5463 NP_705833 L215Q not found in SNVbox database
7294 NP_109597 S21C not found in SNVbox database
407 NP_001070868 I659S not found in SNVbox database
787 NP_001070868 R234P not found in SNVbox database
1652 NP_705833 A670V not found in SNVbox database
2326 NP_001070868 P728A not found in SNVbox database
3023 NP_705833 K25M not found in SNVbox database
3797 NP_001070868 G341E not found in SNVbox database
4163 NP_705833 N562K not found in SNVbox database
4392 NP_705833 G816E not found in SNVbox database
Sequencing variant TCGA-A3-3308-01A-01D-0966-08 chr5:55407416 A>G maps to NM_024669.2 D386D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3308-01A-01D-0966-08 chr3:128757715 C>T maps to NM_024768.2 L545L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3308-01A-01D-0966-08 chr12:119909964 T>C maps to NM_178499.3 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3308-01A-01D-0966-08 chrX:34962087 C>T maps to NM_152631.2 Y380Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3308-01A-01D-0966-08 chr3:100949946 A>G maps to NM_016247.2 C1092C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3308-01A-01D-0966-08 chr10:121587099 T>A maps to NM_014937.2 S1069S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3308-01A-01D-0966-08 chr15:91025443 C>T maps to NM_003870.3 F1162F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3308-01A-01D-0966-08 chr6:168440858 G>A maps to NM_030615.2 T203T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3308-01A-01D-0966-08 chr6:63990711 A>C maps to NM_016571.2 Y248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3308-01A-01D-0966-08 chr6:63990711 A>C maps to NM_016571.2 Y248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3308-01A-01D-0966-08 chr13:76369560 G>A maps to ENST00000357063 V44V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3308-01A-01D-0966-08 chr10:85991772 C>T maps to NM_015613.2 E594E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3308-01A-01D-0966-08 chr8:15967630 G>T maps to ENST00000445506 S458*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3308-01A-01D-0966-08 chr17:30986143 C>T maps to NM_015194.1 T778T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3308-01A-01D-0966-08 chr7:158447320 T>C maps to NM_017760.5 Q904Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3308-01A-01D-0966-08 chr19:55451742 G>A maps to ENST00000446217 D176D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3308-01A-01D-0966-08 chr12:117672373 A>T maps to ENST00000338101 A1111A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3308-01A-01D-0966-08 chr3:98001736 G>A maps to NM_001005482.1 S2S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3308-01A-01D-0966-08 chr9:96415637 C>T maps to NM_005392.3 H260H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3308-01A-01D-0966-08 chr11:57147059 C>T maps to NM_006093.3 R94R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3308-01A-01D-0966-08 chr10:89712016 G>A did not map to a codon.
Sequencing variant TCGA-A3-3308-01A-01D-0966-08 chr8:37756811 C>A maps to NM_001002814.2 E50*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3308-01A-01D-0966-08 chr13:25353867 T>C maps to ENST00000381927 L165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3308-01A-01D-0966-08 chr13:45914268 A>G maps to ENST00000309246 N51N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3308-01A-01D-0966-08 chr8:81399983 T>C maps to NM_001105539.1 S313S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3308-01A-01D-0966-08 chr19:44832083 C>T maps to ENST00000412927 P759P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3308-01A-01D-0966-08 chr14:71067336 G>A maps to ENST00000430055 I6I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3308-01A-01D-0966-08 chr14:71067336 G>A maps to ENST00000430055 I6I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3311-01A-01D-0966-08 chr1:12820748 G>A maps to NM_152290.2 Q150Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3311-01A-01D-0966-08 chr9:139266449 G>C maps to NM_052813.4 P27P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3311-01A-01D-0966-08 chr1:227213827 C>T maps to ENST00000366766 V1486V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3311-01A-01D-0966-08 chr2:97483237 A>C maps to NM_017623.4 R408R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3311-01A-01D-0966-08 chr6:36730738 A>G maps to NM_020939.1 S270S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3311-01A-01D-0966-08 chr15:44751275 A>T maps to NM_016396.2 R22*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3311-01A-01D-0966-08 chr6:91228281 C>A did not map to a codon.
Sequencing variant TCGA-A3-3311-01A-01D-0966-08 chr3:49466657 C>T maps to NM_032316.3 L5L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3311-01A-01D-0966-08 chr8:52359591 C>A maps to NM_144651.4 V499V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3311-01A-01D-0966-08 chr4:83839152 C>T maps to NM_024672.4 V596V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3311-01A-01D-0966-08 chr7:142626640 G>A maps to NM_019841.4 I123I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3311-01A-01D-0966-08 chr2:3391615 C>T maps to NM_016030.5 D74D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3311-01A-01D-0966-08 chr2:179399167 C>T maps to NM_133378.4 R31490R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3316-01A-01D-0966-08 chr7:48556345 C>T maps to NM_152701.3 L4556L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3316-01A-01D-0966-08 chr11:107974930 A>G maps to NM_003478.3 Q721Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3316-01A-01D-0966-08 chr18:28934517 C>T maps to NM_001942.2 Q787*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3316-01A-01D-0966-08 chr11:22646828 C>T maps to NM_022725.3 E176E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3316-01A-01D-0966-08 chr1:39934333 C>T maps to ENST00000361689 T5208T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3316-01A-01D-0966-08 chr1:203816425 C>A maps to NM_014827.4 S386*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3316-01A-01D-0966-08 chr11:66472255 C>A maps to NM_006946.2 E831*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3316-01A-01D-0966-08 chr11:66472255 C>A maps to NM_006946.2 E831*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3317-01A-01D-0966-08 chr12:50453581 C>T maps to NM_020039.2 L135L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3317-01A-01D-0966-08 chr14:33068659 T>A maps to NM_004274.4 A838A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3317-01A-01D-0966-08 chr5:78076226 C>T maps to NM_000046.3 W532*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3317-01A-01D-0966-08 chr11:64673942 G>A maps to ENST00000421419 Q1016*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3317-01A-01D-0966-08 chr3:52438514 C>A maps to NM_004656.2 E402*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3317-01A-01D-0966-08 chr2:175612867 A>T maps to NM_001039523.2 L478*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3317-01A-01D-0966-08 chr1:44684378 A>T maps to NM_019100.4 R224R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3317-01A-01D-0966-08 chr18:28651757 A>G maps to ENST00000438199 Y659Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3317-01A-01D-0966-08 chr5:96139527 G>A maps to NM_016442.3 S34S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3317-01A-01D-0966-08 chr13:99098407 G>A maps to NM_005766.2 K951K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3317-01A-01D-0966-08 chr11:59611469 C>T maps to NM_005142.2 S46S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3317-01A-01D-0966-08 chr6:33374603 G>T maps to NM_002263.3 L643L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3317-01A-01D-0966-08 chr18:47799981 A>T maps to ENST00000424334 P517P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3317-01A-01D-0966-08 chr16:86565765 G>T maps to NM_001159377.1 R335R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3317-01A-01D-0966-08 chr5:140202643 C>T maps to NM_018908.2 D428D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3317-01A-01D-0966-08 chr5:131607571 C>T maps to NM_003687.3 P253P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3317-01A-01D-0966-08 chr2:44554021 T>A maps to NM_001171603.1 L525L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3317-01A-01D-0966-08 chr1:151337663 C>G did not map to a codon.
Sequencing variant TCGA-A3-3317-01A-01D-0966-08 chr2:55813756 T>A maps to NM_001122964.1 V371V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3317-01A-01D-0966-08 chr2:107460217 C>G maps to NM_001142351.1 G72G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3317-01A-01D-0966-08 chr8:15531299 C>T maps to NM_006765.2 I251I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3317-01A-01D-0966-08 chr7:6731606 C>T maps to ENST00000330442 E379E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3317-01A-01D-0966-08 chr14:103389066 C>T maps to NM_030943.3 C14C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3317-01A-01D-0966-08 chr14:103389066 C>T maps to NM_030943.3 C14C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3317-01A-01D-0966-08 chr5:52221112 C>G maps to NM_181501.1 P803P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3317-01A-01D-0966-08 chr5:52221112 C>G maps to NM_181501.1 P803P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3317-01A-01D-0966-08 chr6:161032705 C>A maps to NM_005577.2 G831*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3317-01A-01D-0966-08 chr6:161032705 C>A maps to NM_005577.2 G831*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3317-01A-01D-0966-08 chr21:42551342 G>C maps to NM_182832.2 L71L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3317-01A-01D-0966-08 chr21:42551342 G>C maps to NM_182832.2 L71L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3317-01A-01D-0966-08 chr7:6442070 G>C maps to NM_018890.3 L210L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3317-01A-01D-0966-08 chr7:6442070 G>C maps to NM_018890.3 L210L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3317-01A-01D-0966-08 chr4:177248329 C>T maps to NM_021928.3 V104V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3317-01A-01D-0966-08 chr4:177248329 C>T maps to NM_021928.3 V104V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3319-01A-01D-0966-08 chr4:114213642 T>C maps to NM_001148.4 H783H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3319-01A-01D-0966-08 chr4:114213642 T>C maps to NM_001148.4 H783H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3319-01A-01D-0966-08 chr1:155450215 G>C maps to ENST00000368346 V815V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3319-01A-01D-0966-08 chr17:29161395 G>T maps to NM_024857.3 T99T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3319-01A-01D-0966-08 chr4:15556748 C>T maps to NM_001080522.2 D847D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3319-01A-01D-0966-08 chr16:65038652 C>T maps to NM_001797.2 E40E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3319-01A-01D-0966-08 chr5:98228308 T>C maps to NM_001270.2 K700K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3319-01A-01D-0966-08 chr2:97475199 T>G maps to NM_020184.3 L758L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3319-01A-01D-0966-08 chr4:5733354 C>T maps to NM_153717.2 N196N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3319-01A-01D-0966-08 chr5:90079094 G>A maps to NM_032119.3 G4462G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3319-01A-01D-0966-08 chr19:51466689 G>A maps to NM_001012964.1 Q105*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3319-01A-01D-0966-08 chr11:68193566 C>G maps to NM_002335.2 T1183T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3319-01A-01D-0966-08 chr1:156047264 G>A maps to NM_001093725.1 P221P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3319-01A-01D-0966-08 chr1:156047264 G>A maps to NM_001093725.1 P221P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3319-01A-01D-0966-08 chr22:18368681 C>A maps to NM_015241.2 E735*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3319-01A-01D-0966-08 chr8:66619368 A>G maps to NM_014637.3 R214R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3319-01A-01D-0966-08 chr3:51667704 T>A maps to NM_015106.2 L313*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3319-01A-01D-0966-08 chr4:83788104 T>C maps to ENST00000505472 S351S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3319-01A-01D-0966-08 chr11:75280026 C>T maps to NM_001235.2 I255I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3319-01A-01D-0966-08 chr12:21036503 A>G maps to NM_019844.2 T550T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3320-01A-01D-0966-08 chr16:75276900 C>A maps to NM_001170714.1 E80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3320-01A-01D-0966-08 chr16:75276901 C>A maps to NM_001170714.1 L79L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3320-01A-01D-0966-08 chr1:57258475 C>A maps to NM_001004303.4 E4*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3320-01A-01D-0966-08 chr5:111071195 G>T maps to NM_001142475.1 Y48*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3320-01A-01D-0966-08 chr17:49726540 A>G did not map to a codon.
Sequencing variant TCGA-A3-3320-01A-01D-0966-08 chr12:102107932 T>A maps to NM_020244.2 I113I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3320-01A-01D-0966-08 chr3:128890022 G>A maps to NM_001127192.1 G107G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3320-01A-01D-0966-08 chr3:38163909 G>A maps to NM_007337.2 P1717P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3320-01A-01D-0966-08 chr14:86089640 A>T maps to NM_013231.4 K595*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3320-01A-01D-0966-08 chr15:59910565 G>A maps to NM_004751.2 E43E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3320-01A-01D-0966-08 chr19:1004978 C>T maps to NM_138690.1 F493F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3320-01A-01D-0966-08 chr19:1004978 C>T maps to NM_138690.1 F493F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3320-01A-01D-0966-08 chr15:63915941 G>T maps to ENST00000261887 T4531T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3320-01A-01D-0966-08 chr1:44425961 G>A maps to NM_014652.3 K690K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3320-01A-01D-0966-08 chr17:73745082 C>T maps to NM_001005619.1 H1091H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3320-01A-01D-0966-08 chr9:114134740 A>T maps to NM_001080398.1 L1677*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3320-01A-01D-0966-08 chr22:42180386 T>C maps to NM_152513.3 A1044A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3320-01A-01D-0966-08 chr10:95093559 G>A maps to NM_013451.3 Y1558Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3320-01A-01D-0966-08 chr10:74684102 C>A maps to NM_152635.1 C356*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3320-01A-01D-0966-08 chr11:5841739 C>A maps to NM_001005174.1 R59R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3320-01A-01D-0966-08 chr11:63679956 C>T maps to NM_173587.3 G359G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3320-01A-01D-0966-08 chr3:155546087 C>A maps to NM_004733.3 G521*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3320-01A-01D-0966-08 chr14:23597393 C>G maps to NM_012244.2 L425L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3320-01A-01D-0966-08 chr2:103095412 C>A maps to NM_001011552.3 V124V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3320-01A-01D-0966-08 chr17:37821617 T>A maps to NM_003673.3 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3320-01A-01D-0966-08 chr11:60701063 C>A maps to NM_017870.3 G470G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3320-01A-01D-0966-08 chr13:19999142 G>C maps to NM_199254.2 Y470*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3320-01A-01D-0966-08 chr1:55251691 T>C maps to NM_001114108.1 P328P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3320-01A-01D-0966-08 chr2:179582322 G>A maps to NM_133378.4 H7182H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3320-01A-01D-0966-08 chr6:34789454 A>T maps to NM_017754.3 K24*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3320-01A-01D-0966-08 chr6:43515439 G>A maps to NM_020750.2 L689L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3320-01A-01D-0966-08 chr19:38876473 C>T maps to NM_152657.3 L476L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3320-01A-01D-0966-08 chr19:38876473 C>T maps to NM_152657.3 L476L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3320-01A-01D-0966-08 chr17:72343935 C>T maps to NM_153209.3 S315S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3320-01A-01D-0966-08 chr17:72343935 C>T maps to NM_153209.3 S315S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3320-01A-01D-0966-08 chr3:52649372 T>A maps to ENST00000296302 K640*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3320-01A-01D-0966-08 chr3:52649372 T>A maps to ENST00000296302 K640*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3322-01A-01D-0966-08 chr22:47116100 G>A maps to NM_022766.5 H87H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3322-01A-01D-0966-08 chr2:3691554 C>T maps to ENST00000418971 P235P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3322-01A-01D-0966-08 chr18:3502637 A>G maps to NM_004746.2 P859P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3322-01A-01D-0966-08 chr8:120569904 T>C maps to NM_006209.3 V868V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3322-01A-01D-0966-08 chr17:65184579 T>C maps to NM_014877.3 Q339Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3322-01A-01D-0966-08 chr15:79749415 C>T maps to NM_015206.2 N309N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3322-01A-01D-0966-08 chr1:201354879 T>G maps to NM_005558.3 R360R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3322-01A-01D-0966-08 chr1:201354879 T>G maps to NM_005558.3 R360R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3322-01A-01D-0966-08 chr2:27663339 C>A maps to ENST00000379863 I377I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3322-01A-01D-0966-08 chr2:27663339 C>A maps to ENST00000379863 I377I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3322-01A-01D-0966-08 chr1:154027277 T>A maps to NM_207308.2 K1091*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3322-01A-01D-0966-08 chr6:57185309 C>T maps to NM_000947.2 Y70Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3322-01A-01D-0966-08 chr8:57219233 C>T did not map to a codon.
Sequencing variant TCGA-A3-3322-01A-01D-0966-08 chr7:94257636 T>A maps to NM_001099401.1 T89T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3322-01A-01D-0966-08 chr1:67101649 C>T maps to NM_032291.2 P41P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3322-01A-01D-0966-08 chr19:58198815 T>C maps to ENST00000356715 Y391Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3322-01A-01D-0966-08 chr19:52496684 G>A maps to ENST00000354939 G559G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3322-01A-01D-0966-08 chr16:90099332 G>A did not map to a codon.
Sequencing variant TCGA-A3-3322-01A-01D-0966-08 chr16:90099332 G>A did not map to a codon.
Sequencing variant TCGA-A3-3322-01A-01D-0966-08 chr7:1487213 C>T maps to NM_182924.3 K174K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3322-01A-01D-0966-08 chr7:1487213 C>T maps to NM_182924.3 K174K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3323-01A-01D-0966-08 chr18:12367033 A>T maps to NM_006796.2 L161*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3323-01A-01D-0966-08 chr4:47538704 C>G maps to NM_020453.3 V382V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3323-01A-01D-0966-08 chr1:230991423 C>T maps to NM_032800.2 W125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3323-01A-01D-0966-08 chr15:59407027 C>T maps to NM_004701.2 Q184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3323-01A-01D-0966-08 chr9:131804662 C>T maps to NM_032809.2 A59A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3323-01A-01D-0966-08 chr7:43484070 G>T maps to NM_015052.3 G434*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3323-01A-01D-0966-08 chr5:137902358 C>A maps to NM_004134.6 E310*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3323-01A-01D-0966-08 chr12:54798565 C>G maps to NM_002205.2 L446L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3323-01A-01D-0966-08 chr12:57920769 T>G maps to NM_052897.3 P614P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3323-01A-01D-0966-08 chr7:100686873 T>G maps to NM_001040105.1 S4059S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3323-01A-01D-0966-08 chr1:120612005 G>A maps to NM_024408.2 R5R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3323-01A-01D-0966-08 chr3:52685755 A>G did not map to a codon.
Sequencing variant TCGA-A3-3323-01A-01D-0966-08 chr3:119378937 G>A maps to NM_022135.2 L111L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3323-01A-01D-0966-08 chr7:103130249 G>T maps to ENST00000428762 L3234L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3323-01A-01D-0966-08 chr17:20931912 G>A maps to ENST00000455117 F150F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3323-01A-01D-0966-08 chr17:20931912 G>A maps to ENST00000455117 F150F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3323-01A-01D-0966-08 chr15:41222314 G>T did not map to a codon.
Sequencing variant TCGA-A3-3323-01A-01D-0966-08 chr15:41222314 G>T did not map to a codon.
Sequencing variant TCGA-A3-3323-01A-01D-0966-08 chr12:132445442 A>C maps to ENST00000333577 P93P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3323-01A-01D-0966-08 chr12:132445442 A>C maps to ENST00000333577 P93P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3323-01A-01D-0966-08 chr15:74365098 C>A maps to NM_001038640.2 V495V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3323-01A-01D-0966-08 chr15:74365098 C>A maps to NM_001038640.2 V495V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3326-01A-01D-0966-08 chr16:21261381 C>G maps to NM_145865.2 Y165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3326-01A-01D-0966-08 chr11:128839968 C>T maps to NM_001142685.1 K1699K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3326-01A-01D-0966-08 chr8:11412943 C>G maps to ENST00000427279 L241L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3326-01A-01D-0966-08 chr1:52552414 G>A maps to NM_152265.3 K154K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3326-01A-01D-0966-08 chr17:65021006 C>T maps to NM_014405.3 I112I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3326-01A-01D-0966-08 chr19:35827038 G>T maps to NM_001771.3 P171P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3326-01A-01D-0966-08 chr20:56099122 A>G maps to ENST00000423479 L47L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3326-01A-01D-0966-08 chr1:154995892 G>A maps to NM_144622.2 T637T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3326-01A-01D-0966-08 chr5:150945789 T>C maps to NM_001447.2 K901K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3326-01A-01D-0966-08 chr11:122930667 A>G maps to NM_006597.3 T211T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3326-01A-01D-0966-08 chr17:56285342 A>G maps to NM_017777.3 P395P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3326-01A-01D-0966-08 chr11:59837675 G>A did not map to a codon.
Sequencing variant TCGA-A3-3326-01A-01D-0966-08 chr3:108205347 G>C maps to NM_014981.1 P319P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3326-01A-01D-0966-08 chr3:25824815 C>T maps to NM_018297.3 Q22Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3326-01A-01D-0966-08 chr6:42713802 G>A maps to NM_003192.2 S3S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3326-01A-01D-0966-08 chr2:179593687 A>G maps to NM_133378.4 S5115S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3326-01A-01D-0966-08 chr1:19505690 T>C maps to ENST00000375267 G736G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3326-01A-01D-0966-08 chr11:58384896 C>A maps to NM_053023.4 G477G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3326-01A-01D-0966-08 chr7:148801993 C>G maps to NM_001001661.2 L323L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3326-01A-01D-0966-08 chr19:58018036 A>T maps to NM_198542.1 K192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3326-01A-01D-0966-08 chr19:18234142 C>A maps to NM_015016.1 G143G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3326-01A-01D-0966-08 chr19:18234142 C>A maps to NM_015016.1 G143G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3346-01A-01D-0966-08 chr3:52012053 G>A maps to ENST00000463937 S79S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3346-01A-01D-0966-08 chr17:7990739 C>T maps to NM_001139.2 R7R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3346-01A-01D-0966-08 chr3:33725900 C>A maps to ENST00000359576 V198V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3346-01A-01D-0966-08 chr10:102006677 G>A maps to NM_018294.4 F241F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3346-01A-01D-0966-08 chr1:111734914 A>C maps to NM_024901.3 A273A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3346-01A-01D-0966-08 chr12:51084866 T>C maps to NM_173602.2 V529V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3346-01A-01D-0966-08 chr4:187549317 C>T maps to ENST00000260147 S1600S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3346-01A-01D-0966-08 chr4:187549317 C>T maps to ENST00000260147 S1600S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3346-01A-01D-0966-08 chr8:125072865 C>T maps to NM_001039112.2 C1021C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3346-01A-01D-0966-08 chr19:56109180 G>A maps to NM_032836.2 A17A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3346-01A-01D-0966-08 chr15:40068677 T>A maps to NM_152597.4 S16S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3346-01A-01D-0966-08 chr19:3522954 C>A did not map to a codon.
Sequencing variant TCGA-A3-3346-01A-01D-0966-08 chr1:155753881 T>G did not map to a codon.
Sequencing variant TCGA-A3-3346-01A-01D-0966-08 chr22:38201973 C>A maps to NM_005318.3 T141T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3346-01A-01D-0966-08 chr1:32796450 C>T maps to NM_004964.2 N307N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3346-01A-01D-0966-08 chr5:35871221 G>T maps to NM_002185.2 V148V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3346-01A-01D-0966-08 chr17:60004005 T>G maps to NM_020748.2 I8I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3346-01A-01D-0966-08 chr19:54758769 G>C maps to NM_001081442.1 A361A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3346-01A-01D-0966-08 chr15:52646190 T>G maps to ENST00000358212 V1148V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3346-01A-01D-0966-08 chr2:184016284 A>C maps to NM_138285.3 T149T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3346-01A-01D-0966-08 chr9:125424611 C>T maps to ENST00000373686 V256V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3346-01A-01D-0966-08 chr3:121187275 G>A maps to ENST00000393672 R2377*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3346-01A-01D-0966-08 chr5:64859224 A>T maps to NM_015342.2 R30*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3346-01A-01D-0966-08 chr4:74442419 A>T maps to NM_201431.1 I282I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3346-01A-01D-0966-08 chr4:40428109 A>G maps to NM_001098634.1 I531I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3346-01A-01D-0966-08 chr5:79616636 C>T maps to NM_032567.3 N201N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3346-01A-01D-0966-08 chrX:122758389 A>G did not map to a codon.
Sequencing variant TCGA-A3-3346-01A-01D-0966-08 chr21:19666660 A>G maps to NM_002772.2 Y804Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3346-01A-01D-0966-08 chr13:51825775 G>T maps to NM_145019.2 R127R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3346-01A-01D-0966-08 chr13:51825775 G>T maps to NM_145019.2 R127R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3346-01A-01D-0966-08 chr21:34143766 G>A maps to NM_016631.3 L71L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3346-01A-01D-0966-08 chr21:34143766 G>A maps to NM_016631.3 L71L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3357-01A-02D-1421-08 chr15:50336886 T>A maps to NM_024837.2 L68L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3357-01A-02D-1421-08 chr1:151021075 A>G maps to NM_017860.3 Q251Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3357-01A-02D-1421-08 chr20:2795844 C>T maps to NM_080739.2 C5C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3357-01A-02D-1421-08 chr9:90255296 T>C maps to NM_004938.2 D238D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3357-01A-02D-1421-08 chr5:141025712 C>A maps to ENST00000354789 E365*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3357-01A-02D-1421-08 chr1:157650774 G>A maps to NM_052939.3 S651S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3357-01A-02D-1421-08 chr14:86088730 G>T maps to NM_013231.4 L291L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3357-01A-02D-1421-08 chr4:84374450 A>C maps to NM_133636.2 P315P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3357-01A-02D-1421-08 chr15:63950915 A>T maps to ENST00000261887 G3142G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3357-01A-02D-1421-08 chr1:186064395 C>G maps to NM_031935.2 S3439*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3357-01A-02D-1421-08 chr17:43923234 G>A maps to NM_175882.2 P321P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3357-01A-02D-1421-08 chr20:16316573 T>G maps to NM_024704.4 A1236A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3357-01A-02D-1421-08 chr9:131256863 C>T maps to NM_153435.1 L674L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3357-01A-02D-1421-08 chr11:6806546 C>T maps to NM_001004489.2 S93S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3357-01A-02D-1421-08 chr19:39880355 A>G maps to NM_019088.2 H72H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3357-01A-02D-1421-08 chr5:141243420 G>A maps to NM_032420.2 L825L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3357-01A-02D-1421-08 chr14:71479736 G>A maps to NM_014982.2 L938L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3357-01A-02D-1421-08 chr12:89885861 A>G maps to NM_172240.2 H101H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3357-01A-02D-1421-08 chr4:39324977 T>C maps to ENST00000381897 E234E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3357-01A-02D-1421-08 chr14:93118452 C>A maps to NM_024832.3 P353P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3357-01A-02D-1421-08 chr1:169677786 A>T maps to NM_000655.4 P94P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3357-01A-02D-1421-08 chr12:33579107 C>T maps to NM_198992.3 V158V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3357-01A-02D-1421-08 chr19:51140595 G>T maps to NM_001160329.1 R25R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3357-01A-02D-1421-08 chr22:35719145 T>C maps to ENST00000451197 H123H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3357-01A-02D-1421-08 chr2:179466063 G>A maps to NM_133378.4 R15986*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3357-01A-02D-1421-08 chr12:109935724 T>C maps to NM_183415.1 P272P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3357-01A-02D-1421-08 chr7:123329153 T>C maps to NM_003941.2 G466G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3357-01A-02D-1421-08 chr7:123329153 T>C maps to NM_003941.2 G466G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3357-01A-02D-1421-08 chr19:44661743 G>A maps to NM_006630.2 S525S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3357-01A-02D-1421-08 chr1:247463961 G>C maps to NM_032752.1 R541R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3357-01A-02D-1421-08 chr17:37265508 G>A maps to NM_020405.4 Q131*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3357-01A-02D-1421-08 chr17:37265508 G>A maps to NM_020405.4 Q131*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3363-01A-01D-0966-08 chr9:35736668 A>G maps to NM_006368.4 G354G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3363-01A-01D-0966-08 chr9:35736668 A>G maps to NM_006368.4 G354G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3363-01A-01D-0966-08 chr9:14846002 G>A maps to ENST00000380880 L453L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3363-01A-01D-0966-08 chr12:12618551 C>T maps to NM_058169.3 Q145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3363-01A-01D-0966-08 chr8:86019571 G>T maps to NM_033402.4 V14V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3363-01A-01D-0966-08 chr7:107848032 G>T maps to ENST00000379032 C382*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3363-01A-01D-0966-08 chr10:96043554 C>T maps to ENST00000371380 L1602L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3363-01A-01D-0966-08 chr2:27258868 C>T maps to NM_017727.4 I223I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3363-01A-01D-0966-08 chr6:41002735 A>G maps to NM_173561.2 L26L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3365-01A-01D-0966-08 chr4:83970373 C>A maps to ENST00000503682 C70*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3365-01A-01D-0966-08 chr2:216236991 C>A maps to NM_212482.1 G2118G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3365-01A-01D-0966-08 chr4:843677 A>G did not map to a codon.
Sequencing variant TCGA-A3-3365-01A-01D-0966-08 chr4:843677 A>G did not map to a codon.
Sequencing variant TCGA-A3-3365-01A-01D-0966-08 chr12:49447311 G>A maps to NM_003482.3 A262A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3365-01A-01D-0966-08 chr12:49447311 G>A maps to NM_003482.3 A262A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3365-01A-01D-0966-08 chr5:140869550 T>A maps to NM_018929.2 R248R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3365-01A-01D-0966-08 chr5:140869550 T>A maps to NM_018929.2 R248R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3365-01A-01D-0966-08 chr17:48252716 C>G maps to NM_000023.2 P361P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3365-01A-01D-0966-08 chr3:143297453 C>A maps to NM_173653.3 G289G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3365-01A-01D-0966-08 chr7:100361426 A>G did not map to a codon.
Sequencing variant TCGA-A3-3365-01A-01D-0966-08 chr13:22067483 T>C maps to NM_152726.2 Q403Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3365-01A-01D-0966-08 chr13:22067483 T>C maps to NM_152726.2 Q403Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3367-01A-02D-1421-08 chr2:175614793 A>G maps to NM_001039523.2 I319I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3367-01A-02D-1421-08 chr8:62212688 C>T maps to NM_173519.2 R101R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3367-01A-02D-1421-08 chr3:45988807 C>T maps to NM_006564.1 L279L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3367-01A-02D-1421-08 chr1:16458585 G>A maps to NM_004431.3 D766D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3367-01A-02D-1421-08 chr11:108381262 G>A maps to NM_015065.2 S1657S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3367-01A-02D-1421-08 chr1:240371468 C>T maps to ENST00000406993 P1262P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3367-01A-02D-1421-08 chrX:131234680 C>A maps to NM_194277.2 E41*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3367-01A-02D-1421-08 chr11:62396248 A>G maps to NM_198335.2 P746P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3367-01A-02D-1421-08 chr11:62396248 A>G maps to NM_198335.2 P746P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3367-01A-02D-1421-08 chrX:24006421 C>A maps to NM_030624.2 A477A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3367-01A-02D-1421-08 chr11:111431065 G>A maps to ENST00000375615 V344V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3367-01A-02D-1421-08 chr3:154862149 C>A maps to NM_007289.2 V440V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3367-01A-02D-1421-08 chr20:62850363 G>A maps to NM_004535.2 T649T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3367-01A-02D-1421-08 chr16:4511891 G>A maps to NM_020677.3 F263F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3367-01A-02D-1421-08 chr14:75416058 C>T did not map to a codon.
Sequencing variant TCGA-A3-3367-01A-02D-1421-08 chr19:14829356 C>T maps to NM_032433.2 S406S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3367-01A-02D-1421-08 chr20:32379289 C>T maps to ENST00000375200 L844L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3367-01A-02D-1421-08 chr5:150646945 C>T maps to NM_000405.4 S172S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3367-01A-02D-1421-08 chr5:150646945 C>T maps to NM_000405.4 S172S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3367-01A-02D-1421-08 chr5:86564516 A>G maps to NM_002890.1 G83G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3367-01A-02D-1421-08 chr5:86564516 A>G maps to NM_002890.1 G83G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3370-01A-02D-1421-08 chr9:138703211 G>A maps to ENST00000409386 N1595N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3370-01A-02D-1421-08 chr11:36302300 T>G maps to NM_014186.3 T46T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3370-01A-02D-1421-08 chr15:51837939 A>C maps to NM_001174116.1 L257*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3370-01A-02D-1421-08 chr1:90049714 C>T maps to NM_015350.2 I502I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3370-01A-02D-1421-08 chr15:100269537 C>T maps to NM_152449.2 L228L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3370-01A-02D-1421-08 chr3:31774805 G>T maps to NM_017784.4 T346T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3370-01A-02D-1421-08 chr6:139233901 C>T maps to ENST00000367663 P657P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3370-01A-02D-1421-08 chr21:33043797 T>A maps to NM_020706.2 K1120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3370-01A-02D-1421-08 chr17:33679557 T>C maps to NM_152270.3 A841A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3370-01A-02D-1421-08 chr5:53814576 T>A maps to NM_052870.2 Y265*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3370-01A-02D-1421-08 chr14:103394800 A>T maps to NM_030943.3 G82G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3370-01A-02D-1421-08 chr14:103394800 A>T maps to NM_030943.3 G82G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3372-01A-01D-0966-08 chr1:155491016 T>C maps to ENST00000368346 K98K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3372-01A-01D-0966-08 chr2:203421004 C>T maps to NM_001204.6 R873*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3372-01A-01D-0966-08 chr2:99448879 G>A maps to NM_207362.2 D157D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3372-01A-01D-0966-08 chr3:48607731 G>A maps to NM_000094.3 G2472G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3372-01A-01D-0966-08 chr4:155312410 G>A maps to NM_017639.3 D13D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3372-01A-01D-0966-08 chr9:19063107 T>C maps to NM_017645.3 L509L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3372-01A-01D-0966-08 chr2:227662869 C>T maps to NM_005544.2 V195V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3372-01A-01D-0966-08 chr3:44816790 T>C maps to NM_020242.2 P36P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3372-01A-01D-0966-08 chr6:129799906 T>C maps to NM_000426.3 N2507N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3372-01A-01D-0966-08 chr6:39895284 G>T maps to ENST00000425303 V11V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3372-01A-01D-0966-08 chr18:70417574 C>T maps to NM_153181.2 R420R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3372-01A-01D-0966-08 chr3:52651418 A>T maps to ENST00000296302 Y559*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3372-01A-01D-0966-08 chr1:203452938 C>T maps to NM_201348.1 D209D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3372-01A-01D-0966-08 chr7:155473514 A>T maps to NM_053043.2 I160I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3372-01A-01D-0966-08 chr15:60789778 G>A maps to NM_134260.2 R516*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3372-01A-01D-0966-08 chr17:48195542 C>T maps to NM_174920.2 S64S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3372-01A-01D-0966-08 chr17:48195542 C>T maps to NM_174920.2 S64S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3372-01A-01D-0966-08 chr18:47906544 C>A maps to NM_145060.3 I46I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3372-01A-01D-0966-08 chr15:44858474 C>T maps to NM_025137.3 L2261L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3372-01A-01D-0966-08 chr12:115117392 A>G maps to NM_016569.3 L261L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3372-01A-01D-0966-08 chr19:42820893 T>C did not map to a codon.
Sequencing variant TCGA-A3-3372-01A-01D-0966-08 chr13:38320156 G>T maps to NM_003306.1 R272R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3372-01A-01D-0966-08 chr13:38320156 G>T maps to NM_003306.1 R272R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3372-01A-01D-0966-08 chr11:43429096 A>G maps to NM_018259.5 L678L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3372-01A-01D-0966-08 chr2:20162079 G>A maps to NM_001006657.1 N401N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3372-01A-01D-0966-08 chr6:3850383 C>T maps to NM_012135.1 R113R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3372-01A-01D-0966-08 chr6:3850383 C>T maps to NM_012135.1 R113R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3373-01A-02D-1421-08 chr14:59835513 A>G maps to NM_014992.1 K1058K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3373-01A-02D-1421-08 chrX:32862974 T>C maps to ENST00000357033 P63P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3373-01A-02D-1421-08 chr2:63169916 G>A maps to NM_015252.3 W452*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3373-01A-02D-1421-08 chr17:7214801 T>C did not map to a codon.
Sequencing variant TCGA-A3-3373-01A-02D-1421-08 chr2:210561003 C>T maps to NM_002374.3 D1370D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3373-01A-02D-1421-08 chr2:149227851 T>G maps to ENST00000404807 L780L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3373-01A-02D-1421-08 chr3:52682445 T>A maps to ENST00000296302 K243*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3373-01A-02D-1421-08 chr19:54625913 A>C maps to NM_015629.3 R121R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3373-01A-02D-1421-08 chr2:166898838 T>C maps to NM_001165963.1 A713A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3373-01A-02D-1421-08 chr3:48900023 C>T maps to NM_000387.4 E162E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3373-01A-02D-1421-08 chr2:40342425 G>A maps to NM_021097.2 S963S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3373-01A-02D-1421-08 chr9:119460980 T>C maps to NM_012210.3 V320V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3373-01A-02D-1421-08 chr16:28857317 G>A maps to NM_003321.4 Y54Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3373-01A-02D-1421-08 chr3:10183793 G>A maps to NM_000551.2 W88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3376-01A-02D-1421-08 chr7:92027911 C>A maps to NM_019004.1 I973I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3376-01A-02D-1421-08 chr14:60928114 C>T maps to NM_174978.2 Q358Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3376-01A-02D-1421-08 chr1:112019441 A>C maps to NM_174896.2 T20T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3376-01A-02D-1421-08 chr1:112019441 A>C maps to NM_174896.2 T20T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3376-01A-02D-1421-08 chr9:406988 T>A maps to NM_203447.3 T1150T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3376-01A-02D-1421-08 chr6:93969180 G>C maps to NM_004440.3 T605T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3376-01A-02D-1421-08 chr3:150421526 C>T maps to NM_152394.3 E53E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3376-01A-02D-1421-08 chr16:66966159 C>T maps to NM_016062.2 L146L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3376-01A-02D-1421-08 chr3:189689770 G>T maps to NM_018192.3 L575L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3376-01A-02D-1421-08 chr10:108366995 A>G maps to NM_001013031.1 T1031T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3376-01A-02D-1421-08 chr19:50926245 C>A maps to NM_003121.3 A97A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3376-01A-02D-1421-08 chr20:62275106 G>T did not map to a codon.
Sequencing variant TCGA-A3-3376-01A-02D-1421-08 chrX:104464655 C>T maps to NM_031274.3 E142E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3376-01A-02D-1421-08 chr1:38227125 G>T maps to NM_001099439.1 G267G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3376-01A-02D-1421-08 chr1:38227125 G>T maps to NM_001099439.1 G267G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3376-01A-02D-1421-08 chr1:186276074 T>C maps to NM_005807.3 T408T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3376-01A-02D-1421-08 chr1:186276074 T>C maps to NM_005807.3 T408T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3376-01A-02D-1421-08 chr3:10183871 G>C did not map to a codon.
Sequencing variant TCGA-A3-3376-01A-02D-1421-08 chr3:10183871 G>C did not map to a codon.
Sequencing variant TCGA-A3-3378-01A-01D-0966-08 chr5:14751237 G>A maps to NM_054027.4 C209C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3378-01A-01D-0966-08 chr9:119204735 T>C maps to ENST00000313400 A1198A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3378-01A-01D-0966-08 chr4:81952662 A>T maps to NM_001201.2 T75T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3378-01A-01D-0966-08 chr21:30442607 C>T maps to NM_006585.2 K37K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3378-01A-01D-0966-08 chr2:80097055 C>T maps to ENST00000402739 Q194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3378-01A-01D-0966-08 chr15:78572438 C>G maps to NM_018602.3 P339P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3378-01A-01D-0966-08 chr19:45857990 C>T maps to NM_000400.3 E554E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3378-01A-01D-0966-08 chr2:183731160 G>T maps to NM_001463.3 I40I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3378-01A-01D-0966-08 chr4:22437011 A>T maps to NM_145290.2 S455S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3378-01A-01D-0966-08 chr12:52793885 C>T maps to NM_033033.3 V275V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3378-01A-01D-0966-08 chr1:153177407 C>A maps to NM_001010857.1 T75T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3378-01A-01D-0966-08 chr7:150034456 T>A maps to NM_023942.2 G169G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3378-01A-01D-0966-08 chrX:26212325 C>G maps to NM_173523.2 G121G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3378-01A-01D-0966-08 chr10:115389355 G>C maps to ENST00000369358 L685L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3378-01A-01D-0966-08 chr6:29079900 C>G maps to NM_001005216.2 T78T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3378-01A-01D-0966-08 chr6:51524030 A>G maps to NM_138694.3 Y3631Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3378-01A-01D-0966-08 chr15:90039694 C>T maps to NM_016321.1 G27G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3378-01A-01D-0966-08 chr1:55622656 C>T maps to NM_015306.2 L470L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3378-01A-01D-0966-08 chrX:47836771 T>C maps to NM_006962.1 A238A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3378-01A-01D-0966-08 chr3:44488852 G>A maps to NM_181489.5 A770A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3378-01A-01D-0966-08 chr19:57839654 G>A maps to NM_213598.3 R275R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3378-01A-01D-0966-08 chr1:16361915 G>A did not map to a codon.
Sequencing variant TCGA-A3-3378-01A-01D-0966-08 chr1:16361915 G>A did not map to a codon.
Sequencing variant TCGA-A3-3378-01A-01D-0966-08 chr14:25076507 A>C maps to NM_033423.3 G148G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3378-01A-01D-0966-08 chr14:25076507 A>C maps to NM_033423.3 G148G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3378-01A-01D-0966-08 chr17:56565200 G>T maps to NM_001080439.1 P145P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3378-01A-01D-0966-08 chr17:56565200 G>T maps to NM_001080439.1 P145P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3380-01A-01D-0966-08 chr16:89167562 G>A maps to NM_174917.2 P158P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3380-01A-01D-0966-08 chr6:71665631 C>T maps to NM_080742.2 L167L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3380-01A-01D-0966-08 chr11:73850648 C>T did not map to a codon.
Sequencing variant TCGA-A3-3380-01A-01D-0966-08 chr2:209104722 A>C maps to NM_005896.2 Y285*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3380-01A-01D-0966-08 chr8:57080031 G>T maps to NM_002655.2 T91T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3380-01A-01D-0966-08 chr17:49098648 T>C maps to ENST00000376407 T287T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3380-01A-01D-0966-08 chrX:153008981 C>T maps to NM_000033.3 G677G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3380-01A-01D-0966-08 chrX:153008981 C>T maps to NM_000033.3 G677G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3380-01A-01D-0966-08 chr18:72201785 G>A did not map to a codon.
Sequencing variant TCGA-A3-3380-01A-01D-0966-08 chr18:72201785 G>A did not map to a codon.
Sequencing variant TCGA-A3-3380-01A-01D-0966-08 chr5:140725627 C>G maps to NM_018916.3 G676G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3380-01A-01D-0966-08 chr5:140725627 C>G maps to NM_018916.3 G676G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3380-01A-01D-0966-08 chr16:2018622 C>A maps to NM_174903.4 G145G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3380-01A-01D-0966-08 chr16:2018622 C>A maps to NM_174903.4 G145G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3382-01A-01D-0966-08 chr12:56363266 C>A maps to NM_001798.3 T165T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3382-01A-01D-0966-08 chr5:156746795 G>A maps to ENST00000442283 Q461Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3382-01A-01D-0966-08 chr2:31484437 T>C maps to NM_014600.2 S313S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3382-01A-01D-0966-08 chr7:4796680 C>G maps to ENST00000450194 S347S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3382-01A-01D-0966-08 chr7:2274852 T>A maps to NM_013393.1 V215V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3382-01A-01D-0966-08 chr2:166611169 A>T maps to NM_004482.3 I531I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3382-01A-01D-0966-08 chr7:8126005 T>G maps to NM_138426.2 V494V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3382-01A-01D-0966-08 chr2:189458665 G>A did not map to a codon.
Sequencing variant TCGA-A3-3382-01A-01D-0966-08 chr15:59499175 A>T maps to NM_033195.1 R13*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3382-01A-01D-0966-08 chr20:3845152 C>T maps to NM_020746.3 N292N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3382-01A-01D-0966-08 chr17:29556074 G>A maps to NM_001042492.2 K814K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3382-01A-01D-0966-08 chr17:29687569 C>G maps to NM_001042492.2 Y2742*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3382-01A-01D-0966-08 chr1:248813489 C>T maps to NM_001001824.1 E232E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3382-01A-01D-0966-08 chr3:52662911 G>A maps to ENST00000296302 Q481*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3382-01A-01D-0966-08 chr1:144857633 C>T maps to NM_014644.4 T2140T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3382-01A-01D-0966-08 chr20:44531162 G>T maps to NM_006227.2 G341G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3382-01A-01D-0966-08 chr3:38797337 C>A maps to NM_006514.2 E468*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3382-01A-01D-0966-08 chr7:107329536 G>A maps to NM_000441.1 S347S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3382-01A-01D-0966-08 chr10:112335136 A>G maps to NM_005445.3 P58P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3382-01A-01D-0966-08 chr20:2448398 C>A maps to ENST00000339610 V3V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3382-01A-01D-0966-08 chr9:138586215 C>A maps to NM_001012415.2 G321G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3382-01A-01D-0966-08 chr2:96861118 C>T maps to NM_020151.3 W153*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3382-01A-01D-0966-08 chr11:118948938 C>T maps to NM_021729.4 A605A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3382-01A-01D-0966-08 chr4:85731356 C>G maps to NM_014991.4 V676V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3382-01A-01D-0966-08 chr6:87970889 C>T maps to NM_015021.1 Q2515*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3382-01A-01D-0966-08 chr1:34666596 C>T maps to NM_001134734.1 R412*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3382-01A-01D-0966-08 chr1:34666596 C>T maps to NM_001134734.1 R412*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3382-01A-01D-0966-08 chr6:159653886 G>T maps to NM_032532.2 A781A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3382-01A-01D-0966-08 chr6:159653886 G>T maps to NM_032532.2 A781A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3383-01A-01D-0966-08 chr6:101095126 C>A maps to NM_006828.2 L1151L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3383-01A-01D-0966-08 chr11:375648 C>T maps to NM_178537.4 A287A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3383-01A-01D-0966-08 chr15:40505654 G>A maps to ENST00000412359 R900R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3383-01A-01D-0966-08 chr16:4412075 G>T maps to NM_024535.3 T496T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3383-01A-01D-0966-08 chr10:74100573 C>T maps to NM_017626.4 R266R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3383-01A-01D-0966-08 chr10:87966298 G>C maps to NM_017551.2 L114L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3383-01A-01D-0966-08 chr4:7062875 G>A maps to NM_025196.2 Q123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3383-01A-01D-0966-08 chr19:11224381 G>A maps to NM_000527.4 T510T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3383-01A-01D-0966-08 chr4:1305933 C>T maps to ENST00000505177 S79S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3383-01A-01D-0966-08 chr17:10442758 A>G did not map to a codon.
Sequencing variant TCGA-A3-3383-01A-01D-0966-08 chr22:50954873 A>C did not map to a codon.
Sequencing variant TCGA-A3-3383-01A-01D-0966-08 chr6:17662259 T>C maps to ENST00000430136 E419E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3383-01A-01D-0966-08 chr3:47162161 G>A maps to NM_014159.6 R1322*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3383-01A-01D-0966-08 chr19:38573641 C>T maps to NM_015073.1 P479P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3383-01A-01D-0966-08 chr12:10783737 C>T maps to NM_018423.2 Q119Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3383-01A-01D-0966-08 chr2:27256956 C>A maps to NM_017727.4 T58T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3383-01A-01D-0966-08 chr2:106717552 C>A maps to ENST00000283148 V315V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3383-01A-01D-0966-08 chr3:10191487 C>T maps to NM_000551.2 R161*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3385-01A-02D-1421-08 chr1:155308159 G>C maps to ENST00000368346 R2846R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3385-01A-02D-1421-08 chr7:72892731 C>G maps to NM_032408.3 V353V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3385-01A-02D-1421-08 chr15:40628800 C>T maps to NM_207380.2 K331K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3385-01A-02D-1421-08 chr5:64933558 C>T maps to NM_001093755.1 I84I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3385-01A-02D-1421-08 chr12:100660754 G>A maps to ENST00000422147 L34L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3385-01A-02D-1421-08 chr6:105192485 C>A did not map to a codon.
Sequencing variant TCGA-A3-3385-01A-02D-1421-08 chr7:35678057 C>A maps to NM_022373.4 G173G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3385-01A-02D-1421-08 chr6:80203391 C>A maps to NM_181714.3 E266*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3385-01A-02D-1421-08 chrX:20081683 G>A maps to NM_001168465.1 Q74*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3385-01A-02D-1421-08 chr17:10447216 A>T did not map to a codon.
Sequencing variant TCGA-A3-3385-01A-02D-1421-08 chr5:37006526 G>A maps to NM_133433.3 A1308A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3385-01A-02D-1421-08 chr1:168269665 C>T maps to NM_005149.2 H224H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3385-01A-02D-1421-08 chr5:678107 G>T maps to NM_007030.2 S23*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3385-01A-02D-1421-08 chr2:64196096 T>A maps to NM_016516.2 V162V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3385-01A-02D-1421-08 chr22:20127298 C>A maps to NM_013373.3 R147R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3385-01A-02D-1421-08 chr19:37005750 A>G maps to NM_001166038.1 H130H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3385-01A-02D-1421-08 chr9:139396755 C>A maps to NM_017617.3 R1784R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3385-01A-02D-1421-08 chr9:139396755 C>A maps to NM_017617.3 R1784R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3385-01A-02D-1421-08 chr19:40900147 G>T maps to NM_181882.2 R1371R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3385-01A-02D-1421-08 chr19:40900147 G>T maps to NM_181882.2 R1371R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3444-01A-01D-0966-08 chr1:27097702 C>T maps to NM_006015.4 Q1098*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3444-01A-01D-0966-08 chr11:115102193 C>T maps to NM_014333.3 L147L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3444-01A-01D-0966-08 chr6:31084878 C>G maps to NM_001264.4 G171G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3444-01A-01D-0966-08 chr16:66976069 C>G maps to NM_003869.5 P464P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3444-01A-01D-0966-08 chr6:170627089 C>T maps to NM_032448.1 V204V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3444-01A-01D-0966-08 chr6:52943654 T>C maps to NM_012347.4 T132T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3444-01A-01D-0966-08 chr11:93779078 A>C maps to NM_001098672.1 S137S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3444-01A-01D-0966-08 chr7:4830218 C>T maps to ENST00000450194 S1356S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3444-01A-01D-0966-08 chr7:4830218 C>T maps to ENST00000450194 S1356S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3444-01A-01D-0966-08 chr9:34371723 C>T maps to NM_020702.3 V406V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3444-01A-01D-0966-08 chr10:103565868 C>T maps to NM_012215.3 V228V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3444-01A-01D-0966-08 chr11:6806984 C>T maps to NM_001004489.2 V239V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3444-01A-01D-0966-08 chr10:3151560 A>G maps to NM_002627.3 G326G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3444-01A-01D-0966-08 chr1:153303263 G>C maps to NM_020393.2 T367T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3444-01A-01D-0966-08 chr3:129324803 G>A maps to NM_015103.2 L227L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3444-01A-01D-0966-08 chr1:114394726 C>A did not map to a codon.
Sequencing variant TCGA-AK-3444-01A-01D-0966-08 chr6:150240944 G>A maps to NM_001001788.2 H31H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3444-01A-01D-0966-08 chr2:128757928 A>G maps to NM_001145928.1 S349S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3444-01A-01D-0966-08 chr15:41136787 C>T maps to NM_181642.2 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3444-01A-01D-0966-08 chr2:45832574 T>A maps to NM_018079.4 S2S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3444-01A-01D-0966-08 chr7:99801729 G>A maps to NM_012447.2 L929L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3444-01A-01D-0966-08 chr7:99801730 C>T maps to NM_012447.2 L930L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3444-01A-01D-0966-08 chr12:6442918 G>A maps to NM_001065.3 C102C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3444-01A-01D-0966-08 chr8:144403382 C>A maps to NM_052963.1 P378P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3444-01A-01D-0966-08 chr17:18188465 T>A maps to NM_004618.3 K623*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3444-01A-01D-0966-08 chr17:18188465 T>A maps to NM_004618.3 K623*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3444-01A-01D-0966-08 chr21:43529670 G>A did not map to a codon.
Sequencing variant TCGA-AK-3444-01A-01D-0966-08 chr11:56468429 C>T maps to NM_001013358.1 G189G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3444-01A-01D-0966-08 chr11:56468429 C>T maps to NM_001013358.1 G189G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3444-01A-01D-0966-08 chr3:10183724 C>A maps to NM_000551.2 S65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3444-01A-01D-0966-08 chr3:10183724 C>A maps to NM_000551.2 S65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3455-01A-01D-0966-08 chr18:24436384 T>A maps to NM_001650.4 P254P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3455-01A-01D-0966-08 chr7:120765872 G>T did not map to a codon.
Sequencing variant TCGA-AK-3455-01A-01D-0966-08 chr5:19747189 A>C maps to NM_004934.3 A128A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3455-01A-01D-0966-08 chr2:225637921 C>T maps to NM_014689.2 V2052V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3455-01A-01D-0966-08 chr15:27193283 C>A maps to NM_000810.3 I431I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3455-01A-01D-0966-08 chr11:2606465 C>T maps to NM_000218.2 L353L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3455-01A-01D-0966-08 chr19:9064630 G>A maps to NM_024690.2 P7605P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3455-01A-01D-0966-08 chr19:56473594 A>G maps to NM_176811.2 Q735Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3455-01A-01D-0966-08 chr22:24175873 C>T maps to NM_003073.3 Q368*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3455-01A-01D-0966-08 chr6:132910009 C>T maps to NM_003967.2 T272T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3455-01A-01D-0966-08 chr5:110407686 C>T maps to NM_033035.4 N33N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3455-01A-01D-0966-08 chr6:34826413 C>T maps to NM_017754.3 Q761*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3455-01A-01D-0966-08 chr6:153323723 G>A maps to NM_019041.5 L33L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3455-01A-01D-0966-08 chr6:153323723 G>A maps to NM_019041.5 L33L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AS-3778-01A-01D-0966-08 chr17:4804297 G>A maps to NM_000080.3 F263F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AS-3778-01A-01D-0966-08 chr2:80136836 C>A maps to ENST00000402739 R324R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AS-3778-01A-01D-0966-08 chr14:55625309 T>C maps to NM_014750.4 P601P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AS-3778-01A-01D-0966-08 chr14:102466736 G>A did not map to a codon.
Sequencing variant TCGA-AS-3778-01A-01D-0966-08 chr2:31484488 G>A maps to NM_014600.2 E330E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AS-3778-01A-01D-0966-08 chr17:7909784 T>A maps to NM_000180.3 A377A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AS-3778-01A-01D-0966-08 chr17:7909784 T>A maps to NM_000180.3 A377A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AS-3778-01A-01D-0966-08 chr1:226834968 G>A maps to NM_002221.3 Y715Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AS-3778-01A-01D-0966-08 chr12:53162497 C>T maps to NM_015848.4 *639*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AS-3778-01A-01D-0966-08 chr7:7636021 C>T maps to NM_019005.3 G777G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AS-3778-01A-01D-0966-08 chr12:117681126 C>T maps to ENST00000338101 V1013V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AS-3778-01A-01D-0966-08 chr16:71682849 A>G maps to NM_015020.2 P1305P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AS-3778-01A-01D-0966-08 chr16:71682849 A>G maps to NM_015020.2 P1305P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AS-3778-01A-01D-0966-08 chr22:21073054 G>C maps to NM_058004.2 S1666S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AS-3778-01A-01D-0966-08 chr3:50112705 C>T maps to NM_005777.2 G1063G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AS-3778-01A-01D-0966-08 chr19:39051931 G>A maps to NM_000540.2 P4154P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AS-3778-01A-01D-0966-08 chr12:125397186 G>A maps to NM_021009.5 L377L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AS-3778-01A-01D-0966-08 chr12:64827304 C>T maps to NM_007235.3 Q792*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AS-3778-01A-01D-0966-08 chr1:149871794 G>T maps to NM_016074.3 P61P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AS-3778-01A-01D-0966-08 chr1:149871794 G>T maps to NM_016074.3 P61P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AS-3778-01A-01D-0966-08 chr19:15164765 G>T maps to NM_012114.2 G134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AS-3778-01A-01D-0966-08 chr19:15164765 G>T maps to NM_012114.2 G134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AS-3778-01A-01D-0966-08 chr7:150693875 C>A maps to NM_000603.4 R149R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AS-3778-01A-01D-0966-08 chr7:150693875 C>A maps to NM_000603.4 R149R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AS-3778-01A-01D-0966-08 chr1:35836038 C>A maps to NM_005095.2 S331*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AS-3778-01A-01D-0966-08 chr1:35836038 C>A maps to NM_005095.2 S331*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4823-01A-02D-1421-08 chr12:9000254 C>A maps to NM_144670.3 V598V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4823-01A-02D-1421-08 chr2:27346839 C>G maps to NM_032604.3 P8P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4823-01A-02D-1421-08 chr5:132228041 C>T maps to NM_014423.3 G817G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4823-01A-02D-1421-08 chr14:105416510 G>C maps to NM_138420.2 P1759P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4823-01A-02D-1421-08 chr15:85360310 G>T maps to NM_020778.4 G78G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4823-01A-02D-1421-08 chr15:85360310 G>T maps to NM_020778.4 G78G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4823-01A-02D-1421-08 chr17:65909127 A>T maps to ENST00000321892 K1836*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4823-01A-02D-1421-08 chr7:89937152 C>T maps to NM_001039706.2 N845N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4823-01A-02D-1421-08 chr9:139722994 G>A maps to NM_001173988.1 Q121Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4823-01A-02D-1421-08 chr8:145540324 G>C maps to NM_012079.4 G453G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4823-01A-02D-1421-08 chr2:196753117 A>T maps to NM_018897.2 L1757*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4823-01A-02D-1421-08 chr20:31386265 G>T maps to NM_006892.3 R497R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4823-01A-02D-1421-08 chr1:36372682 C>T maps to NM_012199.2 L515L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4823-01A-02D-1421-08 chr14:74454757 A>G maps to NM_001249.2 C16C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4823-01A-02D-1421-08 chr6:131179362 C>T maps to NM_001431.3 R977R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4823-01A-02D-1421-08 chr10:5948165 T>C maps to NM_032807.3 S159S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4823-01A-02D-1421-08 chr5:153755894 T>G maps to NM_198321.3 L209L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4823-01A-02D-1421-08 chrX:48681370 G>A maps to ENST00000444343 K868K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4823-01A-02D-1421-08 chr12:52967396 C>A maps to NM_175053.3 G55G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4823-01A-02D-1421-08 chr12:96421287 A>G maps to NM_000895.1 A115A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4823-01A-02D-1421-08 chr7:79082435 C>A maps to NM_012301.3 L67L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4823-01A-02D-1421-08 chr9:140002044 C>T maps to NM_016219.3 R609R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4823-01A-02D-1421-08 chr20:33147237 G>T maps to NM_181509.1 E66*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4823-01A-02D-1421-08 chr3:168802757 C>T maps to NM_004991.3 W1220*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4823-01A-02D-1421-08 chr16:68283193 C>T maps to NM_012320.3 V43V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4823-01A-02D-1421-08 chr12:53837460 A>G maps to NM_018457.3 A102A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4823-01A-02D-1421-08 chr7:42964386 C>A maps to NM_002787.4 V87V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4823-01A-02D-1421-08 chr2:89036069 C>T maps to NM_144563.2 L205L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4823-01A-02D-1421-08 chr20:3677900 G>C maps to NM_023068.3 G737G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4823-01A-02D-1421-08 chr5:1073765 C>T maps to NM_006598.2 E741E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4823-01A-02D-1421-08 chr17:40476789 G>A maps to NM_139276.2 S513S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4823-01A-02D-1421-08 chr17:38243107 T>A did not map to a codon.
Sequencing variant TCGA-B0-4823-01A-02D-1421-08 chr6:123545247 C>T maps to NM_006073.2 K668K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4823-01A-02D-1421-08 chr2:179481862 G>T maps to NM_133378.4 T13385T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4823-01A-02D-1421-08 chr1:215820888 C>T maps to ENST00000366943 W4922*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4823-01A-02D-1421-08 chr2:225661098 T>C maps to NM_014689.2 G1624G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4823-01A-02D-1421-08 chr2:225661098 T>C maps to NM_014689.2 G1624G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4827-01A-02D-1421-08 chr7:91668039 C>G maps to NM_005751.4 S1549*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4827-01A-02D-1421-08 chr19:1807165 C>T did not map to a codon.
Sequencing variant TCGA-B0-4827-01A-02D-1421-08 chr10:93768665 T>G maps to NM_003972.2 T1298T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4827-01A-02D-1421-08 chr21:37518698 C>A maps to NM_001236.3 I241I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4827-01A-02D-1421-08 chr3:48474087 C>T maps to NM_024661.3 E322E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4827-01A-02D-1421-08 chr12:56121063 G>A maps to NM_001780.4 T42T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4827-01A-02D-1421-08 chr19:41594409 C>T maps to NM_000766.3 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4827-01A-02D-1421-08 chr9:127690520 G>A maps to NM_002077.3 A115A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4827-01A-02D-1421-08 chrX:83724058 T>C maps to NM_144657.4 P224P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4827-01A-02D-1421-08 chr2:8919169 G>T maps to NM_020738.2 R824R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4827-01A-02D-1421-08 chr2:234775438 T>A did not map to a codon.
Sequencing variant TCGA-B0-4827-01A-02D-1421-08 chr2:234775438 T>A did not map to a codon.
Sequencing variant TCGA-B0-4827-01A-02D-1421-08 chr12:109826582 C>T maps to NM_001101421.3 D20D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4827-01A-02D-1421-08 chr11:6897949 T>G maps to NM_207186.2 L24L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4827-01A-02D-1421-08 chr19:15839671 C>T maps to NM_013939.2 T273T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4827-01A-02D-1421-08 chr15:72542433 C>T did not map to a codon.
Sequencing variant TCGA-B0-4827-01A-02D-1421-08 chr20:39798839 C>T maps to NM_002660.2 A913A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4827-01A-02D-1421-08 chr19:39360339 G>C maps to NM_001195833.1 P449P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4827-01A-02D-1421-08 chr3:170185028 G>A maps to NM_020949.2 Y710Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4827-01A-02D-1421-08 chr16:30734515 C>T maps to NM_006662.2 L1375L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4827-01A-02D-1421-08 chrX:106092529 G>A maps to NM_198881.1 E631E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4827-01A-02D-1421-08 chr1:151751218 A>G maps to NM_001083965.1 S275S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4827-01A-02D-1421-08 chr17:73519836 C>G maps to NM_207346.2 P469P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4827-01A-02D-1421-08 chr12:53708551 A>T maps to NM_015665.5 R176R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4827-01A-02D-1421-08 chr12:53708551 A>T maps to NM_015665.5 R176R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4827-01A-02D-1421-08 chr17:39274414 C>T maps to NM_033059.3 R51R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4827-01A-02D-1421-08 chr17:39274414 C>T maps to NM_033059.3 R51R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4827-01A-02D-1421-08 chr20:62607108 C>T maps to NM_080621.4 V174V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4827-01A-02D-1421-08 chr20:62607108 C>T maps to NM_080621.4 V174V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4842-01A-02D-1421-08 chr8:107773579 G>A maps to NM_139166.4 T277T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4842-01A-02D-1421-08 chr8:107773582 G>A maps to NM_139166.4 S276S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4842-01A-02D-1421-08 chr3:52439305 A>C maps to NM_004656.2 G312G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4842-01A-02D-1421-08 chr1:205041695 A>C maps to NM_005076.3 R939R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4842-01A-02D-1421-08 chr19:1980182 C>A maps to NM_001319.6 S410*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4842-01A-02D-1421-08 chr5:41064634 G>T maps to ENST00000296803 L133L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4842-01A-02D-1421-08 chr17:80394585 C>T maps to NM_173620.2 Y225Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4842-01A-02D-1421-08 chr17:80394585 C>T maps to NM_173620.2 Y225Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4842-01A-02D-1421-08 chrX:153283527 G>A maps to NM_001569.3 Q280*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4842-01A-02D-1421-08 chr13:70681441 C>A maps to NM_020866.2 V130V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4842-01A-02D-1421-08 chr11:21250959 C>T maps to NM_006157.3 T503T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4842-01A-02D-1421-08 chr3:52620673 G>A maps to ENST00000296302 R1052*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4842-01A-02D-1421-08 chr2:1664725 G>A maps to NM_012293.1 D588D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4842-01A-02D-1421-08 chr2:54883107 G>T maps to NM_003128.2 E2007*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4842-01A-02D-1421-08 chr3:10191469 G>A did not map to a codon.
Sequencing variant TCGA-B0-4842-01A-02D-1421-08 chr3:10191469 G>A did not map to a codon.
Sequencing variant TCGA-B0-4945-01A-01D-1421-08 chr1:156821581 T>C did not map to a codon.
Sequencing variant TCGA-B0-4945-01A-01D-1421-08 chr10:126671766 G>A maps to NM_017580.2 T524T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4945-01A-01D-1421-08 chr10:51769498 C>T maps to NM_001077665.2 D538D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4945-01A-01D-1421-08 chr10:51769498 C>T maps to NM_001077665.2 D538D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4945-01A-01D-1421-08 chr1:226836373 T>C maps to NM_002221.3 A677A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4945-01A-01D-1421-08 chr1:226836373 T>C maps to NM_002221.3 A677A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4945-01A-01D-1421-08 chr3:143567236 G>T did not map to a codon.
Sequencing variant TCGA-B0-4945-01A-01D-1421-08 chr3:143567236 G>T did not map to a codon.
Sequencing variant TCGA-B0-4945-01A-01D-1421-08 chr19:1623967 C>T maps to NM_003200.2 P177P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4945-01A-01D-1421-08 chr19:1623967 C>T maps to NM_003200.2 P177P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5075-01A-01D-1462-08 chr17:63532472 G>T maps to NM_004655.3 R702R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5075-01A-01D-1462-08 chr12:27059271 T>A maps to NM_018164.2 R682*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5075-01A-01D-1462-08 chrX:110491969 G>A maps to NM_014289.3 H437H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5075-01A-01D-1462-08 chr18:25591823 G>A maps to NM_001792.3 Q178*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5075-01A-01D-1462-08 chr18:25591823 G>A maps to NM_001792.3 Q178*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5075-01A-01D-1462-08 chr16:30435759 G>A maps to NM_024096.1 L103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5075-01A-01D-1462-08 chr8:142178353 C>A maps to NM_014957.2 R589R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5075-01A-01D-1462-08 chr7:5541299 G>A maps to ENST00000312577 Y200Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5075-01A-01D-1462-08 chr7:5541299 G>A maps to ENST00000312577 Y200Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5075-01A-01D-1462-08 chr3:186364116 A>T maps to NM_014375.2 S225S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5075-01A-01D-1462-08 chr3:186364116 A>T maps to NM_014375.2 S225S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5075-01A-01D-1462-08 chr10:87407077 G>T maps to NM_017551.2 R692R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5075-01A-01D-1462-08 chr1:183197725 G>A maps to NM_005562.2 L562L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5075-01A-01D-1462-08 chr1:87805217 G>C did not map to a codon.
Sequencing variant TCGA-B0-5075-01A-01D-1462-08 chr19:9067240 G>T maps to NM_024690.2 I6735I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5075-01A-01D-1462-08 chr4:40122526 C>T maps to NM_018177.3 G932G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5075-01A-01D-1462-08 chr19:19313199 C>T maps to ENST00000420605 Q81Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5075-01A-01D-1462-08 chr19:10568585 C>T maps to NM_001111307.1 P303P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5075-01A-01D-1462-08 chr19:49362922 A>C maps to NM_020904.2 P165P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5075-01A-01D-1462-08 chr14:39511998 A>C maps to NM_006364.2 Y659*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5075-01A-01D-1462-08 chr9:136340533 G>A maps to NM_017585.3 N254N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5075-01A-01D-1462-08 chr3:17279708 G>A maps to NM_001134381.1 Q512*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5075-01A-01D-1462-08 chr10:98273268 G>A maps to NM_012465.3 A58A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5075-01A-01D-1462-08 chr19:12825696 C>T maps to NM_001136196.1 E276E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5075-01A-01D-1462-08 chr8:103341597 A>G maps to NM_015902.4 A376A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5075-01A-01D-1462-08 chr8:97244061 T>A maps to NM_006294.3 A66A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5075-01A-01D-1462-08 chr20:57766295 C>T maps to NM_178457.1 R74R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5075-01A-01D-1462-08 chr19:40376318 G>A maps to NM_003890.2 Y3995Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5075-01A-01D-1462-08 chr19:40376318 G>A maps to NM_003890.2 Y3995Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5075-01A-01D-1462-08 chr8:145096166 T>G maps to NM_198572.2 G447G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5075-01A-01D-1462-08 chr8:145096166 T>G maps to NM_198572.2 G447G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5075-01A-01D-1462-08 chr19:52942410 G>A maps to NM_001143939.1 A579A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5075-01A-01D-1462-08 chr19:52942410 G>A maps to NM_001143939.1 A579A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5077-01A-01D-1462-08 chr5:129015554 C>T maps to NM_133638.3 R863*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5077-01A-01D-1462-08 chr11:95564237 A>T maps to NM_014679.3 K441*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5077-01A-01D-1462-08 chr3:130287095 C>T maps to NM_001102608.1 S683S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5077-01A-01D-1462-08 chr8:145634428 G>C maps to NM_013291.2 L38L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5077-01A-01D-1462-08 chr5:176893973 C>A maps to ENST00000393565 R215R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5077-01A-01D-1462-08 chr14:94517731 C>A maps to NM_020414.3 L795L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5077-01A-01D-1462-08 chr7:154561187 C>T maps to NM_130797.2 Y315Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5077-01A-01D-1462-08 chr11:92590422 G>A maps to ENST00000298047 P3803P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5077-01A-01D-1462-08 chr6:25509936 C>T maps to NM_017640.5 N483N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5077-01A-01D-1462-08 chr6:25509936 C>T maps to NM_017640.5 N483N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5077-01A-01D-1462-08 chr12:78400325 C>G maps to NM_014903.4 S336S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5077-01A-01D-1462-08 chr7:99474476 A>G maps to NM_001005276.1 Y60Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5077-01A-01D-1462-08 chr9:136233528 G>A maps to NM_033161.2 S86S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5077-01A-01D-1462-08 chr8:9413532 G>T maps to NM_003747.2 P28P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5077-01A-01D-1462-08 chr5:180651529 T>A maps to NM_033549.3 P177P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5077-01A-01D-1462-08 chr9:15211316 C>T maps to NM_152574.2 Q187Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5077-01A-01D-1462-08 chr11:5537652 G>A maps to NM_145053.4 R7*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5077-01A-01D-1462-08 chr17:9559805 A>G maps to NM_153210.3 V197V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5077-01A-01D-1462-08 chr17:9559805 A>G maps to NM_153210.3 V197V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5081-01A-01D-1462-08 chr2:241631446 G>C maps to ENST00000429564 R39R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5081-01A-01D-1462-08 chr18:30795587 T>A maps to NM_001105528.1 I668I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5081-01A-01D-1462-08 chr4:184600618 T>C maps to NM_021942.4 H315H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5081-01A-01D-1462-08 chr4:184600618 T>C maps to NM_021942.4 H315H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5081-01A-01D-1462-08 chr3:48475151 A>G maps to NM_024661.3 L148L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5081-01A-01D-1462-08 chr16:67909956 T>A maps to NM_014329.3 T64T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5081-01A-01D-1462-08 chr5:136974756 G>A maps to NM_017415.2 D368D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5081-01A-01D-1462-08 chr5:136974756 G>A maps to NM_017415.2 D368D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5081-01A-01D-1462-08 chr15:23048906 C>G maps to NM_144599.4 G304G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5081-01A-01D-1462-08 chr3:47163944 G>T maps to NM_014159.6 C727*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5081-01A-01D-1462-08 chr5:94803694 T>C did not map to a codon.
Sequencing variant TCGA-B0-5081-01A-01D-1462-08 chr2:179395675 C>T maps to NM_133378.4 R32654R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5081-01A-01D-1462-08 chr1:216405368 T>C maps to ENST00000366943 Q973Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5081-01A-01D-1462-08 chr16:720685 G>A maps to NM_138769.1 A184A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5081-01A-01D-1462-08 chr16:720685 G>A maps to NM_138769.1 A184A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5081-01A-01D-1462-08 chr1:36553612 G>T maps to NM_014466.2 L373L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5081-01A-01D-1462-08 chr1:36553612 G>T maps to NM_014466.2 L373L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5085-01A-01D-1462-08 chr6:44270801 C>A did not map to a codon.
Sequencing variant TCGA-B0-5085-01A-01D-1462-08 chr3:141011819 G>T maps to NM_001037172.1 E406*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5085-01A-01D-1462-08 chr3:53908275 G>A maps to NM_022899.4 L343L. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-B0-5085-01A-01D-1462-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-B0-5085-01A-01D-1462-08 chr8:1728426 C>G maps to NM_018941.3 S185S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5085-01A-01D-1462-08 chr8:1728426 C>G maps to NM_018941.3 S185S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5085-01A-01D-1462-08 chr13:111102706 C>A maps to NM_001846.2 P415P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5085-01A-01D-1462-08 chr2:27716992 A>G maps to NM_022823.2 N86N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5085-01A-01D-1462-08 chr5:161520981 G>T maps to NM_198903.2 G86*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5085-01A-01D-1462-08 chr7:79764503 A>T maps to NM_002069.5 K10*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5085-01A-01D-1462-08 chr8:145066242 A>T maps to NM_001009184.1 A230A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5085-01A-01D-1462-08 chr8:76456145 A>G maps to NM_004133.4 A63A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5085-01A-01D-1462-08 chr11:17793894 T>C maps to NM_001112741.1 A418A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5085-01A-01D-1462-08 chr12:7023183 C>A maps to NM_006992.3 I296I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5085-01A-01D-1462-08 chr2:71351337 C>A maps to NM_032601.3 E126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5085-01A-01D-1462-08 chr11:5068544 C>T maps to NM_001001916.2 R264*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5085-01A-01D-1462-08 chr3:52643827 T>A maps to ENST00000296302 R690*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5085-01A-01D-1462-08 chr12:123488977 C>T maps to NM_020845.2 S337S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5085-01A-01D-1462-08 chr12:123488977 C>T maps to NM_020845.2 S337S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5085-01A-01D-1462-08 chr10:124742524 C>T maps to NM_153336.2 Q165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5085-01A-01D-1462-08 chr7:127975594 A>C did not map to a codon.
Sequencing variant TCGA-B0-5085-01A-01D-1462-08 chr1:20141318 G>C maps to NM_019062.1 P92P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5085-01A-01D-1462-08 chr6:117681073 T>C maps to NM_002944.2 R1182R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5085-01A-01D-1462-08 chr10:70141060 A>G maps to NM_017987.4 D380D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5085-01A-01D-1462-08 chr19:49129224 G>A maps to NM_020126.3 P39P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5085-01A-01D-1462-08 chr6:169648850 G>C maps to NM_003247.2 L90L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5085-01A-01D-1462-08 chr19:2422195 G>A maps to NM_182973.1 Q799Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5085-01A-01D-1462-08 chr5:145878249 G>A did not map to a codon.
Sequencing variant TCGA-B0-5085-01A-01D-1462-08 chr5:145878249 G>A did not map to a codon.
Sequencing variant TCGA-B0-5088-01A-01D-1462-08 chr12:21960402 G>A maps to NM_005691.2 V1442V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5088-01A-01D-1462-08 chr15:72848194 T>C maps to NM_005744.3 T228T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5088-01A-01D-1462-08 chr17:64875147 G>A maps to NM_014404.1 L85L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5088-01A-01D-1462-08 chr2:135711410 A>G maps to NM_058241.2 E462E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5088-01A-01D-1462-08 chr10:126683132 G>A maps to NM_022802.2 L769L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5088-01A-01D-1462-08 chr14:59113095 G>A maps to NM_016651.5 K585K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5088-01A-01D-1462-08 chr6:56399925 T>C maps to ENST00000361203 E5434E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5088-01A-01D-1462-08 chr3:128060617 G>T maps to NM_021937.3 R443R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5088-01A-01D-1462-08 chr20:37580731 C>T maps to NM_030919.2 Q473*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5088-01A-01D-1462-08 chr1:38059397 G>A maps to NM_013285.2 I38I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5088-01A-01D-1462-08 chr2:170371426 A>T maps to ENST00000419050 S382S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5088-01A-01D-1462-08 chr1:202777265 G>C maps to ENST00000367264 A56A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5088-01A-01D-1462-08 chr2:141773378 T>G maps to NM_018557.2 S692S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5088-01A-01D-1462-08 chr21:16338034 G>A maps to NM_003489.3 Q827*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5088-01A-01D-1462-08 chr3:97887842 A>G maps to NM_001005515.1 Q100Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5088-01A-01D-1462-08 chr2:179253840 C>G maps to ENST00000392505 T779T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5088-01A-01D-1462-08 chr5:140248768 G>A maps to NM_018902.3 G27G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5088-01A-01D-1462-08 chr8:145722669 C>T maps to NM_032902.5 A31A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5088-01A-01D-1462-08 chrX:38182652 G>A maps to NM_001034853.1 T51T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5088-01A-01D-1462-08 chrX:38182652 G>A maps to NM_001034853.1 T51T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5088-01A-01D-1462-08 chr21:34066597 A>T maps to NM_003895.3 V282V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5088-01A-01D-1462-08 chr7:99084909 T>C maps to NM_213603.2 H359H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5088-01A-01D-1462-08 chr4:20490576 G>A maps to ENST00000273739 E249E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5088-01A-01D-1462-08 chr4:20490576 G>A maps to ENST00000273739 E249E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5092-01A-01D-1421-08 chr17:48538730 G>C maps to ENST00000427954 L176L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5092-01A-01D-1421-08 chr3:52440294 G>A maps to NM_004656.2 Q253*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5092-01A-01D-1421-08 chr2:32640715 C>A maps to NM_016252.3 S786*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5092-01A-01D-1421-08 chr13:49852532 C>T maps to NM_030911.3 Y366Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5092-01A-01D-1421-08 chr11:118656897 C>T maps to NM_004397.4 L21L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5092-01A-01D-1421-08 chr1:97564119 C>T maps to NM_000110.3 L897L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5092-01A-01D-1421-08 chr4:126398471 A>G maps to NM_024582.4 A4152A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5092-01A-01D-1421-08 chr22:45929740 G>A maps to ENST00000348697 G249G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5092-01A-01D-1421-08 chr19:33608750 C>T maps to NM_018025.2 D739D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5092-01A-01D-1421-08 chr11:33363110 A>G maps to NM_005734.3 A592A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5092-01A-01D-1421-08 chr12:54893216 A>T maps to NM_005337.4 K61*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5092-01A-01D-1421-08 chr12:76424987 C>T maps to NM_007350.3 G178G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5092-01A-01D-1421-08 chr8:10468847 C>T maps to NM_178857.5 R920R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5092-01A-01D-1421-08 chr1:169565277 A>G maps to NM_003005.3 F662F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5092-01A-01D-1421-08 chr4:7533340 G>T maps to NM_020777.2 P211P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5092-01A-01D-1421-08 chr17:30302575 A>T maps to NM_015355.2 K223*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5092-01A-01D-1421-08 chr22:42605745 C>A maps to NM_005650.1 E1856*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5092-01A-01D-1421-08 chr22:42605745 C>A maps to NM_005650.1 E1856*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5092-01A-01D-1421-08 chr17:7579395 G>A maps to NM_001126112.1 V97V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5092-01A-01D-1421-08 chr2:128927879 G>T maps to NM_020120.3 P980P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5092-01A-01D-1421-08 chr8:38125964 G>C maps to NM_001102559.1 L66L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5092-01A-01D-1421-08 chr8:38125964 G>C maps to NM_001102559.1 L66L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5092-01A-01D-1421-08 chr7:116870008 G>A maps to ENST00000446490 G510G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5092-01A-01D-1421-08 chr7:116870008 G>A maps to ENST00000446490 G510G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5094-01A-01D-1421-08 chr9:116840414 C>T maps to NM_001633.3 P25P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5094-01A-01D-1421-08 chr16:28847660 A>T maps to NM_148414.1 R1052*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5094-01A-01D-1421-08 chr10:96967147 G>A maps to NM_207321.2 W196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5094-01A-01D-1421-08 chr1:169391257 A>G maps to ENST00000367806 L137L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5094-01A-01D-1421-08 chr11:47611594 G>C maps to NM_031909.2 A256A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5094-01A-01D-1421-08 chr7:90355878 A>T did not map to a codon.
Sequencing variant TCGA-B0-5094-01A-01D-1421-08 chr7:24758692 G>A maps to NM_001127453.1 I183I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5094-01A-01D-1421-08 chr6:56484744 C>A maps to ENST00000281662 E1927*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5094-01A-01D-1421-08 chr19:18499471 G>T maps to NM_004864.2 A218A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5094-01A-01D-1421-08 chrX:53227795 C>A maps to NM_004187.3 E798*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5094-01A-01D-1421-08 chr12:81239637 A>T maps to NM_004664.2 L118L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5094-01A-01D-1421-08 chr11:47283270 G>C maps to NM_005693.2 A294A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5094-01A-01D-1421-08 chr11:199996 T>C maps to NM_053280.3 S243S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5094-01A-01D-1421-08 chr2:242063381 G>C maps to ENST00000358649 T962T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5094-01A-01D-1421-08 chr1:210412916 G>A maps to NM_019605.3 E85E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5094-01A-01D-1421-08 chr11:61295624 G>A maps to NM_004200.2 H128H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5094-01A-01D-1421-08 chr15:41194908 G>T maps to NM_020857.2 V764V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5094-01A-01D-1421-08 chr3:166958708 T>A did not map to a codon.
Sequencing variant TCGA-B0-5094-01A-01D-1421-08 chr11:121016493 G>T maps to NM_005422.2 L1258L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5094-01A-01D-1421-08 chr11:121016493 G>T maps to NM_005422.2 L1258L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5095-01A-01D-1421-08 chr18:55319398 G>A maps to NM_005603.4 G1089G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5095-01A-01D-1421-08 chr3:52437781 G>C maps to NM_004656.2 S460*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5095-01A-01D-1421-08 chr8:22037968 G>A maps to NM_006129.4 W350*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5095-01A-01D-1421-08 chr19:40827908 G>T maps to ENST00000357884 V383V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5095-01A-01D-1421-08 chr16:61851426 C>A maps to NM_001796.2 G411G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5095-01A-01D-1421-08 chr4:184367367 G>C maps to NM_017632.2 T177T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5095-01A-01D-1421-08 chr3:121591510 C>A maps to NM_018456.4 S204S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5095-01A-01D-1421-08 chr10:13699458 G>A maps to NM_018027.3 S710S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5095-01A-01D-1421-08 chr5:161302566 C>T maps to NM_001127648.1 L160L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5095-01A-01D-1421-08 chrX:69622532 T>C maps to NM_012310.4 Y869Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5095-01A-01D-1421-08 chr18:2616500 C>T maps to NM_006101.2 L619L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5095-01A-01D-1421-08 chr5:142779612 A>C maps to NM_001024094.1 V264V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5095-01A-01D-1421-08 chr1:248059808 G>A maps to NM_001001957.2 G307G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5095-01A-01D-1421-08 chr12:54962994 G>A maps to NM_000924.3 L85L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5095-01A-01D-1421-08 chr10:98312747 A>T maps to NM_020123.3 I243I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5095-01A-01D-1421-08 chr3:10191469 G>C did not map to a codon.
Sequencing variant TCGA-B0-5095-01A-01D-1421-08 chr3:10191469 G>C did not map to a codon.
Sequencing variant TCGA-B0-5095-01A-01D-1421-08 chr10:31134378 T>C maps to NM_182755.2 L666L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5095-01A-01D-1421-08 chr19:12256408 C>T maps to ENST00000439556 P276P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5095-01A-01D-1421-08 chr11:75160646 C>T maps to NM_030792.6 A161A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5095-01A-01D-1421-08 chr11:75160646 C>T maps to NM_030792.6 A161A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5095-01A-01D-1421-08 chr6:46656687 G>T maps to NM_001010870.2 E275*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5095-01A-01D-1421-08 chr6:46656687 G>T maps to NM_001010870.2 E275*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5096-01A-01D-1421-08 chr4:89016749 A>G maps to NM_004827.2 G553G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5096-01A-01D-1421-08 chr15:30919055 G>T maps to NM_001039841.1 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5096-01A-01D-1421-08 chr8:37967895 G>T did not map to a codon.
Sequencing variant TCGA-B0-5096-01A-01D-1421-08 chrX:119509281 C>T maps to NM_001142447.2 Y206Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5096-01A-01D-1421-08 chr16:56535340 G>A maps to NM_031885.3 L383L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5096-01A-01D-1421-08 chr7:116533093 A>T maps to NM_006136.2 A50A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5096-01A-01D-1421-08 chr22:39262465 C>T maps to NM_014292.3 P329P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5096-01A-01D-1421-08 chr16:2506612 G>A maps to NM_001761.2 Q651Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5096-01A-01D-1421-08 chr4:77969662 G>T maps to NM_006835.2 P281P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5096-01A-01D-1421-08 chr4:77969662 G>T maps to NM_006835.2 P281P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5096-01A-01D-1421-08 chr18:34855138 G>A maps to NM_020180.3 F172F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5096-01A-01D-1421-08 chr15:57836714 C>G maps to NM_032866.3 Y1140*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5096-01A-01D-1421-08 chrX:107935976 G>T did not map to a codon.
Sequencing variant TCGA-B0-5096-01A-01D-1421-08 chr11:61188975 A>C maps to NM_024811.3 P96P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5096-01A-01D-1421-08 chr17:48050512 G>C maps to NM_138281.2 P120P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5096-01A-01D-1421-08 chr3:132245125 G>A did not map to a codon.
Sequencing variant TCGA-B0-5096-01A-01D-1421-08 chr1:167095900 A>C maps to NM_001080426.1 A511A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5096-01A-01D-1421-08 chr19:6896424 C>T maps to ENST00000381407 D37D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5096-01A-01D-1421-08 chr3:150421526 C>T maps to NM_152394.3 E53E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5096-01A-01D-1421-08 chr19:1398923 G>A maps to NM_138924.1 I187I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5096-01A-01D-1421-08 chr1:110129421 C>T maps to NM_006496.2 I264I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5096-01A-01D-1421-08 chr7:107596065 A>G maps to NM_002291.2 A900A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5096-01A-01D-1421-08 chr1:209799285 C>T maps to NM_000228.2 G561G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5096-01A-01D-1421-08 chr5:145557189 C>T maps to NM_020117.9 K15K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5096-01A-01D-1421-08 chr8:20107280 C>T maps to NM_021020.2 L581L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5096-01A-01D-1421-08 chr11:30557622 A>T maps to NM_001584.2 P76P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5096-01A-01D-1421-08 chr1:41218905 T>G maps to ENST00000308733 P125P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5096-01A-01D-1421-08 chr6:32170157 C>T maps to NM_004557.3 T1150T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5096-01A-01D-1421-08 chr3:193355796 C>G maps to NM_130837.2 A364A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5096-01A-01D-1421-08 chr20:1961112 A>T maps to NM_024411.4 Y207*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5096-01A-01D-1421-08 chr19:57327460 G>T maps to NM_006210.2 A783A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5096-01A-01D-1421-08 chr2:114512804 A>C maps to NM_025181.2 A70A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5096-01A-01D-1421-08 chr2:196545177 G>T maps to NM_001127257.1 E138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5096-01A-01D-1421-08 chr6:7605679 G>A maps to NM_152551.3 W256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5096-01A-01D-1421-08 chr15:43748160 G>C maps to NM_001141980.1 S882*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5096-01A-01D-1421-08 chr2:179587902 G>A maps to NM_133378.4 N6033N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5096-01A-01D-1421-08 chr2:234431844 A>G maps to NM_018218.2 I735I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5096-01A-01D-1421-08 chr6:30884693 T>C maps to NM_001167734.1 G267G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5096-01A-01D-1421-08 chr3:10188196 G>T did not map to a codon.
Sequencing variant TCGA-B0-5096-01A-01D-1421-08 chr7:129666109 C>A maps to NM_016478.3 E222*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5096-01A-01D-1421-08 chr1:247322363 G>A maps to NM_003431.2 N54N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5096-01A-01D-1421-08 chrX:120009344 G>T maps to NM_001145718.1 G60G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5096-01A-01D-1421-08 chrX:120009344 G>T maps to NM_001145718.1 G60G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5096-01A-01D-1421-08 chr10:8051124 G>T maps to NM_031923.2 A800A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5096-01A-01D-1421-08 chr10:8051124 G>T maps to NM_031923.2 A800A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5097-01A-01D-1421-08 chr9:116154421 G>T maps to ENST00000277315 I56I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5097-01A-01D-1421-08 chrX:55039930 C>A maps to NM_000032.4 E530*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5097-01A-01D-1421-08 chr2:73677724 T>A maps to NM_015120.4 A1356A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5097-01A-01D-1421-08 chr2:96789863 C>A maps to NM_001002036.3 E341*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5097-01A-01D-1421-08 chr11:108202713 A>T maps to NM_000051.3 R2580*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5097-01A-01D-1421-08 chr4:56314943 A>G did not map to a codon.
Sequencing variant TCGA-B0-5097-01A-01D-1421-08 chr4:56314943 A>G did not map to a codon.
Sequencing variant TCGA-B0-5097-01A-01D-1421-08 chr13:40268841 A>G maps to ENST00000255468 K415K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5097-01A-01D-1421-08 chr14:76045407 C>A maps to NM_017791.2 P31P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5097-01A-01D-1421-08 chr1:94370099 T>C maps to NM_002061.2 Q57Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5097-01A-01D-1421-08 chr20:23347702 C>T maps to NM_022482.3 H476H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5097-01A-01D-1421-08 chr1:166962001 C>T maps to NM_032858.1 L135L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5097-01A-01D-1421-08 chr3:184082990 C>T maps to NM_006232.2 N76N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5097-01A-01D-1421-08 chr9:113241932 C>T maps to ENST00000374463 E823E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5097-01A-01D-1421-08 chr4:68719844 G>A maps to NM_004262.2 Q64*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5097-01A-01D-1421-08 chr5:176402396 G>A maps to ENST00000377219 Q78*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5097-01A-01D-1421-08 chr3:10183752 C>T maps to NM_000551.2 V74V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5097-01A-01D-1421-08 chr1:241875160 G>A maps to NM_144625.4 K334K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5097-01A-01D-1421-08 chr7:99170285 G>A maps to NM_001083956.1 Q220Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5099-01A-01D-1421-08 chr1:159161759 G>A maps to NM_021189.3 V75V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5099-01A-01D-1421-08 chr10:50690812 A>G maps to NM_000124.2 L697L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5099-01A-01D-1421-08 chr2:187559049 A>G maps to NM_177454.3 Q50Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5099-01A-01D-1421-08 chr9:79117315 C>T maps to NM_001097636.1 R7*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5099-01A-01D-1421-08 chr19:35540221 A>G maps to NM_182983.2 R15R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5099-01A-01D-1421-08 chr19:35540221 A>G maps to NM_182983.2 R15R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5099-01A-01D-1421-08 chr11:122930261 G>A maps to NM_006597.3 Q347*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5099-01A-01D-1421-08 chr8:19687915 G>C did not map to a codon.
Sequencing variant TCGA-B0-5099-01A-01D-1421-08 chr7:151877174 G>A maps to ENST00000355193 Q2396*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5099-01A-01D-1421-08 chr15:73575303 G>A did not map to a codon.
Sequencing variant TCGA-B0-5099-01A-01D-1421-08 chr5:131543564 G>A maps to NM_001142599.1 Q306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5099-01A-01D-1421-08 chr5:34757613 C>G maps to NM_001145521.1 A26A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5099-01A-01D-1421-08 chr1:100575994 A>G maps to NM_194292.1 D238D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5099-01A-01D-1421-08 chr22:43625096 G>A maps to NM_173050.2 Y355Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5099-01A-01D-1421-08 chr15:49284863 A>C maps to NM_001193489.1 T961T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5099-01A-01D-1421-08 chr17:17769631 G>T maps to NM_001082968.1 L354L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5099-01A-01D-1421-08 chr17:17769631 G>T maps to NM_001082968.1 L354L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5099-01A-01D-1421-08 chr1:160385971 G>C maps to NM_020335.2 R64R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5099-01A-01D-1421-08 chr19:52942410 G>A maps to NM_001143939.1 A579A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5099-01A-01D-1421-08 chr19:52942410 G>A maps to NM_001143939.1 A579A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5100-01A-01D-1421-08 chr1:159557957 G>A maps to NM_001639.3 P44P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5100-01A-01D-1421-08 chr5:133747410 C>A maps to NM_080656.2 L45L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5100-01A-01D-1421-08 chr3:51198059 C>T maps to NM_004947.4 L322L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5100-01A-01D-1421-08 chr17:39334329 G>T maps to ENST00000458321 T146T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5100-01A-01D-1421-08 chr7:150698929 G>A maps to NM_000603.4 S508S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5100-01A-01D-1421-08 chr5:140563510 C>T maps to NM_020957.1 F459F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5100-01A-01D-1421-08 chr7:98639740 G>C maps to NM_020429.2 P483P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5100-01A-01D-1421-08 chr10:96291126 A>G maps to NM_015188.1 L723L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5100-01A-01D-1421-08 chr10:12071444 G>A maps to NM_015542.2 N148N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5100-01A-01D-1421-08 chr16:72821620 G>A maps to NM_006885.3 G3518G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5100-01A-01D-1421-08 chr7:100867048 A>T maps to NM_006349.2 P123P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5100-01A-01D-1421-08 chr19:58385761 C>G maps to NM_001144989.1 S332S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5100-01A-01D-1421-08 chr19:58385761 C>G maps to NM_001144989.1 S332S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5102-01A-01D-1421-08 chr5:125891621 C>T did not map to a codon.
Sequencing variant TCGA-B0-5102-01A-01D-1421-08 chr12:110720426 G>C did not map to a codon.
Sequencing variant TCGA-B0-5102-01A-01D-1421-08 chr12:110720426 G>C did not map to a codon.
Sequencing variant TCGA-B0-5102-01A-01D-1421-08 chrX:76813065 C>T maps to NM_000489.3 L2185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5102-01A-01D-1421-08 chr15:45398797 G>A maps to NM_014080.4 R625*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5102-01A-01D-1421-08 chr16:70884502 A>G maps to NM_032821.2 L4166L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5102-01A-01D-1421-08 chr11:4510759 G>A maps to NM_001005171.2 V210V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5102-01A-01D-1421-08 chr13:67800363 G>A maps to NM_203487.2 L737L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5102-01A-01D-1421-08 chr5:140202182 G>T maps to NM_018908.2 E275*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5102-01A-01D-1421-08 chr5:140347847 G>A maps to NM_018899.5 K499K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5102-01A-01D-1421-08 chr6:76421099 A>T maps to NM_015571.2 G959G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5102-01A-01D-1421-08 chr3:164905804 C>G maps to NM_014926.2 S938S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5102-01A-01D-1421-08 chr14:65289683 G>A maps to ENST00000389723 S47S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5102-01A-01D-1421-08 chr3:10183724 C>A maps to NM_000551.2 S65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5102-01A-01D-1421-08 chr3:10183724 C>A maps to NM_000551.2 S65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5104-01A-01D-1421-08 chr2:215818762 G>A maps to NM_173076.2 Y2154Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5104-01A-01D-1421-08 chr2:32673958 C>A maps to NM_016252.3 V1527V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5104-01A-01D-1421-08 chr5:40852477 G>A maps to NM_032587.3 K348K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5104-01A-01D-1421-08 chr8:19297428 C>A maps to NM_018371.4 E289*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5104-01A-01D-1421-08 chr8:113358404 C>A maps to NM_198123.1 V2121V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5104-01A-01D-1421-08 chr14:59112840 C>T maps to NM_016651.5 N500N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5104-01A-01D-1421-08 chr2:136678171 T>C did not map to a codon.
Sequencing variant TCGA-B0-5104-01A-01D-1421-08 chr14:24424291 G>T maps to NM_021004.2 V59V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5104-01A-01D-1421-08 chr11:111915860 G>A did not map to a codon.
Sequencing variant TCGA-B0-5104-01A-01D-1421-08 chr10:50732230 C>T maps to ENST00000515869 K415K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5104-01A-01D-1421-08 chr19:3586519 A>T maps to NM_133261.2 K85*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5104-01A-01D-1421-08 chr4:88303418 G>A maps to NM_016245.3 S102S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5104-01A-01D-1421-08 chr2:74725149 C>T maps to NM_001009812.1 L163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5104-01A-01D-1421-08 chr17:10225009 C>A maps to NM_003802.2 E984*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5104-01A-01D-1421-08 chrX:67273542 C>T maps to NM_002547.2 K756K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5104-01A-01D-1421-08 chr3:57542939 T>C maps to NM_177966.5 T278T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5104-01A-01D-1421-08 chr12:100704844 G>A maps to NM_017988.4 L168L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5104-01A-01D-1421-08 chr12:113865885 T>A maps to NM_138432.2 P33P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5104-01A-01D-1421-08 chr22:38476982 G>A maps to NM_013356.2 G354G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5104-01A-01D-1421-08 chr19:10475697 G>A maps to NM_003331.4 N346N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5104-01A-01D-1421-08 chr16:4924864 G>A maps to NM_016936.3 T818T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5104-01A-01D-1421-08 chr11:6977425 C>A maps to NM_013250.2 P406P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5104-01A-01D-1421-08 chr11:6977425 C>A maps to NM_013250.2 P406P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5104-01A-01D-1421-08 chr2:233246012 C>A maps to NM_001632.3 Y415*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5104-01A-01D-1421-08 chr2:233246012 C>A maps to NM_001632.3 Y415*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5104-01A-01D-1421-08 chr17:34093632 G>A maps to NM_024302.3 D482D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5104-01A-01D-1421-08 chr17:34093632 G>A maps to NM_024302.3 D482D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5104-01A-01D-1421-08 chr14:90730103 T>G maps to NM_002802.2 S126S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5104-01A-01D-1421-08 chr14:90730103 T>G maps to NM_002802.2 S126S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5106-01A-01D-1421-08 chr6:151670458 C>A maps to NM_005100.3 T311T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5106-01A-01D-1421-08 chr1:170965677 G>T maps to NM_001163629.1 L456L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5106-01A-01D-1421-08 chr20:61167748 G>A maps to NM_178463.3 Q73Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5106-01A-01D-1421-08 chr20:20123552 G>A maps to ENST00000389655 L304L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5106-01A-01D-1421-08 chr20:20123552 G>A maps to ENST00000389655 L304L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5106-01A-01D-1421-08 chr19:13325350 G>A maps to NM_023035.2 Q1939*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5106-01A-01D-1421-08 chr15:78565449 A>G maps to NM_018602.3 V138V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5106-01A-01D-1421-08 chr18:34192013 A>T maps to NM_025135.2 K305*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5106-01A-01D-1421-08 chr1:53972294 G>T maps to NM_147193.2 T620T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5106-01A-01D-1421-08 chr11:122931840 G>A maps to NM_006597.3 T64T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5106-01A-01D-1421-08 chr4:3138011 A>G maps to NM_002111.6 E919E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5106-01A-01D-1421-08 chr11:1264223 C>A maps to ENST00000447027 T2041T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5106-01A-01D-1421-08 chr21:42778675 G>A maps to NM_002463.1 T552T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5106-01A-01D-1421-08 chr15:23932262 C>T maps to NM_002487.2 P34P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5106-01A-01D-1421-08 chr17:2995984 G>T maps to NM_002548.2 Y102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5106-01A-01D-1421-08 chr6:13206173 G>A maps to NM_030948.1 Q264Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5106-01A-01D-1421-08 chr5:133887863 T>C maps to ENST00000448712 P108P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5106-01A-01D-1421-08 chr8:110530495 T>A maps to ENST00000426474 V3931V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5106-01A-01D-1421-08 chr17:40765979 C>T maps to NM_001070.4 L269L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5106-01A-01D-1421-08 chr19:10468694 G>A maps to NM_003331.4 G765G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5106-01A-01D-1421-08 chr2:234526874 C>A maps to NM_019076.4 C174*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5106-01A-01D-1421-08 chr3:10183866 C>A maps to NM_000551.2 Y112*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5106-01A-01D-1421-08 chr11:102100587 T>C maps to NM_001130145.2 L478L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5106-01A-01D-1421-08 chr11:130131042 A>T maps to ENST00000397753 P242P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5106-01A-01D-1421-08 chr6:160218316 A>C did not map to a codon.
Sequencing variant TCGA-B0-5106-01A-01D-1421-08 chr6:160218316 A>C did not map to a codon.
Sequencing variant TCGA-B0-5106-01A-01D-1421-08 chr5:140794505 C>T maps to NM_018913.2 P588P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5106-01A-01D-1421-08 chr5:140794505 C>T maps to NM_018913.2 P588P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5106-01A-01D-1421-08 chr8:145004391 G>A maps to NM_201380.2 S981S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5106-01A-01D-1421-08 chr8:145004391 G>A maps to NM_201380.2 S981S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5107-01A-01D-1421-08 chr7:134222409 C>T maps to NM_020299.4 A246A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5107-01A-01D-1421-08 chr17:21147502 G>A maps to NM_152914.2 Y46Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5107-01A-01D-1421-08 chr6:157744465 A>G maps to NM_018452.4 N22N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5107-01A-01D-1421-08 chr14:24774972 T>C did not map to a codon.
Sequencing variant TCGA-B0-5107-01A-01D-1421-08 chr17:1326914 A>G maps to NM_016823.2 I269I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5107-01A-01D-1421-08 chr1:161677074 C>A maps to NM_001184866.1 L24L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5107-01A-01D-1421-08 chr18:7026066 C>T maps to NM_005559.2 Q771Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5107-01A-01D-1421-08 chr13:36049372 G>A maps to NM_005584.4 N301N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5107-01A-01D-1421-08 chr13:36049372 G>A maps to NM_005584.4 N301N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5107-01A-01D-1421-08 chr1:224491541 G>A maps to NM_002533.2 L281L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5107-01A-01D-1421-08 chr3:52676062 T>A did not map to a codon.
Sequencing variant TCGA-B0-5107-01A-01D-1421-08 chrX:18836211 C>T maps to NM_006240.2 R484*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5107-01A-01D-1421-08 chr8:48694797 C>T maps to NM_006904.6 W3804*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5107-01A-01D-1421-08 chr19:33493760 A>G maps to NM_033103.4 N302N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5107-01A-01D-1421-08 chr1:38079541 C>T maps to NM_001038633.2 W153*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5107-01A-01D-1421-08 chr9:2116049 G>A did not map to a codon.
Sequencing variant TCGA-B0-5107-01A-01D-1421-08 chr9:120475389 T>C maps to NM_138554.3 Y328Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5107-01A-01D-1421-08 chr1:52492990 C>A maps to NM_015913.2 E81*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5107-01A-01D-1421-08 chr1:52492990 C>A maps to NM_015913.2 E81*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5107-01A-01D-1421-08 chr19:57640817 G>T maps to NM_020903.2 E259*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5107-01A-01D-1421-08 chr10:1149774 A>C maps to ENST00000416775 T321T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5107-01A-01D-1421-08 chr11:1268528 G>A maps to ENST00000447027 S3476S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5107-01A-01D-1421-08 chr11:1268528 G>A maps to ENST00000447027 S3476S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5108-01A-01D-1421-08 chr12:112650434 G>C maps to NM_001109662.2 G2323G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5108-01A-01D-1421-08 chr11:35208448 T>A did not map to a codon.
Sequencing variant TCGA-B0-5108-01A-01D-1421-08 chr5:122685708 A>T maps to NM_153223.3 L885L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5108-01A-01D-1421-08 chr6:54791200 T>C maps to NM_001010872.1 D159D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5108-01A-01D-1421-08 chr3:58128450 G>A maps to NM_001164317.1 P1783P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5108-01A-01D-1421-08 chr5:179047902 C>T maps to NM_005520.2 Q129Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5108-01A-01D-1421-08 chr11:133802055 G>T maps to NM_014987.1 I340I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5108-01A-01D-1421-08 chr12:49420871 G>C maps to NM_003482.3 A4959A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5108-01A-01D-1421-08 chr12:14656714 A>G maps to NM_024829.5 D551D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5108-01A-01D-1421-08 chr20:9374305 G>T maps to NM_001172646.1 L465L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5108-01A-01D-1421-08 chr2:219487601 G>C did not map to a codon.
Sequencing variant TCGA-B0-5108-01A-01D-1421-08 chr14:24731315 G>A maps to NM_000359.2 G81G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5108-01A-01D-1421-08 chr19:35175868 A>G maps to ENST00000221282 Q388Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5108-01A-01D-1421-08 chr1:104160100 C>A maps to NM_000699.2 C13*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5108-01A-01D-1421-08 chr1:104160100 C>A maps to NM_000699.2 C13*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5108-01A-01D-1421-08 chr2:98201806 C>T maps to NM_025190.3 L72L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5108-01A-01D-1421-08 chr2:98201806 C>T maps to NM_025190.3 L72L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5108-01A-01D-1421-08 chr6:56394512 G>T maps to ENST00000361203 G5565G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5108-01A-01D-1421-08 chr6:56394512 G>T maps to ENST00000361203 G5565G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5109-01A-02D-1421-08 chr14:58831551 A>C maps to NM_002892.3 I915I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5109-01A-02D-1421-08 chr4:1804695 C>A maps to NM_001163213.1 S329*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5109-01A-02D-1421-08 chr11:68125160 C>A maps to NM_002335.2 R178R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5109-01A-02D-1421-08 chr12:91502696 G>C maps to NM_002345.3 Y20*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5109-01A-02D-1421-08 chr7:7635994 G>T maps to NM_019005.3 T768T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5109-01A-02D-1421-08 chr3:132416206 C>A did not map to a codon.
Sequencing variant TCGA-B0-5109-01A-02D-1421-08 chr5:140750549 A>T maps to NM_018924.2 K197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5109-01A-02D-1421-08 chr1:151288135 G>A maps to NM_002651.2 R286R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5109-01A-02D-1421-08 chr7:131194327 C>T maps to NM_001018111.2 S273S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5109-01A-02D-1421-08 chr3:170585833 G>T maps to NM_001099645.1 I64I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5109-01A-02D-1421-08 chr3:170585833 G>T maps to NM_001099645.1 I64I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5109-01A-02D-1421-08 chr21:43897416 G>A maps to NM_080860.2 D237D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5109-01A-02D-1421-08 chr18:33689576 G>A maps to NM_012319.3 I749I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5109-01A-02D-1421-08 chr22:38151616 G>T maps to NM_001039141.2 E1880*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5109-01A-02D-1421-08 chr1:247202839 C>T did not map to a codon.
Multiple mappings detected for codon TCGA-B0-5109-01A-02D-1421-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-B0-5109-01A-02D-1421-08 chr7:50467715 C>T maps to NM_006060.3 N317N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5109-01A-02D-1421-08 chr7:50467715 C>T maps to NM_006060.3 N317N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5110-01A-01D-1421-08 chr10:111877146 C>T maps to NM_016824.3 G178G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5110-01A-01D-1421-08 chr17:7385620 C>T maps to NM_001102614.1 F106F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5110-01A-01D-1421-08 chr12:121758186 C>A did not map to a codon.
Sequencing variant TCGA-B0-5110-01A-01D-1421-08 chr17:37333728 C>T maps to NM_000723.3 A402A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5110-01A-01D-1421-08 chr6:100009546 T>A maps to NM_005190.3 A50A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5110-01A-01D-1421-08 chr1:86947887 A>G maps to NM_001285.3 R186R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5110-01A-01D-1421-08 chr16:20802203 C>A maps to NM_080663.2 G261G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5110-01A-01D-1421-08 chr12:123343989 C>T maps to NM_003959.1 S771S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5110-01A-01D-1421-08 chr6:29910621 C>T maps to ENST00000376806 D54D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5110-01A-01D-1421-08 chr8:21985224 C>A maps to NM_005144.4 E244*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5110-01A-01D-1421-08 chr3:183211911 G>T maps to NM_130446.2 I435I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5110-01A-01D-1421-08 chr3:183211911 G>T maps to NM_130446.2 I435I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5110-01A-01D-1421-08 chr10:95076525 G>C maps to NM_013451.3 P1881P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5110-01A-01D-1421-08 chr11:120096480 G>T maps to NM_178507.2 E115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5110-01A-01D-1421-08 chrX:90691349 C>T maps to NM_080832.2 D258D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5110-01A-01D-1421-08 chr10:98405299 G>A maps to NM_152309.2 L435L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5110-01A-01D-1421-08 chr13:30098299 G>A maps to NM_003045.4 A265A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5110-01A-01D-1421-08 chr22:21385822 C>T maps to NM_004173.2 G93G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5110-01A-01D-1421-08 chr15:41865310 T>C did not map to a codon.
Sequencing variant TCGA-B0-5110-01A-01D-1421-08 chr12:95676228 A>G maps to NM_017599.3 Q379Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5110-01A-01D-1421-08 chr11:64854836 C>A maps to NM_006782.3 L226L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5110-01A-01D-1421-08 chr19:56732943 T>C maps to NM_024303.1 *497W. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5110-01A-01D-1421-08 chrX:152954166 C>A maps to NM_005629.3 R46R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5110-01A-01D-1421-08 chrX:152954166 C>A maps to NM_005629.3 R46R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5113-01A-01D-1421-08 chr15:51217399 A>T maps to NM_007347.3 K176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5113-01A-01D-1421-08 chr1:65143847 T>C maps to ENST00000371073 C1033C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5113-01A-01D-1421-08 chr22:36960523 G>A maps to NM_006078.3 T282T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5113-01A-01D-1421-08 chr6:33133476 G>A maps to NM_080680.2 A1533A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5113-01A-01D-1421-08 chr1:38022627 C>T maps to NM_003462.3 Y33Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5113-01A-01D-1421-08 chr1:94335472 G>A maps to NM_014597.4 I735I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5113-01A-01D-1421-08 chr11:78412935 G>A maps to NM_001098816.2 N1574N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5113-01A-01D-1421-08 chr19:50118188 C>T maps to NM_020719.1 F1649F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5113-01A-01D-1421-08 chr19:6501364 G>A maps to NM_006087.2 P70P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5113-01A-01D-1421-08 chr3:10191469 G>T did not map to a codon.
Sequencing variant TCGA-B0-5113-01A-01D-1421-08 chr3:10191469 G>T did not map to a codon.
Sequencing variant TCGA-B0-5113-01A-01D-1421-08 chr1:78045310 T>C maps to NM_015534.4 K661K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5115-01A-01D-1421-08 chr1:236891014 C>T maps to NM_001103.2 R192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5115-01A-01D-1421-08 chr12:7636080 C>G maps to NM_004244.4 P990P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5115-01A-01D-1421-08 chr10:101923758 A>G did not map to a codon.
Sequencing variant TCGA-B0-5115-01A-01D-1421-08 chr12:130649145 C>T maps to NM_007197.3 S553S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5115-01A-01D-1421-08 chr7:2645632 T>A did not map to a codon.
Sequencing variant TCGA-B0-5115-01A-01D-1421-08 chr16:67404968 C>T maps to NM_018296.5 L440L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5115-01A-01D-1421-08 chr4:2254185 G>A maps to NM_006454.2 S86S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5115-01A-01D-1421-08 chr3:52662983 C>A maps to ENST00000296302 E457*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5115-01A-01D-1421-08 chr22:18566232 T>G maps to NM_017929.5 P134P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5115-01A-01D-1421-08 chr22:18566232 T>G maps to NM_017929.5 P134P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5115-01A-01D-1421-08 chr11:129817094 C>T maps to NM_020228.2 T155T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5115-01A-01D-1421-08 chr20:49196425 G>T maps to NM_002827.2 G351*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5115-01A-01D-1421-08 chr12:108920273 G>A maps to NM_014706.3 Q658*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5115-01A-01D-1421-08 chr18:45368210 G>T maps to NM_001003652.2 S464*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5115-01A-01D-1421-08 chr3:121097678 C>T maps to NM_014980.2 R789*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5115-01A-01D-1421-08 chr5:114499349 T>A maps to NM_018700.3 K55*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5115-01A-01D-1421-08 chr9:34241772 C>G maps to NM_001171201.1 S314S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5115-01A-01D-1421-08 chr19:12243968 A>T maps to NM_021143.2 C344*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5116-01A-02D-1421-08 chr12:34179314 C>A maps to NM_032834.3 S296*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5116-01A-02D-1421-08 chr1:70781172 G>C maps to NM_030816.4 A218A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5116-01A-02D-1421-08 chr19:36054146 C>T maps to NM_000704.2 A60A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5116-01A-02D-1421-08 chr19:36054146 C>T maps to NM_000704.2 A60A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5116-01A-02D-1421-08 chr2:29383259 C>T maps to ENST00000379543 L487L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5116-01A-02D-1421-08 chr9:115932897 G>T maps to ENST00000446284 I915I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5116-01A-02D-1421-08 chr12:104390595 A>G maps to NM_031302.3 L173L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5116-01A-02D-1421-08 chr14:63447835 A>T maps to NM_139318.3 V232V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5116-01A-02D-1421-08 chr11:71260167 C>A maps to NM_005553.3 S155S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5116-01A-02D-1421-08 chr5:138643266 T>C maps to ENST00000394800 L55L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5116-01A-02D-1421-08 chr19:9077023 G>A maps to NM_024690.2 L3474L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5116-01A-02D-1421-08 chr19:9077023 G>A maps to NM_024690.2 L3474L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5116-01A-02D-1421-08 chr6:128318043 A>G did not map to a codon.
Sequencing variant TCGA-B0-5116-01A-02D-1421-08 chr15:42147093 C>T maps to ENST00000320955 L3168L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5116-01A-02D-1421-08 chr2:75278448 G>T maps to NM_001058.3 Y287*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5116-01A-02D-1421-08 chr1:184023904 C>A maps to NM_052965.2 L87L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5116-01A-02D-1421-08 chr15:50833302 G>A maps to ENST00000456636 N210N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5116-01A-02D-1421-08 chr12:109530324 T>A maps to NM_001145375.1 V89V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5116-01A-02D-1421-08 chr12:109530324 T>A maps to NM_001145375.1 V89V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5119-01A-02D-1421-08 chr15:89382023 C>G maps to NM_013227.3 A67A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5119-01A-02D-1421-08 chr18:29207085 T>G did not map to a codon.
Sequencing variant TCGA-B0-5119-01A-02D-1421-08 chr10:60558279 A>G maps to NM_001080512.1 T496T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5119-01A-02D-1421-08 chr17:48652947 C>T maps to NM_018896.3 A395A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5119-01A-02D-1421-08 chr22:46807518 G>T maps to NM_014246.1 G1583G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5119-01A-02D-1421-08 chr12:124272411 A>T maps to NM_207437.3 K434*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5119-01A-02D-1421-08 chr5:76028880 C>A maps to NM_001992.3 V277V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5119-01A-02D-1421-08 chr6:33639878 C>T maps to ENST00000374316 S934S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5119-01A-02D-1421-08 chr1:115829227 C>A maps to NM_002506.2 V63V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5119-01A-02D-1421-08 chr10:74673123 T>C maps to NM_152635.1 G283G. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-B0-5119-01A-02D-1421-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-B0-5119-01A-02D-1421-08 chr3:52649436 G>A maps to ENST00000296302 L618L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5119-01A-02D-1421-08 chr1:204380313 C>A maps to NM_032833.3 G76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5119-01A-02D-1421-08 chr11:111624211 G>T maps to NM_181699.2 T373T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5119-01A-02D-1421-08 chr15:40993341 A>T maps to NM_002875.4 P56P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5119-01A-02D-1421-08 chr19:1220428 C>T maps to NM_000455.4 H174H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5119-01A-02D-1421-08 chr16:1552945 G>T maps to NM_016111.3 L595L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5119-01A-02D-1421-08 chr8:100847773 A>G maps to NM_017890.3 P3275P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5119-01A-02D-1421-08 chr14:100847488 T>A maps to NM_001161476.1 Y76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5119-01A-02D-1421-08 chr19:57765249 A>T maps to NM_001023563.3 R355*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5119-01A-02D-1421-08 chr19:57765249 A>T maps to NM_001023563.3 R355*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5120-01A-01D-1421-08 chr22:50303614 C>T maps to NM_024105.3 L197L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5120-01A-01D-1421-08 chr1:201047116 C>A maps to NM_000069.2 V503V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5120-01A-01D-1421-08 chr22:30766352 C>A maps to NM_001017437.2 P153P. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-B0-5120-01A-01D-1421-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-B0-5120-01A-01D-1421-08 chr18:480712 G>T maps to NM_130386.2 R18R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5120-01A-01D-1421-08 chr6:30866811 C>T maps to NM_013994.2 Q873*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5120-01A-01D-1421-08 chr1:223178701 T>C maps to NM_032890.2 A1321A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5120-01A-01D-1421-08 chr11:113295087 C>T did not map to a codon.
Sequencing variant TCGA-B0-5120-01A-01D-1421-08 chr5:180047686 G>A maps to NM_182925.4 I776I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5120-01A-01D-1421-08 chr6:96997452 A>G maps to NM_015323.4 A562A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5120-01A-01D-1421-08 chrX:19410162 C>T maps to NM_001001671.3 S796S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5120-01A-01D-1421-08 chr11:20124910 G>A maps to ENST00000396087 L2235L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5120-01A-01D-1421-08 chr1:229602503 C>A did not map to a codon.
Sequencing variant TCGA-B0-5120-01A-01D-1421-08 chr10:119049790 C>A maps to NM_173791.3 G389G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5120-01A-01D-1421-08 chrX:54982602 C>T maps to NM_002625.2 L207L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5120-01A-01D-1421-08 chr21:38444808 C>A maps to NM_153681.2 E27*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5120-01A-01D-1421-08 chr21:38444808 C>A maps to NM_153681.2 E27*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5120-01A-01D-1421-08 chr2:160813102 A>G maps to NM_007366.4 S980S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5120-01A-01D-1421-08 chr17:1648686 C>T maps to NM_000934.3 Q55*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5120-01A-01D-1421-08 chr11:63057714 C>G maps to NM_001039752.3 P26P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5120-01A-01D-1421-08 chr6:147685199 C>T maps to NM_001127715.1 A993A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5120-01A-01D-1421-08 chrX:48557407 C>A maps to NM_003173.2 V45V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5120-01A-01D-1421-08 chr19:17366334 G>A maps to NM_031941.3 L517L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5120-01A-01D-1421-08 chr7:63981784 A>G maps to NM_178558.4 L449L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5120-01A-01D-1421-08 chr9:99580321 G>A maps to NM_001001662.1 L661L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5120-01A-01D-1421-08 chr9:99580321 G>A maps to NM_001001662.1 L661L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5120-01A-01D-1421-08 chrX:114400840 C>A maps to NM_020871.3 E355*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5120-01A-01D-1421-08 chrX:114400840 C>A maps to NM_020871.3 E355*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5120-01A-01D-1421-08 chr15:81633741 A>G maps to ENST00000454937 F611F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5120-01A-01D-1421-08 chr15:81633741 A>G maps to ENST00000454937 F611F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5120-01A-01D-1421-08 chr13:115047558 C>T maps to NM_023011.2 L91L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5120-01A-01D-1421-08 chr13:115047558 C>T maps to NM_023011.2 L91L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5121-01A-02D-1421-08 chr11:62297274 G>A maps to NM_001620.1 D1538D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5121-01A-02D-1421-08 chr16:1389513 G>A maps to NM_003933.4 E141E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5121-01A-02D-1421-08 chr12:70087466 G>A maps to NM_032735.2 H156H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5121-01A-02D-1421-08 chr22:19076917 C>A maps to NM_005137.2 A55A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5121-01A-02D-1421-08 chr1:62550235 C>T maps to NM_176877.2 V1431V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5121-01A-02D-1421-08 chr16:27732991 T>C maps to NM_015202.2 V573V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5121-01A-02D-1421-08 chr7:135277918 C>A maps to NM_015135.2 L603L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5121-01A-02D-1421-08 chr11:59282456 C>T maps to NM_001004711.1 S24S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5121-01A-02D-1421-08 chr4:55156689 G>T maps to ENST00000507166 E791*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5121-01A-02D-1421-08 chr3:47162786 A>C maps to NM_014159.6 Y1113*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5121-01A-02D-1421-08 chr11:62652669 C>T maps to NM_001012661.1 N412N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5121-01A-02D-1421-08 chr12:101560444 G>T maps to NM_145913.3 A451A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5121-01A-02D-1421-08 chr6:132892287 T>A maps to NM_175067.1 I276I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5121-01A-02D-1421-08 chr12:83526101 A>G maps to NM_152588.1 T815T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5121-01A-02D-1421-08 chr15:54025232 C>T maps to NM_182758.2 E38E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5121-01A-02D-1421-08 chr19:21216890 G>A did not map to a codon.
Sequencing variant TCGA-B0-5121-01A-02D-1421-08 chr18:28720255 G>A maps to NM_024421.2 N423N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5121-01A-02D-1421-08 chr18:28720255 G>A maps to NM_024421.2 N423N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5121-01A-02D-1421-08 chr7:114269990 G>A maps to NM_148898.3 Q201Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5121-01A-02D-1421-08 chr7:114269990 G>A maps to NM_148898.3 Q201Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5121-01A-02D-1421-08 chr2:74732305 C>T maps to NM_032673.2 L248L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5121-01A-02D-1421-08 chr2:74732305 C>T maps to NM_032673.2 L248L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5698-01A-11D-1669-08 chr11:100226890 C>G maps to NM_014361.2 S1081S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5698-01A-11D-1669-08 chr18:77475250 G>C maps to NM_004715.3 L597L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5698-01A-11D-1669-08 chr19:1433801 C>T maps to NM_170711.1 V371V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5698-01A-11D-1669-08 chr13:41507955 G>A maps to NM_172373.3 Q489*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5698-01A-11D-1669-08 chrX:53224221 G>C maps to NM_004187.3 S1110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5698-01A-11D-1669-08 chr19:41120305 G>A maps to ENST00000308370 R989R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5698-01A-11D-1669-08 chr22:50695075 C>T did not map to a codon.
Sequencing variant TCGA-B0-5698-01A-11D-1669-08 chr11:1029577 G>A maps to NM_005961.2 C351C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5698-01A-11D-1669-08 chr17:46134731 A>T maps to ENST00000362042 T299T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5698-01A-11D-1669-08 chr19:16059969 G>A maps to NM_001004465.1 W51*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5698-01A-11D-1669-08 chr4:134071549 C>A maps to NM_032961.1 C85*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5698-01A-11D-1669-08 chr1:84670171 G>C maps to ENST00000370680 *265S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5698-01A-11D-1669-08 chr21:44840176 G>A maps to NM_173354.3 D303D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5698-01A-11D-1669-08 chr12:56745116 G>A maps to NM_005419.3 R300R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5698-01A-11D-1669-08 chr1:223408419 G>A maps to NM_001037175.2 F249F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5698-01A-11D-1669-08 chr12:129558539 G>T maps to NM_133448.2 P1060P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5698-01A-11D-1669-08 chr8:72975791 A>C maps to NM_007332.2 A189A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5698-01A-11D-1669-08 chr2:179404240 G>A maps to NM_133378.4 R30283*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5698-01A-11D-1669-08 chr16:28115914 G>T maps to NM_015171.2 I966I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5710-01A-11D-1669-08 chr19:36362617 G>A maps to NM_001024807.1 G214G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5710-01A-11D-1669-08 chr7:73245665 C>T maps to NM_001305.3 T45T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5710-01A-11D-1669-08 chr11:61511888 C>T maps to NM_006133.2 I1019I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5710-01A-11D-1669-08 chr1:54370441 A>G maps to NM_000792.5 A147A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5710-01A-11D-1669-08 chr17:29687576 G>T maps to NM_001042492.2 G2745*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5710-01A-11D-1669-08 chr5:176728944 A>G maps to NM_130781.2 A176A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5710-01A-11D-1669-08 chr1:76255647 G>A maps to NM_004582.2 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5710-01A-11D-1669-08 chr14:101351020 C>T maps to NM_001134888.2 A35A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5710-01A-11D-1669-08 chr2:179605551 G>A maps to NM_133437.3 G3965G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5710-01A-11D-1669-08 chr11:5528856 G>A maps to NM_017481.2 D644D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5711-01A-11D-1669-08 chr19:39216362 G>A did not map to a codon.
Sequencing variant TCGA-B0-5711-01A-11D-1669-08 chr5:5462476 G>T maps to NM_015325.1 V1010V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5711-01A-11D-1669-08 chr13:21557680 C>A maps to NM_014572.2 E722*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5711-01A-11D-1669-08 chr16:3293875 G>A maps to NM_000243.2 G592G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5711-01A-11D-1669-08 chr16:3293875 G>A maps to NM_000243.2 G592G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5711-01A-11D-1669-08 chr6:29407842 C>T maps to NM_013941.2 S17S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5711-01A-11D-1669-08 chr3:52643897 A>T maps to ENST00000296302 Y666*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5711-01A-11D-1669-08 chr9:72892385 C>T maps to NM_015110.3 Q181*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5711-01A-11D-1669-08 chr12:57485456 T>C maps to NM_005967.3 P211P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5711-01A-11D-1669-08 chr12:57485456 T>C maps to NM_005967.3 P211P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5713-01A-11D-1669-08 chrX:138827925 C>T maps to NM_173694.4 G976G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5713-01A-11D-1669-08 chr18:55399033 A>G maps to NM_005603.4 S2S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5713-01A-11D-1669-08 chr14:99641321 C>T maps to NM_138576.2 K617K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5713-01A-11D-1669-08 chr8:67970383 A>G maps to NM_006837.2 L147L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5713-01A-11D-1669-08 chr16:4408460 C>T maps to NM_024535.3 T788T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5713-01A-11D-1669-08 chr12:53685568 C>T maps to NM_012291.4 L1872L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5713-01A-11D-1669-08 chr12:95546723 C>A maps to NM_018351.3 E878*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5713-01A-11D-1669-08 chrX:48979946 A>T maps to NM_015698.4 S42S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5713-01A-11D-1669-08 chrX:48979946 A>T maps to NM_015698.4 S42S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5713-01A-11D-1669-08 chr1:99767413 T>C maps to NM_014839.4 Y309Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5713-01A-11D-1669-08 chr1:99767413 T>C maps to NM_014839.4 Y309Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5713-01A-11D-1669-08 chr1:76262747 T>C maps to NM_002440.2 P26P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5713-01A-11D-1669-08 chr2:27656878 T>C maps to ENST00000379863 D119D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5713-01A-11D-1669-08 chr8:59506789 C>G did not map to a codon.
Sequencing variant TCGA-B0-5713-01A-11D-1669-08 chr6:52268835 T>A maps to ENST00000361841 C280*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5713-01A-11D-1669-08 chr19:7614965 C>T maps to NM_001166111.1 T603T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5713-01A-11D-1669-08 chr2:131116983 C>T maps to NM_014369.3 S98S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5713-01A-11D-1669-08 chr5:176728924 C>T did not map to a codon.
Sequencing variant TCGA-B0-5713-01A-11D-1669-08 chr2:17699550 G>T maps to NM_001099218.2 V44V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5713-01A-11D-1669-08 chr5:170336744 G>T maps to NM_022897.3 V190V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5713-01A-11D-1669-08 chr11:114314630 T>C maps to NM_015523.3 D95D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5713-01A-11D-1669-08 chr14:62462754 G>A maps to NM_031914.2 A6A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5713-01A-11D-1669-08 chr2:216965264 A>T maps to NM_138390.3 *298Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5713-01A-11D-1669-08 chr3:10191468 A>G did not map to a codon.
Sequencing variant TCGA-B0-5713-01A-11D-1669-08 chr16:68598498 T>C maps to NM_133458.2 H603H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5713-01A-11D-1669-08 chr7:148769509 A>T maps to NM_152411.3 P118P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5713-01A-11D-1669-08 chr12:53670455 C>T maps to NM_012291.4 L585L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5713-01A-11D-1669-08 chr12:53670455 C>T maps to NM_012291.4 L585L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5812-01A-11D-1669-08 chr14:100375764 C>A maps to NM_001008707.1 Y415*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5812-01A-11D-1669-08 chr8:623547 G>A maps to NM_207332.1 D268D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5812-01A-11D-1669-08 chr7:107605112 G>A maps to NM_002291.2 Q528*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5812-01A-11D-1669-08 chr9:133942551 C>T maps to ENST00000355048 Y851Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5812-01A-11D-1669-08 chr2:141812721 A>T maps to NM_018557.2 T505T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5812-01A-11D-1669-08 chr3:182897462 C>T maps to NM_015078.2 Q1041Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5812-01A-11D-1669-08 chr3:173998402 T>G maps to NM_014932.2 V594V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5812-01A-11D-1669-08 chr1:229643912 C>G maps to NM_018230.2 T28T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5812-01A-11D-1669-08 chr17:73096900 A>T maps to ENST00000450736 P421P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5812-01A-11D-1669-08 chr10:18250700 G>A maps to NM_001145195.1 R151R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5812-01A-11D-1669-08 chr17:37369245 A>C did not map to a codon.
Sequencing variant TCGA-B0-5812-01A-11D-1669-08 chr22:31018989 T>A maps to NM_000355.3 L381*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5812-01A-11D-1669-08 chr3:10188289 C>T maps to NM_000551.2 Q145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5812-01A-11D-1669-08 chr9:139959179 A>G maps to NM_178448.3 I372I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5812-01A-11D-1669-08 chr9:139959179 A>G maps to NM_178448.3 I372I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-3924-01A-01D-1458-08 chr15:29346527 G>A maps to NM_005503.3 P147P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-3924-01A-01D-1458-08 chr17:80369359 G>T maps to NM_175902.4 I117I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-3924-01A-01D-1458-08 chr5:82940356 G>T maps to NM_001884.3 G200G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-3924-01A-01D-1458-08 chr11:63670172 G>T maps to NM_001039469.2 R445R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-3924-01A-01D-1458-08 chr2:192250810 G>T did not map to a codon.
Sequencing variant TCGA-B2-3924-01A-01D-1458-08 chr11:123887006 C>T maps to NM_001004462.1 S242S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-3924-01A-01D-1458-08 chr6:32156279 G>T maps to NM_002586.4 G99G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-3924-01A-01D-1458-08 chr6:32156279 G>T maps to NM_002586.4 G99G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-3924-01A-01D-1458-08 chr13:45008836 A>G maps to NM_183422.2 P1049P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-3924-01A-01D-1458-08 chr13:45008836 A>G maps to NM_183422.2 P1049P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-3924-01A-01D-1458-08 chr3:10183724 C>A maps to NM_000551.2 S65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-3924-01A-01D-1458-08 chr3:10183724 C>A maps to NM_000551.2 S65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-4098-01A-01D-1458-08 chr14:68086726 C>G maps to NM_001172.3 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-4098-01A-01D-1458-08 chr2:65299147 T>G maps to NM_015147.2 T306T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-4098-01A-01D-1458-08 chr6:42931106 G>A maps to NM_018960.4 V212V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-4098-01A-01D-1458-08 chr11:2154814 G>A maps to NM_001127598.1 L136L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-4098-01A-01D-1458-08 chr8:56986628 G>A maps to NM_001146227.1 S31S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-4098-01A-01D-1458-08 chr4:83788376 A>G maps to ENST00000505472 D325D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-4098-01A-01D-1458-08 chr2:45171736 C>A maps to NM_005413.3 G279G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-4098-01A-01D-1458-08 chr17:76127731 G>A maps to NM_152468.4 L21L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-4098-01A-01D-1458-08 chr20:61442845 G>A maps to NM_007346.2 R166R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-4098-01A-01D-1458-08 chr20:61442845 G>A maps to NM_007346.2 R166R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-4099-01A-02D-1458-08 chr7:73183929 C>G maps to NM_001306.3 V150V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-4099-01A-02D-1458-08 chr6:27839910 C>T maps to NM_003533.2 L61L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-4101-01A-02D-1458-08 chrX:32834667 A>G maps to ENST00000357033 R149R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-4101-01A-02D-1458-08 chr15:68628033 C>A did not map to a codon.
Sequencing variant TCGA-B2-4101-01A-02D-1458-08 chr20:33328812 C>A maps to NM_014071.2 T1749T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-4101-01A-02D-1458-08 chr10:63999438 G>T maps to NM_145307.2 I152I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-4101-01A-02D-1458-08 chr1:25256116 C>A maps to NM_001031680.2 S95S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-4101-01A-02D-1458-08 chr3:47129721 C>A maps to NM_014159.6 E1720*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-4101-01A-02D-1458-08 chr7:143140756 C>G maps to NM_177437.1 S71*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-4101-01A-02D-1458-08 chr7:143140756 C>G maps to NM_177437.1 S71*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-4101-01A-02D-1458-08 chr3:196053865 C>T maps to NM_138461.2 W80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-4101-01A-02D-1458-08 chr3:196053865 C>T maps to NM_138461.2 W80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-4101-01A-02D-1458-08 chr8:11058308 G>A maps to NM_173683.3 S180S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-4101-01A-02D-1458-08 chr17:41610307 C>T did not map to a codon.
Sequencing variant TCGA-B2-4101-01A-02D-1458-08 chr17:41610307 C>T did not map to a codon.
Sequencing variant TCGA-B2-4101-01A-02D-1458-08 chr11:117785149 G>A maps to ENST00000413475 D211D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-4101-01A-02D-1458-08 chr11:117785149 G>A maps to ENST00000413475 D211D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4146-01B-11D-1669-08 chr19:17405545 G>T maps to NM_024527.4 I290I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4146-01B-11D-1669-08 chr12:48543457 T>C maps to NM_024095.3 T186T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4146-01B-11D-1669-08 chr16:28898564 C>A maps to NM_173201.3 V200V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4146-01B-11D-1669-08 chr5:180376248 C>T maps to NM_001040462.2 D282D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4146-01B-11D-1669-08 chr2:152709961 T>C maps to NM_000726.3 P372P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4146-01B-11D-1669-08 chr17:74018280 G>A maps to NM_001988.2 R212*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4146-01B-11D-1669-08 chr10:120877120 C>A maps to NM_207009.2 G141G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4146-01B-11D-1669-08 chr10:78872136 C>A maps to NM_001161352.1 G316G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4146-01B-11D-1669-08 chr10:78872139 G>A maps to NM_001161352.1 A315A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4146-01B-11D-1669-08 chr11:56954875 G>A maps to NM_001005210.2 V316V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4146-01B-11D-1669-08 chr6:57372298 G>A maps to NM_000947.2 R235R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4146-01B-11D-1669-08 chr7:64168952 C>T maps to NM_016220.3 F757F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4146-01B-11D-1669-08 chr1:247265091 T>C maps to NM_024804.2 G130G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4146-01B-11D-1669-08 chr15:83215271 C>A did not map to a codon.
Sequencing variant TCGA-B8-4146-01B-11D-1669-08 chr15:83215271 C>A did not map to a codon.
Sequencing variant TCGA-B8-4146-01B-11D-1669-08 chr12:31242860 A>C maps to NM_030653.3 R308R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4146-01B-11D-1669-08 chr12:31242860 A>C maps to NM_030653.3 R308R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4146-01B-11D-1669-08 chr1:115828690 T>G maps to NM_002506.2 *242C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4146-01B-11D-1669-08 chr1:115828690 T>G maps to NM_002506.2 *242C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4153-01B-11D-1669-08 chr6:43402468 G>A maps to NM_033450.2 R454R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4153-01B-11D-1669-08 chr6:157520040 G>C maps to ENST00000367148 P1410P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4153-01B-11D-1669-08 chr8:131073178 C>G maps to NM_018482.2 L946L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4153-01B-11D-1669-08 chr12:32369297 G>T maps to NM_001714.2 E111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4153-01B-11D-1669-08 chr16:88958663 C>T maps to NM_005187.5 V203V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4153-01B-11D-1669-08 chr4:56884017 G>T maps to NM_025009.3 E1003*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4153-01B-11D-1669-08 chr16:53320219 T>G maps to ENST00000219084 V1718V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4153-01B-11D-1669-08 chr6:34100943 G>T maps to NM_000841.1 S110S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4153-01B-11D-1669-08 chr6:29910621 C>T maps to ENST00000376806 D54D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4153-01B-11D-1669-08 chr20:60904898 C>G maps to NM_005560.3 L1351L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4153-01B-11D-1669-08 chr17:61762879 C>T maps to NM_203351.1 L245L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4153-01B-11D-1669-08 chr12:56213244 C>T maps to NM_014182.4 S98S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4153-01B-11D-1669-08 chr6:33240469 G>A maps to NM_022551.2 R23R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4153-01B-11D-1669-08 chr18:67872494 C>A maps to NM_173630.3 E30*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4153-01B-11D-1669-08 chr16:51171322 T>C maps to ENST00000251020 S1225S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4153-01B-11D-1669-08 chr14:31122775 A>T maps to ENST00000311943 A287A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4153-01B-11D-1669-08 chr1:153934707 G>T maps to NM_014437.3 A102A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4153-01B-11D-1669-08 chr1:155207293 C>T maps to NM_001005742.2 L279L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4153-01B-11D-1669-08 chr1:155207293 C>T maps to NM_001005742.2 L279L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4620-01A-01D-1553-08 chr11:3681531 C>T maps to NM_004314.2 P261P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4620-01A-01D-1553-08 chr15:65499357 G>T maps to NM_003613.3 I62I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4620-01A-01D-1553-08 chr2:11053934 G>A maps to NM_002236.4 A461A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4620-01A-01D-1553-08 chr3:65425587 C>T maps to NM_001033057.1 Q412Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4622-01A-02D-1553-08 chr7:20682903 A>C maps to NM_001163941.1 R138R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4622-01A-02D-1553-08 chr20:10604012 G>T maps to NM_001009608.1 E405*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4622-01A-02D-1553-08 chr16:2506954 G>A maps to NM_001761.2 V765V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4622-01A-02D-1553-08 chr17:76506510 G>T maps to ENST00000389840 V1393V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4622-01A-02D-1553-08 chr1:240371033 A>C maps to ENST00000406993 G1117G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4622-01A-02D-1553-08 chr17:21318740 C>T maps to NM_021012.4 N29N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4622-01A-02D-1553-08 chr13:61103272 A>G maps to NM_001146070.1 E638E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4622-01A-02D-1553-08 chrX:56310755 T>G maps to NM_007250.4 P303P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4622-01A-02D-1553-08 chrX:56310755 T>G maps to NM_007250.4 P303P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4622-01A-02D-1553-08 chr2:71160066 G>A maps to NM_012476.2 A202A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4622-01A-02D-1553-08 chr2:71160066 G>A maps to NM_012476.2 A202A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5158-01A-01D-1421-08 chr7:117199624 C>A maps to NM_000492.3 G500G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5158-01A-01D-1421-08 chr10:375465 G>C maps to NM_014974.2 A1220A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5158-01A-01D-1421-08 chr1:38192871 C>A maps to NM_001099439.1 G558G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5158-01A-01D-1421-08 chr3:120495383 C>T maps to NM_005513.2 V255V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5158-01A-01D-1421-08 chr2:242179324 G>A maps to NM_005336.3 I794I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5158-01A-01D-1421-08 chr6:27860780 C>G maps to NM_003514.2 P49P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5158-01A-01D-1421-08 chr17:73485345 G>A did not map to a codon.
Sequencing variant TCGA-B8-5158-01A-01D-1421-08 chr20:60921135 C>T did not map to a codon.
Sequencing variant TCGA-B8-5158-01A-01D-1421-08 chr1:183204763 T>G maps to NM_005562.2 Y785*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5158-01A-01D-1421-08 chr4:164050357 A>G maps to NM_138386.2 P392P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5158-01A-01D-1421-08 chr4:164050357 A>G maps to NM_138386.2 P392P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5158-01A-01D-1421-08 chr15:73590936 T>C maps to NM_002499.3 L1384L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5158-01A-01D-1421-08 chr17:5290384 G>A maps to NM_002532.3 L654L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5158-01A-01D-1421-08 chr10:89717761 A>T maps to NM_000314.4 K263*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5158-01A-01D-1421-08 chr22:50903271 T>C maps to ENST00000337034 E479E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5158-01A-01D-1421-08 chr17:56603080 C>A maps to NM_004574.3 R171R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5158-01A-01D-1421-08 chr1:16257993 T>C maps to NM_015001.2 P1753P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5158-01A-01D-1421-08 chr12:58140427 G>C maps to NM_005981.3 L123L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5158-01A-01D-1421-08 chr3:52678805 C>T did not map to a codon.
Sequencing variant TCGA-B8-5158-01A-01D-1421-08 chr3:52678805 C>T did not map to a codon.
Sequencing variant TCGA-B8-5158-01A-01D-1421-08 chr7:5752485 G>T maps to NM_207111.2 L614L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5158-01A-01D-1421-08 chr7:5752485 G>T maps to NM_207111.2 L614L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5159-01A-01D-1421-08 chr2:71190717 C>A maps to NM_001692.3 I359I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5159-01A-01D-1421-08 chr5:68581284 G>C maps to NM_176816.3 S370*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5159-01A-01D-1421-08 chr13:41525465 T>A maps to NM_172373.3 I120I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5159-01A-01D-1421-08 chr1:62330118 A>G maps to NM_176877.2 S883S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5159-01A-01D-1421-08 chr4:62812746 C>T maps to ENST00000506720 V845V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5159-01A-01D-1421-08 chr17:19284304 C>G maps to NM_139034.2 L261L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5159-01A-01D-1421-08 chr1:36926349 G>A maps to NM_031280.3 Q110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5159-01A-01D-1421-08 chr12:57110096 G>A maps to NM_001113203.1 L1739L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5159-01A-01D-1421-08 chr1:176738771 G>C maps to NM_020318.2 G1451G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5159-01A-01D-1421-08 chr3:178921333 T>A maps to NM_006218.2 Y272*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5159-01A-01D-1421-08 chr12:27835399 T>C maps to NM_003622.3 N709N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5159-01A-01D-1421-08 chr12:126135243 C>T maps to NM_052907.2 S548S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5159-01A-01D-1421-08 chr3:33481334 G>T maps to NM_001128161.1 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5159-01A-01D-1421-08 chr3:10191535 A>T maps to NM_000551.2 R177*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5163-01A-01D-1421-08 chr14:74086149 T>C maps to NM_001037162.1 T77T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5163-01A-01D-1421-08 chr3:28368356 T>C maps to NM_022461.3 L244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5163-01A-01D-1421-08 chr12:2566763 A>T maps to NM_199460.2 K217*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5163-01A-01D-1421-08 chr6:43153718 G>A maps to ENST00000354495 L259L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5163-01A-01D-1421-08 chr1:167974002 A>G maps to ENST00000367840 A450A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5163-01A-01D-1421-08 chr10:12142205 C>A maps to NM_018706.5 I567I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5163-01A-01D-1421-08 chr16:67236113 C>T maps to NM_024712.3 H449H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5163-01A-01D-1421-08 chr11:134240283 C>T maps to NM_138342.3 Y402Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5163-01A-01D-1421-08 chr19:46388203 C>A maps to NM_015649.1 E277*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5163-01A-01D-1421-08 chr5:156670645 C>A maps to NM_005546.3 I358I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5163-01A-01D-1421-08 chr17:8274813 T>G maps to NM_213597.2 P13P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5163-01A-01D-1421-08 chr5:126754855 A>T maps to NM_032446.2 I450I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5163-01A-01D-1421-08 chr13:48619889 A>G maps to NM_018283.1 K150K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5163-01A-01D-1421-08 chr1:149920965 A>G maps to NM_020205.2 D381D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5163-01A-01D-1421-08 chr14:73685984 A>G maps to NM_000021.3 Q464Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5163-01A-01D-1421-08 chr17:37815806 G>A did not map to a codon.
Sequencing variant TCGA-B8-5163-01A-01D-1421-08 chr17:28887639 T>C maps to NM_015594.2 S28S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5163-01A-01D-1421-08 chr11:59622279 A>G maps to NM_001062.3 P322P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5163-01A-01D-1421-08 chr6:28294514 T>G maps to NM_030899.4 R217R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5163-01A-01D-1421-08 chr19:58439173 A>T maps to NM_133460.1 R125R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5163-01A-01D-1421-08 chr19:52942410 G>A maps to NM_001143939.1 A579A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5163-01A-01D-1421-08 chr19:52942410 G>A maps to NM_001143939.1 A579A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5164-01A-01D-1421-08 chr9:104192183 G>A maps to NM_000035.3 F59F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5164-01A-01D-1421-08 chr9:104192183 G>A maps to NM_000035.3 F59F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5164-01A-01D-1421-08 chr17:3851043 G>T maps to NM_174953.1 R246R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5164-01A-01D-1421-08 chr1:92470111 G>T maps to ENST00000347608 E856*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5164-01A-01D-1421-08 chr10:127426982 A>T maps to ENST00000356792 L650L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5164-01A-01D-1421-08 chr15:34647721 G>T maps to ENST00000438749 E495*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5164-01A-01D-1421-08 chr6:20781421 G>C maps to NM_017774.3 R188R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5164-01A-01D-1421-08 chr15:93545456 G>A maps to NM_001271.3 E1396E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5164-01A-01D-1421-08 chr3:53853055 C>A maps to NM_018397.4 G425G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5164-01A-01D-1421-08 chr1:36932908 C>T maps to NM_156039.3 R654R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5164-01A-01D-1421-08 chr15:64218209 C>A maps to NM_014326.3 E248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5164-01A-01D-1421-08 chr13:96238361 T>C maps to NM_198968.2 K749K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5164-01A-01D-1421-08 chr10:129536796 C>T maps to NM_207426.2 Y175Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5164-01A-01D-1421-08 chr10:129536796 C>T maps to NM_207426.2 Y175Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5164-01A-01D-1421-08 chr12:53045839 C>A maps to NM_000423.2 V29V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5164-01A-01D-1421-08 chr12:50571731 C>T maps to NM_001113546.1 W466*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5164-01A-01D-1421-08 chr22:20921041 T>C maps to NM_001003891.1 L327L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5164-01A-01D-1421-08 chr17:34093554 G>A maps to NM_024302.3 G508G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5164-01A-01D-1421-08 chr8:59514095 T>C did not map to a codon.
Sequencing variant TCGA-B8-5164-01A-01D-1421-08 chr7:128413771 G>T maps to NM_001708.2 T286T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5164-01A-01D-1421-08 chr19:40873737 G>A maps to NM_012268.2 W127*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5164-01A-01D-1421-08 chr13:29238706 G>T did not map to a codon.
Sequencing variant TCGA-B8-5164-01A-01D-1421-08 chr16:58314589 G>A maps to NM_001080492.1 N242N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5164-01A-01D-1421-08 chr8:53554924 G>A maps to NM_014781.4 S1441S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5164-01A-01D-1421-08 chr9:130167741 A>G maps to NM_014580.3 S398S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5164-01A-01D-1421-08 chr2:48809433 G>A maps to NM_172311.2 Q554Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5164-01A-01D-1421-08 chr3:14964674 G>C maps to NM_152536.3 L1310L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5164-01A-01D-1421-08 chr3:14964674 G>C maps to NM_152536.3 L1310L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5164-01A-01D-1421-08 chr19:56104631 C>T maps to NM_032836.2 V225V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5164-01A-01D-1421-08 chr19:56104631 C>T maps to NM_032836.2 V225V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5164-01A-01D-1421-08 chr2:219146893 G>T did not map to a codon.
Sequencing variant TCGA-B8-5164-01A-01D-1421-08 chr2:219146893 G>T did not map to a codon.
Sequencing variant TCGA-B8-5164-01A-01D-1421-08 chrX:47518229 G>A maps to NM_153477.1 R45*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5164-01A-01D-1421-08 chrX:47518229 G>A maps to NM_153477.1 R45*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5165-01A-01D-1421-08 chr17:35872565 T>C maps to NM_007026.2 P64P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5165-01A-01D-1421-08 chr12:56495608 C>T maps to NM_001982.2 R1267*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5165-01A-01D-1421-08 chr11:108040714 C>G maps to NM_002519.2 G947G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5165-01A-01D-1421-08 chr6:3113550 T>A maps to NM_003804.3 L665*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5165-01A-01D-1421-08 chr5:176825283 C>A maps to NM_003052.4 L639L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5165-01A-01D-1421-08 chr12:46623009 T>C maps to NM_030674.3 L80L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5165-01A-01D-1421-08 chrX:135080322 T>C maps to NM_001042537.1 Y194Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5165-01A-01D-1421-08 chr3:10188320 G>T did not map to a codon.
Sequencing variant TCGA-B8-5165-01A-01D-1421-08 chr9:130475073 C>A maps to NM_001012502.2 L408L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5165-01A-01D-1421-08 chr9:130475073 C>A maps to NM_001012502.2 L408L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5545-01A-01D-1669-08 chr10:61835268 C>T maps to NM_020987.2 Q1790Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5545-01A-01D-1669-08 chr2:39519947 C>A maps to NM_003618.2 E413*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5545-01A-01D-1669-08 chr3:12422836 G>A maps to NM_015869.4 E109E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5545-01A-01D-1669-08 chr4:6349696 C>T maps to NM_181876.2 T222T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5545-01A-01D-1669-08 chr18:42531245 A>G maps to NM_015559.2 K647K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5545-01A-01D-1669-08 chr13:86370303 G>A maps to NM_032229.2 L114L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5545-01A-01D-1669-08 chr8:74858966 G>T maps to NM_005648.2 Y79*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5545-01A-01D-1669-08 chr4:76722352 G>A maps to NM_003715.2 Q611Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5545-01A-01D-1669-08 chr5:94014547 A>G maps to NM_032290.3 G621G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5545-01A-01D-1669-08 chr5:94014547 A>G maps to NM_032290.3 G621G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5545-01A-01D-1669-08 chr10:16919091 A>G maps to NM_001081.3 R2970R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5545-01A-01D-1669-08 chr10:16919091 A>G maps to NM_001081.3 R2970R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5545-01A-01D-1669-08 chrX:54475271 C>T maps to NM_004463.2 Q801Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5545-01A-01D-1669-08 chrX:54475271 C>T maps to NM_004463.2 Q801Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5552-01B-11D-1669-08 chr5:33576383 G>A maps to NM_030955.2 L1249L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5552-01B-11D-1669-08 chr2:37315581 C>T maps to ENST00000379187 Q20*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5552-01B-11D-1669-08 chr2:37315581 C>T maps to ENST00000379187 Q20*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5552-01B-11D-1669-08 chr2:30756118 T>A maps to NM_182551.3 Y139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5552-01B-11D-1669-08 chr11:3846651 G>A maps to NM_014489.2 L304L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5552-01B-11D-1669-08 chr20:48130812 C>T maps to NM_000961.3 S325S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5552-01B-11D-1669-08 chr2:179614715 A>G maps to ENST00000375038 D4139D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5552-01B-11D-1669-08 chr3:126707543 T>G maps to NM_032242.3 G36G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5552-01B-11D-1669-08 chr3:126707543 T>G maps to NM_032242.3 G36G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4782-01A-02D-1421-08 chr22:39441013 T>A maps to NM_145298.5 P80P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4782-01A-02D-1421-08 chr20:23066498 G>A maps to NM_012072.3 L111L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4782-01A-02D-1421-08 chr12:58158258 C>T maps to NM_000785.3 E346E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4782-01A-02D-1421-08 chr7:43503282 T>C maps to NM_015052.3 I892I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4782-01A-02D-1421-08 chr11:77727893 G>T maps to NM_023930.3 C171*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4782-01A-02D-1421-08 chr11:77727893 G>T maps to NM_023930.3 C171*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4782-01A-02D-1421-08 chr14:23891450 C>A maps to NM_000257.2 L1061L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4782-01A-02D-1421-08 chr2:232321357 T>C maps to NM_005381.2 S563S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4782-01A-02D-1421-08 chr16:4953993 C>A maps to NM_002705.4 V70V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4782-01A-02D-1421-08 chr16:31213522 G>T maps to NM_013258.4 G92G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4782-01A-02D-1421-08 chr1:46743872 G>A maps to NM_003579.3 Q721Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4782-01A-02D-1421-08 chr20:34292610 A>G maps to NM_184234.1 L491L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4782-01A-02D-1421-08 chr12:56750312 G>A maps to NM_005419.3 Q15*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4782-01A-02D-1421-08 chr16:67262756 T>A maps to NM_014187.3 S119S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4782-01A-02D-1421-08 chr17:42266746 G>A maps to NM_001076674.1 E131E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4782-01A-02D-1421-08 chr8:141310713 C>T did not map to a codon.
Sequencing variant TCGA-BP-4782-01A-02D-1421-08 chr13:52293352 G>C maps to NM_052950.3 T118T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4782-01A-02D-1421-08 chr9:131021535 C>T maps to NM_004486.4 L642L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4782-01A-02D-1421-08 chr9:131021535 C>T maps to NM_004486.4 L642L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4782-01A-02D-1421-08 chr7:103969250 C>T maps to NM_199000.2 A8A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4782-01A-02D-1421-08 chr7:103969250 C>T maps to NM_199000.2 A8A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4782-01A-02D-1421-08 chr13:79928636 A>C maps to ENST00000438737 G642G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4782-01A-02D-1421-08 chr13:79928636 A>C maps to ENST00000438737 G642G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4782-01A-02D-1421-08 chr6:72960945 T>A maps to NM_014989.4 L858*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4782-01A-02D-1421-08 chr6:72960945 T>A maps to NM_014989.4 L858*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4782-01A-02D-1421-08 chr2:70475611 C>T did not map to a codon.
Sequencing variant TCGA-BP-4782-01A-02D-1421-08 chr2:70475611 C>T did not map to a codon.
Sequencing variant TCGA-BP-4782-01A-02D-1421-08 chr17:73814862 C>T maps to NM_001080419.1 F580F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4782-01A-02D-1421-08 chr17:73814862 C>T maps to NM_001080419.1 F580F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4801-01A-02D-1421-08 chr17:42249678 G>A maps to NM_080863.4 L189L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4801-01A-02D-1421-08 chr19:19014154 G>A maps to NM_007263.3 L219L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4801-01A-02D-1421-08 chr9:304679 G>A maps to NM_203447.3 L168L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4801-01A-02D-1421-08 chr11:117332277 C>G maps to NM_020693.2 L1160L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4801-01A-02D-1421-08 chr20:33703673 A>C maps to NM_018217.2 T433T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4801-01A-02D-1421-08 chr1:190067929 G>A maps to NM_199051.1 R507*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4801-01A-02D-1421-08 chr10:92617161 C>G maps to NM_019859.3 T89T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4801-01A-02D-1421-08 chr2:128262532 C>A maps to NM_017969.2 E316*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4801-01A-02D-1421-08 chr2:128262532 C>A maps to NM_017969.2 E316*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4801-01A-02D-1421-08 chr20:36869595 C>A maps to NM_001029864.1 E313*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4801-01A-02D-1421-08 chr17:21203906 T>C maps to NM_145109.2 R72R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4801-01A-02D-1421-08 chr11:68747867 C>G maps to NM_198923.2 L196L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4801-01A-02D-1421-08 chr3:52696147 C>A did not map to a codon.
Sequencing variant TCGA-BP-4801-01A-02D-1421-08 chr3:52696147 C>A did not map to a codon.
Sequencing variant TCGA-BP-4801-01A-02D-1421-08 chr2:120720266 G>T maps to NM_002830.2 E786*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4801-01A-02D-1421-08 chr12:71029652 G>T maps to NM_001109754.1 I83I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4801-01A-02D-1421-08 chr20:1895841 T>C maps to ENST00000400068 S59S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4801-01A-02D-1421-08 chr16:2126067 G>A did not map to a codon.
Sequencing variant TCGA-BP-4801-01A-02D-1421-08 chr4:68547885 G>A maps to NM_018227.5 A60A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4801-01A-02D-1421-08 chr17:45891938 G>C maps to NM_145798.2 T433T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4801-01A-02D-1421-08 chr17:45891938 G>C maps to NM_145798.2 T433T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4801-01A-02D-1421-08 chr15:38591663 C>T maps to NM_152594.2 S41S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4801-01A-02D-1421-08 chr15:38591663 C>T maps to NM_152594.2 S41S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4960-01A-01D-1462-08 chr14:69349270 C>G maps to NM_001130004.1 T619T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4960-01A-01D-1462-08 chr5:173372084 A>G maps to NM_030627.2 R466R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4960-01A-01D-1462-08 chr15:68596121 C>T maps to ENST00000423218 L1162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4960-01A-01D-1462-08 chr1:82408995 T>C maps to ENST00000370717 Y247Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4960-01A-01D-1462-08 chr1:74575230 C>T maps to NM_001105659.1 V238V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4960-01A-01D-1462-08 chr2:9048797 A>C maps to NM_138799.2 T116T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4960-01A-01D-1462-08 chr8:48874106 T>A maps to NM_182746.1 S34S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4960-01A-01D-1462-08 chr11:281410 C>T maps to NM_138329.1 I559I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4960-01A-01D-1462-08 chr5:41794777 C>G did not map to a codon.
Sequencing variant TCGA-BP-4960-01A-01D-1462-08 chr20:49367003 T>C maps to NM_032521.2 D366D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4960-01A-01D-1462-08 chr6:161139401 T>A maps to NM_000301.3 A288A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4960-01A-01D-1462-08 chr19:54395810 G>A maps to NM_002739.3 W245*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4960-01A-01D-1462-08 chr17:9808161 G>A maps to NM_002903.2 D112D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4960-01A-01D-1462-08 chr6:86258078 A>T maps to NM_153816.3 L269L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4960-01A-01D-1462-08 chr7:134928141 C>T maps to NM_182489.1 S133S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4960-01A-01D-1462-08 chr9:73477849 C>A maps to ENST00000419692 G87*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4960-01A-01D-1462-08 chr8:28214211 A>G maps to NM_018660.2 P186P. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-BP-4960-01A-01D-1462-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-BP-4960-01A-01D-1462-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-BP-4961-01A-01D-1462-08 chr15:89395178 T>A maps to NM_013227.3 T727T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4961-01A-01D-1462-08 chr9:119802149 A>G maps to ENST00000313400 C457C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4961-01A-01D-1462-08 chr22:21990821 C>T maps to NM_152612.2 L435L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4961-01A-01D-1462-08 chr17:7806303 C>T maps to NM_001005271.2 G1199G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4961-01A-01D-1462-08 chr7:130295933 A>G maps to NM_012133.4 L209L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4961-01A-01D-1462-08 chr18:47808971 G>A maps to NM_001101654.1 A658A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4961-01A-01D-1462-08 chr1:120307116 C>A maps to NM_005518.3 V79V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4961-01A-01D-1462-08 chr3:47957987 C>T maps to ENST00000426837 E460E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4961-01A-01D-1462-08 chr7:151851227 G>T maps to ENST00000355193 S4105*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4961-01A-01D-1462-08 chr11:82877717 T>C maps to NM_015885.3 S593S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4961-01A-01D-1462-08 chr10:99120375 C>A did not map to a codon.
Sequencing variant TCGA-BP-4961-01A-01D-1462-08 chr11:3150288 C>T maps to NM_020896.3 R30R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4961-01A-01D-1462-08 chr11:3150288 C>T maps to NM_020896.3 R30R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4961-01A-01D-1462-08 chr3:13921262 G>T maps to NM_004625.3 G17G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4961-01A-01D-1462-08 chr3:13921262 G>T maps to NM_004625.3 G17G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4962-01A-01D-1462-08 chr13:50204840 C>T maps to NM_138450.5 Y86Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4962-01A-01D-1462-08 chr1:8390935 C>T maps to ENST00000377479 D495D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4962-01A-01D-1462-08 chr21:34011315 G>A maps to NM_003895.3 Q1312*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4962-01A-01D-1462-08 chr21:34011315 G>A maps to NM_003895.3 Q1312*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4962-01A-01D-1462-08 chr3:196733605 G>T maps to NM_005929.5 G584G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4962-01A-01D-1462-08 chr3:196733605 G>T maps to NM_005929.5 G584G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4963-01A-01D-1462-08 chr13:32911476 A>T maps to NM_000059.3 G995G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4963-01A-01D-1462-08 chr8:61769233 T>C maps to NM_017780.2 F2465F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4963-01A-01D-1462-08 chr5:134126241 G>A maps to ENST00000452510 Q542Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4963-01A-01D-1462-08 chr14:21238698 C>T maps to NM_022360.4 D130D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4963-01A-01D-1462-08 chr17:19186716 G>A maps to NM_014964.4 Q95Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4963-01A-01D-1462-08 chr15:48779392 G>A maps to NM_000138.4 I1156I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4963-01A-01D-1462-08 chr12:117448165 G>A maps to NM_153348.2 L426L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4963-01A-01D-1462-08 chr17:42477629 G>A maps to NM_001002909.2 G605G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4963-01A-01D-1462-08 chr15:101597209 A>T maps to NM_024652.3 R1494R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4963-01A-01D-1462-08 chr2:27245100 G>A maps to NM_012326.2 V5V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4963-01A-01D-1462-08 chr2:198571442 G>A maps to NM_138395.3 P438P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4963-01A-01D-1462-08 chr6:20144500 G>A maps to NM_001080480.1 I123I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4963-01A-01D-1462-08 chr8:8748227 G>T maps to NM_004225.2 R781R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4963-01A-01D-1462-08 chr17:26449739 T>C maps to NM_016231.4 C190C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4963-01A-01D-1462-08 chr14:73746100 A>G maps to NM_001005743.1 L376L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4963-01A-01D-1462-08 chrX:114880822 G>C maps to NM_001136025.3 L493L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4963-01A-01D-1462-08 chr11:60658694 G>A maps to NM_014502.4 H486H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4963-01A-01D-1462-08 chr17:1840902 G>T maps to NM_178568.2 P71P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4963-01A-01D-1462-08 chr1:156169880 C>A maps to NM_014655.2 T81T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4963-01A-01D-1462-08 chr1:153932642 C>T maps to NM_014437.3 R302R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4963-01A-01D-1462-08 chr19:11129631 G>A did not map to a codon.
Sequencing variant TCGA-BP-4963-01A-01D-1462-08 chr5:79616822 G>A maps to NM_032567.3 E263E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4963-01A-01D-1462-08 chr12:10772766 G>C maps to NM_018423.2 L415L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4963-01A-01D-1462-08 chr3:189604290 G>A maps to NM_003722.4 Q486Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4963-01A-01D-1462-08 chr2:61566796 A>G maps to NM_014709.3 H840H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4963-01A-01D-1462-08 chr19:6853049 C>T maps to NM_005428.2 P764P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4963-01A-01D-1462-08 chr3:126160624 G>A maps to NM_025112.4 Q793*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4963-01A-01D-1462-08 chr1:186276050 C>T maps to NM_005807.3 T400T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4963-01A-01D-1462-08 chr1:186276050 C>T maps to NM_005807.3 T400T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4964-01A-01D-1462-08 chr11:94554896 C>G maps to NM_130847.2 A441A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4964-01A-01D-1462-08 chr7:100085829 G>A maps to ENST00000423930 Q162Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4964-01A-01D-1462-08 chr4:1389121 C>T maps to NM_175918.3 R275*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4964-01A-01D-1462-08 chrX:27998266 G>A maps to NM_001017930.1 C395C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4964-01A-01D-1462-08 chr8:141549417 C>T did not map to a codon.
Sequencing variant TCGA-BP-4964-01A-01D-1462-08 chr5:76128710 C>T maps to NM_005242.4 N93N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4964-01A-01D-1462-08 chr1:45476653 G>C maps to NM_024602.5 A92A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4964-01A-01D-1462-08 chr14:94088744 C>T maps to ENST00000393153 D1744D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4964-01A-01D-1462-08 chr12:49443746 G>A maps to NM_003482.3 I1208I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4964-01A-01D-1462-08 chr12:6602136 A>C maps to NM_016497.3 G27G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4964-01A-01D-1462-08 chr3:135913892 G>A maps to NM_018133.3 D21D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4964-01A-01D-1462-08 chr12:117710300 G>C maps to ENST00000338101 L576L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4964-01A-01D-1462-08 chr11:12518074 G>T maps to NM_018222.4 L157L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4964-01A-01D-1462-08 chr14:68038959 C>A maps to NM_020715.2 S565*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4964-01A-01D-1462-08 chr1:186645101 G>T maps to NM_000963.2 Y395*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4964-01A-01D-1462-08 chr20:43837137 T>C maps to NM_003007.3 G400G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4964-01A-01D-1462-08 chr3:170078220 G>A maps to NM_005414.3 T34T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4964-01A-01D-1462-08 chr1:19480420 G>T maps to ENST00000375267 G2157G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4964-01A-01D-1462-08 chr9:130207058 C>T maps to NM_007135.2 P360P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4964-01A-01D-1462-08 chr17:3921210 C>T maps to NM_015113.3 R2520R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4964-01A-01D-1462-08 chr17:4005689 A>G maps to NM_015113.3 T531T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4964-01A-01D-1462-08 chr12:58204235 C>T maps to NM_006576.3 L219L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4964-01A-01D-1462-08 chr12:58204235 C>T maps to NM_006576.3 L219L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4964-01A-01D-1462-08 chr2:207820278 T>A maps to NM_173077.2 Y86*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4964-01A-01D-1462-08 chr2:207820278 T>A maps to NM_173077.2 Y86*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4964-01A-01D-1462-08 chr8:25158134 G>T maps to NM_024940.6 E270*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4964-01A-01D-1462-08 chr8:25158134 G>T maps to NM_024940.6 E270*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4964-01A-01D-1462-08 chr2:24524883 T>G maps to NM_006277.2 G315G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4964-01A-01D-1462-08 chr2:24524883 T>G maps to NM_006277.2 G315G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4964-01A-01D-1462-08 chr6:26638478 A>G maps to NM_024639.3 C101C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4964-01A-01D-1462-08 chr6:26638478 A>G maps to NM_024639.3 C101C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4967-01A-01D-1462-08 chr1:27874261 G>A maps to NM_001029882.2 H1455H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4967-01A-01D-1462-08 chr19:1993132 C>T maps to NM_017797.3 V190V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4967-01A-01D-1462-08 chr18:24496339 G>T maps to NM_031422.4 T405T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4967-01A-01D-1462-08 chr8:59404309 A>C maps to NM_000780.3 L413L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4967-01A-01D-1462-08 chr6:31939425 T>C maps to NM_005510.3 G9G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4967-01A-01D-1462-08 chr10:71103743 T>C maps to ENST00000439900 S110S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4967-01A-01D-1462-08 chr1:145534207 G>A maps to NM_003637.3 A571A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4967-01A-01D-1462-08 chrX:78618082 G>A maps to NM_004867.4 L183L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4967-01A-01D-1462-08 chr1:215408256 G>A maps to NM_001017425.2 E350E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4967-01A-01D-1462-08 chr12:53207944 G>T maps to NM_002272.2 P40P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4967-01A-01D-1462-08 chrX:75649862 G>T maps to NM_020932.2 E514*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4967-01A-01D-1462-08 chr12:49425038 C>T maps to NM_003482.3 L4483L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4967-01A-01D-1462-08 chr12:44917250 C>T maps to NM_001145107.1 G657G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4967-01A-01D-1462-08 chr12:9305861 G>T maps to NM_002864.2 V1284V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4967-01A-01D-1462-08 chr1:93299159 C>A maps to NM_000969.3 Y44*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4967-01A-01D-1462-08 chr16:67979423 C>A maps to NM_005072.4 L960L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4967-01A-01D-1462-08 chr17:40359717 A>G maps to NM_012448.3 P645P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4967-01A-01D-1462-08 chr2:85828148 G>T maps to NM_001031738.2 L65L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4967-01A-01D-1462-08 chr15:50763850 A>G maps to NM_005154.3 E236E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4967-01A-01D-1462-08 chr8:106813473 C>T maps to NM_012082.3 S388S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4967-01A-01D-1462-08 chr19:57646762 C>T maps to NM_052882.1 K314K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4967-01A-01D-1462-08 chr13:72204835 G>A maps to ENST00000359684 A328A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4967-01A-01D-1462-08 chr13:72204835 G>A maps to ENST00000359684 A328A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4967-01A-01D-1462-08 chr5:65088385 A>C maps to NM_020726.4 S477S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4967-01A-01D-1462-08 chr5:65088385 A>C maps to NM_020726.4 S477S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4968-01A-01D-1462-08 chr9:139906469 C>T maps to ENST00000355090 L1817L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4968-01A-01D-1462-08 chr17:40061041 G>T maps to ENST00000401700 G389G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4968-01A-01D-1462-08 chr4:175896894 G>A maps to NM_014269.4 L73L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4968-01A-01D-1462-08 chr12:7807217 G>A maps to NM_001644.3 T9T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4968-01A-01D-1462-08 chr17:11845735 T>A maps to NM_001372.3 C4259*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4968-01A-01D-1462-08 chr4:139983075 C>T maps to ENST00000379550 W250*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4968-01A-01D-1462-08 chr1:22920117 C>G maps to NM_020526.3 A514A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4968-01A-01D-1462-08 chr6:26124126 A>G maps to NM_003526.2 P2P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4968-01A-01D-1462-08 chr17:40330117 A>G maps to NM_012285.2 N195N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4968-01A-01D-1462-08 chr17:40330117 A>G maps to NM_012285.2 N195N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4968-01A-01D-1462-08 chr10:45959706 T>A maps to NM_145021.4 P74P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4968-01A-01D-1462-08 chr1:6532595 C>G maps to NM_198681.2 V434V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4968-01A-01D-1462-08 chr1:214171380 C>T maps to NM_002763.3 S501S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4968-01A-01D-1462-08 chr11:62744738 A>G maps to NM_004790.3 P494P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4968-01A-01D-1462-08 chr21:34099146 G>A maps to NM_003895.3 L59L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4968-01A-01D-1462-08 chr3:10183733 C>A maps to NM_000551.2 S68*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4968-01A-01D-1462-08 chr2:86389157 A>C maps to NM_006839.2 G279G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4968-01A-01D-1462-08 chr2:86389157 A>C maps to NM_006839.2 G279G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4970-01A-01D-1462-08 chr17:34182252 T>C maps to NM_152781.2 Q509Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4970-01A-01D-1462-08 chr6:70733566 G>T maps to NM_001858.4 E359*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4970-01A-01D-1462-08 chr6:70733566 G>T maps to NM_001858.4 E359*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4970-01A-01D-1462-08 chr19:54744776 C>T maps to ENST00000245620 R295R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4970-01A-01D-1462-08 chr17:45894651 G>A maps to NM_145798.2 I224I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4970-01A-01D-1462-08 chr20:33225753 C>T maps to NM_080476.4 Q118Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4970-01A-01D-1462-08 chr19:434717 G>A maps to NM_012435.2 A367A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4970-01A-01D-1462-08 chr20:44669097 C>T maps to NM_001134771.1 Y256Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4970-01A-01D-1462-08 chr11:5687232 T>C maps to NM_033034.2 K282K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4970-01A-01D-1462-08 chr3:10188320 G>T did not map to a codon.
Sequencing variant TCGA-BP-4970-01A-01D-1462-08 chr22:31520973 A>T maps to ENST00000331075 R83R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4970-01A-01D-1462-08 chr22:31520973 A>T maps to ENST00000331075 R83R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4970-01A-01D-1462-08 chr4:16020104 G>A maps to NM_006017.2 H281H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4970-01A-01D-1462-08 chr4:16020104 G>A maps to NM_006017.2 H281H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4971-01A-01D-1462-08 chr5:14711322 T>A maps to NM_054027.4 R488*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4971-01A-01D-1462-08 chrX:1748788 C>T maps to NM_001171038.1 T173T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4971-01A-01D-1462-08 chr17:30666860 C>A maps to NM_022344.2 G106G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4971-01A-01D-1462-08 chr7:102960088 T>A maps to NM_014377.1 T403T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4971-01A-01D-1462-08 chr11:66255470 T>A maps to NM_005700.3 L220L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4971-01A-01D-1462-08 chr2:233677187 T>C maps to ENST00000373566 A720A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4971-01A-01D-1462-08 chr3:20153264 C>T maps to NM_003884.4 L343L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4971-01A-01D-1462-08 chr16:84516269 C>T maps to NM_020947.3 V335V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4971-01A-01D-1462-08 chr19:47181734 G>A maps to ENST00000449438 N752N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4971-01A-01D-1462-08 chrX:23410646 G>C did not map to a codon.
Sequencing variant TCGA-BP-4971-01A-01D-1462-08 chr12:9321468 A>G maps to NM_002864.2 Y701Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4971-01A-01D-1462-08 chr3:170584195 A>G maps to NM_001099645.1 D114D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4971-01A-01D-1462-08 chr11:77378303 C>T maps to NM_016578.3 R1328R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4971-01A-01D-1462-08 chr12:112580007 A>G maps to NM_006700.2 Q253Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4971-01A-01D-1462-08 chr19:31768040 C>T maps to NM_020856.2 T886T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4971-01A-01D-1462-08 chr19:990273 T>A maps to NM_024100.3 S169S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4971-01A-01D-1462-08 chr19:990273 T>A maps to NM_024100.3 S169S. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-BP-4971-01A-01D-1462-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-BP-4971-01A-01D-1462-08 chr2:237076137 G>A maps to ENST00000415226 E16E. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-BP-4971-01A-01D-1462-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-BP-4971-01A-01D-1462-08 chr2:237076137 G>A maps to ENST00000415226 E16E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4971-01A-01D-1462-08 chr3:12949879 G>T maps to ENST00000429247 L908L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4971-01A-01D-1462-08 chr3:12949879 G>T maps to ENST00000429247 L908L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4971-01A-01D-1462-08 chr18:76753525 G>A maps to NM_171999.2 W512*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4971-01A-01D-1462-08 chr18:76753525 G>A maps to NM_171999.2 W512*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4972-01A-01D-1462-08 chrX:129265758 G>A maps to NM_004208.3 P488P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4972-01A-01D-1462-08 chr6:13470344 T>C maps to NM_033069.2 V56V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4972-01A-01D-1462-08 chr17:37341383 C>T maps to NM_000723.3 S216S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4972-01A-01D-1462-08 chrX:107868986 T>G maps to ENST00000328300 P1023P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4972-01A-01D-1462-08 chr1:155104090 A>G maps to NM_004428.2 G123G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4972-01A-01D-1462-08 chr4:175443218 C>A did not map to a codon.
Sequencing variant TCGA-BP-4972-01A-01D-1462-08 chr15:101528944 G>A maps to NM_024652.3 P180P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4972-01A-01D-1462-08 chr1:11190693 G>A maps to NM_004958.3 A1835A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4972-01A-01D-1462-08 chr6:34499374 A>C did not map to a codon.
Sequencing variant TCGA-BP-4972-01A-01D-1462-08 chr11:16838610 G>A maps to ENST00000448080 H534H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4972-01A-01D-1462-08 chr12:70965010 C>T maps to NM_001109754.1 V1055V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4972-01A-01D-1462-08 chr6:72974722 A>G maps to NM_014989.4 L1054L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4972-01A-01D-1462-08 chr1:9118228 A>T maps to NM_003039.2 A38A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4972-01A-01D-1462-08 chr5:1272326 C>A maps to NM_198253.2 P785P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4972-01A-01D-1462-08 chr15:43552388 G>A maps to NM_201631.3 S99S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4972-01A-01D-1462-08 chr16:67876819 G>A maps to NM_020457.2 Q121Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4973-01A-01D-1462-08 chr5:160061394 G>A maps to NM_025153.2 T449T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4973-01A-01D-1462-08 chr5:160061394 G>A maps to NM_025153.2 T449T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4973-01A-01D-1462-08 chr1:1571828 A>G maps to ENST00000401097 P642P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4973-01A-01D-1462-08 chr19:10610394 A>G maps to NM_203500.1 P105P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4973-01A-01D-1462-08 chr8:101725326 T>C maps to NM_002568.3 E242E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4973-01A-01D-1462-08 chr4:26426099 C>T maps to NM_005349.2 L224L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4973-01A-01D-1462-08 chr5:168098201 C>G did not map to a codon.
Sequencing variant TCGA-BP-4973-01A-01D-1462-08 chr3:10183743 C>T maps to NM_000551.2 P71P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4973-01A-01D-1462-08 chr19:44570595 G>A maps to NM_013361.4 K205K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4974-01A-01D-1462-08 chr4:88106696 A>G maps to NM_020803.3 C157C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4974-01A-01D-1462-08 chr17:37565878 G>A maps to NM_004774.3 F865F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4974-01A-01D-1462-08 chr1:171753286 C>T maps to NM_015935.4 A187A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4974-01A-01D-1462-08 chrX:50350757 C>T maps to NM_020717.3 Q1128Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4974-01A-01D-1462-08 chr12:69756581 T>G maps to NM_006530.2 V22V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4974-01A-01D-1462-08 chr12:69756581 T>G maps to NM_006530.2 V22V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4975-01A-01D-1462-08 chr1:111860637 C>T maps to NM_201653.2 Y212Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4975-01A-01D-1462-08 chr2:238249677 A>C maps to NM_004369.3 A2627A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4975-01A-01D-1462-08 chr5:90025456 A>C did not map to a codon.
Sequencing variant TCGA-BP-4975-01A-01D-1462-08 chr16:1866932 G>A maps to NM_005326.4 P236P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4975-01A-01D-1462-08 chr6:155776181 G>A maps to NM_015718.2 R44*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4975-01A-01D-1462-08 chr9:131256883 A>G maps to NM_153435.1 Q680Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4975-01A-01D-1462-08 chr11:57118270 C>T maps to NM_002559.2 C247C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4975-01A-01D-1462-08 chr16:67318758 G>A maps to NM_001129729.1 L612L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4975-01A-01D-1462-08 chr2:95539854 T>G did not map to a codon.
Sequencing variant TCGA-BP-4975-01A-01D-1462-08 chr7:149990454 T>C maps to NM_001164458.1 T33T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4975-01A-01D-1462-08 chr7:149990454 T>C maps to NM_001164458.1 T33T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4975-01A-01D-1462-08 chr7:2577861 A>G maps to NM_152743.3 P769P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4975-01A-01D-1462-08 chr7:2577861 A>G maps to NM_152743.3 P769P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4976-01A-01D-1462-08 chr12:112186992 C>T maps to NM_001136538.1 V918V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4976-01A-01D-1462-08 chr12:110815265 A>T maps to NM_016238.2 L464*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4976-01A-01D-1462-08 chr11:77314712 T>C maps to NM_173039.2 S244S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4976-01A-01D-1462-08 chr19:42490381 C>A did not map to a codon.
Sequencing variant TCGA-BP-4976-01A-01D-1462-08 chr3:9785379 C>G maps to NM_001003694.1 G810G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4976-01A-01D-1462-08 chr13:50495710 A>G maps to NM_020456.2 I132I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4976-01A-01D-1462-08 chr7:2577852 C>G maps to NM_152743.3 V772V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4976-01A-01D-1462-08 chr7:2577852 C>G maps to NM_152743.3 V772V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4976-01A-01D-1462-08 chr14:55004492 C>T maps to NM_006568.2 C208C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4976-01A-01D-1462-08 chrX:83128528 T>C maps to NM_021118.1 N271N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4976-01A-01D-1462-08 chr5:169494674 C>T maps to NM_004946.2 F1543F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4976-01A-01D-1462-08 chr5:169494674 C>T maps to NM_004946.2 F1543F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4976-01A-01D-1462-08 chr11:6233062 G>T maps to NM_032127.3 L878L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4976-01A-01D-1462-08 chr19:3533329 C>A maps to NM_001136198.1 V427V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4976-01A-01D-1462-08 chr11:67219268 C>A maps to NM_206997.1 V309V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4976-01A-01D-1462-08 chr12:66731857 G>A maps to NM_033647.2 K1080K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4976-01A-01D-1462-08 chr2:48687266 G>T maps to NM_001135629.2 E192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4976-01A-01D-1462-08 chr12:107371721 T>C maps to NM_025198.3 Q257Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4976-01A-01D-1462-08 chr3:195505745 T>G maps to NM_018406.5 T4235T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4976-01A-01D-1462-08 chr12:57112265 A>G maps to NM_001113203.1 P1016P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4976-01A-01D-1462-08 chr10:75520025 C>T maps to NM_198597.1 P244P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4976-01A-01D-1462-08 chr7:37955989 C>A maps to ENST00000223214 T72T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4976-01A-01D-1462-08 chr18:46474802 A>G maps to NM_005904.3 S206S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4976-01A-01D-1462-08 chr20:36024601 C>A maps to ENST00000373558 A203A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4976-01A-01D-1462-08 chr1:229738592 C>A maps to NM_014409.3 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4976-01A-01D-1462-08 chr2:179437361 T>A maps to NM_133378.4 L21931L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4976-01A-01D-1462-08 chr8:87464826 A>G maps to NM_007013.3 E771E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4976-01A-01D-1462-08 chr10:46272803 G>A maps to ENST00000399588 V742V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4976-01A-01D-1462-08 chr10:46272803 G>A maps to ENST00000399588 V742V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4976-01A-01D-1462-08 chr5:176863392 G>T did not map to a codon.
Sequencing variant TCGA-BP-4976-01A-01D-1462-08 chr5:176863392 G>T did not map to a codon.
Sequencing variant TCGA-BP-4976-01A-01D-1462-08 chr3:47038047 G>A maps to NM_015175.1 L813L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4976-01A-01D-1462-08 chr3:47038047 G>A maps to NM_015175.1 L813L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4977-01A-01D-1462-08 chr10:123503287 C>T maps to NM_001001976.1 Q488Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4977-01A-01D-1462-08 chr7:31683359 C>A maps to NM_194300.2 I792I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4977-01A-01D-1462-08 chr16:68862135 C>T maps to NM_004360.3 L742L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4977-01A-01D-1462-08 chr9:139748705 C>T maps to ENST00000392881 N238N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4977-01A-01D-1462-08 chr7:156450263 C>T maps to NM_001184997.1 H149H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4977-01A-01D-1462-08 chr17:71429904 C>T maps to NM_001144952.1 S426S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4977-01A-01D-1462-08 chr2:224866440 C>T maps to NM_001136530.1 A71A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4977-01A-01D-1462-08 chrX:70148385 G>A maps to NM_032803.5 F209F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4977-01A-01D-1462-08 chrX:69825331 C>A maps to NM_001003811.1 L677L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4977-01A-01D-1462-08 chr18:66367640 C>A did not map to a codon.
Sequencing variant TCGA-BP-4981-01A-01D-1462-08 chr7:48313954 C>T maps to NM_152701.3 N1564N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4981-01A-01D-1462-08 chr18:9211597 T>C maps to NM_015208.3 H156H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4981-01A-01D-1462-08 chr2:25967151 G>C maps to NM_018263.4 S685*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4981-01A-01D-1462-08 chr20:5903113 G>A maps to NM_001819.2 G108G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4981-01A-01D-1462-08 chr1:47401232 C>T maps to ENST00000371904 K199K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4981-01A-01D-1462-08 chr19:2214516 G>A maps to ENST00000221482 S615S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4981-01A-01D-1462-08 chr2:109103097 T>A maps to NM_181453.3 A1308A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4981-01A-01D-1462-08 chr2:74684831 C>G maps to ENST00000452361 G304G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4981-01A-01D-1462-08 chr12:442727 A>G maps to NM_001042603.1 F526F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4981-01A-01D-1462-08 chr20:54824096 C>T maps to ENST00000371389 N103N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4981-01A-01D-1462-08 chr16:21611122 G>C maps to NM_016025.3 T23T. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-BP-4981-01A-01D-1462-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-BP-4981-01A-01D-1462-08 chr16:816774 C>G maps to NM_013404.4 P454P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4981-01A-01D-1462-08 chr16:15872667 C>T maps to NM_001040114.1 T260T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4981-01A-01D-1462-08 chr5:140255596 T>G maps to NM_018903.2 L180L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4981-01A-01D-1462-08 chr13:113854791 A>G maps to ENST00000246505 C25C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4981-01A-01D-1462-08 chr20:34487449 A>T maps to NM_016436.4 K481*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4981-01A-01D-1462-08 chr12:32949146 G>A maps to NM_004572.3 A795A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4981-01A-01D-1462-08 chr6:54212216 T>C maps to NM_014464.3 N267N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4981-01A-01D-1462-08 chr17:57915759 T>C did not map to a codon.
Sequencing variant TCGA-BP-4981-01A-01D-1462-08 chr9:134612881 C>T did not map to a codon.
Sequencing variant TCGA-BP-4981-01A-01D-1462-08 chr9:134612881 C>T did not map to a codon.
Sequencing variant TCGA-BP-4982-01A-01D-1462-08 chr1:223568376 C>T maps to NM_152610.2 H520H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4982-01A-01D-1462-08 chr19:49468841 G>A maps to NM_000146.3 Q26Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4982-01A-01D-1462-08 chr10:100481427 G>A maps to NM_021828.4 I314I. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-BP-4982-01A-01D-1462-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-BP-4982-01A-01D-1462-08 chr3:100059917 C>T maps to NM_020202.4 G83G. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-BP-4982-01A-01D-1462-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-BP-4982-01A-01D-1462-08 chr1:226564844 G>C maps to NM_001618.3 P635P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4982-01A-01D-1462-08 chr1:226564844 G>C maps to NM_001618.3 P635P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4982-01A-01D-1462-08 chr3:52702611 T>A maps to ENST00000296302 K96*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4982-01A-01D-1462-08 chr2:28752199 C>A maps to NM_153021.4 I114I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4982-01A-01D-1462-08 chr20:1144991 C>T maps to NM_006814.3 P212P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4982-01A-01D-1462-08 chr3:47455553 T>A maps to NM_012235.2 S1210S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4982-01A-01D-1462-08 chr5:54618205 T>C maps to NM_015360.4 N62N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4982-01A-01D-1462-08 chr10:70967646 C>A maps to NM_003171.3 L625L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4982-01A-01D-1462-08 chr19:44352475 G>T maps to NM_181845.1 E575*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4982-01A-01D-1462-08 chr3:10183793 G>A maps to NM_000551.2 W88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4982-01A-01D-1462-08 chr3:10183793 G>A maps to NM_000551.2 W88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4983-01A-01D-1462-08 chr1:197087082 A>G maps to NM_018136.4 L1301L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4983-01A-01D-1462-08 chr20:31023503 G>T maps to ENST00000375687 E997*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4983-01A-01D-1462-08 chr1:159170639 C>T maps to NM_021189.3 D409D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4983-01A-01D-1462-08 chr17:62009606 C>T maps to NM_001039933.1 A5A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4983-01A-01D-1462-08 chr18:59195204 G>A maps to NM_031891.2 L341L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4983-01A-01D-1462-08 chr1:23191445 C>T maps to ENST00000400191 R348R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4983-01A-01D-1462-08 chr3:50290460 C>T maps to NM_002070.2 D103D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4983-01A-01D-1462-08 chrX:78426731 C>A maps to NM_032553.1 I76I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4983-01A-01D-1462-08 chr1:155252387 T>C maps to NM_020897.1 A155A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4983-01A-01D-1462-08 chr15:28501376 C>T maps to NM_004667.4 T868T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4983-01A-01D-1462-08 chr20:39987125 C>T maps to NM_022896.1 F785F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4983-01A-01D-1462-08 chr12:57600463 G>A maps to NM_002332.2 A3933A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4983-01A-01D-1462-08 chr11:65318873 G>A maps to NM_001130144.2 P540P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4983-01A-01D-1462-08 chr14:51259501 A>C maps to NM_020921.3 P121P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4983-01A-01D-1462-08 chr1:248525255 C>A maps to NM_001004696.1 S125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4983-01A-01D-1462-08 chr15:40594519 T>A maps to NM_004573.2 K135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4983-01A-01D-1462-08 chr9:125760993 G>A maps to NM_012197.3 W441*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4983-01A-01D-1462-08 chr14:36096962 G>A maps to NM_194301.2 Q1558*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4983-01A-01D-1462-08 chr7:155537938 T>G maps to NM_053043.2 L874L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4983-01A-01D-1462-08 chr10:63958098 T>C maps to NM_145307.2 L466L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4983-01A-01D-1462-08 chr15:33988669 T>C maps to NM_001036.3 L2038L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4983-01A-01D-1462-08 chr7:4011188 G>T maps to NM_152744.3 R602R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4983-01A-01D-1462-08 chr17:79220706 G>A maps to NM_001037984.1 D740D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4983-01A-01D-1462-08 chr7:127341300 T>C maps to NM_014390.2 H171H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4983-01A-01D-1462-08 chr22:50660935 G>A maps to NM_020461.3 R786*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4983-01A-01D-1462-08 chr10:27529389 G>A maps to ENST00000375888 S11S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4983-01A-01D-1462-08 chr10:27529389 G>A maps to ENST00000375888 S11S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4983-01A-01D-1462-08 chr12:2800178 G>A maps to NM_199460.2 A2160A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4983-01A-01D-1462-08 chr12:2800178 G>A maps to NM_199460.2 A2160A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4983-01A-01D-1462-08 chr22:31091333 G>A maps to NM_030758.3 A146A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4983-01A-01D-1462-08 chr22:31091333 G>A maps to NM_030758.3 A146A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4983-01A-01D-1462-08 chr4:147560211 C>A did not map to a codon.
Sequencing variant TCGA-BP-4983-01A-01D-1462-08 chr4:147560211 C>A did not map to a codon.
Sequencing variant TCGA-BP-4985-01A-01D-1462-08 chr15:35196563 C>T maps to NM_014691.2 R658R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4985-01A-01D-1462-08 chr11:111754534 T>C maps to NM_022761.2 P128P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4985-01A-01D-1462-08 chr15:90785078 G>T maps to NM_001013657.2 L313L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4985-01A-01D-1462-08 chr1:55166857 C>T maps to ENST00000454855 L1079L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4985-01A-01D-1462-08 chr4:170663224 C>T maps to NM_017867.2 T177T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4985-01A-01D-1462-08 chr3:33648251 T>C did not map to a codon.
Sequencing variant TCGA-BP-4985-01A-01D-1462-08 chr10:129202629 C>T maps to ENST00000398025 I1398I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4985-01A-01D-1462-08 chr21:37603370 C>T maps to NM_005128.2 F763F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4985-01A-01D-1462-08 chr17:42636501 C>T maps to NM_001466.3 Y482Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4985-01A-01D-1462-08 chr8:39775605 G>A did not map to a codon.
Sequencing variant TCGA-BP-4985-01A-01D-1462-08 chr17:17078668 C>A maps to NM_015134.2 G884G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4985-01A-01D-1462-08 chr19:9067639 A>G maps to NM_024690.2 S6602S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4985-01A-01D-1462-08 chr1:248436861 G>T maps to NM_001004695.1 T85T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4985-01A-01D-1462-08 chr3:52623109 C>A maps to ENST00000296302 E981*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4985-01A-01D-1462-08 chr5:140579544 G>C maps to NM_018931.2 V66V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4985-01A-01D-1462-08 chr10:81904025 G>C maps to NM_001012973.1 L70L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4985-01A-01D-1462-08 chr14:24808451 C>T maps to NM_006871.3 E80E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4985-01A-01D-1462-08 chr11:9048917 C>A maps to ENST00000457346 R898R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4985-01A-01D-1462-08 chr11:9048917 C>A maps to ENST00000457346 R898R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4985-01A-01D-1462-08 chr8:87242197 C>T maps to NM_138817.2 L103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4985-01A-01D-1462-08 chrX:123197043 C>T maps to NM_001042750.1 R604*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4985-01A-01D-1462-08 chr2:228228664 A>T maps to NM_024795.3 T155T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4985-01A-01D-1462-08 chr6:32047062 G>A maps to ENST00000375244 L1374L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4985-01A-01D-1462-08 chr1:179833915 C>A maps to NM_022347.3 *132Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4985-01A-01D-1462-08 chr11:118531942 G>A maps to ENST00000264029 N261N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4985-01A-01D-1462-08 chr17:56058036 G>T maps to NM_007146.2 I301I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4985-01A-01D-1462-08 chr7:138764441 G>A maps to ENST00000464606 G415G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4985-01A-01D-1462-08 chr19:53668434 G>T maps to NM_024733.3 G436G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4985-01A-01D-1462-08 chr1:248084573 C>A maps to NM_001005522.1 T85T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4985-01A-01D-1462-08 chr1:248084573 C>A maps to NM_001005522.1 T85T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4986-01A-01D-1462-08 chr4:71510238 C>A maps to NM_031889.2 G1032G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4986-01A-01D-1462-08 chr4:187208886 C>T maps to NM_000128.3 N542N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4986-01A-01D-1462-08 chr13:39451279 T>C maps to NM_207361.4 F2857F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4986-01A-01D-1462-08 chr10:6054845 T>G maps to NM_000417.2 R270R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4986-01A-01D-1462-08 chr1:18807867 G>A maps to NM_152375.2 S131S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4986-01A-01D-1462-08 chr1:183532671 T>A maps to NM_001127651.2 K359*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4986-01A-01D-1462-08 chr15:90815013 A>G maps to NM_001033088.1 R290R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4986-01A-01D-1462-08 chr5:140230077 G>A maps to NM_031857.1 L666L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4986-01A-01D-1462-08 chr19:50905746 G>A maps to ENST00000391817 W265*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4986-01A-01D-1462-08 chr2:179664359 C>T maps to NM_133378.4 R256R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4986-01A-01D-1462-08 chr17:4381895 G>C maps to NM_182538.4 L381L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4986-01A-01D-1462-08 chr17:4381895 G>C maps to NM_182538.4 L381L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4987-01A-01D-1462-08 chr20:30037859 T>A maps to NM_153324.2 Y29*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4987-01A-01D-1462-08 chr3:121415220 T>C maps to ENST00000393667 Q1383Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4987-01A-01D-1462-08 chr17:45377873 G>C maps to NM_000212.2 R648R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4987-01A-01D-1462-08 chr3:52712579 G>A maps to ENST00000296302 R58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4987-01A-01D-1462-08 chr22:21104190 A>G did not map to a codon.
Sequencing variant TCGA-BP-4987-01A-01D-1462-08 chr5:146077635 G>A maps to ENST00000394414 F146F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4987-01A-01D-1462-08 chr14:21771588 C>T maps to NM_020366.3 S229S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4987-01A-01D-1462-08 chr19:38985139 G>A maps to NM_000540.2 A2141A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4987-01A-01D-1462-08 chr14:64447731 G>A maps to NM_182914.2 Q559Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4987-01A-01D-1462-08 chr12:132633360 G>T maps to NM_024078.1 L274L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4987-01A-01D-1462-08 chr12:132633360 G>T maps to NM_024078.1 L274L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4988-01A-01D-1462-08 chr3:184102983 G>T maps to NM_003741.2 T592T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4988-01A-01D-1462-08 chr5:122911472 A>G maps to NM_001044723.1 V163V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4988-01A-01D-1462-08 chr8:88885731 G>A maps to NM_152418.3 A156A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4988-01A-01D-1462-08 chr8:88885731 G>A maps to NM_152418.3 A156A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4988-01A-01D-1462-08 chr1:6741000 G>A maps to NM_018198.3 R57*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4988-01A-01D-1462-08 chr1:6741000 G>A maps to NM_018198.3 R57*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4988-01A-01D-1462-08 chr12:120586151 T>C did not map to a codon.
Sequencing variant TCGA-BP-4988-01A-01D-1462-08 chr17:73729633 G>A maps to NM_001005619.1 E506E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4988-01A-01D-1462-08 chr8:48309112 T>C maps to NM_001080394.1 L235L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4988-01A-01D-1462-08 chr8:48309112 T>C maps to NM_001080394.1 L235L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4988-01A-01D-1462-08 chr2:170060530 C>A maps to NM_004525.2 E2656*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4988-01A-01D-1462-08 chr5:176637817 A>C maps to NM_022455.4 I806I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4988-01A-01D-1462-08 chr3:52643347 G>A maps to ENST00000296302 R850*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4988-01A-01D-1462-08 chr15:72039332 C>T maps to NM_024817.2 C731C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4988-01A-01D-1462-08 chr15:72039332 C>T maps to NM_024817.2 C731C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4988-01A-01D-1462-08 chr8:141415690 A>G maps to NM_031466.5 I429I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4988-01A-01D-1462-08 chr3:10191480 G>C maps to NM_000551.2 L158L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4988-01A-01D-1462-08 chr17:75209463 C>T maps to NM_001039573.2 C644C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4988-01A-01D-1462-08 chr17:75209463 C>T maps to NM_001039573.2 C644C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4988-01A-01D-1462-08 chrX:70472955 A>G maps to ENST00000373988 P50P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4988-01A-01D-1462-08 chrX:70472955 A>G maps to ENST00000373988 P50P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4989-01A-01D-1462-08 chr16:396290 C>T maps to NM_003502.3 E245E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4989-01A-01D-1462-08 chr12:56487572 A>G maps to NM_001982.2 P502P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4989-01A-01D-1462-08 chr2:187559049 A>G maps to NM_177454.3 Q50Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4989-01A-01D-1462-08 chr6:99365255 A>C maps to NM_012160.3 P284P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4989-01A-01D-1462-08 chr20:14307333 G>C maps to NM_198391.2 L273L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4989-01A-01D-1462-08 chr17:46608209 G>T maps to NM_002144.3 P19P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4989-01A-01D-1462-08 chr15:81589273 G>A maps to NM_172217.3 A636A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4989-01A-01D-1462-08 chr19:10799268 C>T maps to NM_017620.2 G826G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4989-01A-01D-1462-08 chr10:24834979 C>A maps to NM_019590.3 L1853L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4989-01A-01D-1462-08 chr6:17898398 C>T maps to NM_022113.4 K53K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4989-01A-01D-1462-08 chr6:17898398 C>T maps to NM_022113.4 K53K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4989-01A-01D-1462-08 chr14:104129225 C>T maps to ENST00000445352 D425D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4989-01A-01D-1462-08 chr12:52756640 G>T maps to NM_002283.3 C358*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4989-01A-01D-1462-08 chr5:153432672 C>T maps to NM_005927.4 L163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4989-01A-01D-1462-08 chr7:104719410 G>A did not map to a codon.
Sequencing variant TCGA-BP-4989-01A-01D-1462-08 chrX:106186436 T>A did not map to a codon.
Sequencing variant TCGA-BP-4989-01A-01D-1462-08 chr4:183714118 C>G maps to NM_001080477.1 L2098L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4989-01A-01D-1462-08 chr5:140182764 C>A maps to NM_018906.2 A661A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4989-01A-01D-1462-08 chr5:140475999 G>A maps to NM_018936.2 A542A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4989-01A-01D-1462-08 chr10:75673066 C>T maps to NM_002658.3 R130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4989-01A-01D-1462-08 chr12:19410395 T>C maps to ENST00000429027 N154N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4989-01A-01D-1462-08 chr3:78706389 G>T maps to NM_002941.3 Y824*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4989-01A-01D-1462-08 chr2:179484438 T>C maps to NM_133378.4 R12967R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4989-01A-01D-1462-08 chr2:179504808 G>A maps to NM_133378.4 L11016L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4989-01A-01D-1462-08 chr17:72249929 C>T maps to NM_032646.5 Y494Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4989-01A-01D-1462-08 chr2:168101916 A>T maps to NM_152381.5 K1339*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4989-01A-01D-1462-08 chr6:131931275 G>T maps to ENST00000403834 L335L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4989-01A-01D-1462-08 chr6:131931275 G>T maps to ENST00000403834 L335L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4989-01A-01D-1462-08 chr7:143929684 G>T maps to NM_001005287.1 L84L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4989-01A-01D-1462-08 chr7:143929684 G>T maps to NM_001005287.1 L84L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4991-01A-01D-1462-08 chr6:31627291 A>G maps to NM_021184.3 L145L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4991-01A-01D-1462-08 chr4:15511766 G>A maps to NM_001080522.2 G148G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4991-01A-01D-1462-08 chr19:10071470 G>T maps to NM_015719.3 Y1649*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4991-01A-01D-1462-08 chr19:11618639 G>A maps to NM_016581.3 A274A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4991-01A-01D-1462-08 chr17:28405488 G>A maps to NM_198529.3 P998P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4991-01A-01D-1462-08 chr17:80046745 G>A maps to NM_004104.4 L771L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4991-01A-01D-1462-08 chr10:49420020 C>T maps to NM_001018071.3 E529E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4991-01A-01D-1462-08 chr22:25010805 G>A maps to NM_005265.2 G76G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4991-01A-01D-1462-08 chr17:46805883 C>T maps to NM_006361.5 G24G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4991-01A-01D-1462-08 chr17:39635601 C>T maps to NM_002280.4 E236E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4991-01A-01D-1462-08 chr9:123476114 G>A maps to ENST00000426959 T166T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4991-01A-01D-1462-08 chr15:89449934 G>A maps to NM_005928.2 Y154Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4991-01A-01D-1462-08 chrX:64959701 C>T maps to NM_002444.2 Q561*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4991-01A-01D-1462-08 chr11:4674481 T>G maps to NM_152430.3 T242T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4991-01A-01D-1462-08 chr15:83805261 T>A maps to NM_023003.3 L317L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4991-01A-01D-1462-08 chr13:47470002 T>A maps to NM_000621.3 S13S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4991-01A-01D-1462-08 chr13:47470002 T>A maps to NM_000621.3 S13S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4992-01A-01D-1462-08 chr2:241631410 C>A maps to ENST00000429564 A27A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4992-01A-01D-1462-08 chr7:42949680 C>T maps to NM_001099858.1 E331E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4992-01A-01D-1462-08 chr2:96993808 C>T maps to ENST00000420728 F511F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4992-01A-01D-1462-08 chr17:2596081 G>A maps to NM_015229.3 Q1063*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4992-01A-01D-1462-08 chr4:674307 C>T maps to NM_002477.1 A101A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4992-01A-01D-1462-08 chr5:140257018 C>T maps to NM_018903.2 H654H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4992-01A-01D-1462-08 chr5:179382656 A>G maps to NM_018434.4 F419F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4992-01A-01D-1462-08 chr2:110053414 G>T maps to NM_001099289.1 G547G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4992-01A-01D-1462-08 chr2:10051036 C>T maps to NM_005680.2 F376F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4992-01A-01D-1462-08 chr11:12316357 T>C maps to NM_032867.2 P460P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4992-01A-01D-1462-08 chr11:12316357 T>C maps to NM_032867.2 P460P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4993-01A-02D-1421-08 chr14:74036024 C>G maps to NM_006821.4 V27V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4993-01A-02D-1421-08 chr12:112673070 C>A did not map to a codon.
Sequencing variant TCGA-BP-4993-01A-02D-1421-08 chr14:77880340 C>T maps to NM_001113475.1 L95L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4993-01A-02D-1421-08 chr4:57842812 C>T maps to NM_032313.2 V313V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4993-01A-02D-1421-08 chr10:12595349 G>T maps to NM_153498.2 L73L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4993-01A-02D-1421-08 chr16:2233882 G>A maps to NM_020764.3 N492N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4993-01A-02D-1421-08 chr17:62496042 A>G maps to NM_004396.3 *615Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4993-01A-02D-1421-08 chr20:29891068 G>A maps to NM_001037731.1 Y85Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4993-01A-02D-1421-08 chr17:7508977 T>C maps to NM_004860.3 E71E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4993-01A-02D-1421-08 chr12:12815271 G>A maps to NM_006143.2 S37S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4993-01A-02D-1421-08 chr12:12815271 G>A maps to NM_006143.2 S37S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4993-01A-02D-1421-08 chr17:60802311 C>A maps to NM_152598.2 V697V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4993-01A-02D-1421-08 chr21:47692475 T>A maps to NM_003906.3 R822*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4993-01A-02D-1421-08 chr22:28192793 C>T maps to NM_002430.2 A1246A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4993-01A-02D-1421-08 chr3:52643347 G>A maps to ENST00000296302 R850*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4993-01A-02D-1421-08 chr4:134071516 C>A maps to NM_032961.1 Y74*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4993-01A-02D-1421-08 chr7:92731888 C>T maps to NM_017654.3 E1174E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4993-01A-02D-1421-08 chr17:33585669 G>A did not map to a codon.
Sequencing variant TCGA-BP-4993-01A-02D-1421-08 chr9:93624626 G>A did not map to a codon.
Sequencing variant TCGA-BP-4993-01A-02D-1421-08 chr9:93624626 G>A did not map to a codon.
Sequencing variant TCGA-BP-4993-01A-02D-1421-08 chr6:86324827 A>G maps to NM_006372.4 A506A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4993-01A-02D-1421-08 chr16:67877044 T>C maps to NM_020457.2 F196F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4993-01A-02D-1421-08 chr16:52478205 C>T maps to ENST00000407228 R323R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4993-01A-02D-1421-08 chr16:52478214 C>T maps to ENST00000407228 A320A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4993-01A-02D-1421-08 chr18:56587465 T>C maps to NM_018181.4 C649C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4993-01A-02D-1421-08 chr8:144654815 T>C maps to NM_001100878.1 A23A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4993-01A-02D-1421-08 chr8:144654815 T>C maps to NM_001100878.1 A23A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4993-01A-02D-1421-08 chr1:100964715 A>T maps to NM_033312.2 P551P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4993-01A-02D-1421-08 chr1:100964715 A>T maps to NM_033312.2 P551P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4993-01A-02D-1421-08 chr20:47989843 A>C maps to NM_004975.2 G751G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4993-01A-02D-1421-08 chr20:47989843 A>C maps to NM_004975.2 G751G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4993-01A-02D-1421-08 chr17:35299576 C>T maps to NM_005568.3 F252F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4993-01A-02D-1421-08 chr17:35299576 C>T maps to NM_005568.3 F252F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4993-01A-02D-1421-08 chr19:36435682 C>A maps to NM_024509.1 S550*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4993-01A-02D-1421-08 chr19:36435682 C>A maps to NM_024509.1 S550*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4993-01A-02D-1421-08 chr15:34113724 T>G maps to NM_001036.3 G3639G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4993-01A-02D-1421-08 chr15:34113724 T>G maps to NM_001036.3 G3639G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4995-01A-01D-1462-08 chr16:16108475 C>T maps to ENST00000399408 A160A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4995-01A-01D-1462-08 chr1:236924370 C>A maps to NM_001103.2 T808T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4995-01A-01D-1462-08 chr14:105418039 G>A maps to NM_138420.2 Q1250*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4995-01A-01D-1462-08 chr4:114277952 C>T maps to NM_001148.4 Q2727*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4995-01A-01D-1462-08 chr1:227227834 C>A maps to ENST00000366766 E1066*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4995-01A-01D-1462-08 chr3:130289956 C>T maps to NM_001102608.1 F899F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4995-01A-01D-1462-08 chr7:99313482 C>A maps to ENST00000292414 G190*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4995-01A-01D-1462-08 chr4:155253990 C>T maps to NM_017639.3 S624S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4995-01A-01D-1462-08 chr11:22646843 C>T maps to NM_022725.3 L171L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4995-01A-01D-1462-08 chr15:43821932 T>A maps to ENST00000382031 A2945A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4995-01A-01D-1462-08 chr11:62366079 C>G maps to NM_004739.2 G74G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4995-01A-01D-1462-08 chr16:4519368 C>T maps to NM_020677.3 E46E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4995-01A-01D-1462-08 chr5:140202820 C>G maps to NM_018908.2 A487A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4995-01A-01D-1462-08 chr5:140553990 G>A maps to NM_018940.2 Q525Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4995-01A-01D-1462-08 chr19:50185318 C>T maps to NM_001536.3 I115I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4995-01A-01D-1462-08 chr6:7231265 T>A maps to NM_001003699.3 S978S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4995-01A-01D-1462-08 chr8:17412116 G>A maps to NM_001164771.1 A408A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4995-01A-01D-1462-08 chr1:154522940 C>T maps to NM_017582.6 W414*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4995-01A-01D-1462-08 chr1:154522940 C>T maps to NM_017582.6 W414*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4995-01A-01D-1462-08 chr2:128927888 G>T maps to NM_020120.3 G983G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4995-01A-01D-1462-08 chr10:31134198 C>T maps to NM_182755.2 L726L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4995-01A-01D-1462-08 chr11:46407570 C>A maps to NM_000741.2 T179T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4995-01A-01D-1462-08 chr11:46407570 C>A maps to NM_000741.2 T179T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4995-01A-01D-1462-08 chr15:42363001 G>A maps to NM_178034.3 I652I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4995-01A-01D-1462-08 chr15:42363001 G>A maps to NM_178034.3 I652I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4995-01A-01D-1462-08 chr11:68853398 G>A did not map to a codon.
Sequencing variant TCGA-BP-4995-01A-01D-1462-08 chr11:68853398 G>A did not map to a codon.
Sequencing variant TCGA-BP-4995-01A-01D-1462-08 chr3:10183733 C>A maps to NM_000551.2 S68*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4995-01A-01D-1462-08 chr3:10183733 C>A maps to NM_000551.2 S68*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4998-01A-01D-1462-08 chr9:133760874 C>T maps to NM_007313.2 F1085F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4998-01A-01D-1462-08 chr12:25264774 A>T maps to NM_018272.3 A570A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4998-01A-01D-1462-08 chr1:15771155 C>T maps to NM_007272.2 H183H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4998-01A-01D-1462-08 chr6:150174137 C>A did not map to a codon.
Sequencing variant TCGA-BP-4998-01A-01D-1462-08 chr7:139724548 G>C maps to NM_022750.2 A639A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4998-01A-01D-1462-08 chrX:54048717 T>C maps to NM_001184896.1 R125R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4998-01A-01D-1462-08 chr7:113559038 C>A maps to NM_002711.3 E5*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4998-01A-01D-1462-08 chr16:2817281 A>T maps to NM_016333.3 P2251P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4998-01A-01D-1462-08 chr2:179598117 A>T maps to NM_133378.4 L4057*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4998-01A-01D-1462-08 chr15:49170495 C>A maps to NM_014335.2 S41S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4998-01A-01D-1462-08 chr15:49170495 C>A maps to NM_014335.2 S41S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4999-01A-01D-1462-08 chr1:160523748 C>T maps to NM_001184879.1 T192T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4999-01A-01D-1462-08 chr22:36693019 C>T maps to NM_002473.4 E1047E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4999-01A-01D-1462-08 chr3:52663034 G>A maps to ENST00000296302 Q440*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4999-01A-01D-1462-08 chr13:33316757 G>A maps to ENST00000400481 W835*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4999-01A-01D-1462-08 chr9:133543579 C>A maps to NM_021619.2 I150I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4999-01A-01D-1462-08 chr5:141019627 G>A maps to NM_173828.4 G215G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4999-01A-01D-1462-08 chr15:56390305 A>G maps to NM_022841.5 V360V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4999-01A-01D-1462-08 chr16:30977376 C>G maps to NM_014712.1 A725A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4999-01A-01D-1462-08 chr1:85117617 G>T maps to NM_001166417.1 T484T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4999-01A-01D-1462-08 chr11:119290971 C>G maps to NM_006288.3 L54L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4999-01A-01D-1462-08 chr2:219140332 G>A maps to NM_022152.4 Y267Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4999-01A-01D-1462-08 chr16:11873153 A>G maps to NM_014153.3 D58D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4999-01A-01D-1462-08 chr2:220073737 G>A maps to NM_138802.1 L232L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4999-01A-01D-1462-08 chr11:747519 C>T maps to NM_006755.1 S13S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4999-01A-01D-1462-08 chr11:747519 C>T maps to NM_006755.1 S13S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5000-01A-01D-1462-08 chr14:24801008 G>C maps to NM_139247.3 T218T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5000-01A-01D-1462-08 chr15:86940774 C>T maps to NM_152336.2 G805G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5000-01A-01D-1462-08 chr8:69351860 G>A maps to NM_052958.2 W152*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5000-01A-01D-1462-08 chr20:39990047 T>G maps to NM_052846.1 R721R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5000-01A-01D-1462-08 chr4:3208254 G>T maps to NM_002111.6 T1917T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5000-01A-01D-1462-08 chr5:61779840 C>T maps to NM_001134779.1 S382S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5000-01A-01D-1462-08 chr5:61779840 C>T maps to NM_001134779.1 S382S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5000-01A-01D-1462-08 chrX:53227750 G>A maps to NM_004187.3 Q813*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5000-01A-01D-1462-08 chr1:225599095 T>A maps to NM_194442.1 R377R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5000-01A-01D-1462-08 chr16:31141807 C>T maps to NM_182958.2 V346V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5000-01A-01D-1462-08 chr13:80094985 G>A maps to NM_019080.2 E121E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5000-01A-01D-1462-08 chr2:152548581 T>C maps to NM_001164507.1 Q699Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5000-01A-01D-1462-08 chr6:57498974 T>C maps to NM_000947.2 D413D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5000-01A-01D-1462-08 chr1:155291905 C>A maps to NM_001105203.1 P114P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5000-01A-01D-1462-08 chr11:64360345 C>A maps to NM_144585.2 A166A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5000-01A-01D-1462-08 chr12:124069275 G>A maps to NM_006815.3 E31E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5000-01A-01D-1462-08 chr19:52918812 T>C maps to NM_032423.2 T236T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5001-01A-01D-1462-08 chr2:234178665 G>T maps to ENST00000392018 L220L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5001-01A-01D-1462-08 chr16:81069750 C>G maps to NM_015251.2 G92G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5001-01A-01D-1462-08 chr7:21639511 C>T maps to NM_003777.3 H925H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5001-01A-01D-1462-08 chr14:86088841 C>T maps to NM_013231.4 I328I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5001-01A-01D-1462-08 chr2:102956733 T>G did not map to a codon.
Sequencing variant TCGA-BP-5001-01A-01D-1462-08 chr6:112513052 C>G did not map to a codon.
Sequencing variant TCGA-BP-5001-01A-01D-1462-08 chr5:140718868 G>T maps to NM_018915.2 E111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5001-01A-01D-1462-08 chr2:43973090 A>T maps to NM_172069.3 T1214T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5001-01A-01D-1462-08 chr9:98209385 C>G maps to NM_000264.3 P1384P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5001-01A-01D-1462-08 chrX:119004754 G>A maps to NM_006978.2 V274V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5001-01A-01D-1462-08 chr2:200193630 T>A maps to NM_001172509.1 G392G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5001-01A-01D-1462-08 chr1:243581286 T>C maps to NM_006642.3 L588L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5001-01A-01D-1462-08 chr1:2234821 G>A maps to NM_003036.3 P398P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5001-01A-01D-1462-08 chr12:21454186 T>A maps to NM_134431.3 G202G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5001-01A-01D-1462-08 chr22:22842517 G>A maps to NM_080764.2 P402P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5004-01A-01D-1462-08 chr17:34185481 G>T maps to NM_152781.2 V329V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5004-01A-01D-1462-08 chr3:129023467 C>T maps to NM_001006109.1 Q289*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5004-01A-01D-1462-08 chr7:76916143 C>T maps to NM_020879.2 D726D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5004-01A-01D-1462-08 chr2:37319306 G>C did not map to a codon.
Sequencing variant TCGA-BP-5004-01A-01D-1462-08 chr2:37319306 G>C did not map to a codon.
Sequencing variant TCGA-BP-5004-01A-01D-1462-08 chr12:51127943 T>C maps to NM_173602.2 T1336T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5004-01A-01D-1462-08 chr6:76570738 G>C did not map to a codon.
Sequencing variant TCGA-BP-5004-01A-01D-1462-08 chr14:73759583 T>C did not map to a codon.
Sequencing variant TCGA-BP-5004-01A-01D-1462-08 chr14:23371267 A>G maps to NM_001077351.1 A389A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5004-01A-01D-1462-08 chr7:122342195 G>C maps to NM_198085.1 A203A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5004-01A-01D-1462-08 chr18:61310790 G>C maps to NM_002974.2 A7A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5004-01A-01D-1462-08 chr7:6190119 C>T maps to ENST00000404835 G728G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5004-01A-01D-1462-08 chr11:75852291 A>T maps to NM_003369.3 S645S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5004-01A-01D-1462-08 chr19:22836215 C>A maps to NM_020855.2 Y5*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5006-01A-01D-1462-08 chr6:107009362 T>C maps to NM_001624.2 C1634C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5006-01A-01D-1462-08 chr12:80650145 A>C maps to NM_173591.3 I530I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5006-01A-01D-1462-08 chr5:153796477 G>A maps to NM_198321.3 Q586Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5006-01A-01D-1462-08 chr10:71868912 G>A maps to NM_018649.2 A301A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5006-01A-01D-1462-08 chr7:129761892 G>A did not map to a codon.
Sequencing variant TCGA-BP-5006-01A-01D-1462-08 chr18:2547513 G>C maps to NM_022840.3 S305*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5006-01A-01D-1462-08 chr11:1258285 C>T maps to ENST00000447027 D1066D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5006-01A-01D-1462-08 chr3:127785927 C>T maps to ENST00000464451 V309V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5006-01A-01D-1462-08 chr19:17760371 G>A maps to ENST00000428389 I576I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5006-01A-01D-1462-08 chr14:103418833 C>A did not map to a codon.
Sequencing variant TCGA-BP-5006-01A-01D-1462-08 chr14:103418833 C>A did not map to a codon.
Sequencing variant TCGA-BP-5006-01A-01D-1462-08 chr3:47161670 C>G did not map to a codon.
Sequencing variant TCGA-BP-5006-01A-01D-1462-08 chr3:47161670 C>G did not map to a codon.
Sequencing variant TCGA-BP-5007-01A-01D-1462-08 chr10:115885643 C>A did not map to a codon.
Sequencing variant TCGA-BP-5007-01A-01D-1462-08 chr14:45537686 C>T maps to ENST00000361462 L1604L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5007-01A-01D-1462-08 chr5:82948368 G>T maps to NM_001884.3 V125V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5007-01A-01D-1462-08 chr17:72340955 C>A maps to NM_153209.3 A213A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5007-01A-01D-1462-08 chr18:57026428 C>T maps to NM_005570.3 L16L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5007-01A-01D-1462-08 chr10:70140990 G>A maps to NM_017987.4 Q404*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5007-01A-01D-1462-08 chr16:30380670 C>T maps to NM_015527.3 G278G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5007-01A-01D-1462-08 chr16:30380670 C>T maps to NM_015527.3 G278G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5008-01A-01D-1462-08 chr1:26663758 G>A maps to NM_001039775.3 L1252L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5008-01A-01D-1462-08 chr12:53700821 C>A maps to NM_021640.3 C340*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5008-01A-01D-1462-08 chr12:56669790 G>A maps to NM_004077.2 L259L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5008-01A-01D-1462-08 chr2:120129818 A>T did not map to a codon.
Sequencing variant TCGA-BP-5008-01A-01D-1462-08 chr20:37632408 T>A maps to NM_021931.3 V290V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5008-01A-01D-1462-08 chr5:147781572 A>G maps to NM_205836.1 L97L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5008-01A-01D-1462-08 chr2:11361379 T>C maps to NM_004850.3 K401K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5008-01A-01D-1462-08 chr22:18021868 C>T maps to ENST00000400579 L658L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5008-01A-01D-1462-08 chr22:18021868 C>T maps to ENST00000400579 L658L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5008-01A-01D-1462-08 chr7:149544911 C>A maps to NM_001099220.1 A110A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5008-01A-01D-1462-08 chr7:149544911 C>A maps to NM_001099220.1 A110A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5009-01A-01D-1462-08 chr6:143094138 T>A maps to NM_006734.3 P579P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5009-01A-01D-1462-08 chr17:39927929 G>A maps to NM_021991.2 T59T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5009-01A-01D-1462-08 chr12:21918782 G>T maps to NM_004982.2 R383R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5009-01A-01D-1462-08 chr1:209799336 C>T maps to NM_000228.2 P544P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5009-01A-01D-1462-08 chr11:56258041 G>A maps to NM_001005282.1 Q269*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5009-01A-01D-1462-08 chr19:57327328 T>C maps to NM_006210.2 G827G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5009-01A-01D-1462-08 chr5:137230169 T>G maps to ENST00000230643 R132R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5009-01A-01D-1462-08 chr2:20403633 C>T maps to NM_001006946.1 E189E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5009-01A-01D-1462-08 chr6:30692125 C>A maps to NM_178014.2 T429T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5009-01A-01D-1462-08 chr3:93643108 C>A did not map to a codon.
Sequencing variant TCGA-BP-5009-01A-01D-1462-08 chr3:93643108 C>A did not map to a codon.
Sequencing variant TCGA-BP-5010-01A-02D-1421-08 chr7:48634310 G>A maps to NM_152701.3 E4882E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5010-01A-02D-1421-08 chr6:7373332 C>T maps to NM_001170692.1 E573E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5010-01A-02D-1421-08 chr1:9801266 C>T maps to NM_001009566.1 P468P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5010-01A-02D-1421-08 chr3:32750280 T>A maps to NM_015442.1 G133G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5010-01A-02D-1421-08 chr6:75947672 C>T maps to NM_001865.3 V107V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5010-01A-02D-1421-08 chr9:35736113 C>T maps to NM_006368.4 S227S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5010-01A-02D-1421-08 chr15:75042327 G>A maps to NM_000761.3 T83T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5010-01A-02D-1421-08 chr6:46563726 A>T maps to NM_016593.3 I354I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5010-01A-02D-1421-08 chr1:21221940 G>A maps to NM_001198801.1 L628L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5010-01A-02D-1421-08 chr9:103002448 C>T maps to NM_014425.2 T241T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5010-01A-02D-1421-08 chr11:56468234 C>T maps to NM_001013358.1 A124A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5010-01A-02D-1421-08 chr16:20380852 G>T maps to NM_174924.1 L359L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5010-01A-02D-1421-08 chr6:117241585 C>T maps to NM_173560.3 S432S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5010-01A-02D-1421-08 chr19:49517739 G>A did not map to a codon.
Sequencing variant TCGA-BP-5010-01A-02D-1421-08 chr3:38798547 G>T maps to NM_006514.2 R351R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5010-01A-02D-1421-08 chr1:232651060 C>A maps to NM_020808.3 E9*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5010-01A-02D-1421-08 chr15:44877929 A>T maps to NM_025137.3 S1675S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5010-01A-02D-1421-08 chr15:102261431 T>A maps to NM_152334.2 K155*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5010-01A-02D-1421-08 chr16:1257813 C>T maps to NM_021098.2 V1036V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5010-01A-02D-1421-08 chr16:1257813 C>T maps to NM_021098.2 V1036V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5168-01A-01D-1421-08 chr12:112167662 G>T maps to NM_001136538.1 E464*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5168-01A-01D-1421-08 chr1:24106409 C>G maps to NM_020362.4 S100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5168-01A-01D-1421-08 chr6:127901449 G>A maps to NM_001010905.1 A143A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5168-01A-01D-1421-08 chr9:114518733 C>A maps to NM_173521.3 E181*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5168-01A-01D-1421-08 chr15:43482263 A>C maps to NM_012142.3 R115R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5168-01A-01D-1421-08 chr12:122826193 T>G maps to ENST00000302528 L519L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5168-01A-01D-1421-08 chr8:120101990 G>A did not map to a codon.
Sequencing variant TCGA-BP-5168-01A-01D-1421-08 chr20:34219485 A>G maps to NM_003915.5 D219D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5168-01A-01D-1421-08 chr20:2775210 C>T maps to NM_019609.4 V645V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5168-01A-01D-1421-08 chr8:113421241 T>C maps to NM_198123.1 V1805V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5168-01A-01D-1421-08 chr7:24738851 T>C maps to NM_001127453.1 V428V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5168-01A-01D-1421-08 chr14:24459471 C>T maps to NM_198083.3 D70D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5168-01A-01D-1421-08 chr3:113858391 T>A maps to NM_000796.3 R226R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5168-01A-01D-1421-08 chr2:207639091 C>A maps to NM_014929.3 L466L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5168-01A-01D-1421-08 chr5:39202846 T>C maps to ENST00000263405 E81E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5168-01A-01D-1421-08 chr12:31944926 G>A maps to NM_001013699.2 T58T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5168-01A-01D-1421-08 chr2:24535239 A>G maps to NM_006277.2 L65L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5168-01A-01D-1421-08 chr15:63419761 C>A maps to NM_032857.3 R276R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5168-01A-01D-1421-08 chr9:133914404 G>A maps to ENST00000355048 R377R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5168-01A-01D-1421-08 chr1:90048979 A>G maps to NM_015350.2 V257V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5168-01A-01D-1421-08 chr1:90048979 A>G maps to NM_015350.2 V257V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5168-01A-01D-1421-08 chr3:169555370 A>G maps to NM_001080460.1 K545K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5168-01A-01D-1421-08 chr11:118352712 G>A maps to NM_001197104.1 P1306P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5168-01A-01D-1421-08 chr11:1017613 G>A maps to NM_005961.2 T1729T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5168-01A-01D-1421-08 chr15:52521377 A>T maps to NM_018728.3 T1053T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5168-01A-01D-1421-08 chr8:71050556 T>C maps to NM_006540.2 E1013E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5168-01A-01D-1421-08 chr19:13192530 C>T maps to ENST00000397661 P372P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5168-01A-01D-1421-08 chr14:52534719 G>C maps to NM_007361.3 P130P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5168-01A-01D-1421-08 chr1:228559758 T>C maps to NM_001098623.1 L7094L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5168-01A-01D-1421-08 chr3:52623266 A>G maps to ENST00000296302 A928A. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-BP-5168-01A-01D-1421-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-BP-5168-01A-01D-1421-08 chr6:30569884 G>A maps to NM_002714.2 P847P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5168-01A-01D-1421-08 chr4:87679431 G>A maps to NM_080685.2 W1081*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5168-01A-01D-1421-08 chr7:157985187 C>T did not map to a codon.
Sequencing variant TCGA-BP-5168-01A-01D-1421-08 chr3:110837734 T>A maps to NM_015480.1 T245T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5168-01A-01D-1421-08 chr5:54701365 T>A maps to NM_015360.4 T865T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5168-01A-01D-1421-08 chr10:71166877 G>A maps to NM_001057.2 T300T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5168-01A-01D-1421-08 chr8:94821183 G>A maps to NM_153704.5 R852R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5168-01A-01D-1421-08 chr8:144411528 G>A maps to NM_052963.1 D117D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5168-01A-01D-1421-08 chr6:133065438 C>T maps to NM_004665.2 *521*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5168-01A-01D-1421-08 chr20:278733 C>T maps to NM_033089.6 R169R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5169-01A-01D-1429-08 chr7:100160276 C>T maps to NM_006076.4 G353G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5169-01A-01D-1429-08 chr18:56202372 T>C maps to NM_052947.3 K1682K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5169-01A-01D-1429-08 chr12:122492741 G>C maps to NM_020993.3 S157S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5169-01A-01D-1429-08 chr22:45601730 C>A maps to NM_001009880.1 L93L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5169-01A-01D-1429-08 chr19:47424188 C>T maps to NM_004491.4 Q753*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5169-01A-01D-1429-08 chrX:51488137 T>A maps to NM_018094.4 V472V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5169-01A-01D-1429-08 chr1:22168730 C>T did not map to a codon.
Sequencing variant TCGA-BP-5169-01A-01D-1429-08 chr3:49160287 G>A maps to NM_002292.3 L1474L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5169-01A-01D-1429-08 chr2:223066807 C>A maps to NM_181459.3 V425V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5169-01A-01D-1429-08 chr3:52595786 A>C maps to ENST00000296302 Y1428*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5169-01A-01D-1429-08 chr11:70218603 T>C maps to NM_003626.2 I1021I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5169-01A-01D-1429-08 chr3:47125379 C>A maps to NM_014159.6 E1964*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5169-01A-01D-1429-08 chr2:103120166 G>A did not map to a codon.
Sequencing variant TCGA-BP-5169-01A-01D-1429-08 chr17:74392797 G>A maps to NM_022066.3 S740S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5169-01A-01D-1429-08 chr7:99668972 G>C maps to NM_032924.3 T378T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5169-01A-01D-1429-08 chr6:100057183 G>A did not map to a codon.
Sequencing variant TCGA-BP-5169-01A-01D-1429-08 chr6:100057183 G>A did not map to a codon.
Sequencing variant TCGA-BP-5170-01A-01D-1429-08 chr1:94953299 T>C maps to ENST00000454898 L364L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5170-01A-01D-1429-08 chr7:92252375 A>G maps to NM_001145306.1 D224D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5170-01A-01D-1429-08 chr11:117265694 C>T maps to NM_014956.4 A940A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5170-01A-01D-1429-08 chr1:156697246 C>T maps to NM_030980.1 T66T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5170-01A-01D-1429-08 chr11:118372560 T>A maps to NM_001197104.1 L2165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5170-01A-01D-1429-08 chr3:52668654 G>A maps to ENST00000296302 Q422*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5170-01A-01D-1429-08 chr3:130454820 T>C maps to NM_014602.2 T253T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5170-01A-01D-1429-08 chr2:109384149 A>G maps to NM_006267.4 R2385R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5170-01A-01D-1429-08 chr5:158603686 A>G maps to NM_144726.2 L220L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5170-01A-01D-1429-08 chr1:153509894 G>A maps to ENST00000359215 I70I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5170-01A-01D-1429-08 chr12:318975 G>C maps to NM_003044.3 V59V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5170-01A-01D-1429-08 chr14:78217739 A>G maps to NM_012245.2 N84N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5170-01A-01D-1429-08 chr4:26741523 T>C maps to NM_018317.2 L386L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5170-01A-01D-1429-08 chr5:176332368 A>G maps to ENST00000377219 L693L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5173-01A-01D-1429-08 chr19:36275073 G>A maps to ENST00000007510 R474R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5173-01A-01D-1429-08 chr4:99064289 C>A maps to NM_174952.2 R4R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5173-01A-01D-1429-08 chr16:71570903 C>A maps to NM_001166395.1 V108V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5173-01A-01D-1429-08 chr5:129520379 G>T maps to NM_175856.4 R515R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5173-01A-01D-1429-08 chr7:146829476 T>C maps to NM_014141.5 G408G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5173-01A-01D-1429-08 chr17:71197741 T>C maps to NM_018714.2 I592I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5173-01A-01D-1429-08 chr9:90321651 C>T maps to NM_004938.2 V1222V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5173-01A-01D-1429-08 chr10:445050 T>A maps to NM_014974.2 K420*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5173-01A-01D-1429-08 chr10:131761927 G>A maps to ENST00000355311 G35G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5173-01A-01D-1429-08 chr5:127782276 G>A maps to NM_001999.3 I283I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5173-01A-01D-1429-08 chr6:90604513 G>A maps to NM_032602.1 R109R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5173-01A-01D-1429-08 chr10:98715213 A>G maps to NM_001170765.1 V279V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5173-01A-01D-1429-08 chr16:79633709 A>G maps to NM_005360.4 F30F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5173-01A-01D-1429-08 chr18:47463680 G>A maps to NM_001080467.2 S613S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5173-01A-01D-1429-08 chr2:204002983 A>T maps to NM_001114132.1 I1526I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5173-01A-01D-1429-08 chr11:123894276 G>A maps to NM_001001953.1 L186L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5173-01A-01D-1429-08 chr5:140559267 G>T maps to NM_019120.2 L551L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5173-01A-01D-1429-08 chr15:44060740 G>A maps to NM_005313.4 L361L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5173-01A-01D-1429-08 chr6:161152840 A>G maps to NM_000301.3 P501P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5173-01A-01D-1429-08 chrX:23803813 G>A maps to NM_002970.2 R119R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5173-01A-01D-1429-08 chr7:122757653 G>A maps to NM_022444.3 A507A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5173-01A-01D-1429-08 chr15:45706845 T>C maps to NM_024063.2 Y504Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5173-01A-01D-1429-08 chr4:119947952 T>A maps to NM_133477.2 A143A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5173-01A-01D-1429-08 chr2:230650535 C>A maps to ENST00000389044 A1650A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5173-01A-01D-1429-08 chr2:230650535 C>A maps to ENST00000389044 A1650A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5173-01A-01D-1429-08 chr4:120182904 T>C maps to NM_019050.2 N286N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5173-01A-01D-1429-08 chr4:120182904 T>C maps to NM_019050.2 N286N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5173-01A-01D-1429-08 chr11:123988557 A>G maps to NM_014622.4 V74V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5173-01A-01D-1429-08 chr19:9578113 A>C maps to NM_152476.2 L503L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5173-01A-01D-1429-08 chr19:17836822 C>T maps to NM_018174.4 F210F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5173-01A-01D-1429-08 chr19:17836822 C>T maps to NM_018174.4 F210F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5173-01A-01D-1429-08 chr3:10183738 G>T maps to NM_000551.2 E70*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5173-01A-01D-1429-08 chr3:10183738 G>T maps to NM_000551.2 E70*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5173-01A-01D-1429-08 chr19:52942410 G>A maps to NM_001143939.1 A579A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5173-01A-01D-1429-08 chr19:52942410 G>A maps to NM_001143939.1 A579A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5174-01A-01D-1429-08 chr3:154022914 T>A maps to NM_020865.2 T312T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5174-01A-01D-1429-08 chr21:41385098 G>A maps to NM_001389.3 A1967A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5174-01A-01D-1429-08 chr1:24666206 C>G maps to NM_021180.3 A339A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5174-01A-01D-1429-08 chr14:23894488 A>T did not map to a codon.
Sequencing variant TCGA-BP-5174-01A-01D-1429-08 chr7:127979813 G>A maps to NM_018077.2 V50V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5174-01A-01D-1429-08 chr9:72131196 G>A maps to NM_001163.3 R310R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5174-01A-01D-1429-08 chr9:72131196 G>A maps to NM_001163.3 R310R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5174-01A-01D-1429-08 chr19:55086975 C>T maps to NM_001130917.1 S303S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5174-01A-01D-1429-08 chr19:55086975 C>T maps to NM_001130917.1 S303S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5175-01A-01D-1429-08 chr5:864639 G>T maps to NM_001009877.2 T526T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5175-01A-01D-1429-08 chr5:21783500 C>T maps to NM_004061.3 A453A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5175-01A-01D-1429-08 chr16:11217729 C>G maps to ENST00000409790 R800R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5175-01A-01D-1429-08 chr1:86453337 C>A did not map to a codon.
Sequencing variant TCGA-BP-5175-01A-01D-1429-08 chr20:57876744 C>T maps to NM_207034.1 C111C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5175-01A-01D-1429-08 chr19:1067421 A>G maps to NM_012292.2 K6K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5175-01A-01D-1429-08 chr2:8953447 A>C maps to NM_020738.2 L108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5175-01A-01D-1429-08 chr10:135012531 G>A maps to ENST00000368572 P840P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5175-01A-01D-1429-08 chr6:43642985 A>T maps to ENST00000372118 P207P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5175-01A-01D-1429-08 chr14:23894067 T>C maps to NM_000257.2 L863L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5175-01A-01D-1429-08 chr20:33575920 C>A maps to NM_020884.3 I523I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5175-01A-01D-1429-08 chr16:50583387 C>T maps to NM_033119.3 I38I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5175-01A-01D-1429-08 chr12:55725603 G>T maps to NM_054104.1 L40L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5175-01A-01D-1429-08 chr5:149240510 C>A maps to NM_000440.2 G844*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5175-01A-01D-1429-08 chr5:32090570 C>T maps to NM_178140.2 I2339I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5175-01A-01D-1429-08 chr22:50724517 G>T maps to NM_012401.2 S629S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5175-01A-01D-1429-08 chr8:92982924 G>A maps to NM_175634.2 D500D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5175-01A-01D-1429-08 chr1:19455527 G>A maps to ENST00000375267 Q2983*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5175-01A-01D-1429-08 chr22:20920818 G>A maps to NM_001003891.1 Q252Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5175-01A-01D-1429-08 chr22:20920818 G>A maps to NM_001003891.1 Q252Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5176-01A-01D-1429-08 chr16:20651788 C>T maps to NM_052956.2 S370S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5176-01A-01D-1429-08 chr14:33292169 G>C maps to NM_004274.4 S1717S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5176-01A-01D-1429-08 chr10:61829376 T>C maps to NM_020987.2 G3754G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5176-01A-01D-1429-08 chr11:30352899 G>A maps to NM_152316.1 Q135Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5176-01A-01D-1429-08 chr22:24451597 C>T maps to NM_012295.3 L357L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5176-01A-01D-1429-08 chr1:201013476 C>G maps to NM_000069.2 A1592A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5176-01A-01D-1429-08 chr16:28944419 C>T maps to NM_001178098.1 Q182*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5176-01A-01D-1429-08 chr14:95557549 C>A maps to NM_177438.2 R1839R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5176-01A-01D-1429-08 chr14:95557549 C>A maps to NM_177438.2 R1839R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5176-01A-01D-1429-08 chr11:111930749 C>G maps to NM_001931.4 T546T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5176-01A-01D-1429-08 chr9:35563217 T>G maps to NM_001164310.1 L77L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5176-01A-01D-1429-08 chr9:35563220 A>G maps to NM_001164310.1 S76S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5176-01A-01D-1429-08 chr9:35563220 A>G maps to NM_001164310.1 S76S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5176-01A-01D-1429-08 chr2:187615885 T>C maps to NM_177454.3 P250P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5176-01A-01D-1429-08 chr10:101163594 G>A maps to NM_002079.2 Q227*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5176-01A-01D-1429-08 chr3:150916819 G>A maps to NM_013308.3 H118H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5176-01A-01D-1429-08 chr21:34721420 A>T maps to NM_000629.2 G271G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5176-01A-01D-1429-08 chr3:197410177 C>T maps to NM_014687.1 K660K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5176-01A-01D-1429-08 chr8:2020500 G>A maps to NM_003970.2 R290R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5176-01A-01D-1429-08 chr1:24434559 T>C maps to ENST00000330966 E56E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5176-01A-01D-1429-08 chr12:93793100 T>C maps to NM_199040.2 N164N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5176-01A-01D-1429-08 chr14:57271022 C>A maps to NM_021728.2 T52T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5176-01A-01D-1429-08 chr5:140773213 A>G maps to NM_032088.1 A278A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5176-01A-01D-1429-08 chr1:7886602 C>A maps to ENST00000377532 S674*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5176-01A-01D-1429-08 chr3:128813981 G>A maps to ENST00000418265 S294S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5176-01A-01D-1429-08 chr11:74546694 A>T maps to NM_001098638.1 L349L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5176-01A-01D-1429-08 chr3:51971259 G>T maps to NM_004704.3 T155T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5176-01A-01D-1429-08 chr9:139360546 G>T maps to NM_014866.1 Y1390*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5176-01A-01D-1429-08 chr6:158541584 T>C maps to NM_032861.3 E346E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5176-01A-01D-1429-08 chr17:19582220 T>C did not map to a codon.
Sequencing variant TCGA-BP-5176-01A-01D-1429-08 chr5:101631680 G>A maps to NM_180991.4 Q96*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5176-01A-01D-1429-08 chrX:106109182 C>G maps to NM_017752.2 S861*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5176-01A-01D-1429-08 chr7:72985070 C>A maps to NM_012453.2 R370R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5176-01A-01D-1429-08 chr17:27896079 G>A maps to NM_138349.2 E39E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5176-01A-01D-1429-08 chr12:113727989 C>A maps to NM_001143819.1 T690T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5176-01A-01D-1429-08 chr12:113727989 C>A maps to NM_001143819.1 T690T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5176-01A-01D-1429-08 chr6:144768772 A>T maps to NM_007124.2 T586T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5176-01A-01D-1429-08 chr3:10191570 G>T maps to NM_000551.2 L188L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5176-01A-01D-1429-08 chr3:10191571 G>T maps to NM_000551.2 E189*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5176-01A-01D-1429-08 chr15:42439927 A>C maps to ENST00000397272 G366G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5176-01A-01D-1429-08 chr15:42439927 A>C maps to ENST00000397272 G366G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5177-01A-01D-1429-08 chr6:106968601 G>A maps to NM_001624.2 P765P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5177-01A-01D-1429-08 chr1:86913357 T>C maps to NM_006536.5 N627N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5177-01A-01D-1429-08 chrX:75397643 A>G maps to NM_016500.3 K201K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5177-01A-01D-1429-08 chr11:62475842 G>T maps to NM_012202.3 E26*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5177-01A-01D-1429-08 chr1:154705481 G>A maps to NM_002249.4 I529I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5177-01A-01D-1429-08 chr1:201751583 C>T maps to ENST00000367296 S648S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5177-01A-01D-1429-08 chr12:57619418 G>A maps to NM_007224.3 K272K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5177-01A-01D-1429-08 chr20:61444724 G>A maps to NM_007346.2 P586P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5177-01A-01D-1429-08 chr15:42446346 G>A maps to ENST00000397272 D131D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5177-01A-01D-1429-08 chr12:64377782 C>T maps to NM_020762.2 R42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5177-01A-01D-1429-08 chr14:102901085 C>T maps to NM_014844.3 L644L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5177-01A-01D-1429-08 chr19:7999039 C>T maps to NM_006351.3 S159S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5177-01A-01D-1429-08 chr17:48941285 T>C maps to NM_005749.2 E31E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5178-01A-01D-1429-08 chr15:100594116 T>C maps to NM_139057.2 L760L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5178-01A-01D-1429-08 chr17:79166552 C>T maps to ENST00000269392 L807L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5178-01A-01D-1429-08 chrX:15790715 C>T maps to NM_007220.3 D146D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5178-01A-01D-1429-08 chr11:128680489 C>T maps to NM_002017.3 G322G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5178-01A-01D-1429-08 chr11:128680489 C>T maps to NM_002017.3 G322G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5178-01A-01D-1429-08 chr22:42482195 G>A maps to NM_002490.3 H152H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5178-01A-01D-1429-08 chrX:70516748 T>G maps to NM_007363.4 Y265*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5178-01A-01D-1429-08 chr16:15126792 G>T maps to NM_015027.2 L549L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5178-01A-01D-1429-08 chr20:8698473 G>T maps to NM_015192.2 E498*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5178-01A-01D-1429-08 chr19:40903259 C>T maps to NM_181882.2 V333V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5178-01A-01D-1429-08 chr5:115803360 C>G maps to ENST00000257414 L621L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5178-01A-01D-1429-08 chr3:101060581 C>A maps to NM_020654.3 L716L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5178-01A-01D-1429-08 chr6:8417151 A>T maps to NM_001142540.1 L317*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5178-01A-01D-1429-08 chr16:67290935 C>T maps to NM_004594.2 L419L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5178-01A-01D-1429-08 chr14:20847177 G>A maps to NM_007110.4 D1738D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5178-01A-01D-1429-08 chr17:53014034 T>C maps to NM_005486.2 L294L. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-BP-5178-01A-01D-1429-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-BP-5178-01A-01D-1429-08 chr10:126670373 A>G maps to NM_017580.2 A508A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5178-01A-01D-1429-08 chr12:55250593 T>A maps to NM_058173.2 T47T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5178-01A-01D-1429-08 chr12:55250593 T>A maps to NM_058173.2 T47T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5178-01A-01D-1429-08 chr7:155465596 A>T maps to NM_053043.2 L53L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5178-01A-01D-1429-08 chr7:155465596 A>T maps to NM_053043.2 L53L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5178-01A-01D-1429-08 chr16:30545835 C>A maps to NM_023931.2 R55R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5178-01A-01D-1429-08 chr16:30545835 C>A maps to NM_023931.2 R55R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5180-01A-01D-1429-08 chr2:24261023 G>C maps to NM_025203.2 T447T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5180-01A-01D-1429-08 chr12:2711090 G>T maps to NM_199460.2 L995L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5180-01A-01D-1429-08 chr17:46628007 C>T maps to NM_002146.4 E328E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5180-01A-01D-1429-08 chr3:52637710 G>A maps to ENST00000296302 Q869*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5180-01A-01D-1429-08 chr11:608266 C>A maps to ENST00000264555 P937P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5180-01A-01D-1429-08 chr11:608266 C>A maps to ENST00000264555 P937P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5180-01A-01D-1429-08 chr12:11035695 C>T did not map to a codon.
Sequencing variant TCGA-BP-5180-01A-01D-1429-08 chr13:21746644 T>G did not map to a codon.
Sequencing variant TCGA-BP-5180-01A-01D-1429-08 chr8:70533275 C>T maps to NM_001128206.1 Q462*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5180-01A-01D-1429-08 chr12:100433379 C>T maps to NM_015054.1 R1423R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5180-01A-01D-1429-08 chr3:10183746 C>A maps to NM_000551.2 S72S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5180-01A-01D-1429-08 chr3:10183747 C>T maps to NM_000551.2 Q73*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5182-01A-01D-1429-08 chr21:46642102 C>A maps to NM_015833.3 L739L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5182-01A-01D-1429-08 chr4:109681435 G>T maps to NM_031279.3 S28*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5182-01A-01D-1429-08 chr2:69045085 C>A maps to NM_001007231.2 L321L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5182-01A-01D-1429-08 chr16:775559 C>T maps to NM_001031737.2 R96R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5182-01A-01D-1429-08 chr5:134153323 G>T maps to ENST00000452510 E918*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5182-01A-01D-1429-08 chr1:111734926 C>T maps to NM_024901.3 Q269Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5182-01A-01D-1429-08 chr4:185138819 T>C maps to NM_153343.3 K51K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5182-01A-01D-1429-08 chr22:38201646 C>T maps to NM_005318.3 I32I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5182-01A-01D-1429-08 chr16:69149148 T>C maps to NM_005329.2 L548L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5182-01A-01D-1429-08 chr1:200959171 C>T did not map to a codon.
Sequencing variant TCGA-BP-5182-01A-01D-1429-08 chr22:31674309 C>A maps to ENST00000438187 S631S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5182-01A-01D-1429-08 chr7:127670480 C>T maps to NM_022143.4 Q71Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5182-01A-01D-1429-08 chr11:118375277 G>T maps to NM_001197104.1 E2891*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5182-01A-01D-1429-08 chr2:86325786 G>A maps to NM_015425.3 L127L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5182-01A-01D-1429-08 chr12:57139903 C>T maps to NM_000946.2 W168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5182-01A-01D-1429-08 chr6:31930532 G>A maps to NM_006929.4 E418E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5182-01A-01D-1429-08 chr3:43389697 C>T maps to NM_017719.4 L649L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5182-01A-01D-1429-08 chr1:16199599 C>T maps to NM_015001.2 R125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5182-01A-01D-1429-08 chr10:98182330 G>T maps to NM_012465.3 T264T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5182-01A-01D-1429-08 chr10:98182330 G>T maps to NM_012465.3 T264T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5182-01A-01D-1429-08 chr15:42512317 T>A maps to ENST00000389834 P473P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5182-01A-01D-1429-08 chr1:211545848 G>A maps to ENST00000427925 K504K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5182-01A-01D-1429-08 chr5:138724268 C>T maps to NM_016459.3 W61*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5182-01A-01D-1429-08 chr5:138724268 C>T maps to NM_016459.3 W61*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5182-01A-01D-1429-08 chr1:8420608 T>G maps to NM_012102.3 P986P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5182-01A-01D-1429-08 chr1:8420608 T>G maps to NM_012102.3 P986P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5182-01A-01D-1429-08 chr13:45008836 A>G maps to NM_183422.2 P1049P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5182-01A-01D-1429-08 chr13:45008836 A>G maps to NM_183422.2 P1049P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5183-01A-01D-1429-08 chr2:231682473 C>T maps to NM_001130850.1 L233L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5183-01A-01D-1429-08 chr22:17690278 G>A maps to NM_017424.2 Q97*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5183-01A-01D-1429-08 chr10:50833614 C>T maps to NM_020549.4 P283P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5183-01A-01D-1429-08 chr1:26514972 G>A maps to ENST00000374253 E530E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5183-01A-01D-1429-08 chr8:113650948 C>A maps to NM_198123.1 E1168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5183-01A-01D-1429-08 chr8:25167944 C>G maps to NM_024940.6 L405L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5183-01A-01D-1429-08 chr8:124204062 T>C maps to NM_032899.4 D167D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5183-01A-01D-1429-08 chr16:20331780 G>A maps to NM_001007240.1 Q224*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5183-01A-01D-1429-08 chr17:7416180 G>A maps to NM_000937.4 W1565*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5183-01A-01D-1429-08 chr19:43376180 G>A maps to NM_006905.2 P149P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5183-01A-01D-1429-08 chr5:130841086 T>G maps to ENST00000514667 G407G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5183-01A-01D-1429-08 chr22:42383653 G>T maps to NM_145733.2 E148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5183-01A-01D-1429-08 chr19:49797186 C>T maps to NM_014037.2 L505L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5183-01A-01D-1429-08 chr1:186302398 T>C maps to NM_003292.2 T1770T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5183-01A-01D-1429-08 chr6:42232447 G>A maps to NM_033502.2 L543L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5183-01A-01D-1429-08 chr17:74392557 G>T maps to NM_022066.3 I820I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5183-01A-01D-1429-08 chr19:3813947 G>T maps to NM_015174.1 T704T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5183-01A-01D-1429-08 chr19:22270899 C>A maps to NM_033468.2 G116G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5184-01A-01D-1429-08 chr11:64875905 C>A maps to NM_013265.2 A321A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5184-01A-01D-1429-08 chr1:65117973 T>C maps to ENST00000371073 T507T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5184-01A-01D-1429-08 chr20:31946923 G>A maps to ENST00000357886 T577T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5184-01A-01D-1429-08 chr8:110567064 G>A maps to ENST00000276658 L90L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5184-01A-01D-1429-08 chr8:110567064 G>A maps to ENST00000276658 L90L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5184-01A-01D-1429-08 chr1:43829742 C>T maps to NM_022821.2 Q228Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5184-01A-01D-1429-08 chrX:137715046 G>A maps to NM_001139500.1 N244N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5184-01A-01D-1429-08 chrX:137715046 G>A maps to NM_001139500.1 N244N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5184-01A-01D-1429-08 chr4:89425490 C>T maps to NM_016323.2 I897I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5184-01A-01D-1429-08 chr5:139232129 G>A maps to NM_013982.2 N485N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5184-01A-01D-1429-08 chr12:110226510 G>A maps to NM_021625.4 S634S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5184-01A-01D-1429-08 chr8:143412302 G>A maps to ENST00000445818 S284S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5184-01A-01D-1429-08 chr13:46584526 A>G maps to ENST00000242848 D234D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5185-01A-01D-1429-08 chr2:236706508 G>A maps to NM_001037131.1 V260V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5185-01A-01D-1429-08 chr12:58207207 T>C did not map to a codon.
Sequencing variant TCGA-BP-5185-01A-01D-1429-08 chr13:26923219 G>A maps to NM_001260.1 E72E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5185-01A-01D-1429-08 chr13:53035797 A>T maps to NM_001098525.1 T280T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5185-01A-01D-1429-08 chr21:37833693 G>A maps to NM_001146077.1 I100I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5185-01A-01D-1429-08 chr7:129938645 A>T maps to NM_016352.3 L43L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5185-01A-01D-1429-08 chr12:113618758 C>T maps to NM_001111322.1 K93K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5185-01A-01D-1429-08 chr9:32488008 C>T maps to NM_014314.3 P382P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5185-01A-01D-1429-08 chr22:31850207 G>A maps to NM_019843.3 D478D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5185-01A-01D-1429-08 chr1:22920015 G>C did not map to a codon.
Sequencing variant TCGA-BP-5185-01A-01D-1429-08 chr13:41704757 G>A maps to NM_152903.4 L630L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5185-01A-01D-1429-08 chr6:150164137 G>A maps to NM_032832.5 R298R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5185-01A-01D-1429-08 chr5:140870295 C>T maps to NM_018929.2 Q497*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5185-01A-01D-1429-08 chr15:99511853 A>T maps to NM_001102612.2 P148P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5185-01A-01D-1429-08 chr2:179428025 T>C maps to NM_133378.4 E25043E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5185-01A-01D-1429-08 chr17:73814847 A>C maps to NM_001080419.1 A575A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5185-01A-01D-1429-08 chr11:17531373 C>T maps to NM_153676.3 G514G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5185-01A-01D-1429-08 chr6:158923757 G>C maps to NM_020245.3 G1021G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5185-01A-01D-1429-08 chr6:158923757 G>C maps to NM_020245.3 G1021G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5186-01A-01D-1429-08 chr1:201017770 T>A maps to NM_000069.2 T1460T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5186-01A-01D-1429-08 chr13:37678646 A>G maps to NM_145203.5 C249C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5186-01A-01D-1429-08 chr19:40420152 G>C maps to NM_003890.2 V947V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5186-01A-01D-1429-08 chr9:111659235 G>A maps to NM_003640.3 Q862*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5186-01A-01D-1429-08 chr11:94731984 T>A maps to NM_018039.2 A483A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5186-01A-01D-1429-08 chr11:12316165 T>G maps to NM_032867.2 L396L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5186-01A-01D-1429-08 chr11:12316165 T>G maps to NM_032867.2 L396L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5186-01A-01D-1429-08 chr1:186278972 T>A maps to NM_005807.3 L1157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5186-01A-01D-1429-08 chrX:55513237 T>A maps to NM_201286.3 *712L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5186-01A-01D-1429-08 chr17:39261864 C>A maps to NM_001146041.1 C75*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5186-01A-01D-1429-08 chr17:39261864 C>A maps to NM_001146041.1 C75*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5187-01A-01D-1429-08 chr12:43862443 T>G maps to ENST00000389420 G394G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5187-01A-01D-1429-08 chr3:11348440 C>A maps to NM_006395.2 C80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5187-01A-01D-1429-08 chr12:76741470 A>G maps to NM_024685.3 H98H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5187-01A-01D-1429-08 chr18:12701061 T>C maps to NM_024899.2 E38E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5187-01A-01D-1429-08 chr11:57573352 G>A did not map to a codon.
Sequencing variant TCGA-BP-5187-01A-01D-1429-08 chr1:153916541 A>T maps to NM_014856.2 V103V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5187-01A-01D-1429-08 chr14:67779287 T>C maps to NM_022474.2 P362P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5187-01A-01D-1429-08 chr19:55497590 G>T maps to NM_017852.3 T758T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5187-01A-01D-1429-08 chr3:52643767 G>A maps to ENST00000296302 R710*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5187-01A-01D-1429-08 chr17:48191586 A>G maps to NM_174920.2 S330S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5187-01A-01D-1429-08 chr22:25251634 T>A maps to NM_001039948.2 V263V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5187-01A-01D-1429-08 chr5:138378409 T>A did not map to a codon.
Sequencing variant TCGA-BP-5187-01A-01D-1429-08 chr2:162815016 A>G maps to NM_001178015.1 L938L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5187-01A-01D-1429-08 chr14:91925214 T>A did not map to a codon.
Sequencing variant TCGA-BP-5187-01A-01D-1429-08 chrX:57162316 C>T maps to NM_019003.3 V238V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5187-01A-01D-1429-08 chr2:84652565 A>G maps to NM_003849.3 P329P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5187-01A-01D-1429-08 chr9:103109628 T>G maps to NM_017746.3 G80G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5187-01A-01D-1429-08 chr2:47221560 C>A maps to ENST00000394850 P303P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5187-01A-01D-1429-08 chr9:32434666 C>T maps to NM_002197.2 N689N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5187-01A-01D-1429-08 chr9:32434666 C>T maps to NM_002197.2 N689N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5187-01A-01D-1429-08 chr2:198508983 C>T maps to NM_144629.2 S112S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5187-01A-01D-1429-08 chr2:198508983 C>T maps to NM_144629.2 S112S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5189-01A-02D-1429-08 chr8:120118231 T>C maps to NM_006438.3 N212N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5189-01A-02D-1429-08 chr8:11703215 G>T maps to NM_147783.2 P292P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5189-01A-02D-1429-08 chr19:49469166 C>T maps to NM_000146.3 D81D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5189-01A-02D-1429-08 chr14:58937441 G>T did not map to a codon.
Sequencing variant TCGA-BP-5189-01A-02D-1429-08 chr15:74239563 G>A maps to NM_005576.2 Q502Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5189-01A-02D-1429-08 chr16:83940608 G>T maps to NM_012213.2 L182L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5189-01A-02D-1429-08 chr11:48346848 T>A maps to NM_001004702.1 Y119*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5189-01A-02D-1429-08 chr1:149920956 A>G maps to NM_020205.2 Y384Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5189-01A-02D-1429-08 chr1:64643610 A>G maps to NM_005012.2 V629V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5189-01A-02D-1429-08 chr9:117848653 G>A maps to NM_002160.2 G452G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5189-01A-02D-1429-08 chr5:158696066 C>G maps to NM_145049.3 L48L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5190-01A-01D-1429-08 chr12:46245700 C>A maps to NM_152641.2 V1265V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5190-01A-01D-1429-08 chr17:12920218 G>A maps to NM_018127.6 F109F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5190-01A-01D-1429-08 chr6:168297598 C>T maps to ENST00000400822 Q421*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5190-01A-01D-1429-08 chr15:22369271 G>T maps to NM_001004719.2 E233*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5190-01A-01D-1429-08 chr5:140174869 G>A maps to NM_018905.2 E107E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5190-01A-01D-1429-08 chr2:175289229 G>A maps to NM_024583.4 V315V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5190-01A-01D-1429-08 chr4:122853761 G>A maps to NM_001130698.1 D217D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5190-01A-01D-1429-08 chr1:12566927 T>A maps to NM_015378.2 I4272I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5190-01A-01D-1429-08 chrX:153236255 C>A maps to ENST00000369984 A12A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5190-01A-01D-1429-08 chrX:153236255 C>A maps to ENST00000369984 A12A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5190-01A-01D-1429-08 chr11:1017646 G>T maps to NM_005961.2 P1718P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5190-01A-01D-1429-08 chr11:1017646 G>T maps to NM_005961.2 P1718P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5191-01A-01D-1429-08 chr1:10502398 A>G maps to NM_199294.2 S118S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5191-01A-01D-1429-08 chr6:170162544 T>A maps to NM_018341.1 L293*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5191-01A-01D-1429-08 chr8:91013752 G>A maps to NM_001359.1 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5191-01A-01D-1429-08 chr5:13753410 A>T maps to NM_001369.2 P3601P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5191-01A-01D-1429-08 chr1:220213564 G>A maps to NM_004446.2 S31S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5191-01A-01D-1429-08 chr14:45468575 G>A maps to ENST00000361462 G738G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5191-01A-01D-1429-08 chr16:23494280 C>A maps to NM_015044.4 R281R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5191-01A-01D-1429-08 chr15:52476834 T>G maps to NM_016194.3 S13S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5191-01A-01D-1429-08 chr11:61897769 C>A maps to NM_001040694.1 L257L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5191-01A-01D-1429-08 chr19:51503867 C>T maps to NM_144505.1 W59*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5191-01A-01D-1429-08 chr21:46047393 C>A maps to NM_198690.2 P102P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5191-01A-01D-1429-08 chr19:2444466 T>A maps to NM_032737.2 R92R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5191-01A-01D-1429-08 chr19:2041089 G>T maps to NM_199054.2 A353A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5191-01A-01D-1429-08 chr19:19329805 G>A maps to NM_004386.2 A52A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5191-01A-01D-1429-08 chr10:60994151 A>C maps to NM_032439.3 S65S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5191-01A-01D-1429-08 chr14:45571776 T>C maps to NM_017922.3 S205S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5191-01A-01D-1429-08 chr2:166170261 T>G maps to NM_001040142.1 L389L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5191-01A-01D-1429-08 chr10:123845032 G>A maps to NM_206862.2 Q1006Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5191-01A-01D-1429-08 chr14:89307273 T>C did not map to a codon.
Sequencing variant TCGA-BP-5191-01A-01D-1429-08 chr22:42054276 C>T maps to NM_001469.3 P481P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5192-01A-01D-1429-08 chr8:113347651 G>T maps to NM_198123.1 T2357T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5192-01A-01D-1429-08 chr11:61070126 T>C maps to NM_001923.3 V1013V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5192-01A-01D-1429-08 chr2:183960370 G>A maps to NM_080876.3 Q213Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5192-01A-01D-1429-08 chr10:125426345 G>A maps to NM_153442.3 A141A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5192-01A-01D-1429-08 chr1:20998503 C>T maps to NM_020816.2 E883E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5192-01A-01D-1429-08 chr16:84211445 A>G maps to NM_178452.4 *726W. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5192-01A-01D-1429-08 chr16:823127 C>T did not map to a codon.
Sequencing variant TCGA-BP-5192-01A-01D-1429-08 chr18:3089565 T>C maps to NM_003803.3 E1346E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5192-01A-01D-1429-08 chr3:46754549 C>T maps to NM_013270.4 W254*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5192-01A-01D-1429-08 chr2:136402958 C>T maps to ENST00000409606 F495F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5192-01A-01D-1429-08 chrX:50341292 G>A maps to NM_020717.3 S1395S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5192-01A-01D-1429-08 chr2:228883286 A>G maps to NM_001142644.1 A761A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5192-01A-01D-1429-08 chr9:130413897 G>T maps to NM_003165.3 V18V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5192-01A-01D-1429-08 chr10:114046094 G>A maps to NM_058222.1 V143V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5192-01A-01D-1429-08 chr19:2418066 C>T maps to NM_182973.1 L661L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5192-01A-01D-1429-08 chr15:40660394 G>A maps to NM_033510.1 L694L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5192-01A-01D-1429-08 chr15:40660394 G>A maps to NM_033510.1 L694L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5192-01A-01D-1429-08 chr1:8420608 T>G maps to NM_012102.3 P986P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5192-01A-01D-1429-08 chr1:8420608 T>G maps to NM_012102.3 P986P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5194-01A-02D-1429-08 chr2:159312933 A>T maps to NM_138803.3 A6A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5194-01A-02D-1429-08 chr2:159312933 A>T maps to NM_138803.3 A6A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5194-01A-02D-1429-08 chrX:49105113 G>A maps to NM_014008.3 L450L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5194-01A-02D-1429-08 chr14:91755524 G>A maps to NM_001080414.2 A1455A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5194-01A-02D-1429-08 chrX:139040296 G>A maps to NM_001013403.2 I56I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5194-01A-02D-1429-08 chr11:65375919 C>A did not map to a codon.
Sequencing variant TCGA-BP-5194-01A-02D-1429-08 chr16:57503111 G>A maps to NM_032940.2 S98S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5194-01A-02D-1429-08 chr15:45559672 C>A maps to NM_004212.3 I321I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5194-01A-02D-1429-08 chr16:4247842 G>A maps to ENST00000330063 N549N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5194-01A-02D-1429-08 chr11:9610145 C>T maps to NM_003390.3 Y646Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5194-01A-02D-1429-08 chr8:67590119 C>A maps to NM_019607.1 V59V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5194-01A-02D-1429-08 chr8:67590119 C>A maps to NM_019607.1 V59V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5194-01A-02D-1429-08 chr3:9957049 C>T maps to NM_153483.2 D561D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5194-01A-02D-1429-08 chr3:9957049 C>T maps to NM_153483.2 D561D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5194-01A-02D-1429-08 chr17:80863899 C>A maps to NM_005993.4 A631A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5194-01A-02D-1429-08 chr17:80863899 C>A maps to NM_005993.4 A631A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5195-01A-02D-1429-08 chr10:37418818 A>G did not map to a codon.
Sequencing variant TCGA-BP-5195-01A-02D-1429-08 chr17:40997545 T>C maps to NM_009590.2 S301S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5195-01A-02D-1429-08 chr10:117024694 A>G maps to NM_207303.2 P571P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5195-01A-02D-1429-08 chr18:60985488 G>A maps to NM_000633.2 L137L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5195-01A-02D-1429-08 chr16:61851420 C>A maps to NM_001796.2 V413V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5195-01A-02D-1429-08 chr15:42632071 G>A maps to NM_198141.2 L683L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5195-01A-02D-1429-08 chr17:28849290 C>T maps to NM_004871.2 N216N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5195-01A-02D-1429-08 chr11:1605897 C>T maps to NM_001005922.1 K194K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5195-01A-02D-1429-08 chr14:24878973 A>T maps to NM_025081.2 A658A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5195-01A-02D-1429-08 chr10:3209165 A>C maps to ENST00000380989 Y76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5195-01A-02D-1429-08 chr19:43243170 A>T maps to NM_021016.3 V45V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5195-01A-02D-1429-08 chr14:94936171 T>C maps to NM_175739.3 A20A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5195-01A-02D-1429-08 chr11:16133397 A>G maps to NM_001145819.1 A296A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5195-01A-02D-1429-08 chr13:20077376 G>A did not map to a codon.
Sequencing variant TCGA-BP-5195-01A-02D-1429-08 chr13:20077376 G>A did not map to a codon.
Sequencing variant TCGA-BP-5196-01A-01D-1429-08 chr1:26664086 C>A maps to NM_001039775.3 E1196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5196-01A-01D-1429-08 chr19:3907732 C>T maps to NM_033064.4 D120D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5196-01A-01D-1429-08 chr1:151496774 C>T maps to NM_020770.2 L448L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5196-01A-01D-1429-08 chr2:201721534 C>A did not map to a codon.
Sequencing variant TCGA-BP-5196-01A-01D-1429-08 chr5:127609607 A>T maps to NM_001999.3 C2588*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5196-01A-01D-1429-08 chr8:80678001 G>A maps to NM_001040708.1 Y116Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5196-01A-01D-1429-08 chr11:614300 G>A maps to NM_004031.2 L197L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5196-01A-01D-1429-08 chr10:99223687 A>G maps to ENST00000422291 P634P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5196-01A-01D-1429-08 chr13:53624773 A>G maps to NM_006418.3 L467L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5196-01A-01D-1429-08 chr5:32052784 C>T maps to NM_178140.2 L578L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5196-01A-01D-1429-08 chr6:79708067 G>A maps to NM_017934.5 I640I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5196-01A-01D-1429-08 chr20:62642792 C>T maps to NM_012469.3 I487I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5196-01A-01D-1429-08 chr5:130897688 C>T maps to ENST00000514667 E161E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5196-01A-01D-1429-08 chr10:72617448 T>C did not map to a codon.
Sequencing variant TCGA-BP-5196-01A-01D-1429-08 chr1:202566076 C>T maps to NM_177402.4 V356V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5196-01A-01D-1429-08 chr11:85409118 T>A maps to ENST00000359152 K1632*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5196-01A-01D-1429-08 chr6:2784576 G>A maps to NM_020135.2 A554A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5196-01A-01D-1429-08 chr8:28206649 A>G maps to NM_018660.2 S474S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5196-01A-01D-1429-08 chr8:77776068 T>C maps to NM_024721.4 A3373A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5196-01A-01D-1429-08 chr8:77776068 T>C maps to NM_024721.4 A3373A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5198-01A-01D-1429-08 chr2:143913196 C>T maps to NM_018460.3 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5198-01A-01D-1429-08 chr20:55101051 C>T maps to NM_001012971.3 R148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5198-01A-01D-1429-08 chr19:17003920 A>C maps to ENST00000443236 *1943E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5198-01A-01D-1429-08 chr5:140954548 G>T maps to ENST00000398557 S542S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5198-01A-01D-1429-08 chr19:2229789 A>C maps to NM_032482.2 *1538S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5198-01A-01D-1429-08 chr19:2229789 A>C maps to NM_032482.2 *1538S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5198-01A-01D-1429-08 chr10:134012455 C>A maps to NM_006426.2 I264I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5198-01A-01D-1429-08 chr16:68109278 C>A maps to NM_017803.3 A318A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5198-01A-01D-1429-08 chr15:48782116 C>A maps to NM_000138.4 E1005*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5198-01A-01D-1429-08 chr12:49315837 T>A maps to NM_016594.2 K179*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5198-01A-01D-1429-08 chr16:27523127 T>C maps to NM_001520.3 T356T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5198-01A-01D-1429-08 chr8:105507334 A>T maps to NM_013437.4 V561V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5198-01A-01D-1429-08 chr1:39908130 C>A maps to ENST00000361689 A4273A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5198-01A-01D-1429-08 chr5:179225512 G>A maps to NM_054013.3 D489D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5198-01A-01D-1429-08 chr8:11142462 C>T maps to NM_015458.3 Y22Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5198-01A-01D-1429-08 chr5:16701662 G>A maps to NM_012334.2 F947F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5198-01A-01D-1429-08 chr14:71462625 T>C maps to NM_014982.2 S871S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5198-01A-01D-1429-08 chr11:77412359 A>T maps to NM_016578.3 C638*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5198-01A-01D-1429-08 chr14:92958091 C>T maps to NM_153646.3 Q541*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5198-01A-01D-1429-08 chr17:42333124 G>A maps to NM_000342.3 L572L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5198-01A-01D-1429-08 chr2:179634603 C>A maps to NM_133378.4 E2902*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5198-01A-01D-1429-08 chr3:195505829 G>C maps to NM_018406.5 T4207T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5198-01A-01D-1429-08 chr3:195505829 G>C maps to NM_018406.5 T4207T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5198-01A-01D-1429-08 chr19:52570737 C>A maps to NM_001136499.1 E133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5198-01A-01D-1429-08 chr19:52570737 C>A maps to NM_001136499.1 E133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5198-01A-01D-1429-08 chr15:85147433 A>T maps to NM_181877.3 V92V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5198-01A-01D-1429-08 chr15:85147433 A>T maps to NM_181877.3 V92V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5198-01A-01D-1429-08 chr10:73499529 G>T did not map to a codon.
Sequencing variant TCGA-BP-5198-01A-01D-1429-08 chr10:73499529 G>T did not map to a codon.
Sequencing variant TCGA-BP-5199-01A-01D-1429-08 chr12:52312802 T>C maps to NM_001077401.1 D427D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5199-01A-01D-1429-08 chr1:27106454 A>C maps to NM_006015.4 P2022P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5199-01A-01D-1429-08 chr4:113510904 A>G maps to NM_018392.4 D1034D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5199-01A-01D-1429-08 chr19:51228702 C>T maps to NM_002975.2 Y317Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5199-01A-01D-1429-08 chrX:107681170 C>A did not map to a codon.
Sequencing variant TCGA-BP-5199-01A-01D-1429-08 chr1:78481810 G>A maps to NM_007034.3 L298L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5199-01A-01D-1429-08 chr15:40268967 C>A maps to NM_001013703.2 P724P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5199-01A-01D-1429-08 chr11:126142904 T>A maps to NM_017547.3 C116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5199-01A-01D-1429-08 chr13:27333001 C>T maps to NM_005288.3 P321P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5199-01A-01D-1429-08 chr1:173703124 A>T maps to NM_014458.3 G99G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5199-01A-01D-1429-08 chr6:10802229 A>T maps to NM_005906.3 V242V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5199-01A-01D-1429-08 chr17:10369588 C>T did not map to a codon.
Sequencing variant TCGA-BP-5199-01A-01D-1429-08 chr5:140229360 G>A maps to NM_031857.1 A427A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5199-01A-01D-1429-08 chr17:61908393 A>G did not map to a codon.
Sequencing variant TCGA-BP-5199-01A-01D-1429-08 chr7:4014045 G>A maps to NM_152744.3 T621T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5199-01A-01D-1429-08 chr10:112764371 A>G maps to NM_007373.3 L327L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5199-01A-01D-1429-08 chr9:140126521 A>T did not map to a codon.
Sequencing variant TCGA-BP-5199-01A-01D-1429-08 chr15:45962136 A>G maps to NM_021199.2 R139R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5199-01A-01D-1429-08 chr9:74305108 C>T maps to NM_013390.2 V1250V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5199-01A-01D-1429-08 chr16:89789583 G>A maps to NM_001113525.1 A183A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5199-01A-01D-1429-08 chr6:43305843 C>T maps to NM_014345.2 K1964K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5199-01A-01D-1429-08 chr1:151263417 C>A maps to NM_020832.1 S1149S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5199-01A-01D-1429-08 chr19:43348719 C>T did not map to a codon.
Sequencing variant TCGA-BP-5199-01A-01D-1429-08 chr19:43348719 C>T did not map to a codon.
Sequencing variant TCGA-BP-5199-01A-01D-1429-08 chr10:89720740 C>T maps to NM_000314.4 Q298*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5199-01A-01D-1429-08 chr10:89720740 C>T maps to NM_000314.4 Q298*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5200-01A-01D-1429-08 chr9:104187207 G>A maps to NM_000035.3 L306L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5200-01A-01D-1429-08 chrX:49173750 G>A maps to NM_001098413.2 V104V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5200-01A-01D-1429-08 chr19:42341276 G>A maps to NM_173506.4 S227S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5200-01A-01D-1429-08 chr11:113133586 T>C maps to ENST00000397960 S741S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5200-01A-01D-1429-08 chr1:247614531 G>A maps to NM_001004492.1 I251I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5200-01A-01D-1429-08 chr14:22133739 C>T maps to NM_001001912.1 L148L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5200-01A-01D-1429-08 chr11:66619325 G>A maps to NM_022172.2 F639F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5200-01A-01D-1429-08 chr10:118305650 G>C did not map to a codon.
Sequencing variant TCGA-BP-5200-01A-01D-1429-08 chr17:56060481 C>T maps to NM_007146.2 V102V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5200-01A-01D-1429-08 chr19:40398045 A>G maps to NM_003890.2 C2307C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5200-01A-01D-1429-08 chr19:40398045 A>G maps to NM_003890.2 C2307C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5200-01A-01D-1429-08 chr10:88466359 A>C maps to NM_007078.2 P323P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5200-01A-01D-1429-08 chr10:88466359 A>C maps to NM_007078.2 P323P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5201-01A-01D-1429-08 chr1:155732097 C>A maps to ENST00000368331 R1598R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5201-01A-01D-1429-08 chrX:44928975 G>A maps to NM_021140.2 Q692Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5201-01A-01D-1429-08 chr1:38323149 C>A maps to NM_005955.2 E61*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5201-01A-01D-1429-08 chr1:38323149 C>A maps to NM_005955.2 E61*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5201-01A-01D-1429-08 chr9:33467190 C>A maps to NM_022917.4 E599*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5201-01A-01D-1429-08 chr8:10396086 C>G maps to NM_198464.3 T281T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5201-01A-01D-1429-08 chr7:92763472 T>C maps to NM_152703.2 L604L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5201-01A-01D-1429-08 chr9:140137407 C>A maps to NM_006088.5 L246L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5202-01A-02D-1429-08 chr12:51696508 G>A maps to NM_016293.2 S91S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5202-01A-02D-1429-08 chr1:203276484 T>A maps to NM_006763.2 C132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5202-01A-02D-1429-08 chr8:68107614 A>G did not map to a codon.
Sequencing variant TCGA-BP-5202-01A-02D-1429-08 chr7:73097663 G>A maps to NM_032317.2 S30S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5202-01A-02D-1429-08 chr3:37032774 A>T maps to NM_014805.3 L598L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5202-01A-02D-1429-08 chr4:79296890 A>T did not map to a codon.
Sequencing variant TCGA-BP-5202-01A-02D-1429-08 chr15:99482524 C>T maps to NM_000875.3 F1131F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5202-01A-02D-1429-08 chr1:203465246 C>T maps to NM_014359.3 G38G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5202-01A-02D-1429-08 chr1:211486236 T>A maps to NM_001136223.1 T417T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4882-01A-02D-1429-08 chr3:137843363 T>C maps to NM_016161.2 L255L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4882-01A-02D-1429-08 chr1:160209813 A>G maps to NM_015726.3 D132D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4882-01A-02D-1429-08 chr1:206822276 C>T maps to NM_003582.2 P578P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4882-01A-02D-1429-08 chr12:132497631 C>T maps to ENST00000333577 R1210*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4882-01A-02D-1429-08 chr11:46880581 G>A maps to ENST00000256991 D1935D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4882-01A-02D-1429-08 chr1:40434357 A>G maps to NM_001136493.1 K503K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4882-01A-02D-1429-08 chr11:102668827 G>A did not map to a codon.
Sequencing variant TCGA-CJ-4882-01A-02D-1429-08 chr17:10247204 G>T maps to NM_003802.2 P602P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4882-01A-02D-1429-08 chr11:63764640 C>A maps to ENST00000422031 G218G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4882-01A-02D-1429-08 chr19:1482901 G>A maps to NM_017573.3 F563F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4882-01A-02D-1429-08 chr17:37829070 C>T maps to NM_033419.3 K316K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4882-01A-02D-1429-08 chr3:150460185 G>C maps to NM_005067.5 Y239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4882-01A-02D-1429-08 chr1:234454500 T>A maps to NM_173508.2 L320*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4882-01A-02D-1429-08 chr17:76354729 C>T maps to NM_003955.3 E149E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4882-01A-02D-1429-08 chr1:115489893 G>T maps to NM_003176.2 E759*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4882-01A-02D-1429-08 chr12:11139224 C>A maps to NM_176890.2 E79*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4882-01A-02D-1429-08 chr7:98457931 G>A maps to NM_001134450.1 Q141*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4882-01A-02D-1429-08 chr2:179424710 T>A maps to NM_133378.4 T26148T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4882-01A-02D-1429-08 chr10:122661796 G>T maps to NM_018117.11 E906*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4882-01A-02D-1429-08 chr7:50070787 A>T maps to NM_007009.2 L202L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4882-01A-02D-1429-08 chr22:20307318 A>G maps to NM_033257.3 S38S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4882-01A-02D-1429-08 chr22:20307318 A>G maps to NM_033257.3 S38S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4882-01A-02D-1429-08 chr19:33882245 G>A maps to NM_000285.3 G369G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4882-01A-02D-1429-08 chr19:33882245 G>A maps to NM_000285.3 G369G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4882-01A-02D-1429-08 chr12:27799071 C>T maps to NM_003622.3 L116L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4882-01A-02D-1429-08 chr12:27799071 C>T maps to NM_003622.3 L116L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4897-01A-03D-1429-08 chr2:233246012 C>T maps to NM_001632.3 Y415Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4897-01A-03D-1429-08 chr6:41021139 G>A maps to NM_006789.3 G18G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4897-01A-03D-1429-08 chr12:6837090 G>C did not map to a codon.
Sequencing variant TCGA-CJ-4897-01A-03D-1429-08 chr10:86132204 G>A maps to ENST00000372088 W466*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4897-01A-03D-1429-08 chr11:65810469 G>A maps to NM_033036.2 N268N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4897-01A-03D-1429-08 chr6:46849805 G>A maps to NM_015234.4 G217G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4897-01A-03D-1429-08 chrX:51487801 C>T maps to NM_018094.4 I360I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4897-01A-03D-1429-08 chr15:63948031 G>A maps to ENST00000261887 N3331N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4897-01A-03D-1429-08 chr10:100177389 G>A maps to NM_000195.2 D678D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4897-01A-03D-1429-08 chrX:53675214 A>C maps to ENST00000276009 V28V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4897-01A-03D-1429-08 chr13:51948839 G>A maps to NM_012141.2 Q608*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4897-01A-03D-1429-08 chr17:38859816 G>A maps to NM_019016.2 F43F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4897-01A-03D-1429-08 chr4:39472862 T>C maps to NM_006859.2 R297R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4897-01A-03D-1429-08 chr15:69328248 C>T maps to NM_024505.3 S387S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4897-01A-03D-1429-08 chr3:121207745 T>A maps to ENST00000393672 A1480A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4897-01A-03D-1429-08 chr2:44556212 A>C maps to NM_001171603.1 T464T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4897-01A-03D-1429-08 chrX:17819212 C>T maps to NM_021785.4 T306T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4897-01A-03D-1429-08 chr15:49320718 G>T maps to NM_001193489.1 C275*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4897-01A-03D-1429-08 chr14:99932085 A>G maps to NM_032233.2 T19T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4897-01A-03D-1429-08 chr20:1460669 T>C maps to NM_001122962.1 L42L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4897-01A-03D-1429-08 chr5:150867781 C>T maps to NM_078483.2 P466P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4897-01A-03D-1429-08 chr6:152599303 G>A maps to NM_182961.2 L6165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4897-01A-03D-1429-08 chr20:42574587 G>A maps to ENST00000348077 A12A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4897-01A-03D-1429-08 chr6:33231656 C>T did not map to a codon.
Sequencing variant TCGA-CJ-4897-01A-03D-1429-08 chr14:64066629 G>A maps to NM_080666.2 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4897-01A-03D-1429-08 chr16:72830805 A>T maps to NM_006885.3 G1925G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4897-01A-03D-1429-08 chr15:79051885 G>A maps to ENST00000258883 C1649C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4897-01A-03D-1429-08 chr15:79051885 G>A maps to ENST00000258883 C1649C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4897-01A-03D-1429-08 chr10:99655167 G>A maps to NM_018058.4 G440G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4897-01A-03D-1429-08 chr10:99655167 G>A maps to NM_018058.4 G440G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4899-01A-01D-1462-08 chr19:50374935 G>A maps to ENST00000391835 P185P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4899-01A-01D-1462-08 chr10:5789076 A>C maps to NM_017782.4 S1231S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4899-01A-01D-1462-08 chr10:5789076 A>C maps to NM_017782.4 S1231S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4899-01A-01D-1462-08 chr4:56825851 C>T maps to NM_025009.3 Q207*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4899-01A-01D-1462-08 chr5:118280325 A>G maps to NM_173666.2 C79C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4899-01A-01D-1462-08 chr17:74721937 C>T did not map to a codon.
Sequencing variant TCGA-CJ-4899-01A-01D-1462-08 chr14:74972835 C>T maps to NM_000428.2 V1364V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4899-01A-01D-1462-08 chr2:85768974 T>C maps to NM_005911.4 T143T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4899-01A-01D-1462-08 chr1:166816821 C>G maps to NM_017542.3 T117T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4899-01A-01D-1462-08 chr1:12854405 G>A maps to NM_023013.2 L210L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4899-01A-01D-1462-08 chr7:138958745 T>A maps to NM_173569.3 S633S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4899-01A-01D-1462-08 chr3:48609478 C>T did not map to a codon.
Sequencing variant TCGA-CJ-4899-01A-01D-1462-08 chr3:48609478 C>T did not map to a codon.
Sequencing variant TCGA-CJ-4901-01A-01D-1429-08 chr13:95862960 C>A maps to NM_005845.3 V202V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4901-01A-01D-1429-08 chr8:113301592 C>A did not map to a codon.
Sequencing variant TCGA-CJ-4901-01A-01D-1429-08 chr22:42524923 A>G maps to NM_000106.4 G176G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4901-01A-01D-1429-08 chr18:11999108 A>T maps to NM_014214.1 A51A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4901-01A-01D-1429-08 chr22:30067835 C>T maps to NM_181832.2 R341*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4901-01A-01D-1429-08 chr1:203472873 G>C did not map to a codon.
Sequencing variant TCGA-CJ-4901-01A-01D-1429-08 chr14:20483199 A>T maps to NM_001004712.1 S51S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4901-01A-01D-1429-08 chr11:5323104 C>G maps to NM_033179.2 R24R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4901-01A-01D-1429-08 chr16:19195339 G>A maps to NM_016524.2 L274L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4901-01A-01D-1429-08 chr1:85564292 A>G maps to NM_145172.3 G477G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4901-01A-01D-1429-08 chr19:22939563 A>G maps to ENST00000397104 F869F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4901-01A-01D-1429-08 chr10:48429219 G>A maps to NM_004962.2 S222S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4901-01A-01D-1429-08 chr10:48429219 G>A maps to NM_004962.2 S222S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4902-01A-01D-1429-08 chr12:9230404 G>A maps to NM_000014.4 I1056I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4902-01A-01D-1429-08 chr16:48244894 G>A maps to NM_032583.3 G524G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4902-01A-01D-1429-08 chr18:56205105 A>T maps to NM_052947.3 P771P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4902-01A-01D-1429-08 chr15:90349607 T>C maps to NM_001150.2 K69K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4902-01A-01D-1429-08 chr10:86130885 A>T maps to ENST00000372088 T26T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4902-01A-01D-1429-08 chr11:118963205 C>A maps to NM_000190.3 I248I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4902-01A-01D-1429-08 chr10:118957019 C>T maps to NM_181840.1 P7P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4902-01A-01D-1429-08 chr2:27322320 C>T maps to NM_006488.2 G229G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4902-01A-01D-1429-08 chr16:85696692 C>T maps to NM_014615.2 S789S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4902-01A-01D-1429-08 chr17:39680197 G>A maps to NM_002276.4 Q334*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4902-01A-01D-1429-08 chr1:70504368 G>A maps to NM_020794.2 P916P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4902-01A-01D-1429-08 chr17:5322724 G>T maps to NM_002532.3 R82R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4902-01A-01D-1429-08 chr17:79257256 C>A maps to NM_001037984.1 V103V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4902-01A-01D-1429-08 chr2:24307099 T>A maps to NM_147184.1 K33*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4902-01A-01D-1429-08 chr2:66667008 G>T maps to ENST00000407092 E92*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4902-01A-01D-1429-08 chr2:66667008 G>T maps to ENST00000407092 E92*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4902-01A-01D-1429-08 chr16:2867458 T>G did not map to a codon.
Sequencing variant TCGA-CJ-4902-01A-01D-1429-08 chr16:2867458 T>G did not map to a codon.
Sequencing variant TCGA-CJ-4903-01A-01D-1429-08 chr14:33293955 C>T maps to NM_004274.4 R2313*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4903-01A-01D-1429-08 chr14:25043507 G>A maps to NM_001911.2 Y179Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4903-01A-01D-1429-08 chr8:145151519 C>T maps to NM_001916.3 L215L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4903-01A-01D-1429-08 chr1:42049238 G>A maps to NM_024503.3 N410N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4903-01A-01D-1429-08 chr3:182871517 A>G maps to NM_014398.3 C237C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4903-01A-01D-1429-08 chr5:71495394 G>A maps to NM_005909.3 K2071K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4903-01A-01D-1429-08 chr11:19735258 C>A maps to ENST00000396087 V6V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4903-01A-01D-1429-08 chr17:3030488 G>A maps to ENST00000381953 A157A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4903-01A-01D-1429-08 chr3:52643359 C>A maps to ENST00000296302 E846*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4903-01A-01D-1429-08 chr1:233150460 G>T maps to NM_014801.3 C1634*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4903-01A-01D-1429-08 chr2:173894948 C>T maps to NM_007023.3 N872N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4903-01A-01D-1429-08 chr2:204305221 T>A maps to ENST00000374493 A949A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4903-01A-01D-1429-08 chr2:178990776 C>G maps to ENST00000456670 A435A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4903-01A-01D-1429-08 chr3:39108072 A>T maps to NM_020839.2 V101V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4904-01A-02D-1429-08 chr16:77387746 C>T maps to NM_199355.2 K499K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4904-01A-02D-1429-08 chr21:41414411 G>A maps to NM_001389.3 L1858L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4904-01A-02D-1429-08 chr12:56142618 C>G maps to NM_005811.3 S232*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4904-01A-02D-1429-08 chr12:53012200 G>T maps to NM_175068.2 G36G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4904-01A-02D-1429-08 chr1:21795328 C>G maps to NM_032264.2 L94L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4904-01A-02D-1429-08 chr19:56459315 C>T maps to NM_176811.2 S16S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4904-01A-02D-1429-08 chr5:43619221 G>A did not map to a codon.
Sequencing variant TCGA-CJ-4904-01A-02D-1429-08 chr11:16876456 C>T maps to ENST00000448080 V167V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4904-01A-02D-1429-08 chr2:86359529 A>G maps to NM_017952.5 Q452Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4904-01A-02D-1429-08 chr4:90743426 A>G maps to NM_001146055.1 T92T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4904-01A-02D-1429-08 chr17:35836945 C>A maps to NM_001166105.1 Y397*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4904-01A-02D-1429-08 chrX:108631718 T>A maps to ENST00000218006 S985S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4904-01A-02D-1429-08 chrX:108631718 T>A maps to ENST00000218006 S985S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4905-01A-02D-1429-08 chr10:116307473 C>T maps to ENST00000277895 Q245Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4905-01A-02D-1429-08 chr3:112969402 C>T maps to ENST00000273395 N33N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4905-01A-02D-1429-08 chr12:112688105 G>C maps to NM_001109662.2 T1092T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4905-01A-02D-1429-08 chr21:47722404 G>A maps to NM_058180.3 A269A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4905-01A-02D-1429-08 chr17:48267075 A>T maps to NM_000088.3 P877P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4905-01A-02D-1429-08 chr20:34778269 C>T maps to NM_012156.2 V366V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4905-01A-02D-1429-08 chr11:108389043 G>T maps to NM_015065.2 V183V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4905-01A-02D-1429-08 chr12:62147528 T>A did not map to a codon.
Sequencing variant TCGA-CJ-4905-01A-02D-1429-08 chrX:108691324 C>T maps to ENST00000218006 T514T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4905-01A-02D-1429-08 chr1:12081815 G>T maps to NM_021933.2 R11R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4905-01A-02D-1429-08 chr20:33345743 C>T maps to NM_014071.2 Q269Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4905-01A-02D-1429-08 chr2:152397300 T>C maps to NM_001164507.1 E6899E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4905-01A-02D-1429-08 chr13:61987112 C>A maps to NM_022843.3 L373L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4905-01A-02D-1429-08 chr20:44049023 G>C maps to NM_015937.4 L274L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4905-01A-02D-1429-08 chr19:50905131 C>T maps to ENST00000391817 C138C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4905-01A-02D-1429-08 chr2:1653136 C>T maps to NM_012293.1 T805T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4905-01A-02D-1429-08 chrX:129306269 G>T maps to NM_004794.2 V78V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4905-01A-02D-1429-08 chr9:6014374 G>A maps to NM_012416.2 S411S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4905-01A-02D-1429-08 chrX:71351147 C>A maps to NM_001024455.3 G81G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4905-01A-02D-1429-08 chr16:30740444 T>C maps to NM_006662.2 R1939R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4905-01A-02D-1429-08 chr2:182757371 G>A maps to NM_001130445.1 W81*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4905-01A-02D-1429-08 chr2:179479673 C>T maps to NM_133378.4 E13652E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4905-01A-02D-1429-08 chr2:179479673 C>T maps to NM_133378.4 E13652E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4905-01A-02D-1429-08 chr4:69188620 C>A maps to NM_001031732.2 E483*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4905-01A-02D-1429-08 chr19:37879643 G>A maps to NM_032453.1 T231T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4905-01A-02D-1429-08 chr22:45683305 A>C maps to NM_006953.3 A154A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4905-01A-02D-1429-08 chr22:45683305 A>C maps to NM_006953.3 A154A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4907-01A-01D-1429-08 chr7:48556329 T>A maps to NM_152701.3 T4550T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4907-01A-01D-1429-08 chr4:100239947 G>C maps to NM_000668.4 R38R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4907-01A-01D-1429-08 chr5:137502345 A>T maps to NM_139199.1 T286T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4907-01A-01D-1429-08 chr13:37014311 C>T maps to NM_003914.3 L364L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4907-01A-01D-1429-08 chr4:68380077 A>G maps to NM_001812.2 A386A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4907-01A-01D-1429-08 chr6:154743777 C>T maps to NM_173515.2 W269*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4907-01A-01D-1429-08 chr4:109783656 C>T maps to ENST00000333642 K399K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4907-01A-01D-1429-08 chr20:56089654 G>A maps to ENST00000423479 S441S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4907-01A-01D-1429-08 chr4:9784912 C>T maps to NM_000798.4 P420P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4907-01A-01D-1429-08 chr6:15627642 C>A maps to NM_032122.4 E96*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4907-01A-01D-1429-08 chr1:26357723 C>T maps to NM_004455.2 P401P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4907-01A-01D-1429-08 chr13:29599345 G>T maps to NM_001033602.2 E181*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4907-01A-01D-1429-08 chr12:103240686 C>A maps to NM_000277.1 E319*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4907-01A-01D-1429-08 chr19:3651894 C>A maps to NM_012398.2 A352A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4907-01A-01D-1429-08 chr20:47258751 C>A maps to NM_020820.3 R1243R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4907-01A-01D-1429-08 chr8:87060712 G>T maps to ENST00000276616 S379*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4907-01A-01D-1429-08 chr19:5219379 C>G maps to NM_002850.3 G1288G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4907-01A-01D-1429-08 chr14:31376114 A>T maps to NM_001083893.1 L619*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4907-01A-01D-1429-08 chr1:1267927 G>A maps to NM_152228.1 K339K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4907-01A-01D-1429-08 chr16:88697619 G>A maps to ENST00000452588 L949L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4907-01A-01D-1429-08 chr11:3109494 G>A maps to NM_020896.3 S860S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4907-01A-01D-1429-08 chr11:3109494 G>A maps to NM_020896.3 S860S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4907-01A-01D-1429-08 chr1:22902867 C>T maps to NM_020526.3 R106R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4907-01A-01D-1429-08 chr1:22902867 C>T maps to NM_020526.3 R106R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4908-01A-01D-1429-08 chr17:35581912 C>T maps to NM_198834.1 Q1158Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4908-01A-01D-1429-08 chr11:67050627 T>C maps to NM_001619.3 P419P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4908-01A-01D-1429-08 chr1:111494479 A>T maps to NM_018372.3 P342P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4908-01A-01D-1429-08 chr21:46912468 G>A maps to ENST00000359759 P1141P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4908-01A-01D-1429-08 chr10:16882523 A>G maps to NM_001081.3 G3279G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4908-01A-01D-1429-08 chr17:44248411 T>C maps to NM_015443.3 G366G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4908-01A-01D-1429-08 chr3:52661376 T>A maps to ENST00000296302 K485*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4908-01A-01D-1429-08 chr6:88210967 T>C maps to NM_006416.4 F149F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4908-01A-01D-1429-08 chr17:27023952 T>C maps to NM_003170.3 D1354D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4912-01A-01D-1429-08 chr8:68111270 A>G maps to NM_006421.3 I1816I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4912-01A-01D-1429-08 chr1:94048424 G>T maps to NM_003567.2 A373A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4912-01A-01D-1429-08 chr4:104000885 G>T maps to NM_020139.3 V237V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4912-01A-01D-1429-08 chr22:30766637 C>G maps to NM_001017437.2 P248P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4912-01A-01D-1429-08 chr7:148454215 C>T maps to NM_003592.2 R153*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4912-01A-01D-1429-08 chr18:28972162 C>T maps to NM_001134453.1 R289*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4912-01A-01D-1429-08 chr12:12629997 A>T maps to NM_030640.2 T589T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4912-01A-01D-1429-08 chr19:14755049 C>T maps to NM_032571.3 W307*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4912-01A-01D-1429-08 chr6:160471665 C>T maps to NM_000876.2 V892V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4912-01A-01D-1429-08 chr9:732500 T>C maps to NM_015158.2 T1043T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4912-01A-01D-1429-08 chrX:43571992 A>G maps to NM_000240.2 K151K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4912-01A-01D-1429-08 chr11:118370616 T>A maps to NM_001197104.1 P2049P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4912-01A-01D-1429-08 chr9:125782627 T>C maps to NM_012197.3 L562L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4912-01A-01D-1429-08 chr7:127961368 T>A maps to NM_018077.2 K505*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4912-01A-01D-1429-08 chr1:182544562 A>G maps to NM_021133.3 A730A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4912-01A-01D-1429-08 chr11:70338535 G>T maps to ENST00000338508 P775P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4912-01A-01D-1429-08 chr18:43212330 G>T maps to NM_007163.3 G180*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4912-01A-01D-1429-08 chr11:26718742 A>G maps to NM_178498.3 L336L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4912-01A-01D-1429-08 chr1:27440752 G>C maps to NM_003047.3 S126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4912-01A-01D-1429-08 chr7:138333762 G>T maps to NM_001139456.1 A218A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4912-01A-01D-1429-08 chr19:36230812 C>T maps to NM_024660.2 L173L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4912-01A-01D-1429-08 chr13:38266298 C>T maps to NM_003306.1 L357L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4912-01A-01D-1429-08 chr4:85664901 G>A maps to NM_014991.4 Y2008Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4912-01A-01D-1429-08 chr1:35580007 C>A maps to NM_024772.3 V859V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4912-01A-01D-1429-08 chr9:139379130 G>A maps to NM_152571.2 Q77Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4912-01A-01D-1429-08 chr9:139379130 G>A maps to NM_152571.2 Q77Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4912-01A-01D-1429-08 chr2:241514016 C>T maps to NM_018226.3 V189V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4912-01A-01D-1429-08 chr2:241514016 C>T maps to NM_018226.3 V189V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4912-01A-01D-1429-08 chr16:67261755 C>T maps to NM_014187.3 G8G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4912-01A-01D-1429-08 chr16:67261755 C>T maps to NM_014187.3 G8G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4912-01A-01D-1429-08 chr16:70834810 G>T did not map to a codon.
Sequencing variant TCGA-CJ-4912-01A-01D-1429-08 chr16:70834810 G>T did not map to a codon.
Sequencing variant TCGA-CJ-4913-01A-01D-1429-08 chr12:63543858 G>T maps to NM_000706.3 S253*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4913-01A-01D-1429-08 chr17:79027520 G>A maps to NM_017451.2 K36K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4913-01A-01D-1429-08 chr10:134261286 C>T maps to NM_173541.2 L54L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4913-01A-01D-1429-08 chr4:4389418 C>G maps to NM_001040101.1 G21G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4913-01A-01D-1429-08 chr5:147778624 G>A maps to NM_205836.1 V64V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4913-01A-01D-1429-08 chr14:94088411 C>A maps to ENST00000393153 S1633S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4913-01A-01D-1429-08 chr3:52621445 C>A maps to ENST00000296302 E1016*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4913-01A-01D-1429-08 chr19:57325906 T>G maps to NM_006210.2 V1301V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4913-01A-01D-1429-08 chr1:10477168 C>A maps to NM_002631.2 R324R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4913-01A-01D-1429-08 chr2:241516159 G>A maps to NM_018226.3 L342L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4913-01A-01D-1429-08 chr16:28993799 C>T maps to NM_032038.2 L363L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4913-01A-01D-1429-08 chr15:43281100 C>A maps to NM_174916.2 G1305*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4913-01A-01D-1429-08 chr7:28319098 C>T did not map to a codon.
Sequencing variant TCGA-CJ-4913-01A-01D-1429-08 chr7:28319098 C>T did not map to a codon.
Sequencing variant TCGA-CJ-4913-01A-01D-1429-08 chr18:60646513 G>A maps to NM_194449.2 P1668P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4913-01A-01D-1429-08 chr18:60646513 G>A maps to NM_194449.2 P1668P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4913-01A-01D-1429-08 chr19:4294618 A>C maps to NM_144615.2 G169G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4913-01A-01D-1429-08 chr19:4294618 A>C maps to NM_144615.2 G169G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4916-01A-01D-1429-08 chr5:56777709 G>A maps to NM_001017992.2 I275I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4916-01A-01D-1429-08 chr3:186335069 G>T maps to ENST00000273784 L169L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4916-01A-01D-1429-08 chr2:118766137 A>G maps to NM_019044.4 L47L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4916-01A-01D-1429-08 chr6:41904302 A>G maps to NM_001760.3 T235T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4916-01A-01D-1429-08 chrX:100381783 G>A maps to NM_006733.2 K258K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4916-01A-01D-1429-08 chr3:100354671 T>A did not map to a codon.
Sequencing variant TCGA-CJ-4916-01A-01D-1429-08 chr2:187500899 G>A maps to NM_002210.3 R241R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4916-01A-01D-1429-08 chr7:116339926 G>T maps to NM_001127500.1 T263T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4916-01A-01D-1429-08 chr14:56757050 G>T maps to NM_021255.2 L191L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4916-01A-01D-1429-08 chr3:38802743 A>G maps to NM_006514.2 N274N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4916-01A-01D-1429-08 chr18:61600418 C>T maps to NM_005024.1 D257D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4916-01A-01D-1429-08 chr11:57087710 G>A maps to NM_033396.2 N190N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4916-01A-01D-1429-08 chr17:72233485 G>T maps to NM_032646.5 R156R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4916-01A-01D-1429-08 chr3:10183747 C>T maps to NM_000551.2 Q73*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4916-01A-01D-1429-08 chr3:9970112 T>G maps to NM_153461.2 G405G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4916-01A-01D-1429-08 chr3:9970112 T>G maps to NM_153461.2 G405G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4916-01A-01D-1429-08 chr20:62839352 A>G maps to NM_004535.2 E268E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4916-01A-01D-1429-08 chr20:62839352 A>G maps to NM_004535.2 E268E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4918-01A-01D-1429-08 chr17:6331787 C>T maps to NM_014336.3 R105R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4918-01A-01D-1429-08 chr1:17990993 C>A maps to NM_018125.3 P971P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4918-01A-01D-1429-08 chr12:58020622 G>A maps to NM_001478.3 A502A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4918-01A-01D-1429-08 chr1:94057947 G>A maps to NM_003567.2 F120F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4918-01A-01D-1429-08 chr11:112064373 T>C maps to NM_031938.4 V157V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4918-01A-01D-1429-08 chr11:61545942 C>T maps to NM_001127392.1 N665N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4918-01A-01D-1429-08 chr6:3723938 G>A maps to NM_183373.3 L204L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4918-01A-01D-1429-08 chr9:97823037 C>T maps to NM_001193329.1 P726P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4918-01A-01D-1429-08 chr9:101829276 T>G maps to NM_001855.3 S1255S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4918-01A-01D-1429-08 chr2:72371135 G>T maps to NM_019885.2 I137I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4918-01A-01D-1429-08 chr9:140695436 G>A did not map to a codon.
Sequencing variant TCGA-CJ-4918-01A-01D-1429-08 chr2:42472704 C>A maps to NM_019063.3 S29*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4918-01A-01D-1429-08 chr14:62211421 G>C did not map to a codon.
Sequencing variant TCGA-CJ-4918-01A-01D-1429-08 chr20:10627596 G>T maps to NM_000214.2 Y625*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4918-01A-01D-1429-08 chr4:100521757 C>T maps to ENST00000511045 T395T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4918-01A-01D-1429-08 chr17:41349124 T>C did not map to a codon.
Sequencing variant TCGA-CJ-4918-01A-01D-1429-08 chr20:46279865 A>G maps to NM_181659.2 Q1264Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4918-01A-01D-1429-08 chr16:53495737 G>T maps to NM_005611.3 E478*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4918-01A-01D-1429-08 chr19:38572297 A>G maps to NM_015073.1 T31T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4918-01A-01D-1429-08 chr6:25779370 A>T maps to NM_005495.2 A483A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4918-01A-01D-1429-08 chr12:113742185 G>A maps to NM_024959.2 I499I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4918-01A-01D-1429-08 chr1:186327743 G>A maps to NM_003292.2 N476N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4918-01A-01D-1429-08 chr10:88230844 A>T maps to ENST00000342368 A767A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4918-01A-01D-1429-08 chr17:39253955 G>A maps to NM_031960.2 P127P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4918-01A-01D-1429-08 chr17:39253955 G>A maps to NM_031960.2 P127P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4918-01A-01D-1429-08 chr5:31423044 C>A maps to NM_013235.4 E1090*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4918-01A-01D-1429-08 chr5:31423044 C>A maps to NM_013235.4 E1090*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4918-01A-01D-1429-08 chr18:42532844 C>A maps to NM_015559.2 G1180G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4918-01A-01D-1429-08 chr18:42532844 C>A maps to NM_015559.2 G1180G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4920-01A-01D-1429-08 chr1:247061602 G>T maps to ENST00000428671 L548L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4920-01A-01D-1429-08 chr11:113270031 C>T maps to NM_178510.1 L447L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4920-01A-01D-1429-08 chr19:19767886 C>A maps to NM_020410.2 V274V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4920-01A-01D-1429-08 chr16:396563 G>A maps to NM_003502.3 G154G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4920-01A-01D-1429-08 chr17:4872276 C>T did not map to a codon.
Sequencing variant TCGA-CJ-4920-01A-01D-1429-08 chr22:21989452 C>T maps to NM_152612.2 R367R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4920-01A-01D-1429-08 chr16:68071946 T>A maps to NM_017803.3 S7S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4920-01A-01D-1429-08 chr6:131995387 A>G maps to NM_005021.3 E243E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4920-01A-01D-1429-08 chr1:226027664 G>A maps to NM_001136018.2 K286K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4920-01A-01D-1429-08 chr1:157105441 G>A maps to NM_001145312.1 I35I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4920-01A-01D-1429-08 chr2:131521735 A>T maps to NM_001105195.1 P697P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4920-01A-01D-1429-08 chr3:68788345 G>C maps to NM_182522.3 S97S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4920-01A-01D-1429-08 chr19:35501011 G>T maps to NM_020895.3 L114L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4920-01A-01D-1429-08 chr14:94129060 G>A did not map to a codon.
Sequencing variant TCGA-CJ-4920-01A-01D-1429-08 chrX:75650468 G>T maps to NM_020932.2 E716*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4920-01A-01D-1429-08 chr5:56160678 T>G maps to NM_005921.1 L318*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4920-01A-01D-1429-08 chr3:182759358 C>G maps to NM_020166.3 R421R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4920-01A-01D-1429-08 chr3:179096585 C>A maps to NM_033540.2 S549*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4920-01A-01D-1429-08 chr7:158447310 G>T maps to NM_017760.5 R908R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4920-01A-01D-1429-08 chr4:149356734 T>G maps to ENST00000511528 P426P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4920-01A-01D-1429-08 chr16:336869 T>A maps to NM_006849.2 T486T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4920-01A-01D-1429-08 chr9:112172525 G>A maps to NM_002829.3 Q495*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4920-01A-01D-1429-08 chr11:32955023 C>T maps to NM_001076786.1 I611I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4920-01A-01D-1429-08 chr17:73657710 A>T maps to NM_004259.5 G283G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4920-01A-01D-1429-08 chr3:38962723 G>T maps to ENST00000302328 A245A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4920-01A-01D-1429-08 chr14:78184795 A>G maps to NM_012245.2 D442D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4920-01A-01D-1429-08 chr19:48385433 A>G maps to NM_003167.3 L127L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4920-01A-01D-1429-08 chr4:65274892 G>A maps to NM_001010874.4 H59H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4920-01A-01D-1429-08 chrX:132351882 G>A maps to NM_016521.2 G135G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4920-01A-01D-1429-08 chr11:113230093 G>T maps to NM_017868.3 E486*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4920-01A-01D-1429-08 chr11:103093808 T>G maps to NM_001080463.1 L3116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4920-01A-01D-1429-08 chr11:103093808 T>G maps to NM_001080463.1 L3116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4920-01A-01D-1429-08 chr11:1643005 G>C maps to ENST00000359229 G106G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4920-01A-01D-1429-08 chr11:1643005 G>C maps to ENST00000359229 G106G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4920-01A-01D-1429-08 chr3:121263751 T>C maps to ENST00000393672 G188G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4920-01A-01D-1429-08 chr3:121263751 T>C maps to ENST00000393672 G188G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4920-01A-01D-1429-08 chr9:131514949 A>C did not map to a codon.
Sequencing variant TCGA-CJ-4920-01A-01D-1429-08 chr9:131514949 A>C did not map to a codon.
Sequencing variant TCGA-CJ-4920-01A-01D-1429-08 chr8:16026113 G>T maps to ENST00000445506 T179T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4920-01A-01D-1429-08 chr8:16026113 G>T maps to ENST00000445506 T179T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4923-01A-01D-1429-08 chr17:66883566 G>C maps to NM_007168.2 S1035S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4923-01A-01D-1429-08 chrX:2835963 G>A maps to NM_001669.2 F248F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4923-01A-01D-1429-08 chr12:107393577 G>A maps to NM_004075.3 F296F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4923-01A-01D-1429-08 chr6:20481596 C>A maps to NM_001949.3 T222T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4923-01A-01D-1429-08 chr11:67219406 G>A maps to NM_206997.1 F263F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4923-01A-01D-1429-08 chr15:65624283 G>A maps to NM_004884.3 N381N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4923-01A-01D-1429-08 chr2:227662245 G>C maps to NM_005544.2 T403T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4923-01A-01D-1429-08 chr20:39984631 T>C maps to NM_022896.1 T587T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4923-01A-01D-1429-08 chr20:39984631 T>C maps to NM_022896.1 T587T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4923-01A-01D-1429-08 chr7:139086942 A>T maps to NM_016019.2 K106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4923-01A-01D-1429-08 chr7:139086942 A>T maps to NM_016019.2 K106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4923-01A-01D-1429-08 chr1:40430906 C>T maps to NM_001136493.1 A139A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4923-01A-01D-1429-08 chr19:46443738 T>G maps to NM_002516.2 A287A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4923-01A-01D-1429-08 chr5:141233714 G>A maps to NM_032420.2 C1202C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4923-01A-01D-1429-08 chr5:141233714 G>A maps to NM_032420.2 C1202C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4923-01A-01D-1429-08 chr3:191179037 G>A maps to NM_001083308.1 L29L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4923-01A-01D-1429-08 chr1:151339306 C>T maps to ENST00000435071 P227P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4923-01A-01D-1429-08 chr1:151339306 C>T maps to ENST00000435071 P227P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4923-01A-01D-1429-08 chr2:197002268 C>A maps to NM_004226.3 E341*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4923-01A-01D-1429-08 chr6:158497794 A>G maps to NM_003898.3 K810K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4923-01A-01D-1429-08 chr6:27420045 G>C maps to NM_007149.2 S431*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4923-01A-01D-1429-08 chr3:52437167 T>A maps to NM_004656.2 K626*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4923-01A-01D-1429-08 chr3:52437167 T>A maps to NM_004656.2 K626*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4923-01A-01D-1429-08 chr11:133807379 G>A maps to NM_014987.1 D190D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4923-01A-01D-1429-08 chr11:133807379 G>A maps to NM_014987.1 D190D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5686-01A-11D-1669-08 chr12:53702265 C>A maps to NM_015665.5 V378V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5686-01A-11D-1669-08 chr3:11354776 G>T did not map to a codon.
Sequencing variant TCGA-CJ-5686-01A-11D-1669-08 chr11:108199912 A>T maps to NM_000051.3 R2419*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5686-01A-11D-1669-08 chr8:69621308 C>G maps to NM_052958.2 S441*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5686-01A-11D-1669-08 chr2:202700486 G>T did not map to a codon.
Sequencing variant TCGA-CJ-5686-01A-11D-1669-08 chr17:73998204 C>A maps to NM_001258.2 L99L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5686-01A-11D-1669-08 chr11:19213959 G>A maps to NM_003476.3 A12A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5686-01A-11D-1669-08 chr5:176894481 C>G maps to ENST00000393565 V159V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5686-01A-11D-1669-08 chr14:53385907 A>G maps to NM_001134999.1 Y108Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5686-01A-11D-1669-08 chr12:130648323 C>T maps to NM_007197.3 I279I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5686-01A-11D-1669-08 chr7:35673461 C>T did not map to a codon.
Sequencing variant TCGA-CJ-5686-01A-11D-1669-08 chr7:99956459 G>A maps to ENST00000413850 W176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5686-01A-11D-1669-08 chr17:6386892 G>A maps to NM_031220.3 L177L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5686-01A-11D-1669-08 chr6:57075109 T>A maps to NM_016277.3 S23S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5686-01A-11D-1669-08 chr12:48143586 C>T maps to NM_001098531.2 G277G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5686-01A-11D-1669-08 chr19:39008077 G>T maps to NM_000540.2 G3255G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5686-01A-11D-1669-08 chr2:228882778 C>A maps to NM_001142644.1 E931*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5686-01A-11D-1669-08 chrX:70602416 T>C maps to ENST00000449580 S522S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5686-01A-11D-1669-08 chr6:32805898 G>A maps to ENST00000452392 L38L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5686-01A-11D-1669-08 chr14:55895568 G>A maps to NM_199047.2 P304P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5686-01A-11D-1669-08 chr8:56652729 T>C maps to ENST00000434581 P312P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5686-01A-11D-1669-08 chr1:12321994 G>T maps to NM_015378.2 S484S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5686-01A-11D-1669-08 chr1:12321994 G>T maps to NM_015378.2 S484S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5686-01A-11D-1669-08 chr8:106810964 T>C maps to NM_012082.3 P251P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5686-01A-11D-1669-08 chr3:143691274 C>A maps to NM_173552.3 S34*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5686-01A-11D-1669-08 chr3:143691274 C>A maps to NM_173552.3 S34*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5686-01A-11D-1669-08 chr6:74228229 G>T maps to NM_001402.5 V292V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5686-01A-11D-1669-08 chr6:74228229 G>T maps to NM_001402.5 V292V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5686-01A-11D-1669-08 chr14:105361168 A>C maps to ENST00000453495 S1549S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5686-01A-11D-1669-08 chr14:105361168 A>C maps to ENST00000453495 S1549S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5686-01A-11D-1669-08 chr9:20414342 A>G maps to NM_004529.2 S167S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5686-01A-11D-1669-08 chr9:20414342 A>G maps to NM_004529.2 S167S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6027-01A-11D-1669-08 chr19:6182802 C>T maps to NM_030924.3 V316V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6027-01A-11D-1669-08 chrX:129289190 G>A maps to NM_145812.2 G59G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6027-01A-11D-1669-08 chr4:41015684 G>A maps to NM_004307.1 I250I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6027-01A-11D-1669-08 chr12:57036240 C>A did not map to a codon.
Sequencing variant TCGA-CJ-6027-01A-11D-1669-08 chr14:35264069 C>A maps to NM_013448.2 V416V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6027-01A-11D-1669-08 chr11:73753115 G>T maps to ENST00000334126 S1881S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6027-01A-11D-1669-08 chr1:117568203 C>T maps to NM_004258.3 C834C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6027-01A-11D-1669-08 chr17:78090844 C>T maps to NM_001079804.1 L756L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6027-01A-11D-1669-08 chrX:48674607 C>T maps to ENST00000444343 G532G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6027-01A-11D-1669-08 chr4:145635413 T>C maps to NM_022475.1 S487S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6027-01A-11D-1669-08 chr1:62237111 A>G maps to NM_176877.2 R178R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6027-01A-11D-1669-08 chr2:27317802 G>A did not map to a codon.
Sequencing variant TCGA-CJ-6027-01A-11D-1669-08 chr12:55026039 C>A maps to NM_033277.1 E80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6027-01A-11D-1669-08 chr1:183177097 C>A maps to NM_005562.2 L54L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6027-01A-11D-1669-08 chr16:55519325 G>A maps to NM_004530.4 L215L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6027-01A-11D-1669-08 chr10:21124509 C>A maps to ENST00000430741 G461*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6027-01A-11D-1669-08 chr9:102590585 G>T maps to NM_173200.1 E99*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6027-01A-11D-1669-08 chr1:28800468 C>A maps to NM_023923.3 P419P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6027-01A-11D-1669-08 chr8:144999884 C>G maps to NM_201380.2 R1541R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6027-01A-11D-1669-08 chr1:153391769 T>C maps to NM_176823.3 S97S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6027-01A-11D-1669-08 chr4:77084505 G>A maps to NM_005506.2 R424*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6027-01A-11D-1669-08 chr2:217342997 A>G maps to NM_014140.3 T867T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6027-01A-11D-1669-08 chr19:44418081 G>A maps to NM_003425.3 C502C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6027-01A-11D-1669-08 chr19:58549264 G>T maps to NM_182572.3 E21*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6027-01A-11D-1669-08 chr5:131630692 C>T maps to NM_003059.2 V128V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6027-01A-11D-1669-08 chr5:131630692 C>T maps to NM_003059.2 V128V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6027-01A-11D-1669-08 chr11:65715208 C>T maps to NM_152762.2 R305*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6027-01A-11D-1669-08 chr11:65715208 C>T maps to NM_152762.2 R305*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6028-01A-11D-1669-08 chrX:135570316 C>A maps to NM_001727.1 S15*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6028-01A-11D-1669-08 chr1:158262060 C>T maps to NM_001765.2 G172G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6028-01A-11D-1669-08 chr10:99640009 G>A maps to NM_018058.4 C605C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6028-01A-11D-1669-08 chr2:80782890 G>T maps to ENST00000402739 R538R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6028-01A-11D-1669-08 chr1:190068173 C>T maps to NM_199051.1 S425S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6028-01A-11D-1669-08 chr9:37733481 A>G maps to NM_014907.2 G336G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6028-01A-11D-1669-08 chr9:37733481 A>G maps to NM_014907.2 G336G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6028-01A-11D-1669-08 chr17:46128662 C>A maps to ENST00000362042 T80T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6028-01A-11D-1669-08 chr17:46128662 C>A maps to ENST00000362042 T80T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6028-01A-11D-1669-08 chr8:144920928 G>A maps to NM_178564.3 Q255*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6028-01A-11D-1669-08 chr6:36922578 C>T maps to NM_153370.2 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6028-01A-11D-1669-08 chr6:36922578 C>T maps to NM_153370.2 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6028-01A-11D-1669-08 chr1:228004908 G>T did not map to a codon.
Sequencing variant TCGA-CJ-6028-01A-11D-1669-08 chr6:160113747 G>T maps to NM_000636.2 A57A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6028-01A-11D-1669-08 chr1:113124710 A>T maps to NM_017744.4 P324P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6028-01A-11D-1669-08 chr8:144550432 G>C maps to NM_015117.2 T707T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6028-01A-11D-1669-08 chr7:44796727 G>A maps to NM_031449.3 G116G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6028-01A-11D-1669-08 chr19:40367840 T>G maps to NM_003890.2 A4373A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6028-01A-11D-1669-08 chr19:40367840 T>G maps to NM_003890.2 A4373A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6028-01A-11D-1669-08 chr1:157789882 C>T did not map to a codon.
Sequencing variant TCGA-CJ-6028-01A-11D-1669-08 chr1:157789882 C>T did not map to a codon.
Sequencing variant TCGA-CJ-6028-01A-11D-1669-08 chr1:220318981 C>T maps to NM_018060.3 L961L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6028-01A-11D-1669-08 chr1:220318981 C>T maps to NM_018060.3 L961L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6028-01A-11D-1669-08 chr5:61649099 A>G did not map to a codon.
Sequencing variant TCGA-CJ-6028-01A-11D-1669-08 chr5:61649099 A>G did not map to a codon.
Sequencing variant TCGA-CJ-6028-01A-11D-1669-08 chr2:220338226 C>A maps to NM_005876.4 G1383G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6028-01A-11D-1669-08 chr2:220338226 C>A maps to NM_005876.4 G1383G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6030-01A-11D-1669-08 chr1:94476402 G>T maps to NM_000350.2 Y1889*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6030-01A-11D-1669-08 chr9:136290646 A>G did not map to a codon.
Sequencing variant TCGA-CJ-6030-01A-11D-1669-08 chr11:66287215 C>G maps to NM_024649.4 A240A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6030-01A-11D-1669-08 chr1:167893735 C>T maps to NM_001143674.1 W50*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6030-01A-11D-1669-08 chr1:167893735 C>T maps to NM_001143674.1 W50*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6030-01A-11D-1669-08 chr3:128998743 C>T maps to NM_001006109.1 L57L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6030-01A-11D-1669-08 chr3:50324294 T>A did not map to a codon.
Sequencing variant TCGA-CJ-6030-01A-11D-1669-08 chr15:42695071 C>T maps to NM_000070.2 N539N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6030-01A-11D-1669-08 chr19:3281240 G>A maps to NM_021938.3 K216K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6030-01A-11D-1669-08 chr1:6212525 G>A maps to NM_015557.2 A272A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6030-01A-11D-1669-08 chr1:103405990 C>A did not map to a codon.
Sequencing variant TCGA-CJ-6030-01A-11D-1669-08 chr3:132193850 A>G maps to NM_015268.3 E789E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6030-01A-11D-1669-08 chr9:23705048 A>G maps to ENST00000359598 S146S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6030-01A-11D-1669-08 chr10:97607249 T>C maps to NM_001098175.1 Y294Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6030-01A-11D-1669-08 chr13:25743822 C>T maps to NM_152704.2 L645L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6030-01A-11D-1669-08 chr19:8194140 G>C maps to NM_032447.3 S718*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6030-01A-11D-1669-08 chr2:198363396 A>C did not map to a codon.
Sequencing variant TCGA-CJ-6030-01A-11D-1669-08 chr6:137528119 G>A maps to NM_000416.2 T60T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6030-01A-11D-1669-08 chr17:37922735 G>T maps to NM_012481.3 R279R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6030-01A-11D-1669-08 chr5:50685529 C>T maps to NM_002202.2 Q177*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6030-01A-11D-1669-08 chr1:153949704 A>T maps to NM_006694.3 P8P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6030-01A-11D-1669-08 chr5:126158525 C>T maps to NM_005573.3 V480V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6030-01A-11D-1669-08 chr5:126158525 C>T maps to NM_005573.3 V480V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6030-01A-11D-1669-08 chr10:129913432 A>C maps to NM_002417.4 T413T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6030-01A-11D-1669-08 chr21:37721694 T>C maps to ENST00000290384 T365T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6030-01A-11D-1669-08 chr5:176720944 C>T maps to NM_022455.4 F2192F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6030-01A-11D-1669-08 chr4:56435976 T>C maps to NM_152401.2 G90G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6030-01A-11D-1669-08 chr6:32808789 T>A maps to NM_148919.3 V259V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6030-01A-11D-1669-08 chr14:21796726 C>T maps to NM_020366.3 Q1014*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6030-01A-11D-1669-08 chr9:35547729 A>T maps to NM_001135999.1 L404L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6030-01A-11D-1669-08 chr22:30856106 G>T maps to NM_174975.4 T368T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6030-01A-11D-1669-08 chr16:30749421 A>T maps to NM_006662.2 P2687P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6030-01A-11D-1669-08 chr2:220465990 C>T maps to NM_052902.2 S43S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6030-01A-11D-1669-08 chr4:70707774 T>C maps to NM_005420.2 K274K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6030-01A-11D-1669-08 chr4:65274994 T>A maps to NM_001010874.4 I25I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6030-01A-11D-1669-08 chr3:196051158 G>A maps to NM_138461.2 F144F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6030-01A-11D-1669-08 chr2:230642130 G>T maps to ENST00000389044 S1783*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6030-01A-11D-1669-08 chr19:41627950 C>T maps to NM_000774.3 I245I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6030-01A-11D-1669-08 chr19:41627950 C>T maps to NM_000774.3 I245I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6030-01A-11D-1669-08 chr15:42175213 C>T maps to ENST00000320955 L624L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6030-01A-11D-1669-08 chr15:42175213 C>T maps to ENST00000320955 L624L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6031-01A-11D-1669-08 chr4:109667937 T>C maps to NM_031279.3 E384E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6031-01A-11D-1669-08 chr3:11389434 G>T maps to NM_006395.2 E404*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6031-01A-11D-1669-08 chr1:169822054 G>A maps to NM_018186.2 W830*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6031-01A-11D-1669-08 chr16:66887325 G>A maps to NM_005182.2 R240R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6031-01A-11D-1669-08 chr22:37769170 C>A maps to NM_052906.3 E802*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6031-01A-11D-1669-08 chr8:125035808 C>T maps to NM_001039112.2 C753C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6031-01A-11D-1669-08 chr6:82950104 A>T maps to NM_015525.2 I33I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6031-01A-11D-1669-08 chr16:85701800 C>T maps to NM_014615.2 H1062H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6031-01A-11D-1669-08 chr20:30897807 G>C maps to NM_004798.3 T76T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6031-01A-11D-1669-08 chr9:5897598 A>G maps to NM_005511.1 L40L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6031-01A-11D-1669-08 chr1:200014590 C>A maps to NM_205860.1 V114V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6031-01A-11D-1669-08 chr2:206640997 C>T maps to NM_018534.3 P823P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6031-01A-11D-1669-08 chr5:176631294 T>C did not map to a codon.
Sequencing variant TCGA-CJ-6031-01A-11D-1669-08 chr5:140594886 G>T maps to NM_018933.2 E398*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6031-01A-11D-1669-08 chr1:109238748 C>T maps to NM_018061.2 Q144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6031-01A-11D-1669-08 chr12:9344840 C>T maps to NM_002864.2 K498K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6031-01A-11D-1669-08 chr3:141278762 A>G maps to ENST00000452898 L263L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6031-01A-11D-1669-08 chr4:1729794 A>G maps to NM_006342.1 E222E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6031-01A-11D-1669-08 chr21:43803191 G>A maps to ENST00000380399 G328G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6031-01A-11D-1669-08 chr15:90616472 C>G maps to NM_198526.2 P543P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6031-01A-11D-1669-08 chr13:115047558 C>T maps to NM_023011.2 L91L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6031-01A-11D-1669-08 chr13:115047558 C>T maps to NM_023011.2 L91L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6032-01A-11D-1669-08 chr12:21991034 T>A maps to NM_005691.2 G1181G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6032-01A-11D-1669-08 chr17:18111565 C>T maps to ENST00000261650 N347N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6032-01A-11D-1669-08 chr1:27094307 G>T maps to NM_006015.4 E1006*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6032-01A-11D-1669-08 chr1:1250911 A>C maps to NM_017871.4 S172S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6032-01A-11D-1669-08 chr3:184001748 T>A maps to NM_014693.3 I449I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6032-01A-11D-1669-08 chr8:144943011 C>T maps to NM_031308.1 W1470*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6032-01A-11D-1669-08 chr15:64380991 C>A maps to NM_032231.4 V61V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6032-01A-11D-1669-08 chr12:32786520 T>G maps to NM_139241.2 L600L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6032-01A-11D-1669-08 chr1:145530385 C>T maps to NM_003637.3 Q201*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6032-01A-11D-1669-08 chr6:168344079 A>G did not map to a codon.
Sequencing variant TCGA-CJ-6032-01A-11D-1669-08 chr11:59949128 T>C maps to NM_152852.1 A24A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6032-01A-11D-1669-08 chr9:32571038 T>C maps to NM_002493.3 V64V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6032-01A-11D-1669-08 chr11:32953803 C>T maps to NM_001076786.1 L205L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6032-01A-11D-1669-08 chr1:40872507 T>A maps to NM_022733.2 V68V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6032-01A-11D-1669-08 chr17:1198810 C>T maps to NM_172367.2 N138N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6032-01A-11D-1669-08 chr11:119510666 G>T maps to NM_203285.1 T353T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6032-01A-11D-1669-08 chr11:119510666 G>T maps to NM_203285.1 T353T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6033-01A-11D-1669-08 chr1:147124276 A>G maps to NM_016361.3 L286L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6033-01A-11D-1669-08 chr12:81647353 C>T maps to NM_024560.2 R634*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6033-01A-11D-1669-08 chr12:81647353 C>T maps to NM_024560.2 R634*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6033-01A-11D-1669-08 chr1:86289365 A>G did not map to a codon.
Sequencing variant TCGA-CJ-6033-01A-11D-1669-08 chr11:117647628 G>T maps to NM_020693.2 R190R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6033-01A-11D-1669-08 chr15:45408397 C>T maps to NM_207581.3 R94R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6033-01A-11D-1669-08 chr8:144941622 C>A maps to NM_031308.1 A1933A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6033-01A-11D-1669-08 chr4:187538910 C>A maps to ENST00000260147 T2946T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6033-01A-11D-1669-08 chr4:8588870 G>A maps to NM_080819.2 P291P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6033-01A-11D-1669-08 chr12:108960982 T>C maps to NM_213595.2 T119T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6033-01A-11D-1669-08 chr5:50685732 G>A maps to NM_002202.2 K244K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6033-01A-11D-1669-08 chr9:5763501 G>A maps to ENST00000414202 Q825Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6033-01A-11D-1669-08 chr17:18135883 C>T maps to NM_004140.3 T85T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6033-01A-11D-1669-08 chr11:94169017 G>A maps to NM_005591.3 T658T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6033-01A-11D-1669-08 chr1:11918767 G>A maps to NM_002521.2 S41S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6033-01A-11D-1669-08 chr3:52610714 C>G did not map to a codon.
Sequencing variant TCGA-CJ-6033-01A-11D-1669-08 chr3:129276045 G>T maps to NM_015103.2 L1822L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6033-01A-11D-1669-08 chr8:141712776 G>T maps to NM_005607.4 I775I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6033-01A-11D-1669-08 chr7:92734660 G>A maps to NM_017654.3 I250I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6033-01A-11D-1669-08 chr2:235950114 G>A maps to NM_014521.2 R234R. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-CJ-6033-01A-11D-1669-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CJ-6033-01A-11D-1669-08 chr8:67546927 T>C maps to NM_025054.4 E1159E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6033-01A-11D-1669-08 chr3:10188289 C>T maps to NM_000551.2 Q145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6033-01A-11D-1669-08 chr3:10188289 C>T maps to NM_000551.2 Q145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6033-01A-11D-1669-08 chr7:134889160 A>G maps to NM_014149.3 N250N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6033-01A-11D-1669-08 chr7:28610068 C>T maps to NM_182898.2 D126D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6033-01A-11D-1669-08 chr7:28610068 C>T maps to NM_182898.2 D126D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6033-01A-11D-1669-08 chr3:126707543 T>G maps to NM_032242.3 G36G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6033-01A-11D-1669-08 chr3:126707543 T>G maps to NM_032242.3 G36G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6033-01A-11D-1669-08 chr19:38027919 G>A maps to NM_001013659.2 G120G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-6033-01A-11D-1669-08 chr19:38027919 G>A maps to NM_001013659.2 G120G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5580-01A-01D-1669-08 chr17:7125373 C>T maps to ENST00000356839 T288T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5580-01A-01D-1669-08 chr15:25959133 C>T maps to NM_024490.3 W677*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5580-01A-01D-1669-08 chr16:49407978 G>A maps to NM_144602.2 G43G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5580-01A-01D-1669-08 chr20:34828158 G>C maps to NM_015511.3 G123G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5580-01A-01D-1669-08 chr17:58234006 C>T maps to NM_000717.3 L67L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5580-01A-01D-1669-08 chr1:160310031 C>A maps to NM_001098398.1 G31G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5580-01A-01D-1669-08 chr22:42524794 A>G maps to NM_000106.4 F219F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5580-01A-01D-1669-08 chrX:125686495 G>A maps to NM_178470.4 D32D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5580-01A-01D-1669-08 chrX:23019820 C>T maps to NM_182699.2 D549D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5580-01A-01D-1669-08 chr5:118560453 T>C maps to NM_005509.4 T2755T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5580-01A-01D-1669-08 chr11:64645858 C>T maps to NM_006795.2 R26R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5580-01A-01D-1669-08 chr7:2404083 A>G maps to ENST00000314800 L359L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5580-01A-01D-1669-08 chr7:2404083 A>G maps to ENST00000314800 L359L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5580-01A-01D-1669-08 chr9:104341504 C>T maps to NM_133445.2 K968K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5580-01A-01D-1669-08 chr17:73736439 G>A maps to NM_001005619.1 V816V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5580-01A-01D-1669-08 chr18:43492337 G>A maps to NM_020964.2 V1300V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5580-01A-01D-1669-08 chr19:54760025 G>A maps to NM_001081442.1 L179L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5580-01A-01D-1669-08 chr15:91449979 C>A maps to NM_006122.2 P282P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5580-01A-01D-1669-08 chr15:91449979 C>A maps to NM_006122.2 P282P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5580-01A-01D-1669-08 chrX:19389074 A>C did not map to a codon.
Sequencing variant TCGA-CW-5580-01A-01D-1669-08 chr20:54824369 C>A maps to ENST00000371389 T194T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5580-01A-01D-1669-08 chr3:195538679 C>T maps to NM_018406.5 G3G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5580-01A-01D-1669-08 chr7:150697630 C>T maps to NM_000603.4 L393L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5580-01A-01D-1669-08 chr17:3195480 G>A maps to ENST00000397187 P138P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5580-01A-01D-1669-08 chr3:129286539 C>T did not map to a codon.
Sequencing variant TCGA-CW-5580-01A-01D-1669-08 chr12:27824428 T>C maps to NM_003622.3 T404T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5580-01A-01D-1669-08 chr3:47162023 G>A maps to NM_014159.6 Q1368*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5580-01A-01D-1669-08 chr6:8422802 C>G maps to NM_001142540.1 G158G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5580-01A-01D-1669-08 chr3:170198276 G>A maps to NM_020949.2 I598I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5580-01A-01D-1669-08 chr12:104071250 C>T maps to NM_017564.9 G889G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5580-01A-01D-1669-08 chr1:156553239 C>T maps to NM_001105669.2 Q384*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5580-01A-01D-1669-08 chr7:71177037 C>T maps to NM_022479.1 C568C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5580-01A-01D-1669-08 chrX:10085337 C>T maps to NM_015691.3 F413F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5580-01A-01D-1669-08 chr2:31598320 G>A maps to NM_000379.3 C509C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5580-01A-01D-1669-08 chr2:31598320 G>A maps to NM_000379.3 C509C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5580-01A-01D-1669-08 chr14:75248500 A>T maps to NM_019589.2 A585A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5580-01A-01D-1669-08 chr5:178293301 C>T maps to NM_058230.2 L31L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5580-01A-01D-1669-08 chr14:23549553 G>T maps to NM_014977.3 S388S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5580-01A-01D-1669-08 chr14:23549553 G>T maps to NM_014977.3 S388S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5580-01A-01D-1669-08 chr12:132547092 A>G maps to ENST00000333577 Q2763Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5580-01A-01D-1669-08 chr12:132547092 A>G maps to ENST00000333577 Q2763Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5580-01A-01D-1669-08 chr19:55451067 C>T maps to ENST00000446217 L401L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5580-01A-01D-1669-08 chr19:55451067 C>T maps to ENST00000446217 L401L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5580-01A-01D-1669-08 chr5:167927654 A>T maps to NM_002887.3 V294V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5580-01A-01D-1669-08 chr5:167927654 A>T maps to NM_002887.3 V294V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6087-01A-11D-1669-08 chr14:77929007 T>C maps to NM_012111.2 D126D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6087-01A-11D-1669-08 chr11:68575042 C>T maps to NM_001876.3 W115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6087-01A-11D-1669-08 chr9:131864767 G>A maps to NM_000755.3 R181*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6087-01A-11D-1669-08 chr1:21268371 C>T maps to NM_001198801.1 T368T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6087-01A-11D-1669-08 chr11:64082234 G>A maps to NM_004451.3 V198V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6087-01A-11D-1669-08 chr1:24484204 T>C maps to NM_170743.2 E326E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6087-01A-11D-1669-08 chr1:62341006 T>A maps to NM_176877.2 L976L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6087-01A-11D-1669-08 chr8:101724673 A>G maps to NM_002568.3 L296L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6087-01A-11D-1669-08 chrX:99662749 G>A maps to NM_001184880.1 N282N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6087-01A-11D-1669-08 chr20:17434532 C>T maps to NM_002594.2 D344D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6087-01A-11D-1669-08 chr7:53103957 C>T maps to NM_182595.3 F198F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6087-01A-11D-1669-08 chr3:38783880 G>T maps to NM_006514.2 L669L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6087-01A-11D-1669-08 chr4:69692198 C>T maps to NM_001075.4 P357P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6087-01A-11D-1669-08 chr5:82834029 T>A maps to NM_004385.4 S1736S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6087-01A-11D-1669-08 chr18:54424322 A>G maps to NM_015285.2 V833V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6087-01A-11D-1669-08 chr5:124079839 C>T maps to NM_020747.2 L281L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6087-01A-11D-1669-08 chr6:90573112 T>A maps to NM_012115.3 L562*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6087-01A-11D-1669-08 chr6:90573112 T>A maps to NM_012115.3 L562*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6087-01A-11D-1669-08 chr1:20470068 G>A maps to NM_022819.3 K100K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6087-01A-11D-1669-08 chr1:20470068 G>A maps to NM_022819.3 K100K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6087-01A-11D-1669-08 chr14:51131953 C>A maps to NM_021818.2 E160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6087-01A-11D-1669-08 chr14:51131953 C>A maps to NM_021818.2 E160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6087-01A-11D-1669-08 chr3:195594609 C>T maps to NM_001010938.1 P916P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6087-01A-11D-1669-08 chr3:195594609 C>T maps to NM_001010938.1 P916P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6090-01A-11D-1669-08 chr2:158595005 T>C maps to NM_001111067.2 V447V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6090-01A-11D-1669-08 chr11:8940959 T>G maps to NM_020642.3 L189*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6090-01A-11D-1669-08 chr16:69199287 C>T maps to NM_032830.2 S564S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6090-01A-11D-1669-08 chr11:72005413 C>T maps to NM_030813.3 E575E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6090-01A-11D-1669-08 chr18:346952 C>A maps to NM_130386.2 L223L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6090-01A-11D-1669-08 chr3:148928071 T>C maps to NM_000096.3 E163E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6090-01A-11D-1669-08 chr15:89056232 C>T maps to NM_017996.3 R545R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6090-01A-11D-1669-08 chr9:114429211 T>C maps to NM_004125.3 L152L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6090-01A-11D-1669-08 chr19:2211149 G>A maps to ENST00000221482 Q468Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6090-01A-11D-1669-08 chr1:36319143 C>T maps to NM_017629.2 Q842*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6090-01A-11D-1669-08 chr19:46119736 G>A maps to NM_001193268.1 S698S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6090-01A-11D-1669-08 chr15:81046665 A>G maps to NM_021214.1 L315L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6090-01A-11D-1669-08 chr16:81118199 C>A did not map to a codon.
Sequencing variant TCGA-CW-6090-01A-11D-1669-08 chr1:35250434 G>A maps to NM_001005752.1 W24*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6090-01A-11D-1669-08 chr14:67147885 C>T maps to NM_020806.4 L42L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6090-01A-11D-1669-08 chr17:3657178 G>C maps to NM_002208.4 S475S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6090-01A-11D-1669-08 chr17:26965109 A>G maps to NM_014680.2 G505G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6090-01A-11D-1669-08 chrX:153130542 G>A maps to NM_000425.3 L958L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6090-01A-11D-1669-08 chr4:129012652 T>C maps to NM_018078.2 Y218Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6090-01A-11D-1669-08 chrX:75648790 C>T maps to NM_020932.2 A156A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6090-01A-11D-1669-08 chr5:71494890 C>A maps to NM_005909.3 G1903G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6090-01A-11D-1669-08 chr11:45925698 C>T maps to NM_005456.2 P551P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6090-01A-11D-1669-08 chr11:92702958 C>A maps to NM_005959.3 S23*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6090-01A-11D-1669-08 chr19:8976795 T>C maps to NM_024690.2 P14090P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6090-01A-11D-1669-08 chr15:52571771 C>A maps to NM_018728.3 E80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6090-01A-11D-1669-08 chr12:124839983 G>A maps to NM_006312.4 I1132I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6090-01A-11D-1669-08 chr9:135102353 C>A maps to NM_032536.2 R326R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6090-01A-11D-1669-08 chr17:2577359 T>C maps to NM_000430.3 C226C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6090-01A-11D-1669-08 chr12:7079387 G>A maps to NM_001144831.1 D61D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6090-01A-11D-1669-08 chr12:57995121 C>G maps to NM_024779.4 V392V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6090-01A-11D-1669-08 chr1:29585158 C>T maps to NM_005704.4 T116T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6090-01A-11D-1669-08 chr1:17748728 G>A maps to NM_018715.2 N238N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6090-01A-11D-1669-08 chr15:90022630 G>A maps to NM_016321.1 T253T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6090-01A-11D-1669-08 chr2:7023568 G>A maps to NM_080657.4 K138K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6090-01A-11D-1669-08 chr19:51215206 G>A maps to ENST00000391814 H319H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6090-01A-11D-1669-08 chr11:22397593 C>A maps to NM_020346.2 S414*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6090-01A-11D-1669-08 chr17:78215585 C>T maps to NM_173626.3 Y334Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6090-01A-11D-1669-08 chr12:46760916 T>C maps to NM_018976.4 A141A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6090-01A-11D-1669-08 chr22:39777741 C>G maps to NM_004711.4 G175G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6090-01A-11D-1669-08 chr6:46660118 C>T maps to NM_001010870.2 C1418C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6090-01A-11D-1669-08 chr12:72068027 T>G maps to NM_031435.3 V39V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6090-01A-11D-1669-08 chr7:5391570 C>T maps to NM_001080495.2 A1783A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6090-01A-11D-1669-08 chr7:5391570 C>T maps to NM_001080495.2 A1783A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6090-01A-11D-1669-08 chr3:50380355 C>T maps to NM_015896.2 R231R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6090-01A-11D-1669-08 chr18:32822820 G>A maps to NM_001135178.2 E129E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6093-01A-11D-1669-08 chr15:87066158 C>A maps to NM_152336.2 R846R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6093-01A-11D-1669-08 chr15:87066158 C>A maps to NM_152336.2 R846R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6093-01A-11D-1669-08 chr10:75884278 G>A maps to NM_207012.2 L339L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6093-01A-11D-1669-08 chr16:28508785 A>G maps to NM_018690.2 E799E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6093-01A-11D-1669-08 chr9:33395102 G>A maps to NM_001170.1 A39A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6093-01A-11D-1669-08 chr14:32619204 A>G maps to NM_001030055.1 P1347P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6093-01A-11D-1669-08 chr16:67166429 T>G did not map to a codon.
Sequencing variant TCGA-CW-6093-01A-11D-1669-08 chr16:67166429 T>G did not map to a codon.
Sequencing variant TCGA-CW-6093-01A-11D-1669-08 chr3:161064027 G>T maps to NM_001040100.1 P28P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6093-01A-11D-1669-08 chr1:160167356 A>G did not map to a codon.
Sequencing variant TCGA-CW-6093-01A-11D-1669-08 chr3:112059810 G>C maps to NM_001004196.2 V50V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6093-01A-11D-1669-08 chr5:137621757 G>A maps to NM_001790.3 L409L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6093-01A-11D-1669-08 chr3:184079225 C>G maps to NM_004366.4 A14A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6093-01A-11D-1669-08 chrX:49851499 C>T maps to NM_001127898.1 V510V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6093-01A-11D-1669-08 chr9:140249169 G>T maps to NM_017820.3 C271*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6093-01A-11D-1669-08 chr18:10697807 C>T maps to NM_022068.2 R2142R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6093-01A-11D-1669-08 chr7:150174243 C>T maps to NM_175571.2 I458I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6093-01A-11D-1669-08 chr12:122656991 T>C maps to NM_001014336.1 S154S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6093-01A-11D-1669-08 chr18:7036006 C>T maps to NM_005559.2 S606S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6093-01A-11D-1669-08 chr6:161507425 G>A maps to NM_005922.2 E796E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6093-01A-11D-1669-08 chr11:94219121 G>T maps to NM_005591.3 L94L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6093-01A-11D-1669-08 chr22:26164740 A>T maps to ENST00000407587 G288G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6093-01A-11D-1669-08 chr15:56208024 G>A maps to ENST00000508342 P335P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6093-01A-11D-1669-08 chr7:156752789 T>G maps to NM_138400.1 A518A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6093-01A-11D-1669-08 chr3:52682458 C>T did not map to a codon.
Sequencing variant TCGA-CW-6093-01A-11D-1669-08 chr11:17118794 A>G maps to NM_002645.2 L1379L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6093-01A-11D-1669-08 chr20:39796505 G>T maps to NM_002660.2 G772G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6093-01A-11D-1669-08 chr9:37500906 C>T maps to NM_022490.1 Y319Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6093-01A-11D-1669-08 chr14:58714514 A>G maps to NM_002788.2 Q23Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6093-01A-11D-1669-08 chr19:49934325 G>A maps to NM_020309.3 G445G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6093-01A-11D-1669-08 chr11:120980197 C>T maps to NM_005422.2 S159S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6093-01A-11D-1669-08 chr1:223983954 C>T maps to NM_001031685.2 R762R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6093-01A-11D-1669-08 chr16:72991476 G>A maps to NM_006885.3 P856P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6093-01A-11D-1669-08 chr5:43161422 A>G maps to ENST00000509156 A148A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6093-01A-11D-1669-08 chr11:123598247 C>T maps to NM_003455.2 W296*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6093-01A-11D-1669-08 chr15:79090323 A>C maps to ENST00000258883 G196G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6093-01A-11D-1669-08 chr15:79090323 A>C maps to ENST00000258883 G196G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6093-01A-11D-1669-08 chr16:1825567 A>C did not map to a codon.
Sequencing variant TCGA-CW-6093-01A-11D-1669-08 chr16:1825567 A>C did not map to a codon.
Sequencing variant TCGA-CW-6093-01A-11D-1669-08 chr12:132547137 A>G maps to ENST00000333577 Q2778Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6093-01A-11D-1669-08 chr12:132547137 A>G maps to ENST00000333577 Q2778Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6093-01A-11D-1669-08 chr8:38827143 C>A maps to NM_021623.1 S374*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-6093-01A-11D-1669-08 chr8:38827143 C>A maps to NM_021623.1 S374*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4853-01A-01D-1429-08 chr2:202598154 G>A maps to NM_020919.3 F808F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4853-01A-01D-1429-08 chr11:61725622 G>A maps to NM_001139443.1 V180V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4853-01A-01D-1429-08 chr12:32491839 C>A maps to NM_001714.2 G897G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4853-01A-01D-1429-08 chr12:32491839 C>A maps to NM_001714.2 G897G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4853-01A-01D-1429-08 chr4:79808403 T>C maps to NM_198892.1 D676D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4853-01A-01D-1429-08 chr16:2481269 C>T maps to NM_001761.2 I52I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4853-01A-01D-1429-08 chr17:28750569 G>C maps to NM_001304.4 V568V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4853-01A-01D-1429-08 chr4:76943923 A>G maps to NM_001565.2 S36S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4853-01A-01D-1429-08 chr3:121554182 C>T maps to NM_018456.4 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4853-01A-01D-1429-08 chr11:92534185 G>T maps to ENST00000298047 L2669L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4853-01A-01D-1429-08 chr12:102179967 T>C maps to NM_024312.4 T131T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4853-01A-01D-1429-08 chr12:111089051 G>T maps to NM_001040107.1 R205R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4853-01A-01D-1429-08 chr1:201843414 G>A maps to NM_018085.4 K916K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4853-01A-01D-1429-08 chr3:160227601 C>A maps to NM_002268.3 G399*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4853-01A-01D-1429-08 chr11:1492591 G>T maps to NM_001172223.1 Y141*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4853-01A-01D-1429-08 chr1:149901784 G>C maps to NM_001145862.1 P557P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4853-01A-01D-1429-08 chr1:40363240 G>A maps to NM_001033082.2 R330*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4853-01A-01D-1429-08 chr12:81101548 G>T maps to NM_002469.2 G17G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4853-01A-01D-1429-08 chr12:81101619 T>A maps to NM_002469.2 L41*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4853-01A-01D-1429-08 chr13:25670548 C>G maps to NM_030979.2 T71T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4853-01A-01D-1429-08 chr5:140559546 G>A maps to NM_019120.2 L644L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4853-01A-01D-1429-08 chr20:44050026 C>T maps to NM_015937.4 A346A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4853-01A-01D-1429-08 chr4:71275488 C>T maps to NM_021225.4 T148T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4853-01A-01D-1429-08 chr2:17697414 T>A maps to NM_001099218.2 V756V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4853-01A-01D-1429-08 chr12:107209025 G>T maps to ENST00000392837 E229*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4853-01A-01D-1429-08 chr15:40865742 G>T maps to NM_152260.1 V307V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4853-01A-01D-1429-08 chrX:50556985 G>A maps to NM_020717.3 V11V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4853-01A-01D-1429-08 chr17:4863166 A>T maps to NM_004890.2 P154P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4853-01A-01D-1429-08 chr4:57333821 G>T maps to NM_006947.3 G7G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4853-01A-01D-1429-08 chr19:39694579 G>T maps to NM_001080468.2 A105A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4853-01A-01D-1429-08 chr5:176084596 G>A maps to NM_012171.2 Q299Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4853-01A-01D-1429-08 chr5:159437681 T>C maps to NM_003314.1 D49D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4853-01A-01D-1429-08 chr2:179591820 T>C maps to NM_133378.4 V5513V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4853-01A-01D-1429-08 chr18:46284643 A>C maps to NM_001142397.1 P313P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4853-01A-01D-1429-08 chr18:46284643 A>C maps to NM_001142397.1 P313P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4853-01A-01D-1429-08 chr18:42281379 C>G maps to NM_015559.2 S23S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4853-01A-01D-1429-08 chr18:42281379 C>G maps to NM_015559.2 S23S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4856-01A-02D-1429-08 chr15:63569839 C>T maps to NM_031301.3 F6F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4856-01A-02D-1429-08 chr6:36185715 A>G maps to NM_015695.2 K1004K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4856-01A-02D-1429-08 chr17:11593687 C>T maps to NM_001372.3 R1517*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4856-01A-02D-1429-08 chr6:56357197 G>A maps to ENST00000361203 Q6651*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4856-01A-02D-1429-08 chrX:101971083 C>A maps to NM_138437.5 S429S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4856-01A-02D-1429-08 chr1:897300 G>T maps to NM_198317.2 L195L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4856-01A-02D-1429-08 chr8:144103076 C>T maps to NM_002346.2 G89G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4856-01A-02D-1429-08 chr1:186839571 G>A maps to NM_024420.2 E13E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4856-01A-02D-1429-08 chr7:131194124 C>T maps to NM_001018111.2 W341*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4856-01A-02D-1429-08 chr20:40944542 C>A maps to ENST00000373198 R653R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4856-01A-02D-1429-08 chr17:6594202 G>A maps to NM_177550.3 P444P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4856-01A-02D-1429-08 chr3:10188321 T>C did not map to a codon.
Sequencing variant TCGA-CZ-4856-01A-02D-1429-08 chr3:10188321 T>C did not map to a codon.
Sequencing variant TCGA-CZ-4856-01A-02D-1429-08 chr1:35870745 G>A maps to NM_005095.2 W1217*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4856-01A-02D-1429-08 chr17:5086702 G>T maps to NM_032530.1 V283V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4856-01A-02D-1429-08 chrX:101858508 A>T maps to NM_022838.3 A480A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4856-01A-02D-1429-08 chrX:101858508 A>T maps to NM_022838.3 A480A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4856-01A-02D-1429-08 chr3:172096212 C>T maps to NM_022763.3 P1054P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4856-01A-02D-1429-08 chr3:172096212 C>T maps to NM_022763.3 P1054P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4856-01A-02D-1429-08 chr19:13211727 C>T maps to NM_005583.4 P86P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4856-01A-02D-1429-08 chr19:13211727 C>T maps to NM_005583.4 P86P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4856-01A-02D-1429-08 chr3:96706397 A>G maps to NM_001080448.2 E225E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4856-01A-02D-1429-08 chr3:96706397 A>G maps to NM_001080448.2 E225E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4859-01A-02D-1429-08 chr7:20739467 A>G maps to NM_001163941.1 K725K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4859-01A-02D-1429-08 chr2:21225675 C>T maps to NM_000384.2 G4206G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4859-01A-02D-1429-08 chr18:76870366 G>A maps to NM_198531.3 W102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4859-01A-02D-1429-08 chr10:105924007 T>C maps to ENST00000389588 A1031A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4859-01A-02D-1429-08 chr20:60971620 G>A maps to NM_031215.2 S130S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4859-01A-02D-1429-08 chrX:151909171 C>A maps to NM_153478.1 P67P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4859-01A-02D-1429-08 chr3:186299284 C>T maps to NM_016306.4 D194D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4859-01A-02D-1429-08 chr13:43652821 A>T maps to NM_013238.2 V103V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4859-01A-02D-1429-08 chr16:1825397 G>T maps to NM_001010865.1 E262*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4859-01A-02D-1429-08 chr13:108518167 G>T maps to NM_001080396.2 T259T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4859-01A-02D-1429-08 chr5:151166244 C>T maps to NM_198395.1 L22L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4859-01A-02D-1429-08 chr11:22707335 G>C did not map to a codon.
Sequencing variant TCGA-CZ-4859-01A-02D-1429-08 chr9:95027314 G>A maps to ENST00000375660 S534S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4859-01A-02D-1429-08 chr9:95027314 G>A maps to ENST00000375660 S534S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4859-01A-02D-1429-08 chr1:65344793 A>T maps to NM_002227.2 Y81*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4859-01A-02D-1429-08 chr1:152732828 C>A maps to NM_001025231.1 C255*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4859-01A-02D-1429-08 chr12:57590880 T>A maps to NM_002332.2 Y3003*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4859-01A-02D-1429-08 chr17:60129920 T>C maps to NM_005121.2 K149K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4859-01A-02D-1429-08 chr11:89223700 A>G maps to NM_016931.3 N26N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4859-01A-02D-1429-08 chr5:140798208 C>T maps to NM_018927.2 I261I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4859-01A-02D-1429-08 chr5:140890568 C>T maps to NM_018915.2 S876S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4859-01A-02D-1429-08 chr5:140890568 C>T maps to NM_018915.2 S876S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4859-01A-02D-1429-08 chr7:44113447 T>C maps to NM_013284.2 R416R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4859-01A-02D-1429-08 chr3:38647615 G>T maps to NM_001099404.1 I388I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4859-01A-02D-1429-08 chr17:27287869 C>T maps to NM_178860.4 R454R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4859-01A-02D-1429-08 chr2:44507852 A>G did not map to a codon.
Sequencing variant TCGA-CZ-4859-01A-02D-1429-08 chr14:64532268 G>C maps to NM_182914.2 S3444S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4859-01A-02D-1429-08 chr7:15433777 T>C maps to NM_001004320.1 E212E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4859-01A-02D-1429-08 chr16:2134518 C>G maps to NM_000548.3 A1432A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4859-01A-02D-1429-08 chr3:122133532 A>T maps to NM_019069.3 I281I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4859-01A-02D-1429-08 chr19:58512736 A>C did not map to a codon.
Sequencing variant TCGA-CZ-4859-01A-02D-1429-08 chr3:57678667 G>A maps to NM_152678.2 G26G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4859-01A-02D-1429-08 chr3:57678667 G>A maps to NM_152678.2 G26G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5982-01A-11D-1669-08 chr3:57283561 T>A maps to NM_012096.2 S346S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5982-01A-11D-1669-08 chr14:77492044 C>G maps to NM_024496.2 V697V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5982-01A-11D-1669-08 chr19:40330953 A>T maps to NM_001436.3 C99*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5982-01A-11D-1669-08 chr22:45931086 C>T maps to ENST00000348697 D264D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5982-01A-11D-1669-08 chr8:37696505 C>T maps to NM_032777.9 G764G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5982-01A-11D-1669-08 chr18:61627534 C>T maps to NM_001123366.1 F122F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5982-01A-11D-1669-08 chr11:47602126 G>T maps to NM_004551.2 G62*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5982-01A-11D-1669-08 chr3:52598157 G>T maps to ENST00000296302 Y1261*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5982-01A-11D-1669-08 chr17:78328248 T>C maps to NM_020914.4 L3628L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5982-01A-11D-1669-08 chr20:50407914 C>A maps to NM_020436.3 V369V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5982-01A-11D-1669-08 chr21:34922736 T>A maps to NM_138927.1 T400T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5982-01A-11D-1669-08 chr10:107015521 G>T maps to NM_014978.1 G1100G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5982-01A-11D-1669-08 chr6:167789487 C>T maps to NM_004610.3 T218T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5982-01A-11D-1669-08 chr6:42604790 C>T maps to NM_015255.2 L573L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5982-01A-11D-1669-08 chr11:63517658 C>A maps to ENST00000377819 G909G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5982-01A-11D-1669-08 chr11:63517658 C>A maps to ENST00000377819 G909G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5984-01A-11D-1669-08 chr1:100336393 G>A maps to ENST00000311030 A310A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5984-01A-11D-1669-08 chr14:74531620 C>A maps to NM_005589.2 V469V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5984-01A-11D-1669-08 chr21:46363675 G>A maps to NM_058190.2 L69L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5984-01A-11D-1669-08 chr19:10090546 G>A maps to NM_015719.3 R894*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5984-01A-11D-1669-08 chr14:74420178 G>T maps to NM_182476.1 E69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5984-01A-11D-1669-08 chr9:79118094 G>T maps to NM_001097636.1 L266L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5984-01A-11D-1669-08 chr7:102106462 G>T maps to NM_152892.1 E94*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5984-01A-11D-1669-08 chr5:140201425 C>T maps to NM_018908.2 Y22Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5984-01A-11D-1669-08 chr2:44436368 T>C maps to NM_002706.4 S289S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5984-01A-11D-1669-08 chr17:27041907 G>A maps to NM_001144943.1 V262V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5984-01A-11D-1669-08 chr18:76753964 G>A maps to NM_171999.2 T658T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5984-01A-11D-1669-08 chr18:76753964 G>A maps to NM_171999.2 T658T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5984-01A-11D-1669-08 chr21:46951438 G>A maps to NM_194255.1 S271S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5984-01A-11D-1669-08 chr6:43146556 G>A maps to NM_003131.2 Q456Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5984-01A-11D-1669-08 chr8:106811084 C>A maps to NM_012082.3 A291A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5984-01A-11D-1669-08 chr1:22913108 G>A maps to NM_020526.3 P320P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5984-01A-11D-1669-08 chr1:22913108 G>A maps to NM_020526.3 P320P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5984-01A-11D-1669-08 chr7:114269972 A>G maps to NM_148898.3 Q195Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5984-01A-11D-1669-08 chr7:114269972 A>G maps to NM_148898.3 Q195Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5985-01A-11D-1669-08 chr1:247081659 T>G maps to ENST00000428671 R43R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5985-01A-11D-1669-08 chr4:42581896 G>T maps to NM_006095.2 V311V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5985-01A-11D-1669-08 chr3:52439310 C>A did not map to a codon.
Sequencing variant TCGA-CZ-5985-01A-11D-1669-08 chr19:14000171 C>T maps to ENST00000454313 Q499Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5985-01A-11D-1669-08 chr22:32198824 G>C did not map to a codon.
Sequencing variant TCGA-CZ-5985-01A-11D-1669-08 chr10:98064449 G>T maps to NM_004088.3 E66*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5985-01A-11D-1669-08 chr11:117309652 C>A maps to NM_020693.2 S1457S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5985-01A-11D-1669-08 chr4:101331486 G>T maps to NM_016242.3 T259T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5985-01A-11D-1669-08 chr9:128099710 A>T maps to NM_015635.2 V933V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5985-01A-11D-1669-08 chr5:137903400 C>T maps to NM_004134.6 L182L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5985-01A-11D-1669-08 chr1:245583032 C>T maps to NM_018012.3 A384A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5985-01A-11D-1669-08 chr1:149901021 T>A maps to NM_001145862.1 *710L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5985-01A-11D-1669-08 chr3:123411690 G>A maps to NM_053025.3 L1152L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5985-01A-11D-1669-08 chr15:23931881 G>A maps to NM_002487.2 H161H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5985-01A-11D-1669-08 chr1:17727909 C>T maps to NM_207421.3 F687F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5985-01A-11D-1669-08 chr7:82785210 G>T maps to NM_033026.5 S249*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5985-01A-11D-1669-08 chr19:47969449 G>T maps to NM_015063.2 R71R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5985-01A-11D-1669-08 chr13:86368848 G>A maps to NM_032229.2 R599*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5985-01A-11D-1669-08 chr13:86368848 G>A maps to NM_032229.2 R599*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5985-01A-11D-1669-08 chr1:44365369 T>C maps to NM_174963.2 L308L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5985-01A-11D-1669-08 chr4:166929188 C>T maps to ENST00000507499 N302N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5985-01A-11D-1669-08 chr21:19716369 G>T maps to NM_002772.2 Y393*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5985-01A-11D-1669-08 chr6:14118277 C>A maps to NM_004233.3 Y45*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5985-01A-11D-1669-08 chr6:14118277 C>A maps to NM_004233.3 Y45*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5986-01A-11D-1669-08 chr7:140373651 G>A maps to NM_052853.3 V174V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5986-01A-11D-1669-08 chr15:83349315 C>T maps to NM_004644.3 V321V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5986-01A-11D-1669-08 chr13:113508718 G>A maps to NM_032189.3 R706R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5986-01A-11D-1669-08 chr11:34478279 T>C maps to NM_001752.3 N324N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5986-01A-11D-1669-08 chr19:42213710 C>A maps to NM_004363.2 P59P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5986-01A-11D-1669-08 chr1:34180250 G>A maps to ENST00000373381 T1074T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5986-01A-11D-1669-08 chr19:46094944 G>A maps to NM_005282.2 S60S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5986-01A-11D-1669-08 chr19:14157045 C>G maps to NM_004843.2 T283T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5986-01A-11D-1669-08 chr19:18377008 C>T maps to NM_001145304.1 G447G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5986-01A-11D-1669-08 chr3:195453060 C>A maps to ENST00000447234 P529P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5986-01A-11D-1669-08 chr19:56363604 A>G maps to NM_134444.4 E53E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5986-01A-11D-1669-08 chr5:140712347 G>A maps to NM_018912.2 A699A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5986-01A-11D-1669-08 chr10:102089624 C>T did not map to a codon.
Sequencing variant TCGA-CZ-5986-01A-11D-1669-08 chr11:45245951 G>A maps to NM_020229.2 L343L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5986-01A-11D-1669-08 chr12:113515328 C>A maps to NM_004416.2 A120A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5986-01A-11D-1669-08 chr12:113515328 C>A maps to NM_004416.2 A120A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5987-01A-11D-1669-08 chr12:109577275 C>A maps to NM_001093.3 I22I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5987-01A-11D-1669-08 chr12:7469735 C>T maps to NM_001080454.1 F208F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5987-01A-11D-1669-08 chr12:53693592 C>T maps to NM_021640.3 R24R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5987-01A-11D-1669-08 chr1:185143986 C>T maps to NM_001105518.1 I236I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5987-01A-11D-1669-08 chr18:63477169 C>T maps to NM_004361.2 N147N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5987-01A-11D-1669-08 chr4:151169527 C>A maps to NM_001040261.4 P666P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5987-01A-11D-1669-08 chr10:123353229 C>T maps to ENST00000351936 E53E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5987-01A-11D-1669-08 chr16:54966435 C>A maps to NM_005853.5 G92G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5987-01A-11D-1669-08 chr17:39579095 G>A maps to NM_003770.4 A222A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5987-01A-11D-1669-08 chr3:33855049 G>A did not map to a codon.
Sequencing variant TCGA-CZ-5987-01A-11D-1669-08 chr17:64731698 C>T maps to NM_002737.2 C383C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5987-01A-11D-1669-08 chr6:33240436 T>C maps to NM_022551.2 I12I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5987-01A-11D-1669-08 chr1:162368718 T>G maps to NM_053282.4 T119T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5987-01A-11D-1669-08 chr10:60128478 G>T did not map to a codon.
Sequencing variant TCGA-CZ-5987-01A-11D-1669-08 chrX:69871298 C>A did not map to a codon.
Sequencing variant TCGA-CZ-5987-01A-11D-1669-08 chrX:69871298 C>A did not map to a codon.
Sequencing variant TCGA-CZ-5987-01A-11D-1669-08 chr19:58385761 C>G maps to NM_001144989.1 S332S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5987-01A-11D-1669-08 chr19:58385761 C>G maps to NM_001144989.1 S332S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5988-01A-11D-1669-08 chr17:15848765 C>T maps to NM_000676.2 S68S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5988-01A-11D-1669-08 chr4:122722620 A>G maps to NM_001034194.1 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5988-01A-11D-1669-08 chr5:41934378 C>T maps to NM_012176.2 F289F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5988-01A-11D-1669-08 chr19:35941422 C>T maps to NM_005306.2 D269D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5988-01A-11D-1669-08 chr19:35941422 C>T maps to NM_005306.2 D269D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5988-01A-11D-1669-08 chr4:17819615 C>G maps to NM_022346.3 A341A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5988-01A-11D-1669-08 chr19:17346353 G>A maps to NM_005234.3 D298D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5988-01A-11D-1669-08 chr19:15198106 C>T maps to NM_001004713.1 T77T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5988-01A-11D-1669-08 chr1:247752395 C>T maps to NM_001001915.1 F245F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5988-01A-11D-1669-08 chr11:5068192 T>C maps to NM_001001916.2 I146I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5988-01A-11D-1669-08 chr9:78774009 C>T maps to NM_001190482.1 I514I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5988-01A-11D-1669-08 chr20:62193087 C>G maps to NM_001037335.2 L2234L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5988-01A-11D-1669-08 chr1:151105697 C>T maps to NM_001178061.1 P717P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5988-01A-11D-1669-08 chr13:88329823 A>G maps to NM_015567.1 P727P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5988-01A-11D-1669-08 chr2:54870208 T>C maps to NM_003128.2 H1316H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5988-01A-11D-1669-08 chr22:24579609 G>T maps to NM_019601.3 L145L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5988-01A-11D-1669-08 chr6:170871084 G>A maps to NM_003194.4 Q87Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5988-01A-11D-1669-08 chr2:179433485 G>A maps to NM_133378.4 A23223A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5989-01A-11D-1669-08 chr17:67023933 G>A maps to NM_080283.3 H546H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5989-01A-11D-1669-08 chr4:8416610 G>A maps to NM_003501.2 L141L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5989-01A-11D-1669-08 chr10:96805618 G>A maps to NM_000770.3 S303S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5989-01A-11D-1669-08 chr12:53242513 C>T maps to NM_173352.2 G67G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5989-01A-11D-1669-08 chr14:71267588 G>A maps to NM_033141.2 A205A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5989-01A-11D-1669-08 chr20:46252828 T>C did not map to a codon.
Sequencing variant TCGA-CZ-5989-01A-11D-1669-08 chr1:247752194 T>C maps to NM_001001915.1 D178D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5989-01A-11D-1669-08 chr9:128724471 C>T maps to ENST00000373487 V388V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5989-01A-11D-1669-08 chr15:42434286 C>T maps to ENST00000397272 L817L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5989-01A-11D-1669-08 chr6:112671197 T>C maps to NM_001013734.2 D96D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5989-01A-11D-1669-08 chr12:56863102 G>A maps to NM_207344.3 W122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5989-01A-11D-1669-08 chr17:3486631 C>T maps to ENST00000399756 G503G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5989-01A-11D-1669-08 chr8:81411970 T>C maps to NM_001105539.1 N405N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5989-01A-11D-1669-08 chr3:141163045 C>T maps to NM_001080412.2 Q606*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5989-01A-11D-1669-08 chr11:1025855 G>T maps to NM_005961.2 I916I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5989-01A-11D-1669-08 chr11:1025855 G>T maps to NM_005961.2 I916I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EU-5904-01A-11D-1669-08 chr6:24528316 T>C maps to NM_170740.1 P435P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EU-5904-01A-11D-1669-08 chr12:49073491 C>A maps to NM_017822.3 E126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EU-5904-01A-11D-1669-08 chr12:49073491 C>A maps to NM_017822.3 E126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EU-5904-01A-11D-1669-08 chr2:56419910 C>T maps to NM_001080433.1 S192S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EU-5904-01A-11D-1669-08 chr9:17416023 T>A maps to NM_017738.2 L984*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EU-5904-01A-11D-1669-08 chr9:140671278 C>T maps to NM_024757.4 A667A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EU-5904-01A-11D-1669-08 chrX:152860112 G>C maps to NM_152274.3 P106P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EU-5904-01A-11D-1669-08 chr2:109099525 C>T maps to NM_181453.3 A1118A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EU-5904-01A-11D-1669-08 chr5:140745222 A>G maps to NM_018918.2 V442V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EU-5904-01A-11D-1669-08 chr1:186277943 C>G maps to NM_005807.3 P1031P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EU-5904-01A-11D-1669-08 chr13:49086879 T>C maps to NM_001268.2 L167L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EU-5904-01A-11D-1669-08 chr4:16165152 G>T maps to NM_153365.2 S494S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EU-5904-01A-11D-1669-08 chr12:58190296 G>A maps to NM_001172696.1 Q324Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EU-5904-01A-11D-1669-08 chr22:18609611 C>A maps to NM_018943.2 A289A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EU-5904-01A-11D-1669-08 chr18:18535178 G>A maps to NM_005406.2 T1180T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EU-5904-01A-11D-1669-08 chr18:18535178 G>A maps to NM_005406.2 T1180T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EU-5904-01A-11D-1669-08 chr2:168105253 C>A maps to NM_152381.5 S2451*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EU-5904-01A-11D-1669-08 chr2:168105253 C>A maps to NM_152381.5 S2451*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EU-5905-01A-11D-1669-08 chr1:161166009 A>T maps to NM_005099.4 I347I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EU-5905-01A-11D-1669-08 chr19:4704157 G>A maps to ENST00000357909 G274G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EU-5905-01A-11D-1669-08 chr16:31201623 T>C maps to NM_004960.3 G399G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EU-5905-01A-11D-1669-08 chr21:34120908 T>C maps to NM_016631.3 K608K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EU-5905-01A-11D-1669-08 chr5:141248527 G>T maps to NM_032420.2 S170*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EU-5905-01A-11D-1669-08 chr1:28785763 C>A maps to NM_023923.3 S72*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EU-5905-01A-11D-1669-08 chr6:146865252 C>T maps to NM_006834.3 I82I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EU-5905-01A-11D-1669-08 chr20:61300315 G>T maps to NM_016354.3 V637V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EU-5905-01A-11D-1669-08 chr3:136170988 C>T maps to NM_005862.2 K438K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EU-5905-01A-11D-1669-08 chr21:32624301 C>A maps to NM_003253.2 R389R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EU-5905-01A-11D-1669-08 chr9:140099455 C>A maps to NM_053045.1 *137Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EU-5905-01A-11D-1669-08 chr7:71175759 C>A maps to NM_022479.1 T505T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EU-5905-01A-11D-1669-08 chr7:71175759 C>A maps to NM_022479.1 T505T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EU-5905-01A-11D-1669-08 chr9:130206350 T>C maps to NM_007135.2 S124S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EU-5906-01A-11D-1669-08 chr22:40742591 C>G maps to NM_000026.2 P10P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EU-5906-01A-11D-1669-08 chr1:234509988 G>T maps to ENST00000424237 G77*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EU-5906-01A-11D-1669-08 chr1:57351709 A>T maps to NM_000562.2 P322P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EU-5906-01A-11D-1669-08 chr2:225342979 T>C maps to NM_003590.3 E704E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EU-5906-01A-11D-1669-08 chr14:94528592 G>A maps to NM_020414.3 Q365*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EU-5906-01A-11D-1669-08 chr12:53685544 C>G maps to NM_012291.4 T1864T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EU-5906-01A-11D-1669-08 chr3:99568695 A>G maps to NM_001042459.1 N608N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EU-5906-01A-11D-1669-08 chr4:46043109 C>T maps to NM_173536.3 R431R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EU-5906-01A-11D-1669-08 chr12:123187634 G>A maps to NM_177551.3 L66L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EU-5906-01A-11D-1669-08 chr9:95062257 G>C maps to NM_017948.5 V1072V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EU-5906-01A-11D-1669-08 chr3:25835879 T>G maps to NM_017897.2 V425V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EU-5906-01A-11D-1669-08 chr9:127789179 T>G maps to NM_173690.4 T164T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EU-5906-01A-11D-1669-08 chr22:30740939 T>A maps to NM_005877.4 L211L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EU-5906-01A-11D-1669-08 chr10:60124535 T>A maps to NM_003338.3 A68A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EU-5906-01A-11D-1669-08 chr3:49337920 G>A maps to NM_003363.3 D497D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EU-5906-01A-11D-1669-08 chr19:53057357 A>T maps to NM_001039886.3 K397*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EU-5906-01A-11D-1669-08 chr7:112724826 T>C did not map to a codon.
Sequencing variant TCGA-EU-5906-01A-11D-1669-08 chr7:112724826 T>C did not map to a codon.
Sequencing variant TCGA-EU-5906-01A-11D-1669-08 chr2:102486843 C>G maps to NM_145686.2 T909T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EU-5906-01A-11D-1669-08 chr2:102486843 C>G maps to NM_145686.2 T909T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EU-5906-01A-11D-1669-08 chr17:18196162 G>A maps to NM_004618.3 Y359Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EU-5906-01A-11D-1669-08 chr17:18196162 G>A maps to NM_004618.3 Y359Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EU-5907-01A-11D-1669-08 chr17:67280185 G>C maps to ENST00000392677 S767*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EU-5907-01A-11D-1669-08 chr13:43362793 A>C maps to NM_182508.2 S96S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EU-5907-01A-11D-1669-08 chr2:238249155 G>C maps to NM_004369.3 S2801S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EU-5907-01A-11D-1669-08 chr2:118577222 A>G did not map to a codon.
Sequencing variant TCGA-EU-5907-01A-11D-1669-08 chr5:32126320 C>T maps to NM_022130.3 K298K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EU-5907-01A-11D-1669-08 chr19:18191684 C>T maps to NM_005535.1 Q122Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EU-5907-01A-11D-1669-08 chr17:39086292 G>A maps to NM_015515.3 R179*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EU-5907-01A-11D-1669-08 chr3:52661324 G>C maps to ENST00000296302 S502*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EU-5907-01A-11D-1669-08 chr20:44045232 A>G maps to NM_015937.4 S88S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EU-5907-01A-11D-1669-08 chr8:110477388 C>T maps to ENST00000426474 D2776D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EU-5907-01A-11D-1669-08 chr12:93134669 T>C maps to NM_001004330.2 Y15Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EU-5907-01A-11D-1669-08 chr12:93134669 T>C maps to NM_001004330.2 Y15Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EU-5907-01A-11D-1669-08 chr12:6981773 C>A maps to NM_032641.3 E98*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EU-5907-01A-11D-1669-08 chr5:176305474 G>A did not map to a codon.
Sequencing variant TCGA-EU-5907-01A-11D-1669-08 chr5:72743653 C>T maps to NM_004472.2 S178S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EU-5907-01A-11D-1669-08 chr5:72743653 C>T maps to NM_004472.2 S178S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3347-01A-02D-1386-10 chr10:101552067 A>G maps to NM_000392.3 T95T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3347-01A-02D-1386-10 chr11:64111335 C>A maps to NM_032251.5 R469R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3347-01A-02D-1386-10 chr19:4433325 C>T maps to NM_005483.2 H821H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3347-01A-02D-1386-10 chr19:4433325 C>T maps to NM_005483.2 H821H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3347-01A-02D-1386-10 chr3:150264606 G>C maps to NM_032025.3 P6P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3347-01A-02D-1386-10 chr3:150264606 G>C maps to NM_032025.3 P6P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3347-01A-02D-1386-10 chr3:52858938 G>A maps to ENST00000485816 P265P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3347-01A-02D-1386-10 chrX:51638669 G>A maps to NM_001005333.1 K245K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3347-01A-02D-1386-10 chr11:74800062 G>C maps to NM_001005285.1 R232R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3347-01A-02D-1386-10 chr11:74800062 G>C maps to NM_001005285.1 R232R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3347-01A-02D-1386-10 chr17:74622131 C>T maps to NM_018414.3 R487R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3347-01A-02D-1386-10 chr17:40371846 C>T maps to NM_012448.3 P188P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3347-01A-02D-1386-10 chr11:4411234 G>A maps to NM_003141.3 Y135Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3347-01A-02D-1386-10 chr3:112993347 C>G maps to ENST00000273395 S454*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3347-01A-02D-1386-10 chr3:112993347 C>G maps to ENST00000273395 S454*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3347-01A-02D-1386-10 chr22:38516842 G>A maps to NM_003560.2 Y555Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3347-01A-02D-1386-10 chr22:38516842 G>A maps to NM_003560.2 Y555Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3347-01A-02D-1386-10 chr19:2245451 C>A maps to NM_007165.4 R85R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3347-01A-02D-1386-10 chr19:2245451 C>A maps to NM_007165.4 R85R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3349-01A-01D-1251-10 chr6:151894313 G>A maps to ENST00000367290 L260L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3349-01A-01D-1251-10 chr1:168034952 A>T maps to ENST00000367840 V855V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3349-01A-01D-1251-10 chr1:168034952 A>T maps to ENST00000367840 V855V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3349-01A-01D-1251-10 chr5:174156376 A>T maps to NM_002449.4 R199*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3349-01A-01D-1251-10 chr7:6042191 A>G maps to NM_000535.5 I143I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3349-01A-01D-1251-10 chr11:66807535 G>A maps to NM_001177880.1 E161E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3349-01A-01D-1251-10 chr17:76795061 A>C maps to NM_025090.3 A1056A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3349-01A-01D-1251-10 chr14:77844366 A>G maps to NM_001010860.1 E202E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3349-01A-01D-1251-10 chr14:77844366 A>G maps to NM_001010860.1 E202E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3358-01A-01D-1534-10 chr4:169085401 T>C maps to NM_007193.3 N121N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3358-01A-01D-1534-10 chr4:169085401 T>C maps to NM_007193.3 N121N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3358-01A-01D-1534-10 chr10:127520152 T>G maps to NM_016567.3 A192A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3358-01A-01D-1534-10 chr2:210889860 C>T maps to NM_152519.2 W844*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3358-01A-01D-1534-10 chr8:23116261 G>A maps to NM_152272.3 Q326Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3358-01A-01D-1534-10 chr2:128036917 C>A maps to NM_000122.1 E521*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3358-01A-01D-1534-10 chrX:71426171 T>A maps to NM_017669.2 P815P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3358-01A-01D-1534-10 chr2:157426663 G>A maps to NM_000408.4 V514V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3358-01A-01D-1534-10 chr2:157426663 G>A maps to NM_000408.4 V514V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3358-01A-01D-1534-10 chr19:1106418 C>T maps to NM_002085.3 G174G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3358-01A-01D-1534-10 chr6:31238125 G>A maps to ENST00000383329 T252T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3358-01A-01D-1534-10 chr1:185985178 G>T maps to NM_031935.2 G1667*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3358-01A-01D-1534-10 chr1:200943294 G>A maps to NM_017596.2 Y1601Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3358-01A-01D-1534-10 chr11:12278354 C>T maps to NM_014632.2 P993P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3358-01A-01D-1534-10 chr6:30954551 C>T maps to NM_001010909.2 S200S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3358-01A-01D-1534-10 chr1:212619209 G>A maps to NM_013349.4 E127E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3358-01A-01D-1534-10 chr21:44427620 A>G maps to NM_004571.3 L24L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3358-01A-01D-1534-10 chr3:47079268 T>A did not map to a codon.
Sequencing variant TCGA-A3-3358-01A-01D-1534-10 chr3:47079268 T>A did not map to a codon.
Sequencing variant TCGA-A3-3358-01A-01D-1534-10 chr19:17756597 G>A maps to ENST00000428389 D835D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3358-01A-01D-1534-10 chrX:48544488 A>T maps to NM_000377.2 P175P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3358-01A-01D-1534-10 chrX:54276545 G>T maps to NM_020922.4 S865*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3358-01A-01D-1534-10 chr2:32517398 A>G maps to NM_032312.3 S129S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3358-01A-01D-1534-10 chr2:32517398 A>G maps to NM_032312.3 S129S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3358-01A-01D-1534-10 chr14:75248650 C>T maps to NM_019589.2 P635P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3358-01A-01D-1534-10 chr20:62596014 C>T maps to NM_020713.1 E363E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3358-01A-01D-1534-10 chr19:58863914 A>T maps to NM_130786.3 L116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3358-01A-01D-1534-10 chr19:58863914 A>T maps to NM_130786.3 L116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3358-01A-01D-1534-10 chr7:140301429 A>C maps to NM_015689.3 G256G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3358-01A-01D-1534-10 chr7:140301429 A>C maps to NM_015689.3 G256G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3358-01A-01D-1534-10 chr16:30036623 G>A maps to NM_031478.4 N235N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3358-01A-01D-1534-10 chr16:30036623 G>A maps to NM_031478.4 N235N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3358-01A-01D-1534-10 chr1:244868991 A>G maps to NM_016076.3 E162E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3358-01A-01D-1534-10 chr1:244868991 A>G maps to NM_016076.3 E162E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3358-01A-01D-1534-10 chr7:66582491 C>T maps to NM_018264.2 L529L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3358-01A-01D-1534-10 chr7:66582491 C>T maps to NM_018264.2 L529L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3362-01A-02D-1386-10 chr7:23728935 C>T maps to NM_199136.3 P96P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3362-01A-02D-1386-10 chr15:44776438 T>G maps to NM_016396.2 P68P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3362-01A-02D-1386-10 chr15:44776438 T>G maps to NM_016396.2 P68P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3362-01A-02D-1386-10 chr11:86662561 G>C maps to NM_012193.2 A412A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3362-01A-02D-1386-10 chr3:151160938 A>C maps to NM_178822.4 L1932L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3362-01A-02D-1386-10 chr1:153637768 A>G maps to NM_004515.2 S168S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3362-01A-02D-1386-10 chr6:52129391 G>A maps to ENST00000419835 L852L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3362-01A-02D-1386-10 chr3:195507128 G>T maps to NM_018406.5 A3774A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3362-01A-02D-1386-10 chr1:154031094 T>A maps to NM_207308.2 T975T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3362-01A-02D-1386-10 chr1:154031094 T>A maps to NM_207308.2 T975T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3362-01A-02D-1386-10 chr5:43555943 A>T maps to NM_006451.4 S141S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3362-01A-02D-1386-10 chr12:57648627 C>G maps to ENST00000438036 V1019V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3362-01A-02D-1386-10 chr3:10188320 G>C did not map to a codon.
Sequencing variant TCGA-A3-3362-01A-02D-1386-10 chr3:10188320 G>C did not map to a codon.
Sequencing variant TCGA-A3-3362-01A-02D-1386-10 chr14:105413708 G>T maps to NM_138420.2 T2693T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3362-01A-02D-1386-10 chr14:105413708 G>T maps to NM_138420.2 T2693T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3362-01A-02D-1386-10 chr21:47409685 G>T maps to NM_001848.2 G308G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3362-01A-02D-1386-10 chr21:47409685 G>T maps to NM_001848.2 G308G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3362-01A-02D-1386-10 chr7:101991205 G>A maps to NM_001146210.1 P239P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3362-01A-02D-1386-10 chr7:101991205 G>A maps to NM_001146210.1 P239P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3365-01A-01W-0898-10 chr3:10183871 G>A did not map to a codon.
Sequencing variant TCGA-A3-3387-01A-01D-1534-10 chr12:27628532 C>T maps to NM_001145010.1 F127F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3387-01A-01D-1534-10 chr12:27628532 C>T maps to NM_001145010.1 F127F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3387-01A-01D-1534-10 chr3:196434642 C>A maps to NM_032898.3 E95*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3387-01A-01D-1534-10 chr1:62979389 A>G maps to ENST00000371140 Y1372Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3387-01A-01D-1534-10 chr18:65181608 A>T maps to NM_032160.2 S89S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3387-01A-01D-1534-10 chr9:88648292 G>A maps to ENST00000376023 L354L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3387-01A-01D-1534-10 chr9:88648292 G>A maps to ENST00000376023 L354L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3387-01A-01D-1534-10 chrX:19026096 C>T did not map to a codon.
Sequencing variant TCGA-A3-3387-01A-01D-1534-10 chr12:13906468 C>A maps to NM_000834.3 G264G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3387-01A-01D-1534-10 chr5:41045850 C>T maps to ENST00000296803 E612E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3387-01A-01D-1534-10 chr9:5763717 C>T maps to ENST00000414202 F897F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3387-01A-01D-1534-10 chr17:10261144 C>T did not map to a codon.
Sequencing variant TCGA-A3-3387-01A-01D-1534-10 chr3:122418639 A>T maps to NM_017554.2 I413I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3387-01A-01D-1534-10 chr3:52643560 G>A maps to ENST00000296302 Q779*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3387-01A-01D-1534-10 chr4:120442143 A>G maps to NM_001083.3 H617H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3387-01A-01D-1534-10 chr1:230461072 G>A maps to ENST00000321327 Y484Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3387-01A-01D-1534-10 chr6:150210679 G>A maps to NM_139165.1 T142T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3387-01A-01D-1534-10 chr6:117674151 C>A did not map to a codon.
Sequencing variant TCGA-A3-3387-01A-01D-1534-10 chr2:1094046 T>G maps to NM_018968.3 S92S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3387-01A-01D-1534-10 chr2:17773469 A>G maps to NM_003385.4 L43L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3387-01A-01D-1534-10 chr2:17773469 A>G maps to NM_003385.4 L43L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3387-01A-01D-1534-10 chr19:44833538 A>T maps to ENST00000412927 Y274*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3387-01A-01D-1534-10 chr1:41012840 T>C maps to NM_152373.3 Y282Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3387-01A-01D-1534-10 chr21:11026721 C>A did not map to a codon.
Sequencing variant TCGA-A3-3387-01A-01D-1534-10 chr21:11026721 C>A did not map to a codon.
Sequencing variant TCGA-A3-3387-01A-01D-1534-10 chr3:187446246 G>A maps to NM_001706.4 Q481*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3387-01A-01D-1534-10 chr3:187446246 G>A maps to NM_001706.4 Q481*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3387-01A-01D-1534-10 chr13:110833683 C>T maps to NM_001845.4 P716P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3387-01A-01D-1534-10 chr13:110833683 C>T maps to NM_001845.4 P716P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3387-01A-01D-1534-10 chr4:780369 C>T maps to NM_006651.3 E108E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3387-01A-01D-1534-10 chr4:780369 C>T maps to NM_006651.3 E108E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3387-01A-01D-1534-10 chr14:105624078 C>A maps to NM_002226.3 E147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3387-01A-01D-1534-10 chr14:105624078 C>A maps to NM_002226.3 E147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3429-01A-02D-1386-10 chr8:108334356 C>G did not map to a codon.
Sequencing variant TCGA-AK-3429-01A-02D-1386-10 chr13:25276071 G>T did not map to a codon.
Sequencing variant TCGA-AK-3429-01A-02D-1386-10 chr13:25276071 G>T did not map to a codon.
Sequencing variant TCGA-AK-3429-01A-02D-1386-10 chr19:17425184 C>A maps to NM_024050.5 Y41*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3429-01A-02D-1386-10 chrX:153736830 C>T maps to ENST00000369641 G83G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3429-01A-02D-1386-10 chr15:28446697 A>G maps to NM_004667.4 S2540S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3429-01A-02D-1386-10 chr15:28446697 A>G maps to NM_004667.4 S2540S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3429-01A-02D-1386-10 chr12:6669890 G>T maps to ENST00000382421 S503S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3429-01A-02D-1386-10 chr7:82580447 C>T maps to NM_033026.5 T3152T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3429-01A-02D-1386-10 chr1:14075879 C>T maps to NM_012231.4 L137L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3429-01A-02D-1386-10 chr19:51919239 C>T maps to NM_033130.4 G312G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3429-01A-02D-1386-10 chr15:99670373 T>C maps to ENST00000336292 A602A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3429-01A-02D-1386-10 chr15:99670373 T>C maps to ENST00000336292 A602A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3429-01A-02D-1386-10 chr3:142037708 A>G maps to NM_019001.3 L1480L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3429-01A-02D-1386-10 chr19:44891002 G>A maps to NM_152354.3 S468S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3429-01A-02D-1386-10 chr19:7964516 C>T maps to NM_025061.3 I370I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3429-01A-02D-1386-10 chr19:7964516 C>T maps to NM_025061.3 I370I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3429-01A-02D-1386-10 chr1:145302695 C>G maps to NM_001039703.4 T378T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3429-01A-02D-1386-10 chr1:145302695 C>G maps to NM_001039703.4 T378T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3429-01A-02D-1386-10 chr19:21992037 A>G maps to NM_003423.2 F267F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3429-01A-02D-1386-10 chr19:21992037 A>G maps to NM_003423.2 F267F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3430-01A-01D-1251-10 chr5:37168940 T>C maps to NM_023073.3 K2395K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3430-01A-01D-1251-10 chr5:66479406 G>A maps to NM_005582.2 L422L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3430-01A-01D-1251-10 chr7:147336209 G>A maps to NM_014141.5 W637*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3430-01A-01D-1251-10 chr4:24572442 G>A maps to NM_001358.2 R179*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3430-01A-01D-1251-10 chr5:158250250 A>G maps to NM_024007.3 N237N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3430-01A-01D-1251-10 chr4:110909738 G>T did not map to a codon.
Sequencing variant TCGA-AK-3430-01A-01D-1251-10 chr22:23915500 G>A maps to NM_020070.2 H198H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3430-01A-01D-1251-10 chr22:23915500 G>A maps to NM_020070.2 H198H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3430-01A-01D-1251-10 chr7:22771125 T>G maps to NM_000600.3 T191T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3430-01A-01D-1251-10 chr2:24469085 A>G maps to NM_006277.2 D1163D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3430-01A-01D-1251-10 chr12:49444843 G>T maps to NM_003482.3 C874*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3430-01A-01D-1251-10 chr11:123886794 C>T maps to NM_001004462.1 Q172*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3430-01A-01D-1251-10 chr7:77256020 G>A did not map to a codon.
Sequencing variant TCGA-AK-3430-01A-01D-1251-10 chr12:86199471 C>A maps to NM_005447.3 E106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3430-01A-01D-1251-10 chr14:21793466 G>A maps to NM_020366.3 A764A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3430-01A-01D-1251-10 chr6:25850133 A>G maps to NM_001098486.1 N390N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3430-01A-01D-1251-10 chr8:110587761 G>A maps to NM_001099744.1 D455D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3430-01A-01D-1251-10 chr21:19725218 C>A did not map to a codon.
Sequencing variant TCGA-AK-3430-01A-01D-1251-10 chr1:111990199 T>A did not map to a codon.
Sequencing variant TCGA-AK-3430-01A-01D-1251-10 chr11:58381763 A>G maps to NM_053023.4 G350G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3430-01A-01D-1251-10 chr10:225961 T>C maps to NM_006624.4 L4L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3430-01A-01D-1251-10 chr19:48977566 C>T maps to NM_017457.4 L226L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3430-01A-01D-1251-10 chr19:48977566 C>T maps to NM_017457.4 L226L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3430-01A-01D-1251-10 chr20:57429459 C>A maps to NM_080425.2 S380S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3430-01A-01D-1251-10 chr20:57429459 C>A maps to NM_080425.2 S380S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3430-01A-01D-1251-10 chr22:50689479 C>A did not map to a codon.
Sequencing variant TCGA-AK-3430-01A-01D-1251-10 chr22:50689479 C>A did not map to a codon.
Sequencing variant TCGA-AK-3436-01A-02D-1386-10 chr20:48273174 G>A maps to NM_004776.3 I60I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3436-01A-02D-1386-10 chr2:210889825 G>A did not map to a codon.
Sequencing variant TCGA-AK-3436-01A-02D-1386-10 chr2:210889825 G>A did not map to a codon.
Sequencing variant TCGA-AK-3436-01A-02D-1386-10 chr3:150659492 G>T maps to NM_001195794.1 L103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3436-01A-02D-1386-10 chr10:104184283 T>A maps to NM_024040.2 S84S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3436-01A-02D-1386-10 chr15:80452757 C>T maps to NM_000137.1 F107F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3436-01A-02D-1386-10 chr2:50149351 T>A maps to ENST00000404971 P1458P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3436-01A-02D-1386-10 chr4:108608292 A>C maps to NM_005443.4 L151*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3436-01A-02D-1386-10 chr3:52621463 G>A maps to ENST00000296302 R1010*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3436-01A-02D-1386-10 chr1:153271693 G>A maps to NM_052891.1 Q248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3436-01A-02D-1386-10 chr7:77469586 C>G maps to ENST00000427986 V5V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3436-01A-02D-1386-10 chrX:49143161 G>A maps to NM_033215.4 G670G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3436-01A-02D-1386-10 chr1:17739592 C>T maps to NM_018715.2 W430*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3436-01A-02D-1386-10 chr17:37360843 G>A maps to NM_000981.3 Q178Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3436-01A-02D-1386-10 chr19:55686304 G>A maps to NM_003180.2 T257T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3436-01A-02D-1386-10 chr15:57458627 C>A maps to NM_207036.1 S118S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3436-01A-02D-1386-10 chr4:103723779 G>A maps to NM_181890.1 Q46*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3436-01A-02D-1386-10 chr4:103723779 G>A maps to NM_181890.1 Q46*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3436-01A-02D-1386-10 chr2:170885901 T>A maps to ENST00000442603 I1529I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3436-01A-02D-1386-10 chr3:195510191 A>C maps to NM_018406.5 L2753L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3436-01A-02D-1386-10 chr3:195510191 A>C maps to NM_018406.5 L2753L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3436-01A-02D-1386-10 chrX:123025167 T>C did not map to a codon.
Sequencing variant TCGA-AK-3436-01A-02D-1386-10 chrX:123025167 T>C did not map to a codon.
Sequencing variant TCGA-AK-3445-01A-02W-1359-10 chr3:10183816 C>T maps to NM_000551.2 Q96*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3450-01A-02W-1359-10 chr3:10183872 T>C did not map to a codon.
Sequencing variant TCGA-AK-3451-01A-02D-1251-10 chr17:78058618 C>T maps to NM_017950.2 D689D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3451-01A-02D-1251-10 chr17:7805977 C>A maps to NM_001005271.2 Y1160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3451-01A-02D-1251-10 chr17:7805977 C>A maps to NM_001005271.2 Y1160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3451-01A-02D-1251-10 chr1:47402389 A>C maps to ENST00000371904 Y152*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3451-01A-02D-1251-10 chr19:45916985 G>T maps to NM_202001.2 I264I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3451-01A-02D-1251-10 chr1:43616486 A>C maps to NM_001101376.2 A63A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3451-01A-02D-1251-10 chr2:173352129 G>A maps to ENST00000264106 T742T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3451-01A-02D-1251-10 chr16:75678247 G>A maps to NM_001130089.1 L27L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3451-01A-02D-1251-10 chr1:200960790 G>T maps to NM_017596.2 T816T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3451-01A-02D-1251-10 chr15:68445965 C>T maps to NM_016166.1 S289S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3451-01A-02D-1251-10 chr16:2158399 C>A maps to NM_001009944.2 L2256L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3451-01A-02D-1251-10 chr18:8113696 T>A maps to NM_001105244.1 T690T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3451-01A-02D-1251-10 chr18:8113696 T>A maps to NM_001105244.1 T690T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3451-01A-02D-1251-10 chr2:74902020 G>T maps to NM_004263.3 G336G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3451-01A-02D-1251-10 chr1:35578966 G>A maps to NM_024772.3 K512K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3451-01A-02D-1251-10 chr5:140256583 G>A maps to NM_018903.2 S509S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3451-01A-02D-1251-10 chr5:140256583 G>A maps to NM_018903.2 S509S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3451-01A-02D-1251-10 chr17:78337080 C>G maps to NM_020914.4 A3894A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3451-01A-02D-1251-10 chr17:78337080 C>G maps to NM_020914.4 A3894A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3456-01A-02D-1386-10 chr6:44274035 C>A maps to NM_020745.2 G427G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3456-01A-02D-1386-10 chr4:42509033 G>A maps to NM_006095.2 I695I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3456-01A-02D-1386-10 chr5:40843665 T>G maps to NM_032587.3 V232V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3456-01A-02D-1386-10 chr1:87045907 T>A maps to ENST00000263723 T881T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3456-01A-02D-1386-10 chr2:165561492 C>A maps to ENST00000392717 P411P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3456-01A-02D-1386-10 chr9:117026663 G>T maps to NM_032888.2 G1075G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3456-01A-02D-1386-10 chr4:1389075 C>T maps to NM_175918.3 P259P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3456-01A-02D-1386-10 chr1:150778607 A>T maps to NM_000396.3 Y71*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3456-01A-02D-1386-10 chr13:39262989 T>C maps to NM_207361.4 A503A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3456-01A-02D-1386-10 chr19:41243661 C>T maps to NM_025194.2 F612F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3456-01A-02D-1386-10 chr3:113376124 C>T maps to NM_001009899.2 Q1468Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3456-01A-02D-1386-10 chr17:39324283 G>A maps to NM_033187.1 S47S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3456-01A-02D-1386-10 chr10:100022770 C>T maps to NM_032211.6 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3456-01A-02D-1386-10 chr7:98256631 C>T maps to NM_002523.2 G348G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3456-01A-02D-1386-10 chr14:52741642 C>T maps to NM_000953.2 S347S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3456-01A-02D-1386-10 chr10:99145672 C>T maps to NM_015179.3 E365E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3456-01A-02D-1386-10 chr3:38888541 G>T maps to ENST00000302328 P1673P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3456-01A-02D-1386-10 chr6:44197390 C>T maps to ENST00000313248 D138D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3456-01A-02D-1386-10 chr1:152975714 C>T maps to NM_005416.2 G73G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3456-01A-02D-1386-10 chrX:101396081 A>G maps to NM_001006938.2 G74G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3456-01A-02D-1386-10 chr16:57775692 C>T maps to NM_005886.2 V45V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3456-01A-02D-1386-10 chr16:57775692 C>T maps to NM_005886.2 V45V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3456-01A-02D-1386-10 chr3:195506372 G>A maps to NM_018406.5 S4026S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3456-01A-02D-1386-10 chr3:195506372 G>A maps to NM_018406.5 S4026S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3456-01A-02D-1386-10 chr4:56448341 T>C maps to NM_152401.2 K23K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3456-01A-02D-1386-10 chr4:56448341 T>C maps to NM_152401.2 K23K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3456-01A-02D-1386-10 chr15:93588746 G>T maps to NM_020211.2 G278G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3456-01A-02D-1386-10 chr15:93588746 G>T maps to NM_020211.2 G278G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3458-01A-01D-1501-10 chr1:32682462 A>T maps to NM_019118.3 S138S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3458-01A-01D-1501-10 chrX:53244974 A>G did not map to a codon.
Sequencing variant TCGA-AK-3458-01A-01D-1501-10 chrX:53244974 A>G did not map to a codon.
Sequencing variant TCGA-AK-3458-01A-01D-1501-10 chr19:57329186 G>A maps to NM_006210.2 D263D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3458-01A-01D-1501-10 chr18:21043936 T>C maps to NM_003831.3 A62A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3458-01A-01D-1501-10 chr7:135370371 C>T maps to NM_012450.2 P501P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3458-01A-01D-1501-10 chr11:113701631 C>A maps to NM_020886.2 V289V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3458-01A-01D-1501-10 chr11:113701631 C>A maps to NM_020886.2 V289V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3458-01A-01D-1501-10 chr18:72234668 G>T did not map to a codon.
Sequencing variant TCGA-AK-3458-01A-01D-1501-10 chr18:72234668 G>T did not map to a codon.
Sequencing variant TCGA-AK-3458-01A-01D-1501-10 chr9:135555165 A>G maps to NM_012204.2 E720E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3458-01A-01D-1501-10 chr9:135555165 A>G maps to NM_012204.2 E720E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3458-01A-01D-1501-10 chr3:195510107 G>A maps to NM_018406.5 H2781H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3458-01A-01D-1501-10 chr3:195510107 G>A maps to NM_018406.5 H2781H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4700-01A-02D-1534-10 chrX:49072840 C>T did not map to a codon.
Sequencing variant TCGA-B0-4700-01A-02D-1534-10 chr5:177166138 C>A did not map to a codon.
Sequencing variant TCGA-B0-4700-01A-02D-1534-10 chrX:153296885 G>C maps to NM_001110792.1 A143A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4700-01A-02D-1534-10 chrX:153296885 G>C maps to NM_001110792.1 A143A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4700-01A-02D-1534-10 chr20:49576092 C>T maps to NM_014484.3 N238N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4700-01A-02D-1534-10 chr20:46279865 A>G maps to NM_181659.2 Q1264Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4700-01A-02D-1534-10 chr7:143633179 G>A maps to NM_001004685.1 L285L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4700-01A-02D-1534-10 chr3:136062773 G>A maps to NM_005862.2 Q1116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4700-01A-02D-1534-10 chr3:136062773 G>A maps to NM_005862.2 Q1116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4700-01A-02D-1534-10 chr16:28607131 G>A maps to NM_001054.3 D40D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4700-01A-02D-1534-10 chr6:132910003 G>T maps to NM_003967.2 V274V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4700-01A-02D-1534-10 chr3:10188196 G>T did not map to a codon.
Sequencing variant TCGA-B0-4700-01A-02D-1534-10 chr1:27874969 C>T maps to NM_001029882.2 W1219*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4700-01A-02D-1534-10 chr1:27874969 C>T maps to NM_001029882.2 W1219*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4700-01A-02D-1534-10 chr12:1755045 C>T maps to NM_032642.2 A236A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4700-01A-02D-1534-10 chr12:1755045 C>T maps to NM_032642.2 A236A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4706-01A-01D-1501-10 chr7:117417735 A>T maps to NM_033427.2 A869A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4706-01A-01D-1501-10 chr2:183623958 T>C maps to NM_018981.1 H690H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4706-01A-01D-1501-10 chr2:153476065 G>A maps to NM_052905.3 P557P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4706-01A-01D-1501-10 chr2:153476068 C>A maps to NM_052905.3 P558P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4706-01A-01D-1501-10 chr19:3533335 G>A maps to NM_001136198.1 K429K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4706-01A-01D-1501-10 chr10:104111128 C>T maps to NM_004193.2 Q138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4706-01A-01D-1501-10 chrX:30260746 C>G maps to NM_002367.3 A165A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4706-01A-01D-1501-10 chr2:95773988 C>A maps to NM_031902.3 E190*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4706-01A-01D-1501-10 chr6:86303400 C>T maps to NM_153816.3 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4706-01A-01D-1501-10 chr1:3545079 C>T maps to NM_182752.3 L244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4706-01A-01D-1501-10 chr9:12698512 C>T maps to NM_000550.2 V257V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4706-01A-01D-1501-10 chrY:2829143 C>T maps to NM_003411.3 Q31*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4706-01A-01D-1501-10 chr15:43653849 A>G maps to NM_152455.3 F660F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4706-01A-01D-1501-10 chr2:131520997 G>A maps to NM_001105195.1 P451P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4706-01A-01D-1501-10 chr2:131520997 G>A maps to NM_001105195.1 P451P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4706-01A-01D-1501-10 chr21:46011525 T>A maps to NM_198688.2 T280T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4706-01A-01D-1501-10 chr21:46011525 T>A maps to NM_198688.2 T280T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4707-01A-01W-1359-10 chr9:21970999 C>A maps to NM_001195132.1 E120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4710-01A-01D-1501-10 chrX:100912451 G>A maps to NM_177949.2 P41P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4710-01A-01D-1501-10 chr13:25266643 C>T maps to NM_001185085.1 L388L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4710-01A-01D-1501-10 chr6:52764812 T>C maps to NM_000847.4 L111L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4710-01A-01D-1501-10 chr19:18286173 G>A maps to NM_006332.3 E123E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4710-01A-01D-1501-10 chr2:113736197 T>A did not map to a codon.
Sequencing variant TCGA-B0-4710-01A-01D-1501-10 chr1:10318552 C>T maps to ENST00000377086 P62P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4710-01A-01D-1501-10 chr19:55085834 C>A maps to NM_001130917.1 T46T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4710-01A-01D-1501-10 chr19:55085834 C>A maps to NM_001130917.1 T46T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4710-01A-01D-1501-10 chr4:99955421 G>T maps to NM_015143.2 E70*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4710-01A-01D-1501-10 chr11:92714907 G>C maps to NM_005959.3 L173L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4710-01A-01D-1501-10 chr19:50812920 C>G maps to NM_001145809.1 T1995T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4710-01A-01D-1501-10 chrX:96139816 A>T maps to NM_013347.4 K170*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4710-01A-01D-1501-10 chr6:35087005 A>T maps to NM_001093728.1 I439I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4710-01A-01D-1501-10 chr1:156552876 C>T maps to NM_001105669.2 S318S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4710-01A-01D-1501-10 chr1:216219776 G>T maps to ENST00000366943 V2107V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4710-01A-01D-1501-10 chr19:994288 C>T maps to NM_024100.3 I415I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4710-01A-01D-1501-10 chr19:44470617 A>C maps to NM_013359.2 R322R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4710-01A-01D-1501-10 chr10:73442208 C>T maps to ENST00000398860 S627S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4710-01A-01D-1501-10 chr10:73442208 C>T maps to ENST00000398860 S627S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4710-01A-01D-1501-10 chr3:195506774 G>A maps to NM_018406.5 T3892T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4710-01A-01D-1501-10 chr3:195506774 G>A maps to NM_018406.5 T3892T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4710-01A-01D-1501-10 chr17:7369781 A>G maps to NM_020899.3 P113P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4710-01A-01D-1501-10 chr17:7369781 A>G maps to NM_020899.3 P113P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4712-01A-01D-1501-10 chr9:33395107 G>A maps to NM_001170.1 L38L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4712-01A-01D-1501-10 chr1:231489082 A>G maps to NM_032018.4 K482K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4712-01A-01D-1501-10 chr1:75101999 G>T maps to NM_001002912.4 T189T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4712-01A-01D-1501-10 chr1:75101999 G>T maps to NM_001002912.4 T189T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4712-01A-01D-1501-10 chr5:149449863 G>T maps to NM_005211.3 Y400*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4712-01A-01D-1501-10 chr10:390775 G>T maps to NM_014974.2 S1142S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4712-01A-01D-1501-10 chr18:2891707 C>G maps to NM_032048.2 S528*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4712-01A-01D-1501-10 chr3:121412703 A>G maps to ENST00000393667 D2222D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4712-01A-01D-1501-10 chr17:21319715 G>A maps to NM_021012.4 T354T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4712-01A-01D-1501-10 chr2:170028540 T>C maps to NM_004525.2 S3749S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4712-01A-01D-1501-10 chr5:176636689 G>A maps to NM_022455.4 Q430Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4712-01A-01D-1501-10 chr5:176636689 G>A maps to NM_022455.4 Q430Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4712-01A-01D-1501-10 chr11:4903716 C>T maps to NM_001004759.1 I223I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4712-01A-01D-1501-10 chr15:65114483 G>A maps to ENST00000333425 T266T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4712-01A-01D-1501-10 chr1:242253368 G>A maps to NM_152666.2 G466G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4712-01A-01D-1501-10 chr12:11546807 A>G maps to NM_006248.3 P68P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4712-01A-01D-1501-10 chr8:70978468 C>A did not map to a codon.
Sequencing variant TCGA-B0-4712-01A-01D-1501-10 chr1:150312942 C>T maps to NM_004698.2 L424L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4712-01A-01D-1501-10 chr19:40480500 C>T maps to NM_006503.2 A180A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4712-01A-01D-1501-10 chrX:135957715 A>G maps to NM_002139.3 Y190Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4712-01A-01D-1501-10 chr3:47165359 G>A maps to NM_014159.6 Q256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4712-01A-01D-1501-10 chr3:47165359 G>A maps to NM_014159.6 Q256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4712-01A-01D-1501-10 chr1:110921781 A>C maps to NM_004696.1 T241T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4712-01A-01D-1501-10 chr13:53231665 G>C did not map to a codon.
Sequencing variant TCGA-B0-4712-01A-01D-1501-10 chr1:166833058 A>T did not map to a codon.
Sequencing variant TCGA-B0-4712-01A-01D-1501-10 chr14:102916036 G>A maps to NM_014844.3 S1049S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4712-01A-01D-1501-10 chr3:9868879 T>C maps to NM_001025930.3 Y501Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4712-01A-01D-1501-10 chr19:58772268 T>C maps to NM_014480.2 A99A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4712-01A-01D-1501-10 chr3:195509126 A>G maps to NM_018406.5 T3108T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4712-01A-01D-1501-10 chr3:195509126 A>G maps to NM_018406.5 T3108T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4712-01A-01D-1501-10 chr14:100809695 A>G maps to NM_173701.1 A285A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4712-01A-01D-1501-10 chr14:100809695 A>G maps to NM_173701.1 A285A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4712-01A-01D-1501-10 chr19:22574467 G>A maps to NM_001098626.1 C523C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4712-01A-01D-1501-10 chr19:22574467 G>A maps to NM_001098626.1 C523C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4713-01A-01D-1361-10 chr3:10183733 C>A maps to NM_000551.2 S68*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4810-01A-01D-1501-10 chr14:23549895 C>T maps to NM_014977.3 E274E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4810-01A-01D-1501-10 chr19:15465830 T>C maps to NM_005858.2 A658A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4810-01A-01D-1501-10 chr19:15465830 T>C maps to NM_005858.2 A658A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4810-01A-01D-1501-10 chr13:26125479 C>A maps to NM_016529.4 S299*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4810-01A-01D-1501-10 chr13:26125479 C>A maps to NM_016529.4 S299*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4810-01A-01D-1501-10 chr10:5789389 G>T maps to NM_017782.4 E1336*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4810-01A-01D-1501-10 chr2:201721414 T>C maps to NM_001162407.1 E391E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4810-01A-01D-1501-10 chr1:103468817 G>A maps to NM_080629.2 R663*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4810-01A-01D-1501-10 chr22:19956114 A>G maps to NM_001135162.1 P224P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4810-01A-01D-1501-10 chr22:19956114 A>G maps to NM_001135162.1 P224P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4810-01A-01D-1501-10 chr2:16742256 C>T did not map to a codon.
Sequencing variant TCGA-B0-4810-01A-01D-1501-10 chr6:137519167 T>A maps to NM_000416.2 *490C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4810-01A-01D-1501-10 chr11:68216348 C>T maps to NM_002335.2 S1553S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4810-01A-01D-1501-10 chr14:47613332 A>T maps to NM_001113498.2 L247*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4810-01A-01D-1501-10 chr4:103971408 A>G maps to NM_178833.4 G191G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4810-01A-01D-1501-10 chr4:103971408 A>G maps to NM_178833.4 G191G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4810-01A-01D-1501-10 chr17:5462473 C>T maps to NM_033004.3 W514*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4810-01A-01D-1501-10 chr10:89725042 G>A did not map to a codon.
Sequencing variant TCGA-B0-4810-01A-01D-1501-10 chrX:38145179 C>T maps to NM_001034853.1 E1024E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4810-01A-01D-1501-10 chr5:132158628 C>A maps to NM_001172700.1 L806L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4810-01A-01D-1501-10 chr5:132158628 C>A maps to NM_001172700.1 L806L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4810-01A-01D-1501-10 chr18:52937098 G>A maps to ENST00000398339 S397S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4811-01A-01D-1501-10 chr20:47604915 C>T maps to NM_006420.2 H784H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4811-01A-01D-1501-10 chr17:4877037 T>C maps to NM_015099.3 E681E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4811-01A-01D-1501-10 chr17:4877037 T>C maps to NM_015099.3 E681E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4811-01A-01D-1501-10 chr2:113509842 C>A did not map to a codon.
Sequencing variant TCGA-B0-4811-01A-01D-1501-10 chr17:40715164 G>A maps to NM_001042532.2 R204R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4811-01A-01D-1501-10 chr6:75864168 G>C maps to ENST00000322507 T1176T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4811-01A-01D-1501-10 chr11:65113419 A>C maps to NM_006268.3 G265G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4811-01A-01D-1501-10 chr8:144668952 T>A maps to NM_032378.4 A387A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4811-01A-01D-1501-10 chr16:71318089 T>A maps to NM_018348.5 I578I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4811-01A-01D-1501-10 chr9:104499649 G>T maps to NM_133445.2 G204G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4811-01A-01D-1501-10 chr20:60895845 G>A maps to NM_005560.3 S2199S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4811-01A-01D-1501-10 chr12:49495926 A>G maps to NM_018113.2 A302A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4811-01A-01D-1501-10 chr18:44137416 C>T maps to NM_144612.6 G1084G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4811-01A-01D-1501-10 chr2:135012081 G>A maps to NM_002410.3 Q36Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4811-01A-01D-1501-10 chr12:49436557 G>C maps to NM_003482.3 G1916G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4811-01A-01D-1501-10 chr11:26582749 C>T maps to NM_001135091.1 P316P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4811-01A-01D-1501-10 chr11:20078103 C>T maps to ENST00000396087 N1643N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4811-01A-01D-1501-10 chr11:20078103 C>T maps to ENST00000396087 N1643N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4811-01A-01D-1501-10 chr1:120497757 G>A maps to NM_024408.2 C708C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4811-01A-01D-1501-10 chr12:95422175 T>C maps to NM_003297.2 V506V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4811-01A-01D-1501-10 chr12:52448381 G>A maps to ENST00000360284 S144S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4811-01A-01D-1501-10 chr8:101725344 T>G maps to NM_002568.3 V236V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4811-01A-01D-1501-10 chr9:131480825 A>C did not map to a codon.
Sequencing variant TCGA-B0-4811-01A-01D-1501-10 chr9:131480825 A>C did not map to a codon.
Sequencing variant TCGA-B0-4811-01A-01D-1501-10 chr14:35777198 G>C did not map to a codon.
Sequencing variant TCGA-B0-4811-01A-01D-1501-10 chr2:219532705 T>C did not map to a codon.
Sequencing variant TCGA-B0-4811-01A-01D-1501-10 chr15:48063501 G>A maps to NM_153618.1 S914S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4811-01A-01D-1501-10 chr6:44224428 C>T maps to NM_178148.2 L66L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4811-01A-01D-1501-10 chr17:18863862 C>T maps to NM_152351.3 I117I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4811-01A-01D-1501-10 chr17:34147196 T>C maps to NM_139215.1 D43D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4811-01A-01D-1501-10 chr4:65147224 A>G maps to NM_001010874.4 F295F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4811-01A-01D-1501-10 chr10:50034822 C>T maps to NM_020945.1 S2030S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4811-01A-01D-1501-10 chr17:5009700 A>G maps to NM_014519.2 T251T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4811-01A-01D-1501-10 chr2:73680748 A>G maps to NM_015120.4 E2364E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4811-01A-01D-1501-10 chr2:73680748 A>G maps to NM_015120.4 E2364E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4811-01A-01D-1501-10 chr11:46388174 G>A maps to NM_001105540.1 Q123Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4811-01A-01D-1501-10 chr11:46388174 G>A maps to NM_001105540.1 Q123Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4811-01A-01D-1501-10 chr16:55362618 T>C maps to NM_024335.2 T243T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4811-01A-01D-1501-10 chr16:55362618 T>C maps to NM_024335.2 T243T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4811-01A-01D-1501-10 chr6:150211276 A>G maps to NM_139165.1 G30G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4811-01A-01D-1501-10 chr6:150211276 A>G maps to NM_139165.1 G30G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4811-01A-01D-1501-10 chr19:58453893 T>A maps to NM_005773.2 I94I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4811-01A-01D-1501-10 chr19:58453893 T>A maps to NM_005773.2 I94I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4815-01A-01D-1501-10 chr11:76750645 C>T maps to ENST00000354301 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4815-01A-01D-1501-10 chr2:85066360 G>T maps to ENST00000409520 I301I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4815-01A-01D-1501-10 chr4:24810061 G>A maps to NM_001130726.2 D513D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4815-01A-01D-1501-10 chr18:63530052 C>T maps to NM_004361.2 D588D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4815-01A-01D-1501-10 chrX:50147056 G>T maps to NM_001013742.1 I356I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4815-01A-01D-1501-10 chr5:161277822 A>T maps to NM_001127648.1 K3*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4815-01A-01D-1501-10 chr6:52622678 G>A maps to NM_000846.4 L23L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4815-01A-01D-1501-10 chr1:59247908 G>C maps to NM_002228.3 A278A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4815-01A-01D-1501-10 chr9:114184458 A>T maps to NM_001080398.1 T607T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4815-01A-01D-1501-10 chr7:91855962 T>C maps to NM_194456.1 L341L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4815-01A-01D-1501-10 chr7:91855962 T>C maps to NM_194456.1 L341L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4815-01A-01D-1501-10 chr12:53216798 C>T did not map to a codon.
Sequencing variant TCGA-B0-4815-01A-01D-1501-10 chr12:53216798 C>T did not map to a codon.
Sequencing variant TCGA-B0-4815-01A-01D-1501-10 chr3:158545108 A>T maps to NM_022736.2 I508I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4815-01A-01D-1501-10 chr11:64427891 T>G maps to NM_015080.3 G767G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4815-01A-01D-1501-10 chr11:64427891 T>G maps to NM_015080.3 G767G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4815-01A-01D-1501-10 chr1:159505239 A>C maps to NM_001004469.1 L186L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4815-01A-01D-1501-10 chr12:121655011 C>T maps to NM_002560.2 G70G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4815-01A-01D-1501-10 chr3:52668806 G>C maps to ENST00000296302 S371*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4815-01A-01D-1501-10 chr5:137257414 T>G maps to ENST00000230643 T473T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4815-01A-01D-1501-10 chr7:75517558 C>T maps to NM_001040456.1 G329G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4815-01A-01D-1501-10 chr7:75517558 C>T maps to NM_001040456.1 G329G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4815-01A-01D-1501-10 chr7:103018051 C>A maps to ENST00000354356 L662L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4815-01A-01D-1501-10 chr1:234458835 C>T maps to NM_173508.2 L440L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4815-01A-01D-1501-10 chr1:234458835 C>T maps to NM_173508.2 L440L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4815-01A-01D-1501-10 chr5:482712 G>A maps to NM_004174.2 L436L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4815-01A-01D-1501-10 chr4:69817430 G>A maps to NM_024743.3 F16F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4815-01A-01D-1501-10 chr1:155932491 C>G maps to NM_001162383.1 A331A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4815-01A-01D-1501-10 chr1:155932491 C>G maps to NM_001162383.1 A331A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4815-01A-01D-1501-10 chr7:141762387 C>T maps to ENST00000475668 A1381A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4815-01A-01D-1501-10 chr7:141762387 C>T maps to ENST00000475668 A1381A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4816-01A-01D-1501-10 chr14:23549880 C>T maps to NM_014977.3 E279E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4816-01A-01D-1501-10 chr14:23549895 C>T maps to NM_014977.3 E274E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4816-01A-01D-1501-10 chr12:7527158 C>T maps to ENST00000416109 G1106G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4816-01A-01D-1501-10 chr12:7527158 C>T maps to ENST00000416109 G1106G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4816-01A-01D-1501-10 chrX:83128363 A>G maps to NM_021118.1 T216T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4816-01A-01D-1501-10 chr11:6592960 C>T maps to NM_144666.2 A4669A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4816-01A-01D-1501-10 chr1:113633958 T>C maps to NM_014813.1 L87L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4816-01A-01D-1501-10 chr15:64448266 G>A maps to NM_000942.4 C202C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4816-01A-01D-1501-10 chr5:57913492 G>A maps to NM_138453.2 R16R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4816-01A-01D-1501-10 chr5:131894989 T>C maps to NM_005732.3 C48C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4816-01A-01D-1501-10 chr1:67340462 C>T did not map to a codon.
Sequencing variant TCGA-B0-4816-01A-01D-1501-10 chr19:37382714 A>G maps to NM_001171979.1 C407C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4818-01A-01D-1501-10 chr2:220075788 G>C maps to NM_005689.2 P670P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4818-01A-01D-1501-10 chr2:220075788 G>C maps to NM_005689.2 P670P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4818-01A-01D-1501-10 chr10:51464816 T>A maps to ENST00000416142 K570*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4818-01A-01D-1501-10 chr10:115894781 T>A maps to NM_018017.2 T515T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4818-01A-01D-1501-10 chr13:21063529 T>C maps to NM_015974.2 V85V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4818-01A-01D-1501-10 chr13:21063529 T>C maps to NM_015974.2 V85V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4818-01A-01D-1501-10 chr2:72411217 C>G maps to NM_015189.1 L765L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4818-01A-01D-1501-10 chr3:100356180 C>T maps to NM_032787.2 L211L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4818-01A-01D-1501-10 chr3:100356180 C>T maps to NM_032787.2 L211L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4818-01A-01D-1501-10 chr16:46950589 G>T maps to NM_133443.2 E291*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4818-01A-01D-1501-10 chr1:119923770 T>C maps to ENST00000361035 T34T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4818-01A-01D-1501-10 chr11:3700798 G>A maps to NM_016320.4 L1686L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4818-01A-01D-1501-10 chr11:3700798 G>A maps to NM_016320.4 L1686L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4818-01A-01D-1501-10 chr3:52637739 G>T maps to ENST00000296302 S859*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4818-01A-01D-1501-10 chr3:52637739 G>T maps to ENST00000296302 S859*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4818-01A-01D-1501-10 chr4:520920 G>A maps to NM_001127178.1 K721K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4818-01A-01D-1501-10 chr4:520920 G>A maps to NM_001127178.1 K721K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4818-01A-01D-1501-10 chr2:136418886 T>A maps to ENST00000409606 P658P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4818-01A-01D-1501-10 chr1:237947722 C>T maps to NM_001035.2 S4237S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4818-01A-01D-1501-10 chr1:109884660 T>C maps to NM_002959.4 V361V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4818-01A-01D-1501-10 chr18:55027489 T>A maps to NM_015879.2 T375T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4818-01A-01D-1501-10 chr5:109940963 A>T maps to NM_001039763.3 T374T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4818-01A-01D-1501-10 chrX:129045755 A>T maps to NM_006649.3 V132V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4818-01A-01D-1501-10 chr3:133119013 G>A maps to NM_003571.2 G29G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4818-01A-01D-1501-10 chr3:133119013 G>A maps to NM_003571.2 G29G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4818-01A-01D-1501-10 chr1:144813814 A>G maps to NM_001037675.2 A353A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4818-01A-01D-1501-10 chr1:144813814 A>G maps to NM_001037675.2 A353A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4818-01A-01D-1501-10 chr6:43742100 A>G maps to NM_001025366.2 A210A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4818-01A-01D-1501-10 chr6:43742100 A>G maps to NM_001025366.2 A210A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4824-01A-01W-1359-10 chr3:10183724 C>A maps to NM_000551.2 S65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4845-01A-01W-1359-10 chr3:10183793 G>A maps to NM_000551.2 W88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4852-01A-01D-1501-10 chr17:35640307 T>C did not map to a codon.
Sequencing variant TCGA-B0-4852-01A-01D-1501-10 chr12:43769951 C>T did not map to a codon.
Sequencing variant TCGA-B0-4852-01A-01D-1501-10 chr5:64483841 C>G did not map to a codon.
Sequencing variant TCGA-B0-4852-01A-01D-1501-10 chr21:40572253 A>G maps to NM_018963.3 S1548S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4852-01A-01D-1501-10 chr21:40572253 A>G maps to NM_018963.3 S1548S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4852-01A-01D-1501-10 chr10:11894169 C>T maps to NM_153256.3 L32L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4852-01A-01D-1501-10 chr15:43021464 G>A maps to NM_138477.2 L835L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4852-01A-01D-1501-10 chr9:123870183 A>T maps to NM_007018.4 K305*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4852-01A-01D-1501-10 chrX:154129669 G>A maps to NM_000132.3 Q2055*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4852-01A-01D-1501-10 chrX:154129669 G>A maps to NM_000132.3 Q2055*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4852-01A-01D-1501-10 chr4:158282179 A>C maps to NM_001083619.1 A770A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4852-01A-01D-1501-10 chr13:77459422 C>G maps to NM_138444.3 S287S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4852-01A-01D-1501-10 chr19:55085804 C>A maps to NM_001130917.1 G36G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4852-01A-01D-1501-10 chr3:150874117 G>T did not map to a codon.
Sequencing variant TCGA-B0-4852-01A-01D-1501-10 chr6:138753024 C>T maps to NM_001144060.1 G819G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4852-01A-01D-1501-10 chrX:128720993 C>T maps to NM_000276.3 Q719*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4852-01A-01D-1501-10 chr11:5969271 C>A maps to NM_001003443.2 L232L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4852-01A-01D-1501-10 chr10:3172144 C>T maps to NM_002627.3 F606F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4852-01A-01D-1501-10 chr15:42386651 C>T maps to NM_178034.3 E2E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4852-01A-01D-1501-10 chr15:42386651 C>T maps to NM_178034.3 E2E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4852-01A-01D-1501-10 chr12:114364984 T>C maps to NM_016196.3 A706A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4852-01A-01D-1501-10 chr4:119718965 C>T did not map to a codon.
Sequencing variant TCGA-B0-4852-01A-01D-1501-10 chr20:45192088 G>A maps to NM_022829.5 I532I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4852-01A-01D-1501-10 chr14:78045380 G>A maps to NM_004863.2 N133N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4852-01A-01D-1501-10 chr4:48148399 A>T maps to NM_003215.2 L341L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4852-01A-01D-1501-10 chr15:41862435 A>G did not map to a codon.
Sequencing variant TCGA-B0-4852-01A-01D-1501-10 chr3:10191468 A>G did not map to a codon.
Sequencing variant TCGA-B0-4852-01A-01D-1501-10 chr3:10191468 A>G did not map to a codon.
Sequencing variant TCGA-B0-4852-01A-01D-1501-10 chr20:62407315 C>T did not map to a codon.
Sequencing variant TCGA-B0-4852-01A-01D-1501-10 chr17:42083123 T>C maps to NM_153006.2 A182A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4852-01A-01D-1501-10 chr17:42083123 T>C maps to NM_153006.2 A182A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5080-01A-01D-1501-10 chr12:7459280 C>A maps to NM_001080454.1 A118A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5080-01A-01D-1501-10 chr1:22973840 C>A maps to NM_172369.3 P101P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5080-01A-01D-1501-10 chr2:225637921 C>G maps to NM_014689.2 V2052V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5080-01A-01D-1501-10 chr2:225637921 C>G maps to NM_014689.2 V2052V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5080-01A-01D-1501-10 chr22:45726593 T>C maps to NM_017911.2 T211T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5080-01A-01D-1501-10 chr22:45726593 T>C maps to NM_017911.2 T211T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5080-01A-01D-1501-10 chr22:45726594 C>T maps to NM_017911.2 Q212*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5080-01A-01D-1501-10 chr22:45726594 C>T maps to NM_017911.2 Q212*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5080-01A-01D-1501-10 chr1:230398727 T>A maps to NM_004481.3 L430L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5080-01A-01D-1501-10 chr5:89986797 G>A maps to NM_032119.3 G2297G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5080-01A-01D-1501-10 chr7:139097304 C>A maps to NM_016019.2 S263*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5080-01A-01D-1501-10 chr7:139097304 C>A maps to NM_016019.2 S263*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5080-01A-01D-1501-10 chr2:60987313 T>C maps to NM_022894.3 I21I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5080-01A-01D-1501-10 chr2:60987313 T>C maps to NM_022894.3 I21I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5080-01A-01D-1501-10 chr17:10728776 G>A maps to NM_001101387.1 G62G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5080-01A-01D-1501-10 chr19:808432 C>T maps to NM_002819.4 D409D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5080-01A-01D-1501-10 chr19:51958702 G>A maps to NM_014442.2 S340S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5080-01A-01D-1501-10 chr11:66813239 G>T maps to NM_001177880.1 L328L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5080-01A-01D-1501-10 chr3:189608581 T>C maps to NM_003722.4 L553L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5080-01A-01D-1501-10 chr3:189608581 T>C maps to NM_003722.4 L553L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5080-01A-01D-1501-10 chr10:73121851 G>A maps to NM_018344.5 T305T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5080-01A-01D-1501-10 chr10:73121851 G>A maps to NM_018344.5 T305T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5080-01A-01D-1501-10 chr19:13260324 T>C maps to NM_003765.1 R96R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5080-01A-01D-1501-10 chr19:13260324 T>C maps to NM_003765.1 R96R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5399-01A-01D-1501-10 chr12:22068793 G>T maps to NM_005691.2 L208L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5399-01A-01D-1501-10 chr20:3655258 G>A maps to NM_025220.2 H164H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5399-01A-01D-1501-10 chr12:657231 G>A maps to NM_173593.3 K250K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5399-01A-01D-1501-10 chr2:71060813 G>C maps to NM_015717.3 G176G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5399-01A-01D-1501-10 chr10:375378 G>T maps to NM_014974.2 S1249S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5399-01A-01D-1501-10 chr19:8148161 G>A maps to NM_032447.3 Y2394Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5399-01A-01D-1501-10 chr11:5068522 A>T maps to NM_001001916.2 S256S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5399-01A-01D-1501-10 chr3:52668816 C>A maps to ENST00000296302 E368*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5399-01A-01D-1501-10 chr6:117647552 C>T maps to NM_002944.2 Q1797Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5399-01A-01D-1501-10 chr3:47164612 C>A maps to NM_014159.6 E505*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5399-01A-01D-1501-10 chr15:62978976 A>G maps to NM_015059.2 S365S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5399-01A-01D-1501-10 chr6:150267505 A>G did not map to a codon.
Sequencing variant TCGA-B0-5400-01A-01D-1501-10 chr3:52246386 G>A maps to ENST00000441729 R588R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5400-01A-01D-1501-10 chr13:26148984 G>T maps to NM_016529.4 E568*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5400-01A-01D-1501-10 chr10:90966989 C>T maps to NM_003956.3 L20L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5400-01A-01D-1501-10 chr10:90966989 C>T maps to NM_003956.3 L20L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5400-01A-01D-1501-10 chr4:153244134 C>G maps to NM_033632.2 R674R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5400-01A-01D-1501-10 chrX:12736619 C>A maps to ENST00000429478 G1215G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5400-01A-01D-1501-10 chrX:12736619 C>A maps to ENST00000429478 G1215G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5400-01A-01D-1501-10 chr2:128263301 G>T maps to NM_017969.2 G59G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5400-01A-01D-1501-10 chr17:39619146 G>A maps to NM_002278.3 D384D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5400-01A-01D-1501-10 chr22:24373818 T>C maps to NM_001144931.1 S106S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5400-01A-01D-1501-10 chr22:24373818 T>C maps to NM_001144931.1 S106S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5400-01A-01D-1501-10 chr10:50121786 G>A maps to NM_001006939.3 T138T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5400-01A-01D-1501-10 chr2:191334580 G>T maps to NM_017694.3 G544*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5400-01A-01D-1501-10 chr1:20233087 A>G maps to NM_015207.1 A333A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5400-01A-01D-1501-10 chrX:54043170 T>C did not map to a codon.
Sequencing variant TCGA-B0-5400-01A-01D-1501-10 chrX:54043170 T>C did not map to a codon.
Sequencing variant TCGA-B0-5400-01A-01D-1501-10 chr12:18649022 T>C maps to NM_004570.4 L900L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5400-01A-01D-1501-10 chr12:18649022 T>C maps to NM_004570.4 L900L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5400-01A-01D-1501-10 chr1:93307321 G>C did not map to a codon.
Sequencing variant TCGA-B0-5400-01A-01D-1501-10 chr1:93307321 G>C did not map to a codon.
Sequencing variant TCGA-B0-5400-01A-01D-1501-10 chr7:82996991 G>A maps to NM_012431.2 P746P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5400-01A-01D-1501-10 chr1:234599595 T>C maps to NM_005646.3 P462P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5400-01A-01D-1501-10 chr2:133175093 G>A maps to NM_001508.2 W160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5400-01A-01D-1501-10 chr2:133175093 G>A maps to NM_001508.2 W160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5400-01A-01D-1501-10 chr20:33345743 C>T maps to NM_014071.2 Q269Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5400-01A-01D-1501-10 chr20:33345743 C>T maps to NM_014071.2 Q269Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5400-01A-01D-1501-10 chr19:39591390 T>G maps to NM_001004318.2 G235G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5400-01A-01D-1501-10 chr19:39591390 T>G maps to NM_001004318.2 G235G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5402-01A-01D-1501-10 chrX:119500535 C>T maps to NM_001142447.2 Q74*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5402-01A-01D-1501-10 chr8:139845295 C>T maps to NM_152888.1 V277V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5402-01A-01D-1501-10 chr5:45262589 C>T maps to NM_021072.2 A702A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5402-01A-01D-1501-10 chr21:44323940 A>G maps to NM_021075.3 R273R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5402-01A-01D-1501-10 chr12:20792853 T>A maps to NM_000921.3 Y738*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5402-01A-01D-1501-10 chr3:10191571 G>T maps to NM_000551.2 E189*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5691-01A-11D-1534-10 chr12:9008180 G>A maps to NM_144670.3 T947T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5691-01A-11D-1534-10 chr3:112969549 G>T maps to ENST00000273395 L82L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5691-01A-11D-1534-10 chr3:112969549 G>T maps to ENST00000273395 L82L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5691-01A-11D-1534-10 chr20:60511820 C>T maps to NM_001794.2 P857P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5691-01A-11D-1534-10 chrX:10180544 C>T maps to NM_001830.3 G476G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5691-01A-11D-1534-10 chr4:1388499 C>T maps to NM_175918.3 H67H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5691-01A-11D-1534-10 chr2:84912546 T>C maps to NM_001370.1 I2338I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5691-01A-11D-1534-10 chrX:37028222 C>A maps to NM_001013736.2 S580S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5691-01A-11D-1534-10 chr19:18497193 C>A maps to NM_004864.2 T65T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5691-01A-11D-1534-10 chr17:40004450 A>C maps to NM_152467.3 P573P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5691-01A-11D-1534-10 chr17:39197613 G>A maps to NM_030967.2 P12P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5691-01A-11D-1534-10 chr17:39197637 A>G maps to NM_030967.2 C4C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5691-01A-11D-1534-10 chrX:78011221 G>T maps to NM_005296.2 E286*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5691-01A-11D-1534-10 chrX:119005936 G>A maps to NM_004541.3 L21L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5691-01A-11D-1534-10 chr6:2836101 C>T maps to NM_030666.2 T241T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5691-01A-11D-1534-10 chr20:21321459 A>T maps to NM_012255.3 A460A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5691-01A-11D-1534-10 chr20:39832046 C>A maps to NM_015035.3 E504*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5692-01A-11D-1534-10 chr7:20685685 T>A maps to NM_001163941.1 Y302*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5692-01A-11D-1534-10 chr16:4776982 G>C maps to NM_133450.2 L122L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5692-01A-11D-1534-10 chr2:69034591 G>A maps to NM_001007231.2 G218G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5692-01A-11D-1534-10 chr6:17556591 A>G maps to NM_006366.2 R451R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5692-01A-11D-1534-10 chr21:19629057 G>A maps to NM_024944.2 W104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5692-01A-11D-1534-10 chr17:48266573 A>G maps to NM_000088.3 P964P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5692-01A-11D-1534-10 chr17:48266573 A>G maps to NM_000088.3 P964P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5692-01A-11D-1534-10 chr7:30701794 G>T maps to ENST00000348438 G272G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5692-01A-11D-1534-10 chr5:39376875 T>A maps to NM_001343.2 G671G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5692-01A-11D-1534-10 chr8:21903770 C>A maps to NM_003867.2 I73I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5692-01A-11D-1534-10 chr11:65653800 C>T maps to NM_198897.1 R168R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5692-01A-11D-1534-10 chr1:35227532 C>T maps to NM_153212.2 C226C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5692-01A-11D-1534-10 chr16:14304163 A>G maps to NM_014048.3 P73P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5692-01A-11D-1534-10 chr16:14304163 A>G maps to NM_014048.3 P73P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5692-01A-11D-1534-10 chr17:10253891 C>T maps to NM_003802.2 A375A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5692-01A-11D-1534-10 chr2:192228922 C>A maps to NM_001130158.1 S318*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5692-01A-11D-1534-10 chr17:36943163 G>A maps to NM_003559.4 L57L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5692-01A-11D-1534-10 chr18:9570185 T>A maps to NM_001042388.1 L514L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5692-01A-11D-1534-10 chr5:139217289 G>A maps to NM_032289.2 R582R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5692-01A-11D-1534-10 chr1:32377373 C>T maps to NM_080391.3 W81*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5692-01A-11D-1534-10 chr15:79264228 G>A maps to NM_002891.4 Y1236Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5692-01A-11D-1534-10 chr10:6143319 C>T maps to NM_001145547.1 D70D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5692-01A-11D-1534-10 chr6:35212547 C>T maps to ENST00000394681 S803S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5692-01A-11D-1534-10 chr7:149485495 G>A maps to NM_198455.2 W1302*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5692-01A-11D-1534-10 chr15:42500324 C>T maps to ENST00000348544 P9P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5692-01A-11D-1534-10 chr19:58805701 C>G maps to NM_021089.2 L176L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5692-01A-11D-1534-10 chr17:26087757 G>A maps to NM_000625.4 F967F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5692-01A-11D-1534-10 chr17:26087757 G>A maps to NM_000625.4 F967F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5693-01A-11D-1534-10 chr7:45725769 G>A maps to NM_021116.2 T761T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5693-01A-11D-1534-10 chr3:119242474 G>T maps to NM_016589.3 E244*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5693-01A-11D-1534-10 chr18:55233772 A>G maps to NM_001012515.2 P174P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5693-01A-11D-1534-10 chr17:39412062 C>A maps to ENST00000431129 P148P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5693-01A-11D-1534-10 chr17:21215482 C>T maps to NM_145109.2 Y268Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5693-01A-11D-1534-10 chr9:112918732 G>T maps to NM_007203.4 E1044*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5693-01A-11D-1534-10 chr9:86276809 G>C maps to NM_013438.4 L554L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5693-01A-11D-1534-10 chr9:86276809 G>C maps to NM_013438.4 L554L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5693-01A-11D-1534-10 chr5:112899758 T>C maps to NM_022828.3 A882A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5693-01A-11D-1534-10 chr10:17195590 T>C maps to NM_004412.5 E330E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5693-01A-11D-1534-10 chr10:17195590 T>C maps to NM_004412.5 E330E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5693-01A-11D-1534-10 chr15:41191987 A>C maps to NM_020857.2 P324P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5693-01A-11D-1534-10 chr15:41191987 A>C maps to NM_020857.2 P324P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5694-01A-11D-1534-10 chr2:216184410 G>T maps to NM_004044.6 E83*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5694-01A-11D-1534-10 chr7:76112182 C>T maps to NM_020892.2 P209P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5694-01A-11D-1534-10 chr15:89859677 A>G maps to NM_001113378.1 K1325K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5694-01A-11D-1534-10 chr5:141028859 G>A maps to ENST00000354789 Q132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5694-01A-11D-1534-10 chr17:39595483 G>A maps to NM_006771.3 Q235*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5694-01A-11D-1534-10 chr1:37975130 G>A maps to NM_022756.4 S73S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5694-01A-11D-1534-10 chr3:52692234 G>A maps to ENST00000296302 Q209*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5694-01A-11D-1534-10 chr3:52692234 G>A maps to ENST00000296302 Q209*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5694-01A-11D-1534-10 chr6:72960118 T>A maps to NM_014989.4 R776R. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-B0-5694-01A-11D-1534-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-B0-5694-01A-11D-1534-10 chr1:151342243 A>C maps to ENST00000435071 A44A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5694-01A-11D-1534-10 chr20:1460663 G>T maps to NM_001122962.1 P44P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5694-01A-11D-1534-10 chr6:43221355 G>T maps to NM_032538.1 T127T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5694-01A-11D-1534-10 chr17:33498339 G>C did not map to a codon.
Sequencing variant TCGA-B0-5694-01A-11D-1534-10 chr2:167760330 C>T maps to NM_152381.5 A113A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5694-01A-11D-1534-10 chr4:145568087 A>C maps to NM_022475.1 L87L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5694-01A-11D-1534-10 chr4:145568087 A>C maps to NM_022475.1 L87L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5694-01A-11D-1534-10 chr16:30750867 A>G maps to NM_006662.2 V3169V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5694-01A-11D-1534-10 chr16:30750867 A>G maps to NM_006662.2 V3169V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5694-01A-11D-1534-10 chr5:124079965 C>G maps to NM_020747.2 G239G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5694-01A-11D-1534-10 chr5:124079965 C>G maps to NM_020747.2 G239G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5695-01A-11D-1534-10 chr2:216211657 T>C maps to NM_004044.6 I499I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5695-01A-11D-1534-10 chr1:174973752 C>T maps to NM_014412.2 Q7*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5695-01A-11D-1534-10 chr7:76829077 T>C maps to NM_006682.2 S11S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5695-01A-11D-1534-10 chr7:4780486 C>T maps to ENST00000450194 P19P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5695-01A-11D-1534-10 chr19:49249007 C>A maps to NM_182575.2 E37*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5695-01A-11D-1534-10 chr19:42930827 C>T maps to NM_005357.2 A158A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5695-01A-11D-1534-10 chr7:156518212 A>G maps to ENST00000354505 L399L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5695-01A-11D-1534-10 chr7:133812164 T>C maps to NM_144648.1 S15S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5695-01A-11D-1534-10 chr15:56208588 A>G maps to ENST00000508342 C147C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5695-01A-11D-1534-10 chr9:8500874 A>T maps to NM_002839.3 T669T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5695-01A-11D-1534-10 chr6:159420741 A>T maps to NM_031924.4 G89G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5695-01A-11D-1534-10 chr14:92470128 C>T maps to NM_004239.3 Q1397Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5695-01A-11D-1534-10 chr7:138822684 G>A maps to NM_024926.2 E78E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5695-01A-11D-1534-10 chr11:17544963 A>C did not map to a codon.
Sequencing variant TCGA-B0-5695-01A-11D-1534-10 chr11:17544963 A>C did not map to a codon.
Sequencing variant TCGA-B0-5695-01A-11D-1534-10 chr4:144106647 G>A maps to NM_032557.5 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5695-01A-11D-1534-10 chr3:10191481 A>T maps to NM_000551.2 K159*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5695-01A-11D-1534-10 chrX:107304758 C>T maps to NM_001170553.1 T105T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5696-01A-11D-1534-10 chr19:6714021 C>A maps to NM_000064.2 E252*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5696-01A-11D-1534-10 chr1:9019021 T>C maps to ENST00000413627 D158D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5696-01A-11D-1534-10 chr17:48647165 T>A did not map to a codon.
Sequencing variant TCGA-B0-5696-01A-11D-1534-10 chr10:16957109 A>G maps to NM_001081.3 N2424N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5696-01A-11D-1534-10 chr8:144940461 G>A maps to NM_031308.1 S2320S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5696-01A-11D-1534-10 chr8:144940473 C>T maps to NM_031308.1 G2316G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5696-01A-11D-1534-10 chr8:144940539 G>A maps to NM_031308.1 G2294G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5696-01A-11D-1534-10 chr2:170411719 T>C maps to NM_024622.3 L376L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5696-01A-11D-1534-10 chr5:127645723 G>A maps to NM_001999.3 C1717C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5696-01A-11D-1534-10 chr22:17449241 T>A maps to NM_001037814.1 G323G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5696-01A-11D-1534-10 chr19:49657753 G>A maps to NM_002152.2 D247D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5696-01A-11D-1534-10 chr6:42832808 G>A maps to NM_015349.1 L955L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5696-01A-11D-1534-10 chr12:50571221 T>C maps to NM_001113546.1 Q636Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5696-01A-11D-1534-10 chr10:129906187 C>A maps to NM_002417.4 E1306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5696-01A-11D-1534-10 chr10:22023040 A>C maps to NM_004641.3 P963P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5696-01A-11D-1534-10 chr20:33337537 A>G maps to NM_014071.2 D820D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5696-01A-11D-1534-10 chrX:123838861 C>A did not map to a codon.
Sequencing variant TCGA-B0-5696-01A-11D-1534-10 chr18:59821798 C>G maps to NM_176787.4 T176T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5696-01A-11D-1534-10 chr7:121651685 G>A maps to NM_002851.2 V862V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5696-01A-11D-1534-10 chr17:71415435 G>T maps to NM_001144952.1 L685L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5696-01A-11D-1534-10 chr1:201860696 G>T did not map to a codon.
Sequencing variant TCGA-B0-5696-01A-11D-1534-10 chr4:123868399 G>T maps to NM_145207.2 G491*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5696-01A-11D-1534-10 chr10:46968664 G>A maps to NM_031912.3 L91L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5696-01A-11D-1534-10 chr19:31770506 G>A maps to NM_020856.2 A64A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5696-01A-11D-1534-10 chr8:24775662 G>A maps to NM_005382.2 G765G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5696-01A-11D-1534-10 chr8:24775662 G>A maps to NM_005382.2 G765G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5696-01A-11D-1534-10 chrY:4966254 G>T did not map to a codon.
Sequencing variant TCGA-B0-5696-01A-11D-1534-10 chrY:4966254 G>T did not map to a codon.
Sequencing variant TCGA-B0-5697-01A-11D-1534-10 chr5:180377359 T>A maps to NM_001040462.2 L440*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5697-01A-11D-1534-10 chr6:110714418 C>T maps to NM_003649.2 K223K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5697-01A-11D-1534-10 chr17:7669720 G>A maps to NM_020877.2 E1199E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5697-01A-11D-1534-10 chrX:9714192 C>T maps to ENST00000380929 R203R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5697-01A-11D-1534-10 chr10:96352149 A>T did not map to a codon.
Sequencing variant TCGA-B0-5697-01A-11D-1534-10 chr14:63473093 G>T maps to NM_139318.3 Y98*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5697-01A-11D-1534-10 chr14:63473093 G>T maps to NM_139318.3 Y98*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5697-01A-11D-1534-10 chr9:73027802 A>G maps to NM_001206.2 H159H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5697-01A-11D-1534-10 chr1:241723980 C>G maps to NM_003679.3 P126P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5697-01A-11D-1534-10 chr6:161781135 T>C maps to NM_004562.2 V423V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5697-01A-11D-1534-10 chr6:161781135 T>C maps to NM_004562.2 V423V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5697-01A-11D-1534-10 chr4:87684096 T>A maps to NM_080685.2 S1257S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5697-01A-11D-1534-10 chr14:73550236 A>G maps to NM_021239.2 Q120Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5697-01A-11D-1534-10 chr17:34249623 C>T maps to NM_145654.3 K208K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5697-01A-11D-1534-10 chr1:213341273 C>T maps to NM_012424.3 I303I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5697-01A-11D-1534-10 chr1:213341273 C>T maps to NM_012424.3 I303I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5697-01A-11D-1534-10 chr4:77941775 T>G maps to ENST00000510515 L312L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5697-01A-11D-1534-10 chr1:53608094 C>T maps to NM_006671.4 R9R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5697-01A-11D-1534-10 chr10:46962002 G>C maps to NM_031912.3 R411R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5697-01A-11D-1534-10 chr8:110131431 C>T maps to NM_003301.4 I315I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5697-01A-11D-1534-10 chr5:140085214 G>T maps to NM_144723.1 A158A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5697-01A-11D-1534-10 chr6:27420476 G>A maps to NM_007149.2 F287F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5697-01A-11D-1534-10 chr20:30432838 C>T maps to NM_004118.3 L169L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5697-01A-11D-1534-10 chr20:30432838 C>T maps to NM_004118.3 L169L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5699-01A-11D-1534-10 chr10:52601745 T>A maps to NM_138932.2 K81*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5699-01A-11D-1534-10 chr15:78486922 G>A maps to NM_015162.4 R126R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5699-01A-11D-1534-10 chr14:32563339 T>G maps to NM_001030055.1 Y1155*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5699-01A-11D-1534-10 chr14:50579392 T>C maps to NM_024558.2 K205K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5699-01A-11D-1534-10 chr2:62934346 A>G maps to NM_015252.3 R7R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5699-01A-11D-1534-10 chr2:62934346 A>G maps to NM_015252.3 R7R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5699-01A-11D-1534-10 chr1:35250611 C>T maps to NM_001005752.1 F83F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5699-01A-11D-1534-10 chr11:122930928 A>G maps to NM_006597.3 S153S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5699-01A-11D-1534-10 chr18:59854884 T>G maps to NM_020854.3 P49P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5699-01A-11D-1534-10 chr17:72769712 A>G did not map to a codon.
Sequencing variant TCGA-B0-5699-01A-11D-1534-10 chr11:19955241 C>A maps to ENST00000396087 G507G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5699-01A-11D-1534-10 chr4:2948136 A>G did not map to a codon.
Sequencing variant TCGA-B0-5699-01A-11D-1534-10 chr6:150094280 A>G maps to NM_005389.2 Q114Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5699-01A-11D-1534-10 chr3:126707666 C>T maps to NM_032242.3 N77N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5699-01A-11D-1534-10 chr3:126707666 C>T maps to NM_032242.3 N77N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5699-01A-11D-1534-10 chr3:47164497 G>T maps to NM_014159.6 S543*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5699-01A-11D-1534-10 chr7:87483611 T>C maps to NM_018843.3 V57V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5699-01A-11D-1534-10 chr6:35922940 G>A maps to NM_052961.3 V740V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5699-01A-11D-1534-10 chr6:33408547 G>A maps to NM_006772.2 R573R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5699-01A-11D-1534-10 chr4:70346628 C>G did not map to a codon.
Sequencing variant TCGA-B0-5699-01A-11D-1534-10 chr20:47887949 C>T maps to NM_021035.2 K133K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5701-01A-11D-1534-10 chr2:242606246 G>T maps to ENST00000337606 T358T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5701-01A-11D-1534-10 chr3:107463493 C>T maps to NM_001142568.1 C229C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5701-01A-11D-1534-10 chr3:107463493 C>T maps to NM_001142568.1 C229C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5701-01A-11D-1534-10 chr19:39233679 C>T maps to NM_144691.3 G100G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5701-01A-11D-1534-10 chr16:65038637 C>T maps to NM_001797.2 G45G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5701-01A-11D-1534-10 chr11:117244471 G>A maps to NM_014956.4 L386L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5701-01A-11D-1534-10 chr15:45453966 G>A maps to NM_175940.1 Q1296Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5701-01A-11D-1534-10 chr14:89168918 C>G maps to ENST00000380664 V703V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5701-01A-11D-1534-10 chr22:26859936 C>G maps to NM_022081.4 L553L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5701-01A-11D-1534-10 chr18:77659530 C>T maps to NM_012283.1 Y372Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5701-01A-11D-1534-10 chr2:44176771 T>A maps to NM_133259.3 G568G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5701-01A-11D-1534-10 chr19:41132931 G>T maps to ENST00000308370 P1412P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5701-01A-11D-1534-10 chr2:1946772 C>T maps to ENST00000399161 E162E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5701-01A-11D-1534-10 chr1:201772832 A>G maps to ENST00000367296 K1210K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5701-01A-11D-1534-10 chr22:50956418 C>T maps to NM_001185011.1 P146P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5701-01A-11D-1534-10 chr11:123909162 G>C maps to NM_001004463.1 P182P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5701-01A-11D-1534-10 chr11:6220794 C>A maps to NM_001005178.1 A114A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5701-01A-11D-1534-10 chr3:155212208 G>A maps to ENST00000340059 L652L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5701-01A-11D-1534-10 chr1:45288275 A>T maps to NM_003738.4 L1141L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5701-01A-11D-1534-10 chr3:125702159 G>A maps to NM_001012337.1 E212E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5701-01A-11D-1534-10 chr16:51174806 G>C maps to ENST00000251020 S442S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5701-01A-11D-1534-10 chr12:56567524 A>G maps to NM_003075.3 A535A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5701-01A-11D-1534-10 chr11:120989264 G>A maps to NM_005422.2 L347L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5701-01A-11D-1534-10 chr1:246707836 T>C maps to NM_022366.2 V335V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5701-01A-11D-1534-10 chr2:179435408 C>T maps to NM_133378.4 Q22582Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5701-01A-11D-1534-10 chr2:179435408 C>T maps to NM_133378.4 Q22582Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5701-01A-11D-1534-10 chr17:61886960 T>C maps to NM_203499.1 L398L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5701-01A-11D-1534-10 chr17:61886960 T>C maps to NM_203499.1 L398L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5702-01A-11D-1534-10 chr17:40054058 C>A maps to ENST00000401700 E512*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5702-01A-11D-1534-10 chr12:76740156 A>G maps to NM_024685.3 Y536Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5702-01A-11D-1534-10 chr1:92470104 G>A maps to ENST00000347608 R853R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5702-01A-11D-1534-10 chr20:31671266 T>C maps to NM_182519.2 G88G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5702-01A-11D-1534-10 chr20:31671266 T>C maps to NM_182519.2 G88G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5702-01A-11D-1534-10 chr6:88074933 C>T maps to NM_001010868.2 I270I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5702-01A-11D-1534-10 chr8:62412011 A>T did not map to a codon.
Sequencing variant TCGA-B0-5702-01A-11D-1534-10 chr1:86362086 T>G maps to NM_152890.5 S928S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5702-01A-11D-1534-10 chr17:27225662 C>T maps to NM_144683.3 L310L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5702-01A-11D-1534-10 chr17:27225662 C>T maps to NM_144683.3 L310L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5702-01A-11D-1534-10 chr2:48050391 A>T maps to NM_001190274.1 T502T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5702-01A-11D-1534-10 chr1:152324077 C>A maps to NM_001014342.2 G2062*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5702-01A-11D-1534-10 chr8:36790509 C>A maps to NM_001031836.2 R1002R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5702-01A-11D-1534-10 chr12:52629133 G>T maps to NM_005556.3 E174*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5702-01A-11D-1534-10 chr18:21441743 C>A maps to ENST00000416669 V1521V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5702-01A-11D-1534-10 chr3:65425578 C>T maps to NM_001033057.1 Q415Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5702-01A-11D-1534-10 chr12:68720391 G>A maps to NM_020128.2 F181F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5702-01A-11D-1534-10 chr22:50558940 C>T maps to NM_018995.2 R489*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5702-01A-11D-1534-10 chr1:226561929 A>G maps to NM_001618.3 Y689Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5702-01A-11D-1534-10 chr1:226561929 A>G maps to NM_001618.3 Y689Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5702-01A-11D-1534-10 chr1:20466688 C>T maps to NM_022819.3 T49T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5702-01A-11D-1534-10 chr2:170806128 T>C maps to ENST00000442603 A1033A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5702-01A-11D-1534-10 chr2:170806129 C>T maps to ENST00000442603 Q1034*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5702-01A-11D-1534-10 chr16:19127312 C>T maps to NM_001034841.3 Y510Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5702-01A-11D-1534-10 chr16:19127312 C>T maps to NM_001034841.3 Y510Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5702-01A-11D-1534-10 chrX:20074910 T>C did not map to a codon.
Sequencing variant TCGA-B0-5702-01A-11D-1534-10 chrX:20074910 T>C did not map to a codon.
Sequencing variant TCGA-B0-5702-01A-11D-1534-10 chr12:11506349 C>T maps to NM_005039.3 Q229Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5702-01A-11D-1534-10 chr12:11506349 C>T maps to NM_005039.3 Q229Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5703-01A-11D-1534-10 chr11:108115599 C>T maps to NM_000051.3 R250*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5703-01A-11D-1534-10 chr11:108115599 C>T maps to NM_000051.3 R250*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5703-01A-11D-1534-10 chr17:30660438 T>C maps to NM_022344.2 L324L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5703-01A-11D-1534-10 chr1:113192052 A>T maps to NM_006135.2 L39L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5703-01A-11D-1534-10 chr1:113192052 A>T maps to NM_006135.2 L39L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5703-01A-11D-1534-10 chr10:101151191 A>G did not map to a codon.
Sequencing variant TCGA-B0-5703-01A-11D-1534-10 chr16:21136610 G>C maps to NM_017539.1 S430*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5703-01A-11D-1534-10 chr9:112005947 A>G maps to NM_019114.3 P453P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5703-01A-11D-1534-10 chr1:169528478 T>C maps to ENST00000367796 L214L. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-B0-5703-01A-11D-1534-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-B0-5703-01A-11D-1534-10 chr2:241662860 C>T maps to ENST00000373308 W1486*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5703-01A-11D-1534-10 chr2:241662860 C>T maps to ENST00000373308 W1486*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5703-01A-11D-1534-10 chr11:56431823 C>A maps to NM_001004730.1 I221I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5703-01A-11D-1534-10 chr22:22893220 A>C maps to NM_206954.1 L104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5703-01A-11D-1534-10 chr9:79325302 G>T maps to NM_015225.2 L629L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5703-01A-11D-1534-10 chr1:240969478 G>A maps to ENST00000407727 N410N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5703-01A-11D-1534-10 chr2:86980657 C>T maps to NM_022780.3 V166V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5703-01A-11D-1534-10 chr19:39965286 C>T maps to NM_003169.3 Q985*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5703-01A-11D-1534-10 chr5:135382105 G>A maps to NM_000358.2 K127K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5703-01A-11D-1534-10 chr5:135382106 C>T maps to NM_000358.2 L128L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5703-01A-11D-1534-10 chr17:33477187 G>A maps to NM_173167.2 R109R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5703-01A-11D-1534-10 chr19:53856729 G>A maps to NM_138374.1 K934K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5703-01A-11D-1534-10 chr5:76348571 T>C maps to NM_018046.4 Y469Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5703-01A-11D-1534-10 chr5:76348571 T>C maps to NM_018046.4 Y469Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5703-01A-11D-1534-10 chr17:19641665 C>T maps to NM_000691.4 L439L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5703-01A-11D-1534-10 chr17:19641665 C>T maps to NM_000691.4 L439L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5703-01A-11D-1534-10 chr6:168377134 T>C maps to NM_001129895.1 Q66Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5703-01A-11D-1534-10 chr6:168377134 T>C maps to NM_001129895.1 Q66Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5703-01A-11D-1534-10 chr20:17640579 T>G maps to ENST00000377813 T191T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5703-01A-11D-1534-10 chr20:17640579 T>G maps to ENST00000377813 T191T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5705-01A-11D-1534-10 chr5:178555035 G>A maps to NM_014244.4 N847N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5705-01A-11D-1534-10 chr7:117876196 C>T maps to ENST00000357099 Q211*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5705-01A-11D-1534-10 chr2:219886631 G>C maps to NM_194302.2 A1000A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5705-01A-11D-1534-10 chr2:219886631 G>C maps to NM_194302.2 A1000A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5705-01A-11D-1534-10 chr18:34833812 C>T maps to NM_020180.3 V474V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5705-01A-11D-1534-10 chr16:53340242 T>C maps to ENST00000219084 N2238N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5705-01A-11D-1534-10 chr4:40356026 C>T maps to NM_017581.2 I310I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5705-01A-11D-1534-10 chr16:3065983 C>T maps to NM_021195.4 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5705-01A-11D-1534-10 chr1:197446955 C>T maps to NM_201253.2 R1390*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5705-01A-11D-1534-10 chr21:45053271 C>A maps to NM_007031.1 E108*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5705-01A-11D-1534-10 chr5:55256362 G>T maps to NM_002184.3 T280T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5705-01A-11D-1534-10 chr2:97267382 T>C maps to ENST00000421845 S897S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5705-01A-11D-1534-10 chr17:16021255 A>G maps to ENST00000395857 F667F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5705-01A-11D-1534-10 chr6:154412360 C>A maps to NM_001145279.1 A399A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5705-01A-11D-1534-10 chr20:30784296 C>T maps to NM_002657.3 L483L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5705-01A-11D-1534-10 chr21:15599584 C>T maps to NM_144770.3 R273*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5705-01A-11D-1534-10 chr14:24617486 A>G maps to NM_017999.4 R120R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5705-01A-11D-1534-10 chr16:67304702 G>T maps to NM_004594.2 E761*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5705-01A-11D-1534-10 chr12:21471821 G>T maps to NM_134431.3 S32S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5705-01A-11D-1534-10 chr1:156243167 T>A maps to NM_015327.2 S206S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5705-01A-11D-1534-10 chr2:179634826 C>T maps to NM_133378.4 V2867V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5705-01A-11D-1534-10 chr2:128878019 G>A maps to NM_020120.3 W321*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5705-01A-11D-1534-10 chr19:57642737 C>A maps to NM_020903.2 R899R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5705-01A-11D-1534-10 chr19:57642745 T>C maps to NM_020903.2 P901P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5705-01A-11D-1534-10 chr15:42743698 A>G maps to NM_022473.1 N234N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5705-01A-11D-1534-10 chr16:49670776 C>T maps to NM_015069.2 E762E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5705-01A-11D-1534-10 chr12:6804738 C>T maps to NM_153685.2 L228L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5705-01A-11D-1534-10 chr12:6804738 C>T maps to NM_153685.2 L228L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5705-01A-11D-1534-10 chr6:108985391 A>G maps to NM_001455.3 Q452Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5705-01A-11D-1534-10 chr6:108985391 A>G maps to NM_001455.3 Q452Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5705-01A-11D-1534-10 chr8:24775662 G>A maps to NM_005382.2 G765G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5705-01A-11D-1534-10 chr8:24775662 G>A maps to NM_005382.2 G765G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5706-01A-11D-1534-10 chr7:150731894 C>T maps to ENST00000297504 S265S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5706-01A-11D-1534-10 chr17:79941540 C>T maps to ENST00000306729 N90N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5706-01A-11D-1534-10 chr1:156628841 G>A maps to NM_021948.3 E884E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5706-01A-11D-1534-10 chr4:128905553 C>T maps to ENST00000454347 S51S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5706-01A-11D-1534-10 chr17:37681092 C>T maps to NM_016507.2 Q1088*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5706-01A-11D-1534-10 chr4:155219150 A>T maps to NM_017639.3 P1650P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5706-01A-11D-1534-10 chr1:65831860 T>C maps to ENST00000371069 T175T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5706-01A-11D-1534-10 chr11:34670584 G>C maps to NM_012153.4 L121L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5706-01A-11D-1534-10 chr4:66467833 C>G maps to NM_004439.5 G145G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5706-01A-11D-1534-10 chr18:43700026 G>A did not map to a codon.
Multiple mappings detected for codon TCGA-B0-5706-01A-11D-1534-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-B0-5706-01A-11D-1534-10 chr5:66459284 C>T maps to NM_001164664.1 H1426H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5706-01A-11D-1534-10 chr19:54377172 C>T maps to NM_001020818.1 H130H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5706-01A-11D-1534-10 chr3:93624945 C>A maps to NM_000313.3 G130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5706-01A-11D-1534-10 chr1:84945168 C>A maps to NM_025065.6 R69R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5706-01A-11D-1534-10 chr19:51219978 G>A maps to ENST00000391814 D66D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5706-01A-11D-1534-10 chr4:69972924 T>C maps to NM_001074.2 D345D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5706-01A-11D-1534-10 chr21:33688960 G>A maps to NM_014825.2 F2150F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5706-01A-11D-1534-10 chr9:74971942 G>A maps to ENST00000437241 Q185*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5706-01A-11D-1534-10 chr9:74971942 G>A maps to ENST00000437241 Q185*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5706-01A-11D-1534-10 chr10:135106636 C>T maps to NM_006659.2 L310L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5706-01A-11D-1534-10 chr10:135106636 C>T maps to NM_006659.2 L310L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5707-01A-11D-1534-10 chr8:144124474 C>G maps to NM_173687.2 T19T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5707-01A-11D-1534-10 chr2:202687538 C>T maps to ENST00000450471 L152L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5707-01A-11D-1534-10 chr1:214830402 T>C maps to NM_016343.3 H2871H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5707-01A-11D-1534-10 chr1:214830402 T>C maps to NM_016343.3 H2871H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5707-01A-11D-1534-10 chr15:71403497 T>G maps to NM_001102658.1 R135R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5707-01A-11D-1534-10 chr15:65957693 C>T maps to ENST00000443035 W1783*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5707-01A-11D-1534-10 chr15:65957693 C>T maps to ENST00000443035 W1783*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5707-01A-11D-1534-10 chr13:33635591 T>C maps to NM_004795.3 D792D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5707-01A-11D-1534-10 chr6:136500188 G>A maps to NM_018945.3 R286R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5707-01A-11D-1534-10 chr19:55713577 C>T maps to NM_002842.3 E333E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5707-01A-11D-1534-10 chr1:237796990 A>G maps to NM_001035.2 E2223E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5707-01A-11D-1534-10 chr7:5396760 C>A maps to NM_001080495.2 G1660G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5707-01A-11D-1534-10 chr19:12060407 T>C maps to NM_144566.1 F523F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5707-01A-11D-1534-10 chr1:171526992 A>C maps to ENST00000392078 P1914P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5707-01A-11D-1534-10 chr1:171526992 A>C maps to ENST00000392078 P1914P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5707-01A-11D-1534-10 chrX:129150164 G>A maps to ENST00000303743 V1139V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5707-01A-11D-1534-10 chrX:129150164 G>A maps to ENST00000303743 V1139V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5707-01A-11D-1534-10 chr9:133799696 C>T maps to NM_001145106.1 L213L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5707-01A-11D-1534-10 chr9:133799696 C>T maps to NM_001145106.1 L213L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5707-01A-11D-1534-10 chr8:24775662 G>A maps to NM_005382.2 G765G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5707-01A-11D-1534-10 chr8:24775662 G>A maps to NM_005382.2 G765G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5707-01A-11D-1534-10 chr9:140137359 T>C maps to NM_006088.5 S230S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5707-01A-11D-1534-10 chr9:140137359 T>C maps to NM_006088.5 S230S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5709-01A-11D-1534-10 chrX:15591565 C>A maps to NM_021804.2 E489*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5709-01A-11D-1534-10 chr11:6423906 G>A maps to ENST00000389906 L385L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5709-01A-11D-1534-10 chr1:201041937 C>T maps to NM_000069.2 E724E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5709-01A-11D-1534-10 chr6:70878566 C>T maps to NM_001858.4 G854G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5709-01A-11D-1534-10 chr15:51778457 G>T maps to NM_001174116.1 S1765*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5709-01A-11D-1534-10 chr15:51778459 A>G maps to NM_001174116.1 T1764T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5709-01A-11D-1534-10 chr5:14693051 C>T maps to NM_138348.4 V318V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5709-01A-11D-1534-10 chr10:104118422 G>T maps to NM_004193.2 G316G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5709-01A-11D-1534-10 chrX:104961378 C>G maps to NM_017416.1 P264P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5709-01A-11D-1534-10 chr21:35144368 G>C maps to NM_003024.2 T349T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5709-01A-11D-1534-10 chr10:133961487 C>G maps to NM_001105521.2 L594L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5709-01A-11D-1534-10 chr11:47599122 T>C maps to NM_018095.4 Q159Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5709-01A-11D-1534-10 chrX:154010063 C>A maps to NM_002436.3 P320P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5709-01A-11D-1534-10 chrX:154010063 C>A maps to NM_002436.3 P320P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5709-01A-11D-1534-10 chr6:29054172 A>G maps to NM_001005226.2 L285L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5709-01A-11D-1534-10 chr7:94540663 C>T maps to NM_001166160.1 D413D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5709-01A-11D-1534-10 chr7:82997338 T>A maps to NM_012431.2 R631*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5709-01A-11D-1534-10 chr7:107334907 C>T maps to NM_000441.1 L442L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5709-01A-11D-1534-10 chr12:23998949 T>A maps to NM_006940.4 K150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5709-01A-11D-1534-10 chr19:47228596 C>G maps to NM_001039877.1 R495R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5709-01A-11D-1534-10 chr19:47228596 C>G maps to NM_001039877.1 R495R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5709-01A-11D-1534-10 chr11:125479361 C>A maps to NM_152713.3 S332*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5709-01A-11D-1534-10 chrX:132351936 C>T maps to NM_016521.2 K117K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5709-01A-11D-1534-10 chr3:12545141 C>T maps to NM_025265.3 L230L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5709-01A-11D-1534-10 chr2:190324064 G>A maps to NM_032168.1 R231R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5709-01A-11D-1534-10 chr6:28329174 A>G maps to NM_024493.2 Q159Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5709-01A-11D-1534-10 chr8:3245040 C>T maps to NM_033225.5 W919*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5709-01A-11D-1534-10 chr8:3245040 C>T maps to NM_033225.5 W919*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5709-01A-11D-1534-10 chr2:70057233 G>A maps to NM_178439.3 E70E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5709-01A-11D-1534-10 chr2:70057233 G>A maps to NM_178439.3 E70E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5709-01A-11D-1534-10 chrX:149639326 G>A maps to NM_005491.3 Q494Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5709-01A-11D-1534-10 chrX:149639326 G>A maps to NM_005491.3 Q494Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-3924-01A-02D-1386-10 chr17:54452061 A>G maps to NM_153228.2 V302V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-3924-01A-02D-1386-10 chr1:228285382 G>A maps to NM_001024228.1 R117R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-3924-01A-02D-1386-10 chr7:97487670 C>A maps to NM_183356.3 L274L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-3924-01A-02D-1386-10 chr7:70228159 G>A maps to NM_015570.2 Q349Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-3924-01A-02D-1386-10 chr11:375477 C>T maps to NM_178537.4 P267P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-3924-01A-02D-1386-10 chr19:44237822 G>A maps to NM_019108.2 L389L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-3924-01A-02D-1386-10 chr12:7177660 T>G maps to NM_001734.3 P591P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-3924-01A-02D-1386-10 chr6:83823097 A>G maps to NM_015018.2 T246T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-3924-01A-02D-1386-10 chr8:145735860 C>A maps to NM_138431.1 S267S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-3924-01A-02D-1386-10 chr17:18044109 C>T maps to ENST00000205890 P1790P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-3924-01A-02D-1386-10 chr2:152348618 A>C maps to NM_001164507.1 T8350T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-3924-01A-02D-1386-10 chr11:55406261 C>A maps to NM_001004124.1 I143I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-3924-01A-02D-1386-10 chr4:30725279 A>T maps to NM_001173523.1 K746*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-3924-01A-02D-1386-10 chr5:140762930 C>T maps to NM_018920.2 S155S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-3924-01A-02D-1386-10 chr13:73482728 C>T maps to NM_006346.2 Q517*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-3924-01A-02D-1386-10 chr20:48760153 C>T maps to NM_199203.2 K42K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-3924-01A-02D-1386-10 chrX:154754204 A>G maps to NM_018196.3 T90T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-3924-01A-02D-1386-10 chr3:130284102 A>G maps to NM_001102608.1 G309G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-3924-01A-02D-1386-10 chr3:130284102 A>G maps to NM_001102608.1 G309G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-3924-01A-02D-1386-10 chr6:168376846 C>G maps to NM_001129895.1 L162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-3924-01A-02D-1386-10 chr6:168376846 C>G maps to NM_001129895.1 L162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-3924-01A-02D-1386-10 chr21:46012290 A>G maps to NM_198688.2 C25C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-3924-01A-02D-1386-10 chr21:46012290 A>G maps to NM_198688.2 C25C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-3924-01A-02D-1386-10 chr22:46654830 A>G maps to NM_006071.1 S1463S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-3924-01A-02D-1386-10 chr22:46654830 A>G maps to NM_006071.1 S1463S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-3924-01A-02D-1386-10 chr19:40723223 A>G maps to NM_152479.5 C160C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-3924-01A-02D-1386-10 chr19:40723223 A>G maps to NM_152479.5 C160C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-4098-01A-02D-1386-10 chr9:138713194 C>T maps to ENST00000409386 P1115P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-4098-01A-02D-1386-10 chr15:49776508 A>G maps to NM_002009.3 K131K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-4098-01A-02D-1386-10 chr6:10529525 C>T maps to NM_145649.4 L128L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-4098-01A-02D-1386-10 chr4:158142837 C>T maps to NM_000826.3 G36G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-4098-01A-02D-1386-10 chr17:39316568 G>T maps to NM_032524.1 Y125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-4098-01A-02D-1386-10 chrX:123839010 C>T maps to NM_001163278.1 S289S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-4098-01A-02D-1386-10 chr1:248059094 G>T maps to NM_001001957.2 L69L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-4098-01A-02D-1386-10 chr5:149499608 G>A maps to NM_002609.3 S888S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-4098-01A-02D-1386-10 chr22:42992338 G>T maps to ENST00000415122 S239S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-4098-01A-02D-1386-10 chr15:55912368 T>A maps to NM_173814.4 T1098T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-4098-01A-02D-1386-10 chr3:128350831 T>A maps to NM_002950.3 R268*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-4098-01A-02D-1386-10 chr19:45996517 G>A maps to NM_005619.3 T311T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-4098-01A-02D-1386-10 chr8:110598353 G>A maps to NM_001099744.1 G155G. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-B2-4098-01A-02D-1386-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-B2-4098-01A-02D-1386-10 chr3:102157366 T>C maps to NM_175056.1 I28I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-4098-01A-02D-1386-10 chr17:76451800 G>A maps to ENST00000389840 Y3351Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-4098-01A-02D-1386-10 chr17:76451800 G>A maps to ENST00000389840 Y3351Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-4098-01A-02D-1386-10 chr22:25007057 A>T maps to NM_005265.2 K4*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-4098-01A-02D-1386-10 chr22:25007057 A>T maps to NM_005265.2 K4*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-4098-01A-02D-1386-10 chr9:35792437 A>G maps to NM_003995.3 A11A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-4098-01A-02D-1386-10 chr9:35792437 A>G maps to NM_003995.3 A11A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-4098-01A-02D-1386-10 chr12:11506581 C>T maps to NM_005039.3 *152*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-4098-01A-02D-1386-10 chr12:11506581 C>T maps to NM_005039.3 *152*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-4098-01A-02D-1386-10 chr17:72209749 C>T maps to NM_032646.5 Y8Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-4098-01A-02D-1386-10 chr17:72209749 C>T maps to NM_032646.5 Y8Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-4099-01A-02D-1251-10 chr4:175898845 C>T maps to NM_014269.4 R724*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-4099-01A-02D-1251-10 chrX:31196784 C>A maps to NM_004019.2 T340T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-4099-01A-02D-1251-10 chr11:6585251 C>T maps to NM_144666.2 C3394C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-4099-01A-02D-1251-10 chr5:149403937 T>C maps to ENST00000421549 N631N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-4099-01A-02D-1251-10 chr1:44128740 T>C maps to NM_014663.2 F202F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-4099-01A-02D-1251-10 chr17:10299726 G>A maps to NM_002472.2 Q1525*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-4099-01A-02D-1251-10 chrX:17746841 C>T maps to NM_198270.2 F1411F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-4099-01A-02D-1251-10 chr11:6024123 G>A maps to NM_001005179.2 P85P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-4099-01A-02D-1251-10 chr5:140532189 C>A maps to NM_018939.2 T784T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-4099-01A-02D-1251-10 chr14:88983530 C>T maps to NM_007039.3 K85K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-4099-01A-02D-1251-10 chr22:32587082 G>C maps to NM_001098527.2 T271T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-4099-01A-02D-1251-10 chr4:71648806 G>T did not map to a codon.
Sequencing variant TCGA-B2-4099-01A-02D-1251-10 chr1:237895426 C>A maps to NM_001035.2 R3673R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-4099-01A-02D-1251-10 chrX:48762339 C>T maps to ENST00000452555 G310G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-4099-01A-02D-1251-10 chr3:27451005 C>T maps to ENST00000454389 L594L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-4099-01A-02D-1251-10 chr14:64683101 C>G maps to NM_182914.2 P6513P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-4099-01A-02D-1251-10 chr1:46156751 C>T maps to NM_016486.3 F4F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-4099-01A-02D-1251-10 chr19:44740520 T>C maps to NM_182490.1 G646G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-4099-01A-02D-1251-10 chr3:183961712 G>T maps to NM_005787.5 R266R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-4099-01A-02D-1251-10 chr3:183961712 G>T maps to NM_005787.5 R266R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-4099-01A-02D-1251-10 chr1:16361874 A>G did not map to a codon.
Sequencing variant TCGA-B2-4099-01A-02D-1251-10 chr1:16361874 A>G did not map to a codon.
Sequencing variant TCGA-B2-4099-01A-02D-1251-10 chr9:35095478 G>A maps to NM_032634.2 F28F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-4099-01A-02D-1251-10 chr9:35095478 G>A maps to NM_032634.2 F28F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-4099-01A-02D-1251-10 chr7:73280190 T>C maps to NM_182504.3 T262T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-4099-01A-02D-1251-10 chr7:73280190 T>C maps to NM_182504.3 T262T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-5633-01A-01D-1534-10 chr3:193039502 C>A maps to NM_198505.2 E628*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-5633-01A-01D-1534-10 chr5:153372625 G>C maps to ENST00000442256 L483L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-5633-01A-01D-1534-10 chr13:99083479 G>T maps to NM_005766.2 E697*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-5633-01A-01D-1534-10 chr13:99083479 G>T maps to NM_005766.2 E697*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-5633-01A-01D-1534-10 chr12:14923793 C>T maps to NM_175054.2 E75E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-5633-01A-01D-1534-10 chr1:220316403 C>T maps to NM_018060.3 I893I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-5633-01A-01D-1534-10 chr11:18738323 G>A maps to NM_173588.3 F399F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-5633-01A-01D-1534-10 chr1:10364567 T>C maps to NM_183416.3 L1109L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-5633-01A-01D-1534-10 chr11:95825382 C>T maps to NM_032427.1 Q604Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-5633-01A-01D-1534-10 chr11:74717077 A>T maps to NM_006656.5 P309P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-5633-01A-01D-1534-10 chr16:69725994 C>A maps to NM_138713.2 S756*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-5633-01A-01D-1534-10 chr11:5152921 T>C maps to NM_001005160.2 *317W. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-5633-01A-01D-1534-10 chrX:50556988 G>A maps to NM_020717.3 Y10Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-5633-01A-01D-1534-10 chr11:60709587 A>C maps to NM_016582.2 L342L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-5633-01A-01D-1534-10 chr11:60709587 A>C maps to NM_016582.2 L342L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-5633-01A-01D-1534-10 chr1:67486081 A>C maps to NM_015139.2 A282A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-5633-01A-01D-1534-10 chr22:41742094 G>A maps to ENST00000351589 R532R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-5635-01A-01D-1534-10 chr1:19611596 A>G maps to NM_012067.2 N173N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-5635-01A-01D-1534-10 chr10:105236263 G>A maps to NM_001129742.1 P110P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-5635-01A-01D-1534-10 chr16:88945788 G>A maps to NM_005187.5 H517H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-5635-01A-01D-1534-10 chr1:6214897 A>C maps to NM_015557.2 G189G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-5635-01A-01D-1534-10 chr1:207685000 T>A did not map to a codon.
Sequencing variant TCGA-B2-5635-01A-01D-1534-10 chr18:28935224 C>T maps to NM_001942.2 H1022H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-5635-01A-01D-1534-10 chr18:28935224 C>T maps to NM_001942.2 H1022H. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-B2-5635-01A-01D-1534-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-B2-5635-01A-01D-1534-10 chr11:118917417 G>A maps to NM_001130991.1 L898L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-5635-01A-01D-1534-10 chr1:19246189 A>G maps to NM_001136265.1 F268F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-5635-01A-01D-1534-10 chr15:99192875 G>A maps to NM_000875.3 A22A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-5635-01A-01D-1534-10 chr3:195508166 G>A maps to NM_018406.5 T3428T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-5635-01A-01D-1534-10 chr3:9792670 G>C maps to NM_016821.2 A60A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-5635-01A-01D-1534-10 chr2:10924425 G>A maps to ENST00000381611 L479L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-5635-01A-01D-1534-10 chr2:10924425 G>A maps to ENST00000381611 L479L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-5635-01A-01D-1534-10 chr21:35467805 G>C maps to NM_006933.4 R103R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-5635-01A-01D-1534-10 chr4:20543096 T>C maps to ENST00000273739 F670F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-5635-01A-01D-1534-10 chr19:22952717 C>A did not map to a codon.
Sequencing variant TCGA-B2-5635-01A-01D-1534-10 chr5:175717636 G>A maps to ENST00000443967 R351R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-5635-01A-01D-1534-10 chr5:175717636 G>A maps to ENST00000443967 R351R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-5635-01A-01D-1534-10 chr4:40440589 G>A maps to NM_001098634.1 D107D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-5635-01A-01D-1534-10 chr4:40440589 G>A maps to NM_001098634.1 D107D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-5641-01A-01D-1534-10 chr15:79585880 C>A maps to NM_001146341.1 G85G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-5641-01A-01D-1534-10 chr12:32134404 T>C maps to NM_018169.3 N172N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-5641-01A-01D-1534-10 chr18:71930703 A>G maps to NM_148923.2 G46G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-5641-01A-01D-1534-10 chr12:56216894 T>C maps to NM_032364.5 A531A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-5641-01A-01D-1534-10 chr1:21226400 T>C maps to NM_001198801.1 V539V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-5641-01A-01D-1534-10 chr5:137278881 C>T maps to NM_016603.2 R766R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-5641-01A-01D-1534-10 chr5:137278881 C>T maps to NM_016603.2 R766R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-5641-01A-01D-1534-10 chr4:159789572 G>C maps to ENST00000379346 P618P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-5641-01A-01D-1534-10 chr16:31193929 G>A maps to NM_004960.3 T45T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-5641-01A-01D-1534-10 chr17:46654167 G>C maps to NM_024015.4 P224P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-5641-01A-01D-1534-10 chr17:46654167 G>C maps to NM_024015.4 P224P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-5641-01A-01D-1534-10 chrX:130410025 C>T maps to NM_001170961.1 E940E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-5641-01A-01D-1534-10 chr16:57785949 C>T maps to NM_005886.2 A205A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-5641-01A-01D-1534-10 chr4:123150304 T>C maps to NM_015312.3 T984T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-5641-01A-01D-1534-10 chr4:123150306 C>A maps to NM_015312.3 S985*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-5641-01A-01D-1534-10 chr20:36978014 C>T maps to NM_004139.2 T63T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-5641-01A-01D-1534-10 chr20:15967709 G>C did not map to a codon.
Sequencing variant TCGA-B2-5641-01A-01D-1534-10 chr15:56735642 A>C maps to NM_018365.2 Y332*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-5641-01A-01D-1534-10 chr12:55523605 A>G maps to NM_001005243.1 Q18Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-5641-01A-01D-1534-10 chr4:649740 C>G maps to NM_000283.3 A335A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-5641-01A-01D-1534-10 chr4:649740 C>G maps to NM_000283.3 A335A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-5641-01A-01D-1534-10 chr18:67871412 C>T maps to NM_173630.3 Q102Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-5641-01A-01D-1534-10 chr1:95286512 A>G maps to NM_001114106.1 A12A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-5641-01A-01D-1534-10 chr1:95286512 A>G maps to NM_001114106.1 A12A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-5641-01A-01D-1534-10 chr17:4389783 C>T maps to NM_182538.4 C452C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-5641-01A-01D-1534-10 chr2:179439167 A>C maps to NM_133378.4 Y21329*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-5641-01A-01D-1534-10 chrX:53247142 C>G maps to NM_004187.3 V119V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-5641-01A-01D-1534-10 chr9:133589642 C>T did not map to a codon.
Sequencing variant TCGA-B2-5641-01A-01D-1534-10 chr9:133589642 C>T did not map to a codon.
Sequencing variant TCGA-B2-5641-01A-01D-1534-10 chr10:43288426 T>C maps to NM_014753.3 S308S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-5641-01A-01D-1534-10 chr10:43288426 T>C maps to NM_014753.3 S308S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B4-5377-01A-01D-1501-10 chr17:28598330 T>C maps to NM_000386.2 S368S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B4-5377-01A-01D-1501-10 chr21:47533974 C>A maps to NM_001849.3 Y263*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B4-5377-01A-01D-1501-10 chr19:18901410 G>A maps to NM_000095.2 I59I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B4-5377-01A-01D-1501-10 chr1:153907296 C>T maps to NM_014856.2 Q904Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B4-5377-01A-01D-1501-10 chr2:230411680 G>T maps to NM_139072.3 C325*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B4-5377-01A-01D-1501-10 chr4:128725180 A>G maps to ENST00000438626 Q338Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B4-5377-01A-01D-1501-10 chr13:25075849 T>C maps to NM_006437.3 R85R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B4-5377-01A-01D-1501-10 chr13:25075849 T>C maps to NM_006437.3 R85R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B4-5377-01A-01D-1501-10 chr3:52692332 T>A did not map to a codon.
Sequencing variant TCGA-B4-5377-01A-01D-1501-10 chr8:17814230 G>T maps to NM_006197.3 E531*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B4-5377-01A-01D-1501-10 chr8:70981666 A>G maps to NM_024504.2 C143C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B4-5377-01A-01D-1501-10 chr8:10396086 C>A maps to NM_198464.3 T281T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B4-5377-01A-01D-1501-10 chr17:33348595 G>A maps to NM_001017368.1 L129L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B4-5377-01A-01D-1501-10 chr8:104513248 T>C maps to NM_001100117.2 D45D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B4-5377-01A-01D-1501-10 chr8:104513248 T>C maps to NM_001100117.2 D45D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B4-5377-01A-01D-1501-10 chr3:77651361 T>C maps to ENST00000332191 D952D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B4-5377-01A-01D-1501-10 chr3:77651361 T>C maps to ENST00000332191 D952D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B4-5377-01A-01D-1501-10 chr9:117803274 G>T maps to NM_002160.2 I1779I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B4-5377-01A-01D-1501-10 chr11:62601146 C>A did not map to a codon.
Sequencing variant TCGA-B4-5377-01A-01D-1501-10 chr3:167045871 A>G maps to ENST00000307529 R240R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B4-5377-01A-01D-1501-10 chr1:146398421 G>A maps to ENST00000442909 P136P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B4-5377-01A-01D-1501-10 chr1:146398421 G>A maps to ENST00000442909 P136P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B4-5377-01A-01D-1501-10 chr10:79814396 C>T maps to NM_001142285.1 Q167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B4-5377-01A-01D-1501-10 chr10:79814396 C>T maps to NM_001142285.1 Q167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B4-5377-01A-01D-1501-10 chr10:96290994 T>C maps to NM_015188.1 D679D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B4-5377-01A-01D-1501-10 chr10:96290994 T>C maps to NM_015188.1 D679D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4143-01A-01D-1806-10 chr2:158443711 C>A maps to NM_145259.2 L97L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4143-01A-01D-1806-10 chr1:115221021 T>A maps to NM_000036.2 K375*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4143-01A-01D-1806-10 chr3:52437162 G>C maps to NM_004656.2 Y627*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4143-01A-01D-1806-10 chr20:3765588 A>G maps to NM_001810.5 S514S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4143-01A-01D-1806-10 chrX:154563724 C>A maps to NM_001289.4 L4L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4143-01A-01D-1806-10 chrX:154563724 C>A maps to NM_001289.4 L4L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4143-01A-01D-1806-10 chr15:65471323 C>T maps to NM_006660.3 Q102Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4143-01A-01D-1806-10 chr2:238280963 C>T maps to NM_004369.3 R1232R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4143-01A-01D-1806-10 chr14:95577718 C>A maps to NM_177438.2 E731*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4143-01A-01D-1806-10 chr7:35029519 C>T maps to NM_015283.1 L193L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4143-01A-01D-1806-10 chr10:82112338 G>A maps to NM_138812.2 Q7*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4143-01A-01D-1806-10 chr12:53686060 G>T did not map to a codon.
Sequencing variant TCGA-B8-4143-01A-01D-1806-10 chr6:136560874 G>A maps to NM_138419.3 Q200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4143-01A-01D-1806-10 chr7:76826153 C>T maps to NM_006682.2 L254L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4143-01A-01D-1806-10 chr7:76826153 C>T maps to NM_006682.2 L254L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4143-01A-01D-1806-10 chr1:149859100 C>T maps to NM_175065.2 E122E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4143-01A-01D-1806-10 chr1:149858592 C>T maps to NM_003517.2 G23G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4143-01A-01D-1806-10 chr1:149858562 C>T maps to NM_003517.2 A13A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4143-01A-01D-1806-10 chr12:39726835 G>C maps to ENST00000395670 S854*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4143-01A-01D-1806-10 chr21:31768457 C>T maps to NM_181599.2 Y18Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4143-01A-01D-1806-10 chr6:25285101 G>T maps to NM_017640.5 E35*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4143-01A-01D-1806-10 chr12:49444337 C>T maps to NM_003482.3 P1011P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4143-01A-01D-1806-10 chr11:102394121 G>A maps to NM_002423.3 F208F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4143-01A-01D-1806-10 chr13:36046543 G>T maps to ENST00000400445 V2152V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4143-01A-01D-1806-10 chr6:51747998 C>A maps to NM_138694.3 L2414L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4143-01A-01D-1806-10 chr11:64029900 G>A maps to NM_000932.2 A687A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4143-01A-01D-1806-10 chr20:34312530 T>C maps to NM_184234.1 Q216Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4143-01A-01D-1806-10 chr11:110150411 C>A maps to ENST00000405097 P2P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4143-01A-01D-1806-10 chr2:162696377 A>G maps to NM_001178015.1 T119T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4143-01A-01D-1806-10 chr9:100326389 G>A maps to NM_003275.3 T186T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4143-01A-01D-1806-10 chr9:131077878 G>A maps to NM_015679.1 L115L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4143-01A-01D-1806-10 chr15:34355730 G>A maps to NM_012125.3 W271*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4143-01A-01D-1806-10 chr15:34355730 G>A maps to NM_012125.3 W271*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4143-01A-01D-1806-10 chr1:149859427 A>G maps to NM_175065.2 A13A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4143-01A-01D-1806-10 chr1:149859427 A>G maps to NM_175065.2 A13A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4143-01A-01D-1806-10 chrX:53586384 G>T maps to ENST00000276009 I2615I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4143-01A-01D-1806-10 chrX:53586384 G>T maps to ENST00000276009 I2615I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4143-01A-01D-1806-10 chr16:1550654 C>T maps to NM_016111.3 V412V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4143-01A-01D-1806-10 chr16:1550654 C>T maps to NM_016111.3 V412V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4148-01A-02D-1386-10 chr4:175899075 A>G maps to NM_014269.4 T800T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4148-01A-02D-1386-10 chr4:175899078 C>T maps to NM_014269.4 P801P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4148-01A-02D-1386-10 chr11:118779363 C>T maps to NM_182557.2 R9R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4148-01A-02D-1386-10 chr11:118779363 C>T maps to NM_182557.2 R9R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4148-01A-02D-1386-10 chr6:12292679 C>T maps to NM_001955.4 S57S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4148-01A-02D-1386-10 chr5:140480793 C>T maps to NM_018937.2 D187D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4148-01A-02D-1386-10 chr1:223994598 T>C maps to NM_001031685.2 A141A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4151-01A-01D-1806-10 chr1:182869150 G>A maps to ENST00000287709 N712N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4151-01A-01D-1806-10 chrX:50213422 T>A maps to NM_001013742.1 P85P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4151-01A-01D-1806-10 chr1:154962042 T>G maps to NM_025207.4 S375S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4151-01A-01D-1806-10 chr17:39190953 G>A maps to NM_030966.1 C40C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4151-01A-01D-1806-10 chr18:48345980 T>C maps to NM_001127176.1 S37S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4151-01A-01D-1806-10 chr11:10624762 C>G maps to NM_001098579.1 R584R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4151-01A-01D-1806-10 chr11:10624762 C>G maps to NM_001098579.1 R584R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4151-01A-01D-1806-10 chr11:66189603 G>A maps to NM_178864.3 A63A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4151-01A-01D-1806-10 chr14:65204094 T>C did not map to a codon.
Sequencing variant TCGA-B8-4151-01A-01D-1806-10 chr4:141302256 A>G maps to NM_001153484.1 *160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4151-01A-01D-1806-10 chr12:57409488 A>T maps to NM_013251.3 V31V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4151-01A-01D-1806-10 chr6:170871066 G>A maps to NM_003194.4 Q81Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4151-01A-01D-1806-10 chr6:170871060 G>A maps to NM_003194.4 Q79Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4151-01A-01D-1806-10 chr8:67047248 C>A maps to NM_184085.1 P122P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4151-01A-01D-1806-10 chr1:159827559 C>T maps to NM_001013661.1 E209E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4151-01A-01D-1806-10 chr19:22154067 T>C maps to NM_007153.3 E1256E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4151-01A-01D-1806-10 chr19:22154067 T>C maps to NM_007153.3 E1256E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4154-01A-01D-1251-10 chr14:77327094 G>A maps to NM_194287.2 P388P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4154-01A-01D-1251-10 chr11:61504730 C>T maps to NM_006133.2 F483F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4154-01A-01D-1251-10 chr1:161093707 C>A maps to ENST00000368005 L118L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4154-01A-01D-1251-10 chr11:65349885 G>A maps to NM_001099409.1 V581V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4154-01A-01D-1251-10 chr11:65349885 G>A maps to NM_001099409.1 V581V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4154-01A-01D-1251-10 chr16:71956528 C>T maps to NM_014761.2 P235P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4154-01A-01D-1251-10 chr10:90497390 G>T did not map to a codon.
Sequencing variant TCGA-B8-4154-01A-01D-1251-10 chr8:55049857 C>G maps to NM_014175.3 L98L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4154-01A-01D-1251-10 chr17:61907490 A>G did not map to a codon.
Sequencing variant TCGA-B8-4154-01A-01D-1251-10 chr18:42530906 C>A maps to NM_015559.2 C534*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4154-01A-01D-1251-10 chr2:220497000 C>T maps to NM_201574.2 N353N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4154-01A-01D-1251-10 chr14:64545254 G>C maps to NM_182914.2 G3698G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4154-01A-01D-1251-10 chr3:10191562 G>T maps to NM_000551.2 E186*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4154-01A-01D-1251-10 chr4:6303444 G>A maps to NM_006005.3 T641T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4154-01A-01D-1251-10 chr19:11979299 G>T maps to NM_152262.2 G472G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4620-01A-02D-1386-10 chr6:105298825 A>G maps to NM_020771.3 Y59Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4620-01A-02D-1386-10 chrX:92927544 T>C maps to NM_004538.5 K253K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4620-01A-02D-1386-10 chr17:26667401 C>T maps to NM_021137.4 T91T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4620-01A-02D-1386-10 chr3:195505871 A>C maps to NM_018406.5 L4193L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4620-01A-02D-1386-10 chr3:195505871 A>C maps to NM_018406.5 L4193L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4621-01A-01D-1501-10 chr7:87795202 C>A maps to NM_021723.3 C711*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4621-01A-01D-1501-10 chr16:24942354 G>C maps to NM_001006634.1 P755P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4621-01A-01D-1501-10 chr9:133333870 C>A maps to NM_000050.4 R86R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4621-01A-01D-1501-10 chr15:73852254 T>A maps to NM_001042367.1 *267K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4621-01A-01D-1501-10 chr5:65288620 T>C maps to ENST00000506030 T25T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4621-01A-01D-1501-10 chr5:65288620 T>C maps to ENST00000506030 T25T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4621-01A-01D-1501-10 chr2:39008931 T>G maps to NM_024775.9 T134T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4621-01A-01D-1501-10 chr12:104341409 G>A did not map to a codon.
Sequencing variant TCGA-B8-4621-01A-01D-1501-10 chr2:231973290 A>G maps to NM_000867.4 D462D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4621-01A-01D-1501-10 chr6:39162420 C>G maps to NM_003740.3 G138G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4621-01A-01D-1501-10 chr12:12483329 T>A maps to NM_018050.2 A309A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4621-01A-01D-1501-10 chr1:11168293 C>T maps to NM_004958.3 E2526E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4621-01A-01D-1501-10 chr1:11168293 C>T maps to NM_004958.3 E2526E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4621-01A-01D-1501-10 chr1:55527081 C>T maps to NM_174936.3 G572G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4621-01A-01D-1501-10 chr14:74180282 A>G maps to NM_006029.4 A20A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4621-01A-01D-1501-10 chr7:142458496 C>A maps to ENST00000486171 G44G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4621-01A-01D-1501-10 chr1:8419867 G>T maps to NM_012102.3 R1192R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4621-01A-01D-1501-10 chr2:39285888 G>T maps to NM_005633.3 A90A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4621-01A-01D-1501-10 chr3:186761060 G>A maps to NM_003032.2 A190A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4621-01A-01D-1501-10 chr20:62698281 G>C maps to NM_003195.4 G50G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4621-01A-01D-1501-10 chr6:41658460 G>A maps to ENST00000343317 G222G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4621-01A-01D-1501-10 chr15:43307884 C>A did not map to a codon.
Sequencing variant TCGA-B8-4621-01A-01D-1501-10 chr13:27680063 G>T maps to NM_182488.3 Y49*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4621-01A-01D-1501-10 chr2:58358986 C>T maps to NM_001130480.2 L241L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4621-01A-01D-1501-10 chr10:51769939 T>C maps to NM_001077665.2 C685C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4621-01A-01D-1501-10 chr10:51769939 T>C maps to NM_001077665.2 C685C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4621-01A-01D-1501-10 chr19:757467 C>A maps to NM_173481.2 G174G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4621-01A-01D-1501-10 chr19:757467 C>A maps to NM_173481.2 G174G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5546-01A-01D-1534-10 chr5:96103642 T>C maps to ENST00000508830 A736A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5546-01A-01D-1534-10 chr1:16386007 T>C maps to NM_182623.2 Q181Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5546-01A-01D-1534-10 chr11:18729751 A>G did not map to a codon.
Sequencing variant TCGA-B8-5546-01A-01D-1534-10 chr12:53189427 C>A maps to ENST00000309505 G133G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5546-01A-01D-1534-10 chr12:53189445 C>T maps to ENST00000309505 G127G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5546-01A-01D-1534-10 chr2:105915064 C>T maps to NM_004257.4 A262A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5549-01A-01D-1534-10 chr10:61833420 A>G maps to NM_020987.2 Y2406Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5549-01A-01D-1534-10 chr15:60641323 T>G maps to NM_001002858.2 R322R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5549-01A-01D-1534-10 chr1:155385551 G>A maps to ENST00000368346 D1997D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5549-01A-01D-1534-10 chr1:43055003 T>C maps to NM_001080850.2 Y411Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5549-01A-01D-1534-10 chr5:19838882 A>T maps to NM_004934.3 P71P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5549-01A-01D-1534-10 chr7:100411569 C>T maps to NM_004444.4 V554V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5549-01A-01D-1534-10 chr13:27333241 C>T maps to NM_005288.3 S241S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5549-01A-01D-1534-10 chr2:103067329 C>T maps to NM_003853.2 F411F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5549-01A-01D-1534-10 chr5:137520632 C>T maps to NM_005733.2 C607C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5549-01A-01D-1534-10 chr3:185195184 G>A did not map to a codon.
Sequencing variant TCGA-B8-5549-01A-01D-1534-10 chr6:28251757 C>T maps to NM_032507.3 H56H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5549-01A-01D-1534-10 chr13:23915482 T>G maps to NM_014363.4 V844V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5549-01A-01D-1534-10 chr15:34546784 A>G maps to NM_133647.1 Y294Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5549-01A-01D-1534-10 chr4:141600355 C>T maps to NM_015130.2 A197A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5549-01A-01D-1534-10 chr8:77776701 G>A maps to NM_024721.4 K3584K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5549-01A-01D-1534-10 chr19:53959770 C>T maps to NM_001008401.3 T670T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5549-01A-01D-1534-10 chr17:39190638 G>A maps to NM_030966.1 R145R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5549-01A-01D-1534-10 chr17:39190638 G>A maps to NM_030966.1 R145R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5549-01A-01D-1534-10 chr16:4727554 G>A maps to NM_015246.2 L349L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5549-01A-01D-1534-10 chr16:4727554 G>A maps to NM_015246.2 L349L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5549-01A-01D-1534-10 chr12:56558429 A>C maps to NM_003075.3 G1075G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5549-01A-01D-1534-10 chr12:56558429 A>C maps to NM_003075.3 G1075G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5549-01A-01D-1534-10 chr6:41001861 C>T maps to NM_173561.2 S148S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5549-01A-01D-1534-10 chr6:41001861 C>T maps to NM_173561.2 S148S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5549-01A-01D-1534-10 chr8:77761276 T>G maps to NM_024721.4 G1186G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5549-01A-01D-1534-10 chr8:77761276 T>G maps to NM_024721.4 G1186G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5550-01A-01D-1534-10 chr9:117130824 T>A maps to NM_030767.4 G489G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5550-01A-01D-1534-10 chr9:75545842 T>C maps to NM_000689.3 L88L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5550-01A-01D-1534-10 chr6:157505417 C>G maps to ENST00000367148 T1173T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5550-01A-01D-1534-10 chrX:39931682 G>T maps to NM_001123385.1 Y972*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5550-01A-01D-1534-10 chr1:92445157 G>A maps to ENST00000347608 P389P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5550-01A-01D-1534-10 chrX:41428919 C>T did not map to a codon.
Sequencing variant TCGA-B8-5550-01A-01D-1534-10 chr11:61113378 A>G maps to NM_015533.3 P512P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5550-01A-01D-1534-10 chr1:225586357 T>A maps to NM_001373.1 L4441*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5550-01A-01D-1534-10 chr6:116757865 C>T maps to NM_013352.2 N745N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5550-01A-01D-1534-10 chr7:100405124 G>C maps to NM_004444.4 A732A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5550-01A-01D-1534-10 chr1:110300153 C>T maps to NM_139053.1 K307K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5550-01A-01D-1534-10 chr1:118166326 G>T maps to NM_017709.3 P279P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5550-01A-01D-1534-10 chrX:24382643 C>T maps to NM_001136234.1 P589P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5550-01A-01D-1534-10 chr1:151079597 C>G maps to NM_144618.2 T274T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5550-01A-01D-1534-10 chr9:127214927 T>A maps to NM_001161808.1 V88V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5550-01A-01D-1534-10 chr17:36495344 T>G maps to ENST00000398597 P287P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5550-01A-01D-1534-10 chr17:36104839 G>T maps to NM_000458.2 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5550-01A-01D-1534-10 chr10:91162802 A>T maps to NM_001548.3 A257A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5550-01A-01D-1534-10 chr6:52054065 C>A maps to NM_002190.2 T148T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5550-01A-01D-1534-10 chr2:73928330 C>T maps to NM_016347.2 R34R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5550-01A-01D-1534-10 chr1:120491749 C>A did not map to a codon.
Sequencing variant TCGA-B8-5550-01A-01D-1534-10 chr19:15289962 G>T maps to NM_000435.2 Y1197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5550-01A-01D-1534-10 chr19:40876045 A>T maps to NM_012268.2 K194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5550-01A-01D-1534-10 chr12:9317896 G>A maps to NM_002864.2 A775A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5550-01A-01D-1534-10 chr11:123513373 G>A maps to NM_018400.3 Y75Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5550-01A-01D-1534-10 chr15:44087391 C>A maps to ENST00000319327 E455*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5550-01A-01D-1534-10 chr3:93733336 C>T maps to NM_001001850.1 E259E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5550-01A-01D-1534-10 chr1:20082230 G>A maps to NM_181719.4 L137L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5550-01A-01D-1534-10 chr12:129180621 C>A maps to NM_001136103.2 R635R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5550-01A-01D-1534-10 chr5:34880313 T>C maps to NM_144725.3 S326S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5550-01A-01D-1534-10 chr2:179595295 T>C maps to NM_133378.4 T4744T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5550-01A-01D-1534-10 chr11:77921085 C>T maps to NM_020798.2 Q729*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5550-01A-01D-1534-10 chr18:14105245 G>A maps to NM_145287.3 H431H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5550-01A-01D-1534-10 chr18:14105248 T>C maps to NM_145287.3 K430K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5551-01A-01D-1534-10 chr16:16256865 G>A maps to NM_001171.5 R1164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5551-01A-01D-1534-10 chr3:52443728 C>T did not map to a codon.
Sequencing variant TCGA-B8-5551-01A-01D-1534-10 chr3:52443728 C>T did not map to a codon.
Sequencing variant TCGA-B8-5551-01A-01D-1534-10 chr20:9495508 C>T maps to NM_012261.3 Q4*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5551-01A-01D-1534-10 chr12:18891594 C>T maps to NM_033328.2 D131D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5551-01A-01D-1534-10 chr12:4398011 T>C maps to NM_001759.3 F192F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5551-01A-01D-1534-10 chr10:96534858 G>A maps to NM_000769.1 L71L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5551-01A-01D-1534-10 chr12:123340839 G>C maps to NM_003959.1 L450L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5551-01A-01D-1534-10 chr12:123340840 A>T maps to NM_003959.1 K451*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5551-01A-01D-1534-10 chr12:68646406 C>A maps to NM_020525.4 L91L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5551-01A-01D-1534-10 chr11:71293817 C>T maps to ENST00000376535 G22G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5551-01A-01D-1534-10 chr16:84101411 C>T maps to NM_003791.2 V696V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5551-01A-01D-1534-10 chr5:140432179 C>T maps to NM_013340.2 D375D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5551-01A-01D-1534-10 chr6:17292139 C>T maps to NM_001143942.1 A167A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5551-01A-01D-1534-10 chr2:62728553 G>T maps to NM_198276.2 L129L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5551-01A-01D-1534-10 chr7:5348897 G>A maps to NM_001080495.2 A2830A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5551-01A-01D-1534-10 chr17:33513508 A>G maps to NM_173167.2 E909E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5551-01A-01D-1534-10 chr10:43088521 G>A maps to NM_006955.1 Q626*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5551-01A-01D-1534-10 chr8:77768348 T>C maps to NM_024721.4 L3064L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5551-01A-01D-1534-10 chr8:77768348 T>C maps to NM_024721.4 L3064L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5551-01A-01D-1534-10 chr19:58386502 A>C maps to NM_001144989.1 G85G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5551-01A-01D-1534-10 chr19:58386502 A>C maps to NM_001144989.1 G85G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5553-01A-01D-1534-10 chr1:112042592 G>A maps to NM_000677.3 S312S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5553-01A-01D-1534-10 chrX:79941023 C>T maps to NM_153252.4 E1339E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5553-01A-01D-1534-10 chr17:76991240 C>A maps to NM_138793.3 E232*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5553-01A-01D-1534-10 chr1:32138104 T>A did not map to a codon.
Sequencing variant TCGA-B8-5553-01A-01D-1534-10 chr8:145623273 C>A maps to NM_013291.2 V656V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5553-01A-01D-1534-10 chrX:24381735 G>T maps to NM_001136234.1 G287*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5553-01A-01D-1534-10 chr16:31202111 A>T maps to NM_004960.3 K448*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5553-01A-01D-1534-10 chr15:50596161 C>A did not map to a codon.
Sequencing variant TCGA-B8-5553-01A-01D-1534-10 chr3:195507851 G>A maps to NM_018406.5 H3533H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5553-01A-01D-1534-10 chr20:33567236 G>T maps to NM_020884.3 E88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5553-01A-01D-1534-10 chr15:52505430 T>C maps to NM_018728.3 Q1365Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5553-01A-01D-1534-10 chr16:23647614 G>T maps to NM_024675.3 I84I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5553-01A-01D-1534-10 chr9:108128707 C>T maps to NM_080546.3 Q498*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5553-01A-01D-1534-10 chr2:37126773 G>A maps to NM_003162.2 S229S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5553-01A-01D-1534-10 chr11:73686107 C>A maps to NM_003355.2 E292*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5553-01A-01D-1534-10 chr19:53611976 T>A maps to NM_001164309.1 K441*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4161-01A-02D-1386-10 chr2:160194249 C>A maps to NM_013450.2 E1830*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4161-01A-02D-1386-10 chr12:51690949 T>A did not map to a codon.
Sequencing variant TCGA-BP-4161-01A-02D-1386-10 chr3:101476745 T>C maps to ENST00000327230 D432D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4161-01A-02D-1386-10 chr6:30917884 C>G maps to NM_080870.3 A548A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4161-01A-02D-1386-10 chr21:45970771 A>G maps to NM_198693.2 P190P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4161-01A-02D-1386-10 chr2:169995116 A>C maps to NM_004525.2 P4496P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4161-01A-02D-1386-10 chr19:43969648 G>A maps to NM_014400.2 R25R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4161-01A-02D-1386-10 chr7:2255570 C>T maps to NM_003550.2 G291G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4161-01A-02D-1386-10 chr12:116549249 G>T maps to NM_015335.4 I126I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4161-01A-02D-1386-10 chr12:116549249 G>T maps to NM_015335.4 I126I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4161-01A-02D-1386-10 chr19:8998752 G>T maps to NM_024690.2 T13610T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4161-01A-02D-1386-10 chr3:195507914 T>C maps to NM_018406.5 S3512S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4161-01A-02D-1386-10 chr17:4442823 T>A maps to NM_001105538.1 P1291P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4161-01A-02D-1386-10 chr3:52702513 C>T maps to ENST00000296302 K128K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4161-01A-02D-1386-10 chr1:144931264 G>A maps to NM_001002811.1 I148I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4161-01A-02D-1386-10 chr5:149505044 G>A maps to NM_002609.3 D590D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4161-01A-02D-1386-10 chr12:18762520 G>A maps to NM_004570.4 E1339E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4161-01A-02D-1386-10 chr17:7415173 G>T maps to NM_000937.4 L1382L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4161-01A-02D-1386-10 chr4:76897075 C>T did not map to a codon.
Sequencing variant TCGA-BP-4161-01A-02D-1386-10 chr12:21032478 G>T maps to NM_019844.2 S415S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4161-01A-02D-1386-10 chr10:115962899 A>T maps to NM_198795.1 R256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4161-01A-02D-1386-10 chr10:115962899 A>T maps to NM_198795.1 R256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4161-01A-02D-1386-10 chr7:100238671 G>A maps to NM_003227.3 L71L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4161-01A-02D-1386-10 chr9:35310689 G>T maps to ENST00000396787 E342*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4161-01A-02W-1382-10 chr3:10183816 C>T maps to NM_000551.2 Q96*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4161-01A-02D-1386-10 chr19:44469418 C>T maps to NM_013359.2 F81F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4161-01A-02D-1386-10 chr10:89725041 A>G did not map to a codon.
Sequencing variant TCGA-BP-4161-01A-02D-1386-10 chr10:89725041 A>G did not map to a codon.
Sequencing variant TCGA-BP-4162-01A-02D-1386-10 chr14:93652728 C>T maps to NM_001098621.1 L75L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4162-01A-02D-1386-10 chr12:2022186 A>G did not map to a codon.
Sequencing variant TCGA-BP-4162-01A-02D-1386-10 chr12:25347861 G>C maps to NM_001082972.1 P45P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4162-01A-02D-1386-10 chr7:101923412 G>T did not map to a codon.
Sequencing variant TCGA-BP-4162-01A-02D-1386-10 chr15:68582266 T>C maps to NM_015322.3 L191L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4162-01A-02D-1386-10 chrX:54839918 A>G did not map to a codon.
Sequencing variant TCGA-BP-4162-01A-02D-1386-10 chr10:26377304 G>T maps to NM_017433.4 L511L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4162-01A-02D-1386-10 chr8:10466018 A>T maps to NM_178857.5 A1863A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4162-01A-02D-1386-10 chr6:25830752 T>C maps to NM_005074.3 K11K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4162-01A-02D-1386-10 chr7:151092873 G>A maps to ENST00000426624 V353V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4162-01A-02D-1386-10 chr7:151092873 G>A maps to ENST00000426624 V353V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4162-01A-02D-1386-10 chr19:38380083 G>A maps to ENST00000447313 G1409G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4162-01A-02D-1386-10 chrX:73524499 C>T maps to NM_203303.2 C133C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4162-01A-02D-1386-10 chr19:52469414 C>G maps to NM_021632.3 V97V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4162-01A-02D-1386-10 chr15:38632096 G>T did not map to a codon.
Sequencing variant TCGA-BP-4162-01A-02D-1386-10 chr15:38632096 G>T did not map to a codon.
Sequencing variant TCGA-BP-4163-01A-02D-1386-10 chr3:193120482 A>G maps to NM_032279.2 S1183S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4163-01A-02D-1386-10 chr3:52439875 G>T maps to NM_004656.2 S279*. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-BP-4163-01A-02W-1382-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-BP-4163-01A-02D-1386-10 chr17:76496392 G>A maps to ENST00000389840 D1864D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4163-01A-02D-1386-10 chr11:92577386 G>T maps to ENST00000298047 L3618L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4163-01A-02D-1386-10 chr16:50120248 T>G maps to NM_182922.2 L499L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4163-01A-02D-1386-10 chr15:101601456 G>A maps to NM_024652.3 Q1587Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4163-01A-02D-1386-10 chr17:40721609 A>G maps to NM_170607.2 L208L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4163-01A-02D-1386-10 chr16:15501818 A>G maps to NM_001128423.1 Q147Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4163-01A-02D-1386-10 chr14:71571969 A>T maps to NM_014982.2 G2038G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4163-01A-02D-1386-10 chr19:4511478 A>T maps to NM_001080400.1 T817T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4163-01A-02D-1386-10 chrX:114864222 A>G maps to NM_001136025.3 P148P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4163-01A-02D-1386-10 chr19:49096054 C>G maps to NM_177973.1 T209T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4163-01A-02D-1386-10 chr19:49096054 C>G maps to NM_177973.1 T209T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4163-01A-02D-1386-10 chr6:159184434 C>A maps to ENST00000297239 G539G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4163-01A-02D-1386-10 chr12:104376607 G>A maps to NM_003211.4 E170E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4163-01A-02D-1386-10 chr3:10005821 T>C maps to NM_018447.2 E239E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4163-01A-02D-1386-10 chr16:72992625 C>T maps to NM_006885.3 E473E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4163-01A-02D-1386-10 chrX:71933735 C>T did not map to a codon.
Sequencing variant TCGA-BP-4163-01A-02D-1386-10 chrX:71933735 C>T did not map to a codon.
Sequencing variant TCGA-BP-4164-01A-02D-1386-10 chr1:207200937 G>C maps to NM_023938.5 P2P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4164-01A-02D-1386-10 chr1:207200937 G>C maps to NM_023938.5 P2P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4164-01A-02D-1386-10 chr17:41582096 G>T maps to NM_004941.1 G544G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4164-01A-02D-1386-10 chr14:80669283 A>G maps to NM_001007023.2 D226D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4164-01A-02D-1386-10 chr1:225288465 A>G maps to NM_001373.1 K1249K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4164-01A-02D-1386-10 chr3:51246203 G>C did not map to a codon.
Sequencing variant TCGA-BP-4164-01A-02D-1386-10 chr14:23826851 C>T maps to NM_005864.2 G423G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4164-01A-02D-1386-10 chr4:71495255 T>G maps to NM_031889.2 P13P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4164-01A-02D-1386-10 chr12:53045596 A>T maps to NM_000423.2 G110G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4164-01A-02D-1386-10 chr1:90049486 T>C maps to NM_015350.2 L426L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4164-01A-02D-1386-10 chr7:151860718 G>A maps to ENST00000355193 Q3315*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4164-01A-02D-1386-10 chr6:30955139 C>T maps to NM_001010909.2 S396S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4164-01A-02D-1386-10 chr3:195507914 T>C maps to NM_018406.5 S3512S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4164-01A-02D-1386-10 chr12:124887095 T>C maps to NM_006312.4 Q498Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4164-01A-02D-1386-10 chr11:123810586 C>T maps to NM_001001965.1 G88G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4164-01A-02D-1386-10 chr3:52584625 G>A maps to ENST00000296302 Q1570*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4164-01A-02D-1386-10 chr13:38162096 G>A maps to NM_006475.2 N156N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4164-01A-02D-1386-10 chr11:66392879 C>T maps to NM_006328.3 T511T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4164-01A-02D-1386-10 chr19:33471128 G>A maps to NM_033103.4 Q612*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4164-01A-02D-1386-10 chr8:121823810 G>C maps to NM_021021.3 V91V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4164-01A-02D-1386-10 chr22:38109336 C>T maps to NM_001039141.2 S125S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4164-01A-02D-1386-10 chr3:10191531 C>A maps to NM_000551.2 Y175*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4164-01A-02D-1386-10 chr7:70255255 C>T maps to NM_015570.2 P1018P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4164-01A-02D-1386-10 chr7:70255255 C>T maps to NM_015570.2 P1018P. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-BP-4164-01A-02D-1386-10. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-BP-4164-01A-02D-1386-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-BP-4164-01A-02D-1386-10 chr3:46477691 C>T maps to NM_002343.3 R709R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4164-01A-02D-1386-10 chr3:46477691 C>T maps to NM_002343.3 R709R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4164-01A-02D-1386-10 chr3:195507716 G>T maps to NM_018406.5 S3578S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4164-01A-02D-1386-10 chr3:195507716 G>T maps to NM_018406.5 S3578S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4167-01A-02D-1386-10 chr14:105418154 G>C maps to NM_138420.2 L1211L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4167-01A-02D-1386-10 chr5:139876771 T>C maps to ENST00000253810 H971H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4167-01A-02D-1386-10 chr5:139876771 T>C maps to ENST00000253810 H971H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4167-01A-02D-1386-10 chr1:150199044 T>C maps to NM_030920.3 E192E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4167-01A-02D-1386-10 chr12:7045893 G>A maps to NM_001940.3 Q488Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4167-01A-02D-1386-10 chr1:103444414 C>A did not map to a codon.
Sequencing variant TCGA-BP-4167-01A-02D-1386-10 chr1:103444414 C>A did not map to a codon.
Sequencing variant TCGA-BP-4167-01A-02D-1386-10 chr18:77488984 T>A maps to NM_004715.3 S832S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4167-01A-02D-1386-10 chr7:14378223 G>A maps to NM_004080.2 R681*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4167-01A-02D-1386-10 chr6:76022976 A>T maps to NM_015687.2 P857P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4167-01A-02D-1386-10 chr22:46712157 C>A maps to NM_016426.6 G427G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4167-01A-02D-1386-10 chr3:15609988 A>G maps to NM_012260.2 N400N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4167-01A-02D-1386-10 chr3:15609988 A>G maps to NM_012260.2 N400N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4167-01A-02D-1386-10 chr11:15243189 C>T maps to NM_001031853.3 L376L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4167-01A-02D-1386-10 chr14:105617707 C>T maps to NM_002226.3 P393P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4167-01A-02D-1386-10 chr11:71276887 T>C maps to ENST00000422553 G142G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4167-01A-02D-1386-10 chr11:1643254 G>A maps to ENST00000359229 G23G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4167-01A-02D-1386-10 chrX:140953291 C>T maps to NM_138702.1 A53A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4167-01A-02D-1386-10 chr5:126778708 T>G maps to NM_032446.2 Y794*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4167-01A-02D-1386-10 chr11:1253968 A>G maps to ENST00000447027 V681V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4167-01A-02D-1386-10 chr3:125286404 A>C maps to NM_022776.4 L234*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4167-01A-02D-1386-10 chr11:36614944 G>A maps to NM_000536.3 V258V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4167-01A-02D-1386-10 chr19:44116656 A>C maps to NM_001145641.1 G128G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4167-01A-02D-1386-10 chrX:100532701 C>A maps to NM_024885.3 E281*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4167-01A-02D-1386-10 chr5:145838652 C>T maps to NM_006706.3 A215A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4167-01A-02D-1386-10 chr16:49672051 A>T maps to NM_015069.2 G337G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4167-01A-02D-1386-10 chr18:14105185 T>C maps to NM_145287.3 Q451Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4167-01A-02D-1386-10 chr18:14105245 G>A maps to NM_145287.3 H431H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4167-01A-02D-1386-10 chr3:40574133 T>A maps to NM_001098414.1 Y291*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4167-01A-02D-1386-10 chr5:140202961 G>A maps to NM_018908.2 V534V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4167-01A-02D-1386-10 chr5:140202961 G>A maps to NM_018908.2 V534V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4167-01A-02D-1386-10 chr12:11506355 G>A maps to NM_005039.3 G227G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4167-01A-02D-1386-10 chr12:11506355 G>A maps to NM_005039.3 G227G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4167-01A-02D-1386-10 chr19:50154203 A>C maps to NM_021228.2 P186P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4167-01A-02D-1386-10 chr19:50154203 A>C maps to NM_021228.2 P186P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4167-01A-02D-1386-10 chr6:31127383 C>T maps to NM_007109.2 P46P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4167-01A-02D-1386-10 chr6:31127383 C>T maps to NM_007109.2 P46P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4167-01A-02D-1386-10 chr6:149855819 T>C maps to NM_139126.2 Q185Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4167-01A-02D-1386-10 chr6:149855819 T>C maps to NM_139126.2 Q185Q. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-BP-4349-01A-01W-1362-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-BP-4355-01A-01W-1362-10 chr3:10183747 C>T maps to NM_000551.2 Q73*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4765-01A-01W-1362-10 chr3:10183733 C>A maps to NM_000551.2 S68*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4770-01A-01D-1501-10 chr2:122488642 G>A maps to NM_032390.4 L130L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4770-01A-01D-1501-10 chr19:9047433 A>G maps to NM_024690.2 D11399D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4770-01A-01D-1501-10 chr19:9074344 T>C maps to NM_024690.2 T4367T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4770-01A-01D-1501-10 chr11:64822096 C>A maps to ENST00000340252 L239L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4770-01A-01D-1501-10 chr1:248525733 T>C maps to NM_001004696.1 Y284Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4770-01A-01D-1501-10 chr11:51412338 A>T maps to NM_001005272.3 P19P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4770-01A-01D-1501-10 chr2:217285019 A>T did not map to a codon.
Sequencing variant TCGA-BP-4770-01A-01D-1501-10 chr9:100963823 C>T maps to NM_018421.3 A798A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4770-01A-01D-1501-10 chr1:175323626 A>T maps to NM_003285.2 I1094I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4770-01A-01D-1501-10 chr17:7577497 C>A did not map to a codon.
Sequencing variant TCGA-BP-4770-01A-01D-1501-10 chr3:51455598 A>C maps to ENST00000273612 L1163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4770-01A-01D-1501-10 chr4:367074 C>T maps to NM_003441.2 I283I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4770-01A-01D-1501-10 chr12:132547140 G>A maps to ENST00000333577 Q2779Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4770-01A-01D-1501-10 chr12:132547140 G>A maps to ENST00000333577 Q2779Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4770-01A-01D-1501-10 chr1:16361918 G>A did not map to a codon.
Sequencing variant TCGA-BP-4770-01A-01D-1501-10 chr1:16361918 G>A did not map to a codon.
Sequencing variant TCGA-BP-4770-01A-01D-1501-10 chr11:551240 G>C maps to NM_198075.3 L245L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4770-01A-01D-1501-10 chr11:551240 G>C maps to NM_198075.3 L245L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4770-01A-01D-1501-10 chr19:36211502 A>C maps to NM_014727.1 P418P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4770-01A-01D-1501-10 chr19:36211502 A>C maps to NM_014727.1 P418P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4770-01A-01D-1501-10 chr9:20414378 G>A maps to NM_004529.2 S155S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4770-01A-01D-1501-10 chr9:20414378 G>A maps to NM_004529.2 S155S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4770-01A-01D-1501-10 chr3:195512213 G>C maps to NM_018406.5 T2079T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4770-01A-01D-1501-10 chr3:195512213 G>C maps to NM_018406.5 T2079T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4770-01A-01D-1501-10 chr11:56057617 T>C maps to NM_001005199.1 R307R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4770-01A-01D-1501-10 chr11:56057617 T>C maps to NM_001005199.1 R307R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4770-01A-01D-1501-10 chr6:51915061 T>G maps to NM_138694.3 P724P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4770-01A-01D-1501-10 chr6:51915061 T>G maps to NM_138694.3 P724P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4770-01A-01D-1501-10 chr11:8662082 T>G maps to ENST00000402157 P466P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4770-01A-01D-1501-10 chr11:8662082 T>G maps to ENST00000402157 P466P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4770-01A-01D-1501-10 chr17:73830528 C>T maps to ENST00000412096 E725E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4770-01A-01D-1501-10 chr17:73830528 C>T maps to ENST00000412096 E725E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4770-01A-01D-1501-10 chr19:53856729 G>A maps to NM_138374.1 K934K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4770-01A-01D-1501-10 chr19:53856729 G>A maps to NM_138374.1 K934K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4770-01A-01D-1501-10 chr7:151970835 G>A maps to ENST00000355193 H322H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4770-01A-01D-1501-10 chr7:151970835 G>A maps to ENST00000355193 H322H. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-BP-4782-01A-02D-2099-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-BP-4789-01A-01W-1369-10 chr3:10183816 C>T maps to NM_000551.2 Q96*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4961-01A-01D-1392-10 chr3:10183724 C>A maps to NM_000551.2 S65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5001-01A-01D-1392-10 chr3:10183810 G>T maps to NM_000551.2 E94*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4634-01A-02D-1386-10 chr17:66924116 A>G maps to NM_007168.2 L405L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4634-01A-02D-1386-10 chr1:112042772 G>A maps to NM_000677.3 I252I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4634-01A-02D-1386-10 chrX:39921478 G>C maps to NM_001123385.1 R1447R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4634-01A-02D-1386-10 chr2:29295854 G>A maps to NM_001029883.1 R425*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4634-01A-02D-1386-10 chr17:8647474 C>T maps to NM_144681.2 S37S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4634-01A-02D-1386-10 chr5:86695280 C>A maps to NM_001239.3 E268*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4634-01A-02D-1386-10 chr19:3293437 C>A maps to NM_021938.3 P484P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4634-01A-02D-1386-10 chr10:71692317 A>T maps to ENST00000356340 G551G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4634-01A-02D-1386-10 chr10:71692318 G>T maps to ENST00000356340 E552*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4634-01A-02D-1386-10 chr13:36521537 C>T maps to NM_004734.4 P260P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4634-01A-02D-1386-10 chr2:71896301 C>A maps to NM_001130987.1 L1869L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4634-01A-02D-1386-10 chr1:152277656 A>G maps to NM_002016.1 A3235A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4634-01A-02D-1386-10 chrX:147088241 C>T maps to NM_152578.2 Q140*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4634-01A-02D-1386-10 chr14:62200985 T>A maps to ENST00000394997 C338*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4634-01A-02D-1386-10 chr5:75886272 A>G maps to NM_006633.2 K227K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4634-01A-02D-1386-10 chr16:67324886 G>C maps to NM_001100915.1 T856T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4634-01A-02D-1386-10 chr16:67324886 G>C maps to NM_001100915.1 T856T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4634-01A-02D-1386-10 chr1:156105093 C>G maps to NM_170707.2 L309L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4634-01A-02D-1386-10 chr13:48669205 C>G maps to NM_014166.2 A3A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4634-01A-02D-1386-10 chr9:134072981 C>G maps to ENST00000451030 G1368G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4634-01A-02D-1386-10 chr1:228528241 C>T maps to NM_001098623.1 P5817P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4634-01A-02D-1386-10 chr5:140531175 C>T maps to NM_018939.2 V446V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4634-01A-02D-1386-10 chr16:24185868 G>C maps to NM_002738.6 L454L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4634-01A-02D-1386-10 chr16:24185868 G>C maps to NM_002738.6 L454L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4634-01A-02D-1386-10 chr6:3081328 T>C maps to NM_003804.3 V146V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4634-01A-02D-1386-10 chr3:9486833 A>C maps to ENST00000407969 P449P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4634-01A-02D-1386-10 chr5:128321006 C>T maps to NM_001017372.1 Y221Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4634-01A-02D-1386-10 chr5:128321006 C>T maps to NM_001017372.1 Y221Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4634-01A-02D-1386-10 chr7:23547079 C>T maps to NM_013293.3 A200A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4634-01A-02D-1386-10 chr6:160176078 C>A maps to NM_004906.3 I209I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4634-01A-02D-1386-10 chr3:183490250 G>C maps to NM_018023.4 V702V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4634-01A-02D-1386-10 chr12:31256927 C>G maps to NM_152438.1 G958G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4634-01A-02D-1386-10 chr12:31256927 C>G maps to NM_152438.1 G958G. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-CJ-4634-01A-02D-1386-10. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-CJ-4634-01A-02D-1386-10. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-CJ-4634-01A-02D-1386-10. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-CJ-4634-01A-02D-1386-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CJ-4634-01A-02D-1386-10 chr19:49216784 C>T maps to NM_001130915.1 L329L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4634-01A-02D-1386-10 chr19:49216784 C>T maps to NM_001130915.1 L329L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4634-01A-02D-1386-10 chr20:3679975 G>A maps to NM_023068.3 H553H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4634-01A-02D-1386-10 chr20:3679975 G>A maps to NM_023068.3 H553H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4634-01A-02D-1386-10 chr8:56015737 C>T maps to NM_052898.1 G230G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4634-01A-02D-1386-10 chr8:56015737 C>T maps to NM_052898.1 G230G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4634-01A-02D-1386-10 chr4:146824029 C>T maps to ENST00000508784 L127L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4634-01A-02D-1386-10 chr4:146824029 C>T maps to ENST00000508784 L127L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4636-01A-02D-1386-10 chr16:4043481 A>T maps to NM_001116.3 A638A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4636-01A-02D-1386-10 chr3:52443567 A>G did not map to a codon.
Sequencing variant TCGA-CJ-4636-01A-02D-1386-10 chr12:21679900 G>T did not map to a codon.
Sequencing variant TCGA-CJ-4636-01A-02D-1386-10 chr12:21679900 G>T did not map to a codon.
Sequencing variant TCGA-CJ-4636-01A-02D-1386-10 chr12:123307923 C>A maps to NM_201435.3 V671V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4636-01A-02D-1386-10 chr1:196918738 G>A maps to ENST00000367421 T71T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4636-01A-02D-1386-10 chr6:56035908 G>A maps to NM_030820.3 R220*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4636-01A-02D-1386-10 chr2:25754450 T>A maps to NM_021907.3 K298*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4636-01A-02D-1386-10 chr2:25754450 T>A maps to NM_021907.3 K298*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4636-01A-02D-1386-10 chr7:102665655 A>G maps to NM_145032.3 L117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4636-01A-02D-1386-10 chr5:178416291 G>C maps to NM_000843.3 S376*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4636-01A-02D-1386-10 chr1:207014375 C>T maps to NM_153758.2 Q169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4636-01A-02D-1386-10 chr17:39197613 G>A maps to NM_030967.2 P12P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4636-01A-02D-1386-10 chr14:21966491 C>T maps to NM_019852.3 L551L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4636-01A-02D-1386-10 chr14:21967448 C>G did not map to a codon.
Sequencing variant TCGA-CJ-4636-01A-02D-1386-10 chr3:195506759 T>A maps to NM_018406.5 A3897A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4636-01A-02D-1386-10 chr12:124887092 C>T maps to NM_006312.4 Q499Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4636-01A-02D-1386-10 chr18:55992364 G>A maps to NM_001144967.1 R217R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4636-01A-02D-1386-10 chr7:4899653 G>A maps to NM_020144.4 H596H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4636-01A-02D-1386-10 chr12:54971105 G>A maps to NM_000924.3 L535L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4636-01A-02D-1386-10 chr8:144942849 G>A maps to NM_031308.1 L1524L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4636-01A-02D-1386-10 chr8:144942849 G>A maps to NM_031308.1 L1524L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4636-01A-02D-1386-10 chr1:16361924 G>A did not map to a codon.
Sequencing variant TCGA-CJ-4636-01A-02D-1386-10 chr1:16361924 G>A did not map to a codon.
Sequencing variant TCGA-CJ-4636-01A-02D-1386-10 chr1:144813814 A>G maps to NM_001037675.2 A353A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4636-01A-02D-1386-10 chr1:144813814 A>G maps to NM_001037675.2 A353A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4636-01A-02D-1386-10 chr15:41769653 A>T did not map to a codon.
Sequencing variant TCGA-CJ-4636-01A-02D-1386-10 chr15:41769653 A>T did not map to a codon.
Sequencing variant TCGA-CJ-4636-01A-02D-1386-10 chr15:49301546 A>C maps to NM_001193489.1 T631T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4636-01A-02D-1386-10 chr15:49301546 A>C maps to NM_001193489.1 T631T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4637-01A-02D-1386-10 chr2:228497786 G>A maps to NM_020161.3 A5A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4637-01A-02D-1386-10 chr6:170179295 T>A maps to NM_018341.1 P586P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4637-01A-02D-1386-10 chr2:218999550 C>T maps to NM_001168298.1 D9D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4637-01A-02D-1386-10 chr2:218999550 C>T maps to NM_001168298.1 D9D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4637-01A-02D-1386-10 chr5:52145319 G>T did not map to a codon.
Sequencing variant TCGA-CJ-4637-01A-02D-1386-10 chr5:52145319 G>T did not map to a codon.
Sequencing variant TCGA-CJ-4637-01A-02D-1386-10 chr9:73027945 C>A maps to NM_001206.2 E112*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4637-01A-02D-1386-10 chr3:195510155 G>A maps to NM_018406.5 H2765H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4637-01A-02D-1386-10 chr2:10262858 G>A maps to NM_001165931.1 G38G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4637-01A-02D-1386-10 chr1:44386569 T>A maps to NM_174963.2 Y405*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4637-01A-02D-1386-10 chr5:140725546 C>T maps to NM_018916.3 H649H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4637-01A-02D-1386-10 chr5:140725546 C>T maps to NM_018916.3 H649H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4637-01A-02D-1386-10 chr17:56651591 T>C maps to ENST00000240361 E1159E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4637-01A-02D-1386-10 chr17:56651591 T>C maps to ENST00000240361 E1159E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4638-01A-02D-1386-10 chr7:121766488 T>A maps to NM_005763.3 K138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4638-01A-02D-1386-10 chr4:114290828 A>T maps to NM_001148.4 I3826I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4638-01A-02D-1386-10 chr4:73956462 T>A maps to NM_032217.3 S2294S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4638-01A-02D-1386-10 chr3:52443573 G>A maps to NM_004656.2 Q40*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4638-01A-02D-1386-10 chr17:58786583 A>T maps to ENST00000407086 T73T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4638-01A-02D-1386-10 chr5:180475149 C>T maps to NM_152547.4 I111I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4638-01A-02D-1386-10 chr1:86957041 G>A maps to NM_001285.3 Q484Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4638-01A-02D-1386-10 chr8:121259909 C>T maps to NM_021110.1 R846R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4638-01A-02D-1386-10 chr1:240371111 G>T maps to ENST00000406993 P1143P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4638-01A-02D-1386-10 chr2:75107667 C>T maps to NM_000189.4 T514T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4638-01A-02D-1386-10 chr2:75107667 C>T maps to NM_000189.4 T514T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4638-01A-02D-1386-10 chr9:6251224 C>G maps to NM_033439.3 V101V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4638-01A-02D-1386-10 chr9:6251224 C>G maps to NM_033439.3 V101V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4638-01A-02D-1386-10 chr8:99028777 T>C maps to ENST00000254898 S528S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4638-01A-02D-1386-10 chr9:35753712 G>A maps to NM_001044264.1 R61R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4638-01A-02D-1386-10 chr4:178283612 T>A maps to NM_018248.2 I602I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4638-01A-02D-1386-10 chr22:30050714 G>C did not map to a codon.
Sequencing variant TCGA-CJ-4638-01A-02D-1386-10 chr11:50003857 G>A maps to NM_001005270.2 F60F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4638-01A-02D-1386-10 chr18:23714009 G>A maps to NM_144662.2 A27A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4638-01A-02D-1386-10 chr11:47593081 C>A maps to NM_175732.2 I169I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4638-01A-02D-1386-10 chr17:33690265 C>T maps to NM_152270.3 S187S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4638-01A-02D-1386-10 chr4:186508840 C>T maps to ENST00000355634 G1181G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4638-01A-02D-1386-10 chr9:131371419 C>T maps to NM_001130438.2 Q1539*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4638-01A-02D-1386-10 chr14:75279328 A>G did not map to a codon.
Sequencing variant TCGA-CJ-4638-01A-02D-1386-10 chrX:111698753 C>T maps to NM_001004308.2 L266L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4638-01A-02D-1386-10 chr22:21385372 G>C maps to NM_004173.2 S243S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4638-01A-02D-1386-10 chr22:21385372 G>C maps to NM_004173.2 S243S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4639-01A-02D-1386-10 chr11:6499970 A>T maps to NM_012402.2 L178L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4639-01A-02D-1386-10 chr11:108106449 A>T maps to NM_000051.3 K129*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4639-01A-02D-1386-10 chr12:2794976 G>A maps to NM_199460.2 P1966P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4639-01A-02D-1386-10 chr2:196750887 G>A maps to NM_018897.2 R1839*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4639-01A-02D-1386-10 chr1:152327666 C>T maps to NM_001014342.2 S865S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4639-01A-02D-1386-10 chr16:58749997 A>C maps to NM_002080.2 R313R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4639-01A-02D-1386-10 chr3:127337929 G>T maps to NM_004526.2 E692*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4639-01A-02D-1386-10 chr10:6257232 C>T maps to NM_004566.3 S84S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4639-01A-02D-1386-10 chr1:167365545 G>A maps to NM_002697.3 G337G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4639-01A-02D-1386-10 chr1:167365545 G>A maps to NM_002697.3 G337G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4639-01A-02D-1386-10 chr1:11594487 C>T maps to NM_020780.1 R1142R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4639-01A-02D-1386-10 chr4:87662969 G>T did not map to a codon.
Sequencing variant TCGA-CJ-4639-01A-02D-1386-10 chr14:23371264 G>A maps to NM_001077351.1 A390A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4639-01A-02D-1386-10 chr6:25913556 A>C maps to NM_005835.2 L426*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4639-01A-02D-1386-10 chr5:53815389 C>T maps to NM_052870.2 I536I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4639-01A-02D-1386-10 chr5:136448174 C>A maps to NM_004598.3 V141V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4639-01A-02D-1386-10 chr3:140401924 C>T maps to NM_152616.4 H321H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4640-01A-02D-1386-10 chr2:37321280 A>G maps to ENST00000379187 E199E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4640-01A-02D-1386-10 chr10:99664545 C>T maps to NM_018058.4 G292G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4640-01A-02D-1386-10 chr10:99664545 C>T maps to NM_018058.4 G292G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4640-01A-02D-1386-10 chr2:116594278 C>A maps to NM_020868.3 G713G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4640-01A-02D-1386-10 chr22:40231925 G>A maps to NM_152512.3 C210C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4640-01A-02D-1386-10 chr1:174418157 C>A maps to NM_005684.4 T303T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4640-01A-02D-1386-10 chr5:75896707 C>G maps to NM_006633.2 A381A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4640-01A-02D-1386-10 chr19:17954626 G>T maps to NM_000215.3 S89S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4640-01A-02D-1386-10 chr19:17954626 G>T maps to NM_000215.3 S89S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4640-01A-02D-1386-10 chr1:150939612 G>T maps to NM_181746.2 A226A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4640-01A-02D-1386-10 chr3:195508298 C>T maps to NM_018406.5 S3384S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4640-01A-02D-1386-10 chr14:56757029 G>T maps to NM_021255.2 G184G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4640-01A-02D-1386-10 chr10:99125880 T>C maps to NM_015179.3 E1167E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4640-01A-02D-1386-10 chr17:18243555 G>T maps to NM_004169.3 Y205*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4640-01A-02D-1386-10 chr1:27648816 C>T maps to NM_032125.2 V43V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4640-01A-02D-1386-10 chr1:225273304 T>C maps to NM_001373.1 A1129A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4640-01A-02D-1386-10 chr1:225273304 T>C maps to NM_001373.1 A1129A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4640-01A-02D-1386-10 chr6:168377134 T>C maps to NM_001129895.1 Q66Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4640-01A-02D-1386-10 chr6:168377134 T>C maps to NM_001129895.1 Q66Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4640-01A-02D-1386-10 chr6:29910606 G>C maps to ENST00000376806 V49V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4640-01A-02D-1386-10 chr6:29910606 G>C maps to ENST00000376806 V49V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4640-01A-02D-1386-10 chr1:13183614 T>C maps to NM_001136561.2 A86A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4640-01A-02D-1386-10 chr1:13183614 T>C maps to NM_001136561.2 A86A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4641-01A-02D-1386-10 chr8:107773723 C>T maps to NM_139166.4 E229E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4641-01A-02D-1386-10 chrX:70824425 T>C maps to NM_052957.4 N433N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4641-01A-02D-1386-10 chrX:70824425 T>C maps to NM_052957.4 N433N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4641-01A-02D-1386-10 chr10:97366698 T>G maps to NM_002860.3 G736G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4641-01A-02D-1386-10 chr3:52441303 G>A maps to NM_004656.2 Q156*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4641-01A-02D-1386-10 chr18:47792750 G>A maps to NM_145020.3 T8T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4641-01A-02D-1386-10 chr15:48748912 C>A maps to NM_000138.4 V1781V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4641-01A-02D-1386-10 chr8:42821724 C>T maps to NM_032410.3 Q297*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4641-01A-02D-1386-10 chr8:48889310 G>T maps to NM_182746.1 V855V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4641-01A-02D-1386-10 chr17:80436688 C>T maps to ENST00000374611 Y178Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4641-01A-02D-1386-10 chr14:24845236 C>T maps to NM_001136022.1 V725V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4641-01A-02D-1386-10 chr13:25670500 G>A maps to NM_030979.2 A55A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4641-01A-02D-1386-10 chr5:140221436 C>T maps to NM_018911.2 Y177Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4641-01A-02D-1386-10 chr5:140764004 C>T maps to NM_018920.2 V513V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4641-01A-02D-1386-10 chr2:28752600 G>A maps to NM_153021.4 L141L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4641-01A-02D-1386-10 chr1:158609797 C>G did not map to a codon.
Sequencing variant TCGA-CJ-4641-01A-02D-1386-10 chr1:158609797 C>G did not map to a codon.
Sequencing variant TCGA-CJ-4641-01A-02D-1386-10 chr3:10005827 G>A maps to NM_018447.2 V237V. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-CJ-4641-01A-02D-1386-10. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-CJ-4641-01A-02D-1386-10. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-CJ-4641-01A-02D-1386-10. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-CJ-4641-01A-02D-1386-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CJ-4641-01A-02D-1386-10 chr12:123343702 C>T maps to NM_003959.1 L752L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4641-01A-02D-1386-10 chr12:123343702 C>T maps to NM_003959.1 L752L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4641-01A-02D-1386-10 chr3:195507050 T>C maps to NM_018406.5 S3800S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4641-01A-02D-1386-10 chr3:195507050 T>C maps to NM_018406.5 S3800S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4643-01A-02D-1386-10 chr14:105412553 T>G maps to NM_138420.2 G3078G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4643-01A-02D-1386-10 chr17:79424536 C>T maps to ENST00000436173 L1654L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4643-01A-02D-1386-10 chr7:26245985 A>T did not map to a codon.
Sequencing variant TCGA-CJ-4643-01A-02D-1386-10 chr17:45234349 C>T maps to NM_001114091.1 Q257Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4643-01A-02D-1386-10 chrX:150912324 G>A maps to NM_005140.1 K450K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4643-01A-02D-1386-10 chrX:150912324 G>A maps to NM_005140.1 K450K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4643-01A-02D-1386-10 chr15:22928511 T>C did not map to a codon.
Sequencing variant TCGA-CJ-4643-01A-02D-1386-10 chr17:37873628 C>T maps to NM_004448.2 A598A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4643-01A-02D-1386-10 chr12:50746021 C>G maps to NM_001145475.1 L1531L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4643-01A-02D-1386-10 chr6:31323127 A>G maps to ENST00000428231 H357H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4643-01A-02D-1386-10 chr6:31323142 T>C maps to ENST00000428231 T352T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4643-01A-02D-1386-10 chr6:31323214 T>C maps to ENST00000428231 R328R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4643-01A-02D-1386-10 chr11:18327002 G>A maps to NM_181507.1 Q288*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4643-01A-02D-1386-10 chr11:18327002 G>A maps to NM_181507.1 Q288*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4643-01A-02D-1386-10 chr19:49657753 G>A maps to NM_002152.2 D247D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4643-01A-02D-1386-10 chr3:183217549 G>T maps to NM_130446.2 G325G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4643-01A-02D-1386-10 chr12:53189409 A>C maps to ENST00000309505 G139G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4643-01A-02D-1386-10 chr17:39340728 G>A maps to ENST00000458321 C122C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4643-01A-02D-1386-10 chr11:1642702 A>G maps to NM_001012709.1 S207S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4643-01A-02D-1386-10 chr19:54872808 C>T maps to NM_002287.3 L26L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4643-01A-02D-1386-10 chr3:195510029 C>G maps to NM_018406.5 S2807S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4643-01A-02D-1386-10 chr11:1017073 A>G maps to NM_005961.2 F1909F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4643-01A-02D-1386-10 chr11:1018381 A>G maps to NM_005961.2 S1473S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4643-01A-02D-1386-10 chr19:56515288 A>G maps to NM_153447.4 E90E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4643-01A-02D-1386-10 chr19:56515288 A>G maps to NM_153447.4 E90E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4643-01A-02D-1386-10 chr2:63283087 C>A maps to NM_014562.3 G234G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4643-01A-02D-1386-10 chr8:52733036 C>T maps to NM_052937.2 E316E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4643-01A-02D-1386-10 chr3:155199833 A>G maps to ENST00000340059 S1335S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4643-01A-02D-1386-10 chr3:155199833 A>G maps to ENST00000340059 S1335S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4643-01A-02D-1386-10 chr12:11506463 C>T maps to NM_005039.3 Q191Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4643-01A-02D-1386-10 chr1:186276623 A>G maps to NM_005807.3 E591E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4643-01A-02D-1386-10 chr7:99022963 C>T maps to NM_001198879.1 G446G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4643-01A-02D-1386-10 chr19:5214436 G>A maps to NM_002850.3 Q1517*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4643-01A-02D-1386-10 chr19:38904045 A>T maps to ENST00000405332 C434*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4643-01A-02D-1386-10 chr3:127816144 G>T maps to NM_003707.2 I338I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4643-01A-02D-1386-10 chr1:110709685 C>T maps to NM_001010898.2 G45G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4643-01A-02D-1386-10 chr13:75936706 T>A maps to ENST00000431480 K179*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4643-01A-02D-1386-10 chr17:16285559 T>C maps to NM_018955.2 P113P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4643-01A-02D-1386-10 chrX:54319686 A>T maps to NM_020922.4 Y589*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4643-01A-02D-1386-10 chr1:35853065 T>C maps to NM_005095.2 F708F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4643-01A-02D-1386-10 chr1:35853065 T>C maps to NM_005095.2 F708F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4643-01A-02D-1386-10 chr19:52857565 C>T maps to NM_001161425.1 L85L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4643-01A-02D-1386-10 chr20:44506357 G>A maps to NM_080752.3 A387A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4643-01A-02D-1386-10 chr1:145301801 C>G maps to NM_001039703.4 L357L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4643-01A-02D-1386-10 chr1:145301801 C>G maps to NM_001039703.4 L357L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4643-01A-02D-1386-10 chr11:6867461 G>A maps to ENST00000379831 P187P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4643-01A-02D-1386-10 chr11:6867461 G>A maps to ENST00000379831 P187P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4643-01A-02D-1386-10 chr12:64812807 C>G maps to NM_007235.3 L141L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4643-01A-02D-1386-10 chr12:64812807 C>G maps to NM_007235.3 L141L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4644-01A-02D-1386-10 chr14:105416366 A>C maps to NM_138420.2 G1807G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4644-01A-02D-1386-10 chr14:105416837 C>A maps to NM_138420.2 A1650A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4644-01A-02D-1386-10 chrX:110987995 A>T maps to NM_001099922.2 P932P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4644-01A-02D-1386-10 chr13:46054426 T>C did not map to a codon.
Sequencing variant TCGA-CJ-4644-01A-02D-1386-10 chrX:149102005 A>G maps to NM_001013845.1 P29P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4644-01A-02D-1386-10 chr11:71504463 C>T maps to NM_018172.2 Y66Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4644-01A-02D-1386-10 chr1:152330074 G>A maps to NM_001014342.2 R63*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4644-01A-02D-1386-10 chr17:43323618 G>T maps to NM_005892.3 E1045*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4644-01A-02D-1386-10 chr2:177033940 C>T maps to NM_006898.4 G33G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4644-01A-02D-1386-10 chr11:15222419 G>C maps to NM_001031853.3 R295R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4644-01A-02D-1386-10 chr3:128848935 G>A maps to ENST00000418265 L282L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4644-01A-02D-1386-10 chr12:53189409 A>C maps to ENST00000309505 G139G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4644-01A-02D-1386-10 chr12:53189427 C>A maps to ENST00000309505 G133G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4644-01A-02D-1386-10 chr17:39254246 A>T maps to NM_031960.2 C30*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4644-01A-02D-1386-10 chr16:3100413 C>T maps to NM_022468.4 R176R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4644-01A-02D-1386-10 chr11:1093271 A>C maps to ENST00000441003 T1697T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4644-01A-02D-1386-10 chr11:1092995 C>A maps to ENST00000441003 T1605T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4644-01A-02D-1386-10 chr11:1093568 A>C maps to ENST00000441003 T1796T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4644-01A-02D-1386-10 chr3:195513539 A>G maps to NM_018406.5 N1637N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4644-01A-02D-1386-10 chr11:1017796 C>G maps to NM_005961.2 A1668A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4644-01A-02D-1386-10 chr18:56033229 G>A did not map to a codon.
Sequencing variant TCGA-CJ-4644-01A-02D-1386-10 chr2:220428158 C>A maps to NM_015311.2 L866L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4644-01A-02D-1386-10 chr1:248737347 G>A maps to NM_001001821.1 A237A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4644-01A-02D-1386-10 chr3:52702661 C>T did not map to a codon.
Sequencing variant TCGA-CJ-4644-01A-02D-1386-10 chr19:4512945 A>G maps to NM_001080400.1 T328T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4644-01A-02D-1386-10 chr19:4511490 A>G maps to NM_001080400.1 G813G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4644-01A-02D-1386-10 chr7:142460414 T>C maps to ENST00000486171 C210C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4644-01A-02D-1386-10 chr9:33798078 T>C maps to NM_007343.3 G208G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4644-01A-02D-1386-10 chr10:27702369 G>A maps to NM_001034842.3 Y270Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4644-01A-02D-1386-10 chr2:20451396 C>T maps to ENST00000361078 K1050K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4644-01A-02D-1386-10 chr2:20451396 C>T maps to ENST00000361078 K1050K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4644-01A-02D-1386-10 chr2:238733022 C>T maps to NM_001080504.2 Q805*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4644-01A-02D-1386-10 chr19:36018433 C>T maps to NM_001166034.1 A250A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4644-01A-02D-1386-10 chr7:107329536 G>A maps to NM_000441.1 S347S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4644-01A-02D-1386-10 chr16:87885387 G>A maps to NM_003486.5 A202A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4644-01A-02D-1386-10 chrX:102864333 G>A maps to NM_032926.2 T114T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4644-01A-02D-1386-10 chr6:35086048 A>G maps to NM_001093728.1 V516V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4644-01A-02D-1386-10 chr3:185212512 A>G maps to NM_080652.3 L158L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4644-01A-02D-1386-10 chr1:19407976 G>A maps to ENST00000375267 D5033D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4644-01A-02D-1386-10 chr3:10191484 G>T maps to NM_000551.2 E160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4644-01A-02D-1386-10 chr5:178139393 T>C maps to NM_005649.2 K495K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4644-01A-02D-1386-10 chr1:238045722 T>A maps to NM_021186.3 *541L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4644-01A-02D-1386-10 chr1:238045722 T>A maps to NM_021186.3 *541L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4644-01A-02D-1386-10 chr12:11506349 C>T maps to NM_005039.3 Q229Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4644-01A-02D-1386-10 chr12:11506349 C>T maps to NM_005039.3 Q229Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4644-01A-02D-1386-10 chr2:107040984 T>C maps to ENST00000304514 R1146R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4644-01A-02D-1386-10 chr2:107040984 T>C maps to ENST00000304514 R1146R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4644-01A-02D-1386-10 chr2:108487876 T>C maps to NM_182588.2 D1139D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4644-01A-02D-1386-10 chr2:108487876 T>C maps to NM_182588.2 D1139D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4644-01A-02D-1386-10 chr14:23635684 C>A maps to NM_012244.2 V72V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4644-01A-02D-1386-10 chr14:23635684 C>A maps to NM_012244.2 V72V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4884-01A-01W-1369-10 chr3:10183724 C>A maps to NM_000551.2 S65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5671-01A-11D-1534-10 chr2:220402024 C>A maps to NM_018674.4 I588I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5671-01A-11D-1534-10 chr1:165652236 G>T maps to NM_000696.3 G146G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5671-01A-11D-1534-10 chr11:77817938 T>C maps to NM_024079.4 R364R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5671-01A-11D-1534-10 chr6:90572531 T>C maps to NM_012115.3 V368V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5671-01A-11D-1534-10 chr11:103091359 C>A maps to NM_001080463.1 V2985V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5671-01A-11D-1534-10 chr12:77444476 C>T maps to NM_203394.2 R139R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5671-01A-11D-1534-10 chr13:47345583 G>A maps to NM_001984.1 H272H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5671-01A-11D-1534-10 chr5:132939625 G>A maps to NM_015082.1 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5671-01A-11D-1534-10 chr15:99192821 C>T maps to NM_000875.3 G4G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5671-01A-11D-1534-10 chr20:33026359 A>G maps to ENST00000262650 S242S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5671-01A-11D-1534-10 chr20:33026359 A>G maps to ENST00000262650 S242S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5671-01A-11D-1534-10 chr6:168443301 G>A maps to NM_030615.2 A297A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5671-01A-11D-1534-10 chrX:86921521 G>T maps to NM_019117.4 V715V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5671-01A-11D-1534-10 chr21:31859595 G>T maps to NM_181608.1 C24*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5671-01A-11D-1534-10 chr12:59276666 T>C maps to NM_153377.3 P488P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5671-01A-11D-1534-10 chr22:50518346 G>A maps to NM_015166.3 N141N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5671-01A-11D-1534-10 chr11:56143438 C>T maps to NM_001005204.1 L114L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5671-01A-11D-1534-10 chr8:52361652 G>C maps to NM_144651.4 P425P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5671-01A-11D-1534-10 chr14:50597306 T>A maps to NM_006939.2 P1083P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5671-01A-11D-1534-10 chr2:242545862 C>A maps to NM_015963.5 V422V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5671-01A-11D-1534-10 chr14:52922173 G>C maps to NM_020784.2 T570T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5671-01A-11D-1534-10 chr1:227842448 A>T maps to NM_178549.3 S221S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5671-01A-11D-1534-10 chr8:144776492 C>T maps to NM_173831.3 L303L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5671-01A-11D-1534-10 chr8:144776492 C>T maps to NM_173831.3 L303L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5671-01A-11D-1534-10 chr7:63537853 A>T maps to NM_001159522.1 K143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5671-01A-11D-1534-10 chr1:151679696 G>T maps to NM_007185.4 Y282*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5671-01A-11D-1534-10 chr1:151679696 G>T maps to NM_007185.4 Y282*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5671-01A-11D-1534-10 chr6:38758104 G>A maps to ENST00000327475 W890*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5671-01A-11D-1534-10 chr6:38758104 G>A maps to ENST00000327475 W890*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5672-01A-11D-1534-10 chr16:77353973 G>A maps to NM_199355.2 V768V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5672-01A-11D-1534-10 chr19:50169187 G>T maps to NM_138639.1 P36P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5672-01A-11D-1534-10 chr12:53700058 G>A maps to NM_021640.3 L240L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5672-01A-11D-1534-10 chr16:19613022 G>T maps to NM_020314.5 V343V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5672-01A-11D-1534-10 chr3:119393996 C>A maps to ENST00000484810 *99L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5672-01A-11D-1534-10 chr5:138261072 A>C maps to ENST00000355078 R626R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5672-01A-11D-1534-10 chr5:138261072 A>C maps to ENST00000355078 R626R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5672-01A-11D-1534-10 chr2:158182139 C>T maps to NM_001009959.1 P18P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5672-01A-11D-1534-10 chr20:13750636 A>G maps to NM_016649.3 D478D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5672-01A-11D-1534-10 chr20:13750636 A>G maps to NM_016649.3 D478D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5672-01A-11D-1534-10 chr13:28913319 C>A maps to NM_002019.4 E825*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5672-01A-11D-1534-10 chr16:46958368 C>T maps to NM_133443.2 V427V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5672-01A-11D-1534-10 chr3:156175240 G>T did not map to a codon.
Sequencing variant TCGA-CJ-5672-01A-11D-1534-10 chr1:70518806 T>C maps to NM_020794.2 P1365P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5672-01A-11D-1534-10 chr1:235969774 C>T maps to NM_000081.2 K887K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5672-01A-11D-1534-10 chr2:73868602 G>A maps to NM_003960.3 L51L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5672-01A-11D-1534-10 chr2:206580919 T>C maps to NM_201266.1 Y85Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5672-01A-11D-1534-10 chr7:44664055 G>T maps to ENST00000444676 R38R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5672-01A-11D-1534-10 chr7:44664055 G>T maps to ENST00000444676 R38R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5672-01A-11D-1534-10 chr21:47850086 G>A maps to NM_006031.5 Q2618Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5672-01A-11D-1534-10 chr3:58416620 G>A maps to NM_000925.3 Q118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5672-01A-11D-1534-10 chr2:200245088 G>A maps to NM_001172509.1 Q199*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5672-01A-11D-1534-10 chr2:200245088 G>A maps to NM_001172509.1 Q199*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5672-01A-11D-1534-10 chr5:150701631 A>G maps to NM_181776.2 I385I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5672-01A-11D-1534-10 chr11:66483387 G>A maps to NM_006946.2 V74V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5672-01A-11D-1534-10 chr2:160080759 G>A maps to NM_033394.2 E1232E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5672-01A-11D-1534-10 chr12:27156168 C>T maps to NM_016551.2 P82P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5672-01A-11D-1534-10 chr12:27156168 C>T maps to NM_016551.2 P82P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5672-01A-11D-1534-10 chr6:7883468 G>A maps to NM_030810.3 R403*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5672-01A-11D-1534-10 chrY:14850171 A>T maps to NM_004654.3 K416*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5672-01A-11D-1534-10 chr3:10191647 G>T maps to NM_000551.2 *214L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5672-01A-11D-1534-10 chr2:220072989 C>A maps to NM_138802.1 I149I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5672-01A-11D-1534-10 chr19:40540305 G>A maps to NM_001005851.2 I820I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5672-01A-11D-1534-10 chr9:91994190 A>G maps to NM_006378.3 L673L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5672-01A-11D-1534-10 chr9:91994190 A>G maps to NM_006378.3 L673L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5675-01A-11D-1534-10 chr5:33881334 G>C maps to NM_030955.2 L126L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5675-01A-11D-1534-10 chr20:896632 G>A maps to NM_015985.2 N75N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5675-01A-11D-1534-10 chr7:138417831 G>A maps to NM_130840.2 F566F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5675-01A-11D-1534-10 chr7:138417831 G>A maps to NM_130840.2 F566F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5675-01A-11D-1534-10 chr11:86097135 G>T maps to NM_001156474.1 R41R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5675-01A-11D-1534-10 chr11:86097135 G>T maps to NM_001156474.1 R41R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5675-01A-11D-1534-10 chr11:86097136 C>T maps to NM_001156474.1 Q42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5675-01A-11D-1534-10 chr11:86097136 C>T maps to NM_001156474.1 Q42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5675-01A-11D-1534-10 chr1:34238248 G>A maps to ENST00000373381 P549P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5675-01A-11D-1534-10 chr1:16577185 G>C maps to NM_018994.1 Y711*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5675-01A-11D-1534-10 chr19:40376808 C>T maps to NM_003890.2 G3871G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5675-01A-11D-1534-10 chr1:202097557 C>T maps to NM_004767.3 G440G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5675-01A-11D-1534-10 chrX:54785276 G>A maps to NM_198510.2 I410I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5675-01A-11D-1534-10 chr8:133141907 C>T maps to NM_004519.2 T740T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5675-01A-11D-1534-10 chr6:37606074 C>T maps to ENST00000297153 G897G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5675-01A-11D-1534-10 chr17:43173563 A>C maps to NM_021079.3 L169L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5675-01A-11D-1534-10 chr3:122247558 G>C maps to NM_031458.2 T739T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5675-01A-11D-1534-10 chr2:20138114 C>G maps to NM_001006657.1 R669R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5675-01A-11D-1534-10 chr2:20138114 C>G maps to NM_001006657.1 R669R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5675-01A-11D-1534-10 chr4:4303968 C>T maps to NM_145291.3 L136L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5675-01A-11D-1534-10 chr18:72346772 T>C maps to NM_017757.2 V1266V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5675-01A-11D-1534-10 chr19:54744734 G>A maps to ENST00000245620 P309P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5675-01A-11D-1534-10 chr19:54744734 G>A maps to ENST00000245620 P309P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5675-01A-11D-1534-10 chr5:16674990 A>G maps to NM_012334.2 I1645I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5675-01A-11D-1534-10 chr5:16674990 A>G maps to NM_012334.2 I1645I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5675-01A-11D-1534-10 chr8:144995867 A>G maps to NM_201380.2 N2844N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5675-01A-11D-1534-10 chr8:144995867 A>G maps to NM_201380.2 N2844N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5675-01A-11D-1534-10 chr3:126733640 C>A maps to NM_032242.3 Y948*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5675-01A-11D-1534-10 chr3:126733640 C>A maps to NM_032242.3 Y948*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5676-01A-11D-1534-10 chr11:62290073 T>A maps to NM_001620.1 K3939*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5676-01A-11D-1534-10 chr9:131587283 A>T maps to NM_016390.2 T228T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5676-01A-11D-1534-10 chr1:11894361 G>T maps to ENST00000376496 G532G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5676-01A-11D-1534-10 chr1:50956259 C>T maps to NM_007051.2 E551E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5676-01A-11D-1534-10 chr1:161599826 T>G did not map to a codon.
Sequencing variant TCGA-CJ-5676-01A-11D-1534-10 chr5:154270985 G>A maps to NM_015465.3 L1359L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5676-01A-11D-1534-10 chr2:11706654 G>A maps to NM_014668.3 E109E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5676-01A-11D-1534-10 chr15:41279358 G>A maps to NM_017553.1 F1254F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5676-01A-11D-1534-10 chr9:5126443 G>T maps to NM_004972.3 E1097*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5676-01A-11D-1534-10 chr12:78401105 C>T maps to NM_014903.4 S596S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5676-01A-11D-1534-10 chr3:52597492 G>A maps to ENST00000296302 Q1298*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5676-01A-11D-1534-10 chr3:52597492 G>A maps to ENST00000296302 Q1298*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5676-01A-11D-1534-10 chr12:130839158 G>T maps to NM_004764.4 G374G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5676-01A-11D-1534-10 chr6:51612745 G>T maps to NM_138694.3 S3223*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5676-01A-11D-1534-10 chr21:46689907 G>A maps to NM_133635.4 G286G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5676-01A-11D-1534-10 chr17:38510747 C>T maps to NM_001145301.2 L334L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5676-01A-11D-1534-10 chr2:20403726 C>T maps to NM_001006946.1 Q158Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5676-01A-11D-1534-10 chr3:47127735 C>T maps to NM_014159.6 W1782*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5676-01A-11D-1534-10 chr3:47127735 C>T maps to NM_014159.6 W1782*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5676-01A-11D-1534-10 chr17:62228233 G>A maps to NM_018469.3 D1083D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5676-01A-11D-1534-10 chr13:103275382 C>T maps to ENST00000376052 T259T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5676-01A-11D-1534-10 chr1:186310210 T>G maps to NM_003292.2 A1323A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5676-01A-11D-1534-10 chr22:24906777 A>G maps to NM_016327.2 A142A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5676-01A-11D-1534-10 chr6:144811220 G>A maps to NM_007124.2 E1383E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5676-01A-11D-1534-10 chr6:144811220 G>A maps to NM_007124.2 E1383E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5676-01A-11D-1534-10 chr3:10191487 C>T maps to NM_000551.2 R161*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5676-01A-11D-1534-10 chr5:150276422 T>C maps to NM_001172831.1 K142K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5676-01A-11D-1534-10 chr5:150276452 T>C maps to NM_001172831.1 T132T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5676-01A-11D-1534-10 chr12:6806816 C>T maps to NM_153685.2 S53S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5676-01A-11D-1534-10 chr12:6806816 C>T maps to NM_153685.2 S53S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5676-01A-11D-1534-10 chr22:38349735 C>A did not map to a codon.
Sequencing variant TCGA-CJ-5676-01A-11D-1534-10 chr22:38349735 C>A did not map to a codon.
Sequencing variant TCGA-CJ-5676-01A-11D-1534-10 chr16:70834810 G>T did not map to a codon.
Sequencing variant TCGA-CJ-5676-01A-11D-1534-10 chr16:70834810 G>T did not map to a codon.
Sequencing variant TCGA-CJ-5676-01A-11D-1534-10 chr11:101984952 T>C maps to NM_001130145.2 L134L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5676-01A-11D-1534-10 chr11:101984952 T>C maps to NM_001130145.2 L134L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5677-01A-11D-1534-10 chrX:49957226 T>A maps to NM_003886.2 K713*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5677-01A-11D-1534-10 chr22:29456414 T>C maps to NM_015370.1 G140G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5677-01A-11D-1534-10 chr3:133302926 T>C maps to NM_017548.4 G133G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5677-01A-11D-1534-10 chr3:133302926 T>C maps to NM_017548.4 G133G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5677-01A-11D-1534-10 chr7:117251653 T>G maps to NM_000492.3 T1053T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5677-01A-11D-1534-10 chr6:49928061 G>T maps to NM_001037499.1 S51S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5677-01A-11D-1534-10 chr11:114442139 C>A maps to NM_001077639.1 V385V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5677-01A-11D-1534-10 chr14:31817064 G>A maps to ENST00000389961 A913A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5677-01A-11D-1534-10 chr2:234749784 A>G maps to NM_018410.3 N547N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5677-01A-11D-1534-10 chr2:33534504 C>T maps to ENST00000354476 I1163I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5677-01A-11D-1534-10 chr17:15952283 T>G maps to ENST00000395857 P2152P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5677-01A-11D-1534-10 chr19:54313325 G>A maps to ENST00000391773 D529D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5677-01A-11D-1534-10 chr5:32089796 C>T maps to NM_178140.2 S2081S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5677-01A-11D-1534-10 chrX:46887396 A>C maps to NM_001077445.1 L193L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5677-01A-11D-1534-10 chrX:46887396 A>C maps to NM_001077445.1 L193L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5677-01A-11D-1534-10 chr19:4013123 G>A maps to NM_015897.2 P77P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5677-01A-11D-1534-10 chr4:148578941 C>T did not map to a codon.
Sequencing variant TCGA-CJ-5677-01A-11D-1534-10 chrX:50350757 C>T maps to NM_020717.3 Q1128Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5677-01A-11D-1534-10 chr11:18636131 T>G maps to NM_194285.2 L563L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5677-01A-11D-1534-10 chr17:80765529 G>A maps to NM_005993.4 W378*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5677-01A-11D-1534-10 chr1:19447689 C>T maps to ENST00000375267 E3378E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5677-01A-11D-1534-10 chr19:38377431 T>C maps to ENST00000447313 E2293E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5677-01A-11D-1534-10 chr20:42788568 G>A maps to NM_020433.4 T286T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5677-01A-11D-1534-10 chr20:42788568 G>A maps to NM_020433.4 T286T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5677-01A-11D-1534-10 chrX:17763602 G>T maps to NM_001037540.1 E21*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5677-01A-11D-1534-10 chrX:17763602 G>T maps to NM_001037540.1 E21*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5678-01A-11D-1534-10 chr6:127902328 T>G maps to NM_001010905.1 Y192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5678-01A-11D-1534-10 chr19:7809903 G>T maps to NM_021155.3 R275R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5678-01A-11D-1534-10 chr6:152382173 G>T maps to NM_001122741.1 L428L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5678-01A-11D-1534-10 chr2:38179039 C>T maps to NM_144713.3 Q228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5678-01A-11D-1534-10 chr11:134188592 G>A maps to NM_001080407.2 Q616Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5678-01A-11D-1534-10 chr1:155160210 G>T maps to ENST00000425082 I442I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5678-01A-11D-1534-10 chr11:50003263 G>T maps to NM_001005270.2 R258R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5678-01A-11D-1534-10 chr11:771045 A>G maps to NM_182612.2 N201N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5678-01A-11D-1534-10 chr8:30651535 G>T maps to NM_001009552.1 S212*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5678-01A-11D-1534-10 chr8:30651535 G>T maps to NM_001009552.1 S212*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5678-01A-11D-1534-10 chr10:133748060 T>G did not map to a codon.
Sequencing variant TCGA-CJ-5678-01A-11D-1534-10 chr6:41752689 C>T maps to NM_013397.5 A86A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5678-01A-11D-1534-10 chr5:179538532 T>C maps to NM_175062.3 K409K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5678-01A-11D-1534-10 chr3:47164729 T>A maps to NM_014159.6 K466*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5678-01A-11D-1534-10 chr15:42742411 G>A maps to NM_022473.1 H663H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5678-01A-11D-1534-10 chr3:119528961 C>A maps to NM_022002.2 C123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5678-01A-11D-1534-10 chr3:119528961 C>A maps to NM_022002.2 C123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5678-01A-11D-1534-10 chr17:15498177 C>T maps to ENST00000455584 V901V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5678-01A-11D-1534-10 chr17:15498177 C>T maps to ENST00000455584 V901V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5679-01A-11D-1534-10 chr7:95157533 C>T maps to NM_016116.2 R299R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5679-01A-11D-1534-10 chr11:6231319 C>T maps to NM_173525.2 R105*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5679-01A-11D-1534-10 chr12:7177888 G>T maps to NM_001734.3 R667R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5679-01A-11D-1534-10 chr6:146975332 C>G maps to NM_024694.3 L131L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5679-01A-11D-1534-10 chrX:135730559 C>T maps to NM_000074.2 D51D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5679-01A-11D-1534-10 chr10:68940122 G>A maps to NM_013266.2 N333N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5679-01A-11D-1534-10 chr12:125435350 C>T did not map to a codon.
Sequencing variant TCGA-CJ-5679-01A-11D-1534-10 chr2:116510750 G>T maps to NM_020868.3 E318*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5679-01A-11D-1534-10 chr19:4719860 A>T did not map to a codon.
Sequencing variant TCGA-CJ-5679-01A-11D-1534-10 chr19:4719860 A>T did not map to a codon.
Sequencing variant TCGA-CJ-5679-01A-11D-1534-10 chr2:212426720 A>T maps to NM_005235.2 L798L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5679-01A-11D-1534-10 chr9:130287412 G>A maps to NM_022833.2 A115A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5679-01A-11D-1534-10 chr5:41927218 G>A maps to NM_012176.2 L98L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5679-01A-11D-1534-10 chr1:146672929 G>A maps to NM_001461.2 A329A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5679-01A-11D-1534-10 chr3:169802071 T>C maps to NM_014373.2 T104T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5679-01A-11D-1534-10 chr7:2629605 C>G maps to NM_152558.3 A370A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5679-01A-11D-1534-10 chr1:15428038 C>T maps to NM_201628.2 S516S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5679-01A-11D-1534-10 chr21:32202005 G>C maps to NM_181606.2 Y4*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5679-01A-11D-1534-10 chr5:66459740 G>A maps to NM_001164664.1 P1578P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5679-01A-11D-1534-10 chr8:98703399 A>C maps to NM_178812.3 S344S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5679-01A-11D-1534-10 chr9:103348312 A>C maps to NM_001018116.1 I225I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5679-01A-11D-1534-10 chr19:4280224 G>A maps to NM_020209.3 P55P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5679-01A-11D-1534-10 chr16:30734025 C>T maps to NM_006662.2 T1283T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5679-01A-11D-1534-10 chr1:23743878 G>A maps to NM_003196.1 S81S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5679-01A-11D-1534-10 chr2:3217939 C>A maps to ENST00000398659 E193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5680-01A-11D-1534-10 chr14:58830900 T>A maps to NM_002892.3 S698S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5680-01A-11D-1534-10 chr19:30500142 T>C maps to NM_003796.2 D306D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5680-01A-11D-1534-10 chr1:87045901 A>T maps to ENST00000263723 T879T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5680-01A-11D-1534-10 chr2:211521331 C>A maps to NM_001122633.1 T1220T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5680-01A-11D-1534-10 chr5:64314066 C>A maps to NM_005869.2 I446I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5680-01A-11D-1534-10 chr19:36003990 G>A maps to NM_033317.4 R129R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5680-01A-11D-1534-10 chr1:26152902 G>T did not map to a codon.
Sequencing variant TCGA-CJ-5680-01A-11D-1534-10 chr2:96993736 C>G maps to ENST00000420728 L487L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5680-01A-11D-1534-10 chr2:96993736 C>G maps to ENST00000420728 L487L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5680-01A-11D-1534-10 chr19:50338352 C>T maps to NM_030973.3 S531S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5680-01A-11D-1534-10 chrX:14891809 G>A did not map to a codon.
Sequencing variant TCGA-CJ-5680-01A-11D-1534-10 chr11:58978850 T>A maps to NM_001039396.1 S496S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5680-01A-11D-1534-10 chr7:24324864 A>G maps to NM_000905.3 L2L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5680-01A-11D-1534-10 chr7:24324864 A>G maps to NM_000905.3 L2L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5680-01A-11D-1534-10 chr11:31816304 C>T maps to NM_001604.4 E199E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5680-01A-11D-1534-10 chr1:151315360 G>T maps to NM_000449.3 I384I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5680-01A-11D-1534-10 chr1:237538045 T>C maps to NM_001035.2 S138S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5680-01A-11D-1534-10 chr9:137006662 G>A maps to NM_052821.3 A74A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5680-01A-11D-1534-10 chr19:53740494 G>A maps to NM_182609.2 A495A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5680-01A-11D-1534-10 chr17:36622484 G>T maps to ENST00000431231 P187P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5680-01A-11D-1534-10 chr17:36622484 G>T maps to ENST00000431231 P187P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5680-01A-11D-1534-10 chr1:158059419 T>G did not map to a codon.
Sequencing variant TCGA-CJ-5680-01A-11D-1534-10 chr1:158059419 T>G did not map to a codon.
Sequencing variant TCGA-CJ-5680-01A-11D-1534-10 chr19:10473018 C>A maps to NM_003331.4 G530G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5680-01A-11D-1534-10 chr19:10473018 C>A maps to NM_003331.4 G530G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5681-01A-11D-1534-10 chr12:120791102 G>A maps to NM_002442.2 P244P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5681-01A-11D-1534-10 chr3:50386815 C>G did not map to a codon.
Sequencing variant TCGA-CJ-5681-01A-11D-1534-10 chr7:100860059 C>A maps to NM_001084.4 L39L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5681-01A-11D-1534-10 chrX:109696031 A>G maps to NM_020769.2 G729G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5681-01A-11D-1534-10 chr17:55058512 C>G maps to NM_021626.2 A49A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5681-01A-11D-1534-10 chr7:83640553 A>G maps to NM_006080.2 R290R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5681-01A-11D-1534-10 chrX:152086677 C>T maps to NM_001178106.1 T137T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5681-01A-11D-1534-10 chr19:18054505 C>T maps to NM_001136203.1 P218P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5681-01A-11D-1534-10 chr19:18054505 C>T maps to NM_001136203.1 P218P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5681-01A-11D-1534-10 chr3:195509393 T>G maps to NM_018406.5 T3019T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5681-01A-11D-1534-10 chr3:195509393 T>G maps to NM_018406.5 T3019T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5682-01A-11D-1534-10 chr1:100964517 A>G maps to NM_033312.2 L485L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5682-01A-11D-1534-10 chr8:142186847 C>A maps to NM_014957.2 A818A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5682-01A-11D-1534-10 chr4:162307411 G>A maps to NM_020116.3 V677V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5682-01A-11D-1534-10 chr19:47491244 G>C did not map to a codon.
Sequencing variant TCGA-CJ-5682-01A-11D-1534-10 chr6:32489793 G>A maps to NM_002125.3 D86D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5682-01A-11D-1534-10 chr12:57588206 C>A maps to NM_002332.2 T2663T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5682-01A-11D-1534-10 chr19:44301841 G>T maps to NM_001031749.2 T219T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5682-01A-11D-1534-10 chr5:56152548 T>A maps to NM_005921.1 L202*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5682-01A-11D-1534-10 chr18:47500799 G>T maps to NM_001080467.2 G414G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5682-01A-11D-1534-10 chr16:68224815 T>A maps to NM_173165.2 I748I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5682-01A-11D-1534-10 chr16:68224815 T>A maps to NM_173165.2 I748I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5682-01A-11D-1534-10 chr1:11579863 C>T maps to NM_020780.1 L709L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5682-01A-11D-1534-10 chr9:116246491 T>C maps to NM_144488.4 A200A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5682-01A-11D-1534-10 chr7:4152924 C>T maps to NM_152744.3 R1147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5682-01A-11D-1534-10 chr3:47098902 A>T maps to NM_014159.6 L2124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5682-01A-11D-1534-10 chr9:91680465 A>C maps to NM_016848.5 A271A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5682-01A-11D-1534-10 chr17:33802319 A>G maps to ENST00000361112 A492A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5682-01A-11D-1534-10 chr9:35608910 G>C maps to NM_006285.2 R351R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5682-01A-11D-1534-10 chr2:179631233 G>A maps to NM_133378.4 R3193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5682-01A-11D-1534-10 chr17:73832899 A>T maps to ENST00000412096 G385G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5682-01A-11D-1534-10 chr19:52619875 T>G maps to NM_178523.3 R181R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5682-01A-11D-1534-10 chr1:16361924 G>A did not map to a codon.
Sequencing variant TCGA-CJ-5682-01A-11D-1534-10 chr1:16361924 G>A did not map to a codon.
Sequencing variant TCGA-CJ-5682-01A-11D-1534-10 chr6:30459115 T>A maps to NM_005516.5 P271P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5682-01A-11D-1534-10 chr6:30459115 T>A maps to NM_005516.5 P271P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5682-01A-11D-1534-10 chr7:23827687 T>C maps to NM_031414.3 N859N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5682-01A-11D-1534-10 chr7:23827687 T>C maps to NM_031414.3 N859N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5683-01A-11D-1534-10 chr17:79426335 G>A maps to ENST00000436173 E1926E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5683-01A-11D-1534-10 chr19:30193855 G>T maps to NM_001031726.2 A74A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5683-01A-11D-1534-10 chr1:78248999 T>C maps to NM_198549.2 F53F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5683-01A-11D-1534-10 chr19:8162184 G>A maps to NM_032447.3 L1759L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5683-01A-11D-1534-10 chr1:155279735 A>G maps to NM_001135821.1 Q52Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5683-01A-11D-1534-10 chr4:175649780 A>G maps to NM_006529.2 P112P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5683-01A-11D-1534-10 chr4:175649780 A>G maps to NM_006529.2 P112P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5683-01A-11D-1534-10 chr12:57548477 C>T maps to NM_002332.2 G407G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5683-01A-11D-1534-10 chr2:170026248 G>A maps to NM_004525.2 S3820S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5683-01A-11D-1534-10 chr11:75438649 G>T maps to NM_025098.2 R147R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5683-01A-11D-1534-10 chr8:17157529 G>A maps to NM_004686.4 D608D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5683-01A-11D-1534-10 chr3:124635227 C>T maps to NM_033049.3 K299K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5683-01A-11D-1534-10 chr15:52720649 C>G maps to ENST00000358212 V85V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5683-01A-11D-1534-10 chr15:52720649 C>G maps to ENST00000358212 V85V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5683-01A-11D-1534-10 chr1:204955081 G>A maps to ENST00000367172 V877V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5683-01A-11D-1534-10 chr1:228403480 G>C maps to NM_001098623.1 L682L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5683-01A-11D-1534-10 chr13:114782718 G>T maps to ENST00000389544 I407I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5683-01A-11D-1534-10 chr1:182551375 G>A maps to NM_021133.3 V528V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5683-01A-11D-1534-10 chr1:182551375 G>A maps to NM_021133.3 V528V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5683-01A-11D-1534-10 chr20:4839998 G>A maps to NM_203327.1 V552V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5683-01A-11D-1534-10 chr5:139946852 T>C maps to NM_080670.2 H33H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5683-01A-11D-1534-10 chr6:35086230 G>A maps to NM_001093728.1 Q456*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5683-01A-11D-1534-10 chr12:125834193 T>C maps to NM_052907.2 I83I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5683-01A-11D-1534-10 chr21:33744826 A>T maps to NM_014825.2 G330G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5683-01A-11D-1534-10 chr17:36636038 C>T maps to ENST00000431231 R848R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5683-01A-11D-1534-10 chr17:36636038 C>T maps to ENST00000431231 R848R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5683-01A-11D-1534-10 chr7:99573622 G>T maps to NM_001185.3 V7V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5683-01A-11D-1534-10 chr7:99573622 G>T maps to NM_001185.3 V7V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5684-01A-11D-1534-10 chr12:4747325 C>A maps to NM_006422.2 G13*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5684-01A-11D-1534-10 chr4:104097154 C>A maps to NM_001813.2 E481*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5684-01A-11D-1534-10 chr4:104097154 C>A maps to NM_001813.2 E481*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5684-01A-11D-1534-10 chr12:77424036 G>T maps to NM_203394.2 L486L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5684-01A-11D-1534-10 chr12:77424036 G>T maps to NM_203394.2 L486L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5684-01A-11D-1534-10 chr18:48510775 C>A maps to NM_018696.2 I156I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5684-01A-11D-1534-10 chr18:48510775 C>A maps to NM_018696.2 I156I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5684-01A-11D-1534-10 chr10:99229885 C>T maps to ENST00000422291 L303L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5684-01A-11D-1534-10 chr3:52610694 G>A maps to ENST00000296302 R1185*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5684-01A-11D-1534-10 chr17:36935737 C>A maps to NM_003559.4 L184L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5684-01A-11D-1534-10 chr22:43614318 C>T maps to NM_173050.2 K611K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5684-01A-11D-1534-10 chr14:95029882 C>T maps to NM_006215.2 L22L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5684-01A-11D-1534-10 chr5:127488498 T>G did not map to a codon.
Sequencing variant TCGA-CJ-5684-01A-11D-1534-10 chr5:127488498 T>G did not map to a codon.
Sequencing variant TCGA-CJ-5684-01A-11D-1534-10 chr1:152084845 G>T maps to NM_007113.2 R283R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5684-01A-11D-1534-10 chr1:152084845 G>T maps to NM_007113.2 R283R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5684-01A-11D-1534-10 chr9:27109632 C>T maps to NM_000459.3 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5684-01A-11D-1534-10 chr11:18722526 C>T maps to NM_153347.1 C23C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5684-01A-11D-1534-10 chr7:66532333 C>T maps to NM_018264.2 R406R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5684-01A-11D-1534-10 chr3:10188204 T>C maps to NM_000551.2 L116L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5684-01A-11D-1534-10 chr12:6091107 C>T maps to NM_000552.3 P2377P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5684-01A-11D-1534-10 chr2:95847046 G>A maps to ENST00000453539 R171R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5684-01A-11D-1534-10 chr3:101038458 C>A maps to NM_016247.2 V101V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5684-01A-11D-1534-10 chr3:101038458 C>A maps to NM_016247.2 V101V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5684-01A-11D-1534-10 chr1:13183479 A>G maps to NM_001136561.2 P131P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-5684-01A-11D-1534-10 chr1:13183479 A>G maps to NM_001136561.2 P131P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5581-01A-02D-1534-10 chr21:47588273 C>T maps to NM_001142854.1 S164S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5581-01A-02D-1534-10 chrX:110494225 G>T maps to NM_014289.3 C359*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5581-01A-02D-1534-10 chr18:25532270 A>T maps to NM_001792.3 L856*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5581-01A-02D-1534-10 chr14:86089420 C>T maps to NM_013231.4 N521N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5581-01A-02D-1534-10 chr6:143081502 A>G maps to NM_006734.3 T1974T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5581-01A-02D-1534-10 chr6:143081502 A>G maps to NM_006734.3 T1974T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5581-01A-02D-1534-10 chr1:227921678 C>T maps to NM_023007.2 W207*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5581-01A-02D-1534-10 chr2:33622347 C>G maps to ENST00000354476 V1662V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5581-01A-02D-1534-10 chr2:99901198 C>A maps to NM_174898.2 E140*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5581-01A-02D-1534-10 chr7:141752122 C>A maps to ENST00000475668 L945L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5581-01A-02D-1534-10 chr6:30954437 C>T maps to NM_001010909.2 A162A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5581-01A-02D-1534-10 chr5:141242927 T>A maps to NM_032420.2 K990*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5581-01A-02D-1534-10 chr17:36523826 A>G maps to NM_014598.2 P418P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5581-01A-02D-1534-10 chr2:29073073 T>C maps to NM_017910.3 Q475Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5581-01A-02W-1584-10 chr3:10183733 C>A maps to NM_000551.2 S68*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5581-01A-02D-1534-10 chr10:103907138 A>C maps to NM_015062.3 R1464R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5581-01A-02D-1534-10 chr10:103907138 A>C maps to NM_015062.3 R1464R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5583-01A-02D-1534-10 chr14:32561312 C>T maps to NM_001030055.1 R480*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5583-01A-02D-1534-10 chr5:140953562 T>A maps to ENST00000398557 P618P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5583-01A-02D-1534-10 chr6:32134516 G>A maps to NM_030652.2 E88E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5583-01A-02D-1534-10 chr1:158988365 G>A maps to ENST00000295809 K299K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5583-01A-02D-1534-10 chr7:94993299 C>A maps to NM_000940.2 L190L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5583-01A-02D-1534-10 chr5:98115299 A>T maps to NM_001012761.2 P92P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5583-01A-02D-1534-10 chr16:68953055 C>A maps to NM_024562.1 T687T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5583-01A-02D-1534-10 chr1:223983852 T>A maps to NM_001031685.2 P796P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5583-01A-02D-1534-10 chr19:46185189 C>T maps to NM_000164.2 C466C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5583-01A-02D-1534-10 chr19:46185189 C>T maps to NM_000164.2 C466C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5585-01A-01D-1534-10 chr3:57291080 T>A did not map to a codon.
Sequencing variant TCGA-CW-5585-01A-01D-1534-10 chr3:148559630 A>T maps to NM_001871.2 K166*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5585-01A-01D-1534-10 chr19:8196480 G>A maps to NM_032447.3 H649H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5585-01A-01D-1534-10 chr12:57619418 G>A maps to NM_007224.3 K272K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5585-01A-01D-1534-10 chr2:179255816 T>G maps to ENST00000392505 S798S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5585-01A-01D-1534-10 chr16:84215641 G>T maps to NM_005679.2 T248T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5585-01A-01D-1534-10 chr1:26609137 A>C did not map to a codon.
Sequencing variant TCGA-CW-5585-01A-01D-1534-10 chr1:26609137 A>C did not map to a codon.
Sequencing variant TCGA-CW-5585-01A-01D-1534-10 chr21:43533906 G>T maps to NM_173568.3 E905*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5585-01A-01D-1534-10 chr2:61575327 G>A maps to NM_014709.3 C654C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5585-01A-01D-1534-10 chr5:82834254 T>C maps to NM_004385.4 S1811S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5585-01A-01D-1534-10 chr13:111125465 T>A maps to NM_001846.2 L798L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5585-01A-01D-1534-10 chr13:111125465 T>A maps to NM_001846.2 L798L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5585-01A-01D-1534-10 chr3:195509321 G>A maps to NM_018406.5 V3043V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5585-01A-01D-1534-10 chr3:195509321 G>A maps to NM_018406.5 V3043V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5585-01A-01D-1534-10 chr11:76814079 C>T maps to NM_006189.1 F65F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5585-01A-01D-1534-10 chr11:76814079 C>T maps to NM_006189.1 F65F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5588-01A-01D-1534-10 chr1:154569309 G>A maps to ENST00000292205 V790V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5588-01A-01D-1534-10 chr11:62296230 G>A maps to NM_001620.1 G1886G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5588-01A-01D-1534-10 chr2:97849371 T>C maps to NM_001164315.1 G640G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5588-01A-01D-1534-10 chr9:33386468 C>T maps to NM_001170.1 P113P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5588-01A-01D-1534-10 chr12:40076778 A>T maps to NM_001031748.2 T351T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5588-01A-01D-1534-10 chr5:54579537 T>C maps to NM_019030.2 K486K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5588-01A-01D-1534-10 chr5:176951609 C>T maps to ENST00000442143 L704L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5588-01A-01D-1534-10 chr1:154956240 T>A maps to NM_025207.4 L24*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5588-01A-01D-1534-10 chr1:154956240 T>A maps to NM_025207.4 L24*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5588-01A-01D-1534-10 chr2:197194347 A>T maps to NM_020760.1 G174G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5588-01A-01D-1534-10 chr10:33217097 G>A maps to ENST00000374956 D157D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5588-01A-01D-1534-10 chr6:29454617 T>A maps to NM_052967.1 P354P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5588-01A-01D-1534-10 chr13:109535456 T>C maps to NM_015011.1 P470P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5588-01A-01D-1534-10 chr8:52733054 C>T maps to NM_052937.2 E310E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5588-01A-01D-1534-10 chr10:119044692 T>C maps to NM_173791.3 S517S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5588-01A-01D-1534-10 chr2:240982051 C>G maps to NM_001080835.1 S116S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5588-01A-01D-1534-10 chr10:112572491 C>T maps to NM_001134363.1 P779P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5588-01A-01D-1534-10 chr1:41092245 G>T maps to NM_014747.2 L290L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5588-01A-01D-1534-10 chr8:10466018 A>T maps to NM_178857.5 A1863A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5588-01A-01D-1534-10 chr9:135173489 G>A maps to ENST00000372169 L1920L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5588-01A-01D-1534-10 chr12:104062491 C>A maps to NM_017564.9 C719*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5588-01A-01D-1534-10 chr19:51845046 C>G maps to NM_001163922.1 L85L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5588-01A-01D-1534-10 chr1:16918652 C>T did not map to a codon.
Sequencing variant TCGA-CW-5588-01A-01D-1534-10 chr1:16918652 C>T did not map to a codon.
Sequencing variant TCGA-CW-5588-01A-01D-1534-10 chr6:41773625 G>A maps to ENST00000373009 R366*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5588-01A-01D-1534-10 chr6:41773625 G>A maps to ENST00000373009 R366*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5589-01A-01D-1534-10 chr8:145759518 G>A maps to NM_025251.1 A894A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5589-01A-01D-1534-10 chr3:142281208 A>T maps to NM_001184.3 A345A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5589-01A-01D-1534-10 chr10:17110703 T>G maps to NM_001081.3 S897S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5589-01A-01D-1534-10 chr22:43024288 T>A did not map to a codon.
Sequencing variant TCGA-CW-5589-01A-01D-1534-10 chr11:687970 C>A maps to NM_021008.2 E202*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5589-01A-01D-1534-10 chr15:66044740 G>A maps to ENST00000443035 V179V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5589-01A-01D-1534-10 chr5:176026121 C>T maps to NM_052899.2 L238L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5589-01A-01D-1534-10 chr14:81682786 C>T maps to NM_015859.2 V34V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5589-01A-01D-1534-10 chr1:15370642 C>T maps to NM_201628.2 A238A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5589-01A-01D-1534-10 chr11:1092815 G>C maps to ENST00000441003 T1545T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5589-01A-01D-1534-10 chr5:37020559 G>T did not map to a codon.
Sequencing variant TCGA-CW-5589-01A-01D-1534-10 chr17:7319144 G>C maps to NM_020795.2 L451L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5589-01A-01D-1534-10 chr11:56431746 G>T maps to NM_001004730.1 E196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5589-01A-01D-1534-10 chr3:52663051 C>A did not map to a codon.
Sequencing variant TCGA-CW-5589-01A-01D-1534-10 chr19:4511478 A>T maps to NM_001080400.1 T817T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5589-01A-01D-1534-10 chr8:43152261 G>A maps to NM_001005365.2 R133R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5589-01A-01D-1534-10 chr1:12837357 G>A maps to NM_001080830.1 E356E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5589-01A-01D-1534-10 chr12:11506646 T>C maps to NM_005039.3 Q130Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5589-01A-01D-1534-10 chr19:18309635 G>C maps to NM_002866.4 S124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5589-01A-01D-1534-10 chr15:63547743 C>G maps to NM_016530.2 S95S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5589-01A-01D-1534-10 chr19:36018412 T>A maps to NM_001166034.1 A257A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5589-01A-01D-1534-10 chr1:156146589 A>G maps to NM_022367.3 S696S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5589-01A-01D-1534-10 chr3:136062786 G>T maps to NM_005862.2 P1111P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5589-01A-01D-1534-10 chr9:93606287 T>C maps to NM_003177.5 D36D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5589-01A-01D-1534-10 chr9:93606287 T>C maps to NM_003177.5 D36D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5589-01A-01D-1534-10 chr19:19380553 G>C maps to NM_001001524.2 L142L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5589-01A-01D-1534-10 chr12:83525987 G>C did not map to a codon.
Sequencing variant TCGA-CW-5589-01A-01D-1534-10 chr10:50108352 T>A did not map to a codon.
Sequencing variant TCGA-CW-5589-01A-01D-1534-10 chr1:144813823 G>C maps to NM_001037675.2 L356L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5589-01A-01D-1534-10 chr1:144813823 G>C maps to NM_001037675.2 L356L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5589-01A-01D-1534-10 chr1:144828609 T>G maps to NM_001037675.2 S884S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5589-01A-01D-1534-10 chr1:144828609 T>G maps to NM_001037675.2 S884S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5589-01A-01D-1534-10 chr11:608821 G>A maps to ENST00000264555 E1122E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5589-01A-01D-1534-10 chr11:608821 G>A maps to ENST00000264555 E1122E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5589-01A-01D-1534-10 chr2:219146893 G>T did not map to a codon.
Sequencing variant TCGA-CW-5589-01A-01D-1534-10 chr2:219146893 G>T did not map to a codon.
Sequencing variant TCGA-CW-5591-01A-01D-1534-10 chr14:86088604 C>T maps to NM_013231.4 L249L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5591-01A-01D-1534-10 chr12:110897605 G>T maps to NM_001164373.1 P83P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5591-01A-01D-1534-10 chr16:57713135 C>A maps to NM_170776.4 R180R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5591-01A-01D-1534-10 chr19:6218034 C>T maps to NM_005934.3 P376P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5591-01A-01D-1534-10 chr3:42679499 T>G maps to NM_005385.3 V768V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5591-01A-01D-1534-10 chr15:72432090 C>T maps to NM_145204.3 Q43*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5591-01A-01D-1534-10 chr16:2546379 C>A maps to ENST00000434757 I77I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5591-01A-01D-1534-10 chr1:55642116 C>A did not map to a codon.
Sequencing variant TCGA-CW-5591-01A-01D-1534-10 chr1:55638067 G>A maps to NM_015306.2 L228L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5591-01A-01D-1534-10 chr3:10191589 C>T maps to NM_000551.2 Q195*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5591-01A-01D-1534-10 chr2:187693067 A>C maps to NM_182521.2 P515P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5591-01A-01D-1534-10 chr19:53911473 A>G maps to NM_001040185.1 K222K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5591-01A-01D-1534-10 chr19:53911473 A>G maps to NM_001040185.1 K222K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4863-01A-01D-1501-10 chr12:27075597 A>G maps to NM_018164.2 D280D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4863-01A-01D-1501-10 chr5:118502424 A>G maps to NM_005509.4 E1695E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4863-01A-01D-1501-10 chr6:46133253 A>G maps to NM_021572.4 N292N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4863-01A-01D-1501-10 chr10:126523419 T>C maps to NM_032182.3 D376D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4863-01A-01D-1501-10 chr4:187629280 A>C maps to ENST00000260147 P567P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4863-01A-01D-1501-10 chr4:187629280 A>C maps to ENST00000260147 P567P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4863-01A-01D-1501-10 chr19:9046548 A>G maps to NM_024690.2 P11694P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4863-01A-01D-1501-10 chr19:9046548 A>G maps to NM_024690.2 P11694P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4863-01A-01D-1501-10 chr2:84660488 C>T maps to NM_003849.3 Q220Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4863-01A-01D-1501-10 chr1:74954919 C>G maps to NM_001112808.2 L824L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4863-01A-01D-1501-10 chr19:18856653 C>T maps to NM_001098482.1 L105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4863-01A-01D-1501-10 chr19:18856653 C>T maps to NM_001098482.1 L105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4863-01A-01D-1501-10 chr16:84050800 C>A maps to NM_001080442.1 R299R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4863-01A-01D-1501-10 chr16:84050800 C>A maps to NM_001080442.1 R299R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4863-01A-01D-1501-10 chr5:176297518 T>C maps to NM_133369.2 S290S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4863-01A-01D-1501-10 chr5:176297518 T>C maps to NM_133369.2 S290S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4865-01A-02D-1501-10 chr5:115350146 G>A maps to NM_173800.4 A791A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4865-01A-02D-1501-10 chr15:90128973 C>T maps to NM_152259.3 P404P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4865-01A-02D-1501-10 chr20:34053566 G>C did not map to a codon.
Sequencing variant TCGA-CZ-4865-01A-02D-1501-10 chr18:5428359 C>T maps to NM_012307.2 K339K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4865-01A-02D-1501-10 chr8:33246864 A>G maps to ENST00000380081 F318F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4865-01A-02D-1501-10 chr19:42566908 C>A did not map to a codon.
Sequencing variant TCGA-CZ-4865-01A-02D-1501-10 chr12:54856985 A>G maps to NM_144594.2 C71C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4865-01A-02D-1501-10 chr7:43351594 C>A maps to NM_015052.3 Y87*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4865-01A-02D-1501-10 chr3:124536467 A>G maps to NM_002213.3 N376N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4865-01A-02D-1501-10 chr1:235884145 A>G maps to NM_000081.2 Y3125Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4865-01A-02D-1501-10 chr1:28660958 C>T maps to NM_017638.2 L35L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4865-01A-02D-1501-10 chr17:10435068 C>A maps to NM_017534.5 E860*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4865-01A-02D-1501-10 chr19:9236855 C>T maps to NM_001001958.1 G257G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4865-01A-02D-1501-10 chr10:95791805 G>T maps to ENST00000371380 E335*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4865-01A-02D-1501-10 chr16:67680180 C>T maps to NM_001013838.1 A114A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4865-01A-02D-1501-10 chr2:62728622 C>G did not map to a codon.
Sequencing variant TCGA-CZ-4865-01A-02D-1501-10 chr1:165859455 A>T maps to NM_012474.4 K39*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4865-01A-02D-1501-10 chr4:70361486 T>C maps to NM_021139.2 T31T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4865-01A-02D-1501-10 chr21:17246742 C>T maps to ENST00000285681 F931F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4866-01A-01D-1501-10 chr7:87196209 C>A maps to NM_000927.3 G141*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4866-01A-01D-1501-10 chr20:50292727 A>T maps to NM_006045.1 V273V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4866-01A-01D-1501-10 chr3:52443567 A>T did not map to a codon.
Sequencing variant TCGA-CZ-4866-01A-01D-1501-10 chr19:10979898 G>A maps to NM_001136482.1 T183T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4866-01A-01D-1501-10 chr4:100443801 G>A maps to NM_032149.2 E91E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4866-01A-01D-1501-10 chr12:69985845 G>T maps to NM_006431.2 L219L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4866-01A-01D-1501-10 chr12:69985845 G>T maps to NM_006431.2 L219L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4866-01A-01D-1501-10 chr4:8613866 G>A maps to NM_001014447.2 A447A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4866-01A-01D-1501-10 chr7:143097035 G>A maps to NM_005232.4 L181L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4866-01A-01D-1501-10 chr7:100281054 T>A maps to NM_022574.4 R689*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4866-01A-01D-1501-10 chr20:30915460 T>C maps to NM_004798.3 Y655Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4866-01A-01D-1501-10 chr19:55019388 G>T maps to NM_002288.3 L118L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4866-01A-01D-1501-10 chr19:55019388 G>T maps to NM_002288.3 L118L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4866-01A-01D-1501-10 chr4:109084819 G>A maps to NM_016269.4 P106P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4866-01A-01D-1501-10 chr19:54721108 C>A did not map to a codon.
Sequencing variant TCGA-CZ-4866-01A-01D-1501-10 chr18:47803543 A>C maps to ENST00000424334 V73V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4866-01A-01D-1501-10 chr11:5068156 C>T maps to NM_001001916.2 Y134Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4866-01A-01D-1501-10 chr8:57354187 C>T maps to NM_001135690.1 S149S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4866-01A-01D-1501-10 chr20:58318177 G>C maps to NM_080672.3 T45T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4866-01A-01D-1501-10 chr1:68903914 G>C maps to NM_000329.2 P361P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4866-01A-01D-1501-10 chr11:47433930 G>A maps to NM_001128225.2 Q150Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4866-01A-01D-1501-10 chr7:47384597 G>T maps to NM_022748.11 I830I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4866-01A-01D-1501-10 chr19:44586258 G>A did not map to a codon.
Sequencing variant TCGA-CZ-4866-01A-01D-1501-10 chr3:56703745 A>C maps to ENST00000447900 V239V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4866-01A-01D-1501-10 chr3:56703745 A>C maps to ENST00000447900 V239V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4866-01A-01D-1501-10 chr2:80136760 G>A maps to ENST00000402739 R298R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4866-01A-01D-1501-10 chr2:80136760 G>A maps to ENST00000402739 R298R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4866-01A-01D-1501-10 chr9:73027889 T>C maps to NM_001206.2 G130G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4866-01A-01D-1501-10 chr9:73027889 T>C maps to NM_001206.2 G130G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5451-01A-01D-1501-10 chr1:154574686 A>T maps to ENST00000292205 L187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5451-01A-01D-1501-10 chr15:50168714 C>T maps to NM_024837.2 V929V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5451-01A-01D-1501-10 chr3:62388784 G>A maps to ENST00000383709 Q1290*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5451-01A-01D-1501-10 chr3:62388784 G>A maps to ENST00000383709 Q1290*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5451-01A-01D-1501-10 chr3:62388785 A>G maps to ENST00000383709 Y1289Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5451-01A-01D-1501-10 chr3:62388785 A>G maps to ENST00000383709 Y1289Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5451-01A-01D-1501-10 chr6:126669609 A>G did not map to a codon.
Sequencing variant TCGA-CZ-5451-01A-01D-1501-10 chr6:126669609 A>G did not map to a codon.
Sequencing variant TCGA-CZ-5451-01A-01D-1501-10 chr4:40337468 G>C did not map to a codon.
Sequencing variant TCGA-CZ-5451-01A-01D-1501-10 chr2:172291645 C>G maps to NM_025000.3 A60A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5451-01A-01D-1501-10 chr2:183616890 A>G maps to NM_018981.1 T509T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5451-01A-01D-1501-10 chr7:111379462 G>T maps to ENST00000428084 S1704*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5451-01A-01D-1501-10 chr10:88930274 G>C maps to ENST00000298786 L558L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5451-01A-01D-1501-10 chr14:55817638 T>G maps to NM_152231.1 P177P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5451-01A-01D-1501-10 chr7:127224746 G>A maps to NM_024523.5 Q164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5451-01A-01D-1501-10 chr17:65141856 A>G did not map to a codon.
Sequencing variant TCGA-CZ-5451-01A-01D-1501-10 chr17:65141856 A>G did not map to a codon.
Sequencing variant TCGA-CZ-5451-01A-01D-1501-10 chr20:33012329 A>C maps to ENST00000262650 R215R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5451-01A-01D-1501-10 chr18:7042147 G>A maps to NM_005559.2 H419H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5451-01A-01D-1501-10 chr6:112441542 A>T maps to NM_001105206.1 G1536G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5451-01A-01D-1501-10 chr9:131669448 T>A maps to NM_001127244.1 I2I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5451-01A-01D-1501-10 chr7:140710229 A>C maps to NM_053035.2 L68L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5451-01A-01D-1501-10 chr14:39645317 T>C maps to NM_002687.3 P50P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5451-01A-01D-1501-10 chr1:220346066 A>G maps to ENST00000358951 V776V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5451-01A-01D-1501-10 chr8:125498659 T>G maps to NM_007218.3 L257*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5451-01A-01D-1501-10 chr18:18546994 G>A maps to NM_005406.2 Q1079*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5451-01A-01D-1501-10 chr1:38455224 G>A maps to NM_006802.2 Q47*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5451-01A-01D-1501-10 chr1:32259421 G>T maps to NM_144569.4 A820A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5451-01A-01D-1501-10 chr12:6439821 G>T maps to NM_001065.3 L227L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5451-01A-01D-1501-10 chr19:46024607 T>G maps to NM_003370.3 L124L. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-CZ-5451-01A-01D-1501-10. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-CZ-5451-01A-01D-1501-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CZ-5451-01A-01D-1501-10 chr10:78709125 T>C did not map to a codon.
Sequencing variant TCGA-CZ-5451-01A-01D-1501-10 chr10:78709125 T>C did not map to a codon.
Sequencing variant TCGA-CZ-5452-01A-01D-1501-10 chr9:75555087 G>A maps to NM_000689.3 L49L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5452-01A-01D-1501-10 chr4:47560000 G>A maps to NM_020453.3 Q715Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5452-01A-01D-1501-10 chr19:6712357 G>A maps to NM_000064.2 G393G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5452-01A-01D-1501-10 chr5:156592755 G>A maps to NM_130899.2 L142L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5452-01A-01D-1501-10 chr5:156592755 G>A maps to NM_130899.2 L142L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5452-01A-01D-1501-10 chr1:235971938 G>A maps to NM_000081.2 Q727*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5452-01A-01D-1501-10 chr2:18765440 C>T maps to ENST00000455492 E345E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5452-01A-01D-1501-10 chrX:38262962 C>T maps to NM_000531.5 F211F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5452-01A-01D-1501-10 chr14:36143765 G>A maps to NM_194301.2 Q1086*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5452-01A-01D-1501-10 chr20:17641023 G>T maps to ENST00000377813 A43A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5452-01A-01D-1501-10 chr20:17641023 G>T maps to ENST00000377813 A43A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5452-01A-01D-1501-10 chr10:49988079 C>T maps to NM_020945.1 H1164H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5452-01A-01D-1501-10 chr19:53577474 C>T maps to NM_001102603.1 G63G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5452-01A-01D-1501-10 chr19:57838031 C>G maps to NM_213598.3 Y59*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5452-01A-01D-1501-10 chr4:9783961 G>T maps to NM_000798.4 V103V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5452-01A-01D-1501-10 chr4:9783961 G>T maps to NM_000798.4 V103V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5453-01A-01D-1501-10 chr10:123683800 G>A maps to NM_001001976.1 L50L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5453-01A-01D-1501-10 chr5:891952 G>A maps to NM_023924.4 P23P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5453-01A-01D-1501-10 chr2:27456648 C>T maps to NM_004341.3 V1124V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5453-01A-01D-1501-10 chr15:69003111 C>T maps to NM_006091.3 N125N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5453-01A-01D-1501-10 chr8:141545587 C>A maps to NM_012154.3 L750L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5453-01A-01D-1501-10 chr8:144940665 G>A maps to NM_031308.1 G2252G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5453-01A-01D-1501-10 chr1:161595992 C>T maps to ENST00000367964 R209R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5453-01A-01D-1501-10 chr17:80706747 T>C maps to NM_022158.3 D162D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5453-01A-01D-1501-10 chr17:80706747 T>C maps to NM_022158.3 D162D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5453-01A-01D-1501-10 chr5:90149226 A>G maps to NM_032119.3 L5777L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5453-01A-01D-1501-10 chr16:30006454 C>T maps to NM_003609.3 E90E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5453-01A-01D-1501-10 chr21:46057624 T>C maps to NM_181688.1 P97P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5453-01A-01D-1501-10 chrX:135328305 T>A maps to NM_024597.3 V57V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5453-01A-01D-1501-10 chr19:15852603 C>T maps to NM_013938.1 N134N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5453-01A-01D-1501-10 chr16:50261848 C>T maps to NM_001040284.2 Q619*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5453-01A-01D-1501-10 chr19:34904639 A>C did not map to a codon.
Sequencing variant TCGA-CZ-5453-01A-01D-1501-10 chr14:50136256 G>A maps to NM_002692.3 S159S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5453-01A-01D-1501-10 chr14:50136256 G>A maps to NM_002692.3 S159S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5453-01A-01D-1501-10 chr7:124503401 A>T did not map to a codon.
Sequencing variant TCGA-CZ-5453-01A-01D-1501-10 chr18:43572168 C>A did not map to a codon.
Sequencing variant TCGA-CZ-5453-01A-01D-1501-10 chr5:137776731 C>T maps to ENST00000378339 A20A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5453-01A-01D-1501-10 chr13:29275083 T>G maps to NM_001135919.1 *464Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5453-01A-01D-1501-10 chr16:68328655 C>A maps to NM_003983.4 S357S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5453-01A-01D-1501-10 chr5:101592956 G>C maps to NM_180991.4 S444*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5453-01A-01D-1501-10 chr19:11113808 G>T maps to NM_001128849.1 L639L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5453-01A-01D-1501-10 chr7:2314822 C>T maps to NM_013321.2 V114V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5453-01A-01D-1501-10 chr7:2314822 C>T maps to NM_013321.2 V114V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5453-01A-01D-1501-10 chr4:68995526 C>T did not map to a codon.
Sequencing variant TCGA-CZ-5453-01A-01D-1501-10 chr9:79936444 C>T maps to ENST00000376646 F1871F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5453-01A-01D-1501-10 chr18:74620407 G>A maps to NM_007345.3 T808T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5453-01A-01D-1501-10 chr15:43661268 T>C maps to NM_152455.3 K125K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5453-01A-01D-1501-10 chr14:74205844 G>A maps to NM_001043318.1 G289G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5453-01A-01D-1501-10 chr14:74205844 G>A maps to NM_001043318.1 G289G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5453-01A-01D-1501-10 chr9:36665414 A>G maps to NM_014791.2 T415T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5453-01A-01D-1501-10 chr9:36665414 A>G maps to NM_014791.2 T415T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5454-01A-01D-1501-10 chr20:33437794 C>T maps to NM_178026.2 P598P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5454-01A-01D-1501-10 chr3:197748372 C>A maps to NM_001136049.2 S511S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5454-01A-01D-1501-10 chr11:46895080 G>A maps to ENST00000256991 D1476D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5454-01A-01D-1501-10 chr3:119528964 G>A maps to NM_022002.2 E124E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5454-01A-01D-1501-10 chr14:97009230 G>A did not map to a codon.
Sequencing variant TCGA-CZ-5454-01A-01D-1501-10 chr3:52696198 C>A maps to ENST00000296302 E160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5454-01A-01D-1501-10 chr4:39297337 C>T maps to ENST00000381897 G951G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5454-01A-01D-1501-10 chr22:39713524 G>A maps to NM_000967.3 F102F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5454-01A-01D-1501-10 chr20:62373330 T>A maps to NM_020062.3 S167S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5454-01A-01D-1501-10 chr5:94876455 T>G maps to NM_014639.3 R161R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5454-01A-01D-1501-10 chr8:64099318 G>A maps to ENST00000339066 P249P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5455-01A-01D-1501-10 chr10:61835850 A>T maps to NM_020987.2 S1596S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5455-01A-01D-1501-10 chr7:132470403 T>A maps to ENST00000448878 G231G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5455-01A-01D-1501-10 chr18:47095826 C>T maps to NM_006033.2 L160L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5455-01A-01D-1501-10 chr11:95825400 C>T maps to NM_032427.1 Q598Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5455-01A-01D-1501-10 chr6:2689125 G>T maps to NM_001012418.3 V100V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5455-01A-01D-1501-10 chr3:52637554 G>A maps to ENST00000296302 R921*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5455-01A-01D-1501-10 chr5:140741741 G>A maps to NM_018923.2 E680E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5455-01A-01D-1501-10 chr17:57078980 G>A maps to NM_015294.3 V930V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5455-01A-01W-1528-10 chr3:10183724 C>A maps to NM_000551.2 S65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5455-01A-01D-1501-10 chr12:118506260 C>T maps to NM_019086.5 K496K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5455-01A-01D-1501-10 chr6:43492325 T>C maps to NM_020750.2 E1120E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5456-01A-01D-1501-10 chr3:53777117 G>T maps to NM_001128840.1 G964G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5456-01A-01D-1501-10 chr8:61757863 C>T maps to NM_017780.2 S1702S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5456-01A-01D-1501-10 chr13:111144510 T>C maps to NM_001846.2 A1183A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5456-01A-01D-1501-10 chr5:179201811 C>G maps to NM_014757.4 S995S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5456-01A-01D-1501-10 chr16:14711479 G>A maps to NM_002582.2 Q119*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5456-01A-01D-1501-10 chr7:124493108 C>T maps to NM_015450.2 E262E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5456-01A-01D-1501-10 chr19:5613493 C>T maps to NM_014649.2 L196L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5456-01A-01D-1501-10 chr19:5613493 C>T maps to NM_014649.2 L196L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5456-01A-01D-1501-10 chr8:17409423 G>A maps to NM_001164771.1 A368A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5456-01A-01D-1501-10 chr4:20512748 T>C maps to ENST00000273739 S353S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5456-01A-01D-1501-10 chr4:20512748 T>C maps to ENST00000273739 S353S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5456-01A-01D-1501-10 chr1:54509108 G>A maps to ENST00000371338 S171S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5456-01A-01D-1501-10 chr1:54509108 G>A maps to ENST00000371338 S171S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5456-01A-01D-1501-10 chr1:152188023 C>G maps to NM_001009931.1 S2027S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5456-01A-01D-1501-10 chr1:152188023 C>G maps to NM_001009931.1 S2027S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5457-01A-01D-1501-10 chr2:207413074 G>T maps to NM_003812.2 V288V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5457-01A-01D-1501-10 chr17:72522163 G>T maps to NM_174892.2 S68S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5457-01A-01D-1501-10 chr1:151688471 G>A maps to NM_007185.4 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5457-01A-01D-1501-10 chr6:43188336 G>A maps to ENST00000354495 K2141K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5457-01A-01D-1501-10 chr1:112308357 G>A did not map to a codon.
Sequencing variant TCGA-CZ-5457-01A-01D-1501-10 chr1:168698361 C>T maps to NM_001937.4 W17*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5457-01A-01D-1501-10 chr2:164468065 C>T maps to NM_018086.2 S92S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5457-01A-01D-1501-10 chr1:166944469 G>A maps to NM_199351.2 F12F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5457-01A-01D-1501-10 chr19:12903493 C>T maps to NM_002229.2 L303L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5457-01A-01D-1501-10 chr17:73058234 C>G maps to NM_015353.1 S219S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5457-01A-01D-1501-10 chr14:24785138 C>T maps to NM_181657.3 H94H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5457-01A-01D-1501-10 chr17:27613673 G>T maps to NM_020772.2 I446I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5457-01A-01D-1501-10 chr9:107367524 G>A maps to NM_001004481.1 N128N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5457-01A-01D-1501-10 chr11:56344846 T>G maps to NM_001004741.1 S117S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5457-01A-01D-1501-10 chr12:121660765 G>A maps to NM_002560.2 R148R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5457-01A-01D-1501-10 chr2:37501594 A>C maps to NM_005813.3 V540V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5457-01A-01D-1501-10 chr9:35811508 G>A maps to NM_001039592.1 G178G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5457-01A-01D-1501-10 chr7:65705727 C>T maps to NM_003596.3 R106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5457-01A-01D-1501-10 chr2:234468566 G>A maps to NM_018218.2 R103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5457-01A-01D-1501-10 chr1:3564111 G>A maps to NM_017818.3 Q28*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5457-01A-01D-1501-10 chr15:56924220 A>C maps to NM_017661.2 V805V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5457-01A-01D-1501-10 chr17:74732523 G>A maps to NM_003016.4 R129*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5457-01A-01D-1501-10 chr17:74732523 G>A maps to NM_003016.4 R129*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5457-01A-01D-1501-10 chr7:2698600 C>T maps to NM_025250.2 P484P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5457-01A-01D-1501-10 chr7:2698600 C>T maps to NM_025250.2 P484P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5458-01A-01D-1501-10 chr15:52844223 C>T maps to NM_006628.4 P82P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5458-01A-01D-1501-10 chr5:137848454 G>A maps to NM_004730.2 Q244*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5458-01A-01D-1501-10 chr11:65480530 T>G did not map to a codon.
Sequencing variant TCGA-CZ-5458-01A-01D-1501-10 chrX:77150868 G>T maps to NM_032121.5 T45T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5458-01A-01D-1501-10 chr17:60813346 T>A maps to NM_152598.2 K628*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5458-01A-01D-1501-10 chr3:47037323 C>G maps to NM_015175.1 A673A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5458-01A-01D-1501-10 chr3:47037323 C>G maps to NM_015175.1 A673A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5458-01A-01D-1501-10 chr7:33055307 G>A maps to NM_001002010.1 L295L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5458-01A-01D-1501-10 chr12:57345980 C>T maps to NM_003708.3 S262S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5458-01A-01D-1501-10 chr15:33873833 C>T maps to NM_001036.3 Y521Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5458-01A-01D-1501-10 chr8:29994915 T>G maps to NM_001128208.1 T136T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5458-01A-01D-1501-10 chr8:29994915 T>G maps to NM_001128208.1 T136T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5459-01A-01D-1501-10 chr1:227192737 A>G maps to ENST00000366766 P1644P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5459-01A-01D-1501-10 chr4:1388535 G>A maps to NM_175918.3 V79V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5459-01A-01D-1501-10 chr4:1388535 G>A maps to NM_175918.3 V79V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5459-01A-01D-1501-10 chr5:138147873 G>T maps to ENST00000355078 V157V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5459-01A-01D-1501-10 chr5:39383076 A>G maps to NM_001343.2 S328S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5459-01A-01D-1501-10 chr8:21563504 C>T maps to NM_001495.4 T281T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5459-01A-01D-1501-10 chr17:40342211 A>G maps to NM_032484.4 N455N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5459-01A-01D-1501-10 chr17:61613154 G>A maps to NM_030779.2 A409A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5459-01A-01D-1501-10 chr9:7013978 G>A maps to NM_015061.3 K720K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5459-01A-01D-1501-10 chr6:161523806 T>C maps to NM_005922.2 S1284S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5459-01A-01D-1501-10 chr3:129152726 A>G maps to NM_003925.1 L459L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5459-01A-01D-1501-10 chr3:129152726 A>G maps to NM_003925.1 L459L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5459-01A-01D-1501-10 chr22:24122847 G>T maps to NM_005940.3 E188*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5459-01A-01D-1501-10 chr5:137222570 T>A maps to NM_006790.2 T403T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5459-01A-01D-1501-10 chr8:125562075 T>A maps to NM_005005.2 G161G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5459-01A-01D-1501-10 chr5:102891794 A>C maps to NM_031438.2 V267V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5459-01A-01D-1501-10 chr7:143657716 C>T maps to NM_012369.2 Y218Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5459-01A-01D-1501-10 chr4:120446850 C>A did not map to a codon.
Sequencing variant TCGA-CZ-5459-01A-01D-1501-10 chr14:68047713 T>A maps to NM_020715.2 S1081S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5459-01A-01D-1501-10 chr16:4940259 T>G maps to NM_002705.4 L746L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5459-01A-01D-1501-10 chr17:80194626 G>C maps to NM_001042423.1 V82V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5459-01A-01D-1501-10 chr17:80194626 G>C maps to NM_001042423.1 V82V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5459-01A-01D-1501-10 chr17:74042205 C>T maps to NM_014230.2 R404R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5459-01A-01D-1501-10 chr22:37469599 G>A maps to ENST00000381792 N509N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5459-01A-01D-1501-10 chr15:43748190 G>T maps to NM_001141980.1 S872*. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-CZ-5459-01A-01D-1501-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CZ-5459-01A-01D-1501-10 chr6:43493657 A>G maps to NM_020750.2 D995D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5459-01A-01D-1501-10 chr7:150714121 C>T did not map to a codon.
Sequencing variant TCGA-CZ-5459-01A-01D-1501-10 chr7:150714121 C>T did not map to a codon.
Sequencing variant TCGA-CZ-5459-01A-01D-1501-10 chr19:42260805 C>T maps to NM_002483.4 T121T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5459-01A-01D-1501-10 chr19:42260805 C>T maps to NM_002483.4 T121T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5459-01A-01D-1501-10 chr12:120128174 G>A maps to ENST00000392521 P1989P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5459-01A-01D-1501-10 chr12:120128174 G>A maps to ENST00000392521 P1989P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5459-01A-01D-1501-10 chr20:22562793 C>T maps to NM_021784.4 P362P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5459-01A-01D-1501-10 chr20:22562793 C>T maps to NM_021784.4 P362P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5459-01A-01D-1501-10 chr1:70505475 G>A maps to NM_020794.2 R1285R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5459-01A-01D-1501-10 chr1:70505475 G>A maps to NM_020794.2 R1285R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5460-01A-01D-1501-10 chr4:178357479 T>A maps to NM_000027.3 G216G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5460-01A-01D-1501-10 chr4:178357479 T>A maps to NM_000027.3 G216G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5460-01A-01D-1501-10 chr19:41932578 G>A maps to NM_198540.2 Y35Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5460-01A-01D-1501-10 chr19:41932578 G>A maps to NM_198540.2 Y35Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5460-01A-01D-1501-10 chr21:40568694 T>C maps to NM_018963.3 R2100R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5460-01A-01D-1501-10 chr21:40568694 T>C maps to NM_018963.3 R2100R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5460-01A-01D-1501-10 chr11:72012969 G>A maps to NM_030813.3 G432G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5460-01A-01D-1501-10 chr11:72012969 G>A maps to NM_030813.3 G432G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5460-01A-01D-1501-10 chr5:64082385 G>A maps to NM_005869.2 R177R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5460-01A-01D-1501-10 chr5:64082385 G>A maps to NM_005869.2 R177R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5460-01A-01D-1501-10 chr1:225266906 A>T did not map to a codon.
Sequencing variant TCGA-CZ-5460-01A-01D-1501-10 chr4:152577468 T>C maps to NM_001109977.1 I879I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5460-01A-01D-1501-10 chr14:20916147 A>G maps to NM_017807.3 T236T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5460-01A-01D-1501-10 chr14:20916147 A>G maps to NM_017807.3 T236T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5460-01A-01D-1501-10 chr6:161155094 C>T maps to NM_000301.3 Y552Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5460-01A-01D-1501-10 chr15:55838991 A>G maps to NM_015617.1 N163N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5460-01A-01D-1501-10 chr17:8658872 C>T maps to NM_001128076.1 S150S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5460-01A-01D-1501-10 chr12:11138583 C>T maps to NM_176890.2 L292L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5460-01A-01D-1501-10 chr3:10191592 A>T maps to NM_000551.2 K196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5460-01A-01D-1501-10 chr9:95997111 C>T maps to ENST00000297954 P366P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5460-01A-01D-1501-10 chr9:95997111 C>T maps to ENST00000297954 P366P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5460-01A-01D-1501-10 chr16:70180076 T>C maps to NM_017990.3 S636S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5460-01A-01D-1501-10 chr16:70180076 T>C maps to NM_017990.3 S636S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5460-01A-01D-1501-10 chr11:66463960 C>A maps to NM_006946.2 S1355S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5460-01A-01D-1501-10 chr11:66463960 C>A maps to NM_006946.2 S1355S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5461-01A-01D-1501-10 chr17:40639357 C>T maps to NM_001130020.1 S339S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5461-01A-01D-1501-10 chr6:55933842 C>A did not map to a codon.
Sequencing variant TCGA-CZ-5461-01A-01D-1501-10 chr13:37679099 T>C maps to NM_145203.5 E98E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5461-01A-01D-1501-10 chr5:83402564 C>A maps to NM_005711.3 G185*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5461-01A-01D-1501-10 chr5:83402564 C>A maps to NM_005711.3 G185*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5461-01A-01D-1501-10 chr17:34935725 G>T maps to NM_024835.3 L299L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5461-01A-01D-1501-10 chr18:19093875 C>A maps to NM_001142966.1 V1610V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5461-01A-01D-1501-10 chr3:52712614 T>C did not map to a codon.
Sequencing variant TCGA-CZ-5461-01A-01D-1501-10 chr3:52712614 T>C did not map to a codon.
Sequencing variant TCGA-CZ-5461-01A-01D-1501-10 chr8:144991672 C>A maps to NM_201380.2 E4243*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5461-01A-01D-1501-10 chr8:144991672 C>A maps to NM_201380.2 E4243*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5461-01A-01D-1501-10 chr16:72158691 C>A maps to NM_031293.2 E855*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5461-01A-01D-1501-10 chr14:101350370 C>T maps to NM_001134888.2 W252*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5461-01A-01D-1501-10 chr8:134107430 C>A maps to NM_003235.4 V2461V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5461-01A-01D-1501-10 chr8:134107430 C>A maps to NM_003235.4 V2461V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5461-01A-01D-1501-10 chr15:52098675 C>T maps to NM_014548.3 R327*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5461-01A-01D-1501-10 chr19:36832151 T>C maps to NM_020917.2 R192R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5461-01A-01D-1501-10 chr2:26717854 C>T maps to NM_194248.2 K284K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5461-01A-01D-1501-10 chr2:26717854 C>T maps to NM_194248.2 K284K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5462-01A-01D-1501-10 chrX:23754069 G>A maps to NM_001037171.1 N28N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5462-01A-01D-1501-10 chr15:78526759 G>A maps to NM_015162.4 S28S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5462-01A-01D-1501-10 chr4:7783207 C>A maps to NM_001134647.1 L559L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5462-01A-01D-1501-10 chr11:33565133 C>T maps to ENST00000389726 S378S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5462-01A-01D-1501-10 chr19:10116390 C>T did not map to a codon.
Sequencing variant TCGA-CZ-5462-01A-01D-1501-10 chr10:125526487 C>T did not map to a codon.
Sequencing variant TCGA-CZ-5462-01A-01D-1501-10 chr11:61081630 T>A maps to NM_001923.3 G547G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5462-01A-01D-1501-10 chr9:990588 C>T maps to NM_021240.2 R335*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5462-01A-01D-1501-10 chr6:105233139 C>A maps to NM_020771.3 E377*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5462-01A-01D-1501-10 chr6:105233139 C>A maps to NM_020771.3 E377*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5462-01A-01D-1501-10 chr5:154394372 C>T maps to NM_001099293.1 S318S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5462-01A-01D-1501-10 chrX:56292016 T>C maps to NM_007250.4 T162T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5462-01A-01D-1501-10 chr2:133540312 G>A maps to NM_207363.2 S1357S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5462-01A-01D-1501-10 chr11:60671328 A>T maps to NM_014502.4 S8S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5462-01A-01D-1501-10 chr20:40713329 G>T maps to ENST00000373198 V1398V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5462-01A-01D-1501-10 chr10:81702177 G>A maps to NM_003019.4 G133G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5462-01A-01D-1501-10 chr9:93636535 G>A maps to NM_003177.5 P322P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5462-01A-01D-1501-10 chr9:93636535 G>A maps to NM_003177.5 P322P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5462-01A-01D-1501-10 chr2:179516237 A>T maps to NM_133378.4 V10729V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5462-01A-01D-1501-10 chr2:179516237 A>T maps to NM_133378.4 V10729V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5462-01A-01D-1501-10 chr4:88583133 C>T maps to NM_004407.3 D68D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5462-01A-01D-1501-10 chr4:88583133 C>T maps to NM_004407.3 D68D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5462-01A-01D-1501-10 chr18:19076570 A>G maps to NM_001142966.1 R1101R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5462-01A-01D-1501-10 chr18:19076570 A>G maps to NM_001142966.1 R1101R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5462-01A-01D-1501-10 chr3:195505838 A>T maps to NM_018406.5 G4204G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5462-01A-01D-1501-10 chr3:195505838 A>T maps to NM_018406.5 G4204G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5462-01A-01D-1501-10 chr8:135521986 G>A maps to NM_020863.3 R1123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5462-01A-01D-1501-10 chr8:135521986 G>A maps to NM_020863.3 R1123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5463-01A-01D-1501-10 chr7:99700546 T>C maps to ENST00000429084 N112N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5463-01A-01D-1501-10 chr12:667219 C>A maps to NM_173593.3 S858*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5463-01A-01D-1501-10 chr11:111179125 T>A maps to NM_001136105.1 Y143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5463-01A-01D-1501-10 chr2:132288326 C>T maps to NM_138770.1 A157A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5463-01A-01D-1501-10 chr4:110737329 C>T maps to NM_018983.3 R4*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5463-01A-01D-1501-10 chr4:110737329 C>T maps to NM_018983.3 R4*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5463-01A-01D-1501-10 chr12:7090782 A>C maps to NM_005768.5 V157V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5463-01A-01D-1501-10 chr19:55450707 G>A maps to ENST00000446217 H521H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5463-01A-01D-1501-10 chr3:186508150 C>T maps to NM_181573.2 Q282Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5463-01A-01D-1501-10 chr7:100479745 C>G maps to NM_015908.5 L157L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5463-01A-01D-1501-10 chr17:31260287 C>A maps to NM_015544.2 A76A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5463-01A-01D-1501-10 chr1:186286644 G>T maps to NM_003292.2 T2303T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5463-01A-01D-1501-10 chr17:4647402 G>T did not map to a codon.
Sequencing variant TCGA-CZ-5463-01A-01D-1501-10 chr15:64967098 C>A maps to NM_015042.1 G682G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5463-01A-01D-1501-10 chr9:134955075 A>G maps to NM_004269.2 F52F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5463-01A-01D-1501-10 chr9:134955075 A>G maps to NM_004269.2 F52F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5463-01A-01D-1501-10 chr9:109689489 A>C maps to NM_021224.4 P1099P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5463-01A-01D-1501-10 chr9:109689489 A>C maps to NM_021224.4 P1099P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5465-01A-01D-1806-10 chr7:44153703 C>T maps to NM_001129.3 P1107P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5465-01A-01D-1806-10 chr14:92537387 T>C maps to ENST00000359819 Q306Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5465-01A-01D-1806-10 chr2:60780393 G>A maps to NM_022893.3 R4R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5465-01A-01D-1806-10 chr19:30500142 T>C maps to NM_003796.2 D306D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5465-01A-01D-1806-10 chr9:123719561 C>T did not map to a codon.
Sequencing variant TCGA-CZ-5465-01A-01D-1806-10 chr1:26524567 G>A maps to NM_198137.1 L226L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5465-01A-01D-1806-10 chr1:26524567 G>A maps to NM_198137.1 L226L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5465-01A-01D-1806-10 chr1:173780411 G>C maps to NM_001127181.2 S9*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5465-01A-01D-1806-10 chr2:122206530 T>C maps to NM_015282.2 L563L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5465-01A-01D-1806-10 chr1:161599724 C>T maps to ENST00000367964 E90E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5465-01A-01D-1806-10 chr8:125052243 A>T maps to NM_001039112.2 T862T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5465-01A-01D-1806-10 chr8:142444933 T>C maps to NM_207414.2 T1257T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5465-01A-01D-1806-10 chr3:151161388 T>A maps to NM_178822.4 A1782A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5465-01A-01D-1806-10 chr7:123119947 A>C maps to NM_178827.4 L437L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5465-01A-01D-1806-10 chr11:71276938 G>A maps to ENST00000422553 G159G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5465-01A-01D-1806-10 chr7:116411637 C>G maps to NM_001127500.1 V957V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5465-01A-01D-1806-10 chr11:1092094 G>A maps to ENST00000441003 W1305*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5465-01A-01D-1806-10 chr8:110460594 T>C maps to ENST00000426474 N2000N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5465-01A-01D-1806-10 chr14:63735886 G>C did not map to a codon.
Sequencing variant TCGA-CZ-5465-01A-01D-1806-10 chr6:151726968 G>T maps to NM_017909.2 V401V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5465-01A-01D-1806-10 chr17:62029158 G>T maps to NM_000334.4 I826I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5465-01A-01D-1806-10 chr3:50310780 C>T maps to NM_004636.2 D238D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5465-01A-01D-1806-10 chr11:60711235 G>A maps to NM_016582.2 I307I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5465-01A-01D-1806-10 chr12:53776831 T>G maps to NM_138473.2 A367A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5465-01A-01D-1806-10 chr6:170871042 G>A maps to NM_003194.4 Q73Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5465-01A-01D-1806-10 chr6:170871054 G>A maps to NM_003194.4 Q77Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5465-01A-01D-1806-10 chr6:170871096 G>A maps to NM_003194.4 Q91Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5465-01A-01D-1806-10 chrX:100297050 T>C maps to NM_001167970.1 L76L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5465-01A-01D-1806-10 chr1:215848922 G>T maps to ENST00000366943 Y4110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5465-01A-01D-1806-10 chr1:215848922 G>T maps to ENST00000366943 Y4110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5465-01A-01D-1806-10 chr1:55642114 A>T maps to NM_015306.2 G164G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5465-01A-01D-1806-10 chr19:58948570 C>T maps to NM_003433.3 W25*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5465-01A-01D-1806-10 chr9:20414342 A>G maps to NM_004529.2 S167S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5465-01A-01D-1806-10 chr9:20414342 A>G maps to NM_004529.2 S167S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5466-01A-01D-1501-10 chr11:47713656 T>C maps to ENST00000357610 R282R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5466-01A-01D-1501-10 chr11:47713656 T>C maps to ENST00000357610 R282R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5466-01A-01D-1501-10 chr22:39380187 G>A maps to ENST00000402182 K42K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5466-01A-01D-1501-10 chr22:24456571 C>T maps to NM_012295.3 L529L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5466-01A-01D-1501-10 chr3:8787537 G>A maps to NM_001234.3 L147L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5466-01A-01D-1501-10 chr3:8787537 G>A maps to NM_001234.3 L147L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5466-01A-01D-1501-10 chr15:59408906 A>T maps to NM_004701.2 K206*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5466-01A-01D-1501-10 chr12:7295477 G>T maps to NM_014718.3 S518S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5466-01A-01D-1501-10 chr12:7295477 G>T maps to NM_014718.3 S518S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5466-01A-01D-1501-10 chr14:94519371 C>T maps to NM_020414.3 E760E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5466-01A-01D-1501-10 chr12:32886680 T>C maps to ENST00000381000 Y506Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5466-01A-01D-1501-10 chr18:65180322 G>C maps to NM_032160.2 S518*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5466-01A-01D-1501-10 chr18:65180322 G>C maps to NM_032160.2 S518*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5466-01A-01D-1501-10 chr12:56076035 G>A maps to NM_152637.2 P166P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5466-01A-01D-1501-10 chr12:53647587 C>G maps to NM_001170790.1 V430V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5466-01A-01D-1501-10 chr19:14165244 C>T maps to NM_001145028.1 A398A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5466-01A-01D-1501-10 chr19:14165244 C>T maps to NM_001145028.1 A398A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5466-01A-01D-1501-10 chr3:52643532 G>T maps to ENST00000296302 S788*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5466-01A-01D-1501-10 chr14:55203898 G>A maps to NM_015589.4 L290L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5466-01A-01D-1501-10 chr6:43272448 C>T maps to ENST00000372585 Q545*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5466-01A-01D-1501-10 chr11:63175622 T>A maps to NM_080866.2 L443*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5466-01A-01D-1501-10 chrX:129483275 G>T maps to ENST00000339231 G120G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5466-01A-01D-1501-10 chr6:138201232 C>T maps to NM_006290.2 V644V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5466-01A-01D-1501-10 chr20:43533771 G>A maps to NM_139323.2 T196T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5466-01A-01D-1501-10 chr11:130131007 A>T maps to ENST00000397753 L254*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5466-01A-01D-1501-10 chr6:116981932 A>C maps to NM_145062.2 V212V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5466-01A-01D-1501-10 chr17:67124894 G>T maps to NM_080284.2 T328T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5466-01A-01D-1501-10 chr17:67124894 G>T maps to NM_080284.2 T328T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5466-01A-01D-1501-10 chr17:4924145 C>T maps to NM_006612.5 A661A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5466-01A-01D-1501-10 chr17:4924145 C>T maps to NM_006612.5 A661A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5467-01A-01D-1501-10 chr5:55412458 G>T maps to NM_024669.2 L316L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5467-01A-01D-1501-10 chr10:28274096 A>G maps to NM_018076.2 N142N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5467-01A-01D-1501-10 chr7:108524165 A>G maps to NM_001024607.1 I82I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5467-01A-01D-1501-10 chr1:62961313 A>T maps to ENST00000371140 S1654S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5467-01A-01D-1501-10 chr9:88692458 C>T maps to ENST00000376023 E58E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5467-01A-01D-1501-10 chr13:94482722 C>T maps to NM_005708.3 T212T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5467-01A-01D-1501-10 chr7:50737541 G>A maps to NM_005311.4 D127D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5467-01A-01D-1501-10 chr12:53594098 C>T maps to NM_000889.1 G43G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5467-01A-01D-1501-10 chrX:53246338 T>A maps to NM_004187.3 R215*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5467-01A-01D-1501-10 chr2:20237322 T>G maps to NM_014713.4 S95S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5467-01A-01D-1501-10 chr22:18376627 G>A maps to NM_015241.2 L498L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5467-01A-01D-1501-10 chr16:56717110 C>T maps to NM_005952.3 C21C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5467-01A-01D-1501-10 chr3:173322837 C>T maps to NM_014932.2 S150S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5467-01A-01D-1501-10 chr19:55489136 C>T maps to NM_017852.3 R115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5467-01A-01D-1501-10 chr19:56243987 A>T maps to NM_176820.2 I403I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5467-01A-01D-1501-10 chr12:104179175 C>A maps to NM_001031701.2 T422T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5467-01A-01D-1501-10 chr22:32589042 C>T maps to NM_001098527.2 G134G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5467-01A-01D-1501-10 chr17:58022844 C>T maps to NM_003161.2 R436*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5467-01A-01D-1501-10 chr14:55218222 G>T maps to NM_015589.4 E381*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5467-01A-01D-1501-10 chr17:26686414 C>T maps to ENST00000457710 N121N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5467-01A-01D-1501-10 chr17:26686414 C>T maps to ENST00000457710 N121N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5467-01A-01D-1501-10 chr1:232607211 T>A maps to NM_020808.3 A716A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5467-01A-01D-1501-10 chr1:232607211 T>A maps to NM_020808.3 A716A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5467-01A-01D-1501-10 chr5:82835014 G>T maps to NM_004385.4 E2065*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5467-01A-01D-1501-10 chr18:45567043 G>A maps to NM_001039360.2 D145D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5468-01A-01D-1501-10 chr1:94568686 G>A maps to NM_000350.2 R152*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5468-01A-01D-1501-10 chr4:185694255 T>C maps to NM_001995.2 S298S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5468-01A-01D-1501-10 chr1:112031473 G>C maps to NM_020683.6 A210A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5468-01A-01D-1501-10 chr2:28532987 C>T maps to NM_199192.1 A376A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5468-01A-01D-1501-10 chr15:40949237 A>T did not map to a codon.
Sequencing variant TCGA-CZ-5468-01A-01D-1501-10 chr7:128434748 G>A maps to NM_022742.3 G91G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5468-01A-01D-1501-10 chr1:227288694 T>C maps to ENST00000366766 E749E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5468-01A-01D-1501-10 chr1:196762627 C>T maps to NM_021023.5 Y326Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5468-01A-01D-1501-10 chr14:39763223 G>A maps to ENST00000396158 R177R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5468-01A-01D-1501-10 chr1:155205089 A>T maps to NM_001005742.2 P467P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5468-01A-01D-1501-10 chr2:97285434 G>T maps to ENST00000421845 R151R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5468-01A-01D-1501-10 chr10:7829794 C>T maps to NM_012311.2 Q34Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5468-01A-01D-1501-10 chr12:53043742 G>A maps to NM_000423.2 I272I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5468-01A-01D-1501-10 chr17:60814439 C>A maps to NM_152598.2 G263G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5468-01A-01D-1501-10 chr18:47799226 T>A maps to ENST00000424334 P612P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5468-01A-01D-1501-10 chr13:53624867 C>T maps to NM_006418.3 L499L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5468-01A-01D-1501-10 chr7:103008446 C>T maps to NM_002803.2 V416V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5468-01A-01D-1501-10 chr16:109254 C>T maps to NM_022450.3 L662L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5468-01A-01D-1501-10 chr16:109254 C>T maps to NM_022450.3 L662L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5468-01A-01D-1501-10 chr17:78321743 A>G maps to NM_020914.4 A3252A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5468-01A-01D-1501-10 chr1:150445628 C>A maps to NM_015203.3 S1402*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5468-01A-01D-1501-10 chr1:150445628 C>A maps to NM_015203.3 S1402*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5468-01A-01D-1501-10 chr21:30380356 A>G maps to NM_016940.2 C150C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5468-01A-01D-1501-10 chr17:71420173 G>A maps to NM_001144952.1 R547R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5468-01A-01D-1501-10 chr19:46319802 G>T maps to NM_004819.2 I1097I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5468-01A-01D-1501-10 chr1:175355201 G>A maps to NM_003285.2 N581N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5468-01A-01D-1501-10 chr1:175355201 G>A maps to NM_003285.2 N581N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5468-01A-01D-1501-10 chr1:19471345 G>A maps to ENST00000375267 Y2667Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5468-01A-01D-1501-10 chr5:82815672 T>G maps to NM_004385.4 T516T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5468-01A-01D-1501-10 chr11:60899491 T>G maps to NM_017966.4 R290R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5468-01A-01D-1501-10 chr2:128477699 T>A maps to NM_018383.4 G633G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5468-01A-01D-1501-10 chr16:17202836 A>G maps to NM_022166.3 N865N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5468-01A-01D-1501-10 chr15:64968214 C>A maps to NM_015042.1 P1054P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5468-01A-01D-1501-10 chr19:41826333 C>T maps to NM_052848.1 H290H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5468-01A-01D-1501-10 chr19:41826333 C>T maps to NM_052848.1 H290H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5468-01A-01D-1501-10 chr11:133789677 C>T maps to NM_014987.1 L1314L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5468-01A-01D-1501-10 chr11:133789677 C>T maps to NM_014987.1 L1314L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5468-01A-01D-1501-10 chr13:48669154 C>T maps to NM_014166.2 V20V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5468-01A-01D-1501-10 chr13:48669154 C>T maps to NM_014166.2 V20V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5468-01A-01D-1501-10 chr12:57618902 G>A maps to NM_007224.3 A100A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5468-01A-01D-1501-10 chr12:57618902 G>A maps to NM_007224.3 A100A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5468-01A-01D-1501-10 chr19:30936490 G>A maps to NM_014717.1 S674S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5468-01A-01D-1501-10 chr19:30936490 G>A maps to NM_014717.1 S674S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5469-01A-01D-1501-10 chr1:155764937 T>C maps to ENST00000368331 E550E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5469-01A-01D-1501-10 chr1:22222713 C>T maps to NM_005529.5 S51S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5469-01A-01D-1501-10 chr12:7947297 C>T maps to NM_024865.2 P175P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5469-01A-01D-1501-10 chr16:3406080 G>A maps to NM_012368.2 L47L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5469-01A-01D-1501-10 chr1:36755252 C>T maps to NM_005119.3 R545*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5469-01A-01D-1501-10 chr7:134212619 G>A did not map to a codon.
Sequencing variant TCGA-CZ-5469-01A-01D-1501-10 chr7:134212619 G>A did not map to a codon.
Sequencing variant TCGA-CZ-5469-01A-01D-1501-10 chr2:97505514 T>C maps to NM_144994.7 K257K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5469-01A-01D-1501-10 chr2:97505514 T>C maps to NM_144994.7 K257K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5469-01A-01D-1501-10 chr6:143093079 C>T maps to NM_006734.3 A932A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5469-01A-01D-1501-10 chr6:143093079 C>T maps to NM_006734.3 A932A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5469-01A-01D-1501-10 chr6:31237139 A>T maps to ENST00000383329 S363S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5469-01A-01D-1501-10 chr6:31237139 A>T maps to ENST00000383329 S363S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5469-01A-01D-1501-10 chrX:70360568 T>C maps to ENST00000333646 R2046R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5469-01A-01D-1501-10 chrX:70360568 T>C maps to ENST00000333646 R2046R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5469-01A-01D-1501-10 chr5:140250598 C>T maps to NM_018902.3 D637D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5469-01A-01D-1501-10 chr5:140250598 C>T maps to NM_018902.3 D637D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5470-01A-01D-1501-10 chr5:139905890 C>T maps to ENST00000253810 C1601C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5470-01A-01D-1501-10 chr22:40062012 T>A did not map to a codon.
Sequencing variant TCGA-CZ-5470-01A-01D-1501-10 chr7:143020427 C>A maps to NM_000083.2 I241I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5470-01A-01D-1501-10 chr7:72849269 G>A maps to NM_003508.2 T311T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5470-01A-01D-1501-10 chr6:12125186 C>A maps to NM_002114.2 S1720*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5470-01A-01D-1501-10 chr1:196254848 G>A maps to NM_198503.2 R879*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5470-01A-01D-1501-10 chr2:241686666 G>A maps to ENST00000373308 Q1017*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5470-01A-01D-1501-10 chrX:140993372 G>A maps to NM_005462.4 E61E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5470-01A-01D-1501-10 chr8:16035393 C>T did not map to a codon.
Sequencing variant TCGA-CZ-5470-01A-01D-1501-10 chr1:149908473 C>T did not map to a codon.
Sequencing variant TCGA-CZ-5470-01A-01D-1501-10 chrX:43809266 C>A maps to NM_000266.3 V60V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5470-01A-01D-1501-10 chrX:43809266 C>A maps to NM_000266.3 V60V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5470-01A-01D-1501-10 chr15:65157276 G>A maps to NM_025201.4 R221R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5470-01A-01D-1501-10 chr3:47163208 T>A maps to NM_014159.6 R973*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5470-01A-01D-1501-10 chr7:98507680 T>C maps to ENST00000359863 V451V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DV-5565-01A-01D-1534-10 chr17:27889658 C>A maps to NM_198147.2 G443*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DV-5565-01A-01D-1534-10 chr18:9254692 G>A maps to NM_015208.3 L476L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DV-5565-01A-01D-1534-10 chr8:444510 T>C maps to NM_175075.3 K65K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DV-5565-01A-01D-1534-10 chr9:21350655 G>T maps to NM_021002.2 I77I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DV-5565-01A-01D-1534-10 chr1:206944317 G>A maps to NM_000572.2 D104D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DV-5565-01A-01D-1534-10 chr20:39802103 G>A maps to NM_002660.2 V1108V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DV-5565-01A-01D-1534-10 chr9:79324115 G>C maps to NM_015225.2 S1025*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DV-5565-01A-01D-1534-10 chr1:40705014 A>G maps to NM_012421.3 T1547T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DV-5565-01A-01D-1534-10 chr2:179667068 C>T did not map to a codon.
Sequencing variant TCGA-DV-5565-01A-01D-1534-10 chr17:16285910 A>G maps to NM_018955.2 *230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DV-5565-01A-01D-1534-10 chr19:35175649 G>A maps to ENST00000221282 K315K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DV-5566-01A-01D-1534-10 chr22:41914521 G>A maps to ENST00000396512 L351L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DV-5566-01A-01D-1534-10 chr17:72700847 T>A maps to ENST00000412086 K51*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DV-5566-01A-01D-1534-10 chr10:105830253 G>T maps to NM_000494.3 S179S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DV-5566-01A-01D-1534-10 chr20:35381211 A>T maps to NM_001145315.1 S350S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DV-5566-01A-01D-1534-10 chrX:153583339 C>A maps to NM_001110556.1 T1690T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DV-5566-01A-01D-1534-10 chr12:51758020 G>C maps to NM_007210.3 P311P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DV-5566-01A-01D-1534-10 chr6:138584326 C>T maps to NM_020340.4 V569V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DV-5566-01A-01D-1534-10 chr11:55999587 T>C maps to NM_001004746.1 K358K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DV-5566-01A-01D-1534-10 chr3:52692297 G>A maps to ENST00000296302 Q188*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DV-5566-01A-01D-1534-10 chr6:161139488 G>T did not map to a codon.
Sequencing variant TCGA-DV-5566-01A-01D-1534-10 chrX:152936427 G>A maps to NM_001039582.3 L334L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DV-5566-01A-01D-1534-10 chr1:110888164 T>C maps to NM_022768.4 F956F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DV-5566-01A-01D-1534-10 chr13:23906941 G>A maps to NM_014363.4 F3691F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DV-5566-01A-01D-1534-10 chr13:53239771 G>A maps to NM_001130912.1 K173K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DV-5566-01A-01D-1534-10 chr6:152470617 G>A maps to NM_182961.2 R8212R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DV-5566-01A-01D-1534-10 chr8:38853912 G>A maps to NM_078473.2 Q16*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DV-5566-01A-01D-1534-10 chr6:41162230 C>T maps to ENST00000373108 S298S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DV-5566-01A-01D-1534-10 chr19:38103227 T>C maps to NM_152606.3 H349H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DV-5568-01A-01D-1534-10 chr15:78922277 C>T maps to NM_000750.3 G123G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DV-5568-01A-01D-1534-10 chr10:89711909 T>G maps to NM_000314.4 Y176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DV-5568-01A-01D-1534-10 chr16:720317 C>T maps to NM_138769.1 P133P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DV-5569-01A-01D-1534-10 chrX:152773749 C>T maps to NM_001711.4 N318N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DV-5569-01A-01D-1534-10 chr1:147231204 C>A maps to NM_005266.5 E48*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DV-5569-01A-01D-1534-10 chr5:179043166 G>A maps to NM_005520.2 Y420Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DV-5569-01A-01D-1534-10 chr17:15974761 G>A maps to ENST00000395857 V1387V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DV-5569-01A-01D-1534-10 chr7:27788295 T>G maps to ENST00000409980 G51G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DV-5569-01A-01D-1534-10 chr15:41862800 G>T did not map to a codon.
Sequencing variant TCGA-DV-5574-01A-01D-1534-10 chr14:105412553 T>G maps to NM_138420.2 G3078G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DV-5574-01A-01D-1534-10 chr3:10088403 C>T maps to NM_033084.3 Y425Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DV-5574-01A-01D-1534-10 chr12:53207605 G>A maps to NM_002272.2 G153G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DV-5574-01A-01D-1534-10 chr9:140320782 G>A did not map to a codon.
Sequencing variant TCGA-DV-5574-01A-01D-1534-10 chr13:25671205 A>G maps to NM_030979.2 R290R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DV-5574-01A-01D-1534-10 chr2:179368496 C>T maps to NM_019091.3 H262H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DV-5574-01A-01D-1534-10 chr1:151317011 C>A maps to NM_000449.3 R118R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DV-5574-01A-01D-1534-10 chr8:10467635 T>C maps to NM_178857.5 E1324E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DV-5574-01A-01D-1534-10 chr8:10465964 T>C maps to NM_178857.5 G1881G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DV-5574-01A-01D-1534-10 chr7:66453384 T>C maps to NM_016038.2 V242V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DV-5574-01A-01D-1534-10 chr11:9875240 A>C maps to NM_030962.3 A794A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DV-5574-01A-01D-1534-10 chr12:71526583 G>A maps to NM_004616.2 V155V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DV-5574-01A-01D-1534-10 chr2:228754593 G>T maps to NM_178821.1 E46*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DV-5574-01A-01D-1534-10 chr4:367266 T>C maps to NM_003441.2 A347A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DV-5575-01A-01D-1534-10 chr11:46625223 G>A maps to NM_173811.3 S302S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DV-5575-01A-01D-1534-10 chr1:201180221 G>A maps to NM_001164586.1 E2067E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DV-5575-01A-01D-1534-10 chr1:201180242 A>G maps to NM_001164586.1 L2074L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DV-5575-01A-01D-1534-10 chr1:248525307 A>G maps to NM_001004696.1 S142S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DV-5575-01A-01D-1534-10 chr11:5068655 C>T maps to NM_001001916.2 R301*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DV-5575-01A-01D-1534-10 chr9:96439003 C>A maps to NM_005392.3 T987T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DV-5575-01A-01D-1534-10 chr2:100019182 T>G maps to NM_016316.2 P1155P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DV-5575-01A-01D-1534-10 chr2:234240286 G>A maps to NM_000541.4 V245V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DV-5575-01A-01D-1534-10 chr8:125527985 C>T did not map to a codon.
Sequencing variant TCGA-DV-5575-01A-01D-1534-10 chr4:48139498 A>G maps to NM_003215.2 P610P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DV-5575-01A-01D-1534-10 chr7:100218518 C>G maps to NM_003227.3 A789A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DV-5576-01A-01D-1534-10 chr7:141336814 A>T maps to NM_018238.3 K242*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DV-5576-01A-01D-1534-10 chr1:181705480 G>A maps to ENST00000357570 V1111V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DV-5576-01A-01D-1534-10 chr3:100170597 C>T maps to ENST00000489752 C77C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DV-5576-01A-01D-1534-10 chr20:2097951 T>A maps to NM_080836.3 A511A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DV-5576-01A-01D-1534-10 chr19:19381022 G>A maps to NM_001001524.2 H120H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DV-5576-01A-01D-1534-10 chr19:22363630 G>A maps to NM_001001411.2 L296L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3425-01A-02D-1361-10 chrX:108912270 A>G maps to NM_022977.2 L419L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3425-01A-02D-1361-10 chr15:29385398 G>T maps to NM_005503.3 A397A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3425-01A-02D-1361-10 chr16:58577564 A>G maps to NM_016284.3 P1460P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3425-01A-02D-1361-10 chrX:139038423 A>G maps to NM_001013403.2 P239P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3425-01A-02D-1361-10 chr11:10825487 A>C maps to ENST00000429377 L293L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3425-01A-02D-1361-10 chr4:186085306 C>A maps to NM_020827.1 V449V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3425-01A-02D-1361-10 chr15:101595296 G>T maps to NM_024652.3 E1401*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3425-01A-02D-1361-10 chr22:18389488 C>T maps to NM_015241.2 K30K. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-AK-3425-01A-02D-1361-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-AK-3425-01A-02D-1361-10 chr13:58299307 G>A maps to NM_001040429.2 Q1120Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3425-01A-02D-1361-10 chr12:80214665 A>G maps to NM_001143885.1 I334I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3425-01A-02D-1361-10 chr6:158565366 A>G maps to NM_032861.3 F191F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3425-01A-02D-1361-10 chr3:164741458 G>A maps to NM_001041.3 Q1000*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3425-01A-02D-1361-10 chr22:21385633 G>A maps to NM_004173.2 H156H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3425-01A-02D-1361-10 chr22:24159113 C>A maps to NM_003073.3 V262V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3425-01A-02D-1361-10 chr7:128849217 C>G maps to NM_005631.4 R482R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3425-01A-02D-1361-10 chr18:12454458 T>C maps to NM_001128626.1 E554E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3425-01A-02D-1361-10 chr7:23821076 G>T maps to NM_031414.3 E669*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3425-01A-02D-1361-10 chr21:45798893 C>A maps to ENST00000397932 A343A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3425-01A-02D-1361-10 chr2:132238285 C>T maps to NM_080386.2 T340T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3425-01A-02D-1361-10 chr20:25655967 C>T maps to NM_015655.2 G652G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3425-01A-02D-1361-10 chr19:53856495 A>G maps to NM_138374.1 E856E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3428-01A-02D-1361-10 chrX:107930859 G>A maps to ENST00000328300 Q1488Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3428-01A-02D-1361-10 chr7:30706863 C>A maps to ENST00000348438 E126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3428-01A-02D-1361-10 chr10:127548369 G>C maps to NM_018180.2 S217S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3428-01A-02D-1361-10 chr20:37597790 G>T maps to NM_021931.3 T36T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3428-01A-02D-1361-10 chr6:38994430 G>A maps to ENST00000327475 T4596T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3428-01A-02D-1361-10 chrX:24086217 T>C maps to NM_001415.3 G335G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3428-01A-02D-1361-10 chr22:31851206 A>T maps to NM_019843.3 I398I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3428-01A-02D-1361-10 chr18:33709980 A>T maps to ENST00000442325 R29*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3428-01A-02D-1361-10 chr22:41536218 T>C maps to NM_001429.3 A612A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3428-01A-02D-1361-10 chr4:126336939 A>C maps to NM_024582.4 T2274T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3428-01A-02D-1361-10 chr17:18156763 A>T maps to NM_002018.2 I288I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3428-01A-02D-1361-10 chr1:78601424 T>C maps to NM_017655.4 *316R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3428-01A-02D-1361-10 chr14:93994954 T>C maps to ENST00000393153 L339L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3428-01A-02D-1361-10 chr1:1897856 C>A maps to ENST00000434971 E452*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3428-01A-02D-1361-10 chr20:10393757 G>A maps to NM_170784.1 T135T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3428-01A-02D-1361-10 chr19:9091028 T>C maps to NM_024690.2 G262G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3428-01A-02D-1361-10 chr10:105164924 C>T maps to NM_014976.1 A183A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3428-01A-02D-1361-10 chr1:144906485 G>A maps to NM_014644.4 Q791*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3428-01A-02D-1361-10 chr1:166818811 G>T maps to NM_017542.3 P332P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3428-01A-02D-1361-10 chr7:100304815 G>A maps to NM_005837.2 L121L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3428-01A-02D-1361-10 chr6:49587013 C>T maps to NM_000324.2 K73K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3428-01A-02D-1361-10 chr2:17922876 A>G did not map to a codon.
Sequencing variant TCGA-AK-3428-01A-02D-1361-10 chr5:150422133 G>C maps to NM_006058.3 L367L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3428-01A-02D-1361-10 chr22:50665214 C>T maps to NM_020461.3 E516E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3428-01A-02D-1361-10 chr12:109541416 G>A did not map to a codon.
Sequencing variant TCGA-AK-3428-01A-02D-1361-10 chr8:124267673 A>G maps to NM_007222.3 V171V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3428-01A-02D-1361-10 chr2:180310275 C>T did not map to a codon.
Sequencing variant TCGA-AK-3431-01A-02D-1361-10 chr19:1049304 C>A maps to NM_019112.3 V807V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3431-01A-02D-1361-10 chr3:48506400 G>T maps to NM_130384.1 E743*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3431-01A-02D-1361-10 chr1:116670805 G>A maps to NM_152367.2 W234*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3431-01A-02D-1361-10 chr9:88844485 C>T maps to NM_001010907.1 E11E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3431-01A-02D-1361-10 chr7:2951853 G>A maps to NM_032415.4 N1032N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3431-01A-02D-1361-10 chr3:112357945 G>T maps to ENST00000447230 I280I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3431-01A-02D-1361-10 chr8:104444936 T>C maps to NM_015420.6 A403A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3431-01A-02D-1361-10 chr11:102991434 G>C maps to NM_001080463.1 A384A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3431-01A-02D-1361-10 chr4:152577543 C>T maps to NM_001109977.1 S904S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3431-01A-02D-1361-10 chr3:186370104 T>G maps to NM_014375.2 L278L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3431-01A-02D-1361-10 chr7:74563752 G>A maps to NM_001003795.2 S500S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3431-01A-02D-1361-10 chr7:138603069 G>T maps to NM_001164665.1 A434A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3431-01A-02D-1361-10 chr22:18389488 C>T maps to NM_015241.2 K30K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3431-01A-02D-1361-10 chr22:30403924 T>C maps to NM_021090.3 L305L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3431-01A-02D-1361-10 chr16:68200895 A>T maps to NM_173165.2 I584I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3431-01A-02D-1361-10 chr1:144864283 C>G maps to NM_014644.4 L1937L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3431-01A-02D-1361-10 chr1:204399129 T>G maps to NM_002646.3 G1439G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3431-01A-02D-1361-10 chr7:100459531 C>T maps to NM_020246.2 L570L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3431-01A-02D-1361-10 chr16:2816399 G>A maps to NM_016333.3 R1957R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3434-01A-02D-1361-10 chr17:66933089 A>G did not map to a codon.
Sequencing variant TCGA-AK-3434-01A-02D-1361-10 chr5:178559877 G>A maps to NM_014244.4 I703I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3434-01A-02D-1361-10 chr8:7754020 T>C maps to NM_004942.2 P28P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3434-01A-02D-1361-10 chr15:41037297 C>T maps to NM_018145.1 E228E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3434-01A-02D-1361-10 chr17:72842987 G>A maps to NM_000835.3 N691N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3434-01A-02D-1361-10 chr4:44700674 C>T maps to NM_021927.2 L663L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3434-01A-02D-1361-10 chr18:29477769 G>A maps to NM_014939.3 L525L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3434-01A-02D-1361-10 chr1:1897856 C>A maps to ENST00000434971 E452*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3434-01A-02D-1361-10 chr6:129796547 T>C did not map to a codon.
Sequencing variant TCGA-AK-3434-01A-02D-1361-10 chr6:168271096 A>G maps to ENST00000400822 L111L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3434-01A-02D-1361-10 chr11:1092237 C>T maps to ENST00000441003 Q1353*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3434-01A-02D-1361-10 chr5:162881023 G>T maps to NM_145266.4 I141I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3434-01A-02D-1361-10 chr3:52610694 G>A maps to ENST00000296302 R1185*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3434-01A-02D-1361-10 chr10:55849760 A>G maps to NM_001142763.1 V665V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3434-01A-02D-1361-10 chr1:144864283 C>G maps to NM_014644.4 L1937L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3434-01A-02D-1361-10 chrX:38180283 T>G maps to NM_001034853.1 S102S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3434-01A-02D-1361-10 chr6:30314293 C>T maps to ENST00000412529 L370L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3434-01A-02D-1361-10 chr22:40803847 G>C did not map to a codon.
Sequencing variant TCGA-AK-3434-01A-02D-1361-10 chr2:220497111 T>C maps to NM_201574.2 V390V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3434-01A-02D-1361-10 chr6:109764750 G>T maps to NM_003080.2 V305V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3434-01A-02D-1361-10 chr2:96959207 A>G maps to NM_014014.3 L628L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3434-01A-02D-1361-10 chr12:56744655 G>A maps to NM_005419.3 Q351*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3434-01A-02D-1361-10 chr1:23751093 G>A maps to NM_003196.1 A11A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3434-01A-02D-1361-10 chr22:42609901 G>T maps to NM_005650.1 V470V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3434-01A-02D-1361-10 chr4:154197263 C>T maps to NM_015271.3 C145C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3434-01A-02D-1361-10 chr17:26697200 G>T maps to NM_000638.3 L8L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3434-01A-02D-1361-10 chr8:123964181 T>A maps to NM_014943.3 I144I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3434-01A-02D-1361-10 chr16:25264265 C>T did not map to a codon.
Sequencing variant TCGA-AK-3445-01A-02D-1361-10 chr14:105207039 C>T maps to NM_199165.1 S236S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3445-01A-02D-1361-10 chr10:92675942 A>T maps to NM_014391.2 I212I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3445-01A-02D-1361-10 chr11:34909859 A>T maps to NM_015957.2 C147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3445-01A-02D-1361-10 chr4:36118734 A>T maps to NM_015230.2 L1329*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3445-01A-02D-1361-10 chr13:43358244 T>C maps to NM_182508.2 V14V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3445-01A-02D-1361-10 chr5:133644046 A>C maps to NM_001113575.1 L382L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3445-01A-02D-1361-10 chr22:37326519 T>C maps to ENST00000262825 F274F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3445-01A-02D-1361-10 chr1:47610116 C>T maps to NM_001010969.2 D293D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3445-01A-02D-1361-10 chr1:223116620 G>A maps to NM_032890.2 P152P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3445-01A-02D-1361-10 chr2:196753008 C>T maps to NM_018897.2 S1793S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3445-01A-02D-1361-10 chr6:127611268 A>G maps to NM_001139510.1 A223A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3445-01A-02D-1361-10 chr2:239038911 T>C maps to NM_194312.2 L519L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3445-01A-02D-1361-10 chr2:96697055 C>T maps to NM_207328.2 T68T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3445-01A-02D-1361-10 chr10:95347224 C>T maps to NM_181745.3 A331A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3445-01A-02D-1361-10 chr12:68647210 T>C maps to NM_020525.4 K6K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3445-01A-02D-1361-10 chr3:52833443 T>C maps to NM_002217.3 P282P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3445-01A-02D-1361-10 chr12:49950161 T>C maps to NM_012284.1 D826D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3445-01A-02D-1361-10 chr10:24832824 G>A maps to NM_019590.3 E1542E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3445-01A-02D-1361-10 chr13:47279241 A>T maps to NM_001164211.1 L480L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3445-01A-02D-1361-10 chr7:141755355 A>G did not map to a codon.
Sequencing variant TCGA-AK-3445-01A-02D-1361-10 chr17:18082102 G>C maps to ENST00000205890 V3504V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3445-01A-02D-1361-10 chr3:50387110 A>G maps to NM_006545.4 Y108Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3445-01A-02D-1361-10 chr13:25876006 G>C maps to NM_014089.3 T32T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3445-01A-02D-1361-10 chr1:247921567 C>A maps to NM_012353.2 A47A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3445-01A-02D-1361-10 chr5:138699538 T>C maps to NM_001033112.1 G22G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3445-01A-02D-1361-10 chr3:52668675 T>A maps to ENST00000296302 K415*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3445-01A-02D-1361-10 chr9:116291499 G>C did not map to a codon.
Sequencing variant TCGA-AK-3445-01A-02D-1361-10 chr8:92972622 G>T maps to NM_175634.2 T554T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3445-01A-02D-1361-10 chr6:35210008 G>A maps to ENST00000394681 R498R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3445-01A-02D-1361-10 chr11:70331567 C>T maps to ENST00000338508 E1604E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3445-01A-02D-1361-10 chr6:109762783 G>A maps to NM_003080.2 L59L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3445-01A-02D-1361-10 chr13:75936578 G>C maps to ENST00000431480 L221L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3445-01A-02D-1361-10 chr13:61084776 C>T maps to NM_001146070.1 G343G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3445-01A-02D-1361-10 chr1:43770961 T>G maps to NM_005424.2 L144L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3445-01A-02D-1361-10 chr11:128807593 A>T maps to NM_022112.2 A40A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3445-01A-02D-1361-10 chr22:28693688 G>T maps to NM_001145418.1 T227T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3445-01A-02D-1361-10 chr10:73044585 C>T maps to NM_170744.3 T138T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3450-01A-02D-1361-10 chr8:54727236 A>G maps to NM_015941.2 T170T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3450-01A-02D-1361-10 chr12:97102552 G>A maps to ENST00000342887 K657K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3450-01A-02D-1361-10 chr2:189863428 A>G maps to NM_000090.3 G669G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3450-01A-02D-1361-10 chr2:209028270 C>T did not map to a codon.
Sequencing variant TCGA-AK-3450-01A-02D-1361-10 chr4:48530032 C>G maps to NM_015030.1 V2365V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3450-01A-02D-1361-10 chr2:96697055 C>T maps to NM_207328.2 T68T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3450-01A-02D-1361-10 chr1:19235150 C>T maps to NM_001136265.1 P486P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3450-01A-02D-1361-10 chr18:5960152 C>G maps to NM_173464.3 V548V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3450-01A-02D-1361-10 chr10:90356596 C>T maps to NM_001010939.2 F209F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3450-01A-02D-1361-10 chr2:202549859 G>T maps to NM_033066.2 T167T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3450-01A-02D-1361-10 chr1:21809749 T>C maps to NM_032264.2 Y591Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3450-01A-02D-1361-10 chr1:21809749 T>C maps to NM_032264.2 Y591Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3450-01A-02D-1361-10 chr1:120539935 C>G maps to NM_024408.2 T145T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3450-01A-02D-1361-10 chr15:41650368 T>C maps to NM_016359.3 A191A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3450-01A-02D-1361-10 chr1:248801911 C>G maps to NM_001001827.1 V216V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3450-01A-02D-1361-10 chr4:4199807 C>T maps to NM_177998.1 Q251Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3450-01A-02D-1361-10 chr1:45268707 C>T maps to NM_004073.2 Y277Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3450-01A-02D-1361-10 chr11:129772384 T>C maps to NM_020228.2 Q1102Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3450-01A-02D-1361-10 chr7:105135689 T>C maps to NM_019042.3 K247K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3450-01A-02D-1361-10 chr12:4655495 C>T maps to NM_001130862.1 L94L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3450-01A-02D-1361-10 chr9:135985693 C>A maps to NM_006266.2 L159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3450-01A-02D-1361-10 chr1:182555818 G>A maps to NM_021133.3 V41V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3450-01A-02D-1361-10 chr16:51174658 G>A maps to ENST00000251020 L492L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3450-01A-02D-1361-10 chr22:30866554 G>T maps to NM_174975.4 V23V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3450-01A-02D-1361-10 chr3:9517396 A>C maps to ENST00000407969 T1336T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3450-01A-02D-1361-10 chr20:34208696 T>G did not map to a codon.
Sequencing variant TCGA-AK-3450-01A-02D-1361-10 chr16:2807931 T>C maps to NM_016333.3 P167P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3450-01A-02D-1361-10 chr1:161198048 G>A maps to NM_032174.4 R186R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3450-01A-02D-1361-10 chr2:210777324 G>A maps to NM_032504.1 K1542K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3454-01A-02D-1361-10 chr16:20570685 A>G maps to NM_182617.3 S87S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3454-01A-02D-1361-10 chr15:90342492 G>C maps to NM_001150.2 A669A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3454-01A-02D-1361-10 chr6:69943307 A>T maps to NM_001704.2 I869I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3454-01A-02D-1361-10 chr6:64776298 A>G maps to ENST00000370616 S2219S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3454-01A-02D-1361-10 chr20:33875699 G>A maps to NM_178468.4 D294D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3454-01A-02D-1361-10 chrX:12734644 C>G maps to ENST00000429478 Y679*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3454-01A-02D-1361-10 chr6:31323295 A>G maps to ENST00000428231 G301G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3454-01A-02D-1361-10 chr5:173534369 C>T maps to NM_015980.3 P126P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3454-01A-02D-1361-10 chr19:51378100 C>A maps to NM_005551.3 P57P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3454-01A-02D-1361-10 chr2:74699715 C>T maps to NM_053050.3 E24E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3454-01A-02D-1361-10 chr5:37064852 A>G maps to NM_133433.3 K2758K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3454-01A-02D-1361-10 chr1:248813291 T>C maps to NM_001001824.1 T298T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3454-01A-02D-1361-10 chr4:4190682 G>A maps to NM_177998.1 A562A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3454-01A-02D-1361-10 chr13:25044067 G>A maps to NM_006437.3 F670F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3454-01A-02D-1361-10 chr5:133533530 G>A maps to NM_002715.2 Q288*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3454-01A-02D-1361-10 chr8:30361882 A>G maps to NM_001008712.1 K109K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3454-01A-02D-1361-10 chr22:32587022 C>G maps to NM_001098527.2 T291T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3454-01A-02D-1361-10 chr6:44224153 C>T maps to NM_178148.2 A95A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3454-01A-02D-1361-10 chr3:137483859 A>T maps to NM_004189.2 R78R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3454-01A-02D-1361-10 chr2:162273244 T>G maps to NM_006593.2 S108S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3454-01A-02D-1361-10 chr6:41655520 C>A maps to ENST00000343317 E319*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3454-01A-02D-1361-10 chr7:75033014 C>T maps to ENST00000430211 R163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3454-01A-02D-1361-10 chr14:100801316 A>C maps to NM_173701.1 V437V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3460-01A-02D-1361-10 chr12:109661639 A>G maps to NM_001093.3 T1271T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3460-01A-02D-1361-10 chr6:166780319 T>C maps to ENST00000360961 K45K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3460-01A-02D-1361-10 chr12:2719718 G>T maps to NM_199460.2 E1211*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3460-01A-02D-1361-10 chr17:62506378 C>A maps to NM_138363.1 V79V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3460-01A-02D-1361-10 chr8:25341647 C>T maps to ENST00000434814 L430L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3460-01A-02D-1361-10 chr8:19263530 A>T maps to NM_018371.4 L453L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3460-01A-02D-1361-10 chr13:77581414 A>G maps to NM_012158.2 G384G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3460-01A-02D-1361-10 chr19:6731510 C>T maps to NM_001080452.1 L441L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3460-01A-02D-1361-10 chr7:2632755 T>C maps to NM_152558.3 L449L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3460-01A-02D-1361-10 chr6:33635705 C>T maps to ENST00000374316 T617T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3460-01A-02D-1361-10 chr6:149918640 A>C did not map to a codon.
Sequencing variant TCGA-AK-3460-01A-02D-1361-10 chr10:95557391 T>C maps to NM_005097.2 Y502Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3460-01A-02D-1361-10 chr1:161953695 G>A maps to ENST00000451379 G675G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3460-01A-02D-1361-10 chr11:55761255 A>G maps to NM_003697.1 I282I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3460-01A-02D-1361-10 chr3:52621463 G>A maps to ENST00000296302 R1010*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3460-01A-02D-1361-10 chr20:58322873 G>A maps to NM_080672.3 L114L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3460-01A-02D-1361-10 chr12:112893797 A>G maps to ENST00000392596 R229R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3460-01A-02D-1361-10 chr12:120650284 A>G maps to NM_001080855.1 S536S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3460-01A-02D-1361-10 chr5:127477608 T>G maps to NM_001046.2 L570*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3460-01A-02D-1361-10 chr4:184930538 C>A maps to NM_020225.1 S183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3460-01A-02D-1361-10 chr2:88485425 G>T maps to NM_018271.3 R413R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3461-01A-02D-1361-10 chr5:7706889 C>T maps to NM_020546.2 N381N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3461-01A-02D-1361-10 chr3:15755031 A>G did not map to a codon.
Sequencing variant TCGA-AK-3461-01A-02D-1361-10 chr19:45322914 T>A maps to NM_005581.3 V565V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3461-01A-02D-1361-10 chr19:48715113 C>A maps to NM_001184900.1 V489V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3461-01A-02D-1361-10 chr7:117188849 G>T maps to NM_000492.3 A455A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3461-01A-02D-1361-10 chr7:135095314 A>T maps to NM_001190850.1 G257G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3461-01A-02D-1361-10 chr11:92600265 G>A maps to ENST00000298047 A4006A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3461-01A-02D-1361-10 chr2:11777870 G>A maps to NM_014668.3 P1792P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3461-01A-02D-1361-10 chr22:46719126 A>G maps to NM_016426.6 A491A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3461-01A-02D-1361-10 chr7:65441160 C>T maps to NM_000181.3 K251K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3461-01A-02D-1361-10 chr22:18304889 A>G maps to NM_015241.2 R1118R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3461-01A-02D-1361-10 chr2:182542618 G>C maps to NM_002500.2 A323A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3461-01A-02D-1361-10 chr5:37051933 C>T maps to NM_133433.3 N2336N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3461-01A-02D-1361-10 chr11:65384726 C>T maps to NM_032223.2 P116P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3461-01A-02D-1361-10 chr1:17743002 T>A maps to NM_018715.2 R333R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3461-01A-02D-1361-10 chr19:4363419 G>A maps to NM_003025.2 Y225Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3461-01A-02D-1361-10 chr15:75702578 A>G maps to NM_001145357.1 L353L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3461-01A-02D-1361-10 chr7:149502985 A>G maps to NM_198455.2 P2831P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3461-01A-02D-1361-10 chr4:119948177 C>T maps to NM_133477.2 L218L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3461-01A-02D-1361-10 chr2:230675715 G>A maps to ENST00000389044 Q701*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4690-01A-01D-1361-10 chr17:67039700 G>C maps to NM_080283.3 V243V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4690-01A-01D-1361-10 chr2:201678002 A>G maps to ENST00000452790 R53R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4690-01A-01D-1361-10 chr5:147821565 G>T maps to NM_205836.1 L1141L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4690-01A-01D-1361-10 chr1:29018199 A>T maps to NM_006582.2 G115G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4690-01A-01D-1361-10 chr12:21711187 G>A maps to NM_021957.3 I456I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4690-01A-01D-1361-10 chr6:112455691 A>G maps to NM_001105206.1 A1178A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4690-01A-01D-1361-10 chr13:25671368 G>T maps to NM_030979.2 E345*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4690-01A-01D-1361-10 chr3:51972150 C>G maps to NM_004704.3 L80L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4690-01A-01D-1361-10 chr16:51174658 G>A maps to ENST00000251020 L492L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4690-01A-01D-1361-10 chr10:7212904 C>T maps to NM_001018039.1 K843K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4690-01A-01D-1361-10 chr18:9399342 G>A did not map to a codon.
Sequencing variant TCGA-B0-4690-01A-01D-1361-10 chr6:28116326 G>T maps to NM_006298.2 E48*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4690-01A-01D-1361-10 chr6:87970403 G>T maps to NM_015021.1 E2353*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4691-01A-01D-1361-10 chr2:202593233 C>G did not map to a codon.
Sequencing variant TCGA-B0-4691-01A-01D-1361-10 chr2:242154263 G>A maps to NM_001001891.3 L645L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4691-01A-01D-1361-10 chrX:3007542 T>C maps to NM_004042.3 S279S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4691-01A-01D-1361-10 chr3:52441469 C>A maps to NM_004656.2 G128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4691-01A-01D-1361-10 chrX:129148821 G>T maps to ENST00000303743 E692*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4691-01A-01D-1361-10 chr13:24895239 G>A maps to NM_178540.3 K112K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4691-01A-01D-1361-10 chr11:14510040 A>C maps to NM_001144061.1 Y232*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4691-01A-01D-1361-10 chr19:11314959 G>A maps to ENST00000319867 P1712P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4691-01A-01D-1361-10 chr4:56738087 A>G maps to NM_018261.3 R346R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4691-01A-01D-1361-10 chr7:148512044 G>A maps to NM_004456.3 Q545*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4691-01A-01D-1361-10 chr12:47630057 T>A maps to NM_138371.1 R404R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4691-01A-01D-1361-10 chr13:32836596 T>C maps to NM_023037.2 I2588I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4691-01A-01D-1361-10 chr17:80391634 C>A maps to NM_173620.2 A128A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4691-01A-01D-1361-10 chr1:207072688 G>A maps to NM_001185156.1 A24A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4691-01A-01D-1361-10 chr13:42460951 C>T maps to NM_015058.1 L277L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4691-01A-01D-1361-10 chr15:101595283 C>A maps to NM_024652.3 S1396S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4691-01A-01D-1361-10 chr10:99220743 G>A maps to ENST00000422291 L799L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4691-01A-01D-1361-10 chr13:77669614 T>C maps to NM_015057.4 E3359E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4691-01A-01D-1361-10 chr18:47518663 G>C maps to NM_001080467.2 V250V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4691-01A-01D-1361-10 chr1:120539836 T>C maps to NM_024408.2 K178K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4691-01A-01D-1361-10 chr11:123909171 G>A maps to NM_001004463.1 D179D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4691-01A-01D-1361-10 chr12:133198302 C>A maps to NM_170683.2 P413P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4691-01A-01D-1361-10 chr10:74806680 A>C did not map to a codon.
Sequencing variant TCGA-B0-4691-01A-01D-1361-10 chr7:142832379 A>G maps to NM_002652.2 K63K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4691-01A-01D-1361-10 chr17:37826359 A>G maps to NM_002686.3 P189P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4691-01A-01D-1361-10 chr14:39650382 C>T maps to NM_002687.3 S490S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4691-01A-01D-1361-10 chr9:135985693 C>A maps to NM_006266.2 L159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4691-01A-01D-1361-10 chr21:37416206 C>T maps to NM_017438.3 T258T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4691-01A-01D-1361-10 chr19:52001299 C>A maps to NM_053003.2 L459L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4691-01A-01D-1361-10 chr15:85451986 G>T maps to NM_004213.3 V252V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4691-01A-01D-1361-10 chr18:12463348 C>G did not map to a codon.
Sequencing variant TCGA-B0-4691-01A-01D-1361-10 chr19:13011344 A>G maps to NM_001105578.1 L142L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4691-01A-01D-1361-10 chr3:10011438 G>A maps to NM_018447.2 A207A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4691-01A-01D-1361-10 chrX:109247113 C>A maps to NM_032227.3 R38R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4691-01A-01D-1361-10 chr17:42265112 T>C did not map to a codon.
Sequencing variant TCGA-B0-4691-01A-01D-1361-10 chr2:113089833 A>G maps to NM_198581.2 P1113P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4691-01A-01D-1361-10 chr6:87970403 G>T maps to NM_015021.1 E2353*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4693-01A-01D-1361-10 chr5:413517 A>G maps to NM_020731.3 A141A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4693-01A-01D-1361-10 chr3:119133103 T>C maps to NM_020754.2 N776N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4693-01A-01D-1361-10 chr11:108153495 T>A maps to NM_000051.3 S1212S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4693-01A-01D-1361-10 chr19:12867046 C>T maps to NM_017682.2 Y347Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4693-01A-01D-1361-10 chr7:100061218 G>A maps to ENST00000426357 Q134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4693-01A-01D-1361-10 chr18:21735911 T>A maps to NM_138644.1 T149T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4693-01A-01D-1361-10 chr11:96104274 T>A maps to NM_024725.3 K371*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4693-01A-01D-1361-10 chr12:56363323 G>A maps to NM_001798.3 V184V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4693-01A-01D-1361-10 chrX:139865946 G>A maps to NM_004065.2 I195I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4693-01A-01D-1361-10 chr9:39103795 G>A maps to NM_033655.3 S827S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4693-01A-01D-1361-10 chr1:152384628 C>T maps to NM_016190.2 A27A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4693-01A-01D-1361-10 chr1:112997121 G>T maps to NM_018704.2 E128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4693-01A-01D-1361-10 chr4:101109220 C>A maps to NM_145244.3 L65L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4693-01A-01D-1361-10 chr17:57656853 C>T maps to NM_024612.4 F365F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4693-01A-01D-1361-10 chr2:183640092 T>C maps to NM_018981.1 A772A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4693-01A-01D-1361-10 chr13:41134061 A>G maps to NM_002015.3 H522H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4693-01A-01D-1361-10 chr1:35226980 G>A maps to NM_153212.2 E42E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4693-01A-01D-1361-10 chr12:54798983 G>T maps to NM_002205.2 T397T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4693-01A-01D-1361-10 chr11:77885168 G>A maps to NM_001029859.1 F144F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4693-01A-01D-1361-10 chr9:133928344 C>T maps to ENST00000355048 S644S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4693-01A-01D-1361-10 chr5:71495733 G>A maps to NM_005909.3 S2184S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4693-01A-01D-1361-10 chr1:36644626 G>A did not map to a codon.
Sequencing variant TCGA-B0-4693-01A-01D-1361-10 chr16:48596216 G>A maps to NM_153029.3 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4693-01A-01D-1361-10 chr9:100409779 C>T maps to NM_002486.4 R206R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4693-01A-01D-1361-10 chr16:81242150 T>C maps to NM_052892.3 G235G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4693-01A-01D-1361-10 chr8:110464466 T>A maps to ENST00000426474 A2155A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4693-01A-01D-1361-10 chr7:77256099 T>G maps to NM_002835.3 P368P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4693-01A-01D-1361-10 chr19:49224072 G>C maps to NM_017805.2 P958P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4693-01A-01D-1361-10 chr2:230914570 C>G maps to NM_152527.4 A103A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4693-01A-01D-1361-10 chr1:9416576 G>A maps to NM_025106.3 L209L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4693-01A-01D-1361-10 chr5:100192025 G>T maps to NM_005668.4 S193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4693-01A-01D-1361-10 chr17:37816463 G>T maps to NM_006804.3 E266*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4693-01A-01D-1361-10 chr4:26640456 G>A did not map to a codon.
Sequencing variant TCGA-B0-4693-01A-01D-1361-10 chr19:6744908 C>T maps to ENST00000313244 S296S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4693-01A-01D-1361-10 chr8:103266716 G>T maps to NM_015902.4 S2738*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4694-01A-01D-1361-10 chr2:69741761 T>C maps to NM_014911.3 Q539Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4694-01A-01D-1361-10 chr17:61557827 G>A maps to NM_000789.3 L262L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4694-01A-01D-1361-10 chr8:39537678 C>G maps to NM_014237.2 S585S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4694-01A-01D-1361-10 chr10:5009192 T>C maps to NM_001353.5 D109D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4694-01A-01D-1361-10 chr4:77817361 T>C maps to NM_001029870.1 L547L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4694-01A-01D-1361-10 chr12:53937185 C>G maps to NM_001130059.1 V64V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4694-01A-01D-1361-10 chr20:47835897 A>G maps to NM_017895.7 V2V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4694-01A-01D-1361-10 chr17:641268 C>A maps to NM_024792.1 V130V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4694-01A-01D-1361-10 chr6:24828488 C>T maps to NM_014722.2 R868R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4694-01A-01D-1361-10 chrX:12736244 G>C maps to ENST00000429478 G1090G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4694-01A-01D-1361-10 chr3:50295031 C>T maps to NM_002070.2 C326C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4694-01A-01D-1361-10 chr1:155735258 T>C maps to ENST00000368331 E1335E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4694-01A-01D-1361-10 chr6:26158750 C>T maps to NM_138720.1 A118A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4694-01A-01D-1361-10 chr2:97278653 A>G maps to ENST00000421845 S271S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4694-01A-01D-1361-10 chr14:56137505 T>A maps to NM_001079521.1 T1109T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4694-01A-01D-1361-10 chrX:153131182 G>A maps to NM_000425.3 V841V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4694-01A-01D-1361-10 chr18:7008501 C>T maps to NM_005559.2 V1369V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4694-01A-01D-1361-10 chr2:28812900 T>C maps to NM_153021.4 R682R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4694-01A-01D-1361-10 chr7:150037575 C>A maps to NM_002889.3 P41P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4694-01A-01D-1361-10 chr1:17743002 T>A maps to NM_018715.2 R333R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4694-01A-01D-1361-10 chr5:145862190 A>G maps to NM_006706.3 E641E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4694-01A-01D-1361-10 chr16:21982910 T>C maps to NM_003366.2 L246L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4694-01A-01D-1361-10 chr3:122133766 T>C maps to NM_019069.3 K203K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4694-01A-01D-1361-10 chr19:36575624 G>T maps to NM_001083961.1 E541*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4694-01A-01D-1361-10 chr9:96002137 C>T maps to ENST00000297954 I474I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4694-01A-01D-1361-10 chr17:4645275 T>C maps to NM_001136046.1 G298G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4694-01A-01D-1361-10 chr8:146107412 G>A maps to NM_021061.3 T390T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4697-01A-01D-1361-10 chr11:134131682 C>T maps to NM_014384.2 L331L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4697-01A-01D-1361-10 chr5:150514008 G>A maps to NM_001155.4 D175D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4697-01A-01D-1361-10 chrX:47428170 A>T maps to ENST00000290277 G380G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4697-01A-01D-1361-10 chr4:139966480 A>G maps to NM_012118.2 K383K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4697-01A-01D-1361-10 chr20:47835942 A>G maps to NM_017895.7 G17G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4697-01A-01D-1361-10 chr17:57676167 T>C maps to NM_024612.4 N551N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4697-01A-01D-1361-10 chr7:73471994 T>C maps to ENST00000358929 A490A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4697-01A-01D-1361-10 chr12:42481608 G>A maps to NM_173601.1 A434A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4697-01A-01D-1361-10 chr11:1606137 T>G maps to NM_001005922.1 G114G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4697-01A-01D-1361-10 chr18:21441701 T>C maps to ENST00000416669 D1507D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4697-01A-01D-1361-10 chr3:49725085 G>A maps to NM_020998.3 N86N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4697-01A-01D-1361-10 chr11:1018288 C>T maps to NM_005961.2 P1504P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4697-01A-01D-1361-10 chr1:179521758 C>A maps to NM_014625.2 A284A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4697-01A-01D-1361-10 chr11:67269465 T>C maps to NM_004910.2 R169R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4697-01A-01D-1361-10 chr8:144996407 T>G maps to NM_201380.2 A2664A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4697-01A-01D-1361-10 chr2:179307991 A>T did not map to a codon.
Sequencing variant TCGA-B0-4697-01A-01D-1361-10 chr2:20647606 C>A maps to NM_004040.2 V127V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4697-01A-01D-1361-10 chr8:19252098 C>T maps to NM_022071.3 L437L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4697-01A-01D-1361-10 chr4:8229880 A>T maps to NM_018986.3 G820G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4697-01A-01D-1361-10 chr16:48396057 T>A maps to NM_001006610.1 V125V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4697-01A-01D-1361-10 chr3:121613337 G>A maps to NM_021082.3 Q5Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4697-01A-01D-1361-10 chr19:1220428 C>T maps to NM_000455.4 H174H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4697-01A-01D-1361-10 chr2:108910185 G>T maps to ENST00000437390 L21L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4697-01A-01D-1361-10 chr22:39826037 C>A maps to NM_006116.2 T442T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4697-01A-01D-1361-10 chr17:17772712 G>A maps to NM_001082968.1 V284V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4697-01A-01D-1361-10 chr5:176084584 G>A maps to NM_012171.2 T295T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4697-01A-01D-1361-10 chr8:67576660 T>G maps to NM_025054.4 R845R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4697-01A-01D-1361-10 chr15:43653321 G>A maps to NM_152455.3 H836H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4703-01A-01D-1361-10 chr16:20696629 G>A maps to NM_052956.2 R96R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4703-01A-01D-1361-10 chr16:20576047 C>A maps to NM_182617.3 V40V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4703-01A-01D-1361-10 chr3:52418903 G>T maps to ENST00000273600 E2809*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4703-01A-01D-1361-10 chr1:35259856 C>T maps to NM_002060.2 Q15*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4703-01A-01D-1361-10 chr19:39108206 C>T did not map to a codon.
Sequencing variant TCGA-B0-4703-01A-01D-1361-10 chr1:85494841 A>T maps to NM_018298.9 L260*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4703-01A-01D-1361-10 chr9:127566583 C>T maps to NM_182487.2 P377P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4703-01A-01D-1361-10 chr11:117076874 G>A maps to NM_004716.2 D732D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4703-01A-01D-1361-10 chr7:6816031 T>C maps to NM_173565.3 I423I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4703-01A-01D-1361-10 chr8:103266716 G>T maps to NM_015902.4 S2738*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4703-01A-01D-1361-10 chr3:52443727 A>C did not map to a codon.
Sequencing variant TCGA-B0-4707-01A-01D-1361-10 chr10:5042783 G>A maps to NM_001354.4 D109D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4707-01A-01D-1361-10 chr22:39421349 T>C maps to NM_152426.3 Y162Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4707-01A-01D-1361-10 chr1:26527919 G>C maps to NM_198137.1 T425T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4707-01A-01D-1361-10 chr2:132289348 A>G maps to NM_138770.1 K219K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4707-01A-01D-1361-10 chr3:49836829 G>A maps to NM_001007540.2 S30S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4707-01A-01D-1361-10 chr10:105792703 G>T maps to NM_000494.3 P1439P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4707-01A-01D-1361-10 chr12:54741559 A>G maps to NM_016057.1 V109V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4707-01A-01D-1361-10 chr10:99642573 T>C maps to NM_018058.4 G548G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4707-01A-01D-1361-10 chr5:150138486 C>T maps to NM_001135643.1 P23P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4707-01A-01D-1361-10 chr1:101487261 T>A maps to NM_015958.2 A65A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4707-01A-01D-1361-10 chr11:1579465 G>T maps to NM_004420.2 L191L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4707-01A-01D-1361-10 chr7:73452037 G>A maps to ENST00000358929 A55A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4707-01A-01D-1361-10 chr3:184294702 C>A maps to NM_004443.3 P362P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4707-01A-01D-1361-10 chr4:5567007 C>A maps to NM_147127.4 L1212L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4707-01A-01D-1361-10 chr13:28979949 A>T maps to NM_002019.4 T506T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4707-01A-01D-1361-10 chr6:112017519 A>T maps to NM_153047.1 S331S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4707-01A-01D-1361-10 chr22:22989280 T>C maps to ENST00000215938 D78D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4707-01A-01D-1361-10 chr14:31626469 A>G maps to NM_015382.2 F554F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4707-01A-01D-1361-10 chr5:55164728 A>C maps to NM_139017.4 R89R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4707-01A-01D-1361-10 chr17:74717894 G>C maps to NM_001081461.1 S309*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4707-01A-01D-1361-10 chr15:81173291 G>A maps to NM_018689.1 G144G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4707-01A-01D-1361-10 chr9:100053694 C>G maps to ENST00000375206 G4G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4707-01A-01D-1361-10 chr13:29600571 C>G maps to NM_001033602.2 R589R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4707-01A-01D-1361-10 chr11:1017439 C>T maps to NM_005961.2 S1787S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4707-01A-01D-1361-10 chr15:88476289 G>T maps to NM_001012338.1 I614I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4707-01A-01D-1361-10 chr1:248813291 T>C maps to NM_001001824.1 T298T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4707-01A-01D-1361-10 chr1:52847346 A>G maps to NM_004153.3 F700F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4707-01A-01D-1361-10 chr7:82474790 C>T maps to NM_033026.5 A4614A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4707-01A-01D-1361-10 chr19:43699378 T>C maps to NM_002780.3 R252R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4707-01A-01D-1361-10 chr2:120221704 G>A maps to NM_002980.2 A210A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4707-01A-01D-1361-10 chr15:42165752 C>G maps to ENST00000320955 L1648L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4707-01A-01D-1361-10 chr13:43155266 T>C maps to NM_003701.3 D75D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4707-01A-01D-1361-10 chr12:49666181 G>A maps to NM_032704.3 A174A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4707-01A-01D-1361-10 chr2:219301348 G>A maps to NM_007127.2 Q657Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4707-01A-01D-1361-10 chr3:183525822 G>T maps to NM_018023.4 G1339G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4713-01A-01D-1361-10 chr21:28327064 G>A maps to NM_007038.3 H410H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4713-01A-01D-1361-10 chr15:101440801 C>A maps to NM_000693.2 A302A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4713-01A-01D-1361-10 chr4:153784770 C>A maps to NM_001025595.1 S36*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4713-01A-01D-1361-10 chrX:11196234 G>A maps to NM_013427.2 S538S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4713-01A-01D-1361-10 chr14:105452998 T>C maps to NM_174891.3 T77T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4713-01A-01D-1361-10 chr20:35395178 T>C maps to NM_001145315.1 R165R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4713-01A-01D-1361-10 chr2:96993826 G>A maps to ENST00000420728 Q517Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4713-01A-01D-1361-10 chr17:21319391 G>A maps to NM_021012.4 L246L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4713-01A-01D-1361-10 chr2:44190791 C>A maps to NM_133259.3 E475*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4713-01A-01D-1361-10 chr2:33412082 G>T maps to ENST00000354476 G454G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4713-01A-01D-1361-10 chr16:58542876 C>T maps to NM_001130487.1 N299N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4713-01A-01D-1361-10 chrX:99551676 G>A maps to NM_001184880.1 F1015F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4713-01A-01D-1361-10 chr5:148747049 C>A maps to NM_024028.3 T270T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4713-01A-01D-1361-10 chr20:5294760 G>A maps to NM_144773.2 R85R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4713-01A-01D-1361-10 chr16:29825763 C>A maps to NM_145239.2 A330A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4713-01A-01D-1361-10 chr11:66100040 A>C maps to NM_004292.2 P686P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4713-01A-01D-1361-10 chr1:205631991 C>A maps to NM_033102.2 P309P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4713-01A-01D-1361-10 chr15:42979925 A>G maps to NM_020759.2 L2050L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4713-01A-01D-1361-10 chr6:123539745 T>G maps to NM_006073.2 *730Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4713-01A-01D-1361-10 chr3:52443728 C>G did not map to a codon.
Sequencing variant TCGA-B0-4714-01A-01D-1361-10 chr17:43333215 G>T maps to NM_152343.2 S111S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4714-01A-01D-1361-10 chr3:85851254 A>C maps to NM_153184.3 A42A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4714-01A-01D-1361-10 chr11:96104274 T>A maps to NM_024725.3 K371*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4714-01A-01D-1361-10 chr1:50610783 G>A maps to NM_021952.3 Q55Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4714-01A-01D-1361-10 chr19:48523090 G>A maps to NM_022142.4 E157E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4714-01A-01D-1361-10 chr2:136608980 G>A maps to NM_005915.4 C636C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4714-01A-01D-1361-10 chr11:34160751 A>T maps to NM_024662.2 G742G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4714-01A-01D-1361-10 chr13:25671368 G>T maps to NM_030979.2 E345*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4714-01A-01D-1361-10 chr15:55912245 C>G maps to NM_173814.4 L1139L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4714-01A-01D-1361-10 chr12:9318748 A>G maps to NM_002864.2 Y719Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4714-01A-01D-1361-10 chr5:176729428 C>A maps to NM_130781.2 V134V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4714-01A-01D-1361-10 chr19:38907760 C>A maps to ENST00000405332 G296G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4714-01A-01D-1361-10 chr1:243480194 G>A maps to NM_006642.3 K356K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4714-01A-01D-1361-10 chr1:169701930 G>C maps to NM_000450.2 V82V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4714-01A-01D-1361-10 chr19:59012064 C>T maps to NM_012254.2 E397E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4714-01A-01D-1361-10 chr17:36523865 T>C maps to NM_014598.2 R431R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4714-01A-01D-1361-10 chr10:114063067 T>C maps to NM_058222.1 *330Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4714-01A-01D-1361-10 chr4:69417569 A>G maps to NM_001076.2 Y355Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4714-01A-01D-1361-10 chr7:12380035 G>A maps to ENST00000275358 C1489C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4714-01A-01D-1361-10 chr1:228113201 G>T maps to NM_003395.2 P38P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4714-01A-01D-1361-10 chr6:43308575 A>T maps to NM_014345.2 I1149I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4718-01A-01D-1361-10 chr2:215845227 G>A maps to NM_173076.2 H1573H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4718-01A-01D-1361-10 chr5:413517 A>G maps to NM_020731.3 A141A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4718-01A-01D-1361-10 chr10:117075205 C>T maps to NM_207303.2 P999P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4718-01A-01D-1361-10 chr2:118732796 G>T maps to NM_019044.4 A239A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4718-01A-01D-1361-10 chr9:90585695 G>T maps to NM_001039803.2 A165A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4718-01A-01D-1361-10 chr2:172409899 T>C maps to NM_024843.3 L149L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4718-01A-01D-1361-10 chr17:57656853 C>T maps to NM_024612.4 F365F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4718-01A-01D-1361-10 chr10:124358419 C>G maps to ENST00000368915 V1029V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4718-01A-01D-1361-10 chr12:77426861 A>G maps to NM_203394.2 A450A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4718-01A-01D-1361-10 chr11:30253598 C>T maps to NM_001018080.1 C50C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4718-01A-01D-1361-10 chr2:121708839 C>T maps to NM_005270.4 S92S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4718-01A-01D-1361-10 chrX:53230751 G>A maps to NM_004187.3 R681*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4718-01A-01D-1361-10 chr1:226566973 T>A maps to NM_001618.3 G538G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4718-01A-01D-1361-10 chr7:75055732 G>C maps to ENST00000257665 L403L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4718-01A-01D-1361-10 chr20:20486075 A>G maps to NM_020343.3 F1677F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4718-01A-01D-1361-10 chr17:30621398 T>G maps to NM_138328.2 V202V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4718-01A-01D-1361-10 chr18:61264229 G>A maps to NM_012397.3 W270*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4718-01A-01D-1361-10 chr3:47155364 C>A did not map to a codon.
Sequencing variant TCGA-B0-4718-01A-01D-1361-10 chr1:232650233 T>G maps to NM_020808.3 S284S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4718-01A-01D-1361-10 chr3:66428111 A>C did not map to a codon.
Sequencing variant TCGA-B0-4718-01A-01D-1361-10 chr11:17523512 A>C maps to NM_153676.3 Y733*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4718-01A-01D-1361-10 chr2:61441706 G>A maps to NM_014709.3 L2724L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4718-01A-01D-1361-10 chr12:58347426 C>T maps to NM_033276.2 V164V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4813-01A-01D-1361-10 chrX:1546875 A>G maps to NM_004192.3 R216R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4813-01A-01D-1361-10 chr2:101009957 C>A maps to NM_004854.3 E274*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4813-01A-01D-1361-10 chr3:130095638 A>G maps to ENST00000312481 V209V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4813-01A-01D-1361-10 chr2:88427488 T>C maps to NM_001443.1 E16E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4813-01A-01D-1361-10 chr3:121544944 G>A maps to NM_001023570.2 L116L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4813-01A-01D-1361-10 chr14:105356096 T>G did not map to a codon.
Sequencing variant TCGA-B0-4813-01A-01D-1361-10 chr21:46032304 T>C maps to NM_198695.2 P96P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4813-01A-01D-1361-10 chr6:161027524 C>T maps to NM_005577.2 E923E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4813-01A-01D-1361-10 chr17:16068361 C>T maps to ENST00000395857 Q183Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4813-01A-01D-1361-10 chr2:209190804 C>A maps to NM_015040.3 L1090L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4813-01A-01D-1361-10 chr20:8713924 C>T maps to NM_015192.2 N643N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4813-01A-01D-1361-10 chr2:113940962 T>G maps to NM_012455.2 A310A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4813-01A-01D-1361-10 chr7:4839089 G>A maps to NM_018059.4 G1049G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4813-01A-01D-1361-10 chr2:61147173 A>C did not map to a codon.
Sequencing variant TCGA-B0-4813-01A-01D-1361-10 chr16:2314217 G>C maps to NM_080594.2 T62T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4813-01A-01D-1361-10 chr20:3210300 G>A maps to NM_001174090.1 N580N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4813-01A-01D-1361-10 chr14:64496674 A>G maps to NM_182914.2 T2259T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4813-01A-01D-1361-10 chr6:169649024 G>T maps to NM_003247.2 I32I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4813-01A-01D-1361-10 chr2:210832286 G>T maps to NM_032504.1 V2578V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4813-01A-01D-1361-10 chr19:21910450 A>C maps to NM_173531.3 T221T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4814-01A-01D-1361-10 chr2:204259530 G>T maps to ENST00000295851 V229V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4814-01A-01D-1361-10 chr2:21224844 C>A maps to NM_000384.2 A4483A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4814-01A-01D-1361-10 chr1:156626161 G>T maps to NM_021948.3 G677G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4814-01A-01D-1361-10 chr5:137488284 T>C maps to NM_139199.1 E914E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4814-01A-01D-1361-10 chr1:26520357 T>C maps to NM_198137.1 N146N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4814-01A-01D-1361-10 chr19:48809520 G>A maps to NM_144577.3 Y182Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4814-01A-01D-1361-10 chr18:50918088 C>G maps to NM_005215.3 L840L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4814-01A-01D-1361-10 chr22:29694786 A>G maps to NM_013986.3 R499R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4814-01A-01D-1361-10 chr8:125015548 C>T maps to NM_001039112.2 T554T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4814-01A-01D-1361-10 chr4:84362514 A>C maps to NM_133636.2 Y535*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4814-01A-01D-1361-10 chr19:15228698 A>T maps to NM_006844.3 A393A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4814-01A-01D-1361-10 chr11:28352292 T>C maps to NM_001113528.1 L377L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4814-01A-01D-1361-10 chr22:30408371 T>C maps to NM_021090.3 L379L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4814-01A-01D-1361-10 chr11:89088167 G>A maps to NM_016931.3 S393S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4814-01A-01D-1361-10 chr5:6749687 C>A maps to NM_006999.4 I285I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4814-01A-01D-1361-10 chr20:44054402 A>C maps to NM_015937.4 T558T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4814-01A-01D-1361-10 chr1:40627265 G>C maps to NM_012421.3 V65V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4814-01A-01D-1361-10 chr17:33875668 G>T maps to NM_001129820.1 A776A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4814-01A-01D-1361-10 chr6:169634862 C>T maps to NM_003247.2 E539E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4814-01A-01D-1361-10 chr1:3624322 C>T maps to NM_005427.2 Q133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4814-01A-01D-1361-10 chr3:10188320 G>T did not map to a codon.
Sequencing variant TCGA-B0-4814-01A-01D-1361-10 chr19:21992280 A>C maps to NM_003423.2 L186L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4817-01A-01D-1361-10 chr7:152522194 C>T maps to NM_020445.4 R313R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4817-01A-01D-1361-10 chr2:233322957 T>C maps to NM_001631.3 G341G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4817-01A-01D-1361-10 chr1:145566759 T>C maps to NM_144698.3 L954L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4817-01A-01D-1361-10 chrX:84310893 A>G maps to NM_198450.4 T119T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4817-01A-01D-1361-10 chr7:120907349 A>G maps to NM_024913.4 L905L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4817-01A-01D-1361-10 chr2:37873388 T>A maps to NM_006449.3 G114G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4817-01A-01D-1361-10 chr16:90025606 A>G maps to NM_017702.2 Q186Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4817-01A-01D-1361-10 chr7:158529818 A>G maps to NM_020728.2 Y800Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4817-01A-01D-1361-10 chr7:148506482 C>T did not map to a codon.
Sequencing variant TCGA-B0-4817-01A-01D-1361-10 chr7:33039810 C>T maps to NM_007270.3 C437C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4817-01A-01D-1361-10 chr7:74129237 T>C did not map to a codon.
Sequencing variant TCGA-B0-4817-01A-01D-1361-10 chr1:234743338 C>A maps to NM_182972.2 G436G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4817-01A-01D-1361-10 chr15:101593135 G>T maps to NM_024652.3 L1233L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4817-01A-01D-1361-10 chr6:39893449 A>T maps to ENST00000425303 L130L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4817-01A-01D-1361-10 chr6:124979432 C>T maps to NM_001040214.1 D125D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4817-01A-01D-1361-10 chr16:18528573 A>G maps to NM_001004060.1 S898S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4817-01A-01D-1361-10 chr12:56720444 T>C maps to NM_001127460.2 T406T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4817-01A-01D-1361-10 chr6:73000564 G>A did not map to a codon.
Sequencing variant TCGA-B0-4817-01A-01D-1361-10 chr6:99848472 A>T maps to NM_032870.2 S787S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4817-01A-01D-1361-10 chr2:182765605 A>T maps to NM_001130445.1 V229V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4817-01A-01D-1361-10 chr7:149516804 G>A did not map to a codon.
Sequencing variant TCGA-B0-4817-01A-01D-1361-10 chrX:102864441 A>G maps to NM_032926.2 Q150Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4817-01A-01D-1361-10 chr3:40528384 A>T maps to NM_001145082.2 G168G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4817-01A-01D-1361-10 chr19:40540305 G>A maps to NM_001005851.2 I820I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4819-01A-01D-1361-10 chr5:141046055 G>T maps to NM_022481.5 S836*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4819-01A-01D-1361-10 chr16:10525096 C>G maps to NM_024997.2 S207*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4819-01A-01D-1361-10 chr5:175740818 T>G maps to ENST00000443967 L601L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4819-01A-01D-1361-10 chr3:47891145 G>A maps to NM_138615.2 W1073*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4819-01A-01D-1361-10 chr6:31237785 A>T maps to ENST00000383329 L324L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4819-01A-01D-1361-10 chr16:68225472 C>T maps to NM_173165.2 T967T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4819-01A-01D-1361-10 chr19:16875872 C>T maps to ENST00000438489 G760G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4819-01A-01D-1361-10 chr2:208795800 C>A maps to NM_001080475.2 E579*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4819-01A-01D-1361-10 chr9:98239879 T>C maps to NM_000264.3 G484G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4819-01A-01D-1361-10 chr9:92017851 C>T maps to NM_006378.3 L62L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4819-01A-01D-1361-10 chr17:79268691 C>T maps to NM_001037984.1 G10G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4819-01A-01D-1361-10 chr8:101196264 A>G maps to NM_003114.3 K190K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4819-01A-01D-1361-10 chr15:69237965 A>G maps to NM_145658.3 Q31Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4819-01A-01D-1361-10 chr1:117660995 C>T maps to NM_025188.3 K294K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4819-01A-01D-1361-10 chr3:10191469 G>A did not map to a codon.
Sequencing variant TCGA-B0-4819-01A-01D-1361-10 chr17:1257622 A>G maps to NM_006761.4 F199F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4819-01A-01D-1361-10 chr8:81577133 G>T maps to NM_001033723.2 A281A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4822-01A-01D-1361-10 chr1:229683266 A>T maps to NM_012089.2 A300A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4822-01A-01D-1361-10 chr1:25569163 A>C maps to NM_020317.3 A263A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4822-01A-01D-1361-10 chr12:8211782 G>A maps to NM_004054.2 L333L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4822-01A-01D-1361-10 chr5:156514239 G>T maps to NM_032782.3 S260*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4822-01A-01D-1361-10 chr15:99482569 T>C maps to NM_000875.3 D1146D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4822-01A-01D-1361-10 chr2:207988750 G>A maps to NM_003709.2 G160G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4822-01A-01D-1361-10 chr15:31266579 A>G maps to NM_017762.2 Y137Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4822-01A-01D-1361-10 chr11:57996083 G>A maps to NM_001004471.2 N88N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4822-01A-01D-1361-10 chr4:79847692 A>T maps to NM_001040202.1 I228I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4822-01A-01D-1361-10 chr17:61906876 A>G maps to NM_002805.5 Q40Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4822-01A-01D-1361-10 chr14:52735099 G>T maps to NM_000953.2 E190*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4822-01A-01D-1361-10 chr11:66407208 G>T maps to NM_002896.3 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4822-01A-01D-1361-10 chr7:122341887 T>A maps to NM_198085.1 *306L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4822-01A-01D-1361-10 chr16:48396057 T>A maps to NM_001006610.1 V125V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4822-01A-01D-1361-10 chr5:145862190 A>G maps to NM_006706.3 E641E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4822-01A-01D-1361-10 chr17:58348759 C>T maps to NM_032582.3 E218E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4822-01A-01D-1361-10 chr1:27587571 C>T maps to ENST00000319394 D9D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4824-01A-01D-1361-10 chr7:121721614 A>T maps to NM_005763.3 L740*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4824-01A-01D-1361-10 chr17:67243706 G>A maps to ENST00000392677 R1635*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4824-01A-01D-1361-10 chr3:35780925 C>T maps to ENST00000458225 Q589*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4824-01A-01D-1361-10 chr17:29161254 G>A maps to NM_024857.3 R52R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4824-01A-01D-1361-10 chr17:17929670 G>T maps to NM_145691.3 I128I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4824-01A-01D-1361-10 chr18:34376767 T>C maps to NM_015476.2 *301W. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4824-01A-01D-1361-10 chr2:200797972 A>G maps to NM_001039693.2 S255S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4824-01A-01D-1361-10 chr10:18629863 C>T maps to NM_201590.2 D3D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4824-01A-01D-1361-10 chr7:2949759 T>G maps to NM_032415.4 R1062R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4824-01A-01D-1361-10 chrX:1409283 G>A maps to NM_001161530.1 V176V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4824-01A-01D-1361-10 chrX:70326250 G>A maps to ENST00000438526 T17T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4824-01A-01D-1361-10 chr17:19232881 G>T maps to NM_014964.4 E445*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4824-01A-01D-1361-10 chr19:55870834 A>C maps to NM_001145402.1 A467A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4824-01A-01D-1361-10 chr19:51462554 C>T maps to NM_001012964.1 P200P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4824-01A-01D-1361-10 chr21:31797888 G>A maps to NM_181622.1 S114S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4824-01A-01D-1361-10 chr6:46787322 A>G maps to NM_005588.2 G146G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4824-01A-01D-1361-10 chr5:16668520 G>T maps to NM_012334.2 V1980V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4824-01A-01D-1361-10 chr1:205280932 C>A maps to ENST00000441520 R128R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4824-01A-01D-1361-10 chr3:52682446 G>C maps to ENST00000296302 Y242*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4824-01A-01D-1361-10 chr7:75055732 G>C maps to ENST00000257665 L403L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4824-01A-01D-1361-10 chr17:61906876 A>G maps to NM_002805.5 Q40Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4824-01A-01D-1361-10 chr1:40702737 T>G maps to NM_012421.3 L788L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4824-01A-01D-1361-10 chr5:134033689 A>T maps to NM_021982.1 R737*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4824-01A-01D-1361-10 chr3:155547677 G>A maps to NM_004733.3 S427S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4824-01A-01D-1361-10 chr13:37422884 C>T maps to NM_001127217.2 G444G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4824-01A-01D-1361-10 chr2:55804448 A>T did not map to a codon.
Sequencing variant TCGA-B0-4824-01A-01D-1361-10 chr6:33408631 G>A maps to NM_006772.2 A601A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4824-01A-01D-1361-10 chr1:114640499 C>T did not map to a codon.
Sequencing variant TCGA-B0-4824-01A-01D-1361-10 chr14:90459806 T>C maps to NM_018319.3 I507I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4824-01A-01D-1361-10 chr15:43525885 C>A did not map to a codon.
Sequencing variant TCGA-B0-4824-01A-01D-1361-10 chr2:132237982 A>G maps to NM_080386.2 T239T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4824-01A-01D-1361-10 chr22:50664351 G>A maps to NM_020461.3 D618D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4824-01A-01D-1361-10 chr11:17544781 C>A maps to NM_153676.3 L284L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4824-01A-01D-1361-10 chr2:61571100 T>C maps to NM_014709.3 A783A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4828-01A-01D-1361-10 chr5:77316581 G>A maps to NM_003664.3 Q976*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4828-01A-01D-1361-10 chrX:79939595 T>C maps to NM_153252.4 G1382G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4828-01A-01D-1361-10 chr10:118424300 G>A maps to ENST00000388884 A144A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4828-01A-01D-1361-10 chr9:26842571 G>A maps to NM_024828.3 N271N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4828-01A-01D-1361-10 chr21:47422536 C>A maps to NM_001848.2 R783R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4828-01A-01D-1361-10 chr12:77417896 G>T maps to NM_203394.2 G878G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4828-01A-01D-1361-10 chr8:25744373 T>C maps to NM_022659.2 R302R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4828-01A-01D-1361-10 chr9:130294040 G>A maps to NM_022833.2 I24I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4828-01A-01D-1361-10 chr5:177161890 A>G maps to ENST00000425383 G236G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4828-01A-01D-1361-10 chr5:177161890 A>G maps to ENST00000425383 G236G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4828-01A-01D-1361-10 chr9:84608501 A>T maps to NM_001001670.2 S1039S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4828-01A-01D-1361-10 chr7:100282979 G>A maps to NM_022574.4 P393P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4828-01A-01D-1361-10 chr2:20824633 T>C maps to NM_022460.3 K214K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4828-01A-01D-1361-10 chr10:118435937 C>T maps to NM_025015.2 P454P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4828-01A-01D-1361-10 chr21:34809268 A>T maps to ENST00000381995 *357C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4828-01A-01D-1361-10 chrX:53245089 C>A maps to NM_004187.3 E284*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4828-01A-01D-1361-10 chr14:56103976 A>G maps to NM_001079521.1 T537T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4828-01A-01D-1361-10 chr15:43621543 G>T maps to NM_014793.4 R382R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4828-01A-01D-1361-10 chr12:59271293 C>A maps to NM_153377.3 V808V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4828-01A-01D-1361-10 chr2:160697358 C>A maps to NM_001198759.1 E1130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4828-01A-01D-1361-10 chr16:71663302 C>T maps to NM_001017967.2 T167T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4828-01A-01D-1361-10 chr6:168273012 A>T maps to ENST00000400822 R177R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4828-01A-01D-1361-10 chr19:50762504 C>T maps to NM_001145809.1 F779F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4828-01A-01D-1361-10 chr19:49167833 A>G did not map to a codon.
Sequencing variant TCGA-B0-4828-01A-01D-1361-10 chr19:9237029 C>A maps to NM_001001958.1 V199V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4828-01A-01D-1361-10 chr8:110464466 T>A maps to ENST00000426474 A2155A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4828-01A-01D-1361-10 chr1:204242840 T>C maps to ENST00000367191 T5T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4828-01A-01D-1361-10 chr11:126080884 T>A maps to NM_032795.2 R85R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4828-01A-01D-1361-10 chr2:20402565 G>C maps to NM_001006946.1 A298A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4828-01A-01D-1361-10 chr1:24995883 C>G maps to NM_005839.3 T670T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4828-01A-01D-1361-10 chr16:1278743 C>T maps to ENST00000445910 G245G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4828-01A-01D-1361-10 chr9:99580431 T>A maps to NM_001001662.1 K625*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4828-01A-01D-1361-10 chr3:10188196 G>C did not map to a codon.
Sequencing variant TCGA-B0-4833-01A-01D-1373-10 chr17:40039401 C>T maps to ENST00000401700 G790G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4833-01A-01D-1373-10 chr4:100205771 T>G maps to NM_000667.3 V117V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4833-01A-01D-1373-10 chr5:139865229 T>A maps to ENST00000253810 S685S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4833-01A-01D-1373-10 chr17:49726558 T>G maps to NM_001082534.1 T206T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4833-01A-01D-1373-10 chrX:149963726 G>T maps to ENST00000438086 R132R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4833-01A-01D-1373-10 chr2:99013012 C>T maps to NM_001298.2 L460L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4833-01A-01D-1373-10 chr12:21699314 T>A maps to NM_021957.3 V504V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4833-01A-01D-1373-10 chr16:75675562 T>A maps to NM_001130089.1 K69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4833-01A-01D-1373-10 chr12:50642462 A>C maps to NM_001113546.1 S24S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4833-01A-01D-1373-10 chr19:821529 G>A maps to NM_024888.1 I10I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4833-01A-01D-1373-10 chr2:135160677 G>A maps to NM_002410.3 R500R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4833-01A-01D-1373-10 chr1:161183973 A>T maps to NM_004550.4 V461V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4833-01A-01D-1373-10 chr1:211451523 G>A maps to NM_001136223.1 R194R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4833-01A-01D-1373-10 chr12:105239708 A>G maps to NM_032148.3 S433S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4833-01A-01D-1373-10 chr20:4158151 C>G maps to ENST00000443211 A121A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4833-01A-01D-1373-10 chr15:39879676 C>A maps to NM_003246.2 S417*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4833-01A-01D-1373-10 chr13:101277908 C>T maps to NM_032813.2 W572*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4833-01A-01D-1373-10 chr2:135988350 T>C maps to NM_032143.2 R562R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4836-01A-01D-1373-10 chrX:1537001 C>G maps to NM_004192.3 T462T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4836-01A-01D-1373-10 chr11:64717340 C>T did not map to a codon.
Sequencing variant TCGA-B0-4836-01A-01D-1373-10 chr17:18156612 A>C did not map to a codon.
Sequencing variant TCGA-B0-4836-01A-01D-1373-10 chr14:44973865 C>A maps to NM_032135.3 S775S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4836-01A-01D-1373-10 chr6:42832829 G>T maps to NM_015349.1 S962S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4836-01A-01D-1373-10 chr2:85769803 T>C maps to NM_005911.4 A295A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4836-01A-01D-1373-10 chr6:51524621 A>G maps to NM_138694.3 T3434T. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-B0-4836-01A-01D-1373-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-B0-4836-01A-01D-1373-10 chr10:119029904 G>T maps to NM_003054.4 G457G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4836-01A-01D-1373-10 chr1:116534698 G>C maps to NM_018420.2 T45T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4836-01A-01D-1373-10 chr13:86369854 C>T maps to NM_032229.2 K263K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4836-01A-01D-1373-10 chr2:241991874 G>A maps to NM_001080437.1 R691R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4836-01A-01D-1373-10 chr11:43427494 A>C maps to NM_018259.5 A585A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4837-01A-01D-1373-10 chr1:94568672 G>T maps to NM_000350.2 I156I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4837-01A-01D-1373-10 chr12:45429898 T>G did not map to a codon.
Sequencing variant TCGA-B0-4837-01A-01D-1373-10 chr10:134013905 C>T maps to NM_006426.2 D286D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4837-01A-01D-1373-10 chr11:6239138 A>G maps to NM_032127.3 R573R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4837-01A-01D-1373-10 chrX:53579771 T>A maps to ENST00000276009 T2861T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4837-01A-01D-1373-10 chr7:45957038 C>G did not map to a codon.
Sequencing variant TCGA-B0-4837-01A-01D-1373-10 chr9:5968195 T>A maps to NM_001017969.2 K679*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4837-01A-01D-1373-10 chr3:186937984 G>A maps to NM_001879.5 G658G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4837-01A-01D-1373-10 chr11:102650296 G>A maps to NM_002425.2 D95D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4837-01A-01D-1373-10 chr2:27663324 C>T maps to ENST00000379863 A372A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4837-01A-01D-1373-10 chr3:53219627 C>T maps to NM_212539.1 S299S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4837-01A-01D-1373-10 chr8:144898830 G>C maps to NM_078480.1 V513V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4837-01A-01D-1373-10 chr4:3432132 G>T did not map to a codon.
Sequencing variant TCGA-B0-4837-01A-01D-1373-10 chr12:56814822 C>G maps to NM_003920.3 G988G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4837-01A-01D-1373-10 chr10:51592503 T>C maps to NM_006327.2 *210W. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4837-01A-01D-1373-10 chr11:5717666 C>T maps to NM_006074.4 R69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4837-01A-01D-1373-10 chr8:11995986 G>A maps to NM_201402.2 L95L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4837-01A-01D-1373-10 chr8:11995986 G>A maps to NM_201402.2 L95L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4838-01A-01D-1373-10 chr20:36940336 C>T maps to NM_001725.2 Q204*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4838-01A-01D-1373-10 chr12:80750653 A>G maps to NM_173591.3 Q1984Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4838-01A-01D-1373-10 chr9:35660624 C>T maps to NM_174923.2 L131L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4838-01A-01D-1373-10 chr12:56221610 G>A maps to NM_032364.5 Q278*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4838-01A-01D-1373-10 chr6:32552078 G>A maps to NM_002124.2 Y59Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4838-01A-01D-1373-10 chr1:219347282 A>G maps to NM_138794.3 A17A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4838-01A-01D-1373-10 chr13:35758116 G>T maps to ENST00000400445 V1612V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4838-01A-01D-1373-10 chr17:76396756 G>A did not map to a codon.
Sequencing variant TCGA-B0-4838-01A-01D-1373-10 chr7:113518386 A>G maps to NM_002711.3 H920H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4838-01A-01D-1373-10 chr19:41009981 C>T maps to NM_020971.2 A536A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4838-01A-01D-1373-10 chr2:159992708 C>G maps to NM_033394.2 P88P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4838-01A-01D-1373-10 chr11:117772954 T>C maps to ENST00000413475 *567*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4838-01A-01D-1373-10 chr2:210794631 A>C maps to NM_032504.1 L1882L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4839-01A-01D-1373-10 chr16:56535331 C>T maps to NM_031885.3 T386T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4839-01A-01D-1373-10 chr2:210896229 A>T maps to NM_152519.2 P690P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4839-01A-01D-1373-10 chr3:112357864 G>A maps to ENST00000447230 D307D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4839-01A-01D-1373-10 chr13:76101978 G>A maps to NM_203497.2 L72L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4839-01A-01D-1373-10 chr10:115609996 T>A maps to NM_014881.3 P289P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4839-01A-01D-1373-10 chr11:120833223 C>T maps to NM_014619.2 S700S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4839-01A-01D-1373-10 chr5:153857037 C>G maps to NM_004821.2 R177R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4839-01A-01D-1373-10 chr8:140631094 G>A maps to NM_016601.2 A177A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4839-01A-01D-1373-10 chr12:53039078 G>T maps to NM_000423.2 S548S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4839-01A-01D-1373-10 chr11:46914587 G>T maps to ENST00000256991 R590R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4839-01A-01D-1373-10 chr19:8996450 G>A maps to NM_024690.2 C13707C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4839-01A-01D-1373-10 chr3:52504924 T>A did not map to a codon.
Sequencing variant TCGA-B0-4839-01A-01D-1373-10 chr13:25671754 G>A maps to NM_030979.2 T473T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4839-01A-01D-1373-10 chr9:79318380 A>T maps to NM_015225.2 A2716A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4839-01A-01D-1373-10 chr5:36301484 G>A maps to NM_001161429.1 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4839-01A-01D-1373-10 chr19:46318215 C>T maps to NM_030785.3 Q73Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4839-01A-01D-1373-10 chr15:42822002 C>T maps to NM_003825.2 R186*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4839-01A-01D-1373-10 chr8:23702338 G>T maps to NM_003155.2 R230R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4839-01A-01D-1373-10 chr3:93733630 C>T maps to NM_001001850.1 K161K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4839-01A-01D-1373-10 chr1:216061914 T>C maps to ENST00000366943 P2692P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4839-01A-01D-1373-10 chr15:62243163 G>A maps to NM_020821.2 L1506L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4839-01A-01D-1373-10 chr8:38205402 G>T maps to NM_023034.1 S96*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4839-01A-01D-1373-10 chr18:56585626 C>T maps to NM_018181.4 D36D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4839-01A-01D-1373-10 chr16:89294594 C>T maps to NM_182531.2 I605I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4841-01A-01D-1361-10 chr1:150531785 C>A maps to ENST00000369039 G952G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4841-01A-01D-1361-10 chr17:33951513 G>A maps to NM_001030006.1 L208L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4841-01A-01D-1361-10 chr7:144070337 A>G maps to NM_005435.3 E1367E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4841-01A-01D-1361-10 chr5:70855947 G>A maps to NM_018429.2 V2460V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4841-01A-01D-1361-10 chr20:31815350 G>A maps to NM_178466.3 E231E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4841-01A-01D-1361-10 chr2:220038161 T>A maps to NM_015680.4 R200R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4841-01A-01D-1361-10 chr4:170671700 G>A maps to NM_017867.2 H128H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4841-01A-01D-1361-10 chr3:9908859 C>T maps to ENST00000430427 K235K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4841-01A-01D-1361-10 chr4:109790279 T>C maps to ENST00000333642 Q349Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4841-01A-01D-1361-10 chr1:47610116 C>T maps to NM_001010969.2 D293D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4841-01A-01D-1361-10 chr14:59113725 G>A maps to NM_016651.5 T795T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4841-01A-01D-1361-10 chr10:124340397 G>T maps to ENST00000368915 P340P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4841-01A-01D-1361-10 chr12:56221620 A>G maps to NM_032364.5 Y274Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4841-01A-01D-1361-10 chr7:37311448 T>C maps to NM_014800.9 L77L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4841-01A-01D-1361-10 chr12:56524687 A>T maps to NM_001184796.1 T182T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4841-01A-01D-1361-10 chr6:71235352 A>T maps to NM_001162529.1 K856*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4841-01A-01D-1361-10 chr9:97365719 T>C maps to NM_001127628.1 G320G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4841-01A-01D-1361-10 chr9:128086082 C>A maps to NM_015635.2 S580*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4841-01A-01D-1361-10 chr19:55539048 C>T maps to NM_001083899.1 T169T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4841-01A-01D-1361-10 chr8:28827802 C>T maps to ENST00000444075 S89S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4841-01A-01D-1361-10 chr2:20838371 A>G maps to NM_022460.3 D149D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4841-01A-01D-1361-10 chr1:153701139 A>C maps to ENST00000428986 A10A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4841-01A-01D-1361-10 chr1:111060344 C>T maps to NM_005549.2 S355S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4841-01A-01D-1361-10 chr4:88099692 G>A maps to NM_020803.3 N344N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4841-01A-01D-1361-10 chr11:1606128 A>C maps to NM_001005922.1 G117G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4841-01A-01D-1361-10 chr22:22142569 G>A maps to NM_138957.2 L278L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4841-01A-01D-1361-10 chr9:134889740 A>G maps to NM_004269.2 T154T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4841-01A-01D-1361-10 chr17:10353951 C>T maps to NM_017533.2 L1333L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4841-01A-01D-1361-10 chr13:33281136 A>T maps to ENST00000400481 P641P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4841-01A-01D-1361-10 chr19:14104646 T>C maps to NM_002918.4 T3T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4841-01A-01D-1361-10 chr18:61471601 A>G maps to NM_001040147.1 R292R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4841-01A-01D-1361-10 chr22:26688759 G>T maps to NM_021115.4 T161T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4841-01A-01D-1361-10 chr5:54645467 A>G maps to NM_015360.4 K436K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4841-01A-01D-1361-10 chr6:167595370 T>C maps to NM_001145121.1 H343H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4841-01A-01D-1361-10 chr8:105360796 C>A maps to NM_030788.2 S6*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4841-01A-01D-1361-10 chr4:68930481 A>G maps to NM_207407.2 V312V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4841-01A-01D-1361-10 chr6:125569530 T>C did not map to a codon.
Sequencing variant TCGA-B0-4841-01A-01D-1361-10 chr2:61571100 T>C maps to NM_014709.3 A783A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4841-01A-01D-1361-10 chr3:14193900 A>T maps to NM_004628.4 T683T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4841-01A-01D-1361-10 chr7:100017326 T>A maps to NM_017984.3 K70*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4843-01A-01D-1361-10 chr5:90671370 T>C maps to NM_020801.2 P190P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4843-01A-01D-1361-10 chrX:63445176 A>G maps to NM_130388.2 H109H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4843-01A-01D-1361-10 chr6:74517870 C>T maps to NM_133493.3 D1085D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4843-01A-01D-1361-10 chr6:44414437 C>A maps to NM_001253.2 S800*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4843-01A-01D-1361-10 chr12:56221610 G>A maps to NM_032364.5 Q278*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4843-01A-01D-1361-10 chr19:45731305 T>C maps to NM_138568.3 A73A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4843-01A-01D-1361-10 chr11:67218863 G>A maps to NM_206997.1 D444D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4843-01A-01D-1361-10 chr17:65119195 A>G maps to NM_014877.3 L1174L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4843-01A-01D-1361-10 chr3:197427933 G>A maps to NM_014687.1 Q271*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4843-01A-01D-1361-10 chr9:27948986 A>C maps to NM_152570.1 L561L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4843-01A-01D-1361-10 chr12:49442447 T>C maps to NM_003482.3 L1375L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4843-01A-01D-1361-10 chr11:118106269 A>G maps to NM_198275.1 L162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4843-01A-01D-1361-10 chr3:195510761 G>A maps to NM_018406.5 V2563V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4843-01A-01D-1361-10 chr17:36895855 C>T maps to NM_007144.2 R64R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4843-01A-01D-1361-10 chr1:186646027 G>A maps to NM_000963.2 Y220Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4843-01A-01D-1361-10 chr6:158565366 A>G maps to NM_032861.3 F191F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4843-01A-01D-1361-10 chr1:85117600 G>C maps to NM_001166417.1 S490*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4843-01A-01D-1361-10 chr7:38256829 T>A maps to NM_032016.2 I159I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4843-01A-01D-1361-10 chr8:74515975 T>C maps to NM_001164380.1 R338R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4843-01A-01D-1361-10 chr4:69403348 C>T maps to NM_001076.2 R529R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4843-01A-01D-1361-10 chr16:21982910 T>C maps to NM_003366.2 L246L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4843-01A-01D-1361-10 chr14:75266223 T>A maps to NM_019589.2 S1408S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4843-01A-01D-1361-10 chr6:28116331 G>A maps to NM_006298.2 V49V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4843-01A-01D-1361-10 chr19:21992280 A>C maps to NM_003423.2 L186L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4843-01A-01D-1361-10 chr16:2050420 T>C maps to ENST00000431526 P421P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4844-01A-01D-1361-10 chr7:123257652 G>T maps to NM_080928.3 E105*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4844-01A-01D-1361-10 chr1:161762091 C>T maps to NM_007348.2 I221I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4844-01A-01D-1361-10 chr11:65650834 T>A maps to NM_001335.3 P320P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4844-01A-01D-1361-10 chr16:31373160 G>T maps to NM_000887.3 T339T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4844-01A-01D-1361-10 chr18:21406682 C>A maps to ENST00000416669 L865L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4844-01A-01D-1361-10 chrX:64744050 C>A maps to NM_031206.4 T395T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4844-01A-01D-1361-10 chr19:8316055 C>T maps to NM_024552.2 V32V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4844-01A-01D-1361-10 chr12:81239679 G>C maps to NM_004664.2 S104S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4844-01A-01D-1361-10 chrX:110366369 T>C maps to NM_001128168.1 A13A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4844-01A-01D-1361-10 chr3:122277191 G>T maps to NM_031458.2 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4844-01A-01D-1361-10 chr11:66392255 C>T maps to NM_006328.3 G303G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4844-01A-01D-1361-10 chr9:4849484 A>G maps to NM_005772.3 L302L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4844-01A-01D-1361-10 chr20:35547820 G>T maps to NM_015474.3 C266*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4844-01A-01D-1361-10 chr6:152779923 G>A maps to NM_182961.2 Q846*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4844-01A-01D-1361-10 chr6:167753862 T>C maps to NM_031949.4 L159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4844-01A-01D-1361-10 chr1:40735724 C>T maps to NM_005857.3 L185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4845-01A-01D-1361-10 chr4:8108314 C>T maps to NM_001130083.1 T20T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4845-01A-01D-1361-10 chr7:134722285 G>A maps to ENST00000458078 Q485Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4845-01A-01D-1361-10 chr7:105516947 T>C maps to NM_020725.1 T19T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4845-01A-01D-1361-10 chr2:160289730 G>A maps to NM_013450.2 H479H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4845-01A-01D-1361-10 chr15:41571547 G>A maps to NM_007236.4 V183V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4845-01A-01D-1361-10 chr7:73245845 C>G maps to NM_001305.3 T105T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4845-01A-01D-1361-10 chr17:74003639 C>T maps to NM_001988.2 A1882A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4845-01A-01D-1361-10 chr11:46760837 T>G maps to NM_000506.3 Y583*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4845-01A-01D-1361-10 chr19:55539048 C>T maps to NM_001083899.1 T169T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4845-01A-01D-1361-10 chr4:100869966 C>A did not map to a codon.
Sequencing variant TCGA-B0-4845-01A-01D-1361-10 chr2:241722487 G>A maps to ENST00000373308 G279G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4845-01A-01D-1361-10 chr10:88476147 C>A maps to NM_001171610.1 S437S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4845-01A-01D-1361-10 chr1:22148090 C>T maps to NM_001013693.2 D264D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4845-01A-01D-1361-10 chr10:27458934 A>C maps to NM_001172303.1 A349A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4845-01A-01D-1361-10 chr20:33587595 G>A maps to NM_020884.3 G1598G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4845-01A-01D-1361-10 chr3:52661387 T>A did not map to a codon.
Sequencing variant TCGA-B0-4845-01A-01D-1361-10 chr8:52773470 C>A maps to NM_052937.2 G81*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4845-01A-01D-1361-10 chr11:65396338 G>A maps to NM_032223.2 T1287T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4845-01A-01D-1361-10 chr17:8722496 G>A maps to NM_001010855.2 C632C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4845-01A-01D-1361-10 chr2:95947010 C>G maps to NM_144707.2 L483L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4845-01A-01D-1361-10 chr10:112579879 C>T maps to NM_001134363.1 G867G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4845-01A-01D-1361-10 chr7:100731747 T>G maps to NM_030961.1 G385G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4845-01A-01D-1361-10 chr19:53770020 T>A maps to NM_173857.2 K300*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4846-01A-01D-1361-10 chr5:7706857 A>T maps to NM_020546.2 K371*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4846-01A-01D-1361-10 chr17:55184150 T>C maps to ENST00000427138 L484L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4846-01A-01D-1361-10 chr22:32113206 C>G maps to NM_173566.2 G206G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4846-01A-01D-1361-10 chr14:95582927 A>G maps to NM_177438.2 D538D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4846-01A-01D-1361-10 chr1:50941222 G>A maps to NM_007051.2 N594N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4846-01A-01D-1361-10 chr11:13734515 A>T maps to NM_032228.5 P297P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4846-01A-01D-1361-10 chr11:63990879 C>T maps to NM_178443.2 F640F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4846-01A-01D-1361-10 chr16:55360270 C>T maps to NM_024335.2 S23S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4846-01A-01D-1361-10 chr9:20758087 G>T did not map to a codon.
Sequencing variant TCGA-B0-4846-01A-01D-1361-10 chr16:18522872 C>T maps to NM_001004060.1 T1072T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4846-01A-01D-1361-10 chr19:18327664 C>A maps to NM_000923.3 L457L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4846-01A-01D-1361-10 chr1:89298944 T>C maps to NM_006256.2 A923A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4846-01A-01D-1361-10 chr5:73144820 T>C maps to NM_001080479.2 V552V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4846-01A-01D-1361-10 chr6:7410656 G>A maps to NM_031480.2 R414R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4846-01A-01D-1361-10 chr1:156169865 G>T maps to NM_014655.2 G76G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4846-01A-01D-1361-10 chr8:56717518 C>T maps to NM_024831.6 F689F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4846-01A-01D-1361-10 chr11:119996483 C>G maps to NM_012101.3 L416L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4846-01A-01D-1361-10 chr8:87424055 T>C maps to NM_007013.3 P338P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4847-01A-01D-1361-10 chr14:105408994 C>A maps to NM_138420.2 E4265*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4847-01A-01D-1361-10 chr8:7754020 T>C maps to NM_004942.2 P28P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4847-01A-01D-1361-10 chr8:49643117 A>T maps to NM_024593.3 S100S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4847-01A-01D-1361-10 chr19:10229836 G>T maps to NM_003755.3 V26V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4847-01A-01D-1361-10 chr15:74370973 T>C maps to NM_001038640.2 Q87Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4847-01A-01D-1361-10 chr12:52797690 G>A maps to NM_033033.3 V138V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4847-01A-01D-1361-10 chr17:49281221 A>G maps to ENST00000389496 N226N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4847-01A-01D-1361-10 chr20:33587602 G>T maps to NM_020884.3 E1601*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4847-01A-01D-1361-10 chr3:52643327 C>T did not map to a codon.
Sequencing variant TCGA-B0-4847-01A-01D-1361-10 chr1:204210580 C>T maps to ENST00000367191 S797S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4847-01A-01D-1361-10 chr9:112151593 G>C maps to NM_002829.3 T724T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4847-01A-01D-1361-10 chr7:5984720 C>T maps to NM_173565.3 A501A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4847-01A-01D-1361-10 chr4:106156074 A>T maps to ENST00000513237 K347*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4847-01A-01D-1361-10 chr3:10191571 G>T maps to NM_000551.2 E189*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4848-01A-01D-1361-10 chr11:6592217 G>T maps to NM_144666.2 L4492L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4848-01A-01D-1361-10 chrX:34148256 A>T maps to NM_203408.3 P713P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4848-01A-01D-1361-10 chr14:45606356 T>C maps to NM_020937.2 L198L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4848-01A-01D-1361-10 chr12:133351771 C>T maps to NM_005895.3 Q1366Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4848-01A-01D-1361-10 chr11:5878041 A>G maps to NM_001005168.1 Y297Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4848-01A-01D-1361-10 chr7:99796169 C>T maps to NM_012447.2 G439G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4848-01A-01D-1361-10 chr19:32844299 C>A maps to NM_014910.4 S188S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4849-01A-01D-1361-10 chr10:115891082 A>G maps to NM_018017.2 L642L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4849-01A-01D-1361-10 chr12:10131626 C>T maps to ENST00000355690 L61L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4849-01A-01D-1361-10 chr11:10825558 C>A maps to ENST00000429377 E270*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4849-01A-01D-1361-10 chr18:2890859 G>T maps to NM_032048.2 T245T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4849-01A-01D-1361-10 chr1:169510436 T>C maps to ENST00000367796 E1302E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4849-01A-01D-1361-10 chr1:209807971 G>A maps to NM_000228.2 P128P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4849-01A-01D-1361-10 chr9:130241214 C>T maps to NM_001005374.2 N251N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4849-01A-01D-1361-10 chr17:10219053 G>A maps to NM_003802.2 Q1314*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4849-01A-01D-1361-10 chr3:52678734 G>T maps to ENST00000296302 S295*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4849-01A-01D-1361-10 chr11:18050850 G>A maps to ENST00000341556 T176T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-4101-01A-02D-1361-10 chr7:6063123 T>A maps to NM_006303.3 V255V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-4101-01A-02D-1361-10 chr3:130125149 T>G maps to ENST00000312481 G1488G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-4101-01A-02D-1361-10 chr1:220157565 A>G maps to NM_004446.2 L1024L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-4101-01A-02D-1361-10 chr1:155256980 A>C maps to NM_020897.1 R499R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-4101-01A-02D-1361-10 chr3:193854201 G>A maps to NM_005524.2 S11S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-4101-01A-02D-1361-10 chr22:41664129 T>G maps to NM_002883.2 R91R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-4101-01A-02D-1361-10 chr9:131550633 C>T maps to NM_018201.3 V15V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-4101-01A-02D-1361-10 chr20:36784288 C>G maps to NM_004613.2 V131V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-4101-01A-02D-1361-10 chr17:79846139 G>A maps to NM_005782.3 Q253*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-4101-01A-02D-1361-10 chr3:141163614 T>C maps to NM_001080412.2 V795V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-4101-01A-02D-1361-10 chr11:110035963 G>A maps to NM_033390.1 R718R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-4101-01A-02D-1361-10 chrX:152085827 G>C did not map to a codon.
Sequencing variant TCGA-B8-4622-01A-02D-1361-10 chr20:3657785 G>T maps to NM_025220.2 S61*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4622-01A-02D-1361-10 chrX:49957014 G>T maps to NM_003886.2 A783A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4622-01A-02D-1361-10 chr14:74539004 A>G maps to NM_005589.2 I83I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4622-01A-02D-1361-10 chr19:42490051 T>A maps to ENST00000441343 P190P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4622-01A-02D-1361-10 chr9:94087666 T>C maps to NM_001698.2 R146R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4622-01A-02D-1361-10 chr19:12867046 C>T maps to NM_017682.2 Y347Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4622-01A-02D-1361-10 chr1:32686771 C>T maps to NM_019118.3 Q65Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4622-01A-02D-1361-10 chr2:37873388 T>A maps to NM_006449.3 G114G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4622-01A-02D-1361-10 chr16:66599817 T>C maps to NM_016951.2 C121C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4622-01A-02D-1361-10 chr19:54646855 T>C maps to NM_014516.3 G9G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4622-01A-02D-1361-10 chr13:110822086 A>G maps to NM_001845.4 P1255P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4622-01A-02D-1361-10 chr6:70942324 T>A maps to NM_001851.4 K822*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4622-01A-02D-1361-10 chr8:2808658 G>T maps to NM_033225.5 S3393*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4622-01A-02D-1361-10 chr18:29102085 G>A maps to NM_001943.3 E188E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4622-01A-02D-1361-10 chr10:74914025 T>G maps to NM_001135752.1 R257R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4622-01A-02D-1361-10 chr7:143095136 T>A maps to NM_005232.4 L497L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4622-01A-02D-1361-10 chr1:110134681 G>T maps to NM_006496.2 E298*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4622-01A-02D-1361-10 chr15:74367322 C>T maps to NM_001038640.2 A289A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4622-01A-02D-1361-10 chr2:86385745 A>T maps to NM_006839.2 T377T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4622-01A-02D-1361-10 chr17:68171452 T>A maps to NM_000891.2 A91A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4622-01A-02D-1361-10 chr9:7015919 G>A maps to NM_015061.3 A750A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4622-01A-02D-1361-10 chr14:74983606 C>A maps to NM_000428.2 G942G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4622-01A-02D-1361-10 chr20:42343845 C>T maps to NM_002466.2 Q633*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4622-01A-02D-1361-10 chr3:52623116 G>C maps to ENST00000296302 V978V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4622-01A-02D-1361-10 chr14:71543030 A>G maps to NM_014982.2 P1744P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4622-01A-02D-1361-10 chr1:12837462 C>T maps to NM_001080830.1 A391A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4622-01A-02D-1361-10 chr10:73579620 T>A maps to ENST00000373120 K348*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4622-01A-02D-1361-10 chr14:24642237 C>T maps to NM_005132.2 Q86*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4622-01A-02D-1361-10 chr12:21624426 A>T maps to NM_032941.2 A534A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4622-01A-02D-1361-10 chr1:183891412 C>T maps to NM_015149.3 L723L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4622-01A-02D-1361-10 chr8:100990284 G>A maps to NM_015668.3 L1127L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4622-01A-02D-1361-10 chr10:104357036 A>G maps to NM_016169.3 R299R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4622-01A-02D-1361-10 chr16:77243353 A>G maps to ENST00000398111 E118E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4622-01A-02D-1361-10 chrX:102529071 C>A maps to NM_001012979.2 L140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4622-01A-02D-1361-10 chr1:46159075 C>A maps to NM_016486.3 A81A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4622-01A-02D-1361-10 chr2:207174279 G>T maps to NM_020923.1 T1676T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4622-01A-02D-1361-10 chr8:77618281 C>A maps to NM_024721.4 Y653*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4622-01A-02D-1361-10 chr22:24086148 G>A maps to NM_021916.2 T393T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4622-01A-02D-1361-10 chr4:146824163 G>A maps to ENST00000508784 L83L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4158-01A-02D-1366-10 chr11:64681628 C>T maps to ENST00000421419 R137R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4158-01A-02D-1366-10 chr10:73521775 C>A maps to NM_022153.1 V30V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4158-01A-02D-1366-10 chr22:37912255 T>C maps to NM_014550.3 R141R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4158-01A-02D-1366-10 chr11:104971441 G>A maps to NM_001007232.1 G24G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4158-01A-02D-1366-10 chr19:42219788 C>A maps to NM_004363.2 L308L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4158-01A-02D-1366-10 chr5:64847409 C>T maps to NM_022145.3 W74*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4158-01A-02D-1366-10 chr2:189860858 C>T maps to NM_000090.3 P539P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4158-01A-02D-1366-10 chr2:242684221 T>A maps to NM_152783.3 T261T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4158-01A-02D-1366-10 chr17:77075666 T>C maps to NM_001042573.1 I171I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4158-01A-02D-1366-10 chr8:101153257 T>C maps to NM_001029860.3 E408E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4158-01A-02D-1366-10 chr3:148789183 C>T maps to NM_003071.3 W250*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4158-01A-02D-1366-10 chr1:62740523 T>G maps to NM_181712.4 A84A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4158-01A-02D-1366-10 chr1:62740523 T>G maps to NM_181712.4 A84A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4158-01A-02D-1366-10 chr9:133942464 C>A maps to ENST00000355048 G822G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4158-01A-02D-1366-10 chr2:141571373 A>G maps to NM_018557.2 G1737G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4158-01A-02D-1366-10 chr3:47050125 C>A maps to NM_015175.1 A2665A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4158-01A-02D-1366-10 chr11:45955638 C>A maps to ENST00000257821 G642G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4158-01A-02D-1366-10 chr6:42975941 C>T maps to NM_006245.2 F287F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4158-01A-02D-1366-10 chr7:103004702 G>T maps to NM_002803.2 A235A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4158-01A-02D-1366-10 chr10:43601999 G>C maps to NM_020975.4 R348R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4158-01A-02D-1366-10 chr16:30773994 C>A maps to NM_014771.2 S43S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4158-01A-02D-1366-10 chrX:9900829 G>T maps to NM_001649.2 S1169S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4158-01A-02D-1366-10 chr1:48694800 C>T maps to NM_001135181.1 D122D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4158-01A-02D-1366-10 chr16:2807886 T>C maps to NM_016333.3 D152D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4158-01A-02D-1366-10 chr7:100478986 A>G maps to NM_015908.5 P68P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4158-01A-02D-1366-10 chr8:119938823 C>T maps to NM_002546.3 R242R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4158-01A-02D-1366-10 chrX:54950146 G>C maps to NM_001039705.1 L394L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4158-01A-02D-1366-10 chr15:31318394 C>T maps to NM_002420.4 K1170K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4159-01A-02D-1366-10 chr2:202589117 G>A maps to NM_020919.3 L1138L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4159-01A-02D-1366-10 chr7:150028095 G>A maps to NM_138434.2 W201*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4159-01A-02D-1366-10 chrX:18622765 G>T maps to NM_001037343.1 P574P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4159-01A-02D-1366-10 chr19:36142195 T>C maps to ENST00000392201 F34F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4159-01A-02D-1366-10 chr8:65517237 C>A did not map to a codon.
Sequencing variant TCGA-BP-4159-01A-02D-1366-10 chr19:13080509 G>A maps to NM_152654.2 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4159-01A-02D-1366-10 chr12:57910756 A>G maps to NM_001195056.1 A138A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4159-01A-02D-1366-10 chr10:131671767 C>A maps to ENST00000355311 R243R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4159-01A-02D-1366-10 chr9:134136483 G>A maps to NM_033387.3 L193L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4159-01A-02D-1366-10 chrX:12701705 G>T maps to ENST00000429478 S181S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4159-01A-02D-1366-10 chr7:126086264 G>T maps to NM_001127323.1 T864T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4159-01A-02D-1366-10 chrX:53240704 T>A maps to NM_004187.3 K459*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4159-01A-02D-1366-10 chr9:73027904 G>A maps to NM_001206.2 S125S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4159-01A-02D-1366-10 chr1:153659770 C>A maps to NM_000906.3 T677T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4159-01A-02D-1366-10 chr2:192550346 T>G maps to NM_001031716.2 P156P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4159-01A-02D-1366-10 chr20:43541487 T>C maps to NM_001124756.1 S127S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4159-01A-02D-1366-10 chr2:113942577 C>T maps to NM_012455.2 D367D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4159-01A-02D-1366-10 chr4:1075244 G>A maps to NM_001131034.3 H142H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4159-01A-02D-1366-10 chr2:234959666 C>A maps to NM_006944.2 A46A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4159-01A-02D-1366-10 chr17:17722890 A>G maps to NM_001005291.2 P254P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4160-01A-02D-1366-10 chr10:52575930 C>A maps to NM_138932.2 E326*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4160-01A-02D-1366-10 chr9:18906803 G>A maps to NM_001040272.4 V1692V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4160-01A-02D-1366-10 chrX:2833630 A>G maps to NM_001669.2 Y322Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4160-01A-02D-1366-10 chr12:32481359 G>C maps to NM_001714.2 R657R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4160-01A-02D-1366-10 chr2:20990105 A>T maps to ENST00000381090 S69S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4160-01A-02D-1366-10 chr22:24434872 C>A maps to NM_012295.3 A58A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4160-01A-02D-1366-10 chr2:219892422 A>G maps to NM_194302.2 P720P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4160-01A-02D-1366-10 chr19:3964715 C>T maps to NM_001348.1 T112T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4160-01A-02D-1366-10 chr4:107846994 G>T maps to NM_014421.2 R112R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4160-01A-02D-1366-10 chr2:25498412 C>T did not map to a codon.
Sequencing variant TCGA-BP-4160-01A-02D-1366-10 chr6:32629145 G>A maps to ENST00000374943 I250I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4160-01A-02D-1366-10 chr15:77756617 C>T maps to NM_018200.2 A42A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4160-01A-02D-1366-10 chr12:26784954 C>T maps to NM_002223.2 E926E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4160-01A-02D-1366-10 chr9:5072559 C>T maps to NM_004972.3 Y570Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4160-01A-02D-1366-10 chr11:47644273 A>G maps to NM_014342.3 C268C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4160-01A-02D-1366-10 chr4:140280991 C>T maps to NM_057175.3 Y451Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4160-01A-02D-1366-10 chr19:50187292 C>T maps to NM_001536.3 L174L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4160-01A-02D-1366-10 chr18:18600157 G>A maps to NM_005406.2 L439L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4160-01A-02D-1366-10 chr10:7239536 C>A maps to NM_001018039.1 P557P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4160-01A-02D-1366-10 chr10:104352444 C>A maps to NM_016169.3 P187P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4160-01A-02D-1366-10 chr22:18640564 C>T maps to NM_017414.3 P45P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4160-01A-02D-1366-10 chrX:41047252 A>G maps to NM_001039590.2 R1231R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4165-01A-02D-1366-10 chr6:24520669 T>C maps to NM_170740.1 S317S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4165-01A-02D-1366-10 chr1:95538418 T>A maps to NM_144988.3 G12G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4165-01A-02D-1366-10 chr12:96350641 G>T maps to NM_152435.2 L163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4165-01A-02D-1366-10 chr8:41577247 G>T maps to ENST00000415018 A346A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4165-01A-02D-1366-10 chr19:33119746 T>C maps to NM_032139.2 A406A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4165-01A-02D-1366-10 chr15:90342492 G>C maps to NM_001150.2 A669A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4165-01A-02D-1366-10 chr20:55088388 G>T maps to ENST00000357348 E196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4165-01A-02D-1366-10 chr9:132084484 A>T maps to NM_001012715.3 V131V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4165-01A-02D-1366-10 chr5:10290760 G>A maps to NM_138809.3 P38P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4165-01A-02D-1366-10 chr10:131671767 C>A maps to ENST00000355311 R243R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4165-01A-02D-1366-10 chr1:11159822 T>A maps to NM_001001998.1 G22G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4165-01A-02D-1366-10 chr2:27730175 C>T maps to NM_001486.3 Q381*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4165-01A-02D-1366-10 chr5:176024672 G>C maps to NM_052899.2 S721S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4165-01A-02D-1366-10 chr17:3628887 A>C maps to NM_031965.2 T553T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4165-01A-02D-1366-10 chr6:168376846 C>G maps to NM_001129895.1 L162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4165-01A-02D-1366-10 chr19:50394325 G>T maps to NM_172374.1 A247A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4165-01A-02D-1366-10 chr17:39579167 G>C maps to NM_003770.4 S198S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4165-01A-02D-1366-10 chr8:99030306 G>A maps to ENST00000254898 E594E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4165-01A-02D-1366-10 chr11:76873960 C>T maps to NM_000260.3 I539I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4165-01A-02D-1366-10 chr1:158735944 G>A maps to NM_001005185.1 H176H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4165-01A-02D-1366-10 chr1:144871741 A>T maps to NM_014644.4 A1740A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4165-01A-02D-1366-10 chr2:229890656 G>T maps to NM_017933.4 L146L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4165-01A-02D-1366-10 chr20:44054402 A>C maps to NM_015937.4 T558T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4165-01A-02D-1366-10 chr19:14574544 A>T maps to NM_213560.1 K502*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4165-01A-02D-1366-10 chr15:90210172 G>A maps to NM_002666.4 Y401Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4165-01A-02D-1366-10 chr6:89793881 A>G maps to NM_006813.2 V317V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4165-01A-02D-1366-10 chr1:110882644 T>C maps to NM_022768.4 H206H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4165-01A-02D-1366-10 chr22:50904776 A>C did not map to a codon.
Sequencing variant TCGA-BP-4165-01A-02D-1366-10 chr19:51919239 C>T maps to NM_033130.4 G312G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4165-01A-02D-1366-10 chr8:145638894 A>C did not map to a codon.
Sequencing variant TCGA-BP-4165-01A-02D-1366-10 chr4:56236194 C>T maps to NM_024592.3 F298F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4165-01A-02D-1366-10 chr8:134488009 C>T maps to NM_173344.2 L86L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4165-01A-02D-1366-10 chr19:39936542 G>T maps to NM_003169.3 E5*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4165-01A-02D-1366-10 chr7:76143371 T>C maps to NM_030570.2 L245L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4165-01A-02D-1366-10 chr1:173839524 C>G maps to NM_001122770.1 S54S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4165-01A-02D-1366-10 chr5:178373910 C>G maps to NM_182594.2 P58P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4166-01A-02D-1366-10 chr16:16142000 C>A maps to ENST00000399408 A407A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4166-01A-02D-1366-10 chr16:89348395 G>A maps to NM_013275.4 S1518S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4166-01A-02D-1366-10 chr12:56363323 G>A maps to NM_001798.3 V184V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4166-01A-02D-1366-10 chr16:53352218 T>A maps to ENST00000219084 R2560R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4166-01A-02D-1366-10 chr3:38141826 G>A maps to NM_007335.2 G925G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4166-01A-02D-1366-10 chr12:53684664 G>A maps to NM_012291.4 W1802*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4166-01A-02D-1366-10 chr1:166135389 C>A maps to NM_001017961.3 T32T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4166-01A-02D-1366-10 chr1:172635131 G>T maps to NM_000639.1 T274T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4166-01A-02D-1366-10 chr4:84240607 C>A maps to NM_006665.5 G130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4166-01A-02D-1366-10 chr3:101571993 C>T maps to NM_031419.3 P208P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4166-01A-02D-1366-10 chr10:91348468 C>T maps to NM_148977.1 L559L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4166-01A-02D-1366-10 chr12:3921405 T>C maps to NM_020367.4 K300K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4166-01A-02D-1366-10 chr19:52716325 G>A maps to NM_014225.5 W257*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4166-01A-02D-1366-10 chr17:31323912 C>A maps to NM_173847.3 Y132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4166-01A-02D-1366-10 chr19:39962249 A>G maps to NM_003169.3 R610R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4166-01A-02D-1366-10 chr22:42610519 G>A maps to NM_005650.1 Y264Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4166-01A-02D-1366-10 chr4:106180796 G>A maps to ENST00000513237 G1296G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4166-01A-02D-1366-10 chr16:72124572 A>G maps to NM_001142318.1 L26L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4166-01A-02D-1366-10 chr7:149174658 G>T maps to NM_001163474.1 T236T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4166-01A-02D-1366-10 chr19:22939930 C>T maps to ENST00000397104 K800K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4169-01A-02D-1366-10 chr16:53358032 G>A maps to ENST00000219084 K2640K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4169-01A-02D-1366-10 chr13:113769995 T>A maps to NM_000131.3 C151*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4169-01A-02D-1366-10 chr3:49210261 C>T maps to NM_173546.2 C20C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4169-01A-02D-1366-10 chr17:25919597 G>T maps to ENST00000268763 V338V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4169-01A-02D-1366-10 chr12:48961739 T>C maps to NM_002289.2 *143W. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4169-01A-02D-1366-10 chr12:91502420 G>A maps to NM_002345.3 F112F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4169-01A-02D-1366-10 chr18:48190483 C>T maps to NM_002747.3 A52A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4169-01A-02D-1366-10 chr11:64577152 G>A maps to NM_130804.2 L143L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4169-01A-02D-1366-10 chr14:22038053 G>A maps to NM_001005465.1 A274A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4169-01A-02D-1366-10 chr2:239185782 T>C maps to NM_022817.2 T94T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4169-01A-02D-1366-10 chr3:53223225 C>A maps to NM_212539.1 R569R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4169-01A-02D-1366-10 chr9:131570109 T>C maps to NM_018201.3 D385D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4169-01A-02D-1366-10 chr9:100991263 C>T maps to NM_018421.3 L316L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4170-01A-02D-1366-10 chr20:44483906 G>T maps to NM_005469.3 A51A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4170-01A-02D-1366-10 chr12:46230713 T>C maps to NM_152641.2 H321H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4170-01A-02D-1366-10 chr14:54996812 A>G maps to NM_006568.2 T97T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4170-01A-02D-1366-10 chr1:203188446 C>T maps to NM_003465.2 W309*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4170-01A-02D-1366-10 chr1:32146504 C>T did not map to a codon.
Sequencing variant TCGA-BP-4170-01A-02D-1366-10 chr20:61526430 A>G maps to NM_033081.2 L767L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4170-01A-02D-1366-10 chr1:46878795 G>T maps to NM_001441.2 G505G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4170-01A-02D-1366-10 chr7:925700 C>T maps to ENST00000457861 V380V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4170-01A-02D-1366-10 chr16:58437162 C>T maps to NM_001126129.1 F155F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4170-01A-02D-1366-10 chrX:135581830 A>C maps to NM_014500.4 A87A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4170-01A-02D-1366-10 chr8:144801566 G>C maps to NM_139021.2 L212L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4170-01A-02D-1366-10 chr1:21808125 G>A maps to NM_032264.2 E490E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4170-01A-02D-1366-10 chr6:32188641 T>C maps to NM_004557.3 P271P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4170-01A-02D-1366-10 chr8:103573036 G>C maps to NM_024410.3 P226P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4170-01A-02D-1366-10 chr9:134385418 C>G maps to NM_007171.3 A245A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4170-01A-02D-1366-10 chr2:1667442 C>A maps to NM_012293.1 E501*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4170-01A-02D-1366-10 chr6:111711295 G>A maps to NM_002912.3 D250D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4170-01A-02D-1366-10 chr19:52000157 G>A maps to NM_053003.2 N525N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4170-01A-02D-1366-10 chr22:18640564 C>A maps to NM_017414.3 P45P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4170-01A-02D-1366-10 chr1:32936275 G>A maps to NM_001145720.1 Q17Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4173-01A-02D-1366-10 chr1:197055988 A>G maps to NM_018136.4 S3425S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4173-01A-02D-1366-10 chr20:31024480 G>T maps to ENST00000375687 P1322P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4173-01A-02D-1366-10 chr19:39225511 T>A did not map to a codon.
Sequencing variant TCGA-BP-4173-01A-02D-1366-10 chr7:126173362 A>G maps to NM_001127323.1 S691S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4173-01A-02D-1366-10 chr1:210857393 C>T maps to NM_172362.2 P733P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4173-01A-02D-1366-10 chr12:53207989 G>A maps to NM_002272.2 P25P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4173-01A-02D-1366-10 chr6:41304035 T>C maps to NM_004828.3 D88D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4173-01A-02D-1366-10 chr16:3614349 C>T maps to ENST00000448023 S243S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4173-01A-02D-1366-10 chr16:28922428 C>T maps to NM_024816.2 R322R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4173-01A-02D-1366-10 chr17:62291517 G>A maps to NM_018469.3 A20A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4173-01A-02D-1366-10 chr2:158958550 G>A did not map to a codon.
Sequencing variant TCGA-BP-4174-01A-02D-1366-10 chr15:89402127 C>A maps to NM_013227.3 S2104S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4174-01A-02D-1366-10 chr13:42875948 C>T maps to NM_016248.2 L1023L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4174-01A-02D-1366-10 chr20:61981904 G>A maps to NM_000744.5 T286T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4174-01A-02D-1366-10 chr9:101777793 A>C maps to NM_001855.3 T483T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4174-01A-02D-1366-10 chr2:116510851 C>G maps to NM_020868.3 T351T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4174-01A-02D-1366-10 chr19:5843821 T>C maps to NM_001097641.1 K343K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4174-01A-02D-1366-10 chr22:50961540 G>A maps to NM_001185011.1 V542V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4174-01A-02D-1366-10 chr2:152552136 A>T maps to NM_001164507.1 T543T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4174-01A-02D-1366-10 chr2:220431630 G>T maps to NM_015311.2 A685A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4174-01A-02D-1366-10 chr9:125140797 G>T maps to NM_000962.2 E100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4174-01A-02D-1366-10 chr8:51705387 G>T maps to NM_018967.2 *518L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4174-01A-02D-1366-10 chr2:1500517 C>T maps to NM_000547.5 F789F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4174-01A-02D-1366-10 chr16:67428939 T>A maps to NM_013304.2 K399*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4176-01A-02D-1366-10 chr11:8959459 G>T maps to NM_020646.1 Y83*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4176-01A-02D-1366-10 chr6:33545339 G>A maps to ENST00000360661 C14C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4176-01A-02D-1366-10 chr11:73814556 T>A maps to ENST00000334126 L733L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4176-01A-02D-1366-10 chr16:76509833 A>T did not map to a codon.
Sequencing variant TCGA-BP-4176-01A-02D-1366-10 chr19:36142195 T>C maps to ENST00000392201 F34F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4176-01A-02D-1366-10 chrX:100088268 G>A maps to ENST00000415585 E456E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4176-01A-02D-1366-10 chr15:28414718 A>G maps to NM_004667.4 L3380L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4176-01A-02D-1366-10 chr6:168376846 C>G maps to NM_001129895.1 L162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4176-01A-02D-1366-10 chr6:32497904 G>A maps to NM_002125.3 R33*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4176-01A-02D-1366-10 chr15:52254682 T>C maps to NM_138792.2 A274A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4176-01A-02D-1366-10 chr2:102490652 C>A maps to NM_145686.2 T996T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4176-01A-02D-1366-10 chr11:1018288 C>T maps to NM_005961.2 P1504P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4176-01A-02D-1366-10 chr1:21798205 A>G maps to NM_032264.2 G197G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4176-01A-02D-1366-10 chr1:248801632 A>G maps to NM_001001827.1 G309G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4176-01A-02D-1366-10 chr7:142457346 C>T maps to ENST00000486171 L4L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4176-01A-02D-1366-10 chr9:79318380 A>T maps to NM_015225.2 A2716A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4176-01A-02D-1366-10 chr8:141745399 G>T maps to NM_005607.4 A682A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4176-01A-02D-1366-10 chr8:144899130 C>A maps to NM_078480.1 S443S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4176-01A-02D-1366-10 chr11:563218 C>T maps to NM_003475.3 R285*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4176-01A-02D-1366-10 chr11:124741006 C>A maps to NM_022370.3 A377A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4176-01A-02D-1366-10 chr7:5972411 C>G did not map to a codon.
Sequencing variant TCGA-BP-4176-01A-02D-1366-10 chr6:28543056 T>C maps to NM_052923.1 Q475Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4176-01A-02D-1366-10 chr2:198257041 A>C maps to NM_012433.2 L1300L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4176-01A-02D-1366-10 chr5:145428751 C>T maps to NM_152550.3 S422S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4176-01A-02D-1366-10 chr4:25667855 C>A maps to NM_006424.2 T162T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4176-01A-02D-1366-10 chr19:56029542 C>T maps to NM_001144950.1 H1300H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4176-01A-02D-1366-10 chr19:56029605 G>A maps to NM_001144950.1 T1321T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4176-01A-02D-1366-10 chr3:36872706 C>T maps to NM_014831.2 A2745A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4326-01A-01D-1366-10 chr10:24886904 G>A maps to NM_020824.3 R1056*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4326-01A-01D-1366-10 chr2:10923346 T>C maps to NM_001039362.1 F414F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4326-01A-01D-1366-10 chrX:110494189 T>G maps to NM_014289.3 S371S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4326-01A-01D-1366-10 chrX:49113205 A>T did not map to a codon.
Sequencing variant TCGA-BP-4326-01A-01D-1366-10 chr8:133111177 C>T maps to NM_001145095.1 A77A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4326-01A-01D-1366-10 chr14:23844832 G>A did not map to a codon.
Sequencing variant TCGA-BP-4326-01A-01D-1366-10 chr22:38823675 C>G maps to NM_152868.1 V154V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4326-01A-01D-1366-10 chr21:33684177 C>G maps to ENST00000445271 T132T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4326-01A-01D-1366-10 chr12:48526704 C>T maps to NM_001166686.1 R169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4326-01A-01D-1366-10 chr8:142437879 T>C maps to NM_032611.1 I120I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4326-01A-01D-1366-10 chr1:169701066 T>C maps to NM_000450.2 T146T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4326-01A-01D-1366-10 chr15:78385102 G>A did not map to a codon.
Sequencing variant TCGA-BP-4326-01A-01D-1366-10 chr1:153750665 G>T maps to ENST00000271857 R525R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4326-01A-01D-1366-10 chr8:87229701 A>G maps to NM_138817.2 Y392Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4326-01A-01D-1366-10 chr15:42985731 C>T maps to NM_020759.2 Q3986*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4326-01A-01D-1366-10 chr2:98373847 T>C did not map to a codon.
Sequencing variant TCGA-BP-4326-01A-01D-1366-10 chr15:64717796 T>C maps to NM_016213.4 I514I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4326-01A-01D-1366-10 chr9:77436727 C>A maps to NM_017662.4 V289V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4326-01A-01D-1366-10 chr2:179464024 C>T maps to NM_133378.4 W16264*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4326-01A-01D-1366-10 chr4:85724466 A>T maps to NM_014991.4 S861S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4326-01A-01D-1366-10 chr7:55991393 T>A did not map to a codon.
Sequencing variant TCGA-BP-4329-01A-02D-1366-10 chr2:100623381 G>A maps to NM_001025108.1 T220T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4329-01A-02D-1366-10 chr1:19202925 T>C maps to NM_003748.3 A407A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4329-01A-02D-1366-10 chr17:47246987 C>A maps to NM_153446.2 A533A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4329-01A-02D-1366-10 chr16:74506245 C>T did not map to a codon.
Sequencing variant TCGA-BP-4329-01A-02D-1366-10 chr19:10394733 T>C maps to NM_000201.2 L221L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4329-01A-02D-1366-10 chr9:139399348 G>A maps to NM_017617.3 R1598R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4329-01A-02D-1366-10 chr12:113405907 C>G maps to NM_006187.2 Y1011*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4329-01A-02D-1366-10 chr3:52712579 G>A maps to ENST00000296302 R58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4329-01A-02D-1366-10 chr16:81232573 T>C maps to NM_052892.3 R412R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4329-01A-02D-1366-10 chr22:30888521 G>T maps to NM_174977.3 A201A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4329-01A-02D-1366-10 chr3:47155364 C>T did not map to a codon.
Sequencing variant TCGA-BP-4330-01A-01D-1366-10 chr5:133655129 T>C maps to NM_001113575.1 V237V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4330-01A-01D-1366-10 chr5:39381654 G>A maps to NM_001343.2 Q469*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4330-01A-01D-1366-10 chr21:47987405 G>T maps to ENST00000318711 V1530V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4330-01A-01D-1366-10 chr15:41228879 G>A maps to NM_019074.3 R565R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4330-01A-01D-1366-10 chr11:94862592 T>G maps to NM_015036.2 V451V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4330-01A-01D-1366-10 chr5:60183306 C>T maps to NM_000082.3 W361*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4330-01A-01D-1366-10 chr20:42355034 G>A maps to NM_176791.3 S100S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4330-01A-01D-1366-10 chr6:32634330 G>A maps to ENST00000374943 V18V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4330-01A-01D-1366-10 chr10:64975353 G>A maps to NM_032776.1 R261*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4330-01A-01D-1366-10 chr7:1480279 C>T maps to NM_182924.3 P584P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4330-01A-01D-1366-10 chr7:1480285 G>A maps to NM_182924.3 D582D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4330-01A-01D-1366-10 chr6:31729358 A>G maps to ENST00000375742 Q733Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4330-01A-01D-1366-10 chr8:2033422 C>T maps to NM_003970.2 T515T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4330-01A-01D-1366-10 chr5:141517332 G>T maps to NM_030571.3 L135L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4330-01A-01D-1366-10 chr8:103573036 G>C maps to NM_024410.3 P226P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4330-01A-01D-1366-10 chr1:12837651 C>T maps to NM_001080830.1 V454V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4330-01A-01D-1366-10 chr1:12837663 C>T maps to NM_001080830.1 R458R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4330-01A-01D-1366-10 chr9:98211563 G>A maps to NM_000264.3 S1197S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4330-01A-01D-1366-10 chr12:46760865 G>A maps to NM_018976.4 N158N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4330-01A-01D-1366-10 chr11:63965324 G>A did not map to a codon.
Sequencing variant TCGA-BP-4330-01A-01D-1366-10 chr13:19751273 G>A maps to NM_006001.1 H283H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4330-01A-01D-1366-10 chr9:35061686 C>G did not map to a codon.
Sequencing variant TCGA-BP-4330-01A-01D-1366-10 chr7:148768359 G>T maps to NM_152411.3 R502R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4331-01A-01D-1366-10 chr1:235345428 C>T maps to NM_016374.5 W935*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4331-01A-01D-1366-10 chrX:138908946 T>C maps to NM_173694.4 T24T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4331-01A-01D-1366-10 chr11:14520432 C>T maps to NM_001144061.1 V14V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4331-01A-01D-1366-10 chr2:120128349 C>A maps to NM_001178017.1 A115A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4331-01A-01D-1366-10 chr11:20177782 G>A maps to ENST00000227256 Q376*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4331-01A-01D-1366-10 chr9:117165102 G>T maps to NM_015404.3 A885A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4331-01A-01D-1366-10 chr1:157062695 G>T maps to NM_001004341.2 L277L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4331-01A-01D-1366-10 chr2:242203955 A>C maps to NM_005336.3 L47L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4331-01A-01D-1366-10 chr6:26056014 C>T maps to NM_005319.3 *214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4331-01A-01D-1366-10 chr15:81224217 A>T maps to NM_018689.1 G877G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4331-01A-01D-1366-10 chr19:51378100 C>A maps to NM_005551.3 P57P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4331-01A-01D-1366-10 chr19:51378100 C>A maps to NM_005551.3 P57P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4331-01A-01D-1366-10 chr13:77730191 C>A did not map to a codon.
Sequencing variant TCGA-BP-4331-01A-01D-1366-10 chr3:108224620 T>C maps to NM_014981.1 V68V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4331-01A-01D-1366-10 chr12:54963141 C>T maps to NM_000924.3 F134F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4331-01A-01D-1366-10 chr2:113420442 G>T maps to NM_005415.3 V627V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4331-01A-01D-1366-10 chr5:79351851 A>T maps to NM_003248.4 P179P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4331-01A-01D-1366-10 chr17:27075314 C>A maps to NM_004295.3 Y166*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4331-01A-01D-1366-10 chr13:115067469 A>G maps to NM_023011.2 P424P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4337-01A-01D-1366-10 chr17:48548423 A>G maps to ENST00000427954 T442T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4337-01A-01D-1366-10 chr5:139941189 T>C maps to ENST00000354402 L250L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4337-01A-01D-1366-10 chr14:58790269 G>T maps to NM_002892.3 E173*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4337-01A-01D-1366-10 chr3:52442566 G>A maps to NM_004656.2 R60*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4337-01A-01D-1366-10 chr2:159033037 G>A maps to NM_138803.3 Q542*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4337-01A-01D-1366-10 chr1:36205124 A>T maps to NM_022111.3 L1050*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4337-01A-01D-1366-10 chr21:47420242 A>C did not map to a codon.
Sequencing variant TCGA-BP-4337-01A-01D-1366-10 chr4:105393488 C>T maps to NM_025212.1 W196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4337-01A-01D-1366-10 chrX:79698229 T>C maps to NM_001170574.1 N64N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4337-01A-01D-1366-10 chr9:114182376 C>G maps to NM_001080398.1 V671V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4337-01A-01D-1366-10 chr2:15326914 A>T maps to NM_015909.2 L2221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4337-01A-01D-1366-10 chr3:135745813 C>T maps to NM_002718.4 F712F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4337-01A-01D-1366-10 chr1:192150458 A>G maps to NM_130782.2 E107E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4337-01A-01D-1366-10 chr20:62275588 G>A maps to NM_015894.2 P31P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4337-01A-01D-1366-10 chr1:19181060 G>A maps to NM_152232.2 S301S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4337-01A-01D-1366-10 chr11:60689309 A>T maps to NM_024092.2 G135G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4337-01A-01D-1366-10 chr19:52659378 A>T maps to NM_001102657.1 I519I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4338-01A-01D-1806-10 chr2:68772384 C>T maps to NM_173545.2 I409I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4338-01A-01D-1806-10 chr6:36175214 A>T maps to NM_015695.2 R577R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4338-01A-01D-1806-10 chr15:30664488 A>G maps to NM_139320.1 P128P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4338-01A-01D-1806-10 chr10:12139742 G>A maps to NM_018706.5 T473T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4338-01A-01D-1806-10 chr6:108985340 C>T maps to NM_001455.3 F435F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4338-01A-01D-1806-10 chr11:18424450 C>T maps to NM_001165414.1 S190S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4338-01A-01D-1806-10 chr1:120548024 G>A maps to NM_024408.2 P114P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4338-01A-01D-1806-10 chr17:45656825 A>G maps to NM_006310.3 K163K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4338-01A-01D-1806-10 chr2:219501272 G>A maps to ENST00000432688 Q786Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4338-01A-01D-1806-10 chr19:4510614 G>A maps to NM_001080400.1 D1105D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4338-01A-01D-1806-10 chr13:25419106 G>C maps to ENST00000381927 L1046L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4338-01A-01D-1806-10 chr1:223284111 G>T maps to NM_003268.5 I754I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4338-01A-01D-1806-10 chr8:100871684 C>A maps to NM_017890.3 S3699*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4338-01A-01D-1806-10 chr16:71512808 C>A maps to NM_006961.3 E45*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4338-01A-01D-1806-10 chr17:15620444 C>T maps to NM_020652.2 S469S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4340-01A-01D-1366-10 chr5:7706889 C>T maps to NM_020546.2 N381N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4340-01A-01D-1366-10 chr19:15367029 C>T maps to NM_058243.2 Q532Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4340-01A-01D-1366-10 chr15:24922519 C>T maps to NM_018958.2 S502S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4340-01A-01D-1366-10 chr8:143927976 T>G maps to NM_002066.2 T116T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4340-01A-01D-1366-10 chr9:86585174 G>T maps to NM_031262.2 I421I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4340-01A-01D-1366-10 chr2:176973806 G>A maps to NM_021192.2 R318R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4340-01A-01D-1366-10 chr12:50615811 G>A maps to NM_001113546.1 Q208*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4340-01A-01D-1366-10 chr4:80246575 C>A maps to NM_032693.2 S152S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4340-01A-01D-1366-10 chr12:53848637 A>T maps to NM_005016.5 L18L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4340-01A-01D-1366-10 chr7:82595119 T>C maps to NM_033026.5 K1328K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4340-01A-01D-1366-10 chr11:74081945 C>T did not map to a codon.
Sequencing variant TCGA-BP-4340-01A-01D-1366-10 chr3:47059127 C>T maps to NM_014159.6 K2511K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4341-01A-01D-1366-10 chr12:43896208 C>T did not map to a codon.
Sequencing variant TCGA-BP-4341-01A-01D-1366-10 chr16:61761057 G>A maps to NM_001796.2 N492N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4341-01A-01D-1366-10 chr16:53358032 G>A maps to ENST00000219084 K2640K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4341-01A-01D-1366-10 chr4:151000430 C>T maps to NM_001040261.4 F84F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4341-01A-01D-1366-10 chr21:34955917 A>C maps to NM_017613.2 Y280*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4341-01A-01D-1366-10 chr2:25754364 T>C maps to NM_021907.3 K326K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4341-01A-01D-1366-10 chr9:97081993 G>A maps to NM_017561.1 H462H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4341-01A-01D-1366-10 chr19:8193951 G>A maps to NM_032447.3 P752P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4341-01A-01D-1366-10 chr15:33358816 C>T maps to NM_001103184.2 E423E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4341-01A-01D-1366-10 chr20:36869004 G>A maps to NM_001029864.1 R510*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4341-01A-01D-1366-10 chr17:39658937 C>T did not map to a codon.
Sequencing variant TCGA-BP-4341-01A-01D-1366-10 chr3:52621463 G>A maps to ENST00000296302 R1010*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4341-01A-01D-1366-10 chr20:56136505 C>T maps to NM_002591.3 A13A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4341-01A-01D-1366-10 chr5:149506121 G>C maps to NM_002609.3 T545T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4341-01A-01D-1366-10 chr16:71689234 C>T maps to NM_015020.2 L831L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4341-01A-01D-1366-10 chr4:57873144 C>T maps to NM_000938.1 Q461*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4341-01A-01D-1366-10 chr15:91523520 C>T maps to NM_003981.2 Q307Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4341-01A-01D-1366-10 chr6:107069325 C>A maps to NM_032730.4 E157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4341-01A-01D-1366-10 chr12:21355423 G>T did not map to a codon.
Sequencing variant TCGA-BP-4341-01A-01D-1366-10 chr1:6640755 T>A maps to NM_005341.2 T29T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4341-01A-01D-1366-10 chr2:180383278 G>A maps to NM_152520.4 V161V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4342-01A-01D-1366-10 chr1:158152833 C>T maps to NM_001766.3 D258D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4342-01A-01D-1366-10 chr5:78328556 C>T maps to NM_013391.2 W490*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4342-01A-01D-1366-10 chr5:92956818 C>T maps to NM_032042.5 E375E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4342-01A-01D-1366-10 chr17:27902333 G>T maps to NM_001085454.1 R670R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4342-01A-01D-1366-10 chr19:16910746 C>T maps to ENST00000438489 V1170V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4342-01A-01D-1366-10 chr11:55735575 G>A maps to NM_001005491.1 Q122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4342-01A-01D-1366-10 chr7:82581463 C>A maps to NM_033026.5 G2935G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4342-01A-01D-1366-10 chr5:149506139 C>T maps to NM_002609.3 L539L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4342-01A-01D-1366-10 chr1:204399060 A>G maps to NM_002646.3 P1462P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4342-01A-01D-1366-10 chr13:23912563 C>T maps to NM_014363.4 T1817T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4342-01A-01D-1366-10 chr14:70480127 G>A maps to NM_001034852.1 E322E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4342-01A-01D-1366-10 chr4:7677814 C>T maps to NM_020777.2 F400F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4342-01A-01D-1366-10 chr1:36814313 G>T maps to ENST00000373130 P247P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4342-01A-01D-1366-10 chr15:53815520 T>A did not map to a codon.
Sequencing variant TCGA-BP-4343-01A-02D-1366-10 chr1:1403813 C>T maps to NM_001039211.2 D380D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4343-01A-02D-1366-10 chr16:84495697 G>C maps to ENST00000416219 L924L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4343-01A-02D-1366-10 chr10:105893488 T>C maps to ENST00000389588 K1496K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4343-01A-02D-1366-10 chr3:138669386 C>T maps to NM_001040061.2 S167S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4343-01A-02D-1366-10 chr20:61987734 T>C maps to NM_000744.5 V87V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4343-01A-02D-1366-10 chr1:46976716 C>T maps to NM_147192.2 A153A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4343-01A-02D-1366-10 chr19:48239720 C>A maps to NM_014601.3 V337V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4343-01A-02D-1366-10 chr3:184041028 G>T maps to NM_001194947.1 P703P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4343-01A-02D-1366-10 chr10:8115904 C>T maps to NM_001002295.1 T418T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4343-01A-02D-1366-10 chr2:128262647 T>C maps to NM_017969.2 E277E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4343-01A-02D-1366-10 chr12:39695436 C>A maps to ENST00000395670 V1593V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4343-01A-02D-1366-10 chr10:88476147 C>A maps to NM_001171610.1 S437S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4343-01A-02D-1366-10 chr3:47079154 C>G did not map to a codon.
Sequencing variant TCGA-BP-4343-01A-02D-1366-10 chr17:26817925 T>G did not map to a codon.
Sequencing variant TCGA-BP-4343-01A-02D-1366-10 chr10:70450817 A>G maps to NM_030625.2 G1886G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4343-01A-02D-1366-10 chr21:45502924 G>A maps to NM_003274.4 E660E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4343-01A-02D-1366-10 chr8:110100373 T>A maps to NM_003301.4 Y211*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4343-01A-02D-1366-10 chr15:31355417 G>A maps to NM_002420.4 L268L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4343-01A-02D-1366-10 chr1:12403072 C>T maps to NM_015378.2 P2950P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4345-01A-01D-1366-10 chr15:90342656 C>A maps to NM_001150.2 S651S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4345-01A-01D-1366-10 chr11:92600265 G>A maps to ENST00000298047 A4006A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4345-01A-01D-1366-10 chr6:155451457 T>C maps to ENST00000456144 V367V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4345-01A-01D-1366-10 chr2:207169575 C>G maps to NM_020923.1 S108S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4346-01A-01D-1366-10 chr3:118865299 C>A maps to NM_152539.2 G88G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4346-01A-01D-1366-10 chr9:101748183 C>A maps to NM_001855.3 S146S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4346-01A-01D-1366-10 chr14:45514043 A>G maps to ENST00000361462 A1375A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4346-01A-01D-1366-10 chr6:32632776 C>T maps to ENST00000374943 V59V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4346-01A-01D-1366-10 chr6:17637569 A>G maps to ENST00000430136 L791L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4346-01A-01D-1366-10 chr4:121631519 G>T maps to NM_018699.2 R558R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4346-01A-01D-1366-10 chr6:27216900 A>C maps to NM_005865.3 P120P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4346-01A-01D-1366-10 chrX:18660195 G>A maps to NM_000330.3 L201L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4346-01A-01D-1366-10 chr14:50312884 G>C maps to NM_004713.3 Y110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4346-01A-01D-1366-10 chr3:167508175 C>T maps to NM_005025.4 F89F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4346-01A-01D-1366-10 chr21:37418056 C>T maps to NM_017438.3 L183L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4346-01A-01D-1366-10 chr16:55734211 T>C maps to NM_001043.3 L584L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4346-01A-01D-1366-10 chr7:43918275 G>C maps to NM_001077663.1 A262A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4347-01A-01D-1366-10 chr16:58585657 A>T maps to NM_016284.3 P1012P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4347-01A-01D-1366-10 chr2:71838424 C>A maps to NM_001130987.1 I1336I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4347-01A-01D-1366-10 chr1:110086264 T>C maps to NM_031936.4 L207L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4347-01A-01D-1366-10 chr19:12975919 G>T maps to NM_014975.2 G522G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4347-01A-01D-1366-10 chr2:46203637 G>A maps to NM_005400.2 R161R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4347-01A-01D-1366-10 chr2:231937036 T>A maps to NM_002807.3 S263S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4347-01A-01D-1366-10 chr10:16547024 T>C maps to NM_030664.3 I235I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4347-01A-01D-1366-10 chr10:99148127 C>A maps to NM_015179.3 E300*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4347-01A-01D-1366-10 chr19:56011914 G>A maps to NM_001144950.1 V787V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4347-01A-01D-1366-10 chr2:179665290 G>T maps to NM_133378.4 Y138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4347-01A-01D-1366-10 chr16:4924284 C>G maps to NM_016936.3 S625*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4347-01A-01D-1366-10 chr16:88644134 G>A did not map to a codon.
Sequencing variant TCGA-BP-4349-01A-01D-1366-10 chr4:88029313 T>C maps to NM_001166693.1 A460A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4349-01A-01D-1366-10 chr4:165118361 C>A maps to NM_012403.1 E168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4349-01A-01D-1366-10 chrX:3007534 A>G did not map to a codon.
Sequencing variant TCGA-BP-4349-01A-01D-1366-10 chr7:105672875 A>T maps to NM_152750.4 G797G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4349-01A-01D-1366-10 chr16:11001466 G>A maps to NM_000246.3 L706L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4349-01A-01D-1366-10 chr2:238243368 G>A maps to NM_004369.3 R3043R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4349-01A-01D-1366-10 chr3:101540500 G>A maps to NM_145037.2 R461R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4349-01A-01D-1366-10 chr17:37898908 A>C maps to ENST00000445327 P105P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4349-01A-01D-1366-10 chr19:603873 C>T maps to NM_001194.3 R321R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4349-01A-01D-1366-10 chr10:91497906 G>A maps to ENST00000416354 K1133K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4349-01A-01D-1366-10 chr16:15931772 G>A maps to NM_001040114.1 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4349-01A-01D-1366-10 chr22:26291195 C>T maps to ENST00000407587 C1541C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4349-01A-01D-1366-10 chr1:169588409 G>T maps to NM_003005.3 V17V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4349-01A-01D-1366-10 chr11:118531933 G>C maps to ENST00000264029 V264V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4349-01A-01D-1366-10 chr6:167753862 T>C maps to NM_031949.4 L159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4351-01A-01D-1366-10 chr11:116703545 T>C maps to ENST00000360377 S100S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4351-01A-01D-1366-10 chr11:72418404 G>T maps to NM_001040118.2 S513*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4351-01A-01D-1366-10 chr9:138387376 G>A maps to NM_001048265.1 L103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4351-01A-01D-1366-10 chr1:11894063 T>C maps to ENST00000376496 R501R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4351-01A-01D-1366-10 chr1:197390460 G>C maps to NM_201253.2 V501V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4351-01A-01D-1366-10 chr11:61505672 G>A maps to NM_006133.2 K550K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4351-01A-01D-1366-10 chr2:109513431 G>T maps to ENST00000376651 S458S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4351-01A-01D-1366-10 chr12:4553397 C>G maps to NM_020996.1 L117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4351-01A-01D-1366-10 chr20:33450695 G>A maps to NM_178026.2 Q160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4351-01A-01D-1366-10 chr19:14591228 A>G maps to NM_202470.1 I181I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4351-01A-01D-1366-10 chr1:949653 A>G maps to NM_005101.3 V98V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4351-01A-01D-1366-10 chr17:21319844 C>T maps to NM_021012.4 D397D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4351-01A-01D-1366-10 chr1:53792605 G>T maps to NM_004631.3 P61P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4351-01A-01D-1366-10 chr16:813649 G>A maps to NM_013404.4 A46A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4351-01A-01D-1366-10 chr1:71873191 G>A maps to NM_173808.2 Y334Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4351-01A-01D-1366-10 chr19:16910779 G>T maps to ENST00000438489 G1181G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4351-01A-01D-1366-10 chr7:44747513 C>T maps to ENST00000444676 T1011T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4351-01A-01D-1366-10 chr8:52773606 C>A maps to NM_052937.2 A35A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4351-01A-01D-1366-10 chr10:124189324 T>A maps to NM_021622.4 S362S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4351-01A-01D-1366-10 chr17:171097 T>G maps to NM_006987.3 A62A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4351-01A-01D-1366-10 chr2:220414018 T>C maps to NM_001005209.1 P296P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4351-01A-01D-1366-10 chr18:77733687 G>T maps to NM_006701.2 Y142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4351-01A-01D-1366-10 chr16:22122216 C>T maps to NM_173615.3 I197I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4351-01A-01D-1366-10 chr3:40529518 C>G maps to NM_001145082.2 P546P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4352-01A-01D-1366-10 chrX:74290343 A>C maps to NM_004299.3 V408V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4352-01A-01D-1366-10 chrX:153662579 C>T maps to NM_001183.4 A237A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4352-01A-01D-1366-10 chr6:147022202 T>C maps to NM_024694.3 S568S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4352-01A-01D-1366-10 chr19:13366049 G>T maps to NM_023035.2 I1542I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4352-01A-01D-1366-10 chr9:130548495 C>G maps to ENST00000373265 A140A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4352-01A-01D-1366-10 chr4:49034690 C>T maps to NM_025087.2 G539G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4352-01A-01D-1366-10 chr15:22956551 C>T maps to NM_014608.2 R597*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4352-01A-01D-1366-10 chr20:61527635 G>A maps to NM_033081.2 Y721Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4352-01A-01D-1366-10 chr15:27772597 C>T maps to NM_033223.4 T295T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4352-01A-01D-1366-10 chr10:15714683 C>T maps to NM_003638.1 R247R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4352-01A-01D-1366-10 chr1:113652930 G>A maps to NM_014813.1 V515V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4352-01A-01D-1366-10 chr21:22652946 A>G maps to NM_004540.2 G35G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4352-01A-01D-1366-10 chr13:52707348 C>A maps to NM_002498.2 E484*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4352-01A-01D-1366-10 chr14:80130118 A>G did not map to a codon.
Sequencing variant TCGA-BP-4352-01A-01D-1366-10 chr6:161135848 G>T maps to NM_000301.3 E191*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4352-01A-01D-1366-10 chr6:105800845 C>T did not map to a codon.
Sequencing variant TCGA-BP-4352-01A-01D-1366-10 chr14:21024784 A>G maps to NM_001110361.1 F153F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4352-01A-01D-1366-10 chr18:43249306 C>T maps to NM_007163.3 S691S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4352-01A-01D-1366-10 chr2:132237982 A>G maps to NM_080386.2 T239T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4352-01A-01D-1366-10 chr3:141163201 G>T maps to NM_001080412.2 E658*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4354-01A-02D-1366-10 chr12:43777459 C>A maps to ENST00000389420 V1566V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4354-01A-02D-1366-10 chr17:58952031 C>A maps to ENST00000407086 V198V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4354-01A-02D-1366-10 chr3:45127492 C>T maps to NM_022842.3 P716P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4354-01A-02D-1366-10 chr12:22826446 A>G maps to NM_018638.4 V355V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4354-01A-02D-1366-10 chr9:37537373 T>A maps to NM_012166.2 V384V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4354-01A-02D-1366-10 chr15:64005709 C>T maps to ENST00000261887 Q1435Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4354-01A-02D-1366-10 chr1:236143953 C>T did not map to a codon.
Sequencing variant TCGA-BP-4354-01A-02D-1366-10 chrX:105197101 G>A maps to NM_198465.2 L1530L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4354-01A-02D-1366-10 chr12:57627118 C>A maps to NM_005412.5 A338A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4354-01A-02D-1366-10 chr13:103718248 A>T maps to NM_000452.2 Y117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4354-01A-02D-1366-10 chr11:126283464 C>T maps to ENST00000356132 A285A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4354-01A-02D-1366-10 chr19:55690358 G>A maps to NM_003180.2 P17P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4355-01A-01D-1366-10 chr20:60419770 G>T maps to NM_001794.2 T208T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4355-01A-01D-1366-10 chrX:153131182 G>A maps to NM_000425.3 V841V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4355-01A-01D-1366-10 chr21:42771181 G>A maps to NM_002463.1 R444R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4355-01A-01D-1366-10 chr8:134296521 A>T maps to NM_006096.3 A11A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4355-01A-01D-1366-10 chr3:10188243 G>T maps to NM_000551.2 L129L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4756-01A-01D-1366-10 chr3:58512374 T>C maps to NM_003500.3 A388A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4756-01A-01D-1366-10 chrX:127185830 G>A maps to NM_138289.3 R119*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4756-01A-01D-1366-10 chr7:134136493 C>A maps to NM_001628.2 G26G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4756-01A-01D-1366-10 chr11:102239262 T>C maps to NM_001166.3 A450A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4756-01A-01D-1366-10 chr1:201058499 C>A maps to NM_000069.2 R262R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4756-01A-01D-1366-10 chr4:148463688 C>T maps to NM_001957.3 N401N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4756-01A-01D-1366-10 chr2:27671790 A>G maps to NM_015662.1 A1473A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4756-01A-01D-1366-10 chr12:53162772 A>G maps to NM_015848.4 S547S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4756-01A-01D-1366-10 chr1:114157262 T>A maps to NM_001142782.1 Y353*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4756-01A-01D-1366-10 chr7:151882664 G>T maps to ENST00000355193 S1687*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4756-01A-01D-1366-10 chr10:76788757 A>G maps to NM_012330.2 E1392E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4756-01A-01D-1366-10 chr11:78565191 G>A maps to NM_001098816.2 D546D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4756-01A-01D-1366-10 chr17:171081 G>A maps to NM_006987.3 L68L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4756-01A-01D-1366-10 chrX:134992604 G>A maps to NM_018666.2 E632E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4756-01A-01D-1366-10 chr17:73279617 G>A maps to NM_021734.4 A115A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4756-01A-01D-1366-10 chr3:49321433 T>A maps to NM_003363.3 V842V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4758-01A-01D-1366-10 chr20:33501581 A>G maps to NM_001076552.2 L199L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4758-01A-01D-1366-10 chr19:1507321 C>T maps to NM_213604.2 T257T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4758-01A-01D-1366-10 chr1:154544123 G>A maps to NM_000748.2 A275A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4758-01A-01D-1366-10 chr1:60139709 G>C did not map to a codon.
Sequencing variant TCGA-BP-4758-01A-01D-1366-10 chr1:155726847 C>A maps to ENST00000368331 V1806V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4758-01A-01D-1366-10 chr6:32628021 A>G maps to ENST00000374943 L267L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4758-01A-01D-1366-10 chr17:21215551 C>T maps to NM_145109.2 A291A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4758-01A-01D-1366-10 chr12:112305373 A>C did not map to a codon.
Sequencing variant TCGA-BP-4758-01A-01D-1366-10 chr21:43287444 G>A maps to NM_022115.3 L195L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4758-01A-01D-1366-10 chr1:19414402 G>A maps to ENST00000375267 V4817V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4759-01A-01D-1366-10 chr9:139568308 G>A maps to NM_006412.3 L244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4759-01A-01D-1366-10 chrX:2836059 G>A maps to NM_001669.2 A216A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4759-01A-01D-1366-10 chrX:152815549 G>A maps to NM_001001344.2 T543T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4759-01A-01D-1366-10 chr17:20769898 G>T maps to NM_001004306.1 S178*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4759-01A-01D-1366-10 chr20:61526430 A>G maps to NM_033081.2 L767L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4759-01A-01D-1366-10 chr6:74228563 C>T maps to NM_001402.5 W210*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4759-01A-01D-1366-10 chr19:45917283 T>C maps to NM_202001.2 E237E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4759-01A-01D-1366-10 chr1:46878795 G>T maps to NM_001441.2 G505G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4759-01A-01D-1366-10 chrX:49173717 C>G maps to NM_001098413.2 G93G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4759-01A-01D-1366-10 chr1:168073746 G>A maps to NM_153832.1 S114S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4759-01A-01D-1366-10 chr5:176026142 C>T maps to NM_052899.2 R231R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4759-01A-01D-1366-10 chr5:176026145 C>T maps to NM_052899.2 P230P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4759-01A-01D-1366-10 chr2:48896937 C>T maps to NM_172311.2 S1056S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4759-01A-01D-1366-10 chr12:42481608 G>A maps to NM_173601.1 A434A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4759-01A-01D-1366-10 chr6:32552099 C>T maps to NM_002124.2 R52R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4759-01A-01D-1366-10 chr6:32489838 G>A maps to NM_002125.3 S71S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4759-01A-01D-1366-10 chr6:32497904 G>A maps to NM_002125.3 R33*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4759-01A-01D-1366-10 chr6:39285597 G>A maps to NM_032115.3 A153A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4759-01A-01D-1366-10 chr19:44276214 G>C maps to NM_002250.2 G252G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4759-01A-01D-1366-10 chr12:27944775 G>A maps to NM_020782.1 E336E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4759-01A-01D-1366-10 chr12:53045614 A>G maps to NM_000423.2 G104G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4759-01A-01D-1366-10 chr12:53185579 C>A maps to ENST00000309505 T403T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4759-01A-01D-1366-10 chr8:99028831 G>A maps to ENST00000254898 S546S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4759-01A-01D-1366-10 chr18:47799781 C>T maps to ENST00000424334 K553K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4759-01A-01D-1366-10 chr18:2555004 C>T maps to NM_022840.3 Q164Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4759-01A-01D-1366-10 chr4:2254227 G>A maps to NM_006454.2 Y72Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4759-01A-01D-1366-10 chr20:33589106 G>A maps to NM_020884.3 K1887K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4759-01A-01D-1366-10 chr12:57485234 G>C maps to NM_005967.3 R137R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4759-01A-01D-1366-10 chr12:54925590 C>T maps to NM_005337.4 A921A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4759-01A-01D-1366-10 chr2:43991494 A>G maps to NM_172069.3 A1429A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4759-01A-01D-1366-10 chr16:67943578 C>A maps to NM_006742.2 I309I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4759-01A-01D-1366-10 chr10:43613843 C>A maps to NM_020975.4 R770R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4759-01A-01D-1366-10 chr16:57261304 C>A maps to NM_133368.1 R405R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4759-01A-01D-1366-10 chr3:47164513 C>A maps to NM_014159.6 G538*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4759-01A-01D-1366-10 chr5:140682765 G>A maps to NM_031947.2 L223L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4759-01A-01D-1366-10 chrX:118604411 G>A maps to NM_001152.4 G225G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4759-01A-01D-1366-10 chr18:33706898 T>C maps to NM_012319.3 L24L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4759-01A-01D-1366-10 chr17:2203199 G>A maps to NM_017575.4 Q283*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4759-01A-01D-1366-10 chr8:110590176 C>T maps to NM_001099744.1 L268L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4759-01A-01D-1366-10 chr18:5891546 G>A maps to NM_001080209.1 I172I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4759-01A-01D-1366-10 chr7:128802361 G>T maps to NM_178562.3 T96T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4759-01A-01D-1366-10 chr19:6828446 G>A maps to NM_005428.2 T347T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4759-01A-01D-1366-10 chr19:36940080 G>T maps to NM_001145343.1 S353*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4761-01A-01D-1366-10 chr16:88052145 C>T maps to NM_001173543.1 A248A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4761-01A-01D-1366-10 chr3:85961676 G>A maps to NM_153184.3 Q221Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4761-01A-01D-1366-10 chr8:121021275 T>C maps to NM_022783.2 G335G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4761-01A-01D-1366-10 chr1:167096183 G>T maps to NM_001080426.1 E606*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4761-01A-01D-1366-10 chr2:37374006 T>A maps to NM_001135651.1 K77*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4761-01A-01D-1366-10 chr16:88802747 C>T maps to NM_001142864.2 T455T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4761-01A-01D-1366-10 chr1:155733232 T>C maps to ENST00000368331 A1532A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4761-01A-01D-1366-10 chr17:42475997 C>T maps to NM_001002909.2 G1149G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4761-01A-01D-1366-10 chr19:605089 C>T maps to NM_001194.3 S362S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4761-01A-01D-1366-10 chr1:210573840 G>T maps to NM_001170580.1 G101G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4761-01A-01D-1366-10 chr1:245022574 A>G did not map to a codon.
Sequencing variant TCGA-BP-4761-01A-01D-1366-10 chr14:24632647 G>A maps to NM_006084.4 R142R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4761-01A-01D-1366-10 chr2:24493590 A>G maps to NM_006277.2 F768F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4761-01A-01D-1366-10 chr1:209796912 G>A maps to NM_000228.2 P765P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4761-01A-01D-1366-10 chr12:50589646 C>T maps to NM_001113546.1 L332L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4761-01A-01D-1366-10 chr1:117984947 G>A did not map to a codon.
Sequencing variant TCGA-BP-4761-01A-01D-1366-10 chr1:46083163 A>G maps to NM_002482.3 K729K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4761-01A-01D-1366-10 chr6:142409627 C>T maps to NM_002511.2 V56V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4761-01A-01D-1366-10 chr11:64417941 G>A maps to NM_015080.3 G1029G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4761-01A-01D-1366-10 chr22:39621820 C>A maps to NM_002608.2 R211R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4761-01A-01D-1366-10 chr4:76787407 T>C maps to NM_006239.2 S618S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4761-01A-01D-1366-10 chr8:30643765 T>G maps to NM_001009552.1 P305P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4761-01A-01D-1366-10 chr19:52729233 A>G maps to NM_014225.5 *590W. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4761-01A-01D-1366-10 chr20:41385108 G>A maps to ENST00000373198 I284I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4761-01A-01D-1366-10 chr16:24580911 A>G maps to NM_006910.4 E967E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4761-01A-01D-1366-10 chr1:237778052 G>A maps to NM_001035.2 L1875L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4761-01A-01D-1366-10 chr1:169831810 G>A maps to NM_181093.2 I361I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4761-01A-01D-1366-10 chr22:42383240 G>A maps to NM_145733.2 L121L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4761-01A-01D-1366-10 chr3:155547593 C>T maps to NM_004733.3 V455V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4761-01A-01D-1366-10 chr1:149883491 G>A maps to NM_014849.3 L221L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4762-01A-02D-1366-10 chr9:135413021 C>A maps to NM_207417.1 R223R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4762-01A-02D-1366-10 chr1:203149654 T>G maps to NM_001276.2 S279S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4762-01A-02D-1366-10 chrX:107923919 C>T maps to ENST00000328300 G1318G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4762-01A-02D-1366-10 chr16:1706434 C>T maps to NM_020825.3 D559D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4762-01A-02D-1366-10 chr1:34083217 C>T did not map to a codon.
Sequencing variant TCGA-BP-4762-01A-02D-1366-10 chr2:74173853 T>A maps to NM_080916.1 T88T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4762-01A-02D-1366-10 chr6:11105372 A>C maps to NM_207582.2 A57A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4762-01A-02D-1366-10 chr17:26861923 G>A maps to NM_003593.2 G445G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4762-01A-02D-1366-10 chr11:134217317 G>A maps to NM_138342.3 V183V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4762-01A-02D-1366-10 chr17:21319391 G>A maps to NM_021012.4 L246L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4762-01A-02D-1366-10 chr8:140630791 C>T maps to NM_016601.2 E278E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4762-01A-02D-1366-10 chr3:195506036 G>T maps to NM_018406.5 S4138S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4762-01A-02D-1366-10 chr1:120384042 C>T maps to NM_001047980.1 R173R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4762-01A-02D-1366-10 chr7:31378183 G>T maps to NM_022728.2 P233P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4762-01A-02D-1366-10 chr19:51875454 G>T maps to NM_005601.3 G88G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4762-01A-02D-1366-10 chr5:167617458 G>A maps to NM_001122679.1 W887*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4762-01A-02D-1366-10 chr13:61986575 G>T maps to NM_022843.3 A552A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4762-01A-02D-1366-10 chr5:140553792 T>C maps to NM_018940.2 F459F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4762-01A-02D-1366-10 chr8:27295367 C>A maps to NM_004103.3 A538A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4762-01A-02D-1366-10 chr1:198704329 C>T maps to ENST00000271610 N784N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4762-01A-02D-1366-10 chr12:48091481 A>T maps to NM_024604.2 L105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4762-01A-02D-1366-10 chrX:118604408 C>T maps to NM_001152.4 A224A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4762-01A-02D-1366-10 chr22:24176328 C>A maps to NM_003073.3 R374R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4762-01A-02D-1366-10 chrX:53436013 C>T maps to NM_006306.2 K508K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4762-01A-02D-1366-10 chr14:64516355 A>T maps to NM_182914.2 K2469*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4762-01A-02D-1366-10 chr9:71867780 G>A maps to NM_004817.3 T1124T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4762-01A-02D-1366-10 chr16:24788557 T>A maps to NM_014494.2 P156P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4762-01A-02D-1366-10 chr1:40313332 C>A did not map to a codon.
Sequencing variant TCGA-BP-4762-01A-02D-1366-10 chr3:141163554 G>A maps to NM_001080412.2 K775K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4762-01A-02D-1366-10 chr1:35871037 C>G maps to NM_005095.2 L1255L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4763-01A-01D-1366-10 chr21:45717549 T>C maps to NM_000383.2 D526D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4763-01A-01D-1366-10 chr20:35431378 C>T maps to NM_080627.2 R1073R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4763-01A-01D-1366-10 chr19:33439253 C>A maps to NM_032816.3 V171V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4763-01A-01D-1366-10 chr16:83378558 G>T maps to ENST00000268613 P243P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4763-01A-01D-1366-10 chr3:52084902 C>A maps to NM_001947.3 S396S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4763-01A-01D-1366-10 chr16:2035867 C>T maps to NM_005262.2 L153L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4763-01A-01D-1366-10 chr1:38058355 A>G maps to NM_013285.2 A67A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4763-01A-01D-1366-10 chr8:133142093 G>A maps to NM_004519.2 S678S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4763-01A-01D-1366-10 chr1:47144228 A>G maps to NM_014774.2 G464G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4763-01A-01D-1366-10 chr8:105544139 G>C maps to NM_013437.4 S44*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4763-01A-01D-1366-10 chr1:90179730 C>T maps to NM_032270.4 T534T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4763-01A-01D-1366-10 chrX:123654382 G>T maps to NM_001163278.1 G1095G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4763-01A-01D-1366-10 chr6:147830069 C>A maps to NM_001030060.2 C2*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4763-01A-01D-1366-10 chr15:65946266 C>T maps to NM_004727.2 L1050L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4763-01A-01D-1366-10 chr7:123594562 G>A maps to NM_001174046.1 L313L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4763-01A-01D-1366-10 chr16:69967968 C>A maps to NM_007014.3 P593P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4765-01A-01D-1366-10 chrX:49957701 G>T maps to NM_003886.2 Y554*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4765-01A-01D-1366-10 chr10:73450273 G>A maps to ENST00000398860 E708E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4765-01A-01D-1366-10 chrX:83128981 A>G maps to NM_021118.1 E422E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4765-01A-01D-1366-10 chr1:197030047 A>T maps to NM_001994.2 S203S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4765-01A-01D-1366-10 chrX:70320887 C>A maps to NM_005938.3 R270R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4765-01A-01D-1366-10 chrX:44922759 C>T maps to NM_021140.2 Q541*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4765-01A-01D-1366-10 chr11:65310997 C>A maps to NM_001130144.2 G792G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4765-01A-01D-1366-10 chr9:134464198 C>A maps to NM_198679.1 G846G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4765-01A-01D-1366-10 chr1:159922169 G>T maps to NM_033438.3 G182G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4765-01A-01D-1366-10 chr12:129559172 G>T maps to NM_133448.2 L849L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4765-01A-01D-1366-10 chr2:220414018 T>C maps to NM_001005209.1 P296P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4765-01A-01D-1366-10 chr8:23049491 G>T maps to NM_003844.3 I374I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4765-01A-01D-1366-10 chr1:160389235 C>T maps to NM_020335.2 Q213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4766-01A-01D-1366-10 chr9:33387072 G>A maps to NM_001170.1 S54S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4766-01A-01D-1366-10 chr9:86570340 C>T maps to NM_032307.3 L184L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4766-01A-01D-1366-10 chr16:90075258 C>T maps to ENST00000392973 S204S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4766-01A-01D-1366-10 chr2:105859153 G>A maps to NM_007227.3 W280*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4766-01A-01D-1366-10 chr19:15229992 A>G maps to NM_006844.3 D345D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4766-01A-01D-1366-10 chr15:68661591 A>G maps to ENST00000423218 N65N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4766-01A-01D-1366-10 chr16:82203741 T>C maps to NM_005792.2 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4766-01A-01D-1366-10 chr5:7897259 G>T maps to NM_024010.2 E645*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4766-01A-01D-1366-10 chr1:148004721 C>T maps to ENST00000310701 S869S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4766-01A-01D-1366-10 chr1:21806630 G>T maps to NM_032264.2 L432L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4766-01A-01D-1366-10 chr17:4576619 C>T maps to ENST00000301396 P734P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4766-01A-01D-1366-10 chrX:54957275 T>A maps to NM_001039705.1 T1373T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4766-01A-01D-1366-10 chr2:179405008 T>A maps to NM_133378.4 G30060G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4768-01A-01D-1366-10 chr19:3754019 G>C maps to NM_004886.3 S282S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4768-01A-01D-1366-10 chr15:50154546 C>T maps to NM_024837.2 Q1064Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4768-01A-01D-1366-10 chr22:39966975 C>T maps to NM_021096.3 I73I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4768-01A-01D-1366-10 chr20:31946926 G>T maps to ENST00000357886 I576I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4768-01A-01D-1366-10 chr19:4428836 G>A maps to NM_005483.2 L518L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4768-01A-01D-1366-10 chr12:49233686 C>T maps to NM_004818.2 Q140Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4768-01A-01D-1366-10 chr5:154278062 C>T maps to NM_015465.3 E1094E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4768-01A-01D-1366-10 chr19:17945470 G>A maps to NM_000215.3 A753A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4768-01A-01D-1366-10 chr2:8891617 G>C maps to NM_020738.2 P1056P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4768-01A-01D-1366-10 chr18:13885199 G>T maps to NM_000529.2 I106I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4768-01A-01D-1366-10 chr2:178096051 C>A maps to NM_006164.3 E427*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4768-01A-01D-1366-10 chr19:15300135 A>G maps to NM_000435.2 P380P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4768-01A-01D-1366-10 chr5:41807504 T>A maps to NM_000436.3 P256P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4768-01A-01D-1366-10 chr6:30570686 T>A maps to NM_002714.2 P631P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4768-01A-01D-1366-10 chr11:18787396 G>T maps to NM_032781.3 S18S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4768-01A-01D-1366-10 chr10:43608352 C>T maps to NM_020975.4 D567D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4768-01A-01D-1366-10 chr6:28543263 C>T maps to NM_052923.1 L406L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4768-01A-01D-1366-10 chr4:72313419 C>T maps to NM_001098484.2 G341G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4768-01A-01D-1366-10 chr15:42977627 T>C maps to NM_020759.2 H1284H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4768-01A-01D-1366-10 chr16:2052324 C>T maps to ENST00000431526 E259E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4771-01A-01D-1366-10 chr1:33478919 G>A maps to NM_001625.3 T194T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4771-01A-01D-1366-10 chr1:207644229 G>T maps to NM_001006658.2 G457G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4771-01A-01D-1366-10 chr17:74023228 G>A maps to NM_001988.2 G17G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4771-01A-01D-1366-10 chr5:150897290 G>T maps to NM_001447.2 R3785R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4771-01A-01D-1366-10 chr9:139837901 C>A maps to NM_018998.2 E84*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4771-01A-01D-1366-10 chr12:7843114 C>A maps to NM_020634.1 E152*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4771-01A-01D-1366-10 chr10:71048513 C>A maps to ENST00000439900 C5*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4771-01A-01D-1366-10 chr17:38977370 T>A did not map to a codon.
Sequencing variant TCGA-BP-4771-01A-01D-1366-10 chr3:195512342 G>A maps to NM_018406.5 T2036T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4771-01A-01D-1366-10 chr10:26385321 T>C maps to NM_017433.4 N525N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4771-01A-01D-1366-10 chr2:232393299 G>C maps to NM_006056.4 V144V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4771-01A-01D-1366-10 chr1:78958514 C>A maps to NM_000959.3 S29S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4771-01A-01D-1366-10 chr15:77407252 G>A maps to NM_024776.2 L1496L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4771-01A-01D-1366-10 chr8:126448322 T>C maps to NM_025195.2 H243H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4771-01A-01D-1366-10 chr17:9604522 C>A maps to NM_153210.3 T541T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4774-01A-01D-1366-10 chr19:1049304 C>A maps to NM_019112.3 V807V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4774-01A-01D-1366-10 chr2:220075155 C>T maps to NM_005689.2 Q766Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4774-01A-01D-1366-10 chr22:51065092 C>G maps to ENST00000395624 V260V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4774-01A-01D-1366-10 chr1:25569163 A>C maps to NM_020317.3 A263A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4774-01A-01D-1366-10 chr6:49696472 G>T maps to NM_001190986.1 A259A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4774-01A-01D-1366-10 chr4:5827341 A>T maps to NM_001014809.1 P616P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4774-01A-01D-1366-10 chr13:43652745 A>G did not map to a codon.
Sequencing variant TCGA-BP-4774-01A-01D-1366-10 chr2:225761076 A>G maps to NM_014689.2 S117S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4774-01A-01D-1366-10 chr4:155487150 G>T maps to NM_005141.4 L102L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4774-01A-01D-1366-10 chr1:91726879 C>T maps to NM_001017975.3 K1425K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4774-01A-01D-1366-10 chr4:57182388 C>T maps to NM_020722.1 P907P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4774-01A-01D-1366-10 chr10:24832824 G>A maps to NM_019590.3 E1542E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4774-01A-01D-1366-10 chr9:133942398 C>T maps to ENST00000355048 L800L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4774-01A-01D-1366-10 chr2:182542618 G>C maps to NM_002500.2 A323A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4774-01A-01D-1366-10 chr1:86851138 A>C did not map to a codon.
Sequencing variant TCGA-BP-4774-01A-01D-1366-10 chr19:15918526 G>A maps to NM_013940.2 F107F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4774-01A-01D-1366-10 chrX:110406198 T>C maps to NM_001128168.1 D211D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4774-01A-01D-1366-10 chr13:25016007 C>T maps to NM_006437.3 E1214E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4774-01A-01D-1366-10 chr3:52651291 C>A maps to ENST00000296302 E602*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4774-01A-01D-1366-10 chr3:71830710 G>A maps to NM_001126128.1 G43G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4774-01A-01D-1366-10 chr15:55912368 T>A maps to NM_173814.4 T1098T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4774-01A-01D-1366-10 chr4:189026065 C>T maps to ENST00000326754 L20L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4775-01A-01D-1366-10 chr3:141011926 T>C maps to NM_001037172.1 R441R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4775-01A-01D-1366-10 chr8:75924704 G>A maps to NM_031461.5 W99*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4775-01A-01D-1366-10 chr16:67644948 C>T maps to NM_006565.3 Q72*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4775-01A-01D-1366-10 chr15:44067733 C>T maps to NM_025165.2 Q186Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4775-01A-01D-1366-10 chr12:132471270 C>A maps to ENST00000333577 P750P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4775-01A-01D-1366-10 chr1:242030290 C>T maps to NM_006027.4 R401*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4775-01A-01D-1366-10 chr1:157765909 C>T maps to NM_052938.4 V423V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4775-01A-01D-1366-10 chr1:27941091 T>C maps to NM_005248.2 V366V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4775-01A-01D-1366-10 chr9:35748455 A>T maps to NM_020944.2 P82P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4775-01A-01D-1366-10 chr10:96354516 T>G maps to NM_018063.3 V718V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4775-01A-01D-1366-10 chr12:55356979 G>A maps to NM_001098815.1 F234F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4775-01A-01D-1366-10 chr11:7064162 C>G maps to NM_176822.3 S302S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4775-01A-01D-1366-10 chr21:47832896 C>T maps to NM_006031.5 D2047D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4775-01A-01D-1366-10 chr17:6381330 G>A maps to NM_031220.3 A288A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4775-01A-01D-1366-10 chr15:90768608 C>T maps to NM_198925.2 L501L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4775-01A-01D-1366-10 chr15:74483210 T>C maps to ENST00000449139 S338S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4775-01A-01D-1366-10 chr15:31295001 C>A maps to NM_002420.4 G1279*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4777-01A-01D-1366-10 chr16:7726798 C>G maps to NM_145891.2 Y339*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4777-01A-01D-1366-10 chrX:107420104 C>T maps to NM_033641.2 G884G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4777-01A-01D-1366-10 chr1:154401717 T>A maps to NM_000565.2 T44T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4777-01A-01D-1366-10 chr5:71493193 C>T maps to NM_005909.3 Q1338*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4781-01A-01D-1373-10 chr12:43825140 C>T maps to ENST00000389420 W1085*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4781-01A-01D-1373-10 chrX:2832695 T>C maps to NM_009589.2 P373P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4781-01A-01D-1373-10 chr2:170505753 C>A maps to NM_001085447.1 E419*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4781-01A-01D-1373-10 chr7:107395873 G>A maps to NM_024814.2 K126K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4781-01A-01D-1373-10 chr8:86118417 C>A maps to ENST00000256117 S172S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4781-01A-01D-1373-10 chr16:14041532 G>T maps to NM_005236.2 E694*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4781-01A-01D-1373-10 chr14:67671484 A>T maps to NM_173526.3 T197T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4781-01A-01D-1373-10 chr10:103534501 G>A maps to NM_033163.3 D108D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4781-01A-01D-1373-10 chr6:143825090 G>C maps to NM_032020.4 Y237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4781-01A-01D-1373-10 chr12:13906648 T>A maps to NM_000834.3 L204L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4781-01A-01D-1373-10 chr2:141259354 G>A maps to NM_018557.2 G2917G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4781-01A-01D-1373-10 chr12:112498997 A>G maps to NM_024953.3 H448H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4781-01A-01D-1373-10 chr13:52649896 T>C maps to NM_199289.1 E598E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4781-01A-01D-1373-10 chr17:79866842 G>T maps to NM_001184917.1 I83I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4781-01A-01D-1373-10 chr4:39905678 G>A maps to NM_001100399.1 Q456*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4781-01A-01D-1373-10 chr12:6436887 G>A maps to NM_001144856.1 G713G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4781-01A-01D-1373-10 chr11:244166 C>T maps to NM_002817.3 N72N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4781-01A-01D-1373-10 chr6:28543263 C>T maps to NM_052923.1 L406L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4781-01A-01D-1373-10 chr5:236652 C>A maps to NM_004168.2 L457L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4781-01A-01D-1373-10 chrX:142718801 G>C maps to NM_001184749.1 V41V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4781-01A-01D-1373-10 chr17:8660583 G>C maps to NM_001128076.1 L112L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4781-01A-01D-1373-10 chr9:100437765 C>T maps to NM_000380.3 K259K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4787-01A-01D-1373-10 chr12:81503484 T>C did not map to a codon.
Sequencing variant TCGA-BP-4787-01A-01D-1373-10 chr11:47195001 A>C maps to NM_032389.3 L198L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4787-01A-01D-1373-10 chr9:134308049 C>G maps to NM_013318.3 A54A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4787-01A-01D-1373-10 chr1:160167357 G>C did not map to a codon.
Sequencing variant TCGA-BP-4787-01A-01D-1373-10 chr16:83816958 C>A maps to ENST00000268613 I672I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4787-01A-01D-1373-10 chr16:61935248 C>T maps to NM_001796.2 E127E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4787-01A-01D-1373-10 chr10:16873254 G>T maps to NM_001081.3 P3508P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4787-01A-01D-1373-10 chr7:76828960 T>C maps to NM_006682.2 E50E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4787-01A-01D-1373-10 chr2:216295546 C>T maps to NM_212482.1 G192G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4787-01A-01D-1373-10 chr14:52174836 T>A maps to ENST00000344768 I200I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4787-01A-01D-1373-10 chr11:118106269 A>G maps to NM_198275.1 L162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4787-01A-01D-1373-10 chr11:66100154 T>C maps to NM_004292.2 P648P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4787-01A-01D-1373-10 chr11:70349009 G>A maps to ENST00000338508 V697V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4787-01A-01D-1373-10 chr12:113737764 T>G maps to NM_024959.2 G524G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4787-01A-01D-1373-10 chr12:22440139 G>A maps to NM_003034.3 D108D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4787-01A-01D-1373-10 chr15:66824727 C>T maps to NM_017975.3 I433I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4789-01A-01D-1373-10 chr17:20108592 G>T maps to NM_001033553.1 E411*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4789-01A-01D-1373-10 chr12:104328065 G>A did not map to a codon.
Sequencing variant TCGA-BP-4789-01A-01D-1373-10 chr11:63276053 A>G maps to NM_001142535.1 G55G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4789-01A-01D-1373-10 chr7:100844111 C>T maps to NM_178176.2 Q8Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4789-01A-01D-1373-10 chr14:64886599 A>G maps to NM_005956.3 K228K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4789-01A-01D-1373-10 chr12:78400502 T>C maps to NM_014903.4 T395T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4789-01A-01D-1373-10 chr17:5461894 C>A maps to NM_033004.3 L707L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4789-01A-01D-1373-10 chr11:73978333 G>A maps to NM_182904.3 Q532*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4789-01A-01D-1373-10 chr1:204411749 G>C maps to NM_002646.3 R1020R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4789-01A-01D-1373-10 chr2:128775372 G>A maps to NM_001145928.1 Q103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4789-01A-01D-1373-10 chr11:62650392 T>C maps to NM_001012661.1 I336I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4789-01A-01D-1373-10 chr5:14364825 T>A maps to NM_007118.2 L885L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4789-01A-01D-1373-10 chr1:52703735 T>A maps to NM_004799.2 L216*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4790-01A-01D-1373-10 chr19:42893090 G>A maps to NM_032488.3 N33N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4790-01A-01D-1373-10 chr9:92220936 T>C maps to NM_006705.3 F141F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4790-01A-01D-1373-10 chr7:126883201 G>A maps to NM_001127323.1 A19A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4790-01A-01D-1373-10 chr17:68172169 C>G maps to NM_000891.2 L330L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4790-01A-01D-1373-10 chr4:6862717 C>T maps to NM_014743.2 Y203Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4790-01A-01D-1373-10 chr10:50725061 A>T maps to ENST00000515869 A501A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4790-01A-01D-1373-10 chr3:47142964 A>C maps to NM_014159.6 Y1666*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4790-01A-01D-1373-10 chr17:62542418 A>T maps to NM_022739.3 I703I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4790-01A-01D-1373-10 chr18:23637607 T>A maps to ENST00000415083 V113V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4790-01A-01D-1373-10 chr1:224586647 G>T maps to NM_025160.6 S503*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4797-01A-01D-1373-10 chr4:123332502 C>T maps to NM_139243.3 Y325Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4797-01A-01D-1373-10 chrX:1537001 C>G maps to NM_004192.3 T462T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4797-01A-01D-1373-10 chr14:77844690 A>G maps to NM_001010860.1 P310P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4797-01A-01D-1373-10 chr17:171097 T>G maps to NM_006987.3 A62A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4797-01A-01D-1373-10 chrX:54953022 C>A maps to NM_001039705.1 I555I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4798-01A-01D-1373-10 chr9:100079447 C>T maps to ENST00000375206 R482R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4798-01A-01D-1373-10 chr17:5462052 T>A maps to NM_033004.3 K655*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4798-01A-01D-1373-10 chr4:55141030 G>A maps to NM_006206.4 W559*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4798-01A-01D-1373-10 chr6:149826603 T>C maps to NM_139126.2 K488K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4798-01A-01D-1373-10 chr17:18814496 G>C maps to NM_002767.2 V222V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4798-01A-01D-1373-10 chr9:74360415 A>G maps to NM_013390.2 G184G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4798-01A-01D-1373-10 chr7:138732447 A>G maps to ENST00000464606 C989C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4798-01A-01D-1373-10 chr3:52439311 T>C did not map to a codon.
Sequencing variant TCGA-BP-4799-01A-01D-1373-10 chr1:100349948 G>T maps to ENST00000311030 E831*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4799-01A-01D-1373-10 chr1:92518078 C>T maps to NM_173567.4 L241L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4799-01A-01D-1373-10 chr6:133804174 G>A maps to ENST00000452339 V377V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4799-01A-01D-1373-10 chr20:61040458 G>A maps to NM_080473.4 A325A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4799-01A-01D-1373-10 chr2:240011716 T>C maps to NM_006037.3 T787T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4799-01A-01D-1373-10 chr5:23526897 C>T maps to NM_020227.2 L567L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4799-01A-01D-1373-10 chr17:62024486 G>T maps to NM_000334.4 S1120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4799-01A-01D-1373-10 chr17:57181740 A>G maps to NM_015294.3 V12V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4799-01A-01D-1373-10 chr21:45798893 C>A maps to ENST00000397932 A343A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4803-01A-01D-1373-10 chr3:195013056 T>C maps to NM_012287.5 A630A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4803-01A-01D-1373-10 chr4:79516572 G>A maps to NM_005139.2 L174L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4803-01A-01D-1373-10 chr10:120085697 C>A maps to NM_022063.2 E171*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4803-01A-01D-1373-10 chr9:140146887 G>T did not map to a codon.
Sequencing variant TCGA-BP-4803-01A-01D-1373-10 chr17:46053333 A>G maps to NM_176096.1 E251E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4803-01A-01D-1373-10 chr16:21117846 G>T maps to NM_017539.1 R750R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4803-01A-01D-1373-10 chr2:183622507 G>A maps to NM_018981.1 E633E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4803-01A-01D-1373-10 chr10:102697178 C>T maps to NM_001136123.1 D819D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4803-01A-01D-1373-10 chr1:92944148 G>A maps to NM_005263.3 H362H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4803-01A-01D-1373-10 chr20:2641179 C>A maps to NM_006899.2 R196R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4803-01A-01D-1373-10 chr11:68483355 A>G maps to NM_004923.3 N323N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4803-01A-01D-1373-10 chr22:50960439 G>A maps to NM_001185011.1 R378R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4803-01A-01D-1373-10 chr6:142397015 A>G maps to NM_002511.2 F314F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4803-01A-01D-1373-10 chr19:4511364 C>G maps to NM_001080400.1 V855V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4803-01A-01D-1373-10 chr12:42854245 T>G maps to NM_153026.2 R621R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4803-01A-01D-1373-10 chr11:10536462 T>A maps to NM_016422.3 *231C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4803-01A-01D-1373-10 chr8:92982929 C>A maps to NM_175634.2 E499*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4803-01A-01D-1373-10 chr3:125769794 G>C maps to NM_001008485.1 L124L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4803-01A-01D-1373-10 chr2:85866456 C>T maps to NM_006590.2 I409I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4804-01A-02D-1373-10 chr5:176942815 A>G maps to NM_016222.2 T147T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4804-01A-02D-1373-10 chr17:21318911 C>A maps to NM_021012.4 I86I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4804-01A-02D-1373-10 chr22:39883402 G>C maps to NM_001098270.1 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4804-01A-02D-1373-10 chr5:38886146 T>G maps to NM_003999.2 S282S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4807-01A-01D-1373-10 chr4:109810855 C>T did not map to a codon.
Sequencing variant TCGA-BP-4807-01A-01D-1373-10 chr10:67726368 C>A did not map to a codon.
Sequencing variant TCGA-BP-4807-01A-01D-1373-10 chr7:6474528 A>T maps to NM_139179.3 L181*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4807-01A-01D-1373-10 chr1:223178161 T>C maps to NM_032890.2 G1141G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4807-01A-01D-1373-10 chr7:21784606 A>T maps to NM_003777.3 T2819T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4807-01A-01D-1373-10 chr2:88874520 A>T maps to NM_004836.5 L827*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4807-01A-01D-1373-10 chrX:119562464 A>G maps to NM_001122606.1 A370A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4807-01A-01D-1373-10 chr6:150001248 A>G maps to NM_004690.2 I785I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4807-01A-01D-1373-10 chr17:79986135 C>T maps to NM_144999.2 L358L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4807-01A-01D-1373-10 chr12:49442447 T>C maps to NM_003482.3 L1375L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4807-01A-01D-1373-10 chr19:56320979 G>C maps to NM_145007.3 L332L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4807-01A-01D-1373-10 chr5:50093024 T>G maps to ENST00000505697 V511V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4807-01A-01D-1373-10 chr3:53219627 C>T maps to NM_212539.1 S299S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4807-01A-01D-1373-10 chr17:29311738 A>T maps to NM_032322.3 S159S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4807-01A-01D-1373-10 chr15:75143006 T>G maps to NM_005697.3 S160S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4807-01A-01D-1373-10 chr21:34929510 T>C maps to NM_138927.1 C2070C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4807-01A-01D-1373-10 chr15:39887563 T>C maps to NM_003246.2 D1169D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4807-01A-01D-1373-10 chr16:68893911 A>C maps to NM_024562.1 R74R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4807-01A-01D-1373-10 chr6:123539745 T>G maps to NM_006073.2 *730Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4807-01A-01D-1373-10 chr8:125987896 A>G maps to NM_152412.2 K5K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4635-01A-02D-1373-10 chr20:25038483 G>T maps to NM_032501.2 T85T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4635-01A-02D-1373-10 chr14:58701184 C>T maps to NM_018477.2 L390L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4635-01A-02D-1373-10 chr2:70008702 C>A maps to NM_001153.3 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4635-01A-02D-1373-10 chr11:102248742 G>A maps to NM_001166.3 L562L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4635-01A-02D-1373-10 chr20:34611537 C>A maps to ENST00000373973 A428A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4635-01A-02D-1373-10 chr20:61537211 G>A maps to NM_022105.4 L539L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4635-01A-02D-1373-10 chr2:183622507 G>A maps to NM_018981.1 E633E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4635-01A-02D-1373-10 chr15:45387205 G>A maps to NM_014080.4 H1441H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4635-01A-02D-1373-10 chr11:58877130 A>C maps to NM_198947.3 S11S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4635-01A-02D-1373-10 chr12:117627029 A>G did not map to a codon.
Sequencing variant TCGA-CJ-4635-01A-02D-1373-10 chr17:80680692 G>A maps to NM_024619.3 G133G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4635-01A-02D-1373-10 chr13:32798430 C>T maps to NM_023037.2 Q1609*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4635-01A-02D-1373-10 chr5:131821388 C>T maps to NM_002198.2 E229E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4635-01A-02D-1373-10 chr18:29437669 G>A maps to NM_014939.3 G1007G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4635-01A-02D-1373-10 chr6:2678596 A>G maps to NM_001012418.3 G299G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4635-01A-02D-1373-10 chr12:112516502 G>A maps to NM_024953.3 L174L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4635-01A-02D-1373-10 chr8:103573000 C>G maps to NM_024410.3 P214P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4635-01A-02D-1373-10 chr20:18005498 C>T maps to NM_021220.2 Q203Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4635-01A-02D-1373-10 chr1:43124122 G>A maps to NM_006347.3 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4635-01A-02D-1373-10 chr1:52385646 C>T maps to NM_002867.3 T204T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4635-01A-02D-1373-10 chr2:103148952 G>T maps to NM_001011552.3 E735*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4635-01A-02D-1373-10 chr16:2816399 G>A maps to NM_016333.3 R1957R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4635-01A-02D-1373-10 chr17:73818636 A>T maps to NM_001080419.1 L715L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4868-01A-01D-1373-10 chr10:17169881 A>G maps to NM_001081.3 S98S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4868-01A-01D-1373-10 chr4:100738084 A>G maps to NM_014395.2 E5E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4868-01A-01D-1373-10 chr3:38139263 C>A maps to NM_007335.2 A865A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4868-01A-01D-1373-10 chr3:113890722 G>T maps to NM_000796.3 L39L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4868-01A-01D-1373-10 chr2:97278027 C>T maps to ENST00000421845 V359V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4868-01A-01D-1373-10 chr1:150938647 A>G maps to NM_181746.2 N373N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4870-01A-01D-1373-10 chr12:22065832 G>T maps to NM_005691.2 T328T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4870-01A-01D-1373-10 chr12:110825590 A>G maps to NM_016238.2 Y243Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4870-01A-01D-1373-10 chr5:141046055 G>T maps to NM_022481.5 S836*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4870-01A-01D-1373-10 chr17:7330113 G>A maps to NM_175734.4 W268*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4870-01A-01D-1373-10 chr2:15746320 A>C maps to NM_004939.1 P250P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4870-01A-01D-1373-10 chr9:135538025 T>C maps to NM_022779.7 K149K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4870-01A-01D-1373-10 chrX:30236765 G>A maps to NM_002364.4 R23R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4870-01A-01D-1373-10 chr11:95825796 A>G maps to NM_032427.1 S466S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4870-01A-01D-1373-10 chr11:1082314 C>T maps to ENST00000441003 L590L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4870-01A-01D-1373-10 chr2:44429132 T>A maps to NM_002706.4 S265S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4870-01A-01D-1373-10 chr14:94697033 C>A maps to NM_058237.1 L135L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4870-01A-01D-1373-10 chr16:4812664 G>A maps to NM_021646.1 S169S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4871-01A-01D-1373-10 chr9:33385666 A>G maps to NM_001170.1 G241G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4871-01A-01D-1373-10 chr1:116936277 T>C maps to NM_000701.7 D531D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4871-01A-01D-1373-10 chr12:121444124 A>G maps to NM_022895.1 D120D. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-CJ-4871-01A-01D-1373-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CJ-4871-01A-01D-1373-10 chr3:48623283 C>T maps to NM_000094.3 Q1255Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4871-01A-01D-1373-10 chr15:31206243 C>T maps to NM_014967.4 Y587Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4871-01A-01D-1373-10 chr3:50387110 A>G maps to NM_006545.4 Y108Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4871-01A-01D-1373-10 chr3:52643503 T>A maps to ENST00000296302 R798*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4871-01A-01D-1373-10 chr19:40902611 C>G maps to NM_181882.2 P549P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4871-01A-01D-1373-10 chr10:89690805 T>A maps to NM_000314.4 C71*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4871-01A-01D-1373-10 chr12:112892408 T>C maps to ENST00000392596 S189S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4871-01A-01D-1373-10 chr20:42969921 C>T maps to NM_178491.2 Y116Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4871-01A-01D-1373-10 chr20:35842246 G>A maps to NM_002951.3 R357R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4871-01A-01D-1373-10 chr9:114304000 A>G maps to NM_133464.2 E262E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4871-01A-01D-1373-10 chr1:45484290 G>A maps to NM_020883.1 S1131S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4872-01A-01D-1373-10 chr2:21225279 A>G maps to NM_000384.2 S4338S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4872-01A-01D-1373-10 chr1:44401721 T>A maps to ENST00000438616 G23G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4872-01A-01D-1373-10 chr11:67274953 G>C maps to NM_005851.3 P65P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4872-01A-01D-1373-10 chr1:103428246 G>A maps to NM_080629.2 Q1008*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4872-01A-01D-1373-10 chr1:152384628 C>T maps to NM_016190.2 A27A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4872-01A-01D-1373-10 chr17:37899215 T>A maps to ENST00000445327 A147A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4872-01A-01D-1373-10 chr7:43531768 A>G maps to NM_015052.3 S1110S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4872-01A-01D-1373-10 chr17:61622983 A>C maps to NM_030779.2 G902G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4872-01A-01D-1373-10 chr17:39150328 T>G maps to NM_033185.2 R7R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4872-01A-01D-1373-10 chr7:55466149 C>T maps to NM_018697.3 V119V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4872-01A-01D-1373-10 chr19:8316055 C>T maps to NM_024552.2 V32V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4872-01A-01D-1373-10 chr22:30824552 C>A maps to NM_001003704.1 A100A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4872-01A-01D-1373-10 chr1:226555204 A>T maps to NM_001618.3 Y794*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4872-01A-01D-1373-10 chr3:52661287 C>A did not map to a codon.
Sequencing variant TCGA-CJ-4872-01A-01D-1373-10 chr11:16838757 C>G maps to ENST00000448080 S485S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4872-01A-01D-1373-10 chr2:17698113 A>G maps to NM_001099218.2 N523N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4872-01A-01D-1373-10 chr2:45800363 T>C maps to NM_018079.4 R429R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4872-01A-01D-1373-10 chr10:75294439 G>T maps to NM_152586.3 V411V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4872-01A-01D-1373-10 chr3:47164927 G>A maps to NM_014159.6 R400*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4873-01A-01D-1373-10 chr15:79090347 G>A maps to ENST00000258883 A188A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4873-01A-01D-1373-10 chr7:134261182 G>A did not map to a codon.
Sequencing variant TCGA-CJ-4873-01A-01D-1373-10 chr6:69685177 A>G maps to NM_001704.2 E560E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4873-01A-01D-1373-10 chr16:15977976 A>G maps to NM_144600.2 D38D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4873-01A-01D-1373-10 chr6:151857577 T>C maps to ENST00000367290 S61S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4873-01A-01D-1373-10 chr5:39382722 A>C maps to NM_001343.2 A446A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4873-01A-01D-1373-10 chr1:36474309 T>A maps to NM_024852.2 T271T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4873-01A-01D-1373-10 chr2:42510109 A>G maps to NM_019063.3 K313K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4873-01A-01D-1373-10 chr4:89702426 G>T maps to NM_014883.2 V449V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4873-01A-01D-1373-10 chr1:15695982 C>T maps to NM_052929.1 F1122F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4873-01A-01D-1373-10 chr14:89656757 A>G maps to NM_001085471.1 L261L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4873-01A-01D-1373-10 chr7:43484309 T>C maps to NM_015052.3 S513S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4873-01A-01D-1373-10 chr2:213872773 A>G maps to ENST00000342002 I303I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4873-01A-01D-1373-10 chr19:39688860 C>T maps to NM_001001414.1 Y140Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4873-01A-01D-1373-10 chr11:5322936 C>T maps to NM_033179.2 L80L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4873-01A-01D-1373-10 chr12:103246687 A>G maps to NM_000277.1 L249L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4873-01A-01D-1373-10 chr19:10565502 A>C did not map to a codon.
Sequencing variant TCGA-CJ-4873-01A-01D-1373-10 chr13:33306262 A>T maps to ENST00000400481 K717*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4873-01A-01D-1373-10 chr18:61264229 G>A maps to NM_012397.3 W270*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4873-01A-01D-1373-10 chr12:100796247 T>C maps to NM_139319.2 V298V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4873-01A-01D-1373-10 chr11:64326671 C>T maps to NM_018484.2 I153I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4873-01A-01D-1373-10 chr20:23016317 C>A maps to NM_001052.2 A66A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4873-01A-01D-1373-10 chrX:132161105 G>A maps to NM_031907.1 N381N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4873-01A-01D-1373-10 chr12:6180475 A>G maps to NM_000552.3 N381N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4873-01A-01D-1373-10 chr12:6180484 G>T maps to NM_000552.3 I378I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4873-01A-01D-1373-10 chr15:42749283 A>G maps to NM_022473.1 S40S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4873-01A-01D-1373-10 chr1:35576004 T>C maps to NM_024772.3 N306N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4874-01A-01D-1373-10 chr15:89398668 T>A maps to NM_013227.3 V951V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4874-01A-01D-1373-10 chr11:44104722 G>A maps to NM_032592.3 W372*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4874-01A-01D-1373-10 chr19:42384962 T>C maps to NM_001783.3 Y199Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4874-01A-01D-1373-10 chr17:40844514 A>T did not map to a codon.
Sequencing variant TCGA-CJ-4874-01A-01D-1373-10 chr3:128181551 G>A maps to NM_153330.2 F179F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4874-01A-01D-1373-10 chr7:158590761 T>G maps to NM_020728.2 V174V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4874-01A-01D-1373-10 chr19:40408821 G>A maps to NM_003890.2 P1339P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4874-01A-01D-1373-10 chr9:14859187 T>G maps to ENST00000380880 P208P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4874-01A-01D-1373-10 chr6:32497900 C>T did not map to a codon.
Sequencing variant TCGA-CJ-4874-01A-01D-1373-10 chr1:21100039 G>T maps to NM_016287.3 T138T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4874-01A-01D-1373-10 chr9:5968931 A>G maps to NM_001017969.2 L433L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4874-01A-01D-1373-10 chr14:50249622 T>G maps to NM_014315.2 L391L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4874-01A-01D-1373-10 chr19:55176301 T>A did not map to a codon.
Sequencing variant TCGA-CJ-4874-01A-01D-1373-10 chrX:70756091 A>G maps to NM_181672.2 A34A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4874-01A-01D-1373-10 chr6:41711089 G>T maps to NM_002630.3 T122T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4874-01A-01D-1373-10 chr12:18446880 C>T maps to NM_004570.4 C322C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4874-01A-01D-1373-10 chr16:81934321 C>G maps to NM_002661.2 P433P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4874-01A-01D-1373-10 chr19:36290975 C>T maps to NM_021232.1 R525R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4874-01A-01D-1373-10 chr14:24808387 A>G maps to NM_006871.3 L102L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4874-01A-01D-1373-10 chr5:177574746 C>T maps to NM_022762.3 G327G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4874-01A-01D-1373-10 chr2:166847874 T>C maps to NM_001165963.1 T1970T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4874-01A-01D-1373-10 chr2:55804448 A>T did not map to a codon.
Sequencing variant TCGA-CJ-4874-01A-01D-1373-10 chr1:226037700 C>T maps to NM_014698.2 K661K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4874-01A-01D-1373-10 chr19:6744587 C>T maps to ENST00000313244 R222R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4874-01A-01D-1373-10 chrX:54957275 T>A maps to NM_001039705.1 T1373T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4874-01A-01D-1373-10 chr20:51870957 A>T maps to NM_173485.5 K321*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4874-01A-01D-1373-10 chr16:17221642 C>T maps to NM_022166.3 K701K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4874-01A-01D-1373-10 chr19:58118341 A>T maps to NM_020880.3 T483T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4875-01A-01D-1373-10 chr10:52569666 A>T maps to NM_138932.2 A540A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4875-01A-01D-1373-10 chrX:15585871 T>A maps to NM_021804.2 V658V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4875-01A-01D-1373-10 chr19:36370070 C>A maps to NM_001024807.1 L603L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4875-01A-01D-1373-10 chr1:116943757 G>T maps to NM_000701.7 E909*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4875-01A-01D-1373-10 chr14:74825561 C>G maps to NM_018228.2 A692A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4875-01A-01D-1373-10 chr7:26678852 A>G maps to NM_001145531.1 T30T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4875-01A-01D-1373-10 chr16:89246669 T>C maps to NM_004933.2 D88D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4875-01A-01D-1373-10 chr19:42132311 G>A maps to NM_001817.2 H29H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4875-01A-01D-1373-10 chr6:70639450 C>A maps to NM_001858.4 G175G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4875-01A-01D-1373-10 chr11:125791251 C>A maps to NM_013264.3 L456L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4875-01A-01D-1373-10 chr1:167097706 A>T maps to NM_001080426.1 A1113A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4875-01A-01D-1373-10 chr22:37769177 G>T maps to NM_052906.3 A799A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4875-01A-01D-1373-10 chr9:140330188 G>A maps to NM_001033113.1 C381C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4875-01A-01D-1373-10 chr2:239033942 G>A maps to NM_194312.2 P340P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4875-01A-01D-1373-10 chr11:69514320 A>T maps to NM_005117.2 C120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4875-01A-01D-1373-10 chrX:135290018 C>T maps to NM_001159699.1 Q150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4875-01A-01D-1373-10 chr2:233680349 G>A maps to ENST00000373566 W726*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4875-01A-01D-1373-10 chr11:134147735 C>A maps to NM_001080407.2 R98R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4875-01A-01D-1373-10 chr12:54792403 G>A maps to NM_002205.2 Q974*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4875-01A-01D-1373-10 chr2:187521115 A>T maps to NM_002210.3 I569I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4875-01A-01D-1373-10 chr13:42461383 G>T maps to NM_015058.1 P255P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4875-01A-01D-1373-10 chr15:41988560 A>G maps to ENST00000219905 S451S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4875-01A-01D-1373-10 chr20:42340165 G>T maps to NM_002466.2 V548V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4875-01A-01D-1373-10 chr7:44579791 A>C maps to NM_013389.2 G68G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4875-01A-01D-1373-10 chr11:124310504 G>A maps to NM_012378.1 H159H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4875-01A-01D-1373-10 chr1:44086830 C>T maps to NM_002840.3 Y1861Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4875-01A-01D-1373-10 chr6:155145480 A>G maps to NM_014892.3 R680R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4875-01A-01D-1373-10 chr14:23371267 A>G maps to NM_001077351.1 A389A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4875-01A-01D-1373-10 chr5:121758632 T>C maps to ENST00000379533 A114A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4875-01A-01D-1373-10 chr11:66466956 C>T maps to NM_006946.2 L1232L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4875-01A-01D-1373-10 chr11:66483324 G>A maps to NM_006946.2 L95L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4875-01A-01D-1373-10 chr4:57366825 G>C maps to NM_006947.3 G601G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4875-01A-01D-1373-10 chr1:155979423 A>G maps to ENST00000368312 F172F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4875-01A-01D-1373-10 chr12:102125402 T>C maps to ENST00000449403 R206R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4875-01A-01D-1373-10 chr8:109796775 G>A maps to NM_153015.1 F184F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4875-01A-01D-1373-10 chr17:74398735 C>T maps to NM_022066.3 G211G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4875-01A-01D-1373-10 chr8:100514006 T>G maps to NM_017890.3 R1321R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4875-01A-01D-1373-10 chr10:49983816 A>T maps to NM_020945.1 S943S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4875-01A-01D-1373-10 chr1:52703735 T>A maps to NM_004799.2 L216*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4875-01A-01D-1373-10 chr19:9407409 G>A maps to NM_198535.1 Q224*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4876-01A-01D-1373-10 chr15:86198697 C>T maps to NM_006738.4 T1475T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4876-01A-01D-1373-10 chr18:29218624 C>T maps to NM_004775.3 A190A. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-CJ-4876-01A-01D-1373-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CJ-4876-01A-01D-1373-10 chr11:66359724 G>A maps to NM_018219.2 S254S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4876-01A-01D-1373-10 chr16:70546245 T>A maps to NM_015386.2 K212*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4876-01A-01D-1373-10 chr5:135228121 A>G maps to NM_000590.1 I131I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4876-01A-01D-1373-10 chr3:4730229 C>T maps to ENST00000356617 Q1248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4876-01A-01D-1373-10 chr17:64800058 T>C maps to NM_002737.2 D641D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4876-01A-01D-1373-10 chr5:34824235 G>C maps to NM_001145521.1 V763V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4876-01A-01D-1373-10 chr16:67428939 T>A maps to NM_013304.2 K399*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4878-01A-01D-1373-10 chr7:48452146 G>A maps to NM_152701.3 T4142T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4878-01A-01D-1373-10 chr8:39666985 C>T did not map to a codon.
Sequencing variant TCGA-CJ-4878-01A-01D-1373-10 chr2:21224730 A>G maps to NM_000384.2 I4521I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4878-01A-01D-1373-10 chr4:100756842 C>T maps to NM_014395.2 D55D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4878-01A-01D-1373-10 chr16:460351 T>G maps to NM_020664.3 Y149*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4878-01A-01D-1373-10 chr11:18738273 C>T did not map to a codon.
Sequencing variant TCGA-CJ-4878-01A-01D-1373-10 chr1:54477873 C>T maps to NM_001010978.2 G94G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4878-01A-01D-1373-10 chr6:136879990 T>C maps to NM_005923.3 L1337L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4878-01A-01D-1373-10 chr16:24573317 T>G maps to NM_006910.4 S375S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4878-01A-01D-1373-10 chr2:227771559 T>C maps to NM_001167608.1 T206T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4878-01A-01D-1373-10 chr5:9629742 C>G maps to NM_019599.2 L134L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4881-01A-01D-1373-10 chr8:107773282 C>G maps to NM_139166.4 V376V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4881-01A-01D-1373-10 chr12:43825221 G>A maps to ENST00000389420 G1058G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4881-01A-01D-1373-10 chrX:49963343 G>A maps to NM_003886.2 Y29Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4881-01A-01D-1373-10 chr17:65942186 C>T maps to ENST00000321892 Q2581*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4881-01A-01D-1373-10 chr1:226180617 T>C maps to NM_152608.3 R108R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4881-01A-01D-1373-10 chr12:56478807 C>T maps to NM_001982.2 L88L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4881-01A-01D-1373-10 chr1:154960801 G>A maps to NM_025207.4 E198E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4881-01A-01D-1373-10 chr1:230410255 G>C maps to NM_004481.3 R502R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4881-01A-01D-1373-10 chr12:52863662 C>T maps to NM_173086.4 L405L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4881-01A-01D-1373-10 chr19:9296954 A>G maps to NM_175883.2 L166L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4881-01A-01D-1373-10 chr19:14580587 G>A maps to NM_213560.1 L732L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4881-01A-01D-1373-10 chr4:76797628 G>A maps to NM_006239.2 C377C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4881-01A-01D-1373-10 chr1:78958514 C>A maps to NM_000959.3 S29S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4881-01A-01D-1373-10 chr6:47251932 G>A maps to NM_014452.3 I328I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4881-01A-01D-1373-10 chr22:30134341 C>A maps to NM_019103.2 R120R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4884-01A-01D-1373-10 chr3:49694176 G>A maps to NM_003458.3 R2396R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4884-01A-01D-1373-10 chr12:97137565 C>T maps to ENST00000342887 L904L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4884-01A-01D-1373-10 chr17:7850943 A>C maps to NM_001037144.4 P683P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4884-01A-01D-1373-10 chr20:35060890 C>T maps to ENST00000339266 T257T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4884-01A-01D-1373-10 chrX:49173717 C>G maps to NM_001098413.2 G93G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4884-01A-01D-1373-10 chr12:42491288 G>A maps to NM_173601.1 D372D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4884-01A-01D-1373-10 chr15:89002954 A>G maps to NM_022163.3 F243F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4884-01A-01D-1373-10 chr19:9018478 G>T maps to NM_024690.2 G12565G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4884-01A-01D-1373-10 chr1:21808125 G>A maps to NM_032264.2 E490E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4884-01A-01D-1373-10 chr8:103573000 C>G maps to NM_024410.3 P214P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4884-01A-01D-1373-10 chr1:176740167 T>C maps to NM_020318.2 L1523L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4884-01A-01D-1373-10 chr1:226566973 T>A maps to NM_001618.3 G538G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4884-01A-01D-1373-10 chr3:52620645 G>T maps to ENST00000296302 S1061*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4884-01A-01D-1373-10 chr1:12010477 C>T maps to ENST00000376369 Q170*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4884-01A-01D-1373-10 chr5:38958912 T>A maps to ENST00000296782 T733T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4884-01A-01D-1373-10 chr9:127789089 C>G did not map to a codon.
Sequencing variant TCGA-CJ-4884-01A-01D-1373-10 chr14:94909002 C>T maps to NM_001080451.1 W403*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4884-01A-01D-1373-10 chr19:7997585 G>T maps to NM_006351.3 R305R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4884-01A-01D-1373-10 chr16:1306920 G>A maps to NM_012217.2 G126G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4884-01A-01D-1373-10 chr14:68251806 T>C maps to NM_015346.3 A1164A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4885-01A-01D-1373-10 chr2:215831607 G>A maps to NM_173076.2 R1950*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4885-01A-01D-1373-10 chr9:140773612 T>A did not map to a codon.
Sequencing variant TCGA-CJ-4885-01A-01D-1373-10 chr5:154185451 C>A maps to ENST00000377643 S853*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4885-01A-01D-1373-10 chr4:2935292 C>A did not map to a codon.
Sequencing variant TCGA-CJ-4885-01A-01D-1373-10 chr17:41345366 C>G maps to NM_005899.3 L412L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4885-01A-01D-1373-10 chr5:36955610 T>A maps to NM_133433.3 A34A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4885-01A-01D-1373-10 chr9:87635221 G>T maps to NM_006180.3 V758V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4885-01A-01D-1373-10 chr11:59481180 T>G maps to NM_001005324.1 A46A. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-CJ-4885-01A-01D-1373-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CJ-4885-01A-01D-1373-10 chr1:53453707 T>G maps to NM_002979.4 G327G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4885-01A-01D-1373-10 chr17:4020302 C>A maps to NM_015113.3 L219L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4886-01A-01D-1373-10 chr10:97371064 G>A maps to NM_002860.3 D686D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4886-01A-01D-1373-10 chr22:50751528 G>C maps to NM_001001794.3 P452P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4886-01A-01D-1373-10 chr19:7675368 C>T maps to NM_001080429.2 C283C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4886-01A-01D-1373-10 chr16:87871507 G>A maps to NM_003486.5 S361S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4886-01A-01D-1373-10 chr9:33989091 C>T maps to NM_018449.2 K107K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4886-01A-01D-1373-10 chr22:30134341 C>A maps to NM_019103.2 R120R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4887-01A-01D-1373-10 chr3:57280132 C>A maps to NM_012096.2 Y168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4887-01A-01D-1373-10 chr7:105254437 C>T maps to NM_020725.1 K781K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4887-01A-01D-1373-10 chr13:46918948 G>A maps to NM_025113.2 G601G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4887-01A-01D-1373-10 chr1:181453104 T>C maps to ENST00000357570 D75D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4887-01A-01D-1373-10 chr18:64172225 A>G maps to NM_021153.2 P714P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4887-01A-01D-1373-10 chr20:31291228 C>A maps to NM_053041.2 L186L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4887-01A-01D-1373-10 chr5:176308430 G>T maps to NM_002115.2 S833S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4887-01A-01D-1373-10 chr6:32629145 G>A maps to ENST00000374943 I250I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4887-01A-01D-1373-10 chr6:160218372 T>C maps to NM_014161.3 N98N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4887-01A-01D-1373-10 chr3:52620673 G>A maps to ENST00000296302 R1052*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4887-01A-01D-1373-10 chr11:70200405 G>T did not map to a codon.
Sequencing variant TCGA-CJ-4887-01A-01D-1373-10 chr17:34171884 C>A maps to NM_139215.1 R528R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4888-01A-01D-1373-10 chr4:126241252 G>C maps to NM_024582.4 V1229V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4888-01A-01D-1373-10 chr4:8582798 C>T maps to NM_080819.2 C30C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4888-01A-01D-1373-10 chr6:31323253 G>C maps to ENST00000428231 G315G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4888-01A-01D-1373-10 chrX:123554561 G>A maps to NM_001163278.1 T1527T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4888-01A-01D-1373-10 chr2:108910185 G>T maps to ENST00000437390 L21L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4888-01A-01D-1373-10 chr4:1738985 G>A maps to NM_006342.1 E589E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4888-01A-01D-1373-10 chr7:141952103 A>T maps to NM_001001317.2 V221V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4888-01A-01D-1373-10 chr3:52613193 C>A maps to ENST00000296302 E1137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4889-01A-01D-1373-10 chr9:133738355 G>A maps to NM_007313.2 Q271Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4889-01A-01D-1373-10 chr2:187367290 A>T maps to NM_018471.2 K171*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4889-01A-01D-1373-10 chr8:144522388 G>A maps to NM_015117.2 S879S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4890-01A-01D-1373-10 chr2:242610737 T>C maps to ENST00000337606 L458L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4890-01A-01D-1373-10 chr4:81967318 C>T maps to NM_001201.2 A248A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4890-01A-01D-1373-10 chr14:95657992 G>A maps to NM_024734.3 Q973*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4890-01A-01D-1373-10 chr6:70942324 T>A maps to NM_001851.4 K822*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4890-01A-01D-1373-10 chrX:13618145 T>C maps to NM_001167890.1 N111N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4890-01A-01D-1373-10 chr5:175388334 T>C maps to NM_032361.2 A244A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4891-01A-01D-1373-10 chr22:29091807 G>A maps to NM_001005735.1 T426T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4891-01A-01D-1373-10 chr1:36358771 T>C maps to NM_012199.2 I135I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4891-01A-01D-1373-10 chr4:2934200 C>G maps to NM_001146069.1 L190L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4891-01A-01D-1373-10 chr17:8701340 G>A maps to NM_152599.3 P366P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4891-01A-01D-1373-10 chr16:81242150 T>C maps to NM_052892.3 G235G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4891-01A-01D-1373-10 chr6:35922961 G>A maps to NM_052961.3 Y733Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4891-01A-01D-1373-10 chr10:70450815 G>T maps to NM_030625.2 G1886*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4891-01A-01D-1373-10 chr1:175334170 C>T maps to NM_003285.2 E854E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4892-01A-01D-1373-10 chr20:25038483 G>T maps to NM_032501.2 T85T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4892-01A-01D-1373-10 chr18:55321262 G>T maps to NM_005603.4 Y992*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4892-01A-01D-1373-10 chr1:244735875 A>G maps to NM_001130957.1 P584P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4892-01A-01D-1373-10 chr17:72522082 G>T maps to NM_174892.2 C95*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4892-01A-01D-1373-10 chr4:1388349 G>A maps to NM_175918.3 T17T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4892-01A-01D-1373-10 chr12:56217259 A>C maps to NM_032364.5 A480A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4892-01A-01D-1373-10 chr8:124820572 C>T maps to NM_144963.2 V698V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4892-01A-01D-1373-10 chr6:32552015 C>A maps to NM_002124.2 T80T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4892-01A-01D-1373-10 chr19:18377980 C>G maps to NM_001145304.1 L123L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4892-01A-01D-1373-10 chr19:871986 G>A maps to NM_005481.2 T679T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4892-01A-01D-1373-10 chr13:38143503 G>T maps to NM_006475.2 T788T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4892-01A-01D-1373-10 chr9:33797832 C>T maps to NM_007343.3 I126I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4892-01A-01D-1373-10 chr1:109824318 T>G maps to ENST00000409138 R147R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4892-01A-01D-1373-10 chr5:131940609 T>C maps to NM_005732.3 T879T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4892-01A-01D-1373-10 chr16:24581248 A>T maps to NM_006910.4 K1080*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4892-01A-01D-1373-10 chr2:27887263 C>T maps to NM_018158.2 H215H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4892-01A-01D-1373-10 chr12:119583247 G>A maps to NM_194286.2 S278S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4892-01A-01D-1373-10 chr3:183952129 A>G maps to ENST00000413060 T266T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4893-01A-01D-1373-10 chr13:103418815 C>A maps to NM_138779.3 E207*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4893-01A-01D-1373-10 chr13:95121258 G>A maps to NM_001129889.1 G112G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4893-01A-01D-1373-10 chr5:59895074 C>A maps to NM_018369.2 G419*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4893-01A-01D-1373-10 chr17:73235513 C>G maps to NM_138619.2 P574P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4893-01A-01D-1373-10 chr12:13716544 C>G maps to NM_000834.3 R1209R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4893-01A-01D-1373-10 chr3:154898166 G>A maps to NM_007289.2 Q724Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4893-01A-01D-1373-10 chr5:80074599 C>T maps to NM_002439.3 Q794*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4893-01A-01D-1373-10 chr11:16816508 C>T maps to ENST00000448080 L822L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4893-01A-01D-1373-10 chr20:37150281 G>A maps to NM_020336.2 L520L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4893-01A-01D-1373-10 chr21:36259169 G>T maps to NM_001754.4 R107R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4893-01A-01D-1373-10 chr5:176382975 T>C maps to ENST00000377219 E441E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4894-01A-01D-1373-10 chr1:156264684 T>G maps to NM_144580.1 V81V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4894-01A-01D-1373-10 chr20:40116334 C>T maps to NM_032221.3 E657E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4894-01A-01D-1373-10 chr12:92816353 T>G maps to NM_001025232.1 A37A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4894-01A-01D-1373-10 chr20:42935613 C>T maps to NM_001080472.1 W147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4894-01A-01D-1373-10 chr5:72743760 T>A maps to NM_004472.2 K143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4894-01A-01D-1373-10 chr5:151208499 C>T maps to NM_001146040.1 R347R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4894-01A-01D-1373-10 chr17:45006906 T>C maps to NM_054022.2 S17S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4894-01A-01D-1373-10 chr12:54383106 C>T maps to NM_017409.3 S302S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4894-01A-01D-1373-10 chr6:111587970 T>A maps to NM_153369.2 P402P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4894-01A-01D-1373-10 chr12:6859056 C>T maps to NM_005439.2 T172T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4894-01A-01D-1373-10 chr17:18022776 G>A maps to ENST00000205890 K221K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4894-01A-01D-1373-10 chr8:110456095 G>T maps to ENST00000426474 G1586*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4894-01A-01D-1373-10 chr2:46211701 C>A maps to NM_005400.2 R236R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4894-01A-01D-1373-10 chr6:128643198 C>T maps to ENST00000368210 W160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4894-01A-01D-1373-10 chr3:120428687 G>A maps to NM_173825.3 G69G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4894-01A-01D-1373-10 chr2:101898369 C>T maps to NM_173647.3 Q370Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4894-01A-01D-1373-10 chr1:177927419 A>C maps to NM_033127.2 P404P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4894-01A-01D-1373-10 chr6:31930350 A>G maps to NM_006929.4 T400T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4894-01A-01D-1373-10 chr17:2195863 A>T maps to NM_017575.4 A773A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4894-01A-01D-1373-10 chr11:85438960 G>T maps to ENST00000359152 G37G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4894-01A-01D-1373-10 chr17:56638927 T>A maps to ENST00000240361 P1416P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4894-01A-01D-1373-10 chr12:27152582 T>A maps to NM_016551.2 T91T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4894-01A-01D-1373-10 chr20:57782031 A>G maps to NM_178457.1 R1316R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4895-01A-01D-1373-10 chr2:24108652 G>A maps to NM_017552.1 Q207*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4895-01A-01D-1373-10 chr1:17313020 G>A maps to NM_022089.2 T1114T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4895-01A-01D-1373-10 chr6:16328274 C>T maps to NM_000332.3 P89P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4895-01A-01D-1373-10 chr1:156264684 T>G maps to NM_144580.1 V81V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4895-01A-01D-1373-10 chr19:13325356 G>A maps to NM_023035.2 L1937L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4895-01A-01D-1373-10 chr11:67017708 G>A maps to NM_012308.2 V736V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4895-01A-01D-1373-10 chr19:7675368 C>T maps to NM_001080429.2 C283C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4895-01A-01D-1373-10 chr2:136566909 G>A maps to NM_002299.2 L1003L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4895-01A-01D-1373-10 chr2:133403818 C>T maps to ENST00000409034 A98A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4895-01A-01D-1373-10 chr8:17612772 G>A maps to NM_001001924.2 Q182*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4895-01A-01D-1373-10 chr19:9061084 G>T maps to NM_024690.2 I8787I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4895-01A-01D-1373-10 chr19:13058666 G>A maps to NM_005053.2 K26K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4895-01A-01D-1373-10 chr1:35454279 T>C maps to NM_007167.3 V801V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4854-01A-01D-1373-10 chr8:11415474 C>T maps to ENST00000427279 C319C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4854-01A-01D-1373-10 chr19:1986501 G>A maps to NM_017797.3 V521V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4854-01A-01D-1373-10 chr19:33444681 T>A maps to NM_032816.3 R111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4854-01A-01D-1373-10 chr2:130897217 T>C maps to NM_207310.1 A351A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4854-01A-01D-1373-10 chr19:34180262 G>A maps to NM_022467.3 Q32Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4854-01A-01D-1373-10 chr9:115931604 G>A maps to ENST00000446284 V1153V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4854-01A-01D-1373-10 chr1:230338992 A>T maps to NM_004481.3 K111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4854-01A-01D-1373-10 chr12:42491288 G>A maps to NM_173601.1 D372D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4854-01A-01D-1373-10 chr3:185376128 A>C maps to NM_006548.4 S423S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4854-01A-01D-1373-10 chr16:84529459 C>A maps to NM_020947.3 R71R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4854-01A-01D-1373-10 chr2:170029717 G>A maps to NM_004525.2 L3677L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4854-01A-01D-1373-10 chr6:30672174 C>G maps to NM_014641.2 R1595R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4854-01A-01D-1373-10 chr16:82203741 T>C maps to NM_005792.2 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4854-01A-01D-1373-10 chr8:144658710 G>A maps to ENST00000276844 L305L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4854-01A-01D-1373-10 chr1:21808098 A>G maps to NM_032264.2 R481R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4854-01A-01D-1373-10 chr12:113448225 C>T maps to NM_016817.2 V699V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4854-01A-01D-1373-10 chr13:25670872 A>G maps to NM_030979.2 R179R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4854-01A-01D-1373-10 chr12:11420894 C>T maps to NM_006249.4 P96P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4854-01A-01D-1373-10 chr6:125366367 C>G maps to NM_152553.2 G6G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4854-01A-01D-1373-10 chrX:118604408 C>T maps to NM_001152.4 A224A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4854-01A-01D-1373-10 chr16:68877597 G>T maps to NM_024562.1 L26L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4854-01A-01D-1373-10 chr8:74893387 A>G did not map to a codon.
Sequencing variant TCGA-CZ-4854-01A-01D-1373-10 chr17:5038558 C>A maps to NM_004505.2 A175A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4854-01A-01D-1373-10 chr19:47575278 G>C maps to NM_015168.1 P634P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4854-01A-01D-1373-10 chr19:35435240 G>A maps to NM_001099438.1 E458E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4857-01A-01D-1373-10 chr1:27106544 C>A maps to NM_006015.4 C2052*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4857-01A-01D-1373-10 chrX:2832695 T>C maps to NM_009589.2 P373P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4857-01A-01D-1373-10 chr3:193174888 C>T maps to NM_032279.2 L605L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4857-01A-01D-1373-10 chr11:89956062 G>A maps to NM_012124.2 S20S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4857-01A-01D-1373-10 chr2:162865774 G>A maps to NM_001935.3 N621N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4857-01A-01D-1373-10 chr17:48618638 G>A maps to NM_017957.2 E433E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4857-01A-01D-1373-10 chr11:64054435 G>C did not map to a codon.
Sequencing variant TCGA-CZ-4857-01A-01D-1373-10 chr10:87379670 C>A maps to NM_017551.2 G771G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4857-01A-01D-1373-10 chr6:26056470 C>T maps to NM_005319.3 L62L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4857-01A-01D-1373-10 chr3:44816878 G>T maps to NM_020242.2 E66*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4857-01A-01D-1373-10 chr12:53009993 C>T maps to NM_175068.2 S206S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4857-01A-01D-1373-10 chrX:140993876 C>A maps to NM_005462.4 A229A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4857-01A-01D-1373-10 chr19:50333062 T>C maps to NM_030973.3 I182I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4857-01A-01D-1373-10 chr7:151848092 C>G did not map to a codon.
Sequencing variant TCGA-CZ-4857-01A-01D-1373-10 chr1:11189850 C>T maps to NM_004958.3 Q1886Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4857-01A-01D-1373-10 chr19:54312935 G>A maps to ENST00000391773 S659S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4857-01A-01D-1373-10 chr1:12837651 C>T maps to NM_001080830.1 V454V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4857-01A-01D-1373-10 chr11:63681730 A>T did not map to a codon.
Sequencing variant TCGA-CZ-4857-01A-01D-1373-10 chr2:224862979 G>A maps to NM_001136530.1 A125A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4857-01A-01D-1373-10 chr16:18844383 A>T maps to ENST00000389467 L2890L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4857-01A-01D-1373-10 chr7:128848597 A>T did not map to a codon.
Sequencing variant TCGA-CZ-4857-01A-01D-1373-10 chr9:131374048 G>A maps to NM_001130438.2 R1610R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4857-01A-01D-1373-10 chr7:149512018 C>G maps to NM_198455.2 S3526S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4857-01A-01D-1373-10 chr10:71166859 G>T maps to NM_001057.2 I306I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4857-01A-01D-1373-10 chr16:30370550 G>A maps to NM_015527.3 F528F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4857-01A-01D-1373-10 chr15:74174088 G>A did not map to a codon.
Sequencing variant TCGA-CZ-4857-01A-01D-1373-10 chr12:44782259 A>G maps to NM_032256.1 R450R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4857-01A-01D-1373-10 chr13:19751273 G>A maps to NM_006001.1 H283H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4857-01A-01D-1373-10 chr8:100832148 G>A maps to NM_017890.3 R2956R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4858-01A-01D-1373-10 chr3:183899958 G>T maps to ENST00000411763 L353L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4858-01A-01D-1373-10 chr1:155319243 A>T maps to ENST00000368346 A2481A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4858-01A-01D-1373-10 chr12:12974948 T>C maps to NM_016355.3 L165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4858-01A-01D-1373-10 chr17:11725795 C>G maps to NM_001372.3 V2964V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4858-01A-01D-1373-10 chr3:51400101 C>T maps to NM_004947.4 R1764*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4858-01A-01D-1373-10 chr8:623640 A>G maps to NM_207332.1 A237A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4858-01A-01D-1373-10 chr4:1806216 C>T maps to NM_000142.4 H412H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4858-01A-01D-1373-10 chr19:34890919 G>A maps to NM_000175.3 Q552Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4858-01A-01D-1373-10 chr6:32634330 G>A maps to ENST00000374943 V18V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4858-01A-01D-1373-10 chr1:6661905 C>A maps to NM_014851.2 L324L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4858-01A-01D-1373-10 chr5:136963989 G>A maps to NM_017415.2 N529N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4858-01A-01D-1373-10 chr17:21215551 C>T maps to NM_145109.2 A291A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4858-01A-01D-1373-10 chr11:129739925 T>A maps to NM_006165.3 G1023G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4858-01A-01D-1373-10 chr11:47282967 C>A maps to NM_005693.2 R226R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4858-01A-01D-1373-10 chr11:111941953 C>A maps to NM_138789.3 E119*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4858-01A-01D-1373-10 chr12:93135274 T>C maps to NM_001004330.2 L36L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4858-01A-01D-1373-10 chr10:89720743 G>T maps to NM_000314.4 E299*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4858-01A-01D-1373-10 chr2:198266831 T>C maps to NM_012433.2 K700K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4858-01A-01D-1373-10 chr21:44841004 G>T maps to NM_173354.3 G211G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4858-01A-01D-1373-10 chr17:61473211 C>T maps to ENST00000389520 Q980*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4858-01A-01D-1373-10 chr17:7578238 C>A maps to NM_001126112.1 E204*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4858-01A-01D-1373-10 chr8:146157098 G>A maps to NM_006958.2 F358F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4861-01A-01D-1373-10 chr2:207457433 C>T maps to NM_003812.2 Y684Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4861-01A-01D-1373-10 chr3:85851254 A>C maps to NM_153184.3 A42A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4861-01A-01D-1373-10 chr18:64172300 G>A maps to NM_021153.2 G689G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4861-01A-01D-1373-10 chr3:9984519 G>T maps to NM_001077415.2 G253*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4861-01A-01D-1373-10 chr16:21065765 C>T maps to NM_017539.1 G1338G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4861-01A-01D-1373-10 chr17:40857162 G>A maps to ENST00000264646 G629G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4861-01A-01D-1373-10 chr3:169802563 G>A maps to NM_014373.2 Q268Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4861-01A-01D-1373-10 chr15:58838058 C>T maps to NM_000236.2 S231S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4861-01A-01D-1373-10 chr11:86198483 T>G did not map to a codon.
Sequencing variant TCGA-CZ-4861-01A-01D-1373-10 chr19:56565045 G>A maps to NM_153447.4 L1057L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4861-01A-01D-1373-10 chr3:195955791 G>A did not map to a codon.
Sequencing variant TCGA-CZ-4861-01A-01D-1373-10 chr1:144856851 C>T maps to NM_014644.4 A2211A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4861-01A-01D-1373-10 chr1:14106782 A>G maps to NM_012231.4 K831K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4861-01A-01D-1373-10 chr13:79190196 A>G maps to NM_024546.3 L567L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4861-01A-01D-1373-10 chr8:93004068 T>G maps to NM_175634.2 P263P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4861-01A-01D-1373-10 chr4:77095295 C>T did not map to a codon.
Sequencing variant TCGA-CZ-4861-01A-01D-1373-10 chr12:109017990 G>A maps to ENST00000228463 A31A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4861-01A-01D-1373-10 chr3:47098444 G>A maps to NM_014159.6 Q2277*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4861-01A-01D-1373-10 chr14:72169178 G>A maps to NM_015556.1 T1201T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4861-01A-01D-1373-10 chr19:11145750 C>A maps to NM_001128849.1 S1371S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4861-01A-01D-1373-10 chr7:19738223 G>A maps to NM_001002926.1 T244T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4861-01A-01D-1373-10 chr17:5066235 C>A maps to NM_004505.2 A991A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4861-01A-01D-1373-10 chrX:41025334 A>G maps to NM_001039590.2 L732L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4861-01A-01D-1373-10 chr18:60242637 T>C maps to NM_017742.4 Y1108Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4861-01A-01D-1373-10 chr7:99631798 G>A maps to NM_003439.1 A557A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4861-01A-01D-1373-10 chr19:11892093 T>C maps to NM_152355.2 S485S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4862-01A-01D-1373-10 chrX:2835992 G>A maps to NM_001669.2 L239L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4862-01A-01D-1373-10 chr19:41932062 A>G maps to NM_198540.2 S207S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4862-01A-01D-1373-10 chr15:83933198 C>T maps to NM_001717.3 Q268Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4862-01A-01D-1373-10 chr11:3022345 A>C maps to NM_001014437.2 *832G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4862-01A-01D-1373-10 chr15:43478361 T>A maps to NM_012142.3 A60A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4862-01A-01D-1373-10 chr15:57816813 C>T maps to NM_032866.3 T968T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4862-01A-01D-1373-10 chr14:39783948 A>G maps to ENST00000396158 R439R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4862-01A-01D-1373-10 chr1:36358771 T>C maps to NM_012199.2 I135I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4862-01A-01D-1373-10 chrX:153609310 C>T maps to NM_000117.2 S173S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4862-01A-01D-1373-10 chr4:91230367 G>A maps to NM_001145065.1 T311T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4862-01A-01D-1373-10 chr5:150924101 G>T maps to NM_001447.2 R2196R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4862-01A-01D-1373-10 chr7:20371477 C>T maps to NM_002214.2 Q17*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4862-01A-01D-1373-10 chr1:202710613 T>G maps to ENST00000367264 I978I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4862-01A-01D-1373-10 chr1:202273685 G>A did not map to a codon.
Sequencing variant TCGA-CZ-4862-01A-01D-1373-10 chrX:114357119 A>T maps to NM_020871.3 L716L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4862-01A-01D-1373-10 chr18:77211776 C>T maps to NM_172387.1 L609L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4862-01A-01D-1373-10 chr7:44687317 C>A maps to ENST00000444676 S159S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4862-01A-01D-1373-10 chr11:5221675 G>C maps to NM_001004760.2 S85S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4862-01A-01D-1373-10 chr11:35016593 C>T maps to NM_003477.2 L461L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4862-01A-01D-1373-10 chr3:52454990 A>G maps to ENST00000454052 L162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4862-01A-01D-1373-10 chr17:8792002 C>G maps to NM_001142633.1 S367S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4862-01A-01D-1373-10 chr15:56032871 G>A maps to NM_173814.4 C35C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4862-01A-01D-1373-10 chr9:112151593 G>C maps to NM_002829.3 T724T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4862-01A-01D-1373-10 chr8:94746442 A>C maps to NM_203390.2 R732R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4862-01A-01D-1373-10 chr12:114397158 C>T maps to NM_016196.3 R143R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4862-01A-01D-1373-10 chr1:39305248 A>G maps to NM_022157.2 N392N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4862-01A-01D-1373-10 chr6:99858628 C>T maps to NM_032870.2 Q163Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4862-01A-01D-1373-10 chr14:72055086 T>C maps to NM_015556.1 A166A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4862-01A-01D-1373-10 chr17:73096579 C>T maps to ENST00000450736 A314A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4862-01A-01D-1373-10 chr1:32557362 G>C maps to NM_018056.2 R226R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4862-01A-01D-1373-10 chr17:5036760 A>C maps to NM_004505.2 G100G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4862-01A-01D-1373-10 chr14:68256096 A>G maps to NM_015346.3 L992L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3308-01A-01D-0966-08 chr12:82746874 T>A did not map to a codon.
Sequencing variant TCGA-A3-3311-01A-01D-0966-08 chrX:153770606 G>T maps to NM_001099856.2 G43G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3311-01A-01D-0966-08 chrX:153770606 G>T maps to NM_001099856.2 G43G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3320-01A-01D-0966-08 chr2:178097098 A>G did not map to a codon.
Sequencing variant TCGA-A3-3323-01A-01D-0966-08 chr8:28651298 A>C did not map to a codon.
Sequencing variant TCGA-A3-3323-01A-01D-0966-08 chr7:116963051 C>A did not map to a codon.
Sequencing variant TCGA-A3-3326-01A-01D-0966-08 chr21:11012922 T>C did not map to a codon.
Sequencing variant TCGA-A3-3326-01A-01D-0966-08 chr21:11012922 T>C did not map to a codon.
Sequencing variant TCGA-A3-3346-01A-01D-0966-08 chr17:48452556 A>C did not map to a codon.
Sequencing variant TCGA-A3-3346-01A-01D-0966-08 chr17:48452558 A>G did not map to a codon.
Sequencing variant TCGA-A3-3357-01A-02D-1421-08 chr16:87394001 A>T did not map to a codon.
Sequencing variant TCGA-A3-3363-01A-01D-0966-08 chr1:52525495 T>C did not map to a codon.
Sequencing variant TCGA-A3-3367-01A-02D-1421-08 chr4:69817502 T>A did not map to a codon.
Sequencing variant TCGA-A3-3372-01A-01D-0966-08 chr6:33259864 A>G maps to ENST00000421215 L646L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3372-01A-01D-0966-08 chrX:41307151 C>T maps to NM_022567.2 R4*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3372-01A-01D-0966-08 chrX:41307151 C>T maps to NM_022567.2 R4*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3373-01A-02D-1421-08 chr14:104643366 G>A maps to NM_015656.1 R1414R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3373-01A-02D-1421-08 chr14:104643366 G>A maps to NM_015656.1 R1414R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A3-3378-01A-01D-0966-08 chr2:175612766 T>A did not map to a codon.
Sequencing variant TCGA-A3-3378-01A-01D-0966-08 chr2:175612766 T>A did not map to a codon.
Sequencing variant TCGA-B0-4823-01A-02D-1421-08 chr20:2637723 C>G did not map to a codon.
Sequencing variant TCGA-B0-5075-01A-01D-1462-08 chr20:15412102 A>T did not map to a codon.
Sequencing variant TCGA-B0-5077-01A-01D-1462-08 chr19:1913029 G>T maps to NM_138422.1 S312S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5081-01A-01D-1462-08 chr16:2070177 C>A maps to NM_001099456.2 P92P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5081-01A-01D-1462-08 chr16:2070177 C>A maps to NM_001099456.2 P92P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5092-01A-01D-1421-08 chr3:52439912 G>A maps to NM_004656.2 Q267*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5095-01A-01D-1421-08 chr22:21968851 C>T did not map to a codon.
Sequencing variant TCGA-B0-5097-01A-01D-1421-08 chr4:56314944 C>A did not map to a codon.
Sequencing variant TCGA-B0-5097-01A-01D-1421-08 chr4:56314944 C>A did not map to a codon.
Sequencing variant TCGA-B0-5097-01A-01D-1421-08 chr10:12209850 G>A did not map to a codon.
Sequencing variant TCGA-B0-5116-01A-02D-1421-08 chr6:128318044 C>T did not map to a codon.
Sequencing variant TCGA-B0-5116-01A-02D-1421-08 chr6:128318044 C>T did not map to a codon.
Sequencing variant TCGA-B0-5119-01A-02D-1421-08 chr3:169492075 A>G did not map to a codon.
Sequencing variant TCGA-B0-5120-01A-01D-1421-08 chr2:58313464 T>A did not map to a codon.
Sequencing variant TCGA-B2-4098-01A-01D-1458-08 chr3:127399685 T>C did not map to a codon.
Sequencing variant TCGA-B8-4153-01B-11D-1669-08 chr3:52620361 T>C did not map to a codon.
Sequencing variant TCGA-B8-4153-01B-11D-1669-08 chr3:52620361 T>C did not map to a codon.
Sequencing variant TCGA-B8-5159-01A-01D-1421-08 chrX:101615562 C>A maps to NM_022053.1 E614*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5159-01A-01D-1421-08 chrX:101615562 C>A maps to NM_022053.1 E614*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4782-01A-02D-1421-08 chr17:43517525 T>C did not map to a codon.
Sequencing variant TCGA-BP-4960-01A-01D-1462-08 chr15:66797732 A>C did not map to a codon.
Sequencing variant TCGA-BP-4967-01A-01D-1462-08 chr19:53926629 C>T did not map to a codon.
Sequencing variant TCGA-BP-4967-01A-01D-1462-08 chr19:53926629 C>T did not map to a codon.
Sequencing variant TCGA-BP-4976-01A-01D-1462-08 chr15:44087847 G>T did not map to a codon.
Sequencing variant TCGA-BP-4982-01A-01D-1462-08 chr3:112732115 T>C did not map to a codon.
Sequencing variant TCGA-BP-4983-01A-01D-1462-08 chr7:86811527 C>G did not map to a codon.
Sequencing variant TCGA-BP-4989-01A-01D-1462-08 chr1:169076144 C>T maps to NM_001677.3 G26G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4989-01A-01D-1462-08 chr1:169076144 C>T maps to NM_001677.3 G26G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4998-01A-01D-1462-08 chr6:4125470 G>T did not map to a codon.
Sequencing variant TCGA-BP-5004-01A-01D-1462-08 chr15:42678048 G>T did not map to a codon.
Sequencing variant TCGA-BP-5006-01A-01D-1462-08 chr2:27851882 C>A did not map to a codon.
Sequencing variant TCGA-BP-5168-01A-01D-1421-08 chr9:116171063 C>T did not map to a codon.
Sequencing variant TCGA-BP-5168-01A-01D-1421-08 chr14:21944785 C>T did not map to a codon.
Sequencing variant TCGA-BP-5168-01A-01D-1421-08 chr20:656173 G>A maps to NM_033129.3 T24T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5168-01A-01D-1421-08 chr20:656173 G>A maps to NM_033129.3 T24T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5170-01A-01D-1429-08 chr1:167887489 A>T did not map to a codon.
Sequencing variant TCGA-BP-5173-01A-01D-1429-08 chrX:151896333 G>A did not map to a codon.
Sequencing variant TCGA-BP-5173-01A-01D-1429-08 chrX:151896333 G>A did not map to a codon.
Sequencing variant TCGA-BP-5175-01A-01D-1429-08 chr15:59417124 T>C did not map to a codon.
Sequencing variant TCGA-BP-5175-01A-01D-1429-08 chr15:59417124 T>C did not map to a codon.
Sequencing variant TCGA-BP-5178-01A-01D-1429-08 chr11:126146918 C>T maps to ENST00000442061 V165V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5182-01A-01D-1429-08 chr3:112724333 C>A did not map to a codon.
Sequencing variant TCGA-BP-5185-01A-01D-1429-08 chr17:74077511 A>G did not map to a codon.
Sequencing variant TCGA-BP-5187-01A-01D-1429-08 chr17:263665 C>A maps to NM_001013672.4 G344G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5187-01A-01D-1429-08 chr17:263665 C>A maps to NM_001013672.4 G344G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-5195-01A-02D-1429-08 chr19:53116220 T>A did not map to a codon.
Sequencing variant TCGA-BP-5200-01A-01D-1429-08 chr16:89753116 G>C did not map to a codon.
Sequencing variant TCGA-CJ-4897-01A-03D-1429-08 chrX:135961596 T>C did not map to a codon.
Sequencing variant TCGA-CJ-4902-01A-01D-1429-08 chr20:15948280 T>C did not map to a codon.
Sequencing variant TCGA-CJ-4903-01A-01D-1429-08 chr1:33476403 T>G did not map to a codon.
Sequencing variant TCGA-CJ-4904-01A-02D-1429-08 chr6:1313356 T>C maps to NM_033260.3 L140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4905-01A-02D-1429-08 chr1:169100954 A>T did not map to a codon.
Sequencing variant TCGA-CJ-4905-01A-02D-1429-08 chr1:169100954 A>T did not map to a codon.
Sequencing variant TCGA-CJ-4912-01A-01D-1429-08 chr13:50489190 A>G did not map to a codon.
Sequencing variant TCGA-CJ-4912-01A-01D-1429-08 chr2:219127644 G>T maps to NM_170699.2 L66L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4918-01A-01D-1429-08 chr7:127031544 G>T did not map to a codon.
Sequencing variant TCGA-CJ-4918-01A-01D-1429-08 chr7:127031545 T>A did not map to a codon.
Sequencing variant TCGA-CZ-4853-01A-01D-1429-08 chr1:148017562 A>G maps to ENST00000310701 S245S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4853-01A-01D-1429-08 chr1:148017562 A>G maps to ENST00000310701 S245S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-4859-01A-02D-1429-08 chr12:6979621 C>T did not map to a codon.
Sequencing variant TCGA-CZ-5986-01A-11D-1669-08 chr7:6048686 G>C did not map to a codon.
Sequencing variant TCGA-AK-3429-01A-02D-1386-10 chr9:95069938 T>C did not map to a codon.
Sequencing variant TCGA-AK-3429-01A-02D-1386-10 chr3:47058512 G>A did not map to a codon.
Sequencing variant TCGA-AK-3429-01A-02D-1386-10 chr3:47058512 G>A did not map to a codon.
Sequencing variant TCGA-B0-4706-01A-01D-1501-10 chr3:47108556 T>A did not map to a codon.
Sequencing variant TCGA-B0-4710-01A-01D-1501-10 chr3:71804018 G>T maps to NM_018971.1 L273L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4712-01A-01D-1501-10 chr14:50779729 C>T did not map to a codon.
Sequencing variant TCGA-B0-4815-01A-01D-1501-10 chr21:33979946 A>G did not map to a codon.
Sequencing variant TCGA-B0-4816-01A-01D-1501-10 chr20:13769226 T>C did not map to a codon.
Sequencing variant TCGA-B0-4852-01A-01D-1501-10 chr2:87015622 G>A did not map to a codon.
Sequencing variant TCGA-B0-5080-01A-01D-1501-10 chr11:64988530 C>T maps to ENST00000454680 T233T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5399-01A-01D-1501-10 chr9:95070140 G>A did not map to a codon.
Sequencing variant TCGA-B0-5399-01A-01D-1501-10 chr3:47127736 C>T maps to NM_014159.6 W1782*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5399-01A-01D-1501-10 chr3:47127736 C>T maps to NM_014159.6 W1782*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5402-01A-01D-1501-10 chr12:123005001 A>T did not map to a codon.
Sequencing variant TCGA-B0-5694-01A-11D-1534-10 chr19:918607 C>T maps to NM_032551.4 Y103Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5694-01A-11D-1534-10 chr19:918607 C>T maps to NM_032551.4 Y103Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5694-01A-11D-1534-10 chr7:23749853 C>T did not map to a codon.
Sequencing variant TCGA-B0-5694-01A-11D-1534-10 chr7:23749853 C>T did not map to a codon.
Sequencing variant TCGA-B0-5696-01A-11D-1534-10 chr19:41945824 G>T did not map to a codon.
Sequencing variant TCGA-B0-5696-01A-11D-1534-10 chr6:44240819 C>T maps to NM_001137560.1 P51P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-5707-01A-11D-1534-10 chr3:196674754 C>T maps to NM_025163.2 W338*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B2-5633-01A-01D-1534-10 chr12:56194627 T>A did not map to a codon.
Sequencing variant TCGA-B8-4143-01A-01D-1806-10 chr1:10494764 T>C did not map to a codon.
Sequencing variant TCGA-B8-4154-01A-01D-1251-10 chrX:151896049 G>T did not map to a codon.
Sequencing variant TCGA-B8-4154-01A-01D-1251-10 chrX:151896049 G>T did not map to a codon.
Sequencing variant TCGA-B8-5549-01A-01D-1534-10 chr16:89757046 G>T did not map to a codon.
Sequencing variant TCGA-B8-5549-01A-01D-1534-10 chr17:4837665 A>C maps to NM_000173.5 T589T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-5549-01A-01D-1534-10 chr17:4837665 A>C maps to NM_000173.5 T589T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4161-01A-02D-1386-10 chr19:1369579 C>T did not map to a codon.
Sequencing variant TCGA-BP-4161-01A-02D-1386-10 chr12:117513064 G>T did not map to a codon.
Sequencing variant TCGA-BP-4162-01A-02D-1386-10 chr7:74298856 T>C did not map to a codon.
Sequencing variant TCGA-BP-4162-01A-02D-1386-10 chr7:74298856 T>C did not map to a codon.
Sequencing variant TCGA-BP-4163-01A-02D-1386-10 chr2:39993263 A>G did not map to a codon.
Sequencing variant TCGA-BP-4770-01A-01D-1501-10 chr20:47605056 T>A maps to NM_006420.2 Y797*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4634-01A-02D-1386-10 chr1:71328116 A>T did not map to a codon.
Sequencing variant TCGA-CJ-4636-01A-02D-1386-10 chr2:27861048 T>A did not map to a codon.
Sequencing variant TCGA-CJ-4637-01A-02D-1386-10 chr7:23750184 C>A did not map to a codon.
Sequencing variant TCGA-CJ-4637-01A-02D-1386-10 chr7:23750184 C>A did not map to a codon.
Sequencing variant TCGA-CJ-4639-01A-02D-1386-10 chr12:52216198 T>G did not map to a codon.
Sequencing variant TCGA-CJ-4639-01A-02D-1386-10 chr4:95503858 T>G did not map to a codon.
Sequencing variant TCGA-CJ-5677-01A-11D-1534-10 chr7:151168453 G>C did not map to a codon.
Sequencing variant TCGA-CJ-5683-01A-11D-1534-10 chr19:52723428 G>A did not map to a codon.
Sequencing variant TCGA-CJ-5683-01A-11D-1534-10 chr21:33058543 A>C did not map to a codon.
Sequencing variant TCGA-CW-5581-01A-02D-1534-10 chr15:42701962 C>G did not map to a codon.
Sequencing variant TCGA-CW-5583-01A-02D-1534-10 chr14:32561315 G>T maps to NM_001030055.1 E481*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CW-5583-01A-02D-1534-10 chr1:169665717 G>A did not map to a codon.
Sequencing variant TCGA-CW-5591-01A-01D-1534-10 chr1:201398086 A>T did not map to a codon.
Sequencing variant TCGA-CW-5591-01A-01D-1534-10 chr1:201398086 A>T did not map to a codon.
Sequencing variant TCGA-CZ-4865-01A-02D-1501-10 chr11:61135390 T>A did not map to a codon.
Sequencing variant TCGA-CZ-5460-01A-01D-1501-10 chr1:182825718 T>C did not map to a codon.
Sequencing variant TCGA-CZ-5460-01A-01D-1501-10 chr6:24719010 G>T did not map to a codon.
Sequencing variant TCGA-CZ-5460-01A-01D-1501-10 chr6:24719010 G>T did not map to a codon.
Sequencing variant TCGA-CZ-5461-01A-01D-1501-10 chr6:3152713 T>G did not map to a codon.
Sequencing variant TCGA-CZ-5461-01A-01D-1501-10 chr2:218935327 C>A did not map to a codon.
Sequencing variant TCGA-CZ-5467-01A-01D-1501-10 chr6:56469945 C>T maps to ENST00000361203 W2949*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CZ-5467-01A-01D-1501-10 chr2:48692135 A>G did not map to a codon.
Sequencing variant TCGA-CZ-5468-01A-01D-1501-10 chr12:31850289 A>G did not map to a codon.
Sequencing variant TCGA-CZ-5468-01A-01D-1501-10 chr2:178095479 A>T did not map to a codon.
Sequencing variant TCGA-CZ-5468-01A-01D-1501-10 chr2:178095479 A>T did not map to a codon.
Sequencing variant TCGA-DV-5569-01A-01D-1534-10 chr5:180431708 C>G did not map to a codon.
Sequencing variant TCGA-AK-3454-01A-02D-1361-10 chrX:101581403 A>G maps to NM_022053.1 A619A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AK-3454-01A-02D-1361-10 chrX:101581403 A>G maps to NM_022053.1 A619A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4694-01A-01D-1361-10 chr19:56614565 G>C maps to NM_001002836.2 A7A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4714-01A-01D-1361-10 chr19:33792420 G>A maps to NM_004364.3 R300R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4824-01A-01D-1361-10 chr16:28736316 T>G maps to NM_003752.3 T462T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B0-4839-01A-01D-1373-10 chr3:47122555 C>A did not map to a codon.
Sequencing variant TCGA-B0-4843-01A-01D-1361-10 chr22:24300633 G>T maps to NM_000854.3 P121P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B8-4622-01A-02D-1361-10 chr10:47158881 G>A maps to ENST00000414655 G379G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4173-01A-02D-1366-10 chr19:33792386 G>A maps to NM_004364.3 Q312*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4174-01A-02D-1366-10 chr22:21742388 G>C maps to NM_001128635.1 V1414V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4338-01A-01D-1806-10 chr1:12977625 A>G maps to NM_001012277.1 T38T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BP-4774-01A-01D-1366-10 chrX:101615545 C>T maps to NM_022053.1 A619A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4881-01A-01D-1373-10 chr9:40704226 C>T maps to NM_001083124.1 D628D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4881-01A-01D-1373-10 chr9:40704226 C>T maps to NM_001083124.1 D628D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CJ-4889-01A-01D-1373-10 chr19:33792411 G>T maps to NM_004364.3 A303A. Only missense variants will be evaluated by CHASM.
