-09 chr17:7578289 C>G did not map to a codon.
Sequencing variant TCGA-R6-A6DQ-01B-11D-A31U-09 chr17:7576872 C>A maps to NM_001126112.1 G325*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6Y0-01B-11D-A33E-09 chr17:7577016 A>C did not map to a codon.
Sequencing variant TCGA-R6-A8W8-01B-11D-A37C-09 chr17:7579535 C>A maps to NM_001126112.1 E51*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-A7RC-01B-11D-A403-09 chr17:7577017 C>T did not map to a codon.
Sequencing variant TCGA-V5-A7RE-01A-11D-A351-09 chr17:7577016 A>C did not map to a codon.
Sequencing variant TCGA-VR-A8EW-01A-11D-A36J-09 chr17:7578555 T>C did not map to a codon.
Sequencing variant TCGA-VR-A8EX-01A-11D-A36J-09 chr17:7573999 C>A maps to NM_001126112.1 E343*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA4G-01A-11D-A37C-09 chr17:7579405 G>T maps to NM_001126112.1 S94*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA7B-01A-31D-A403-09 chr17:7576651 C>T maps to NM_001126114.1 Q333Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X8-AAAR-01A-11D-A403-09 chr17:7574002 G>A maps to NM_001126112.1 R342*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XP-A8T6-01A-11D-A36J-09 chr17:7578211 G>A maps to NM_001126112.1 R213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GN-01A-11D-A37C-09 chr15:43699687 G>A maps to NM_001141980.1 Q1943*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr15:43748968 C>A maps to NM_001141980.1 E613*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr8:95952410 T>C maps to NM_033285.3 E50E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GM-01A-11D-A37C-09 chr3:189584486 T>C maps to NM_003722.4 P261P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6F8-01A-11D-A33E-09 chr3:189587177 G>T maps to NM_003722.4 E399*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A8I0-01A-11D-A36J-09 chr8:80992547 A>G did not map to a codon.
Sequencing variant TCGA-LN-A49M-01A-21D-A27G-09 chr1:154155546 G>A maps to NM_001043351.1 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr2:1544473 C>A maps to NM_000547.5 A909A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OJ-01A-11D-A27G-09 chr2:1459993 C>T maps to NM_000547.5 F253F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6L4-01A-11D-A31U-09 chr2:1440108 T>C maps to NM_000547.5 T145T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6Y2-01B-11D-A33E-09 chr2:1488581 G>A maps to NM_000547.5 W518*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA7D-01A-11D-A403-09 chr2:1500467 G>T maps to NM_000547.5 E773*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr11:6638870 G>T maps to ENST00000453338 C131*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A893-01A-11D-A36J-09 chr11:6640088 G>T maps to ENST00000453338 L58L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A4-01A-11D-A27G-09 chr13:103330575 G>A did not map to a codon.
Sequencing variant TCGA-IG-A3I8-01A-11D-A247-09 chr1:186302443 G>T maps to NM_003292.2 V1755V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr1:186312522 C>A maps to NM_003292.2 E1229*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RF-01A-13D-A33E-09 chr16:1291205 C>G maps to ENST00000461509 P45P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L7-A56G-01A-21D-A27G-09 chr16:1306352 C>T maps to NM_012217.2 Y24Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GF-01A-11D-A37C-09 chr16:1272739 G>T maps to NM_012467.3 I141I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA4D-01A-11D-A37C-09 chr7:65705855 G>A maps to NM_003596.3 K148K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NH-01A-11D-A37C-09 chr21:10914362 C>T maps to NM_199261.2 S452S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASX-01A-11D-A387-09 chr21:10943020 C>A did not map to a codon.
Sequencing variant TCGA-JY-A6F8-01A-11D-A33E-09 chr13:20025335 A>G maps to NM_199254.2 H257H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FO-01A-11D-A387-09 chr13:20025335 A>G maps to NM_199254.2 H257H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-A7RE-01A-11D-A351-09 chr13:20048097 G>T maps to NM_199254.2 G116G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4MQ-01A-11D-A28B-09 chr20:30385275 C>T maps to ENST00000340513 Q671*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-AAPN-01A-11D-A403-09 chr20:30358169 G>A maps to ENST00000340513 Q127Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HV-01A-21D-A351-09 chr3:185639915 T>C did not map to a codon.
Sequencing variant TCGA-IG-A4P3-01A-11D-A27G-09 chr2:239257448 G>T maps to NM_015650.3 E443*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6L6-01B-11D-A33E-09 chr6:111887730 G>T maps to ENST00000340026 P473P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HX-01A-11D-A33E-09 chr1:211526730 G>A maps to ENST00000427925 S50S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr11:36522833 G>A maps to NM_145803.1 R78*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49R-01A-11D-A247-09 chr16:2225836 C>T maps to NM_032271.2 I543I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93C-01A-11D-A387-09 chr3:49881277 G>A maps to NM_005879.2 Q122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr3:42264487 G>A maps to NM_001042646.1 T707T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr3:42166921 C>T maps to NM_001042646.1 N34N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OS-01A-11D-A28B-09 chr3:36931319 G>A maps to NM_014831.2 R259*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X8-AAAR-01A-11D-A403-09 chr3:36900335 G>A maps to NM_014831.2 C471C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A8JE-01A-11D-A37C-09 chr3:36873774 G>A maps to NM_014831.2 F2389F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr8:141468444 G>T maps to NM_031466.5 S73S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8Q7-01A-11D-A37C-09 chr8:141461321 G>A maps to NM_031466.5 R149*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NJ-01A-11D-A36J-09 chr6:123653048 T>C maps to NM_006073.2 K482K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49W-01A-11D-A27G-09 chr6:123576224 C>A did not map to a codon.
Sequencing variant TCGA-LN-A49U-01A-31D-A27G-09 chr6:41250445 C>T maps to NM_018643.2 L31L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NJ-01A-11D-A36J-09 chr6:41126734 G>A maps to NM_018965.2 L184L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EW-01A-11D-A36J-09 chr6:41168695 G>A maps to ENST00000373108 V76V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr6:42237238 G>A maps to NM_033502.2 S30S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NW-01A-11D-A37C-09 chr6:42211038 G>T maps to NM_033502.2 R936R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49S-01A-11D-A247-09 chr6:42233491 G>T maps to NM_033502.2 S494*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HV-01A-21D-A351-09 chr3:48508869 T>C maps to NM_016381.3 D327D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OG-01A-11D-A27G-09 chr12:73014976 C>T maps to NM_013381.2 Y808Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OJ-01A-11D-A27G-09 chr12:72969050 T>A maps to NM_013381.2 T671T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49M-01A-21D-A27G-09 chr12:72956809 C>T maps to NM_013381.2 Q633*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RE-A7BO-01A-11D-A33E-09 chr12:72956793 T>C maps to NM_013381.2 T627T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EQ-01A-11D-A36J-09 chr12:72667154 G>T maps to NM_013381.2 A199A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FG-01A-11D-A33E-09 chr20:377202 C>T maps to ENST00000422053 R343*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A5B8-01A-11D-A28B-09 chr6:30128404 G>A maps to NM_006778.3 N77N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L7-A6VZ-01A-12D-A33E-09 chr6:30123536 C>A did not map to a codon.
Sequencing variant TCGA-R6-A6Y2-01B-11D-A33E-09 chr6:30122003 C>G maps to NM_006778.3 L396L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6Y0-01B-11D-A33E-09 chr9:100857152 C>T maps to NM_033219.1 K232K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XP-A8T6-01A-11D-A36J-09 chr6:30136084 C>A maps to NM_033229.2 I162I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3Y9-01A-12D-A247-09 chr11:5717812 G>A maps to NM_006074.4 W117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FP-01A-31D-A387-09 chr7:138255645 G>C maps to NM_015905.2 T592T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EY-01A-11D-A36J-09 chr6:30166679 G>T maps to NM_003449.3 P67P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q9-A6FW-01A-31D-A31U-09 chr11:6478031 C>T maps to NM_033278.2 S308S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GK-01A-11D-A37C-09 chr9:119460512 G>A maps to NM_012210.3 Q164Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q9-A6FU-01A-11D-A31U-09 chr11:5655907 G>A maps to NM_001003819.3 Q543Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3YA-01A-11D-A247-09 chr8:27168551 G>C maps to NM_171982.3 A67A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr5:114499431 G>A maps to NM_018700.3 I27I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GH-01A-11D-A37C-09 chr17:57079001 C>A maps to NM_015294.3 G923G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HZ-01A-31D-A351-09 chr17:57109425 G>A maps to NM_015294.3 S593S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OJ-01A-11D-A27G-09 chr6:25972224 G>T maps to NM_006355.2 L212L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A1-01A-21D-A27G-09 chr6:25983524 C>G maps to NM_006355.2 V336V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EX-01A-11D-A36J-09 chr6:25983830 G>T maps to NM_006355.2 P438P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4ON-01A-11D-A27G-09 chr3:140406765 T>C maps to NM_152616.4 Y414Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8W8-01B-11D-A37C-09 chr3:140401780 A>G maps to NM_152616.4 Q273Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8WC-01A-11D-A37C-09 chr3:140407023 A>G maps to NM_152616.4 S500S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA4G-01A-11D-A37C-09 chr3:140397292 C>T maps to NM_152616.4 P74P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr2:96262095 A>G maps to NM_138800.1 K218K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A8I1-01A-11D-A36J-09 chr2:96265164 C>T maps to NM_138800.1 Y395Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6XQ-01B-11D-A33E-09 chr2:96265164 C>T maps to NM_138800.1 Y395Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr1:117661013 A>G maps to NM_025188.3 I288I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6DQ-01B-11D-A31U-09 chr1:117661117 C>A maps to NM_025188.3 E254*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr1:155156329 G>A maps to NM_025058.3 S648S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NS-01A-12D-A37C-09 chr11:89537598 G>C maps to NM_020358.2 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6XG-01B-11D-A33E-09 chr11:5701290 G>T maps to NM_033034.2 L39L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GK-01A-11D-A37C-09 chr5:180687427 C>T maps to NM_032765.2 E129E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr5:180687592 G>T maps to NM_032765.2 A74A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q9-A6FU-01A-11D-A31U-09 chr5:180687601 C>T maps to NM_032765.2 A71A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A5S3-01A-11D-A28B-09 chr2:27529351 C>T maps to NM_032546.3 A382A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FR-01A-11D-A387-09 chr8:67066570 T>C did not map to a codon.
Sequencing variant TCGA-L5-A4OU-01A-11D-A28B-09 chr7:100730994 G>A maps to NM_030961.1 G134G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88W-01A-11D-A351-09 chr7:100730775 G>A maps to NM_030961.1 E61E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GK-01A-11D-A37C-09 chr1:248039701 T>C maps to NM_015431.3 L458L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RF-01A-13D-A33E-09 chr1:248039250 C>T maps to NM_015431.3 T307T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OU-01A-11D-A28B-09 chr1:248039572 T>C maps to NM_015431.3 L415L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NE-01A-11D-A37C-09 chr1:248039763 T>C maps to NM_015431.3 A478A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASX-01A-11D-A387-09 chr4:165962597 C>T maps to NM_152620.2 S458S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3YA-01A-11D-A247-09 chr4:165891023 C>T maps to NM_001012414.2 W44*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A97I-01A-11D-A387-09 chr1:33612834 C>T maps to NM_018207.2 Q457Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NE-01A-11D-A37C-09 chr1:33613223 G>A maps to NM_018207.2 Q328*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NL-01A-12D-A37C-09 chr1:26386783 C>T maps to NM_032588.2 Q190Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XP-A8T7-01A-11D-A36J-09 chr1:26392820 G>A maps to NM_032588.2 Y90Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NR-01A-11D-A37C-09 chr1:231335943 C>T maps to NM_001004342.3 T438T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FP-01A-31D-A387-09 chr15:45047270 C>T maps to NM_182985.3 F60F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FB-01A-11D-A33E-09 chr5:180630634 G>T maps to NM_203293.1 L176L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88S-01A-11D-A36J-09 chr3:32859628 C>T maps to NM_001039111.1 C19C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HZ-01A-31D-A351-09 chr3:32932231 C>T maps to NM_001039111.1 H512H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49X-01A-31D-A27G-09 chr10:104404514 C>T maps to NM_030912.2 S47S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OJ-01A-11D-A27G-09 chr4:189060789 A>G maps to NM_178556.3 P26P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OJ-01A-11D-A27G-09 chr4:189012835 G>A maps to ENST00000326754 S310S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FG-01A-11D-A33E-09 chr5:14358417 C>T maps to NM_007118.2 N726N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr5:14419945 C>T maps to NM_007118.2 N1673N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-AAPN-01A-11D-A403-09 chr5:14369613 G>A maps to NM_007118.2 Q1066Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A97H-01A-11D-A387-09 chr22:38130533 G>A maps to NM_001039141.2 R1397R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr22:38122336 C>T maps to NM_001039141.2 P1258P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr22:38129303 G>T did not map to a codon.
Sequencing variant TCGA-L5-A8NS-01A-12D-A37C-09 chr22:38130718 G>A maps to NM_001039141.2 W1459*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6F8-01A-11D-A33E-09 chr19:6751164 G>T maps to ENST00000313244 R583R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A2-01A-31D-A27G-09 chr19:6751204 C>T maps to ENST00000313244 R597*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OE-01A-11D-A27G-09 chr14:92472506 C>A maps to NM_004239.3 E605*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GR-01A-12D-A37C-09 chr2:230664050 T>C maps to ENST00000389044 P1058P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr2:230668380 G>A maps to ENST00000389044 S941S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43C-01A-11D-A247-09 chr15:64687621 C>T maps to NM_016213.4 G99G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA7D-01A-11D-A403-09 chr15:64692981 C>G maps to NM_016213.4 S220*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NK-01A-21D-A37C-09 chr6:126329536 G>T did not map to a codon.
Sequencing variant TCGA-LN-A9FQ-01A-31D-A387-09 chr6:126334175 G>A maps to NM_001031712.2 L356L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EQ-01A-11D-A36J-09 chr6:126319385 G>A maps to NM_001031712.2 S104S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43I-01A-11D-A247-09 chr22:46751483 A>G maps to NM_018006.4 L339L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88Z-01A-11D-A36J-09 chr22:46748165 G>A maps to NM_018006.4 L237L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OR-01A-11D-A27G-09 chr23:54949884 G>T did not map to a codon.
Sequencing variant TCGA-LN-A8I0-01A-11D-A36J-09 chr23:54950122 C>T did not map to a codon.
Sequencing variant TCGA-R6-A6XQ-01B-11D-A33E-09 chr23:54951450 G>A did not map to a codon.
Sequencing variant TCGA-R6-A6Y2-01B-11D-A33E-09 chr23:54957318 G>T did not map to a codon.
Sequencing variant TCGA-XP-A8T7-01A-11D-A36J-09 chr23:54953051 G>A did not map to a codon.
Sequencing variant TCGA-IG-A6QS-01A-12D-A33E-09 chr1:193045170 G>T did not map to a codon.
Sequencing variant TCGA-L5-A4OR-01A-11D-A27G-09 chr1:193051320 C>G maps to NM_004600.5 V403V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RE-01A-11D-A33E-09 chr8:72964919 G>C maps to NM_007332.2 V575V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88W-01A-11D-A351-09 chr8:72935275 G>A maps to NM_007332.2 I1075I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NG-01A-11D-A37C-09 chr8:72966068 C>A maps to NM_007332.2 A521A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NU-01A-11D-A36J-09 chr8:72969980 C>T maps to NM_007332.2 W355*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZR-A9CJ-01B-11D-A387-09 chr8:72964955 G>A maps to NM_007332.2 A563A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GQ-01A-11D-A37C-09 chr3:142467209 A>G maps to ENST00000476941 K180K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8Q7-01A-11D-A37C-09 chr3:142511808 G>A maps to ENST00000476941 Q527Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GM-01A-11D-A37C-09 chr4:122800992 A>T maps to NM_001130698.1 R888R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NN-01A-11D-A37C-09 chr4:122853923 G>A maps to NM_001130698.1 T163T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NF-01A-11D-A37C-09 chr13:38320270 C>A maps to NM_003306.1 E234*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NQ-01A-11D-A36J-09 chr13:38211353 G>A maps to NM_003306.1 Q879*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XP-A8T8-01A-11D-A36J-09 chr20:33632410 T>C maps to NM_015638.2 S254S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3I8-01A-11D-A247-09 chr23:111195501 C>A did not map to a codon.
Sequencing variant TCGA-IG-A6QS-01A-12D-A33E-09 chr23:111078314 C>G did not map to a codon.
Sequencing variant TCGA-L5-A8NV-01A-11D-A37C-09 chr23:111078236 G>T did not map to a codon.
Sequencing variant TCGA-LN-A7HY-01A-12D-A351-09 chr23:111155530 G>A did not map to a codon.
Sequencing variant TCGA-LN-A4A9-01A-11D-A28B-09 chr11:101323835 C>A maps to NM_004621.5 G882G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6KZ-01A-11D-A31U-09 chr11:101374847 A>G maps to NM_004621.5 A284A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-AAPN-01A-11D-A403-09 chr11:101341988 C>T maps to NM_004621.5 L778L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GN-01A-11D-A37C-09 chr15:31330033 T>C maps to NM_002420.4 A795A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HY-01A-12D-A351-09 chr15:31352746 C>A maps to NM_002420.4 P399P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FA-01A-11D-A33E-09 chr21:45820224 G>T maps to ENST00000397932 P764P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GF-01A-11D-A37C-09 chr9:73399028 T>C maps to ENST00000419692 E346E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A4P3-01A-11D-A27G-09 chr9:73164473 G>T maps to ENST00000419692 R1185R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A6QS-01A-12D-A33E-09 chr9:73240145 G>A maps to ENST00000419692 R544R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NE-01A-11D-A37C-09 chr9:73206022 T>C maps to ENST00000419692 S1003S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A8HZ-01A-11D-A36J-09 chr9:73213385 G>T maps to ENST00000419692 I953I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA4D-01A-11D-A37C-09 chr9:73225652 G>A maps to ENST00000419692 R801*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A891-01A-11D-A36J-09 chr19:49699774 C>T maps to NM_017636.3 C763C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EQ-01A-11D-A36J-09 chr11:2428370 A>G maps to ENST00000452833 A1034A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43H-01A-11D-A247-09 chr9:77377815 G>A maps to NM_017662.4 I1257I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3I8-01A-11D-A247-09 chr15:50955213 C>T maps to NM_017672.4 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49L-01A-11D-A247-09 chr15:50903478 G>A maps to NM_017672.4 S697S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NR-01A-11D-A37C-09 chr8:116616854 G>T maps to NM_014112.2 Y447*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6Y0-01B-11D-A33E-09 chr8:116617052 G>C maps to NM_014112.2 S381S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L7-A6VZ-01A-12D-A33E-09 chr17:3494369 G>T maps to ENST00000399756 L164L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A50L-01A-11D-A27G-09 chr7:142622701 G>A maps to NM_019841.4 V348V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49M-01A-21D-A27G-09 chr7:142612478 G>A maps to NM_019841.4 I428I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q9-A6FU-01A-11D-A31U-09 chr7:142574199 G>A maps to NM_018646.2 L241L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr7:98490093 C>T maps to ENST00000359863 N103N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A9-01A-11D-A28B-09 chr7:141952040 T>A maps to NM_001001317.2 *242C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr9:135779171 G>A maps to NM_000368.4 R692*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NS-01A-12D-A37C-09 chr16:2130298 G>A maps to NM_000548.3 V1177V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4MQ-01A-11D-A28B-09 chr16:2126083 C>T maps to NM_000548.3 I885I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A5U5-01A-21D-A28B-09 chr16:2111976 G>T maps to NM_000548.3 E409*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EQ-01A-11D-A36J-09 chr16:2134648 G>T maps to NM_000548.3 E1476*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZR-A9CJ-01B-11D-A387-09 chr16:2121820 C>T maps to NM_000548.3 G661G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GL-01A-12D-A37C-09 chr13:45008869 C>T maps to NM_183422.2 Q1038Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OX-01A-21D-A28B-09 chr3:150127664 A>G maps to NM_014779.2 R176R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EX-01A-11D-A36J-09 chr7:100075403 G>T maps to NM_030935.3 R86R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43I-01A-11D-A247-09 chr11:18502113 G>T maps to NM_006292.2 A384A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4MR-01A-11D-A28B-09 chr2:99634812 C>T did not map to a codon.
Sequencing variant TCGA-JY-A6FD-01A-11D-A33E-09 chr1:115576686 G>T maps to NM_000549.3 G86*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OU-01A-11D-A28B-09 chr1:115576591 A>C did not map to a codon.
Sequencing variant TCGA-R6-A8W8-01B-11D-A37C-09 chr14:81558919 T>C maps to NM_000369.2 A171A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S8-A6BW-01A-11D-A31U-09 chr14:81609997 G>A maps to NM_000369.2 K532K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A5B8-01A-11D-A28B-09 chr20:51872036 C>A maps to NM_173485.5 C680*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OU-01A-11D-A28B-09 chr20:51871025 T>G maps to NM_173485.5 S343S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HX-01A-11D-A33E-09 chr20:51871833 G>T maps to NM_173485.5 E613*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GG-01A-11D-A37C-09 chr19:31768322 C>T maps to NM_020856.2 L792L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FG-01A-11D-A33E-09 chr19:31770038 G>A maps to NM_020856.2 S220S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A891-01A-11D-A36J-09 chr19:31768919 A>G maps to NM_020856.2 S593S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NJ-01A-11D-A36J-09 chr19:31769654 G>T maps to NM_020856.2 T348T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASX-01A-11D-A387-09 chr19:31770617 G>A maps to NM_020856.2 D27D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NQ-01A-11D-A36J-09 chr19:50251726 C>G did not map to a codon.
Sequencing variant TCGA-JY-A6FH-01A-11D-A33E-09 chr5:110411738 T>G maps to NM_033035.4 R149R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A8I0-01A-11D-A36J-09 chr1:231672956 A>G did not map to a codon.
Sequencing variant TCGA-XP-A8T7-01A-11D-A36J-09 chr12:31106946 C>T maps to NM_001080509.2 Q8*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88V-01A-11D-A351-09 chr1:115604800 G>A maps to NM_005725.4 F75F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OX-01A-21D-A28B-09 chr7:128807244 G>T maps to NM_178562.3 V198V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KH-A6WC-01A-11D-A33E-09 chr23:99887532 C>G did not map to a codon.
Sequencing variant TCGA-LN-A8I0-01A-11D-A36J-09 chr23:99888428 C>A did not map to a codon.
Sequencing variant TCGA-L5-A8NR-01A-11D-A37C-09 chr23:38525450 A>G did not map to a codon.
Sequencing variant TCGA-IG-A50L-01A-11D-A27G-09 chr12:3390479 G>A maps to ENST00000407263 T183T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EP-01A-31D-A403-09 chr12:3387723 G>A maps to ENST00000407263 T67T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GI-01A-11D-A37C-09 chr24:6114770 C>T did not map to a codon.
Sequencing variant TCGA-VR-A8EP-01A-31D-A403-09 chr23:53114915 C>G did not map to a codon.
Sequencing variant TCGA-VR-AA4G-01A-11D-A37C-09 chr23:53114891 A>G did not map to a codon.
Sequencing variant TCGA-IG-A3YA-01A-11D-A247-09 chr6:116574349 G>A maps to ENST00000368611 D324D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88W-01A-11D-A351-09 chr17:2236266 C>T maps to NM_018128.4 E431E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FP-01A-31D-A387-09 chr23:54467181 G>T did not map to a codon.
Sequencing variant TCGA-IG-A51D-01A-11D-A27G-09 chr5:112770524 A>G maps to NM_032028.3 A4A. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-L5-A4OW-01A-11D-A28B-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-X8-AAAR-01A-11D-A403-09 chr1:32828358 G>T maps to NM_052841.3 G19G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8WC-01A-11D-A37C-09 chr9:100367119 T>A maps to NM_139246.4 K381*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr6:43221341 C>T maps to NM_032538.1 R123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr6:43250472 C>T maps to NM_032538.1 S665S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr6:43251750 G>A maps to NM_032538.1 R1091R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NS-01A-12D-A37C-09 chr2:3483160 C>T maps to NM_016030.5 Q713*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NG-01A-11D-A37C-09 chr10:75056898 G>T maps to NM_145170.3 Y585*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-A7RC-01B-11D-A403-09 chr10:75091009 G>A maps to NM_145170.3 C304C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8ER-01A-11D-A36J-09 chr3:39172256 C>A maps to ENST00000301819 G803G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GM-01A-11D-A37C-09 chr2:166771919 G>T maps to NM_024753.3 A643A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3YB-01A-11D-A247-09 chr2:166756356 G>A maps to NM_024753.3 Q931*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr1:55252653 G>A maps to NM_001114108.1 T278T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr1:156552851 G>A maps to NM_001105669.2 W310*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88T-01A-11D-A351-09 chr1:156551657 G>T maps to NM_001105669.2 G168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A8I0-01A-11D-A36J-09 chr1:156551464 G>A maps to NM_001105669.2 L103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FP-01A-31D-A387-09 chr1:156554757 C>A maps to NM_001105669.2 V447V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6DN-01B-11D-A31U-09 chr1:156552115 G>A maps to NM_001105669.2 W267*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NE-01A-11D-A37C-09 chr2:32859030 C>T maps to NM_017735.4 Q119*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XP-A8T8-01A-11D-A36J-09 chr4:147795958 A>T maps to ENST00000513335 T262T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NG-01A-11D-A37C-09 chr21:38460553 C>T maps to NM_003316.3 C82C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3Y9-01A-12D-A247-09 chr2:178417446 G>A maps to NM_152517.2 T15T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OU-01A-11D-A28B-09 chr2:74718459 C>A maps to NM_022492.4 S214S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GN-01A-11D-A37C-09 chr5:94833130 G>T maps to NM_014639.3 R1209R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A625-01A-11D-A31U-09 chr5:94803578 C>T maps to NM_014639.3 E1537E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A893-01A-11D-A36J-09 chr1:51756282 G>T maps to ENST00000447632 I463I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NV-01A-11D-A37C-09 chr9:15307093 C>T maps to NM_152574.2 L76L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EO-01A-11D-A36J-09 chr9:15211355 G>T maps to NM_152574.2 T174T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49W-01A-11D-A27G-09 chr14:89291074 G>T maps to NM_144596.2 L8L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GG-01A-11D-A37C-09 chr9:135277917 G>A maps to NM_007344.2 D97D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr9:135277548 C>T maps to NM_007344.2 K220K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NS-01A-12D-A37C-09 chr6:80721266 T>A did not map to a codon.
Sequencing variant TCGA-R6-A6Y2-01B-11D-A33E-09 chr1:1119335 G>A maps to NM_001130045.1 K375K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr9:124632948 G>A maps to NM_001139442.1 N610N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8WC-01A-11D-A37C-09 chr9:124855628 G>T maps to NM_001139442.1 L23L. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-L5-A4OI-01A-11D-A27G-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-LN-A49P-01A-11D-A247-09 chr15:90801305 C>T maps to ENST00000438251 H324H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4MQ-01A-11D-A28B-09 chr6:167754287 C>T maps to NM_031949.4 S300S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NI-01A-11D-A37C-09 chr14:76173978 C>T maps to NM_015072.4 D223D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr14:76259373 G>A maps to NM_015072.4 Q1034Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NQ-01A-11D-A36J-09 chr17:46882290 C>A maps to NM_001130918.1 E56*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EQ-01A-11D-A36J-09 chr1:84356014 G>A maps to NM_024686.4 F786F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43E-01A-11D-A247-09 chr22:50470516 G>A maps to NM_001080447.1 N435N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GI-01A-11D-A37C-09 chr2:179402366 G>A maps to NM_133378.4 L30621L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GI-01A-11D-A37C-09 chr2:179429644 C>A maps to NM_133378.4 E24504*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RF-01A-13D-A33E-09 chr2:179643818 G>T maps to NM_133378.4 R1330R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A625-01A-11D-A31U-09 chr2:179647000 G>A maps to NM_133378.4 G1106G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A97H-01A-11D-A387-09 chr2:179474465 C>A maps to NM_133378.4 A14660A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FH-01A-11D-A33E-09 chr2:179407889 A>G maps to NM_133378.4 G29702G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93D-01A-11D-A387-09 chr2:179393710 G>T maps to NM_133378.4 V33021V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93D-01A-11D-A387-09 chr2:179437625 G>T maps to NM_133378.4 A21843A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93E-01A-11D-A37C-09 chr2:179585678 G>A maps to NM_133378.4 D6445D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93F-01A-21D-A37C-09 chr2:179504468 G>T maps to NM_133378.4 P11043P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43E-01A-11D-A247-09 chr2:179500729 G>A maps to NM_133378.4 N11288N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OE-01A-11D-A27G-09 chr2:179431595 G>T maps to NM_133378.4 Y23853*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OM-01A-11D-A27G-09 chr2:179593014 A>G maps to NM_133378.4 A5268A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OR-01A-11D-A27G-09 chr2:179489320 T>A maps to NM_133378.4 K12328*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88T-01A-11D-A351-09 chr2:179428547 A>G maps to NM_133378.4 G24869G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88T-01A-11D-A351-09 chr2:179644144 A>T maps to NM_133378.4 I1258I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A891-01A-11D-A36J-09 chr2:179418691 G>A maps to NM_133378.4 Q27148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A891-01A-11D-A36J-09 chr2:179468903 T>C maps to NM_133378.4 P15602P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A893-01A-11D-A36J-09 chr2:179391939 G>C maps to NM_133378.4 T33357T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A893-01A-11D-A36J-09 chr2:179417236 T>C maps to NM_133378.4 E27562E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NE-01A-11D-A37C-09 chr2:179596612 A>G maps to NM_133378.4 T4419T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NI-01A-11D-A37C-09 chr2:179458715 C>T maps to NM_133378.4 R16900R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NK-01A-21D-A37C-09 chr2:179408015 G>A maps to NM_133378.4 Y29660Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NL-01A-12D-A37C-09 chr2:179602911 G>A maps to NM_133378.4 S3512S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NV-01A-11D-A37C-09 chr2:179418787 G>A maps to NM_133378.4 L27116L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NW-01A-11D-A37C-09 chr2:179424742 G>T maps to NM_133378.4 R26138R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NW-01A-11D-A37C-09 chr2:179476866 G>T maps to NM_133378.4 A14189A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49K-01A-11D-A247-09 chr2:179606442 C>T maps to NM_133437.3 L3668L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49M-01A-21D-A27G-09 chr2:179667000 G>A maps to NM_133378.4 G53G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49N-01A-11D-A247-09 chr2:179571595 G>A maps to NM_133378.4 V8465V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49Y-01A-11D-A27G-09 chr2:179579778 C>A maps to NM_133378.4 E7468*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A2-01A-31D-A27G-09 chr2:179575993 G>T maps to NM_133378.4 A8079A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A5-01A-21D-A27G-09 chr2:179444678 A>C maps to NM_133378.4 A19877A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A5-01A-21D-A27G-09 chr2:179455005 A>G maps to NM_133378.4 C17914C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A8-01A-32D-A27G-09 chr2:179595753 G>A maps to NM_133378.4 L4636L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A5U5-01A-21D-A28B-09 chr2:179588637 G>A maps to NM_133378.4 C5872C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A8HZ-01A-11D-A36J-09 chr2:179451854 T>C maps to NM_133378.4 S18793S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FP-01A-31D-A387-09 chr2:179479480 C>G did not map to a codon.
Sequencing variant TCGA-M9-A5M8-01A-11D-A28B-09 chr2:179611820 A>G maps to ENST00000375038 T5104T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6L4-01A-11D-A31U-09 chr2:179590367 T>G maps to NM_133378.4 R5611R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6XG-01B-11D-A33E-09 chr2:179396212 G>T maps to NM_133378.4 R32475R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6XG-01B-11D-A33E-09 chr2:179401680 G>T maps to NM_133378.4 I30817I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6XG-01B-11D-A33E-09 chr2:179404445 G>T maps to NM_133378.4 G30214G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6XG-01B-11D-A33E-09 chr2:179453426 G>T maps to NM_133378.4 R18441R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S8-A6BW-01A-11D-A31U-09 chr2:179399176 C>G maps to NM_133378.4 V31487V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-A7RB-01A-11D-A351-09 chr2:179419248 G>A maps to NM_133378.4 R27041*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-A7RB-01A-11D-A351-09 chr2:179480172 G>A maps to NM_133378.4 R13599*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-A7RB-01A-11D-A351-09 chr2:179604930 T>C maps to NM_133437.3 E4172E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASW-01A-11D-A403-09 chr2:179658217 G>A maps to NM_133378.4 A483A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EU-01A-11D-A36J-09 chr2:179408973 G>A maps to NM_133378.4 S29426S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EU-01A-11D-A36J-09 chr2:179460408 A>G maps to NM_133378.4 R16656R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EZ-01A-11D-A36J-09 chr2:179593287 G>T maps to NM_133378.4 Y5211*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EZ-01A-11D-A36J-09 chr2:179638019 G>T maps to NM_133378.4 S2557S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8Q7-01A-11D-A37C-09 chr2:179428349 G>T maps to NM_133378.4 G24935G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA4D-01A-11D-A37C-09 chr2:179428955 G>A maps to NM_133378.4 G24733G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA7B-01A-31D-A403-09 chr2:179486303 G>T maps to NM_133378.4 R12515R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X8-AAAR-01A-11D-A403-09 chr2:179639843 A>C maps to NM_133378.4 T2198T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A8JE-01A-11D-A37C-09 chr2:179402297 G>T maps to NM_133378.4 S30644S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A9VB-01A-21D-A37C-09 chr2:179611958 C>A maps to ENST00000375038 G5058G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OT-01A-11D-A28B-09 chr8:63976809 G>T maps to NM_000370.3 V206V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OW-01A-11D-A28B-09 chr20:43118106 C>T maps to NM_024331.3 P318P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43C-01A-11D-A247-09 chr19:54942050 C>T maps to ENST00000391739 R334*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GK-01A-11D-A37C-09 chr17:72218721 C>T maps to NM_032646.5 D76D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FP-01A-31D-A387-09 chr7:2687176 G>C maps to NM_025250.2 T177T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FA-01A-11D-A33E-09 chr12:49521824 A>G maps to NM_006082.2 D424D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FA-01A-11D-A33E-09 chr12:49521827 T>C maps to NM_006082.2 E423E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OW-01A-11D-A28B-09 chr12:49521905 C>T maps to NM_006082.2 L397L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GI-01A-11D-A37C-09 chr13:19751309 G>T maps to NM_006001.1 T271T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3I8-01A-11D-A247-09 chr13:19748203 G>A maps to NM_006001.1 I384I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NI-01A-11D-A37C-09 chr13:19751405 C>T maps to NM_006001.1 T239T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OE-01A-11D-A27G-09 chr2:132238132 C>T maps to NM_080386.2 A289A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FP-01A-31D-A387-09 chr2:132235780 C>T maps to NM_080386.2 I16I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A5B8-01A-11D-A28B-09 chr2:130949565 G>C maps to NM_207312.2 L397L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NJ-01A-11D-A36J-09 chr20:57599433 C>A maps to NM_030773.3 R318R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HX-01A-11D-A33E-09 chr20:57598916 C>T maps to NM_030773.3 S145S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OX-01A-21D-A28B-09 chr16:90002058 C>T maps to ENST00000304984 G747G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GR-01A-12D-A37C-09 chr10:135103367 C>T maps to NM_006659.2 P440P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr10:135107235 C>A maps to NM_006659.2 V218V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr10:135116331 C>T maps to NM_006659.2 P38P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88W-01A-11D-A351-09 chr13:113158951 G>T maps to NM_006322.4 Y721*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6KZ-01A-11D-A31U-09 chr13:113140381 G>A maps to NM_006322.4 N883N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA7D-01A-11D-A403-09 chr13:113201972 G>A maps to NM_006322.4 R377*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6KZ-01A-11D-A31U-09 chr15:43678413 G>A maps to ENST00000399460 L300L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6XG-01B-11D-A33E-09 chr15:43678000 G>T maps to ENST00000399460 E246*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr22:50656443 C>G maps to NM_020461.3 G1757G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NS-01A-12D-A37C-09 chr16:28857356 G>A maps to NM_003321.4 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6DQ-01B-11D-A31U-09 chr6:35477489 T>C maps to NM_003322.3 P213P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OE-01A-11D-A27G-09 chr19:49387033 G>T maps to NM_003323.2 R418R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88V-01A-11D-A351-09 chr19:49388730 G>A maps to NM_003323.2 D345D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NQ-01A-11D-A36J-09 chr19:49385304 G>T maps to NM_003323.2 I477I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RE-01A-11D-A33E-09 chr6:158923469 G>A maps to NM_020245.3 L925L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FA-01A-11D-A33E-09 chr6:158735105 C>T maps to NM_020245.3 L20L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49Y-01A-11D-A27G-09 chr6:158922785 G>A maps to NM_020245.3 S697S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8W5-01B-11D-A37C-09 chr6:158900955 G>T maps to NM_020245.3 L400L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8Q7-01A-11D-A37C-09 chr11:62346472 C>T maps to NM_022830.2 S278S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93D-01A-11D-A387-09 chr12:44194270 G>A maps to NM_002822.3 G149G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XP-A8T8-01A-11D-A36J-09 chr12:44191173 T>A maps to NM_002822.3 K265*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FE-01A-11D-A33E-09 chr3:52265238 G>T maps to NM_007284.3 L129L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OH-01A-11D-A27G-09 chr4:48088567 G>T maps to NM_003328.2 R291R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr4:48088567 G>T maps to NM_003328.2 R291R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A891-01A-11D-A36J-09 chr4:48114498 G>T maps to NM_003328.2 R69R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L7-A6VZ-01A-12D-A33E-09 chr1:32647153 G>T maps to NM_175852.3 E161*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A97I-01A-11D-A387-09 chr22:36863943 C>T maps to NM_012473.3 V136V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr16:11773554 G>A maps to ENST00000356957 S818S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASX-01A-11D-A387-09 chr16:11785932 G>A maps to ENST00000356957 T398T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FD-01A-11D-A33E-09 chr18:9886733 C>T maps to NM_001098529.1 G86G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OJ-01A-11D-A27G-09 chr18:9887084 G>A maps to NM_001098529.1 Q203Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49S-01A-11D-A247-09 chr18:9887036 C>T maps to NM_001098529.1 I187I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GI-01A-11D-A37C-09 chr7:37924816 A>C maps to NM_016616.4 R404R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr18:54278225 G>A maps to NM_004786.2 R280*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GQ-01A-11D-A37C-09 chr16:72122989 C>T maps to NM_001142318.1 L60L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L7-A6VZ-01A-12D-A33E-09 chr12:104682730 A>C maps to NM_001093771.1 G109G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49M-01A-21D-A27G-09 chr12:104742132 A>G maps to NM_001093771.1 V628V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4ON-01A-11D-A27G-09 chr22:19902751 C>T maps to NM_006440.3 P192P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FP-01A-31D-A387-09 chr19:10463208 C>G maps to NM_003331.4 L1073L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S8-A6BW-01A-11D-A31U-09 chr18:671441 G>A maps to NM_001071.2 L265L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3Y9-01A-12D-A247-09 chr11:88911210 G>C maps to NM_000372.4 L30L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43M-01A-11D-A247-09 chr11:88911366 C>T maps to NM_000372.4 S82S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43I-01A-11D-A247-09 chr15:41862355 T>C did not map to a codon.
Sequencing variant TCGA-L5-A43I-01A-11D-A247-09 chr15:41865874 A>T did not map to a codon.
Sequencing variant TCGA-L5-A8NV-01A-11D-A37C-09 chr15:41859735 G>C did not map to a codon.
Sequencing variant TCGA-R6-A6DN-01B-11D-A31U-09 chr15:41865874 A>T did not map to a codon.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr21:44515595 G>A maps to NM_001025203.1 N100N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8WC-01A-11D-A37C-09 chr21:44513331 C>T maps to NM_001025203.1 E201E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A8I0-01A-11D-A36J-09 chr15:70976775 G>T maps to NM_018003.2 L204L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A8JD-01A-11D-A36J-09 chr9:139973474 G>T maps to NM_207309.2 E240*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NF-01A-11D-A37C-09 chr23:47065780 G>T did not map to a codon.
Sequencing variant TCGA-L5-A8NS-01A-12D-A37C-09 chr23:47058626 G>A did not map to a codon.
Sequencing variant TCGA-Q9-A6FU-01A-11D-A31U-09 chr23:47074031 C>G did not map to a codon.
Sequencing variant TCGA-XP-A8T7-01A-11D-A36J-09 chr23:47072571 C>T did not map to a codon.
Sequencing variant TCGA-LN-A9FO-01A-11D-A387-09 chr9:33941665 G>C maps to NM_018449.2 S637*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-AAPN-01A-11D-A403-09 chr9:33927919 G>C maps to NM_018449.2 S749*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49V-01A-11D-A247-09 chr11:122667712 G>T maps to NM_032873.4 V443V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A50L-01A-11D-A27G-09 chr12:125397206 A>G maps to NM_021009.5 L371L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA4G-01A-11D-A37C-09 chr12:125396397 A>G maps to NM_021009.5 D640D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr20:44443030 C>T maps to NM_007019.2 G46G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8W5-01B-11D-A37C-09 chr10:60124622 G>T maps to NM_003338.3 L97L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A5B8-01A-11D-A28B-09 chr5:138979985 A>T maps to NM_003339.2 P18P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-AAPN-01A-11D-A403-09 chr2:181846834 G>A maps to NM_182678.1 A22A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GQ-01A-11D-A37C-09 chr4:39776477 G>T maps to NM_005339.4 T108T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49R-01A-11D-A247-09 chr11:57322081 G>T maps to NM_004223.3 Y46*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr19:59067560 G>A maps to NM_003969.3 A149A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GG-01A-11D-A37C-09 chr23:142967286 G>A did not map to a codon.
Sequencing variant TCGA-L5-A8NH-01A-11D-A37C-09 chr1:64680521 G>T maps to ENST00000371077 E122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8Q7-01A-11D-A37C-09 chr1:11333869 G>A maps to NM_013319.2 V94V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S8-A6BV-01A-21D-A31U-09 chr23:153714146 G>A did not map to a codon.
Sequencing variant TCGA-VR-A8EX-01A-11D-A36J-09 chr16:4921227 T>A maps to NM_016936.3 A544A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EY-01A-11D-A36J-09 chr16:4927080 C>G maps to NM_016936.3 A1078A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A8I1-01A-11D-A36J-09 chr20:3102654 C>A maps to NM_014948.2 L210L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NR-01A-11D-A37C-09 chr23:56591386 G>T did not map to a codon.
Sequencing variant TCGA-LN-A9FQ-01A-31D-A387-09 chr23:56591894 C>G did not map to a codon.
Sequencing variant TCGA-VR-A8EZ-01A-11D-A36J-09 chr23:56591113 C>T did not map to a codon.
Sequencing variant TCGA-VR-AA7B-01A-31D-A403-09 chr1:156018299 G>T maps to NM_020131.3 R298R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8WG-01A-11D-A37C-09 chr15:43339471 G>A maps to NM_174916.2 R519*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8ER-01A-11D-A36J-09 chr15:43367260 G>A maps to NM_174916.2 F148F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GG-01A-11D-A37C-09 chr2:170735084 G>T did not map to a codon.
Sequencing variant TCGA-2H-A9GN-01A-11D-A37C-09 chr1:19499497 C>T maps to ENST00000375267 A1127A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A5B8-01A-11D-A28B-09 chr1:19510630 G>T maps to ENST00000375267 T659T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6F8-01A-11D-A33E-09 chr1:19443866 G>T maps to ENST00000375267 T3557T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49P-01A-11D-A247-09 chr1:19422059 G>C maps to ENST00000375267 V4535V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6Y0-01B-11D-A33E-09 chr1:19510611 G>T maps to ENST00000375267 R666R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr8:103271267 G>A maps to NM_015902.4 C2682C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49P-01A-11D-A247-09 chr14:93676301 A>T maps to NM_175748.3 R95*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GO-01A-11D-A37C-09 chr17:42290222 G>T maps to NM_014233.2 T208T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6XQ-01B-11D-A33E-09 chr17:42284615 G>T maps to NM_014233.2 S763S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X8-AAAR-01A-11D-A403-09 chr11:62444459 C>T maps to NM_015853.3 G223G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GK-01A-11D-A37C-09 chr2:136519419 C>T maps to NM_014607.3 Q181*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A938-01A-11D-A37C-09 chr2:136513151 T>C maps to NM_014607.3 T133T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FA-01A-11D-A33E-09 chr13:76179917 A>G maps to NM_006002.3 R221R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49O-01A-11D-A247-09 chr20:62572377 G>A maps to NM_017859.3 R347R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NR-01A-11D-A37C-09 chr3:48600421 C>A maps to NM_033199.3 E46*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZR-A9CJ-01B-11D-A387-09 chr11:73686624 G>T maps to NM_003355.2 Y242*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr11:18566188 G>A maps to NM_001040697.1 G347G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EZ-01A-11D-A36J-09 chr11:18566292 G>A maps to NM_001040697.1 R313*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A8O2-01A-11D-A36J-09 chr1:161123889 G>T maps to NM_016406.3 E35*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr2:128900741 G>A maps to NM_020120.3 P598P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OF-01A-11D-A27G-09 chr2:128936113 A>G maps to NM_020120.3 A1262A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49Y-01A-11D-A27G-09 chr2:128877947 G>T maps to NM_020120.3 L297L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GR-01A-12D-A37C-09 chr2:234622056 C>T maps to NM_019078.1 H140H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43I-01A-11D-A247-09 chr4:70080139 G>T maps to NM_001073.1 R101R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A9VB-01A-21D-A37C-09 chr4:69403557 G>A maps to NM_001076.2 R460*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NF-01A-11D-A37C-09 chr4:70156481 G>C maps to NM_053039.1 S421S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GF-01A-11D-A37C-09 chr4:70361096 G>A maps to NM_021139.2 A161A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93D-01A-11D-A387-09 chr5:35957434 C>T maps to NM_152404.3 Q310Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASV-01A-11D-A387-09 chr5:36066849 G>A maps to NM_174914.3 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr19:4910890 C>T maps to ENST00000398240 A11A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr19:4944159 C>A maps to ENST00000398240 R377R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A8I1-01A-11D-A36J-09 chr19:4954400 C>T maps to ENST00000398240 R633*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr6:34831895 A>G maps to NM_017754.3 S1111S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NV-01A-11D-A37C-09 chr6:34802095 G>A maps to NM_017754.3 L147L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OT-01A-11D-A28B-09 chr12:100452003 C>T maps to NM_015054.1 S1017S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93E-01A-11D-A37C-09 chr12:132396488 C>T maps to NM_003565.2 S317S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8W5-01B-11D-A37C-09 chr3:41795926 T>C maps to NM_017886.2 R749R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8WG-01A-11D-A37C-09 chr3:41497035 C>A maps to NM_017886.2 L1148L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GO-01A-11D-A37C-09 chr16:20360415 G>T maps to ENST00000424589 C102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FD-01A-11D-A33E-09 chr16:20355413 G>T maps to ENST00000424589 I454I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr16:20352507 G>A maps to ENST00000424589 G527G. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-2H-A9GF-01A-11D-A37C-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr21:43547904 C>T maps to NM_173568.3 R1346R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NS-01A-12D-A37C-09 chr21:43531563 C>G maps to NM_173568.3 T744T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GL-01A-12D-A37C-09 chr17:26875685 G>T maps to NM_005148.3 I86I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A8I0-01A-11D-A36J-09 chr17:26875694 G>T maps to NM_005148.3 I83I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3QL-01A-11D-A247-09 chr19:17767142 C>A maps to ENST00000428389 E366*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A4QS-01A-11D-A27G-09 chr19:17758182 G>T maps to ENST00000428389 I733I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93D-01A-11D-A387-09 chr19:17750316 G>A maps to ENST00000428389 S1046S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6XQ-01B-11D-A33E-09 chr19:17760329 G>T maps to ENST00000428389 L590L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8WC-01A-11D-A37C-09 chr19:17738352 G>A maps to ENST00000428389 N1383N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49Y-01A-11D-A27G-09 chr9:35398977 G>T maps to ENST00000396787 A1270A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FH-01A-11D-A33E-09 chr15:54590123 G>A maps to ENST00000260323 E1368E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93E-01A-11D-A37C-09 chr15:54305909 C>G maps to ENST00000260323 L270L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OE-01A-11D-A27G-09 chr15:54306905 G>A maps to ENST00000260323 K602K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASV-01A-11D-A387-09 chr15:54307296 C>T maps to ENST00000260323 Q733*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49N-01A-11D-A247-09 chr17:73827329 G>A maps to ENST00000412096 A849A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr15:91485758 G>A maps to NM_018671.3 L260L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EW-01A-11D-A36J-09 chr15:91489924 C>T maps to NM_018671.3 D427D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FG-01A-11D-A33E-09 chr17:33481675 G>A maps to NM_173167.2 L185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-A7RB-01A-11D-A351-09 chr17:33504596 C>T maps to NM_173167.2 L743L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZR-A9CJ-01B-11D-A387-09 chr17:33513523 C>T maps to NM_173167.2 A914A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93F-01A-21D-A37C-09 chr5:176289623 G>T did not map to a codon.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr10:73051549 G>T maps to NM_170744.3 L552L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RF-01A-13D-A33E-09 chr8:35624505 C>A maps to ENST00000416672 T805T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43E-01A-11D-A247-09 chr8:35606062 T>C maps to ENST00000416672 S600S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43I-01A-11D-A247-09 chr8:35616887 A>G maps to ENST00000416672 P743P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6Y2-01B-11D-A33E-09 chr7:1273297 G>A maps to NM_001080461.1 A139A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FO-01A-11D-A387-09 chr12:109547653 G>A maps to NM_080911.2 Q274Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A5B8-01A-11D-A28B-09 chr16:1463959 G>C maps to ENST00000508903 L58L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FP-01A-31D-A387-09 chr22:24919602 C>A maps to NM_016327.2 G311G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA7B-01A-31D-A403-09 chr22:24896221 C>A maps to NM_016327.2 P84P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3Y9-01A-12D-A247-09 chr19:18972826 G>A maps to ENST00000418384 E833E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr10:12070973 G>C maps to NM_015542.2 V305V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OR-01A-11D-A27G-09 chr10:11994104 C>T maps to NM_015542.2 R998R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GI-01A-11D-A37C-09 chr13:115067490 G>A maps to NM_023011.2 L431L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-AAPN-01A-11D-A403-09 chr13:115067485 C>T maps to NM_023011.2 R430*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3I8-01A-11D-A247-09 chr23:118975733 C>T did not map to a codon.
Sequencing variant TCGA-LN-A4A9-01A-11D-A28B-09 chr23:118979253 C>T did not map to a codon.
Sequencing variant TCGA-R6-A8WG-01A-11D-A37C-09 chr11:118828378 G>A did not map to a codon.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr3:48637504 G>A maps to NM_003365.2 S431S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr16:21980006 G>T did not map to a codon.
Sequencing variant TCGA-2H-A9GH-01A-11D-A37C-09 chr1:229771577 G>A maps to NM_014777.2 P406P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A8JD-01A-11D-A36J-09 chr1:229771163 G>T maps to NM_014777.2 T268T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4MR-01A-11D-A28B-09 chr7:43917444 C>T maps to NM_001077663.1 Q539Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EZ-01A-11D-A36J-09 chr7:43918838 C>A maps to NM_001077663.1 E75*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-AAPN-01A-11D-A403-09 chr9:131133691 C>T maps to NM_001135947.1 F11F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q9-A6FU-01A-11D-A31U-09 chr1:45479617 C>G maps to NM_000374.4 S171*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3QL-01A-11D-A247-09 chr19:17330465 G>A maps to NM_018467.3 A208A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-A7RC-01B-11D-A403-09 chr11:17546006 C>A maps to NM_153676.3 V250V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3QL-01A-11D-A247-09 chr17:72915949 G>A maps to NM_173477.2 H327H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GH-01A-11D-A37C-09 chr1:216373261 G>T maps to ENST00000366943 S1173*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RE-01A-11D-A33E-09 chr1:216074200 G>T maps to ENST00000366943 T2449T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A5B8-01A-11D-A28B-09 chr1:215848442 C>T maps to ENST00000366943 V4270V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FA-01A-11D-A33E-09 chr1:216073501 G>A maps to ENST00000366943 Y2503Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NI-01A-11D-A37C-09 chr1:216462678 G>T maps to ENST00000366943 C638*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A6-01A-11D-A27G-09 chr1:216258049 G>A maps to ENST00000366943 F1719F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HW-01A-22D-A351-09 chr1:215987081 T>C maps to ENST00000366943 L3245L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A8HZ-01A-11D-A36J-09 chr1:216052368 G>A maps to ENST00000366943 H2765H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6XQ-01B-11D-A33E-09 chr1:215802170 G>T maps to ENST00000366943 G5192G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EW-01A-11D-A36J-09 chr1:216595332 G>A maps to ENST00000366943 L116L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A6QS-01A-12D-A33E-09 chr1:62916243 A>T maps to NM_003368.4 G650G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr16:84797821 G>A maps to NM_005153.2 A595A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NT-01A-11D-A37C-09 chr16:84779187 C>T maps to NM_005153.2 P367P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HX-01A-11D-A33E-09 chr16:84778243 G>T maps to NM_005153.2 E53*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NG-01A-11D-A37C-09 chr23:47104087 C>T did not map to a codon.
Sequencing variant TCGA-L5-A8NQ-01A-11D-A36J-09 chr23:47101641 C>G did not map to a codon.
Sequencing variant TCGA-V5-A7RE-01A-11D-A351-09 chr23:47104173 G>T did not map to a codon.
Sequencing variant TCGA-IG-A8O2-01A-11D-A36J-09 chr3:179481947 C>T maps to NM_003940.2 R751*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8WG-01A-11D-A37C-09 chr3:179474858 G>A maps to NM_003940.2 L647L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASV-01A-11D-A387-09 chr3:179426665 C>T maps to NM_003940.2 N242N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A8I0-01A-11D-A36J-09 chr18:203114 G>T maps to NM_005151.3 L320L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6L6-01B-11D-A33E-09 chr18:197624 G>T maps to NM_005151.3 E202*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L7-A6VZ-01A-12D-A33E-09 chr12:62783637 A>T maps to ENST00000280377 R572*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43E-01A-11D-A247-09 chr21:30426151 C>G maps to NM_006447.2 L741L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A893-01A-11D-A36J-09 chr21:30402976 G>T maps to NM_006447.2 V41V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OR-01A-11D-A27G-09 chr8:11995297 G>C maps to NM_201402.2 V324V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NG-01A-11D-A37C-09 chr8:11995084 G>A maps to NM_201402.2 G395G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASX-01A-11D-A387-09 chr8:11996158 G>A maps to NM_201402.2 L37L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NE-01A-11D-A37C-09 chr9:132637911 G>T maps to NM_001008563.3 L764L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KH-A6WC-01A-11D-A33E-09 chr1:55599819 G>T maps to NM_015306.2 R1102R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NR-01A-11D-A37C-09 chr1:55560967 G>T maps to NM_015306.2 R2055R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA7I-01A-11D-A403-09 chr1:55595243 G>A maps to NM_015306.2 L1181L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OE-01A-11D-A27G-09 chr23:132161454 A>G did not map to a codon.
Sequencing variant TCGA-L5-A8NF-01A-11D-A37C-09 chr23:132160962 C>A did not map to a codon.
Sequencing variant TCGA-L5-A43C-01A-11D-A247-09 chr11:113698016 G>A maps to NM_020886.2 S375S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GG-01A-11D-A37C-09 chr15:63866316 T>A maps to NM_006537.2 C327*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A8JD-01A-11D-A36J-09 chr15:63862740 G>T maps to NM_006537.2 E291*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FG-01A-11D-A33E-09 chr16:23091493 T>G did not map to a codon.
Sequencing variant TCGA-R6-A8W8-01B-11D-A37C-09 chr17:58372091 G>A maps to NM_032582.3 H121H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr1:78207075 A>G maps to NM_015017.3 L71L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr2:61438923 G>A maps to NM_014709.3 C2941C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49L-01A-11D-A247-09 chr2:61468741 C>A maps to NM_014709.3 E2244*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3Y9-01A-12D-A247-09 chr11:77907299 G>A maps to NM_020798.2 K3K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-AAPN-01A-11D-A403-09 chr11:77924690 G>T did not map to a codon.
Sequencing variant TCGA-VR-A8EY-01A-11D-A36J-09 chr2:219346827 T>C maps to NM_020935.2 P600P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NV-01A-11D-A37C-09 chr2:85875087 G>A maps to NM_006590.2 Q533Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93C-01A-11D-A387-09 chr2:234438129 T>C maps to NM_018218.2 P511P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EP-01A-31D-A403-09 chr2:234405456 G>A maps to NM_018218.2 L924L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43I-01A-11D-A247-09 chr7:6183718 T>C maps to ENST00000404835 C294C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr7:6185157 C>T maps to ENST00000404835 Y334Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GR-01A-12D-A37C-09 chr17:9578206 G>T did not map to a codon.
Sequencing variant TCGA-Z6-A8JE-01A-11D-A37C-09 chr17:9549131 C>T maps to NM_153210.3 F61F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-A7RE-01A-11D-A351-09 chr6:99936084 G>A maps to NM_001080481.1 D235D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RE-01A-11D-A33E-09 chr4:53470743 G>A maps to NM_022832.3 F215F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8ER-01A-11D-A36J-09 chr4:53494204 C>T maps to NM_022832.3 A81A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr11:11969621 C>T maps to ENST00000399455 S1081S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr1:22016514 G>T maps to NM_032236.5 A987A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EO-01A-11D-A36J-09 chr1:22074728 G>A maps to NM_032236.5 C270C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NR-01A-11D-A37C-09 chr12:6965535 G>A maps to NM_001098536.1 W169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3Y9-01A-12D-A247-09 chr15:50792992 G>A maps to ENST00000456636 F335F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NS-01A-12D-A37C-09 chr15:50793016 C>T maps to ENST00000456636 L327L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA4G-01A-11D-A37C-09 chr15:50792967 A>G maps to ENST00000456636 *344R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RF-01A-13D-A33E-09 chr23:55515326 G>C did not map to a codon.
Sequencing variant TCGA-JY-A93D-01A-11D-A387-09 chr23:55515145 C>T did not map to a codon.
Sequencing variant TCGA-L5-A43M-01A-11D-A247-09 chr23:55515359 G>T did not map to a codon.
Sequencing variant TCGA-L5-A8NI-01A-11D-A37C-09 chr4:120192514 A>G maps to NM_019050.2 K500K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NS-01A-12D-A37C-09 chr10:75305349 G>A maps to NM_152586.3 F107F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43I-01A-11D-A247-09 chr17:5042961 C>T maps to NM_004505.2 C497C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NN-01A-11D-A37C-09 chr10:11504477 G>T maps to NM_001080491.2 R834R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6F8-01A-11D-A33E-09 chr16:8997211 G>C maps to NM_003470.2 Y584*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88Z-01A-11D-A36J-09 chr16:8998323 G>T maps to NM_003470.2 R558R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A2-01A-31D-A27G-09 chr15:50785053 C>T maps to NM_005154.3 N797N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A939-01A-12D-A37C-09 chr23:41084050 C>T did not map to a codon.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr23:41029817 T>C did not map to a codon.
Sequencing variant TCGA-L5-A891-01A-11D-A36J-09 chr23:41007637 C>T did not map to a codon.
Sequencing variant TCGA-LN-A4A4-01A-11D-A27G-09 chr23:41057780 G>T did not map to a codon.
Sequencing variant TCGA-M9-A5M8-01A-11D-A28B-09 chr23:41000019 A>C did not map to a codon.
Sequencing variant TCGA-ZR-A9CJ-01B-11D-A387-09 chr23:41057805 C>T did not map to a codon.
Sequencing variant TCGA-JY-A6FH-01A-11D-A33E-09 chr24:14954276 C>T did not map to a codon.
Sequencing variant TCGA-L5-A8NI-01A-11D-A37C-09 chr24:14951884 A>C did not map to a codon.
Sequencing variant TCGA-R6-A6L4-01A-11D-A31U-09 chr24:14924809 C>T did not map to a codon.
Sequencing variant TCGA-R6-A6L6-01B-11D-A33E-09 chr24:14821395 C>G did not map to a codon.
Sequencing variant TCGA-Z6-A8JE-01A-11D-A37C-09 chr24:14898608 G>T did not map to a codon.
Sequencing variant TCGA-L5-A8NE-01A-11D-A37C-09 chr13:31233168 G>T maps to NM_005800.4 L985L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NL-01A-12D-A37C-09 chr6:149208143 C>T maps to NM_005715.2 D90D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A5B8-01A-11D-A28B-09 chr13:52604064 C>T maps to NM_021645.5 F375F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr12:101739436 G>T maps to NM_014503.2 E1571*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OR-01A-11D-A27G-09 chr12:101774934 C>T maps to NM_014503.2 L2534L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A893-01A-11D-A36J-09 chr12:101702063 G>A maps to NM_014503.2 L699L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NF-01A-11D-A37C-09 chr12:101764853 C>T maps to NM_014503.2 L2236L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NI-01A-11D-A37C-09 chr12:101777367 G>C maps to NM_014503.2 G2659G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6XQ-01B-11D-A33E-09 chr12:101706007 G>T maps to NM_014503.2 E836*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FG-01A-11D-A33E-09 chr6:145124229 C>T maps to NM_007124.2 R3102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XP-A8T8-01A-11D-A36J-09 chr6:144800994 G>T maps to NM_007124.2 A1128A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A8JE-01A-11D-A37C-09 chr6:144814580 C>T maps to NM_007124.2 L1528L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43I-01A-11D-A247-09 chr3:190995875 T>G maps to NM_198152.3 R63R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FB-01A-11D-A33E-09 chr24:15417344 C>G did not map to a codon.
Sequencing variant TCGA-L5-A8NI-01A-11D-A37C-09 chr24:15582099 A>T did not map to a codon.
Sequencing variant TCGA-LN-A49S-01A-11D-A247-09 chr24:15591137 C>A did not map to a codon.
Sequencing variant TCGA-V5-A7RB-01A-11D-A351-09 chr24:15448173 A>C did not map to a codon.
Sequencing variant TCGA-V5-AASW-01A-11D-A403-09 chr2:106710607 C>T maps to ENST00000283148 P384P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OJ-01A-11D-A27G-09 chr16:70819616 G>A maps to NM_018052.3 D137D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A8JD-01A-11D-A36J-09 chr16:70796487 G>A maps to NM_018052.3 S442S. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-LN-A4A4-01A-11D-A27G-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-L5-A8NH-01A-11D-A37C-09 chr1:160394066 G>A maps to NM_020335.2 T433T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr1:160394993 C>T maps to NM_020335.2 S464S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HW-01A-22D-A351-09 chr1:160389225 G>A maps to NM_020335.2 E209E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NQ-01A-11D-A36J-09 chr18:9945045 G>A maps to NM_003574.5 E181E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6F8-01A-11D-A33E-09 chr6:31760767 G>T maps to NM_006295.2 R173R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EZ-01A-11D-A36J-09 chr6:31759424 A>G maps to NM_006295.2 H354H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S8-A6BW-01A-11D-A31U-09 chr6:30888138 G>A maps to NM_001167734.1 K471K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6F8-01A-11D-A33E-09 chr1:213161895 G>T maps to NM_001136474.1 L281L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr19:46025799 C>T maps to NM_003370.3 A227A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8WG-01A-11D-A37C-09 chr19:46029232 G>A maps to NM_003370.3 L359L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3YC-01A-11D-A247-09 chr17:41168410 C>G maps to NM_006373.3 L337L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GF-01A-11D-A37C-09 chr16:78005823 T>A maps to NM_020927.1 T385T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EQ-01A-11D-A36J-09 chr16:77850904 T>C maps to NM_020927.1 S107S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XP-A8T8-01A-11D-A36J-09 chr19:6848008 G>A maps to NM_005428.2 W671*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr9:136726533 C>T maps to NM_001134398.1 R114R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OJ-01A-11D-A27G-09 chr9:136671267 G>T maps to NM_001134398.1 A257A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OJ-01A-11D-A27G-09 chr10:118893719 C>T maps to NM_001112704.1 A268A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OT-01A-11D-A28B-09 chr10:118896156 G>T maps to NM_001112704.1 S85S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93F-01A-21D-A37C-09 chr2:71160033 G>T maps to NM_012476.2 L191L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6F8-01A-11D-A33E-09 chr23:154444769 T>C did not map to a codon.
Sequencing variant TCGA-2H-A9GJ-01A-11D-A37C-09 chr5:82841390 G>T maps to NM_004385.4 G3101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43C-01A-11D-A247-09 chr5:82837980 T>C maps to NM_004385.4 T3053T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr5:82786220 G>A maps to NM_004385.4 A125A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NE-01A-11D-A37C-09 chr5:82815483 A>G maps to NM_004385.4 S453S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L7-A6VZ-01A-12D-A33E-09 chr5:82833725 C>A maps to NM_004385.4 S1635*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S8-A6BV-01A-21D-A31U-09 chr5:82836372 C>T maps to NM_004385.4 D2517D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A8JD-01A-11D-A36J-09 chr5:82818042 G>A maps to NM_004385.4 A1306A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GF-01A-11D-A37C-09 chr10:75867025 C>T maps to NM_014000.2 L825L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49M-01A-21D-A27G-09 chr10:75802873 C>T maps to NM_014000.2 Q68*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KH-A6WC-01A-11D-A33E-09 chr9:35062126 G>T maps to NM_007126.3 G318G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6Y2-01B-11D-A33E-09 chr9:35059170 C>A maps to NM_007126.3 G684*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GO-01A-11D-A37C-09 chr23:8434031 G>A did not map to a codon.
Sequencing variant TCGA-LN-A4A4-01A-11D-A27G-09 chr4:177650745 G>C maps to NM_005429.2 S101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A5B8-01A-11D-A28B-09 chr10:135053602 C>T maps to NM_014468.2 S190S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6Y2-01B-11D-A33E-09 chr10:135053542 C>T maps to NM_014468.2 Y170Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NS-01A-12D-A37C-09 chr17:56060673 A>C maps to NM_007146.2 P38P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A4P3-01A-11D-A27G-09 chr12:95656734 G>T maps to NM_017599.3 L104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88W-01A-11D-A351-09 chr2:219294099 G>T maps to NM_007127.2 P220P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NT-01A-11D-A37C-09 chr2:219303391 C>T maps to NM_007127.2 S724S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A893-01A-11D-A36J-09 chr6:153075358 G>T maps to NM_003381.2 E56*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L7-A6VZ-01A-12D-A33E-09 chr6:153073407 T>G maps to NM_003381.2 P32P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6F8-01A-11D-A33E-09 chr3:42567436 G>A maps to NM_004624.3 P117P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NK-01A-21D-A37C-09 chr16:31104657 G>A maps to ENST00000319788 I86I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HY-01A-12D-A351-09 chr19:53761867 C>T maps to NM_173856.2 H80H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49Y-01A-11D-A27G-09 chr19:53770336 G>C maps to NM_173857.2 L194L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88T-01A-11D-A351-09 chr6:133032957 A>C maps to NM_004666.2 T77T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A2-01A-31D-A27G-09 chr6:133015314 G>A maps to NM_004666.2 G116G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A2-01A-31D-A27G-09 chr6:133072385 G>A maps to NM_004665.2 C366C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASX-01A-11D-A387-09 chr9:79954670 G>A maps to ENST00000376646 Q2206Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93D-01A-11D-A387-09 chr8:100286533 C>A maps to NM_017890.3 S875*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8W5-01B-11D-A37C-09 chr8:100865816 G>A maps to NM_017890.3 P3425P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3I8-01A-11D-A247-09 chr15:62209683 G>T maps to NM_020821.2 L2637L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr15:62202413 G>A maps to NM_020821.2 R2936*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RF-01A-13D-A33E-09 chr1:12313874 G>T maps to NM_015378.2 E221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A9VB-01A-21D-A37C-09 chr1:12336368 T>A maps to NM_015378.2 T908T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RE-01A-11D-A33E-09 chr20:2845629 G>T maps to NM_022575.2 E645*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49S-01A-11D-A247-09 chr20:2846871 C>T maps to NM_022575.2 I762I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49V-01A-11D-A247-09 chr15:41192272 C>T maps to NM_020857.2 P419P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8W8-01B-11D-A37C-09 chr15:41195001 C>T maps to NM_020857.2 F795F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr11:134109962 C>T maps to NM_052875.3 S153S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OX-01A-21D-A28B-09 chr13:52997735 G>T maps to NM_016075.2 C271*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88Z-01A-11D-A36J-09 chr11:60899315 C>T maps to NM_017966.4 P348P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr15:42479522 C>T maps to ENST00000348544 A171A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49S-01A-11D-A247-09 chr15:42470517 C>A maps to ENST00000348544 V297V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A51D-01A-11D-A27G-09 chr1:150048326 C>T maps to NM_007259.3 I102I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FQ-01A-31D-A387-09 chr1:150082616 G>A maps to NM_007259.3 Q500Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr16:69355061 C>T maps to NM_013245.2 H320H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8ER-01A-11D-A36J-09 chr16:69349972 G>A maps to NM_013245.2 A28A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EX-01A-11D-A36J-09 chr16:69352762 C>T maps to NM_013245.2 N127N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OJ-01A-11D-A27G-09 chr18:61064443 G>A maps to NM_004869.3 A305A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49K-01A-11D-A247-09 chr18:61077551 T>C maps to NM_004869.3 E89E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EX-01A-11D-A36J-09 chr18:61070964 A>G maps to NM_004869.3 P153P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A4P3-01A-11D-A27G-09 chr1:151158057 G>T maps to ENST00000354473 T103T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FB-01A-11D-A33E-09 chr23:107320558 G>T did not map to a codon.
Sequencing variant TCGA-2H-A9GJ-01A-11D-A37C-09 chr12:118506353 T>C maps to NM_019086.5 E465E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GJ-01A-11D-A37C-09 chr23:65244938 T>G did not map to a codon.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr23:65244880 T>C did not map to a codon.
Sequencing variant TCGA-LN-A4A1-01A-21D-A27G-09 chr23:65259807 C>T did not map to a codon.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr1:159827703 G>A maps to NM_001013661.1 N161N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr2:17836615 C>T maps to NM_003385.4 S177S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NV-01A-11D-A37C-09 chr19:54544289 G>A maps to NM_198481.3 S212S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A5U6-01A-11D-A28B-09 chr7:54617840 C>A maps to ENST00000404951 I204I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KH-A6WC-01A-11D-A33E-09 chr20:25057115 G>T maps to NM_014588.4 G293G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HX-01A-11D-A33E-09 chr20:25058369 G>A maps to NM_014588.4 L253L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HZ-01A-31D-A351-09 chr10:114220328 A>G maps to NM_145206.2 E47E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NK-01A-21D-A37C-09 chr10:116045740 G>A maps to NM_198496.1 L347L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HY-01A-12D-A351-09 chr10:116048823 C>T maps to NM_198496.1 D566D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X8-AAAR-01A-11D-A403-09 chr10:116048898 G>A maps to NM_198496.1 R591R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49M-01A-21D-A27G-09 chr16:22149767 C>T maps to NM_173615.3 Q743*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6Y0-01B-11D-A33E-09 chr16:22159580 G>T maps to NM_173615.3 E980*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L7-A6VZ-01A-12D-A33E-09 chr2:98709642 G>T maps to NM_144992.4 E30*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr11:123994432 C>T maps to NM_014622.4 A362A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EZ-01A-11D-A36J-09 chr11:61048111 G>A maps to NM_152718.2 C436C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RE-01A-11D-A33E-09 chr12:6058966 A>G maps to NM_000552.3 D2746D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A625-01A-11D-A31U-09 chr12:6153591 G>T maps to NM_000552.3 P769P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FG-01A-11D-A33E-09 chr12:6132812 C>T maps to NM_000552.3 R1121R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NR-01A-11D-A37C-09 chr12:6182794 G>A maps to NM_000552.3 C329C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L7-A6VZ-01A-12D-A33E-09 chr12:6167090 G>A maps to NM_000552.3 N551N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A5U7-01A-11D-A31U-09 chr12:6167104 C>A maps to NM_000552.3 E547*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HZ-01A-31D-A351-09 chr12:6103139 G>T maps to NM_000552.3 I2162I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FO-01A-11D-A387-09 chr12:6161848 G>T maps to NM_000552.3 A682A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NE-01A-11D-A37C-09 chr6:110428321 C>T maps to NM_003931.2 L166L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RF-01A-13D-A33E-09 chr13:27216439 G>A maps to NM_006646.5 R11R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88W-01A-11D-A351-09 chr13:27255247 G>T maps to NM_006646.5 L258L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FP-01A-31D-A387-09 chr13:27256797 G>T maps to NM_006646.5 P346P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZR-A9CJ-01B-11D-A387-09 chr13:27256995 T>G maps to NM_006646.5 S412S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6L6-01B-11D-A33E-09 chr13:41642796 A>G maps to NM_007187.3 K121K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HX-01A-11D-A33E-09 chr7:74486514 G>T maps to NM_030798.3 V131V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr7:71135006 A>G maps to NM_022479.1 K439K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NS-01A-12D-A37C-09 chr7:71036302 C>G maps to NM_022479.1 V332V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASX-01A-11D-A387-09 chr7:70885938 G>C maps to NM_022479.1 V270V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A893-01A-11D-A36J-09 chr2:224760339 G>A maps to NM_020830.3 V202V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49S-01A-11D-A247-09 chr13:52333895 C>T maps to NM_052950.3 V398V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GH-01A-11D-A37C-09 chr4:85696070 A>C maps to NM_014991.4 T1552T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6F8-01A-11D-A33E-09 chr4:85715780 C>T maps to NM_014991.4 V1126V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49L-01A-11D-A247-09 chr4:85711027 C>A maps to NM_014991.4 E1174*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HX-01A-11D-A33E-09 chr4:85724487 G>A maps to NM_014991.4 A854A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EU-01A-11D-A36J-09 chr4:10099382 G>T maps to NM_017491.3 C170*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49L-01A-11D-A247-09 chr23:48458002 G>T did not map to a codon.
Sequencing variant TCGA-IG-A4QS-01A-11D-A27G-09 chr4:177046414 T>C maps to NM_170710.4 S257S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A891-01A-11D-A36J-09 chr4:177037077 C>A maps to NM_170710.4 I109I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NU-01A-11D-A36J-09 chr4:177061047 A>T maps to NM_170710.4 G479G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6L4-01A-11D-A31U-09 chr4:177098796 A>T maps to NM_170710.4 K1281*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6XQ-01B-11D-A33E-09 chr4:177072974 G>T maps to NM_170710.4 E797*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A3-01A-11D-A27G-09 chr16:736117 G>T maps to ENST00000248142 L597L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OH-01A-11D-A27G-09 chr1:224621664 G>T maps to NM_025160.6 S48*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A939-01A-12D-A37C-09 chr6:170043853 C>T maps to NM_182552.3 L562L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A4P3-01A-11D-A27G-09 chr1:118477289 G>T maps to NM_006784.2 L122L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GG-01A-11D-A37C-09 chr9:116082778 C>A did not map to a codon.
Sequencing variant TCGA-L5-A8NQ-01A-11D-A36J-09 chr9:116085327 G>A maps to NM_001012361.2 G144G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GK-01A-11D-A37C-09 chr2:128477672 C>T maps to NM_018383.4 L642L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43E-01A-11D-A247-09 chr2:128477432 C>T maps to NM_018383.4 P722P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NR-01A-11D-A37C-09 chr9:131403137 C>T maps to NM_052844.3 T89T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr2:20137694 A>C maps to NM_001006657.1 A703A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GF-01A-11D-A37C-09 chr5:110459843 A>C maps to NM_139281.2 S825S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GF-01A-11D-A37C-09 chr21:44283654 C>T maps to NM_018669.4 K116K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FD-01A-11D-A33E-09 chr23:48935400 C>A did not map to a codon.
Sequencing variant TCGA-L5-A4OS-01A-11D-A28B-09 chr3:113125832 G>A maps to NM_001164496.1 R316*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A2-01A-31D-A27G-09 chr3:113025139 G>A maps to NM_001164496.1 R1556*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A8-01A-32D-A27G-09 chr3:113145024 G>T maps to NM_001164496.1 S118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NT-01A-11D-A37C-09 chr16:74946164 G>A maps to NM_030581.3 N440N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49V-01A-11D-A247-09 chr7:158695218 T>C maps to NM_018051.4 I430I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FP-01A-31D-A387-09 chr19:36573984 C>G maps to NM_001083961.1 Y464*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A939-01A-12D-A37C-09 chr1:43675419 C>T maps to NM_001195831.1 R588*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GH-01A-11D-A37C-09 chr12:122359576 A>G maps to NM_144668.4 S122S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FE-01A-11D-A33E-09 chr12:122361695 G>T maps to NM_144668.4 E183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr12:122405916 A>T maps to NM_144668.4 G871G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NN-01A-11D-A37C-09 chr12:122359235 C>T maps to NM_144668.4 R9*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8WG-01A-11D-A37C-09 chr12:122398615 G>T maps to NM_144668.4 L753L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr8:124153105 G>T maps to NM_145647.3 E869*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88T-01A-11D-A351-09 chr8:124089434 C>T maps to NM_145647.3 G54G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GH-01A-11D-A37C-09 chr2:228750091 T>C maps to NM_178821.1 H22H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6F8-01A-11D-A33E-09 chr18:54346667 G>T maps to NM_015285.2 G89*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NE-01A-11D-A37C-09 chr18:54426149 T>C maps to NM_015285.2 T938T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NL-01A-12D-A37C-09 chr15:54003576 G>A maps to NM_182758.2 I271I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GH-01A-11D-A37C-09 chr11:62606982 C>T maps to NM_018093.2 L20L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EO-01A-11D-A36J-09 chr2:190320167 G>T maps to NM_032168.1 E166*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8W8-01B-11D-A37C-09 chr1:67288088 A>T maps to NM_024763.4 S817S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr1:3548108 C>T maps to NM_017818.3 R387R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3QL-01A-11D-A247-09 chr17:1639331 G>T did not map to a codon.
Sequencing variant TCGA-R6-A8W8-01B-11D-A37C-09 chr17:1637130 C>T maps to NM_001163809.1 N1600N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr19:33623176 C>A maps to NM_173479.3 S34S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FG-01A-11D-A33E-09 chr16:708984 C>A maps to NM_145294.4 L995L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr16:708574 C>T maps to NM_145294.4 D939D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49M-01A-21D-A27G-09 chr7:134878361 G>A maps to NM_014149.3 L486L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XP-A8T6-01A-11D-A36J-09 chr7:134882798 G>T maps to NM_014149.3 R332R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GG-01A-11D-A37C-09 chr2:68384440 G>T maps to NM_138458.2 V45V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr1:27622890 G>T maps to ENST00000319394 G316G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8ET-01A-11D-A403-09 chr1:27609832 C>T maps to ENST00000319394 L62L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NK-01A-21D-A37C-09 chr11:9603161 C>T maps to NM_003390.3 Q409*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OP-01A-11D-A27G-09 chr7:141427102 G>A did not map to a codon.
Sequencing variant TCGA-L5-A8NG-01A-11D-A37C-09 chr7:141424036 G>T maps to NM_001105558.1 G395*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NJ-01A-11D-A36J-09 chr20:44258463 G>A maps to NM_080753.2 Q4Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OP-01A-11D-A27G-09 chr16:682589 G>A maps to NM_053284.2 A60A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GO-01A-11D-A37C-09 chr8:38135882 T>A maps to NM_023034.1 R1270*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4MR-01A-11D-A28B-09 chr8:38173481 G>T maps to NM_023034.1 S645*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OJ-01A-11D-A27G-09 chr2:175436911 G>A maps to NM_003387.4 P207P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GJ-01A-11D-A37C-09 chr17:38421088 C>T maps to NM_133264.4 R221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3YB-01A-11D-A247-09 chr19:15538261 G>A maps to ENST00000389282 H1061H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RE-01A-11D-A33E-09 chr12:977759 T>C maps to NM_001184985.1 T956T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A4QS-01A-11D-A27G-09 chr12:1005334 G>T maps to NM_001184985.1 V2154V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EU-01A-11D-A36J-09 chr12:977828 A>G maps to NM_001184985.1 G979G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OT-01A-11D-A28B-09 chr23:54259371 T>A did not map to a codon.
Sequencing variant TCGA-LN-A49M-01A-21D-A27G-09 chr2:219757941 C>T maps to NM_025216.2 F401F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASX-01A-11D-A387-09 chr11:75905724 G>T maps to NM_004626.2 L161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93E-01A-11D-A37C-09 chr1:113062920 C>T maps to NM_024494.2 G322G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OP-01A-11D-A27G-09 chr17:44851046 G>A maps to NM_030753.3 P103P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S8-A6BV-01A-21D-A31U-09 chr22:46327148 G>A maps to NM_058238.2 C133C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A891-01A-11D-A36J-09 chr10:102240761 G>T maps to NM_003393.3 R83R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr21:40762673 G>A maps to NM_004627.4 A51A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GK-01A-11D-A37C-09 chr8:30999100 C>T maps to NM_000553.4 C1041C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr8:30921933 C>T maps to NM_000553.4 H113H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr8:30946427 T>C maps to NM_000553.4 N533N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr8:30977865 T>C maps to NM_000553.4 I852I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FP-01A-31D-A387-09 chr8:31004644 G>T did not map to a codon.
Sequencing variant TCGA-2H-A9GL-01A-12D-A37C-09 chr6:2779581 C>T maps to NM_020135.2 Q448*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XP-A8T8-01A-11D-A36J-09 chr6:2783658 C>T maps to NM_020135.2 C502C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GL-01A-12D-A37C-09 chr17:6021338 C>T maps to NM_015253.1 S402S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A8HZ-01A-11D-A36J-09 chr11:32456396 G>T maps to NM_024426.4 S165S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L7-A6VZ-01A-12D-A33E-09 chr6:160176453 G>A maps to NM_004906.3 A334A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RE-01A-11D-A33E-09 chr23:10096086 G>C did not map to a codon.
Sequencing variant TCGA-JY-A93E-01A-11D-A37C-09 chr23:10046904 G>T did not map to a codon.
Sequencing variant TCGA-L5-A4OJ-01A-11D-A27G-09 chr23:10096178 C>T did not map to a codon.
Sequencing variant TCGA-VR-A8EO-01A-11D-A36J-09 chr23:10035343 G>T did not map to a codon.
Sequencing variant TCGA-JY-A6FH-01A-11D-A33E-09 chr8:87473461 G>T maps to NM_007013.3 E837*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8W5-01B-11D-A37C-09 chr8:87424099 C>G maps to NM_007013.3 S353*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GK-01A-11D-A37C-09 chr3:149260123 G>A maps to NM_001168278.1 Q257*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3I8-01A-11D-A247-09 chr3:149290714 G>C maps to NM_001168278.1 L168L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S8-A6BV-01A-21D-A31U-09 chr3:149260150 G>A maps to NM_001168278.1 R248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HZ-01A-31D-A351-09 chr19:7684914 C>A maps to NM_020196.2 L771L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OW-01A-11D-A28B-09 chr3:46062566 C>T maps to NM_005283.2 G291G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FB-01A-11D-A33E-09 chr2:31569642 C>A maps to NM_000379.3 E1115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OU-01A-11D-A28B-09 chr2:31567571 A>G maps to NM_000379.3 L1128L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HV-01A-21D-A351-09 chr2:31620584 G>A maps to NM_000379.3 C148C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr23:2670326 G>C did not map to a codon.
Sequencing variant TCGA-R6-A6Y0-01B-11D-A33E-09 chr3:39225950 G>T maps to NM_194293.2 S1662S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A9VB-01A-21D-A37C-09 chr3:39227195 C>T maps to NM_194293.2 P1247P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3Y9-01A-12D-A247-09 chr2:168101828 A>G maps to NM_152381.5 V1309V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6F8-01A-11D-A33E-09 chr2:168102104 A>G maps to NM_152381.5 E1401E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OP-01A-11D-A27G-09 chr2:168107318 C>T maps to NM_152381.5 N3139N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NN-01A-11D-A37C-09 chr2:168099624 C>T maps to NM_152381.5 Q575*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NW-01A-11D-A37C-09 chr2:168115787 T>A maps to ENST00000420519 L944*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49W-01A-11D-A27G-09 chr2:168097246 G>T did not map to a codon.
Sequencing variant TCGA-V5-A7RE-01A-11D-A351-09 chr2:168099200 C>A maps to NM_152381.5 V433V. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-VR-A8EQ-01A-11D-A36J-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-IG-A5B8-01A-11D-A28B-09 chr22:17288834 G>T maps to NM_175878.3 L43L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GG-01A-11D-A37C-09 chr8:56436614 C>A maps to NM_052898.1 V594V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49Y-01A-11D-A27G-09 chr8:56436365 C>G maps to NM_052898.1 A511A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GR-01A-12D-A37C-09 chr8:6669804 G>T maps to NM_207411.4 I325I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NF-01A-11D-A37C-09 chr20:30584966 G>T maps to NM_001011718.1 E483*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FP-01A-31D-A387-09 chr20:30585019 C>A maps to NM_001011718.1 V500V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q9-A6FW-01A-31D-A31U-09 chr20:30584920 C>T maps to NM_001011718.1 D467D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FP-01A-31D-A387-09 chr1:28293101 G>A maps to NM_018053.2 P193P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GI-01A-11D-A37C-09 chr3:14187440 T>C maps to NM_004628.4 *941W. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OQ-01A-11D-A27G-09 chr10:111647945 A>G maps to NM_020383.3 Y171Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6XQ-01B-11D-A33E-09 chr10:111640656 G>T maps to NM_020383.3 I358I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A938-01A-11D-A37C-09 chr23:128888455 C>T did not map to a codon.
Sequencing variant TCGA-L5-A4OJ-01A-11D-A27G-09 chr23:128888488 G>T did not map to a codon.
Sequencing variant TCGA-LN-A49M-01A-21D-A27G-09 chr23:128885743 G>C did not map to a codon.
Sequencing variant TCGA-XP-A8T6-01A-11D-A36J-09 chr23:128881661 G>T did not map to a codon.
Sequencing variant TCGA-R6-A6XG-01B-11D-A33E-09 chr2:61719268 G>T maps to NM_003400.3 R596R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q9-A6FU-01A-11D-A31U-09 chr13:21417978 G>C maps to NM_022459.4 S168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NQ-01A-11D-A36J-09 chr6:43528001 G>A maps to NM_020750.2 L378L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A8HZ-01A-11D-A36J-09 chr6:43501710 T>C maps to NM_020750.2 L792L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A8HZ-01A-11D-A36J-09 chr6:43528717 T>C maps to NM_020750.2 P346P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GN-01A-11D-A37C-09 chr16:28133017 G>T maps to NM_015171.2 S611*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OP-01A-11D-A27G-09 chr8:21840252 G>T maps to ENST00000434536 E412*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NS-01A-12D-A37C-09 chr12:64811878 C>G maps to NM_007235.3 S85*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S8-A6BW-01A-11D-A31U-09 chr12:64823864 C>T maps to NM_007235.3 Q592*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GR-01A-12D-A37C-09 chr19:44056235 G>A maps to NM_006297.2 R339*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A97H-01A-11D-A387-09 chr19:44055805 C>T maps to NM_006297.2 Q372Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8Q7-01A-11D-A37C-09 chr7:152345899 T>A maps to NM_005431.1 R224*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6Y2-01B-11D-A33E-09 chr3:38437042 G>T maps to NM_005108.3 E447*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr16:17292231 T>G maps to NM_022166.3 R376R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49S-01A-11D-A247-09 chr16:17202584 C>T maps to NM_022166.3 L949L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NT-01A-11D-A37C-09 chr1:33241584 G>A maps to NM_003680.3 S528S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FE-01A-11D-A33E-09 chr5:143545144 G>T maps to NM_030799.7 S45*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-A7RE-01A-11D-A351-09 chr23:67751766 G>A did not map to a codon.
Sequencing variant TCGA-JY-A938-01A-11D-A37C-09 chr14:75247266 C>T maps to NM_019589.2 Q424*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr14:75248114 C>T maps to NM_019589.2 R457*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FQ-01A-31D-A387-09 chr14:75266004 G>A maps to NM_019589.2 P1335P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XP-A8T6-01A-11D-A36J-09 chr14:75265986 A>G maps to NM_019589.2 P1329P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A5B8-01A-11D-A28B-09 chr10:27434387 G>C maps to NM_139312.1 V157V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6F8-01A-11D-A33E-09 chr2:135756497 C>T maps to NM_025052.3 T128T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr2:135763095 G>A maps to NM_025052.3 F48F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49O-01A-11D-A247-09 chr2:135749142 C>T maps to NM_025052.3 S194S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-A7RC-01B-11D-A403-09 chr2:135722472 G>A maps to NM_025052.3 R1312*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr5:112889314 T>G maps to NM_022828.3 Y632*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA4D-01A-11D-A37C-09 chr5:112903394 C>A maps to NM_022828.3 P1031P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6L6-01B-11D-A33E-09 chr7:75959219 C>A maps to NM_012479.3 G140*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8WG-01A-11D-A37C-09 chr17:74076365 C>T maps to NM_180990.3 P135P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93C-01A-11D-A387-09 chr2:174074530 T>C maps to NM_016653.2 C273C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GJ-01A-11D-A37C-09 chr7:100350073 C>T maps to ENST00000349350 I782I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NH-01A-11D-A37C-09 chr7:100377344 C>T maps to ENST00000349350 P2198P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NV-01A-11D-A37C-09 chr7:100369491 G>A maps to ENST00000349350 V1758V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr2:98351784 C>T maps to NM_001079.3 R385R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OS-01A-11D-A28B-09 chr2:98349435 G>A maps to NM_001079.3 A218A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GG-01A-11D-A37C-09 chr3:166958583 A>C maps to ENST00000307529 T839T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GO-01A-11D-A37C-09 chr3:167023730 A>G maps to ENST00000307529 T475T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A4P3-01A-11D-A27G-09 chr3:166958593 G>T maps to ENST00000307529 S836*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GH-01A-11D-A37C-09 chr23:2406810 G>A did not map to a codon.
Sequencing variant TCGA-JY-A93C-01A-11D-A387-09 chr23:2408325 G>A did not map to a codon.
Sequencing variant TCGA-L5-A4OJ-01A-11D-A27G-09 chr23:2407850 G>T did not map to a codon.
Sequencing variant TCGA-R6-A6XG-01B-11D-A33E-09 chr23:2407511 G>A did not map to a codon.
Sequencing variant TCGA-L5-A8NN-01A-11D-A37C-09 chr22:50279479 G>T maps to NM_014838.2 E724*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8WC-01A-11D-A37C-09 chr20:56179775 A>T maps to NM_030776.2 I381I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OT-01A-11D-A28B-09 chr11:114112973 G>A maps to NM_001018011.1 A513A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A8I0-01A-11D-A36J-09 chr11:113934618 C>A maps to NM_001018011.1 T199T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8W8-01B-11D-A37C-09 chr11:114118001 G>A maps to NM_001018011.1 T569T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49M-01A-21D-A27G-09 chr1:16271286 G>A maps to ENST00000375733 I325I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OM-01A-11D-A27G-09 chr3:114099154 C>T maps to NM_001164342.1 L36L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A5-01A-21D-A27G-09 chr6:33284414 G>A maps to NM_001145338.1 S93S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FP-01A-31D-A387-09 chr6:33283127 G>A maps to NM_001145338.1 F522F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8WC-01A-11D-A37C-09 chr6:33284639 C>A maps to NM_001145338.1 S18S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A8I1-01A-11D-A36J-09 chr23:119388905 G>T did not map to a codon.
Sequencing variant TCGA-IG-A5B8-01A-11D-A28B-09 chr3:141162093 C>G maps to NM_001080412.2 S288S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88T-01A-11D-A351-09 chr3:141163938 C>T maps to NM_001080412.2 F903F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A8HZ-01A-11D-A36J-09 chr3:141161328 C>T maps to NM_001080412.2 C33C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q9-A6FU-01A-11D-A31U-09 chr12:57398626 G>C maps to NM_014830.2 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RE-01A-11D-A33E-09 chr17:7369676 G>A maps to NM_020899.3 L148L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EQ-01A-11D-A36J-09 chr17:7366572 G>A maps to NM_020899.3 G576G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X8-AAAR-01A-11D-A403-09 chr17:7365492 G>T maps to NM_020899.3 Y936*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FP-01A-31D-A387-09 chr1:22839480 G>T maps to NM_014870.3 G842G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA7I-01A-11D-A403-09 chr20:62421603 C>T maps to NM_025224.2 P169P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OE-01A-11D-A27G-09 chr3:42700677 C>T maps to NM_145166.3 D277D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8W8-01B-11D-A37C-09 chr3:42701320 G>A did not map to a codon.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr1:6649031 G>A maps to NM_005341.2 R609R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6Y0-01B-11D-A33E-09 chr4:4304044 C>G maps to NM_145291.3 S161*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FA-01A-11D-A33E-09 chr9:37440550 G>T maps to NM_014872.2 R666R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NT-01A-11D-A37C-09 chr9:37442365 G>T maps to NM_014872.2 T61T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A625-01A-11D-A31U-09 chr19:4054660 C>T maps to NM_015898.2 A190A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GI-01A-11D-A37C-09 chr1:154987711 G>T maps to ENST00000417934 P226P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3I8-01A-11D-A247-09 chr23:64709205 C>A did not map to a codon.
Sequencing variant TCGA-JY-A6FG-01A-11D-A33E-09 chr23:64709146 G>T did not map to a codon.
Sequencing variant TCGA-L7-A6VZ-01A-12D-A33E-09 chr23:64718910 A>G did not map to a codon.
Sequencing variant TCGA-LN-A49M-01A-21D-A27G-09 chr23:64722231 T>C did not map to a codon.
Sequencing variant TCGA-LN-A9FQ-01A-31D-A387-09 chr23:64709052 G>A did not map to a codon.
Sequencing variant TCGA-VR-A8EY-01A-11D-A36J-09 chr23:64721860 A>G did not map to a codon.
Sequencing variant TCGA-LN-A4A3-01A-11D-A27G-09 chr11:110008025 G>A maps to NM_033390.1 R220R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASW-01A-11D-A403-09 chr11:110035942 G>T maps to NM_033390.1 P711P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88V-01A-11D-A351-09 chr13:46559747 C>T maps to ENST00000242848 R468R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NE-01A-11D-A37C-09 chr13:46549565 G>A maps to ENST00000242848 R774*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FP-01A-31D-A387-09 chr13:46549673 C>A maps to ENST00000242848 E738*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8WC-01A-11D-A37C-09 chr13:46562990 G>A maps to ENST00000242848 R396*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASW-01A-11D-A403-09 chr13:46559794 G>A maps to ENST00000242848 R453*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EW-01A-11D-A36J-09 chr13:46549820 G>T maps to ENST00000242848 R689R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3I8-01A-11D-A247-09 chr8:144522385 T>G maps to NM_015117.2 S880S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OU-01A-11D-A28B-09 chr8:144621395 G>T maps to NM_015117.2 G47G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr8:144621272 G>A maps to NM_015117.2 A88A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASV-01A-11D-A387-09 chr8:144620513 A>G maps to NM_015117.2 S341S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93F-01A-21D-A37C-09 chr2:113074097 C>T maps to NM_198581.2 Q267*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49U-01A-31D-A27G-09 chr22:41723331 C>T maps to ENST00000351589 Y136Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FO-01A-11D-A387-09 chr22:41739431 C>A maps to ENST00000351589 G453G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OF-01A-11D-A27G-09 chr1:52991244 C>T maps to NM_001009881.2 S236S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NG-01A-11D-A37C-09 chr23:117959805 C>T did not map to a codon.
Sequencing variant TCGA-R6-A6KZ-01A-11D-A31U-09 chr23:117959407 A>G did not map to a codon.
Sequencing variant TCGA-JY-A6FH-01A-11D-A33E-09 chr23:111698081 A>G did not map to a codon.
Sequencing variant TCGA-VR-A8EQ-01A-11D-A36J-09 chr23:111698081 A>C did not map to a codon.
Sequencing variant TCGA-LN-A4MQ-01A-11D-A28B-09 chr23:103359996 G>A did not map to a codon.
Sequencing variant TCGA-LN-A8HZ-01A-11D-A36J-09 chr23:103359000 C>A did not map to a codon.
Sequencing variant TCGA-LN-A4A6-01A-11D-A27G-09 chr18:60241387 C>T maps to NM_017742.4 Q692*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A8HZ-01A-11D-A36J-09 chr10:81154163 G>A maps to NM_153367.3 Y160Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GM-01A-11D-A37C-09 chr23:77912709 T>G did not map to a codon.
Sequencing variant TCGA-IG-A4QS-01A-11D-A27G-09 chr23:77913150 A>C did not map to a codon.
Sequencing variant TCGA-L5-A4OJ-01A-11D-A27G-09 chr23:77912921 G>T did not map to a codon.
Sequencing variant TCGA-L5-A8NH-01A-11D-A37C-09 chr23:77913194 A>C did not map to a codon.
Sequencing variant TCGA-L5-A8NW-01A-11D-A37C-09 chr23:77913423 T>A did not map to a codon.
Sequencing variant TCGA-R6-A6DN-01B-11D-A31U-09 chr23:77912926 G>T did not map to a codon.
Sequencing variant TCGA-2H-A9GH-01A-11D-A37C-09 chr9:88967670 G>A maps to NM_024617.3 C148C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RF-01A-13D-A33E-09 chr12:122962496 C>A maps to NM_017612.2 V412V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L7-A6VZ-01A-12D-A33E-09 chr5:80604423 C>T maps to NM_032280.2 C143C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr12:42707710 C>T maps to NM_033114.3 K137K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr7:100016811 C>A maps to NM_017984.3 E95*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-A7RE-01A-11D-A351-09 chr2:207171384 G>T maps to NM_020923.1 P711P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA7B-01A-31D-A403-09 chr2:207172017 C>A maps to NM_020923.1 I922I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A5S3-01A-11D-A28B-09 chr16:67440126 G>A maps to NM_013304.2 H76H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A97I-01A-11D-A387-09 chr5:840628 G>A maps to NM_024786.2 L255L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FD-01A-11D-A33E-09 chr23:74644565 C>A did not map to a codon.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr23:74636972 G>T did not map to a codon.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr23:74636980 G>T did not map to a codon.
Sequencing variant TCGA-IG-A97H-01A-11D-A387-09 chr12:77239523 G>T maps to NM_015336.2 V455V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-A7RC-01B-11D-A403-09 chr12:77243229 G>A maps to NM_015336.2 T580T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GL-01A-12D-A37C-09 chr3:195934292 C>T maps to NM_001039617.1 S221S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr3:195934355 G>A maps to NM_001039617.1 S200S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EZ-01A-11D-A36J-09 chr3:195937565 A>G maps to NM_001039617.1 V63V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A5B8-01A-11D-A28B-09 chr10:31809969 T>C maps to NM_001174096.1 P570P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr10:31810287 A>G maps to NM_001174096.1 V676V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NQ-01A-11D-A36J-09 chr10:31791291 C>T maps to NM_001174096.1 C113C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NV-01A-11D-A37C-09 chr10:31810441 C>T maps to NM_001174096.1 Q728*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A8HZ-01A-11D-A36J-09 chr10:31810431 T>C maps to NM_001174096.1 A724A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASX-01A-11D-A387-09 chr2:145156008 G>T maps to NM_014795.3 T915T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A8I0-01A-11D-A36J-09 chr8:82629518 C>A maps to NM_024699.2 E35*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASV-01A-11D-A387-09 chr2:220071744 G>A maps to NM_138802.1 E12E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GF-01A-11D-A37C-09 chr6:38029502 C>T maps to NM_021943.2 Q83*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NK-01A-21D-A37C-09 chr8:135614788 G>A maps to NM_020863.3 L391L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GO-01A-11D-A37C-09 chr12:72004483 C>T maps to NM_144982.4 L1941L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr16:72822520 C>T maps to NM_006885.3 P3218P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A893-01A-11D-A36J-09 chr16:72992172 G>T maps to NM_006885.3 G624G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A2-01A-31D-A27G-09 chr16:72828726 C>T maps to NM_006885.3 L2618L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A8I1-01A-11D-A36J-09 chr16:72831381 T>C maps to NM_006885.3 Q1733Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6XQ-01B-11D-A33E-09 chr16:72984826 G>A maps to NM_006885.3 G919G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A8JE-01A-11D-A37C-09 chr16:72828296 C>A maps to NM_006885.3 G2762*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FA-01A-11D-A33E-09 chr8:77618140 C>T maps to NM_024721.4 D606D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OW-01A-11D-A28B-09 chr8:77616565 C>A maps to NM_024721.4 P81P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6XG-01B-11D-A33E-09 chr8:77766810 C>T maps to NM_024721.4 L2552L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6XQ-01B-11D-A33E-09 chr8:77765709 C>T maps to NM_024721.4 R2185*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr16:75203736 G>A maps to NM_153688.2 P243P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A4QS-01A-11D-A27G-09 chr19:44832454 G>A maps to ENST00000412927 Q636*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8Q7-01A-11D-A37C-09 chr19:36831605 C>T maps to NM_020917.2 G374G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A5B8-01A-11D-A28B-09 chr18:5291264 G>A maps to NM_003409.3 F314F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A625-01A-11D-A31U-09 chr18:5291774 A>C maps to NM_003409.3 Y144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OG-01A-11D-A27G-09 chr5:178359070 C>T maps to NM_030613.2 Q253*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GO-01A-11D-A37C-09 chr19:57066421 T>G maps to NM_020828.1 P756P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NR-01A-11D-A37C-09 chr19:57065437 T>C maps to NM_020828.1 T428T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q9-A6FW-01A-31D-A31U-09 chr19:57066742 C>G maps to NM_020828.1 S863S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GK-01A-11D-A37C-09 chr19:38126130 G>T maps to NM_014898.2 P437P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FG-01A-11D-A33E-09 chr4:188924335 A>G maps to NM_174900.3 K125K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49S-01A-11D-A247-09 chr4:188924011 G>T maps to NM_174900.3 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A8JE-01A-11D-A37C-09 chr4:188924575 G>A maps to NM_174900.3 L205L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FP-01A-31D-A387-09 chr6:29641134 G>C maps to NM_001109809.2 R251R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8Q7-01A-11D-A37C-09 chr20:50701304 G>A maps to NM_199427.2 Q577*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA7B-01A-31D-A403-09 chr11:58384872 C>T maps to NM_053023.4 L469L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HW-01A-22D-A351-09 chr5:32407028 A>T maps to NM_016107.3 A294A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZR-A9CJ-01B-11D-A387-09 chr5:32407028 A>T maps to NM_016107.3 A294A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GR-01A-12D-A37C-09 chr19:3819164 C>T maps to NM_015174.1 T603T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A938-01A-11D-A37C-09 chr23:24228808 C>T did not map to a codon.
Sequencing variant TCGA-LN-A8I0-01A-11D-A36J-09 chr23:24197366 A>G did not map to a codon.
Sequencing variant TCGA-S8-A6BW-01A-11D-A31U-09 chr5:79733701 C>T maps to NM_014733.3 Q400*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NJ-01A-11D-A36J-09 chr3:15124115 C>A did not map to a codon.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr14:68229513 G>A maps to NM_015346.3 L2012L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EX-01A-11D-A36J-09 chr14:68228957 C>A maps to NM_015346.3 E2111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49X-01A-31D-A27G-09 chr10:99509264 C>T maps to NM_001002261.3 L196L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA4G-01A-11D-A37C-09 chr10:99511158 G>T maps to NM_001002261.3 P277P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GQ-01A-11D-A37C-09 chr1:52747420 G>T maps to NM_004799.2 P986P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NS-01A-12D-A37C-09 chr1:52805902 G>A maps to NM_004799.2 E1313E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GL-01A-12D-A37C-09 chr20:62365092 T>C did not map to a codon.
Sequencing variant TCGA-L5-A4OS-01A-11D-A28B-09 chr8:124266851 T>A maps to NM_007222.3 A445A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A891-01A-11D-A36J-09 chr8:124268117 C>T maps to NM_007222.3 E23E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr8:124266179 A>G maps to NM_007222.3 P669P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A6QS-01A-12D-A33E-09 chr13:100637593 G>A maps to NM_007129.2 P419P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8W8-01B-11D-A37C-09 chr23:136649851 C>A did not map to a codon.
Sequencing variant TCGA-V5-A7RC-01B-11D-A403-09 chr3:147120550 G>A maps to NM_001168379.1 R50*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA7D-01A-11D-A403-09 chr13:100622678 C>T maps to NM_033132.3 P417P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FB-01A-11D-A33E-09 chr19:58096318 G>T did not map to a codon.
Sequencing variant TCGA-L5-A43I-01A-11D-A247-09 chr19:57648268 T>C maps to NM_052882.1 E71E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GM-01A-11D-A37C-09 chr16:25258514 T>C maps to NM_001012981.4 E334E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93F-01A-21D-A37C-09 chr16:25251910 T>C maps to NM_001012981.4 S710S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49L-01A-11D-A247-09 chr6:28327647 G>T maps to NM_024493.2 L95L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49U-01A-31D-A27G-09 chr6:28331512 A>G maps to NM_024493.2 E226E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NS-01A-12D-A37C-09 chr6:28213172 A>G maps to NM_019110.3 I453I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GH-01A-11D-A37C-09 chr23:101152885 C>T did not map to a codon.
Sequencing variant TCGA-IG-A4QS-01A-11D-A27G-09 chr23:101138900 T>G did not map to a codon.
Sequencing variant TCGA-IG-A4QS-01A-11D-A27G-09 chr23:101138907 T>A did not map to a codon.
Sequencing variant TCGA-L5-A88Z-01A-11D-A36J-09 chr23:101153103 A>G did not map to a codon.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr8:40554908 G>A maps to NM_024645.2 A68A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RF-01A-13D-A33E-09 chr10:81050765 C>T maps to NM_020338.3 G197G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XP-A8T8-01A-11D-A36J-09 chr7:44795880 G>C maps to NM_031449.3 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A51D-01A-11D-A27G-09 chr1:35570261 G>A maps to NM_024772.3 E233E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OF-01A-11D-A27G-09 chr1:35578790 C>T maps to NM_024772.3 R454*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49U-01A-31D-A27G-09 chr1:35576031 G>A maps to NM_024772.3 K315K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A8JD-01A-11D-A36J-09 chr1:35563127 C>A maps to NM_024772.3 S127*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr13:20610979 A>G maps to NM_001190965.1 E741E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RF-01A-13D-A33E-09 chr23:70462089 G>T did not map to a codon.
Sequencing variant TCGA-IG-A3Y9-01A-12D-A247-09 chr23:70471430 C>T did not map to a codon.
Sequencing variant TCGA-KH-A6WC-01A-11D-A33E-09 chr23:70473059 G>T did not map to a codon.
Sequencing variant TCGA-L5-A4OG-01A-11D-A27G-09 chr23:70469459 G>A did not map to a codon.
Sequencing variant TCGA-L5-A8NE-01A-11D-A37C-09 chr23:70463795 G>T did not map to a codon.
Sequencing variant TCGA-L5-A8NN-01A-11D-A37C-09 chr23:70472900 C>T did not map to a codon.
Sequencing variant TCGA-R6-A6L6-01B-11D-A33E-09 chr23:70471417 G>T did not map to a codon.
Sequencing variant TCGA-R6-A6XG-01B-11D-A33E-09 chr23:70473040 C>A did not map to a codon.
Sequencing variant TCGA-IG-A3YB-01A-11D-A247-09 chr1:35480666 C>T maps to NM_007167.3 E175E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A8JD-01A-11D-A36J-09 chr1:35472674 G>A maps to NM_007167.3 R564*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A5U7-01A-11D-A31U-09 chr3:50379080 G>T maps to NM_015896.2 R391R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3I8-01A-11D-A247-09 chr10:287977 G>T maps to NM_006624.4 L283L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A4QS-01A-11D-A27G-09 chr10:283565 G>A maps to NM_006624.4 P186P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr9:140481422 G>A maps to NM_138462.2 Q119*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FR-01A-11D-A387-09 chr9:140482239 A>T maps to NM_138462.2 A49A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A4-01A-11D-A27G-09 chr12:133727693 G>T maps to NM_015394.4 V38V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6F8-01A-11D-A33E-09 chr19:48785719 G>T maps to NM_153608.1 V34V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X8-AAAR-01A-11D-A403-09 chr19:48789138 A>G maps to NM_153608.1 L86L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43C-01A-11D-A247-09 chr19:58945570 G>A maps to NM_003433.3 R414*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OE-01A-11D-A27G-09 chr19:58574826 G>A maps to NM_007134.1 P70P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FP-01A-31D-A387-09 chr7:64291961 G>C maps to ENST00000307355 V114V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43M-01A-11D-A247-09 chr23:47269755 C>A did not map to a codon.
Sequencing variant TCGA-R6-A6L6-01B-11D-A33E-09 chr19:53571670 G>A maps to NM_001102603.1 R706*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8Q7-01A-11D-A37C-09 chr19:53571878 A>G maps to NM_001102603.1 L636L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-A7RE-01A-11D-A351-09 chr3:44611891 C>A maps to NM_018651.2 L430L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EZ-01A-11D-A36J-09 chr3:44598658 C>T maps to NM_018651.2 S40S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8W8-01B-11D-A37C-09 chr19:57931204 G>A maps to NM_006959.2 L115L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FG-01A-11D-A33E-09 chr16:3454445 G>T maps to NM_003450.2 G141G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43H-01A-11D-A247-09 chr19:9492425 C>T maps to NM_001172651.1 I473I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FB-01A-11D-A33E-09 chr17:11881519 G>T maps to NM_144680.2 Y468*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FG-01A-11D-A33E-09 chr19:44980660 A>G maps to NM_013256.3 H679H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr19:44981823 C>A maps to NM_013256.3 E292*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KH-A6WC-01A-11D-A33E-09 chr19:35232846 G>T maps to ENST00000392232 E565*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EQ-01A-11D-A36J-09 chr6:27419795 G>T maps to NM_007149.2 L514L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GG-01A-11D-A37C-09 chr23:152087568 C>T did not map to a codon.
Sequencing variant TCGA-2H-A9GK-01A-11D-A37C-09 chr23:152097179 G>T did not map to a codon.
Sequencing variant TCGA-L5-A43H-01A-11D-A247-09 chr23:152101492 G>T did not map to a codon.
Sequencing variant TCGA-L5-A4OE-01A-11D-A27G-09 chr23:152097181 G>T did not map to a codon.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr23:152105005 A>G did not map to a codon.
Sequencing variant TCGA-L5-A4OQ-01A-11D-A27G-09 chr23:152091292 G>A did not map to a codon.
Sequencing variant TCGA-VR-A8EX-01A-11D-A36J-09 chr9:104170479 G>T maps to NM_003452.2 E144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-A7RB-01A-11D-A351-09 chr6:28121230 A>T maps to NM_006298.2 T391T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q9-A6FU-01A-11D-A31U-09 chr11:3380465 G>C maps to NM_001130520.1 S591*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OS-01A-11D-A28B-09 chr19:12243539 G>A maps to NM_021143.2 A487A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49Y-01A-11D-A27G-09 chr16:3283512 C>T maps to NM_198088.2 Q81Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93D-01A-11D-A387-09 chr16:3168963 G>A maps to NM_001042428.1 S181S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr16:3170160 C>T maps to NM_001042428.1 G500G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GK-01A-11D-A37C-09 chr19:22155411 T>C maps to NM_007153.3 E808E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A4QS-01A-11D-A27G-09 chr19:22155861 A>G maps to NM_007153.3 I658I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43E-01A-11D-A247-09 chr19:22157547 T>C maps to NM_007153.3 Q96Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4MR-01A-11D-A28B-09 chr19:22157330 C>A maps to NM_007153.3 G169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6Y0-01B-11D-A33E-09 chr10:45498856 C>G maps to NM_006963.4 S14*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EO-01A-11D-A36J-09 chr10:45498899 G>T maps to NM_006963.4 R28R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A938-01A-11D-A37C-09 chr19:44470959 C>T maps to NM_013359.2 R436*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49O-01A-11D-A247-09 chr19:44470082 C>T maps to NM_013359.2 S143S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A5U7-01A-11D-A31U-09 chr19:44536477 A>G maps to NM_001129996.1 K257K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA4G-01A-11D-A37C-09 chr19:44636225 G>T maps to NM_013362.2 E487*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EU-01A-11D-A36J-09 chr19:44680326 A>C maps to NM_001032372.1 G304G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KH-A6WC-01A-11D-A33E-09 chr19:44739246 G>T maps to NM_182490.1 E222*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93C-01A-11D-A387-09 chr16:71482559 G>A maps to NM_145911.1 A456A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OX-01A-21D-A28B-09 chr16:71482988 A>G maps to NM_145911.1 C313C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr16:71482628 G>A maps to NM_145911.1 S433S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A5U7-01A-11D-A31U-09 chr19:44777238 G>A maps to NM_181756.1 Q142Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93C-01A-11D-A387-09 chr19:44662022 C>T maps to NM_006630.2 H618H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GM-01A-11D-A37C-09 chr18:74607161 C>T maps to NM_007345.3 I535I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr18:74583779 A>C maps to NM_007345.3 T220T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6Y2-01B-11D-A33E-09 chr18:32917381 G>T maps to NM_006965.2 Y307*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASX-01A-11D-A387-09 chr18:32917453 C>T maps to NM_006965.2 E283E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA7B-01A-31D-A403-09 chr8:146115387 G>T maps to NM_021061.3 R38R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NG-01A-11D-A37C-09 chr19:24310679 A>G maps to NM_203282.2 G626G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FR-01A-11D-A387-09 chr19:24310229 C>A maps to NM_203282.2 T476T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NU-01A-11D-A36J-09 chr19:58452306 G>A maps to NM_005773.2 N623N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8W8-01B-11D-A37C-09 chr19:58452837 C>T maps to NM_005773.2 R446R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GK-01A-11D-A37C-09 chr19:22271913 T>G maps to NM_033468.2 T454T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A8O2-01A-11D-A36J-09 chr19:22272087 G>A maps to NM_033468.2 E512E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FH-01A-11D-A33E-09 chr19:22270891 A>C maps to NM_033468.2 R114R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OG-01A-11D-A27G-09 chr19:22270891 A>C maps to NM_033468.2 R114R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HZ-01A-31D-A351-09 chr19:22271019 G>A maps to NM_033468.2 K156K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8ER-01A-11D-A36J-09 chr19:22271248 G>T maps to NM_033468.2 E233*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OU-01A-11D-A28B-09 chr16:3333829 C>T maps to NM_005741.4 G4G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3QL-01A-11D-A247-09 chr19:57724046 C>T maps to NM_003417.4 R528*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KH-A6WC-01A-11D-A33E-09 chr7:64388283 C>A maps to NM_021148.2 S193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HX-01A-11D-A33E-09 chr7:64388068 G>A maps to NM_021148.2 K121K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A5B8-01A-11D-A28B-09 chr19:58698338 G>T maps to NM_133502.1 V62V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6Y2-01B-11D-A33E-09 chr23:152612274 A>C did not map to a codon.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr7:111967770 G>T did not map to a codon.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr22:22842652 C>T maps to NM_080764.2 Q357Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q9-A6FW-01A-31D-A31U-09 chr15:56946581 C>T did not map to a codon.
Sequencing variant TCGA-RE-A7BO-01A-11D-A33E-09 chr1:200378071 G>T maps to NM_012482.3 L254L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr7:148895517 C>T maps to NM_003575.2 R87*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NH-01A-11D-A37C-09 chr19:44352454 G>T maps to NM_181845.1 E568*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GJ-01A-11D-A37C-09 chr19:44891311 T>C maps to NM_152354.3 V365V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GJ-01A-11D-A37C-09 chr19:44892265 T>C did not map to a codon.
Sequencing variant TCGA-L5-A4OU-01A-11D-A28B-09 chr19:44890665 G>A maps to NM_152354.3 Q581*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OU-01A-11D-A28B-09 chr19:44892265 T>C did not map to a codon.
Sequencing variant TCGA-V5-AASW-01A-11D-A403-09 chr19:44892205 C>A maps to NM_152354.3 S67S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASW-01A-11D-A403-09 chr19:44892265 T>C did not map to a codon.
Sequencing variant TCGA-LN-A9FQ-01A-31D-A387-09 chr17:16456270 C>T maps to NM_020653.2 S395S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RE-01A-11D-A33E-09 chr6:87968020 T>G maps to NM_015021.1 T1558T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A5B8-01A-11D-A28B-09 chr6:87966127 T>A maps to NM_015021.1 T927T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FR-01A-11D-A387-09 chr7:99672872 G>A maps to NM_032924.3 T52T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NE-01A-11D-A37C-09 chr19:57868052 C>A maps to ENST00000391705 I319I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3Y9-01A-12D-A247-09 chr6:28963075 G>C maps to NM_001010877.2 S568*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A6QS-01A-12D-A33E-09 chr19:9271727 G>T maps to NM_020933.4 T469T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FG-01A-11D-A33E-09 chr10:44139886 G>T maps to NM_006973.2 R145R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GG-01A-11D-A37C-09 chr19:53384007 A>T maps to NM_207333.2 I457I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49U-01A-31D-A27G-09 chr19:53385225 G>A maps to NM_207333.2 S51S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HX-01A-11D-A33E-09 chr19:53384796 G>T maps to NM_207333.2 C194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A4QS-01A-11D-A27G-09 chr19:58640555 G>A maps to NM_024620.3 P105P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FQ-01A-31D-A387-09 chr19:54081017 G>T maps to NM_001079907.1 E402*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NK-01A-21D-A37C-09 chr19:14829422 G>T maps to NM_032433.2 G428G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr20:44588004 G>A maps to NM_022095.3 H696H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49M-01A-21D-A27G-09 chr20:44579099 G>A maps to NM_022095.3 C1108C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A4P3-01A-11D-A27G-09 chr20:25655910 G>T maps to NM_015655.2 L671L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A8O2-01A-11D-A36J-09 chr10:38345269 C>T maps to NM_006954.1 Q740*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GF-01A-11D-A37C-09 chr20:32346607 C>T maps to ENST00000375200 R342*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A3-01A-11D-A27G-09 chr20:32377395 T>A did not map to a codon.
Sequencing variant TCGA-LN-A4A9-01A-11D-A28B-09 chr20:32341070 C>T maps to ENST00000375200 Q195*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FO-01A-11D-A387-09 chr20:32376684 A>G maps to ENST00000375200 K623K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A97I-01A-11D-A387-09 chr20:2464528 G>A maps to NM_024325.4 R360*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EW-01A-11D-A36J-09 chr20:2465210 G>A maps to NM_024325.4 F132F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GF-01A-11D-A37C-09 chr5:176449766 C>T maps to ENST00000503039 Q10*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GR-01A-12D-A37C-09 chr19:53644919 G>A maps to NM_001172674.1 S388S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6KZ-01A-11D-A31U-09 chr19:53644628 A>C maps to NM_001172674.1 P485P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88W-01A-11D-A351-09 chr5:178506867 C>T maps to NM_014594.1 Q479*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA4G-01A-11D-A37C-09 chr10:64219516 C>T maps to NM_199451.2 G314G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EU-01A-11D-A36J-09 chr19:37117923 G>A maps to NM_032825.3 T375T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FE-01A-11D-A33E-09 chr19:37721364 G>T did not map to a codon.
Sequencing variant TCGA-L5-A891-01A-11D-A36J-09 chr19:37733515 C>T maps to NM_152604.1 H126H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr12:6788169 C>T maps to NM_001135734.1 A82A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NQ-01A-11D-A36J-09 chr12:6787384 C>G maps to NM_001135734.1 R198R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OM-01A-11D-A27G-09 chr12:54764421 G>A maps to NM_001130967.1 A306A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GK-01A-11D-A37C-09 chr3:21466995 C>T maps to NM_024697.2 T280T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6F8-01A-11D-A33E-09 chr3:21467078 C>A maps to NM_024697.2 G253*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4MQ-01A-11D-A28B-09 chr7:99097548 A>C maps to NM_032164.2 A56A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A8O2-01A-11D-A36J-09 chr8:28218518 G>A maps to NM_018660.2 A41A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr18:72632565 C>A maps to NM_017757.2 T1782T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GO-01A-11D-A37C-09 chr11:46726044 C>T maps to NM_024741.2 C265C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OH-01A-11D-A27G-09 chr11:46727346 G>T maps to NM_024741.2 V699V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KH-A6WC-01A-11D-A33E-09 chr23:47308820 G>T did not map to a codon.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr23:47307382 C>T did not map to a codon.
Sequencing variant TCGA-IC-A6RE-01A-11D-A33E-09 chr14:74371667 G>A maps to NM_021188.1 R265R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A8JD-01A-11D-A36J-09 chr14:74371760 G>A maps to NM_021188.1 L296L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NW-01A-11D-A37C-09 chr19:37618366 A>G maps to NM_144689.3 Q158Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr16:49669798 G>T maps to NM_015069.2 P1088P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6F8-01A-11D-A33E-09 chr7:148802514 C>A maps to NM_001001661.2 E150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49Y-01A-11D-A27G-09 chr7:148800754 C>A maps to NM_001001661.2 A736A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8WG-01A-11D-A37C-09 chr7:148802200 G>A maps to NM_001001661.2 S254S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NJ-01A-11D-A36J-09 chr19:44111801 C>T maps to NM_182498.3 G178G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8W8-01B-11D-A37C-09 chr19:21719847 T>C maps to NM_001001415.2 H331H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EY-01A-11D-A36J-09 chr19:21240140 A>T maps to NM_025189.3 K343*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A51D-01A-11D-A27G-09 chr19:21365979 G>T maps to NM_133473.2 E292*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4MQ-01A-11D-A28B-09 chr19:21366095 C>T maps to NM_133473.2 T330T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HY-01A-12D-A351-09 chr19:12127156 G>A maps to NM_001080411.1 C175C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A3-01A-11D-A27G-09 chr16:3433043 C>T maps to ENST00000396852 K634K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NQ-01A-11D-A36J-09 chr1:23688649 G>A maps to NM_001077195.1 Q409*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A8I0-01A-11D-A36J-09 chr1:23689411 G>T maps to NM_001077195.1 R155R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EZ-01A-11D-A36J-09 chr10:31138754 C>T maps to NM_182755.2 A193A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NR-01A-11D-A37C-09 chr19:11979018 G>T maps to NM_152262.2 E379*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q9-A6FW-01A-31D-A31U-09 chr19:11978919 A>C maps to NM_152262.2 R346R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43I-01A-11D-A247-09 chr19:11941177 C>T maps to NM_152357.2 L28L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NF-01A-11D-A37C-09 chr19:12461333 C>A maps to NM_030824.2 G355G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4MR-01A-11D-A28B-09 chr19:12541041 T>C maps to NM_005815.4 P648P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FR-01A-11D-A387-09 chr19:12541472 C>A maps to NM_005815.4 E505*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49Y-01A-11D-A27G-09 chr3:44491966 C>A maps to NM_181489.5 L264L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EZ-01A-11D-A36J-09 chr23:134481195 C>G did not map to a codon.
Sequencing variant TCGA-LN-A49U-01A-31D-A27G-09 chr6:57018676 C>T maps to NM_001031623.2 Q968*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OJ-01A-11D-A27G-09 chr5:178392571 T>C maps to NM_182594.2 C389C. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-L5-A893-01A-11D-A36J-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-L5-A8NW-01A-11D-A37C-09 chr5:178392571 T>A maps to NM_182594.2 C389*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A5U7-01A-11D-A31U-09 chr5:178373439 G>C maps to NM_182594.2 L38L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43E-01A-11D-A247-09 chr19:37130775 T>C maps to NM_153257.2 Q157Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EO-01A-11D-A36J-09 chr9:109687208 C>A maps to NM_021224.4 S339*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6DQ-01B-11D-A31U-09 chr19:53344547 A>G maps to NM_001008801.1 D333D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr19:57089371 G>A maps to NM_001001668.3 A525A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NV-01A-11D-A37C-09 chr19:57036329 C>T maps to NM_020813.2 A298A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GH-01A-11D-A37C-09 chr5:121487981 C>T maps to NM_207317.1 I99I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6XG-01B-11D-A33E-09 chr16:30409329 C>A maps to ENST00000495929 P382P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88W-01A-11D-A351-09 chr19:52825737 C>G maps to NM_144684.2 S412*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NS-01A-12D-A37C-09 chr9:114305074 G>T maps to NM_133464.2 T620T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6Y0-01B-11D-A33E-09 chr9:114303962 G>T maps to NM_133464.2 E250*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASX-01A-11D-A387-09 chr9:114304807 C>A maps to NM_133464.2 P531P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A4P3-01A-11D-A27G-09 chr9:95608569 G>T maps to NM_031486.1 S833S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NS-01A-12D-A37C-09 chr10:44112086 C>G maps to NM_145312.3 S199*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3QL-01A-11D-A247-09 chr19:20308433 T>C maps to ENST00000428290 H299H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NL-01A-12D-A37C-09 chr10:48371119 C>A maps to NM_153034.2 L196L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6KZ-01A-11D-A31U-09 chr19:11917122 C>T maps to NM_152356.3 R119*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GR-01A-12D-A37C-09 chr19:22848043 A>C maps to NM_020855.2 R525R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4ON-01A-11D-A27G-09 chr1:247464405 G>A maps to NM_032752.1 T393T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4MR-01A-11D-A28B-09 chr7:99226868 G>A maps to NM_145115.2 A287A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr19:32844629 G>A maps to NM_014910.4 A298A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A5U7-01A-11D-A31U-09 chr19:32843901 G>T maps to NM_014910.4 E56*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S8-A6BV-01A-21D-A31U-09 chr19:32845529 A>C maps to NM_014910.4 T598T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A4P3-01A-11D-A27G-09 chr9:99521731 A>T maps to NM_014930.1 Y460*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OM-01A-11D-A27G-09 chr20:62594468 C>T maps to NM_020713.1 V649V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6XQ-01B-11D-A33E-09 chr20:62594453 C>A maps to NM_020713.1 T654T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FB-01A-11D-A33E-09 chr2:27603101 G>A maps to NM_144631.4 D23D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FA-01A-11D-A33E-09 chr18:74154845 C>T maps to ENST00000443185 K55K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6Y0-01B-11D-A33E-09 chr8:146029025 G>T maps to NM_213605.2 E12*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A4P3-01A-11D-A27G-09 chr4:10446496 G>A maps to NM_053042.2 L486L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A9-01A-11D-A28B-09 chr18:14105542 G>A maps to NM_145287.3 G332G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A9-01A-11D-A28B-09 chr18:14105575 C>T maps to NM_145287.3 K321K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GH-01A-11D-A37C-09 chr18:22806876 C>A maps to NM_015461.2 P335P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NR-01A-11D-A37C-09 chr18:22806600 A>G maps to NM_015461.2 T427T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GN-01A-11D-A37C-09 chr19:52919152 G>T maps to NM_032423.2 E350*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FE-01A-11D-A33E-09 chr19:52909832 C>T maps to NM_032423.2 Q70*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43C-01A-11D-A247-09 chr19:52919181 C>T maps to NM_032423.2 G359G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr19:58117514 C>T maps to NM_020880.3 R208*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NE-01A-11D-A37C-09 chr18:56585941 C>T maps to NM_018181.4 D141D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A8-01A-32D-A27G-09 chr18:56651289 G>A maps to NM_018181.4 L1166L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6L6-01B-11D-A33E-09 chr19:52942557 C>T maps to NM_001143939.1 F628F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A891-01A-11D-A36J-09 chr19:31040155 G>A maps to NM_014717.1 Q1210Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8WG-01A-11D-A37C-09 chr19:31039198 T>G maps to NM_014717.1 P891P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8Q7-01A-11D-A37C-09 chr19:30936427 C>T maps to NM_014717.1 H653H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr19:38103491 A>G maps to NM_152606.3 K437K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NK-01A-21D-A37C-09 chr19:38102735 G>A maps to NM_152606.3 V185V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-A7RB-01A-11D-A351-09 chr19:38102846 A>G maps to NM_152606.3 K222K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GG-01A-11D-A37C-09 chr19:58773549 G>A maps to NM_014480.2 G526G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GN-01A-11D-A37C-09 chr19:58757715 G>A maps to NM_014480.2 W28*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8ER-01A-11D-A36J-09 chr19:57910926 C>T maps to NM_001172773.1 S436S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GF-01A-11D-A37C-09 chr19:2833991 C>T maps to NM_001102651.1 S253S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EX-01A-11D-A36J-09 chr19:2878077 G>A maps to NM_024967.1 T374T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GO-01A-11D-A37C-09 chr19:8932676 A>G did not map to a codon.
Sequencing variant TCGA-L5-A4OR-01A-11D-A27G-09 chr19:9449866 A>C did not map to a codon.
Sequencing variant TCGA-V5-AASV-01A-11D-A387-09 chr19:9763999 G>A maps to NM_001130032.1 S302S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FP-01A-31D-A387-09 chr19:12430082 C>A maps to NM_145276.2 P252P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GN-01A-11D-A37C-09 chr19:37440439 A>T maps to NM_198539.2 K129*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93D-01A-11D-A387-09 chr19:37441137 T>G maps to NM_198539.2 P361P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FO-01A-11D-A387-09 chr19:37416129 C>T maps to NM_198539.2 S35S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr19:2915521 C>T maps to NM_173480.2 D2D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GK-01A-11D-A37C-09 chr19:37975772 C>T maps to NM_144694.1 Q417*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A891-01A-11D-A36J-09 chr19:38074876 G>C maps to NM_016536.3 S44*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NJ-01A-11D-A36J-09 chr8:125989784 C>A maps to NM_152412.2 S425S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6Y2-01B-11D-A33E-09 chr19:42583429 G>A maps to ENST00000222339 Q314Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr19:53013903 G>A maps to NM_001099694.1 L90L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A8-01A-32D-A27G-09 chr19:53014447 C>T maps to NM_001099694.1 R272*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A9-01A-11D-A28B-09 chr19:56089493 G>T maps to NM_152600.2 L504L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A9VB-01A-21D-A37C-09 chr19:56090029 G>A maps to NM_152600.2 L326L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6XG-01B-11D-A33E-09 chr19:56156512 G>A maps to NM_016535.3 T192T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3I8-01A-11D-A247-09 chr19:56895666 T>C maps to NM_144690.1 G373G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49X-01A-31D-A27G-09 chr19:56895795 C>T maps to NM_144690.1 Q330Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GK-01A-11D-A37C-09 chr19:37643364 G>C maps to ENST00000356958 S479*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GL-01A-12D-A37C-09 chr19:37676374 T>C maps to NM_152279.3 K688K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr19:37677211 C>T maps to NM_152279.3 S409S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NJ-01A-11D-A36J-09 chr19:37676129 C>G maps to NM_152279.3 *770S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-S8-A6BV-01A-21D-A31U-09 chr19:37676371 A>C maps to NM_152279.3 P689P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr19:58291094 A>G maps to NM_017652.2 K380K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6DQ-01B-11D-A31U-09 chr19:58369949 G>A maps to NM_032828.2 W57*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-A7RB-01A-11D-A351-09 chr19:58370469 C>T maps to NM_032828.2 H230H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FP-01A-31D-A387-09 chr15:85326475 G>T maps to NM_014630.2 P190P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OW-01A-11D-A28B-09 chr17:5085462 G>A maps to NM_032530.1 Q697*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A4P3-01A-11D-A27G-09 chr16:2053039 C>T maps to ENST00000431526 R139R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GL-01A-12D-A37C-09 chr19:35258287 G>T maps to NM_001007248.2 I58I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43H-01A-11D-A247-09 chr19:58491629 C>A maps to NM_025027.3 E140*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88W-01A-11D-A351-09 chr19:38190338 G>T maps to NM_032689.4 G231G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr19:38189876 A>G maps to NM_032689.4 G385G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr5:124036908 G>T maps to NM_020747.2 L320L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A50L-01A-11D-A27G-09 chr15:64967548 A>T maps to NM_015042.1 G832G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L7-A6VZ-01A-12D-A33E-09 chr15:64792329 G>T maps to NM_015042.1 E238*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8ET-01A-11D-A403-09 chr15:64966760 C>T maps to NM_015042.1 R570*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GK-01A-11D-A37C-09 chr19:52869350 C>T maps to NM_001161425.1 V240V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA4G-01A-11D-A37C-09 chr19:53209055 T>G maps to NM_001161500.1 R418R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3YC-01A-11D-A247-09 chr19:52447930 T>C maps to NM_001031721.3 C265C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EO-01A-11D-A36J-09 chr19:52520063 C>A maps to NM_025040.3 E263*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RE-01A-11D-A33E-09 chr19:52505105 A>G maps to ENST00000354939 T66T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA4D-01A-11D-A37C-09 chr19:52496999 G>T maps to ENST00000354939 L454L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RE-01A-11D-A33E-09 chr19:52620092 A>G maps to NM_178523.3 D108D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A50L-01A-11D-A27G-09 chr19:52619108 A>G maps to NM_178523.3 T436T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GL-01A-12D-A37C-09 chr3:40528734 C>A maps to NM_001145082.2 S285*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A97H-01A-11D-A387-09 chr8:144733439 A>G maps to NM_014789.3 K466K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HX-01A-11D-A33E-09 chr8:144733631 G>T maps to NM_014789.3 G530G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NW-01A-11D-A37C-09 chr19:12256138 C>T maps to ENST00000439556 S366S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OH-01A-11D-A27G-09 chr19:20807353 A>G maps to NM_001076675.2 H443H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88Z-01A-11D-A36J-09 chr19:20807455 G>A maps to NM_001076675.2 S409S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NQ-01A-11D-A36J-09 chr19:20807473 G>T maps to NM_001076675.2 G403G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HX-01A-11D-A33E-09 chr19:20808427 A>C maps to NM_001076675.2 L85L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EW-01A-11D-A36J-09 chr19:11728169 C>T maps to NM_145295.3 C284C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr16:30794961 C>T maps to NM_001080417.1 T229T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HX-01A-11D-A33E-09 chr16:30793914 G>A maps to NM_001080417.1 F578F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FD-01A-11D-A33E-09 chr2:71626764 G>T maps to NM_014497.3 V859V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GN-01A-11D-A37C-09 chr1:91406697 C>T maps to NM_201269.1 T71T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NH-01A-11D-A37C-09 chr1:91403315 T>G maps to NM_201269.1 S1138S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L7-A6VZ-01A-12D-A33E-09 chr1:91405547 G>T maps to NM_201269.1 R455R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49S-01A-11D-A247-09 chr1:91406271 C>T maps to NM_201269.1 K213K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6F8-01A-11D-A33E-09 chr16:31090990 G>T maps to NM_014699.3 E1116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A2-01A-31D-A27G-09 chr16:31091868 G>A maps to NM_014699.3 A1408A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OJ-01A-11D-A27G-09 chr19:52394845 A>G maps to NM_023074.3 T181T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6DQ-01B-11D-A31U-09 chr17:47376269 G>T maps to NM_014897.2 I442I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RF-01A-13D-A33E-09 chr12:124497200 C>A maps to NM_152437.1 P170P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZR-A9CJ-01B-11D-A387-09 chr12:124497177 A>C maps to NM_152437.1 R163R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93F-01A-21D-A37C-09 chr19:56952916 G>T maps to ENST00000342634 R611R. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-VR-A8EU-01A-11D-A36J-09. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-VR-A8EU-01A-11D-A36J-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-LN-A49U-01A-31D-A27G-09 chr19:58232612 C>A maps to ENST00000335820 G281*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASX-01A-11D-A387-09 chr19:58238832 G>A maps to ENST00000335820 R22*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A5B8-01A-11D-A28B-09 chr1:249141563 C>T maps to NM_024836.1 R31*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr1:249142522 C>T maps to NM_024836.1 C350C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88W-01A-11D-A351-09 chr1:249142288 C>G maps to NM_024836.1 R272R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8W8-01B-11D-A37C-09 chr1:249141661 G>A maps to NM_024836.1 T63T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93E-01A-11D-A37C-09 chr19:23836453 T>C maps to NM_138330.2 E427E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-A7RB-01A-11D-A351-09 chr19:23836408 A>G maps to NM_138330.2 H442H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A50L-01A-11D-A27G-09 chr19:22363759 G>T maps to NM_001001411.2 Y253*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FD-01A-11D-A33E-09 chr19:22363642 C>T maps to NM_001001411.2 S292S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NE-01A-11D-A37C-09 chr19:22363723 G>T maps to NM_001001411.2 V265V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NQ-01A-11D-A36J-09 chr19:22363285 A>G maps to NM_001001411.2 H411H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NW-01A-11D-A37C-09 chr19:22363519 T>G maps to NM_001001411.2 G333G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NW-01A-11D-A37C-09 chr19:22363525 A>G maps to NM_001001411.2 H331H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OO-01A-11D-A27G-09 chr19:53747129 A>G maps to NM_182609.2 D12D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q9-A6FU-01A-11D-A31U-09 chr1:227842419 G>T maps to NM_178549.3 E212*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A2-01A-31D-A27G-09 chr7:63726928 C>T maps to NM_153363.2 S306S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RE-A7BO-01A-11D-A33E-09 chr7:63721261 G>T maps to NM_153363.2 E73*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4ON-01A-11D-A27G-09 chr7:63981862 T>C maps to NM_178558.4 R423R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L7-A6VZ-01A-12D-A33E-09 chr7:63982351 A>G maps to NM_178558.4 H260H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GI-01A-11D-A37C-09 chr19:23927699 T>G maps to NM_138286.2 R218R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NU-01A-11D-A36J-09 chr19:23927145 A>C maps to NM_138286.2 A402A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASV-01A-11D-A387-09 chr19:20117175 T>A maps to NM_033196.2 K379*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EX-01A-11D-A36J-09 chr1:26688514 T>C did not map to a codon.
Sequencing variant TCGA-VR-A8EZ-01A-11D-A36J-09 chr16:30581254 G>T maps to NM_145271.3 I271I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NL-01A-12D-A37C-09 chr1:247150386 G>T maps to NM_020394.3 S477*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49M-01A-21D-A27G-09 chr1:247151123 C>T maps to NM_020394.3 K231K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GQ-01A-11D-A37C-09 chr1:120165819 G>A maps to NM_001080470.1 G382G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RE-A7BO-01A-11D-A33E-09 chr1:120165645 G>A maps to NM_001080470.1 R440R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr19:9413156 C>A maps to NM_198535.1 V24V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88Z-01A-11D-A36J-09 chr19:9407536 T>A maps to NM_198535.1 P181P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6Y2-01B-11D-A33E-09 chr19:9406192 G>C maps to NM_198535.1 Y629*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8Q7-01A-11D-A37C-09 chr22:24087104 G>A maps to NM_021916.2 Q75*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XP-A8T6-01A-11D-A36J-09 chr22:24086331 G>A maps to NM_021916.2 G332G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A3Y9-01A-12D-A247-09 chr19:12059540 C>T maps to NM_144566.1 F234F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A5U7-01A-11D-A31U-09 chr19:12060417 G>T maps to NM_144566.1 E527*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A8I1-01A-11D-A36J-09 chr19:12060146 C>T maps to NM_144566.1 H436H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A8I1-01A-11D-A36J-09 chr19:12060158 C>T maps to NM_144566.1 H440H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4MQ-01A-11D-A28B-09 chr19:53086052 A>T maps to NM_001172655.1 V313V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A4QS-01A-11D-A27G-09 chr8:37556149 T>G maps to NM_025069.1 Y577*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr8:37554829 C>T maps to NM_025069.1 A137A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6Y0-01B-11D-A33E-09 chr19:21493354 C>T maps to NM_021269.2 Q26Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-AASX-01A-11D-A387-09 chr19:57134061 C>T maps to NM_021216.4 G469G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43H-01A-11D-A247-09 chr15:90623057 A>G maps to NM_198526.2 L664L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NS-01A-12D-A37C-09 chr15:90611142 G>A maps to NM_198526.2 T258T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6DN-01B-11D-A31U-09 chr15:90610956 G>T maps to NM_198526.2 R196R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93E-01A-11D-A37C-09 chr23:84502617 G>T did not map to a codon.
Sequencing variant TCGA-LN-A8I1-01A-11D-A36J-09 chr23:84526288 C>T did not map to a codon.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr19:21300891 T>C maps to NM_182515.3 H474H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EQ-01A-11D-A36J-09 chr7:57529024 C>T maps to NM_001159279.1 Y286Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NF-01A-11D-A37C-09 chr4:265859 G>T maps to ENST00000419098 S262S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A939-01A-12D-A37C-09 chr7:63808651 G>A maps to NM_001170905.1 L137L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49L-01A-11D-A247-09 chr7:63797360 G>T did not map to a codon.
Sequencing variant TCGA-2H-A9GI-01A-11D-A37C-09 chr7:149190004 G>T maps to NM_001163474.1 C155*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43J-01A-12D-A247-09 chr7:149172341 A>G maps to NM_001163474.1 G357G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A8O2-01A-11D-A36J-09 chr17:80790166 A>C maps to NM_024702.2 L55*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49Y-01A-11D-A27G-09 chr17:80789737 G>T maps to NM_024702.2 S198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FP-01A-31D-A387-09 chr17:80790121 G>T maps to NM_024702.2 S70*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OJ-01A-11D-A27G-09 chr23:134427909 A>C did not map to a codon.
Sequencing variant TCGA-IG-A3I8-01A-11D-A247-09 chr19:52793496 A>G maps to NM_001010851.2 R151R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FA-01A-11D-A33E-09 chr19:52794069 C>A maps to NM_001010851.2 L342L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43H-01A-11D-A247-09 chr19:52794163 C>T maps to NM_001010851.2 Q374*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OW-01A-11D-A28B-09 chr19:52793490 T>G maps to NM_001010851.2 L149L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A4P3-01A-11D-A27G-09 chr15:35274939 C>T maps to NM_014106.3 L232L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A4P3-01A-11D-A27G-09 chr15:35275226 C>A maps to NM_014106.3 E137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A4P3-01A-11D-A27G-09 chr15:35275229 C>A maps to NM_014106.3 E136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A4P3-01A-11D-A27G-09 chr15:35275344 C>A maps to NM_014106.3 V97V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A4P3-01A-11D-A27G-09 chr15:35275356 C>T maps to NM_014106.3 L93L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4MR-01A-11D-A28B-09 chr19:57985076 A>T maps to NM_001024596.2 T345T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-V5-A7RB-01A-11D-A351-09 chr19:57984812 A>G maps to NM_001024596.2 P433P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XP-A8T6-01A-11D-A36J-09 chr19:57986506 T>A maps to NM_001024596.2 T69T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NH-01A-11D-A37C-09 chr19:58016676 A>G maps to NM_198542.1 A57A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FG-01A-11D-A33E-09 chr7:150093754 C>T maps to NM_173680.3 A62A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A938-01A-11D-A37C-09 chr19:58258456 C>T maps to NM_173632.3 Q11*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49X-01A-31D-A27G-09 chr19:40580617 T>C maps to NM_001142577.1 K578K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HX-01A-11D-A33E-09 chr19:40540575 G>A maps to NM_001005851.2 C730C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GK-01A-11D-A37C-09 chr19:38160929 C>T maps to NM_152605.3 K40K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HW-01A-22D-A351-09 chr16:30594219 G>A maps to NM_152458.6 F293F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NH-01A-11D-A37C-09 chr7:99081749 C>A maps to NM_213603.2 S83S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GM-01A-11D-A37C-09 chr19:37314261 C>A maps to NM_206894.2 E52*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EQ-01A-11D-A36J-09 chr19:37309757 G>A maps to NM_206894.2 H496H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X8-AAAR-01A-11D-A403-09 chr19:37310183 A>G maps to NM_206894.2 T354T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EX-01A-11D-A36J-09 chr19:12738586 G>T maps to NM_153358.2 E82*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NQ-01A-11D-A36J-09 chr19:35451801 G>A maps to NM_175872.4 L44L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HZ-01A-31D-A351-09 chr19:35449654 G>A maps to NM_175872.4 C368C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FQ-01A-31D-A387-09 chr19:38023299 G>T maps to NM_001013659.2 E20*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EX-01A-11D-A36J-09 chr19:12501411 G>C maps to NM_001080821.2 L600L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZR-A9CJ-01B-11D-A387-09 chr7:127026123 G>T maps to NM_176814.3 C49*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FG-01A-11D-A33E-09 chr2:185801664 A>G maps to NM_194250.1 G514G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr2:185803527 C>A maps to NM_194250.1 I1135I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OX-01A-21D-A28B-09 chr2:185800767 T>G maps to NM_194250.1 S215S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8WG-01A-11D-A37C-09 chr2:185803449 T>C maps to NM_194250.1 A1109A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA4D-01A-11D-A37C-09 chr2:185803170 T>C maps to NM_194250.1 T1016T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GG-01A-11D-A37C-09 chr7:88965049 A>G maps to NM_181646.2 G918G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FD-01A-11D-A33E-09 chr19:53058172 G>A maps to NM_001039886.3 W668*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OP-01A-11D-A27G-09 chr19:53058028 G>A maps to NM_001039886.3 E620E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43M-01A-11D-A247-09 chr23:47775627 G>T did not map to a codon.
Sequencing variant TCGA-L5-A4OG-01A-11D-A27G-09 chr23:47774636 A>G did not map to a codon.
Sequencing variant TCGA-L5-A8NS-01A-12D-A37C-09 chr23:47775830 C>G did not map to a codon.
Sequencing variant TCGA-LN-A49U-01A-31D-A27G-09 chr23:47775249 A>G did not map to a codon.
Sequencing variant TCGA-R6-A6XG-01B-11D-A33E-09 chr23:47775682 C>A did not map to a codon.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr19:53994004 A>G maps to NM_001004301.3 S173S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6XQ-01B-11D-A33E-09 chr19:53994703 C>T maps to NM_001004301.3 T406T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GQ-01A-11D-A37C-09 chr19:58384288 A>G maps to NM_001144989.1 T823T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-M9-A5M8-01A-11D-A28B-09 chr19:53453724 G>T maps to NM_001031665.1 R435R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A5U7-01A-11D-A31U-09 chr16:71894142 C>T maps to ENST00000425432 R339R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q9-A6FW-01A-31D-A31U-09 chr19:11833222 G>A maps to NM_001080493.2 R376*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZR-A9CJ-01B-11D-A387-09 chr19:11833535 G>A maps to NM_001080493.2 T271T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IC-A6RE-01A-11D-A33E-09 chr13:115091141 G>T maps to NM_032436.2 E609*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NI-01A-11D-A37C-09 chr13:115090508 C>T maps to NM_032436.2 R398*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A939-01A-12D-A37C-09 chr19:37382573 G>T maps to NM_001171979.1 I454I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A893-01A-11D-A36J-09 chr19:37382648 A>C maps to NM_001171979.1 G429G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NF-01A-11D-A37C-09 chr19:37382912 T>C maps to NM_001171979.1 R341R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NF-01A-11D-A37C-09 chr19:37382963 C>T maps to NM_001171979.1 K324K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GM-01A-11D-A37C-09 chr19:53116986 T>A maps to NM_018300.3 A277A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FA-01A-11D-A33E-09 chr19:53116854 C>T maps to NM_018300.3 E321E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4ON-01A-11D-A27G-09 chr20:57766157 T>C maps to NM_178457.1 G28G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43C-01A-11D-A247-09 chr19:57175633 G>A maps to NM_001005850.1 C333C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-M9-A5M8-01A-11D-A28B-09 chr19:57175696 G>A maps to NM_001005850.1 I312I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A4P3-01A-11D-A27G-09 chr3:32031298 C>G maps to NM_001137674.1 S243*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A4A5-01A-21D-A27G-09 chr3:32030981 C>T maps to NM_001137674.1 S137S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A5B8-01A-11D-A28B-09 chr19:52877591 G>A maps to NM_001145434.1 E60E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NG-01A-11D-A37C-09 chr19:52876491 T>A did not map to a codon.
Sequencing variant TCGA-LN-A49L-01A-11D-A247-09 chr19:52887706 G>T maps to NM_001145434.1 G292*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A6Y0-01B-11D-A33E-09 chr19:52887243 T>C maps to NM_001145434.1 P137P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RE-A7BO-01A-11D-A33E-09 chr19:52887526 A>C maps to NM_001145434.1 R232R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A43E-01A-11D-A247-09 chr19:20215064 A>G maps to NM_007138.1 R7R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OI-01A-11D-A27G-09 chr19:23543032 G>T maps to NM_003430.2 G916G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z6-A8JD-01A-11D-A36J-09 chr19:23544104 G>C maps to NM_003430.2 S559*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FP-01A-31D-A387-09 chr19:22574496 C>A maps to NM_001098626.1 G514*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GO-01A-11D-A37C-09 chr19:22952778 A>G maps to ENST00000397104 S2S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OW-01A-11D-A28B-09 chr19:22940991 A>G maps to ENST00000397104 A482A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49U-01A-31D-A27G-09 chr19:22940565 G>A maps to ENST00000397104 S624S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A8I0-01A-11D-A36J-09 chr19:22941057 G>T maps to ENST00000397104 T460T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8WG-01A-11D-A37C-09 chr19:22940885 T>A maps to ENST00000397104 R518*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A97I-01A-11D-A387-09 chr20:47864703 G>A maps to NM_021035.2 C1619C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-R6-A8W8-01B-11D-A37C-09 chr20:47882795 G>T maps to NM_021035.2 T626T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA7D-01A-11D-A403-09 chr20:47866095 G>A maps to NM_021035.2 T1155T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A625-01A-11D-A31U-09 chr7:100867223 G>A maps to NM_006349.2 L150L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OX-01A-21D-A28B-09 chr7:100865990 C>T maps to NM_006349.2 D43D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KH-A6WC-01A-11D-A33E-09 chr1:86173817 C>T maps to NM_017953.3 G50G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NM-01A-11D-A37C-09 chr6:30030077 G>A maps to NM_170783.2 G108G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-AA7B-01A-31D-A403-09 chr22:29446743 C>T maps to NM_032173.2 R759*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A97I-01A-11D-A387-09 chr19:5456255 C>T maps to NM_181710.3 L252L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X8-AAAR-01A-11D-A403-09 chr16:21212847 G>A maps to NM_003460.1 N512N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GI-01A-11D-A37C-09 chr7:76069837 A>T maps to NM_001110354.1 K324*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A93C-01A-11D-A387-09 chr1:238051807 G>T maps to NM_021186.3 R135R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GR-01A-12D-A37C-09 chr7:50121487 C>T maps to NM_007009.2 A72A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A9FQ-01A-31D-A387-09 chr23:15817994 G>T did not map to a codon.
Sequencing variant TCGA-L5-A891-01A-11D-A36J-09 chr19:58549513 C>T maps to NM_182572.3 R104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NW-01A-11D-A37C-09 chr19:58551836 G>A maps to NM_182572.3 S130S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A8NW-01A-11D-A37C-09 chr19:58565406 C>T maps to NM_182572.3 H405H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A49S-01A-11D-A247-09 chr19:58565136 C>T maps to NM_182572.3 R315R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GF-01A-11D-A37C-09 chr19:58596075 G>A maps to NM_001145542.1 P559P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EX-01A-11D-A36J-09 chr15:85164082 G>A maps to NM_181877.3 E219E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-2H-A9GF-01A-11D-A37C-09 chr6:28403282 C>T maps to NM_001012455.1 E170E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8EX-01A-11D-A36J-09 chr20:44511254 G>A maps to NM_080603.4 P8P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OJ-01A-11D-A27G-09 chr2:187693009 C>A maps to NM_182521.2 G535*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IG-A4P3-01A-11D-A27G-09 chr19:13919936 C>G maps to NM_023072.2 L305L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A4OO-01A-11D-A27G-09 chr1:45553565 G>A maps to NM_020883.1 I313I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JY-A6FE-01A-11D-A33E-09 chr11:113631035 A>G maps to NM_004724.2 L159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L5-A88V-01A-11D-A351-09 chr15:66806414 A>G maps to NM_017975.3 E65E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A7HZ-01A-31D-A351-09 chr10:58118340 C>T maps to NM_032997.2 G256G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VR-A8ET-01A-11D-A403-09 chr10:58119777 C>T did not map to a codon.
Sequencing variant TCGA-JY-A93E-01A-11D-A37C-09 chr23:57935853 G>A did not map to a codon.
Sequencing variant TCGA-IG-A50L-01A-11D-A27G-09 chr23:57619960 T>C did not map to a codon.
Sequencing variant TCGA-LN-A8I0-01A-11D-A36J-09 chr23:57619665 C>T did not map to a codon.
Sequencing variant TCGA-VR-A8ER-01A-11D-A36J-09 chr23:57620062 C>T did not map to a codon.
Sequencing variant TCGA-LN-A4MR-01A-11D-A28B-09 chr17:3981249 T>C maps to NM_015113.3 L972L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LN-A8I1-01A-11D-A36J-09 chr17:3992102 G>T maps to NM_015113.3 R704R. Only missense variants will be evaluated by CHASM.
