Sequencing variant TCGA-N5-A4R8-01A-11D-A28R-08 chr20:60913125 C>A maps to NM_005560.3 G613*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4R8-01A-11D-A28R-08 chr1:67148014 C>T maps to ENST00000237247 P430P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4R8-01A-11D-A28R-08 chr8:2021506 C>T maps to NM_003970.2 D349D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4R8-01A-11D-A28R-08 chr1:151490982 A>T did not map to a codon.
Sequencing variant TCGA-N5-A4R8-01A-11D-A28R-08 chr16:21261507 C>A maps to NM_145865.2 I207I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4R8-01A-11D-A28R-08 chr6:144093532 C>T maps to NM_001100164.1 D457D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4R8-01A-11D-A28R-08 chr6:121768820 T>C maps to NM_000165.3 A276A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4R8-01A-11D-A28R-08 chr12:98987869 C>G maps to NM_213611.2 G38G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4R8-01A-11D-A28R-08 chr17:7578290 T>G did not map to a codon.
Sequencing variant TCGA-N5-A4R8-01A-11D-A28R-08 chr2:179597446 T>G did not map to a codon.
Sequencing variant TCGA-N5-A4R8-01A-11D-A28R-08 chr3:183995213 C>T maps to NM_014693.3 S264S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4R8-01A-11D-A28R-08 chr10:115402733 G>A maps to ENST00000369358 Q392*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4R8-01A-11D-A28R-08 chr1:154987607 C>T maps to ENST00000417934 R192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4R8-01A-11D-A28R-08 chr7:141736711 C>T maps to ENST00000475668 Y722Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4R8-01A-11D-A28R-08 chr12:4737295 C>A maps to NM_006422.2 G258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RA-01A-11D-A28R-08 chr2:24438917 C>T maps to NM_006277.2 K1330K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RA-01A-11D-A28R-08 chr11:65380918 A>C maps to NM_002419.3 G103G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RA-01A-11D-A28R-08 chr6:138584323 G>T maps to NM_020340.4 T568T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RA-01A-11D-A28R-08 chr1:16342194 G>A maps to ENST00000375714 D219D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RA-01A-11D-A28R-08 chr18:14543049 G>A maps to ENST00000444806 F32F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RA-01A-11D-A28R-08 chr2:176964702 C>T maps to NM_021193.3 C58C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RA-01A-11D-A28R-08 chr3:124418864 C>T maps to NM_001024660.3 R2661*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RA-01A-11D-A28R-08 chr1:216595498 G>A maps to ENST00000366943 L60L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RA-01A-11D-A28R-08 chr2:166908388 C>T maps to NM_001165963.1 L268L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RA-01A-11D-A28R-08 chr20:46279832 G>A maps to NM_181659.2 Q1253Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RA-01A-11D-A28R-08 chr5:80626632 G>T maps to NM_130767.2 I506I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RA-01A-11D-A28R-08 chr14:59793304 A>T maps to NM_014992.1 K418*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RA-01A-11D-A28R-08 chr20:57766697 C>A maps to NM_178457.1 G208G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RD-01A-11D-A28R-08 chr17:67193232 T>C maps to NM_080282.3 G402G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RD-01A-11D-A28R-08 chr9:37745608 C>T maps to NM_014907.2 Q1194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RD-01A-11D-A28R-08 chr1:65352022 C>T did not map to a codon.
Sequencing variant TCGA-N5-A4RD-01A-11D-A28R-08 chr17:73661199 G>A maps to NM_004259.5 C61C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RD-01A-11D-A28R-08 chr5:140237390 G>A maps to NM_018901.2 A586A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RD-01A-11D-A28R-08 chr1:149858535 T>G maps to NM_003517.2 R4R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RD-01A-11D-A28R-08 chr15:44048890 C>T maps to NM_005313.4 V97V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RD-01A-11D-A28R-08 chr6:33541651 G>A maps to ENST00000360661 I193I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RD-01A-11D-A28R-08 chr1:62237127 C>T maps to NM_176877.2 Q184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RD-01A-11D-A28R-08 chr11:68854002 C>T maps to NM_139075.3 I672I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RD-01A-11D-A28R-08 chr4:186263242 T>C maps to NM_031953.2 F556F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RD-01A-11D-A28R-08 chr19:14817511 T>A maps to NM_032433.2 A146A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RD-01A-11D-A28R-08 chr16:88677690 C>T maps to ENST00000452588 R432*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RD-01A-11D-A28R-08 chr4:16900018 G>A maps to NM_001290.3 Y30Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RD-01A-11D-A28R-08 chr3:62259444 C>T maps to NM_002841.3 Q1131*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RF-01A-11D-A28R-08 chrX:153581769 G>T maps to NM_001110556.1 P1972P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RF-01A-11D-A28R-08 chr7:134853625 G>A maps to NM_024033.2 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RF-01A-11D-A28R-08 chrX:123538967 G>A maps to NM_001163278.1 P1768P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RF-01A-11D-A28R-08 chr10:89720876 T>G did not map to a codon.
Sequencing variant TCGA-N5-A4RF-01A-11D-A28R-08 chr17:2228661 C>T maps to NM_018128.4 A652A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RF-01A-11D-A28R-08 chr5:140176606 C>T maps to NM_018905.2 A686A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RF-01A-11D-A28R-08 chrX:154490294 G>A maps to NM_171998.2 Y145Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RF-01A-11D-A28R-08 chr10:113928672 G>A maps to NM_020918.4 R278*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RF-01A-11D-A28R-08 chr20:13763374 T>A maps to NM_016649.3 K138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RF-01A-11D-A28R-08 chr1:27057893 C>G maps to NM_006015.4 Y534*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RF-01A-11D-A28R-08 chr17:46700471 G>A maps to NM_024017.4 H181H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RF-01A-11D-A28R-08 chrX:107976124 G>A maps to NM_003604.2 A1150A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RF-01A-11D-A28R-08 chr3:39150701 G>T maps to ENST00000301819 E52*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RF-01A-11D-A28R-08 chr5:7727299 G>A maps to NM_020546.2 A599A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RF-01A-11D-A28R-08 chr15:91795209 C>T maps to NM_014848.4 R205*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RF-01A-11D-A28R-08 chr7:8258021 C>T maps to ENST00000422063 T164T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RF-01A-11D-A28R-08 chr14:65008091 C>T maps to NM_021979.3 N175N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RF-01A-11D-A28R-08 chr1:241094032 C>T maps to ENST00000407727 P123P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RJ-01A-11D-A28R-08 chr19:15198439 C>T maps to NM_001004713.1 S188S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RJ-01A-11D-A28R-08 chr6:24596358 C>T maps to NM_014809.3 E181E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RJ-01A-11D-A28R-08 chr2:32983376 C>T maps to NM_017735.4 Q491*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RJ-01A-11D-A28R-08 chr13:28009311 A>T maps to NM_002097.2 K306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RJ-01A-11D-A28R-08 chr22:29879421 G>A maps to NM_021076.3 A314A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RJ-01A-11D-A28R-08 chr11:66082812 A>G maps to NM_020404.2 G562G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RJ-01A-11D-A28R-08 chr7:150269568 C>A maps to ENST00000430830 I151I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RJ-01A-11D-A28R-08 chr7:14741317 G>A maps to NM_004080.2 F168F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RJ-01A-11D-A28R-08 chr19:59074527 C>T maps to NM_198055.1 L372L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RJ-01A-11D-A28R-08 chr22:32784074 G>T maps to NM_014306.4 S474S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RJ-01A-11D-A28R-08 chr6:161530807 G>T maps to NM_005922.2 E1420*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RJ-01A-11D-A28R-08 chr22:17488842 C>T maps to NM_001037814.1 K54K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RJ-01A-11D-A28R-08 chr4:153251906 G>A maps to NM_033632.2 R367*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RJ-01A-11D-A28R-08 chr2:128757878 A>C did not map to a codon.
Sequencing variant TCGA-N5-A4RJ-01A-11D-A28R-08 chrX:139865784 G>A maps to NM_004065.2 T249T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RM-01A-11D-A28R-08 chr1:43772664 G>T maps to NM_005424.2 R213R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RM-01A-11D-A28R-08 chr5:140793311 C>T maps to NM_018913.2 A190A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RM-01A-11D-A28R-08 chr8:26627887 G>A maps to ENST00000356368 G393G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RM-01A-11D-A28R-08 chr17:3638131 C>T maps to NM_002208.4 L878L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RM-01A-11D-A28R-08 chr10:49395265 G>A maps to NM_001018071.3 L745L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RM-01A-11D-A28R-08 chr2:3341869 G>T maps to ENST00000398659 V59V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RM-01A-11D-A28R-08 chr12:7249403 G>A maps to NM_016546.2 I349I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RM-01A-11D-A28R-08 chr2:136575372 C>T maps to NM_002299.2 R415R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RM-01A-11D-A28R-08 chr20:52612493 G>A maps to NM_003657.2 D273D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RM-01A-11D-A28R-08 chr13:27257059 C>T maps to NM_006646.5 Q434*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RM-01A-11D-A28R-08 chr11:64112226 G>A maps to NM_032251.5 R738R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RM-01A-11D-A28R-08 chr12:132633384 G>A maps to NM_024078.1 P282P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RM-01A-11D-A28R-08 chr14:105418190 G>A maps to NM_138420.2 L1199L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RM-01A-11D-A28R-08 chr3:42448440 G>A maps to NM_144634.2 Y63Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RM-01A-11D-A28R-08 chr14:20404415 T>C maps to NM_001004063.2 I197I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RM-01A-11D-A28R-08 chr6:160999635 G>A maps to NM_005577.2 R1464*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RM-01A-11D-A28R-08 chr5:78280983 G>A maps to NM_000046.3 L30L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RM-01A-11D-A28R-08 chr3:52324394 C>T maps to NM_145262.3 R13*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RN-01A-12D-A28R-08 chr16:67579899 C>T maps to NM_001193523.1 R1166*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RN-01A-12D-A28R-08 chr2:55463903 C>A maps to NM_002453.2 T688T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RN-01A-12D-A28R-08 chr20:57564965 C>T maps to NM_198976.1 S246S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RN-01A-12D-A28R-08 chr4:144445585 C>T maps to NM_003601.2 T162T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RN-01A-12D-A28R-08 chr19:41220035 C>G maps to NM_024876.3 L75L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RN-01A-12D-A28R-08 chr4:128878654 C>A did not map to a codon.
Sequencing variant TCGA-N5-A4RN-01A-12D-A28R-08 chr11:117969703 C>G maps to NM_019894.3 V16V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RN-01A-12D-A28R-08 chr22:32232997 T>C maps to NM_001136029.1 C728C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RN-01A-12D-A28R-08 chr8:86038970 T>G maps to NM_033402.4 A440A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RN-01A-12D-A28R-08 chr18:8380346 A>C maps to NM_001105244.1 T1280T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RN-01A-12D-A28R-08 chr19:39962346 C>T maps to NM_003169.3 L643L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RN-01A-12D-A28R-08 chr10:75554071 C>T maps to NM_015037.2 D931D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RN-01A-12D-A28R-08 chr3:195508193 T>G maps to NM_018406.5 T3419T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RN-01A-12D-A28R-08 chr8:95403997 G>A maps to NM_012415.2 R550*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RN-01A-12D-A28R-08 chr11:5443751 G>T maps to NM_001004757.2 G108*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RN-01A-12D-A28R-08 chr14:50249132 T>G maps to NM_014315.2 V334V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RN-01A-12D-A28R-08 chr15:72608245 G>A maps to NM_052840.4 C95C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RN-01A-12D-A28R-08 chr20:44856147 G>T maps to NM_021248.1 T223T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RN-01A-12D-A28R-08 chr7:63981661 G>A maps to NM_178558.4 Y490Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RN-01A-12D-A28R-08 chr16:71701132 G>A maps to NM_015020.2 Q578*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RN-01A-12D-A28R-08 chr13:48881413 A>G did not map to a codon.
Sequencing variant TCGA-N5-A4RN-01A-12D-A28R-08 chr14:94770859 C>T maps to NM_001756.3 T371T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RN-01A-12D-A28R-08 chr6:27100484 G>A maps to NM_021058.3 S15S. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-N5-A4RN-01A-12D-A28R-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-N5-A4RN-01A-12D-A28R-08 chr16:76587180 A>G maps to NM_033401.3 E1147E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RN-01A-12D-A28R-08 chr11:56468603 C>A maps to NM_001013358.1 V247V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RN-01A-12D-A28R-08 chr16:27503991 G>A maps to NM_001520.3 C973C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RN-01A-12D-A28R-08 chr19:41072111 T>C maps to NM_020971.2 D2061D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RO-01A-11D-A28R-08 chr10:16882376 G>C maps to NM_001081.3 T3328T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RO-01A-11D-A28R-08 chr2:207569604 G>A maps to NM_001093730.1 R149*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RO-01A-11D-A28R-08 chr3:179332846 G>A maps to NM_002492.2 L71L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RO-01A-11D-A28R-08 chr15:38811526 C>T maps to NM_005739.3 K124K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RO-01A-11D-A28R-08 chr7:127235408 C>T maps to NM_020369.2 R65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RO-01A-11D-A28R-08 chr6:57512488 T>C maps to NM_000947.2 F439F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RO-01A-11D-A28R-08 chr14:103400063 C>T maps to NM_006035.3 P1707P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RO-01A-11D-A28R-08 chr4:1232003 G>A maps to NM_001328.2 C54C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RO-01A-11D-A28R-08 chr9:18775889 T>C maps to NM_001040272.4 C849C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RO-01A-11D-A28R-08 chr9:109765633 G>A maps to NM_021224.4 K2372K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RO-01A-11D-A28R-08 chr13:100634934 C>A maps to NM_007129.2 S206*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RO-01A-11D-A28R-08 chr10:14939227 T>C maps to NM_001193424.1 A187A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RO-01A-11D-A28R-08 chr15:54003561 A>G maps to NM_182758.2 G276G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RO-01A-11D-A28R-08 chr7:150094610 C>T maps to NM_173680.3 Q348*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RO-01A-11D-A28R-08 chrX:105876450 G>A maps to NM_018015.5 S424S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RO-01A-11D-A28R-08 chr11:105483156 C>T maps to NM_000829.3 N81N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RO-01A-11D-A28R-08 chr8:139164616 G>A maps to NM_015912.3 R701*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RO-01A-11D-A28R-08 chr11:57335060 C>A maps to NM_004223.3 V8V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RS-01A-11D-A28R-08 chr15:89021194 G>A maps to NM_022839.3 K190K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RS-01A-11D-A28R-08 chrX:112022453 C>T maps to NM_001113490.1 P976P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RS-01A-11D-A28R-08 chr6:169626325 G>A maps to NM_003247.2 D829D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RS-01A-11D-A28R-08 chr22:42299023 C>T maps to NM_004599.2 L986L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RS-01A-11D-A28R-08 chr10:5144363 T>C maps to NM_003739.4 V214V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RS-01A-11D-A28R-08 chr17:7578555 T>G did not map to a codon.
Sequencing variant TCGA-N5-A4RS-01A-11D-A28R-08 chr15:40398007 G>A maps to NM_001003940.1 R94*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RS-01A-11D-A28R-08 chr1:22986092 C>T maps to NM_000491.3 G48G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RT-01A-11D-A28R-08 chr17:21075509 G>T did not map to a codon.
Sequencing variant TCGA-N5-A4RT-01A-11D-A28R-08 chrX:215881 C>T maps to NM_018390.3 V284V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RT-01A-11D-A28R-08 chr4:10445495 C>T maps to NM_053042.2 A819A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RT-01A-11D-A28R-08 chr9:134379640 G>C maps to NM_007171.3 T12T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RT-01A-11D-A28R-08 chr16:70575649 A>G maps to NM_012426.4 G382G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RT-01A-11D-A28R-08 chr15:34018591 C>A maps to NM_001036.3 I2306I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RT-01A-11D-A28R-08 chr9:104086317 G>A maps to NM_017753.2 A319A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RT-01A-11D-A28R-08 chr19:49228097 G>A maps to NM_017805.2 G749G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RT-01A-11D-A28R-08 chr12:49999202 G>A maps to NM_032130.2 L20L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RT-01A-11D-A28R-08 chr15:96880649 C>T maps to NM_021005.3 Y348Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RT-01A-11D-A28R-08 chrX:70356868 A>G maps to ENST00000333646 P1847P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RT-01A-11D-A28R-08 chr1:205053391 C>G maps to NM_203376.1 L19L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RT-01A-11D-A28R-08 chr5:45396743 C>A maps to NM_021072.2 G360G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RT-01A-11D-A28R-08 chr4:73930518 G>A maps to NM_173827.2 G232G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RT-01A-11D-A28R-08 chr3:131404726 G>A maps to ENST00000502818 R213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RT-01A-11D-A28R-08 chr2:179639015 G>C maps to NM_133378.4 V2325V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RT-01A-11D-A28R-08 chr17:54558121 C>G maps to NM_153228.2 Y681*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RT-01A-11D-A28R-08 chr2:85577955 C>A maps to NM_017750.3 E182*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RT-01A-11D-A28R-08 chr21:44840173 G>A maps to NM_173354.3 Y304Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RT-01A-11D-A28R-08 chr2:86274380 G>T maps to NM_015425.3 C880*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RT-01A-11D-A28R-08 chr1:237957189 A>G maps to NM_001035.2 R4602R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RT-01A-11D-A28R-08 chrX:85211372 C>T maps to NM_000390.2 E317E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RT-01A-11D-A28R-08 chr6:70646732 C>A maps to NM_001858.4 A268A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RT-01A-11D-A28R-08 chr11:12315220 T>G maps to NM_032867.2 Y81*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RT-01A-11D-A28R-08 chr1:182850452 C>T maps to NM_001357.4 F893F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RT-01A-11D-A28R-08 chr8:28574907 C>T maps to NM_001440.2 S444S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RT-01A-11D-A28R-08 chr2:74491272 C>T did not map to a codon.
Sequencing variant TCGA-N5-A4RT-01A-11D-A28R-08 chr7:44574198 G>T maps to NM_013389.2 G671G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RT-01A-11D-A28R-08 chr6:74363525 C>A maps to NM_012434.4 R28R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RT-01A-11D-A28R-08 chr21:32513670 C>T maps to NM_003253.2 A1209A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RT-01A-11D-A28R-08 chr11:6129436 T>G maps to NM_001005181.1 T143T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RT-01A-11D-A28R-08 chr5:23526780 G>A maps to NM_020227.2 E528E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RT-01A-11D-A28R-08 chrX:129630082 A>C did not map to a codon.
Sequencing variant TCGA-N5-A4RU-01A-31D-A28R-08 chr19:42223864 C>G maps to NM_004363.2 P503P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RU-01A-31D-A28R-08 chr10:91162763 A>G maps to NM_001548.3 L244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RU-01A-31D-A28R-08 chr11:65729346 C>T maps to NM_005146.4 H32H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RU-01A-31D-A28R-08 chr19:50154614 C>T maps to NM_021228.2 D323D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RU-01A-31D-A28R-08 chr3:126132949 G>A maps to ENST00000505024 A51A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RU-01A-31D-A28R-08 chr10:102689754 G>A did not map to a codon.
Sequencing variant TCGA-N5-A4RU-01A-31D-A28R-08 chr3:55038788 G>C did not map to a codon.
Sequencing variant TCGA-N5-A4RU-01A-31D-A28R-08 chr5:150405019 G>A maps to NM_002084.3 V69V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RU-01A-31D-A28R-08 chr6:132910255 G>T maps to NM_003967.2 G190G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RU-01A-31D-A28R-08 chr6:79918281 C>G maps to NM_004242.2 R26R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RU-01A-31D-A28R-08 chr4:140272381 C>T maps to NM_057175.3 A283A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RU-01A-31D-A28R-08 chr16:3613452 G>A maps to ENST00000448023 F542F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RU-01A-31D-A28R-08 chr1:4772160 G>T maps to NM_018836.3 P77P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RU-01A-31D-A28R-08 chr6:7585360 C>T maps to NM_004415.2 I2622I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RU-01A-31D-A28R-08 chr17:42478775 T>C maps to NM_001002909.2 V223V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RV-01A-21D-A28R-08 chr5:41904474 G>C maps to NM_175921.4 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RV-01A-21D-A28R-08 chr3:196736582 G>A maps to NM_005929.5 H477H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RV-01A-21D-A28R-08 chr12:109696794 A>G maps to NM_001093.3 G2126G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RV-01A-21D-A28R-08 chr3:40231701 A>G maps to NM_015460.2 R471R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RV-01A-21D-A28R-08 chr3:133664064 G>T maps to NM_005630.2 R445R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RV-01A-21D-A28R-08 chr6:31848028 G>A maps to ENST00000395728 G1212G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RV-01A-21D-A28R-08 chr17:42398462 G>A maps to NM_001143780.1 G218G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RV-01A-21D-A28R-08 chr4:159140503 G>A maps to NM_018342.4 P125P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RV-01A-21D-A28R-08 chr5:76115088 G>T maps to NM_005242.4 G28*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RV-01A-21D-A28R-08 chr20:61951482 C>T maps to ENST00000326996 P1010P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RV-01A-21D-A28R-08 chr9:93375838 G>A maps to NM_017594.3 R91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RV-01A-21D-A28R-08 chr17:76490707 G>A maps to ENST00000389840 D2065D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RV-01A-21D-A28R-08 chr8:113585823 G>A maps to NM_198123.1 R1316R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RV-01A-21D-A28R-08 chrX:132161819 A>T maps to NM_031907.1 S143S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RV-01A-21D-A28R-08 chr7:143792721 C>T maps to NM_001004135.1 N174N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RV-01A-21D-A28R-08 chr19:35941554 C>T maps to NM_005306.2 D313D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RV-01A-21D-A28R-08 chr11:103182701 T>C maps to NM_001080463.1 A3870A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RV-01A-21D-A28R-08 chr16:76555942 A>T maps to NM_033401.3 T847T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RV-01A-21D-A28R-08 chr8:113358407 A>C maps to NM_198123.1 G2120G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RV-01A-21D-A28R-08 chr9:139400312 A>T maps to NM_017617.3 C1345*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RV-01A-21D-A28R-08 chr3:52431060 G>A did not map to a codon.
Sequencing variant TCGA-N5-A4RV-01A-21D-A28R-08 chr8:124250154 G>T maps to NM_032847.1 I80I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A59E-01A-11D-A28R-08 chr16:31434761 C>A maps to ENST00000444228 V999V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A59E-01A-11D-A28R-08 chr22:50216635 G>A maps to ENST00000342989 L444L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A59E-01A-11D-A28R-08 chr16:56792512 G>T maps to NM_014669.3 L81L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A59E-01A-11D-A28R-08 chr1:196397291 C>T maps to NM_198503.2 L309L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A59E-01A-11D-A28R-08 chr1:152278955 G>A maps to NM_002016.1 H2802H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A59E-01A-11D-A28R-08 chr8:22106725 C>G maps to NM_001722.2 L275L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A59E-01A-11D-A28R-08 chr22:50216636 G>T maps to ENST00000342989 V443V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A59E-01A-11D-A28R-08 chr13:101266663 G>A maps to NM_032813.2 H619H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A59E-01A-11D-A28R-08 chr6:51889955 G>T maps to NM_138694.3 S1551*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A59E-01A-11D-A28R-08 chr3:195511814 G>A maps to NM_018406.5 T2212T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A59E-01A-11D-A28R-08 chr1:19712042 C>T maps to ENST00000375145 K119K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A59E-01A-11D-A28R-08 chr13:113748840 G>T maps to NM_001112732.1 T1046T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A59E-01A-11D-A28R-08 chr2:40656142 G>A maps to NM_021097.2 A426A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A59E-01A-11D-A28R-08 chr12:13061635 A>G maps to NM_003979.3 E151E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A59E-01A-11D-A28R-08 chr3:194181554 A>G maps to NM_024524.3 I19I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A59E-01A-11D-A28R-08 chr2:131099730 C>T maps to ENST00000409127 R24R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A59E-01A-11D-A28R-08 chr6:26033562 G>A maps to NM_003513.2 R78R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A59E-01A-11D-A28R-08 chr2:234847658 C>A maps to NM_024080.4 C122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A59E-01A-11D-A28R-08 chr17:79180596 C>T maps to ENST00000269392 P154P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A59E-01A-11D-A28R-08 chr20:23016959 G>C maps to NM_001052.2 L280L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A59E-01A-11D-A28R-08 chr1:44075092 G>C maps to NM_002840.3 S1299S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A59E-01A-11D-A28R-08 chr22:31658194 G>A maps to NM_001031801.1 G188G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A59F-01A-11D-A28R-08 chr12:120637129 G>A maps to NM_053275.3 N71N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A59F-01A-11D-A28R-08 chr1:75608913 C>A maps to NM_001001933.1 C167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A59F-01A-11D-A28R-08 chr1:13716935 G>A maps to NM_001099851.1 T141T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A59F-01A-11D-A28R-08 chr5:179263547 G>A maps to NM_003900.4 A426A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A59F-01A-11D-A28R-08 chr2:179569234 A>G did not map to a codon.
Sequencing variant TCGA-N5-A59F-01A-11D-A28R-08 chr3:49726194 T>G did not map to a codon.
Sequencing variant TCGA-N5-A59F-01A-11D-A28R-08 chr19:47572490 C>A maps to NM_015168.1 P752P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A59F-01A-11D-A28R-08 chr4:517576 C>A maps to NM_001127178.1 G648G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A59F-01A-11D-A28R-08 chr20:37634872 C>A maps to NM_021931.3 R366R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A59F-01A-11D-A28R-08 chr2:9519168 G>C maps to NM_003887.2 G643G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A59F-01A-11D-A28R-08 chr5:180048620 G>A maps to NM_182925.4 H647H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A59F-01A-11D-A28R-08 chr7:70853250 G>A maps to NM_022479.1 L151L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A59F-01A-11D-A28R-08 chr8:12285187 G>A maps to NM_001137610.1 C290C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A59F-01A-11D-A28R-08 chr15:28474382 G>A maps to NM_004667.4 R1744*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4V9-01A-11D-A28R-08 chr19:36259087 C>G maps to NM_001039887.2 P417P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4V9-01A-11D-A28R-08 chr19:34936016 T>C maps to NM_005499.2 L254L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4V9-01A-11D-A28R-08 chr17:80040212 G>T maps to NM_004104.4 T1999T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4V9-01A-11D-A28R-08 chr3:138290179 C>A maps to NM_024491.2 E30*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4V9-01A-11D-A28R-08 chr2:165969451 A>T maps to NM_006922.3 Y1262*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4V9-01A-11D-A28R-08 chr17:40839787 C>T maps to NM_003632.2 F365F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4V9-01A-11D-A28R-08 chr11:66191698 C>G maps to NM_178864.3 T446T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4V9-01A-11D-A28R-08 chr7:48411970 A>G maps to NM_152701.3 A3670A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4V9-01A-11D-A28R-08 chr17:72473653 C>T maps to NM_007261.2 Q205*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4V9-01A-11D-A28R-08 chr5:161128592 G>T maps to NM_000811.2 T392T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4V9-01A-11D-A28R-08 chr8:37993283 G>A maps to NM_004674.3 T573T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4V9-01A-11D-A28R-08 chr7:86468806 G>A maps to NM_000840.2 L659L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4V9-01A-11D-A28R-08 chr5:39377322 A>G maps to NM_001343.2 N522N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VC-01A-11D-A28R-08 chr19:53762413 T>A maps to NM_173856.2 Y262*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VC-01A-11D-A28R-08 chr9:37784999 G>A maps to NM_016042.2 G14G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VC-01A-11D-A28R-08 chr5:160721269 G>A maps to NM_021911.2 R453*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VC-01A-11D-A28R-08 chr9:137808191 A>G did not map to a codon.
Sequencing variant TCGA-N6-A4VC-01A-11D-A28R-08 chrX:11139869 A>G maps to NM_005333.4 L249L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VC-01A-11D-A28R-08 chrX:70607292 T>C maps to ENST00000449580 H802H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VC-01A-11D-A28R-08 chrX:70823663 C>T maps to NM_052957.4 P179P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VC-01A-11D-A28R-08 chr17:44953960 G>A maps to NM_003396.1 G317G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VC-01A-11D-A28R-08 chr6:160977178 G>A maps to NM_005577.2 Y1617Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VC-01A-11D-A28R-08 chr1:248637451 G>A maps to NM_001005495.1 P267P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VC-01A-11D-A28R-08 chr20:22563664 G>T maps to NM_021784.4 S72*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VC-01A-11D-A28R-08 chr5:145719784 G>A maps to NM_002700.2 K265K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VC-01A-11D-A28R-08 chr4:56847394 T>C maps to NM_025009.3 A543A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VC-01A-11D-A28R-08 chr6:7585588 C>T maps to NM_004415.2 F2698F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VC-01A-11D-A28R-08 chr14:45623209 A>C maps to NM_020937.2 R380R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VC-01A-11D-A28R-08 chr12:72030370 T>A maps to NM_144982.4 R667*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VC-01A-11D-A28R-08 chr21:41648104 C>A maps to NM_001389.3 E759*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VC-01A-11D-A28R-08 chr19:11327691 G>A maps to ENST00000319867 T1264T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VC-01A-11D-A28R-08 chr16:29917115 C>T maps to NM_181718.3 P357P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VC-01A-11D-A28R-08 chrX:37028480 C>A maps to NM_001013736.2 L666L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VC-01A-11D-A28R-08 chr6:31526159 G>A maps to NM_005007.3 G306G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VC-01A-11D-A28R-08 chr10:135439076 T>C maps to ENST00000443774 S122S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VC-01A-11D-A28R-08 chr2:179449408 C>A maps to NM_133378.4 A19085A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VD-01A-11D-A28R-08 chr2:1457505 C>T maps to NM_000547.5 R175*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VD-01A-11D-A28R-08 chr7:93065413 C>T maps to NM_001164737.1 A367A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VD-01A-11D-A28R-08 chr5:171509416 G>A maps to NM_005990.3 R634R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VD-01A-11D-A28R-08 chr2:100266098 A>T maps to NM_001025108.1 A416A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VD-01A-11D-A28R-08 chr1:157551319 C>T did not map to a codon.
Sequencing variant TCGA-N6-A4VD-01A-11D-A28R-08 chr2:170557639 G>A maps to NM_001008489.3 K53K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VD-01A-11D-A28R-08 chr7:86542400 C>T maps to NM_001142749.2 S617S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VD-01A-11D-A28R-08 chr1:158618427 C>T maps to NM_003126.2 T1195T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VD-01A-11D-A28R-08 chr4:38138874 G>A maps to NM_015173.2 T1142T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VD-01A-11D-A28R-08 chr19:17338750 T>C maps to NM_024578.1 C185C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VD-01A-11D-A28R-08 chrX:55757848 C>T maps to NM_016656.3 R144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VD-01A-11D-A28R-08 chr6:22290510 C>T maps to ENST00000397199 T129T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VD-01A-11D-A28R-08 chr16:89922601 C>A maps to NM_032451.1 R354R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VD-01A-11D-A28R-08 chr10:127724803 G>A maps to NM_003474.4 R817*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VD-01A-11D-A28R-08 chr5:149497299 G>A maps to NM_002609.3 S1006S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VD-01A-11D-A28R-08 chr13:28537413 C>T maps to NM_001265.3 P260P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VD-01A-11D-A28R-08 chr8:77766791 G>A maps to NM_024721.4 P2545P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VD-01A-11D-A28R-08 chr6:27833146 C>T maps to NM_003511.2 G5G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VD-01A-11D-A28R-08 chr7:80290414 C>T maps to NM_001127444.1 D106D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VD-01A-11D-A28R-08 chr2:21256328 G>A maps to NM_000384.2 A322A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VD-01A-11D-A28R-08 chr8:113254009 A>G maps to NM_198123.1 G3469G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VD-01A-11D-A28R-08 chr1:44474143 G>A maps to NM_201649.2 A230A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VD-01A-11D-A28R-08 chr11:126306736 G>A maps to NM_032531.3 S507S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VD-01A-11D-A28R-08 chr1:57206383 C>T maps to NM_001004303.4 S563S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VD-01A-11D-A28R-08 chr20:58569314 G>T maps to NM_177980.2 P479P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VD-01A-11D-A28R-08 chr17:44782177 G>A maps to NM_006178.2 T476T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VD-01A-11D-A28R-08 chr17:76395555 C>T maps to NM_024419.3 N213N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VD-01A-11D-A28R-08 chr5:140515027 G>A maps to NM_015669.2 A4A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VD-01A-11D-A28R-08 chr10:124389945 C>T maps to ENST00000368915 R1989*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VE-01A-11D-A28R-08 chr20:59829993 G>T did not map to a codon.
Sequencing variant TCGA-N6-A4VE-01A-11D-A28R-08 chr9:33295249 C>T maps to NM_002504.4 L286L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VE-01A-11D-A28R-08 chr3:115805174 T>C maps to NM_002338.3 V128V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VE-01A-11D-A28R-08 chr4:39230232 T>C maps to NM_025132.3 H635H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VE-01A-11D-A28R-08 chr19:58438843 A>G maps to NM_133460.1 C235C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VE-01A-11D-A28R-08 chr6:29323300 G>T maps to NM_030876.5 T224T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VE-01A-11D-A28R-08 chr7:86416019 C>T maps to NM_000840.2 G304G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VE-01A-11D-A28R-08 chr7:98457842 G>C maps to NM_001134450.1 L170L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VE-01A-11D-A28R-08 chr6:159642726 A>T maps to NM_032532.2 S255S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VE-01A-11D-A28R-08 chr21:27277387 A>T maps to NM_000484.3 V637V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VE-01A-11D-A28R-08 chr19:53058028 G>A maps to NM_001039886.3 E620E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VE-01A-11D-A28R-08 chr5:138282943 G>C maps to ENST00000509534 P423P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VE-01A-11D-A28R-08 chr5:40691916 T>C maps to NM_000958.2 L302L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VE-01A-11D-A28R-08 chr4:87696406 T>A maps to NM_080685.2 V1869V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VE-01A-11D-A28R-08 chr19:33604671 G>T did not map to a codon.
Sequencing variant TCGA-N6-A4VE-01A-11D-A28R-08 chr4:140278709 G>A did not map to a codon.
Sequencing variant TCGA-N6-A4VE-01A-11D-A28R-08 chr6:42689571 G>T maps to NM_000322.4 G167G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VE-01A-11D-A28R-08 chr13:77713330 G>A maps to NM_015057.4 D2553D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VE-01A-11D-A28R-08 chr11:48347055 C>A maps to NM_001004702.1 V188V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VE-01A-11D-A28R-08 chr16:2042102 C>G maps to NM_004209.5 L76L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VE-01A-11D-A28R-08 chr7:82764633 C>T maps to NM_033026.5 Q744Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VF-01A-31D-A28R-08 chr11:18755101 C>T did not map to a codon.
Sequencing variant TCGA-N6-A4VF-01A-31D-A28R-08 chr1:10715750 G>A maps to NM_001079843.1 H540H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VF-01A-31D-A28R-08 chr5:140751622 C>T maps to NM_018924.2 D554D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VF-01A-31D-A28R-08 chr5:140183010 C>T maps to NM_018906.2 S743S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VF-01A-31D-A28R-08 chr13:113803455 C>T maps to NM_000504.3 F364F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VF-01A-31D-A28R-08 chrX:67433757 A>C maps to NM_002547.2 Y181*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VF-01A-31D-A28R-08 chr6:7845379 C>T maps to NM_001718.4 Y224Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VF-01A-31D-A28R-08 chr7:150094402 G>A maps to NM_173680.3 P278P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VF-01A-31D-A28R-08 chr12:56816662 C>T maps to NM_003920.3 E802E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VF-01A-31D-A28R-08 chr18:76754279 C>T maps to NM_171999.2 G763G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VF-01A-31D-A28R-08 chr2:234601883 T>G maps to NM_001072.3 Y78*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VF-01A-31D-A28R-08 chr12:57871400 G>T maps to ENST00000393797 R270R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VF-01A-31D-A28R-08 chr6:134491531 G>C maps to NM_001143676.1 T485T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VF-01A-31D-A28R-08 chr1:22161367 G>A maps to NM_005529.5 F3508F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VG-01A-31D-A28R-08 chr21:31045467 T>C maps to ENST00000327783 Q187Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VG-01A-31D-A28R-08 chr4:147204389 G>A maps to ENST00000507030 D267D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VG-01A-31D-A28R-08 chr2:152321301 C>T maps to NM_018151.4 D1756D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VG-01A-31D-A28R-08 chr17:7578289 C>T did not map to a codon.
Sequencing variant TCGA-N6-A4VG-01A-31D-A28R-08 chr17:7702524 C>T maps to NM_020877.2 I2888I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VG-01A-31D-A28R-08 chr9:87635191 G>A maps to NM_006180.3 T748T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VG-01A-31D-A28R-08 chr17:40847635 G>A maps to NM_003632.2 R1030R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VG-01A-31D-A28R-08 chr21:10969072 A>T did not map to a codon.
Sequencing variant TCGA-N6-A4VG-01A-31D-A28R-08 chr2:242380726 A>C maps to NM_014808.2 S389S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VG-01A-31D-A28R-08 chr22:42128267 G>A maps to NM_152513.3 R372R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VG-01A-31D-A28R-08 chr20:62598841 G>A maps to NM_020713.1 P52P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VG-01A-31D-A28R-08 chr8:124243796 C>T maps to NM_032847.1 A186A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VG-01A-31D-A28R-08 chr5:9043071 A>G maps to NM_003966.2 H1054H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VG-01A-31D-A28R-08 chr8:86193463 C>G maps to NM_198584.2 A225A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VG-01A-31D-A28R-08 chr1:34192254 G>A maps to ENST00000373381 S760S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VG-01A-31D-A28R-08 chrX:52677446 C>G did not map to a codon.
Sequencing variant TCGA-N6-A4VG-01A-31D-A28R-08 chr19:47935655 C>T maps to NM_015063.2 P719P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VG-01A-31D-A28R-08 chr6:42986289 G>C maps to NM_057161.2 S243S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VG-01A-31D-A28R-08 chr5:50045993 C>A maps to ENST00000505697 Y52*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VG-01A-31D-A28R-08 chr19:1828424 G>A maps to NM_020695.3 S121S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N6-A4VG-01A-31D-A28R-08 chr3:40251349 G>A maps to NM_015460.2 S557S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr1:152188527 G>A maps to NM_001009931.1 G1859G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr15:54625987 T>C maps to ENST00000260323 T1506T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr1:205290639 C>T maps to ENST00000441520 A83A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr22:19959450 G>A maps to NM_001670.2 G913G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr15:42162109 G>A maps to ENST00000320955 L1928L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr1:228474714 C>T maps to NM_001098623.1 C3173C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr16:20974800 C>A maps to NM_017539.1 G3469*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr14:24033539 A>G did not map to a codon.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr1:892378 C>T maps to NM_015658.3 A127A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr16:67863713 G>A maps to NM_025082.3 D380D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr18:44036490 C>A maps to NM_152470.2 P311P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr11:92624209 C>T maps to ENST00000298047 S4567S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr10:25464417 C>T maps to NM_020752.2 G23G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr9:98238410 C>A maps to NM_000264.3 G545*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr22:43570303 G>A maps to NM_015140.3 G380G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr8:52336135 C>A maps to NM_144651.4 T598T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr7:45930297 C>A maps to NM_000596.2 T167T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chrX:83129488 A>G maps to NM_021118.1 K591K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr8:26481665 C>T maps to NM_001197293.1 H212H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr22:41654016 G>A maps to NM_002883.2 L237L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr10:104241926 A>G maps to NM_005736.3 G252G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr6:36359627 A>G maps to NM_152990.3 D108D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr17:43474151 C>T maps to ENST00000428638 A652A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr17:25976005 T>C maps to NM_009587.2 *356Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr6:43276524 G>A maps to ENST00000449267 S2S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chrX:138882231 C>A maps to NM_173694.4 E236*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr10:115410305 T>C did not map to a codon.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr3:196733482 G>A maps to NM_005929.5 H625H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr19:46815487 C>T maps to NM_152795.2 L281L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr8:1581003 G>A maps to ENST00000357934 A476A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr9:37740147 C>T maps to NM_014907.2 D541D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr1:233515337 A>G maps to NM_032435.2 S862S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr8:17611441 G>A maps to NM_001001924.2 C625C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr9:125424189 C>T maps to ENST00000373686 L116L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr10:27494153 C>T maps to ENST00000375888 L485L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr2:219883882 G>A maps to NM_194302.2 P1164P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr5:108203562 C>T maps to NM_005246.2 Q193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr8:54163549 G>A maps to NM_000912.3 C16C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr3:149684299 T>C maps to NM_053024.3 K133K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr5:115783142 C>T maps to ENST00000257414 T770T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr14:23887558 C>T maps to NM_000257.2 L1343L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr16:72822571 C>T maps to NM_006885.3 Q3201Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr19:47260140 C>T maps to NM_024301.4 I478I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr14:105643363 G>A maps to NM_177533.3 S42S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr14:68215287 T>C maps to NM_015346.3 S2495S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr17:37899523 C>T maps to ENST00000445327 F208F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr19:13879656 C>T maps to NM_001031727.2 D248D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr19:17691985 G>A maps to NM_024656.2 V534V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr9:138011984 C>T maps to NM_014279.4 N455N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr3:127335928 C>T maps to NM_004526.2 R581*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr12:102468811 G>A maps to NM_024057.2 S278S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr19:49845738 G>A maps to NM_003598.1 R396*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr15:62201258 G>A maps to NM_020821.2 Y2970Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chrX:30578298 G>T maps to NM_025159.2 C58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr8:56863329 T>C maps to NM_002350.2 S158S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr14:105518407 C>T maps to NM_013345.2 P22P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr1:29189254 C>T maps to NM_000911.3 D193D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr18:21484615 C>T maps to ENST00000416669 D2193D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr18:47811721 C>A did not map to a codon.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr2:227661890 G>A maps to NM_005544.2 R522*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr13:52676359 C>T maps to NM_199289.1 P226P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr5:145252291 C>T maps to NM_001080516.1 L80L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr10:94408153 C>T maps to NM_004523.3 C911C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr3:121190984 T>C maps to ENST00000393672 L2326L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr10:101163311 G>A maps to NM_002079.2 I291I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr9:138392883 G>A maps to NM_016034.3 K28K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr20:60927342 G>A maps to NM_005560.3 I214I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr5:140564302 C>T maps to NM_020957.1 G723G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr7:147914500 G>A maps to NM_014141.5 P1044P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr2:219895831 A>G maps to NM_194302.2 A337A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr7:97846803 G>A maps to ENST00000379795 D1134D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr13:23914021 A>G maps to NM_014363.4 H1331H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr8:88885770 C>T maps to NM_152418.3 L143L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr20:17581477 G>A maps to NM_006870.3 K33K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr17:7736212 T>C maps to NM_020877.2 T4315T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr18:33800115 C>T maps to NM_017947.2 P632P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr4:1729656 C>T maps to NM_006342.1 G176G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr16:87445611 G>A maps to NM_015144.2 H768H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr10:68686814 T>C maps to NM_178011.3 C47C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr15:35273865 A>G maps to NM_014106.3 G590G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr7:5645074 C>T maps to ENST00000340250 T490T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr8:144945054 G>A maps to NM_031308.1 P789P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr2:47707955 G>A maps to NM_000251.1 S860S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chrX:2828697 A>G did not map to a codon.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr9:139418328 G>A maps to NM_017617.3 G81G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr8:144649982 G>A maps to NM_001100878.1 L614L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr3:167754716 A>G maps to NM_014498.3 P250P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr20:62571739 G>A maps to NM_017859.3 R467R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr4:84502844 C>T maps to NM_032717.3 T113T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr16:17228505 G>A maps to NM_022166.3 Y617Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr11:55890693 T>C maps to NM_001005201.1 I282I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr9:131670970 C>T maps to NM_001127244.1 L510L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr19:18378025 C>T maps to NM_001145304.1 T108T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chrX:50085295 A>G maps to NM_033031.2 Q1204Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chrX:151900215 G>A maps to NM_005367.5 I195I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr5:476345 G>A maps to NM_004174.2 L680L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr20:57767906 G>A maps to NM_178457.1 R611R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr14:102506037 C>T maps to NM_001376.4 L3887L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr12:105282850 A>G maps to NM_032148.3 S280S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr1:47728787 G>A maps to NM_001048166.1 N872N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chrX:152845674 G>A maps to NM_001001344.2 T1194T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr12:6703715 C>T maps to ENST00000309577 W741*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr7:2687614 C>T maps to NM_025250.2 L217L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr8:133923761 T>C maps to NM_003235.4 P1381P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr20:62839358 G>A maps to NM_004535.2 E270E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr22:19776480 C>G maps to NM_053004.2 V245V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr10:24831987 G>A maps to NM_019590.3 V1263V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr15:41099852 C>G maps to NM_001077268.1 S22S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr13:52365372 C>A maps to NM_001031719.1 V49V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr9:134382767 C>T maps to NM_007171.3 N98N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr4:83788041 C>T maps to ENST00000505472 Q372Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr6:102372595 T>C did not map to a codon.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr5:112824030 G>A maps to NM_001085377.1 S27S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr2:198274671 G>A maps to NM_012433.2 S242S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr7:143087015 T>C maps to NM_001010972.1 T520T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr3:8609223 G>A maps to NM_014583.2 A346A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr8:81553672 G>A maps to NM_001033723.2 Y389Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr5:155040 C>T maps to NM_052909.3 Q326*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chrX:107420158 G>A maps to NM_033641.2 G866G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr1:151261868 C>T maps to NM_020832.1 C829C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr19:50979570 G>T maps to ENST00000391816 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr9:33053231 G>A maps to NM_018225.2 T393T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr4:6031487 G>A maps to NM_001099433.1 D800D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr17:4534906 A>G maps to NM_001140.3 S659S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr2:120388229 C>T maps to NM_001029996.3 R320*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr8:28314408 C>T maps to NM_172366.2 Q127Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr17:72470734 T>C maps to NM_007261.2 F148F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr3:32778913 T>C maps to NM_015442.1 H509H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr2:120438731 G>T maps to NM_030577.2 G101G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr12:100709496 G>A maps to NM_017988.4 Q419Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr6:83806835 T>C did not map to a codon.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr16:29912570 G>A maps to NM_181718.3 W93*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chrX:153179297 G>A maps to NM_001164741.1 D396D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr12:120878306 G>A maps to NM_004373.2 V99V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr8:124266661 T>A maps to NM_007222.3 K509*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chrX:47085769 C>T maps to NM_001170460.1 N369N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr11:33581396 C>T maps to ENST00000389726 Q1029*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr21:45994015 C>A maps to NM_198687.1 P127P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr3:155206446 A>G did not map to a codon.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr11:67790204 G>A maps to NM_001161473.1 L363L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr4:77091019 A>C maps to NM_005506.2 P371P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr5:176696630 C>T maps to NM_022455.4 R1778*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr13:32351560 G>A maps to NM_130806.3 T230T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chrX:79973118 C>T maps to NM_153252.4 A728A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr15:50152665 G>T maps to NM_024837.2 R1102R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr10:26436414 C>T maps to NM_017433.4 D854D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr3:128181452 G>A maps to NM_153330.2 D212D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr7:128037025 G>A maps to NM_000883.3 I375I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr17:10555850 G>A maps to NM_002470.2 Y78Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr1:16456083 G>A maps to NM_004431.3 R890R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr1:23767954 G>T maps to NM_017707.3 A253A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr3:169846642 C>T maps to NM_024947.3 Q539Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr4:1017701 C>T maps to NM_021923.3 H177H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr6:99283718 C>T maps to NM_005604.2 L324L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chrX:132092543 G>A maps to NM_001077188.1 R29R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chrX:153129470 G>A maps to NM_000425.3 G1108G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr7:142749857 C>T maps to NM_001001667.1 Q141*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chrX:114536596 T>C maps to NM_016383.3 A44A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr10:96162513 G>A maps to NM_015188.1 P48P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr1:152784987 C>A maps to NM_178349.1 P22P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr4:1988037 C>T maps to NM_005663.3 P253P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr16:76528915 C>T maps to NM_033401.3 C729C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr11:60718780 G>A maps to NM_016582.2 G81G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr19:58850388 G>A maps to NM_181846.2 Q391Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr20:37546948 T>C maps to NM_015568.2 H448H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr2:27423871 G>A maps to NM_021095.2 Y586Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr1:230907845 G>A did not map to a codon.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr15:79058094 G>A maps to ENST00000258883 H1386H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr12:52451180 G>A maps to ENST00000360284 V523V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr7:1976421 G>A maps to NM_003550.2 R570*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr11:12246316 C>T maps to NM_014632.2 R546R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr1:20141294 G>A maps to NM_019062.1 R100R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr5:176004717 G>A maps to NM_001171976.1 R477R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr15:85383001 A>G maps to NM_020778.4 S366S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr6:100896034 G>A maps to ENST00000262901 C279C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr9:139836498 G>A maps to NM_018998.2 I365I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr11:66298468 G>A maps to NM_024649.4 A526A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr7:26192150 C>T maps to NM_004289.6 G11G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr7:111423965 G>A maps to ENST00000428084 G1157G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr1:179078367 C>T maps to NM_007314.3 Q678Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr3:196730856 T>C maps to NM_005929.5 G684G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr12:12483293 C>T maps to NM_018050.2 P321P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr3:179107815 C>T maps to NM_033540.2 R679R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr6:35424066 C>T maps to NM_021922.2 D264D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr19:47856556 C>A maps to NM_014681.5 I90I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr19:36574053 A>G maps to NM_001083961.1 T487T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr7:134252968 C>T maps to ENST00000418096 H42H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr19:10078752 A>G maps to NM_015719.3 G1439G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr11:46724533 C>T maps to NM_024741.2 S131S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr2:128471557 C>T maps to NM_018383.4 P969P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr17:74469405 A>G maps to NM_024599.5 C608C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr19:40316672 C>T maps to NM_004714.1 K524K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr2:242036780 A>G maps to NM_182501.3 I194I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr19:6417015 G>A maps to NM_003685.2 D388D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr10:79552203 C>T maps to NM_004747.3 P1918P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr4:110384777 G>A maps to NM_006323.2 A285A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr19:42351809 C>T maps to ENST00000427618 R77R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr1:26527325 C>T maps to NM_198137.1 G331G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr19:54684566 G>A maps to NM_024298.3 A259A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr11:6478960 C>T maps to NM_033278.2 A160A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr19:55497517 G>T did not map to a codon.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr2:112786407 C>T maps to NM_006343.2 D989D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr2:135119888 G>A maps to NM_002410.3 Q430Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr13:24860368 C>T maps to ENST00000424834 N810N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr12:99145153 G>A maps to NM_152788.3 R1217R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr8:120850596 C>T maps to NM_024094.2 L325L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr7:42949407 C>T maps to NM_001099858.1 T422T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr22:39883621 C>T maps to NM_001098270.1 A90A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr8:30560724 G>T maps to NM_000637.3 A175A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr7:150490214 C>T maps to NM_014020.3 W187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chrX:152960289 C>T maps to NM_005629.3 C571C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr6:111409146 C>T maps to NM_018593.4 P64P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr6:31079316 C>T maps to NM_014070.2 G273G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr11:1265996 G>A maps to ENST00000447027 T2632T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr16:2282536 C>T maps to NM_004424.3 R230R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr8:38835512 T>C maps to NM_153692.3 L271L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr6:53787464 A>G maps to NM_018214.4 P483P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr10:133958681 G>A maps to NM_001105521.2 A558A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chrX:12693028 T>C did not map to a codon.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr5:174151739 G>C maps to NM_002449.4 P26P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr4:9784645 C>T maps to NM_000798.4 A331A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr11:6238901 C>T maps to NM_032127.3 V652V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr15:40502377 G>A maps to ENST00000412359 A798A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr11:119044560 C>T maps to NM_024618.2 D201D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr13:35624438 T>A maps to ENST00000400445 A293A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr11:117779387 G>A maps to ENST00000413475 T406T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr4:8588798 C>A maps to NM_080819.2 P267P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr19:17836816 C>T maps to NM_018174.4 C208C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr12:7090984 A>T maps to NM_005768.5 T149T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr5:92929319 G>A maps to NM_005654.4 S348S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr19:56249560 G>A maps to NM_176820.2 D60D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr6:42036323 C>T maps to NM_138572.2 N253N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr7:120386009 C>T maps to NM_012281.2 S548S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr1:160141102 G>A maps to NM_144699.3 P518P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr3:121415163 C>T maps to ENST00000393667 L1402L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chrX:73960122 G>A maps to NM_001008537.2 R1423R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chrX:103495019 C>T maps to NM_153448.3 P370P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr9:116356772 T>C maps to NM_144488.4 P1048P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr1:97235319 T>C maps to ENST00000370197 R59R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr8:87165042 A>G did not map to a codon.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr3:43122425 G>A maps to NM_032806.4 H166H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr17:4200056 G>A maps to NM_003342.4 R68*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr5:83239261 C>A maps to NM_005711.3 L473L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr12:81102658 C>T maps to NM_002469.2 R217*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr19:48848476 C>T maps to NM_018273.2 P168P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr19:9964924 G>A maps to NM_058164.2 N434N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr1:36788048 C>A maps to NM_018166.1 S115S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr7:137339500 C>A maps to NM_004717.2 G239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr7:99998669 G>A maps to NM_017984.3 G638G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr5:40964970 T>A maps to NM_000587.2 C626*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr19:33095252 G>A maps to NM_032139.2 F857F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y0-01A-12D-A28R-08 chr9:71491649 C>T maps to NM_003558.2 Y86Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y5-01A-12D-A28R-08 chr4:123855465 G>T maps to NM_145207.2 L240L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y5-01A-12D-A28R-08 chr1:190067522 C>T maps to NM_199051.1 E642E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y5-01A-12D-A28R-08 chr11:64453156 G>A maps to NM_015080.3 N371N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y5-01A-12D-A28R-08 chr7:142562259 C>A maps to NM_004445.3 A234A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y5-01A-12D-A28R-08 chr1:110754450 C>T maps to NM_004978.4 Y110Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y5-01A-12D-A28R-08 chr11:75439190 T>C did not map to a codon.
Sequencing variant TCGA-N7-A4Y5-01A-12D-A28R-08 chr2:101011978 A>G maps to NM_004854.3 I175I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y5-01A-12D-A28R-08 chr5:44305204 C>A maps to NM_004465.1 G173G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y5-01A-12D-A28R-08 chr16:3406725 G>A maps to NM_012368.2 P262P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y5-01A-12D-A28R-08 chr6:154360936 C>T maps to NM_001145279.1 F179F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y5-01A-12D-A28R-08 chr8:145735979 G>A did not map to a codon.
Sequencing variant TCGA-N7-A4Y5-01A-12D-A28R-08 chr2:135012114 C>T maps to NM_002410.3 R47R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y5-01A-12D-A28R-08 chr9:129853994 G>A maps to NM_012098.2 N412N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y5-01A-12D-A28R-08 chr1:173907981 T>C maps to NM_172071.2 T1093T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y5-01A-12D-A28R-08 chr20:9343592 C>T maps to NM_001172646.1 N140N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y5-01A-12D-A28R-08 chr19:58965694 C>T maps to NM_207395.2 Y74Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y5-01A-12D-A28R-08 chr5:32712484 A>C maps to ENST00000265074 A201A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y5-01A-12D-A28R-08 chr12:105543427 C>T maps to NM_015275.1 F850F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y5-01A-12D-A28R-08 chr1:19018401 C>T maps to NM_002584.2 R247R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y5-01A-12D-A28R-08 chr2:173355989 G>A maps to ENST00000264106 P979P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y5-01A-12D-A28R-08 chr20:25277118 C>T maps to NM_002862.3 S831S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y5-01A-12D-A28R-08 chr16:67189312 C>T maps to NM_003789.3 E132E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y5-01A-12D-A28R-08 chr2:40342515 G>A maps to NM_021097.2 I933I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y8-01A-11D-A28R-08 chr6:170871039 A>G maps to NM_003194.4 Q72Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y8-01A-11D-A28R-08 chr1:44057542 C>A maps to NM_002840.3 S531*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y8-01A-11D-A28R-08 chr4:156135432 G>A maps to NM_000910.2 G114G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y8-01A-11D-A28R-08 chr8:110590122 C>T maps to NM_001099744.1 K286K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y8-01A-11D-A28R-08 chr12:13103267 G>A maps to NM_018654.1 D17D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y8-01A-11D-A28R-08 chr14:74407729 G>A maps to NM_152445.1 P433P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y8-01A-11D-A28R-08 chr8:87229899 T>G maps to NM_138817.2 L326L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y8-01A-11D-A28R-08 chr11:65302777 C>T maps to NM_020680.3 A437A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y8-01A-11D-A28R-08 chr10:43317507 A>G did not map to a codon.
Sequencing variant TCGA-N7-A4Y8-01A-11D-A28R-08 chr3:195510995 G>A maps to NM_018406.5 D2485D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y8-01A-11D-A28R-08 chr1:229568732 C>A did not map to a codon.
Sequencing variant TCGA-N7-A4Y8-01A-11D-A28R-08 chr12:6664976 G>A maps to NM_001193457.1 N73N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y8-01A-11D-A28R-08 chr1:204588976 G>A maps to NM_201630.1 R48R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y8-01A-11D-A28R-08 chr7:127958087 C>T maps to NM_018077.2 A545A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y8-01A-11D-A28R-08 chr6:109815250 T>C maps to NM_001145128.2 L1822L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y8-01A-11D-A28R-08 chr16:14980688 C>T maps to ENST00000456867 F1098F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A59B-01A-11D-A28R-08 chr19:18376864 G>C maps to NM_001145304.1 T495T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A59B-01A-11D-A28R-08 chr20:31381339 A>G did not map to a codon.
Sequencing variant TCGA-N7-A59B-01A-11D-A28R-08 chrX:18660258 C>T maps to NM_000330.3 S180S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A59B-01A-11D-A28R-08 chr5:170819813 T>A maps to NM_002520.6 V151V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A59B-01A-11D-A28R-08 chr7:139715630 G>A maps to NM_001166253.1 W492*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A59B-01A-11D-A28R-08 chr19:12501522 T>C maps to NM_001080821.2 Q563Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A59B-01A-11D-A28R-08 chr13:98829046 C>T maps to NM_178861.4 R148R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A59B-01A-11D-A28R-08 chr9:35381191 C>T maps to ENST00000396787 Q754*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A59B-01A-11D-A28R-08 chr17:16285415 G>T maps to NM_018955.2 S65S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A59B-01A-11D-A28R-08 chr2:33036104 A>T maps to NM_017735.4 L671L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A59B-01A-11D-A28R-08 chr9:107331462 C>T maps to NM_001004483.1 N5N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A59B-01A-11D-A28R-08 chr8:125082753 G>A maps to NM_001039112.2 W1294*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A59B-01A-11D-A28R-08 chr19:36526380 G>T maps to NM_152658.2 A262A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A59B-01A-11D-A28R-08 chr10:107015548 G>A maps to NM_014978.1 Q1109Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A59B-01A-11D-A28R-08 chr19:7585558 A>G maps to NM_018083.4 K477K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PI-01A-21D-A28R-08 chr8:1871978 G>A maps to ENST00000398564 T834T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PI-01A-21D-A28R-08 chr9:2039778 G>A maps to NM_003070.3 Q223Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PI-01A-21D-A28R-08 chr21:47552222 C>T maps to NM_001849.3 H939H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PI-01A-21D-A28R-08 chr3:136323150 C>T maps to NM_005862.2 Q99Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PI-01A-21D-A28R-08 chr1:117491979 G>A maps to NM_020440.2 R333R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PI-01A-21D-A28R-08 chr5:13865874 G>T maps to NM_001369.2 Y1419*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PI-01A-21D-A28R-08 chr3:35778808 G>A maps to ENST00000458225 Q499Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PI-01A-21D-A28R-08 chr17:7577497 C>T did not map to a codon.
Sequencing variant TCGA-N8-A4PI-01A-21D-A28R-08 chr7:135080617 C>T maps to NM_001190850.1 T299T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PI-01A-21D-A28R-08 chr11:132180093 A>C maps to NM_001144058.1 S250S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PI-01A-21D-A28R-08 chr3:121260218 T>A maps to ENST00000393672 K284*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PI-01A-21D-A28R-08 chr8:65527730 C>T maps to NM_004820.3 W303*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PI-01A-21D-A28R-08 chr7:150269307 C>T maps to ENST00000430830 I64I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PI-01A-21D-A28R-08 chrX:20185862 T>C maps to NM_004586.2 V482V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PI-01A-21D-A28R-08 chr11:46397945 C>T maps to NM_001105540.1 D908D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PI-01A-21D-A28R-08 chr9:90584734 G>A maps to NM_001039803.2 G221G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PI-01A-21D-A28R-08 chr17:70120194 G>A maps to NM_000346.3 T399T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PI-01A-21D-A28R-08 chr10:89692903 C>T maps to NM_000314.4 R130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PI-01A-21D-A28R-08 chr1:207679360 C>T maps to NM_000651.4 S78S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PI-01A-21D-A28R-08 chr1:85656052 A>G maps to NM_032184.1 P376P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PI-01A-21D-A28R-08 chr19:38976496 C>T maps to NM_000540.2 I1734I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PI-01A-21D-A28R-08 chr5:177156484 C>G did not map to a codon.
Sequencing variant TCGA-N8-A4PI-01A-21D-A28R-08 chr12:54645938 A>T maps to NM_012117.2 Y70*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PI-01A-21D-A28R-08 chr17:1563259 C>T maps to NM_006445.3 E1607E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PI-01A-21D-A28R-08 chr2:27801238 C>T maps to NM_032266.3 I600I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PI-01A-21D-A28R-08 chr12:6710696 C>T did not map to a codon.
Sequencing variant TCGA-N8-A4PL-01A-11D-A28R-08 chr16:4949274 G>A maps to NM_002705.4 Y239Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PL-01A-11D-A28R-08 chr6:29012268 C>T maps to NM_030903.3 T228T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PL-01A-11D-A28R-08 chr5:150646987 C>T maps to NM_000405.4 I186I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PL-01A-11D-A28R-08 chr14:24709662 C>T maps to NM_001099274.1 K341K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PL-01A-11D-A28R-08 chr1:22073589 A>G maps to NM_032236.5 L321L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PL-01A-11D-A28R-08 chr17:10304251 C>T maps to NM_002472.2 L1093L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PL-01A-11D-A28R-08 chr4:20760462 C>T maps to ENST00000382152 S113S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PL-01A-11D-A28R-08 chr17:6900278 G>A maps to NM_000697.2 A90A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PL-01A-11D-A28R-08 chr2:130832626 G>A maps to NM_001099771.2 T806T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PL-01A-11D-A28R-08 chr10:127585026 C>A did not map to a codon.
Sequencing variant TCGA-N8-A4PL-01A-11D-A28R-08 chr8:142175304 C>T maps to NM_014957.2 F410F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PL-01A-11D-A28R-08 chr4:6064098 G>A maps to NM_001099433.1 R500R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PL-01A-11D-A28R-08 chr14:20344722 C>A maps to NM_001005501.1 T99T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PL-01A-11D-A28R-08 chr8:92346558 C>A maps to NM_134266.1 R227R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PL-01A-11D-A28R-08 chr6:30639045 T>C maps to NM_003587.4 P71P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PL-01A-11D-A28R-08 chr4:3475358 C>T maps to ENST00000389653 G109G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PL-01A-11D-A28R-08 chr17:21731269 T>C did not map to a codon.
Sequencing variant TCGA-N8-A4PL-01A-11D-A28R-08 chr6:24473847 A>G maps to NM_001503.2 F163F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PL-01A-11D-A28R-08 chr1:151205103 C>T maps to NM_001135638.1 D188D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PL-01A-11D-A28R-08 chr2:179213991 C>A maps to ENST00000392505 S368S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PL-01A-11D-A28R-08 chr11:13393791 C>T maps to ENST00000403290 D301D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PM-01A-11D-A28R-08 chr13:97639791 G>A maps to NM_080818.3 N74N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PM-01A-11D-A28R-08 chr13:36686232 G>A maps to NM_004734.4 L166L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PM-01A-11D-A28R-08 chr2:102805587 T>C maps to NM_003854.2 P37P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PM-01A-11D-A28R-08 chr13:113777239 G>A did not map to a codon.
Sequencing variant TCGA-N8-A4PM-01A-11D-A28R-08 chr5:140215890 C>T maps to NM_018910.2 D641D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PM-01A-11D-A28R-08 chr2:179702419 G>A maps to NM_173648.3 R1176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PM-01A-11D-A28R-08 chr9:35660817 T>C maps to NM_174923.2 D162D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PM-01A-11D-A28R-08 chr1:11589624 C>T maps to NM_020780.1 F937F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PM-01A-11D-A28R-08 chr15:23006810 A>G maps to NM_030922.6 L165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PM-01A-11D-A28R-08 chr1:11985517 C>A maps to ENST00000376576 V259V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PM-01A-11D-A28R-08 chr11:55110832 T>C maps to NM_001005274.1 L53L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PM-01A-11D-A28R-08 chr5:65370849 A>G did not map to a codon.
Sequencing variant TCGA-N8-A4PM-01A-11D-A28R-08 chr10:135346209 T>C maps to NM_000773.3 F221F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PM-01A-11D-A28R-08 chr1:154493951 G>A maps to NM_001098475.1 P122P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PM-01A-11D-A28R-08 chr17:42636255 C>G maps to NM_001466.3 G400G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PM-01A-11D-A28R-08 chrX:69489950 C>T maps to NM_004312.2 D34D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PM-01A-11D-A28R-08 chr19:56466005 G>A maps to NM_176811.2 L194L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PM-01A-11D-A28R-08 chr12:81111291 A>T maps to NM_005593.2 G150G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PM-01A-11D-A28R-08 chr7:142641780 G>A maps to NM_000420.2 L454L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PM-01A-11D-A28R-08 chr18:6965301 G>A maps to NM_005559.2 R2394*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PM-01A-11D-A28R-08 chr10:75597240 C>T maps to ENST00000423381 S346S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PM-01A-11D-A28R-08 chr14:23885020 G>A maps to NM_000257.2 D1658D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PN-01A-11D-A28R-08 chr2:135745258 G>A maps to NM_025052.3 Q395*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PN-01A-11D-A28R-08 chr4:149356962 A>G maps to ENST00000511528 A350A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PN-01A-11D-A28R-08 chr3:194081583 C>T maps to NM_001135057.2 T69T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PN-01A-11D-A28R-08 chr13:103698524 C>T maps to NM_000452.2 S335S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PN-01A-11D-A28R-08 chrX:30236897 C>A maps to NM_002364.4 T67T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PN-01A-11D-A28R-08 chrX:63410057 G>A maps to NM_152424.3 Q1037*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PN-01A-11D-A28R-08 chr3:38050772 G>A maps to NM_001130964.1 L553L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PN-01A-11D-A28R-08 chr12:99106174 C>T maps to NM_181861.1 Q974*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PN-01A-11D-A28R-08 chr3:65425584 C>T maps to NM_001033057.1 Q413Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PN-01A-11D-A28R-08 chr10:114919685 C>T maps to NM_030756.4 S436S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PN-01A-11D-A28R-08 chr12:44124454 T>C maps to NM_031292.3 V610V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PN-01A-11D-A28R-08 chr4:84348766 G>A maps to NM_133636.2 P875P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PN-01A-11D-A28R-08 chr22:41077055 C>T maps to NM_005297.3 I131I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PN-01A-11D-A28R-08 chr11:70505947 C>G maps to ENST00000338508 G683G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PN-01A-11D-A28R-08 chr11:55798809 G>T maps to NM_001001921.1 E306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PN-01A-11D-A28R-08 chrX:17770058 C>T maps to NM_001037540.1 C276C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PN-01A-11D-A28R-08 chr8:48873763 C>T maps to NM_182746.1 P20P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PO-01A-11D-A28R-08 chr8:38095662 G>A maps to NM_001164232.1 T186T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PO-01A-11D-A28R-08 chr9:128003020 C>T maps to NM_005347.4 K96K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PO-01A-11D-A28R-08 chr3:195510911 T>A maps to NM_018406.5 L2513L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PO-01A-11D-A28R-08 chr8:52773450 C>A maps to NM_052937.2 L87L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PO-01A-11D-A28R-08 chr11:48511045 C>A maps to NM_001005512.2 A234A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PO-01A-11D-A28R-08 chr11:57114098 C>T maps to NM_002559.2 S67S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PO-01A-11D-A28R-08 chr2:95954316 T>C maps to NM_144707.2 R807R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PO-01A-11D-A28R-08 chr7:100355877 C>T maps to ENST00000349350 P1121P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PO-01A-11D-A28R-08 chr8:66525566 G>T maps to NM_018120.4 S126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PO-01A-11D-A28R-08 chrX:129629215 G>T did not map to a codon.
Sequencing variant TCGA-N8-A4PO-01A-11D-A28R-08 chr5:128362946 C>G maps to NM_001017372.1 Y459*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PO-01A-11D-A28R-08 chr5:101576466 G>T maps to NM_180991.4 R611R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PO-01A-11D-A28R-08 chr9:77415319 C>G maps to NM_017662.4 T696T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PO-01A-11D-A28R-08 chr10:119027212 C>A maps to NM_003054.4 L384L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PO-01A-11D-A28R-08 chr8:3216671 A>C did not map to a codon.
Sequencing variant TCGA-N8-A4PO-01A-11D-A28R-08 chr3:195511688 G>T maps to NM_018406.5 T2254T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PO-01A-11D-A28R-08 chr11:72552577 G>A maps to ENST00000409314 Y683Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PO-01A-11D-A28R-08 chr6:4892428 C>T maps to ENST00000328908 V223V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PO-01A-11D-A28R-08 chr19:41622200 C>A maps to NM_000774.3 P36P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PO-01A-11D-A28R-08 chr1:204588891 G>A maps to NM_201630.1 Q77*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PO-01A-11D-A28R-08 chr11:617617 A>G maps to NM_021924.4 G757G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PO-01A-11D-A28R-08 chr3:13612328 G>T maps to NM_001165035.1 R158R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PO-01A-11D-A28R-08 chr12:109494589 A>C maps to NM_032663.3 R63R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PO-01A-11D-A28R-08 chr6:150267592 G>A maps to NM_025217.2 G145G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PO-01A-11D-A28R-08 chr7:158468183 A>G maps to NM_017760.5 R437R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PO-01A-11D-A28R-08 chr17:48545805 G>A maps to NM_001267.2 T123T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PO-01A-11D-A28R-08 chr5:1075523 G>A maps to NM_006598.2 L643L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PO-01A-11D-A28R-08 chr17:15884459 T>A did not map to a codon.
Sequencing variant TCGA-N8-A4PO-01A-11D-A28R-08 chr13:40297489 A>C maps to ENST00000255468 T568T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PO-01A-11D-A28R-08 chr19:46094974 G>A maps to NM_005282.2 N50N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PO-01A-11D-A28R-08 chr10:74096298 C>T maps to NM_017626.4 W364*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PO-01A-11D-A28R-08 chr6:64394336 T>C maps to NM_015153.2 H238H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PO-01A-11D-A28R-08 chr9:102595039 C>T maps to NM_173200.1 R352*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PP-01A-11D-A28R-08 chr3:193188756 G>A maps to NM_032279.2 R278R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PP-01A-11D-A28R-08 chr17:6946802 A>G maps to NM_153357.1 D34D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PP-01A-11D-A28R-08 chr12:56568508 T>G maps to NM_003075.3 R474R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PP-01A-11D-A28R-08 chr22:41320469 A>C maps to NM_022098.2 V447V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PP-01A-11D-A28R-08 chr13:27827918 G>A maps to NM_000982.3 T2T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PP-01A-11D-A28R-08 chr16:57717866 C>G maps to NM_170776.4 S302*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PP-01A-11D-A28R-08 chr13:28931760 T>C maps to NM_002019.4 E726E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PP-01A-11D-A28R-08 chr16:3107136 C>A maps to NM_022468.4 Y255*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PP-01A-11D-A28R-08 chr3:182584219 A>G maps to NM_014616.1 E536E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PP-01A-11D-A28R-08 chr7:48319343 T>C maps to NM_152701.3 I2851I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PP-01A-11D-A28R-08 chr2:230667107 A>G maps to ENST00000389044 C995C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PP-01A-11D-A28R-08 chr9:137620520 G>T maps to NM_000093.3 T264T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PP-01A-11D-A28R-08 chr8:77767178 T>C maps to NM_024721.4 H2674H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PP-01A-11D-A28R-08 chr12:103352600 C>A maps to NM_004316.3 I193I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PP-01A-11D-A28R-08 chr1:153660532 C>A maps to NM_000906.3 I751I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PP-01A-11D-A28R-08 chr2:176987825 C>T maps to NM_014213.3 S110S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PP-01A-11D-A28R-08 chr19:13039264 G>T maps to NM_004461.2 T244T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PP-01A-11D-A28R-08 chr11:61511822 G>C maps to NM_006133.2 S997S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PP-01A-11D-A28R-08 chr10:108366949 T>A maps to NM_001013031.1 K1047*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PP-01A-11D-A28R-08 chr10:103900433 C>A maps to NM_015062.3 I723I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PP-01A-11D-A28R-08 chr5:171849419 C>T maps to NM_001017995.2 Q52Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PP-01A-11D-A28R-08 chr19:11462748 G>A maps to ENST00000427879 E284E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PP-01A-11D-A28R-08 chr17:8092944 G>A maps to NM_017622.2 L172L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PP-01A-11D-A28R-08 chr11:120925928 C>A maps to NM_152715.3 A208A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PP-01A-11D-A28R-08 chr1:152733336 C>T maps to NM_001025231.1 R425*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PP-01A-11D-A28R-08 chr5:140229831 G>A maps to NM_031857.1 S584S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PP-01A-11D-A28R-08 chr5:86668013 T>C did not map to a codon.
Sequencing variant TCGA-N8-A4PP-01A-11D-A28R-08 chr7:38431441 C>T maps to NM_001635.3 Q595Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PP-01A-11D-A28R-08 chr10:7605312 T>C maps to ENST00000256861 E854E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PP-01A-11D-A28R-08 chr14:20925651 A>T maps to NM_080649.1 L314L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PP-01A-11D-A28R-08 chr3:36874296 T>G maps to NM_014831.2 T2215T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PP-01A-11D-A28R-08 chr7:106508092 G>A maps to NM_002649.2 A29A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PP-01A-11D-A28R-08 chr10:50901854 G>T maps to NM_182554.2 E45*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PP-01A-11D-A28R-08 chr1:152191668 G>A maps to NM_001009931.1 G812G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PP-01A-11D-A28R-08 chr1:177199125 G>A maps to NM_021165.2 A38A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PP-01A-11D-A28R-08 chr6:150210551 G>T maps to NM_139165.1 S185*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PP-01A-11D-A28R-08 chr12:48468233 G>T maps to ENST00000004980 S271S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PP-01A-11D-A28R-08 chr19:46443288 G>T maps to NM_002516.2 G437G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PQ-01A-11D-A28R-08 chr11:7950116 G>A maps to NM_001004461.1 F31F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PQ-01A-11D-A28R-08 chr6:45390465 A>G maps to ENST00000359524 Q133Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PQ-01A-11D-A28R-08 chr13:40175116 G>A maps to NM_005780.2 S79S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PQ-01A-11D-A28R-08 chr8:143996606 C>A maps to NM_000498.3 S150S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PQ-01A-11D-A28R-08 chr9:34978095 G>A maps to NM_015297.1 K397K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PQ-01A-11D-A28R-08 chr20:60736499 G>A maps to NM_198935.1 T80T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PQ-01A-11D-A28R-08 chrX:601570 C>A maps to NM_000451.3 R168R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PQ-01A-11D-A28R-08 chr4:169049236 G>A maps to NM_007193.3 V7V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PQ-01A-11D-A28R-08 chr1:55277786 C>A maps to NM_001110533.1 V229V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PQ-01A-11D-A28R-08 chr6:2893764 C>T maps to NM_004155.4 P149P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PQ-01A-11D-A28R-08 chr19:51022477 C>T maps to NM_001080457.1 W164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PQ-01A-11D-A28R-08 chr2:16742750 G>T maps to NM_030797.3 I162I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PQ-01A-11D-A28R-08 chr10:909779 G>A maps to NM_015155.1 A111A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PQ-01A-11D-A28R-08 chr12:123703046 C>A did not map to a codon.
Sequencing variant TCGA-N8-A4PQ-01A-11D-A28R-08 chr14:95921743 G>A maps to NM_152592.3 D369D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PQ-01A-11D-A28R-08 chr16:227403 C>A maps to NM_000558.3 Y141*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PQ-01A-11D-A28R-08 chr17:46847314 G>A maps to NM_001130918.1 Q729*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PQ-01A-11D-A28R-08 chr2:29158460 G>A maps to NM_015131.1 P504P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PQ-01A-11D-A28R-08 chr1:159505383 C>T maps to NM_001004469.1 K138K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PQ-01A-11D-A28R-08 chr5:161318009 C>G maps to NM_001127648.1 V270V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PQ-01A-11D-A28R-08 chr10:46964008 G>C maps to NM_031912.3 V318V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PQ-01A-11D-A28R-08 chr17:38711152 G>A maps to NM_001838.3 Y326Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PQ-01A-11D-A28R-08 chr9:8331733 G>A maps to NM_002839.3 D1794D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PQ-01A-11D-A28R-08 chr10:133758847 C>A maps to ENST00000455566 I204I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PQ-01A-11D-A28R-08 chr3:44611528 A>T maps to NM_018651.2 A309A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PQ-01A-11D-A28R-08 chr7:90895679 C>G maps to NM_003505.1 L495L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PQ-01A-11D-A28R-08 chr5:9630015 C>T maps to NM_019599.2 P43P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PQ-01A-11D-A28R-08 chr20:50139906 C>T maps to NM_012340.3 P291P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A4PQ-01A-11D-A28R-08 chr10:129905828 T>C maps to NM_002417.4 G1425G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A56S-01A-11D-A28R-08 chr17:79653377 C>T maps to NM_004712.4 V53V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A56S-01A-11D-A28R-08 chr12:110234488 C>T maps to NM_021625.4 R391R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A56S-01A-11D-A28R-08 chrX:49845342 G>A maps to NM_001127898.1 A232A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A56S-01A-11D-A28R-08 chr20:60885520 C>A maps to NM_005560.3 L3518L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A56S-01A-11D-A28R-08 chr14:52521020 G>T maps to NM_007361.3 I262I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A56S-01A-11D-A28R-08 chr7:27237843 G>A maps to NM_000522.4 V380V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A56S-01A-11D-A28R-08 chr12:6101113 G>A maps to NM_000552.3 N2223N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A56S-01A-11D-A28R-08 chr17:7579388 G>A maps to NM_001126112.1 Q100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A56S-01A-11D-A28R-08 chr3:47050734 G>A maps to NM_015175.1 K2730K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A56S-01A-11D-A28R-08 chr6:84234377 C>T maps to NM_153362.2 N406N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A56S-01A-11D-A28R-08 chr17:65916137 C>T maps to ENST00000321892 S1938S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A56S-01A-11D-A28R-08 chr5:43675665 A>C maps to NM_182977.2 S896S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A56S-01A-11D-A28R-08 chr12:6031878 G>A maps to ENST00000356134 L34L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A56S-01A-11D-A28R-08 chrX:17710477 C>T maps to NM_198270.2 R248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N8-A56S-01A-11D-A28R-08 chr19:16872831 C>T maps to ENST00000438489 S672S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4PZ-01A-22D-A28R-08 chr17:80788320 C>T maps to NM_024702.2 A623A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4PZ-01A-22D-A28R-08 chr17:71344824 C>G maps to NM_001144952.1 S2026S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4PZ-01A-22D-A28R-08 chr5:35084593 A>C maps to NM_000949.4 L117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4PZ-01A-22D-A28R-08 chr12:101561909 G>A maps to NM_145913.3 F428F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4PZ-01A-22D-A28R-08 chr19:40411751 G>A maps to NM_003890.2 A1292A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4PZ-01A-22D-A28R-08 chr16:31927690 G>T maps to NM_003414.4 R707R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4PZ-01A-22D-A28R-08 chrX:47074219 G>A maps to NM_153280.2 S1023S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4PZ-01A-22D-A28R-08 chr5:94891002 G>C maps to NM_198150.2 S7S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4PZ-01A-22D-A28R-08 chr1:202915579 C>T maps to NM_015999.3 W139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4PZ-01A-22D-A28R-08 chr16:3543945 G>A maps to NM_001080524.1 Q148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4PZ-01A-22D-A28R-08 chr6:158923247 G>C maps to NM_020245.3 P851P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4PZ-01A-22D-A28R-08 chr22:22842865 A>G maps to NM_080764.2 S286S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4PZ-01A-22D-A28R-08 chr1:197411422 G>T did not map to a codon.
Sequencing variant TCGA-N9-A4PZ-01A-22D-A28R-08 chr2:239103470 G>A maps to NM_030768.2 L32L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4PZ-01A-22D-A28R-08 chr19:7516087 C>T maps to NM_001130955.1 L409L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4PZ-01A-22D-A28R-08 chr5:140764736 C>G maps to NM_018920.2 V757V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4PZ-01A-22D-A28R-08 chr7:141736742 C>T maps to ENST00000475668 R733*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4PZ-01A-22D-A28R-08 chr19:8609288 G>A maps to NM_012335.3 G472G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4PZ-01A-22D-A28R-08 chrX:21674487 G>A maps to NM_153270.1 R473R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4PZ-01A-22D-A28R-08 chr3:195974348 C>T maps to NM_005017.2 T125T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4PZ-01A-22D-A28R-08 chrX:70360622 A>G maps to ENST00000333646 Q2064Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4PZ-01A-22D-A28R-08 chr4:77290770 A>G maps to NM_001042784.1 D385D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4PZ-01A-22D-A28R-08 chr19:49671541 G>T maps to NM_017636.3 L158L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4PZ-01A-22D-A28R-08 chr8:38178628 G>T maps to NM_023034.1 S590S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4PZ-01A-22D-A28R-08 chr4:81123236 C>T maps to NM_001099403.1 G207G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4PZ-01A-22D-A28R-08 chr2:242062239 G>A maps to ENST00000358649 G993G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4PZ-01A-22D-A28R-08 chr19:22375866 T>C maps to NM_001001411.2 G27G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4PZ-01A-22D-A28R-08 chr11:126305175 G>A maps to NM_032531.3 A525A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4PZ-01A-22D-A28R-08 chr3:77595593 G>A maps to ENST00000332191 W347*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q1-01A-11D-A28R-08 chrX:83724415 G>T maps to NM_144657.4 V105V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q1-01A-11D-A28R-08 chr3:195511838 A>T maps to NM_018406.5 G2204G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q1-01A-11D-A28R-08 chr19:39330768 G>A maps to ENST00000221419 F400F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q1-01A-11D-A28R-08 chr3:98002238 A>C maps to NM_001005482.1 R170R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q1-01A-11D-A28R-08 chr12:39735321 C>A maps to ENST00000395670 E636*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q3-01A-11D-A28R-08 chr17:39521742 G>A maps to ENST00000394004 P218P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q3-01A-11D-A28R-08 chr12:369128 C>A maps to NM_016615.3 L30L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q3-01A-11D-A28R-08 chr5:36118006 C>A maps to NM_001007527.1 E378*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q3-01A-11D-A28R-08 chr1:92178080 C>A maps to NM_003243.4 E629*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q3-01A-11D-A28R-08 chr13:73357693 T>C maps to NM_006346.2 V29V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q3-01A-11D-A28R-08 chrX:8553428 G>A maps to NM_000216.2 D245D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q3-01A-11D-A28R-08 chr6:29856317 C>G did not map to a codon.
Sequencing variant TCGA-N9-A4Q3-01A-11D-A28R-08 chr3:142168366 C>T maps to NM_001184.3 P2613P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q3-01A-11D-A28R-08 chr19:8555520 G>A maps to NM_032152.4 F621F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q3-01A-11D-A28R-08 chr3:189582067 C>T maps to NM_003722.4 C209C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q3-01A-11D-A28R-08 chr17:7579590 C>G did not map to a codon.
Sequencing variant TCGA-N9-A4Q3-01A-11D-A28R-08 chr3:100364804 C>T maps to NM_032787.2 C321C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q4-01A-11D-A28R-08 chrX:48458031 G>A maps to NM_017883.4 G150G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q4-01A-11D-A28R-08 chr2:228882545 G>A maps to NM_001142644.1 D1008D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q4-01A-11D-A28R-08 chr19:55363702 G>A maps to NM_006737.2 S107S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q4-01A-11D-A28R-08 chr17:42171101 G>A maps to NM_001015053.1 G66G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q4-01A-11D-A28R-08 chr8:144885554 C>A maps to NM_182706.3 E1201*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q4-01A-11D-A28R-08 chr1:31347423 T>C maps to NM_014654.3 P294P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q4-01A-11D-A28R-08 chrX:78010755 C>A maps to NM_005296.2 T130T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q4-01A-11D-A28R-08 chr22:30682352 C>T maps to NM_001037666.2 E214E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q4-01A-11D-A28R-08 chr2:135745372 G>A maps to NM_025052.3 R357*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q4-01A-11D-A28R-08 chr19:52569973 A>T maps to NM_001136499.1 S387S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q4-01A-11D-A28R-08 chr15:72492886 G>A maps to ENST00000419739 L547L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q4-01A-11D-A28R-08 chr15:86225392 A>G maps to NM_006738.4 S1706S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q4-01A-11D-A28R-08 chrX:152226401 G>T maps to NM_013364.4 L330L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q4-01A-11D-A28R-08 chr19:1802612 C>A maps to NM_138813.2 R312R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q4-01A-11D-A28R-08 chr1:248308943 C>A maps to NM_001004690.1 S165S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q4-01A-11D-A28R-08 chrX:12735884 G>A maps to ENST00000429478 P970P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q4-01A-11D-A28R-08 chr19:42509902 G>T maps to NM_002088.3 T745T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q4-01A-11D-A28R-08 chr1:158670013 C>A maps to NM_001005279.1 L143L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q4-01A-11D-A28R-08 chr11:56043797 C>A maps to NM_001004745.1 I228I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q4-01A-11D-A28R-08 chr7:143175363 C>G maps to NM_176883.2 L133L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr3:194080439 A>G maps to NM_001135057.2 L451L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr1:55349323 C>G maps to NM_014762.3 L118L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr19:46332274 G>A maps to NM_004819.2 L646L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr6:44224542 C>A maps to NM_178148.2 P28P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr2:96690525 G>A maps to NM_207328.2 Q475*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr19:3656426 C>T maps to NM_012398.2 Q199Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr1:231935885 G>A maps to NM_001164537.1 L606L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr5:180374587 C>T maps to NM_001040462.2 G250G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr12:78400499 G>T maps to NM_014903.4 R394R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr17:33904941 C>T maps to NM_000286.2 V33V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr7:112129967 C>T maps to NM_182597.2 L120L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chrX:153595789 C>T maps to NM_001110556.1 P281P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr20:32677667 G>A maps to NM_003908.3 I290I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr1:11589955 C>G maps to NM_020780.1 V1014V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr12:56566437 C>T maps to NM_003075.3 E567E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr1:1152960 G>C maps to NM_016176.3 L340L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chrX:65483501 C>T maps to NM_138737.3 L1126L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr12:111886102 C>A maps to NM_005475.2 L575L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr20:19956198 G>A maps to ENST00000255006 P559P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr2:227662587 G>C maps to NM_005544.2 L289L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chrX:21581354 G>C did not map to a codon.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr1:226125368 G>A maps to NM_003240.3 Y291Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr7:15725700 G>A maps to NM_005924.4 C109C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr6:90371186 C>T maps to NM_014611.1 K4892K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr5:176519358 C>T maps to NM_213647.1 L255L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr19:21588647 C>G maps to NM_001076678.2 V81V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chrX:54955688 A>G maps to NM_001039705.1 G844G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr6:7571653 A>T maps to NM_004415.2 I580I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr1:207222907 G>A maps to NM_018566.3 V168V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr16:70548412 C>T did not map to a codon.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr22:21081547 G>A maps to NM_058004.2 Y1579Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr18:61468143 C>T maps to NM_001040147.1 F214F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr19:1460849 C>G maps to NM_005883.2 L505L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr12:55688183 G>T maps to NM_001005493.1 S278*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr15:90167616 C>G maps to NM_152259.3 S1359*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr19:52394224 T>C maps to NM_023074.3 G388G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr1:176525514 C>G maps to NM_020318.2 L19L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr16:71898076 G>A maps to ENST00000425432 C127C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr10:103825881 C>G maps to NM_024747.4 L217L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr13:24895246 C>T maps to NM_178540.3 R115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr7:6441992 C>T maps to NM_018890.3 L184L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr15:42021387 C>T maps to ENST00000219905 V1228V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr8:125076586 G>T did not map to a codon.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr6:30955307 G>A maps to NM_001010909.2 L452L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr20:2844650 G>T maps to NM_022575.2 L511L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr7:2188794 G>A maps to NM_003550.2 V355V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr1:118629492 C>A did not map to a codon.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr4:39304133 G>A maps to ENST00000381897 Q809*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr12:85450932 C>T maps to NM_001079910.1 R788*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr4:46252591 C>T maps to ENST00000507069 Q423Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr1:111216486 G>A maps to NM_002232.3 F315F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr12:20905331 C>G maps to NM_017435.4 S670*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr2:37291993 G>C maps to NM_019024.1 L491L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr22:31042915 C>T maps to NM_001001479.2 L317L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr11:62549790 C>G maps to NM_006473.2 L271L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr1:158909027 C>T maps to NM_152501.3 S190S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr19:2233839 C>T maps to NM_018049.1 *150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr1:248737521 G>A maps to NM_001001821.1 I179I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr4:77969710 G>A maps to NM_006835.2 L265L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr4:87724874 G>C maps to NM_080685.2 L2178L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr7:130356586 G>C maps to NM_052933.2 S191*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr20:13463938 G>C maps to NM_017714.2 S307*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr4:3318235 C>T maps to NM_198229.2 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr17:2303969 G>A maps to NM_020310.2 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr2:63053310 C>A maps to NM_015252.3 V134V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr10:134563348 G>A maps to NM_005539.3 A301A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr7:92765170 G>A maps to NM_152703.2 L38L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr8:25715960 G>A maps to NM_022659.2 Q468*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr2:233393336 C>T maps to NM_000751.1 F160F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr1:158984676 C>T maps to ENST00000295809 F69F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr11:65088725 C>T maps to NM_006779.2 L119L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr17:62291463 G>A maps to NM_018469.3 F38F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr17:6499536 C>A maps to NM_014804.2 E767*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr11:121393332 C>T maps to NM_003105.5 L481L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr14:76928924 C>T maps to NM_004452.3 C145C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr17:10363564 G>C maps to NM_017533.2 V407V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr15:52416725 G>A maps to NM_016194.3 R374*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chrX:19507019 G>A maps to NM_001001671.3 R143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr12:6981729 G>T maps to NM_032641.3 L112L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr1:179320590 G>A maps to NM_003101.4 L530L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr12:121570868 C>T maps to NM_002562.5 F32F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr3:113955900 C>T maps to NM_007136.3 G7G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr2:178095659 G>C maps to NM_006164.3 L557L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr22:42607448 G>C maps to NM_005650.1 S1288*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr11:102272783 G>T maps to NM_052932.2 S104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr5:5306708 G>A maps to NM_139056.2 K1093K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr19:34960011 C>A maps to NM_005499.2 V603V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr10:108412180 C>A maps to NM_001013031.1 E812*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr19:1234624 G>C maps to ENST00000382477 S211*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr11:73850727 G>C maps to ENST00000334126 S210*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr6:27805760 C>T maps to NM_003510.2 K119K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chrX:106034390 G>A maps to NM_024539.3 E334E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr11:117090318 G>A maps to NM_004716.2 F437F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr10:103921998 C>T maps to ENST00000405356 V701V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr1:84967542 G>C maps to NM_005274.2 V64V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr16:57180016 C>T maps to NM_152727.5 I441I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr15:31323321 G>A maps to NM_002420.4 V975V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr17:7660534 C>T maps to NM_020877.2 L677L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chrX:138630628 C>T maps to NM_000133.3 Q167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr17:39846028 G>C did not map to a codon.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr2:191844514 G>T maps to NM_007315.3 L570L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr22:42968532 G>T maps to NM_014509.3 E275*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr12:116460309 G>A maps to NM_015335.4 I192I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q7-01A-11D-A28R-08 chr1:248637187 C>T maps to NM_001005495.1 I179I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q8-01A-31D-A28R-08 chr1:26150121 C>G maps to ENST00000336146 V37V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q8-01A-31D-A28R-08 chr9:38411521 C>A maps to NM_001007563.1 E238*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q8-01A-31D-A28R-08 chr11:125301239 G>A maps to NM_022062.2 T457T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q8-01A-31D-A28R-08 chr10:124608783 G>A maps to NM_152644.2 C88C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q8-01A-31D-A28R-08 chr1:145293413 A>G maps to NM_001039703.4 V3V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q8-01A-31D-A28R-08 chr19:19741120 G>C maps to NM_016573.2 S855*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q8-01A-31D-A28R-08 chr2:108868908 C>T maps to NM_001008743.1 H87H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q8-01A-31D-A28R-08 chr11:111753231 T>C maps to NM_022761.2 N62N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q8-01A-31D-A28R-08 chr7:21805152 G>A maps to NM_003777.3 Q3023Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q8-01A-31D-A28R-08 chr12:54799461 G>A maps to NM_002205.2 D334D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q8-01A-31D-A28R-08 chr12:55615302 C>T maps to NM_001005280.1 A165A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q8-01A-31D-A28R-08 chr6:136597334 G>C maps to NM_014739.2 S443*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q8-01A-31D-A28R-08 chr1:32694779 C>A maps to NM_003757.2 T258T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q8-01A-31D-A28R-08 chr3:27475587 T>A maps to ENST00000454389 V199V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q8-01A-31D-A28R-08 chr17:7573981 C>A maps to NM_001126112.1 E349*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q8-01A-31D-A28R-08 chr8:95518909 A>T maps to NM_015496.3 G1305G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q8-01A-31D-A28R-08 chr4:145580926 T>C maps to NM_022475.1 P256P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q8-01A-31D-A28R-08 chr7:113518496 G>A maps to NM_002711.3 Q884*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4QV-01A-11D-A28R-08 chr1:196714953 A>G maps to NM_000186.3 T1106T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4QV-01A-11D-A28R-08 chr12:120876299 C>T maps to NM_004373.2 Y74Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4QV-01A-11D-A28R-08 chr19:42880632 A>G maps to ENST00000251268 G2748G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4QV-01A-11D-A28R-08 chr19:35804290 G>T maps to NM_002361.3 R605R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4QV-01A-11D-A28R-08 chr2:116593797 C>T maps to NM_020868.3 S672S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4QV-01A-11D-A28R-08 chr10:123810032 G>T maps to NM_206862.2 T38T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4QV-01A-11D-A28R-08 chr1:6692464 G>A maps to NM_001195753.1 A116A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4QV-01A-11D-A28R-08 chr16:46993253 G>A maps to NM_005880.3 F284F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4QV-01A-11D-A28R-08 chr10:105657467 G>A maps to NM_024928.4 G197G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4QV-01A-11D-A28R-08 chr21:27141431 C>T maps to NM_002040.3 V418V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4QV-01A-11D-A28R-08 chr17:32963036 G>A maps to NM_207313.1 P573P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4QV-01A-11D-A28R-08 chr14:69256295 G>C maps to NM_004926.2 S324*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4QV-01A-11D-A28R-08 chr11:60694715 G>A maps to NM_017870.3 P47P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4QV-01A-11D-A28R-08 chr2:50723041 C>A did not map to a codon.
Sequencing variant TCGA-NA-A4QV-01A-11D-A28R-08 chr12:78362440 G>A maps to NM_014903.4 S210S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4QV-01A-11D-A28R-08 chr19:38633332 C>G maps to NM_015073.1 Y1172*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4QW-01A-11D-A28R-08 chr4:189022257 C>T maps to ENST00000326754 A94A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4QW-01A-11D-A28R-08 chr6:150067547 G>A maps to NM_198887.1 T28T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4QW-01A-11D-A28R-08 chr1:148594543 T>C maps to NM_001170755.1 H639H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4QW-01A-11D-A28R-08 chr19:14938183 A>G maps to NM_017506.1 Y290Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4QW-01A-11D-A28R-08 chr17:57057476 C>T maps to NM_014906.3 S451S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4QW-01A-11D-A28R-08 chr17:79994777 G>A maps to NM_016286.3 L88L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4QW-01A-11D-A28R-08 chr7:23391159 C>T maps to NM_006547.2 L149L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4QW-01A-11D-A28R-08 chr16:1995898 G>A maps to NM_005061.2 N328N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4QW-01A-11D-A28R-08 chr14:20483157 C>T maps to NM_001004712.1 G65G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4QW-01A-11D-A28R-08 chr1:114483988 C>A maps to ENST00000426820 R399R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4QW-01A-11D-A28R-08 chr7:56140698 C>G maps to ENST00000395437 V100V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4QW-01A-11D-A28R-08 chr10:91198854 G>A maps to NM_213606.3 I178I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4QW-01A-11D-A28R-08 chr8:144940731 C>T maps to NM_031308.1 L2230L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4QW-01A-11D-A28R-08 chr1:89730614 G>A maps to NM_052942.3 A301A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4QW-01A-11D-A28R-08 chr6:26200067 G>A maps to NM_003522.3 E94E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4QW-01A-11D-A28R-08 chr1:226827356 T>C maps to NM_002221.3 K818K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4QW-01A-11D-A28R-08 chr15:75653472 G>C maps to NM_006715.2 L458L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4QW-01A-11D-A28R-08 chr5:26881649 G>A maps to NM_016279.3 N655N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4QX-01A-11D-A28R-08 chr1:24186287 C>T maps to NM_000147.4 K256K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4QX-01A-11D-A28R-08 chr16:3707024 C>T maps to NM_005223.3 P154P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4QX-01A-11D-A28R-08 chr5:140573706 G>T maps to NM_018930.3 E528*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4QX-01A-11D-A28R-08 chr17:18023598 G>A maps to ENST00000205890 V495V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4QX-01A-11D-A28R-08 chrX:64719784 T>C maps to NM_001010888.3 L336L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4QX-01A-11D-A28R-08 chrX:153051889 G>A maps to NM_004135.2 T313T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4QX-01A-11D-A28R-08 chr3:12531436 C>T maps to NM_025265.3 N46N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4QX-01A-11D-A28R-08 chr21:34053868 G>A maps to NM_003895.3 S469S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4QX-01A-11D-A28R-08 chrX:153716853 C>T maps to ENST00000440701 L197L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4QX-01A-11D-A28R-08 chr19:38230643 C>T maps to NM_001172690.1 Q249Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4QX-01A-11D-A28R-08 chrX:18338511 C>A maps to NM_006089.2 P142P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4QX-01A-11D-A28R-08 chr16:68200784 T>C maps to NM_173165.2 D547D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4QX-01A-11D-A28R-08 chr15:43891377 C>T maps to ENST00000413657 I418I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4QY-01A-11D-A28R-08 chr19:39869207 C>T maps to NM_018028.2 I503I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4QY-01A-11D-A28R-08 chr3:47889848 A>G maps to NM_138615.2 Q822Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4QY-01A-11D-A28R-08 chr17:43907498 C>A maps to NM_001145146.1 L187L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4QY-01A-11D-A28R-08 chr1:24417410 G>A maps to ENST00000330966 G437G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4QY-01A-11D-A28R-08 chr10:101715316 C>G maps to ENST00000342239 V638V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4QY-01A-11D-A28R-08 chr10:128785805 G>A maps to ENST00000398025 P83P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4QY-01A-11D-A28R-08 chr5:38451443 C>T maps to ENST00000354891 F865F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4QY-01A-11D-A28R-08 chr6:71501408 T>A maps to NM_001044305.1 A144A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4QY-01A-11D-A28R-08 chr11:22396404 G>A maps to NM_020346.2 T382T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4R0-01A-11D-A28R-08 chr10:101491746 G>A maps to NM_078470.4 L20L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4R0-01A-11D-A28R-08 chr1:150478147 C>A maps to NM_025150.3 R659R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4R0-01A-11D-A28R-08 chr12:57882856 C>T maps to NM_004990.2 S55S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4R0-01A-11D-A28R-08 chr2:121732501 C>A maps to NM_005270.4 G395G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4R0-01A-11D-A28R-08 chr16:23654274 G>C did not map to a codon.
Sequencing variant TCGA-NA-A4R0-01A-11D-A28R-08 chr1:157665944 C>A maps to NM_052939.3 L339L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4R0-01A-11D-A28R-08 chr7:148718138 T>C maps to NM_004911.4 G63G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4R0-01A-11D-A28R-08 chr12:120652777 C>T maps to NM_001080855.1 T376T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4R0-01A-11D-A28R-08 chr3:13896247 G>A maps to NM_004625.3 H117H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4R0-01A-11D-A28R-08 chr15:24921415 G>A maps to NM_018958.2 A134A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4R0-01A-11D-A28R-08 chrX:10066583 C>A maps to NM_015691.3 V232V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4R0-01A-11D-A28R-08 chr3:38798314 T>G maps to NM_006514.2 V380V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4R0-01A-11D-A28R-08 chrX:53575114 G>A maps to ENST00000276009 C3387C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4R0-01A-11D-A28R-08 chr20:47605194 G>A maps to NM_006420.2 K843K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4R0-01A-11D-A28R-08 chr5:82940356 G>A maps to NM_001884.3 G200G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4R0-01A-11D-A28R-08 chr16:89351377 C>A maps to NM_013275.4 S524S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4R0-01A-11D-A28R-08 chr15:23931764 C>G maps to NM_002487.2 V200V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4R0-01A-11D-A28R-08 chr19:37210153 T>C maps to ENST00000423498 T175T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4R0-01A-11D-A28R-08 chr15:56209011 T>A maps to ENST00000508342 R6R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4R0-01A-11D-A28R-08 chr1:24120730 C>G maps to NM_007260.2 L129L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4R0-01A-11D-A28R-08 chr7:77378906 A>G maps to NM_198467.2 Q290Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4R1-01A-11D-A28R-08 chr1:9661176 C>T maps to NM_001130924.2 A207A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4R1-01A-11D-A28R-08 chr10:89717671 C>T maps to NM_000314.4 R233*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4R1-01A-11D-A28R-08 chr1:190067974 G>A maps to NM_199051.1 L492L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4R1-01A-11D-A28R-08 chr16:17292082 G>A maps to NM_022166.3 A425A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4R1-01A-11D-A28R-08 chr7:107417135 C>T maps to NM_000111.2 T510T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4R1-01A-11D-A28R-08 chr1:97217024 G>A maps to ENST00000370197 P28P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4R1-01A-11D-A28R-08 chr19:31040263 G>A maps to NM_014717.1 A1246A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4R1-01A-11D-A28R-08 chr2:143718290 T>C maps to NM_003937.2 T227T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4R1-01A-11D-A28R-08 chr2:38301892 G>A maps to NM_000104.3 R213R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4R1-01A-11D-A28R-08 chr1:176709278 G>A maps to NM_020318.2 S1366S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4R1-01A-11D-A28R-08 chr1:119985582 G>T did not map to a codon.
Sequencing variant TCGA-NA-A4R1-01A-11D-A28R-08 chr3:69093747 T>C did not map to a codon.
Sequencing variant TCGA-NA-A4R1-01A-11D-A28R-08 chr5:140209478 A>G maps to NM_018909.2 S601S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4R1-01A-11D-A28R-08 chr10:60154713 C>T maps to NM_003201.1 D207D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4R1-01A-11D-A28R-08 chr6:158923253 T>C maps to NM_020245.3 P853P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4R1-01A-11D-A28R-08 chr18:52265363 C>T maps to NM_173629.1 T207T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4R1-01A-11D-A28R-08 chr20:61981955 G>A maps to NM_000744.5 S269S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4R1-01A-11D-A28R-08 chr18:672901 C>T maps to NM_001071.2 R283*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4R1-01A-11D-A28R-08 chr12:133225984 G>A maps to ENST00000455752 P1307P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4R1-01A-11D-A28R-08 chr9:139972956 C>T maps to NM_207309.2 Y166Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4R1-01A-11D-A28R-08 chr17:36707583 G>T maps to NM_025248.2 T923T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4R1-01A-11D-A28R-08 chr5:138456751 C>T maps to ENST00000509534 P79P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4R1-01A-11D-A28R-08 chrX:153296732 T>C maps to NM_001110792.1 P194P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4R1-01A-11D-A28R-08 chr14:55429737 G>A maps to NM_007086.3 A821A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4R1-01A-11D-A28R-08 chr18:28651724 G>A maps to ENST00000438199 G670G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4R1-01A-11D-A28R-08 chr9:5787227 A>G maps to NM_024896.2 P877P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4R1-01A-11D-A28R-08 chr1:1391259 C>T maps to NM_001039211.2 Y176Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4R1-01A-11D-A28R-08 chr13:73346314 G>A maps to NM_014953.3 L495L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4R1-01A-11D-A28R-08 chr15:33261468 G>T maps to NM_001103184.2 T588T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4R1-01A-11D-A28R-08 chr1:24484263 G>A maps to NM_170743.2 R307*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4R1-01A-11D-A28R-08 chr8:21986671 C>T maps to NM_005144.4 T4T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4R1-01A-11D-A28R-08 chr15:86259070 C>T maps to NM_006738.4 T1888T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4R1-01A-11D-A28R-08 chr2:242078092 C>T maps to ENST00000358649 S239S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4R1-01A-11D-A28R-08 chr2:95537620 C>T maps to NM_144705.2 H99H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4R1-01A-11D-A28R-08 chr2:182543458 G>A maps to NM_002500.2 L43L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4R1-01A-11D-A28R-08 chr16:1270129 C>T maps to NM_021098.2 S2066S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4R1-01A-11D-A28R-08 chr7:44530145 C>T maps to NM_015332.3 Q18Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4R1-01A-11D-A28R-08 chr12:111064169 C>T maps to NM_001082538.2 G115G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4R1-01A-11D-A28R-08 chr7:135304340 T>C maps to NM_015135.2 P1378P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4R1-01A-11D-A28R-08 chr3:65342631 T>C maps to NM_001033057.1 R1270R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4R1-01A-11D-A28R-08 chrX:46913858 G>A maps to NM_001077445.1 T424T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4R1-01A-11D-A28R-08 chr18:56274660 C>T maps to NM_052947.3 K40K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4R1-01A-11D-A28R-08 chr13:48953759 C>T maps to NM_000321.2 R455*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4R1-01A-11D-A28R-08 chr4:7725500 C>T maps to NM_020777.2 T834T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4R1-01A-11D-A28R-08 chr4:119621740 C>T maps to NM_020961.2 R228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4R1-01A-11D-A28R-08 chr15:86122534 G>A maps to NM_006738.4 T412T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4R1-01A-11D-A28R-08 chr9:19786015 G>A maps to NM_020344.2 N283N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4R1-01A-11D-A28R-08 chr6:46623608 C>T maps to NM_004277.3 R46*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4R1-01A-11D-A28R-08 chr14:104124026 C>T maps to ENST00000445352 Q308*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4R1-01A-11D-A28R-08 chrX:151935380 G>A maps to NM_005362.3 P262P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4R1-01A-11D-A28R-08 chr1:22928122 C>T maps to NM_020526.3 D969D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4R1-01A-11D-A28R-08 chr20:43043172 C>T maps to ENST00000338692 N203N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4R1-01A-11D-A28R-08 chr19:53116461 A>G maps to NM_018300.3 T452T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4R1-01A-11D-A28R-08 chr1:17570623 C>T maps to NM_013358.2 H626H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4R1-01A-11D-A28R-08 chr12:122672354 C>A maps to NM_001098519.1 P210P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4R1-01A-11D-A28R-08 chr4:187509883 G>A maps to ENST00000260147 T4546T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4R1-01A-11D-A28R-08 chr3:188590443 C>T maps to NM_005578.3 R535*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A4R1-01A-11D-A28R-08 chr7:120590816 T>C did not map to a codon.
Sequencing variant TCGA-NA-A5I1-01A-21D-A28R-08 chr6:38942306 T>C did not map to a codon.
Sequencing variant TCGA-NA-A5I1-01A-21D-A28R-08 chr1:152278697 T>G maps to NM_002016.1 G2888G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A5I1-01A-21D-A28R-08 chr18:32428343 G>C maps to NM_001390.4 S450S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A5I1-01A-21D-A28R-08 chr19:33077793 A>T maps to NM_004708.3 K97*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A5I1-01A-21D-A28R-08 chr4:110866381 A>C maps to NM_001963.4 V297V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A5I1-01A-21D-A28R-08 chrX:131573525 G>T maps to NM_018388.3 A38A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A5I1-01A-21D-A28R-08 chr1:152325749 G>A maps to NM_001014342.2 S1504S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A5I1-01A-21D-A28R-08 chr2:158594951 C>T maps to NM_001111067.2 P465P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A5I1-01A-21D-A28R-08 chr22:21377576 G>T maps to NM_005446.3 E218*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A5I1-01A-21D-A28R-08 chr19:55789013 G>A maps to NM_012267.4 A137A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A5I1-01A-21D-A28R-08 chr16:23366759 C>G maps to ENST00000307331 G287G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A5I1-01A-21D-A28R-08 chr9:368134 G>A maps to NM_203447.3 P599P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A5I1-01A-21D-A28R-08 chr12:70963617 C>A maps to NM_001109754.1 T1157T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A5I1-01A-21D-A28R-08 chr11:62291940 G>C maps to NM_001620.1 P3316P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A5I1-01A-21D-A28R-08 chr1:152284532 T>G maps to NM_002016.1 G943G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A5I1-01A-21D-A28R-08 chr3:45877082 G>A maps to NM_020347.2 R108*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NA-A5I1-01A-21D-A28R-08 chr4:110384636 G>A maps to NM_006323.2 S238S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4W6-01A-11D-A28R-08 chr1:205126442 G>A maps to NM_015375.2 S770S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4W6-01A-11D-A28R-08 chrX:71684475 T>C maps to NM_018486.2 P281P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4W6-01A-11D-A28R-08 chr14:24040295 C>T maps to NM_032452.2 E548E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4W6-01A-11D-A28R-08 chr19:44352094 C>T maps to NM_181845.1 Q448*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4W6-01A-11D-A28R-08 chr11:68170952 G>A maps to NM_002335.2 V529V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4W6-01A-11D-A28R-08 chr5:161113260 G>T maps to NM_000811.2 E22*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4W6-01A-11D-A28R-08 chr18:61654203 C>T maps to NM_198833.1 L273L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4W6-01A-11D-A28R-08 chr8:145749617 C>G maps to NM_001024678.3 L161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4W6-01A-11D-A28R-08 chr1:27106464 C>T maps to NM_006015.4 Q2026*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4W6-01A-11D-A28R-08 chr17:73096693 C>G maps to ENST00000450736 L352L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4W6-01A-11D-A28R-08 chr8:56435861 C>T maps to NM_052898.1 L343L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4W6-01A-11D-A28R-08 chr13:31233270 T>C maps to NM_005800.4 H1019H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4W6-01A-11D-A28R-08 chr17:73096219 C>T maps to ENST00000450736 L194L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4W6-01A-11D-A28R-08 chr6:170181479 C>T maps to NM_018341.1 Y636Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4W6-01A-11D-A28R-08 chr1:228481946 G>A maps to NM_001098623.1 P3742P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4W6-01A-11D-A28R-08 chr16:5122950 G>T did not map to a codon.
Sequencing variant TCGA-ND-A4W6-01A-11D-A28R-08 chr17:73096838 C>T maps to ENST00000450736 Q401*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4W6-01A-11D-A28R-08 chr21:10921995 C>T did not map to a codon.
Sequencing variant TCGA-ND-A4W6-01A-11D-A28R-08 chr7:82584376 C>T maps to NM_033026.5 T1964T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4W6-01A-11D-A28R-08 chr5:140516677 C>T maps to NM_015669.2 N554N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4W6-01A-11D-A28R-08 chr17:73096513 C>T maps to ENST00000450736 F292F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4W6-01A-11D-A28R-08 chr10:67862962 G>A maps to NM_013266.2 H643H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4W6-01A-11D-A28R-08 chr1:206821769 C>T maps to NM_003582.2 F409F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4W6-01A-11D-A28R-08 chr2:196573522 C>T maps to NM_001127257.1 I510I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4W6-01A-11D-A28R-08 chr3:44612303 C>T maps to NM_018651.2 R568*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4W6-01A-11D-A28R-08 chr7:28547288 C>T maps to NM_182898.2 F75F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4W6-01A-11D-A28R-08 chr22:24561545 C>T maps to NM_012295.3 F1653F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4W6-01A-11D-A28R-08 chr2:21229149 C>A maps to NM_000384.2 V3530V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4W6-01A-11D-A28R-08 chr15:42374008 G>C maps to NM_178034.3 L269L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4W6-01A-11D-A28R-08 chr16:71823358 C>A maps to ENST00000423132 R31R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4W6-01A-11D-A28R-08 chr11:55579556 G>A maps to NM_001004738.1 L205L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4W6-01A-11D-A28R-08 chr3:179095161 C>T maps to NM_033540.2 R419*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WA-01A-12D-A28R-08 chrX:34962327 G>A maps to NM_152631.2 S460S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WA-01A-12D-A28R-08 chrX:91090728 C>T maps to NM_032968.3 R76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WA-01A-12D-A28R-08 chrX:47101056 G>T maps to NM_004651.3 E423*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WA-01A-12D-A28R-08 chr19:6678425 G>A maps to NM_000064.2 D1557D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WA-01A-12D-A28R-08 chr7:84628908 G>A maps to NM_152754.2 L727L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WA-01A-12D-A28R-08 chr3:20082164 G>T maps to NM_003884.4 G66*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WA-01A-12D-A28R-08 chrX:83359666 T>A did not map to a codon.
Sequencing variant TCGA-ND-A4WA-01A-12D-A28R-08 chr19:55284833 A>G maps to ENST00000291633 K40K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WA-01A-12D-A28R-08 chr1:52258047 C>A did not map to a codon.
Sequencing variant TCGA-ND-A4WA-01A-12D-A28R-08 chr1:55527144 G>A maps to NM_174936.3 E593E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WA-01A-12D-A28R-08 chr18:13741540 A>G maps to NM_003799.1 Q275Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WA-01A-12D-A28R-08 chr19:15512056 G>A maps to NM_014371.2 G240G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WA-01A-12D-A28R-08 chr19:52496398 G>A maps to ENST00000354939 R655*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WA-01A-12D-A28R-08 chr6:26271423 G>A maps to NM_003534.2 I63I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WA-01A-12D-A28R-08 chr11:4703776 G>A maps to NM_030774.3 H55H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WA-01A-12D-A28R-08 chr1:47495699 T>C maps to NM_178033.1 I72I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WF-01A-11D-A28R-08 chr3:62188854 G>A maps to NM_002841.3 A462A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WF-01A-11D-A28R-08 chr3:139078197 A>G maps to NM_004766.2 D739D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WF-01A-11D-A28R-08 chr6:15497072 G>T maps to NM_004973.2 S539S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WF-01A-11D-A28R-08 chr11:57076215 G>C maps to NM_033396.2 T1323T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WF-01A-11D-A28R-08 chr10:28023622 C>T maps to NM_173576.2 A200A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WF-01A-11D-A28R-08 chr9:18622330 C>T maps to NM_001040272.4 R189*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WF-01A-11D-A28R-08 chr20:58533810 G>C maps to NM_177980.2 S10S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WF-01A-11D-A28R-08 chr5:110438052 A>G maps to NM_139281.2 L240L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WF-01A-11D-A28R-08 chr17:34310905 G>A maps to NM_032962.4 G87G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WF-01A-11D-A28R-08 chr5:108203562 C>T maps to NM_005246.2 Q193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WF-01A-11D-A28R-08 chr18:55102968 C>G maps to NM_004852.2 A7A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WF-01A-11D-A28R-08 chr21:17250146 A>G maps to ENST00000285681 E976E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WF-01A-11D-A28R-08 chr2:170494026 C>T maps to NM_004792.2 S753S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WF-01A-11D-A28R-08 chr1:236746149 T>C maps to NM_018072.5 E816E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WF-01A-11D-A28R-08 chr3:49847419 G>A maps to NM_003335.2 H610H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WF-01A-11D-A28R-08 chr5:177031296 C>T maps to NM_007255.2 D56D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WF-01A-11D-A28R-08 chr3:121435638 G>A maps to ENST00000393667 L411L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WF-01A-11D-A28R-08 chr4:39229837 C>T maps to NM_025132.3 D546D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WF-01A-11D-A28R-08 chr14:39556160 G>A maps to NM_006364.2 Q219*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WF-01A-11D-A28R-08 chrX:95940098 C>A maps to NM_006729.4 G14G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NF-A4WU-01A-11D-A28R-08 chr6:26104423 A>T maps to NM_003542.3 T83T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NF-A4WU-01A-11D-A28R-08 chr6:27834839 C>A maps to NM_005322.2 P156P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NF-A4WU-01A-11D-A28R-08 chr9:129453153 C>T maps to NM_001174147.1 I122I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NF-A4WU-01A-11D-A28R-08 chr8:124037228 G>T maps to NM_024295.4 I109I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NF-A4WU-01A-11D-A28R-08 chr19:37643368 G>T maps to ENST00000356958 R478R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NF-A4WU-01A-11D-A28R-08 chr5:1420692 G>A maps to NM_001044.4 C306C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NF-A4WU-01A-11D-A28R-08 chr14:51101950 G>A maps to NM_021818.2 R368*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NF-A4WU-01A-11D-A28R-08 chr9:100403881 T>A maps to NM_002486.4 A54A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NF-A4WU-01A-11D-A28R-08 chr6:29856426 G>T did not map to a codon.
Sequencing variant TCGA-NF-A4WU-01A-11D-A28R-08 chr10:23292318 C>T maps to NM_173081.3 N569N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NF-A4WU-01A-11D-A28R-08 chr7:21757422 G>A maps to NM_003777.3 R2345R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NF-A4WU-01A-11D-A28R-08 chr3:195511814 G>A maps to NM_018406.5 T2212T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NF-A4WU-01A-11D-A28R-08 chr3:195511910 G>A maps to NM_018406.5 T2180T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NF-A4WU-01A-11D-A28R-08 chr16:81197273 G>A maps to NM_052892.3 V1136V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NF-A4WU-01A-11D-A28R-08 chr1:18809451 C>T maps to NM_152375.2 A659A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NF-A4WU-01A-11D-A28R-08 chrX:103499130 G>A maps to NM_153448.3 D70D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NF-A4WU-01A-11D-A28R-08 chr17:30293183 G>A maps to NM_015355.2 Q158Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NF-A4WX-01A-11D-A28R-08 chr19:4859937 G>A maps to NM_005817.4 H55H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NF-A4WX-01A-11D-A28R-08 chr11:122805247 C>T maps to NM_024806.2 R367*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NF-A4WX-01A-11D-A28R-08 chr2:160807931 T>C maps to NM_007366.4 T1153T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NF-A4WX-01A-11D-A28R-08 chr14:89628876 C>A maps to NM_001085471.1 E452*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NF-A4WX-01A-11D-A28R-08 chr22:50955911 G>A did not map to a codon.
Sequencing variant TCGA-NF-A4WX-01A-11D-A28R-08 chrX:133700505 G>A maps to NM_021796.3 H69H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NF-A4WX-01A-11D-A28R-08 chr11:55563681 C>T maps to NM_001004735.1 L217L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NF-A4WX-01A-11D-A28R-08 chr6:26091202 C>T maps to NM_000410.3 R71*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NF-A4WX-01A-11D-A28R-08 chr8:18258040 T>A maps to NM_000015.2 L176L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NF-A4WX-01A-11D-A28R-08 chr17:45911900 T>C did not map to a codon.
Sequencing variant TCGA-NF-A4WX-01A-11D-A28R-08 chr5:10403622 C>T maps to NM_005885.2 Y434Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NF-A4WX-01A-11D-A28R-08 chr10:28822964 T>A did not map to a codon.
Sequencing variant TCGA-NF-A4WX-01A-11D-A28R-08 chr17:74046598 G>A maps to NM_014230.2 S329S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NF-A4WX-01A-11D-A28R-08 chr17:80545020 G>T maps to NM_004514.3 P553P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NF-A4X2-01A-11D-A28R-08 chr10:29843733 G>A maps to NM_021738.2 S46S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NF-A4X2-01A-11D-A28R-08 chr13:36242542 C>T maps to ENST00000400445 T2879T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NF-A4X2-01A-11D-A28R-08 chr11:74985230 C>A maps to NM_004041.3 T267T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NF-A4X2-01A-11D-A28R-08 chr6:41165845 C>T did not map to a codon.
Sequencing variant TCGA-NF-A4X2-01A-11D-A28R-08 chr1:212964985 G>T maps to NM_015471.3 C40*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NF-A4X2-01A-11D-A28R-08 chr17:6676463 A>G maps to NM_017523.2 G294G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NF-A4X2-01A-11D-A28R-08 chr17:13504290 G>A maps to NM_006042.1 P52P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NF-A4X2-01A-11D-A28R-08 chr15:24922693 C>T maps to NM_018958.2 N560N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NF-A4X2-01A-11D-A28R-08 chr19:57956697 G>T maps to NM_001023561.2 E728*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NF-A4X2-01A-11D-A28R-08 chr10:119003728 C>T maps to NM_003054.4 D123D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NF-A4X2-01A-11D-A28R-08 chr10:103901270 G>A maps to NM_015062.3 L1002L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NF-A4X2-01A-11D-A28R-08 chr19:49174006 G>A maps to NM_145807.1 S79S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NF-A4X2-01A-11D-A28R-08 chr9:119582945 C>T maps to ENST00000313400 T719T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NF-A4X2-01A-11D-A28R-08 chr2:197707533 A>C maps to NM_024989.3 L847L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NF-A4X2-01A-11D-A28R-08 chr11:18158856 C>T maps to NM_054031.3 I36I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NF-A4X2-01A-11D-A28R-08 chr10:71874718 G>A maps to NM_032797.5 I309I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NF-A4X2-01A-11D-A28R-08 chr3:132202304 C>G maps to NM_015268.3 S1022S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NF-A4X2-01A-11D-A28R-08 chr8:23167293 G>A maps to NM_002318.2 P589P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NF-A4X2-01A-11D-A28R-08 chr4:149356601 C>A maps to ENST00000511528 G471*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NF-A4X2-01A-11D-A28R-08 chr19:46274874 G>A maps to NM_004409.3 V517V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NF-A4X2-01A-11D-A28R-08 chr3:142840558 C>T maps to NM_004267.3 L301L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NF-A4X2-01A-11D-A28R-08 chr11:108385312 T>C maps to NM_015065.2 K307K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NF-A4X2-01A-11D-A28R-08 chr17:27945806 C>G did not map to a codon.
Sequencing variant TCGA-NF-A4X2-01A-11D-A28R-08 chr7:134851482 C>A maps to NM_024033.2 L118L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NF-A4X2-01A-11D-A28R-08 chr9:135762850 C>T maps to ENST00000372136 C80C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NF-A4X2-01A-11D-A28R-08 chr14:42360909 G>T maps to NM_152447.3 E615*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NF-A4X2-01A-11D-A28R-08 chrX:26212811 G>A maps to NM_173523.2 P283P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NF-A4X2-01A-11D-A28R-08 chr7:102760562 C>T maps to ENST00000455523 T207T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NF-A4X2-01A-11D-A28R-08 chr1:207499028 T>C maps to NM_001114752.1 L181L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NF-A4X2-01A-11D-A28R-08 chr8:97172605 G>C maps to NM_001001557.2 Y105*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NF-A4X2-01A-11D-A28R-08 chr1:159505080 G>A maps to NM_001004469.1 T239T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NF-A5CP-01A-12D-A28R-08 chr6:32609249 G>A maps to NM_002122.3 P82P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NF-A5CP-01A-12D-A28R-08 chr1:115143530 G>A maps to ENST00000393274 Y622Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NF-A5CP-01A-12D-A28R-08 chrX:108911497 G>A maps to NM_022977.2 L424L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NF-A5CP-01A-12D-A28R-08 chr15:25928531 C>T maps to NM_024490.3 S1131S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NF-A5CP-01A-12D-A28R-08 chr13:42763365 C>G maps to NM_178009.2 A611A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NF-A5CP-01A-12D-A28R-08 chr12:117723944 C>T maps to ENST00000338101 S418S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NF-A5CP-01A-12D-A28R-08 chr2:62067001 A>G maps to ENST00000404929 Y379Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NF-A5CP-01A-12D-A28R-08 chr7:86468551 C>T maps to NM_000840.2 D574D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NF-A5CP-01A-12D-A28R-08 chr13:75884162 T>C maps to ENST00000431480 S836S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NF-A5CP-01A-12D-A28R-08 chr1:247614474 G>A maps to NM_001004492.1 Y270Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NF-A5CP-01A-12D-A28R-08 chr2:224831612 A>G maps to NM_022915.3 E287E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NF-A5CP-01A-12D-A28R-08 chr17:72541015 G>A maps to NM_006678.3 R44R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NF-A5CP-01A-12D-A28R-08 chr11:134009764 A>G maps to NM_032801.3 V77V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NF-A5CP-01A-12D-A28R-08 chr3:119013765 T>A maps to NM_020754.2 G5G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NF-A5CP-01A-12D-A28R-08 chr10:70748845 C>G maps to NM_015634.3 P86P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NF-A5CP-01A-12D-A28R-08 chrX:30236751 C>T maps to NM_002364.4 R19*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NF-A5CP-01A-12D-A28R-08 chr2:220421347 G>A maps to NM_015311.2 A1388A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NF-A5CP-01A-12D-A28R-08 chrX:151899864 C>T maps to NM_005367.5 G312G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NF-A5CP-01A-12D-A28R-08 chr8:10470755 C>T maps to NM_178857.5 P284P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NF-A5CP-01A-12D-A28R-08 chr10:127464288 C>T maps to NM_147191.1 S34S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NF-A5CP-01A-12D-A28R-08 chr3:47451556 C>T maps to NM_015466.2 R757*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NF-A5CP-01A-12D-A28R-08 chr12:57572303 C>T maps to NM_002332.2 T1508T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NF-A5CP-01A-12D-A28R-08 chr9:134385762 C>T maps to NM_007171.3 H294H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NF-A5CP-01A-12D-A28R-08 chr17:79974987 G>A maps to ENST00000306729 P643P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NG-A4VU-01A-11D-A28R-08 chr22:36919949 C>T maps to NM_003753.3 Q128Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NG-A4VU-01A-11D-A28R-08 chr1:103453187 C>A did not map to a codon.
Sequencing variant TCGA-NG-A4VU-01A-11D-A28R-08 chr5:147281274 G>A maps to NM_206966.2 D44D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NG-A4VU-01A-11D-A28R-08 chr1:207110845 G>A maps to NM_002644.3 S213S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NG-A4VU-01A-11D-A28R-08 chr1:145293413 A>G maps to NM_001039703.4 V3V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NG-A4VU-01A-11D-A28R-08 chr2:137917825 G>A maps to ENST00000272643 P471P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NG-A4VU-01A-11D-A28R-08 chr22:29754888 C>T maps to NM_001127.3 K117K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NG-A4VU-01A-11D-A28R-08 chr19:14090341 G>A maps to NM_002918.4 Q251*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NG-A4VU-01A-11D-A28R-08 chr14:21423972 C>T maps to NM_002934.2 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NG-A4VU-01A-11D-A28R-08 chr3:4716885 G>A maps to ENST00000356617 A907A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NG-A4VU-01A-11D-A28R-08 chr17:40557061 C>T maps to NM_012232.5 K272K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NG-A4VU-01A-11D-A28R-08 chr17:7129435 C>G maps to NM_004422.2 G653G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NG-A4VU-01A-11D-A28R-08 chr10:126682515 G>A maps to NM_022802.2 G813G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NG-A4VW-01A-11D-A28R-08 chr1:24390562 G>A maps to ENST00000330966 D1210D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NG-A4VW-01A-11D-A28R-08 chr17:34073282 G>A maps to NM_139285.2 L411L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NG-A4VW-01A-11D-A28R-08 chr18:12725486 G>A maps to NM_020232.4 W251*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NG-A4VW-01A-11D-A28R-08 chr9:127300414 G>A maps to NM_033334.2 A260A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NG-A4VW-01A-11D-A28R-08 chr13:48916758 G>T maps to NM_000321.2 E97*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NG-A4VW-01A-11D-A28R-08 chr12:92821901 G>A maps to NM_001025232.1 N7N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NG-A4VW-01A-11D-A28R-08 chr17:6023653 C>T maps to NM_015253.1 Y467Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NG-A4VW-01A-11D-A28R-08 chr3:52395769 G>A maps to ENST00000273600 A1656A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NG-A4VW-01A-11D-A28R-08 chr7:100281656 C>T maps to NM_022574.4 A618A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NG-A4VW-01A-11D-A28R-08 chr1:207790016 C>T maps to NM_000651.4 C2253C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NG-A4VW-01A-11D-A28R-08 chr15:75684735 G>A maps to NM_001145357.1 Q900*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NG-A4VW-01A-11D-A28R-08 chr17:66873703 G>A maps to NM_007168.2 A1345A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NG-A4VW-01A-11D-A28R-08 chr11:71155947 G>A maps to NM_001360.2 G17G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NG-A4VW-01A-11D-A28R-08 chr9:137653811 C>T maps to NM_000093.3 D659D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NG-A4VW-01A-11D-A28R-08 chrX:153578522 G>A maps to NM_001110556.1 D2403D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NG-A4VW-01A-11D-A28R-08 chr15:74623363 C>T maps to ENST00000321288 Q733*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NG-A4VW-01A-11D-A28R-08 chr3:111797604 C>T maps to ENST00000443106 L735L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-NG-A4VW-01A-11D-A28R-08 chr7:101747647 C>T maps to ENST00000360264 R158*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QM-A5NM-01A-11D-A28R-08 chr5:161277799 A>T did not map to a codon.
Sequencing variant TCGA-QM-A5NM-01A-11D-A28R-08 chr10:89624274 C>T maps to NM_000314.4 Q17*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QM-A5NM-01A-11D-A28R-08 chr8:41363428 G>A did not map to a codon.
Sequencing variant TCGA-QM-A5NM-01A-11D-A28R-08 chr8:19682373 T>C maps to NM_018142.2 D299D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QM-A5NM-01A-11D-A28R-08 chr20:2377167 G>T maps to NM_198994.2 L147L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QM-A5NM-01A-11D-A28R-08 chr12:4855405 C>T maps to NM_017417.1 N385N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QM-A5NM-01A-11D-A28R-08 chr20:18477787 C>T maps to NM_006606.2 V8V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QM-A5NM-01A-11D-A28R-08 chr7:149418076 C>T maps to NM_032534.2 P102P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QM-A5NM-01A-11D-A28R-08 chr5:639301 C>T maps to NM_018140.3 G435G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QM-A5NM-01A-11D-A28R-08 chr11:55587890 G>T maps to ENST00000395203 V264V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QM-A5NM-01A-11D-A28R-08 chr4:151504555 G>A maps to NM_006439.4 A125A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QM-A5NM-01A-11D-A28R-08 chr19:34263304 T>C maps to NM_022467.3 N204N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QM-A5NM-01A-11D-A28R-08 chr20:61637711 G>A maps to NM_080606.3 L123L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QM-A5NM-01A-11D-A28R-08 chr11:14535161 T>C maps to NM_148976.2 Q172Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QM-A5NM-01A-11D-A28R-08 chr11:1092953 G>A maps to ENST00000441003 T1591T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QM-A5NM-01A-11D-A28R-08 chr18:61449728 G>T maps to NM_001040147.1 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QN-A5NN-01A-11D-A28R-08 chr8:121238998 T>A maps to NM_021110.1 T666T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QN-A5NN-01A-11D-A28R-08 chr7:127721494 C>T maps to NM_014390.2 P684P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QN-A5NN-01A-11D-A28R-08 chr11:76813926 G>A maps to NM_006189.1 P14P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QN-A5NN-01A-11D-A28R-08 chr5:72364496 T>G maps to NM_138782.2 P490P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QN-A5NN-01A-11D-A28R-08 chr18:45556035 C>T maps to NM_001039360.2 A485A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QN-A5NN-01A-11D-A28R-08 chr14:20692035 A>G maps to NM_001004480.1 T56T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QN-A5NN-01A-11D-A28R-08 chr16:30021384 G>A maps to NM_003586.2 P53P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QN-A5NN-01A-11D-A28R-08 chr7:20682947 C>T maps to NM_001163941.1 I152I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QN-A5NN-01A-11D-A28R-08 chr10:5141028 A>G maps to NM_003739.4 G135G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QN-A5NN-01A-11D-A28R-08 chr14:75265353 C>T maps to NM_019589.2 G1118G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QN-A5NN-01A-11D-A28R-08 chr2:133174752 G>A maps to NM_001508.2 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QN-A5NN-01A-11D-A28R-08 chr7:2962373 G>A maps to NM_032415.4 G721G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QN-A5NN-01A-11D-A28R-08 chrX:54955076 C>T maps to NM_001039705.1 R640R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QN-A5NN-01A-11D-A28R-08 chr16:20331091 T>C did not map to a codon.
Sequencing variant TCGA-QN-A5NN-01A-11D-A28R-08 chr12:122361823 G>T maps to NM_144668.4 R225R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QN-A5NN-01A-11D-A28R-08 chr15:53957933 T>C maps to NM_182758.2 R599R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QN-A5NN-01A-11D-A28R-08 chr5:53467718 G>A maps to NM_019087.2 R30*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QN-A5NN-01A-11D-A28R-08 chr17:29528440 C>T maps to NM_001042492.2 Q400*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QN-A5NN-01A-11D-A28R-08 chr11:71693850 A>C maps to NM_018320.4 T96T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QN-A5NN-01A-11D-A28R-08 chr8:121535575 A>G maps to NM_022045.3 *905W. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QN-A5NN-01A-11D-A28R-08 chr11:6643540 G>T maps to NM_003737.2 G3122G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QN-A5NN-01A-11D-A28R-08 chr10:102054718 A>G maps to NM_016112.2 F506F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QN-A5NN-01A-11D-A28R-08 chr6:117686851 T>A maps to NM_002944.2 S955S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QN-A5NN-01A-11D-A28R-08 chr3:122247219 A>T maps to NM_031458.2 P852P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RF-01A-11D-A28R-08 chr1:212798593 G>A maps to NM_153606.3 R125R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A4RS-01A-11D-A28R-08 chr21:14982926 C>T maps to NM_174981.3 S126S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N5-A59F-01A-11D-A28R-08 chr7:74298938 G>C did not map to a codon.
Sequencing variant TCGA-N6-A4VE-01A-11D-A28R-08 chr7:74299553 C>T maps to ENST00000359898 E121E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N7-A4Y8-01A-11D-A28R-08 chr1:115078571 G>T did not map to a codon.
Sequencing variant TCGA-N8-A4PI-01A-21D-A28R-08 chr17:7578381 G>C maps to NM_001126112.1 S183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N9-A4Q3-01A-11D-A28R-08 chr20:590482 C>T maps to NM_004609.3 S133S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ND-A4WA-01A-12D-A28R-08 chr15:30938494 G>T did not map to a codon.
