Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr3:151461923 G>A maps to NM_207365.3 T135T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZL-A9V6-01A-11D-A428-09 chr19:1043090 C>T maps to NM_019112.3 R211*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3G-AB14-01A-11D-A423-09 chr7:96747040 G>A maps to NM_020186.2 P2P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A961-01A-11D-A428-09 chr17:73947522 A>C maps to NM_004035.6 G360G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5U-AB0D-01A-11D-A423-09 chr11:47266388 C>T maps to NM_001610.2 W223*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZL-A9V6-01A-11D-A428-09 chr8:39587435 G>T maps to NM_014237.2 E733*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XM-AAZ2-01A-11D-A423-09 chr4:175897903 G>T maps to NM_014269.4 E410*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr9:136291137 C>T maps to NM_139025.3 D165D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A962-01A-11D-A428-09 chr5:5146384 C>T maps to NM_139056.2 H106H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A96Q-01A-11D-A428-09 chr3:64592728 G>T maps to NM_182920.1 Y1127*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XU-A930-01A-11D-A423-09 chr15:84639318 C>T maps to NM_207517.2 L858L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr1:150532262 G>A maps to ENST00000369039 T1013T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4V-A9QW-01A-11D-A423-09 chr1:203134441 G>A maps to NM_001048230.1 W132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XU-A933-01A-11D-A423-09 chr23:148069068 C>A did not map to a codon.
Alternatively spliced codon TCGA-X7-A8D8-01A-11D-A423-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-YT-A95H-01A-11D-A428-09 chr10:51225553 A>G maps to ENST00000425119 C476C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr14:105419321 G>A maps to NM_138420.2 A822A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XU-A92T-01A-11D-A423-09 chr23:129270036 G>A did not map to a codon.
Sequencing variant TCGA-5U-AB0D-01A-11D-A423-09 chr23:55042030 T>A did not map to a codon.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr19:49971696 G>T maps to NM_153329.3 V666V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XU-A936-01A-11D-A428-09 chr17:6909879 G>A maps to NM_000697.2 W498*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XU-A933-01A-11D-A423-09 chr15:85405948 C>T maps to NM_020778.4 R1607*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr2:233274419 C>T maps to NM_031313.2 H479H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr12:53819609 G>A maps to NM_020547.2 Q253Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr11:118076602 G>A maps to NM_001098526.1 R176R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3G-AB0T-01A-11D-A423-09 chr12:121756195 G>A maps to NM_016237.4 R593*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3G-AB14-01A-11D-A423-09 chr10:61932687 C>T maps to NM_020987.2 Q784Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr10:61840357 G>A maps to NM_020987.2 R1457*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr10:61843306 C>T maps to NM_020987.2 Q1381Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZC-AAAF-01A-11D-A428-09 chr18:9257209 C>T maps to NM_015208.3 V1315V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr9:69391188 C>T maps to NM_001098805.1 R233*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4V-A9QT-01A-11D-A423-09 chr2:97830035 G>A maps to NM_001164315.1 P482P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A96V-01A-11D-A428-09 chr12:99640642 C>T did not map to a codon.
Sequencing variant TCGA-XU-A92R-01A-11D-A423-09 chr2:21227521 A>G maps to NM_000384.2 D3938D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr23:130215767 C>T did not map to a codon.
Sequencing variant TCGA-XU-A936-01A-11D-A428-09 chr23:11157086 G>A did not map to a codon.
Sequencing variant TCGA-4V-A9QJ-01A-11D-A423-09 chr9:34621493 G>A maps to NM_001017363.1 P400P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3S-A8YW-01A-11D-A423-09 chr10:28233762 G>A maps to NM_018076.2 T505T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XU-A933-01A-11D-A423-09 chr23:100911456 C>T did not map to a codon.
Sequencing variant TCGA-5K-AAAP-01A-11D-A423-09 chr2:220091610 G>T maps to NM_024085.3 I64I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XU-A933-01A-11D-A423-09 chr15:25971101 T>G maps to NM_024490.3 A325A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XM-A8RE-01A-11D-A423-09 chr5:160071154 G>A maps to NM_025153.2 V286V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5V-A9RR-01A-11D-A423-09 chr23:138886757 C>A did not map to a codon.
Sequencing variant TCGA-X7-A8M1-01A-11D-A423-09 chr13:25274966 C>A maps to NM_001185085.1 S602S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XU-A936-01A-11D-A428-09 chr3:113497641 A>G maps to NM_001690.3 K14K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A96C-01A-11D-A428-09 chr20:50221407 C>G maps to NM_006045.1 L985L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr3:142269027 C>T maps to NM_001184.3 T974T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3G-AB19-01A-21D-A423-09 chr23:153171713 C>T did not map to a codon.
Sequencing variant TCGA-ZB-A969-01A-11D-A428-09 chr21:30699273 G>T maps to NM_206866.1 E377*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X7-A8M3-01A-11D-A423-09 chr6:57048768 C>G maps to NM_004282.3 Y139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZC-AAA7-01A-11D-A428-09 chr4:102751112 G>A maps to NM_017935.4 L73L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XM-A8RC-01A-11D-A423-09 chr23:39933499 A>T did not map to a codon.
Sequencing variant TCGA-XM-A8RI-01A-12D-A423-09 chr23:39932170 G>A did not map to a codon.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr23:39934418 C>T did not map to a codon.
Sequencing variant TCGA-ZB-A961-01A-11D-A428-09 chr11:102198821 C>A maps to NM_182962.1 I331I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4V-A9QX-01A-11D-A423-09 chr2:32582264 T>A maps to NM_016252.3 T12T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XU-A930-01A-11D-A423-09 chr6:55638912 G>A maps to NM_021073.2 R321*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XU-A933-01A-11D-A423-09 chr16:50357575 A>C maps to NM_001173984.2 Y455*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A965-01A-11D-A428-09 chr3:9786001 G>T maps to NM_001003694.1 P910P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4X-A9FA-01A-11D-A423-09 chr10:50532899 G>A maps to NM_001135196.1 K770K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr10:50532272 C>T maps to NM_001135196.1 P561P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr12:112750857 C>T maps to NM_001109662.2 A149A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A96L-01A-11D-A428-09 chr12:112752331 G>A maps to NM_001109662.2 F94F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr17:80401909 A>G maps to NM_001193657.1 S178S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A96Q-01A-11D-A428-09 chr19:3620800 C>G did not map to a codon.
Sequencing variant TCGA-4V-A9QM-01A-11D-A423-09 chr19:14001020 C>T maps to ENST00000454313 G216G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr1:223568376 C>T maps to NM_152610.2 H520H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4X-A9FD-01A-11D-A423-09 chr20:31876667 C>T maps to NM_033197.2 T79T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X7-A8D8-01A-11D-A423-09 chr20:18794488 G>A maps to NM_178483.2 K10K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr3:14711555 T>C maps to NM_016474.4 P356P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XM-A8RC-01A-11D-A423-09 chr3:56657535 T>C maps to ENST00000447900 E1514E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XM-A8RI-01A-12D-A423-09 chr6:43970529 G>A maps to NM_153246.4 A132A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XU-A92V-01A-11D-A423-09 chr7:40173956 G>A maps to NM_138701.3 G70G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XU-A92R-01A-11D-A423-09 chr7:150028150 C>T maps to NM_138434.2 R220*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr7:120740102 G>A maps to NM_024913.4 T291T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A96V-01A-11D-A428-09 chr8:67589948 G>A maps to NM_019607.1 R2R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr8:67422331 G>T maps to NM_152765.3 V94V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A96F-01A-11D-A428-09 chr9:116183408 G>A maps to ENST00000451722 T140T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XM-AAZ2-01A-11D-A423-09 chr23:15790685 C>G did not map to a codon.
Sequencing variant TCGA-5V-A9RR-01A-11D-A423-09 chr19:13340903 G>A maps to NM_023035.2 P1844P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr19:44130990 C>T maps to NM_145296.1 P148P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A96D-01A-11D-A428-09 chr11:14991620 C>T maps to NM_001741.2 R29R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XU-A92Q-01A-11D-A423-09 chr23:110494929 C>T did not map to a codon.
Sequencing variant TCGA-X7-A8M3-01A-11D-A423-09 chr22:39069239 G>T maps to NM_015373.3 *127L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A96C-01A-11D-A428-09 chr2:219870258 T>G maps to NM_194302.2 R1650R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A96L-01A-11D-A428-09 chr2:159312933 A>C maps to NM_138803.3 A6A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XM-A8RF-01A-11D-A423-09 chr23:49106159 C>T did not map to a codon.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr17:78069069 C>T maps to NM_017950.2 L947L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr3:113187078 G>A maps to NM_144718.3 R354R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZC-AAA7-01A-11D-A428-09 chr11:66358914 C>T maps to NM_018219.2 S524S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr23:50055545 C>T did not map to a codon.
Sequencing variant TCGA-XM-AAZ1-01A-11D-A423-09 chr12:7548910 G>A maps to ENST00000416109 D620D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A961-01A-11D-A428-09 chr15:73994735 C>T maps to NM_001024736.1 Q74*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5U-AB0D-01A-11D-A423-09 chr20:3783594 C>T maps to NM_021873.2 D411D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A965-01A-11D-A428-09 chr20:44869800 G>A maps to NM_021248.1 G117G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr23:139865787 C>G did not map to a codon.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr22:46835084 C>T did not map to a codon.
Sequencing variant TCGA-XU-A92R-01A-11D-A423-09 chr23:100387418 T>G did not map to a codon.
Sequencing variant TCGA-5U-AB0E-01A-11D-A423-09 chr2:182413584 C>T did not map to a codon.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr16:66974546 C>T maps to NM_003869.5 G319G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4V-A9QS-01A-11D-A423-09 chr16:75428995 G>A maps to NM_006324.2 A214A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3G-AB0Q-01A-11D-A423-09 chr17:7798459 C>T maps to NM_001005271.2 R558*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr20:40033424 G>A maps to NM_032221.3 S2652S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XM-A8RI-01A-12D-A423-09 chr11:125514477 A>G maps to NM_001274.4 Q391Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A96V-01A-11D-A428-09 chr22:29090048 C>A maps to NM_001005735.1 E521*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZC-AAA7-01A-11D-A428-09 chr3:440068 G>C did not map to a codon.
Sequencing variant TCGA-ZC-AAA7-01A-11D-A428-09 chr7:136699905 T>C maps to NM_001006628.1 L98L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5U-AB0D-01A-11D-A423-09 chr2:101019054 C>A maps to NM_004854.3 E55*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr19:19654910 G>A maps to NM_153221.2 R519R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A96K-01A-11D-A428-09 chr16:74452070 G>A maps to NM_001011880.2 P114P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZC-AAA7-01A-11D-A428-09 chr12:122763583 C>G maps to ENST00000302528 L1252L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5V-A9RR-01A-11D-A423-09 chr10:105796367 T>C maps to NM_000494.3 L1100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XU-A932-01A-11D-A423-09 chr21:47417639 C>T maps to NM_001848.2 A496A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr6:70961828 C>A maps to NM_001851.4 G622G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr6:36711477 G>A maps to NM_020939.1 R517R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr16:89653461 G>A maps to NM_014427.4 V368V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5V-A9RR-01A-11D-A423-09 chr8:3855579 G>A maps to NM_033225.5 S221S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4V-A9QJ-01A-11D-A423-09 chr1:85040023 C>T maps to NM_004388.2 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A96E-01A-11D-A428-09 chr16:67670754 G>T did not map to a codon.
Sequencing variant TCGA-XM-A8RF-01A-11D-A423-09 chr23:16711301 C>T did not map to a codon.
Sequencing variant TCGA-XU-A92T-01A-11D-A423-09 chr10:17085824 C>T did not map to a codon.
Sequencing variant TCGA-ZC-AAA7-01A-11D-A428-09 chr10:16957097 G>A maps to NM_001081.3 V2428V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XM-A8RC-01A-11D-A423-09 chr23:35959478 A>G did not map to a codon.
Sequencing variant TCGA-4V-A9QR-01A-11D-A423-09 chr23:19983215 C>G did not map to a codon.
Sequencing variant TCGA-4V-A9QQ-01A-11D-A423-09 chr23:23957370 C>T did not map to a codon.
Sequencing variant TCGA-XM-A8RI-01A-12D-A423-09 chr1:202931735 C>T maps to NM_016243.2 G279G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X7-A8D9-01A-11D-A423-09 chr5:156712385 C>A maps to ENST00000442283 V5V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A96V-01A-11D-A428-09 chr16:50811825 C>A maps to ENST00000311559 S371*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr10:94833786 C>T maps to NM_000783.3 C32C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A96V-01A-11D-A428-09 chr10:135341998 C>T maps to NM_000773.3 F64F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XM-A8RI-01A-12D-A423-09 chr7:99459366 G>A maps to NM_022820.3 V386V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZC-AAAF-01A-11D-A428-09 chr19:15806748 C>T maps to NM_023944.2 D373D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr9:34089565 G>A maps to NM_015397.3 Y349Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X7-A8M5-01A-11D-A423-09 chr23:125299319 C>A did not map to a codon.
Sequencing variant TCGA-XM-A8RC-01A-11D-A423-09 chr10:115609246 A>C maps to NM_014881.3 P539P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X7-A8M1-01A-11D-A423-09 chr23:134713736 A>G did not map to a codon.
Sequencing variant TCGA-ZC-AAAF-01A-11D-A428-09 chr23:134655183 G>A did not map to a codon.
Sequencing variant TCGA-ZC-AAAF-01A-11D-A428-09 chr17:57654625 G>A did not map to a codon.
Sequencing variant TCGA-X7-A8M3-01A-11D-A423-09 chr2:232952372 C>A maps to NM_152383.4 I181I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A96V-01A-11D-A428-09 chr23:69670113 C>G did not map to a codon.
Sequencing variant TCGA-3S-A8YW-01A-11D-A423-09 chr23:31986628 T>G did not map to a codon.
Sequencing variant TCGA-XM-A8RF-01A-11D-A423-09 chr23:32482814 T>G did not map to a codon.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr23:32834700 C>A did not map to a codon.
Sequencing variant TCGA-4V-A9QX-01A-11D-A423-09 chr7:21906095 C>T maps to NM_003777.3 A3842A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4V-A9QQ-01A-11D-A423-09 chr16:21156602 A>T maps to NM_017539.1 L116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XU-A92U-01A-11D-A423-09 chr2:196912089 A>G maps to NM_018897.2 L128L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4V-A9QJ-01A-11D-A423-09 chr17:11757405 C>A maps to NM_001372.3 P3198P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr1:65860701 G>A maps to ENST00000371069 S675S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr17:40146919 C>A maps to NM_003315.3 E150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr11:6578412 C>T maps to NM_144666.2 R2630*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YT-A95E-01A-11D-A428-09 chr16:89696826 C>T maps to NM_004413.3 S3S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A96L-01A-11D-A428-09 chr3:109031470 G>A maps to NM_138815.3 D34D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A96C-01A-11D-A428-09 chr18:28622607 G>T maps to NM_001941.3 R7R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr21:41446993 G>T maps to NM_001389.3 R1620R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4V-A9QW-01A-11D-A423-09 chr18:28916465 T>C maps to NM_001942.2 F385F. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-XM-A8RF-01A-11D-A423-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-ZB-A965-01A-11D-A428-09 chr11:103019259 G>T maps to NM_001080463.1 E954*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A96E-01A-11D-A428-09 chr12:4714231 C>T maps to NM_003845.1 Q312*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X7-A8M1-01A-11D-A423-09 chr2:71738995 G>A maps to NM_001130987.1 P135P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr2:71825778 G>A maps to NM_001130987.1 T1220T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X7-A8M3-01A-11D-A423-09 chr5:158523986 C>A maps to NM_024007.3 E96*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3S-A8YW-01A-11D-A423-09 chr1:245285220 G>T did not map to a codon.
Sequencing variant TCGA-3S-A8YW-01A-11D-A423-09 chr6:52344481 T>C maps to NM_018100.3 L513L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr5:38352385 G>A maps to ENST00000354891 A166A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3G-AB19-01A-21D-A423-09 chr6:31850562 C>A did not map to a codon.
Sequencing variant TCGA-XM-AAZ1-01A-11D-A423-09 chr23:20159747 T>C did not map to a codon.
Sequencing variant TCGA-X7-A8M5-01A-11D-A423-09 chr8:141572625 T>C maps to NM_012154.3 S148S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XU-A92R-01A-11D-A423-09 chr13:41515205 C>T maps to NM_172373.3 R369R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZC-AAAF-01A-11D-A428-09 chr19:6919661 G>A maps to ENST00000381407 K510K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4V-A9QM-01A-11D-A423-09 chr22:41521971 T>C maps to NM_001429.3 T278T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3S-A8YW-01A-11D-A423-09 chr9:102784464 G>T maps to NM_015051.1 L110L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr23:103495106 G>A did not map to a codon.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr3:138183252 C>T maps to NM_031913.3 R328*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr2:176947100 G>A maps to NM_001080458.1 G168G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XU-A92O-01A-11D-A423-09 chr23:154159466 C>A did not map to a codon.
Sequencing variant TCGA-3G-AB19-01A-21D-A423-09 chr19:1881262 G>A maps to NM_031213.3 C101C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4X-A9FB-01A-11D-A423-09 chr19:1881346 A>G maps to NM_031213.3 R73R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4V-A9QX-01A-11D-A423-09 chr23:54099528 A>G did not map to a codon.
Sequencing variant TCGA-ZB-A965-01A-11D-A428-09 chr23:63411802 G>T did not map to a codon.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr23:134166466 T>C did not map to a codon.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr23:134166470 A>G did not map to a codon.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr23:134185996 A>C did not map to a codon.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr23:134186033 T>G did not map to a codon.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr23:134186093 G>C did not map to a codon.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr23:68725181 C>T did not map to a codon.
Sequencing variant TCGA-XM-AAZ3-01A-11D-A423-09 chr11:6233062 G>A maps to NM_032127.3 L878L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4V-A9QJ-01A-11D-A423-09 chr1:222919976 C>T maps to NM_207468.2 D30D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr1:43621890 C>T maps to NM_001101376.2 R104R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A962-01A-11D-A428-09 chr9:97083467 G>A maps to NM_017561.1 Q297*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YT-A95D-01A-11D-A428-09 chr23:153741209 C>T did not map to a codon.
Sequencing variant TCGA-5U-AB0D-01A-11D-A423-09 chr23:34149545 C>T did not map to a codon.
Sequencing variant TCGA-ZB-A96K-01A-11D-A428-09 chr23:37026798 A>G did not map to a codon.
Sequencing variant TCGA-ZB-A961-01A-11D-A428-09 chr1:78332036 T>C maps to NM_198549.2 S508S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XM-A8RC-01A-11D-A423-09 chr20:3128198 A>C maps to NM_021826.4 T506T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZC-AAA7-01A-11D-A428-09 chr19:8191231 C>G did not map to a codon.
Sequencing variant TCGA-XU-A92V-01A-11D-A423-09 chr19:55396875 C>T maps to NM_002000.2 C100C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A96H-01A-11D-A428-09 chr19:40366439 G>T maps to NM_003890.2 R4598R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XM-A8RG-01A-11D-A423-09 chr8:125107170 C>A maps to NM_001039112.2 L1529L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3S-A8YW-01A-11D-A423-09 chr19:35849878 C>T maps to NM_005304.3 L29L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr4:1807582 G>A maps to NM_000142.4 P584P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5V-A9RR-01A-11D-A423-09 chr6:110062668 A>G maps to NM_014845.5 P266P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XU-A92T-01A-11D-A423-09 chr6:32096723 C>T maps to NM_022110.3 V278V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A96V-01A-11D-A428-09 chr1:152278163 C>T maps to NM_002016.1 V3066V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr15:33357215 C>T maps to NM_001103184.2 W478*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A961-01A-11D-A428-09 chr9:70918631 C>G maps to NM_199135.4 P255P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3G-AB0Q-01A-11D-A423-09 chr9:70177485 G>A maps to NM_001126334.1 F166F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr7:4799131 G>A maps to ENST00000450194 S512S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A96V-01A-11D-A428-09 chr1:74665348 C>T maps to NM_001112808.2 G28G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XU-A92O-01A-11D-A423-09 chr10:95429585 T>C maps to NM_145246.4 L315L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr10:49440314 G>T maps to NM_001018071.3 S337S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5V-A9RR-01A-11D-A423-09 chr7:127240362 C>G maps to NM_020369.2 A469A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XM-A8RC-01A-11D-A423-09 chr2:186665768 G>A maps to NM_173651.2 L4001L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YT-A95E-01A-11D-A428-09 chr23:31089832 G>T did not map to a codon.
Sequencing variant TCGA-5U-AB0D-01A-11D-A423-09 chr17:42636534 G>A maps to NM_001466.3 S493S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr6:89890145 G>A maps to NM_002042.3 R337R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A96V-01A-11D-A428-09 chr22:29704682 C>T maps to NM_152236.1 R196R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X7-A8M3-01A-11D-A423-09 chr22:30681674 C>A maps to ENST00000434291 V459V. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-ZB-A966-01A-11D-A428-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-XU-A933-01A-11D-A423-09 chr8:97157552 C>G maps to NM_001001557.2 L202L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr23:69644871 G>A did not map to a codon.
Sequencing variant TCGA-3S-A8YW-01A-11D-A423-09 chr8:95262573 G>T maps to NM_181702.2 L285L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XU-A92R-01A-11D-A423-09 chr3:158399828 T>A maps to ENST00000264263 Y568*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr22:38025515 G>T maps to ENST00000381756 G398*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4V-A9QL-01A-11D-A423-09 chr7:100284305 C>T maps to NM_022574.4 R220R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3S-A8YW-01A-11D-A423-09 chr6:87994414 G>C maps to NM_198568.2 S72S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr7:42004803 G>A maps to NM_000168.5 S1289S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr6:39033980 G>A maps to NM_002062.3 P137P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A96M-01A-11D-A428-09 chr1:183913442 C>T maps to NM_015101.2 E428E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr22:23437977 C>T maps to NM_002073.2 R32R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr15:75586104 C>T maps to NM_001145224.1 D543D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XU-A92V-01A-11D-A423-09 chr23:135428326 G>A did not map to a codon.
Sequencing variant TCGA-ZB-A96Q-01A-11D-A428-09 chr23:135427619 T>C did not map to a codon.
Sequencing variant TCGA-ZB-A969-01A-11D-A428-09 chr23:129519406 G>T did not map to a codon.
Sequencing variant TCGA-ZB-A96V-01A-11D-A428-09 chr10:134942642 C>T maps to ENST00000368577 A977A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4V-A9QT-01A-11D-A423-09 chr4:22517361 A>G maps to NM_145290.2 L16L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A96V-01A-11D-A428-09 chr4:22456538 T>G maps to NM_145290.2 I141I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr1:6314014 G>A maps to NM_207370.2 S183S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A96C-01A-11D-A428-09 chr23:53106205 A>G did not map to a codon.
Sequencing variant TCGA-4V-A9QL-01A-11D-A423-09 chr23:19017306 C>G did not map to a codon.
Sequencing variant TCGA-XU-A933-01A-11D-A423-09 chr5:90059168 G>C maps to NM_032119.3 V4056V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A96E-01A-11D-A428-09 chr16:19883615 G>A maps to NM_016235.1 T184T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XM-A8RC-01A-11D-A423-09 chr10:46999614 C>G maps to NM_014696.3 G245G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XM-AAZ3-01A-11D-A423-09 chr3:113658829 G>T maps to NM_017577.4 E597*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A96K-01A-11D-A428-09 chr10:87362203 C>T maps to NM_017551.2 P952P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr23:48840260 G>A did not map to a codon.
Sequencing variant TCGA-ZB-A96I-01A-11D-A428-09 chr1:119934842 T>C maps to ENST00000361035 A307A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr5:140075193 C>T maps to NM_012208.2 G167G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4V-A9QL-01A-11D-A423-09 chr15:73617503 C>A maps to NM_005477.2 V590V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr23:83724351 C>T did not map to a codon.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr15:63967236 G>A maps to ENST00000261887 R2384*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZC-AAAA-01A-11D-A428-09 chr6:26124471 T>C maps to NM_003512.3 R4R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XM-A8RG-01A-11D-A423-09 chr6:26250542 G>A maps to NM_021018.2 C97C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr6:143092793 G>A maps to NM_006734.3 R1028*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4V-A9QU-01A-11D-A423-09 chr1:221054596 C>G maps to NM_021958.3 P218P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X7-A8M1-01A-11D-A423-09 chr1:186052061 T>C maps to NM_031935.2 S2951S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5U-AB0E-01A-11D-A423-09 chr7:27134901 G>A maps to NM_005522.4 V210V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X7-A8D9-01A-11D-A423-09 chr7:27135318 G>A maps to NM_005522.4 H71H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XU-A92Q-01A-11D-A423-09 chr1:152189037 A>G maps to NM_001009931.1 Y1689Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A96R-01A-11D-A428-09 chr16:25703803 G>A maps to NM_006040.2 P22P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X7-A8M3-01A-11D-A423-09 chr16:67470563 G>A maps to NM_000196.3 L292L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5U-AB0D-01A-11D-A423-09 chr23:135593718 C>A did not map to a codon.
Sequencing variant TCGA-XU-AAY0-01A-11D-A428-09 chr23:135582343 A>G did not map to a codon.
Sequencing variant TCGA-4V-A9QR-01A-11D-A423-09 chr10:92508879 G>A maps to NM_019859.3 T337T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A96V-01A-11D-A428-09 chr20:2639396 C>G maps to NM_006899.2 *386Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr8:39847305 C>T maps to NM_194294.2 R219*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XU-A933-01A-11D-A423-09 chr23:148564526 C>T did not map to a codon.
Sequencing variant TCGA-X7-A8M5-01A-11D-A423-09 chr9:27524942 A>G maps to NM_020124.2 L203L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XU-A92O-01A-11D-A423-09 chr23:130409532 G>A did not map to a codon.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr12:57828743 G>A maps to NM_005538.2 Q25Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A96E-01A-11D-A428-09 chr1:46165727 T>A maps to NM_005897.2 S555S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr3:121500718 C>T maps to NM_001023570.2 A427A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3S-A8YW-01A-11D-A423-09 chr3:12944296 C>T maps to ENST00000429247 A927A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YT-A95F-01A-11D-A428-09 chr23:53272535 C>T did not map to a codon.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr13:110434872 G>A maps to NM_003749.2 S1176S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr23:107979450 C>T did not map to a codon.
Sequencing variant TCGA-ZB-A969-01A-11D-A428-09 chr13:102227853 C>T maps to NM_004791.1 D181D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A969-01A-11D-A428-09 chr3:52858574 C>A maps to ENST00000485816 E295*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A96A-01A-11D-A428-09 chr23:78618444 A>C did not map to a codon.
Sequencing variant TCGA-4X-A9F9-01A-11D-A423-09 chr1:152882980 A>T maps to NM_005547.2 P236P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr23:8522067 G>A did not map to a codon.
Sequencing variant TCGA-5U-AB0D-01A-11D-A423-09 chr19:49573388 G>A maps to NM_031886.2 D434D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr11:17757797 C>T maps to NM_001112741.1 C83C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YT-A95E-01A-11D-A428-09 chr17:40318360 G>A maps to NM_012285.2 S598S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XU-A92Q-01A-11D-A423-09 chr12:70760621 C>G maps to NM_014505.4 G36G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3G-AB0O-01A-22D-A423-09 chr5:113698627 C>T maps to NM_021614.2 A52A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A96D-01A-11D-A428-09 chr1:196438173 G>A maps to NM_198503.2 R137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A963-01A-11D-A428-09 chr11:67018080 G>A maps to NM_012308.2 E860E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A961-01A-11D-A428-09 chr14:24901147 C>G maps to NM_015299.2 P227P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr17:26961697 T>C maps to NM_014680.2 A969A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A961-01A-11D-A428-09 chr20:36642125 C>T maps to NM_014657.1 E31E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr20:36625223 C>T maps to NM_014657.1 S975S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A96V-01A-11D-A428-09 chr16:15706471 G>C maps to NM_014647.3 S1139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr13:42481720 C>T did not map to a codon.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr23:118217054 G>A did not map to a codon.
Sequencing variant TCGA-YT-A95G-01A-11D-A428-09 chr18:43497644 G>A maps to NM_020964.2 Q1080*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr1:233497905 C>T maps to NM_032435.2 D473D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X7-A8M0-01A-11D-A423-09 chr23:73961371 C>A did not map to a codon.
Sequencing variant TCGA-X7-A8M5-01A-11D-A423-09 chr23:73960472 C>T did not map to a codon.
Sequencing variant TCGA-X7-A8M5-01A-11D-A423-09 chr23:73961544 C>A did not map to a codon.
Sequencing variant TCGA-ZB-A96V-01A-11D-A428-09 chr23:73963427 G>T did not map to a codon.
Sequencing variant TCGA-4V-A9QJ-01A-11D-A423-09 chr20:30918005 T>C maps to NM_004798.3 G677G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3G-AB19-01A-21D-A423-09 chr2:26204456 G>C maps to NM_002254.6 T110T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr23:69510594 A>G did not map to a codon.
Sequencing variant TCGA-X7-A8M5-01A-11D-A423-09 chr3:47286393 A>G maps to NM_182902.3 D467D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4X-A9FC-01A-11D-A423-09 chr19:55255453 A>G maps to NM_015868.2 G194G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5K-AAAP-01A-11D-A423-09 chr19:55363630 C>T maps to NM_006737.2 G83G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XU-A92O-01A-11D-A423-09 chr11:126316677 G>T maps to NM_032531.3 V367V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr1:204159761 G>T maps to ENST00000306118 P89P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A96L-01A-11D-A428-09 chr16:87743033 C>T maps to NM_017566.3 G428G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5U-AB0E-01A-11D-A423-09 chr19:51503885 C>T maps to NM_144505.1 S53S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5U-AB0F-01A-11D-A423-09 chr12:53295732 G>A maps to NM_002273.3 Q150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XU-AAXZ-01A-11D-A428-09 chr21:45959694 G>T maps to NM_198691.2 T113T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A96K-01A-11D-A428-09 chr21:45994462 C>T maps to NM_198687.1 C276C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XM-A8RD-01A-11D-A423-09 chr17:39324103 A>G maps to NM_033187.1 S107S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4V-A9QX-01A-11D-A423-09 chr11:1606281 T>C maps to NM_001005922.1 K66K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X7-A8D8-01A-11D-A423-09 chr6:130374130 G>T maps to NM_032438.2 E193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3S-A8YW-01A-11D-A423-09 chr20:60895896 G>A maps to NM_005560.3 G2182G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr20:60921236 G>A maps to NM_005560.3 T439T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A96V-01A-11D-A428-09 chr15:59499261 C>A maps to NM_033195.1 T41T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A96V-01A-11D-A428-09 chr14:93178265 C>T maps to NM_005606.6 S215S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4V-A9QU-01A-11D-A423-09 chr7:103969250 C>T maps to NM_199000.2 A8A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XU-A92W-01A-11D-A423-09 chr13:76335144 A>G maps to ENST00000357063 L26L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XM-A8RC-01A-11D-A423-09 chr1:165218732 G>A maps to NM_177398.3 V136V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr17:56321400 C>T maps to NM_006151.2 A41A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XM-AAZ3-01A-11D-A423-09 chr17:62855862 C>T maps to NM_199340.2 S1467S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A961-01A-11D-A428-09 chr4:52883539 C>G maps to NM_001024611.1 T80T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A96E-01A-11D-A428-09 chr3:37154408 T>A maps to NM_006309.2 L145L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr1:204588190 G>A maps to NM_201630.1 P310P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr12:96394808 G>A maps to NM_000895.1 P598P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4X-A9FD-01A-11D-A423-09 chr17:48823272 C>T maps to ENST00000393227 R296*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr1:23420408 G>A maps to NM_001142546.1 R116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A96E-01A-11D-A428-09 chr23:151935506 T>A did not map to a codon.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr23:27840013 C>T did not map to a codon.
Sequencing variant TCGA-X7-A8M3-01A-11D-A423-09 chr23:35820518 G>T did not map to a codon.
Sequencing variant TCGA-ZB-A961-01A-11D-A428-09 chr23:26157792 G>A did not map to a codon.
Sequencing variant TCGA-ZB-A96C-01A-11D-A428-09 chr9:139750226 C>T maps to ENST00000392881 D505D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr6:136934281 A>G maps to NM_005923.3 N797N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZC-AAA7-01A-11D-A428-09 chr16:29821497 G>A maps to NM_002383.2 S460S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr6:90359894 G>A maps to NM_014611.1 R5352*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A96Q-01A-11D-A428-09 chr6:90405581 C>T maps to NM_014611.1 Q3171Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5U-AB0D-01A-11D-A423-09 chr23:153297696 G>A did not map to a codon.
Sequencing variant TCGA-XU-A936-01A-11D-A428-09 chr23:153296827 C>T did not map to a codon.
Sequencing variant TCGA-YT-A95G-01A-11D-A428-09 chr12:116445403 G>A maps to NM_015335.4 Q684*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr23:40572272 C>T did not map to a codon.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr2:112751862 C>T maps to NM_006343.2 S444S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A96I-01A-11D-A428-09 chr15:41991096 G>T maps to ENST00000219905 E684*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr14:50088615 C>T maps to NM_002408.3 C210C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XU-A933-01A-11D-A423-09 chr23:10427744 A>G did not map to a codon.
Sequencing variant TCGA-ZB-A96M-01A-11D-A428-09 chr10:129905996 A>G maps to NM_002417.4 T1369T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr3:37035146 G>T maps to NM_000249.3 E37*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZT-A8OM-01A-11D-A428-09 chr3:154832819 G>A maps to NM_007289.2 E78E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5K-AAAP-01A-11D-A423-09 chr4:90856010 C>T maps to NM_007351.2 Q394*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X7-A8D7-01A-11D-A423-09 chr22:28194935 C>T maps to NM_002430.2 Q532Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr19:2078277 G>C maps to NM_130807.2 G94G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr23:154033629 C>T did not map to a codon.
Sequencing variant TCGA-3S-A8YW-01A-11D-A423-09 chr7:24727231 G>C maps to ENST00000409253 *583S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr17:60743590 C>T maps to NM_006039.3 Y219Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr11:18158925 C>T maps to NM_054031.3 N59N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3S-A8YW-01A-11D-A423-09 chr8:16026356 C>T maps to ENST00000445506 T98T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A96D-01A-11D-A428-09 chr23:149931162 G>A did not map to a codon.
Sequencing variant TCGA-ZB-A96V-01A-11D-A428-09 chr8:17228599 G>A maps to NM_004686.4 Q86*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XM-AAZ2-01A-11D-A423-09 chr23:63488808 T>G did not map to a codon.
Sequencing variant TCGA-4V-A9QS-01A-11D-A423-09 chr5:79284998 G>T maps to ENST00000512528 L99L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A965-01A-11D-A428-09 chr19:9063746 G>C maps to NM_024690.2 S7900*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A962-01A-11D-A428-09 chr11:1090372 G>A maps to ENST00000441003 P1223P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XU-A92R-01A-11D-A423-09 chr6:30955022 C>T maps to NM_001010909.2 A357A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XM-A8RD-01A-11D-A423-09 chr16:29848215 C>T maps to NM_017458.3 C282C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A96C-01A-11D-A428-09 chr23:3235592 C>G did not map to a codon.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr19:54376794 G>A maps to NM_001020818.1 T4T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XU-A933-01A-11D-A423-09 chr20:42331284 C>T maps to NM_002466.2 T369T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A96V-01A-11D-A428-09 chr12:102046902 G>A maps to NM_002465.2 K548K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X7-A8M1-01A-11D-A423-09 chr17:10248530 C>T maps to NM_003802.2 E524E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr19:50713828 G>A maps to NM_001145809.1 A69A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZC-AAA7-01A-11D-A428-09 chr14:23902824 C>A maps to NM_000257.2 V39V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr4:673724 C>T maps to NM_002477.1 D70D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZC-AAA7-01A-11D-A428-09 chr17:18036681 C>T maps to ENST00000205890 V1488V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X7-A8M1-01A-11D-A423-09 chr15:59523987 G>A maps to NM_004998.2 H141H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A96V-01A-11D-A428-09 chr19:8615521 G>A maps to NM_012335.3 L276L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XU-A92T-01A-11D-A423-09 chr2:128384561 C>T maps to ENST00000389524 Q1384*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XU-A92R-01A-11D-A423-09 chr23:153199410 T>C did not map to a codon.
Sequencing variant TCGA-XU-A930-01A-11D-A423-09 chr13:41932576 G>T maps to NM_024561.4 E409*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZC-AAA7-01A-11D-A428-09 chr13:41885702 C>T maps to NM_024561.4 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5K-AAAP-01A-11D-A423-09 chr13:35738642 A>C maps to ENST00000400445 P1410P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr13:35729942 A>G maps to ENST00000400445 V826V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XU-A92U-01A-11D-A423-09 chr11:134028285 A>G maps to NM_015261.2 H1324H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X7-A8M0-01A-11D-A423-09 chr4:115760704 C>T did not map to a codon.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr11:77790745 A>G maps to NM_004549.4 D15D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A96C-01A-11D-A428-09 chr1:16785394 G>A maps to NM_001145277.1 T242T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A96I-01A-11D-A428-09 chr12:55420927 G>A maps to NM_021191.2 S235S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A962-01A-11D-A428-09 chr17:29677283 G>T maps to NM_001042492.2 E2469*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XU-A92Z-01A-11D-A423-09 chr22:30050678 G>T maps to NM_181832.2 G161*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5G-A9ZZ-01A-31D-A423-09 chr23:17745001 C>A did not map to a codon.
Sequencing variant TCGA-ZB-A96I-01A-11D-A428-09 chr3:52524089 G>T did not map to a codon.
Sequencing variant TCGA-ZC-AAA7-01A-11D-A428-09 chr23:119077213 C>G did not map to a codon.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr16:50583396 G>A maps to NM_033119.3 Q41Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A96B-01A-11D-A428-09 chr5:1038421 G>A maps to NM_033120.2 R430R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XM-A8RI-01A-12D-A423-09 chr23:5821677 G>T did not map to a codon.
Sequencing variant TCGA-ZB-A969-01A-11D-A428-09 chr23:5947400 C>A did not map to a codon.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr17:26370219 A>T maps to NM_016231.4 A107A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr19:54308673 G>T maps to ENST00000391773 A759A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XU-A92V-01A-11D-A423-09 chr19:56539530 C>T maps to NM_153447.4 D644D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A962-01A-11D-A428-09 chr19:56465978 C>T maps to NM_176811.2 H185H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr7:30492632 G>A maps to NM_006092.2 R134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XU-A933-01A-11D-A423-09 chr1:145281624 C>G maps to ENST00000454606 P197P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A964-01A-11D-A428-09 chr11:108043016 A>T maps to NM_002519.2 T898T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XM-A8RF-01A-11D-A423-09 chr1:179528896 C>A did not map to a codon.
Sequencing variant TCGA-ZB-A965-01A-11D-A428-09 chr23:30326467 G>A did not map to a codon.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr23:30326503 C>T did not map to a codon.
Sequencing variant TCGA-ZT-A8OM-01A-11D-A428-09 chr3:24018735 C>A maps to NM_005126.4 V522V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XM-AAZ2-01A-11D-A423-09 chr3:119534624 C>T maps to NM_022002.2 F408F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X7-A8DJ-01A-11D-A423-09 chr3:15084512 T>C maps to NM_003298.3 *616Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XU-A92Y-01A-11D-A423-09 chr10:115374702 C>T maps to ENST00000369358 T1035T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5U-AB0D-01A-11D-A423-09 chr1:52276076 C>T did not map to a codon.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr8:32621337 G>A maps to NM_013956.3 S452S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZL-A9V6-01A-11D-A428-09 chr23:105156724 T>C did not map to a codon.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr2:18765848 G>A maps to ENST00000455492 Y295Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5U-AB0F-01A-11D-A423-09 chr9:87342743 C>T maps to NM_006180.3 H343H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5V-A9RR-01A-11D-A423-09 chr9:87285830 G>A maps to NM_006180.3 P56P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XU-A932-01A-11D-A423-09 chr11:47839661 T>C maps to NM_015231.1 Q459Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X7-A8M3-01A-11D-A423-09 chr23:101581400 C>T did not map to a codon.
Sequencing variant TCGA-XU-A936-01A-11D-A428-09 chr1:228466565 C>T maps to NM_001098623.1 L2346L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3S-A8YW-01A-11D-A423-09 chr15:28263683 G>A maps to NM_000275.2 H222H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YT-A95D-01A-11D-A428-09 chr23:128692700 C>A did not map to a codon.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr5:167551990 G>A maps to NM_001122679.1 T715T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr11:78380639 G>A maps to NM_001098816.2 D2250D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5U-AB0D-01A-11D-A423-09 chr23:70787884 G>A did not map to a codon.
Sequencing variant TCGA-XU-A933-01A-11D-A423-09 chr1:248059454 C>T maps to NM_001001957.2 C189C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X7-A8M0-01A-11D-A423-09 chr11:55111500 T>C maps to NM_001005274.1 I275I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XM-AAZ2-01A-11D-A423-09 chr11:56230565 G>A maps to NM_001004743.1 A104A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4V-A9QX-01A-11D-A423-09 chr11:56184916 T>C maps to NM_001004744.1 S264S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr12:55715135 C>T maps to NM_001005182.1 G251G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5K-AAAP-01A-11D-A423-09 chr12:55794549 C>T maps to NM_001005518.1 L80L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X7-A8M5-01A-11D-A423-09 chr19:9325420 G>A maps to NM_001005191.2 F31F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr12:122079266 G>A maps to NM_032790.3 Q210Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3G-AB19-01A-21D-A423-09 chr23:90691712 G>T did not map to a codon.
Sequencing variant TCGA-ZL-A9V6-01A-11D-A428-09 chr10:135193683 C>T maps to NM_152911.2 S121S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A965-01A-11D-A428-09 chr20:21690062 C>T maps to NM_006192.3 F421F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr5:140256943 C>T maps to NM_018903.2 G629G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XU-A92R-01A-11D-A423-09 chr5:140262572 G>A maps to NM_018904.2 P240P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr5:140215416 C>T maps to NM_018910.2 D483D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X7-A8D6-01A-11D-A423-09 chr5:140229924 G>T maps to NM_031857.1 T615T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XM-A8RE-01A-11D-A423-09 chr5:140482341 T>C maps to NM_018937.2 F703F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XU-AAXW-01A-11D-A428-09 chr5:140482341 T>C maps to NM_018937.2 F703F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZC-AAA7-01A-11D-A428-09 chr5:140554629 C>T maps to NM_018940.2 S738S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XU-A936-01A-11D-A428-09 chr5:140736821 C>T maps to NM_018917.2 D685D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr5:140774368 C>T maps to NM_032088.1 A663A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XU-A92Y-01A-11D-A423-09 chr5:140730597 C>T maps to NM_018922.2 S257S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A96I-01A-11D-A428-09 chr15:101971524 A>G maps to NM_002570.3 Y218Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZC-AAA7-01A-11D-A428-09 chr4:56428639 T>A maps to NM_152401.2 K168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A969-01A-11D-A428-09 chr1:66384467 G>A maps to NM_001037341.1 L77L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XU-A92O-01A-11D-A423-09 chr1:144852463 G>A maps to NM_014644.4 A2345A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr1:144874777 G>T maps to NM_014644.4 T1610T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A962-01A-11D-A428-09 chr7:95223078 A>G maps to NM_002612.3 Y92Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZC-AAAF-01A-11D-A428-09 chr1:10689945 C>T maps to NM_004565.2 Q346*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr1:10477497 C>T maps to NM_002631.2 T347T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4V-A9QX-01A-11D-A423-09 chr11:74058311 G>A maps to NM_173582.3 Q274*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr23:22051241 G>A did not map to a codon.
Sequencing variant TCGA-ZB-A96C-01A-11D-A428-09 chr23:22129591 G>A did not map to a codon.
Sequencing variant TCGA-ZB-A96H-01A-11D-A428-09 chr9:96435986 C>T maps to NM_005392.3 S823S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr1:120263833 C>T maps to NM_006623.3 T60T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4X-A9FD-01A-11D-A423-09 chr23:18966937 C>T did not map to a codon.
Sequencing variant TCGA-ZB-A96V-01A-11D-A428-09 chr3:111685489 A>G maps to NM_001134438.1 E1036E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A96E-01A-11D-A428-09 chr11:609649 C>T maps to ENST00000264555 A1398A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XM-A8RD-01A-11D-A423-09 chr5:67588085 G>A did not map to a codon.
Sequencing variant TCGA-ZC-AAAF-01A-11D-A428-09 chr8:110451153 T>C maps to ENST00000426474 Y1263Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4V-A9QX-01A-11D-A423-09 chr16:3024071 C>T maps to NM_004203.4 P413P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3S-A8YW-01A-11D-A423-09 chr1:89250346 C>T maps to NM_006256.2 G337G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XM-A8R9-01A-31D-A423-09 chr21:44450114 G>A maps to NM_004571.3 E405E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4V-A9QM-01A-11D-A423-09 chr10:96066441 C>T maps to ENST00000371380 R1961*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZC-AAA7-01A-11D-A428-09 chr16:81965141 C>T maps to NM_002661.2 F874F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A96V-01A-11D-A428-09 chr8:144995483 G>A maps to NM_201380.2 F2972F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A96E-01A-11D-A428-09 chr5:174163 G>A maps to NM_052909.3 W1095*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZC-AAA7-01A-11D-A428-09 chr1:907767 G>A maps to ENST00000379409 P374P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A965-01A-11D-A428-09 chr9:19120929 G>T maps to NM_001122.2 T181T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A96V-01A-11D-A428-09 chr1:12018610 C>T maps to ENST00000376369 I341I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr3:126708479 C>T maps to NM_032242.3 R348R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X7-A8M3-01A-11D-A423-09 chr23:153696249 C>A did not map to a codon.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr3:48465011 G>A maps to NM_001130082.1 R337*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XM-A8R9-01A-31D-A423-09 chr22:50719925 C>T maps to NM_012401.2 V1175V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XM-AAZ2-01A-11D-A423-09 chr22:50721177 G>C maps to NM_012401.2 P983P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr7:131195724 G>A maps to NM_001018111.2 R190*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZC-AAA7-01A-11D-A428-09 chr14:50120763 G>A maps to NM_002692.3 I385I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr6:43572405 G>A maps to NM_006502.2 R313R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3T-AA9L-01A-11D-A423-09 chr2:130832170 G>A maps to NM_001099771.2 P958P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XM-A8RF-01A-11D-A423-09 chr12:27835370 C>T maps to NM_003622.3 Q700*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XU-A92T-01A-11D-A423-09 chr17:57057843 C>T maps to NM_014906.3 Q574*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YT-A95E-01A-11D-A428-09 chr11:64014016 C>G maps to NM_138689.2 G43G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr8:26227707 C>T maps to NM_001177591.1 R385*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3G-AB19-01A-21D-A423-09 chr12:110989714 T>A maps to NM_139283.1 S94S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr23:48931615 C>T did not map to a codon.
Sequencing variant TCGA-5V-A9RR-01A-11D-A423-09 chr1:186275526 T>C maps to NM_005807.3 L226L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr1:186276065 A>G maps to NM_005807.3 A405A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr6:41752670 A>T did not map to a codon.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr8:48805843 G>A maps to NM_006904.6 G1234G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr14:23395918 C>T maps to NM_006109.3 T185T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZL-A9V6-01A-11D-A428-09 chr19:50098912 C>T maps to NM_020719.1 Q441*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5U-AB0D-01A-11D-A423-09 chr9:79325398 G>A maps to NM_015225.2 S597S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X7-A8M5-01A-11D-A423-09 chr14:73640273 A>C maps to NM_000021.3 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr2:54163924 C>T maps to NM_014614.2 V245V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5U-AB0D-01A-11D-A423-09 chr9:132502126 G>A maps to NM_004878.4 N74N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A96C-01A-11D-A428-09 chr19:49926533 C>A maps to NM_178449.3 L21L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A96I-01A-11D-A428-09 chr10:129869095 A>T maps to NM_006504.4 K440*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZC-AAA7-01A-11D-A428-09 chr7:157369456 G>A maps to NM_002847.3 S877S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A96G-01A-11D-A428-09 chr7:121652081 G>C maps to NM_002851.2 G994G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X7-A8M3-01A-11D-A423-09 chr12:9353545 C>A maps to NM_002864.2 V204V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XM-A8RC-01A-11D-A423-09 chr15:55522663 C>A maps to NM_183235.1 P58P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XU-AAXZ-01A-11D-A428-09 chr5:34811967 A>G maps to NM_001145521.1 G218G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XM-A8RF-01A-11D-A423-09 chr9:129815131 C>T maps to NM_014636.2 L133L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YT-A95G-01A-11D-A428-09 chr7:5104286 T>G maps to NM_021163.3 L400L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr1:145509001 C>A maps to NM_005105.2 P143P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr11:63682648 C>T did not map to a codon.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr23:17080624 T>A did not map to a codon.
Sequencing variant TCGA-X7-A8M3-01A-11D-A423-09 chr13:37393922 C>G maps to NM_000538.3 Y143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XU-A92T-01A-11D-A423-09 chr23:71351031 G>C did not map to a codon.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr10:86017731 C>T maps to ENST00000358110 D244D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr9:116268674 G>A maps to NM_144488.4 P329P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr7:75511246 C>T maps to NM_001040456.1 T93T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XM-A8RG-01A-11D-A423-09 chr3:49400048 T>G maps to NM_001664.2 P96P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A96F-01A-11D-A428-09 chr12:130935796 G>A maps to NM_015347.4 S132S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3G-AB19-01A-21D-A423-09 chr8:104948817 A>G maps to NM_001100117.2 T805T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4X-A9FA-01A-11D-A423-09 chr11:66101498 T>C maps to NM_004292.2 Q494Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr11:66103855 C>T maps to NM_004292.2 E6E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X7-A8M5-01A-11D-A423-09 chr14:24807632 G>A maps to NM_006871.3 V204V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XM-A8RF-01A-11D-A423-09 chr19:14141520 G>A did not map to a codon.
Sequencing variant TCGA-ZB-A96K-01A-11D-A428-09 chr16:67691318 T>A maps to NM_001013838.1 L1402L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr23:105970575 A>G did not map to a codon.
Sequencing variant TCGA-3S-A8YW-01A-11D-A423-09 chr18:29706741 A>G maps to NM_001191324.1 Q253Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X7-A8D8-01A-11D-A423-09 chr5:63510130 T>C maps to NM_001113561.1 T326T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr17:78247136 G>A maps to NM_020914.4 P65P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZC-AAA7-01A-11D-A428-09 chr17:78318572 G>C maps to NM_020914.4 L2195L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A96C-01A-11D-A428-09 chr23:38146389 T>C did not map to a codon.
Sequencing variant TCGA-3G-AB0Q-01A-11D-A423-09 chr19:49120072 C>T maps to NM_000979.2 K69K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X7-A8M3-01A-11D-A423-09 chr23:83359601 C>A did not map to a codon.
Sequencing variant TCGA-ZB-A96V-01A-11D-A428-09 chr18:67733067 G>A maps to NM_173630.3 Q1582*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X7-A8M1-01A-11D-A423-09 chr4:184577087 A>T maps to ENST00000326397 I17I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3S-A8YW-01A-11D-A423-09 chr19:39075659 C>T maps to NM_000540.2 D4908D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZC-AAAF-01A-11D-A428-09 chr2:166848732 G>A maps to NM_001165963.1 Y1684Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A96Q-01A-11D-A428-09 chr2:166188029 C>T maps to NM_001040142.1 H780H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr2:165947439 A>G maps to NM_006922.3 C1741C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr12:6471269 C>T maps to NM_001159576.1 T333T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4V-A9QT-01A-11D-A423-09 chr6:35199577 C>T maps to ENST00000394681 H137H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YT-A95F-01A-11D-A428-09 chr12:100691877 T>C maps to NM_017988.4 N135N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5U-AB0E-01A-11D-A423-09 chr17:71382582 C>A did not map to a codon.
Sequencing variant TCGA-XU-A92O-01A-11D-A423-09 chr17:71394218 C>T maps to NM_001144952.1 V1103V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZC-AAA7-01A-11D-A428-09 chr16:5057390 C>G maps to NM_014692.1 L492L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5U-AB0D-01A-11D-A423-09 chr10:102247372 T>C maps to NM_015490.3 *1180*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5V-A9RR-01A-11D-A423-09 chr4:25780762 C>T maps to NM_015187.3 W840*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A96A-01A-11D-A428-09 chr6:76343305 C>A maps to NM_015571.2 R73R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr22:42383763 G>A did not map to a codon.
Sequencing variant TCGA-ZB-A96K-01A-11D-A428-09 chr17:75398453 C>T maps to NM_001113491.1 F130F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr13:50056924 C>T maps to NM_031915.2 N415N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YT-A95D-01A-11D-A428-09 chr3:4358834 G>T maps to NM_006515.3 E654*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5U-AB0F-01A-11D-A423-09 chr22:26693011 C>T maps to NM_021115.4 D376D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3G-AB0Q-01A-11D-A423-09 chr2:198273162 G>A maps to NM_012433.2 S349S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A96K-01A-11D-A428-09 chr5:171881341 G>T maps to NM_001017995.2 R5R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X7-A8M5-01A-11D-A423-09 chr4:8229316 G>A maps to NM_018986.3 L632L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr4:8229976 G>A maps to NM_018986.3 R852R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr22:51159899 C>T maps to NM_001080420.1 H1229H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4X-A9FD-01A-11D-A423-09 chr23:9864182 G>A did not map to a codon.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr23:50438918 C>T did not map to a codon.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr11:124509730 G>A maps to NM_170601.3 D333D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XU-A936-01A-11D-A428-09 chr14:72117204 C>T maps to NM_015556.1 R658*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X7-A8D9-01A-11D-A423-09 chr23:153716217 G>A did not map to a codon.
Sequencing variant TCGA-3G-AB19-01A-21D-A423-09 chr15:48551474 C>T maps to NM_000338.2 N707N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr17:6609989 C>T maps to NM_177550.3 T113T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XM-A8RF-01A-11D-A423-09 chr14:23816666 A>C did not map to a codon.
Sequencing variant TCGA-X7-A8M3-01A-11D-A423-09 chr11:62931390 C>A maps to NM_199352.3 E517*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr1:43394958 G>A maps to NM_006516.2 F298F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr9:99122449 G>A maps to NM_007001.2 S111S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A96F-01A-11D-A428-09 chr23:48326270 G>A did not map to a codon.
Sequencing variant TCGA-ZB-A96V-01A-11D-A428-09 chr17:19451347 T>C maps to ENST00000395585 S119S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr2:74474313 G>A maps to NM_021196.3 T636T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr2:74512934 A>G maps to NM_021196.3 H122H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A96L-01A-11D-A428-09 chr3:111940003 T>C maps to NM_183061.1 A547A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XU-A930-01A-11D-A423-09 chr2:103324902 G>A maps to NM_003048.3 S798S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A962-01A-11D-A428-09 chr16:67298984 C>T maps to NM_004594.2 R686*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr3:164907220 G>A maps to NM_014926.2 N466N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4V-A9QX-01A-11D-A423-09 chr23:142718488 T>C did not map to a codon.
Sequencing variant TCGA-XM-A8RI-01A-12D-A423-09 chr5:159833627 G>T maps to NM_006425.4 G378G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr1:183511426 G>T maps to ENST00000367537 V587V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr9:139289752 G>A maps to NM_003086.2 G156G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XU-A933-01A-11D-A423-09 chr2:241992588 G>A maps to NM_001080437.1 P701P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XM-A8RI-01A-12D-A423-09 chr11:130784292 G>A maps to NM_014758.2 A514A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5U-AB0D-01A-11D-A423-09 chr4:7533319 C>T maps to NM_020777.2 I204I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A965-01A-11D-A428-09 chr14:50697941 C>G maps to NM_006939.2 R20R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XM-A8RI-01A-12D-A423-09 chr13:112722166 G>A maps to NM_005986.2 Q65Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A96V-01A-11D-A428-09 chr11:16068113 G>A maps to NM_001145819.1 D536D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A96I-01A-11D-A428-09 chr7:20825174 A>T maps to NM_182700.4 A87A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A962-01A-11D-A428-09 chr3:172631486 T>C maps to NM_031955.5 R517R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4V-A9QX-01A-11D-A423-09 chr2:228883769 G>A maps to NM_001142644.1 P600P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A96C-01A-11D-A428-09 chr16:89936635 C>T maps to NM_032451.1 Q701*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XU-A92T-01A-11D-A423-09 chr16:29675930 C>T maps to NM_003123.3 G294G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X7-A8M4-01A-11D-A423-09 chr16:1827256 C>T maps to NM_080861.3 P303P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A96F-01A-11D-A428-09 chr19:41029462 C>G maps to NM_020971.2 A1258A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A96B-01A-11D-A428-09 chr23:153050280 C>A did not map to a codon.
Sequencing variant TCGA-XU-A930-01A-11D-A423-09 chr23:99925837 A>C did not map to a codon.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr1:24979466 G>A maps to NM_005839.3 P328P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr20:23016416 C>T maps to NM_001052.2 S99S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X7-A8D8-01A-11D-A423-09 chr3:136068117 T>C maps to NM_005862.2 S1051S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr3:136221538 G>A maps to NM_005862.2 A253A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4V-A9QQ-01A-11D-A423-09 chr23:123182925 C>A did not map to a codon.
Sequencing variant TCGA-XU-A92X-01A-11D-A423-09 chr15:81614805 T>C maps to NM_181900.2 L75L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4X-A9F9-01A-11D-A423-09 chr18:51855781 A>T maps to NM_139171.1 P138P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A969-01A-11D-A428-09 chr23:67943846 G>A did not map to a codon.
Sequencing variant TCGA-3G-AB0T-01A-11D-A423-09 chr5:171520784 G>A maps to NM_005990.3 V395V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr11:67925889 C>T maps to NM_017635.3 A641A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YT-A95F-01A-11D-A428-09 chr9:113259211 G>A maps to ENST00000374463 D561D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4V-A9QS-01A-11D-A423-09 chr22:32923932 G>A maps to NM_003490.3 G430G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr14:64468723 G>A maps to NM_182914.2 S1237S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5G-A9ZZ-01A-31D-A423-09 chr23:37979639 A>G did not map to a codon.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr10:123842740 G>A maps to NM_206862.2 G242G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YT-A95E-01A-11D-A428-09 chr12:118599687 C>A maps to NM_016281.3 E682*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr23:48419276 C>T did not map to a codon.
Sequencing variant TCGA-YT-A95F-01A-11D-A428-09 chr23:106064108 G>A did not map to a codon.
Sequencing variant TCGA-XU-A92O-01A-11D-A423-09 chr12:64858241 G>A maps to NM_013254.3 V119V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr19:3595730 C>T maps to NM_001060.5 S329S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr2:85532523 C>T maps to NM_031283.2 S329S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr12:110353317 G>A maps to NM_032300.4 A477A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr6:46656323 C>T maps to NM_001010870.2 D153D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr10:70406646 A>G maps to NM_030625.2 T1387T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A96V-01A-11D-A428-09 chr3:30733030 G>A maps to NM_001024847.2 S573S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr14:24729875 C>T maps to NM_000359.2 T179T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XU-A930-01A-11D-A423-09 chr15:43525532 G>T maps to NM_201631.3 V673V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YT-A95G-01A-11D-A428-09 chr11:2185540 G>A maps to NM_199292.2 P503P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A96C-01A-11D-A428-09 chr16:67876807 G>A maps to NM_020457.2 Q117Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XU-A92Y-01A-11D-A423-09 chr12:56817403 G>T maps to NM_003920.3 S685*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr22:33253241 C>T maps to NM_000362.4 R71*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr4:187000161 T>C maps to NM_003265.2 L204L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XM-A8RB-01A-11D-A423-09 chr8:38851119 A>G maps to NM_031940.3 D82D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr1:205238454 C>T maps to NM_014858.3 D375D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XU-A92R-01A-11D-A423-09 chr19:5772831 C>T maps to NM_152784.3 D599D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr4:947093 G>T maps to NM_032326.2 P193P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A96C-01A-11D-A428-09 chr23:148692969 C>T did not map to a codon.
Sequencing variant TCGA-ZC-AAAH-01A-11D-A428-09 chr23:34675057 G>T did not map to a codon.
Sequencing variant TCGA-ZB-A96V-01A-11D-A428-09 chr2:112854653 C>T maps to NM_032824.2 L380L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X7-A8D7-01A-11D-A423-09 chr16:24788443 G>A maps to NM_014494.2 Q118Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XU-A936-01A-11D-A428-09 chr6:32029976 G>A maps to ENST00000375244 H2375H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr20:39690074 C>A maps to NM_003286.2 R34R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X7-A8M3-01A-11D-A423-09 chr9:32543744 G>A maps to NM_005802.4 R260*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr15:43714074 G>T maps to NM_001141980.1 R1360R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr1:186313620 C>T maps to NM_003292.2 E1101E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZT-A8OM-01A-11D-A428-09 chr1:186313051 A>T maps to NM_003292.2 I1196I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3G-AB0T-01A-11D-A423-09 chr16:1306553 G>A maps to NM_012217.2 G40G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XU-A92O-01A-11D-A423-09 chr21:10910351 G>A maps to NM_199261.2 D468D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XU-A936-01A-11D-A428-09 chr1:155149535 C>G maps to NM_025058.3 A266A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5U-AB0D-01A-11D-A423-09 chr11:5624748 G>A maps to NM_001003819.3 R97R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XU-A92T-01A-11D-A423-09 chr23:54956353 A>G did not map to a codon.
Sequencing variant TCGA-ZB-A961-01A-11D-A428-09 chr9:73736099 A>T maps to NM_001007471.2 L57L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X7-A8M1-01A-11D-A423-09 chr16:2126080 C>G maps to NM_000548.3 Y884*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A96H-01A-11D-A428-09 chr8:98289253 T>A maps to NM_033512.2 V273V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4V-A9QX-01A-11D-A423-09 chr8:144695459 A>G maps to NM_003313.3 D272D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4X-A9FB-01A-11D-A423-09 chr6:43250760 A>G maps to NM_032538.1 E761E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XU-A933-01A-11D-A423-09 chr2:179560832 G>A maps to NM_133378.4 D9078D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XM-A8RC-01A-11D-A423-09 chr18:12308714 C>T maps to NM_032525.1 G29G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A96A-01A-11D-A428-09 chr22:50968039 G>C maps to ENST00000395681 P33P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr19:55912863 G>A maps to NM_014501.2 R203R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XU-A92U-01A-11D-A423-09 chr7:138968002 T>A maps to NM_173569.3 P784P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A96E-01A-11D-A428-09 chr23:56590759 G>C did not map to a codon.
Sequencing variant TCGA-5U-AB0D-01A-11D-A423-09 chr15:43281143 G>T maps to NM_174916.2 I1290I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr4:141484595 T>C maps to NM_021833.4 T134T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A96V-01A-11D-A428-09 chr11:18554025 A>T maps to NM_001040697.1 Y419*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XM-AAZ3-01A-11D-A423-09 chr2:234638521 T>C maps to NM_019093.2 S250S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XM-AAZ3-01A-11D-A423-09 chr2:234638554 T>C maps to NM_019093.2 F261F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XM-AAZ3-01A-11D-A423-09 chr2:234638575 A>G maps to NM_019093.2 P268P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X7-A8DI-01A-11D-A423-09 chr4:70361045 G>A maps to NM_021139.2 Y178Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr4:115544173 C>T maps to NM_003360.3 H46H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5G-A9ZZ-01A-31D-A423-09 chr19:18968184 G>A maps to ENST00000418384 A686A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4X-A9FC-01A-11D-A423-09 chr23:74494111 C>T did not map to a codon.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr1:229771118 C>A maps to NM_014777.2 S253S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZC-AAA7-01A-11D-A428-09 chr1:215916611 G>A maps to ENST00000366943 L3819L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A963-01A-11D-A428-09 chr11:119230313 G>T maps to NM_004205.4 Y294*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr4:144106795 C>T maps to NM_032557.5 L65L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZC-AAA7-01A-11D-A428-09 chr7:6189290 C>T maps to ENST00000404835 S488S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A96V-01A-11D-A428-09 chr23:41082534 G>A did not map to a codon.
Sequencing variant TCGA-3G-AB0T-01A-11D-A423-09 chr1:38488444 T>G maps to NM_016037.3 V214V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr8:117782506 C>T maps to NM_032334.2 R89*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XU-A92V-01A-11D-A423-09 chr6:144744741 C>T maps to NM_007124.2 Q98*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5U-AB0D-01A-11D-A423-09 chr23:154448564 C>T did not map to a codon.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr15:62300906 C>T maps to NM_020821.2 A355A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr12:6132809 C>T maps to NM_000552.3 T1122T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZL-A9V6-01A-11D-A428-09 chr4:177071054 A>C maps to NM_170710.4 V689V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr1:118483746 C>T maps to NM_006784.2 R264*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr17:1637358 G>A maps to NM_001163809.1 P1676P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr12:118480646 G>A maps to ENST00000441406 H203H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr17:5984032 C>T maps to NM_015253.1 L19L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr23:10062287 C>T did not map to a codon.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr23:10104701 G>A did not map to a codon.
Sequencing variant TCGA-4V-A9QN-01A-11D-A423-09 chr2:61706053 T>C maps to NM_003400.3 E1039E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YT-A95D-01A-11D-A428-09 chr12:32908583 G>A maps to NM_001040436.1 T75T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XU-A930-01A-11D-A423-09 chr7:100395208 C>T maps to ENST00000349350 R2792R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr19:59028857 C>T maps to NM_032792.2 K61K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X7-A8D9-01A-11D-A423-09 chr5:825359 T>C maps to NM_024786.2 K314K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X7-A8D8-01A-11D-A423-09 chr10:114204969 G>A maps to NM_022494.1 A75A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr8:77775726 C>T maps to NM_024721.4 G3259G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3G-AB14-01A-11D-A423-09 chr23:70468141 G>T did not map to a codon.
Sequencing variant TCGA-5U-AB0D-01A-11D-A423-09 chr19:22154451 A>G maps to NM_007153.3 L1128L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-YT-A95F-01A-11D-A428-09 chr19:22154190 G>A maps to NM_007153.3 H1215H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr17:15619436 A>G maps to NM_020652.2 S133S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr20:2464360 G>A maps to NM_024325.4 R416*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5U-AB0D-01A-11D-A423-09 chr19:52537806 G>A maps to NM_014650.2 C375C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr19:11878012 T>C did not map to a codon.
Sequencing variant TCGA-X7-A8M3-01A-11D-A423-09 chr19:22847764 C>T maps to NM_020855.2 Q432*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3T-AA9L-01A-11D-A423-09 chr19:19905795 A>G maps to NM_001099269.2 L300L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-XM-A8RI-01A-12D-A423-09 chr2:27600981 G>C maps to NM_144631.4 P352P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A96E-01A-11D-A428-09 chr19:58773096 T>G maps to NM_014480.2 T375T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A969-01A-11D-A428-09 chr19:42584755 C>G maps to ENST00000222339 R756R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr19:58371213 C>T maps to NM_032828.2 S478S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A96V-01A-11D-A428-09 chr19:53269289 A>C maps to NM_198457.2 R573R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr16:30793647 G>A maps to NM_001080417.1 C667C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZT-A8OM-01A-11D-A428-09 chr23:22291396 C>T did not map to a codon.
Sequencing variant TCGA-ZL-A9V6-01A-11D-A428-09 chr19:21301035 C>A maps to NM_182515.3 I522I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5U-AB0D-01A-11D-A423-09 chr7:57528595 T>C maps to NM_001159279.1 N143N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr19:53058424 C>T maps to NM_001039886.3 C752C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-4V-A9QQ-01A-11D-A423-09 chr23:47774779 C>T did not map to a codon.
Sequencing variant TCGA-ZB-A96I-01A-11D-A428-09 chr4:146791433 T>G maps to ENST00000508784 S648S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr19:57175294 G>A maps to NM_001005850.1 G446G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A966-01A-11D-A428-09 chr1:238053866 A>G maps to NM_021186.3 P23P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-5V-A9RR-01A-11D-A423-09 chr6:28358989 G>A maps to ENST00000396827 H359H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ZB-A96C-01A-11D-A428-09 chr6:28097442 C>T maps to NM_025231.1 H254H. Only missense variants will be evaluated by CHASM.
