5995 NP_109597 Q69K not found in SNVbox database
6015 NP_109597 R485Q not found in SNVbox database
6140 NP_109597 R262Q not found in SNVbox database
7217 NP_705833 T658A not found in SNVbox database
7880 NP_705833 E56K not found in SNVbox database
8777 NP_109597 L263I not found in SNVbox database
9067 NP_705833 S67P not found in SNVbox database
9130 NP_705833 G653D not found in SNVbox database
200 NP_705833 A723E not found in SNVbox database
1205 NP_705833 L592R not found in SNVbox database
1374 NP_705833 F692Y not found in SNVbox database
1390 NP_705833 R185C not found in SNVbox database
1586 NP_705833 R934Q not found in SNVbox database
2481 NP_705833 L19I not found in SNVbox database
2854 NP_705833 Q239R not found in SNVbox database
3321 NP_705833 L829V not found in SNVbox database
4435 NP_705833 G386D not found in SNVbox database
4546 NP_705833 A83T not found in SNVbox database
4701 NP_705833 E56K not found in SNVbox database
4870 NP_705833 M86T not found in SNVbox database
Sequencing variant TCGA-KL-8323-01A-21D-2310-10 chr15:88727493 G>A maps to NM_001012338.1 N95N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8323-01A-21D-2310-10 chr15:88727493 G>A maps to NM_001012338.1 N95N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8323-01A-21D-2310-10 chr3:38040854 C>T maps to NM_015873.3 D369D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8323-01A-21D-2310-10 chr3:38040854 C>T maps to NM_015873.3 D369D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8323-01A-21D-2310-10 chrX:64137683 C>T maps to NM_018684.2 P218P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8323-01A-21D-2310-10 chrX:64137683 C>T maps to NM_018684.2 P218P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8323-01A-21D-2310-10 chr22:32000341 C>T maps to NM_001007467.1 D643D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8323-01A-21D-2310-10 chr22:32000341 C>T maps to NM_001007467.1 D643D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8323-01A-21D-2310-10 chr19:1084343 A>G maps to NM_012292.2 R1021R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8323-01A-21D-2310-10 chr19:1084343 A>G maps to NM_012292.2 R1021R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8323-01A-21D-2310-10 chr10:16967261 G>A maps to NM_001081.3 I2208I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8323-01A-21D-2310-10 chr10:16967261 G>A maps to NM_001081.3 I2208I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8323-01A-21D-2310-10 chr17:19284373 C>T maps to NM_139034.2 A284A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8323-01A-21D-2310-10 chr17:19284373 C>T maps to NM_139034.2 A284A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8323-01A-21D-2310-10 chr17:78082575 G>A maps to NM_001079804.1 P425P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8323-01A-21D-2310-10 chr17:78082575 G>A maps to NM_001079804.1 P425P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8324-01A-11D-2310-10 chr4:187527259 G>T maps to ENST00000260147 P3441P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8324-01A-11D-2310-10 chr4:187527259 G>T maps to ENST00000260147 P3441P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8324-01A-11D-2310-10 chr8:99440359 G>A maps to NM_020697.2 S51S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8324-01A-11D-2310-10 chr8:99440359 G>A maps to NM_020697.2 S51S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8324-01A-11D-2310-10 chr3:38739265 G>A maps to NM_006514.2 S1815S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8324-01A-11D-2310-10 chr3:38739265 G>A maps to NM_006514.2 S1815S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8324-01A-11D-2310-10 chrX:130219619 C>A maps to NM_144967.3 P338P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8324-01A-11D-2310-10 chrX:130219619 C>A maps to NM_144967.3 P338P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8324-01A-11D-2310-10 chr11:30601905 A>G maps to NM_001584.2 I5I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8324-01A-11D-2310-10 chr11:30601905 A>G maps to NM_001584.2 I5I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8324-01A-11D-2310-10 chr4:123663958 T>C maps to NM_152618.2 C304C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8324-01A-11D-2310-10 chr4:123663958 T>C maps to NM_152618.2 C304C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8324-01A-11D-2310-10 chr11:5969445 C>A maps to NM_001003443.2 A290A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8324-01A-11D-2310-10 chr11:5969445 C>A maps to NM_001003443.2 A290A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8324-01A-11D-2310-10 chr11:5510049 T>C maps to NM_001005163.2 Y38Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8324-01A-11D-2310-10 chr11:5510049 T>C maps to NM_001005163.2 Y38Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8324-01A-11D-2310-10 chr2:11922577 C>T maps to ENST00000396099 P409P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8324-01A-11D-2310-10 chr2:11922577 C>T maps to ENST00000396099 P409P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8324-01A-11D-2310-10 chr5:95746663 G>A maps to NM_000439.4 F303F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8324-01A-11D-2310-10 chr5:95746663 G>A maps to NM_000439.4 F303F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8324-01A-11D-2310-10 chr12:120510406 G>A maps to NM_207311.2 T394T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8324-01A-11D-2310-10 chr12:120510406 G>A maps to NM_207311.2 T394T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8324-01A-11D-2310-10 chr4:46976324 C>T maps to NM_000809.2 P215P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8324-01A-11D-2310-10 chr4:46976324 C>T maps to NM_000809.2 P215P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8324-01A-11D-2310-10 chr7:116411694 A>G maps to NM_001127500.1 R976R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8324-01A-11D-2310-10 chr7:116411694 A>G maps to NM_001127500.1 R976R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8324-01A-11D-2310-10 chr5:140569000 T>C maps to NM_019119.3 S703S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8324-01A-11D-2310-10 chr5:140569000 T>C maps to NM_019119.3 S703S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8324-01A-11D-2310-10 chrX:152956888 C>T maps to NM_005629.3 T175T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8324-01A-11D-2310-10 chrX:152956888 C>T maps to NM_005629.3 T175T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8324-01A-11D-2310-10 chr16:30435592 C>T maps to NM_024096.1 A158A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8324-01A-11D-2310-10 chr16:30435592 C>T maps to NM_024096.1 A158A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8324-01A-11D-2310-10 chr11:17408681 T>C maps to NM_000525.3 V319V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8324-01A-11D-2310-10 chr11:17408681 T>C maps to NM_000525.3 V319V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8324-01A-11D-2310-10 chr13:52686430 T>C maps to NM_199289.1 Q95Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8324-01A-11D-2310-10 chr13:52686430 T>C maps to NM_199289.1 Q95Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8324-01A-11D-2310-10 chr10:129899863 T>C maps to NM_002417.4 E3121E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8324-01A-11D-2310-10 chr10:129899863 T>C maps to NM_002417.4 E3121E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8324-01A-11D-2310-10 chr1:100353593 A>G maps to ENST00000311030 E915E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8324-01A-11D-2310-10 chr1:100353593 A>G maps to ENST00000311030 E915E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8324-01A-11D-2310-10 chr17:57775084 C>T maps to ENST00000409433 Q86Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8324-01A-11D-2310-10 chr17:57775084 C>T maps to ENST00000409433 Q86Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8324-01A-11D-2310-10 chrX:138698452 A>G maps to ENST00000370578 S538S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8324-01A-11D-2310-10 chrX:138698452 A>G maps to ENST00000370578 S538S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8324-01A-11D-2310-10 chr15:31779680 G>A maps to ENST00000382902 D420D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8324-01A-11D-2310-10 chr15:31779680 G>A maps to ENST00000382902 D420D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8325-01A-11D-2310-10 chr12:2783695 C>T maps to NM_001129829.1 F1613F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8325-01A-11D-2310-10 chr12:2783695 C>T maps to NM_001129829.1 F1613F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8325-01A-11D-2310-10 chr8:27779571 G>A maps to NM_173833.5 G144G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8325-01A-11D-2310-10 chr8:27779571 G>A maps to NM_173833.5 G144G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8325-01A-11D-2310-10 chr3:37523096 A>G maps to NM_002207.2 E181E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8325-01A-11D-2310-10 chr3:37523096 A>G maps to NM_002207.2 E181E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8325-01A-11D-2310-10 chr7:33028127 G>A maps to NM_007270.3 R301R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8325-01A-11D-2310-10 chr7:33028127 G>A maps to NM_007270.3 R301R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8325-01A-11D-2310-10 chr20:39708802 A>G maps to NM_003286.2 R138R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8325-01A-11D-2310-10 chr20:39708802 A>G maps to NM_003286.2 R138R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8325-01A-11D-2310-10 chr15:101427814 C>A maps to NM_000693.2 A81A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8325-01A-11D-2310-10 chr15:101427814 C>A maps to NM_000693.2 A81A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8325-01A-11D-2310-10 chr9:103004867 C>T maps to NM_014425.2 V271V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8325-01A-11D-2310-10 chr9:103004867 C>T maps to NM_014425.2 V271V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8325-01A-11D-2310-10 chr3:185783821 A>G maps to NM_004454.2 P230P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8325-01A-11D-2310-10 chr3:185783821 A>G maps to NM_004454.2 P230P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8325-01A-11D-2310-10 chr14:68052684 C>A maps to NM_020715.2 Y1268*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8325-01A-11D-2310-10 chr14:68052684 C>A maps to NM_020715.2 Y1268*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8325-01A-11D-2310-10 chr3:77526692 C>T maps to ENST00000332191 R173*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8325-01A-11D-2310-10 chr3:77526692 C>T maps to ENST00000332191 R173*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8325-01A-11D-2310-10 chr13:61989198 T>G maps to NM_022843.3 L31L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8325-01A-11D-2310-10 chr13:61989198 T>G maps to NM_022843.3 L31L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8325-01A-11D-2310-10 chr17:43215197 G>A did not map to a codon.
Sequencing variant TCGA-KL-8325-01A-11D-2310-10 chr17:43215197 G>A did not map to a codon.
Sequencing variant TCGA-KL-8325-01A-11D-2310-10 chr3:183028732 T>C maps to NM_015078.2 Q321Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8325-01A-11D-2310-10 chr3:183028732 T>C maps to NM_015078.2 Q321Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8325-01A-11D-2310-10 chr12:7802196 C>T maps to NM_001644.3 P219P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8325-01A-11D-2310-10 chr12:7802196 C>T maps to NM_001644.3 P219P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8325-01A-11D-2310-10 chr22:20302560 C>T did not map to a codon.
Sequencing variant TCGA-KL-8325-01A-11D-2310-10 chr22:20302560 C>T did not map to a codon.
Sequencing variant TCGA-KL-8326-01A-11D-2310-10 chr11:123814284 C>T maps to NM_001005187.1 T87T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8326-01A-11D-2310-10 chr11:123814284 C>T maps to NM_001005187.1 T87T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8326-01A-11D-2310-10 chr14:75301974 G>A maps to NM_019589.2 W2101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8326-01A-11D-2310-10 chr14:75301974 G>A maps to NM_019589.2 W2101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8326-01A-11D-2310-10 chr15:69320700 C>T maps to NM_024505.3 I107I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8326-01A-11D-2310-10 chr15:69320700 C>T maps to NM_024505.3 I107I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8326-01A-11D-2310-10 chr9:128246856 T>G maps to NM_001006617.1 R358R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8326-01A-11D-2310-10 chr9:128246856 T>G maps to NM_001006617.1 R358R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8326-01A-11D-2310-10 chr7:128483326 C>T maps to NM_001458.4 H865H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8326-01A-11D-2310-10 chr7:128483326 C>T maps to NM_001458.4 H865H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8326-01A-11D-2310-10 chr15:49052451 A>T maps to NM_001194998.1 A858A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8326-01A-11D-2310-10 chr15:49052451 A>T maps to NM_001194998.1 A858A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8326-01A-11D-2310-10 chr7:116759715 T>C maps to ENST00000323984 S112S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8326-01A-11D-2310-10 chr7:116759715 T>C maps to ENST00000323984 S112S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8326-01A-11D-2310-10 chrX:91090724 G>T maps to NM_032968.3 L74L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8326-01A-11D-2310-10 chrX:91090724 G>T maps to NM_032968.3 L74L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8326-01A-11D-2310-10 chr13:36167553 A>G maps to ENST00000400445 R2422R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8326-01A-11D-2310-10 chr13:36167553 A>G maps to ENST00000400445 R2422R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8326-01A-11D-2310-10 chr6:147646105 C>A maps to NM_001127715.1 S605*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8326-01A-11D-2310-10 chr6:147646105 C>A maps to NM_001127715.1 S605*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8326-01A-11D-2310-10 chr2:239090746 A>C maps to NM_030768.2 Y265*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8326-01A-11D-2310-10 chr2:239090746 A>C maps to NM_030768.2 Y265*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8326-01A-11D-2310-10 chrX:44703527 C>T maps to NM_022076.3 A50A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8326-01A-11D-2310-10 chrX:44703527 C>T maps to NM_022076.3 A50A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8326-01A-11D-2310-10 chr2:88383882 C>T maps to NM_198274.3 L62L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8326-01A-11D-2310-10 chr2:88383882 C>T maps to NM_198274.3 L62L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8326-01A-11D-2310-10 chr6:30139747 C>T maps to NM_033229.2 G340G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8326-01A-11D-2310-10 chr6:30139747 C>T maps to NM_033229.2 G340G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8327-01A-11D-2310-10 chrX:17745122 C>A maps to NM_198270.2 S945*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8327-01A-11D-2310-10 chrX:17745122 C>A maps to NM_198270.2 S945*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8327-01A-11D-2310-10 chr19:34710314 T>G maps to NM_001114093.1 A267A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8327-01A-11D-2310-10 chr19:34710314 T>G maps to NM_001114093.1 A267A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8327-01A-11D-2310-10 chr17:37657500 A>G did not map to a codon.
Sequencing variant TCGA-KL-8327-01A-11D-2310-10 chr17:37657500 A>G did not map to a codon.
Sequencing variant TCGA-KL-8327-01A-11D-2310-10 chr17:9808239 G>A maps to NM_002903.2 Y86Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8327-01A-11D-2310-10 chr17:9808239 G>A maps to NM_002903.2 Y86Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8327-01A-11D-2310-10 chr4:47667068 G>A maps to NM_006587.2 G523G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8327-01A-11D-2310-10 chr4:47667068 G>A maps to NM_006587.2 G523G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8327-01A-11D-2310-10 chrX:23874421 T>C maps to NM_024122.4 Q186Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8327-01A-11D-2310-10 chrX:23874421 T>C maps to NM_024122.4 Q186Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8327-01A-11D-2310-10 chr1:231471904 G>A maps to NM_175876.3 C529C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8327-01A-11D-2310-10 chr1:231471904 G>A maps to NM_175876.3 C529C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8328-01A-11D-2310-10 chr2:149226186 G>A maps to ENST00000404807 A225A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8328-01A-11D-2310-10 chr2:149226186 G>A maps to ENST00000404807 A225A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8328-01A-11D-2310-10 chr1:32101117 G>A maps to NM_012392.3 C10C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8328-01A-11D-2310-10 chr1:32101117 G>A maps to NM_012392.3 C10C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8328-01A-11D-2310-10 chr4:88986630 C>T maps to NM_000297.2 R742*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8328-01A-11D-2310-10 chr4:88986630 C>T maps to NM_000297.2 R742*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8328-01A-11D-2310-10 chr9:2056811 T>A maps to NM_003070.3 I438I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8328-01A-11D-2310-10 chr9:2056811 T>A maps to NM_003070.3 I438I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8328-01A-11D-2310-10 chr6:151673068 C>T maps to NM_005100.3 D1181D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8328-01A-11D-2310-10 chr6:151673068 C>T maps to NM_005100.3 D1181D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8328-01A-11D-2310-10 chr9:107367648 G>C maps to NM_001004481.1 S87*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8328-01A-11D-2310-10 chr9:107367648 G>C maps to NM_001004481.1 S87*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8328-01A-11D-2310-10 chr3:56649271 C>T maps to NM_001141947.1 D561D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8328-01A-11D-2310-10 chr3:56649271 C>T maps to NM_001141947.1 D561D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8328-01A-11D-2310-10 chr15:81216981 C>T maps to NM_018689.1 N741N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8328-01A-11D-2310-10 chr15:81216981 C>T maps to NM_018689.1 N741N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8328-01A-11D-2310-10 chr2:168100983 C>T maps to NM_152381.5 Q1028*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8328-01A-11D-2310-10 chr2:168100983 C>T maps to NM_152381.5 Q1028*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8328-01A-11D-2310-10 chr18:72234589 T>C maps to NM_032649.5 I226I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8328-01A-11D-2310-10 chr18:72234589 T>C maps to NM_032649.5 I226I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8328-01A-11D-2310-10 chr7:150932431 C>T maps to NM_019015.1 Q188*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8328-01A-11D-2310-10 chr7:150932431 C>T maps to NM_019015.1 Q188*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8328-01A-11D-2310-10 chrX:15657839 A>G maps to NM_020665.4 N119N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8328-01A-11D-2310-10 chrX:15657839 A>G maps to NM_020665.4 N119N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8328-01A-11D-2310-10 chr5:177421250 C>T maps to NM_006261.4 P66P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8328-01A-11D-2310-10 chr5:177421250 C>T maps to NM_006261.4 P66P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8328-01A-11D-2310-10 chr10:124457697 C>A maps to NM_001010912.1 E187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8328-01A-11D-2310-10 chr10:124457697 C>A maps to NM_001010912.1 E187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8328-01A-11D-2310-10 chr3:77571940 C>T maps to ENST00000332191 D274D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8328-01A-11D-2310-10 chr3:77571940 C>T maps to ENST00000332191 D274D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8329-01A-11D-2310-10 chr4:155219312 C>T maps to NM_017639.3 S1596S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8329-01A-11D-2310-10 chr4:155219312 C>T maps to NM_017639.3 S1596S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8329-01A-11D-2310-10 chr6:36652170 C>A maps to ENST00000448526 S132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8329-01A-11D-2310-10 chr6:36652170 C>A maps to ENST00000448526 S132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8329-01A-11D-2310-10 chr11:65048557 G>A maps to NM_002689.2 S280S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8329-01A-11D-2310-10 chr11:65048557 G>A maps to NM_002689.2 S280S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8329-01A-11D-2310-10 chr6:170627575 C>T maps to NM_032448.1 P366P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8329-01A-11D-2310-10 chr6:170627575 C>T maps to NM_032448.1 P366P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8329-01A-11D-2310-10 chr12:105504981 C>T maps to NM_015275.1 D47D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8329-01A-11D-2310-10 chr12:105504981 C>T maps to NM_015275.1 D47D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8329-01A-11D-2310-10 chr7:27672040 A>G maps to NM_152740.3 V92V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8329-01A-11D-2310-10 chr7:27672040 A>G maps to NM_152740.3 V92V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8329-01A-11D-2310-10 chr6:151671481 A>G maps to NM_005100.3 E652E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8329-01A-11D-2310-10 chr6:151671481 A>G maps to NM_005100.3 E652E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8329-01A-11D-2310-10 chr3:29925684 T>G maps to NM_001003793.2 A259A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8329-01A-11D-2310-10 chr3:29925684 T>G maps to NM_001003793.2 A259A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8329-01A-11D-2310-10 chr2:99449444 C>T maps to NM_207362.2 T85T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8329-01A-11D-2310-10 chr2:99449444 C>T maps to NM_207362.2 T85T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8329-01A-11D-2310-10 chr4:2952918 T>C maps to NM_003703.1 K308K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8329-01A-11D-2310-10 chr4:2952918 T>C maps to NM_003703.1 K308K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8329-01A-11D-2310-10 chr17:7577593 A>T maps to NM_001126112.1 C229*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8329-01A-11D-2310-10 chr17:7577593 A>T maps to NM_001126112.1 C229*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8329-01A-11D-2310-10 chrX:53222785 A>G maps to NM_004187.3 L1384L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8329-01A-11D-2310-10 chrX:53222785 A>G maps to NM_004187.3 L1384L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8329-01A-11D-2310-10 chr11:17121507 A>G maps to NM_002645.2 P1339P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8329-01A-11D-2310-10 chr11:17121507 A>G maps to NM_002645.2 P1339P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8330-01A-11D-2310-10 chr11:102709282 T>G maps to NM_002422.3 R410R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8330-01A-11D-2310-10 chr11:102709282 T>G maps to NM_002422.3 R410R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8330-01A-11D-2310-10 chr15:52562049 G>A maps to NM_018728.3 A280A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8330-01A-11D-2310-10 chr15:52562049 G>A maps to NM_018728.3 A280A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8330-01A-11D-2310-10 chr1:120462210 A>G maps to NM_024408.2 A1835A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8330-01A-11D-2310-10 chr1:120462210 A>G maps to NM_024408.2 A1835A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8330-01A-11D-2310-10 chr2:224462647 C>T maps to NM_003469.4 S451S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8330-01A-11D-2310-10 chr2:224462647 C>T maps to NM_003469.4 S451S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8330-01A-11D-2310-10 chr4:69978238 C>T maps to NM_001074.2 R459*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8330-01A-11D-2310-10 chr4:69978238 C>T maps to NM_001074.2 R459*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8330-01A-11D-2310-10 chr2:210683985 G>T did not map to a codon.
Sequencing variant TCGA-KL-8330-01A-11D-2310-10 chr2:210683985 G>T did not map to a codon.
Sequencing variant TCGA-KL-8330-01A-11D-2310-10 chr19:53619569 G>T maps to NM_001164309.1 S44S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8330-01A-11D-2310-10 chr19:53619569 G>T maps to NM_001164309.1 S44S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8330-01A-11D-2310-10 chr1:85718362 A>G maps to NM_198077.3 T166T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8330-01A-11D-2310-10 chr1:85718362 A>G maps to NM_198077.3 T166T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8330-01A-11D-2310-10 chr18:19379922 A>G maps to NM_020774.2 R453R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8330-01A-11D-2310-10 chr18:19379922 A>G maps to NM_020774.2 R453R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8330-01A-11D-2310-10 chr5:140857473 C>T maps to NM_002588.2 D597D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8330-01A-11D-2310-10 chr5:140857473 C>T maps to NM_002588.2 D597D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8330-01A-11D-2310-10 chr12:21918736 G>T maps to NM_004982.2 R399R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8330-01A-11D-2310-10 chr12:21918736 G>T maps to NM_004982.2 R399R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8331-01A-11D-2310-10 chrX:151303810 G>A maps to NM_021048.3 P94P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8331-01A-11D-2310-10 chrX:151303810 G>A maps to NM_021048.3 P94P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8331-01A-11D-2310-10 chr17:19823385 T>C maps to NM_007202.2 R599R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8331-01A-11D-2310-10 chr17:19823385 T>C maps to NM_007202.2 R599R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8331-01A-11D-2310-10 chrX:99661924 G>A maps to NM_001184880.1 N557N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8331-01A-11D-2310-10 chrX:99661924 G>A maps to NM_001184880.1 N557N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8331-01A-11D-2310-10 chr10:124399734 C>T maps to ENST00000368915 V2374V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8331-01A-11D-2310-10 chr10:124399734 C>T maps to ENST00000368915 V2374V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8331-01A-11D-2310-10 chrX:152091353 G>T did not map to a codon.
Sequencing variant TCGA-KL-8331-01A-11D-2310-10 chrX:152091353 G>T did not map to a codon.
Sequencing variant TCGA-KL-8331-01A-11D-2310-10 chr16:69786143 C>T maps to NM_014062.1 K109K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8331-01A-11D-2310-10 chr16:69786143 C>T maps to NM_014062.1 K109K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8331-01A-11D-2310-10 chrX:150817085 G>A did not map to a codon.
Sequencing variant TCGA-KL-8331-01A-11D-2310-10 chrX:150817085 G>A did not map to a codon.
Sequencing variant TCGA-KL-8331-01A-11D-2310-10 chr19:51828627 G>A maps to NM_001101372.1 S140S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8331-01A-11D-2310-10 chr19:51828627 G>A maps to NM_001101372.1 S140S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8331-01A-11D-2310-10 chr21:30963506 C>T maps to ENST00000327783 T430T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8331-01A-11D-2310-10 chr21:30963506 C>T maps to ENST00000327783 T430T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8331-01A-11D-2310-10 chr7:5342509 C>T maps to NM_153247.2 D511D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8331-01A-11D-2310-10 chr7:5342509 C>T maps to NM_153247.2 D511D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8331-01A-11D-2310-10 chr6:30623373 C>T maps to NM_003587.4 K833K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8331-01A-11D-2310-10 chr6:30623373 C>T maps to NM_003587.4 K833K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8331-01A-11D-2310-10 chr12:53517644 C>T maps to NM_003578.3 C502C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8331-01A-11D-2310-10 chr12:53517644 C>T maps to NM_003578.3 C502C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8332-01A-11D-2310-10 chr16:50348997 T>A maps to NM_001114.3 T1015T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8332-01A-11D-2310-10 chr16:50348997 T>A maps to NM_001114.3 T1015T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8332-01A-11D-2310-10 chr11:56237918 G>A maps to NM_001004742.1 R19*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8332-01A-11D-2310-10 chr11:56237918 G>A maps to NM_001004742.1 R19*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8332-01A-11D-2310-10 chr13:19751675 G>A maps to NM_006001.1 F149F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8332-01A-11D-2310-10 chr13:19751675 G>A maps to NM_006001.1 F149F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8332-01A-11D-2310-10 chr2:131813239 C>T maps to NM_001009993.2 V61V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8332-01A-11D-2310-10 chr2:131813239 C>T maps to NM_001009993.2 V61V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8332-01A-11D-2310-10 chr17:2228034 A>G maps to NM_018128.4 P703P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8332-01A-11D-2310-10 chr17:2228034 A>G maps to NM_018128.4 P703P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8332-01A-11D-2310-10 chr16:67325 G>A maps to ENST00000326592 V183V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8332-01A-11D-2310-10 chr16:67325 G>A maps to ENST00000326592 V183V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8333-01A-11D-2310-10 chr6:84884490 T>C maps to NM_014895.2 K660K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8333-01A-11D-2310-10 chr6:84884490 T>C maps to NM_014895.2 K660K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8333-01A-11D-2310-10 chrX:51076023 G>A maps to NM_153183.2 E69E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8333-01A-11D-2310-10 chrX:51076023 G>A maps to NM_153183.2 E69E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8333-01A-11D-2310-10 chr1:248343934 T>C maps to NM_001004688.1 A216A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8333-01A-11D-2310-10 chr1:248343934 T>C maps to NM_001004688.1 A216A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8333-01A-11D-2310-10 chr7:23825128 A>G maps to NM_031414.3 E727E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8333-01A-11D-2310-10 chr7:23825128 A>G maps to NM_031414.3 E727E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8333-01A-11D-2310-10 chr2:206037068 G>A maps to ENST00000406610 Q585Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8333-01A-11D-2310-10 chr2:206037068 G>A maps to ENST00000406610 Q585Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8333-01A-11D-2310-10 chr4:1821160 G>A maps to NM_012318.2 S549S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8333-01A-11D-2310-10 chr4:1821160 G>A maps to NM_012318.2 S549S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8333-01A-11D-2310-10 chr8:22079279 G>T maps to NM_014759.3 G193G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8333-01A-11D-2310-10 chr8:22079279 G>T maps to NM_014759.3 G193G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8333-01A-11D-2310-10 chr5:177580962 G>A did not map to a codon.
Sequencing variant TCGA-KL-8333-01A-11D-2310-10 chr5:177580962 G>A did not map to a codon.
Sequencing variant TCGA-KL-8333-01A-11D-2310-10 chr11:76804732 C>T maps to ENST00000360841 I97I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8333-01A-11D-2310-10 chr11:76804732 C>T maps to ENST00000360841 I97I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8333-01A-11D-2310-10 chr8:125074106 C>T maps to NM_001039112.2 N1054N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8333-01A-11D-2310-10 chr8:125074106 C>T maps to NM_001039112.2 N1054N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8333-01A-11D-2310-10 chr2:169842724 A>C maps to NM_003742.2 T326T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8333-01A-11D-2310-10 chr2:169842724 A>C maps to NM_003742.2 T326T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8333-01A-11D-2310-10 chrX:135429077 T>C maps to NM_153834.3 A1071A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8333-01A-11D-2310-10 chrX:135429077 T>C maps to NM_153834.3 A1071A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8334-01A-11D-2310-10 chr6:36759869 A>G maps to NM_020939.1 G156G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8334-01A-11D-2310-10 chr6:36759869 A>G maps to NM_020939.1 G156G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8334-01A-11D-2310-10 chr14:76118233 T>C did not map to a codon.
Sequencing variant TCGA-KL-8334-01A-11D-2310-10 chr14:76118233 T>C did not map to a codon.
Sequencing variant TCGA-KL-8334-01A-11D-2310-10 chr19:2207666 C>T maps to ENST00000221482 I317I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8334-01A-11D-2310-10 chr19:2207666 C>T maps to ENST00000221482 I317I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8334-01A-11D-2310-10 chr2:238004480 A>G maps to NM_006710.4 G152G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8334-01A-11D-2310-10 chr2:238004480 A>G maps to NM_006710.4 G152G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8334-01A-11D-2310-10 chr12:100377919 G>A maps to NM_152788.3 G32G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8334-01A-11D-2310-10 chr12:100377919 G>A maps to NM_152788.3 G32G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8334-01A-11D-2310-10 chr1:47653016 G>A maps to NM_005764.3 V50V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8334-01A-11D-2310-10 chr1:47653016 G>A maps to NM_005764.3 V50V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8334-01A-11D-2310-10 chr12:9242557 C>T maps to NM_000014.4 E886E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8334-01A-11D-2310-10 chr12:9242557 C>T maps to NM_000014.4 E886E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8334-01A-11D-2310-10 chr2:228112293 A>G maps to NM_000091.4 G154G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8334-01A-11D-2310-10 chr2:228112293 A>G maps to NM_000091.4 G154G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8334-01A-11D-2310-10 chr5:180276229 T>C maps to NM_001172638.1 K755K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8334-01A-11D-2310-10 chr5:180276229 T>C maps to NM_001172638.1 K755K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8334-01A-11D-2310-10 chr13:49719942 A>G maps to NM_001079673.1 V283V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8334-01A-11D-2310-10 chr13:49719942 A>G maps to NM_001079673.1 V283V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8334-01A-11D-2310-10 chr19:33697007 C>T maps to NM_002333.3 P444P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8334-01A-11D-2310-10 chr19:33697007 C>T maps to NM_002333.3 P444P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8334-01A-11D-2310-10 chrX:50376363 A>G maps to NM_020717.3 Y903Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8334-01A-11D-2310-10 chrX:50376363 A>G maps to NM_020717.3 Y903Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8335-01A-11D-2310-10 chr17:7577017 C>T did not map to a codon.
Sequencing variant TCGA-KL-8335-01A-11D-2310-10 chr17:7577017 C>T did not map to a codon.
Sequencing variant TCGA-KL-8335-01A-11D-2310-10 chr9:109691640 G>A maps to NM_021224.4 E1816E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8335-01A-11D-2310-10 chr9:109691640 G>A maps to NM_021224.4 E1816E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8335-01A-11D-2310-10 chr4:100234995 G>A maps to NM_000668.4 I270I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8335-01A-11D-2310-10 chr4:100234995 G>A maps to NM_000668.4 I270I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8335-01A-11D-2310-10 chr19:37006029 G>A maps to NM_001166038.1 S37S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8335-01A-11D-2310-10 chr19:37006029 G>A maps to NM_001166038.1 S37S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8335-01A-11D-2310-10 chr11:49175929 G>A maps to NM_004476.1 R580*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8335-01A-11D-2310-10 chr11:49175929 G>A maps to NM_004476.1 R580*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8335-01A-11D-2310-10 chr9:6460651 C>T maps to NM_152896.1 L242L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8335-01A-11D-2310-10 chr9:6460651 C>T maps to NM_152896.1 L242L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8335-01A-11D-2310-10 chr11:57886019 G>A maps to NM_001005211.1 D299D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8335-01A-11D-2310-10 chr11:57886019 G>A maps to NM_001005211.1 D299D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8335-01A-11D-2310-10 chr17:6606362 G>T maps to NM_177550.3 Y214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8335-01A-11D-2310-10 chr17:6606362 G>T maps to NM_177550.3 Y214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8335-01A-11D-2310-10 chr15:26825478 A>T maps to NM_021912.4 V223V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8335-01A-11D-2310-10 chr15:26825478 A>T maps to NM_021912.4 V223V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8335-01A-11D-2310-10 chr18:13049582 A>G maps to NM_032142.3 R931R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8335-01A-11D-2310-10 chr18:13049582 A>G maps to NM_032142.3 R931R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8335-01A-11D-2310-10 chr1:245021519 G>A maps to NM_031844.2 G429G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8335-01A-11D-2310-10 chr1:245021519 G>A maps to NM_031844.2 G429G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8335-01A-11D-2310-10 chr9:94808321 C>T maps to NM_006415.2 V365V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8335-01A-11D-2310-10 chr9:94808321 C>T maps to NM_006415.2 V365V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8335-01A-11D-2310-10 chr5:5489407 G>T maps to NM_015325.1 E2256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8335-01A-11D-2310-10 chr5:5489407 G>T maps to NM_015325.1 E2256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8335-01A-11D-2310-10 chr2:220473922 C>T maps to NM_052902.2 H649H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8335-01A-11D-2310-10 chr2:220473922 C>T maps to NM_052902.2 H649H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8335-01A-11D-2310-10 chr14:51375669 G>A maps to NM_002863.4 Y727Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8335-01A-11D-2310-10 chr14:51375669 G>A maps to NM_002863.4 Y727Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8335-01A-11D-2310-10 chr10:5254674 C>T maps to NM_001818.2 R223*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8335-01A-11D-2310-10 chr10:5254674 C>T maps to NM_001818.2 R223*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8335-01A-11D-2310-10 chr12:20522511 G>A maps to NM_000921.3 A98A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8335-01A-11D-2310-10 chr12:20522511 G>A maps to NM_000921.3 A98A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8335-01A-11D-2310-10 chr4:25415321 G>A maps to ENST00000510092 R528R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8335-01A-11D-2310-10 chr4:25415321 G>A maps to ENST00000510092 R528R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8335-01A-11D-2310-10 chr8:18725566 T>C maps to ENST00000440756 Q417Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8335-01A-11D-2310-10 chr8:18725566 T>C maps to ENST00000440756 Q417Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8336-01A-11D-2310-10 chr5:37721278 A>G maps to NM_018034.2 G493G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8336-01A-11D-2310-10 chr5:37721278 A>G maps to NM_018034.2 G493G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8336-01A-11D-2310-10 chr18:28611061 C>A maps to NM_001941.3 G77G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8336-01A-11D-2310-10 chr18:28611061 C>A maps to NM_001941.3 G77G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8336-01A-11D-2310-10 chr11:1651411 G>C maps to NM_001001480.2 G114G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8336-01A-11D-2310-10 chr11:1651411 G>C maps to NM_001001480.2 G114G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8336-01A-11D-2310-10 chr16:71885172 C>T maps to NM_001137675.2 V510V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8336-01A-11D-2310-10 chr16:71885172 C>T maps to NM_001137675.2 V510V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8336-01A-11D-2310-10 chr7:150763998 T>C maps to NM_003040.3 G295G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8336-01A-11D-2310-10 chr7:150763998 T>C maps to NM_003040.3 G295G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8337-01A-11D-2310-10 chr15:69238205 A>G maps to NM_145658.3 G111G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8337-01A-11D-2310-10 chr15:69238205 A>G maps to NM_145658.3 G111G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8337-01A-11D-2310-10 chr11:2168964 C>T maps to NM_001042376.2 S160S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8337-01A-11D-2310-10 chr11:2168964 C>T maps to NM_001042376.2 S160S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8337-01A-11D-2310-10 chr18:77513732 C>T maps to NM_004715.3 S943S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8337-01A-11D-2310-10 chr18:77513732 C>T maps to NM_004715.3 S943S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8337-01A-11D-2310-10 chr2:61415631 G>T maps to NM_014709.3 R3416R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8337-01A-11D-2310-10 chr2:61415631 G>T maps to NM_014709.3 R3416R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8337-01A-11D-2310-10 chr7:7278069 A>G maps to NM_020156.3 K135K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8337-01A-11D-2310-10 chr7:7278069 A>G maps to NM_020156.3 K135K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8337-01A-11D-2310-10 chr3:16633628 C>T maps to NM_001190811.1 T274T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8337-01A-11D-2310-10 chr3:16633628 C>T maps to NM_001190811.1 T274T. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-KL-8338-01A-11D-2310-10. Mapping will be selected arbitrarily.
Alternatively spliced codon TCGA-KL-8338-01A-11D-2310-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-KL-8338-01A-11D-2310-10 chr19:55824238 C>T maps to NM_001085488.1 P230P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8338-01A-11D-2310-10 chr19:55824238 C>T maps to NM_001085488.1 P230P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8338-01A-11D-2310-10 chr5:82841437 G>T maps to NM_004385.4 V3116V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8338-01A-11D-2310-10 chr5:82841437 G>T maps to NM_004385.4 V3116V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8338-01A-11D-2310-10 chr7:80458055 G>A maps to NM_006379.2 R37*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8338-01A-11D-2310-10 chr7:80458055 G>A maps to NM_006379.2 R37*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8338-01A-11D-2310-10 chr7:99084963 G>A maps to NM_213603.2 T377T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8338-01A-11D-2310-10 chr7:99084963 G>A maps to NM_213603.2 T377T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8338-01A-11D-2310-10 chr3:179336310 T>C did not map to a codon.
Sequencing variant TCGA-KL-8338-01A-11D-2310-10 chr3:179336310 T>C did not map to a codon.
Sequencing variant TCGA-KL-8338-01A-11D-2310-10 chr1:22839531 C>T maps to NM_014870.3 T859T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8338-01A-11D-2310-10 chr1:22839531 C>T maps to NM_014870.3 T859T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8339-01A-11D-2310-10 chr17:6515463 C>T maps to NM_014804.2 K440K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8339-01A-11D-2310-10 chr17:6515463 C>T maps to NM_014804.2 K440K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8339-01A-11D-2310-10 chr1:1391259 C>T maps to NM_001039211.2 Y176Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8339-01A-11D-2310-10 chr1:1391259 C>T maps to NM_001039211.2 Y176Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8339-01A-11D-2310-10 chr19:46443969 G>A maps to NM_002516.2 L210L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8339-01A-11D-2310-10 chr19:46443969 G>A maps to NM_002516.2 L210L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8339-01A-11D-2310-10 chr2:11053757 C>T maps to NM_002236.4 I402I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8339-01A-11D-2310-10 chr2:11053757 C>T maps to NM_002236.4 I402I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8339-01A-11D-2310-10 chr10:99342110 C>T maps to NM_020349.2 Q259*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8339-01A-11D-2310-10 chr10:99342110 C>T maps to NM_020349.2 Q259*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8339-01A-11D-2310-10 chr2:129025736 T>A maps to NM_004807.2 *412L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8339-01A-11D-2310-10 chr2:129025736 T>A maps to NM_004807.2 *412L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8339-01A-11D-2310-10 chr4:56319288 C>A maps to NM_004898.2 E380*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8339-01A-11D-2310-10 chr4:56319288 C>A maps to NM_004898.2 E380*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8339-01A-11D-2310-10 chr3:38739682 G>T maps to NM_006514.2 P1676P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8339-01A-11D-2310-10 chr3:38739682 G>T maps to NM_006514.2 P1676P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8339-01A-11D-2310-10 chr1:1647843 G>A maps to NM_024011.2 R143R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8339-01A-11D-2310-10 chr1:1647843 G>A maps to NM_024011.2 R143R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8339-01A-11D-2310-10 chr8:139674281 G>A maps to NM_152888.1 A1077A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8339-01A-11D-2310-10 chr8:139674281 G>A maps to NM_152888.1 A1077A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8339-01A-11D-2310-10 chr8:133141625 G>A maps to NM_004519.2 A834A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8339-01A-11D-2310-10 chr8:133141625 G>A maps to NM_004519.2 A834A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8339-01A-11D-2310-10 chr3:73657757 C>G maps to NM_015009.1 R267R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8339-01A-11D-2310-10 chr3:73657757 C>G maps to NM_015009.1 R267R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8339-01A-11D-2310-10 chr9:80049324 G>A maps to NM_004297.3 Y141Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8339-01A-11D-2310-10 chr9:80049324 G>A maps to NM_004297.3 Y141Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8339-01A-11D-2310-10 chr3:150421547 T>C maps to NM_152394.3 E46E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8339-01A-11D-2310-10 chr3:150421547 T>C maps to NM_152394.3 E46E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8339-01A-11D-2310-10 chr3:49755707 G>A maps to NM_198722.2 L397L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8339-01A-11D-2310-10 chr3:49755707 G>A maps to NM_198722.2 L397L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8340-01A-11D-2310-10 chr17:21730915 G>T did not map to a codon.
Sequencing variant TCGA-KL-8340-01A-11D-2310-10 chr17:21730915 G>T did not map to a codon.
Sequencing variant TCGA-KL-8340-01A-11D-2310-10 chr7:42079818 G>T maps to NM_000168.5 P282P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8340-01A-11D-2310-10 chr7:42079818 G>T maps to NM_000168.5 P282P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8340-01A-11D-2310-10 chr10:18957459 T>C maps to NM_178815.3 L37L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8340-01A-11D-2310-10 chr10:18957459 T>C maps to NM_178815.3 L37L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8340-01A-11D-2310-10 chr9:136231847 T>C maps to NM_033161.2 E137E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8340-01A-11D-2310-10 chr9:136231847 T>C maps to NM_033161.2 E137E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8340-01A-11D-2310-10 chr2:71653714 T>A maps to NM_014497.3 V1572V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8340-01A-11D-2310-10 chr2:71653714 T>A maps to NM_014497.3 V1572V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8340-01A-11D-2310-10 chr6:160200277 C>T maps to NM_030752.2 L490L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8340-01A-11D-2310-10 chr6:160200277 C>T maps to NM_030752.2 L490L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8340-01A-11D-2310-10 chr21:32639201 G>T maps to NM_003253.2 S29S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8340-01A-11D-2310-10 chr21:32639201 G>T maps to NM_003253.2 S29S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8340-01A-11D-2310-10 chr5:140720556 C>T maps to NM_018915.2 A673A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8340-01A-11D-2310-10 chr5:140720556 C>T maps to NM_018915.2 A673A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8341-01A-11D-2310-10 chr17:48184156 G>C did not map to a codon.
Sequencing variant TCGA-KL-8341-01A-11D-2310-10 chr17:48184156 G>C did not map to a codon.
Sequencing variant TCGA-KL-8341-01A-11D-2310-10 chr4:71509878 C>T maps to NM_031889.2 D912D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8341-01A-11D-2310-10 chr4:71509878 C>T maps to NM_031889.2 D912D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8341-01A-11D-2310-10 chr15:48518685 C>G maps to NM_000338.2 L214L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8341-01A-11D-2310-10 chr15:48518685 C>G maps to NM_000338.2 L214L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8341-01A-11D-2310-10 chr5:180276711 C>A maps to NM_001172638.1 E595*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8341-01A-11D-2310-10 chr5:180276711 C>A maps to NM_001172638.1 E595*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8341-01A-11D-2310-10 chr8:144550601 G>A maps to NM_015117.2 G685G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8341-01A-11D-2310-10 chr8:144550601 G>A maps to NM_015117.2 G685G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8341-01A-11D-2310-10 chr3:148583132 T>C maps to NM_001870.2 T13T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8341-01A-11D-2310-10 chr3:148583132 T>C maps to NM_001870.2 T13T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8341-01A-11D-2310-10 chr20:33345743 C>T maps to NM_014071.2 Q269Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8341-01A-11D-2310-10 chr20:33345743 C>T maps to NM_014071.2 Q269Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8341-01A-11D-2310-10 chr1:8424202 C>T maps to NM_012102.3 P551P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8341-01A-11D-2310-10 chr1:8424202 C>T maps to NM_012102.3 P551P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8341-01A-11D-2310-10 chr8:24170912 T>C maps to NM_014265.4 S132S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8341-01A-11D-2310-10 chr8:24170912 T>C maps to NM_014265.4 S132S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8341-01A-11D-2310-10 chr6:117013532 A>G maps to NM_002269.2 K106K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8341-01A-11D-2310-10 chr6:117013532 A>G maps to NM_002269.2 K106K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8341-01A-11D-2310-10 chr5:59894910 T>C maps to NM_018369.2 K473K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8341-01A-11D-2310-10 chr5:59894910 T>C maps to NM_018369.2 K473K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8341-01A-11D-2310-10 chr5:92923830 G>A maps to NM_005654.4 A224A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8341-01A-11D-2310-10 chr5:92923830 G>A maps to NM_005654.4 A224A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8341-01A-11D-2310-10 chr15:58004286 C>T maps to NM_001018090.3 I470I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8341-01A-11D-2310-10 chr15:58004286 C>T maps to NM_001018090.3 I470I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8341-01A-11D-2310-10 chr12:69140525 G>A maps to NM_018656.2 Q123Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8341-01A-11D-2310-10 chr12:69140525 G>A maps to NM_018656.2 Q123Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8341-01A-11D-2310-10 chr6:152642497 G>A maps to NM_182961.2 R5371*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8341-01A-11D-2310-10 chr6:152642497 G>A maps to NM_182961.2 R5371*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8341-01A-11D-2310-10 chr5:170239018 C>T maps to NM_014211.2 S360S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8341-01A-11D-2310-10 chr5:170239018 C>T maps to NM_014211.2 S360S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8341-01A-11D-2310-10 chr11:56756939 T>A maps to NM_001005323.1 I184I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8341-01A-11D-2310-10 chr11:56756939 T>A maps to NM_001005323.1 I184I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8341-01A-11D-2310-10 chr16:68325150 G>A maps to NM_003983.4 V278V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8341-01A-11D-2310-10 chr16:68325150 G>A maps to NM_003983.4 V278V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8341-01A-11D-2310-10 chr9:107367737 G>C maps to NM_001004481.1 T57T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8341-01A-11D-2310-10 chr9:107367737 G>C maps to NM_001004481.1 T57T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8341-01A-11D-2310-10 chr22:24472139 C>T maps to NM_012295.3 L885L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8341-01A-11D-2310-10 chr22:24472139 C>T maps to NM_012295.3 L885L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8341-01A-11D-2310-10 chr17:7577063 T>A maps to NM_001126112.1 K292*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8341-01A-11D-2310-10 chr17:7577063 T>A maps to NM_001126112.1 K292*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8341-01A-11D-2310-10 chr1:230372422 T>C maps to NM_004481.3 L187L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8341-01A-11D-2310-10 chr1:230372422 T>C maps to NM_004481.3 L187L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8341-01A-11D-2310-10 chr15:42742930 C>T maps to NM_022473.1 S490S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8341-01A-11D-2310-10 chr15:42742930 C>T maps to NM_022473.1 S490S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8342-01A-11D-2310-10 chr8:26196503 G>T did not map to a codon.
Sequencing variant TCGA-KL-8342-01A-11D-2310-10 chr8:26196503 G>T did not map to a codon.
Sequencing variant TCGA-KL-8342-01A-11D-2310-10 chr12:51072519 A>G maps to NM_173602.2 K325K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8342-01A-11D-2310-10 chr12:51072519 A>G maps to NM_173602.2 K325K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8342-01A-11D-2310-10 chr21:19751609 C>T maps to NM_002772.2 L174L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8342-01A-11D-2310-10 chr21:19751609 C>T maps to NM_002772.2 L174L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8342-01A-11D-2310-10 chr3:172165984 C>T maps to NM_198407.2 E73E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8342-01A-11D-2310-10 chr3:172165984 C>T maps to NM_198407.2 E73E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8342-01A-11D-2310-10 chr5:78672017 T>C maps to NM_004272.3 E293E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8342-01A-11D-2310-10 chr5:78672017 T>C maps to NM_004272.3 E293E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8342-01A-11D-2310-10 chr5:140073222 A>G maps to NM_012208.2 K52K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8342-01A-11D-2310-10 chr5:140073222 A>G maps to NM_012208.2 K52K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8342-01A-11D-2310-10 chr6:162394347 C>A maps to NM_004562.2 T240T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8342-01A-11D-2310-10 chr6:162394347 C>A maps to NM_004562.2 T240T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8342-01A-11D-2310-10 chr16:23716451 C>T maps to NM_033266.3 A250A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8342-01A-11D-2310-10 chr16:23716451 C>T maps to NM_033266.3 A250A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8342-01A-11D-2310-10 chr1:24122441 G>A maps to NM_001008216.1 A348A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8342-01A-11D-2310-10 chr1:24122441 G>A maps to NM_001008216.1 A348A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8342-01A-11D-2310-10 chrX:149638777 A>T maps to NM_005491.3 A311A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8342-01A-11D-2310-10 chrX:149638777 A>T maps to NM_005491.3 A311A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8342-01A-11D-2310-10 chr12:50746921 T>G maps to NM_001145475.1 L1231L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8342-01A-11D-2310-10 chr12:50746921 T>G maps to NM_001145475.1 L1231L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8342-01A-11D-2310-10 chr1:26509851 C>T maps to ENST00000374253 R234*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8342-01A-11D-2310-10 chr1:26509851 C>T maps to ENST00000374253 R234*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8342-01A-11D-2310-10 chr19:10091505 A>C maps to NM_015719.3 G845G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8342-01A-11D-2310-10 chr19:10091505 A>C maps to NM_015719.3 G845G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8342-01A-11D-2310-10 chrX:39913557 A>G maps to NM_001123385.1 N1590N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8342-01A-11D-2310-10 chrX:39913557 A>G maps to NM_001123385.1 N1590N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8342-01A-11D-2310-10 chr22:18029227 T>C maps to ENST00000400579 P1396P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8342-01A-11D-2310-10 chr22:18029227 T>C maps to ENST00000400579 P1396P. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-KL-8343-01A-11D-2310-10. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-KL-8343-01A-11D-2310-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-KL-8343-01A-11D-2310-10 chr5:79968624 C>G maps to NM_002439.3 L325L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8343-01A-11D-2310-10 chr5:79968624 C>G maps to NM_002439.3 L325L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8343-01A-11D-2310-10 chr5:36985237 A>G maps to NM_133433.3 K652K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8343-01A-11D-2310-10 chr5:36985237 A>G maps to NM_133433.3 K652K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8343-01A-11D-2310-10 chr1:110168779 A>T did not map to a codon.
Sequencing variant TCGA-KL-8343-01A-11D-2310-10 chr1:110168779 A>T did not map to a codon.
Sequencing variant TCGA-KL-8343-01A-11D-2310-10 chr12:122672369 C>T maps to NM_001098519.1 Y215Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8343-01A-11D-2310-10 chr12:122672369 C>T maps to NM_001098519.1 Y215Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8343-01A-11D-2310-10 chr3:133368473 A>G maps to NM_007027.3 P419P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8343-01A-11D-2310-10 chr3:133368473 A>G maps to NM_007027.3 P419P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8343-01A-11D-2310-10 chr8:144680423 G>T maps to NM_032862.4 R117R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8343-01A-11D-2310-10 chr8:144680423 G>T maps to NM_032862.4 R117R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8343-01A-11D-2310-10 chr10:73767937 C>T maps to NM_004273.4 R383R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8343-01A-11D-2310-10 chr10:73767937 C>T maps to NM_004273.4 R383R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8343-01A-11D-2310-10 chr6:43020112 A>G maps to NM_001168370.1 L190L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8343-01A-11D-2310-10 chr6:43020112 A>G maps to NM_001168370.1 L190L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8344-01A-11D-2310-10 chr17:15930769 C>T maps to NM_017775.2 H480H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8344-01A-11D-2310-10 chr17:15930769 C>T maps to NM_017775.2 H480H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8344-01A-11D-2310-10 chr20:55208517 G>A maps to NM_003222.3 S232S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8344-01A-11D-2310-10 chr20:55208517 G>A maps to NM_003222.3 S232S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8344-01A-11D-2310-10 chr2:183791546 A>G maps to NM_205842.1 D1095D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8344-01A-11D-2310-10 chr2:183791546 A>G maps to NM_205842.1 D1095D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8344-01A-11D-2310-10 chr17:34942390 A>G maps to NM_024835.3 E496E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8344-01A-11D-2310-10 chr17:34942390 A>G maps to NM_024835.3 E496E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8344-01A-11D-2310-10 chr16:70161180 C>T maps to NM_017990.3 T82T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8344-01A-11D-2310-10 chr16:70161180 C>T maps to NM_017990.3 T82T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8344-01A-11D-2310-10 chr15:42034894 A>G maps to ENST00000219905 T1628T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8344-01A-11D-2310-10 chr15:42034894 A>G maps to ENST00000219905 T1628T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8344-01A-11D-2310-10 chr11:763427 T>G maps to NM_006755.1 G182G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8344-01A-11D-2310-10 chr11:763427 T>G maps to NM_006755.1 G182G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8344-01A-11D-2310-10 chr11:40136543 C>G maps to NM_020929.1 G433G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8344-01A-11D-2310-10 chr11:40136543 C>G maps to NM_020929.1 G433G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8344-01A-11D-2310-10 chr12:122406015 C>T maps to NM_144668.4 C904C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8344-01A-11D-2310-10 chr12:122406015 C>T maps to NM_144668.4 C904C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8345-01A-11D-2310-10 chr14:24773483 G>A did not map to a codon.
Sequencing variant TCGA-KL-8345-01A-11D-2310-10 chr14:24773483 G>A did not map to a codon.
Sequencing variant TCGA-KL-8345-01A-11D-2310-10 chr21:41514494 G>A maps to NM_001389.3 L1132L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8345-01A-11D-2310-10 chr21:41514494 G>A maps to NM_001389.3 L1132L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8345-01A-11D-2310-10 chr5:148407014 A>G maps to NM_024577.3 C760C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8345-01A-11D-2310-10 chr5:148407014 A>G maps to NM_024577.3 C760C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8345-01A-11D-2310-10 chrX:19854347 C>T maps to NM_031892.2 T19T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8345-01A-11D-2310-10 chrX:19854347 C>T maps to NM_031892.2 T19T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8345-01A-11D-2310-10 chr4:3417848 G>A did not map to a codon.
Sequencing variant TCGA-KL-8345-01A-11D-2310-10 chr4:3417848 G>A did not map to a codon.
Sequencing variant TCGA-KL-8345-01A-11D-2310-10 chr2:8871659 G>A maps to NM_020738.2 L1502L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8345-01A-11D-2310-10 chr2:8871659 G>A maps to NM_020738.2 L1502L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8345-01A-11D-2310-10 chr11:47653264 T>C did not map to a codon.
Sequencing variant TCGA-KL-8345-01A-11D-2310-10 chr11:47653264 T>C did not map to a codon.
Sequencing variant TCGA-KL-8345-01A-11D-2310-10 chr4:169837135 T>C maps to NM_001166108.1 D936D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8345-01A-11D-2310-10 chr4:169837135 T>C maps to NM_001166108.1 D936D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8345-01A-11D-2310-10 chr2:179480473 A>G maps to NM_133378.4 D13550D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8345-01A-11D-2310-10 chr2:179480473 A>G maps to NM_133378.4 D13550D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8345-01A-11D-2310-10 chr19:35800934 G>T maps to NM_002361.3 E464*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8345-01A-11D-2310-10 chr19:35800934 G>T maps to NM_002361.3 E464*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8345-01A-11D-2310-10 chr7:100174728 C>A maps to NM_002319.3 V448V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8345-01A-11D-2310-10 chr7:100174728 C>A maps to NM_002319.3 V448V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8346-01A-11D-2310-10 chr3:17415992 C>T maps to NM_001134381.1 W264*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8346-01A-11D-2310-10 chr3:17415992 C>T maps to NM_001134381.1 W264*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8346-01A-11D-2310-10 chr22:37888768 C>T maps to NM_014550.3 P839P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8346-01A-11D-2310-10 chr22:37888768 C>T maps to NM_014550.3 P839P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8346-01A-11D-2310-10 chr18:9954093 T>A maps to NM_003574.5 P257P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8346-01A-11D-2310-10 chr18:9954093 T>A maps to NM_003574.5 P257P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8346-01A-11D-2310-10 chr12:7045494 A>C maps to NM_001940.3 S355S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8346-01A-11D-2310-10 chr12:7045494 A>C maps to NM_001940.3 S355S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8346-01A-11D-2310-10 chr1:108769306 G>A maps to NM_001143989.2 S623S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8346-01A-11D-2310-10 chr1:108769306 G>A maps to NM_001143989.2 S623S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8346-01A-11D-2310-10 chr4:114290873 G>A maps to NM_001148.4 P3841P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8346-01A-11D-2310-10 chr4:114290873 G>A maps to NM_001148.4 P3841P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8346-01A-11D-2310-10 chr1:158647557 G>T maps to NM_003126.2 G293G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8346-01A-11D-2310-10 chr1:158647557 G>T maps to NM_003126.2 G293G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8346-01A-11D-2310-10 chr8:26722372 A>C maps to ENST00000356368 L38L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8346-01A-11D-2310-10 chr8:26722372 A>C maps to ENST00000356368 L38L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8346-01A-11D-2310-10 chr17:73727412 G>T maps to NM_001005619.1 T393T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8346-01A-11D-2310-10 chr17:73727412 G>T maps to NM_001005619.1 T393T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8438-01A-11D-2310-10 chr1:102269841 C>T maps to ENST00000338858 L463L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8438-01A-11D-2310-10 chr1:102269841 C>T maps to ENST00000338858 L463L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8438-01A-11D-2310-10 chr8:16935351 C>T maps to NM_181723.2 R210*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8438-01A-11D-2310-10 chr8:16935351 C>T maps to NM_181723.2 R210*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8438-01A-11D-2310-10 chr14:103941507 G>A maps to ENST00000335102 A504A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8438-01A-11D-2310-10 chr14:103941507 G>A maps to ENST00000335102 A504A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8438-01A-11D-2310-10 chr12:11506382 C>T maps to NM_005039.3 K218K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8438-01A-11D-2310-10 chr12:11506382 C>T maps to NM_005039.3 K218K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8438-01A-11D-2310-10 chr1:207896963 T>C maps to NM_175710.1 G548G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8438-01A-11D-2310-10 chr1:207896963 T>C maps to NM_175710.1 G548G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8438-01A-11D-2310-10 chr3:47084093 G>A maps to NM_014159.6 R2399*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8438-01A-11D-2310-10 chr3:47084093 G>A maps to NM_014159.6 R2399*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8438-01A-11D-2310-10 chr20:30584473 G>A maps to NM_001011718.1 A318A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8438-01A-11D-2310-10 chr20:30584473 G>A maps to NM_001011718.1 A318A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8438-01A-11D-2310-10 chr17:11833187 T>C maps to NM_001372.3 I3961I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8438-01A-11D-2310-10 chr17:11833187 T>C maps to NM_001372.3 I3961I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8438-01A-11D-2310-10 chr11:7324615 G>A maps to NM_175733.3 S164S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8438-01A-11D-2310-10 chr11:7324615 G>A maps to NM_175733.3 S164S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8438-01A-11D-2310-10 chr20:37126160 T>C did not map to a codon.
Sequencing variant TCGA-KM-8438-01A-11D-2310-10 chr20:37126160 T>C did not map to a codon.
Sequencing variant TCGA-KM-8438-01A-11D-2310-10 chr17:79102326 G>A maps to NM_001080395.2 D119D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8438-01A-11D-2310-10 chr17:79102326 G>A maps to NM_001080395.2 D119D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8438-01A-11D-2310-10 chr15:78921470 G>A maps to NM_000750.3 P392P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8438-01A-11D-2310-10 chr15:78921470 G>A maps to NM_000750.3 P392P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8439-01A-11D-2310-10 chr10:14890640 G>A maps to NM_016299.2 A85A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8439-01A-11D-2310-10 chr10:14890640 G>A maps to NM_016299.2 A85A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8439-01A-11D-2310-10 chr18:72997838 A>C maps to NM_005786.4 T114T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8439-01A-11D-2310-10 chr18:72997838 A>C maps to NM_005786.4 T114T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8439-01A-11D-2310-10 chr1:145299778 C>T maps to NM_001039703.4 A276A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8439-01A-11D-2310-10 chr1:145299778 C>T maps to NM_001039703.4 A276A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8439-01A-11D-2310-10 chr4:151842426 A>G maps to NM_006726.3 L190L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8439-01A-11D-2310-10 chr4:151842426 A>G maps to NM_006726.3 L190L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8439-01A-11D-2310-10 chr13:103328695 A>G maps to ENST00000376052 R1210R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8439-01A-11D-2310-10 chr13:103328695 A>G maps to ENST00000376052 R1210R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8440-01A-11D-2310-10 chr22:46653501 C>T maps to NM_006071.1 W1906*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8440-01A-11D-2310-10 chr22:46653501 C>T maps to NM_006071.1 W1906*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8440-01A-11D-2310-10 chr13:41134355 A>T maps to NM_002015.3 Y424*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8440-01A-11D-2310-10 chr13:41134355 A>T maps to NM_002015.3 Y424*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8440-01A-11D-2310-10 chr4:88379167 T>C maps to NM_024047.3 L350L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8440-01A-11D-2310-10 chr4:88379167 T>C maps to NM_024047.3 L350L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8440-01A-11D-2310-10 chr4:961062 G>A maps to NM_001347.2 D358D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8440-01A-11D-2310-10 chr4:961062 G>A maps to NM_001347.2 D358D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8440-01A-11D-2310-10 chr15:65916546 A>G maps to NM_004727.2 R43R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8440-01A-11D-2310-10 chr15:65916546 A>G maps to NM_004727.2 R43R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8440-01A-11D-2310-10 chr2:32694460 A>G did not map to a codon.
Sequencing variant TCGA-KM-8440-01A-11D-2310-10 chr2:32694460 A>G did not map to a codon.
Sequencing variant TCGA-KM-8440-01A-11D-2310-10 chr11:62294616 C>T maps to NM_001620.1 G2424G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8440-01A-11D-2310-10 chr11:62294616 C>T maps to NM_001620.1 G2424G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8440-01A-11D-2310-10 chr3:51690164 C>T maps to NM_015106.2 Q1069*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8440-01A-11D-2310-10 chr3:51690164 C>T maps to NM_015106.2 Q1069*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8440-01A-11D-2310-10 chr7:99514381 G>A maps to NM_033017.3 H138H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8440-01A-11D-2310-10 chr7:99514381 G>A maps to NM_033017.3 H138H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8441-01A-11D-2310-10 chr1:47717421 G>A maps to NM_001048166.1 R1085*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8441-01A-11D-2310-10 chr1:47717421 G>A maps to NM_001048166.1 R1085*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8441-01A-11D-2310-10 chr14:20389391 C>T maps to NM_001005483.1 S209S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8441-01A-11D-2310-10 chr14:20389391 C>T maps to NM_001005483.1 S209S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8441-01A-11D-2310-10 chr8:48882494 C>T maps to NM_182746.1 Q438*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8441-01A-11D-2310-10 chr8:48882494 C>T maps to NM_182746.1 Q438*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8441-01A-11D-2310-10 chr3:186395000 G>T maps to NM_000412.2 E303*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8441-01A-11D-2310-10 chr3:186395000 G>T maps to NM_000412.2 E303*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8441-01A-11D-2310-10 chr16:31072730 A>C maps to NM_001172669.1 G529G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8441-01A-11D-2310-10 chr16:31072730 A>C maps to NM_001172669.1 G529G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8441-01A-11D-2310-10 chr17:48629512 G>T maps to NM_022827.2 G643G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8441-01A-11D-2310-10 chr17:48629512 G>T maps to NM_022827.2 G643G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8441-01A-11D-2310-10 chr14:86088694 A>G maps to NM_013231.4 E279E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8441-01A-11D-2310-10 chr14:86088694 A>G maps to NM_013231.4 E279E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8441-01A-11D-2310-10 chr9:118950339 C>T maps to NM_002581.3 R441R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8441-01A-11D-2310-10 chr9:118950339 C>T maps to NM_002581.3 R441R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8442-01A-11D-2310-10 chr6:11185613 C>T maps to NM_006403.3 T762T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8442-01A-11D-2310-10 chr6:11185613 C>T maps to NM_006403.3 T762T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8442-01A-11D-2310-10 chrX:49084508 G>A maps to NM_005183.2 G369G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8442-01A-11D-2310-10 chrX:49084508 G>A maps to NM_005183.2 G369G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8442-01A-11D-2310-10 chr14:105412334 C>T maps to NM_138420.2 P3151P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8442-01A-11D-2310-10 chr14:105412334 C>T maps to NM_138420.2 P3151P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8442-01A-11D-2310-10 chr15:40257896 A>G maps to NM_001013703.2 E290E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8442-01A-11D-2310-10 chr15:40257896 A>G maps to NM_001013703.2 E290E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8442-01A-11D-2310-10 chr5:23521145 G>A maps to NM_020227.2 A122A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8442-01A-11D-2310-10 chr5:23521145 G>A maps to NM_020227.2 A122A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8442-01A-11D-2310-10 chr11:34074125 C>T maps to NM_005898.4 A53A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8442-01A-11D-2310-10 chr11:34074125 C>T maps to NM_005898.4 A53A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8442-01A-11D-2310-10 chr11:118111081 G>A maps to NM_198275.1 I28I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8442-01A-11D-2310-10 chr11:118111081 G>A maps to NM_198275.1 I28I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8442-01A-11D-2310-10 chr1:2268197 C>T maps to NM_024848.1 P376P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8442-01A-11D-2310-10 chr1:2268197 C>T maps to NM_024848.1 P376P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8443-01A-11D-2310-10 chr3:126071788 G>A did not map to a codon.
Sequencing variant TCGA-KM-8443-01A-11D-2310-10 chr3:126071788 G>A did not map to a codon.
Sequencing variant TCGA-KM-8443-01A-11D-2310-10 chr8:27468112 C>T maps to NM_001831.2 A44A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8443-01A-11D-2310-10 chr8:27468112 C>T maps to NM_001831.2 A44A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8443-01A-11D-2310-10 chr2:25966454 C>T maps to NM_018263.4 S917S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8443-01A-11D-2310-10 chr2:25966454 C>T maps to NM_018263.4 S917S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8443-01A-11D-2310-10 chr22:43459836 G>A maps to NM_012263.4 V243V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8443-01A-11D-2310-10 chr22:43459836 G>A maps to NM_012263.4 V243V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8443-01A-11D-2310-10 chr8:60031453 A>T maps to NM_014729.2 Y31*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8443-01A-11D-2310-10 chr8:60031453 A>T maps to NM_014729.2 Y31*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8443-01A-11D-2310-10 chr5:158526462 G>T maps to NM_024007.3 I8I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8443-01A-11D-2310-10 chr5:158526462 G>T maps to NM_024007.3 I8I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8443-01A-11D-2310-10 chr3:47041770 G>A maps to NM_015175.1 G1394G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8443-01A-11D-2310-10 chr3:47041770 G>A maps to NM_015175.1 G1394G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8476-01A-11D-2310-10 chr6:146720022 G>T maps to NM_000838.3 L616L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8476-01A-11D-2310-10 chr6:146720022 G>T maps to NM_000838.3 L616L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8476-01A-11D-2310-10 chr19:53086656 C>T maps to NM_001172655.1 R515*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8476-01A-11D-2310-10 chr19:53086656 C>T maps to NM_001172655.1 R515*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8476-01A-11D-2310-10 chr18:77090009 A>G did not map to a codon.
Sequencing variant TCGA-KM-8476-01A-11D-2310-10 chr18:77090009 A>G did not map to a codon.
Sequencing variant TCGA-KM-8476-01A-11D-2310-10 chr11:224194 G>A maps to NM_012239.5 T284T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8476-01A-11D-2310-10 chr11:224194 G>A maps to NM_012239.5 T284T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8476-01A-11D-2310-10 chr22:22842484 C>T maps to NM_080764.2 S413S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8476-01A-11D-2310-10 chr22:22842484 C>T maps to NM_080764.2 S413S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8476-01A-11D-2310-10 chr12:109577281 G>A maps to NM_001093.3 G24G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8476-01A-11D-2310-10 chr12:109577281 G>A maps to NM_001093.3 G24G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8476-01A-11D-2310-10 chr5:140683387 C>T maps to NM_031947.2 A15A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8476-01A-11D-2310-10 chr5:140683387 C>T maps to NM_031947.2 A15A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8476-01A-11D-2310-10 chr7:150555108 C>T maps to ENST00000416793 R517R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8476-01A-11D-2310-10 chr7:150555108 C>T maps to ENST00000416793 R517R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8476-01A-11D-2310-10 chr5:175511994 A>G maps to NM_001079529.2 E10E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8476-01A-11D-2310-10 chr5:175511994 A>G maps to NM_001079529.2 E10E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8476-01A-11D-2310-10 chr4:159780274 G>A maps to ENST00000379346 R331R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8476-01A-11D-2310-10 chr4:159780274 G>A maps to ENST00000379346 R331R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8476-01A-11D-2310-10 chr16:70432187 G>A maps to NM_006927.3 S82S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8476-01A-11D-2310-10 chr16:70432187 G>A maps to NM_006927.3 S82S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8476-01A-11D-2310-10 chr10:132932682 T>C maps to NM_174937.3 E406E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8476-01A-11D-2310-10 chr10:132932682 T>C maps to NM_174937.3 E406E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8476-01A-11D-2310-10 chr15:52613682 A>G maps to ENST00000358212 S1608S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8476-01A-11D-2310-10 chr15:52613682 A>G maps to ENST00000358212 S1608S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8476-01A-11D-2310-10 chr22:39884299 C>T maps to NM_001098270.1 D316D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8476-01A-11D-2310-10 chr22:39884299 C>T maps to NM_001098270.1 D316D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8476-01A-11D-2310-10 chr19:10823282 C>T maps to NM_031209.2 C280C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8476-01A-11D-2310-10 chr19:10823282 C>T maps to NM_031209.2 C280C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8476-01A-11D-2310-10 chr20:33575695 C>T maps to NM_020884.3 I507I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8476-01A-11D-2310-10 chr20:33575695 C>T maps to NM_020884.3 I507I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8476-01A-11D-2310-10 chr12:53416355 T>C maps to ENST00000438209 A204A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8476-01A-11D-2310-10 chr12:53416355 T>C maps to ENST00000438209 A204A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8476-01A-11D-2310-10 chr2:143959764 A>G maps to NM_018460.3 E76E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8476-01A-11D-2310-10 chr2:143959764 A>G maps to NM_018460.3 E76E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8476-01A-11D-2310-10 chr5:153065876 C>T maps to NM_001114183.1 D374D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8476-01A-11D-2310-10 chr5:153065876 C>T maps to NM_001114183.1 D374D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8476-01A-11D-2310-10 chr11:57268328 C>T did not map to a codon.
Sequencing variant TCGA-KM-8476-01A-11D-2310-10 chr11:57268328 C>T did not map to a codon.
Sequencing variant TCGA-KM-8476-01A-11D-2310-10 chr16:27374338 C>T maps to NM_000418.2 R556*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8476-01A-11D-2310-10 chr16:27374338 C>T maps to NM_000418.2 R556*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8477-01A-11D-2310-10 chr20:61386086 G>T maps to NM_002531.2 L255L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8477-01A-11D-2310-10 chr20:61386086 G>T maps to NM_002531.2 L255L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8477-01A-11D-2310-10 chr10:75519463 G>A maps to NM_198597.1 P131P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8477-01A-11D-2310-10 chr10:75519463 G>A maps to NM_198597.1 P131P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8477-01A-11D-2310-10 chr8:102705064 C>T maps to NM_032041.2 E146E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8477-01A-11D-2310-10 chr8:102705064 C>T maps to NM_032041.2 E146E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8477-01A-11D-2310-10 chr19:33702228 G>A maps to NM_019849.2 F306F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8477-01A-11D-2310-10 chr19:33702228 G>A maps to NM_019849.2 F306F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8477-01A-11D-2310-10 chr2:84928426 G>T maps to NM_001370.1 L2675L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8477-01A-11D-2310-10 chr2:84928426 G>T maps to NM_001370.1 L2675L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8477-01A-11D-2310-10 chr20:33345743 C>T maps to NM_014071.2 Q269Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8477-01A-11D-2310-10 chr20:33345743 C>T maps to NM_014071.2 Q269Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8477-01A-11D-2310-10 chr2:202901004 C>T maps to NM_003507.1 G545G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8477-01A-11D-2310-10 chr2:202901004 C>T maps to NM_003507.1 G545G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8477-01A-11D-2310-10 chr11:55762020 G>A maps to NM_003697.1 L27L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8477-01A-11D-2310-10 chr11:55762020 G>A maps to NM_003697.1 L27L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8477-01A-11D-2310-10 chr8:25744301 G>T maps to NM_022659.2 C326*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8477-01A-11D-2310-10 chr8:25744301 G>T maps to NM_022659.2 C326*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8477-01A-11D-2310-10 chr5:138209475 T>G maps to NM_015564.2 L258L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8477-01A-11D-2310-10 chr5:138209475 T>G maps to NM_015564.2 L258L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8477-01A-11D-2310-10 chr12:1742018 G>A maps to NM_032642.2 W92*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8477-01A-11D-2310-10 chr12:1742018 G>A maps to NM_032642.2 W92*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8477-01A-11D-2310-10 chrX:47041265 G>A did not map to a codon.
Sequencing variant TCGA-KM-8477-01A-11D-2310-10 chrX:47041265 G>A did not map to a codon.
Sequencing variant TCGA-KM-8477-01A-11D-2310-10 chr10:129866454 C>T maps to NM_006504.4 F304F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8477-01A-11D-2310-10 chr10:129866454 C>T maps to NM_006504.4 F304F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8639-01A-11D-2397-10 chr7:135079030 T>C maps to NM_001190850.1 E422E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8639-01A-11D-2397-10 chr7:135079030 T>C maps to NM_001190850.1 E422E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8639-01A-11D-2397-10 chr10:25464833 G>A maps to NM_020752.2 W162*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8639-01A-11D-2397-10 chr10:25464833 G>A maps to NM_020752.2 W162*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8639-01A-11D-2397-10 chr20:42825742 G>C maps to NM_016470.6 Y276*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8639-01A-11D-2397-10 chr20:42825742 G>C maps to NM_016470.6 Y276*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8639-01A-11D-2397-10 chr1:39987054 C>T maps to NM_181809.3 S227S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8639-01A-11D-2397-10 chr1:39987054 C>T maps to NM_181809.3 S227S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8639-01A-11D-2397-10 chr14:63174363 C>T maps to NM_139318.3 S943S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8639-01A-11D-2397-10 chr14:63174363 C>T maps to NM_139318.3 S943S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8418-01A-11D-2310-10 chr17:65889529 C>T maps to ENST00000321892 T826T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8418-01A-11D-2310-10 chr17:65889529 C>T maps to ENST00000321892 T826T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8418-01A-11D-2310-10 chr21:34727797 T>C maps to NM_000629.2 S539S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8418-01A-11D-2310-10 chr21:34727797 T>C maps to NM_000629.2 S539S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8418-01A-11D-2310-10 chr5:40775605 C>T did not map to a codon.
Sequencing variant TCGA-KN-8418-01A-11D-2310-10 chr5:40775605 C>T did not map to a codon.
Sequencing variant TCGA-KN-8418-01A-11D-2310-10 chr2:242283309 C>A maps to ENST00000391972 L315L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8418-01A-11D-2310-10 chr2:242283309 C>A maps to ENST00000391972 L315L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8418-01A-11D-2310-10 chr6:16326645 G>A maps to NM_000332.3 A632A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8418-01A-11D-2310-10 chr6:16326645 G>A maps to NM_000332.3 A632A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8418-01A-11D-2310-10 chr19:13340906 G>A maps to NM_023035.2 D1843D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8418-01A-11D-2310-10 chr19:13340906 G>A maps to NM_023035.2 D1843D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8418-01A-11D-2310-10 chr22:42456378 G>A maps to NM_000262.2 L380L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8418-01A-11D-2310-10 chr22:42456378 G>A maps to NM_000262.2 L380L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8418-01A-11D-2310-10 chr5:79945301 G>A maps to NM_000791.3 L50L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8418-01A-11D-2310-10 chr5:79945301 G>A maps to NM_000791.3 L50L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8418-01A-11D-2310-10 chr3:53139766 G>A maps to NM_052859.3 F293F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8418-01A-11D-2310-10 chr3:53139766 G>A maps to NM_052859.3 F293F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8418-01A-11D-2310-10 chr19:38782513 G>A maps to NM_021102.3 L209L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8418-01A-11D-2310-10 chr19:38782513 G>A maps to NM_021102.3 L209L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8418-01A-11D-2310-10 chr2:99163145 G>A maps to NM_001134224.1 E384E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8418-01A-11D-2310-10 chr2:99163145 G>A maps to NM_001134224.1 E384E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8418-01A-11D-2310-10 chr5:41045850 C>T maps to ENST00000296803 E612E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8418-01A-11D-2310-10 chr5:41045850 C>T maps to ENST00000296803 E612E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8418-01A-11D-2310-10 chr3:195507050 T>C maps to NM_018406.5 S3800S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8418-01A-11D-2310-10 chr3:195507050 T>C maps to NM_018406.5 S3800S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8419-01A-11D-2310-10 chr8:142175379 G>A maps to NM_014957.2 E435E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8419-01A-11D-2310-10 chr8:142175379 G>A maps to NM_014957.2 E435E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8419-01A-11D-2310-10 chrX:51076023 G>A maps to NM_153183.2 E69E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8419-01A-11D-2310-10 chrX:51076023 G>A maps to NM_153183.2 E69E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8419-01A-11D-2310-10 chr1:70897871 C>A maps to NM_001902.5 A277A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8419-01A-11D-2310-10 chr1:70897871 C>A maps to NM_001902.5 A277A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8419-01A-11D-2310-10 chr19:1073205 C>A maps to NM_012292.2 V160V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8419-01A-11D-2310-10 chr19:1073205 C>A maps to NM_012292.2 V160V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8419-01A-11D-2310-10 chr12:52777474 G>A maps to NM_033045.3 I218I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8419-01A-11D-2310-10 chr12:52777474 G>A maps to NM_033045.3 I218I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8419-01A-11D-2310-10 chr5:154394948 T>C maps to NM_001099293.1 A510A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8419-01A-11D-2310-10 chr5:154394948 T>C maps to NM_001099293.1 A510A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8419-01A-11D-2310-10 chr17:56693672 C>T maps to ENST00000240361 W216*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8419-01A-11D-2310-10 chr17:56693672 C>T maps to ENST00000240361 W216*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8419-01A-11D-2310-10 chr22:31266428 C>T maps to NM_030758.3 D289D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8419-01A-11D-2310-10 chr22:31266428 C>T maps to NM_030758.3 D289D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8419-01A-11D-2310-10 chr4:57182676 G>A maps to NM_020722.1 P1003P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8419-01A-11D-2310-10 chr4:57182676 G>A maps to NM_020722.1 P1003P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8419-01A-11D-2310-10 chr14:65245964 C>T did not map to a codon.
Sequencing variant TCGA-KN-8419-01A-11D-2310-10 chr14:65245964 C>T did not map to a codon.
Sequencing variant TCGA-KN-8421-01A-11D-2310-10 chr21:19744528 G>A maps to NM_002772.2 D215D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8421-01A-11D-2310-10 chr21:19744528 G>A maps to NM_002772.2 D215D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8421-01A-11D-2310-10 chr2:179401231 C>T maps to NM_133378.4 K30846K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8421-01A-11D-2310-10 chr2:179401231 C>T maps to NM_133378.4 K30846K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8421-01A-11D-2310-10 chr1:84876611 A>T maps to NM_021233.2 P159P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8421-01A-11D-2310-10 chr1:84876611 A>T maps to NM_021233.2 P159P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8421-01A-11D-2310-10 chr11:123886664 G>A maps to NM_001004462.1 P128P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8421-01A-11D-2310-10 chr11:123886664 G>A maps to NM_001004462.1 P128P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8421-01A-11D-2310-10 chr2:136473265 T>A did not map to a codon.
Sequencing variant TCGA-KN-8421-01A-11D-2310-10 chr2:136473265 T>A did not map to a codon.
Sequencing variant TCGA-KN-8421-01A-11D-2310-10 chr12:51757966 G>A maps to NM_007210.3 F329F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8421-01A-11D-2310-10 chr12:51757966 G>A maps to NM_007210.3 F329F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8421-01A-11D-2310-10 chr8:143694489 G>A maps to NM_015193.3 P381P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8421-01A-11D-2310-10 chr8:143694489 G>A maps to NM_015193.3 P381P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8421-01A-11D-2310-10 chr17:59118254 T>G did not map to a codon.
Sequencing variant TCGA-KN-8421-01A-11D-2310-10 chr17:59118254 T>G did not map to a codon.
Sequencing variant TCGA-KN-8421-01A-11D-2310-10 chrX:119072772 C>T maps to NM_024528.3 K129K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8421-01A-11D-2310-10 chrX:119072772 C>T maps to NM_024528.3 K129K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8421-01A-11D-2310-10 chr2:165987816 G>T maps to NM_006922.3 L834L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8421-01A-11D-2310-10 chr2:165987816 G>T maps to NM_006922.3 L834L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8422-01A-11D-2310-10 chr5:137524672 C>T maps to NM_004661.3 T596T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8422-01A-11D-2310-10 chr5:137524672 C>T maps to NM_004661.3 T596T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8422-01A-11D-2310-10 chr8:25203088 C>T maps to NM_024940.6 L906L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8422-01A-11D-2310-10 chr8:25203088 C>T maps to NM_024940.6 L906L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8423-01A-11D-2310-10 chr1:245022135 T>C maps to NM_031844.2 E375E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8423-01A-11D-2310-10 chr1:245022135 T>C maps to NM_031844.2 E375E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8423-01A-11D-2310-10 chr3:16638274 A>G maps to NM_001190811.1 P180P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8423-01A-11D-2310-10 chr3:16638274 A>G maps to NM_001190811.1 P180P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8423-01A-11D-2310-10 chr19:18879482 C>T maps to NM_001098482.1 P416P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8423-01A-11D-2310-10 chr19:18879482 C>T maps to NM_001098482.1 P416P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8423-01A-11D-2310-10 chr1:225477666 T>C maps to NM_001373.1 P2691P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8423-01A-11D-2310-10 chr1:225477666 T>C maps to NM_001373.1 P2691P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8423-01A-11D-2310-10 chr13:37678604 A>G maps to NM_145203.5 C263C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8423-01A-11D-2310-10 chr13:37678604 A>G maps to NM_145203.5 C263C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8423-01A-11D-2310-10 chr9:125620199 A>G did not map to a codon.
Sequencing variant TCGA-KN-8423-01A-11D-2310-10 chr9:125620199 A>G did not map to a codon.
Sequencing variant TCGA-KN-8423-01A-11D-2310-10 chr4:3234984 C>G maps to NM_002111.6 L2787L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8423-01A-11D-2310-10 chr4:3234984 C>G maps to NM_002111.6 L2787L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8424-01A-11D-2310-10 chr9:131730828 A>G maps to NM_015354.1 E210E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8424-01A-11D-2310-10 chr9:131730828 A>G maps to NM_015354.1 E210E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8424-01A-11D-2310-10 chr3:51475087 C>T did not map to a codon.
Sequencing variant TCGA-KN-8424-01A-11D-2310-10 chr3:51475087 C>T did not map to a codon.
Sequencing variant TCGA-KN-8424-01A-11D-2310-10 chr9:3856039 A>G maps to NM_001042413.1 S814S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8424-01A-11D-2310-10 chr9:3856039 A>G maps to NM_001042413.1 S814S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8424-01A-11D-2310-10 chr1:152127951 T>C maps to NM_001122965.1 Q541Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8424-01A-11D-2310-10 chr1:152127951 T>C maps to NM_001122965.1 Q541Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8424-01A-11D-2310-10 chr10:135346308 T>C maps to NM_000773.3 H254H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8424-01A-11D-2310-10 chr10:135346308 T>C maps to NM_000773.3 H254H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8424-01A-11D-2310-10 chr7:143748123 G>A maps to NM_012365.1 P210P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8424-01A-11D-2310-10 chr7:143748123 G>A maps to NM_012365.1 P210P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8424-01A-11D-2310-10 chr7:76828558 G>A maps to NM_006682.2 V184V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8424-01A-11D-2310-10 chr7:76828558 G>A maps to NM_006682.2 V184V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8424-01A-11D-2310-10 chr10:31138700 A>G maps to NM_182755.2 H211H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8424-01A-11D-2310-10 chr10:31138700 A>G maps to NM_182755.2 H211H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8424-01A-11D-2310-10 chr3:52233379 C>A maps to ENST00000441729 A58A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8424-01A-11D-2310-10 chr3:52233379 C>A maps to ENST00000441729 A58A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8424-01A-11D-2310-10 chr16:1265530 C>T maps to NM_021098.2 L1728L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8424-01A-11D-2310-10 chr16:1265530 C>T maps to NM_021098.2 L1728L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8424-01A-11D-2310-10 chr19:1236021 C>T maps to ENST00000382477 S20S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8424-01A-11D-2310-10 chr19:1236021 C>T maps to ENST00000382477 S20S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8424-01A-11D-2310-10 chr1:158056510 G>A maps to ENST00000368173 E212E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8424-01A-11D-2310-10 chr1:158056510 G>A maps to ENST00000368173 E212E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8424-01A-11D-2310-10 chr3:150421568 T>C maps to NM_152394.3 E39E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8424-01A-11D-2310-10 chr3:150421568 T>C maps to NM_152394.3 E39E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8424-01A-11D-2310-10 chr2:179497286 T>C maps to NM_133378.4 E11914E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8424-01A-11D-2310-10 chr2:179497286 T>C maps to NM_133378.4 E11914E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8424-01A-11D-2310-10 chr2:119731957 G>A maps to NM_006770.3 P170P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8424-01A-11D-2310-10 chr2:119731957 G>A maps to NM_006770.3 P170P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8424-01A-11D-2310-10 chr5:54329717 G>A maps to NM_002104.2 W253*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8424-01A-11D-2310-10 chr5:54329717 G>A maps to NM_002104.2 W253*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8424-01A-11D-2310-10 chr7:34724246 A>G maps to NM_207172.1 R77R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8424-01A-11D-2310-10 chr7:34724246 A>G maps to NM_207172.1 R77R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8424-01A-11D-2310-10 chr7:156437190 A>G did not map to a codon.
Sequencing variant TCGA-KN-8424-01A-11D-2310-10 chr7:156437190 A>G did not map to a codon.
Sequencing variant TCGA-KN-8425-01A-11D-2310-10 chr3:114070435 T>C maps to NM_001164342.1 L163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8425-01A-11D-2310-10 chr3:114070435 T>C maps to NM_001164342.1 L163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8425-01A-11D-2310-10 chr19:56243851 G>A maps to NM_176820.2 Q449*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8425-01A-11D-2310-10 chr19:56243851 G>A maps to NM_176820.2 Q449*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8425-01A-11D-2310-10 chr12:117624288 C>A maps to NM_033624.2 E155*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8425-01A-11D-2310-10 chr12:117624288 C>A maps to NM_033624.2 E155*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8425-01A-11D-2310-10 chr10:74952369 A>G maps to NM_173348.1 E113E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8425-01A-11D-2310-10 chr10:74952369 A>G maps to NM_173348.1 E113E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8425-01A-11D-2310-10 chr16:1705978 A>G maps to NM_020825.3 T407T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8425-01A-11D-2310-10 chr16:1705978 A>G maps to NM_020825.3 T407T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8425-01A-11D-2310-10 chr6:27368215 C>T maps to NM_001076781.1 Q23*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8425-01A-11D-2310-10 chr6:27368215 C>T maps to NM_001076781.1 Q23*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8426-01A-11D-2310-10 chr19:8966764 C>T maps to NM_024690.2 S14396S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8426-01A-11D-2310-10 chr19:8966764 C>T maps to NM_024690.2 S14396S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8426-01A-11D-2310-10 chr10:29759269 G>A maps to NM_021738.2 H1926H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8426-01A-11D-2310-10 chr10:29759269 G>A maps to NM_021738.2 H1926H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8426-01A-11D-2310-10 chr13:73572976 A>G maps to NM_006346.2 K689K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8426-01A-11D-2310-10 chr13:73572976 A>G maps to NM_006346.2 K689K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8426-01A-11D-2310-10 chr12:8618082 G>A maps to NM_001007033.1 W76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8426-01A-11D-2310-10 chr12:8618082 G>A maps to NM_001007033.1 W76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8426-01A-11D-2310-10 chr17:30207664 T>C maps to NM_018428.2 K298K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8426-01A-11D-2310-10 chr17:30207664 T>C maps to NM_018428.2 K298K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8426-01A-11D-2310-10 chr12:57957253 C>T maps to NM_004984.2 P54P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8426-01A-11D-2310-10 chr12:57957253 C>T maps to NM_004984.2 P54P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8426-01A-11D-2310-10 chr5:139189306 G>A maps to NM_032289.2 A94A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8426-01A-11D-2310-10 chr5:139189306 G>A maps to NM_032289.2 A94A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8426-01A-11D-2310-10 chr15:42734361 T>C maps to NM_022473.1 Q1201Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8426-01A-11D-2310-10 chr15:42734361 T>C maps to NM_022473.1 Q1201Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8426-01A-11D-2310-10 chr16:21049159 C>A maps to NM_017539.1 E1625*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8426-01A-11D-2310-10 chr16:21049159 C>A maps to NM_017539.1 E1625*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8426-01A-11D-2310-10 chr12:82747060 C>A maps to NM_014167.4 E199*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8426-01A-11D-2310-10 chr12:82747060 C>A maps to NM_014167.4 E199*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8426-01A-11D-2310-10 chr8:68939494 T>C maps to NM_024870.2 V160V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8426-01A-11D-2310-10 chr8:68939494 T>C maps to NM_024870.2 V160V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8426-01A-11D-2310-10 chr22:40552183 A>G maps to ENST00000454349 K15K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8426-01A-11D-2310-10 chr22:40552183 A>G maps to ENST00000454349 K15K. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-KN-8426-01A-11D-2310-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-KN-8426-01A-11D-2310-10 chr19:54875935 C>T maps to NM_002287.3 V12V. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-KN-8426-01A-11D-2310-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-KN-8426-01A-11D-2310-10 chr19:54875935 C>T maps to NM_002287.3 V12V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8426-01A-11D-2310-10 chr7:24931998 T>C maps to NM_015550.2 R31R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8426-01A-11D-2310-10 chr7:24931998 T>C maps to NM_015550.2 R31R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8426-01A-11D-2310-10 chr4:114278578 T>C maps to NM_001148.4 S2935S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8426-01A-11D-2310-10 chr4:114278578 T>C maps to NM_001148.4 S2935S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8426-01A-11D-2310-10 chr1:13183836 G>A maps to NM_001136561.2 H12H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8426-01A-11D-2310-10 chr1:13183836 G>A maps to NM_001136561.2 H12H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8426-01A-11D-2310-10 chr22:24226119 G>A maps to ENST00000407566 P99P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8426-01A-11D-2310-10 chr22:24226119 G>A maps to ENST00000407566 P99P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8426-01A-11D-2310-10 chr19:42225040 C>G maps to NM_004363.2 V657V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8426-01A-11D-2310-10 chr19:42225040 C>G maps to NM_004363.2 V657V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8427-01A-11D-2310-10 chr1:171072966 C>T maps to NM_006894.5 V58V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8427-01A-11D-2310-10 chr1:171072966 C>T maps to NM_006894.5 V58V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8427-01A-11D-2310-10 chr1:160275562 C>G maps to NM_001098398.1 R481R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8427-01A-11D-2310-10 chr1:160275562 C>G maps to NM_001098398.1 R481R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8427-01A-11D-2310-10 chr9:27556770 C>T maps to NM_018325.2 L293L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8427-01A-11D-2310-10 chr9:27556770 C>T maps to NM_018325.2 L293L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8427-01A-11D-2310-10 chr9:124936965 C>A did not map to a codon.
Sequencing variant TCGA-KN-8427-01A-11D-2310-10 chr9:124936965 C>A did not map to a codon.
Sequencing variant TCGA-KN-8427-01A-11D-2310-10 chr15:86808033 C>A maps to NM_152336.2 T498T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8427-01A-11D-2310-10 chr15:86808033 C>A maps to NM_152336.2 T498T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8427-01A-11D-2310-10 chr11:102737124 A>C maps to ENST00000326227 S322S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8427-01A-11D-2310-10 chr11:102737124 A>C maps to ENST00000326227 S322S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8427-01A-11D-2310-10 chr3:44489836 C>T maps to NM_181489.5 G442G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8427-01A-11D-2310-10 chr3:44489836 C>T maps to NM_181489.5 G442G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8427-01A-11D-2310-10 chr8:143958437 C>T did not map to a codon.
Sequencing variant TCGA-KN-8427-01A-11D-2310-10 chr8:143958437 C>T did not map to a codon.
Sequencing variant TCGA-KN-8427-01A-11D-2310-10 chr9:94487338 C>G maps to NM_004560.2 L479L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8427-01A-11D-2310-10 chr9:94487338 C>G maps to NM_004560.2 L479L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8427-01A-11D-2310-10 chr8:110530423 T>C maps to ENST00000426474 T3907T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8427-01A-11D-2310-10 chr8:110530423 T>C maps to ENST00000426474 T3907T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8427-01A-11D-2310-10 chr8:113988243 A>G maps to NM_198123.1 H388H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8427-01A-11D-2310-10 chr8:113988243 A>G maps to NM_198123.1 H388H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8427-01A-11D-2310-10 chr19:33113432 G>T maps to NM_032139.2 R574R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8427-01A-11D-2310-10 chr19:33113432 G>T maps to NM_032139.2 R574R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8427-01A-11D-2310-10 chr19:12911997 T>C maps to NM_005809.4 K26K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8427-01A-11D-2310-10 chr19:12911997 T>C maps to NM_005809.4 K26K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8427-01A-11D-2310-10 chr6:117248565 G>T maps to NM_173560.3 P754P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8427-01A-11D-2310-10 chr6:117248565 G>T maps to NM_173560.3 P754P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8427-01A-11D-2310-10 chr2:179644741 A>C maps to NM_133378.4 T1238T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8427-01A-11D-2310-10 chr2:179644741 A>C maps to NM_133378.4 T1238T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8427-01A-11D-2310-10 chr19:56952704 T>C maps to ENST00000342634 K681K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8427-01A-11D-2310-10 chr19:56952704 T>C maps to ENST00000342634 K681K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8427-01A-11D-2310-10 chr22:43565505 C>T maps to NM_015140.3 Q548Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8427-01A-11D-2310-10 chr22:43565505 C>T maps to NM_015140.3 Q548Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8427-01A-11D-2310-10 chr1:34209064 A>G maps to ENST00000373381 I623I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8427-01A-11D-2310-10 chr1:34209064 A>G maps to ENST00000373381 I623I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8427-01A-11D-2310-10 chrX:128886302 C>T maps to NM_003399.5 I333I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8427-01A-11D-2310-10 chrX:128886302 C>T maps to NM_003399.5 I333I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8427-01A-11D-2310-10 chr10:30318484 G>A maps to NM_020848.2 Q198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8427-01A-11D-2310-10 chr10:30318484 G>A maps to NM_020848.2 Q198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8427-01A-11D-2310-10 chr17:46000416 C>G maps to NM_003110.5 T383T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8427-01A-11D-2310-10 chr17:46000416 C>G maps to NM_003110.5 T383T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8427-01A-11D-2310-10 chr7:83590704 C>T maps to NM_006080.2 R766R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8427-01A-11D-2310-10 chr7:83590704 C>T maps to NM_006080.2 R766R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr1:167088686 G>A maps to NM_001080426.1 A213A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr1:167088686 G>A maps to NM_001080426.1 A213A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr16:4940316 G>A maps to NM_002705.4 S727S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr16:4940316 G>A maps to NM_002705.4 S727S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr16:3334015 C>T maps to NM_005741.4 C66C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr16:3334015 C>T maps to NM_005741.4 C66C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chrX:2933299 C>A maps to NM_001011719.1 S210S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chrX:2933299 C>A maps to NM_001011719.1 S210S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr17:59445724 C>T maps to ENST00000407086 C851C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr17:59445724 C>T maps to ENST00000407086 C851C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr1:22902936 G>A maps to NM_020526.3 S129S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr1:22902936 G>A maps to NM_020526.3 S129S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr11:66039635 G>A maps to NM_030981.2 T32T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr11:66039635 G>A maps to NM_030981.2 T32T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr22:21082094 C>T maps to NM_058004.2 P1522P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr22:21082094 C>T maps to NM_058004.2 P1522P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr8:120628542 G>A maps to NM_006209.3 R247*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr8:120628542 G>A maps to NM_006209.3 R247*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr15:48755318 C>T maps to NM_000138.4 A1728A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr15:48755318 C>T maps to NM_000138.4 A1728A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr8:82571602 G>A maps to NM_001144878.1 R332*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr8:82571602 G>A maps to NM_001144878.1 R332*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr11:72404806 G>A maps to NM_001040118.2 H1246H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr11:72404806 G>A maps to NM_001040118.2 H1246H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr19:51738930 G>A maps to NM_001772.3 P308P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr19:51738930 G>A maps to NM_001772.3 P308P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr4:155254287 G>A maps to NM_017639.3 G525G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr4:155254287 G>A maps to NM_017639.3 G525G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr1:6646762 G>A maps to NM_005341.2 T351T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr1:6646762 G>A maps to NM_005341.2 T351T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr17:39411912 C>T maps to ENST00000431129 G98G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr17:39411912 C>T maps to ENST00000431129 G98G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr12:52449896 G>A maps to ENST00000360284 Q374Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr12:52449896 G>A maps to ENST00000360284 Q374Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr1:20005812 C>T maps to NM_000871.1 P425P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr1:20005812 C>T maps to NM_000871.1 P425P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr6:106553249 G>A maps to NM_001198.3 S405S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr6:106553249 G>A maps to NM_001198.3 S405S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr3:122420028 C>T maps to NM_017554.2 H876H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr3:122420028 C>T maps to NM_017554.2 H876H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr1:180135638 C>A maps to NM_002826.4 A93A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr1:180135638 C>A maps to NM_002826.4 A93A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr2:168100184 C>T maps to NM_152381.5 D761D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr2:168100184 C>T maps to NM_152381.5 D761D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr8:30436511 G>A maps to NM_002095.4 R268*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr8:30436511 G>A maps to NM_002095.4 R268*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chrX:138884414 C>T maps to NM_173694.4 Q216Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chrX:138884414 C>T maps to NM_173694.4 Q216Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr4:3107130 G>A maps to NM_002111.6 E192E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr4:3107130 G>A maps to NM_002111.6 E192E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr8:103848545 C>T maps to NM_148174.2 L174L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr8:103848545 C>T maps to NM_148174.2 L174L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr17:54672234 G>A maps to NM_005450.4 W217*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr17:54672234 G>A maps to NM_005450.4 W217*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr8:21924624 C>T maps to ENST00000265800 S16S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr8:21924624 C>T maps to ENST00000265800 S16S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr10:95168569 T>G maps to NM_013451.3 R235R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr10:95168569 T>G maps to NM_013451.3 R235R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr1:151641044 T>C maps to ENST00000458013 L361L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr1:151641044 T>C maps to ENST00000458013 L361L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr4:1746486 G>A maps to NM_006342.1 A793A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr4:1746486 G>A maps to NM_006342.1 A793A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr9:103064526 G>A maps to NM_017746.3 N912N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr9:103064526 G>A maps to NM_017746.3 N912N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr11:111938615 G>A maps to NM_138789.3 I309I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr11:111938615 G>A maps to NM_138789.3 I309I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr5:79366536 C>T maps to NM_003248.4 D508D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr5:79366536 C>T maps to NM_003248.4 D508D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr8:26513188 C>T maps to NM_001197293.1 P667P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr8:26513188 C>T maps to NM_001197293.1 P667P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr22:42341238 G>A maps to NM_024053.3 L100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr22:42341238 G>A maps to NM_024053.3 L100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr12:131466489 G>A maps to NM_198827.3 A124A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr12:131466489 G>A maps to NM_198827.3 A124A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr12:49251931 C>T maps to NM_014470.3 T182T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr12:49251931 C>T maps to NM_014470.3 T182T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr22:42987961 G>A maps to ENST00000415122 D357D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr22:42987961 G>A maps to ENST00000415122 D357D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr19:50548035 C>T maps to NM_015428.1 F112F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr19:50548035 C>T maps to NM_015428.1 F112F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr22:50720399 G>A maps to NM_012401.2 D1076D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr22:50720399 G>A maps to NM_012401.2 D1076D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr9:35396916 C>T maps to ENST00000396787 R1102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr9:35396916 C>T maps to ENST00000396787 R1102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr5:169931584 C>T maps to NM_001034837.1 A3A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr5:169931584 C>T maps to NM_001034837.1 A3A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr19:52941907 C>T maps to NM_001143939.1 R412*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr19:52941907 C>T maps to NM_001143939.1 R412*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr4:7725500 C>T maps to NM_020777.2 T834T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr4:7725500 C>T maps to NM_020777.2 T834T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr16:28603674 C>T maps to NM_001054.3 S228S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr16:28603674 C>T maps to NM_001054.3 S228S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr3:184038752 G>A maps to NM_001194947.1 T230T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr3:184038752 G>A maps to NM_001194947.1 T230T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr19:11568979 C>T maps to NM_001420.3 A203A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr19:11568979 C>T maps to NM_001420.3 A203A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr3:3179091 G>C maps to NM_182916.2 R99R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr3:3179091 G>C maps to NM_182916.2 R99R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr5:179192793 G>A maps to NM_014757.4 S261S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr5:179192793 G>A maps to NM_014757.4 S261S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr12:52910638 G>A maps to NM_000424.3 C407C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr12:52910638 G>A maps to NM_000424.3 C407C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr4:155254035 C>T maps to NM_017639.3 A609A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr4:155254035 C>T maps to NM_017639.3 A609A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr19:4409548 G>A maps to NM_005483.2 P251P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr19:4409548 G>A maps to NM_005483.2 P251P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr11:134009776 C>A maps to NM_032801.3 S81S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr11:134009776 C>A maps to NM_032801.3 S81S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr15:66214757 G>A maps to NM_032445.2 C625C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr15:66214757 G>A maps to NM_032445.2 C625C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr6:30864434 C>T maps to NM_013994.2 G554G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr6:30864434 C>T maps to NM_013994.2 G554G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr14:100141821 G>A maps to NM_001127258.1 L736L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr14:100141821 G>A maps to NM_001127258.1 L736L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr5:140250127 C>T maps to NM_018902.3 D480D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr5:140250127 C>T maps to NM_018902.3 D480D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr13:36909382 T>C maps to NM_001142294.1 S195S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr13:36909382 T>C maps to NM_001142294.1 S195S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr12:40689346 C>A maps to NM_198578.3 A999A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr12:40689346 C>A maps to NM_198578.3 A999A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr11:133800912 C>T maps to NM_014987.1 T495T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr11:133800912 C>T maps to NM_014987.1 T495T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr19:15752326 C>A maps to NM_000896.2 I34I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr19:15752326 C>A maps to NM_000896.2 I34I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr2:25799754 G>A maps to NM_021907.3 A276A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr2:25799754 G>A maps to NM_021907.3 A276A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr1:201060822 G>A maps to NM_000069.2 I213I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr1:201060822 G>A maps to NM_000069.2 I213I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr5:38510728 T>C maps to NM_002310.5 K276K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr5:38510728 T>C maps to NM_002310.5 K276K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr15:75980708 C>T maps to NM_001897.4 A899A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr15:75980708 C>T maps to NM_001897.4 A899A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr7:7472277 G>A maps to NM_001037763.2 G638G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr7:7472277 G>A maps to NM_001037763.2 G638G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr16:1306310 C>T maps to NM_012217.2 S10S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr16:1306310 C>T maps to NM_012217.2 S10S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr3:52552012 C>T maps to NM_015136.2 V1585V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr3:52552012 C>T maps to NM_015136.2 V1585V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr1:156814311 G>T maps to NM_014215.2 T893T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr1:156814311 G>T maps to NM_014215.2 T893T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr11:65744158 C>T maps to NM_005146.4 N593N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr11:65744158 C>T maps to NM_005146.4 N593N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr16:2093637 C>T maps to NM_002528.5 A213A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr16:2093637 C>T maps to NM_002528.5 A213A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr5:139251391 G>T maps to NM_013982.2 A342A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr5:139251391 G>T maps to NM_013982.2 A342A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr16:1612075 G>A maps to NM_014714.3 H703H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr16:1612075 G>A maps to NM_014714.3 H703H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr9:79322500 T>C maps to NM_015225.2 Q1563Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr9:79322500 T>C maps to NM_015225.2 Q1563Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr12:118588924 G>A maps to NM_016281.3 S858S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr12:118588924 G>A maps to NM_016281.3 S858S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr11:67925895 G>A maps to NM_017635.3 D639D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr11:67925895 G>A maps to NM_017635.3 D639D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr7:1588278 G>A maps to NM_001097620.1 S230S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr7:1588278 G>A maps to NM_001097620.1 S230S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr19:33666432 G>A maps to NM_173479.3 S458S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr19:33666432 G>A maps to NM_173479.3 S458S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr1:151339348 G>A maps to ENST00000435071 F213F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr1:151339348 G>A maps to ENST00000435071 F213F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr10:91371797 T>C maps to NM_148977.1 P237P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr10:91371797 T>C maps to NM_148977.1 P237P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr3:12858740 G>A maps to NM_001162499.1 P770P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr3:12858740 G>A maps to NM_001162499.1 P770P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr5:76645326 C>T maps to NM_003719.3 S320S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr5:76645326 C>T maps to NM_003719.3 S320S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr19:40730406 G>A maps to NM_024877.3 C167C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr19:40730406 G>A maps to NM_024877.3 C167C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr2:179578855 C>T maps to NM_133378.4 T7599T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr2:179578855 C>T maps to NM_133378.4 T7599T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr16:51173804 C>T maps to ENST00000251020 T776T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr16:51173804 C>T maps to ENST00000251020 T776T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr10:45485140 C>T maps to NM_032023.3 F219F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr10:45485140 C>T maps to NM_032023.3 F219F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr15:63966708 G>A maps to ENST00000261887 R2560*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr15:63966708 G>A maps to ENST00000261887 R2560*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr19:12865477 C>T maps to NM_017682.2 R120R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr19:12865477 C>T maps to NM_017682.2 R120R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr11:19170817 C>A maps to NM_019028.2 I153I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr11:19170817 C>A maps to NM_019028.2 I153I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr16:15711250 G>A maps to NM_014647.3 H954H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr16:15711250 G>A maps to NM_014647.3 H954H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr16:49671193 G>A maps to NM_015069.2 S623S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr16:49671193 G>A maps to NM_015069.2 S623S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr19:40366433 G>A maps to NM_003890.2 R4600R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr19:40366433 G>A maps to NM_003890.2 R4600R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr6:90661557 C>T maps to NM_001170794.1 P89P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr6:90661557 C>T maps to NM_001170794.1 P89P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr11:128781257 C>T maps to NM_000890.3 R30R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr11:128781257 C>T maps to NM_000890.3 R30R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr16:72822643 C>T maps to NM_006885.3 S3177S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr16:72822643 C>T maps to NM_006885.3 S3177S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr17:8044490 G>A maps to NM_002616.2 G1256G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr17:8044490 G>A maps to NM_002616.2 G1256G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr16:21734299 G>A did not map to a codon.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr16:21734299 G>A did not map to a codon.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr8:144995546 G>A maps to NM_201380.2 G2951G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr8:144995546 G>A maps to NM_201380.2 G2951G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr11:66101540 G>A maps to NM_004292.2 F480F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr11:66101540 G>A maps to NM_004292.2 F480F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr5:140750095 G>A maps to NM_018924.2 S45S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr5:140750095 G>A maps to NM_018924.2 S45S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr1:91809064 A>G maps to NM_001017975.3 L753L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr1:91809064 A>G maps to NM_001017975.3 L753L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr6:44329697 G>A maps to NM_145026.3 T181T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr6:44329697 G>A maps to NM_145026.3 T181T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr20:56185304 G>A maps to NM_030776.2 D331D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr20:56185304 G>A maps to NM_030776.2 D331D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr15:65157909 C>T maps to NM_025201.4 G432G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr15:65157909 C>T maps to NM_025201.4 G432G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr2:42720407 G>A maps to NM_133329.5 R78R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr2:42720407 G>A maps to NM_133329.5 R78R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr1:3807423 G>A maps to NM_207356.2 G109G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr1:3807423 G>A maps to NM_207356.2 G109G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr19:46308229 G>A maps to NM_030785.3 F311F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr19:46308229 G>A maps to NM_030785.3 F311F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr16:55360357 C>T maps to NM_024335.2 Y52Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr16:55360357 C>T maps to NM_024335.2 Y52Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr19:58264680 C>T maps to NM_173632.3 D61D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr19:58264680 C>T maps to NM_173632.3 D61D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr17:62291322 G>A maps to NM_018469.3 P85P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr17:62291322 G>A maps to NM_018469.3 P85P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr20:62065202 C>T maps to NM_172107.2 T359T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr20:62065202 C>T maps to NM_172107.2 T359T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr9:135073708 G>A maps to NM_032536.2 A190A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr9:135073708 G>A maps to NM_032536.2 A190A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr6:155450719 C>T maps to ENST00000456144 H121H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr6:155450719 C>T maps to ENST00000456144 H121H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr20:46365621 G>A maps to NM_001161841.1 N80N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr20:46365621 G>A maps to NM_001161841.1 N80N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr12:6078502 G>A maps to NM_000552.3 R2535*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr12:6078502 G>A maps to NM_000552.3 R2535*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr3:50005641 C>T maps to NM_005777.2 R262*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr3:50005641 C>T maps to NM_005777.2 R262*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr16:84778425 C>T maps to NM_005153.2 I113I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr16:84778425 C>T maps to NM_005153.2 I113I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr12:119968787 C>T maps to NM_178499.3 R491*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr12:119968787 C>T maps to NM_178499.3 R491*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr7:100484813 C>T maps to NM_015908.5 H656H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr7:100484813 C>T maps to NM_015908.5 H656H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr20:420957 G>A maps to ENST00000246077 H259H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr20:420957 G>A maps to ENST00000246077 H259H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr12:104391268 G>A maps to NM_031302.3 H149H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr12:104391268 G>A maps to NM_031302.3 H149H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr10:101716911 G>A maps to ENST00000342239 R107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr10:101716911 G>A maps to ENST00000342239 R107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr8:95541375 G>A maps to NM_015496.3 R268*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr8:95541375 G>A maps to NM_015496.3 R268*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr19:7521289 G>A did not map to a codon.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr19:7521289 G>A did not map to a codon.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr9:2191374 C>T maps to NM_003070.3 S1568S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr9:2191374 C>T maps to NM_003070.3 S1568S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr9:139908707 G>A maps to ENST00000355090 G1414G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr9:139908707 G>A maps to ENST00000355090 G1414G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr22:19839715 G>A maps to NM_024627.5 N23N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr22:19839715 G>A maps to NM_024627.5 N23N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr18:56191245 C>T maps to NM_052947.3 P1850P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr18:56191245 C>T maps to NM_052947.3 P1850P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr17:38512459 G>T maps to NM_001145301.2 P457P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr17:38512459 G>T maps to NM_001145301.2 P457P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr5:178454553 G>A maps to NM_001136116.1 L38L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr5:178454553 G>A maps to NM_001136116.1 L38L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr16:55690629 G>A maps to NM_001043.3 P8P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr16:55690629 G>A maps to NM_001043.3 P8P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr10:124172504 C>T maps to NM_021622.4 Q138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr10:124172504 C>T maps to NM_021622.4 Q138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr7:111368530 C>T maps to ENST00000428084 P1909P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr7:111368530 C>T maps to ENST00000428084 P1909P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr22:51117230 C>T maps to NM_001080420.1 N161N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr22:51117230 C>T maps to NM_001080420.1 N161N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr19:57765509 T>G maps to NM_001023563.3 T441T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr19:57765509 T>G maps to NM_001023563.3 T441T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr19:8209800 G>A maps to NM_032447.3 C167C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr19:8209800 G>A maps to NM_032447.3 C167C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr7:14620498 G>A maps to NM_004080.2 R534*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr7:14620498 G>A maps to NM_004080.2 R534*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr18:216575 G>A maps to NM_005131.2 S504S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr18:216575 G>A maps to NM_005131.2 S504S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr11:76506752 C>T maps to NM_015516.3 F31F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr11:76506752 C>T maps to NM_015516.3 F31F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr20:44641957 G>A maps to NM_004994.2 P465P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr20:44641957 G>A maps to NM_004994.2 P465P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr3:49059934 C>A maps to NM_199069.1 P78P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr3:49059934 C>A maps to NM_199069.1 P78P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr20:61878937 G>A maps to NM_152864.3 L155L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr20:61878937 G>A maps to NM_152864.3 L155L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr5:43613076 A>G maps to NM_182977.2 A73A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr5:43613076 A>G maps to NM_182977.2 A73A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr10:21097514 G>A maps to ENST00000430741 D897D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr10:21097514 G>A maps to ENST00000430741 D897D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr20:16021923 G>A did not map to a codon.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr20:16021923 G>A did not map to a codon.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr4:2950031 G>A maps to NM_003703.1 L462L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr4:2950031 G>A maps to NM_003703.1 L462L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr7:150648044 G>A maps to NM_000238.2 H703H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr7:150648044 G>A maps to NM_000238.2 H703H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr19:49473832 G>A maps to NM_002103.4 S593S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr19:49473832 G>A maps to NM_002103.4 S593S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr5:168096803 G>A maps to NM_003062.2 G1440G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr5:168096803 G>A maps to NM_003062.2 G1440G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr3:149093474 G>A maps to ENST00000383054 R87*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr3:149093474 G>A maps to ENST00000383054 R87*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr17:61497779 A>G maps to ENST00000389520 R1489R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr17:61497779 A>G maps to ENST00000389520 R1489R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr4:983646 C>T maps to NM_213613.2 A360A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr4:983646 C>T maps to NM_213613.2 A360A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr19:2249495 C>T maps to NM_000479.3 C55C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr19:2249495 C>T maps to NM_000479.3 C55C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr20:2560636 C>T maps to NM_080751.2 R257*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr20:2560636 C>T maps to NM_080751.2 R257*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr10:6063567 G>A maps to NM_000417.2 C152C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr10:6063567 G>A maps to NM_000417.2 C152C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr1:151377514 G>A maps to NM_015100.3 P1332P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr1:151377514 G>A maps to NM_015100.3 P1332P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr20:52601912 G>A maps to NM_003657.2 S351S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr20:52601912 G>A maps to NM_003657.2 S351S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr11:4624491 G>A maps to NM_018073.5 R169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr11:4624491 G>A maps to NM_018073.5 R169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr15:48703306 A>G maps to NM_000138.4 S2832S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr15:48703306 A>G maps to NM_000138.4 S2832S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr8:145139220 G>A maps to NM_003801.3 T267T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr8:145139220 G>A maps to NM_003801.3 T267T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr14:103988668 G>A maps to NM_001823.3 D54D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr14:103988668 G>A maps to NM_001823.3 D54D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr1:49208390 C>A maps to NM_024603.2 P266P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr1:49208390 C>A maps to NM_024603.2 P266P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr12:52681794 G>A maps to NM_002281.3 A291A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr12:52681794 G>A maps to NM_002281.3 A291A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr22:38536029 G>A maps to NM_003560.2 N252N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr22:38536029 G>A maps to NM_003560.2 N252N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr3:53757944 C>T maps to NM_001128840.1 G673G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr3:53757944 C>T maps to NM_001128840.1 G673G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr12:8083894 A>T maps to NM_006931.2 G152G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr12:8083894 A>T maps to NM_006931.2 G152G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr5:442634 C>T maps to NM_138464.2 A101A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr5:442634 C>T maps to NM_138464.2 A101A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr16:1291623 C>G maps to ENST00000461509 T148T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr16:1291623 C>G maps to ENST00000461509 T148T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr1:39951258 C>T maps to ENST00000361689 A5362A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr1:39951258 C>T maps to ENST00000361689 A5362A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr11:46911058 G>A maps to ENST00000256991 N751N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr11:46911058 G>A maps to ENST00000256991 N751N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr9:135553527 C>T maps to NM_012204.2 C174C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr9:135553527 C>T maps to NM_012204.2 C174C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr16:89169103 G>A maps to NM_174917.2 A253A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr16:89169103 G>A maps to NM_174917.2 A253A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr17:36521269 G>A maps to NM_014598.2 P346P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr17:36521269 G>A maps to NM_014598.2 P346P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr1:14107223 G>A maps to NM_012231.4 P978P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr1:14107223 G>A maps to NM_012231.4 P978P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr18:44057527 G>A maps to NM_144612.6 S2181S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr18:44057527 G>A maps to NM_144612.6 S2181S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr8:113657335 A>G did not map to a codon.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr8:113657335 A>G did not map to a codon.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr7:30662009 G>A maps to NM_002047.2 V515V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr7:30662009 G>A maps to NM_002047.2 V515V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr11:6632969 G>A maps to NM_006284.2 N104N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr11:6632969 G>A maps to NM_006284.2 N104N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr3:189526149 C>T maps to NM_003722.4 H138H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr3:189526149 C>T maps to NM_003722.4 H138H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr14:34145547 C>T maps to NM_001164749.1 A230A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr14:34145547 C>T maps to NM_001164749.1 A230A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr19:10818002 C>T maps to NM_031209.2 D159D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr19:10818002 C>T maps to NM_031209.2 D159D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr11:92086238 T>C maps to ENST00000298047 L321L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr11:92086238 T>C maps to ENST00000298047 L321L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr6:88853688 G>A maps to NM_016083.4 H435H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr6:88853688 G>A maps to NM_016083.4 H435H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr3:88105045 G>A maps to NM_001195308.1 V27V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr3:88105045 G>A maps to NM_001195308.1 V27V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr19:35941486 C>T maps to NM_005306.2 L291L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr19:35941486 C>T maps to NM_005306.2 L291L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr17:7578262 G>A maps to NM_001126112.1 R196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr17:7578262 G>A maps to NM_001126112.1 R196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr17:65134097 G>A maps to NM_014877.3 R968*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr17:65134097 G>A maps to NM_014877.3 R968*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chrX:54012316 G>A maps to NM_001184896.1 G723G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chrX:54012316 G>A maps to NM_001184896.1 G723G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr19:36210430 C>T maps to NM_014727.1 R142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr19:36210430 C>T maps to NM_014727.1 R142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr12:53685529 C>T maps to NM_012291.4 Y1859Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr12:53685529 C>T maps to NM_012291.4 Y1859Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr12:51752020 G>A maps to NM_007210.3 R465*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr12:51752020 G>A maps to NM_007210.3 R465*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr2:74327958 C>T maps to ENST00000409262 D1255D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr2:74327958 C>T maps to ENST00000409262 D1255D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr20:30231237 G>A maps to NM_032609.2 A93A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr20:30231237 G>A maps to NM_032609.2 A93A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr4:79236853 C>T maps to NM_025074.6 G595G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr4:79236853 C>T maps to NM_025074.6 G595G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr15:74315582 C>T maps to NM_033238.2 Y339Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr15:74315582 C>T maps to NM_033238.2 Y339Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr20:62571653 G>A maps to NM_017859.3 H472H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr20:62571653 G>A maps to NM_017859.3 H472H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr1:978745 C>T maps to NM_198576.2 S504S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr1:978745 C>T maps to NM_198576.2 S504S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr3:133553467 C>T maps to NM_016577.3 A171A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr3:133553467 C>T maps to NM_016577.3 A171A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr3:182681754 A>G maps to NM_020640.2 S101S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr3:182681754 A>G maps to NM_020640.2 S101S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr6:126210642 G>A maps to NM_181782.4 A481A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr6:126210642 G>A maps to NM_181782.4 A481A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr18:19070218 C>T maps to NM_001142966.1 R979R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr18:19070218 C>T maps to NM_001142966.1 R979R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr15:49030736 G>A maps to NM_001194998.1 S1614S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr15:49030736 G>A maps to NM_001194998.1 S1614S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr19:12574913 G>A maps to ENST00000428311 R608*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr19:12574913 G>A maps to ENST00000428311 R608*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr7:141619430 C>T maps to NM_001001656.1 Y252Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr7:141619430 C>T maps to NM_001001656.1 Y252Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr19:13186459 C>T maps to ENST00000397661 S310S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr19:13186459 C>T maps to ENST00000397661 S310S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr19:56024480 G>T maps to NM_001144950.1 G963G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr19:56024480 G>T maps to NM_001144950.1 G963G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr7:101259534 G>A maps to NM_138403.4 F166F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr7:101259534 G>A maps to NM_138403.4 F166F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr20:61981544 C>T maps to NM_000744.5 P406P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr20:61981544 C>T maps to NM_000744.5 P406P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr11:62286930 G>A maps to NM_001620.1 S4986S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr11:62286930 G>A maps to NM_001620.1 S4986S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr8:19363315 C>T maps to NM_018371.4 A10A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr8:19363315 C>T maps to NM_018371.4 A10A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr8:123964436 C>T maps to NM_014943.3 L229L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr8:123964436 C>T maps to NM_014943.3 L229L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr3:10960100 C>T maps to NM_014229.1 Y361Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr3:10960100 C>T maps to NM_014229.1 Y361Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr1:44303968 G>A maps to NM_174963.2 T165T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr1:44303968 G>A maps to NM_174963.2 T165T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr16:818455 G>A maps to NM_013404.4 P566P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr16:818455 G>A maps to NM_013404.4 P566P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr9:129870869 C>T maps to NM_012098.2 A47A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr9:129870869 C>T maps to NM_012098.2 A47A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr19:7606948 C>T maps to NM_001166111.1 I425I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr19:7606948 C>T maps to NM_001166111.1 I425I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr2:27802447 G>A maps to NM_032266.3 T1003T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr2:27802447 G>A maps to NM_032266.3 T1003T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr9:104153052 G>A maps to NM_019051.2 R58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr9:104153052 G>A maps to NM_019051.2 R58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr16:1574678 G>A maps to NM_014714.3 N1005N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr16:1574678 G>A maps to NM_014714.3 N1005N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr12:50185654 G>A maps to NM_001037806.3 Y1324Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr12:50185654 G>A maps to NM_001037806.3 Y1324Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr19:41072216 G>A maps to NM_020971.2 A2096A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr19:41072216 G>A maps to NM_020971.2 A2096A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr3:88040985 C>T maps to NM_000866.3 R363*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr3:88040985 C>T maps to NM_000866.3 R363*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr22:40717183 C>T maps to ENST00000454349 R1703*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr22:40717183 C>T maps to ENST00000454349 R1703*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr9:139915956 G>A maps to ENST00000355090 Q292*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr9:139915956 G>A maps to ENST00000355090 Q292*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr7:89854551 C>T maps to NM_152999.3 C52C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr7:89854551 C>T maps to NM_152999.3 C52C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr15:67358663 C>T maps to NM_005902.3 Q58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr15:67358663 C>T maps to NM_005902.3 Q58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr17:18923132 C>T maps to NM_152351.3 A522A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr17:18923132 C>T maps to NM_152351.3 A522A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr17:5436263 G>A maps to NM_033004.3 C1058C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr17:5436263 G>A maps to NM_033004.3 C1058C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr17:78320903 C>T maps to NM_020914.4 L2972L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr17:78320903 C>T maps to NM_020914.4 L2972L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chrX:83599462 A>C maps to NM_144657.4 T485T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chrX:83599462 A>C maps to NM_144657.4 T485T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr15:23889370 A>T maps to NM_019066.4 P1173P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr15:23889370 A>T maps to NM_019066.4 P1173P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr14:21834650 G>A maps to NM_007192.3 D331D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr14:21834650 G>A maps to NM_007192.3 D331D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr10:124057336 C>T maps to ENST00000368994 Y216Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr10:124057336 C>T maps to ENST00000368994 Y216Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr19:10794617 C>T maps to NM_017620.2 Y681Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr19:10794617 C>T maps to NM_017620.2 Y681Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr16:77228769 C>A maps to NM_014940.2 A338A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr16:77228769 C>A maps to NM_014940.2 A338A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr3:49940430 G>A maps to NM_002447.2 D204D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr3:49940430 G>A maps to NM_002447.2 D204D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr1:227921192 G>A maps to NM_023007.2 G294G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr1:227921192 G>A maps to NM_023007.2 G294G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr19:51646039 G>A maps to NM_014385.2 Q138Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr19:51646039 G>A maps to NM_014385.2 Q138Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr6:56044472 A>G maps to NM_030820.3 A181A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr6:56044472 A>G maps to NM_030820.3 A181A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr19:6733231 G>A maps to NM_001080452.1 S268S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr19:6733231 G>A maps to NM_001080452.1 S268S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr13:41657032 C>T maps to NM_007187.3 R372*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr13:41657032 C>T maps to NM_007187.3 R372*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr9:135919148 G>A maps to NM_001122823.1 T136T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr9:135919148 G>A maps to NM_001122823.1 T136T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr11:61906226 G>A maps to NM_001040694.1 A386A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr11:61906226 G>A maps to NM_001040694.1 A386A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr10:129216675 G>A maps to ENST00000398025 T1566T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr10:129216675 G>A maps to ENST00000398025 T1566T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr9:8485822 C>T maps to NM_002839.3 T998T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr9:8485822 C>T maps to NM_002839.3 T998T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr18:21474919 C>T maps to ENST00000416669 G1839G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr18:21474919 C>T maps to ENST00000416669 G1839G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr6:41767667 G>A maps to ENST00000373009 R524*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr6:41767667 G>A maps to ENST00000373009 R524*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr22:51064678 G>A maps to ENST00000395624 G294G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr22:51064678 G>A maps to ENST00000395624 G294G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chrX:70080717 G>A maps to NM_001003811.1 R120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chrX:70080717 G>A maps to NM_001003811.1 R120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr19:55239155 G>A maps to NM_153443.3 W145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr19:55239155 G>A maps to NM_153443.3 W145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr4:155163875 C>T maps to NM_017639.3 T1875T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr4:155163875 C>T maps to NM_017639.3 T1875T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr18:44554923 C>T maps to NM_145653.3 V430V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr18:44554923 C>T maps to NM_145653.3 V430V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr7:76024630 C>T maps to NM_080744.1 T295T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr7:76024630 C>T maps to NM_080744.1 T295T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr8:142477561 G>A maps to NM_207414.2 R753R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr8:142477561 G>A maps to NM_207414.2 R753R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr14:89817013 A>G did not map to a codon.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr14:89817013 A>G did not map to a codon.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr14:88945932 C>T maps to NM_007039.3 A614A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr14:88945932 C>T maps to NM_007039.3 A614A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr4:187629556 G>A maps to ENST00000260147 N475N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr4:187629556 G>A maps to ENST00000260147 N475N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr19:36349604 G>A did not map to a codon.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr19:36349604 G>A did not map to a codon.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr4:141481157 T>C maps to NM_021833.4 V272V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr4:141481157 T>C maps to NM_021833.4 V272V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr20:20475758 A>G did not map to a codon.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr20:20475758 A>G did not map to a codon.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr5:153795446 C>T maps to NM_198321.3 Y536Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr5:153795446 C>T maps to NM_198321.3 Y536Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr19:51021775 C>T maps to NM_001080457.1 T398T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr19:51021775 C>T maps to NM_001080457.1 T398T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr19:11892621 T>C maps to NM_152355.2 H661H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr19:11892621 T>C maps to NM_152355.2 H661H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr4:11401503 G>A maps to NM_005114.2 R42R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr4:11401503 G>A maps to NM_005114.2 R42R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr5:87494938 G>A maps to NM_153354.3 R315*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr5:87494938 G>A maps to NM_153354.3 R315*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr9:129642635 C>T maps to ENST00000319119 R320*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr9:129642635 C>T maps to ENST00000319119 R320*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr15:99454670 G>A did not map to a codon.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr15:99454670 G>A did not map to a codon.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr20:57769703 C>T maps to NM_178457.1 H1210H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr20:57769703 C>T maps to NM_178457.1 H1210H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr19:57647365 A>G maps to NM_052882.1 T113T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr19:57647365 A>G maps to NM_052882.1 T113T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr3:44684293 C>T maps to NM_006991.3 R558*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr3:44684293 C>T maps to NM_006991.3 R558*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr14:20763922 G>A maps to NM_138376.2 R263*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr14:20763922 G>A maps to NM_138376.2 R263*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr5:149212385 G>A maps to NM_133263.3 P250P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr5:149212385 G>A maps to NM_133263.3 P250P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr1:21887144 C>T maps to NM_000478.4 R30*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr1:21887144 C>T maps to NM_000478.4 R30*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr8:27097421 G>A did not map to a codon.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr8:27097421 G>A did not map to a codon.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr8:25341584 G>A maps to ENST00000434814 L409L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr8:25341584 G>A maps to ENST00000434814 L409L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr17:56290441 C>T maps to NM_017777.3 T253T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr17:56290441 C>T maps to NM_017777.3 T253T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chrX:154197603 A>G did not map to a codon.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chrX:154197603 A>G did not map to a codon.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr20:45355543 C>T maps to NM_030777.3 R444*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr20:45355543 C>T maps to NM_030777.3 R444*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr19:36120478 G>A maps to NM_024321.3 A62A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr19:36120478 G>A maps to NM_024321.3 A62A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr19:15063792 C>T maps to NM_005071.1 S482S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr19:15063792 C>T maps to NM_005071.1 S482S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr20:48744629 C>T maps to NM_199203.2 T191T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr20:48744629 C>T maps to NM_199203.2 T191T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr12:27933685 G>A maps to NM_020782.1 G141G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr12:27933685 G>A maps to NM_020782.1 G141G. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-KN-8428-01A-11D-2310-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr16:15818056 G>A maps to NM_001143979.1 T319T. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-KN-8428-01A-11D-2310-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr16:15818056 G>A maps to NM_001143979.1 T319T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr14:89307766 A>G did not map to a codon.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr14:89307766 A>G did not map to a codon.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr15:42193091 C>T maps to NM_139265.3 S459S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr15:42193091 C>T maps to NM_139265.3 S459S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr8:72129050 T>C maps to NM_000503.4 A412A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr8:72129050 T>C maps to NM_000503.4 A412A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr8:143746610 C>T maps to NM_003724.2 P289P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr8:143746610 C>T maps to NM_003724.2 P289P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr9:86895779 G>A maps to NM_022127.2 I555I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr9:86895779 G>A maps to NM_022127.2 I555I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr19:50399427 G>T did not map to a codon.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr19:50399427 G>T did not map to a codon.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr1:10713845 G>A maps to NM_001079843.1 A756A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr1:10713845 G>A maps to NM_001079843.1 A756A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr19:38386819 G>A maps to ENST00000447313 F68F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr19:38386819 G>A maps to ENST00000447313 F68F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr4:159076876 C>T maps to NM_001128424.1 Q337Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr4:159076876 C>T maps to NM_001128424.1 Q337Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr14:24879315 C>T maps to NM_025081.2 H772H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr14:24879315 C>T maps to NM_025081.2 H772H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chrX:49106625 C>T maps to NM_014008.3 G596G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chrX:49106625 C>T maps to NM_014008.3 G596G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr5:39377145 G>T maps to NM_001343.2 P581P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr5:39377145 G>T maps to NM_001343.2 P581P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr12:52867038 G>A maps to NM_173086.4 A161A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr12:52867038 G>A maps to NM_173086.4 A161A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr1:16053892 C>T maps to ENST00000420314 P545P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr1:16053892 C>T maps to ENST00000420314 P545P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr22:43236981 G>A maps to NM_014570.4 R77*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr22:43236981 G>A maps to NM_014570.4 R77*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr22:50617543 G>A maps to NM_052839.3 P624P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr22:50617543 G>A maps to NM_052839.3 P624P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr13:35733451 A>G maps to ENST00000400445 V1048V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr13:35733451 A>G maps to ENST00000400445 V1048V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr5:94005882 T>C maps to NM_032290.3 C520C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr5:94005882 T>C maps to NM_032290.3 C520C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr11:33770353 G>A maps to NM_012175.3 D339D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr11:33770353 G>A maps to NM_012175.3 D339D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr16:19236098 T>C maps to NM_016524.2 N389N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr16:19236098 T>C maps to NM_016524.2 N389N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr12:48185381 G>A maps to NM_015401.3 N640N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr12:48185381 G>A maps to NM_015401.3 N640N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr9:139730291 C>T maps to NM_001173988.1 Y269Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr9:139730291 C>T maps to NM_001173988.1 Y269Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr9:86571235 G>A maps to NM_032307.3 A60A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr9:86571235 G>A maps to NM_032307.3 A60A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr19:37916857 C>T maps to NM_152484.2 P50P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr19:37916857 C>T maps to NM_152484.2 P50P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr15:75949417 C>T maps to NM_153271.1 A529A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr15:75949417 C>T maps to NM_153271.1 A529A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8429-01A-11D-2310-10 chr1:154315637 C>T maps to NM_020452.3 T534T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8429-01A-11D-2310-10 chr1:154315637 C>T maps to NM_020452.3 T534T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8429-01A-11D-2310-10 chr7:37136305 T>C maps to NM_014800.9 E406E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8429-01A-11D-2310-10 chr7:37136305 T>C maps to NM_014800.9 E406E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8429-01A-11D-2310-10 chr3:195509690 T>A maps to NM_018406.5 S2920S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8429-01A-11D-2310-10 chr3:195509690 T>A maps to NM_018406.5 S2920S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8429-01A-11D-2310-10 chr4:107154197 A>G maps to NM_001163436.1 C512C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8429-01A-11D-2310-10 chr4:107154197 A>G maps to NM_001163436.1 C512C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8429-01A-11D-2310-10 chr10:115973823 T>C maps to NM_198795.1 C721C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8429-01A-11D-2310-10 chr10:115973823 T>C maps to NM_198795.1 C721C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8429-01A-11D-2310-10 chr1:50162980 T>C did not map to a codon.
Sequencing variant TCGA-KN-8429-01A-11D-2310-10 chr1:50162980 T>C did not map to a codon.
Sequencing variant TCGA-KN-8429-01A-11D-2310-10 chr4:73205261 A>G maps to NM_014243.1 R270R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8429-01A-11D-2310-10 chr4:73205261 A>G maps to NM_014243.1 R270R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8429-01A-11D-2310-10 chr8:8998707 G>A maps to NM_024607.2 Q152*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8429-01A-11D-2310-10 chr8:8998707 G>A maps to NM_024607.2 Q152*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8430-01A-11D-2310-10 chr7:156742688 G>A maps to NM_138400.1 R86R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8430-01A-11D-2310-10 chr7:156742688 G>A maps to NM_138400.1 R86R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8430-01A-11D-2310-10 chr7:149480235 C>T maps to NM_198455.2 D706D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8430-01A-11D-2310-10 chr7:149480235 C>T maps to NM_198455.2 D706D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8430-01A-11D-2310-10 chr4:89408221 C>T maps to NM_016323.2 D618D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8430-01A-11D-2310-10 chr4:89408221 C>T maps to NM_016323.2 D618D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8430-01A-11D-2310-10 chr2:131486933 G>A maps to NM_207364.2 L70L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8430-01A-11D-2310-10 chr2:131486933 G>A maps to NM_207364.2 L70L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8430-01A-11D-2310-10 chr5:79025640 A>G maps to NM_153610.3 A351A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8430-01A-11D-2310-10 chr5:79025640 A>G maps to NM_153610.3 A351A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8430-01A-11D-2310-10 chr21:46000293 C>T maps to NM_198694.2 A54A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8430-01A-11D-2310-10 chr21:46000293 C>T maps to NM_198694.2 A54A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8430-01A-11D-2310-10 chr2:171709232 A>C maps to NM_000817.2 S398S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8430-01A-11D-2310-10 chr2:171709232 A>C maps to NM_000817.2 S398S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8430-01A-11D-2310-10 chr6:43746625 A>G maps to NM_001025366.2 R311R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8430-01A-11D-2310-10 chr6:43746625 A>G maps to NM_001025366.2 R311R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8430-01A-11D-2310-10 chr3:16630167 C>G maps to NM_001190811.1 *316S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8430-01A-11D-2310-10 chr3:16630167 C>G maps to NM_001190811.1 *316S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8430-01A-11D-2310-10 chr2:179426291 A>G maps to NM_133378.4 Y25621Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8430-01A-11D-2310-10 chr2:179426291 A>G maps to NM_133378.4 Y25621Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8430-01A-11D-2310-10 chr12:12871757 G>C did not map to a codon.
Sequencing variant TCGA-KN-8430-01A-11D-2310-10 chr12:12871757 G>C did not map to a codon.
Sequencing variant TCGA-KN-8430-01A-11D-2310-10 chr2:136558374 G>A maps to NM_002299.2 V1556V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8430-01A-11D-2310-10 chr2:136558374 G>A maps to NM_002299.2 V1556V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8430-01A-11D-2310-10 chr11:92543183 T>A maps to ENST00000298047 Y3141*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8430-01A-11D-2310-10 chr11:92543183 T>A maps to ENST00000298047 Y3141*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8431-01A-11D-2310-10 chr4:122743633 A>G maps to NM_001237.3 A127A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8431-01A-11D-2310-10 chr4:122743633 A>G maps to NM_001237.3 A127A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8431-01A-11D-2310-10 chr5:61653553 C>T maps to NM_001098511.1 R231*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8431-01A-11D-2310-10 chr5:61653553 C>T maps to NM_001098511.1 R231*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8431-01A-11D-2310-10 chr1:16383401 C>T maps to NM_000085.3 A685A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8431-01A-11D-2310-10 chr1:16383401 C>T maps to NM_000085.3 A685A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8431-01A-11D-2310-10 chr14:50626455 T>A maps to NM_006939.2 V515V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8431-01A-11D-2310-10 chr14:50626455 T>A maps to NM_006939.2 V515V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8431-01A-11D-2310-10 chr9:2039814 G>A maps to NM_003070.3 Q235Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8431-01A-11D-2310-10 chr9:2039814 G>A maps to NM_003070.3 Q235Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8431-01A-11D-2310-10 chr7:105182934 T>C maps to NM_021930.4 N118N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8431-01A-11D-2310-10 chr7:105182934 T>C maps to NM_021930.4 N118N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8431-01A-11D-2310-10 chr17:7578211 G>A maps to NM_001126112.1 R213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8431-01A-11D-2310-10 chr17:7578211 G>A maps to NM_001126112.1 R213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8431-01A-11D-2310-10 chr19:44980906 T>C maps to NM_013256.3 R597R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8431-01A-11D-2310-10 chr19:44980906 T>C maps to NM_013256.3 R597R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8432-01A-11D-2310-10 chr4:52861444 G>A maps to NM_001024611.1 S581S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8432-01A-11D-2310-10 chr4:52861444 G>A maps to NM_001024611.1 S581S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8432-01A-11D-2310-10 chr16:71419535 C>T maps to NM_001740.4 Y228Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8432-01A-11D-2310-10 chr16:71419535 C>T maps to NM_001740.4 Y228Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8432-01A-11D-2310-10 chr2:169999256 T>C maps to NM_004525.2 R4345R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8432-01A-11D-2310-10 chr2:169999256 T>C maps to NM_004525.2 R4345R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8432-01A-11D-2310-10 chrX:54837699 G>A maps to NM_201222.1 K288K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8432-01A-11D-2310-10 chrX:54837699 G>A maps to NM_201222.1 K288K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8432-01A-11D-2310-10 chr18:56414968 C>T maps to NM_006785.2 F790F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8432-01A-11D-2310-10 chr18:56414968 C>T maps to NM_006785.2 F790F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8432-01A-11D-2310-10 chr1:183885723 G>A maps to NM_015149.3 T666T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8432-01A-11D-2310-10 chr1:183885723 G>A maps to NM_015149.3 T666T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8432-01A-11D-2310-10 chr3:63649636 A>T maps to NM_001080537.1 R104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8432-01A-11D-2310-10 chr3:63649636 A>T maps to NM_001080537.1 R104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8432-01A-11D-2310-10 chr7:50444369 C>T maps to NM_006060.3 G100G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8432-01A-11D-2310-10 chr7:50444369 C>T maps to NM_006060.3 G100G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8432-01A-11D-2310-10 chr19:57724078 C>T maps to NM_003417.4 P538P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8432-01A-11D-2310-10 chr19:57724078 C>T maps to NM_003417.4 P538P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8432-01A-11D-2310-10 chrX:37028120 C>T maps to NM_001013736.2 L546L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8432-01A-11D-2310-10 chrX:37028120 C>T maps to NM_001013736.2 L546L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8432-01A-11D-2310-10 chr4:48513001 C>G did not map to a codon.
Sequencing variant TCGA-KN-8432-01A-11D-2310-10 chr4:48513001 C>G did not map to a codon.
Sequencing variant TCGA-KN-8432-01A-11D-2310-10 chr3:127323459 C>T maps to NM_004526.2 R82R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8432-01A-11D-2310-10 chr3:127323459 C>T maps to NM_004526.2 R82R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8432-01A-11D-2310-10 chr6:112480082 C>G did not map to a codon.
Sequencing variant TCGA-KN-8432-01A-11D-2310-10 chr6:112480082 C>G did not map to a codon.
Sequencing variant TCGA-KN-8432-01A-11D-2310-10 chr19:36632119 C>T maps to NM_001749.2 I69I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8432-01A-11D-2310-10 chr19:36632119 C>T maps to NM_001749.2 I69I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8432-01A-11D-2310-10 chr12:46633472 A>G maps to NM_030674.3 G37G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8432-01A-11D-2310-10 chr12:46633472 A>G maps to NM_030674.3 G37G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8432-01A-11D-2310-10 chr1:223936793 G>C maps to NM_001748.4 G261G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8432-01A-11D-2310-10 chr1:223936793 G>C maps to NM_001748.4 G261G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8432-01A-11D-2310-10 chr17:38346942 C>T maps to ENST00000456989 R421*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8432-01A-11D-2310-10 chr17:38346942 C>T maps to ENST00000456989 R421*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8432-01A-11D-2310-10 chr16:89838100 C>T maps to NM_000135.2 E712E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8432-01A-11D-2310-10 chr16:89838100 C>T maps to NM_000135.2 E712E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8432-01A-11D-2310-10 chr8:19680920 T>C maps to NM_018142.2 T211T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8432-01A-11D-2310-10 chr8:19680920 T>C maps to NM_018142.2 T211T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8432-01A-11D-2310-10 chr17:62021159 G>A maps to NM_000334.4 N1321N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8432-01A-11D-2310-10 chr17:62021159 G>A maps to NM_000334.4 N1321N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8432-01A-11D-2310-10 chr11:63988120 C>T maps to NM_178443.2 R513*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8432-01A-11D-2310-10 chr11:63988120 C>T maps to NM_178443.2 R513*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8433-01A-11D-2310-10 chr8:144890885 G>A maps to NM_182706.3 Q670*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8433-01A-11D-2310-10 chr8:144890885 G>A maps to NM_182706.3 Q670*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8433-01A-11D-2310-10 chr17:7579698 C>A did not map to a codon.
Sequencing variant TCGA-KN-8433-01A-11D-2310-10 chr17:7579698 C>A did not map to a codon.
Sequencing variant TCGA-KN-8433-01A-11D-2310-10 chr10:101969425 G>A maps to NM_001278.3 Q352*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8433-01A-11D-2310-10 chr10:101969425 G>A maps to NM_001278.3 Q352*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8433-01A-11D-2310-10 chr7:45123696 C>T maps to NM_001146334.1 S694S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8433-01A-11D-2310-10 chr7:45123696 C>T maps to NM_001146334.1 S694S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8433-01A-11D-2310-10 chr19:39421913 A>G did not map to a codon.
Sequencing variant TCGA-KN-8433-01A-11D-2310-10 chr19:39421913 A>G did not map to a codon.
Sequencing variant TCGA-KN-8433-01A-11D-2310-10 chr12:126138172 C>T maps to NM_052907.2 Y718Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8433-01A-11D-2310-10 chr12:126138172 C>T maps to NM_052907.2 Y718Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8433-01A-11D-2310-10 chr20:35262936 G>A maps to NM_032214.2 A49A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8433-01A-11D-2310-10 chr20:35262936 G>A maps to NM_032214.2 A49A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8433-01A-11D-2310-10 chr3:109129036 C>T maps to NM_001145553.1 G8G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8433-01A-11D-2310-10 chr3:109129036 C>T maps to NM_001145553.1 G8G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8433-01A-11D-2310-10 chr19:34818400 C>T maps to NM_014686.3 Q261*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8433-01A-11D-2310-10 chr19:34818400 C>T maps to NM_014686.3 Q261*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8433-01A-11D-2310-10 chr7:73184304 C>T maps to NM_001306.3 A25A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8433-01A-11D-2310-10 chr7:73184304 C>T maps to NM_001306.3 A25A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8434-01A-11D-2310-10 chrX:48418348 C>A maps to NM_002536.2 A351A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8434-01A-11D-2310-10 chrX:48418348 C>A maps to NM_002536.2 A351A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8434-01A-11D-2310-10 chr11:119024754 G>A maps to NM_001142505.1 K86K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8434-01A-11D-2310-10 chr11:119024754 G>A maps to NM_001142505.1 K86K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8434-01A-11D-2310-10 chr3:48669761 G>A maps to NM_022911.2 N167N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8434-01A-11D-2310-10 chr3:48669761 G>A maps to NM_022911.2 N167N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8434-01A-11D-2310-10 chr7:70231280 C>T maps to NM_015570.2 I550I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8434-01A-11D-2310-10 chr7:70231280 C>T maps to NM_015570.2 I550I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8434-01A-11D-2310-10 chr13:99476684 T>C maps to ENST00000428223 E1699E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8434-01A-11D-2310-10 chr13:99476684 T>C maps to ENST00000428223 E1699E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8434-01A-11D-2310-10 chr22:28193288 C>T maps to NM_002430.2 S1081S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8434-01A-11D-2310-10 chr22:28193288 C>T maps to NM_002430.2 S1081S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8434-01A-11D-2310-10 chr17:7534019 C>T maps to NM_001040.3 R76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8434-01A-11D-2310-10 chr17:7534019 C>T maps to NM_001040.3 R76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8435-01A-11D-2310-10 chr22:37875490 C>T maps to NM_002405.3 A151A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8435-01A-11D-2310-10 chr22:37875490 C>T maps to NM_002405.3 A151A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8435-01A-11D-2310-10 chr9:95991991 C>G maps to ENST00000297954 T232T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8435-01A-11D-2310-10 chr9:95991991 C>G maps to ENST00000297954 T232T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8435-01A-11D-2310-10 chr17:58156292 G>C did not map to a codon.
Sequencing variant TCGA-KN-8435-01A-11D-2310-10 chr17:58156292 G>C did not map to a codon.
Sequencing variant TCGA-KN-8435-01A-11D-2310-10 chr16:4431909 C>T maps to NM_138440.2 Y344Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8435-01A-11D-2310-10 chr16:4431909 C>T maps to NM_138440.2 Y344Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8435-01A-11D-2310-10 chr22:50216912 A>G maps to ENST00000342989 H351H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8435-01A-11D-2310-10 chr22:50216912 A>G maps to ENST00000342989 H351H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8435-01A-11D-2310-10 chr19:17036077 A>G maps to ENST00000443236 L1216L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8435-01A-11D-2310-10 chr19:17036077 A>G maps to ENST00000443236 L1216L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8435-01A-11D-2310-10 chr17:41244424 T>C maps to ENST00000471181 S1041S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8435-01A-11D-2310-10 chr17:41244424 T>C maps to ENST00000471181 S1041S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8435-01A-11D-2310-10 chr11:57982413 G>A maps to NM_001004458.1 T66T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8435-01A-11D-2310-10 chr11:57982413 G>A maps to NM_001004458.1 T66T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8436-01A-11D-2310-10 chr19:2515019 T>A maps to NM_052847.2 *69Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8436-01A-11D-2310-10 chr19:2515019 T>A maps to NM_052847.2 *69Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8436-01A-11D-2310-10 chr12:81503374 C>T maps to NM_024560.2 A116A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8436-01A-11D-2310-10 chr12:81503374 C>T maps to NM_024560.2 A116A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8436-01A-11D-2310-10 chr1:155112593 C>A maps to NM_018973.3 L71L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8436-01A-11D-2310-10 chr1:155112593 C>A maps to NM_018973.3 L71L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8436-01A-11D-2310-10 chr12:32136954 T>A maps to NM_018169.3 P1022P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8436-01A-11D-2310-10 chr12:32136954 T>A maps to NM_018169.3 P1022P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8436-01A-11D-2310-10 chr11:66335106 C>T maps to NM_003793.3 E113E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8436-01A-11D-2310-10 chr11:66335106 C>T maps to NM_003793.3 E113E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8436-01A-11D-2310-10 chr14:51196405 C>T maps to NM_020921.3 P1971P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8436-01A-11D-2310-10 chr14:51196405 C>T maps to NM_020921.3 P1971P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8436-01A-11D-2310-10 chr1:8922982 G>A maps to NM_001428.2 R400*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8436-01A-11D-2310-10 chr1:8922982 G>A maps to NM_001428.2 R400*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8437-01A-11D-2310-10 chr10:72293730 C>G maps to NM_014431.2 L308L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8437-01A-11D-2310-10 chr10:72293730 C>G maps to NM_014431.2 L308L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8437-01A-11D-2310-10 chr1:14107868 T>C maps to NM_012231.4 C1193C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8437-01A-11D-2310-10 chr1:14107868 T>C maps to NM_012231.4 C1193C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8437-01A-11D-2310-10 chr6:84233684 G>A maps to NM_153362.2 K175K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8437-01A-11D-2310-10 chr6:84233684 G>A maps to NM_153362.2 K175K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8437-01A-11D-2310-10 chr19:44117019 C>T maps to NM_001145641.1 I249I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8437-01A-11D-2310-10 chr19:44117019 C>T maps to NM_001145641.1 I249I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8437-01A-11D-2310-10 chr18:22930910 C>A did not map to a codon.
Sequencing variant TCGA-KN-8437-01A-11D-2310-10 chr18:22930910 C>A did not map to a codon.
Multiple mappings detected for codon TCGA-KN-8437-01A-11D-2310-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-KN-8437-01A-11D-2310-10 chr16:31073369 C>G maps to ENST00000417110 L186L. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-KN-8437-01A-11D-2310-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-KN-8437-01A-11D-2310-10 chr16:31073369 C>G maps to ENST00000417110 L186L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8403-01A-11D-2310-10 chr11:1075669 C>T maps to ENST00000441003 H32H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8403-01A-11D-2310-10 chr11:1075669 C>T maps to ENST00000441003 H32H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8403-01A-11D-2310-10 chr11:117307844 G>A maps to NM_020693.2 Y1631Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8403-01A-11D-2310-10 chr11:117307844 G>A maps to NM_020693.2 Y1631Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8403-01A-11D-2310-10 chr3:57431083 G>T maps to NM_178504.4 L1391L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8403-01A-11D-2310-10 chr3:57431083 G>T maps to NM_178504.4 L1391L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8403-01A-11D-2310-10 chr22:32797732 C>A did not map to a codon.
Sequencing variant TCGA-KO-8403-01A-11D-2310-10 chr22:32797732 C>A did not map to a codon.
Sequencing variant TCGA-KO-8403-01A-11D-2310-10 chr5:140480871 C>T maps to NM_018937.2 T213T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8403-01A-11D-2310-10 chr5:140480871 C>T maps to NM_018937.2 T213T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8403-01A-11D-2310-10 chr14:20019956 G>A maps to ENST00000439503 D88D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8403-01A-11D-2310-10 chr14:20019956 G>A maps to ENST00000439503 D88D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8403-01A-11D-2310-10 chr19:49656871 C>T maps to NM_002152.2 E541E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8403-01A-11D-2310-10 chr19:49656871 C>T maps to NM_002152.2 E541E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8404-01A-11D-2310-10 chr3:121659850 C>A maps to NM_021082.3 L729L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8404-01A-11D-2310-10 chr3:121659850 C>A maps to NM_021082.3 L729L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8404-01A-11D-2310-10 chr20:56087701 A>G maps to ENST00000423479 T479T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8404-01A-11D-2310-10 chr20:56087701 A>G maps to ENST00000423479 T479T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8404-01A-11D-2310-10 chr17:71375626 C>A maps to NM_001144952.1 G1608G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8404-01A-11D-2310-10 chr17:71375626 C>A maps to NM_001144952.1 G1608G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8404-01A-11D-2310-10 chr1:1389870 C>T maps to NM_001039211.2 H123H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8404-01A-11D-2310-10 chr1:1389870 C>T maps to NM_001039211.2 H123H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8404-01A-11D-2310-10 chr18:8609871 C>A maps to NM_001025300.2 G49G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8404-01A-11D-2310-10 chr18:8609871 C>A maps to NM_001025300.2 G49G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8404-01A-11D-2310-10 chr16:4029167 G>A maps to NM_001116.3 P876P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8404-01A-11D-2310-10 chr16:4029167 G>A maps to NM_001116.3 P876P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8404-01A-11D-2310-10 chr1:172037990 G>A maps to ENST00000359070 T456T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8404-01A-11D-2310-10 chr1:172037990 G>A maps to ENST00000359070 T456T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8404-01A-11D-2310-10 chr15:68624720 G>A maps to ENST00000423218 N507N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8404-01A-11D-2310-10 chr15:68624720 G>A maps to ENST00000423218 N507N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8404-01A-11D-2310-10 chr4:69795704 T>G maps to NM_024743.3 G470G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8404-01A-11D-2310-10 chr4:69795704 T>G maps to NM_024743.3 G470G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8404-01A-11D-2310-10 chr19:18507173 C>T maps to NM_145256.2 E200E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8404-01A-11D-2310-10 chr19:18507173 C>T maps to NM_145256.2 E200E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8404-01A-11D-2310-10 chr17:7577608 C>T did not map to a codon.
Sequencing variant TCGA-KO-8404-01A-11D-2310-10 chr17:7577608 C>T did not map to a codon.
Sequencing variant TCGA-KO-8404-01A-11D-2310-10 chr19:49001438 C>A maps to NM_001080434.1 E992*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8404-01A-11D-2310-10 chr19:49001438 C>A maps to NM_001080434.1 E992*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8404-01A-11D-2310-10 chr6:70873232 A>T did not map to a codon.
Sequencing variant TCGA-KO-8404-01A-11D-2310-10 chr6:70873232 A>T did not map to a codon.
Sequencing variant TCGA-KO-8404-01A-11D-2310-10 chr1:94639722 C>T maps to NM_004815.3 W1163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8404-01A-11D-2310-10 chr1:94639722 C>T maps to NM_004815.3 W1163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8405-01A-11D-2310-10 chr16:3817814 T>C maps to NM_004380.2 K1052K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8405-01A-11D-2310-10 chr16:3817814 T>C maps to NM_004380.2 K1052K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8405-01A-11D-2310-10 chr9:136550313 C>A did not map to a codon.
Sequencing variant TCGA-KO-8405-01A-11D-2310-10 chr9:136550313 C>A did not map to a codon.
Sequencing variant TCGA-KO-8405-01A-11D-2310-10 chr20:2686301 C>T maps to ENST00000342725 L73L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8405-01A-11D-2310-10 chr20:2686301 C>T maps to ENST00000342725 L73L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8405-01A-11D-2310-10 chr1:16386094 G>A maps to NM_182623.2 V152V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8405-01A-11D-2310-10 chr1:16386094 G>A maps to NM_182623.2 V152V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8405-01A-11D-2310-10 chr17:43523002 C>G maps to NM_014798.2 L890L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8405-01A-11D-2310-10 chr17:43523002 C>G maps to NM_014798.2 L890L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8405-01A-11D-2310-10 chr11:64664286 G>A maps to ENST00000421419 D1737D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8405-01A-11D-2310-10 chr11:64664286 G>A maps to ENST00000421419 D1737D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8406-01A-11D-2310-10 chr9:139262145 C>T maps to NM_052813.4 A404A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8406-01A-11D-2310-10 chr9:139262145 C>T maps to NM_052813.4 A404A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8406-01A-11D-2310-10 chr12:91550948 C>T maps to NM_133503.2 P185P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8406-01A-11D-2310-10 chr12:91550948 C>T maps to NM_133503.2 P185P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8406-01A-11D-2310-10 chr11:61537796 A>C maps to NM_001127392.1 P180P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8406-01A-11D-2310-10 chr11:61537796 A>C maps to NM_001127392.1 P180P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8406-01A-11D-2310-10 chr6:139164270 G>A maps to NM_001195037.2 T166T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8406-01A-11D-2310-10 chr6:139164270 G>A maps to NM_001195037.2 T166T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8406-01A-11D-2310-10 chr18:9887447 C>T maps to NM_001098529.1 P324P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8406-01A-11D-2310-10 chr18:9887447 C>T maps to NM_001098529.1 P324P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8406-01A-11D-2310-10 chr16:57984388 T>C maps to NM_001297.4 E310E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8406-01A-11D-2310-10 chr16:57984388 T>C maps to NM_001297.4 E310E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8407-01A-11D-2310-10 chr11:7439308 C>T maps to NM_175733.3 P429P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8407-01A-11D-2310-10 chr11:7439308 C>T maps to NM_175733.3 P429P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8407-01A-11D-2310-10 chr6:75843573 C>A maps to ENST00000322507 L1888L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8407-01A-11D-2310-10 chr6:75843573 C>A maps to ENST00000322507 L1888L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8407-01A-11D-2310-10 chr19:55107717 C>T maps to NM_006863.1 N341N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8407-01A-11D-2310-10 chr19:55107717 C>T maps to NM_006863.1 N341N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8407-01A-11D-2310-10 chr5:140222357 G>A maps to NM_018911.2 A484A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8407-01A-11D-2310-10 chr5:140222357 G>A maps to NM_018911.2 A484A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8407-01A-11D-2310-10 chr18:31325883 T>C maps to NM_030632.1 P2024P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8407-01A-11D-2310-10 chr18:31325883 T>C maps to NM_030632.1 P2024P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8407-01A-11D-2310-10 chr20:1276942 C>A maps to ENST00000381876 G20G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8407-01A-11D-2310-10 chr20:1276942 C>A maps to ENST00000381876 G20G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8407-01A-11D-2310-10 chr9:139946005 G>T maps to NM_203468.1 G114G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8407-01A-11D-2310-10 chr9:139946005 G>T maps to NM_203468.1 G114G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8407-01A-11D-2310-10 chr5:13708237 C>T maps to NM_001369.2 W4444*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8407-01A-11D-2310-10 chr5:13708237 C>T maps to NM_001369.2 W4444*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8408-01A-11D-2310-10 chr10:63700093 G>A maps to NM_032199.2 L143L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8408-01A-11D-2310-10 chr10:63700093 G>A maps to NM_032199.2 L143L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8408-01A-11D-2310-10 chr8:90802424 G>A maps to NM_003821.5 L468L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8408-01A-11D-2310-10 chr8:90802424 G>A maps to NM_003821.5 L468L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8408-01A-11D-2310-10 chr17:39623193 G>A maps to NM_002278.3 I128I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8408-01A-11D-2310-10 chr17:39623193 G>A maps to NM_002278.3 I128I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8408-01A-11D-2310-10 chr16:28128692 G>A maps to NM_015171.2 F650F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8408-01A-11D-2310-10 chr16:28128692 G>A maps to NM_015171.2 F650F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8408-01A-11D-2310-10 chr14:21992202 C>T maps to NM_005407.1 L553L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8408-01A-11D-2310-10 chr14:21992202 C>T maps to NM_005407.1 L553L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8408-01A-11D-2310-10 chr15:72954854 G>A maps to NM_018652.4 Q370Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8408-01A-11D-2310-10 chr15:72954854 G>A maps to NM_018652.4 Q370Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8408-01A-11D-2310-10 chr4:79301067 C>T maps to NM_025074.6 Q1161*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8408-01A-11D-2310-10 chr4:79301067 C>T maps to NM_025074.6 Q1161*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8408-01A-11D-2310-10 chr11:15267582 G>T maps to NM_001031853.3 V579V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8408-01A-11D-2310-10 chr11:15267582 G>T maps to NM_001031853.3 V579V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8408-01A-11D-2310-10 chr10:89693002 A>T maps to NM_000314.4 K163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8408-01A-11D-2310-10 chr10:89693002 A>T maps to NM_000314.4 K163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8408-01A-11D-2310-10 chr15:99671286 A>T maps to ENST00000336292 K907*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8408-01A-11D-2310-10 chr15:99671286 A>T maps to ENST00000336292 K907*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8408-01A-11D-2310-10 chr5:134782501 C>T maps to NM_130848.2 S99S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8408-01A-11D-2310-10 chr5:134782501 C>T maps to NM_130848.2 S99S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8408-01A-11D-2310-10 chr1:214171242 T>A maps to NM_002763.3 P455P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8408-01A-11D-2310-10 chr1:214171242 T>A maps to NM_002763.3 P455P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8408-01A-11D-2310-10 chr13:39266097 C>T maps to NM_207361.4 H1539H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8408-01A-11D-2310-10 chr13:39266097 C>T maps to NM_207361.4 H1539H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8408-01A-11D-2310-10 chr2:88125233 T>C maps to NM_001078170.2 K5K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8408-01A-11D-2310-10 chr2:88125233 T>C maps to NM_001078170.2 K5K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8408-01A-11D-2310-10 chr19:44418133 G>C maps to NM_003425.3 S485*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8408-01A-11D-2310-10 chr19:44418133 G>C maps to NM_003425.3 S485*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8408-01A-11D-2310-10 chr20:30408124 C>T maps to NM_033118.3 G83G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8408-01A-11D-2310-10 chr20:30408124 C>T maps to NM_033118.3 G83G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8408-01A-11D-2310-10 chr3:48694701 G>A maps to NM_001407.2 T1276T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8408-01A-11D-2310-10 chr3:48694701 G>A maps to NM_001407.2 T1276T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8408-01A-11D-2310-10 chr14:91044470 G>A maps to NM_001010854.1 H763H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8408-01A-11D-2310-10 chr14:91044470 G>A maps to NM_001010854.1 H763H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8408-01A-11D-2310-10 chr12:21242949 A>G maps to ENST00000381541 V632V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8408-01A-11D-2310-10 chr12:21242949 A>G maps to ENST00000381541 V632V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8409-01A-11D-2310-10 chr11:26465369 C>T maps to NM_031418.2 S100S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8409-01A-11D-2310-10 chr11:26465369 C>T maps to NM_031418.2 S100S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8409-01A-11D-2310-10 chr1:21014270 C>T maps to NM_020816.2 Q516Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8409-01A-11D-2310-10 chr1:21014270 C>T maps to NM_020816.2 Q516Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8409-01A-11D-2310-10 chr11:22291962 G>A maps to NM_213599.2 G668G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8409-01A-11D-2310-10 chr11:22291962 G>A maps to NM_213599.2 G668G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8409-01A-11D-2310-10 chr2:86374839 C>T maps to NM_006839.2 K506K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8409-01A-11D-2310-10 chr2:86374839 C>T maps to NM_006839.2 K506K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8409-01A-11D-2310-10 chr16:23546344 C>A maps to NM_001083614.1 L274L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8409-01A-11D-2310-10 chr16:23546344 C>A maps to NM_001083614.1 L274L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8409-01A-11D-2310-10 chr10:25887314 C>G maps to NM_020752.2 T920T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8409-01A-11D-2310-10 chr10:25887314 C>G maps to NM_020752.2 T920T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8409-01A-11D-2310-10 chr17:4575432 C>T maps to ENST00000301396 E1095E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8409-01A-11D-2310-10 chr17:4575432 C>T maps to ENST00000301396 E1095E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8409-01A-11D-2310-10 chrX:109698464 A>G maps to NM_020769.2 K1361K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8409-01A-11D-2310-10 chrX:109698464 A>G maps to NM_020769.2 K1361K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8409-01A-11D-2310-10 chr8:42294727 C>T maps to NM_006749.3 S434S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8409-01A-11D-2310-10 chr8:42294727 C>T maps to NM_006749.3 S434S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8409-01A-11D-2310-10 chr7:75617797 G>C maps to NM_031925.2 L138L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8409-01A-11D-2310-10 chr7:75617797 G>C maps to NM_031925.2 L138L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8409-01A-11D-2310-10 chr18:6898506 G>A maps to ENST00000400091 S701S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8409-01A-11D-2310-10 chr18:6898506 G>A maps to ENST00000400091 S701S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8409-01A-11D-2310-10 chr3:150127404 C>T maps to NM_014779.2 L90L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8409-01A-11D-2310-10 chr3:150127404 C>T maps to NM_014779.2 L90L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8409-01A-11D-2310-10 chr6:73102465 A>G maps to NM_014989.4 G1524G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8409-01A-11D-2310-10 chr6:73102465 A>G maps to NM_014989.4 G1524G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8410-01A-11D-2310-10 chrX:134294441 G>A maps to NM_001031705.2 P106P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8410-01A-11D-2310-10 chrX:134294441 G>A maps to NM_001031705.2 P106P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8410-01A-11D-2310-10 chr21:41384993 G>A maps to NM_001389.3 N2002N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8410-01A-11D-2310-10 chr21:41384993 G>A maps to NM_001389.3 N2002N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8410-01A-11D-2310-10 chr1:115220102 G>C maps to NM_000036.2 Y452*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8410-01A-11D-2310-10 chr1:115220102 G>C maps to NM_000036.2 Y452*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8410-01A-11D-2310-10 chr4:156638324 C>T maps to NM_001130684.1 G529G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8410-01A-11D-2310-10 chr4:156638324 C>T maps to NM_001130684.1 G529G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8410-01A-11D-2310-10 chr4:79403633 C>T maps to NM_025074.6 A2899A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8410-01A-11D-2310-10 chr4:79403633 C>T maps to NM_025074.6 A2899A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8410-01A-11D-2310-10 chrX:79989614 A>G did not map to a codon.
Sequencing variant TCGA-KO-8410-01A-11D-2310-10 chrX:79989614 A>G did not map to a codon.
Sequencing variant TCGA-KO-8410-01A-11D-2310-10 chr12:77216265 A>G maps to NM_015336.2 K284K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8410-01A-11D-2310-10 chr12:77216265 A>G maps to NM_015336.2 K284K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8411-01A-11D-2310-10 chr4:187541478 G>A maps to ENST00000260147 Y2090Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8411-01A-11D-2310-10 chr4:187541478 G>A maps to ENST00000260147 Y2090Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8411-01A-11D-2310-10 chr12:58152574 C>T maps to NM_138396.4 R312R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8411-01A-11D-2310-10 chr12:58152574 C>T maps to NM_138396.4 R312R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8411-01A-11D-2310-10 chr19:52660554 A>G maps to NM_001102657.1 H127H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8411-01A-11D-2310-10 chr19:52660554 A>G maps to NM_001102657.1 H127H. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-KO-8411-01A-11D-2310-10. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-KO-8411-01A-11D-2310-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-KO-8411-01A-11D-2310-10 chr11:47356592 G>A maps to ENST00000399249 Q969*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8411-01A-11D-2310-10 chr11:47356592 G>A maps to ENST00000399249 Q969*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8411-01A-11D-2310-10 chr6:29910606 G>C maps to ENST00000376806 V49V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8411-01A-11D-2310-10 chr6:29910606 G>C maps to ENST00000376806 V49V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8411-01A-11D-2310-10 chr7:47968828 C>T maps to NM_138295.3 A344A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8411-01A-11D-2310-10 chr7:47968828 C>T maps to NM_138295.3 A344A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8411-01A-11D-2310-10 chr20:23728527 C>T maps to NM_001898.2 L117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8411-01A-11D-2310-10 chr20:23728527 C>T maps to NM_001898.2 L117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8411-01A-11D-2310-10 chr1:185891567 C>T maps to NM_031935.2 R320*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8411-01A-11D-2310-10 chr1:185891567 C>T maps to NM_031935.2 R320*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8413-01A-11D-2310-10 chr5:45267263 G>A maps to NM_021072.2 N570N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8413-01A-11D-2310-10 chr5:45267263 G>A maps to NM_021072.2 N570N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8413-01A-11D-2310-10 chrX:12735001 C>T maps to ENST00000429478 A798A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8413-01A-11D-2310-10 chrX:12735001 C>T maps to ENST00000429478 A798A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8413-01A-11D-2310-10 chr17:7578211 G>A maps to NM_001126112.1 R213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8413-01A-11D-2310-10 chr17:7578211 G>A maps to NM_001126112.1 R213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8413-01A-11D-2310-10 chr11:4903764 C>T maps to NM_001004759.1 D239D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8413-01A-11D-2310-10 chr11:4903764 C>T maps to NM_001004759.1 D239D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8413-01A-11D-2310-10 chr3:99514922 G>A maps to ENST00000429802 L727L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8413-01A-11D-2310-10 chr3:99514922 G>A maps to ENST00000429802 L727L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8413-01A-11D-2310-10 chr16:70405335 G>A maps to NM_018332.3 G415G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8413-01A-11D-2310-10 chr16:70405335 G>A maps to NM_018332.3 G415G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8413-01A-11D-2310-10 chrX:79932728 T>C maps to NM_153252.4 K1596K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8413-01A-11D-2310-10 chrX:79932728 T>C maps to NM_153252.4 K1596K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8413-01A-11D-2310-10 chr12:124819112 T>G maps to NM_006312.4 A2161A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8413-01A-11D-2310-10 chr12:124819112 T>G maps to NM_006312.4 A2161A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8414-01A-11D-2310-10 chr1:170004686 G>A maps to NM_014970.2 A175A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8414-01A-11D-2310-10 chr1:170004686 G>A maps to NM_014970.2 A175A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8414-01A-11D-2310-10 chr6:56417322 C>A maps to ENST00000361203 E5212*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8414-01A-11D-2310-10 chr6:56417322 C>A maps to ENST00000361203 E5212*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8414-01A-11D-2310-10 chr11:1092623 C>A maps to ENST00000441003 T1481T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8414-01A-11D-2310-10 chr11:1092623 C>A maps to ENST00000441003 T1481T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8414-01A-11D-2310-10 chr3:11301061 G>A maps to NM_001098211.1 A113A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8414-01A-11D-2310-10 chr3:11301061 G>A maps to NM_001098211.1 A113A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8414-01A-11D-2310-10 chr11:95561020 A>G maps to NM_014679.3 K319K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8414-01A-11D-2310-10 chr11:95561020 A>G maps to NM_014679.3 K319K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8414-01A-11D-2310-10 chr3:167039951 T>C maps to ENST00000307529 E312E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8414-01A-11D-2310-10 chr3:167039951 T>C maps to ENST00000307529 E312E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8414-01A-11D-2310-10 chr7:72863960 A>G maps to NM_032408.3 C1213C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8414-01A-11D-2310-10 chr7:72863960 A>G maps to NM_032408.3 C1213C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8414-01A-11D-2310-10 chr11:125359541 G>A maps to NM_005103.4 S44S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8414-01A-11D-2310-10 chr11:125359541 G>A maps to NM_005103.4 S44S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8414-01A-11D-2310-10 chr19:15839689 C>T maps to NM_013939.2 Y279Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8414-01A-11D-2310-10 chr19:15839689 C>T maps to NM_013939.2 Y279Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8414-01A-11D-2310-10 chr10:72496470 C>T maps to NM_139155.2 C510C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8414-01A-11D-2310-10 chr10:72496470 C>T maps to NM_139155.2 C510C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8414-01A-11D-2310-10 chr3:48697289 G>T maps to NM_001407.2 T926T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8414-01A-11D-2310-10 chr3:48697289 G>T maps to NM_001407.2 T926T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8415-01A-11D-2310-10 chr2:144765014 A>G maps to NM_001164629.2 P203P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8415-01A-11D-2310-10 chr2:144765014 A>G maps to NM_001164629.2 P203P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8415-01A-11D-2310-10 chr19:40331123 A>G maps to NM_001436.3 G71G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8415-01A-11D-2310-10 chr19:40331123 A>G maps to NM_001436.3 G71G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8415-01A-11D-2310-10 chr2:218713274 C>T maps to NM_022648.4 E530E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8415-01A-11D-2310-10 chr2:218713274 C>T maps to NM_022648.4 E530E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8415-01A-11D-2310-10 chr3:195510065 T>G maps to NM_018406.5 T2795T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8415-01A-11D-2310-10 chr3:195510065 T>G maps to NM_018406.5 T2795T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8415-01A-11D-2310-10 chr2:219350460 T>C maps to NM_020935.2 E532E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8415-01A-11D-2310-10 chr2:219350460 T>C maps to NM_020935.2 E532E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8415-01A-11D-2310-10 chr5:140736272 C>T maps to NM_018917.2 S502S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8415-01A-11D-2310-10 chr5:140736272 C>T maps to NM_018917.2 S502S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8415-01A-11D-2310-10 chr12:13828723 C>T maps to NM_000834.3 P360P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8415-01A-11D-2310-10 chr12:13828723 C>T maps to NM_000834.3 P360P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8415-01A-11D-2310-10 chr12:53169329 C>T maps to NM_015848.4 Q219Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8415-01A-11D-2310-10 chr12:53169329 C>T maps to NM_015848.4 Q219Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8415-01A-11D-2310-10 chr2:31621475 G>A maps to NM_000379.3 P132P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8415-01A-11D-2310-10 chr2:31621475 G>A maps to NM_000379.3 P132P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8415-01A-11D-2310-10 chr19:52505117 T>G maps to ENST00000354939 R62R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8415-01A-11D-2310-10 chr19:52505117 T>G maps to ENST00000354939 R62R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8415-01A-11D-2310-10 chr20:10629265 A>G maps to NM_000214.2 G500G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8415-01A-11D-2310-10 chr20:10629265 A>G maps to NM_000214.2 G500G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8416-01A-11D-2310-10 chr6:27114568 T>C maps to NM_080593.2 E3E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8416-01A-11D-2310-10 chr6:27114568 T>C maps to NM_080593.2 E3E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8416-01A-11D-2310-10 chr16:58030678 G>A maps to NM_020807.1 Y497Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8416-01A-11D-2310-10 chr16:58030678 G>A maps to NM_020807.1 Y497Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8416-01A-11D-2310-10 chr12:50045189 A>T maps to NM_175736.4 S549S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8416-01A-11D-2310-10 chr12:50045189 A>T maps to NM_175736.4 S549S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8416-01A-11D-2310-10 chr20:2306575 T>C maps to NM_003245.3 A355A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8416-01A-11D-2310-10 chr20:2306575 T>C maps to NM_003245.3 A355A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8416-01A-11D-2310-10 chrX:9900607 A>C maps to NM_001649.2 P1095P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8416-01A-11D-2310-10 chrX:9900607 A>C maps to NM_001649.2 P1095P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8416-01A-11D-2310-10 chr1:16383401 C>T maps to NM_000085.3 A685A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8416-01A-11D-2310-10 chr1:16383401 C>T maps to NM_000085.3 A685A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8416-01A-11D-2310-10 chr1:148010986 T>C maps to ENST00000310701 S550S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8416-01A-11D-2310-10 chr1:148010986 T>C maps to ENST00000310701 S550S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8416-01A-11D-2310-10 chr10:5415961 C>T maps to NM_053049.2 T93T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8416-01A-11D-2310-10 chr10:5415961 C>T maps to NM_053049.2 T93T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8416-01A-11D-2310-10 chr17:7578211 G>A maps to NM_001126112.1 R213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8416-01A-11D-2310-10 chr17:7578211 G>A maps to NM_001126112.1 R213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8416-01A-11D-2310-10 chr12:9885605 G>A maps to NM_172004.2 Y85Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8416-01A-11D-2310-10 chr12:9885605 G>A maps to NM_172004.2 Y85Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8417-01A-11D-2310-10 chrX:83361950 A>G maps to NM_014496.4 P403P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8417-01A-11D-2310-10 chrX:83361950 A>G maps to NM_014496.4 P403P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8417-01A-11D-2310-10 chr5:157078492 G>A maps to NM_178424.1 G198G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8417-01A-11D-2310-10 chr5:157078492 G>A maps to NM_178424.1 G198G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8417-01A-11D-2310-10 chr15:58837950 C>T maps to NM_000236.2 A195A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8417-01A-11D-2310-10 chr15:58837950 C>T maps to NM_000236.2 A195A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8417-01A-11D-2310-10 chr1:35223026 C>T maps to NM_005268.2 R32R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8417-01A-11D-2310-10 chr1:35223026 C>T maps to NM_005268.2 R32R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8417-01A-11D-2310-10 chr14:75265324 C>T maps to NM_019589.2 R1109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8417-01A-11D-2310-10 chr14:75265324 C>T maps to NM_019589.2 R1109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8417-01A-11D-2310-10 chr9:127915853 G>A maps to NM_001123355.1 P246P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8417-01A-11D-2310-10 chr9:127915853 G>A maps to NM_001123355.1 P246P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8417-01A-11D-2310-10 chr17:12898342 C>T maps to NM_018127.6 E615E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8417-01A-11D-2310-10 chr17:12898342 C>T maps to NM_018127.6 E615E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8417-01A-11D-2310-10 chr1:214171102 C>T maps to NM_002763.3 L409L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8417-01A-11D-2310-10 chr1:214171102 C>T maps to NM_002763.3 L409L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8417-01A-11D-2310-10 chr1:38463082 C>A maps to NM_004468.3 G279G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8417-01A-11D-2310-10 chr1:38463082 C>A maps to NM_004468.3 G279G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8323-01A-21D-2310-10 chr1:178421770 C>T maps to ENST00000263528 L647L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8325-01A-11D-2310-10 chr5:180687430 T>C maps to NM_032765.2 E128E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8326-01A-11D-2310-10 chrX:139038873 G>A maps to NM_001013403.2 A89A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8326-01A-11D-2310-10 chr11:113934294 G>T maps to NM_001018011.1 T91T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8328-01A-11D-2310-10 chr4:94411802 G>A maps to NM_001510.2 P624P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8328-01A-11D-2310-10 chr2:170129473 G>A maps to NM_004525.2 F693F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8328-01A-11D-2310-10 chr7:73020309 G>A maps to NM_032951.2 S250S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8328-01A-11D-2310-10 chr14:24646405 G>A maps to NM_005132.2 E227E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8329-01A-11D-2310-10 chr7:91851359 T>C maps to NM_194456.1 Q473Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8329-01A-11D-2310-10 chr11:95825382 C>T maps to NM_032427.1 Q604Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8329-01A-11D-2310-10 chr17:7579311 C>T maps to NM_001126112.1 T125T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8329-01A-11D-2310-10 chr10:64415146 A>T maps to NM_199452.3 P49P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8330-01A-11D-2310-10 chr4:114275927 C>T maps to NM_001148.4 R2052*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8330-01A-11D-2310-10 chrX:135956573 C>G maps to NM_002139.3 P301P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8331-01A-11D-2310-10 chr13:28840990 A>G maps to NM_175854.7 P517P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8331-01A-11D-2310-10 chr2:130832596 G>A maps to NM_001099771.2 R816R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8331-01A-11D-2310-10 chr8:10467236 G>T maps to NM_178857.5 L1457L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8332-01A-11D-2310-10 chr3:37360553 A>T maps to NM_001172713.1 K494*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8333-01A-11D-2310-10 chr17:56448328 G>T maps to NM_017763.4 I106I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8334-01A-11D-2310-10 chr4:1389129 G>A maps to NM_175918.3 G277G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8334-01A-11D-2310-10 chr17:48245012 C>T maps to NM_000023.2 L76L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8334-01A-11D-2310-10 chr16:2819138 C>T maps to NM_016333.3 S2625S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8335-01A-11D-2310-10 chr11:62417410 G>A maps to NM_030628.1 G47G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8335-01A-11D-2310-10 chr2:85573122 C>A maps to NM_017750.3 L364L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8335-01A-11D-2310-10 chr22:40802518 C>T maps to NM_015705.4 D346D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8336-01A-11D-2310-10 chr12:52774145 C>T did not map to a codon.
Sequencing variant TCGA-KL-8336-01A-11D-2310-10 chr11:6477761 C>A maps to NM_033278.2 L398L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8337-01A-11D-2310-10 chr1:1290407 A>G maps to NM_032348.2 A201A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8337-01A-11D-2310-10 chr6:42946489 C>A maps to NM_000287.3 V133V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8337-01A-11D-2310-10 chr9:124751434 C>T maps to NM_194252.2 L526L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8338-01A-11D-2310-10 chr3:65425593 C>T maps to NM_001033057.1 Q410Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8339-01A-11D-2310-10 chr14:24788627 G>T maps to NM_139247.3 P916P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8339-01A-11D-2310-10 chr2:239147554 A>G maps to NM_018645.4 A196A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8339-01A-11D-2310-10 chr14:23790863 G>A maps to NM_004643.3 L62L. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-KL-8340-01A-11D-2310-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-KL-8340-01A-11D-2310-10 chr12:6777080 C>T maps to ENST00000407384 L129L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8341-01A-11D-2310-10 chr4:843562 C>T did not map to a codon.
Sequencing variant TCGA-KL-8341-01A-11D-2310-10 chr12:64436721 T>A maps to NM_020762.2 S214S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8341-01A-11D-2310-10 chr7:5428641 G>A maps to NM_001080495.2 T271T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8341-01A-11D-2310-10 chr15:62261605 G>A maps to NM_020821.2 L935L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8342-01A-11D-2310-10 chr12:56491705 G>A maps to NM_001982.2 L866L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8342-01A-11D-2310-10 chr12:76424939 C>T maps to NM_007350.3 Q194Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8343-01A-11D-2310-10 chr1:203188923 G>T maps to NM_003465.2 I261I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8343-01A-11D-2310-10 chr4:115544545 T>G maps to NM_003360.3 A170A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8344-01A-11D-2310-10 chr4:113066759 G>A maps to NM_152400.2 L8L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8344-01A-11D-2310-10 chr14:95579560 T>C maps to NM_177438.2 R636R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8344-01A-11D-2310-10 chr18:40850386 T>C maps to NM_020783.3 G399G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8345-01A-11D-2310-10 chr4:114276400 G>A maps to NM_001148.4 G2209G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8345-01A-11D-2310-10 chr10:37486215 C>T maps to ENST00000374660 P937P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8345-01A-11D-2310-10 chr1:196744040 C>T maps to NM_021023.5 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8438-01A-11D-2310-10 chr15:22743234 A>G maps to NM_001001413.3 R540R. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-KM-8439-01A-11D-2310-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-KM-8440-01A-11D-2310-10 chr11:1643254 G>A maps to ENST00000359229 G23G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8440-01A-11D-2310-10 chr5:145838640 C>T maps to NM_006706.3 A211A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8441-01A-11D-2310-10 chr10:21805485 C>T maps to NM_207371.3 E422E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8441-01A-11D-2310-10 chr22:30681818 A>C did not map to a codon.
Sequencing variant TCGA-KM-8442-01A-11D-2310-10 chr19:40719457 C>T maps to NM_002446.3 S624S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8443-01A-11D-2310-10 chr5:9629358 G>A maps to NM_019599.2 F262F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8476-01A-11D-2310-10 chr11:73073257 G>T maps to NM_014786.3 V1556V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8476-01A-11D-2310-10 chr18:19116140 G>A maps to NM_052911.2 D683D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8476-01A-11D-2310-10 chr14:31844039 G>A maps to ENST00000389961 R609*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8476-01A-11D-2310-10 chr16:82032716 C>A maps to NM_145168.2 *394L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8477-01A-11D-2310-10 chr5:612535 C>T maps to NM_018140.3 G20G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8477-01A-11D-2310-10 chr11:71932760 C>T maps to NM_001113536.1 L241L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KM-8477-01A-11D-2310-10 chr9:79324153 A>T maps to NM_015225.2 P1012P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8418-01A-11D-2310-10 chr2:220354241 G>A maps to NM_005876.4 S2834S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8419-01A-11D-2310-10 chr7:155251200 G>A maps to NM_001427.3 G43G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8419-01A-11D-2310-10 chr22:37603326 G>A maps to NM_001051.2 A172A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8419-01A-11D-2310-10 chr19:22156869 G>A maps to NM_007153.3 F322F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8421-01A-11D-2310-10 chr2:153573941 G>A maps to ENST00000410080 G68G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8421-01A-11D-2310-10 chr1:180945771 T>C maps to NM_005819.4 Q234Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8421-01A-11D-2310-10 chr3:113114595 C>T did not map to a codon.
Sequencing variant TCGA-KN-8422-01A-11D-2310-10 chr11:117214945 G>T maps to NM_014956.4 L49L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8423-01A-11D-2310-10 chr19:36033312 T>C did not map to a codon.
Sequencing variant TCGA-KN-8423-01A-11D-2310-10 chr12:120972754 G>A maps to ENST00000458409 E47E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8424-01A-11D-2310-10 chr12:62954343 A>T maps to ENST00000393630 V1162V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8424-01A-11D-2310-10 chr8:144874054 C>T maps to NM_182706.3 P1562P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8424-01A-11D-2310-10 chr21:19770213 G>T maps to NM_002772.2 S109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8425-01A-11D-2310-10 chr19:55869901 C>T maps to NM_001145402.1 Q778Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8425-01A-11D-2310-10 chr9:135546020 G>A maps to NM_012204.2 A12A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8426-01A-11D-2310-10 chr5:76326663 C>T maps to NM_018046.4 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8427-01A-11D-2310-10 chr8:104427571 T>A maps to NM_015420.6 T118T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8427-01A-11D-2310-10 chr1:155036406 C>T maps to NM_182689.1 N36N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8427-01A-11D-2310-10 chr1:176709218 A>C maps to NM_020318.2 S1346S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8427-01A-11D-2310-10 chr10:63957975 A>C maps to NM_145307.2 P507P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8427-01A-11D-2310-10 chr1:158596632 C>T maps to NM_003126.2 W1943*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8427-01A-11D-2310-10 chr6:170871042 G>A maps to NM_003194.4 Q73Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8427-01A-11D-2310-10 chr2:20189770 G>A maps to NM_001006657.1 F2F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr6:90333670 T>C maps to ENST00000339746 P371P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr19:50305239 G>A maps to NM_014203.2 S652S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr3:142272664 A>G did not map to a codon.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr10:50534402 C>T maps to NM_001135196.1 P1271P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr9:34661942 A>G maps to NM_006664.2 *113R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr10:73768162 C>T maps to NM_004273.4 D458D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr1:10510333 C>T maps to ENST00000377049 T68T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr7:117407221 T>C maps to NM_033427.2 L929L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr2:67637128 C>T maps to NM_019002.3 R914*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr9:71668177 T>C did not map to a codon.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr19:52217096 G>A maps to NM_001523.2 G440G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr1:236762780 A>G did not map to a codon.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr4:174254649 C>T did not map to a codon.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr17:3649158 G>A maps to NM_002208.4 L740L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr12:26581016 T>C maps to NM_002223.2 T2258T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr16:19126838 A>C maps to NM_001034841.3 A352A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr1:109735385 C>T maps to NM_020775.3 R613*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr19:43965541 T>C maps to NM_014400.2 A334A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr3:49723816 G>A maps to NM_020998.3 G315G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr17:7228700 G>A maps to NM_032442.2 N486N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chrX:71360544 C>T maps to NM_001013627.2 G1049G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr7:143807470 C>T maps to NM_001005480.2 R266*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr9:130684386 C>T maps to NM_001135219.1 V308V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr22:50726134 G>A maps to NM_012401.2 S523S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr15:74327977 C>T maps to NM_033239.2 R726*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr1:161139814 G>T did not map to a codon.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr5:40681715 C>T maps to NM_000958.2 C207C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr7:4876099 G>A maps to NM_018059.4 N224N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr3:78666911 G>A maps to NM_002941.3 S1385S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr17:4500238 C>T maps to NM_001114974.1 L358L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr4:119951252 C>T maps to NM_133477.2 S441S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr19:1621855 G>A maps to NM_003200.2 S312S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr11:60689598 C>T maps to NM_024092.2 R232*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr19:2425066 C>T maps to NM_182973.1 L895L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr7:12396888 A>G did not map to a codon.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr15:41105575 C>T maps to NM_001077268.1 D357D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8429-01A-11D-2310-10 chr4:25005582 C>T maps to NM_018176.3 A376A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8429-01A-11D-2310-10 chr22:28194899 T>C maps to NM_002430.2 Q544Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8430-01A-11D-2310-10 chr2:187559046 G>A maps to NM_177454.3 Q49Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8430-01A-11D-2310-10 chr19:55870549 G>T maps to NM_001145402.1 G562G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8430-01A-11D-2310-10 chr13:21742125 C>A did not map to a codon.
Sequencing variant TCGA-KN-8430-01A-11D-2310-10 chr17:56056603 T>C maps to NM_007146.2 Q349Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8431-01A-11D-2310-10 chr6:39159434 C>T maps to NM_003740.3 W244*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8432-01A-11D-2310-10 chr7:17369577 T>A maps to NM_001621.4 S151S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8432-01A-11D-2310-10 chr2:233274093 C>T maps to NM_031313.2 Y412Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8432-01A-11D-2310-10 chr16:18806887 C>T maps to NM_015161.1 Q102Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8432-01A-11D-2310-10 chr7:74563944 C>A maps to NM_001003795.2 A564A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8432-01A-11D-2310-10 chr17:27028051 C>T maps to NM_003170.3 Q1634*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8432-01A-11D-2310-10 chr1:223465988 G>A maps to NM_017982.3 F51F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8433-01A-11D-2310-10 chr1:62675663 G>A maps to NM_019079.4 E406E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8434-01A-11D-2310-10 chr9:35044752 G>A maps to NM_203299.2 V709V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8434-01A-11D-2310-10 chr11:64600191 C>A maps to NM_017525.2 R963R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8434-01A-11D-2310-10 chr19:1108865 G>A maps to NM_014963.2 G1176G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8434-01A-11D-2310-10 chr7:143078855 C>T maps to NM_001010972.1 P64P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8403-01A-11D-2310-10 chr9:88897334 C>A maps to ENST00000452279 V60V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8403-01A-11D-2310-10 chr22:21982829 C>T maps to NM_001017964.1 R283R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8404-01A-11D-2310-10 chr6:28542930 A>T maps to NM_052923.1 T517T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8405-01A-11D-2310-10 chrX:19983777 T>A maps to ENST00000379682 R220*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8405-01A-11D-2310-10 chr19:11558366 G>A maps to ENST00000436195 E321E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8406-01A-11D-2310-10 chr19:41173903 T>C maps to NM_004756.3 Q433Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8407-01A-11D-2310-10 chr1:87045901 A>T maps to ENST00000263723 T879T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8407-01A-11D-2310-10 chr1:153907296 C>T maps to NM_014856.2 Q904Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8407-01A-11D-2310-10 chr15:44881588 G>A maps to NM_025137.3 V1589V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8407-01A-11D-2310-10 chr6:159173010 G>A maps to ENST00000297239 K362K. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-KO-8408-01A-11D-2310-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-KO-8408-01A-11D-2310-10 chr17:40049425 T>C maps to ENST00000401700 G531G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8408-01A-11D-2310-10 chr12:88465165 A>G maps to NM_025114.3 D1972D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8408-01A-11D-2310-10 chr19:17088186 G>A maps to ENST00000443236 F640F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8408-01A-11D-2310-10 chr15:41501705 C>T maps to NM_152596.2 W118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8410-01A-11D-2310-10 chr11:1092890 C>A maps to ENST00000441003 T1570T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8411-01A-11D-2310-10 chr12:10205355 C>T maps to NM_207345.2 L24L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8411-01A-11D-2310-10 chr22:28194932 T>C maps to NM_002430.2 Q533Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8411-01A-11D-2310-10 chr18:55143924 G>A maps to NM_004852.2 S495S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8411-01A-11D-2310-10 chr1:68697907 T>C maps to NM_024911.6 Q25Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8413-01A-11D-2310-10 chr17:45234385 G>T maps to NM_001114091.1 V245V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8413-01A-11D-2310-10 chr12:11546873 T>C maps to NM_006248.3 K46K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8413-01A-11D-2310-10 chr7:100780309 C>T maps to NM_000602.3 P372P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8414-01A-11D-2310-10 chr11:74800083 G>A maps to NM_001005285.1 H225H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8415-01A-11D-2310-10 chr1:190067564 G>A maps to NM_199051.1 Y628Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8415-01A-11D-2310-10 chr17:39324346 G>T maps to NM_033187.1 R26R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8415-01A-11D-2310-10 chr19:16982118 G>A maps to NM_015260.1 T866T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8416-01A-11D-2310-10 chr5:145838655 G>A maps to NM_006706.3 Q216Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8417-01A-11D-2310-10 chr14:105416789 T>C maps to NM_138420.2 P1666P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8323-01A-21D-2310-10 chr15:81295652 G>A maps to NM_022566.2 R347R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8323-01A-21D-2310-10 chr15:81295652 G>A maps to NM_022566.2 R347R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8324-01A-11D-2310-10 chr2:186689202 A>G maps to NM_173651.2 L6912L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8324-01A-11D-2310-10 chr2:186689202 A>G maps to NM_173651.2 L6912L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8346-01A-11D-2310-10 chr6:31977380 T>C maps to NM_032470.3 G477G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KL-8346-01A-11D-2310-10 chr6:31977380 T>C maps to NM_032470.3 G477G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr15:81295559 C>T maps to NM_022566.2 G316G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr15:81295559 C>T maps to NM_022566.2 G316G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr3:71804264 C>T maps to NM_018971.1 C355C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr3:71804264 C>T maps to NM_018971.1 C355C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KO-8415-01A-11D-2310-10 chr21:11012927 A>T did not map to a codon.
Sequencing variant TCGA-KO-8415-01A-11D-2310-10 chr21:11012927 A>T did not map to a codon.
Sequencing variant TCGA-KL-8330-01A-11D-2310-10 chr22:19137289 G>A maps to NM_005315.1 F133F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KN-8428-01A-11D-2310-10 chr20:21376974 G>A maps to NM_033176.1 Y213Y. Only missense variants will be evaluated by CHASM.
